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Sample records for surface seawater concentrations

  1. Temporal variations of 137Cs concentrations in the surface seawater and marine organisms collected from the Japanese coast during the 1980's

    International Nuclear Information System (INIS)

    Yamada, M.; Nagaya, Y.

    1998-01-01

    The surface seawater and marine organisms were collected on the Japanese coast and analyzed for their 137 Cs concentrations during the 1980's. The 137 Cs concentrations in surface seawater decreased almost exponentially with time and the 137 Cs removal rate constant was estimated to be 0.0445 y -1 . The 137 Cs concentrations in marine organisms also decreased almost exponentially with time. The environmental half-lives of 137 Cs in muscle and viscera of fish, crustacea, and seaweed were estimated from the measured decreases of 137 Cs concentrations. (author)

  2. Dynamic Bubble Surface Tension Measurements in Northwest Atlantic Seawater

    Science.gov (United States)

    Kieber, D. J.; Long, M. S.; Keene, W. C.; Kinsey, J. D.; Frossard, A. A.; Beaupre, S. R.; Duplessis, P.; Maben, J. R.; Lu, X.; Chang, R.; Zhu, Y.; Bisgrove, J.

    2017-12-01

    Numerous reports suggest that most organic matter (OM) associated with newly formed primary marine aerosol (PMA) originates from the sea-surface microlayer. However, surface-active OM rapidly adsorbs onto bubble surfaces in the water column and is ejected into the atmosphere when bubbles burst at the air-water interface. Here we present dynamic surface tension measurements of bubbles produced in near surface seawater from biologically productive and oligotrophic sites and in deep seawater collected from 2500 m in the northwest Atlantic. In all cases, the surface tension of bubble surfaces decreased within seconds after the bubbles were exposed to seawater. These observations demonstrate that bubble surfaces are rapidly saturated by surfactant material scavenged from seawater. Spatial and diel variability in bubble surface evolution indicate corresponding variability in surfactant concentrations and/or composition. Our results reveal that surface-active OM is found throughout the water column, and that at least some surfactants are not of recent biological origin. Our results also support the hypothesis that the surface microlayer is a minor to negligible source of OM associated with freshly produced PMA.

  3. Stabilization of arsenic and lead by magnesium oxide (MgO) in different seawater concentrations.

    Science.gov (United States)

    Kameda, Kentaro; Hashimoto, Yohey; Ok, Yong Sik

    2018-02-01

    Ongoing sea level rise will have a major impact on mobility and migration of contaminants by changing a number of natural phenomena that alter geochemistry and hydrology of subsurface environment. In-situ immobilization techniques may be a promising remediation strategy for mitigating contaminant mobility induced by sea level rise. This study investigated the reaction mechanisms of magnesium oxide (MgO) with aqueous Pb and As under freshwater and seawater using XAFS spectroscopy. Initial concentrations of Pb and As in freshwater strongly controlled the characteristics of the reaction product of MgO. Our study revealed that i) the removal of aqueous Pb and As by MgO was increased by the elevation of seawater concentration, and ii) the removal of As was attributed primarily to (inner-sphere) surface adsorption on MgO, independent on seawater concentrations, and iii) the retention mechanism of Pb was dependent on seawater concentrations where formations of Pb oxides and adsorption on the MgO surface were predominant in solutions with low and high salinity, respectively. The release of As fixed with MgO significantly increased in seawater compared to freshwater, although the amount of As desorbed accounted for <0.2% of total As. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Concentrations and activity ratios of 228Ra and 226Ra in surface seawater along the Pacific coast of Japan

    International Nuclear Information System (INIS)

    Ohta, T.; Mahara, Y.; Kubota, T.; Sato, J.; Gamo, T.

    2011-01-01

    We measured the 228 Ra/ 226 Ra activity ratios in surface seawater along the Pacific coast of Japan at five ports around the island of Izu-Oshima (n = 29), at Atami in Sagami Bay (n = 13), and at Umizuri Park in Tokyo Bay (n = 14). We also conducted these measurements along a transect from the open Pacific Ocean across the Kuroshio to the mouth of Tokyo Bay (n = 7). The activity ratios decreased with increasing salinity of the sampling sites. The 228 Ra/ 226 Ra activity ratios in surface seawater along the coast gradually decreased after at the end of autumn and were lowest in winter and the beginning of spring. The surface salinity along the coast decreased from summer into autumn and increased from winter to the beginning of spring. The activity ratios decreased with the increase of salinity. The variation in activity ratios at the three coastal sites is possibly caused by differing contributions of surface seawater from the Kuroshio and surrounding open ocean. The different patterns and ranges of variation in the 228 Ra/ 226 Ra activity ratios in surface seawater at Izu-Oshima, Atami, and Umizuri Park may reflect both the amount of water from the Kuroshio and vicinity, and the local bathymetry, because continental shelf sediment is the source of Ra isotopes in surface seawater. (orig.)

  5. Distribution of 137Cs in surface seawater and sediment around Sabahs Sulu-Sulawesi Sea

    International Nuclear Information System (INIS)

    Mohd Izwan Abdul Aziz; Ahmad Sanadi Abu Bakar; Yii, Mei Wo; Nurrul Assyikeen Jaffary; Zaharudin Ahmad

    2010-01-01

    The studies on distribution of 137 Cs in surface seawater and sediment around Sabahs Sulu-Sulawesi Sea were carried out during Ekspedisi Pelayaran Saintifik Perdana (EPSP) in July 2009. About sixteen and twenty five sampling locations were identified for surface seawater and sediment respectively in Sabahs Sulu-Sulawesi Sea. Large volumes of seawater samples are collected and co-precipitation technique was employed to concentrate cesium content before known amounts of 134 Cs tracer were added as yield determinant. Grab sampler were used to collect surface sediment sample. The caesium precipitate and sediment were dried and finely ground before counted using gamma-ray spectrometry system at 661 keV. The activity of 137 Cs was found in surface seawater and sediment to be in the range 1.73 Bq/ m 3 to 5.50 Bq/ m 3 and 1.15 Bq/ kg to 4.53 Bq/ kg respectively. (author)

  6. Determination of 226Ra and 228Ra in surface seawater around Sagami bay and its vicinity

    International Nuclear Information System (INIS)

    Nakano-Ohta, T.; Kubota, T.; Mahara, Y.; Yoshikawa, M.; Sato, J.

    2006-01-01

    Activity ratios of 228 Ra/ 226 Ra in surface seawaters were observed at 5 ports of Izu-Oshima, Ajiro port of Sagami bay and Umizuri park of Tokyo bay. The 228 Ra/ 226 Ra activity ratio in surface seawaters were from 0.2 to 0.7 for Izu-Oshima, from 0.2 to 0.7 for Ajiro port and from 0.6 to 0.8 for Tokyo bay. The activity ratio in surface seawaters of Izu-Oshima and Atami of Sagami bay showed lower in spring and highly in autumn, while narrow variation pattern was observed in Umizuri park of Tokyo bay. The observed variation patterns of 228 Ra/ 226 Ra in surface seawaters at Izu-oshima, Ajiro park and Umizuri park may be reflected by difference of contribution from amount of seawater far off coast with low 228 Ra concentration. (author)

  7. Fast concentration of dissolved forms of cesium radioisotopes from large seawater samples

    International Nuclear Information System (INIS)

    Jan Kamenik; Henrieta Dulaiova; Ferdinand Sebesta; Kamila St'astna; Czech Technical University, Prague

    2013-01-01

    The method developed for cesium concentration from large freshwater samples was tested and adapted for analysis of cesium radionuclides in seawater. Concentration of dissolved forms of cesium in large seawater samples (about 100 L) was performed using composite absorbers AMP-PAN and KNiFC-PAN with ammonium molybdophosphate and potassium–nickel hexacyanoferrate(II) as active components, respectively, and polyacrylonitrile as a binding polymer. A specially designed chromatography column with bed volume (BV) 25 mL allowed fast flow rates of seawater (up to 1,200 BV h -1 ). The recovery yields were determined by ICP-MS analysis of stable cesium added to seawater sample. Both absorbers proved usability for cesium concentration from large seawater samples. KNiFC-PAN material was slightly more effective in cesium concentration from acidified seawater (recovery yield around 93 % for 700 BV h -1 ). This material showed similar efficiency in cesium concentration also from natural seawater. The activity concentrations of 137 Cs determined in seawater from the central Pacific Ocean were 1.5 ± 0.1 and 1.4 ± 0.1 Bq m -3 for an offshore (January 2012) and a coastal (February 2012) locality, respectively, 134 Cs activities were below detection limit ( -3 ). (author)

  8. Bacterial biofilms utilization of low concentrations of organic matter on hydrophile surfaces submerged in seawater

    Directory of Open Access Journals (Sweden)

    Aurelia Manuela Moldoveanu

    2011-12-01

    Full Text Available A series of experiments were designed to determine the effect and the metabolic rate utilization of various types of organic matter in low concentration by heterotrophic marine bacteria using as Henrici slide technique as culture method and “in vitro” static conditions in sterile containers in order to obtain bacterial biofilms on the hydrophile surface of glass. The bacteria attachment and biofilm formation was analyzed for a period from 2 hours to 72 hours in order to observe de first phase of biofilm formation in condition of seawater supplied  with organic matter and noninvasive optic microscopy analysis. The utilization of five different  types of organic substances (amino-acid mixture, yeast extract, tryptone, glucose and starch reveled that bacteria multiply and are otherwise physiologically active in this very dilute nutrient solutions of 0.1% and also the results revealed that the bacterial growth was considerable in the case of the substances like amino-acid mixture with a total density of 30.9∙103 cells/mm2  and tryptone with a total density of 28.85∙103 cells/mm2  comparable to the other types of organic matter used to supply the seawater

  9. Comparison of techniques for pre-concentrating radium from seawater

    International Nuclear Information System (INIS)

    Bourquin, M.; Van Beek, P.; Souhaut, M.; Jeandel, C.; Reyss, J.L.; Charette, M.A.

    2008-01-01

    In the framework of the KEOPS project (Kerguelen: compared study of the Ocean and the Plateau in Surface water), we aimed to provide information on the water mass pathways and vertical mixing on the Kerguelen Plateau, Southern Ocean, based on 228 Ra profiles. Because 228 Ra activities are extremely low in this area (∼ 0.1 dpm/100 kg or ∼ 2.10 -18 g kg -1 ), the filtration of large volumes of seawater was required in order to be able to detect it with minimal uncertainty. This challenging study was an opportunity for us to test and compare methods aimed at removing efficiently radium isotopes from seawater. We used Mn-fiber that retains radium and that allows the measurement of all four radium isotopes ( 226 Ra, 228 Ra, 223 Ra, 224 Ra). First, we used Niskin bottles or the ship's seawater intake to collect large volumes of seawater that were passed onto Mn-fiber in the laboratory. Second, we filled cartridges with Mn-fiber that we placed in tandem on in situ pumps. Finally, we fixed nylon nets filled with Mn-fiber on the frame of in situ pumps to allow the passive filtration of seawater during the pump deployment. Yields of radium fixation on the cartridges filled with Mn-fiber and placed on in situ pumps are ca. 30% when combining the two cartridges. Because large volumes of seawater can be filtered with these pumps, this yields to effective volumes of 177-280 kg (that is, higher than that recovered from fourteen 12-1 Niskin bottles). Finally, the effective volume of seawater that passed through Mn-fiber placed in nylon nets and deployed during 4 h ranged between 125 and 364 kg. Consequently, the two techniques that separate Ra isotopes in situ are good alternatives for pre-concentrating radium from seawater. They can save ship-time by avoiding repeated CTD casts to obtain the large volumes of seawater. This is especially true when in situ pumps are deployed to collect suspended particles. However, both methods only provide 228 Ra/ 226 Ra ratios. The

  10. Concentration of enteric virus indicator from seawater using granular activated carbon.

    Science.gov (United States)

    Cormier, Jiemin; Gutierrez, Miguel; Goodridge, Lawrence; Janes, Marlene

    2014-02-01

    Fecal contamination of shellfish growing seawater with enteric viruses is often associated with human outbreaks of gastroenteritis. Male specific bacteriophage MS2 is correlated with those of enteric viruses in a wide range of water environments and has been used widely as a surrogate for pathogenic waterborne viruses. Since viruses in contaminated water are usually at low levels, the development of methods to concentrate viruses from water is crucial for detection purposes. In the present study, granular activated carbon was evaluated for concentration of MS2 from artificial seawater, and different parameters of the seawater were also compared. Recovery of MS2 from warm seawater (37°C) was found to be significantly greater than from cold seawater (4 and 20°C), and even greater than from fresh water (4, 20 and 37°C); the difference between seawater and fresh water became less profound when the temperatures of both were below 37°C. Although not of statistical significance, recovery of MS2 from low salinity seawater (10 and 20 parts per thousand, ppt) was greater than from high salinity seawater (30 and 40ppt). One gram of granular activated carbon was able to extract 6-log plaque forming units (PFU) of MS2 from 500ml seawater at 37°C. This study demonstrated that granular activated carbon can concentrate an enteric virus indicator from shellfish growing seawater effectively. Copyright © 2013 Elsevier B.V. All rights reserved.

  11. Predicting and measurement of pH of seawater reverse osmosis concentrates

    KAUST Repository

    Waly, Tarek; Kennedy, Maria Dolores; Witkamp, Geert-Jan; Amy, Gary L.; Schippers, Jan Cornelis

    2011-01-01

    The pH of seawater reverse osmosis plants (SWRO) is the most influential parameter in determining the degree of supersaturation of CaCO3 in the concentrate stream. For this, the results of pH measurements of the concentrate of a seawater reverse

  12. Concentration of uranium in seawater by flotation

    International Nuclear Information System (INIS)

    Nozaki, Toru; Yamashita, Hiroshi

    1986-01-01

    A method has been developed for the concentration of uranium in seawater by precipitation flotation-carbonate extraction-ion flotation. Uranium in seawater was coprecipitated with hydrated iron (III) oxide by adjusting the pH to 5.5 after addition of 1.0 x 10 -3 mol/l of iron (III) and agitating for 1 hr, and the precipitate was floated with 1.0 x 10 -5 mol/l of sodium oleate and 5.0 x 10 -5 mol/l of sodium lauryl sulfate by bubbling nitrogen through the seawater for 15 min. Uranium was extracted from the precipitate scum at the yield of 89 % with 100 ml of 1.8 % of ammonium carbonate solution by agitating for 2 hr, and floated with 1.2 x 10 -3 mol/l of cetylpyridinium chloride by bubbling nitrogen through the extract diluted 5-fold for 30 min in the recovery of about 100 %. The fairly selective recovery of uranium was obtained from 4 l of seawater at the yield of 87 % throughout the entire process. (author)

  13. Predicting and measurement of pH of seawater reverse osmosis concentrates

    KAUST Repository

    Waly, Tarek

    2011-10-01

    The pH of seawater reverse osmosis plants (SWRO) is the most influential parameter in determining the degree of supersaturation of CaCO3 in the concentrate stream. For this, the results of pH measurements of the concentrate of a seawater reverse osmosis pilot plant were compared with pH calculations based on the CO2-HCO3 --CO3 2- system equilibrium equations. Results were compared with two commercial software programs from membrane suppliers and also the software package Phreeqc. Results suggest that the real concentrate pH is lower than that of the feed and that none of the used programs was able to predict correctly real pH values. In addition, the effect of incorporating the acidity constant calculated for NaCl medium or seawater medium showed a great influence on the concentrate pH determination. The HCO3 - and CO3 2- equilibrium equation using acidity constants developed for seawater medium was the only method able to predict correctly the concentrate pH. The outcome of this study indicated that the saturation level of the concentrate was lower than previously anticipated. This was confirmed by shutting down the acid and the antiscalants dosing without any signs of scaling over a period of 12 months. © 2011 Elsevier B.V.

  14. The use of algorithms to predict surface seawater dimethyl sulphide concentrations in the SE Pacific, a region of steep gradients in primary productivity, biomass and mixed layer depth

    Directory of Open Access Journals (Sweden)

    A. J. Hind

    2011-01-01

    Full Text Available Dimethyl sulphide (DMS is an important precursor of cloud condensation nuclei (CCN, particularly in the remote marine atmosphere. The SE Pacific is consistently covered with a persistent stratocumulus layer that increases the albedo over this large area. It is not certain whether the source of CCN to these clouds is natural and oceanic or anthropogenic and terrestrial. This unknown currently limits our ability to reliably model either the cloud behaviour or the oceanic heat budget of the region. In order to better constrain the marine source of CCN, it is necessary to have an improved understanding of the sea-air flux of DMS. Of the factors that govern the magnitude of this flux, the greatest unknown is the surface seawater DMS concentration. In the study area, there is a paucity of such data, although previous measurements suggest that the concentration can be substantially variable. In order to overcome such data scarcity, a number of climatologies and algorithms have been devised in the last decade to predict seawater DMS. Here we test some of these in the SE Pacific by comparing predictions with measurements of surface seawater made during the Vamos Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx in October and November of 2008. We conclude that none of the existing algorithms reproduce local variability in seawater DMS in this region very well. From these findings, we recommend the best algorithm choice for the SE Pacific and suggest lines of investigation for future work.

  15. Determination of thorium concentration in seawater by neutron activation analysis

    International Nuclear Information System (INIS)

    Huh, C.A.; Bacon, M.P.

    1985-01-01

    A sensitive neutron activation analysis method has been successfully developed to determine 232 Th concentration in seawater. The method involves both preirradiation and postirradiation radiochemical separations. The isotopes were separated from the samples and purified during the preirradiation chemistry. 233 Pa was extracted and counted after the irradiation. Yields were monitored with 230 Th and 231 Pa tracers. The separation and purification schemes include ion exchange chromatography and solvent extraction. By this method the authors have measured 232 Th concentrations in some seawater samples that are 1 order of magnitude lower than most previously reported values. 21 references, 3 figures, 2 tables

  16. Contribution of Seawater Surfactants to Generated Primary Marine Aerosol Particles

    Science.gov (United States)

    Frossard, A. A.; Gerard, V.; Duplessis, P.; Kinsey, J. D.; Lu, X.; Zhu, Y.; Bisgrove, J.; Maben, J. R.; Long, M. S.; Chang, R.; Beaupre, S. R.; Kieber, D. J.; Keene, W. C.; Noziere, B.; Cohen, R. C.

    2017-12-01

    Surfactants account for minor fractions of total organic carbon in the ocean but may have major impacts on the surface tension of bursting bubbles at the sea surface that drive the production of primary marine aerosol particles (PMA). Surfactants associated with marine aerosol may also significantly reduce the surface tension of water thereby increasing the potential for cloud droplet activation and growth. During September and October 2016, PMA were produced from bursting bubbles in seawater using a high capacity generator at two biologically productive and two oligotrophic stations in the western North Atlantic, as part of a cruise on the R/V Endeavor. Surfactants were extracted from paired PMA and seawater samples, and their ionic compositions, total concentrations, and critical micelle concentrations (CMC) were quantified and compared for the four hydrographic stations. Higher surfactant concentrations were determined in the aerosol produced from biologically productive seawater compared to oligotrophic seawater, and the surfactants extracted from productive seawater were stronger (had lower CMCs) than those in the oligotrophic seawater. Surfactants associated with PMA and seawater in productive regions also varied over diel cycles, whereas those in the oligotrophic regions did not. This work demonstrates a direct link between surfactants in seawater and those in PMA.

  17. Temporal annual changes of 210Po concentrations in coastal seawater at Kyushu Island

    International Nuclear Information System (INIS)

    Tolmachyov, S.; Maeda, Y.; Momoshima, N.

    2001-01-01

    Polonium-210 ( 210 Po, T 1/2 =138.4 d) arises from the decay of 210 Pb (T 1/2 =22.3 yr) via intermediary 210 Bi (T 1/2 =5.03 d). Virtually, all of 210 Po in seawater is originated by in situ decay of 210 Pb, which in turn originated due to in situ decay of 226 Ra, and decay of 222 Rn in the sea and in the atmosphere followed by deposition. In seawater, 210 Po is considered an insoluble element, therefore the concentration of dissolved 210 Po is very low. The concentration levels of 210 Po in marine environmental samples are well documented, however, scanty information is available about long-scale 210 Po behavior in open oceans and/or coastal seawater. Few studies have quantified temporal variation of 210 Po concentrations with relation to environmental parameters and seasonality. Nevertheless, seasonal detail allows us to make inferences about what geochemical parameters can effected on 210 Po behavior in the marine environment that will obviously improve our present understanding of the rates and mechanisms of 210 Po scavenging from seawater column. This paper presents the results of annual observation of 210 Po concentration in the coastal seawater at Kyushu Island (Japan). Besides the 210 Po concentrations, concentration of Chlorophyll-a (Chl-a), which is generally used as an indicator of plankton activity, fluctuations of loaded suspended particulate matter (SPM) concentration (C p ) and monthly rainfall collected at the place close to the sampling area were examined to confirm if their behavior mirrors that of 210 Po. (author)

  18. Development of pre-concentration procedure for the determination of Hg isotope ratios in seawater samples

    International Nuclear Information System (INIS)

    Štrok, Marko; Hintelmann, Holger; Dimock, Brian

    2014-01-01

    Highlights: • The method for the quantitative pre-concentration of Hg from seawater was developed. • First report of Hg isotope ratios in seawater is presented. • A unique mass independent 200 Hg isotope fractionation was observed. • This fractionation has unique potential to distinguish anthropogenic and natural Hg. - Abstract: Hg concentrations in seawater are usually too low to allow direct (without pre-concentration and removal of salt matrix) measurement of its isotope ratios with multicollector-inductively coupled plasma mass spectrometry (MC-ICP-MS). Therefore, a new method for the pre-concentration of Hg from large volumes of seawater was developed. The final method allows for relatively fast (about 2.5 L h −1 ) and quantitative pre-concentration of Hg from seawater samples with an average Hg recovery of 98 ± 6%. Using this newly developed method we determined Hg isotope ratios in seawater. Reference seawater samples were compared to samples potentially impacted by anthropogenic activity. The results show negative mass dependent fractionation relative to the NIST 3133 Hg standard with δ 202 Hg values in the range from −0.50‰ to −1.50‰. In addition, positive mass independent fractionation of 200 Hg was observed for samples from reference sites, while impacted sites did not show significant Δ 200 Hg values. Although the influence of the impacted sediments is limited to the seawater and particulate matter in very close proximity to the sediment, this observation may raise the possibility of using Δ 200 Hg to distinguish between samples from impacted and reference sites

  19. Efficient purification and concentration of viruses from a large body of high turbidity seawater.

    Science.gov (United States)

    Sun, Guowei; Xiao, Jinzhou; Wang, Hongming; Gong, Chaowen; Pan, Yingjie; Yan, Shuling; Wang, Yongjie

    2014-01-01

    Marine viruses are the most abundant entities in the ocean and play crucial roles in the marine ecological system. However, understanding of viral diversity on large scale depends on efficient and reliable viral purification and concentration techniques. Here, we report on developing an efficient method to purify and concentrate viruses from large body of high turbidity seawater. The developed method characterizes with high viral recovery efficiency, high concentration factor, high viral particle densities and high-throughput, and is reliable for viral concentration from high turbidity seawater. Recovered viral particles were used directly for subsequent analysis by epifluorescence microscopy, transmission electron microscopy and metagenomic sequencing. Three points are essential for this method:•The sampled seawater (>150 L) was initially divided into two parts, water fraction and settled matter fraction, after natural sedimentation.•Both viruses in the water fraction concentrated by tangential flow filtration (TFF) and viruses isolated from the settled matter fraction were considered as the whole viral community in high turbidity seawater.•The viral concentrates were re-concentrated by using centrifugal filter device in order to obtain high density of viral particles.

  20. Trace elements release from volcanic ash to seawater. Natural concentrations in Central Mediterranean sea

    Science.gov (United States)

    Randazzo, L. A.; Censi, P.; Saiano, F.; Zuddas, P.; Aricò, P.; Mazzola, S.

    2009-04-01

    Distributions and concentrations of many minor and trace elements in epicontinental basins, as Mediterranean Sea, are mainly driven to atmospheric fallout from surroundings. This mechanism supplies an estimated yearly flux of about 1000 kg km-2 of terrigenous matter of different nature on the whole Mediterranean basin. Dissolution of these materials and processes occurring at solid-liquid interface along the water column drive the distributions of many trace elements as V, Cr, Mn, Co, Cu, and Pb with contents ranging from pmol l-1 (Co, Cd, Pb) to nmol l-1 scale in Mediterranean seawater, with some local differences in the basin. The unwinding of an oceanographic cruise in the coastal waters of Ionian Sea during the Etna's eruptive activity in summer 2001 led to the almost unique chance to test the effects of large delivery of volcanic ash to a coastal sea water system through the analyses of distribution of selected trace elements along several seawater columns. The collection of these waters and their analyses about V, Cr, Mn, Co, Cu, and Pb contents evidenced trace element concentrations were always higher (about 1 order of magnitude at least) than those measured concentrations in the recent past in Mediterranean seawater, apart from Pb. Progressive increase of concentrations of some elements with depth, sometimes changing in a "conservative" behaviour without any clear reason and the observed higher concentrations required an investigation about interaction processes occurring at solid-liquid interface between volcanic ash and seawater along water columns. This investigation involving kinetic evaluation of trace element leaching to seawater, was carried out during a 6 months time period under laboratory conditions. X-ray investigations, SEM-EDS observations and analyses on freshly-erupted volcanic ash evidenced formation of alteration clay minerals onto glass fraction surfaces. Chemical analyses carried out on coexisting liquid phase demonstrated that trace

  1. Radioactivity in the Exclusive Economic Zone of east coast Peninsular Malaysia. Distribution trends of 137Cs in surface seawater

    International Nuclear Information System (INIS)

    Zaharudin Ahmad; Zal U'yun Wan Mahmood; Hidayah Shahar; Mei Wo Yii; Ahmad Sanadi Abu Bakar

    2011-01-01

    Large volumes of surface seawater samples were collected from thirty locations in the Exclusive Economic Zone (EEZ) of the east coast Peninsular Malaysia on June 2008 to study the activity concentrations of 137 Cs. The results will serve as additional information to the existing baseline data and is very useful for monitoring fresh input of anthropogenic radionuclide into Malaysian marine environment. In this study, the activity concentrations of 137 Cs were determined using co-precipitation technique, followed by Gamma Spectrometry measurement. The mean activity concentration of 137 Cs ranged between 3.40 and 5.89 Bq/m 3 . Higher activity concentrations were observed at the coastal and towards the south of Peninsular Malaysia and were aligned with the high turbidity. These may due to the rapid diffusion of 137 Cs from suspended particulates and fine sediments into surface seawater. The activity concentrations of 137 Cs observed in this study were slightly higher than the concentrations reported in seawater at the Straits of Malacca, Vietnam and Philippines. This might be because the study area received more input of 137 Cs that originated from global fallout and then deposited on land which later being transported subsequently into the coastal zone due to siltation and erosion processes. It could also be attributed to the intrusion of river waters containing higher concentrations of 137 Cs. (author)

  2. Concentration and detection of hepatitis A virus and its indicator from artificial seawater using zeolite.

    Science.gov (United States)

    Cormier, Jiemin; Janes, Marlene

    2016-09-01

    Hepatitis A virus (HAV) infection is the leading worldwide cause of acute viral hepatitis, and outbreaks caused by this virus often occur in fecal polluted waters. Rapid concentration and detection of viral contamination in water environments can prevent economic loss and can identify the source of contamination within a short time. However, conventional methods for virus concentration are often laborious, time consuming, and subject to clogging. Furthermore, most methods require a secondary concentration step to reduce the final volume of samples. We developed a method to concentrate HAV from seawater using zeolite in aid of rapid detection. In this method,artificial seawater was inoculated with HAV (7-8 log TCID50) and filtered with zeolite. The viruses were then eluted from zeolite with sodium dodecyl sulfate and detected via real-time PCR (qPCR). Zeolite was able to concentrate HAV from artificial seawater with ∼99% efficiency in less than 5min and was more efficient in seawater than in fresh water. The entire concentration and detection can be done in approximately 2h. Compared to existing methods, this method eliminated the need for a secondary concentration step as well as the necessity to modify the pH or salinity of the seawater during concentration, and was simple and inexpensive. Copyright © 2016 Elsevier B.V. All rights reserved.

  3. Different Planctomycetes diversity patterns in latitudinal surface seawater of the open sea and in sediment.

    Science.gov (United States)

    Shu, Qinglong; Jiao, Nianzhi

    2008-04-01

    The 16S rRNA gene approach was applied to investigate the diversity of Planctomycetes in latitudinal surface seawater of the Western Pacific Ocean. The results revealed that the Pirellula-Rhodopirellula-Blastopirellula clade dominated the Planctomycetes community at all surface seawater sites while the minority genera Gemmata and Planctomyces were only found at sites H5 and H2 respectively. Although the clone frequency of the PRB clade seemed stable (between 83.3% and 94.1%) for all surface seawater sites, the retrieved Pirellula-Rhodopirellula-Blastopirellula clade presented unexpected diversity. Interestingly, low latitude seawater appeared to have higher diversity than mid-latitudes. integral-LIBSHUFF software analysis revealed significantly different diversity patterns between in latitudinal surface seawater and in the sediment of South China Sea station M2896. Our data suggested that different hydrological and geographic features contributed to the shift of Planctomycetes diversity in marine environments. This is, to our knowledge, the first systematic assessment of Planctomycetes in latitudinal surface seawater of the open sea and the first comparison of diversity pattern between surface seawater and sediments and has broadened our understanding of Planctomycetes diversity in marine environments.

  4. Development of pre-concentration procedure for the determination of Hg isotope ratios in seawater samples.

    Science.gov (United States)

    Štrok, Marko; Hintelmann, Holger; Dimock, Brian

    2014-12-03

    Hg concentrations in seawater are usually too low to allow direct (without pre-concentration and removal of salt matrix) measurement of its isotope ratios with multicollector-inductively coupled plasma mass spectrometry (MC-ICP-MS). Therefore, a new method for the pre-concentration of Hg from large volumes of seawater was developed. The final method allows for relatively fast (about 2.5Lh(-1)) and quantitative pre-concentration of Hg from seawater samples with an average Hg recovery of 98±6%. Using this newly developed method we determined Hg isotope ratios in seawater. Reference seawater samples were compared to samples potentially impacted by anthropogenic activity. The results show negative mass dependent fractionation relative to the NIST 3133 Hg standard with δ(202)Hg values in the range from -0.50‰ to -1.50‰. In addition, positive mass independent fractionation of (200)Hg was observed for samples from reference sites, while impacted sites did not show significant Δ(200)Hg values. Although the influence of the impacted sediments is limited to the seawater and particulate matter in very close proximity to the sediment, this observation may raise the possibility of using Δ(200)Hg to distinguish between samples from impacted and reference sites. Copyright © 2014 Elsevier B.V. All rights reserved.

  5. Distribution of trace metals in surface seawater and zooplankton of the Bay of Bengal, off Rushikulya estuary, East Coast of India.

    Science.gov (United States)

    Srichandan, Suchismita; Panigrahy, R C; Baliarsingh, S K; Rao B, Srinivasa; Pati, Premalata; Sahu, Biraja K; Sahu, K C

    2016-10-15

    Concentrations of trace metals such as iron (Fe), copper (Cu), zinc (Zn), cobalt (Co), nickel (Ni), manganese (Mn), lead (Pb), cadmium (Cd), chromium (Cr), arsenic (As), vanadium (V), and selenium (Se) were determined in seawater and zooplankton from the surface waters off Rushikulya estuary, north-western Bay of Bengal. During the study period, the concentration of trace metals in seawater and zooplankton showed significant spatio-temporal variation. Cu and Co levels in seawater mostly remained non-detectable. Other elements were found at higher concentrations and exhibited marked variations. The rank order distribution of trace metals in terms of their average concentration in seawater was observed as Fe>Ni>Mn>Pb>As>Zn>Cr>V>Se>Cd while in zooplankton it was Fe>Mn>Cd>As>Pb>Ni>Cr>Zn>V>Se. The bioaccumulation factor (BAF) of Fe was highest followed by Zn and the lowest value was observed with Ni. Results of correlation analysis discerned positive affinity and good relationship among the majority of the trace metals, both in seawater and zooplankton suggesting their strong affinity and coexistence. Copyright © 2016 Elsevier Ltd. All rights reserved.

  6. Distribution of trace metals in surface seawater and zooplankton of the Bay of Bengal, off Rushikulya estuary, East Coast of India

    International Nuclear Information System (INIS)

    Srichandan, Suchismita; Panigrahy, R.C.; Baliarsingh, S.K.; Srinivasa, Rao B.; Pati, Premalata; Sahu, Biraja K.; Sahu, K.C.

    2016-01-01

    Concentrations of trace metals such as iron (Fe), copper (Cu), zinc (Zn), cobalt (Co), nickel (Ni), manganese (Mn), lead (Pb), cadmium (Cd), chromium (Cr), arsenic (As), vanadium (V), and selenium (Se) were determined in seawater and zooplankton from the surface waters off Rushikulya estuary, north-western Bay of Bengal. During the study period, the concentration of trace metals in seawater and zooplankton showed significant spatio-temporal variation. Cu and Co levels in seawater mostly remained non-detectable. Other elements were found at higher concentrations and exhibited marked variations. The rank order distribution of trace metals in terms of their average concentration in seawater was observed as Fe > Ni > Mn > Pb > As > Zn > Cr > V > Se > Cd while in zooplankton it was Fe > Mn > Cd > As > Pb > Ni > Cr > Zn > V > Se. The bioaccumulation factor (BAF) of Fe was highest followed by Zn and the lowest value was observed with Ni. Results of correlation analysis discerned positive affinity and good relationship among the majority of the trace metals, both in seawater and zooplankton suggesting their strong affinity and coexistence. - Highlights: • First-hand report on trace metal concentration in zooplankton and seawater covering 2 years from this eco-sensitive region. • In seawater trace metals followed the rank order of Fe > Ni > Mn > Pb > As > Zn > Cr > V > Se > Cd. • In zooplankton the rank order was Fe > Mn > Cd > As > Pb > Ni > Cr > Zn > V > Se. • The bioaccumulation factor of Fe was highest followed by Zn. • Strong affinity, coexistence, and similar source of trace metals in the study area.

  7. Electrochemical behaviour of aluminum alloy containing various stanum concentration tested in tropical seawater

    International Nuclear Information System (INIS)

    Siti Radiah Mohd Kamarudin; Muhamad Daud; Mohd Shariff Satar

    2004-01-01

    A study has been carried out to investigate the electrochemical behaviour of sacrificial anodes with different Sh concentration in tropical seawater environment. In this work, samples of Aluminum alloy with the addition of Sn in a range of 1. 0% - 1. 7% were tested in tropical seawater at room temperature. Tafel technique was used to produce a graph of the measured current versus potential for each different Sh concentration of aluminum alloy. The results show that the variation in alloy compositions affected the values of corrosion rate, corrosion current density and potential compared to alloy without Sn content. Furthermore, it was found that small addition of Sn successfully increased aluminum ion dissolution into seawater by producing a higher value of corrosion current density and corrosion rate. (Author)

  8. Concentration of infectious aquatic rhabdoviruses from freshwater and seawater using ultrafiltration.

    Science.gov (United States)

    Grant, Amelia A M; Jakob, Eva; Richard, Jon; Garver, Kyle A

    2011-12-01

    Infectious hematopoietic necrosis virus (IHNV), viral hemorrhagic septicemia virus, and spring viremia of carp virus were concentrated and detected from freshwater and seawater samples by using hollow-fiber ultrafiltration. Within 60 min, virus in a 50-L freshwater or saltwater sample was concentrated more than 70-fold, and virus retention efficiencies were consistently greater than 88%. Retention efficiency was highly dependent upon concentrations of column blocking and sample stabilization solutions. A large column with a surface area of 1.15 m2 and a filtration capacity of 5-200 L exhibited optimal viral retention when blocked with 2% fetal bovine serum (FBS) and when the samples were supplemented with 0.1% FBS. Conversely, a small column with 100-fold less surface area and a filtering capacity of 0.5-2.0 L was optimized when blocked with 1% FBS and when the samples were supplemented with 0.1% FBS. The optimized ultrafiltration procedure was further validated with water from a tank that contained IHNV-exposed juvenile sockeye salmon Oncorhynchus nerka, resulting in an average virus retention efficiency of 91.6 +/- 4.1% (mean +/- SE). Virus quantification of concentrated samples demonstrated that IHNV shedding in sockeye salmon preceded mortality; shedding of the virus was observed to increase significantly as early as 7 d postchallenge and peaked at day 14, when virus levels reached 4.87 x 10(3) plaque-forming units/mL. We conclude that ultrafiltration is a reliable and effective method for concentrating viable aquatic rhabdoviruses from large volumes of water and has application for the analysis of environmental water samples.

  9. Vertical variability of seawater DMS in the South Pacific Ocean and its implication for atmospheric and surface seawater DMS.

    Science.gov (United States)

    Lee, Gangwoong; Park, Jooyoung; Jang, Yuwoon; Lee, Meehye; Kim, Kyung-Ryul; Oh, Jae-Ryoung; Kim, Dongseon; Yi, Hi-Il; Kim, Tong-Yup

    2010-02-01

    Shipboard measurements of atmospheric dimethylsulfide (DMS) and sea surface water DMS were performed aboard the R/V Onnuri across the South Pacific from Santiago, Chile to Fiji in February 2000. Hydrographic profiles of DMS, dissolved dimethylsulfoniopropionate (DMSP(d)), and particulate DMSP(p) in the upper 200m were obtained at 16 stations along the track. Atmospheric and sea surface water DMS concentrations ranged from 3 to 442pptv and from 0.1 to 19.9nM, respectively; the mean values of 61pptv and 2.1nM, respectively, were comparable to those from previous studies in the South Pacific. The South Pacific Gyre was distinguished by longitudinal-vertical distributions of DMS, DMSP(d), and DMSP(p), which was thought to be associated with the characteristic modification of biological activities that occurs mainly due to significant change in water temperature. The averaged DMS maximum appeared at 40m depth, whereas DMSP(p) and DMSP(d) maxima coincided with that of dissolved oxygen content at 60-80m. The sea-to-air fluxes of DMS were estimated to be 0.4-11.3micromold(-1)m(-2) (mean=2.8micromold(-1)m(-2)). A fairly good correlation between atmospheric DMS and sea-to-air DMS flux indicated that atmospheric DMS concentration was more sensitive to change in physical parameters than its photochemical removal process or surface seawater DMS concentrations.

  10. Ocean anoxia and the concentrations of molybdenum and vanadium in seawater

    International Nuclear Information System (INIS)

    Emerson, S.R.; Huested, S.S.

    1991-01-01

    Molybdenum and vanadium are relatively unreactive in seawater and are preferentially concentrated in sediments overlain by anoxic or near-anoxic water. The geochemistry of these metals is investigated by interpreting measurements from anoxic basins and sediment porewater. The concentrations of Mo and V in the water column of anoxic basins are usually lower than in oxic seawater because of uptake into highly anoxic sediments. The mechanism of removal from solution appears to be diffusion across the sediment-water interface and immobilization within the sediments. Measurements from open ocean porewater imply fluxes of vanadium from sediments that are greater than 10 times the dissolved and particulate river inflow, which is consistent with the distribution of vanadium in deep waters of the ocean and previous geochemical studies; this inconsistency shows that early diagenesis of this element is poorly understood. The authors estimate that the area of ocean sediment at present overlain by anoxic and near-anoxic water is accumulating 25±15% and 8±5% of the river influx of Mo and V, respectively. This fraction is 17±10% for uranium, which has been shown to share some of the redox behavior of Mo and V. A case is made that changes in the concentrations of these elements in the ocean should be sensitive indicators of the portion of the ocean bottom overlain by anoxic seawater through geologic time. (author). 65 refs.; 3 figs.; 5 tabs

  11. Concentration of 99Tc in seawater by coprecipitation with iron hydroxide

    International Nuclear Information System (INIS)

    Momoshima, Noriyuki; Eto, Ichiro; Muhammad Sayad; Takashima, Yoshimasa

    1991-01-01

    A method for accumulation of 99 Tc in seawater has been developed. Technetium tracer in +VII oxidation state was added to the seawater together with reducing agent, potassium pyrosulfite, and coprecipitation agent, ferric chloride. After reduction of Tc(VII) at pH 4, Tc(IV) was coprecipitated as iron hydroxide by addition of sodium hydroxide to pH 9. The reduction and coprecipitation was quantitative and overall recovery of Tc was more than 98%. The green color of iron precipitate formed at pH 9 suggested that Tc(VII) as well as ferric ion was reduced under this condition. Adsorption of Tc(IV), however, was poor for iron hydroxide which was prepared in advance indicating active surface of freshly precipitated iron hydroxide is necessary for quantitative recovery of Tc(IV). A repeating coprecipitation technique was examined for enrichment of Tc in seawater that the same iron was used repeatedly as coprecipitater. After separation of iron hydroxide with Tc(IV) from supernatant, the precipitate was dissolved by addition of acid and then new seawater which contained reducing agent and Tc(VII) was added. Reduction and coprecipitation was again carried out. Good recovery was attained for 7 repeats. The proposed repeating coprecipitation technique was applicable to a large amount of seawater without increasing the amount of iron hydroxide which is subjected to radiochemical analysis. (author)

  12. Use of a two-step ultrafiltration procedure to concentrate viral hemorrhagic septicemia virus (VHSV) in seawater.

    Science.gov (United States)

    Kim, Soo-Jin; Kim, Jong-Oh; Kim, Wi-Sik; Oh, Myung-Joo

    2015-11-01

    Viral hemorrhagic septicemia virus (VHSV) has been reported to be stable in both fresh as well as seawater, suggesting that VHSV exists in natural aquatic environments and might have an effect on the wild and cultured fish. However, VHSV is below the detectable limits of laboratory tests in natural seawater. In this study, a two-step ultrafiltration (UF) procedure was used to concentration of VHSV in seawater, providing samples that were tested for infectivity by cell culture and the presence of VHSV by quantitative reverse transcriptase PCR (qRT-PCR) methods. Overall, VHSV was approximately concentrated 100-1000 times in 1, 5 and 10 L, seawater volumes respectively: from 2.81×10(6) to 6.53×10(7)/mL and 10(3.3) to 10(3.8)TCID50/mL prior to the UF procedure, to 3.78×10(8), 1.16 × 10(11), and 9.12 × 10(10)/mL after the procedure. This is the first report of concentrating VHSV using an UF method that was specifically designed for seawater samples. In addition, the two-step UF procedure appears to be compatible with viral cell culture and qRT-PCR methods. Copyright © 2015 Elsevier B.V. All rights reserved.

  13. Perfluoroalkyl acids in surface seawater from the North Pacific to the Arctic Ocean: Contamination, distribution and transportation.

    Science.gov (United States)

    Li, Lei; Zheng, Hongyuan; Wang, Tieyu; Cai, Minghong; Wang, Pei

    2018-03-16

    The bioaccumulative, persistent and toxic properties of long-chain perfluoroalkyl acids (PFAAs) resulted in strict regulations on PFAAs, especially in developed countries. Consequently, the industry manufacturing of PFAAs shifts from long-chain to short-chain. In order to better understand the pollution situation of PFAAs in marine environment under this new circumstance, the occurrence of 17 linear PFAAs was investigated in 30 surface seawater samples from the North Pacific to Arctic Ocean (123°E to 24°W, 32 to 82°N) during the sixth Chinese Arctic Expedition in 2014. Total concentrations of PFAAs (∑PFAAs) were between 346.9 pg per liter (pg/L) to 3045.3 pg/L. The average concentrations of ∑PFAAs decreased in the order of East China Sea (2791.4 pg/L, n = 2), Sea of Japan (East Sea) (832.8 pg/L, n = 6), Arctic Ocean (516.9 pg/L, n = 7), Chukchi Sea (505.2 pg/L, n = 4), Bering Sea (501.2 pg/L, n = 8) and Sea of Okhotsk (417.7 pg/L, n = 3). C4 to C9 perfluoroalkyl carboxylic acids (PFCAs) were detected in more than 80% of the surface water samples. Perfluorobutanoic acid (PFBA) was the most prevalent compound and perfluorooctanoic acid (PFOA) was the second abundant homolog. The concentration of individual PFAAs in the surface seawater of East China Sea was much higher than other sampling seas. As the spatial distribution of PFAAs in the marine environment was mainly influenced by the river inflow from the basin countries, which proved the large input from China. Furthermore, the marginal seas of China were found with the greatest burden of PFOA comparing the pollution level in surface seawater worldwide. PFBA concentration in the surrounding seas of China was also high, but distributed more evenly with an obvious increase in recent years. This large-scale monitoring survey will help the improvement and development of PFAAs regulations and management, where production shift should be taken into consideration. Copyright

  14. Determination of trace metals in coastal seawater around Okinawa and its multielement profiling analysis

    International Nuclear Information System (INIS)

    Itoh, Akihide; Ishigaki, Teruyuki; Arakaki, Teruo; Yamada, Ayako; Yamaguchi, Mami; Kabe, Noriko

    2009-01-01

    In the present study, trace metals in coastal surface seawater around Okinawa were determined by inductively coupled plasma mass spectrometry (ICP-MS) with chelating disk preconcentration. As a result, the concentrations of V, Mn, Co, Ni, Cu, Zn, Mo, Cd, Pb, and U were obtained in the range from 10 μgL -1 to 0.001 μgL -1 for 6 samples. In addition, multielement profiling analyses were carried out using analytical values obtained in order to elucidate the features of trace metals in each coastal sea area. For coastal surface seawater near an urban area, the analytical values for Zn, Cu, Mn, and Pb were higher by more than 10-fold the literature values for open-surface seawater, and those of Cd were also relatively high. Such a trend concerning the multi-element profile was almost similar to the literature values for coastal seawater of the main island of Japan. On the other hand, the analytical values of most elements for coastal surface seawater near a suburb area were in the range from 0.5 to 5 fold, compared to the literature values for open surface seawater. From multielement profiling analyses for nutrient type elements in marine chemistry, it was suggested that the concentrations of Zn and Cd in a coral sea area normalized to literature values for open surface-seawater were higher than those of Ni and Cu. (author)

  15. Disk mini-adsorbers with radial flow for determination of 234Th concentration in seawater

    International Nuclear Information System (INIS)

    Gulin, S.B.; Gorelov, Yu.S.; Sidorov, I.G.; Proskurnin, V.Yu.

    2013-01-01

    A modified method has been developed for measuring the 234 Th concentration in seawater, which is based upon the use of MnO 2 -impregnated disk mini adsorbers with radial flow connected in-line and the direct beta counting of 234 Th and/or its daughter 234m Pa. This allows determining the 234 Th concentration in a relatively small volume of seawater (20-50 L) with the possibility to check the extraction efficiency in every individual sample. The field testing, which was carried out at different areas of Sevastopol Bay during different seasons, has shown applicability of the proposed method to evaluate particle fluxes in marine environments within a wide range of concentrations of suspended matter. (author)

  16. A rapid approach for measuring silver nanoparticle concentration and dissolution in seawater by UV-Vis.

    Science.gov (United States)

    Sikder, Mithun; Lead, Jamie R; Chandler, G Thomas; Baalousha, Mohammed

    2018-03-15

    Detection and quantification of engineered nanoparticles (NPs) in environmental systems is challenging and requires sophisticated analytical equipment. Furthermore, dissolution is an important environmental transformation process for silver nanoparticles (AgNPs) which affects the size, speciation and concentration of AgNPs in natural water systems. Herein, we present a simple approach for the detection, quantification and measurement of dissolution of PVP-coated AgNPs (PVP-AgNPs) based on monitoring their optical properties (extinction spectra) using UV-vis spectroscopy. The dependence of PVP-AgNPs extinction coefficient (ɛ) and maximum absorbance wavelength (λ max ) on NP size was experimentally determined. The concentration, size, and extinction spectra of PVP-AgNPs were characterized during dissolution in 30ppt synthetic seawater. AgNPs concentration was determined as the difference between the total and dissolved Ag concentrations measured by inductively coupled plasma-mass spectroscopy (ICP-MS); extinction spectra of PVP-AgNPs were monitored by UV-vis; and size evolution was monitored by atomic force microscopy (AFM) over a period of 96h. Empirical equations for the dependence of maximum absorbance wavelength (λ max ) and extinction coefficient (ɛ) on NP size were derived. These empirical formulas were then used to calculate the size and concentration of PVP-AgNPs, and dissolved Ag concentration released from PVP-AgNPs in synthetic seawater at variable particle concentrations (i.e. 25-1500μgL -1 ) and in natural seawater at particle concentration of 100μgL -1 . These results suggest that UV-vis can be used as an easy and quick approach for detection and quantification (size and concentration) of sterically stabilized PVP-AgNPs from their extinction spectra. This approach can also be used to monitor the release of Ag from PVP-AgNPs and the concurrent NP size change. Finally, in seawater, AgNPs dissolve faster and to a higher extent with the decrease in NP

  17. Surfactant induced complex formation and their effects on the interfacial properties of seawater.

    Science.gov (United States)

    Guzmán, Eduardo; Santini, Eva; Benedetti, Alessandro; Ravera, Francesca; Ferrari, Michele; Liggieri, Libero

    2014-11-01

    The effect of a cationic surfactant, hexadecyltrimethylammonium bromide (CTAB), on the interfacial properties of seawater has been studied by dynamic and equilibrium surface tension and by dilational rheology essays. Important modifications of the surface tension and dilational rheology response have been observed already at the very low CTAB concentrations, where the effects due to the high ionic strength are negligible. The comparison with the effects of CTAB in different seawater models, or in natural seawater fractions, points out the establishment of strong interactions between the surfactant molecules and the lipophilic fraction of organic material dispersed/dissolved in seawater, affecting the interfacial activity of the molecules. Considering the biochemical richness of seawater, these results can be explained assuming interaction mechanisms and adsorption schemes similar to those speculated for protein and other macromolecules in the presence of surfactants, which in fact show similar features. Thus already at the low concentrations the surfactant molecules form highly surface-active complexes with part of the organic fraction of seawater. At the larger surfactant concentrations these complexes compete for adsorption with an excess of free CTAB molecules which, according to the thermodynamic conditions, are most favoured to occupy the liquid interface. The results of this study underline the important role of the sea organic content in enhancing the surface-activity of surfactants, which is relevant for a deeper understand of the direct and indirect effects of these types of pollutants on the physico-chemical environment in the sea coastal areas and develop mitigation strategies. Copyright © 2014 Elsevier B.V. All rights reserved.

  18. Strontium (Sr) separation from seawater using titanate adsorbents: Effects of seawater matrix ions on Sr sorption behavior

    Science.gov (United States)

    Ryu, Jungho; Hong, Hye-jin; Ryu, Taegong; Park, In-Su

    2017-04-01

    Strontium (Sr) which has many industrial applications such as ferrite magnet, ceramic, and fire works exists in seawater with the concentration of approximately 7 mg/L. In previous report estimating economic potential on recovery of various elements from seawater in terms of their commercial values and concentrations in seawater, Sr locates upper than approximate break-even line, which implies Sr recovery from seawater can be potentially profitable. Recently, Sr separation from seawater has received great attention in the environmental aspect after Fukushima Nuclear Power Plant (NPP) accident which released much amount of radioactive Sr and Cs. Accordingly, the efficient separation of radioactive elements released to seawater has become critical as an important technological need as well as their removal from radioactive wastes. So far, it has been introduced to separate Sr from aqueous media by various methods including solvent extraction, adsorption by solid materials, and ion exchange. Among them, the adsorption technique using solid adsorbents is of great interest for selectively separating Sr from seawater with respect to low concentration level of Sr. In this study, we synthesized titanate nanotube (TiNT) by simple hydrothermal reaction, characterized its physicochemical properties, and systematically evaluated Sr sorption behavior under various reaction conditions corresponding to seawater environment. The synthesized TiNT exhibited the fibril-type nanotube structure with high specific surface area of 260 m2/g. The adsorption of Sr on TiNT rapidly occurred following pseudo-second-order kinetic model, and was in good agreement with Langmuir isotherm model, indicating maximum adsorption capacity of 97 mg/g. Based on Sr uptake and Na release with stoichiometric balance, sorption mechanism of Sr on TiNT was found to be ion-exchange between Na in TiNT lattice and Sr in solution phase, which was also confirmed by XRD and Raman analysis. Among competitive ions, Ca

  19. Standard practice for exposing and evaluating metals and alloys in surface seawater

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2000-01-01

    1.1 This practice covers conditions for the exposure of metals, alloys, and other materials in natural surface seawater such as those typically found in bays, harbors, channels, and so forth, as contrasted with deep ocean testing. This practice covers full immersion, tidal zone and related splash, and spray zone exposures. 1.2 This practice sets forth general procedures that should be followed in conducting seawater exposure tests so that meaningful comparisons may be made from one location to another. 1.3 This practice identifies recommended procedures for evaluating the effects of natural surface seawater on the materials exposed. 1.4 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only. This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regula...

  20. Chlorine-36 in seawater

    International Nuclear Information System (INIS)

    Argento, David C.; Stone, John O.; Keith Fifield, L.; Tims, Stephen G.

    2010-01-01

    Natural cosmogenic 36 Cl found in seawater originates from spallation of atmospheric 40 Ar, capture of secondary cosmic-ray neutrons by dissolved 35 Cl, and river runoff which contains 36 Cl produced in situ over the surface of the continents. The long residence time of chloride in the ocean and long half-life of 36 Cl compared to the oceanic mixing time should result in a homogenous 36 Cl/Cl ratio throughout the ocean. Production by neutron capture in the course of nuclear weapons testing should be insignificant averaged over the oceans as a whole, but may have led to regions of elevated 36 Cl concentration. Previous attempts to measure the 36 Cl/Cl ratio of seawater have been hindered by interferences, contamination, or insufficient analytic sensitivity. Here we report preliminary measurements on seawater samples, which demonstrate that the 36 Cl/Cl ratio is 0.5 ± 0.3 x 10 -15 , in reasonable agreement with calculated contributions from the sources listed above.

  1. Determining subnanomolar iron concentrations in oceanic seawater using a siderophore-modified film analyzed by infrared spectroscopy.

    Science.gov (United States)

    Roy, Eric G; Jiang, Cuihong; Wells, Mark L; Tripp, Carl

    2008-06-15

    Iron is a bioactive trace element in seawater that regulates photosynthetic carbon dioxide drawdown and export from surface waters by phytoplankton in upward of 40% of the world's oceans. While autonomous sensor arrays are beginning to provide high-resolution data on temporal and spatial scales for some key oceanographic parameters, current analytical methods for iron are not amenable to autonomous platforms because of the need for user involvement and wet chemistry-based approaches. As a result, very large gaps remain in our understanding of iron distribution and chemistry in seawater. Here we present a straightforward nanostructure-based method to measure dissolved iron in natural seawater. The device comprises an iron-specific chelating biomolecule, desferrioxamine B (DFB), covalently immobilized on a mesoporous silica film. Changes in infrared spectral signatures of the immobilized DFB upon Fe(III) complexation provide an accurate and precise measure of iron on the surface of a chip exposed to seawater. The current system has a detection limit of approximately 50 pM for a 1-L sample at pH 1.7 and was used to measure dissolved iron in subarctic Pacific waters without interference from other elements in seawater. This technology provides a major step toward obtaining accurate iron measurements on autonomous research platforms.

  2. Diversity of bacterioplankton in the surface seawaters of Drake Passage near the Chinese Antarctic station.

    Science.gov (United States)

    Xing, Mengxin; Li, Zhao; Wang, Wei; Sun, Mi

    2015-07-01

    The determination of relative abundances and distribution of different bacterial groups is a critical step toward understanding the functions of various bacteria and its surrounding environment. Few studies focus on the taxonomic composition and functional diversity of microbial communities in Drake Passage. In this study, marine bacterioplankton communities from surface seawaters at five locations in Drake Passage were examined by 16S rRNA gene sequence analyses. The results indicated that psychrophilic bacteria were the most abundant group in Drake Passage, and mainly made up of Bacillus, Aeromonas, Psychrobacter, Pseudomonas and Halomonas. Diversity analysis showed that surface seawater communities had no significant correlation with latitudinal gradient. Additionally, a clear difference among five surface seawater communities was evident, with 1.8% OTUs (only two) belonged to Bacillus consistent across five locations and 71% OTUs (80) existed in only one location. However, the few cosmopolitans had the largest population sizes. Our results support the hypothesis that the dominant bacterial groups appear to be analogous between geographical sites, but significant differences may be detected among rare bacterial groups. The microbial diversity of surface seawaters would be liable to be affected by environmental factors. © FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

  3. Radionuclides and particles in seawater with the large volume in situ filtration and concentration system in the coastal waters off Japan

    International Nuclear Information System (INIS)

    Aono, Tatsuo; Nakanishi, Takahiro; Okubo, Ayako; Zheng, Jian; Yamada, Masatoshi; Kusakabe, Masashi

    2008-01-01

    It is necessary to determine the radionuclides in dissolved and particulate state in order to clarify the distributions and behavior of these in seawater. Because the concentrations of radionuclides and particles are very low in the ocean, it is difficult to concentrate and fractionate the particulate matters with the filtration systems in seawater. The large volume in situ filtration and concentration system (LV-FiCS) was developed to collect various forms of trace radionuclides and particles in seawater. The LV-FiCS has been operated during several cruises in the coastal waters off Japan, and several m 3 of seawaters were filtered through different kinds of filters and then pass through the adsorbents to concentrate radionuclides simultaneously. This system could be shown the vertical profiles of thorium with the size-fractionated method and the behavior of these nuclides in the ocean. (author)

  4. Monitoring of uranium isotopes in seaweeds and seawater

    International Nuclear Information System (INIS)

    Meena, Balram; Mehendarge, S.T.; Baburajan, A.; Rao, D.D.

    2012-01-01

    The paper deals with the concentration of uranium in seawater and different types of seaweed found along the coast line of Tarapur marine environment. The seaweeds are the trend indicators of heavy metals and radionuclides present in the aquatic environment. Seaweeds also serve as a food to the marine organisms and thus can enter the human being through food chain. The higher concentration of uranium in seafood may have radiological impact on human health. The Tarapur Atomic Power Station is adjoined to the sea and has a rocky surface area, which act as a good dwelling for the growth and survival of marine biota. In present study, separation and measurements were made to determine the uranium concentration in seaweed seawater at Tarapur coastal environment

  5. Seawater Polluted with Highly Concentrated Polycyclic Aromatic Hydrocarbons Suppresses Osteoblastic Activity in the Scales of Goldfish, Carassius auratus.

    Science.gov (United States)

    Suzuki, Nobuo; Sato, Masayuki; Nassar, Hossam F; Abdel-Gawad, Fagr Kh; Bassem, Samah M; Yachiguchi, Koji; Tabuchi, Yoshiaki; Endo, Masato; Sekiguchi, Toshio; Urata, Makoto; Hattori, Atsuhiko; Mishima, Hiroyuki; Shimasaki, Youhei; Oshima, Yuji; Hong, Chun-Sang; Makino, Fumiya; Tang, Ning; Toriba, Akira; Hayakawa, Kazuichi

    2016-08-01

    We have developed an original in vitro bioassay using teleost scale, that has osteoclasts, osteoblasts, and bone matrix as each marker: alkaline phosphatase (ALP) for osteoblasts and tartrate-resistant acid phosphatase (TRAP) for osteoclasts. Using this scale in vitro bioassay, we examined the effects of seawater polluted with highly concentrated polycyclic aromatic hydrocarbons (PAHs) and nitro-polycyclic aromatic hydrocarbons (NPAHs) on osteoblastic and osteoclastic activities in the present study. Polluted seawater was collected from two sites (the Alexandria site on the Mediterranean Sea and the Suez Canal site on the Red Sea). Total levels of PAHs in the seawater from the Alexandria and Suez Canal sites were 1364.59 and 992.56 ng/l, respectively. We were able to detect NPAHs in both seawater samples. Total levels of NPAHs were detected in the seawater of the Alexandria site (12.749 ng/l) and the Suez Canal site (3.914 ng/l). Each sample of polluted seawater was added to culture medium at dilution rates of 50, 100, and 500, and incubated with the goldfish scales for 6 hrs. Thereafter, ALP and TRAP activities were measured. ALP activity was significantly suppressed by both polluted seawater samples diluted at least 500 times, but TRAP activity did not change. In addition, mRNA expressions of osteoblastic markers (ALP, osteocalcin, and the receptor activator of the NF-κB ligand) decreased significantly, as did the ALP enzyme activity. In fact, ALP activity decreased on treatment with PAHs and NPAHs. We conclude that seawater polluted with highly concentrated PAHs and NPAHs influences bone metabolism in teleosts.

  6. Effect of different seawater Mg2 + concentrations on calcification in two benthic foraminifers

    Science.gov (United States)

    Mewes, Antje; Langer, Gerald; de Nooijer, Lennart Jan; Bijma, Jelle; Reichart, Gert-Jan

    2014-01-01

    Magnesium, incorporated in foraminiferal calcite (Mg/CaCC), is used intensively to reconstruct past seawater temperatures but, in addition to temperature, the Mg/CaCC of foraminiferal tests also depends on the ratio of Mg and Ca in seawater (Mg/CaSW). The physiological mechanisms responsible for these proxy relationships are still unknown. This culture study investigates the impact of different seawater [Mg2 +] on calcification in two benthic foraminiferal species precipitating contrasting Mg/CaCC: Ammonia aomoriensis, producing low-Mg calcite and Amphistegina lessonii, producing intermediate-Mg calcite. Foraminiferal growth and test thickness were determined and, Mg/Ca was analyzed using Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS). Results show that at present-day seawater Mg/CaSW of ~ 5, both species have highest growth rates, reflecting their adaptation to modern seawater element concentrations. Test thickness is not significantly affected by different Mg/CaSW. The relationship between Mg/CaSW and Mg/CaCC shows a distinct positive y-axis intercept, possibly reflecting at least two processes involved in foraminiferal biomineralization. The associated Mg partition (DMg) changes non-linearly with increasing Mg/CaSW, hence suggesting that the DMg is best described by an exponential function approaching an asymptote. PMID:26089590

  7. Naphthalene degradation in seawater by UV irradiation: The effects of fluence rate, salinity, temperature and initial concentration

    International Nuclear Information System (INIS)

    Jing, Liang; Chen, Bing; Zhang, Baiyu; Zheng, Jisi; Liu, Bo

    2014-01-01

    Highlights: • The removal of naphthalene follows first order kinetics in seawater. • Irradiance and temperature are the most influential factors. • An increase in irradiance can linearly promote photodegradation. • High salinity suppresses the photodegradation of naphthalene. - Abstract: A large amount of oil pollution at sea is produced by the operational discharge of oily wastewater. The removal of polycyclic aromatic hydrocarbons (PAHs) from such sources using UV irradiation has become attractive, yet the photolysis mechanism in seawater has remained unclear. This study examines the photodegradation kinetics of naphthalene in natural seawater through a full factorial design of experiments (DOE). The effects of fluence rate, salinity, temperature and initial concentration are investigated. Results show that fluence rate, temperature and the interaction between temperature and initial concentration are the most influential factors. An increase in fluence rate can linearly promote the photodegradation process. Salinity increasingly impedes the removal of naphthalene because of the existence of free-radical scavengers and photon competitors. The results will help understand the photolysis mechanism of PAHs and develop more effective methods for treating oily seawater generated from offshore industries

  8. Distribution of radionuclides in surface seawater obtained by an aerial radiological survey

    International Nuclear Information System (INIS)

    Inomata, Yayoi; Aoyama, Michio; Hirose, Katsumi; Sanada, Yukihisa; Torii, Tatsuo; Tsubono, Takaki; Tsumune, Daisuke; Yamada, Masatoshi

    2014-01-01

    We investigated the distribution in seawater of anthropogenic radionuclides from the Fukushima Daiichi Nuclear Power Plant (FNPP1) as preliminary attempt using a rapid aerial radiological survey performed by the U.S. Department of Energy National Nuclear Security Administration on 18 April 2011. We found strong correlations between in-situ activities of 131 I, 134 Cs, and 137 Cs measured in surface seawater samples and gamma-ray peak count rates determined by the aerial survey (correlation coefficients were 0.89 for 131 I, 0.96 for 134 Cs, and 0.92 for 137 Cs). The offshore area of high radionuclide activity extended south and southeast from the FNPP1. The maximum activities of 131 I, 134 Cs, and 137 Cs were 329, 650, and 599 Bq L -1 , respectively. The 131 I/ 137 Cs ratio in surface water of the high-activity area ranged from 0.6 to 0.7. Considering the radioactive decay of 131 I (half-life 8.02 d), we determined that the radionuclides in this area were directly released from FNPP1 to the ocean. We confirm that aerial radiological surveys can be effective for investigating the surface distribution of anthropogenic radionuclides in seawater. Our model reproduced the distribution pattern of radionuclides derived from the FNPP1, although results simulated by a regional ocean model were underestimated. (author)

  9. Identification and characterization of 1,4-dioxane-degrading microbe separated from surface seawater by the seawater-charcoal perfusion apparatus.

    Science.gov (United States)

    Matsui, Ryotaro; Takagi, Kazuhiro; Sakakibara, Futa; Abe, Tomoko; Shiiba, Kiwamu

    2016-06-01

    To determine the concentration of soluble 1,4-dioxane during biodegradation, a new method using of high-performance liquid chromatography equipped with a hydrophilic interaction chromatography column was developed. The developed method enabled easy and rapid determination of 1,4-dioxane, even in saline medium. Microbes capable of degrading 1,4-dioxane were selected from the seawater samples by the seawater-charcoal perfusion apparatus. Among 32 candidate 1,4-dioxane degraders,, strain RM-31 exhibited the strongest 1,4-dioxane degradation ability. 16S rDNA sequencing and the similarity analysis of strain RM-31 suggested that this organism was most closely related to Pseudonocardia carboxydivorans. This species is similar to Pseudonocardia dioxanivorans, which has previously been reported as a 1,4-dioxane degrader. Strain RM-31 could degrade 300 mg/L within 2 days. As culture incubation times increasing, the residual 1,4-dioxane concentration was decreasing and the total protein contents extracted from growth cells were increasing. The optimum initial pH of the broth medium and incubation temperature for 1,4-dioxane degradation were pH 6-8 and 25 °C. The biodegradation rate of 1,4-dioxane by strain RM-31 at 25 °C in broth medium with 3 % NaCl was almost 20 % faster than that without NaCl. It was probably a first bacteria from the seawater that can exert a strong degrading ability.

  10. Plutonium determination in seawater by inductively coupled plasma mass spectrometry: A review.

    Science.gov (United States)

    Cao, Liguo; Bu, Wenting; Zheng, Jian; Pan, Shaoming; Wang, Zhongtang; Uchida, Shigeo

    2016-05-01

    Knowing the concentration and isotopic ratio of Pu in seawater is of critical importance for assessing Pu contamination and investigating oceanic processes. In recent decades, the concentration of (239+240)Pu in seawater, particularly for surface seawater, has presented an exponential decreasing trend with time; thus determination of Pu in seawater has become a challenge nowadays. Here, we have summarized and critically discussed a variety of reported analytical methods for Pu determination in seawater sample based on inductively coupled plasma mass spectrometry (ICP-MS) analytical technique for rapid ultra-trace detection of Pu. Generally, pretreatments for seawater sample include co-precipitation, valence adjustment and chemical separation and purification procedures, all of which are comprehensively reviewed. Overall, the selected anion-exchange, extraction resins and operation condition are important for decontamination of interference from matrix elements and achieving satisfactory chemical yields. In addition, other mass spectrometric and radiometric detections are briefly addressed and compared with the focus on assessing ICP-MS. Finally, we discuss some issues and prospects in determination and application of Pu isotopes in seawater samples for future research. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Studies on rare earth elements in seawater and uptake by marine organisms

    International Nuclear Information System (INIS)

    Suzuki, H.; Koyanagi, T.; Saiki, M.

    1975-01-01

    The contents of rare earth elements in marine environmental samples were determined by neutron activation analysis to examine the existing state in coastal seawater and the concentration by marine organisms of the elements. Seawater was filtered through a Millipore filter GS (pore size 0.22 μm), before the analysis. Some of the seawater was treated with HC1 solution before filtration and some after filtration. Certain marine organisms were also analysed for determination of rare earth elements. These were: flounder (Paralichthys olivaceus); yellowtails (Seriola quinqueradiata); immature anchovy (Engraulis japonica); clams (Meretrix lusoria); green algae (Ulva pertusa); brown algae (Hizikia fusiforme, Sargassum fulvellum, Undaria pinnatifida). In the seawater without HC1 treatment before filtration, considerable amounts of the elements existed in residue on the filter, whereas in the seawater treated with HC1 before filtration, the greater part remained in the dissolved state. Concentration factors calculated from the contents of stable elements, therefore, are affected remarkably by the existing state of the elements in seawater. If only the dissolved state is assumed available for marine organisms, values one order higher are attained compared with the case where total amounts of the elements were used for the calculation. However, the contribution of the insoluble state seems to be not negligible with some organisms. The higher concentration factors for immature anchovy and clams observed in this study were considered to be caused by surface adsorption of elements in particulate form and also ingested sediment with high element concentration. (author)

  12. Inorganic speciation of dissolved elements in seawater: the influence of pH on concentration ratios

    Directory of Open Access Journals (Sweden)

    Byrne Robert H

    2002-01-01

    Full Text Available Assessments of inorganic elemental speciation in seawater span the past four decades. Experimentation, compilation and critical review of equilibrium data over the past forty years have, in particular, considerably improved our understanding of cation hydrolysis and the complexation of cations by carbonate ions in solution. Through experimental investigations and critical evaluation it is now known that more than forty elements have seawater speciation schemes that are strongly influenced by pH. In the present work, the speciation of the elements in seawater is summarized in a manner that highlights the significance of pH variations. For elements that have pH-dependent species concentration ratios, this work summarizes equilibrium data (S = 35, t = 25°C that can be used to assess regions of dominance and relative species concentrations. Concentration ratios of complex species are expressed in the form log[A]/[B] = pH - C where brackets denote species concentrations in solution, A and B are species important at higher (A and lower (B solution pH, and C is a constant dependent on salinity, temperature and pressure. In the case of equilibria involving complex oxy-anions (MOx(OHy or hydroxy complexes (M(OHn, C is written as pKn = -log Kn or pKn* = -log Kn* respectively, where Kn and Kn* are equilibrium constants. For equilibria involving carbonate complexation, the constant C is written as pQ = -log(K2lKn [HCO3-] where K2l is the HCO3 - dissociation constant, Kn is a cation complexation constant and [HCO3-] is approximated as 1.9 × 10-3 molar. Equilibrium data expressed in this manner clearly show dominant species transitions, ranges of dominance, and relative concentrations at any pH.

  13. Ultra-trace plutonium determination in small volume seawater by sector field inductively coupled plasma mass spectrometry with application to Fukushima seawater samples.

    Science.gov (United States)

    Bu, Wenting; Zheng, Jian; Guo, Qiuju; Aono, Tatsuo; Tagami, Keiko; Uchida, Shigeo; Tazoe, Hirofumi; Yamada, Masatoshi

    2014-04-11

    Long-term monitoring of Pu isotopes in seawater is required for assessing Pu contamination in the marine environment from the Fukushima Dai-ichi Nuclear Power Plant accident. In this study, we established an accurate and precise analytical method based on anion-exchange chromatography and SF-ICP-MS. This method was able to determine Pu isotopes in seawater samples with small volumes (20-60L). The U decontamination factor was 3×10(7)-1×10(8), which provided sufficient removal of interfering U from the seawater samples. The estimated limits of detection for (239)Pu and (240)Pu were 0.11fgmL(-1) and 0.08fgmL(-1), respectively, which corresponded to 0.01mBqm(-3) for (239)Pu and 0.03mBqm(-3) for (240)Pu when a 20L volume of seawater was measured. We achieved good precision (2.9%) and accuracy (0.8%) for measurement of the (240)Pu/(239)Pu atom ratio in the standard Pu solution with a (239)Pu concentration of 11fgmL(-1) and (240)Pu concentration of 2.7fgmL(-1). Seawater reference materials were used for the method validation and both the (239+240)Pu activities and (240)Pu/(239)Pu atom ratios agreed well with the expected values. Surface and bottom seawater samples collected off Fukushima in the western North Pacific since March 2011 were analyzed. Our results suggested that there was no significant variation of the Pu distribution in seawater in the investigated areas compared to the distribution before the accident. Copyright © 2014 Elsevier B.V. All rights reserved.

  14. Spatial distributions of (137)Cs and (239+240)Pu in surface seawater within the Exclusive Economic Zone of East Coast Peninsular Malaysia.

    Science.gov (United States)

    Ahmad, Zaharudin; Mei-Wo, Yii; Abu Bakar, Ahmad Sanadi; Shahar, Hidayah

    2010-09-01

    The studies of (137)Cs and (239+240)Pu distributions in surface seawater at South China Sea within the Exclusive Economic Zone (EEZ) of Peninsular Malaysia were carried out in June 2008. The analysis results will serve as additional information to the expanded baseline data for Malaysia's marine environment. Thirty locations from extended study area were identified in the EEZ from which large volumes of surface seawater samples were collected. Different co-precipitation techniques were employed to concentrate cesium and plutonium separately. A known amount of (134)Cs and (242)Pu tracers were used as yield determinant. The precipitate slurry was collected and oven dried at 60(o)C for 1-2 days. Cesium precipitate was fine-ground and counted using gamma-ray spectrometry system at 661.62keV, while plutonium was separated from other radionuclides using anion exchange, electrodeposited and counted using alpha spectrometry. The activity concentrations of (137)Cs and (239+240)Pu were in the range of 3.40-5.89Bq/m(3) and 2.3-7.9mBq/m(3), respectively. The (239+240)Pu/(137)Cs ratios indicate that there are no new inputs of these radionuclides into the area.

  15. Recovery of uranium from seawater

    International Nuclear Information System (INIS)

    Hirotsu, Takahiro; Takagi, Norio; Katoh, Shunsaku

    1995-01-01

    Present status of the development of chelating adsorbents for the recovery of uranium from seawater is outlined with emphasis on the research by the author. Uranium is estimated to exist as stable tri (carbonate) uranylate (6) ion in seawater in a very low concentration. The adsorbent for uranium from seawater in a very low concentration. The adsorbent for uranium from seawater should have high selectivity and affinity for uranium around pH 8. The required characteristics for uranium adsorbent are examined. Various chelating adsorbents have been proposed for the uranium adsorbent and their structures are discussed. Amidoxime type adsorbents have the highest adsorbing power for uranium among the adsorbents hitherto developed and fibrous amidoxime adsorbents are most promising for the practical application. Synthesis, structure and suitable shape of the amidoxime adsorbents are discussed. Uranium adsorption behavior and the amount of saturated adsorption are examined theoretically based on the complexation of an amidoxime monomer and the formula for the adsorption equiliburium is derived. The adsorption and recovery process for uranium from seawater is composed of adsorption, desorption, separation and concentration and finally, uranium is recovered as the yellow cake. A floating body mooring system is proposed by Nobukawa. (T.H.)

  16. Assessment of Selected Heavy Metals in Seawater and Sediment at Klang Coastal Area Malaysia

    International Nuclear Information System (INIS)

    Noor Aziatul Aini Hamzan; Farah Fardiana Mohamad Zaini; Mohd Ismail Ibrahim; Nik Azlin Nik Ariffin

    2015-01-01

    Sediments are capable of transporting loads of adsorbed nutrients, pesticides, heavy metals, and other toxins. In this study, the samples of sediment were collected from four sampling points (Kapar, Sungai Puloh, Sementa and North Port) using sediment core sampler. The cores then was sub-sampled by slicing into 1 cm slices and dried at 60 degree Celsius until mass become constant and the weight recorded. The samples were pulverized and sieved through 220 μm stainless steel sieves. Each sub-sample digested using aqua regia acids. For seawater, the samples were evaporated using the hotplate at 60 degree Celsius. The concentration of heavy metals was determined by inductively coupled plasma optical emission spectrometry (ICP-OES). The highest concentration of copper, zinc, iron and lead was observed from seawater samples obtained from Sementa while highest concentration of cadmium was found from Kapar samples). Most of the bottom seawater gives high concentration of the heavy metal compare to the surface. For sediment, the overall concentration of heavy metal in each layer was fluctuated. From the analysis, there is a significant correlation for overall selected heavy metals and the samples (seawater and sediment) that study in this area. (author)

  17. Atmospheric Aerosol Emissions Related to the Mediterranean Seawater Biogeochemistry

    Science.gov (United States)

    Sellegri, K.; Schwier, A.; Rose, C.; Gazeau, F. P. H.; Guieu, C.; D'anna, B.; Ebling, A. M.; Pey, J.; Marchand, N.; Charriere, B.; Sempéré, R.; Mas, S.

    2016-02-01

    Marine aerosols contribute significantly to the global aerosol load and consequently has an important impact on the Earth's climate. Different factors influence the way they are produced at the air/seawater interface. The sea state (whitecap coverage, temperature, etc. ) influence the size and concentration of primarily produced particles but also biogeochemical characteristics of the seawater influence both the physical and chemical primary fluxes to the atmosphere. An additional aerosol source of marine aerosol to the atmosphere is the formation of new particles by gaz-to-particle conversion, i.e. nucleation. How the seawater and surface microlayer biogeochemical compositions influences the aerosol emissions is still a large debate. In order to study marine emissions, one approach is to use semi-controlled environments such as mesocosms. Within the MedSea and SAM projects, we characterize the primary Sea Spray Aerosol (SSA) during mesocosms experiments performed during different seasons in the Mediteranean Sea. Mesocosms were either left unchanged as control or enriched by addition of nutriments in order to create different levels of phytoplanctonic activities. The mesocosms waters were daily analyzed for their chemical and biological composition (DOC, CDOM, TEP, Chl-a, virus, bacteria, phytoplankton and zooplankton concentrations). SSA production by bubble bursting was daily simulated in a dedicated set-up. The size segregated SSA number fluxes, cloud condensation nuclei (CCN) properties, and chemical composition were determined as a function of the seawater characteristics. We show that the SSA organic content was clearly correlated to the seawater Chl-a level, provided that the mesocosm was not enriched to create an artificial phytoplanctonic bloom. In our experiments, the enrichment of the seawater with natural surface microlayer did not impact the SSA organic content nor its CCN properties. At last, nucleation of secondary particles were observed to occur in

  18. Isolation and Characterization of Surface and Subsurface Bacteria in Seawater of Mantanani Island, Kota Belud, Sabah by Direct and Enrichment Techniques

    International Nuclear Information System (INIS)

    Benard, L D; Tuah, P M; Suadin, E G; Jamian, N

    2015-01-01

    The distribution of hydrocarbon-utilizing bacterial may vary between surface and subsurface of the seawater. One of the identified contributors is the Total Petroleum Hydrocarbon. The isolation and characterization of bacteria using Direct and Enrichment techniques helps in identifying dominant bacterial populations in seawater of Mantanani Island, Kota Belud, Sabah, potential of further investigation as hydrocarbon degrader. Crude oil (5% v/v) was added as the carbon source for bacteria in Enrichment technique. For surface seawater, the highest population of bacteria identified for both Direct and Enrichment technique were 2.60 × 10 7 CFU/mL and 3.84 × 10 6 CFU/mL respectively. Meanwhile, for subsurface seawater, the highest population of bacteria identified for both Direct and Enrichment technique were 5.21 × 10 6 CFU/mL and 8.99 × 10 7 CFU/mL respectively. Dominant species in surface seawater were characterized as Marinobacter hydrocarbonoclasticus-RMSF-C1 and RMSF-C2 and Alcanivorax borkumensis-RMSF-C3, RMSF-C4 and RMSF-C5. As for subsurface seawater, dominant species were characterized as Pseudomonas luteola-SSBR-W1, Burkholderia cepacia-SSBR-C1, Rhizobium radiobacter- SSBR-C3 and Leuconostoc-cremois -SSBR-C4. (paper)

  19. Radiation-induced reactions of Cl-, CO32-, and Br- in seawater, - Model calculation of gamma radiolysis of seawater

    International Nuclear Information System (INIS)

    Hata, Kuniki; Hanawa, Satoshi; Kasahara, Shigeki; Muroya, Yusa; Katsumura, Yosuke

    2012-09-01

    Gamma-radiolysis of seawater has been simulated to estimate the concentrations of radiolysis products. Although gas products such as H 2 , O 2 and H 2 O 2 in irradiated pure water quickly attain the steady state with very low concentrations, the products in seawater monotonically increase with dose. It was found that H 2 is produced almost linearly with dose, and corresponding G-value was 4.4 x 10 -8 mol J -1 . As similar result was obtained from the calculation of 8 x 10 -4 mol dm -3 NaBr solution, the origin of the linear increase in seawater was attributable to be the reactions of Br - . According to the sensitivity analysis, three reactions, 1: Br - + ·OH → BrOH· - , 2: BrOH· - → Br - + ·OH, and 3: BrOH· - → Br· + OH - , determined the concentrations of the products. The presence of Cl - and HCO 3 - in seawater hardly affected the concentrations of the radiolysis products. Oxyanions derived from Cl - and Br - were not obtained at observable concentration. (authors)

  20. Rate of mass deposition of scaling compounds from seawater on the outer surface of heat exchangers in MED evaporators

    Energy Technology Data Exchange (ETDEWEB)

    Omar, W. [Department of Natural Resources and Chemical Engineering, Tafila Technical University, Tafila (Jordan); Ulrich, J. [FB Ingenieurwissenschaften, Institut fuer Verfahrenstechnik/TVT, Martin-Luther-Universitaet Halle-Wittenberg, Halle (Germany)

    2006-08-15

    The scaling problem in Multi Effect Distillation (MED) evaporators is investigated by the experimental measurement of the deposition rate under different operating conditions. The measurements are conducted in a batch vessel containing artificial seawater, which is allowed to contact the outer surface of a hot pipe under controlled temperature, salinity and pH. The rate of mass deposition is higher at elevated temperature. The salinity of the seawater also influences the scaling process - an increase in salinity from 47-59 g/L leads to an increase of 75.6 % in the deposition rate. Decreasing the pH value of seawater to 2.01 results in a complete inhibition of scaling, whereas the severity of the scaling increases in neutral and basic mediums. Polyacrylic acid is tested as an antifoulant and it was found that its presence in seawater reduces the scaling process. The nature of the heat transfer surface material also plays an important role in the scaling process. It is found experimentally that the rate of scaling is higher in the case of a Cu-Ni alloy as the surface material of the tube rather than stainless steel. (Abstract Copyright [2006], Wiley Periodicals, Inc.)

  1. Wireless Sensor Node for Surface Seawater Density Measurements

    Directory of Open Access Journals (Sweden)

    Roberto Saletti

    2012-03-01

    Full Text Available An electronic meter to measure surface seawater density is presented. It is based on the measurement of the difference in displacements of a surface level probe and a weighted float, which according to Archimedes’ law depends on the density of the water. The displacements are simultaneously measured using a high-accuracy magnetostrictive sensor, to which a custom electronic board provides a wireless connection and power supply so that it can become part of a wireless sensor network. The electronics are designed so that different kinds of wireless networks can be used, by simply changing the wireless module and the relevant firmware of the microcontroller. Lastly, laboratory and at-sea tests are presented and discussed in order to highlight the functionality and the performance of a prototype of the wireless density meter node in a Bluetooth radio network. The experimental results show a good agreement of the values of the calculated density compared to reference hydrometer readings.

  2. Wireless sensor node for surface seawater density measurements.

    Science.gov (United States)

    Baronti, Federico; Fantechi, Gabriele; Roncella, Roberto; Saletti, Roberto

    2012-01-01

    An electronic meter to measure surface seawater density is presented. It is based on the measurement of the difference in displacements of a surface level probe and a weighted float, which according to Archimedes' law depends on the density of the water. The displacements are simultaneously measured using a high-accuracy magnetostrictive sensor, to which a custom electronic board provides a wireless connection and power supply so that it can become part of a wireless sensor network. The electronics are designed so that different kinds of wireless networks can be used, by simply changing the wireless module and the relevant firmware of the microcontroller. Lastly, laboratory and at-sea tests are presented and discussed in order to highlight the functionality and the performance of a prototype of the wireless density meter node in a Bluetooth radio network. The experimental results show a good agreement of the values of the calculated density compared to reference hydrometer readings.

  3. Chemical effect on ozone deposition over seawater

    Science.gov (United States)

    Surface layer resistance plays an important role in determining ozone deposition velocity over seawater. Recent studies suggest that surface layer resistance over sea-water is influenced by wind-speed and chemical interaction at the air-water interface. Here, we investigate the e...

  4. assessment of Seawater Intrusion in Concrete by Measuring Chlorine Concentration

    International Nuclear Information System (INIS)

    Abdel-Monem, A.M.; Kansouh, W.A.; Osman, A.M.; Bashter, I.I.

    2011-01-01

    The object of this work is to measure water intrusion in concrete using a new methodology based on neutron activation technique. The applied method depends on measuring the activated gamma energy lines emitted from 38 Cl using a gamma spectrometer with Ge(Li) and HPGe detectors. Concrete samples with different percentages of silica fume (SF), up to 20 % submerged in seawater for different period of time were used to perform the investigation. Samples of concrete taken from different positions along the direction of water intrusion in concrete block were irradiated by thermal neutrons using the irradiation cell of 252 Cf neutron source and one of the vertical channels of search reactor at Delft University. The measured 38 Cl concentrations of the irradiated samples were used to plot groups of water profiles distribution in concrete samples with different SF % and submerged in seawater for different periods. These profiles were compared with the others which use here measured by neutron back emitted method where a satisfactory agreement was observed between the two. Further, the displayed measured results; show that the diffusivity for all water contents decreases with increasing the silica fume percentage up to 15 %. However, for concrete samples with silica fume 20 % the observed phenomenon is reversed due to the deterioration of concrete physical and mechanical properties

  5. Flow cytometric assessment of microbial abundance in the near-field area of seawater reverse osmosis concentrate discharge

    KAUST Repository

    Van Der Merwe, Riaan; Hammes, Frederik A.; Lattemann, Sabine; Amy, Gary L.

    2014-01-01

    The discharge of concentrate and other process waters from seawater reverse osmosis (SWRO) plant operations into the marine environment may adversely affect water quality in the near-field area surrounding the outfall. The main concerns

  6. Mercury in the marine boundary layer and seawater of the South China Sea: Concentrations, sea/air flux, and implication for land outflow

    Science.gov (United States)

    Fu, Xuewu; Feng, Xinbin; Zhang, Gan; Xu, Weihai; Li, Xiangdong; Yao, Hen; Liang, Peng; Li, Jun; Sommar, Jonas; Yin, Runsheng; Liu, Na

    2010-03-01

    Using R/V Shiyan 3 as a sampling platform, measurements of gaseous elemental mercury (GEM), surface seawater total mercury (THg), methyl mercury (MeHg), and dissolved gaseous mercury (DGM) were carried out above and in the South China Sea (SCS). Measurements were collected for 2 weeks (10 to 28 August 2007) during an oceanographic expedition, which circumnavigated the northern SCS from Guangzhou (Canton), Hainan Inland, the Philippines, and back to Guangzhou. GEM concentrations over the northern SCS ranged from 1.04 to 6.75 ng m-3 (mean: 2.62 ng m-3, median: 2.24 ng m-3). The spatial distribution of GEM was characterized by elevated concentrations near the coastal sites adjacent to mainland China and lower concentrations at stations in the open sea. Trajectory analysis revealed that high concentrations of GEM were generally related to air masses from south China and the Indochina peninsula, while lower concentrations of GEM were related to air masses from the open sea area, reflecting great Hg emissions from south China and Indochina peninsula. The mean concentrations of THg, MeHg, and DGM in surface seawater were 1.2 ± 0.3 ng L-1, 0.12 ± 0.05 ng L-1, and 36.5 ± 14.9 pg L-1, respectively. In general, THg and MeHg levels in the northern SCS were higher compared to results reported from most other oceans/seas. Elevated THg levels in the study area were likely attributed to significant Hg delivery from surrounding areas of the SCS primarily via atmospheric deposition and riverine input, whereas other sources like in situ production by various biotic and abiotic processes may be important for MeHg. Average sea/air flux of Hg in the study area was estimated using a gas exchange method (4.5 ± 3.4 ng m-2 h-1). This value was comparable to those from other coastal areas and generally higher than those from open sea environments, which may be attributed to the reemission of Hg previously transported to this area.

  7. Preparation of Pt deposited nanotubular TiO2 as cathodes for enhanced photoelectrochemical hydrogen production using seawater electrolytes

    International Nuclear Information System (INIS)

    Nam, Wonsik; Oh, Seichang; Joo, Hyunku; Yoon, Jaekyung

    2011-01-01

    The purpose of this study was to develop effective cathodes to increase the production of hydrogen and use the seawater, an abundant resource in the earth as the electrolyte in photoelectrochemical systems. In order to fabricate the Pt/TiO 2 cathodes, various contents of the Pt precursor (0-0.4 wt%) deposited by the electrodeposition method were used. On the basis of the hydrogen evolution rate, 0.2 wt% Pt/TiO 2 was observed to exhibit the best performance among the various Pt/TiO 2 cathodes with the natural seawater and two concentrated seawater electrolytes obtained from single (nanofiltration) and combined membrane (nanofiltration and reverse osmosis) processes. The surface characterizations exhibited that crystal structures and morphological properties of Pt and TiO 2 found the results of XRD pattern and SEM/TEM images, respectively. - Graphical abstract: On the basis of photoelectrochemical hydrogen production, 0.2 wt% Pt/TiO 2 was observed to exhibit the best performance among the various Pt/TIO 2 cathodes with natural seawater. In comparison of hydrogen evolution rate with various seawater electrolytes, 0.2 wt% Pt/TiO 2 was found to show the better performance as cathode with the concentrated seawater electrolytes obtained from membrane. Highlights: → Pt deposited TiO 2 electrodes are used as cathode in PEC H 2 production. → Natural and concentrated seawater by membranes are used as electrolytes in PEC. → Pt/TiO 2 shows a good performance as cathode with seawater electrolytes. → H 2 evolution rate increases with more concentrated seawater electrolyte. → Highly saline seawater is useful resource for H 2 production.

  8. Biomass production of Tetraselmis suecica using seawater with sanguaza

    Directory of Open Access Journals (Sweden)

    Juan Silva B.

    2011-03-01

    Full Text Available The growth of Tetraselmis suecica was evaluated. The experiment was realized using the Response Surface Methodology (RSM with Central Composite Rotational Design (CCRD with two factors, pH and sanguaza/seawater concentration in the range of 7 - 9 and 2 - 5 % (v/v, respectively. The culture media were stirred by bubbling air constantly (0.07 L/s and continuously illuminated with 40 W of fluorescent light in glass containers of 1.5 L capacity at a temperature of 22.5 ± 2.1 °C. Using the Gompertz mathematical model was determined that from an 8.0 of pH and a ratio of 3.5% of sanguaza/seawater, the Tetraselmis suecica achieves maximum growth. An 8.71 of pH and a ratio of 4.56% of sanguaza/seawater allow the Tetraselmis suecica maximum growth (logN/N0 of 0.659, with a 12.3% of prediction error by applying a mathematical model of 2nd order. According to the study, the values obtained in sanguaza/seawater as a culture medium outperformed the traditionally used culture medium (Guillard F/2 with seawater. The results demonstrate the potential use of the sanguaza/seawater medium in scalable studies on pilot scale production of Tetraselmis suecica, with a view to the production of biodiesel

  9. Determination of radioactivity levels and heavy metal concentrations in seawater, sediment and anchovy (Engraulis encrasicolus) from the Black Sea in Rize, Turkey.

    Science.gov (United States)

    Baltas, Hasan; Kiris, Erkan; Sirin, Murat

    2017-03-15

    Seawater, sediment and fish (anchovy) samples consumed in the Rize province of the Eastern Black Sea region of Turkey were collected from five different stations. The radioactivity levels ( 226 Ra, 232 Th, 40 K and 137 Cs) were determined in all the samples using a high-purity germanium detector. While 226 Ra, 232 Th and 40 K radionuclides were detected in all samples, the radionuclide concentration of 137 Cs, except for the sediment samples (mean activity is 9±1.4Bqkg -1 ), was not detected for the seawater and fish samples. The total annual effective dose rates from the ingestion of these radionuclides for fish were calculated using the measured activity concentrations in radionuclides and their ingested dose conversion factor. Also, the concentrations of some heavy metals in all the samples were determined. The activity and heavy metal concentration values that were determined for the seawater, sediment and fish samples were compared among the locations themselves and with literature values. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Holographic interferometry as electrochemical emission spectroscopy of carbon steel in seawater with low concentration of RA-41 corrosion inhibitor

    International Nuclear Information System (INIS)

    Habib, K.; Al-Muhana, K.; Habib, A.

    2009-01-01

    In the present investigation, holographic interferometry was utilized for the first time to determine the rate change of the number of the fringe evolutions during the corrosion test of carbon steel in blank seawater and with seawater with different concentrations of a corrosion inhibitor. In other words, the anodic dissolution behaviors (corrosion) of the carbon steel were determined simultaneously by holographic interferometry, an electromagnetic method, and by the electrochemical impedance (EI) spectroscopy, an electronic method. So, the abrupt rate change of the number of the fringe evolutions during corrosion test (EI) spectroscopy, of the carbon steel is called electrochemical emission spectroscopy. The corrosion process of the steel samples was carried out in blank seawater and seawater with different concentrations, 5-20 ppm, of RA-41 corrosion inhibitor using the EI spectroscopy method, at room temperature. The electrochemical emission spectra of the carbon steel in different solutions represent a detailed picture of the rate change of the anodic dissolution of the steel throughout the corrosion processes. Furthermore, the optical interferometry data of the carbon steel were compared to the data, which were obtained from the EI spectroscopy. Consequently, holographic interferometric is found very useful for monitoring the anodic dissolution behaviors of metals, in which the number of the fringe evolutions of the steel samples can be determined in situ. (Author)

  11. The effect of changing seawater Ca and Mg concentrations upon the distribution coefficients of Mg and Sr in the skeletons of the scleractinian coral Pocillopora damicornis

    Science.gov (United States)

    Giri, Sharmila J.; Swart, Peter K.; Devlin, Quinn B.

    2018-02-01

    The skeletal composition of calcifying organisms, in particular Mg/Ca and Sr/Ca ratios, have been widely used to understand fluctuations in seawater chemistry throughout the Phanerozoic. While the success of applying these data to the geologic record depends on a knowledge of the distribution coefficients for these elements (DMg and DSr), there are scarcely any studies which have described how these values vary as a result of changing seawater Mg/Ca ratios. To address this, we have cultured the scleractinian coral, Pocillopora damicornis, in seawater with ranges of Mg and Ca concentrations. Here, we demonstrate that Mg/Ca and Sr/Ca ratios of coral skeletons correlate with total seawater Mg/Ca and Sr/Ca molar ratios, but that apparent DMg and DSr values do not remain constant across the range of experimental seawater treatments, with DMg values significantly increasing with seawater Mg/Ca ratios and DSr values significantly increasing with seawater Ca concentrations. These trends are not rate dependent and may be best explained by a Rayleigh distillation model, in which the calcifying space is semi-isolated from seawater during skeletogenesis (i.e. leaky). As there is a slight increase in DMg and decrease in DSr values between our "Jurassic" and "Modern" seawater treatments, the application of a constant distribution coefficient to estimate changes in ancient seawater chemistry may underestimate seawater Mg/Ca ratios and overestimate Sr/Ca throughout the Mesozoic and Cenozoic. We suggest that interpretations of seawater chemistry from fossil corals may be improved by using the relationships derived for skeletal and seawater Mg/Ca and Sr/Ca ratios established by our experiments, as they incorporate the effect of seawater Mg/Ca ratios on skeletal Mg/Ca and Sr/Ca ratios.

  12. Sulfate was a trace constituent of Archean seawater

    DEFF Research Database (Denmark)

    Crowe, Sean Andrew; Paris, Guillaume; Katsev, Sergei

    2014-01-01

    In the low-oxygen Archean world (>2400 million years ago), seawater sulfate concentrations were much lower than today, yet open questions frustrate the translation of modern measurements of sulfur isotope fractionations into estimates of Archean seawater sulfate concentrations. In the water column...

  13. SRB seawater corrosion project

    Science.gov (United States)

    Bozack, M. J.

    1991-01-01

    The corrosion behavior of 2219 aluminum when exposed to seawater was characterized. Controlled corrosion experiments at three different temperatures (30, 60 and 100 C) and two different environments (seawater and 3.5 percent salt solution) were designed to elucidate the initial stages in the corrosion process. It was found that 2219 aluminum is an active catalytic surface for growth of Al2O3, NaCl, and MgO. Formation of Al2O3 is favored at lower temperatures, while MgO is favored at higher temperatures. Visible corrosion products are formed within 30 minutes after seawater exposure. Corrosion characteristics in 3.5 percent salt solution are different than corrosion in seawater. Techniques utilized were: (1) scanning electron microscopy, (2) energy dispersive x-ray spectroscopy, and (3) Auger electron spectroscopy.

  14. Uranium from seawater

    International Nuclear Information System (INIS)

    Gregg, D.; Folkendt, M.

    1982-01-01

    A novel process for recovering uranium from seawater is proposed and some of the critical technical parameters are evaluated. The process, in summary, consists of two different options for contacting adsorbant pellets with seawater without pumping the seawater. It is expected that this will reduce the mass handling requirements, compared to pumped seawater systems, by a factor of approximately 10 5 , which should also result in a large reduction in initial capital investment. Activated carbon, possibly in combination with a small amount of dissolved titanium hydroxide, is expected to be the preferred adsorbant material instead of the commonly assumed titanium hydroxide alone. The activated carbon, after exposure to seawater, can be stripped of uranium with an appropriate eluant (probably an acid) or can be burned for its heating value (possible in a power plant) leaving the uranium further enriched in its ash. The uranium, representing about 1% of the ash, is then a rich ore and would be recovered in a conventional manner. Experimental results have indicated that activated carbon, acting alone, is not adequately effective in adsorbing the uranium from seawater. We measured partition coefficients (concentration ratios) of approximately 10 3 in seawater instead of the reported values of 10 5 . However, preliminary tests carried out in fresh water show considerable promise for an extraction system that uses a combination of dissolved titanium hydroxide (in minute amounts) which forms an insoluble compound with the uranyl ion, and the insoluble compound then being sorbed out on activated carbon. Such a system showed partition coefficients in excess of 10 5 in fresh water. However, the system was not tested in seawater

  15. Novel Fluorometric Method for the Determination of Production Rate and Steady-State Concentration of Photochemically Generated Superoxide Radical in Seawater Using 3',6'-(Diphenylphosphinyl)fluorescein.

    Science.gov (United States)

    Anifowose, Adebanjo Jacob; Takeda, Kazuhiko; Sakugawa, Hiroshi

    2015-12-15

    Superoxide radical (O2(•-)) is an important reactive oxygen species in seawater. Measurements of its production rates and steady-state concentrations generated by photochemical processes have been a Herculean task over the years. In this study, a probe - 3'6'-(diphenylphosphinyl)fluorescein (PF-1) - was used to trap photochemically generated O2(•-) in seawater, thereby yielding fluorescein. The fluorescein produced was measured by an isocratic fluorescence HPLC at excitation/emission wavelengths of 490/513 nm, respectively. The reaction rate constant of PF-1 with O2(•-) (kPF-1) was pH-dependent: (3.2-23.5) × 10(7) M(-1) s(-1) at pHTOT 7.65-8.50. By applying appropriate equations, both the production rate and the steady-state concentration of O2(•-) generated by photochemical reactions in the seawater were quantified. Under the optimized experimental conditions, fluorescein standards (3-50 nM) exhibited linearity in the seawater by HPLC. The photoformation of fluorescein, due to the reaction of PF-1 with the O2(•-) photochemically produced in the seawater, was linear within the 20 min irradiation. The detection limit of the fluorescein photoformation rate was 0.03 pM s(-1), defined as 3σ of the lowest standard fluorescein concentration per 20 min irradiation. Using this value, the yield of fluorescein, and the fraction of O2(•-) that reacted with PF-1 in the seawater, the detection limit of the O2(•-) photoformation rate was 1.78 pM s(-1). Superoxide measurements using the proposed method were relatively unaffected by the potential interfering species in seawater. Application of the proposed method to ten (10) seawater samples from the Seto Inland Sea, Japan, resulted in measured O2(•-) photoformation rates of 3.1-8.5 nM s(-1), with steady-state concentrations ranging (0.06-0.3) × 10(-10) M. The method is simple, requires no technical sample preparation, and can be used to analyze a large number of samples.

  16. Status of technology of uranium recovery from seawater

    International Nuclear Information System (INIS)

    Sugo, Takanobu; Saito, Kyoichi.

    1990-01-01

    By bringing the solid material called adsorbent in contact with seawater, uranium can be collected, therefore, the adsorbent to which uranium was adsorbed in seawater can be regarded as the resource of uranium storing. To the adsorbent, also rare metals are concentrated in addition to uranium. From such viewpoint, the development of the technology for collecting seawater uranium is important for the Japanese energy policy. The uranium concentration in seawater is about 3 mg/m 3 and its form of dissolution is uranyl tricarbonate ions. The technology of collecting seawater uranium is the separation technology for extracting the component of very low concentration from the aqueous solution containing many components. The total amount of uranium in the whole oceans reaches about 4 billion t, which is about 1000 times as much as the uranium commercially mined on land. It is the target of the technology to make artificial uranium ore of as high quality as possible quickly. The process of collecting seawater uranium comprises adsorption, desorption, separation and enrichment. As the adsorbents, hydrated titanium oxide and chelate resin represented by amidoxime are promising. The adsorption system is described. (K.I.)

  17. Use of experimentally determined Henry's Law and salting-out constants for ethanol in seawater for determination of the saturation state of ethanol in coastal waters.

    Science.gov (United States)

    Willey, Joan D; Powell, Jacqueline P; Avery, G Brooks; Kieber, Robert J; Mead, Ralph N

    2017-09-01

    The Henry's law constant for ethanol in seawater was experimentally determined to be 221 ± 4 M/atm at 22 °C compared with 247 ± 6 M/atm in pure water. The salting out coefficient for ethanol was 0.13 M -1 . In seawater ln(K H ) = -(12.8 ± 0.7) + (5310 ± 197)/T where K H is in M atm -1 and temperature is in K. This plus the salting out coefficient allow calculation of K H for any estuarine or sea water between 1 and 35 °C. High concentrations of dissolved organic carbon do not affect K H values in fresh or seawater. Nearshore surface waters were usually undersaturated with respect to gas phase ethanol except when air concentrations decreased, whereas surface seawater 40 km from shore was supersaturated. The percent saturation in surface waters is driven primarily by changes in air concentrations because these change quickly (hours) and more extensively than surface water. This study allows calculation of ethanol saturation states from air and surface water concentrations which is a necessary step to define the role of surface oceans in the global biogeochemical cycling of ethanol both now and in the future as use of ethanol biofuel continues to grow. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Dissolved Platinum Concentrations in Coastal Seawater: Boso to Sanriku Areas, Japan.

    Science.gov (United States)

    Mashio, Asami Suzuki; Obata, Hajime; Gamo, Toshitaka

    2017-08-01

    Platinum, one of the rarest elements in the earth's crust, is now widely used in a range of products, such as catalytic converters in automobiles and anticancer drugs. Increasing use and dispersal of platinum has the potential to affect aquatic environments. Platinum concentrations in open ocean seawater have been found to be very low (approximately 0.2 pmol/L); however, Pt distributions and biogeochemical cycles in coastal areas are unknown. In this study, we investigated Pt concentrations in coastal waters between the Boso and Sanriku areas, Japan, after the 2011 tsunami. We determined sub-picomolar levels of dissolved Pt using isotope-dilution Inductively coupled plasma mass spectrometry after column preconcentration with an anion exchange resin. Dissolved Pt concentrations were found to be in the range 0.20-1.5 pmol/L, with the highest concentration in bottom water of the Boso coastal area, and at stations close to Tokyo Bay. Assuming thermodynamical equilibrium, Pt was determined to be present in the form PtCl 5 (OH) 2- , even in low-oxygen coastal waters. Vertical profiles indicated Pt levels increased toward seafloors near coastal stations and were similar to those of the open ocean at trench stations. High concentrations of dissolved Pt are thought to be derived from coastal sediments.

  19. Seawater bicarbonate removal during hydrothermal circulation

    Science.gov (United States)

    Proskurowski, G. K.; Seewald, J.; Sylva, S. P.; Reeves, E.; Lilley, M. D.

    2013-12-01

    High temperature fluids sampled at hydrothermal vents represent a complex alteration product of water-rock reactions on a multi-component mixture of source fluids. Sources to high-temperature hydrothermal samples include the 'original' seawater present in the recharge limb of circulation, magmatically influenced fluids added at depth as well as any seawater entrained during sampling. High-temperature hydrothermal fluids are typically enriched in magmatic volatiles, with CO2 the dominant species, characterized by concentrations of 10's-100's of mmol/kg (1, 2). Typically, the high concentration of CO2 relative to background seawater bicarbonate concentrations (~2.3 mmol/kg) obscures a full analysis of the fate of seawater bicarbonate during high-temperature hydrothermal circulation. Here we present data from a suite of samples collected over the past 15 years from high-temperature hydrothermal vents at 9N, Endeavour, Lau Basin, and the MAR that have endmember CO2 concentrations less than 10 mmol/kg. Using stable and radiocarbon isotope measurements these samples provide a unique opportunity to examine the balance between 'original' seawater bicarbonate and CO2 added from magmatic sources. Multiple lines of evidence from multiple hydrothermal settings consistently points to the removal of ~80% of the 'original' 2.3 mmol/kg seawater bicarbonate. Assuming that this removal occurs in the low-temperature, 'recharge' limb of hydrothermal circulation, this removal process is widely occurring and has important contributions to the global carbon cycle over geologic time. 1. Lilley MD, Butterfield DA, Lupton JE, & Olson EJ (2003) Magmatic events can produce rapid changes in hydrothermal vent chemistry. Nature 422(6934):878-881. 2. Seewald J, Cruse A, & Saccocia P (2003) Aqueous volatiles in hydrothermal fluids from the Main Endeavour Field, northern Juan de Fuca Ridge: temporal variability following earthquake activity. Earth and Planetary Science Letters 216(4):575-590.

  20. Determination of picomolar beryllium levels in seawater with inductively coupled plasma mass spectrometry following silica-gel preconcentration

    Energy Technology Data Exchange (ETDEWEB)

    Tazoe, Hirofumi, E-mail: tazoe@cc.hirosaki-u.ac.jp [Department of Radiation Chemistry, Institute of Radiation Emergency Mediation, Hirosaki University, 66-1 Hon-cho, Hirosaki, Aomori 036-8564 (Japan); College of Humanities and Sciences, Nihon University, 3-25-40, Sakurajosui, Setagaya-ku, Tokyo 156-8550 (Japan); Yamagata, Takeyasu [College of Humanities and Sciences, Nihon University, 3-25-40, Sakurajosui, Setagaya-ku, Tokyo 156-8550 (Japan); Obata, Hajime [Atmosphere and Ocean Research Institute, The Tokyo University, 5-1-5 Kashiwanoha, Kashiwa-shi, Chiba 277-8564 (Japan); Nagai, Hisao [College of Humanities and Sciences, Nihon University, 3-25-40, Sakurajosui, Setagaya-ku, Tokyo 156-8550 (Japan)

    2014-12-10

    Highlights: • We developesd the simplest and robust SPE method for ultra low picomolar level beryllium in seawater. • Just silica gel column can quantitatively adsorb beryllium in neutral pH condition containing natural seawater. • EDTA solution can eliminate seawater matrixes retaining Be in the column, which optimize to ICP-MS detemination. • Accurate and precise Be data have been obtained for natural seawater from North Pacific Ocean. - Abstract: A robust and rapid method for the determination of natural levels of beryllium (Be) in seawater was developed to facilitate mapping Be concentrations in the ocean. A solid-phase extraction method using a silica gel column was applied for preconcentration and purification of Be in seawater prior to determination of Be concentrations with inductively coupled plasma mass spectrometry (ICP-MS). Be was quantitatively adsorbed onto silica gel from solutions with pH values ranging from 6.3 to 9, including natural seawater. The chelating agent ethylenediamine tetraacetic acid was used to remove other ions in the seawater matrix (Na, Mg, and Ca) that interfere with the ICP-MS analysis. The reproducibility of the method was 3% based on triplicate analyses of natural seawater samples, and the detection limit was 0.4 pmol kg{sup −1} for 250 mL of seawater, which is sufficient for the analysis of seawater in the open ocean. The method was then used to determine the vertical profile of Be in the eastern North Pacific Ocean, which was found to be a recycled-type profile in which the Be concentration increased with depth from the surface (7.2 pmol kg{sup −1} at <200 m) to deep water (29.2 pmol kg{sup −1} from 3500 m to the bottom)

  1. Determination of picomolar beryllium levels in seawater with inductively coupled plasma mass spectrometry following silica-gel preconcentration

    International Nuclear Information System (INIS)

    Tazoe, Hirofumi; Yamagata, Takeyasu; Obata, Hajime; Nagai, Hisao

    2014-01-01

    Highlights: • We developesd the simplest and robust SPE method for ultra low picomolar level beryllium in seawater. • Just silica gel column can quantitatively adsorb beryllium in neutral pH condition containing natural seawater. • EDTA solution can eliminate seawater matrixes retaining Be in the column, which optimize to ICP-MS detemination. • Accurate and precise Be data have been obtained for natural seawater from North Pacific Ocean. - Abstract: A robust and rapid method for the determination of natural levels of beryllium (Be) in seawater was developed to facilitate mapping Be concentrations in the ocean. A solid-phase extraction method using a silica gel column was applied for preconcentration and purification of Be in seawater prior to determination of Be concentrations with inductively coupled plasma mass spectrometry (ICP-MS). Be was quantitatively adsorbed onto silica gel from solutions with pH values ranging from 6.3 to 9, including natural seawater. The chelating agent ethylenediamine tetraacetic acid was used to remove other ions in the seawater matrix (Na, Mg, and Ca) that interfere with the ICP-MS analysis. The reproducibility of the method was 3% based on triplicate analyses of natural seawater samples, and the detection limit was 0.4 pmol kg −1 for 250 mL of seawater, which is sufficient for the analysis of seawater in the open ocean. The method was then used to determine the vertical profile of Be in the eastern North Pacific Ocean, which was found to be a recycled-type profile in which the Be concentration increased with depth from the surface (7.2 pmol kg −1 at <200 m) to deep water (29.2 pmol kg −1 from 3500 m to the bottom)

  2. Electrochemical and Corrosion Properties of Aluminum Brass in Seawater Desalination Environments

    Directory of Open Access Journals (Sweden)

    Hong JU

    2017-11-01

    Full Text Available The corrosion behavior and mechanism of aluminum brass (HAl77-2 in seawater desalination plant were investigated using electrochemical measurement, Scanning Electronic Microscope (SEM and Energy Dispersive X-ray spectroscopy (EDX analysis. The electrochemical results revealed that the corrosion of HAl77-2 in the desalination artificial seawater depended on chloride ion concentrations, displaying a maximum with a chloride ion concentration of 2.3 wt.%. Corrosion rate of HAl77-2 initial increased and subsequently decreased with the increasing of chloride ion concentration. Moreover, corrosion of HAl77-2 becomes more severe when temperature rises. The above results obtained by electrochemical impedance spectroscopy and potentiodynamic polarization tests were in a good agreement. The results of SEM and EDX methods showed selective localized corrosion appeared remarkably on the surface of HAl77-2.DOI: http://dx.doi.org/10.5755/j01.ms.23.4.17170

  3. Leaching behavior of gamma-emitting fission products and Np from neutron-irradiated UO_2-ZrO_2 solid solutions in non-filtered surface seawater

    International Nuclear Information System (INIS)

    Sasaki, Takayuki; Takeno, Yuu; Kobayashi, Taishi; Kirishima, Akira; Sato, Nobuaki

    2016-01-01

    The gamma ray radionuclides Cs-137, Ba-140, I-131, Ce-141, Ru-103, Zr-95, and Np-239 were produced by neutron irradiation of UO_2-ZrO_2 solid solutions that were synthesized as simulated fuel debris under reducing and oxidizing conditions. The leaching ratio of radionuclides was investigated under atmospheric conditions at 25°C for non-filtered natural surface seawater, as well as deionized water after filtration with a membrane of 0.45-μm pore size or that of nominal molecular weight limit of 3 kDa. The uranium molar concentration was affected by the oxidation state in the solid solution samples. The congruent dissolution of Cs, I, and Ba with the hexavalent uranium of U_3O_8 was facilitated in the seawater samples, whereas a lower leaching ratio of nuclides was observed in the deionized water samples. Neptunium-239, originally produced from uranium-238 in U_3O_8, showed behavior that was similar to that of Cs, I, and Ba. However, the dissolution of Np (as a parent nuclide of Pu-239) in the debris of UO_2 and UO_2-ZrO_2 was suppressed in the same manner as Zr(IV) and Ce(IV). The concentration exhibited no filtration dependence after 15 d, which shows that most of the leached nuclides can exist in their ionic form in seawater. (author)

  4. Development of an Assessment Procedure for Seawater Intrusion Mitigation

    Science.gov (United States)

    Hsi Ting, F.; Yih Chi, T.

    2017-12-01

    The Pingtung Plain is one of the areas with extremely plentiful groundwater resources in Taiwan. Due to that the application of the water resource is restricted by significant variation of precipitation between wet and dry seasons, groundwater must be used as a recharge source to implement the insufficient surface water resource during dry seasons. In recent years, the coastal aquaculture rises, and the over withdrawn of groundwater by private well results in fast drop of groundwater level. Then it causes imbalance of groundwater supply and leads to serious seawater intrusion in the coastal areas. The purpose of this study is to develop an integrated numerical model of groundwater resources and seawater intrusion. Soil and Water Assessment Tool (SWAT), MODFLOW and MT3D models were applied to analyze the variation of the groundwater levels and salinity concentration to investigate the correlation of parameters, which are used to the model applications in order to disposal saltwater intrusion. The data of groundwater levels, pumping capacity and hydrogeological data to were collected to build an integrated numerical model. Firstly, we will collect the information of layered aquifer and the data of hydrological parameters to build the groundwater numerical model at Pingtung Plain, and identify the amount of the groundwater which flow into the sea. In order to deal with the future climate change conditions or extreme weather conditions, we will consider the recharge with groundwater model to improve the seawater intrusion problem. The integrated numerical model which describes that seawater intrusion to deep confined aquifers and shallow unsaturated aquifers. Secondly, we will use the above model to investigate the weights influenced by different factors to the amount area of seawater intrusion, and predict the salinity concentration distribution of evaluation at coastal area of Pingtung Plain. Finally, we will simulate groundwater recharge/ injection at the coastal

  5. Chemical Characteristics of Seawater and Sediment in the Yap Trench

    Science.gov (United States)

    Ding, H.; Sun, C.; Yang, G.

    2017-12-01

    In June 2016, seawater samples at sediment-seawater interface and sediment samples were collected by the he Jiaolong, China's manned submersible, at four sampling sites located in the Yap Trench. Seawater samples from different depths of the trench were also collected by CTD. Chemical parameters, including pH, alkanility, concentrations of dissolved inorganic carbon, dissolved and total organic carbon, methane, dimethylsulfoniopropionate, nutrients, carbohydrates, and amino acids were analyzed in the seawater samples. Concentrations of total organic carbon, six constant elements and nine trace elements were determined in the sediment samples. All the vertical profiles of the chemical parameters in the seawater have unique characteristics. Our resluts also showed that the carbonate compensation depth (CCD) was between 4500 m and 5000 m in the trench. The hadal sediment at 6500 m depth under the CCD line was siliceous ooze favored for the burial of orgaic carbon, attributed to accumulation of surface sediment by gravity flow. The abyssal sediment at the 4500 m depth was calcareous ooze. Various microfossils, such as discoasters and diatoms, were identified in different sediment layers of the sediment samples.Based on the ratios of Fe/Al and Ti/Al, and the correlation between different elements, the sediment in the Yap Trench were derived from biogenic, terrestrial, volcanic and autogenic sources. The ratios of Ni/Co and V/Cr showed that the deposition environment of the trench should be oxidative, arributed to inflow of the Antractic bottom oxygen-rich seawater.The high concentraiont of Ca in the sediment from the station 371-Yap-S02 below 4 cm depth indicated that there was no large-scale volcanic eruption in the research area and the volcanic materials in the sediment might orginated from the Mariana Volcanic Arc, and the Carolyn Ridge has been slowly sinking on the east side of the trench due to plate subduction. This study is the first systematic study of

  6. Amnesic shellfish poisoning biotoxin detection in seawater using pure or amino-functionalized Ag nanoparticles and SERS.

    Science.gov (United States)

    Müller, Csilla; Glamuzina, Branko; Pozniak, Iva; Weber, Karina; Cialla, Dana; Popp, Jürgen; Cîntă Pînzaru, Simona

    2014-12-01

    Domoic acid (DA) biotoxin responsible for the amnesic shellfish poisoning (ASP) has been unambiguously detected in seawater in a broad range of concentration, with both pure and amino-functionalized Ag nanoparticles employed for surface enhanced Raman scattering (SERS). To achieve this, a comprehensive SERS study on DA dissolved in distilled water has been conducted. SERS of DA dissolved in seawater in concentrations ranging from 3.3 × 10(-4) to 3.3 × 10(-8) mol l(-1) exhibited specific signal, completely different to those of the corresponding DA aqueous solutions, due to the seawater interference in the overall SERS effect. In order to assess the capability of the technique as a cheaper alternative for rapid and unambiguous detection of the DA biotoxin in seawater, three detection schemes have been proposed. DA was detectable at 0.33 nmoll(-1) concentration (0.33) dissolved in distilled water and 0.033 nmol l(-1) (0.033 ppb) in seawater respectively, much lower than the admitted level by the current regulation. A solvent specific interaction of DA with the NPs was concluded, since DA aqueous solution added to Ag nanoparticles provided different SERS signal compared to that of DA directly dissolved in seawater. Employing amino-functionalized Ag nanoparticles with 4-aminothiophenol as SERS tag, SERS signal of DA on amino-AgNPs revealed significant specificity associated with the aromatic primary amine interaction of the SERS tag with DA, thus allowing DA detection in seawater at 4.16 × 10(-4) mol l(-1) concentration, much higher than in the case of pure NPs. To highlight the findings, a brief literature review to date on the DA biotoxin detection was also provided. Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Perchlorate in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Martinelango, P. Kalyani [Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409-1061 (United States); Tian Kang [Institute of Environmental and Human Health, Texas Tech University, Lubbock, TX 79409 (United States); Dasgupta, Purnendu K. [Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409-1061 (United States)]. E-mail: Sandyd@ttu.edu

    2006-05-10

    There has been no reliable published data on the presence of perchlorate in seawater. Seaweeds are among the most important plant life in the ocean and are good sources of iodine and have been widely used as food and nutritional supplement. Perchlorate is known to inhibit the transport of iodide by the sodium iodide symporter (NIS), present e.g., in the thyroid and mammary glands. With perchlorate being increasingly detected in drinking water, milk and various other foods, increasing the iodide intake through inexpensive natural supplements may be an attractive solution for maintaining iodine assimilation. We report here measurable concentrations of perchlorate in several samples of seawater (detectable in about half the samples analyzed). We also report the iodide and perchlorate concentrations of 11 different species of seaweed and the corresponding bioconcentration factors (BCF) for perchlorate and iodide, relative to the seawater from which they were harvested. All seaweed samples came from the same region, off the coast of Northeastern Maine. Concentrations of iodide and perchlorate in four seawater samples collected from the region near harvest time were 30 {+-} 11 and 0.16 {+-} 0.084 {mu}g l{sup -1}, respectively. Concentrations of both iodide and perchlorate varied over a wide range for different seaweed species; iodide ranging from 16 to 3134 mg kg{sup -1} and perchlorate from 0.077 to 3.2 mg kg{sup -1}. The Laminaria species had the highest iodide concentration; Laminaria digitata is the seaweed species most commonly used in the kelp tablets sold in health food stores. Our sample of L. digitata contained 3134 {+-} 15 mg iodide/kg dry weight. The BCF varied widely for different species, with Laminaria species concentrating iodide preferentially over perchlorate. The iodide BCF (BCF{sub i}) to perchlorate BCF (BCF{sub p}) quotient ranged from 0.66 to 53; L. digitata and L. saccarina having a BCF{sub i}/BCF{sub p} value of 45 and 53, respectively, far

  8. Perchlorate in seawater

    International Nuclear Information System (INIS)

    Martinelango, P. Kalyani; Tian Kang; Dasgupta, Purnendu K.

    2006-01-01

    There has been no reliable published data on the presence of perchlorate in seawater. Seaweeds are among the most important plant life in the ocean and are good sources of iodine and have been widely used as food and nutritional supplement. Perchlorate is known to inhibit the transport of iodide by the sodium iodide symporter (NIS), present e.g., in the thyroid and mammary glands. With perchlorate being increasingly detected in drinking water, milk and various other foods, increasing the iodide intake through inexpensive natural supplements may be an attractive solution for maintaining iodine assimilation. We report here measurable concentrations of perchlorate in several samples of seawater (detectable in about half the samples analyzed). We also report the iodide and perchlorate concentrations of 11 different species of seaweed and the corresponding bioconcentration factors (BCF) for perchlorate and iodide, relative to the seawater from which they were harvested. All seaweed samples came from the same region, off the coast of Northeastern Maine. Concentrations of iodide and perchlorate in four seawater samples collected from the region near harvest time were 30 ± 11 and 0.16 ± 0.084 μg l -1 , respectively. Concentrations of both iodide and perchlorate varied over a wide range for different seaweed species; iodide ranging from 16 to 3134 mg kg -1 and perchlorate from 0.077 to 3.2 mg kg -1 . The Laminaria species had the highest iodide concentration; Laminaria digitata is the seaweed species most commonly used in the kelp tablets sold in health food stores. Our sample of L. digitata contained 3134 ± 15 mg iodide/kg dry weight. The BCF varied widely for different species, with Laminaria species concentrating iodide preferentially over perchlorate. The iodide BCF (BCF i ) to perchlorate BCF (BCF p ) quotient ranged from 0.66 to 53; L. digitata and L. saccarina having a BCF i /BCF p value of 45 and 53, respectively, far greater than a simple anion exchange process

  9. Inhibition of Sodium Benzoate on Stainless Steel in Tropical Seawater

    International Nuclear Information System (INIS)

    Seoh, S. Y.; Senin, H. B.; Nik, W. N. Wan; Amin, M. M.

    2007-01-01

    The inhibition of sodium benzoate for stainless steel controlling corrosion was studied in seawater at room temperature. Three sets of sample have been immersed in seawater containing sodium benzoate with the concentrations of 0.3M, 0.6M and 1.0M respectively. One set of sample has been immersed in seawater without adding any sodium benzoate. It was found that the highest corrosion rate was observed for the stainless steel with no inhibitor was added to the seawater. As the concentration of sodium benzoate being increased, the corrosion rate is decreases. Results show that by the addition of 1.0M of sodium benzoate in seawater samples, it giving ≥ 90% efficiencies

  10. Influence of glacial meltwater on global seawater δ234U

    Science.gov (United States)

    Arendt, Carli A.; Aciego, Sarah M.; Sims, Kenneth W. W.; Das, Sarah B.; Sheik, Cody; Stevenson, Emily I.

    2018-03-01

    We present the first published uranium-series measurements from modern Greenland Ice Sheet (GrIS) runoff and proximal seawater, and investigate the influence of glacial melt on global seawater δ234U over glacial-interglacial (g-ig) timescales. Climate reconstructions based on closed-system uranium-thorium (U/Th) dating of fossil corals assume U chemistry of seawater has remained stable over time despite notable fluctuations in major elemental compositions, concentrations, and isotopic compositions of global seawater on g-ig timescales. Deglacial processes increase weathering, significantly increasing U-series concentrations and changing the δ234U of glacial meltwater. Analyses of glacial discharge from GrIS outlet glaciers indicate that meltwater runoff has elevated U concentrations and differing 222Rn concentrations and δ234U compositions, likely due to variations in subglacial residence time. Locations with high δ234U have the potential to increase proximal seawater δ234U. To better understand the impact of bulk glacial melt on global seawater δ234U over time, we use a simple box model to scale these processes to periods of extreme deglaciation. We account for U fluxes from the GrIS, Antarctica, and large Northern Hemisphere Continental Ice Sheets, and assess sensitivity by varying melt volumes, duration and U flux input rates based on modern subglacial water U concentrations and compositions. All scenarios support the hypothesis that global seawater δ234U has varied by more than 1‰ through time as a function of predictable perturbations in continental U fluxes during g-ig periods.

  11. Flux patterns and membrane fouling propensity during desalination of seawater by forward osmosis

    KAUST Repository

    Li, Zhenyu; Yangali-Quintanilla, Victor; Valladares Linares, Rodrigo; Li, Qingyu; Zhan, Tong; Amy, Gary L.

    2012-01-01

    The membrane fouling propensity of natural seawater during forward osmosis was studied. Seawater from the Red Sea was used as the feed in a forward osmosis process while a 2. M sodium chloride solution was used as the draw solution. The process was conducted in a semi-batch mode under two crossflow velocities, 16.7. cm/s and 4.2. cm/s. For the first time reported, silica scaling was found to be the dominant inorganic fouling (scaling) on the surface of membrane active layer during seawater forward osmosis. Polymerization of dissolved silica was the major mechanism for the formation of silica scaling. After ten batches of seawater forward osmosis, the membrane surface was covered by a fouling layer of assorted polymerized silica clusters and natural organic matter, especially biopolymers. Moreover, the absorbed biopolymers also provided bacterial attachment sites. The accumulated organic fouling could be partially removed by water flushing while the polymerized silica was difficult to remove. The rate of flux decline was about 53% with a crossflow velocity of 16.7. cm/s while reaching more than 70% with a crossflow velocity of 4.2. cm/s. Both concentration polarization and fouling played roles in the decrease of flux. The salt rejection was stable at about 98% during seawater forward osmosis. In addition, an almost complete rejection of natural organic matter was attained. The results from this study are valuable for the design and development of a successful protocol for a pretreatment process before seawater forward osmosis and a cleaning method for fouled membranes. © 2011 Elsevier Ltd.

  12. Analysis of selected antibiotics in surface freshwater and seawater using direct injection in liquid chromatography electrospray ionization tandem mass spectrometry.

    Science.gov (United States)

    Bayen, Stéphane; Yi, Xinzhu; Segovia, Elvagris; Zhou, Zhi; Kelly, Barry C

    2014-04-18

    Emerging contaminants such as antibiotics have received recent attention as they have been detected in natural waters and health concerns over potential antibiotic resistance. With the purpose to investigate fast and high-throughput analysis, and eventually the continuous on-line analysis of emerging contaminants, this study presents results on the analysis of seven selected antibiotics (sulfadiazine, sulfamethazine, sulfamerazine, sulfamethoxazole, chloramphenicol, lincomycin, tylosin) in surface freshwater and seawater using direct injection of a small sample volume (20μL) in liquid chromatography electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). Notably, direct injection of seawater in the LC-ESI-MS/MS was made possible on account of the post-column switch on the system, which allows diversion of salt-containing solutions flushed out of the column to the waste. Mean recoveries based on the isotope dilution method average 95±14% and 96±28% amongst the compounds for spiked freshwater and seawater, respectively. Linearity across six spiking levels was assessed and the response was linear (r(2)>0.99) for all compounds. Direct injection concentrations were compared for real samples to those obtained with the conventional SPE-based analysis and both techniques concurs on the presence/absence and levels of the compounds in real samples. These results suggest direct injection is a reliable method to detect antibiotics in both freshwater and seawater. Method detection limits for the direct injection technique (37pg/L to 226ng/L in freshwater, and from 16pg/to 26ng/L in seawater) are sufficient for a number of environmental applications, for example the fast screening of water samples for ecological risk assessments. In the present study of real samples, this new method allowed for example the positive detection of some compounds (e.g. lincomycin) down to the sub ng/L range. The direct injection method appears to be relatively cheaper and faster

  13. Impacts of seawater rise on seawater intrusion in the Nile Delta Aquifer, Egypt.

    Science.gov (United States)

    Sefelnasr, Ahmed; Sherif, Mohsen

    2014-01-01

    Several investigations have recently considered the possible impacts of climate change and seawater level rise on seawater intrusion in coastal aquifers. All have revealed the severity of the problem and the significance of the landward movement of the dispersion zone under the condition of seawater level rise. Most of the studies did not consider the possible effects of the seawater rise on the inland movement of the shoreline and the associate changes in the boundary conditions at the seaside and the domain geometry. Such effects become more evident in flat, low land, coastal alluvial plans where large areas might be submerged with seawater under a relatively small increase in the seawater level. None of the studies combined the effect of increased groundwater pumping, due to the possible decline in precipitation and shortage in surface water resources, with the expected landward shift of the shore line. In this article, the possible effects of seawater level rise in the Mediterranean Sea on the seawater intrusion problem in the Nile Delta Aquifer are investigated using FEFLOW. The simulations are conducted in horizontal view while considering the effect of the shoreline landward shift using digital elevation models. In addition to the basic run (current conditions), six different scenarios are considered. Scenarios one, two, and three assume a 0.5 m seawater rise while the total pumping is reduced by 50%, maintained as per the current conditions and doubled, respectively. Scenarios four, five, and six assume a 1.0 m seawater rise and the total pumping is changed as in the first three scenarios. The shoreline is moved to account for the seawater rise and hence the study domain and the seaside boundary are modified accordingly. It is concluded that, large areas in the coastal zone of the Nile Delta will be submerged by seawater and the coast line will shift landward by several kilometers in the eastern and western sides of the Delta. Scenario six represents

  14. Concentrating cesium-137 from seawater using resorcinol-formaldehyde resin for radioecological monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Egorin, Andrei; Tokar, Eduard; Tutov, Mikhail; Avramenko, Valentin [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation); Far Eastern Federal Univ., Vladivostok (Russian Federation); Palamarchuk, Marina; Marinin, Dmitry [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation)

    2017-04-01

    A method of preconcentrating cesium-137 from seawater using a resorcinol-formaldehyde resin, which enables one to optimize the ecological monitoring procedure, has been suggested. Studies of sorption of cesium-137 from seawater by resorcinol-formaldehyde resin have been performed, and it has been demonstrated that the cation exchanger is characterized by high selectivity with respect to cesium-137. It was found that the selectivity depended on the temperature of resin solidification and the seawater pH value. The maximal value of the cesium-137 distribution coefficient is equal to 4.1-4.5 x 10{sup 3} cm{sup 3} g{sup -1}. Under dynamic conditions, the ion-exchange resin capacity is 310-910 bed volumes depending on the seawater pH, whereas the efficiency of cesium removal exceeds 95%. The removal of more than 95% of cesium-137 has been attained using 1-3 M solutions of nitric acid: here, the eluate volume was 8-8.4 bed volumes. Application of 3 M solution of nitric acid results in resin degradation with the release of gaseous products.

  15. Effects of dissolved species on radiolysis of diluted seawater

    International Nuclear Information System (INIS)

    Hata, Kuniki; Hanawa, Satoshi; Kasahara, Shigeki; Motooka, Takafumi; Tsukada, Takashi; Muroya, Yusa; Yamashita, Shinichi; Katsumura, Yosuke

    2014-01-01

    Fukushima Daiichi Nuclear Power Plants (NPPs) experienced seawater injection into the cores and fuel pools as an emergent measure after the accident. After the accident, retained water has been continuously desalinized, and subsequently the concentration of chloride ion (Cl"-) has been kept at a lower level these days. These ions in seawater are known to affect water radiolysis, which causes the production of radiolytic products, such as hydrogen peroxide (H_2O_2), molecular hydrogen (H_2) and molecular oxygen (O_2). However, the effects of dissolved ions relating seawater on the production of the stable radiolytic products are not well understood in the diluted seawater. To understand of the production behavior in diluted seawater under radiation, radiolysis calculations were carried out. Production of H_2 is effectively suppressed by diluting by up to vol10%. The concentrations of oxidants (H_2O_2 and O_2) are also suppressed by dilution of dissolved species. The effect of oxidants on corrosion of materials is thought to be low when the seawater was diluted by less than 1 vol% by water. It is also shown that deaeration is one of the effective measure to suppress the concentrations of oxidants at a lower level for any dilution conditions. (author)

  16. Influence of sulfide concentration on the corrosion behavior of pure copper in synthetic seawater

    International Nuclear Information System (INIS)

    Taniguchi, Naoki; Kawasaki, Manabu

    2008-01-01

    Corrosion rate and stress corrosion cracking (SCC) behavior of pure copper under anaerobic conditions were studied by immersion tests and slow strain rate tests (SSRT) in synthetic seawater containing Na 2 S. The corrosion rate was increased with sulfide concentration both in simple saline solution and in bentnite-sand mixture. The results of SSRT showed that copper was susceptible to intergranular attack; selective dissolution at lower sulfide concentration (less than 0.005 M) and SCC at higher sulfide concentration (0.01 M). It was expected that if the sulfide concentration in groundwater is less than 0.001 M, pure copper is possible to exhibit superior corrosion resistance under anaerobic condition evident by very low corrosion rates and immunity to SCC. In such a low sulfide environment, copper overpack has the potential to achieve super-long lifetimes exceeding several tens of thousands years according to long-term simulations of corrosion based on diffusion of sulfide in buffer material

  17. Effects of seawater components on radiolysis of water at elevated temperature

    International Nuclear Information System (INIS)

    Wada, Yoichi; Tachibana, Masahiko; Ishida, Kazushige; Ota, Nobuyuki; Shigenaka, Naoto; Inagaki, Hiromitsu; Noda, Hiroshi

    2014-01-01

    Effects of seawater components on radiolysis of water at elevated temperature have been studied with a radiolysis model in order to evaluate influence on integrity of materials used in an ABWR. In 2011, seawater flowed into a wide part of the nuclear power plant system of the Hamaoka Nuclear Power Station Reactor No. 5 owned by Chubu Electric Power Co., Inc. after condenser tubes broke during the plant shutdown operation. The reactor water temperature was 250°C and its maximum Cl − concentration was ca. 450 ppm when seawater was mixed with reactor water. In order to clarify effects of the sea water components on radiolysis of water at elevated temperature, a radiolysis model calculation was conducted with Hitachi's radiolysis analysis code 'SIMFONY'. For the calculation, the temperature range was set from 50 to 250°C with 50°C increments and the gamma dose rate was set at 60 Gys −1 to see the effect of gamma irradiation from fuels under shutdown conditions. Concentrations of radiolytic species were calculated for 10 5 s. Dilution ratio of seawater was changed to see the effects of concentration of seawater components. Reaction rate constants of the Cl − , Br − , HCO 3 − , and SO 4 2− systems were considered. The main radiolytic species were predicted to be hydrogen and oxygen. Hydrogen peroxide of low concentration was produced in seawater-mixed water at elevated temperatures. Compared with these main products, concentrations of radiolytic products originating from chloride ion and other seawater components were found to be rather low. The dominant product among them was ClO 3 − and its concentration was found to be below 0.01ppm at 10 5 s. Then, during the plant shutdown operation, the harmful influence from radiolytic species originating from seawater components on integrity of fuel materials must be smaller than that of chloride ion which is the main ionic species in seawater. (author)

  18. Methane-oxidizing seawater microbial communities from an Arctic shelf

    Science.gov (United States)

    Uhlig, Christiane; Kirkpatrick, John B.; D'Hondt, Steven; Loose, Brice

    2018-06-01

    Marine microbial communities can consume dissolved methane before it can escape to the atmosphere and contribute to global warming. Seawater over the shallow Arctic shelf is characterized by excess methane compared to atmospheric equilibrium. This methane originates in sediment, permafrost, and hydrate. Particularly high concentrations are found beneath sea ice. We studied the structure and methane oxidation potential of the microbial communities from seawater collected close to Utqiagvik, Alaska, in April 2016. The in situ methane concentrations were 16.3 ± 7.2 nmol L-1, approximately 4.8 times oversaturated relative to atmospheric equilibrium. The group of methane-oxidizing bacteria (MOB) in the natural seawater and incubated seawater was > 97 % dominated by Methylococcales (γ-Proteobacteria). Incubations of seawater under a range of methane concentrations led to loss of diversity in the bacterial community. The abundance of MOB was low with maximal fractions of 2.5 % at 200 times elevated methane concentration, while sequence reads of non-MOB methylotrophs were 4 times more abundant than MOB in most incubations. The abundances of MOB as well as non-MOB methylotroph sequences correlated tightly with the rate constant (kox) for methane oxidation, indicating that non-MOB methylotrophs might be coupled to MOB and involved in community methane oxidation. In sea ice, where methane concentrations of 82 ± 35.8 nmol kg-1 were found, Methylobacterium (α-Proteobacteria) was the dominant MOB with a relative abundance of 80 %. Total MOB abundances were very low in sea ice, with maximal fractions found at the ice-snow interface (0.1 %), while non-MOB methylotrophs were present in abundances similar to natural seawater communities. The dissimilarities in MOB taxa, methane concentrations, and stable isotope ratios between the sea ice and water column point toward different methane dynamics in the two environments.

  19. Branchial ionocyte organization and ion-transport protein expression in juvenile alewives acclimated to freshwater or seawater

    Science.gov (United States)

    Christensen, A.K.; Hiroi, J.; Schultz, E.T.; McCormick, S.D.

    2012-01-01

    The alewife (Alosa pseudoharengus) is a clupeid that undergoes larval and juvenile development in freshwater preceding marine habitation. The purpose of this study was to investigate osmoregulatory mechanisms in alewives that permit homeostasis in different salinities. To this end, we measured physiological, branchial biochemical and cellular responses in juvenile alewives acclimated to freshwater (0.5p.p.t.) or seawater (35.0p.p.t.). Plasma chloride concentration was higher in seawater-acclimated than freshwater-acclimated individuals (141mmoll -1 vs 134mmoll -1), but the hematocrit remained unchanged. In seawateracclimated individuals, branchial Na +/K +-ATPase (NKA) activity was higher by 75%. Western blot analysis indicated that the abundance of the NKA subunit and a Na+/K+/2Cl- cotransporter (NKCC1) were greater in seawater-acclimated individuals by 40% and 200%, respectively. NKA and NKCC1 were localized on the basolateral surface and tubular network of ionocytes in both acclimation groups. Immunohistochemical labeling for the cystic fibrosis transmembrane conductance regulator (CFTR) was restricted to the apical crypt of ionocytes in seawater-acclimated individuals, whereas sodium/hydrogen exchanger 3 (NHE3) labeling was present on the apical surface of ionocytes in both acclimation groups. Ionocytes were concentrated on the trailing edge of the gill filament, evenly distributed along the proximal 75% of the filamental axis and reduced distally. Ionocyte size and number on the gill filament were not affected by salinity; however, the number of lamellar ionocytes was significantly lower in seawater-acclimated fish. Confocal z-series reconstructions revealed that mature ionocytes in seawater-acclimated alewives occurred in multicellular complexes. These complexes might reduce paracellular Na + resistance, hence facilitating Na+ extrusion in hypo-osmoregulating juvenile alewives after seaward migration. ?? 2012. Published by The Company of Biologists Ltd.

  20. Spatial distributions of and diurnal variations in low molecular weight carbonyl compounds in coastal seawater, and the controlling factors

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, Kazuhiko, E-mail: takedaq@hiroshima-u.ac.jp [Graduate School of Biosphere Science, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8521 (Japan); Katoh, Shinya; Mitsui, Yumi; Nakano, Shinichi [Graduate School of Biosphere Science, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8521 (Japan); Nakatani, Nobutake [Graduate School of Biosphere Science, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8521 (Japan); Department of Environmental and Symbiotic Sciences, Rakuno Gakuen University, 582 Bunkyodai-Midorimachi, Ebetsu, Hokkaido 069-8501 (Japan); Sakugawa, Hiroshi [Graduate School of Biosphere Science, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8521 (Japan)

    2014-09-15

    We studied the spatial distributions of and the diurnal variations in four low molecular weight (LMW) carbonyl compounds, formaldehyde, acetaldehyde, propionaldehyde, and glyoxal, in coastal seawater. The samples were taken from the coastal areas of Hiroshima Bay, the Iyo Nada, and the Bungo Channel, western Japan. The formaldehyde, acetaldehyde, and glyoxal concentrations were higher in the northern part of Hiroshima Bay than at offshore sampling points in the Iyo Nada and the Bungo Channel. These three compounds were found at much higher concentrations in the surface water than in deeper water layers in Hiroshima Bay. It is noteworthy that propionaldehyde was not detected in any of the seawater samples, the concentrations present being lower than the detection limit (1 nanomole per liter (nM)) of the high performance liquid chromatography (HPLC) system we used. Photochemical and biological experiments were performed in the laboratory to help understand the characteristic distributions and fates of the LMW carbonyl compounds. The primary process controlling their fate in the coastal environment appears to be their biological consumption. The direct photo degradation of propionaldehyde, initiated by ultraviolet (UV) absorption, was observed, although formaldehyde and acetaldehyde were not degraded by UV irradiation. Our results suggest that the degradation of the LMW carbonyl compounds by photochemically formed hydroxyl radicals is relatively insignificant in the study area. Atmospheric deposition is a possible source of soluble carbonyl compounds in coastal surface seawater, but it may not influence the carbonyl concentrations in offshore waters. - Highlights: • Low molecular weight (LMW) carbonyl compounds in coastal seawater were determined. • Photochemical productions of LMW carbonyl compounds in seawater were observed. • LMW carbonyl compounds were largely consumed biologically. • Photochemical degradation was relatively insignificant in the study area.

  1. Spatial distributions of and diurnal variations in low molecular weight carbonyl compounds in coastal seawater, and the controlling factors

    International Nuclear Information System (INIS)

    Takeda, Kazuhiko; Katoh, Shinya; Mitsui, Yumi; Nakano, Shinichi; Nakatani, Nobutake; Sakugawa, Hiroshi

    2014-01-01

    We studied the spatial distributions of and the diurnal variations in four low molecular weight (LMW) carbonyl compounds, formaldehyde, acetaldehyde, propionaldehyde, and glyoxal, in coastal seawater. The samples were taken from the coastal areas of Hiroshima Bay, the Iyo Nada, and the Bungo Channel, western Japan. The formaldehyde, acetaldehyde, and glyoxal concentrations were higher in the northern part of Hiroshima Bay than at offshore sampling points in the Iyo Nada and the Bungo Channel. These three compounds were found at much higher concentrations in the surface water than in deeper water layers in Hiroshima Bay. It is noteworthy that propionaldehyde was not detected in any of the seawater samples, the concentrations present being lower than the detection limit (1 nanomole per liter (nM)) of the high performance liquid chromatography (HPLC) system we used. Photochemical and biological experiments were performed in the laboratory to help understand the characteristic distributions and fates of the LMW carbonyl compounds. The primary process controlling their fate in the coastal environment appears to be their biological consumption. The direct photo degradation of propionaldehyde, initiated by ultraviolet (UV) absorption, was observed, although formaldehyde and acetaldehyde were not degraded by UV irradiation. Our results suggest that the degradation of the LMW carbonyl compounds by photochemically formed hydroxyl radicals is relatively insignificant in the study area. Atmospheric deposition is a possible source of soluble carbonyl compounds in coastal surface seawater, but it may not influence the carbonyl concentrations in offshore waters. - Highlights: • Low molecular weight (LMW) carbonyl compounds in coastal seawater were determined. • Photochemical productions of LMW carbonyl compounds in seawater were observed. • LMW carbonyl compounds were largely consumed biologically. • Photochemical degradation was relatively insignificant in the study area

  2. Sulphide production and corrosion in seawaters during exposure to FAME diesel.

    Science.gov (United States)

    Lee, Jason S; Ray, Richard I; Little, Brenda J; Duncan, Kathleen E; Oldham, Athenia L; Davidova, Irene A; Suflita, Joseph M

    2012-01-01

    Experiments were designed to evaluate the corrosion-related consequences of storing/transporting fatty acid methyl ester (FAME) alternative diesel fuel in contact with natural seawater. Coastal Key West, FL (KW), and Persian Gulf (PG) seawaters, representing an oligotrophic and a more organic- and inorganic mineral-rich environment, respectively, were used in 60 day incubations with unprotected carbon steel. The original microflora of the two seawaters were similar with respect to major taxonomic groups but with markedly different species. After exposure to FAME diesel, the microflora of the waters changed substantially, with Clostridiales (Firmicutes) becoming dominant in both. Despite low numbers of sulphate-reducing bacteria in the original waters and after FAME diesel exposure, sulphide levels and corrosion increased markedly due to microbial sulphide production. Corrosion morphology was in the form of isolated pits surrounded by an intact, passive surface with the deepest pits associated with the fuel/seawater interface in the KW exposure. In the presence of FAME diesel, the highest corrosion rates measured by linear polarization occurred in the KW exposure correlating with significantly higher concentrations of sulphur and chlorine (presumed sulphide and chloride, respectively) in the corrosion products.

  3. Colloidal nature of radionuclides in seawater

    International Nuclear Information System (INIS)

    Feldman, I.

    1976-01-01

    There is considerable doubt that equilibrium calculations, i.e., employing solubility products and complex-ion stability constants, are valid for the submicro concentrations of radionuclides in seawater. The existence of radiocolloids should be expected in seawater. The great tendency of radiocolloids to adsorb onto finely-divided hydrous oxides makes their formation of significance in seawater, especially for artificial radionuclides. The subject of radiocolloid formation is reviewed in this chapter. It is shown that the 226 Ra/ 230 Th/U relationship found in seawater can be explained from the fact that the tendencies of these elements to form radiocolloids in seawater should decrease in order thorium > radium much greater than uranium. This explanation is much simpler than the prevailing oceanographic one. The theories for radiocolloid formation are discussed. The recent theory of Jones and Healy for the adsorption of hydrolyzable metal ions onto hydrous oxides is reviewed briefly, and its relevance to radiocolloid formation is pointed out

  4. Seasonal variations of total 234Th and dissolved 238U concentration activities in surface water of Bransfield Strait, Antarctica, from March to October 2011

    International Nuclear Information System (INIS)

    Lapa, Flavia V.; Oliveira, Joselene de; Costa, Alice M.R.; Braga, Elisabete S.

    2013-01-01

    In this study the naturally occurring radionuclides 234 Th and 238 U were used to investigate the magnitude of upper ocean particulate organic carbon export in Bransfield Strait, Southern Ocean. This region is the largest oceanic high-nitrate low-chlorophyll (HNLC) area in the world and is known to contribute to regulate of the atmospheric CO 2 via the biological pump. Due to its different geochemical behavior in seawater, the resulting U/Th disequilibria can be easily used to constrain the transport rates of particles and reaction processes between solution and particulate phases. Sampling occurred during the summer (March and November) 2011. Total 234 Th activities in surface seawater samples ranged from 1.3 to 3.7 dpm L -1 (station EB 011) during March/11 campaign, while in October/11 total 234 Th activity concentrations varied from 1.4 to 2.9 dpm L -1 . Highest total 234 Th activities were found late in the austral summer season. Activity concentrations of dissolved 238 U in surface seawater varied from 2.1 to 2.4 dpm L -1 . Taking into account all sampling stations established in March and October/11 the relative variability of total 234 Th distribution was 22%. (author)

  5. Enhancement of Extraction of Uranium from Seawater

    International Nuclear Information System (INIS)

    Al-Sheikhly, Mohamad; Dietz, Travis; Tsinas, Zois; Tomaszewski, Claire; Pazos, Ileana M.; Nigliazzo, Olga; Li, Weixing; Adel-Hadadi, Mohamad; Barkatt, Aaron

    2016-01-01

    Even at a concentration of 3 @@g/L, the world@@@s oceans contain a thousand times more uranium than currently know terrestrial sources. In order to take advantage of this stockpile, methods and materials must be developed to extract it efficiently, a difficult task considering the very low concentration of the element and the competition for extraction by other atoms in seawater such as sodium, calcium, and vanadium. The majority of current research on methods to extract uranium from seawater are vertical explorations of the grafting of amidoxime ligand, which was originally discovered and promoted by Japanese studies in the late 1980s. Our study expands on this research horizontally by exploring the effectiveness of novel uranium extraction ligands grafted to the surface of polymer substrates using radiation. Through this expansion, a greater understanding of uranium binding chemistry and radiation grafting effects on polymers has been obtained. While amidoxime-functionalized fabrics have been shown to have the greatest extraction efficiency so far, they suffer from an extensive chemical processing step which involves treatment with powerful basic solutions. Not only does this add to the chemical waste produced in the extraction process and add to the method@@@s complexity, but it also significantly impacts the regenerability of the amidoxime fabric. The approach of this project has been to utilize alternative, commercially available monomers capable of extracting uranium and containing a carbon-carbon double bond to allow it to be grafted using radiation, specifically phosphate, oxalate, and azo monomers. The use of commercially available monomers and radiation grafting with electron beam or gamma irradiation will allow for an easily scalable fabrication process once the technology has been optimized. The need to develop a cheap and reliable method for extracting uranium from seawater is extremely valuable to energy independence and will extend the quantity of

  6. Coagulation and ultrafiltration in seawater reverse osmosis pretreatment

    NARCIS (Netherlands)

    Tabatabai, S.A.A.

    2014-01-01

    Seawater desalination is a globally expanding coastal industry with an installed capacity of over 80 million m3/day. Algal blooms pose a challenge to the operation of seawater reverse osmosis (SWRO) membranes and pre-treatment systems due to high concentrations of algal cells and algal organic

  7. A new approach for determination of fouling potential by colloidal nanoparticles during reverse osmosis (RO) membrane filtration of seawater

    International Nuclear Information System (INIS)

    Park, Ji Yeon; Lim, Sungil; Park, Kihong

    2013-01-01

    A direct measurement of number concentration of colloidal nanoparticles (15–450 nm) in water was made with the membrane filtration-differential mobility analyzer technique, and its corresponding flux decline rate (FDR) was determined by laboratory-scale RO fouling test unit using varying number concentrations of silica nanoparticles in artificial seawaters. This relationship was used to predict fouling potential of colloidal nanoparticles in reverse osmosis (RO) membrane process of seawaters in RO plant. It was found that the FDR linearly increased with the increasing number of colloidal nanoparticles for the given concentration range and that the relationship between the number concentration and the FDR also depended on RO membrane surface properties. Data for estimated FDR values for natural seawaters after pretreatment showed a clear difference among samples, which is contrary to the pre-existing index such as silt density index and modified fouling index. Our data suggest that measurement of colloidal nanoparticles is useful for selection of proper pretreatment and successful operation of RO membrane process along with other particle fouling predictors accounting for large particles (>450 nm).

  8. A new approach for determination of fouling potential by colloidal nanoparticles during reverse osmosis (RO) membrane filtration of seawater

    Energy Technology Data Exchange (ETDEWEB)

    Park, Ji Yeon; Lim, Sungil; Park, Kihong, E-mail: kpark@gist.ac.kr [Gwangju Institute of Science and Technology (GIST), School of Environmental Science and Engineering (Korea, Republic of)

    2013-04-15

    A direct measurement of number concentration of colloidal nanoparticles (15-450 nm) in water was made with the membrane filtration-differential mobility analyzer technique, and its corresponding flux decline rate (FDR) was determined by laboratory-scale RO fouling test unit using varying number concentrations of silica nanoparticles in artificial seawaters. This relationship was used to predict fouling potential of colloidal nanoparticles in reverse osmosis (RO) membrane process of seawaters in RO plant. It was found that the FDR linearly increased with the increasing number of colloidal nanoparticles for the given concentration range and that the relationship between the number concentration and the FDR also depended on RO membrane surface properties. Data for estimated FDR values for natural seawaters after pretreatment showed a clear difference among samples, which is contrary to the pre-existing index such as silt density index and modified fouling index. Our data suggest that measurement of colloidal nanoparticles is useful for selection of proper pretreatment and successful operation of RO membrane process along with other particle fouling predictors accounting for large particles (>450 nm).

  9. Organic Carbon Reduction in Seawater Reverse Osmosis (SWRO) Plants, Jeddah, Saudi Arabia

    KAUST Repository

    Alshahri, Abdullah

    2015-12-01

    Desalination is considered to be a major source of usable water in the Middle East, especially the Gulf countries which lack fresh water resources. A key and sometimes the only solution to produce high quality water in these countries is through the use of seawater reverse osmosis (SWRO) desalination technology. Membrane fouling is an economic and operational defect that impacts the performance of SWRO desalination technology. To limit this fouling phenomenon, it is important to implement the appropriate type of intake and pre-treatment system design. In this study, two types of systems were investigated, a vertical well system and a surface-water intake at a 9m depth. The purpose of this investigation is to study the impact of the different intake systems and pre-treatment stages in minimizing the concentrations of algae, bacteria, natural organic matter (NOM) and transparent exopolymer particles (TEP), in the feed water prior to pre-treatment, through the pre-treatment stages, and in the product water and concentrate. Water samples were collected from the surface seawater, the intakes (wells for site A, 9 m depth open ocean intake at site B), after the media filter, after the cartridge filter, and from the permeate and reject streams. The measured parameters included physical parameters, algae, bacteria, total organic carbon (TOC), fractions of dissolved NOM, particulate and colloidal TEP. The results of this study prove that the natural filtration and biological treatment of the seawater which occur in the aquifer matrix are very effective in improving the raw water quality to a significant degree. The results demonstrated that algae and biopolymers were 100% removed, the bacterial concentrations were significantly removed and roughly 50% or greater of TOC concentrations was eliminated by the aquifer matrix at site A. The aquifer feeding the vertical wells reduced TEP concentrations, but to differing degree. There is a slight decrease in the concentrations of

  10. Extraction of uranium from seawater: evaluation of uranium resources and plant siting

    International Nuclear Information System (INIS)

    Rodman, M.R.; Gordon, L.I.; Chen, A.C.T.

    1979-02-01

    This report deals with the evaluation of U.S. coastal waters as a uranium resource and with the selection of a suitable site for construction of a large-scale plant for uranium extraction. Evaluation of the resource revealed that although the concentration of uranium is quite low, about 3.3 ppB in seawater of average oceanic salinity, the amount present in the total volume of the oceans is very great, some 4.5 billion metric tons. Of this, perhaps only that uranium contained in the upper 100 meters or so of the surface well-mixed layer should be considered accessible for recovery, some 160 million tonnes. The study indicated that open ocean seawater acquired for the purpose of uranium extraction would be a more favorable resource than rivers entering the sea, cooling water of power plants, or the feed or effluent streams of existing plants producing other products such as magnesium, bromine, or potable and/or agricultural water from seawater. Various considerations led to the selection of a site for a pumped seawater coastal plant at a coastal location. Puerto Yabucoa, Puerto Rico was selected. Recommendations are given for further studies. 21 figures, 8 tables

  11. Extraction of uranium from seawater: evaluation of uranium resources and plant siting

    Energy Technology Data Exchange (ETDEWEB)

    Rodman, M.R.; Gordon, L.I.; Chen, A.C.T.

    1979-02-01

    This report deals with the evaluation of U.S. coastal waters as a uranium resource and with the selection of a suitable site for construction of a large-scale plant for uranium extraction. Evaluation of the resource revealed that although the concentration of uranium is quite low, about 3.3 ppB in seawater of average oceanic salinity, the amount present in the total volume of the oceans is very great, some 4.5 billion metric tons. Of this, perhaps only that uranium contained in the upper 100 meters or so of the surface well-mixed layer should be considered accessible for recovery, some 160 million tonnes. The study indicated that open ocean seawater acquired for the purpose of uranium extraction would be a more favorable resource than rivers entering the sea, cooling water of power plants, or the feed or effluent streams of existing plants producing other products such as magnesium, bromine, or potable and/or agricultural water from seawater. Various considerations led to the selection of a site for a pumped seawater coastal plant at a coastal location. Puerto Yabucoa, Puerto Rico was selected. Recommendations are given for further studies. 21 figures, 8 tables.

  12. Seawater ultrafiltration fouling control: Backwashing with demineralized water/SWRO permeate

    KAUST Repository

    Li, Sheng; Heijman, Sebastiaan G J; Verberk, J. Q J C; Amy, Gary L.; Van Dijk, Johannis C.

    2012-01-01

    In this study, the effect of demineralized water backwashing on fouling control of seawater ultrafiltration was investigated. Seawater from Scheveningen beach in The Hague and a desalination plant of Evides Company at Zeeland in the Netherlands was used as feed water, while demineralized water and UF permeate were used as backwash water for a fouling control efficiency comparison under different fluxes and backwash durations. Furthermore, demineralized waters with 5 or 50 mmol/l NaCl were applied for backwashing as well, to check the influence of monovalent cations on UF fouling control. Additionally, SWRO permeate was used for backwashes in long-term experiments to check the possibility of it replacing demineralized water. Results show that seawater UF fouling control is substantially improved by demineralized water backwashing. However, due to the high salinity of seawater, more water was required to dilute the cation concentration and limit the dispersion effect near the membrane surface than was needed for surface water. A 2-min demineralized water backwash showed better fouling control efficiency than a 1-min backwash. Furthermore, the presence of monovalent cations in the backwash water deteriorated the fouling control efficiency of the backwash, indicating the existence of a charge screening effect. The demineralized water with 5 and 50 mmol/l NaCl both showed a similar fouling control efficiency which is better than the UF permeate backwash. The calcium ions in UF permeate probably deteriorates the fouling control efficiency by maintaining a Ca-bridging effect between the membranes and NOM. SWRO permeate backwashing successfully controls membrane fouling as well. © 2012 Elsevier B.V. All rights reserved.

  13. Seawater ultrafiltration fouling control: Backwashing with demineralized water/SWRO permeate

    KAUST Repository

    Li, Sheng

    2012-09-01

    In this study, the effect of demineralized water backwashing on fouling control of seawater ultrafiltration was investigated. Seawater from Scheveningen beach in The Hague and a desalination plant of Evides Company at Zeeland in the Netherlands was used as feed water, while demineralized water and UF permeate were used as backwash water for a fouling control efficiency comparison under different fluxes and backwash durations. Furthermore, demineralized waters with 5 or 50 mmol/l NaCl were applied for backwashing as well, to check the influence of monovalent cations on UF fouling control. Additionally, SWRO permeate was used for backwashes in long-term experiments to check the possibility of it replacing demineralized water. Results show that seawater UF fouling control is substantially improved by demineralized water backwashing. However, due to the high salinity of seawater, more water was required to dilute the cation concentration and limit the dispersion effect near the membrane surface than was needed for surface water. A 2-min demineralized water backwash showed better fouling control efficiency than a 1-min backwash. Furthermore, the presence of monovalent cations in the backwash water deteriorated the fouling control efficiency of the backwash, indicating the existence of a charge screening effect. The demineralized water with 5 and 50 mmol/l NaCl both showed a similar fouling control efficiency which is better than the UF permeate backwash. The calcium ions in UF permeate probably deteriorates the fouling control efficiency by maintaining a Ca-bridging effect between the membranes and NOM. SWRO permeate backwashing successfully controls membrane fouling as well. © 2012 Elsevier B.V. All rights reserved.

  14. The isotope composition of inorganic germanium in seawater and deep sea sponges

    Science.gov (United States)

    Guillermic, Maxence; Lalonde, Stefan V.; Hendry, Katharine R.; Rouxel, Olivier J.

    2017-09-01

    Although dissolved concentrations of germanium (Ge) and silicon (Si) in modern seawater are tightly correlated, uncertainties still exist in the modern marine Ge cycle. Germanium stable isotope systematics in marine systems should provide additional constraints on marine Ge sources and sinks, however the low concentration of Ge in seawater presents an analytical challenge for isotopic measurement. Here, we present a new method of pre-concentration of inorganic Ge from seawater which was applied to measure three Ge isotope profiles in the Southern Ocean and deep seawater from the Atlantic and Pacific Oceans. Germanium isotopic measurements were performed on Ge amounts as low as 2.6 ng using a double-spike approach and a hydride generation system coupled to a MC-ICP-MS. Germanium was co-precipitated with iron hydroxide and then purified through anion-exchange chromatography. Results for the deep (i.e. >1000 m depth) Pacific Ocean off Hawaii (nearby Loihi Seamount) and the deep Atlantic off Bermuda (BATS station) showed nearly identical δ74/70Ge values at 3.19 ± 0.31‰ (2SD, n = 9) and 2.93 ± 0.10‰ (2SD, n = 2), respectively. Vertical distributions of Ge concentration and isotope composition in the deep Southern Ocean for water depth > 1300 m yielded an average δ74/70Ge = 3.13 ± 0.25‰ (2SD, n = 14) and Ge/Si = 0.80 ± 0.09 μmol/mol (2SD, n = 12). Significant variations in δ74/70Ge, from 2.62 to 3.71‰, were measured in the first 1000 m in one station of the Southern Ocean near Sars Seamount in the Drake Passage, with the heaviest values measured in surface waters. Isotope fractionation by diatoms during opal biomineralization may explain the enrichment in heavy isotopes for both Ge and Si in surface seawater. However, examination of both oceanographic parameters and δ74/70Ge values suggest also that water mass mixing and potential contribution of shelf-derived Ge also could contribute to the variations. Combining these results with new Ge isotope data

  15. Substrate Use of Pseudovibrio sp. Growing in Ultra-Oligotrophic Seawater

    Science.gov (United States)

    Schwedt, Anne; Seidel, Michael; Dittmar, Thorsten; Simon, Meinhard; Bondarev, Vladimir; Romano, Stefano; Lavik, Gaute; Schulz-Vogt, Heide N.

    2015-01-01

    Marine planktonic bacteria often live in habitats with extremely low concentrations of dissolved organic matter (DOM). To study the use of trace amounts of DOM by the facultatively oligotrophic Pseudovibrio sp. FO-BEG1, we investigated the composition of artificial and natural seawater before and after growth. We determined the concentrations of dissolved organic carbon (DOC), total dissolved nitrogen (TDN), free and hydrolysable amino acids, and the molecular composition of DOM by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR-MS). The DOC concentration of the artificial seawater we used for cultivation was 4.4 μmol C L-1, which was eight times lower compared to the natural oligotrophic seawater we used for parallel experiments (36 μmol C L -1). During the three-week duration of the experiment, cell numbers increased from 40 cells mL-1 to 2x104 cells mL -1 in artificial and to 3x105 cells mL -1 in natural seawater. No nitrogen fixation and minor CO2 fixation (seawater, using unexpected organic compounds to fuel their energy, carbon and nitrogen requirements. PMID:25826215

  16. Boron Removal from Seawater by Thin-Film Composite Reverse Osmosis Membranes

    KAUST Repository

    Al Sunbul, Yasmeen

    2018-04-01

    Reverse Osmosis membranes have been successfully proven to remove almost 99% of chemicals dissolved in seawater. However, removal of certain trace elements, such as boron is challenging and relatively low for seawater reverse osmosis desalination plants compared to thermal desalination plants. Boron is naturally occurring and is present in seawater at an average concentration of 4.5-5 mg/L. While boron is a vital element, its toxicity has been proven on crops, animals and possibly humans. Additionally, boron should be removed to comply with the current guideline value of 0.5 mg/L, for drinking water, issued by the World Health Organization (WHO), which is barely attained by a single-pass process seawater reverse osmosis plant. Currently, multipass reverse osmosis membrane operations with pH modifications are the only valid method for boron removal. However, this is not economically efficient as it requires higher energy and chemicals consumptions. The objective of this study was to investigate boron removal by commercial TFC RO membranes in addition to custom-made KAUST-synthesized TFC membrane. Five membrane samples were examined: Toray, Sepro, Koch, and KAUST in-house synthesized membrane. Three different feed pH conditions were used: pH6, pH8, and pH10. Filtration experiments were conducted in two parts. In experiment 1, all five membranes were examined for boron rejection in a dead-end permeation system, whereas in experiment 2 the two membranes with the highest boron rejection from experiment 1 were tested in a cross-flow system. Permeate and feed samples were taken continuously and analyzed for boron concentration, rejection calculation. Membrane surfaces were characterized according to hydrophilicity, roughness and surface charge. The results showed for all the tested membranes that boron rejection increased as the feed pH increased. KAUST, defect-free TFC, showed the highest performance for boron rejection for all pH conditions, although, it shows the

  17. Process for enriching uranium from seawater

    International Nuclear Information System (INIS)

    Heitkamp, D.; Inden, P.

    1982-01-01

    In selective elutriation of uranium deposited on titanium oxide hydrate by carbonate solution, only uranium should be dissolved from the absorption material forming carbonate compounds, without the deposited ballast ions, above all of magnesium, calcium and sodium being elutriated. The uranium elutriation according to the invention is therefore carried out in the presence of these ballast ions in the same concentrations as those in seawater. The carbonate concentration can only be raised as far as the solubility product of the basic magnesium carbonate permits, so that magnesium remains in the solution, as well as carbonate, in the concentration present in seawater. One must accept the absence of calcium ions in the elutriation solution, as their solubility product with carbonate is considerably less than that for magnesium. (orig./PW) [de

  18. A critical look at the calculation of the binding characteristics and concentration of iron complexing ligands in seawater with suggested improvements

    NARCIS (Netherlands)

    Gerringa, L.J.A.; Rijkenberg, M.J.A.; Thuróczy, C.-E.; Maas, L.R.M.

    2014-01-01

    Environmental context
    The low concentration of iron in the oceans limits growth of phytoplankton. Dissolved organic molecules, called ligands, naturally present in seawater, bind iron thereby increasing its solubility and, consequently, its availability for biological uptake by phytoplankton. The

  19. Seasonal variations of total {sup 234}Th and dissolved {sup 238}U concentration activities in surface water of Bransfield Strait, Antarctica, from March to October 2011

    Energy Technology Data Exchange (ETDEWEB)

    Lapa, Flavia V.; Oliveira, Joselene de; Costa, Alice M.R., E-mail: fvlapa@ipen.br, E-mail: jolivei@ipen.br, E-mail: lice_mrc@hotmail.com [Instituto de Pesquisas Energeticas e Nucleares (IPEN-CNEN/SP), Sao Paulo, SP (Brazil). Laboratorio de Radiometria Ambiental; Braga, Elisabete S., E-mail: edsbraga@usp.br [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Inst. Oceanografico. Lab. de Nutrientes, Micronutrientes e Tracos nos Oceanos

    2013-07-01

    In this study the naturally occurring radionuclides {sup 234}Th and {sup 238}U were used to investigate the magnitude of upper ocean particulate organic carbon export in Bransfield Strait, Southern Ocean. This region is the largest oceanic high-nitrate low-chlorophyll (HNLC) area in the world and is known to contribute to regulate of the atmospheric CO{sub 2} via the biological pump. Due to its different geochemical behavior in seawater, the resulting U/Th disequilibria can be easily used to constrain the transport rates of particles and reaction processes between solution and particulate phases. Sampling occurred during the summer (March and November) 2011. Total {sup 234}Th activities in surface seawater samples ranged from 1.3 to 3.7 dpm L{sup -1} (station EB 011) during March/11 campaign, while in October/11 total {sup 234}Th activity concentrations varied from 1.4 to 2.9 dpm L{sup -1}. Highest total {sup 234}Th activities were found late in the austral summer season. Activity concentrations of dissolved {sup 238}U in surface seawater varied from 2.1 to 2.4 dpm L{sup -1}. Taking into account all sampling stations established in March and October/11 the relative variability of total {sup 234}Th distribution was 22%. (author)

  20. Conceptual design on uranium recovery plant from seawater

    International Nuclear Information System (INIS)

    Kato, Toshiaki; Okugawa, Katsumi; Sugihara, Yutaka; Matsumura, Tsuyoshi

    1999-01-01

    Uranium containing in seawater is extremely low concentration, which is about 3 mg (3 ppb) per 1 ton of seawater. Recently, a report on development of a more effective collector of uranium in seawater (a radiation graft polymerization product of amidoxime onto polyethylene fiber) was issued by Japan Atomic Energy Research Institute. In this paper, an outline design of a uranium recovery plant from seawater was conducted on a base of the collector. As a result of cost estimation, the collection cost of seawater uranium using this method was much higher than that of uranium mine on land and described in the Red Book for mineral uranium cost. In order to make the seawater uranium cost comparable to the on-land uranium cost, it is necessary to establish comprehensive efforts in future technical development, such as development in absorption property of uranium with the collector, resolution method using less HCl, and so forth. (G.K.)

  1. Rapid determination of actinides in seawater samples

    International Nuclear Information System (INIS)

    Maxwell, S.L.; Culligan, B.K.; Hutchison, J.B.; Utsey, R.C.; McAlister, D.R.

    2014-01-01

    A new rapid method for the determination of actinides in seawater samples has been developed at the Savannah River National Laboratory. The actinides can be measured by alpha spectrometry or inductively-coupled plasma mass spectrometry. The new method employs novel pre-concentration steps to collect the actinide isotopes quickly from 80 L or more of seawater. Actinides are co-precipitated using an iron hydroxide co-precipitation step enhanced with Ti +3 reductant, followed by lanthanum fluoride co-precipitation. Stacked TEVA Resin and TRU Resin cartridges are used to rapidly separate Pu, U, and Np isotopes from seawater samples. TEVA Resin and DGA Resin were used to separate and measure Pu, Am and Cm isotopes in seawater volumes up to 80 L. This robust method is ideal for emergency seawater samples following a radiological incident. It can also be used, however, for the routine analysis of seawater samples for oceanographic studies to enhance efficiency and productivity. In contrast, many current methods to determine actinides in seawater can take 1-2 weeks and provide chemical yields of ∼30-60 %. This new sample preparation method can be performed in 4-8 h with tracer yields of ∼85-95 %. By employing a rapid, robust sample preparation method with high chemical yields, less seawater is needed to achieve lower or comparable detection limits for actinide isotopes with less time and effort. (author)

  2. Cl-36 in polar ice, rainwater and seawater

    Science.gov (United States)

    Finkel, R. C.; Nishiizumi, K.; Elmore, D.; Ferraro, R. D.; Gove, H. E.

    1980-01-01

    Concentrations of the cosmogenic radioisotope Cl-36 in Antarctic ice, rain, and an upper limit of the seawater value are determined using van de Graaff accelerator high energy mass spectrometry. Cl-36 concentrations in Antarctic ice range between 2.5 to 8.7 x 10 to the 6th atoms Cl-36/kg, while those concentrations in samples collected at the Alan Hills ice field locations where meteorites have been brought to the surface by glacial flow and ablation are found to vary by more than a factor of three. This variation is attributed either to the effects of atmospheric mixing and scavenging or to radioactive decay in old ice. The Cl-36 concentration found in a present sample of rainwater is much lower than that reported in samples collected in the early 1960's, suggesting the occurrence of a decrease in the concentration of atmospheric Cl-36 derived from nuclear weapons tests over this time period.

  3. Decomposition of dilute residual active chlorine in sea-water

    International Nuclear Information System (INIS)

    Yoshinaga, Tetsutaro; Kawano, Kentaro; Yanagase, Kenjiro; Shiga, Akira

    1985-01-01

    Coastal industries such as power stations require enormous quantities of sea-water for cooling, but the marine organisms in it often result in fouling and/or blockade of the circulating water condenser and pipeworks. To prevent this, chlorine, or hypochlorite by the direct electrolysis of sea-water have been added. Environmental concerns, however, dictate that the residual chlorine concentration at the outlet should be less than the regulated value (0.02 ppm). Methods for decomposing dilute residual chlorine solutions were therefore studied. It was found that: 1) The addition of (raw) sea-water to the sea-water which passed through the condenser lowered the residual chlorine concentration to an greater extent than could be expected by dilution only. 2) Ozonation of the residual chlorine solution led to degradation of OCl - , but in solutions with a residual chlorine concentrations of less than 3 -- 4 ppm, ozonation had no effect. 3) Irradiation with ultra violet light (254 nm) decomposed the residual chlorine. Under the present work conditions (25 0 C: pH 8; depth 10 mm), nearly first order kinetics were to hold [da/dt = ksub((1)) (1-a)sup(n)]. There is a proportional relationship between the kinetic constant (k) and illuminous intensity (L), i.e., ksub((1))[C 0 sup(Cl 2 ): 10 ppm] = 6.56 x 10 -5 L (L = 0 -- 1000 lx). Thus, the use of both sea-water addition and UV irradiation provides a probable method for decomposing a residual chlorine to the expected concentration. (author)

  4. Rare earth element geochemistry characteristics of seawater and porewater from deep sea in western Pacific.

    Science.gov (United States)

    Deng, Yinan; Ren, Jiangbo; Guo, Qingjun; Cao, Jun; Wang, Haifeng; Liu, Chenhui

    2017-11-28

    Deep-sea sediments contain high concentrations of rare earth element (REE) which have been regarded as a huge potential resource. Understanding the marine REE cycle is important to reveal the mechanism of REE enrichment. In order to determine the geochemistry characteristics and migration processes of REE, seawater, porewater and sediment samples were systematically collected from the western Pacific for REE analysis. The results show a relatively flat REE pattern and the HREE (Heavy REE) enrichment in surface and deep seawater respectively. The HREE enrichment distribution patterns, low concentrations of Mn and Fe and negative Ce anomaly occur in the porewater, and high Mn/Al ratios and low U concentrations were observed in sediment, indicating oxic condition. LREE (Light REE) and MREE (Middle REE) enrichment in upper layer and depletion of MREE in deeper layer were shown in porewater profile. This study suggests that porewater flux in the western Pacific basin is a minor source of REEs to seawater, and abundant REEs are enriched in sediments, which is mainly caused by the extensive oxic condition, low sedimentation rate and strong adsorption capacity of sediments. Hence, the removal of REEs of porewater may result in widespread REE-rich sediments in the western Pacific basin.

  5. Spatial variations in microbial community composition in surface seawater from the ultra-oligotrophic center to rim of the South Pacific Gyre.

    Directory of Open Access Journals (Sweden)

    Qi Yin

    Full Text Available Surface seawater in the South Pacific Gyre (SPG is one of the cleanest oceanic environments on earth, and the photosynthetic primary production is extremely low. Despite the ecological significance of the largest aquatic desert on our planet, microbial community composition in the ultra-oligotrophic seawater remain largely unknown. In this study, we collected surface seawater along a southern transect of the SPG during the Integrated Ocean Drilling Program (IODP Expedition 329. Samples from four distinct sites (Sites U1368, U1369, U1370 and U1371 were examined, representing ~5400 kilometers of transect line from the gyre heart to the edge area. Real-time PCR analysis showed 16S rRNA gene abundance in the gyre seawater, ranging from 5.96×10(5 to 2.55×10(6 copies ml(-1 for Bacteria and 1.17×10(3 to 1.90×10(4 copies ml(-1 for Archaea. The results obtained by statistic analyses of 16S rRNA gene clone libraries revealed the community composition in the southern SPG area: diversity richness estimators in the gyre center (Sites U1368 & U1369 are generally lower than those at sites in the gyre edge (Sites U1370 & U1371 and their community structures are clearly distinguishable. Phylogenetic analysis showed the predominance of Proteobacteria (especially Alphaproteobacteria and Cyanobacteria in bacterial 16S rRNA gene clone libraries, whereas phylotypes of Betaproteobacteria were only detected in the central gyre. Archaeal 16S rRNA genes in the clone libraries were predominated by the sequences of Marine Group II within the Euryarchaeota, and the Crenarchaeota sequences were rarely detected, which is consistent with the real-time PCR data (only 9.9 to 22.1 copies ml(-1. We also performed cultivation of heterotrophic microbes onboard, resulting in 18.9% of phylogenetically distinct bacterial isolates at least at the species level. Our results suggest that the distribution and diversity of microbial communities in the SPG surface seawater are closely

  6. Extracting Minerals from Seawater: An Energy Analysis

    Directory of Open Access Journals (Sweden)

    Ugo Bardi

    2010-04-01

    Full Text Available The concept of recovering minerals from seawater has been proposed as a way of counteracting the gradual depletion of conventional mineral ores. Seawater contains large amounts of dissolved ions and the four most concentrated metal ones (Na, Mg, Ca, K are being commercially extracted today. However, all the other metal ions exist at much lower concentrations. This paper reports an estimate of the feasibility of the extraction of these metal ions on the basis of the energy needed. In most cases, the result is that extraction in amounts comparable to the present production from land mines would be impossible because of the very large amount of energy needed. This conclusion holds also for uranium as fuel for the present generation of nuclear fission plants. Nevertheless, in a few cases, mainly lithium, extraction from seawater could provide amounts of metals sufficient for closing the cycle of metal use in the economy, provided that an increased level of recycling can be attained.

  7. Enhancement of Extraction of Uranium from Seawater

    Energy Technology Data Exchange (ETDEWEB)

    Al-Sheikhly, Mohamad [Univ. of Maryland, College Park, MD (United States); Dietz, Travis [Univ. of Maryland, College Park, MD (United States); Tsinas, Zois [Univ. of Maryland, College Park, MD (United States); Tomaszewski, Claire [Univ. of Maryland, College Park, MD (United States); Pazos, Ileana M. [Univ. of Maryland, College Park, MD (United States); Nigliazzo, Olga [The Catholic Univ. of America, Washington, DC (United States); Li, Weixing [The Catholic Univ. of America, Washington, DC (United States); Adel-Hadadi, Mohamad [Univ. of Maryland, College Park, MD (United States); Barkatt, Aaron [Univ. of Palermo (Italy)

    2016-04-01

    Even at a concentration of 3 μg/L, the world’s oceans contain a thousand times more uranium than currently know terrestrial sources. In order to take advantage of this stockpile, methods and materials must be developed to extract it efficiently, a difficult task considering the very low concentration of the element and the competition for extraction by other atoms in seawater such as sodium, calcium, and vanadium. The majority of current research on methods to extract uranium from seawater are vertical explorations of the grafting of amidoxime ligand, which was originally discovered and promoted by Japanese studies in the late 1980s. Our study expands on this research horizontally by exploring the effectiveness of novel uranium extraction ligands grafted to the surface of polymer substrates using radiation. Through this expansion, a greater understanding of uranium binding chemistry and radiation grafting effects on polymers has been obtained. While amidoxime-functionalized fabrics have been shown to have the greatest extraction efficiency so far, they suffer from an extensive chemical processing step which involves treatment with powerful basic solutions. Not only does this add to the chemical waste produced in the extraction process and add to the method’s complexity, but it also significantly impacts the regenerability of the amidoxime fabric. The approach of this project has been to utilize alternative, commercially available monomers capable of extracting uranium and containing a carbon-carbon double bond to allow it to be grafted using radiation, specifically phosphate, oxalate, and azo monomers. The use of commercially available monomers and radiation grafting with electron beam or gamma irradiation will allow for an easily scalable fabrication process once the technology has been optimized. The need to develop a cheap and reliable method for extracting uranium from seawater is extremely valuable to energy independence and will extend the quantity of

  8. Aragonite coating solutions (ACS) based on artificial seawater

    International Nuclear Information System (INIS)

    Tas, A. Cuneyt

    2015-01-01

    Graphical abstract: - Highlights: • Developed completely inorganic solutions for the deposition of monolayers of aragonite spherules (or ooids). • Solutions mimicked the artificial seawater. • Biomimetic crystallization was performed at the tropical sea surface temperature of 30 °C. - Abstract: Aragonite (CaCO 3 , calcium carbonate) is an abundant biomaterial of marine life. It is the dominant inorganic phase of coral reefs, mollusc bivalve shells and the stalactites or stalagmites of geological sediments. Inorganic and initially precipitate-free aragonite coating solutions (ACS) of pH 7.4 were developed in this study to deposit monolayers of aragonite spherules or ooids on biomaterial (e.g., UHMWPE, ultrahigh molecular weight polyethylene) surfaces soaked in ACS at 30 °C. The ACS solutions of this study have been developed for the surface engineering of synthetic biomaterials. The abiotic ACS solutions, enriched with calcium and bicarbonate ions at different concentrations, essentially mimicked the artificial seawater composition and started to deposit aragonite after a long (4 h) incubation period at the tropical sea surface temperature of 30 °C. While numerous techniques for the solution deposition of calcium hydroxyapatite (Ca 10 (PO 4 ) 6 (OH) 2 ), of low thermodynamic solubility, on synthetic biomaterials have been demonstrated, procedures related to the solution-based surface deposition of high solubility aragonite remained uncommon. Monolayers of aragonite ooids deposited at 30 °C on UHMWPE substrates soaked in organic-free ACS solutions were found to possess nano-structures similar to the mortar-and-brick-type botryoids observed in biogenic marine shells. Samples were characterized using SEM, XRD, FTIR, ICP-AES and contact angle goniometry

  9. Aragonite coating solutions (ACS) based on artificial seawater

    Energy Technology Data Exchange (ETDEWEB)

    Tas, A. Cuneyt, E-mail: c_tas@hotmail.com

    2015-03-01

    Graphical abstract: - Highlights: • Developed completely inorganic solutions for the deposition of monolayers of aragonite spherules (or ooids). • Solutions mimicked the artificial seawater. • Biomimetic crystallization was performed at the tropical sea surface temperature of 30 °C. - Abstract: Aragonite (CaCO{sub 3}, calcium carbonate) is an abundant biomaterial of marine life. It is the dominant inorganic phase of coral reefs, mollusc bivalve shells and the stalactites or stalagmites of geological sediments. Inorganic and initially precipitate-free aragonite coating solutions (ACS) of pH 7.4 were developed in this study to deposit monolayers of aragonite spherules or ooids on biomaterial (e.g., UHMWPE, ultrahigh molecular weight polyethylene) surfaces soaked in ACS at 30 °C. The ACS solutions of this study have been developed for the surface engineering of synthetic biomaterials. The abiotic ACS solutions, enriched with calcium and bicarbonate ions at different concentrations, essentially mimicked the artificial seawater composition and started to deposit aragonite after a long (4 h) incubation period at the tropical sea surface temperature of 30 °C. While numerous techniques for the solution deposition of calcium hydroxyapatite (Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}), of low thermodynamic solubility, on synthetic biomaterials have been demonstrated, procedures related to the solution-based surface deposition of high solubility aragonite remained uncommon. Monolayers of aragonite ooids deposited at 30 °C on UHMWPE substrates soaked in organic-free ACS solutions were found to possess nano-structures similar to the mortar-and-brick-type botryoids observed in biogenic marine shells. Samples were characterized using SEM, XRD, FTIR, ICP-AES and contact angle goniometry.

  10. Coral calcifying fluid pH is modulated by seawater carbonate chemistry not solely seawater pH.

    Science.gov (United States)

    Comeau, S; Tambutté, E; Carpenter, R C; Edmunds, P J; Evensen, N R; Allemand, D; Ferrier-Pagès, C; Tambutté, S; Venn, A A

    2017-01-25

    Reef coral calcification depends on regulation of pH in the internal calcifying fluid (CF) in which the coral skeleton forms. However, little is known about calcifying fluid pH (pH CF ) regulation, despite its importance in determining the response of corals to ocean acidification. Here, we investigate pH CF in the coral Stylophora pistillata in seawater maintained at constant pH with manipulated carbonate chemistry to alter dissolved inorganic carbon (DIC) concentration, and therefore total alkalinity (A T ). We also investigate the intracellular pH of calcifying cells, photosynthesis, respiration and calcification rates under the same conditions. Our results show that despite constant pH in the surrounding seawater, pH CF is sensitive to shifts in carbonate chemistry associated with changes in [DIC] and [A T ], revealing that seawater pH is not the sole driver of pH CF Notably, when we synthesize our results with published data, we identify linear relationships of pH CF with the seawater [DIC]/[H + ] ratio, [A T ]/ [H + ] ratio and [[Formula: see text

  11. Organic sources in the Egyptian seawater around Alexandria coastal area as integrated from polycyclic aromatic hydrocarbons (PAHs

    Directory of Open Access Journals (Sweden)

    Omayma E. Ahmed

    2017-09-01

    Full Text Available This paper represents the first comprehensive survey and provides important data on PAHs concentration and composition in Alexandria coastal seawater. The compositions of PAHs determined in all samples are to be used as chemical markers for identifying different sources of PAH pollution in the surface seawater of Alexandria coastal area. The quantitative analysis of PAHs showed a concentration ranging from 8970.939 to 1254756.00 ng/L, which exceeds the maximum admissible concentrations of PAHs (200 ng/L for the water standard of European Union. The calculated diagnostic ratios suggested that the sources of PAHs at the majority of the studied area are derived primarily from pyrogenic sources from incomplete fuel combustion of the boats and vehicle engines with lesser amounts of PAHs contributed from petrogenic sources. Some stations displayed mixed sources in comparison to many other studied marine systems, the PAH concentrations detected at Alexandria area were considered to be higher and pose health risks to aquatic bodies.

  12. Radionuclides in sediments and seawater at Rongelap Atoll

    Energy Technology Data Exchange (ETDEWEB)

    Noshkin, V.E.; Robison, W.L.; Eagle, R.J.; Brunk, J.L.

    1998-03-01

    The present concentrations and distributions of long-lived, man-made radionuclides in Rongelap Atoll lagoon surface sediments, based on samples collected and analyzed in this report. The radionuclides were associated with debris generated with the 1954 Bravo thermonuclear test at Bikini Atoll. Presently, only {sup 90}Sr and the transuranic radionuclides are found associated with the surface sediments in any quantity. Other radionuclides, including {sup 60}Co and {sup 137} Cs, are virtually absent and have either decayed or migrated from the deposits to the overlying seawater. Present inventories of {sup 241}Am and {sup 249+240}Pu in the surface layer at Rongelap are estimated to be 3% of the respective inventories in surface sediments from Bikini Atoll. There is a continuous slow release of the transuranics from the sediments back to the water column. The inventories will only slowly change with time unless the chemical-physical processes that now regulate this release to the water column are changed or altered.

  13. Study of Henna (Lawsonia inermis) as Natural Corrosion Inhibitor for Aluminum Alloy in Seawater

    International Nuclear Information System (INIS)

    Nik, W B Wan; Zulkifli, F; Sulaiman, O; Samo, K B; Rosliza, R

    2012-01-01

    Commercial henna (Lawsonia inermis) was investigated to inhibit the corrosion of aluminum alloy through immersion in seawater. The aluminum alloy (5083) was prepared in size of 25mm × 25mm × 3mm. The immersion test was conducted in seawater with different concentration of henna, 100ppm, 300ppm, 500ppm for duration of 60 days. Four characterizations were performed in this study which was weight loss study, Fourier Transform Infrared (FTIR), Electrochemical Impedance Spectroscopy (EIS) and adsorption isotherm. The results indicated that henna has major constituents of lawsone which contributed to the chemisorptions or adsorption process by forming an isolation layers on the aluminum alloy surface which follows the Langmuir adsorption isotherm. It was found that the protection layer attached on metal was not permanent and precipitation occurred as the time increases. The highest inhibition efficiency was found at 88% (500ppm). This research found that henna is an excellent natural inhibitor for aluminum alloy in seawater.

  14. A field study of physico-chemical states of artificial radionuclides in seawater

    International Nuclear Information System (INIS)

    Nagaya, Yutaka; Nakamura, Kiyoshi

    1974-01-01

    The physico-chemical states of artificial radionuclides, 90 Sr, 137 Cs and 144 Ce in seawater were investigated by radiochemical analysis of filtered and unfiltered seawater. The difference of radionuclide concentrations between unfiltered and filtered seawaters was defined as the ''particulate form'' radioisotope and its ''particle ratio'' was discussed. Practically no particulate 90 Sr, greater than 0.22 μ in size, was observed in both coastal and open seawaters, but some of 137 Cs seemed to be insoluble in some circumstances, especially in coastal waters. A considerable amount of 144 Ce was found to be particulate. An estimation of the radionuclides in particulate form was made for Kashima-nada seawaters collected in 1970 to 1972, and it was shown that the possible occurrence of particulate radionuclides, greater than 0.22 μ in size, were 1% or less for 90 Sr and 6% for 137 Cs. In the coastal water, 80% of 144 Ce were seemed to be in particulate form, but in the open seawater only a few %. The influences of suspended materials to 137 Cs and 144 Ce concentration levels in seawater were not negligible and further investigations are desirable. (auth.)

  15. Rapid determination of total phenols in seawater by 4-aminoantipyrine colorimetry

    Digital Repository Service at National Institute of Oceanography (India)

    Kadam, A.N.; Bhangale, V.P.

    A rapid and efficient 4-aminoantipyrine (4-AAP) colorimetric method without any cleanup step to determine total phenols in seawater is described. Efficiency of the method for seawater using external addition of phenol concentrations with working...

  16. Speciation and spectrophotometric determination of uranium in seawater

    Directory of Open Access Journals (Sweden)

    M. KONSTANTINOU

    2004-06-01

    Full Text Available A series of ion-exchange and extraction procedures for the separation of uranium from seawater samples and subsequent spectrophotometric determination of uranium in seawater by means of arsenazo(III is described. According to the measurements performed by means of traced samples at every stage of separation, the yield of the pre-analytical procedures is generally over 90% and the separation of uranium very selective. The mean uranium concentration in seawater samples collected from five different coastal areas in Cyprus was found to be 3.2 ± 0.2 & micro; g L-1. Uranium in seawater is stable in its hexavalent oxidation state and UO2 (CO334- is the predominant species under normal coastal conditions (pH ≥ 8, EH ≥ 0.35 mV, 1 atm and 0.03% CO2.

  17. Uranium from seawater

    International Nuclear Information System (INIS)

    1974-12-01

    The report concerns the possibilities of extracting uranium from seawater using either 'tidal' and 'pumped' schemes. It was decided to undertake an initial exercise on the pumped scheme. It was to take into account not only the direct energy requirements, but also the indirect energy inputs needed to produce the capital equipment, operating materials, etc. The report begins with a discussion of the technique of energy accounting, and the merits and limitations of the two principal approaches are compared. These are: 'Process Analysis' (or 'Energy Cost of Materials') and 'Input-Output Analysis' (or 'Energy Cost of Money'). A comparison is made between the energy cost of the tidal and pumped schemes, by both methods of analysis. A 'Best Estimate' is compiled calling on both methods, and this indicates that on an energy cost basis the pumped scheme is three times as expensive as the tidal scheme. Intermediate schemes are feasible, however. There is some evidence that the energy cost of an ore refining process with an initial concentration of 0.007% would be of the same order as that of the pumped seawater scheme. The energy cost of generating electricity using seawater uranium in an SGHWR is compared with the present UK generating system as a whole. (U.K.)

  18. Substrate use of Pseudovibrio sp. growing in ultra-oligotrophic seawater.

    Directory of Open Access Journals (Sweden)

    Anne Schwedt

    Full Text Available Marine planktonic bacteria often live in habitats with extremely low concentrations of dissolved organic matter (DOM. To study the use of trace amounts of DOM by the facultatively oligotrophic Pseudovibrio sp. FO-BEG1, we investigated the composition of artificial and natural seawater before and after growth. We determined the concentrations of dissolved organic carbon (DOC, total dissolved nitrogen (TDN, free and hydrolysable amino acids, and the molecular composition of DOM by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR-MS. The DOC concentration of the artificial seawater we used for cultivation was 4.4 μmol C L(-1, which was eight times lower compared to the natural oligotrophic seawater we used for parallel experiments (36 μmol C L(-1. During the three-week duration of the experiment, cell numbers increased from 40 cells mL(-1 to 2x10(4 cells mL(-1 in artificial and to 3x10(5 cells mL(-1 in natural seawater. No nitrogen fixation and minor CO2 fixation (< 1% of cellular carbon was observed. Our data show that in both media, amino acids were not the main substrate for growth. Instead, FT-ICR-MS analysis revealed usage of a variety of different dissolved organic molecules, belonging to a wide range of chemical compound groups, also containing nitrogen. The present study shows that marine heterotrophic bacteria are able to proliferate with even lower DOC concentrations than available in natural ultra-oligotrophic seawater, using unexpected organic compounds to fuel their energy, carbon and nitrogen requirements.

  19. Surface functionalization of Cu-Ni alloys via grafting of a bactericidal polymer for inhibiting biocorrosion by Desulfovibrio desulfuricans in anaerobic seawater.

    Science.gov (United States)

    Yuan, S J; Liu, C K; Pehkonen, S O; Bai, R B; Neoh, K G; Ting, Y P; Kang, E T

    2009-01-01

    A novel surface modification technique was developed to provide a copper nickel alloy (M) surface with bactericidal and anticorrosion properties for inhibiting biocorrosion. 4-(chloromethyl)-phenyl tricholorosilane (CTS) was first coupled to the hydroxylated alloy surface to form a compact silane layer, as well as to confer the surface with chloromethyl functional groups. The latter allowed the coupling of 4-vinylpyridine (4VP) to generate the M-CTS-4VP surface with biocidal functionality. Subsequent surface graft polymerization of 4VP, in the presence of benzoyl peroxide (BPO) initiator, from the M-CTS-4VP surface produced the poly(4-vinylpyridine) (P(4VP)) grafted surface, or the M-CTS-P(4VP) surface. The pyridine nitrogen moieties on the M-CTS-P(4VP) surface were quaternized with hexylbromide to produce a high concentration of quaternary ammonium groups. Each surface functionalization step was ascertained by X-ray photoelectron spectroscopy (XPS) and static water contact angle measurements. The alloy with surface-quaternized pyridinium cation groups (N+) exhibited good bactericidal efficiency in a Desulfovibrio desulfuricans-inoculated seawater-based modified Barr's medium, as indicated by viable cell counts and fluorescence microscopy (FM) images of the surface. The anticorrosion capability of the organic layers was verified by the polarization curve and electrochemical impedance spectroscopy (EIS) measurements. In comparison, the pristine (surface hydroxylated) Cu-Ni alloy was found to be readily susceptible to biocorrosion under the same environment.

  20. Sorption of lead onto two gram-negative marine bacteria in seawater

    Science.gov (United States)

    Harvey, Ronald W.; Leckie, James O.

    1985-01-01

    Laboratory adsorption experiments performed at environmentally significant lead (Pb) and cell concentrations indicate that the marine bacteria examined have significant binding capacities for Pb. However, the behavior governing Pb sorption onto gram-negative bacteria in seawater may be quite complex. The sorption kinetics appear to involve two distinct phases, i.e., a rapid removal of Pb from solution within the first few minutes, followed by a slow but nearly constant removal over many hours. Also, the average binding coefficient, calculated for Pb sorption onto bacteria and a measure of binding intensity, increases with decreasing sorption density (amounts of bacteria-associated Pb per unit bacterial surface) at low cell concentrations (105 cells ml−1), but decreases with decreasing sorption density at higher cell concentrations (107 cells ml−1). The latter effect is apparently due to the production of significant amounts of extra-cellular organics at high cell concentrations that compete directly with bacterial surfaces for available lead. Lead toxicity and active uptake by marine bacteria did not appear significant at the Pb concentrations used.

  1. Lawrence Livermore Laboratory concept for uranium recovery from seawater

    International Nuclear Information System (INIS)

    Gregg, D.; Wang, F.

    1980-01-01

    The Lawrence Livermore Laboratory concept for uranium recovery from seawater involves the following process steps: (1) produce activated carbon via a coal gasification plant; (2) contact activated carbon sorbent with seawater using a settling process (no pumping of seawater); (3) vacuum activated carbon from sea floor; (4) gasify or burn activated carbon (further concentrating the uranium in the ash); (5) extract the uranium from the rich ash ore by conventional techniques. The process advantages are: (1) eliminates seawater pumping, the need for an illuent, and the need for a fresh water wash; (2) should result in much lower capital investment and regional process energy. Major process issues are: (1) uranium loading on activated carbon; (2) activated carbon modifications required to improve the sorbtion performance; (3) activated carbon particle size needed to meet system requirements; (4) minimization of sorbent losses when contacted with seawater

  2. Mercury isotope signatures of seawater discharged from a coal-fired power plant equipped with a seawater flue gas desulfurization system.

    Science.gov (United States)

    Lin, Haiying; Peng, Jingji; Yuan, Dongxing; Lu, Bingyan; Lin, Kunning; Huang, Shuyuan

    2016-07-01

    Seawater flue gas desulfurization (SFGD) systems are commonly used to remove acidic SO2 from the flue gas with alkaline seawater in many coastal coal-fired power plants in China. However, large amount of mercury (Hg) originated from coal is also transferred into seawater during the desulfurization (De-SO2) process. This research investigated Hg isotopes in seawater discharged from a coastal plant equipped with a SFGD system for the first time. Suspended particles of inorganic minerals, carbon residuals and sulfides are enriched in heavy Hg isotopes during the De-SO2 process. δ(202)Hg of particulate mercury (PHg) gradually decreased from -0.30‰ to -1.53‰ in study sea area as the distance from the point of discharge increased. The results revealed that physical mixing of contaminated De-SO2 seawater and uncontaminated fresh seawater caused a change in isotopic composition of PHg isotopes in the discharging area; and suggested that both De-SO2 seawater and local background contributed to PHg. The impacted sea area predicted with isotopic tracing technique was much larger than that resulted from a simple comparison of pollutant concentration. It was the first attempt to apply mercury isotopic composition signatures with two-component mixing model to trace the mercury pollution and its influence in seawater. The results could be beneficial to the coal-fired plants with SFGD systems to assess and control Hg pollution in sea area. Copyright © 2016 Elsevier Ltd. All rights reserved.

  3. Rapid and gradual modes of aerosol trace metal dissolution in seawater

    Directory of Open Access Journals (Sweden)

    Katherine Rose Marie Mackey

    2015-01-01

    Full Text Available Atmospheric deposition is a major source of trace metals in marine surface waters and supplies vital micronutrients to phytoplankton, yet measured aerosol trace metal solubility values are operationally defined and there are relatively few multi-element studies on aerosol-metal solubility in seawater. Here we measure the solubility of aluminum (Al, cadmium (Cd, cobalt (Co, copper (Cu, iron (Fe, manganese (Mn, nickel (Ni, lead (Pb, and zinc (Zn from natural aerosol samples in seawater over a 7 day period to (1 evaluate the role of extraction time in trace metal dissolution behavior and (2 explore how the individual dissolution patterns could influence biota. Dissolution behavior occurs over a continuum ranging from rapid dissolution, in which the majority of soluble metal dissolved immediately upon seawater exposure (Cd and Co in our samples, to gradual dissolution, where metals dissolved slowly over time (Zn, Mn, Cu, and Al in our samples. Additionally, dissolution affected by interactions with particles was observed in which a decline in soluble metal concentration over time occurred (Fe and Pb in our samples. Natural variability in aerosol chemistry between samples can cause metals to display different dissolution kinetics in different samples, and this was particularly evident for Ni, for which samples showed a broad range of dissolution rates. The elemental molar ratio of metals in the bulk aerosols was 23,189Fe: 22,651Al: 445Mn: 348Zn: 71Cu: 48Ni: 23Pb: 9Co: 1Cd, whereas the seawater soluble molar ratio after 7 days of leaching was 11Fe: 620Al: 205Mn: 240Zn: 20Cu: 14Ni: 9Pb: 2Co: 1Cd. The different kinetics and ratios of aerosol metal dissolution have implications for phytoplankton nutrition, and highlight the need for unified extraction protocols that simulate aerosol metal dissolution in the surface ocean.

  4. Uranium from Seawater Program Review; Fuel Resources Uranium from Seawater Program DOE Office of Nuclear Energy

    Energy Technology Data Exchange (ETDEWEB)

    None

    2013-07-01

    For nuclear energy to remain sustainable in the United States, economically viable sources of uranium beyond terrestrial ores must be developed. The goal of this program is to develop advanced adsorbents that can extract uranium from seawater at twice the capacity of the best adsorbent developed by researchers at the Japan Atomic Energy Agency (JAEA), 1.5 mg U/g adsorbent. A multidisciplinary team from Oak Ridge National Laboratory, Lawrence Berkeley National Laboratory, Pacific Northwest National Laboratory, and the University of Texas at Austin was assembled to address this challenging problem. Polymeric adsorbents, based on the radiation grafting of acrylonitrile and methacrylic acid onto high surface-area polyethylene fibers followed by conversion of the nitriles to amidoximes, have been developed. These poly(acrylamidoxime-co-methacrylic acid) fibers showed uranium adsorption capacities for the extraction of uranium from seawater that exceed 3 mg U/g adsorbent in testing at the Pacific Northwest National Laboratory Marine Sciences Laboratory. The essence of this novel technology lies in the unique high surface-area trunk material that considerably increases the grafting yield of functional groups without compromising its mechanical properties. This technology received an R&D100 Award in 2012. In addition, high surface area nanomaterial adsorbents are under development with the goal of increasing uranium adsorption capacity by taking advantage of the high surface areas and tunable porosity of carbon-based nanomaterials. Simultaneously, de novo structure-based computational design methods are being used to design more selective and stable ligands and the most promising candidates are being synthesized, tested and evaluated for incorporation onto a support matrix. Fundamental thermodynamic and kinetic studies are being carried out to improve the adsorption efficiency, the selectivity of uranium over other metals, and the stability of the adsorbents. Understanding

  5. Laboratory experiments to investigate radionuclide enrichment in the sea-surface microlayer

    International Nuclear Information System (INIS)

    Hickmott, S.J.B.

    1982-02-01

    Samples of simulated seawater, and seawater from the Irish Sea, were contained in a plastic tank in the laboratory, and bubbles were passed through them to burst at the water surface. The emitted jet droplets, as representing the surface microlayer, were collected on filter papers. Such measurements are easier to perform than similar measurements at sea, and the lack of waves enables greater collection efficiencies to be obtained. The droplet samples were analysed for stable Na, 137 Cs and actinides, and compared with the concentrations in the bulk tank water, in order to examine possible concentration factors for radionuclides in the surface microlayer. (author)

  6. Calcium extraction from brine water and seawater using oxalic acid

    Science.gov (United States)

    Natasha, Nadia Chrisayu; Lalasari, Latifa Hanum

    2017-01-01

    Calcium can be extracted not only from rocks but also from natural liquor such as seawater and brine water. In order to extract the calcium from seawater and brine water, oxalic acid was used in this research. Effect of variations of the volume of the oxalic acid at a constant concentration in seawater and brine water to produce calcium was investigated. The concentration of oxalic acid was 100 g/l and the variations of its volume were 2 ml, 4 ml, 6 ml, 8 ml, 10 ml, 20 ml, 30 ml, 40 ml, and 50 ml. The used seawater and brine water were firstly evaporated from 100 ml into 50 ml and then the oxalic acid was added into them with mixing to produce the calcium precipitates. The precipitates were analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM) and the filtrates were analyzed by inductively coupled plasma-optical emission spectrometry (ICP-OES). The SEM analysis showed that the precipitates from brine water were consisted of only calcium compound while from seawater sodium one was also found along with calcium compound. The XRD analysis showed that the calcium was present in the form of calcium oxalate for both seawater and brine water. The ICP-OES analysis of the filtrate from seawater precipitation showed that the its calcium content was decreased from 826.20 ppm to 0.04 ppm while from brine water, it decreased from 170.06 ppm to 1.96 ppm. These results showed that both seawater and brine water have the potential to be a raw material for calcium production.

  7. Biodegradation of Halloysite Nanotubes-Polyester Nanocomposites Exposed to Short Term Seawater Immersion

    Directory of Open Access Journals (Sweden)

    Mohd Shahneel Saharudin

    2017-07-01

    Full Text Available Halloysite nanotubes (HNTs-polyester nanocomposites with four different concentrations were produced using solution casting technique and the biodegradation effect of short-term seawater exposure (120 h was studied. Monolithic polyester was observed to have the highest seawater absorption with 1.37%. At 0.3 wt % HNTs reinforcement, the seawater absorption dropped significantly to the lowest value of 0.77% due to increase of liquid diffusion path. For samples tested in dry conditions, the Tg, storage modulus, tensile properties and flexural properties were improved. The highest improvement of Tg was from 79.3 to 82.4 °C (increase 3.1 °C in the case of 0.3 wt % HNTs. This can be associated with the exfoliated HNTs particles, which restrict the mobility of polymer chains and thus raised the Tg. After seawater exposure, the Tg, storage modulus, tensile properties and flexural properties of polyester and its nanocomposites were decreased. The Young’s modulus of 0.3 wt % HNTs-polyester dropped 20% while monolithic polyester dropped up to 24% compared to their values in dry condition. Apart from that, 29% flexural modulus reduction was observed, which was 18% higher than monolithic polyester. In contrast, fracture toughness and surface roughness increased due to plasticization effect. The presence of various microbial communities caused gradual biodegradation on the microstructure of the polyester matrix as also evidently shown by SEM images.

  8. Transport and fate of hexachlorocyclohexanes in the oceanic air and surface seawater

    Directory of Open Access Journals (Sweden)

    Z. Xie

    2011-09-01

    Full Text Available Hexachlorocyclohexanes (HCHs are ubiquitous organic pollutants derived from pesticide application. They are subject to long-range transport, persistent in the environment, and capable of accumulation in biota. Shipboard measurements of HCH isomers (α-, γ- and β-HCH in surface seawater and boundary layer atmospheric samples were conducted in the Atlantic and the Southern Ocean in October to December of 2008. ΣHCHs concentrations (the sum of α-, γ- and β-HCH in the lower atmosphere ranged from 12 to 37 pg m−3 (mean: 27 ± 11 pg m−3 in the Northern Hemisphere (NH, and from 1.5 to 4.0 pg m−3 (mean: 2.8 ± 1.1 pg m−3 in the Southern Hemisphere (SH, respectively. Water concentrations were: α-HCH 0.33–47 pg l−1, γ-HCH 0.02–33 pg l−1 and β-HCH 0.11–9.5 pg l−1. Dissolved HCH concentrations decreased from the North Atlantic to the Southern Ocean, indicating historical use of HCHs in the NH. Spatial distribution showed increasing concentrations from the equator towards North and South latitudes illustrating the concept of cold trapping in high latitudes and less interhemispheric mixing process. In comparison to concentrations measured in 1987–1999/2000, gaseous HCHs were slightly lower, while dissolved HCHs decreased by factor of 2–3 orders of magnitude. Air-water exchange gradients suggested net deposition for α-HCH (mean: 3800 pg m−2 day−1 and γ-HCH (mean: 2000 pg m−2 day−1, whereas β-HCH varied between equilibrium (volatilization: <0–12 pg m−2 day−1 and net deposition (range: 6–690 pg m−2 day−1. Climate change may significantly accelerate the release of "old" HCHs from continental storage (e.g. soil, vegetation and high mountains and drive long-range transport from sources to deposition in the open oceans. Biological productivities may

  9. Uptake of elements from seawater by ferromanganese crusts: Solid-phase associations and seawater speciation

    Science.gov (United States)

    Koschinsky, A.; Hein, J.R.

    2003-01-01

    Marine Fe-Mn oxyhydroxide crusts form by precipitation of dissolved components from seawater. Three hydrogenetic crust samples (one phosphatized) and two hydrothermal Mn-oxide samples were subjected to a sequential-leaching procedure in order to determine the host phases of 40 elements. Those host-phase associations are discussed with respect to element speciation in seawater. The partitioning of elements between the two major phases, Mn oxide and Fe oxyhydroxide, can in a first-order approximation be explained by a simple sorption model related to the inorganic speciation of the elements in seawater, as has been proposed in earlier models. Free and weakly complexed cations, such as alkali and alkaline earth metals, Mn, Co, Ni, Zn, T1(I), and partly Y, are sorbed preferentially on the negatively charged surface of the MnO2 in hydrogenetic crusts. The driving force is a strong coulombic interaction. All neutral or negatively charged chloro (Cd, Hg, T1), carbonate (Cu, Y, Pb, and U), and hydroxide (Be, Sc, Ti, Fe, Zr, Nb, In, Sn, Sb, Te, Hf, Ta, Bi, Th, and T1(III)) complexes and oxyanions (V, Cr, As, Se, Mo, and W) bind to the slightly positively charged surface of the amorphous FeOOH phase. While coulombic interaction can explain the sorption of the negatively charged species, the binding of neutral species is based on specific chemical interaction. Organic complexation of elements in deep-ocean water seems to be at most of minor importance. Surface oxidation can explain some strong metal associations, e.g. of Co and T1 with the MnO2 and Te with the FeOOH. Sorption reactions initially driven by coulombic forces are often followed by the formation of specific bonds between the adsorbate and the atoms of the oxide surface. Differences in the associations of some metals between the non-phosphatized and phosphatized hydrogenetic crusts and between the hydrogenetic and the hydrothermal samples reflect the different physico-chemical environments of formation and

  10. Multi-elemental determination of trace elements in deep seawater by inductively coupled plasma mass spectrometry with resin preconcentration

    International Nuclear Information System (INIS)

    Sumida, Takashi; Nakazato, Tetsuya; Tao, Hiroaki

    2003-01-01

    A miniaturized column (ca. 3 mm i.d., 40 mm length), packed with a chelating resin (0.2 g) with iminodiacetic acid groups (Muromac A-1), was tested for the preconcentration of trace elements in seawater. After preconcentration, the column was washed with ammonium acetate buffer (pH 5.5) and water to remove the major elements, such as Ca and Mg, and was then eluted with 4 ml of 2 mol l -1 nitric acid. Twenty-six trace elements were determined by inductively coupled plasma mass spectrometry and inductively coupled plasma emission spectrometry. The necessary volume of the seawater sample was only 200 ml. The recoveries for most of the elements tested were over 90%, although those for Al, V and Th were around 70%. The trueness and precision were evaluated by analyzing a standard reference material of seawater (NASS-4, NRC Canada). The observed values obtained with the present method showed good agreement with the certified values. The present method was also applied to deep seawater samples collected at Muroto, Japan. A difference in the rare earth element pattern, especially the Ce anomaly, between the deep seawater sample and the surface seawater sample was observed, as well as the differences of the concentrations of many trace elements. (author)

  11. Standardization of solvent extraction procedure for determination of uranium in seawater

    International Nuclear Information System (INIS)

    Sukanta Maity; Sahu, S.K.; Pandit, G.G.

    2015-01-01

    Solvent extraction procedure using ammonium pyrolidine dithiocarbamate complexing agent in methyl isobutyl ketone organic phase and acid exchange back-extraction is described for the simultaneous quantitative pre-concentration of uranium in seawater followed by its determination by differential pulse adsorptive stripping voltammetry. Solvent extraction time is optimized for extraction of uranium from seawater. Solvent extraction efficiency for uranium in seawater at different pH was carried out. The method gives a recovery of 98 ± 2 % for 400 mL sample at pH 3.0 ± 0.02, facilitating the rapid and interference free analysis of seawater samples. (author)

  12. Fuel Production from Seawater and Fuel Cells Using Seawater.

    Science.gov (United States)

    Fukuzumi, Shunichi; Lee, Yong-Min; Nam, Wonwoo

    2017-11-23

    Seawater is the most abundant resource on our planet and fuel production from seawater has the notable advantage that it would not compete with growing demands for pure water. This Review focuses on the production of fuels from seawater and their direct use in fuel cells. Electrolysis of seawater under appropriate conditions affords hydrogen and dioxygen with 100 % faradaic efficiency without oxidation of chloride. Photoelectrocatalytic production of hydrogen from seawater provides a promising way to produce hydrogen with low cost and high efficiency. Microbial solar cells (MSCs) that use biofilms produced in seawater can generate electricity from sunlight without additional fuel because the products of photosynthesis can be utilized as electrode reactants, whereas the electrode products can be utilized as photosynthetic reactants. Another important source for hydrogen is hydrogen sulfide, which is abundantly found in Black Sea deep water. Hydrogen produced by electrolysis of Black Sea deep water can also be used in hydrogen fuel cells. Production of a fuel and its direct use in a fuel cell has been made possible for the first time by a combination of photocatalytic production of hydrogen peroxide from seawater and dioxygen in the air and its direct use in one-compartment hydrogen peroxide fuel cells to obtain electric power. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. XAS and TRLIF spectroscopy of uranium and neptunium in seawater.

    Science.gov (United States)

    Maloubier, Melody; Solari, Pier Lorenzo; Moisy, Philippe; Monfort, Marguerite; Den Auwer, Christophe; Moulin, Christophe

    2015-03-28

    Seawater contains radionuclides at environmental levels; some are naturally present and others come from anthropogenic nuclear activity. In this report, the molecular speciation in seawater of uranium(VI) and neptunium(V) at a concentration of 5 × 10(-5) M has been investigated for the first time using a combination of two spectroscopic techniques: Time-resolved laser-induced fluorescence (TRLIF) for U and extended X-ray absorption fine structure (EXAFS) for U and Np at the LIII edge. In parallel, the theoretical speciation of uranium and neptunium in seawater at the same concentration is also discussed and compared to spectroscopic data. The uranium complex was identified as the neutral carbonato calcic complex UO2(CO3)3Ca2, which has been previously described in other natural systems. In the case of neptunium, the complex identified is mainly a carbonato complex whose exact stoichiometry is more difficult to assess. The knowledge of the actinide molecular speciation and reactivity in seawater is of fundamental interest in the particular case of uranium recovery and more generally regarding the actinide life cycle within the biosphere in the case of accidental release. This is the first report of actinide direct speciation in seawater medium that can complement inventory data.

  14. Concentration and distribution of 14C in aquatic environment around Qinshan nuclear power plant

    International Nuclear Information System (INIS)

    Wang Zhongtang; Guo Qiuju; Hu Dan; Xu Hong

    2015-01-01

    In order to study the concentration and distribution of 14 C in aquatic environment in the vicinity of Qinshan Nuclear Power Plant (NPP) after twenty years' operation, an apparatus extracting dissolved inorganic carbon from water was set up and applied to pretreat the water samples collected around Qinshan NPP. The 14 C concentration was measured by accelerator mass spectrometer (AMS). The results show that the 14 C specific activities in surface seawater samples range from 196.8 to 206.5 Bq/kg 203.4 ± 5.6) Bq/kg in average), which are close to the background. The 14 C concentrations in cooling water discharged from Qinshan NPP are close to the 14 C values in near shore seawater samples out of liquid radioactive effluent discharge period. It can be further concluded that the 14 C discharged previously is diluted and diffused well, and no 14 C enrichment in seawater is found. Also, no obvious increment in the 14 C specific activities of surface water and underground water samples are found between Qinshan NPP region and the reference region. (authors)

  15. Mercury isotope fractionation during transfer from post-desulfurized seawater to air.

    Science.gov (United States)

    Huang, Shuyuan; Lin, Kunning; Yuan, Dongxing; Gao, Yaqin; Sun, Lumin

    2016-12-15

    Samples of dissolved gaseous mercury (DGM) in the post-desulfurized seawater discharged from a coal-fired power plant together with samples of gaseous elemental mercury (GEM) over the post-desulfurized seawater surface were collected and analyzed to study the mercury isotope fractionation during transfer from post-desulfurized seawater to air. Experimental results showed that when DGM in the seawater was converted to GEM in the air, the δ 202 Hg and Δ 199 Hg values were changed, ranging from -2.98 to -0.04‰ and from -0.31 to 0.64‰, respectively. Aeration played a key role in accelerating the transformation of DGM to GEM, and resulted in light mercury isotopes being more likely to be enriched in the GEM. The ratio Δ 199 Hg/Δ 201 Hg was 1.626 in all samples, suggesting that mercury mass independent fractionation occurred owing to the nuclear volume effect during the transformation. In addition, mass independent fractionation of mercury even isotopes was found in the GEM above the post-desulfurized seawater surface in the aeration pool. Copyright © 2016 Elsevier Ltd. All rights reserved.

  16. Influence of non-smooth surface on tribological properties of glass fiber-epoxy resin composite sliding against stainless steel under natural seawater lubrication

    Science.gov (United States)

    Wu, Shaofeng; Gao, Dianrong; Liang, Yingna; Chen, Bo

    2015-11-01

    With the development of bionics, the bionic non-smooth surfaces are introduced to the field of tribology. Although non-smooth surface has been studied widely, the studies of non-smooth surface under the natural seawater lubrication are still very fewer, especially experimental research. The influences of smooth and non-smooth surface on the frictional properties of the glass fiber-epoxy resin composite (GF/EPR) coupled with stainless steel 316L are investigated under natural seawater lubrication in this paper. The tested non-smooth surfaces include the surfaces with semi-spherical pits, the conical pits, the cone-cylinder combined pits, the cylindrical pits and through holes. The friction and wear tests are performed using a ring-on-disc test rig under 60 N load and 1000 r/min rotational speed. The tests results show that GF/EPR with bionic non-smooth surface has quite lower friction coefficient and better wear resistance than GF/EPR with smooth surface without pits. The average friction coefficient of GF/EPR with semi-spherical pits is 0.088, which shows the largest reduction is approximately 63.18% of GF/EPR with smooth surface. In addition, the wear debris on the worn surfaces of GF/EPR are observed by a confocal scanning laser microscope. It is shown that the primary wear mechanism is the abrasive wear. The research results provide some design parameters for non-smooth surface, and the experiment results can serve as a beneficial supplement to non-smooth surface study.

  17. A coastal surface seawater analyzer for nitrogenous nutrient mapping

    Science.gov (United States)

    Masserini, Robert T.; Fanning, Kent A.; Hendrix, Steven A.; Kleiman, Brittany M.

    2017-11-01

    Satellite-data-based modeling of chlorophyll indicates that ocean waters in the mesosphere category are responsible for the majority of oceanic net primary productivity. Coastal waters, which frequently have surface chlorophyll values in the mesosphere range and have strong horizontal chlorophyll gradients and large temporal variations. Thus programs of detailed coastal nutrient surveys are essential to the study of the dynamics of oceanic net primary productivity, along with land use impacts on estuarine and coastal ecosystems. The degree of variability in these regions necessitates flexible instrumentation capable of near real-time analysis to detect and monitor analytes of interest. This work describes the development of a portable coastal surface seawater analyzer for nutrient mapping that can simultaneously elucidate with high resolution the distribution of nitrate, nitrite, and ammonium - the three principal nitrogenous inorganic nutrients in coastal systems. The approach focuses on the use of pulsed xenon flash lamps to construct an analyzer which can be adapted to any automated chemistry with fluorescence detection. The system has two heaters, on-the-fly standardization, on-board data logging, an independent 24 volt direct current power supply, internal local operating network, a 12 channel peristaltic pump, four rotary injection/selection valves, and an intuitive graphical user interface. Using the methodology of Masserini and Fanning (2000) the detection limits for ammonium, nitrite, and nitrate plus nitrite were 11, 10, and 22 nM, respectively. A field test of the analyzer in Gulf of Mexico coastal waters demonstrated its ability to monitor and delineate the complexity of inorganic nitrogen nutrient enrichments within a coastal system.

  18. Speciation of cadmium in seawater - a direct voltammetric approach

    International Nuclear Information System (INIS)

    Helmers, E.

    1994-01-01

    The present report deals with differential pulse anodic stripping voltammetry (DPASV) applied for the analysis of cadmium in open ocean seawater. Evaluation of different Cd species can generate information about distribution and speciation of Cd in the open ocean. Distribution of Cd was investigated in surface waters of the Atlantic Ocean over a wide geographical range as well as in the water column. Surface water sampling on board the research vessel Polarstern was performed from the bow boom of the ship as well as with a snorkel system which allowed continuous sample-taking. Two different Cd species could be differentiated in the voltammograms. UV-irradiation experiments allowed the identification of an inorganic and organic Cd form, the latter caused by the association between Cd and organic matter as e.g. humic substances (HS). Atlantic ocean surface seawater normally contains between 2 and 4 ng organically complexed Cd/kg and no detectable inorganic Cd. Some areas however showed readings of up to 14 ng inorganic Cd/kg in addition. Water column samples exhibited an enrichment of inorganic Cd by depth. Occurrence of inorganic Cd at the surface could be related to specific oceanographical conditions. Together with analytical results of trace metal contents in the particulate phases of surface seawater, new aspects could be established about the biogeochemical cycling of Cd in the sea. (orig.)

  19. A study on antifouling technique through seawater electrolyzing reaction on ship hull surface 【Article】

    OpenAIRE

    Huang, Yi; Saito, Kimio; Usami, Masahiro

    2003-01-01

    The antifouling technique through seawater electrolysis for ship hulls may be realized by an antifoul-ing system consisting of a power unit and the electro-conductive film. In the electric field formed bysuch an antifouling system, besides that both the electro-conductive film layer sub-region and the sea-water sub-region are included, polarization occurs on the interface between electro-conductive film layerand seawater. Therefore, based on the Interface Electro-Double Layer theory, a numeri...

  20. Enhancement of Extraction of Uranium from Seawater - Final Report

    International Nuclear Information System (INIS)

    Dietz, Travis Cameron; Tsinas, Zois; Tomaszewski, Claire; Pazos, Ileana; Nigliazzo, Olga; Li, Weixing; Adel-Hadadi, Mohammad; Barkatt, Aaron; Al-Sheikhly, Mohamad

    2016-01-01

    Even at a concentration of 3 μg/L, the world's oceans contain a thousand times more uranium than currently know terrestrial sources. In order to take advantage of this stockpile, methods and materials must be developed to extract it efficiently, a difficult task considering the very low concentration of the element and the competition for extraction by other atoms in seawater such as sodium, calcium, and vanadium. The majority of current research on methods to extract uranium from seawater are vertical explorations of the grafting of amidoxime ligand, which was originally discovered and promoted by Japanese studies in the late 1980s. Our study expands on this research horizontally by exploring the effectiveness of novel uranium extraction ligands grafted to the surface of polymer substrates using radiation. Through this expansion, a greater understanding of uranium binding chemistry and radiation grafting effects on polymers has been obtained. While amidoxime-functionalized fabrics have been shown to have the greatest extraction efficiency so far, they suffer from an extensive chemical processing step which involves treatment with powerful basic solutions. Not only does this add to the chemical waste produced in the extraction process and add to the method's complexity, but it also significantly impacts the regenerability of the amidoxime fabric. The approach of this project has been to utilize alternative, commercially available monomers capable of extracting uranium and containing a carbon-carbon double bond to allow it to be grafted using radiation, specifically phosphate, oxalate, and azo monomers. The use of commercially available monomers and radiation grafting with electron beam or gamma irradiation will allow for an easily scalable fabrication process once the technology has been optimized. The need to develop a cheap and reliable method for extracting uranium from seawater is extremely valuable to energy independence, and will extend the

  1. Assessing the pollution risk of a groundwater source field at western Laizhou Bay under seawater intrusion

    International Nuclear Information System (INIS)

    Zeng, Xiankui; Wu, Jichun; Wang, Dong; Zhu, Xiaobin

    2016-01-01

    Coastal areas have great significance for human living, economy and society development in the world. With the rapid increase of pressures from human activities and climate change, the safety of groundwater resource is under the threat of seawater intrusion in coastal areas. The area of Laizhou Bay is one of the most serious seawater intruded areas in China, since seawater intrusion phenomenon was firstly recognized in the middle of 1970s. This study assessed the pollution risk of a groundwater source filed of western Laizhou Bay area by inferring the probability distribution of groundwater Cl − concentration. The numerical model of seawater intrusion process is built by using SEAWAT4. The parameter uncertainty of this model is evaluated by Markov Chain Monte Carlo (MCMC) simulation, and DREAM (ZS) is used as sampling algorithm. Then, the predictive distribution of Cl - concentration at groundwater source field is inferred by using the samples of model parameters obtained from MCMC. After that, the pollution risk of groundwater source filed is assessed by the predictive quantiles of Cl - concentration. The results of model calibration and verification demonstrate that the DREAM (ZS) based MCMC is efficient and reliable to estimate model parameters under current observation. Under the condition of 95% confidence level, the groundwater source point will not be polluted by seawater intrusion in future five years (2015–2019). In addition, the 2.5% and 97.5% predictive quantiles show that the Cl − concentration of groundwater source field always vary between 175 mg/l and 200 mg/l. - Highlights: • The parameter uncertainty of seawater intrusion model is evaluated by MCMC. • Groundwater source field won’t be polluted by seawater intrusion in future 5 years. • The pollution risk is assessed by the predictive quantiles of Cl − concentration

  2. Assessing the pollution risk of a groundwater source field at western Laizhou Bay under seawater intrusion

    Energy Technology Data Exchange (ETDEWEB)

    Zeng, Xiankui; Wu, Jichun; Wang, Dong, E-mail: wangdong@nju.edu.cn; Zhu, Xiaobin

    2016-07-15

    Coastal areas have great significance for human living, economy and society development in the world. With the rapid increase of pressures from human activities and climate change, the safety of groundwater resource is under the threat of seawater intrusion in coastal areas. The area of Laizhou Bay is one of the most serious seawater intruded areas in China, since seawater intrusion phenomenon was firstly recognized in the middle of 1970s. This study assessed the pollution risk of a groundwater source filed of western Laizhou Bay area by inferring the probability distribution of groundwater Cl{sup −} concentration. The numerical model of seawater intrusion process is built by using SEAWAT4. The parameter uncertainty of this model is evaluated by Markov Chain Monte Carlo (MCMC) simulation, and DREAM{sub (ZS)} is used as sampling algorithm. Then, the predictive distribution of Cl{sup -} concentration at groundwater source field is inferred by using the samples of model parameters obtained from MCMC. After that, the pollution risk of groundwater source filed is assessed by the predictive quantiles of Cl{sup -} concentration. The results of model calibration and verification demonstrate that the DREAM{sub (ZS)} based MCMC is efficient and reliable to estimate model parameters under current observation. Under the condition of 95% confidence level, the groundwater source point will not be polluted by seawater intrusion in future five years (2015–2019). In addition, the 2.5% and 97.5% predictive quantiles show that the Cl{sup −} concentration of groundwater source field always vary between 175 mg/l and 200 mg/l. - Highlights: • The parameter uncertainty of seawater intrusion model is evaluated by MCMC. • Groundwater source field won’t be polluted by seawater intrusion in future 5 years. • The pollution risk is assessed by the predictive quantiles of Cl{sup −} concentration.

  3. Efficient Functionalization of Polyethylene Fibers for the Uranium Extraction from Seawater through Atom Transfer Radical Polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Neti, Venkata S. [Chemical; Das, Sadananda [Chemical; Brown, Suree [Department; Janke, Christopher J. [Materials; Kuo, Li-Jung [Marine; Gill, Gary A. [Marine; Dai, Sheng [Chemical; Department; Mayes, Richard T. [Chemical

    2017-09-14

    Brush-on-brush structures are proposed as one method to overcome support effects in grafted polymers. Utilizing glycidyl methacrylate (GMA) grafted on polyethylene (PE) fibers using radiation-induced graft polymerization (RIGP) provides a hydrophilic surface on the hydrophobic PE. When integrated with atom transfer radical polymerization (ATRP), the grafting of acrylonitrile (AN) and hydroxyethyl acrylate (HEA) can be controlled and manipulated more easily than with RIGP. Poly(acrylonitrile)-co-poly(hydroxyethyl acrylate) chains were grown via ATRP on PE-GMA fibers to generate an adsorbent for the extraction of uranium from seawater. The prepared adsorbents in this study demonstrated promise (159.9 g- U/kg of adsorbent) in laboratory screening tests using a high uranium concentration brine and 1.24 g-U/Kg of adsorbent in the filtered natural seawater in 21-days. The modest capacity in 21- days exceeds previous efforts to generate brush-on-brush adsorbents by ATRP while manipulating the apparent surface hydrophilicity of the trunk material (PE).

  4. Manganese in the shell of the bivalve Mytilus edulis: Seawater Mn or physiological control?

    Science.gov (United States)

    Freitas, Pedro S.; Clarke, Leon J.; Kennedy, Hilary; Richardson, Christopher A.

    2016-12-01

    Manganese in the shell calcite of marine bivalves has been suggested to reflect ambient seawater Mn concentrations, thus providing a high-resolution archive of past seawater Mn concentrations. However, a quantitative relationship between seawater Mn and shell Mn/Ca ratios, as well as clear understanding of which process(es) control(s) shell Mn/Ca, are still lacking. Blue mussels, Mytilus edulis, were grown in a one-year duration field experiment in the Menai Strait, U.K., to study the relationship between seawater particulate and dissolved Mn2+ concentrations and shell calcite Mn/Ca ratios. Shell Mn/Ca showed a well-defined intra-annual double-peak, with maximum values during early spring and early summer and low values during autumn and winter. Seawater particulate Mn peaked during winter and autumn, with a series of smaller peaks during spring and summer, whereas dissolved Mn2+ exhibited a marked single maximum during late-spring to early-summer, being low during the remainder of the year. Consequently, neither seawater particulate Mn nor dissolved Mn2+ concentrations explain the intra-annual variation of shell Mn/Ca ratios. A physiological control on shell Mn/Ca ratios is evident from the strong similarity and timing of the double-peaked intra-annual variations of Mn/Ca and shell growth rate (SGR), the latter corresponding to periods of increased metabolic activity (as indicated by respiration rate). It is thus likely that in M. edulis SGR influences shell Mn/Ca by altering the concentration or activity of Mn2+ within the extra-pallial fluid (EPF), by changing the flux of Mn into or the proportion of protein bound Mn within the EPF. By linking shell Mn/Ca ratios to the endogenous and environmental factors that determine growth and metabolic activity, this study helps to explain the lack of a consistent relationship between shell Mn/Ca in marine bivalve shell calcite and seawater particulate and dissolved Mn2+ concentrations. The use of Mn content from M. edulis

  5. Biological fate of cobalt-60 released during the corrosion of neutron-activated stanless steel in seawater

    International Nuclear Information System (INIS)

    Young, J.S.

    1982-03-01

    Passing seawater over radioactive Type 347 stainless steel in a sediment/seawater laboratory system and exposing marine animals to this environment provided information on the bioaccumulation of 60 Co from radioactive structural material. Exposure of marine organisms to radioactive corrosion products and directly to radioactive stainless steel in seawater simulated some of the possible conditions which could arise from the deposition of radioactive stainless steel on the ocean floor. Detectable levels of 60 Co in marine animals were not observed on a short term basis (5 weeks). Longterm (13 months) exposure of marine animals in a sediment/seawater system resulted in 60 Co bioaccumulation. The specific activity of 60 Co in the organisms was as much as one million times less than that initially present in the radioactive stainless steel. This was due to the dilution of 60 Co by stable cobalt in the seawater, sediments and organisms. As expected the 60 Co specific activity of the organisms never increased above that of the radioactive source. This is because 60 Co is chemicaly indistinguishable from stable Co. Increasing 60 Co concentration factors with decreasing 60 Co concentrations in the seawater and sediment media coupled with relatively constant 60 Co specific activities suggest a possible homeostatic control of cobalt concentrations in certain marine organisms. The evidence indicates that the marine animals derived more of the accumulated 60 Co from the sediments and interstitial water than from seawater. Cobalt-60 concentration factors were generally found to be lower than published cobalt concentration factors due to the predominantly insoluble nature of the corrosion products. Baseline information is provided on trace element concentrations in deep-sea organisms. Stable Co and twenty other elements were measured in abyssal invertebrates and a fish

  6. Corrosion of aluminum alloys in ocean thermal energy conversion seawaters

    International Nuclear Information System (INIS)

    Larsen-Basse, J.

    1984-01-01

    Aluminum alloys 5052, 3004, and Alclad 3003 and 3004 were exposed to flowing seawater at 2.44 m/s (8 fps) at the Seacoast Test Facility on Hawaii. One year data for warm surface water and three mouth data for cold water from 600 m depth are reported for free fouling, chlorinated and sponge ball cleaned conditions. All alloys pit in deep seawater, but show no pitting in warm surface water. Uniform corrosion in the warm water is initially rapid, but after 25 to 30 days the rate becomes slower and extrapolated 30 year material losses are in the 125 to 215 μm range. Chlorination at a level of 0.05 ppm for one hour per day has only a minor effect on corrosion rates, while sponge ball cleaning leads to erosion-corrosion of the Alclad surfaces and has no effect on alloy 5052. The need for additional testing in tropical seawater is discussed, as is the need for an improved understanding of the formation of inorganic scale films, their properties, and their effect on corrosion rates and heat transfer

  7. Bioaccumulation of PCBs in the cuttlefish Sepia officinalis from seawater, sediment and food pathways

    International Nuclear Information System (INIS)

    Danis, B.; Bustamante, P.; Cotret, O.; Teyssie, J.L.; Fowler, S.W.; Warnau, M.

    2005-01-01

    The cuttlefish Sepia officinalis was selected as a model cephalopod to study PCB bioaccumulation via seawater, sediments and food. Newly hatched, juvenile cuttlefish were exposed for 17 days to environmentally realistic concentrations of 14 C-labeled 2,2',4,4',5,5'-hexachlorobiphenyl (PCB no. 153) (18 ng PCB l -1 seawater; 30 ng PCB g -1 dry wt sediments; Artemia salina exposed to 18 ng PCB l -1 seawater). Accumulation of PCB no. 153 was followed in three body compartments: digestive gland, cuttlebone and the combined remaining tissues. Results showed that (1) uptake kinetics were source- and body compartment-dependent, (2) for each body compartment, the accumulation was far greater when S. officinalis was exposed via seawater, (3) the cuttlebone accumulated little of the contaminant regardless of the source, and (4) the PCB congener showed a similar distribution pattern among the different body compartments following exposure to contaminated seawater, sediment or food with the lowest concentrations in the cuttlebone and the highest in the remaining tissues. The use of radiotracer techniques allowed delineating PCB kinetics in small whole organisms as well as in their separate tissues. The results underscore the enhanced ability of cephalopods to concentrate organic pollutants such as PCBs, and raise the question of potential risk to their predators in contaminated areas. - Bioaccumulation of PCBs by cuttlefish is studied, via seawater, sediments and their food

  8. Radiolytic removal of trihalomethane in chlorinated seawater

    International Nuclear Information System (INIS)

    Rajamohan, R.; Rajesh, Puspalata; Venugopalan, V.P.; Rangarajan, S.; Natesan, Usha

    2015-01-01

    Biofouling is one of the major operational problems in seawater cooling systems. It is controlled by application of chlorine based biocides in the range of 0.5-2.0 mg L -1 . The bromide in seawater reacts with the added chlorine and forms hypobromous acid. The brominated residual biocides react with natural organic matter present in the seawater, resulting in the formation of trihalomethanes (THM) such as bromoform (CHBr 3 ), dibromochloromethane (CHBr 2 Cl) bromodichloromethane (CHBrCl 2 ). Though THMs represent a small fraction of the added chlorine, they are relatively more persistent than residual chlorine, and hence pose a potential hazard to marine life because of their reported mutagenicity. There have been few reports on removal of THMs from chlorinated seawater. In this work, the efficacy of gamma irradiation technique for the removal of THMs from chlorine-dosed seawater was investigated. Experiments were carried out using seawater collected from Kalpakkam. Irradiation study was conducted in chlorinated (1, 3, and 5 mg L -1 of Cl 2 ) seawater by applying various dosages (0.4-5.0 kGy) of gamma radiation using a 60 Co Gamma Chamber 5000. Bromoform showed a faster rate of degradation as compared to other halocarbons like bromodichloromethane and dibromochloromethane. This shows the change in total THM concentration with variation in the radiation dose and initial Cl 2 dosing. When the percentage degradation of all the three trihalomethane species was compared with applied doses, it was found that the maximum reduction occurred at a dose of 2.5 kGy. The reduction was almost similar for all the three doses (1, 3, 5 ppm of Cl 2 ) used for chlorination. With a further increase in radiation dose to 5.0 kGy, a slight increase in reduction was observed

  9. A solvent extraction technique for the isotopic measurement of dissolved copper in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Thompson, Claire M., E-mail: claire.thompson@anu.edu.au; Ellwood, Michael J., E-mail: michael.ellwood@anu.edu.au; Wille, Martin, E-mail: martin.wille@uni-tuebingen.de

    2013-05-02

    Graphical abstract: -- Highlights: •A new sample preparation method for seawater copper isotopic analysis (δ{sup 65}Cu). •Solvent-extraction was used to pre-concentrate metals from seawater samples. •Anion-exchange was used to purify copper from the metal-rich extract. •δ{sup 65}Cu was measured in the north Tasman Sea. •Seawater δ{sup 65}Cu may be linked to marine biological activity. -- Abstract: Stable copper (Cu) isotope geochemistry provides a new perspective for investigating and understanding Cu speciation and biogeochemical Cu cycling in seawater. In this work, sample preparation for isotopic analysis employed solvent-extraction with amino pyrollidine dithiocarbamate/diethyl dithiocarbamate (APDC/DDC), coupled with a nitric acid back-extraction, to concentrate Cu from seawater. This was followed by Cu-purification using anion-exchange. This straightforward technique is high yielding and fractionation free for Cu and allows precise measurement of the seawater Cu isotopic composition using multi-collector inductively coupled plasma mass-spectrometry. A deep-sea profile measured in the oligotrophic north Tasman Sea shows fractionation in the Cu isotopic signature in the photic zone but is relatively homogenised at depth. A minima in the Cu isotopic profile correlates with the chlorophyll a maximum at the site. These results indicate that a range of processes are likely to fractionate stable Cu isotopes in seawater.

  10. Activation of TRPV1-dependent calcium oscillation exacerbates seawater inhalation-induced acute lung injury.

    Science.gov (United States)

    Li, Congcong; Bo, Liyan; Liu, Qingqing; Liu, Wei; Chen, Xiangjun; Xu, Dunquan; Jin, Faguang

    2016-03-01

    Calcium is an important second messenger and it is widely recognized that acute lung injury (ALI) is often caused by oscillations of cytosolic free Ca2+. Previous studies have indicated that the activation of transient receptor potential‑vanilloid (TRPV) channels and subsequent Ca2+ entry initiates an acute calcium‑dependent permeability increase during ALI. However, whether seawater exposure induces such an effect through the activation of TRPV channels remains unknown. In the current study, the effect of calcium, a component of seawater, on the inflammatory reactions that occur during seawater drowning‑induced ALI, was examined. The results demonstrated that a high concentration of calcium ions in seawater increased lung tissue myeloperoxidase activity and the secretion of inflammatory mediators, such as tumor necrosis factor‑α (TNF‑α) and interleukin (IL)‑1β and IL‑6. Further study demonstrated that the seawater challenge elevated cytosolic Ca2+ concentration, indicated by [Ca2+]c, by inducing calcium influx from the extracellular medium via TRPV1 channels. The elevated [Ca2+c] may have resulted in the increased release of TNF‑α and IL‑1β via increased phosphorylation of nuclear factor‑κB (NF‑κB). It was concluded that a high concentration of calcium in seawater exacerbated lung injury, and TRPV1 channels were notable mediators of the calcium increase initiated by the seawater challenge. Calcium influx through TRPV1 may have led to greater phosphorylation of NF‑κB and increased release of TNF‑α and IL‑1β.

  11. Symbiotic Role of the Viable but Nonculturable State of Vibrio fischeri in Hawaiian Coastal Seawater.

    Science.gov (United States)

    Lee, K; Ruby, E G

    1995-01-01

    To achieve functional bioluminescence, the developing light organ of newly hatched juveniles of the Hawaiian squid Euprymna scolopes must become colonized by luminous, symbiosis-competent Vibrio fischeri present in the ambient seawater. This benign infection occurs rapidly in animals placed in seawater from the host's natural habitat. Therefore, it was surprising that colony hybridization studies with a V. fischeri-specific luxA gene probe indicated the presence of only about 2 CFU of V. fischeri per ml of this infective seawater. To examine this paradox, we estimated the total concentration of V. fischeri cells present in seawater from the host's habitat in two additional ways. In the first approach, the total bacterial assemblage in samples of seawater was collected on polycarbonate membrane filters and used as a source of both a crude cell lysate and purified DNA. These preparations were then assayed by quantitative DNA-DNA hybridization with the luxA gene probe. The results suggested the presence of between 200 and 400 cells of V. fischeri per ml of natural seawater, a concentration more than 100 times that revealed by colony hybridization. In the second approach, we amplified V. fischeri-specific luxA sequences from microliter volumes of natural seawater by PCR. Most-probable-number analyses of the frequency of positive PCR results from cell lysates in these small volumes gave an estimate of the concentration of V. fischeri luxA gene targets of between 130 and 1,680 copies per ml. From these measurements, we conclude that in their natural seawater environment, the majority of V. fischeri cells become nonculturable while remaining viable and symbiotically infective. Experimental studies indicated that V. fischeri cells suspended in natural Hawaiian seawater enter such a state within a few days.

  12. Technical note: Examining ozone deposition over seawater

    Science.gov (United States)

    Surface layer resistance plays an important role in determining ozone deposition velocity over sea-water and can be influenced by chemical interactions at the air-water interface. Here, we examine the effect of chemical interactions of iodide, dimethylsulfide, dissolved organic c...

  13. Radiation influence on heterogenous processes in stainless steel contact with sea-water

    International Nuclear Information System (INIS)

    Agayev, T.N.; Garibov, A.A.; Velibekova, G.Z.; Aliyev, A.Q.; Aliyev, S.M.

    2005-01-01

    Full text: Austenitic stainless steel (s.s.) with Cr content 16 %, Ni - 15 % is widely used in nuclear reactors as construction material, for fuel cladding production and also is used in oil and gas production and transportation. They possess comparatively large section of slow neutron capture and as a result high corrosion resistance. In real exploitation condition of nuclear reactors s.s. are exposed to ionizing radiation influence in contact of different media. That's why during their corrosion and destruction processes the surface defect formation processes and further heterogenous processes with their participation are of great importance. The research results of mechanism during radiation-heterogenous processes in nuclear reactor stainless steel contact with sea-water under the influence of γ-radiation in temperature interval 300-1074 K are represented in the given work. Radiolytic processes in water are comprehensively studied and therefore it was taken as model system for dating the surface defects and secondary electrons emitted from metal. The same model system was applied also in sea-water radiolysis processes. It's been established that radiation processes in s.s. lead to molecular hydrogen yield increase and at T=300 K up to 6.5 molec./100 eV. With the temperature increase molecular hydrogen yield increase up to 25.3 molec./100 eV at T≤773 K. During the further temperature increase up to 1073 K radiation constituent of radiation-thermal process in comparison with thermal becomes unnoticeable and W T (H 2 )≅W p (H 2 ). The kinetics of oxide phase formation of investigated sample surface in the result of thermal and radiation-thermal processes in their contact with sea-water has been studied. At that it's been shown that radiation leads to protective oxidation process rate increase and promotes the beginning of stainless steel destruction oxidation in contact with sea-water. At T≥573 K insoluble oxide phase is formed on metal surface that promotes

  14. Tritium concentration in fresh, brackish and sea-water samples in Rokkasho-Village, Japan, bordered by nuclear fuel cycle facilities

    International Nuclear Information System (INIS)

    Ueda, S.; Kakiuchi, H.; Kondo, K.; Inaba, J.

    2006-01-01

    In order to identify the concentration of tritium ( 3 H) in areas of fresh, brackish and sea water, bordered by nuclear fuel facilities at Rokkasho-Village, Aomori, Japan, water samples were collected from 2001 to 2004 at six points in those areas. Concentration ranges of tritium in fresh river water, brackish lake and seawater samples were 0.60 to 1.1 Bq x l -1 (mean value 0.79 Bq x l -1 ), 0.20 to 0.87 Bq x l -1 (mean value 0.41 Bq x l -1 ), and 0.08 to 0.25 Bq x l -1 (mean value 0.15 Bq x l -1 ), respectively. Relationships between tritium concentrations and salinity in the samples showed a clear negative correlation. Moreover, the seasonal variation of tritium in water from Rokkasho-Village was high in spring and low in fall. (author)

  15. An updated climatology of surface dimethlysulfide concentrations and emission fluxes in the global ocean

    Science.gov (United States)

    Lana, A.; Bell, T. G.; Simó, R.; Vallina, S. M.; Ballabrera-Poy, J.; Kettle, A. J.; Dachs, J.; Bopp, L.; Saltzman, E. S.; Stefels, J.; Johnson, J. E.; Liss, P. S.

    2011-03-01

    The potentially significant role of the biogenic trace gas dimethylsulfide (DMS) in determining the Earth's radiation budget makes it necessary to accurately reproduce seawater DMS distribution and quantify its global flux across the sea/air interface. Following a threefold increase of data (from 15,000 to over 47,000) in the global surface ocean DMS database over the last decade, new global monthly climatologies of surface ocean DMS concentration and sea-to-air emission flux are presented as updates of those constructed 10 years ago. Interpolation/extrapolation techniques were applied to project the discrete concentration data onto a first guess field based on Longhurst's biogeographic provinces. Further objective analysis allowed us to obtain the final monthly maps. The new climatology projects DMS concentrations typically in the range of 1-7 nM, with higher levels occurring in the high latitudes, and with a general trend toward increasing concentration in summer. The increased size and distribution of the observations in the DMS database have produced in the new climatology substantially lower DMS concentrations in the polar latitudes and generally higher DMS concentrations in regions that were severely undersampled 10 years ago, such as the southern Indian Ocean. Using the new DMS concentration climatology in conjunction with state-of-the-art parameterizations for the sea/air gas transfer velocity and climatological wind fields, we estimate that 28.1 (17.6-34.4) Tg of sulfur are transferred from the oceans into the atmosphere annually in the form of DMS. This represents a global emission increase of 17% with respect to the equivalent calculation using the previous climatology. This new DMS climatology represents a valuable tool for atmospheric chemistry, climate, and Earth System models.

  16. Hydrochemical and isotopic characteristics of estuarial seawater and river water of Bailanghe in Laizhou Bay, China

    Science.gov (United States)

    Yang, Qiaofeng; Xu, Suning; Wang, Ruijiu; Li, Wenpeng; Wang, Zhiyi; Mei, Junjun; Ding, Zhilei; Yang, Peijie; Yu, Liangju; Lv, Tieying; Bai, Gang; Kang, Wei

    2016-04-01

    In the study of seawater intrusion, seawater is usually taken as an end-member that mixes with other source(s). However, compared to standard seawater, the coastal seawater particularly that near the estuary, can be strongly influenced by the rivers into the sea and by coastal human activities. Their composition can be thus continuously changed and redistributed with space and time. Therefore, before investigating seawater intrusion in a certain area, it is essentially important to determine the features of the estuarine seawater (e.g. the mixture percentage between standard seawater and river water). In this study, we aimed to gain a clear situation of the seawater intrusion in Laizhou Bay, Southern Bohai, China. The issue aforementioned was investigated by comparing the stable isotopic and hydrochemical composition of the marine and river water collected in this area. Samples investigated include 5 surface water samples collected at the downstream of the Bailanghe and 7 seawater samples near the estuary of Laizhou Bay. Inert tracers (δD, δ18O, Cl, Br) and reaction tracers (Na, Mg, SO4, HCO3, Ca, NO3) are particularly analyzed. The major results are as follows: 1) All the river water samples fall below the Global Meteoric Water Line in the δD - δ18O diagram, reflecting evaporation of the upstream reservoir water. The seawater samples fall on the mixing line of standard seawater and the river water in the stable isotopic diagram. 2) The Cl-δ18O diagram indicates widespread dissolution of evaporate into the river, while high concentration of Ca and HCO3-, as well as the SO42- - Cl relation of the river water samples reflect the dissolution of CO2 , carbonate and sulfate in the atmosphere and on the ground. 3) The Br/Cl ratios of seawater samples are closed to the marine ratios. This together with the plots of major ions vs. Cl suggest that the seawater samples are originated from the mixture of standard seawater and river water. Therefore, when referring to the

  17. Selective uptake of manganese in seawater by hybrid microcapsules

    International Nuclear Information System (INIS)

    Kuzumaki, Takenori; Yan, Wu; Mimura, Hitoshi; Niibori, Yuichi

    2008-01-01

    The selective separation and recovery of low concentrated elements in seawater are very important subjects for the advancement of environmental monitoring. Selective uptake of manganese from seawater was carried out by using two kinds of microcapsules (MCs) including activated carbon (AC) and insoluble tannin (T). The adsorbents, AC and T, having affinity for manganese, were enclosed into MCs (ACMS, TMC) by sol-gel method using matrices of biopolymer (calcium alginate gel polymer, CaALG). The uptake properties and selectivity of Mn 2+ (1 ppm) for MCs were examined by batch method. Relatively large uptake percentages of Mn 2+ above 80% were obtained within 1 h, and the uptake percentage above 80% was kept at pH 3-6. The uptake order was found to be T, AC, CaALG > ACMC, TMC. The uptake of Mn 2+ decreased with increasing Na + ion concentration. This tendency depends on the swelling property of CaALG; it tends to solate in the presence of highly concentrated Na + ions. The manganese ions were adsorbed on CaALG, ACMC and TMC from seawater containing 1,000 ppm Mn 2+ . ACMC and TMC had selectivity to Mn 2+ , and, especially, the matrices of CaALG also had an excellent uptake and selectivity properties. (author)

  18. Overview of the nuclear fuel resources – seawater uranium recovery program sponsored by the U.S. Department of Energy

    International Nuclear Information System (INIS)

    Kung, S.

    2014-01-01

    For nuclear energy to remain a sustainable energy source, there must be assurance that an economically viable supply of nuclear fuel is available. One major goal of the Fuel Cycle Technology Research and Development (R&D) Program in the United States Department of Energy (DOE), Office of Nuclear Energy (NE) is to develop sustainable fuel cycles options. The development of technology to recover uranium from seawater has the potential to fulfill this program goal. Seawater uranium recovery technology is identified in the U.S. DOE NE Roadmap as an area most appropriate for federal involvement to support long-term, “game-changing” approach. Seawater contains more than 4 billion metric tons of dissolved uranium. This unconventional uranium resource, combined with a suitable extraction cost, can potentially meet the uranium demands for centuries to come. The challenge, however, is the low concentration of uranium in seawater – approximately 3.3 ppb. A multidisciplinary team from the U.S. national laboratories, universities, and research institutes has been assembled to address this challenge. Polymeric adsorbents materials containing amidoxime ligands, developed at the Oak Ridge National Laboratory (ORNL), have demonstrated great promise for the extraction of uranium from seawater. These ORNL adsorbents showed adsorption capacities for the extraction of uranium from seawater that exceed 3 mg U/g adsorbent in testing at the Pacific Northwest National Laboratory Marine Sciences Laboratory. A key component of this novel technology lies in the unique high surface-area polyethylene fibers that considerably increase the surface area and thus the grafting yield of functional groups without compromising its mechanical properties. In addition, high surface area nanomaterial adsorbents are under development at ORNL with the goal of increasing uranium adsorption capacity by taking advantage of the high surface areas and tunable porosity of carbon-based nanomaterials

  19. Seawater spray injury to Quercus acutissima leaves: crystal deposition, stomatal clogging, and chloroplast degeneration.

    Science.gov (United States)

    Kim, Ki Woo; Koo, Kyosang; Kim, Pan-Gi

    2011-05-01

    Effects of seawater spray on leaf structure were investigated in Quercus acutissima by electron microscopy and X-ray microanalysis. Two-year-old seedlings of Q. acutissima were sprayed with seawater and kept in a greenhouse maintained at 25°C. The most recognizable symptoms of seawater-sprayed seedlings included leaf necrosis, crystal deposition, stomatal clogging, and chloroplast degeneration. Field emission scanning electron microscopy revealed that the leaf surface was covered with additional layers of remnants of seawater spray. Composed of sodium and chloride, cube-shaped crystals (halite) were prevalently found on trichomes and epidermis, and formed aggregates. Meanwhile, wedge-shaped crystals were deposited on epidermis and consisted of calcium and sulfur. As a result of stomatal clogging by crystal deposition on the abaxial surface, it was conceivable that plant respiration became severely hampered. Transmission electron microscopy showed degenerated cytoplasm of seawater-sprayed leaves. It was common to observe severe plasmolysis and disrupted chloroplasts with a reduced number of thylakoids in grana. These results indicate that foliar applications of seawater were sufficient to induce necrosis of Q. acutissima seedlings as an abiotic disturbance factor. Copyright © 2010 Wiley-Liss, Inc.

  20. Enhancement of Extraction of Uranium from Seawater – Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Dietz, Travis Cameron [Univ. of Maryland, College Park, MD (United States); Tsinas, Zois [Univ. of Maryland, College Park, MD (United States); Tomaszewski, Claire [Univ. of Maryland, College Park, MD (United States); Pazos, Ileana [Univ. of Maryland, College Park, MD (United States); Nigliazzo, Olga [University of Palermo, Palermo (Italy); Li, Weixing [Univ. of Maryland, College Park, MD (United States); Adel-Hadadi, Mohammad [Univ. of Maryland, College Park, MD (United States); Barkatt, Aaron [The Catholic Univ. of America, Washington, DC (United States); Al-Sheikhly, Mohamad [Univ. of Maryland, College Park, MD (United States)

    2016-05-16

    Even at a concentration of 3 μg/L, the world’s oceans contain a thousand times more uranium than currently know terrestrial sources. In order to take advantage of this stockpile, methods and materials must be developed to extract it efficiently, a difficult task considering the very low concentration of the element and the competition for extraction by other atoms in seawater such as sodium, calcium, and vanadium. The majority of current research on methods to extract uranium from seawater are vertical explorations of the grafting of amidoxime ligand, which was originally discovered and promoted by Japanese studies in the late 1980s. Our study expands on this research horizontally by exploring the effectiveness of novel uranium extraction ligands grafted to the surface of polymer substrates using radiation. Through this expansion, a greater understanding of uranium binding chemistry and radiation grafting effects on polymers has been obtained. While amidoxime-functionalized fabrics have been shown to have the greatest extraction efficiency so far, they suffer from an extensive chemical processing step which involves treatment with powerful basic solutions. Not only does this add to the chemical waste produced in the extraction process and add to the method’s complexity, but it also significantly impacts the regenerability of the amidoxime fabric. The approach of this project has been to utilize alternative, commercially available monomers capable of extracting uranium and containing a carbon-carbon double bond to allow it to be grafted using radiation, specifically phosphate, oxalate, and azo monomers. The use of commercially available monomers and radiation grafting with electron beam or gamma irradiation will allow for an easily scalable fabrication process once the technology has been optimized. The need to develop a cheap and reliable method for extracting uranium from seawater is extremely valuable to energy independence, and will extend the quantity of

  1. Electrochemical formation of green rusts in deaerated seawater-like solutions

    Energy Technology Data Exchange (ETDEWEB)

    Refait, Ph., E-mail: prefait@univ-lr.fr [Laboratoire d' etude des materiaux en milieux agressifs (LEMMA), EA 3167, Universite de La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Fed. de Recherche en Environnement et Developpement Durable, FR CNRS 3097 (France); Nguyen, D.D. [Laboratoire d' etude des materiaux en milieux agressifs (LEMMA), EA 3167, Universite de La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Hue University' s College of Education, Hue (Viet Nam); Jeannin, M. [Laboratoire d' etude des materiaux en milieux agressifs (LEMMA), EA 3167, Universite de La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Fed. de Recherche en Environnement et Developpement Durable, FR CNRS 3097 (France); Sable, S. [Littoral, Environnement et Societe (LiENSs), UMR 6250, CNRS-Univ. La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Fed. de Recherche en Environnement et Developpement Durable, FR CNRS 3097 (France); Langumier, M. [Laboratoire d' etude des materiaux en milieux agressifs (LEMMA), EA 3167, Universite de La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Littoral, Environnement et Societe (LiENSs), UMR 6250, CNRS-Univ. La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Fed. de Recherche en Environnement et Developpement Durable, FR CNRS 3097 (France); Sabot, R. [Laboratoire d' etude des materiaux en milieux agressifs (LEMMA), EA 3167, Universite de La Rochelle, Bat. Marie Curie, Av. Michel Crepeau, F-17 042 La Rochelle Cedex 01 (France); Fed. de Recherche en Environnement et Developpement Durable, FR CNRS 3097 (France)

    2011-07-15

    Highlights: > Sulphated green rust could be electro-generated on carbon steel in anoxic seawater-like electrolytes. > Rust layers grown during 11 years on carbon steel in natural seawater were thoroughly characterised by {mu}-Raman spectroscopy. > The mechanism of marine corrosion of carbon steel in anoxic conditions could be specified. - Abstract: Carbon steel electrodes were polarised at a potential {approx}150 mV higher than the open circuit potential, in a deaerated seawater-like electrolyte (0.5 mol dm{sup -3} NaCl, 0.03 mol dm{sup -3} Na{sub 2}SO{sub 4}, 0.003 mol dm{sup -3} NaHCO{sub 3}). X-ray diffraction and {mu}-Raman analysis demonstrated that a layer mainly composed of GR(SO{sub 4}{sup 2-}) had grown on the steel surface. GR(SO{sub 4}{sup 2-}) was accompanied by traces of GR(CO{sub 3}{sup 2-}). Similar experiments performed in a solution composed of 0.3 mol dm{sup -3} of Na{sub 2}SO{sub 4} and 0.03 mol dm{sup -3} of NaHCO{sub 3} led to the same result. The nature of the GR forming on steel is thus mainly linked to the sulphate to carbonate concentration ratio. Finally, carbon steel coupons immersed for 11 years in the harbour of La Rochelle (Atlantic coast) were removed from seawater for analysis. The inner part of the rust layer proved to be mainly composed of magnetite, GR(SO{sub 4}{sup 2-}) and iron sulphide FeS. This definitively confirms that GR(SO{sub 4}{sup 2-}), as Fe{sub 3}O{sub 4} and FeS, can form from steel in O{sub 2}-depleted environments.

  2. Post-Mesozoic Rapid Increase of Seawater Mg/Ca due to Enhanced Mantle-Seawater Interaction

    Science.gov (United States)

    Ligi, Marco; Bonatti, Enrico; Cuffaro, Marco; Brunelli, Daniele

    2013-01-01

    The seawater Mg/Ca ratio increased significantly from ~ 80 Ma to present, as suggested by studies of carbonate veins in oceanic basalts and of fluid inclusions in halite. We show here that reactions of mantle-derived peridotites with seawater along slow spreading mid-ocean ridges contributed to the post-Cretaceous Mg/Ca increase. These reactions can release to modern seawater up to 20% of the yearly Mg river input. However, no significant peridotite-seawater interaction and Mg-release to the ocean occur in fast spreading, East Pacific Rise-type ridges. The Mesozoic Pangean superocean implies a hot fast spreading ridge system. This prevented peridotite-seawater interaction and Mg release to the Mesozoic ocean, but favored hydrothermal Mg capture and Ca release by the basaltic crust, resulting in a low seawater Mg/Ca ratio. Continent dispersal and development of slow spreading ridges allowed Mg release to the ocean by peridotite-seawater reactions, contributing to the increase of the Mg/Ca ratio of post-Mesozoic seawater. PMID:24067442

  3. Bicarbonate Elution of Uranium from Amidoxime-Based Polymer Adsorbents for Sequestering Uranium from Seawater

    Energy Technology Data Exchange (ETDEWEB)

    Pan, Horng-Bin [Department of Chemistry, University of Idaho, Moscow, Idaho 83844 USA; Wai, Chien M. [Department of Chemistry, University of Idaho, Moscow, Idaho 83844 USA; Kuo, Li-Jung [Pacific Northwest National Laboratory, Marine Sciences Laboratory, Sequim, Washington 98382 USA; Gill, Gary [Pacific Northwest National Laboratory, Marine Sciences Laboratory, Sequim, Washington 98382 USA; Tian, Guoxin [Lawrence Berkeley National Laboratory, Berkeley, California 94720 USA; Rao, Linfeng [Lawrence Berkeley National Laboratory, Berkeley, California 94720 USA; Das, Sadananda [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA; Mayes, Richard T. [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA; Janke, Christopher J. [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA

    2017-05-02

    Uranium adsorbed on amidoxime-based polyethylene fibers in simulated seawater can be quantitatively eluted using 3 M KHCO3 at 40°C. Thermodynamic calculations are in agreement with the experimental observation that at high bicarbonate concentrations (3 M) uranyl ions bound to amidoxime molecules are converted to uranyl tris-carbonato complex in the aqueous solution. The elution process is basically the reverse reaction of the uranium adsorption process which occurs at a very low bicarbonate concentration (~10-3 M) in seawater. In real seawater experiments, the bicarbonate elution is followed by a NaOH treatment to remove natural organic matter adsorbed on the polymer adsorbent. Using the sequential bicarbonate and NaOH elution, the adsorbent is reusable after rinsing with deionized water and the recycled adsorbent shows no loss of uranium loading capacity based on real seawater experiments.

  4. Anthropogenic 236U in Danish Seawater: Global Fallout versus Reprocessing Discharge.

    Science.gov (United States)

    Qiao, Jixin; Steier, Peter; Nielsen, Sven; Hou, Xiaolin; Roos, Per; Golser, Robin

    2017-06-20

    This work focuses on the occurrence of 236 U in seawater along Danish coasts, which is the sole water-exchange region between the North Sea-Atlantic Ocean and the Baltic Sea. Seawater collected in 2013 and 2014 were analyzed for 236 U (as well as 238 U and 137 Cs). Our results indicate that 236 U concentrations in Danish seawater are distributed within a relatively narrow range of (3.6-8.2) × 10 7 atom/L and, to a certain extent, independent of salinity. 236 U/ 238 U atomic ratios in Danish seawater are more than 4 times higher than the estimated global fallout value of 1× 10 -9 . The levels of 236 U/ 238 U atomic ratios obtained are comparable to those reported for the open North Sea and much higher than several other open oceans worldwide. This indicates that besides the global fallout input, the discharges from the two major European nuclear reprocessing plants are dominating sources of 236 U in Danish seawater. However, unexpectedly high 236 U/ 238 U ratios as well as high 236 U concentrations were observed at low-salinity locations of the Baltic Sea. While this feature might be interpreted as a clue for another significant 236 U input in the Baltic Sea, it may also be caused by the complexity of water currents or slow turnover rate.

  5. Occurrence of perchlorate in drinking water and seawater in South Korea.

    Science.gov (United States)

    Her, Namguk; Jeong, Hyunchan; Kim, Jongsung; Yoon, Yeomin

    2011-08-01

    Concentrations of perchlorate were determined by both liquid-chromatography-mass spectrometry (LC-MS) and ion chromatography tandem mass spectrometry (IC-MS/MS) in 520 tap-water, 48 bottled-water, and 9 seawater samples obtained or purchased from >100 different locations in South Korea. The method detection limits were 0.013 μg/L for LC-MS and 0.005 μg/L for IC-MS/MS, and the limits of quantification (LOQs) were 0.10 μg/L for LC-MS and 0.032 μg/L for IC-MS/MS. Perchlorate was detected in most (80%) of the tap-water samples, with concentrations higher than the LOQ; the concentrations ranged from water samples, with concentrations higher then the LOQ, ranging from 0.04 to 0.29 μg/L (mean 0.07 ± 0.01). The concentrations of perchlorate in all seawater samples collected from the various locations were higher than the LOQ, with a mean concentration of 1.15 ± 0.01 μg/L (maximum 6.11 and minimum 0.11). This study provides further evidence that drinking-water sources have been contaminated by perchlorate. To the best of our knowledge, this is the first comprehensive study on perchlorate assessment in drinking water and seawater in South Korea.

  6. Nature/culture/seawater.

    Science.gov (United States)

    Helmreich, Stefan

    2011-01-01

    Seawater has occupied an ambiguous place in anthropological categories of "nature" and "culture." Seawater as nature appears as potentiality of form and uncontainable flux; it moves faster than culture - with culture frequently figured through land-based metaphors - even as culture seeks to channel water's (nature's) flow. Seawater as culture manifests as a medium of pleasure, sustenance, travel, disaster. I argue that, although seawater's qualities in early anthropology were portrayed impressionistically, today technical, scientific descriptions of water's form prevail. For example, processes of globalization - which may also be called "oceanization" - are often described as "currents," "flows," and "circulations." Examining sea-set ethnography, maritime anthropologies, and contemporary social theory, I propose that seawater has operated as a “theory machine” for generating insights about human cultural organization. I develop this argument with ethnography from the Sargasso Sea and in the Sea Islands. I conclude with a critique of appeals to water's form in social theory.

  7. Development of adsorbents for recovery of uranium from seawater

    International Nuclear Information System (INIS)

    Egawa, Hiroaki; Furusaki, Shintaro.

    1987-01-01

    The largest subject for putting the extraction of uranium from seawater in practical use is the development of high performance adsorbents for uranium. In this paper, the way of thinking about the development of adsorbents for extracting uranium from seawater and the recent reports on this subject are described. Next, the research on the adsorbing capacity and adsorbing rate of the adsorbents developed so far is summarized, and the way of thinking about the evaluation of adsorbent performance which is the base of the design of a system for extracting uranium from seawater is explained, taking amidoxime type adsorbent as the example. For Japan where energy resources are scant, the uranium contained in seawater, which is estimated to be about 4.2 billion t, is the most luring important element. Uranium is contained in seawater is very low concentration of 3 ppb, and exists as anion complex salt. In 1960s, the Harwell Atomic Energy Research Establishment in UK found out that titanium oxide hydrate is the most promising as the adsorbent. Also a number of organic absorbents have been developed. In order to bring adsorbents in contact with seawater, pumping, ocean current and wave force are utilized. Adsorbents are in spherical, fiber and film forms, and held as fixed beds and fluidized beds. (Kako, I.) 48 refs

  8. Materials resistant to seawater

    International Nuclear Information System (INIS)

    Lunde, L.

    1986-03-01

    The report is a summary of the topics discussed at a two-day seminar at Institute for Energy Technology, Kjeller in August 1985. Experience with seawater corrosion in Nordic power reactor plants was discussed. There was also input from Danish experience with seawater corrosion in coal fired power plants. The following topics were dealt with: Experience in seawater cooling system materials, chlorination of seawater systems, and accelerated laboratory tests for stainless steels

  9. Global Cr-isotope distributions in surface seawater and incorporation of Cr isotopes into carbonate shells

    DEFF Research Database (Denmark)

    Paulukat, Cora Stefanie; Frei, Robert; Vögelin, Andrea Regula

    produced carbonate shells (bivalves, gastropods) and corals. Our preliminary data set ranges approximately from d53Cr = -0.2 to +0.7‰. They are isotopically lighter than local seawater. This is in good agreement with [6], who measured a negative offset from seawater in corals. These offsets indicate some...

  10. Biofouling control of industrial seawater cooling towers

    KAUST Repository

    Al-Bloushi, Mohammed

    2017-01-01

    In this study, the research focuses on biofouling control in seawater cooling towers by investigating two different approaches. The first strategy addresses the use of alternative oxidants (i.e. ozone micro-bubbles and chlorine dioxide) in treatment of cooling towers. The second strategy investigates removing nutrients in seawater using granular activated carbon filter column and ultrafiltration to prevent the growth of microorganisms. Laboratory bench-scale tests in terms of temperature, cycle of concentration, dosage, etc. indicated that, at lower oxidant dosages (total residual oxidant (TRO) equivalent = 0.1 mg/l Cl2), chlorine dioxide had a better disinfection effect than chlorine and ozone. The performance of oxidizing biocides at pilot scale, operating at assorted conditions, showed that for the disinfectants tested, ozone could remove 95 % bioactivity of total number of bacteria and algae followed by chlorine dioxide at 85%, while conventional chlorine dosing only gave 60% reduction in bioactivities. Test results of GAC bio-filter showed that around 70 % removal of total organic carbon in the seawater feed was achieved and was effective in keeping the microbial growth to a minimum. The measured results from this study enable designers of seawater cooling towers to manage the biofouling problems when such cooling towers are extrapolated to a pilot scale.

  11. A Survey of Tritium in Irish Seawater

    International Nuclear Information System (INIS)

    Currivan, L.; Kelleher, K.; McGinnity, P.; Wong, J.; McMahon, C.

    2013-07-01

    This report provides a comprehensive record of the study and measurements of tritium in Irish seawater undertaken by the Radiological Protection Institute of Ireland RPII. The majority of the samples analysed were found to have tritium concentrations below the limit of detection and a conservative assessment of radiation dose arising showed a negligible impact to the public. Tritium is discharged in large quantities from various nuclear facilities, and mostly in liquid form. For this reason it is included in the list of radioactive substances of interest to the OSPAR (Oslo-Paris) Convention to protect the marine environment of the North-East Atlantic. To fulfil its role within OSPAR, to provide technical support to the Irish Government, RPII carried out a project to determine the levels of tritium in seawater from around the Irish coast to supplement its routine marine monitoring programme. A total of 85 seawater samples were collected over a three year period and analysed at the RPII's laboratory. Given that the operational discharges for tritium from the nuclear fuel reprocessing plant at Sellafield, UK, are expected to increase due to current and planned decommissioning activities RPII will continue to monitor tritium levels in seawater around the Irish coast, including the Irish Sea, as part of its routine marine monitoring programme

  12. Biofouling control of industrial seawater cooling towers

    KAUST Repository

    Albloushi, Mohammed

    2017-11-01

    The use of seawater in cooling towers for industrial applications has much merit in the Gulf Cooperation Council countries due to the scarcity and availability of fresh water. Seawater make-up in cooling towers is deemed the most feasible because of its unlimited supply in coastal areas. Such latent-heat removal with seawater in cooling towers is several folds more efficient than sensible heat extraction via heat exchangers. Operational challenges such as scaling, corrosion, and biofouling are a major challenge in conventional cooling towers, where the latter is also a major issue in seawater cooling towers. Biofouling can significantly hamper the efficiency of cooling towers. The most popular methods used in cooling treatment to control biofouling are disinfection by chlorination. However, the disadvantages of chlorination are formation of harmful disinfection byproducts in the presence of high organic loading and safety concerns in the storage of chlorine gas. In this study, the research focuses on biofouling control in seawater cooling towers by investigating two different approaches. The first strategy addresses the use of alternative oxidants (i.e. ozone micro-bubbles and chlorine dioxide) in treatment of cooling towers. The second strategy investigates removing nutrients in seawater using granular activated carbon filter column and ultrafiltration to prevent the growth of microorganisms. Laboratory bench-scale tests in terms of temperature, cycle of concentration, dosage, etc. indicated that, at lower oxidant dosages (total residual oxidant (TRO) equivalent = 0.1 mg/l Cl2), chlorine dioxide had a better disinfection effect than chlorine and ozone. The performance of oxidizing biocides at pilot scale, operating at assorted conditions, showed that for the disinfectants tested, ozone could remove 95 % bioactivity of total number of bacteria and algae followed by chlorine dioxide at 85%, while conventional chlorine dosing only gave 60% reduction in bioactivities

  13. Concentration and retention of Toxoplasma gondii surrogates from seawater by red abalone (Haliotis rufescens)

    Science.gov (United States)

    Schott, Kristen C; Krusor, Colin; Tinker, M. Tim; Moore, James G.; Conrad, Patricia A.; Shapiro, Karen

    2016-01-01

    Small marine snails and abalone have been identified as high- and low-risk prey items, respectively, for exposure of threatened southern sea otters to Toxoplasma gondii, a zoonotic parasite that can cause fatal encephalitis in animals and humans. While recent work has characterized snails as paratenic hosts for T. gondii, the ability of abalone to vector the parasite has not been evaluated. To further elucidate why abalone predation may be protective against T. gondii exposure, this study aimed to determine whether: (1) abalone are physiologically capable of acquiring T. gondii; and (2) abalone and snails differ in their ability to concentrate and retain the parasite. Abalone were exposed to T. gondii surrogate microspheres for 24 h, and fecal samples were examined for 2 weeks following exposure. Concentration of surrogates was 2–3 orders of magnitude greater in abalone feces than in the spiked seawater, and excretion of surrogates continued for 14 days post-exposure. These results indicate that, physiologically, abalone and snails can equally vector T. gondii as paratenic hosts. Reduced risk of T. gondii infection in abalone-specializing otters may therefore result from abalone's high nutritional value, which implies otters must consume fewer animals to meet their caloric needs.

  14. Concentration and retention of Toxoplasma gondii surrogates from seawater by red abalone (Haliotis rufescens).

    Science.gov (United States)

    Schott, Kristen C; Krusor, Colin; Tinker, M Tim; Moore, James; Conrad, Patricia A; Shapiro, Karen

    2016-11-01

    Small marine snails and abalone have been identified as high- and low-risk prey items, respectively, for exposure of threatened southern sea otters to Toxoplasma gondii, a zoonotic parasite that can cause fatal encephalitis in animals and humans. While recent work has characterized snails as paratenic hosts for T. gondii, the ability of abalone to vector the parasite has not been evaluated. To further elucidate why abalone predation may be protective against T. gondii exposure, this study aimed to determine whether: (1) abalone are physiologically capable of acquiring T. gondii; and (2) abalone and snails differ in their ability to concentrate and retain the parasite. Abalone were exposed to T. gondii surrogate microspheres for 24 h, and fecal samples were examined for 2 weeks following exposure. Concentration of surrogates was 2-3 orders of magnitude greater in abalone feces than in the spiked seawater, and excretion of surrogates continued for 14 days post-exposure. These results indicate that, physiologically, abalone and snails can equally vector T. gondii as paratenic hosts. Reduced risk of T. gondii infection in abalone-specializing otters may therefore result from abalone's high nutritional value, which implies otters must consume fewer animals to meet their caloric needs.

  15. Spatial distribution, ecological and health risk assessment of heavy metals in marine surface sediments and coastal seawaters of fringing coral reefs of the Persian Gulf, Iran.

    Science.gov (United States)

    Ranjbar Jafarabadi, Ali; Riyahi Bakhtiyari, Alireza; Shadmehri Toosi, Amirhossein; Jadot, Catherine

    2017-10-01

    Concentrations of 13 heavy metals (Al, Fe, Mn, Zn, Cu, Cr, Co, Ni, V, As, Cd, Hg, Pb) in 360 reef surface sediments (0-5 cm) and coastal seawater samples from ten coral Islands in the Persian Gulf were analyzed to determine their spatial distribution and potential ecological risks. Different sediment quality indices were applied to assess the surface sediment quality. The mean concentrations of metals in studied sediments followed the order: Al > Fe > Ni > V > Mn > Zn > Cu > Cr > Co > As > Cd > Pb > As. Average Cd and Hg exceeded coastal background levels at most sampling sites. With the exception of As, concentrations of heavy metals decreased progressively from the west to the east of the Persian Gulf. Based on the Enrichment Factor (EF) and Potential Ecological Risk Index (RI), concentrations of V, Ni, Hg and Cd indicated moderate contamination and is of some concern. The mean values of heavy metals Toxic Units (TUs) were calculated in the following order: Hg (0.75)> Cr (0.41)> Cd (0.27)> As (0.23)> Cu (0.12)> Zn (0.05)> Pb (0.009). Furthermore, the mean contributing ratios of six heavy metals to Toxic Risk Index (TRI) values were 79% for Hg, 11.48% for Cd, 6.16% for Cr, 3.27% for Cu, 0.07% for Zn and 0.01% for Pb. Calculated values of potential ecological risk factor, revealed that the risk of the heavy metals followed the order Cd > Pb > Ni > Cr > V > Cu > Zn. The results reflected that the level of heavy metals, especially Hg and Cd, are on rise due to emerging oil exploration, industrial development, and oil refineries along the entire Gulf. Fe, Mn, Cu, Zn, V and Ni concentrations in seawater were significantly higher (p heavy metals in the sampling sites. A health risk assessment using the hazard quotient index (HQ) recommended by the USEPA suggests that there is no adverse health effect through dermal exposure, and there is no carcinogenic and non-carcinogenic harm to human health. Copyright © 2017 Elsevier Ltd. All

  16. Surface modification of commercial seawater reverse osmosis membranes by grafting of hydrophilic monomer blended with carboxylated multiwalled carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Vatanpour, Vahid, E-mail: vahidvatanpour@khu.ac.ir; Zoqi, Naser

    2017-02-28

    Highlights: • A commercial PA RO membrane was modified by grafting of hydrophilic acrylic acid. • COOH-MWCNTs were mixed in grafting layer to increase permeability and antifouling. • However, more increase of CNTs caused in reduction of flux of the membranes. • Effect of acrylic acid amount, contact time and curing time was optimized. - Abstract: In this study, modification of commercial seawater reverse osmosis membranes was carried out with simultaneous use of surface grafting and nanoparticle incorporation. Membrane grafting with a hydrophilic acrylic acid monomer and thermal initiator was used to increase membrane surface hydrophilicity. The used nanomaterial was carboxylated multiwalled carbon nanotubes (MWCNTs), which were dispersed in the grafting solution and deposited on membrane surface to reduce fouling by creating polymer brushes and hydrodynamic resistance. Effectiveness of the grafting process (formation of graft layer on membrane surface) was proved by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) analyses. Increase of membrane surface hydrophilicity was approved with contact angle test. First, the grafting was performed on the membrane surfaces with different monomer concentrations, various contact times and several membrane curing times (three variables for optimization). The modified membranes were tested by a cross-flow setup using saline solution for permeability and rejection tests, and bovine serum albumin (BSA) solution for fouling test. The results showed that the modified membranes with 0.75 M of monomer, 3 min contact time and 80 min curing time in an oven at 50 °C presented the highest flux and lowest rejection decline related to the commercial reverse osmosis membrane. In the next step, the optimum grafting condition was selected and the nanotubes with different weight percentages were dispersed in the acrylic acid monomer solution. The membrane containing 0.25 wt% COOH-MWCNTs showed the

  17. Surface modification of commercial seawater reverse osmosis membranes by grafting of hydrophilic monomer blended with carboxylated multiwalled carbon nanotubes

    International Nuclear Information System (INIS)

    Vatanpour, Vahid; Zoqi, Naser

    2017-01-01

    Highlights: • A commercial PA RO membrane was modified by grafting of hydrophilic acrylic acid. • COOH-MWCNTs were mixed in grafting layer to increase permeability and antifouling. • However, more increase of CNTs caused in reduction of flux of the membranes. • Effect of acrylic acid amount, contact time and curing time was optimized. - Abstract: In this study, modification of commercial seawater reverse osmosis membranes was carried out with simultaneous use of surface grafting and nanoparticle incorporation. Membrane grafting with a hydrophilic acrylic acid monomer and thermal initiator was used to increase membrane surface hydrophilicity. The used nanomaterial was carboxylated multiwalled carbon nanotubes (MWCNTs), which were dispersed in the grafting solution and deposited on membrane surface to reduce fouling by creating polymer brushes and hydrodynamic resistance. Effectiveness of the grafting process (formation of graft layer on membrane surface) was proved by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) analyses. Increase of membrane surface hydrophilicity was approved with contact angle test. First, the grafting was performed on the membrane surfaces with different monomer concentrations, various contact times and several membrane curing times (three variables for optimization). The modified membranes were tested by a cross-flow setup using saline solution for permeability and rejection tests, and bovine serum albumin (BSA) solution for fouling test. The results showed that the modified membranes with 0.75 M of monomer, 3 min contact time and 80 min curing time in an oven at 50 °C presented the highest flux and lowest rejection decline related to the commercial reverse osmosis membrane. In the next step, the optimum grafting condition was selected and the nanotubes with different weight percentages were dispersed in the acrylic acid monomer solution. The membrane containing 0.25 wt% COOH-MWCNTs showed the

  18. Aerobic methanotrophic communities at the Red Sea brine-seawater interface

    Directory of Open Access Journals (Sweden)

    Rehab Z. Abdallah

    2014-09-01

    Full Text Available The central rift of the Red Sea contains 25 brine pools with different physicochemical conditions, dictating the diversity and abundance of the microbial community. Three of these pools, the Atlantis II, Kebrit and Discovery Deeps, are uniquely characterized by a high concentration of hydrocarbons. The brine-seawater interface, described as an anoxic-oxic (brine-seawater boundary, is characterized by a high methane concentration, thus favoring aerobic methane oxidation. The current study analyzed the aerobic free–living methane-oxidizing bacterial communities that potentially contribute to methane oxidation at the brine-seawater interfaces of the three aforementioned brine pools, using metagenomic pyrosequencing, 16S rRNA pyrotags and pmoA library constructs. The sequencing of 16S rRNA pyrotags revealed that these interfaces are characterized by high microbial community diversity. Signatures of aerobic methane-oxidizing bacteria were detected in the Atlantis II Interface (ATII-I and the Kebrit Deep Upper (KB-U and Lower (KB-L brine-seawater interfaces. Through phylogenetic analysis of pmoA, we further demonstrated that the ATII-I aerobic methanotroph community is highly diverse. We propose four ATII-I pmoA clusters. Most importantly, cluster 2 groups with marine methane seep methanotrophs, and cluster 4 represent a unique lineage of an uncultured bacterium with divergent alkane monooxygenases. Moreover, non-metric multidimensional scaling (NMDS based on the ordination of putative enzymes involved in methane metabolism showed that the Kebrit interface layers were distinct from the ATII-I and DD-I brine-seawater interfaces.

  19. Butterfly valves for seawater

    International Nuclear Information System (INIS)

    Yamanaka, Katsuto

    1991-01-01

    Recently in thermal and nuclear power stations and chemical plants which have become large capacity, large quantity of cooling water is required, and mostly seawater is utilized. In these cooling water systems, considering thermal efficiency and economy, the pipings become complex, and various control functions are demanded. For the purpose, the installation of shut-off valves and control valves for pipings is necessary. The various types of valves have been employed, and in particular, butterfly valves have many merits in their function, size, structure, operation, maintenance, usable period, price and so on. The corrosion behavior of seawater is complicated due to the pollution of seawater, therefore, the environment of the valves used for seawater became severe. The structure and the features of the butterfly valves for seawater, the change of the structure of the butterfly valves for seawater and the checkup of the butterfly valves for seawater are reported. The corrosion of metallic materials is complicatedly different due to the locating condition of plants, the state of pipings and the condition of use. The corrosion countermeasures for butterfly valves must be examined from the synthetic viewpoints. (K.I.)

  20. Nucleation from seawater emissions during mesocosm experiments

    Science.gov (United States)

    Rose, Clémence; Culot, Anais; Pey, Jorge; Schwier, Allison; Mas, Sébastien; Charriere, Bruno; Sempéré, Richard; Marchand, Nicolas; D'Anna, Barbara; Sellegri, Karine

    2015-04-01

    Nucleation and new particle formation in the marine atmosphere is usually associated to the presence of macroalgea emerged at low tides in coastal areas, while these processes were very rarely detected away from coastlines. In the present study, we evidence the formation of new particles from the 1 nm size above the seawater surface in the absence of any macroalgea population. Within the SAM project (Sources of marine Aerosol in the Mediterranean),seawater mesocosms experiments were deployed in May 2013 at the STARESO in western Corsica, with the goal of investigating the relationship between marine aerosol emissions and the seawater biogeochemical properties. Three mesocosms imprisoned 3,3 m3 of seawater each and their emerged part was flushed with aerosol-filtered natural air. One of these mesocosms was left unchanged as control and the two others were enriched by addition of nitrates and phosphates respecting Redfield ratio (N:P = 16) in order to create different levels of phytoplanctonic activities. We followed both water and air characteristics of three mesocosms during a period of three weeks by using online water and atmospheric probes as well as seawater daily samples for chemical and biological analysis. Secondary new particle formation was followed on-line in the emerged parts of the mesocosms, using a SMPS for the size distribution above 6 nm and a Particle Size Magnifyer (PSM) for the number of cluster particles between 1 and 6 nm. We will present how the cluster formation rates and early growth rates relate to the gaz-phase emissions from the seawater and to its biogeochemical properties. Aknowledgemnts: The authors want to acknowledge the financial support of the ANR "Source of marine Aerosol in the Mediterranean" (SAM), and the support of MISTRAL CHARMEX and MERMEX programs.

  1. Application of a bacterial whole cell biosensor for the rapid detection of cytotoxicity in heavy metal contaminated seawater.

    Science.gov (United States)

    Cui, Zhisong; Luan, Xiao; Jiang, Huichao; Li, Qian; Xu, Guangfei; Sun, Chengjun; Zheng, Li; Song, Yizhi; Davison, Paul A; Huang, Wei E

    2018-06-01

    A toxicity biosensor Acinetobacter baylyi Tox2 was constructed with the host strain A. baylyi ADP1 harboring a new and medium-copy-number plasmid pWH1274_lux, and was applied to detect the cytotoxicity of heavy metal contaminated seawater. The gene cassette luxCDABE was controlled by constitutively expressed promoter P tet on pWH1274_lux and the bioluminescence intensity of the biosensor reduces in proportional to the concentrations of toxic compounds. A. baylyi Tox2 exhibits tolerance to salinity, hence it is applicable to seawater samples. A. baylyi Tox2 and Mugilogobius chulae were exposed to different concentrations of heavy metals (Hg 2+ , Zn 2+ , Cu 2+ , and Cd 2+ ) in artificial seawater for performance comparison and Pearson correlation analysis showed a significant correlation (p heavy metal contaminated seawater. Furthermore, A. baylyi Tox2 was used to evaluate cytotoxicity of field-collected seawater samples. The results indicate that there was a significant correlation between the luminescence inhibition ratio (IR) of A. baylyi Tox2 and heavy metal concentrations detected by ICP-MS in the samples. Two seawater samples, which contained a high concentration of total heavy metals, exhibited stronger cytotoxicity than the samples containing low concentrations of heavy metals. In conclusion, A. baylyi Tox2 can be used as an alternative tool to aquatic animals for the evaluation of the cytotoxicity of heavy metal contamination in the marine environment. Copyright © 2018 Elsevier Ltd. All rights reserved.

  2. Modification of Optical Properties of Seawater Exposed to Oil Contaminants Based on Excitation-Emission Spectra

    Science.gov (United States)

    Baszanowska, E.; Otremba, Z.

    2015-10-01

    The optical behaviour of seawater exposed to a residual amount of oil pollution is presented and a comparison of the fluorescence spectra of oil dissolved in both n-hexane and seawater is discussed based on excitation-emission spectra. Crude oil extracted from the southern part of the Baltic Sea was used to characterise petroleum properties after contact with seawater. The wavelength-independent fluorescence maximum for natural seawater and seawater artificially polluted with oil were determined. Moreover, the specific excitation-emission peaks for natural seawater and polluted water were analysed to identify the natural organic matter composition. It was found that fluorescence spectra identification is a promising method to detect even an extremely low concentration of petroleum residues directly in the seawater. In addition, alien substances disturbing the fluorescence signatures of natural organic substances in a marine environment is also discussed.

  3. Radiochemical determination of cesium-137 in seawater

    International Nuclear Information System (INIS)

    Cunha, I.I.L.; Munita, C.S.; Paiva, R.P.

    1990-01-01

    Seawater samples were collected from the Atlantic Ocean, in the vicinity of Ubatuba (Sao Paulo State - Brazil), acidified to pH 1 and stored in polyethylene containers. Cesium was precipitated with ammonium phospho molybdate (AMP), synthesized in our laboratory. The elements potassium and rubidium present in the seawater are also coprecipitated by AMP and adequate decontamination of the cesium is made by preparing a column by mixing Cs-137 AMP precipitate and asbestos. The interfering elements were eluted with 1.0 M ammonium nitrate solution whereas cesium was eluted with 1.0 M sodium hydroxide solution. Cesium was reprecipitated by acidifying the solution with concentrated hydrochloric acid. The overall chemical yield of cesium was of 75%. (author)

  4. Organophosphate Esters in Air, Snow, and Seawater in the North Atlantic and the Arctic.

    Science.gov (United States)

    Li, Jing; Xie, Zhiyong; Mi, Wenying; Lai, Senchao; Tian, Chongguo; Emeis, Kay-Christian; Ebinghaus, Ralf

    2017-06-20

    The concentrations of eight organophosphate esters (OPEs) have been investigated in air, snow and seawater samples collected during the cruise of ARK-XXVIII/2 from sixth June to third July 2014 across the North Atlantic and the Arctic. The sum of gaseous and particle concentrations (ΣOPE) ranged from 35 to 343 pg/m 3 . The three chlorinated OPEs accounted for 88 ± 5% of the ΣOPE. The most abundant OPE was tris(2-chloroethyl) phosphate (TCEP), with concentrations ranging from 30 to 227 pg/m 3 , followed by three major OPEs, such as tris(1-chloro-2-propyl) phosphate (TCPP, 0.8 to 82 pg/m 3 ), tri-n-butyl phosphate (TnBP, 2 to 19 pg/m 3 ), and tri-iso-butyl phosphate (TiBP, 0.3 to 14 pg/m 3 ). The ΣOPE concentrations in snow and seawater ranged from 4356 to 10561 pg/L and from 348 to 8396 pg/L, respectively. The atmospheric particle-bound dry depositions of TCEP ranged from 2 to 12 ng/m 2 /day. The air-seawater gas exchange fluxes were dominated by net volatilization from seawater to air for TCEP (mean, 146 ± 239 ng/m 2 /day), TCPP (mean, 1670 ± 3031 ng/m 2 /day), TiBP (mean, 537 ± 581 ng/m 2 /day) and TnBP (mean, 230 ± 254 ng/m 2 /day). This study highlighted that OPEs are subject to long-range transport via both air and seawater from the European continent and seas to the North Atlantic and the Arctic.

  5. Assessing the pollution risk of a groundwater source field at western Laizhou Bay under seawater intrusion.

    Science.gov (United States)

    Zeng, Xiankui; Wu, Jichun; Wang, Dong; Zhu, Xiaobin

    2016-07-01

    Coastal areas have great significance for human living, economy and society development in the world. With the rapid increase of pressures from human activities and climate change, the safety of groundwater resource is under the threat of seawater intrusion in coastal areas. The area of Laizhou Bay is one of the most serious seawater intruded areas in China, since seawater intrusion phenomenon was firstly recognized in the middle of 1970s. This study assessed the pollution risk of a groundwater source filed of western Laizhou Bay area by inferring the probability distribution of groundwater Cl(-) concentration. The numerical model of seawater intrusion process is built by using SEAWAT4. The parameter uncertainty of this model is evaluated by Markov Chain Monte Carlo (MCMC) simulation, and DREAM(ZS) is used as sampling algorithm. Then, the predictive distribution of Cl(-) concentration at groundwater source field is inferred by using the samples of model parameters obtained from MCMC. After that, the pollution risk of groundwater source filed is assessed by the predictive quantiles of Cl(-) concentration. The results of model calibration and verification demonstrate that the DREAM(ZS) based MCMC is efficient and reliable to estimate model parameters under current observation. Under the condition of 95% confidence level, the groundwater source point will not be polluted by seawater intrusion in future five years (2015-2019). In addition, the 2.5% and 97.5% predictive quantiles show that the Cl(-) concentration of groundwater source field always vary between 175mg/l and 200mg/l. Copyright © 2015 Elsevier Inc. All rights reserved.

  6. Full utilization of silt density index (SDI) measurements for seawater pre-treatment

    KAUST Repository

    Wei, Chunhai

    2012-07-01

    In order to clarify the fouling mechanism during silt density index (SDI) measurements of seawater in the seawater reverse osmosis (SWRO) desalination process, 11 runs were conducted under constant-pressure (207kPa) dead-end filtration mode according to the standard protocol for SDI measurement, in which two kinds of 0.45μm membranes of different material and seawater samples from the Mediterranean including raw seawater and seawater pre-treated by coagulation followed by sand filtration (CSF) and coagulation followed by microfiltration (CMF) technologies were tested. Fouling mechanisms based on the constant-pressure filtration equation were fully analyzed. For all runs, only t/(V/A)∼t showed very good linearity (correlation coefficient R 2>0.99) since the first moment of the filtration, indicating that standard blocking rather than cake filtration was the dominant fouling mechanism during the entire filtration process. The very low concentration of suspended solids rejected by MF of 0.45μm in seawater was the main reason why a cake layer was not formed. High turbidity removal during filtration indicated that organic colloids retained on and/or adsorbed in membrane pores governed the filtration process (i.e., standard blocking) due to the important contribution of organic substances to seawater turbidity in this study. Therefore the standard blocking coefficient k s, i.e., the slope of t/(V/A)∼t, could be used as a good fouling index for seawater because it showed good linearity with feed seawater turbidity. The correlation of SDI with k s and feed seawater quality indicated that SDI could be reliably used for seawater with low fouling potential (SDI 15min<5) like pre-treated seawater in this study. From both k s and SDI, the order of fouling potential was raw seawater>seawater pre-treated by CSF>seawater pre-treated by CMF, indicating the better performance of CMF than CSF. © 2012 Elsevier B.V.

  7. The impact of changing surface ocean conditions on the dissolution of aerosol iron

    Science.gov (United States)

    Fishwick, Matthew P.; Sedwick, Peter N.; Lohan, Maeve C.; Worsfold, Paul J.; Buck, Kristen N.; Church, Thomas M.; Ussher, Simon J.

    2014-11-01

    The proportion of aerosol iron (Fe) that dissolves in seawater varies greatly and is dependent on aerosol composition and the physicochemical conditions of seawater, which may change depending on location or be altered by global environmental change. Aerosol and surface seawater samples were collected in the Sargasso Sea and used to investigate the impact of these changing conditions on aerosol Fe dissolution in seawater. Our data show that seawater temperature, pH, and oxygen concentration, within the range of current and projected future values, had no significant effect on the dissolution of aerosol Fe. However, the source and composition of aerosols had the most significant effect on the aerosol Fe solubility, with the most anthropogenically influenced samples having the highest fractional solubility (up to 3.2%). The impact of ocean warming and acidification on aerosol Fe dissolution is therefore unlikely to be as important as changes in land usage and fossil fuel combustion. Our experimental results also reveal important changes in the size distribution of soluble aerosol Fe in solution, depending on the chemical conditions of seawater. Under typical conditions, the majority (77-100%) of Fe released from aerosols into ambient seawater existed in the colloidal (0.02-0.4 µm) size fraction. However, in the presence of a sufficient concentration of strong Fe-binding organic ligands (10 nM) most of the aerosol-derived colloidal Fe was converted to soluble Fe (<0.02 µm). This finding highlights the potential importance of organic ligands in retaining aerosol Fe in a biologically available form in the surface ocean.

  8. Physiological, molecular, and cellular mechanisms of impaired seawater tolerance following exposure of Atlantic salmon, Salmo salar, smolts to acid and aluminum

    Energy Technology Data Exchange (ETDEWEB)

    Monette, Michelle Y., E-mail: michelle.monette@yale.edu [Organismic and Evolutionary Biology Program, University of Massachusetts, Amherst, MA 01003 (United States); USGS, Conte Anadromous Fish Research Center, Turners Falls, MA 01376 (United States); Yada, Takashi [Freshwater Fisheries Research Department, National Research Institute of Fisheries Science, Nikko (Japan); Matey, Victoria [Department of Biology, San Diego State University, San Diego, CA 92182 (United States); McCormick, Stephen D. [Organismic and Evolutionary Biology Program, University of Massachusetts, Amherst, MA 01003 (United States); USGS, Conte Anadromous Fish Research Center, Turners Falls, MA 01376 (United States)

    2010-08-01

    We examined the physiological, molecular, and cellular mechanisms of impaired ion regulation in Atlantic salmon, Salmo salar, smolts following acute acid and aluminum (Al) exposure. Smolts were exposed to: control (pH 6.5, 3.4 {mu}g l{sup -1} Al), acid and low Al (LAl: pH 5.4, 11 {mu}g l{sup -1} Al), acid and moderate Al (MAl: pH 5.3, 42 {mu}g l{sup -1} Al), and acid and high Al (HAl: pH 5.4, 56 {mu}g l{sup -1} Al) for two and six days. At each time-point, smolts were sampled directly from freshwater treatment tanks and after a 24 h seawater challenge. Exposure to acid/MAl and acid/HAl led to accumulation of gill Al, substantial alterations in gill morphology, reduced gill Na{sup +}/K{sup +}-ATPase (NKA) activity, and impaired ion regulation in both freshwater and seawater. Exposure to acid/MAl for six days also led to a decrease in gill mRNA expression of the apical Cl{sup -} channel (cystic fibrosis transmembrane conductance regulator I), increased apoptosis upon seawater exposure, an increase in the surface expression of mitochondria-rich cells (MRCs) within the filament epithelium of the gill, but reduced abundance of gill NKA-positive MRCs. By contrast, smolts exposed to acid and the lowest Al concentration exhibited minor gill Al accumulation, slight morphological modifications in the gill, and impaired seawater tolerance in the absence of a detectable effect on freshwater ion regulation. These impacts were accompanied by decreased cell proliferation, a slight increase in the surface expression of MRCs within the filament epithelium, but no impact on gill apoptosis or total MRC abundance was observed. However, MRCs in the gills of smolts exposed to acid/LAl exhibited morphological alterations including decreased size, staining intensity, and shape factor. We demonstrate that the seawater tolerance of Atlantic salmon smolts is extremely sensitive to acute exposure to acid and low levels of Al, and that the mechanisms underlying this depend on the time

  9. Physiological, molecular, and cellular mechanisms of impaired seawater tolerance following exposure of Atlantic salmon, Salmo salar, smolts to acid and aluminum

    International Nuclear Information System (INIS)

    Monette, Michelle Y.; Yada, Takashi; Matey, Victoria; McCormick, Stephen D.

    2010-01-01

    We examined the physiological, molecular, and cellular mechanisms of impaired ion regulation in Atlantic salmon, Salmo salar, smolts following acute acid and aluminum (Al) exposure. Smolts were exposed to: control (pH 6.5, 3.4 μg l -1 Al), acid and low Al (LAl: pH 5.4, 11 μg l -1 Al), acid and moderate Al (MAl: pH 5.3, 42 μg l -1 Al), and acid and high Al (HAl: pH 5.4, 56 μg l -1 Al) for two and six days. At each time-point, smolts were sampled directly from freshwater treatment tanks and after a 24 h seawater challenge. Exposure to acid/MAl and acid/HAl led to accumulation of gill Al, substantial alterations in gill morphology, reduced gill Na + /K + -ATPase (NKA) activity, and impaired ion regulation in both freshwater and seawater. Exposure to acid/MAl for six days also led to a decrease in gill mRNA expression of the apical Cl - channel (cystic fibrosis transmembrane conductance regulator I), increased apoptosis upon seawater exposure, an increase in the surface expression of mitochondria-rich cells (MRCs) within the filament epithelium of the gill, but reduced abundance of gill NKA-positive MRCs. By contrast, smolts exposed to acid and the lowest Al concentration exhibited minor gill Al accumulation, slight morphological modifications in the gill, and impaired seawater tolerance in the absence of a detectable effect on freshwater ion regulation. These impacts were accompanied by decreased cell proliferation, a slight increase in the surface expression of MRCs within the filament epithelium, but no impact on gill apoptosis or total MRC abundance was observed. However, MRCs in the gills of smolts exposed to acid/LAl exhibited morphological alterations including decreased size, staining intensity, and shape factor. We demonstrate that the seawater tolerance of Atlantic salmon smolts is extremely sensitive to acute exposure to acid and low levels of Al, and that the mechanisms underlying this depend on the time-course and severity of Al exposure. We propose

  10. Physiological, molecular, and cellular mechanisms of impaired seawater tolerance following exposure of Atlantic salmon, Salmo salar, smolts to acid and aluminum

    Science.gov (United States)

    Monette, M.Y.; Yada, T.; Matey, V.; McCormick, S.D.

    2010-01-01

    We examined the physiological, molecular, and cellular mechanisms of impaired ion regulation in Atlantic salmon, Salmo salar, smolts following acute acid and aluminum (Al) exposure. Smolts were exposed to: control (pH 6.5, 3.4??gl-1 Al), acid and low Al (LAl: pH 5.4, 11??gl-1 Al), acid and moderate Al (MAl: pH 5.3, 42??gl-1 Al), and acid and high Al (HAl: pH 5.4, 56??gl-1 Al) for two and six days. At each time-point, smolts were sampled directly from freshwater treatment tanks and after a 24h seawater challenge. Exposure to acid/MAl and acid/HAl led to accumulation of gill Al, substantial alterations in gill morphology, reduced gill Na+/K+-ATPase (NKA) activity, and impaired ion regulation in both freshwater and seawater. Exposure to acid/MAl for six days also led to a decrease in gill mRNA expression of the apical Cl- channel (cystic fibrosis transmembrane conductance regulator I), increased apoptosis upon seawater exposure, an increase in the surface expression of mitochondria-rich cells (MRCs) within the filament epithelium of the gill, but reduced abundance of gill NKA-positive MRCs. By contrast, smolts exposed to acid and the lowest Al concentration exhibited minor gill Al accumulation, slight morphological modifications in the gill, and impaired seawater tolerance in the absence of a detectable effect on freshwater ion regulation. These impacts were accompanied by decreased cell proliferation, a slight increase in the surface expression of MRCs within the filament epithelium, but no impact on gill apoptosis or total MRC abundance was observed. However, MRCs in the gills of smolts exposed to acid/LAl exhibited morphological alterations including decreased size, staining intensity, and shape factor. We demonstrate that the seawater tolerance of Atlantic salmon smolts is extremely sensitive to acute exposure to acid and low levels of Al, and that the mechanisms underlying this depend on the time-course and severity of Al exposure. We propose that when smolts are

  11. Variable response of three Trifolium repens ecotypes to soil flooding by seawater.

    Science.gov (United States)

    White, Anissia C; Colmer, Timothy D; Cawthray, Greg R; Hanley, Mick E

    2014-08-01

    Despite concerns about the impact of rising sea levels and storm surge events on coastal ecosystems, there is remarkably little information on the response of terrestrial coastal plant species to seawater inundation. The aim of this study was to elucidate responses of a glycophyte (white clover, Trifolium repens) to short-duration soil flooding by seawater and recovery following leaching of salts. Using plants cultivated from parent ecotypes collected from a natural soil salinity gradient, the impact of short-duration seawater soil flooding (8 or 24 h) on short-term changes in leaf salt ion and organic solute concentrations was examined, together with longer term impacts on plant growth (stolon elongation) and flowering. There was substantial Cl(-) and Na(+) accumulation in leaves, especially for plants subjected to 24 h soil flooding with seawater, but no consistent variation linked to parent plant provenance. Proline and sucrose concentrations also increased in plants following seawater flooding of the soil. Plant growth and flowering were reduced by longer soil immersion times (seawater flooding followed by drainage and freshwater inputs), but plants originating from more saline soil responded less negatively than those from lower salinity soil. The accumulation of proline and sucrose indicates a potential for solute accumulation as a response to the osmotic imbalance caused by salt ions, while variation in growth and flowering responses between ecotypes points to a natural adaptive capacity for tolerance of short-duration seawater soil flooding in T. repens. Consequently, it is suggested that selection for tolerant ecotypes is possible should the predicted increase in frequency of storm surge flooding events occur. © The Author 2014. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

  12. Changes in feedwater organic matter concentrations based on intake type and pretreatment processes at SWRO facilities, Red Sea, Saudi Arabia

    KAUST Repository

    Dehwah, Abdullah

    2015-03-01

    Transparent exopolymer particles (TEP), natural organic matter, and bacterial concentrations in feedwater are important factors that can lead to membrane biofouling in seawater reverse osmosis (SWRO) systems. Two methods for controlling these concentrations in the feedwater prior to pretreatment have been suggested; use of subsurface intake systems or placement of the intake at a greater depth in the sea. These proposed solutions were tested at two SWRO facilities located along the Red Sea of Saudi Arabia. A shallow well intake system was very effective in reducing the algae and bacterial concentrations and somewhat effective in reducing TEP concentrations. An intake placed at a depth of 9. m below the surface was found to have limited impact on improving water quality compared to a surface intake. The algae and bacteria concentration in the feedwater (deep) was lower compared to the surface seawater, but the overall TEP concentration was higher. Bacteria and TEP measurements made in the pretreatment process train in the plant and after the cartridge filters suggest that regrowth of bacteria is occurring within the cartridge filters.

  13. Changes in feedwater organic matter concentrations based on intake type and pretreatment processes at SWRO facilities, Red Sea, Saudi Arabia

    KAUST Repository

    Dehwah, Abdullah; Li, Sheng; Almashharawi, Samir; Winters, Harvey; Missimer, Thomas M.

    2015-01-01

    Transparent exopolymer particles (TEP), natural organic matter, and bacterial concentrations in feedwater are important factors that can lead to membrane biofouling in seawater reverse osmosis (SWRO) systems. Two methods for controlling these concentrations in the feedwater prior to pretreatment have been suggested; use of subsurface intake systems or placement of the intake at a greater depth in the sea. These proposed solutions were tested at two SWRO facilities located along the Red Sea of Saudi Arabia. A shallow well intake system was very effective in reducing the algae and bacterial concentrations and somewhat effective in reducing TEP concentrations. An intake placed at a depth of 9. m below the surface was found to have limited impact on improving water quality compared to a surface intake. The algae and bacteria concentration in the feedwater (deep) was lower compared to the surface seawater, but the overall TEP concentration was higher. Bacteria and TEP measurements made in the pretreatment process train in the plant and after the cartridge filters suggest that regrowth of bacteria is occurring within the cartridge filters.

  14. Seasonal levels of the Vibrio predator Bacteriovorax in Atlantic, Pacific and Gulf Coast Seawater

    Science.gov (United States)

    Bacteriovorax were quantified in US Atlantic, Gulf and Pacific seawater to determine baseline levels of these predatory bacteria and possible seasonal fluctuations in levels. Surface seawater was analyzed monthly for 1 year from Kailua-Kona, Hawaii; the Gulf Coast of Alabama; and four sites along t...

  15. Coupled sea surface temperature-seawater delta O-18 reconstructions in the Arabian Sea at the millennial scale for the last 35 ka

    NARCIS (Netherlands)

    Anand, P.; Kroon, D.; Singh, A.D.; Ganssen, G.M.

    2008-01-01

    Two sediment cores from the western (905; 10.46°9′N, 51.56°4′E, water depth 1586 m) and eastern (SK17; 15°15′N, 72°58′E, water depth 840 m) Arabian Sea were used to study past sea surface temperatures (SST) and seawater δ

  16. Effects of acidified seawater on coral calcification and variations of U/Ca ratio in their skeletons

    Science.gov (United States)

    Inoue, M.; Ozaki, S.; Iguchi, A.; Sakai, K.; Suzuki, A.; Kawahata, H.

    2011-12-01

    The rising CO2 concentration in the atmosphere is changing the carbonate chemistry of the ocean. Elevated partial pressure of CO2 (pCO2) has caused significant decrease in surface seawater pH and carbonate ion concentration. Therefore, ocean acidification has a negative effect on calcification of marine calcifying organisms. Especially, hermatypic corals are dominant organisms in coral reef ecosystems, so their calcificication is a key to determine the health of reef ecosystems. On the other hand, recent study has suggested that there is a negative correlation between U/Ca ratio in coral skeleton and seawater pH, based on the culture experiment using primary polyps of Acropora digitifera. In this study, primary polyps and adult colonies of A. digitifera and adult colonies of Porites australiensis, which are the dominant species around the Ryukyu Islands, Japan, were reared in seawater with different pCO2 (300, 400, 600, 800, 1000ppm) and pH (7.4, 7.6, 8.0) settings controlled by CO2 bubbling. Calcification rate of adult coral was estimated by buoyant method, while skeletal growth of polyps was evaluated by measuring the dry weight of each skeleton after the experiments. In order to evaluate the relationship between U/Ca ratios in coral skeletons and seawater pH, U/Ca ratios in reared corals were analyzed by Inductively Coupled Plasma Mass Spectrometry (ICP-MS). The results of A. digitifera showed that the growth rate of adult corals had no significant correlation against pCO2, but dry weight of polyp skeletons decreased with increase in pCO2. Growth rate of P. australiensis typically showed a positive correlation with pH. However, growth rates were different among colonies, suggesting that their responses to acidification may vary among the colonies. Regarding the variations of U/Ca ratios, there were positive correlations between U/Ca ratios in adults of A. digitifera and P. australiensis and seawater pCO2 (pH), while no relation was observed in polyp corals.

  17. Development of Alloy Coating Process of Steel Pipe for Seawater service

    Energy Technology Data Exchange (ETDEWEB)

    Han, Jong Man; Kwon, Taeg Kyu; Lee, Sang Hyeog [Daewoo Shipbuilding and Marine Engineering Co., Ltd., Okpo (Korea)

    2001-02-01

    The new alloy coating process was developed to apply steel pipe for seawater service. This process consists of Zn-Al hot-dip coating treatment immediately following after normal galvanizing treatment. The alloy coating process formed double layer after surface treatment, and the surface layer was similar to that of Galfan steel and the intermetallic layer was also similar to that of aluminized steel. The alloy coating layer protect steel pipe galvanically and provide steel pipe with high resistance to general corrosion of seawater. This new alloy coated steel pipe had also good weldability and adhesion strength of paints compared to galvanized steel. 5 refs., 14 figs.

  18. The major-ion composition of Carboniferous seawater

    Science.gov (United States)

    Holt, Nora M.; García-Veigas, Javier; Lowenstein, Tim K.; Giles, Peter S.; Williams-Stroud, Sherilyn

    2014-06-01

    The major-ion chemistry (Na+, Mg2+, Ca2+, K+, SO42-, and Cl-) of Carboniferous seawater was determined from chemical analyses of fluid inclusions in marine halites, using the cryo scanning electron microscopy (Cryo-SEM) X-ray energy-dispersive spectrometry (EDS) technique. Fluid inclusions in halite from the Mississippian Windsor and Mabou Groups, Shubenacadie Basin, Nova Scotia, Canada (Asbian and Pendleian Substages, 335.5-330 Ma), and from the Pennsylvanian Paradox Formation, Utah, USA, (Desmoinesian Stage 309-305 Ma) contain Na+-Mg2+-K+-Ca2+-Cl- brines, with no measurable SO42-, which shows that the Carboniferous ocean was a “CaCl2 sea”, relatively enriched in Ca2+ and low in SO42- with equivalents Ca2+ > SO42- + HCO3-. δ34S values from anhydrite in the Mississippian Shubenacadie Basin (13.2-14.0 ‰) and the Pennsylvanian Paradox Formation (11.2-12.6 ‰) support seawater sources. Br in halite from the Shubenacadie Basin (53-111 ppm) and the Paradox Basin (68-147 ppm) also indicate seawater parentages. Carboniferous seawater, modeled from fluid inclusions, contained ∼22 mmol Ca2+/kg H2O (Mississippian) and ∼24 mmol Ca2+/kg H2O (Pennsylvanian). Estimated sulfate concentrations are ∼14 mmol SO42-/kg H2O (Mississippian), and ∼12 mmol SO42-/kg H2O (Pennsylvanian). Calculated Mg2+/Ca2+ ratios are 2.5 (Mississippian) and 2.3 (Pennsylvanian), with an estimated range of 2.0-3.2. The fluid inclusion record of seawater chemistry shows a long period of CaCl2 seas in the Paleozoic, from the Early Cambrian through the Carboniferous, when seawater was enriched in Ca2+ and relatively depleted in SO42-. During this ∼200 Myr interval, Ca2+ decreased and SO42- increased, but did not cross the Ca2+-SO42- chemical divide to become a MgSO4 sea (when SO42- in seawater became greater than Ca2+) until the latest Pennsylvanian or earliest Permian (∼309-295 Ma). Seawater remained a MgSO4 sea during the Permian and Triassic, for ∼100 Myr. Fluid inclusions also record

  19. Development of a process for continuous extraction of uranium from seawater

    International Nuclear Information System (INIS)

    Yun, C.K.

    1982-03-01

    Hydrous titanium oxide, titanium phosphate, galena (PbS), polystyrene beads containing TBP were preliminarily tested, using artificial seawater. Galena indicated the capacity of 1.1mg U/g PbS and faster reaction rates, whereas, hydrous titanium oxide showed 0.6mg U/g Ti and slow rates. The adsorption performance of galena was not changed after repeated use and regeneration with dil. HCl solutions. The effective surface of galena beads was 0.4mm in depth. Elution of uranium form adsorbents was examined by both acid and alkali methods; the latter showed preferred condition. Secondary concentration of uranium by Amberlite IRA-400 was also studies. Eventually, two types of packed systems with galena (columns and panels) were installed in the seawater channel of a thermal power plant. The maximum adsorption of 150μg U/g PbS was obtained using the packed column. Based on the experimental data, the authors made a conceptual design for a test plant of the production capacity 12Kg U 3 O 8 /y. The construction would cost about $1 million and the operation cost is estimated at $115.20/lb U 3 O 8

  20. Post-Mesozoic Rapid Increase of Seawater Mg/Ca due to Enhanced Mantle-Seawater Interaction

    OpenAIRE

    Marco Ligi; Enrico Bonatti; Marco Cuffaro; Daniele Brunelli

    2013-01-01

    The seawater Mg/Ca ratio increased significantly from ~ 80?Ma to present, as suggested by studies of carbonate veins in oceanic basalts and of fluid inclusions in halite. We show here that reactions of mantle-derived peridotites with seawater along slow spreading mid-ocean ridges contributed to the post-Cretaceous Mg/Ca increase. These reactions can release to modern seawater up to 20% of the yearly Mg river input. However, no significant peridotite-seawater interaction and Mg-release to the ...

  1. The status quo and the prospect of extraction of resources in seawater

    International Nuclear Information System (INIS)

    Katoh, Shunsaku

    1991-01-01

    Sea is the natural storage, and the enormous quantity of river water which contains the large amount of ions and compositions flows into sea, accordingly it has been calculated that seawater is replaced with new water in about 4 x 10 4 years. Sea is always agitated by tidal current, therefore, the composition of seawater is nearly uniform in most sea areas. Almost all elements existing in nature are dissolved in seawater, and the state of dissolution of main elements and their concentration are shown. The total quantity of seawater is as enormous as 1.35 x 10 9 km 3 , accordingly even in the trace elements in seawater, the total dissolved amount is enormous. For Japan which lacks resources, it is the important subject to develop the technology of effectively utilizing the resources in sea. The methods of obtaining sodium chloride, magnesium, bromine and potassium, which are the main components of seawater, are briefly explained. As the extraction of trace components, gold and silver, uranium, lithium, boron, strontium, vanadium, molybdenum, yttrium and heavy water are taken up. The optimal system must be built including the development of high performance adsorbents. (K.I.)

  2. Temperature profile data from surface seawater intake, bucket, and XBT casts in a world wide distribution from 1995-02-24 to 1996-06-23 (NODC Accession 9700060)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using surface seawater intake, bucket, and XBT casts from several vessels in a world wide distribution from February 24,...

  3. Temperature profile data from surface seawater intake, bucket, and XBT casts in a world wide distribution from 1996-09-30 to 1997-05-27 (NODC Accession 9700161)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using surface seawater intake, bucket, and XBT casts from several vessels in a world wide distribution from September 30,...

  4. Temperature profile data from surface seawater intake, bucket, and XBT casts in a world wide distribution from 1996-09-19 to 1997-03-25 (NODC Accession 9700061)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using surface seawater intake, bucket, and XBT casts from several vessels in a world wide distribution from September 19,...

  5. Preliminary design and analysis of a process for the extraction of lithium from seawater

    International Nuclear Information System (INIS)

    Steinberg, M.; Dang, V.D.

    1975-09-01

    The U.S. demand for lithium by the industrial sector and by a fusion power economy in the future is discussed. For a one million MW(e) CTR (D-T fuel cycle) economy, growing into the beginning of the next century (the years 2000 to 2030), the cumulative demand for lithium is estimated to range from (0.55 to 4.7) x 10 7 to 1.0 x 10 9 kg. Present estimates of the available U.S. supply are 6.9 x 10 8 kg of lithium from mineral resources and 4.0 x 10 9 kg of lithium from concentrated natural brines. There is, however, a vast supply of lithium in seawater: 2.5 x 10 14 kg. A preliminary process design for the extraction of lithium from seawater is presented: seawater is first evaporated by solar energy to increase the concentration of lithium and to decrease the concentration of other cations in the bittern which then passes into a Dowex-50 ion exchange bed for cation adsorption. Lithium ions are then eluted with dilute hydrochloric acid forming an aqueous lithium chloride which is subsequently concentrated and electrolyzed. The energy requirement for lithium extraction varies between 0.08 and 2.46 kWh(e)/gm for a range of production rates varying between 10 4 and 10 8 kg/y; this is small compared to the energy produced from the use of lithium in a CTR having a value of 3400 kWh(e)/g Li. Production cost of the process is estimated to be in the range of 2.2 to 3.2 cents/g Li. As a basis for the process design, it is recommended that a phase equilibria study of the solid--liquid crystallization processes of seawater be conducted. Uncertainties exist in the operation of large solar ponds for concentrating large quantities of seawater. A search for a highly selective adsorbent or extractant for Li from low concentration aqueous solutions should be made. Other physical separation processes such as using membranes should be investigated. 9 tables

  6. Temperature profile data from bucket, surface seawater intake, and XBT casts in a world wide distribution from 07 December 1995 to 18 October 1996 (NODC Accession 9600167)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using bucket, surface seawater intake, and XBT casts from several vessels in a world wide distribution from December 07, 1995...

  7. Spatial variation of PAHs and PCBs in coastal air, seawater, and sediments in a heavily industrialized region.

    Science.gov (United States)

    Odabasi, Mustafa; Dumanoglu, Yetkin; Kara, Melik; Altiok, Hasan; Elbir, Tolga; Bayram, Abdurrahman

    2017-05-01

    Concurrent coastal seawater (n = 22), sediment (n = 22), and atmospheric samples (n = 10) were collected in the Aliaga industrial region, Turkey, to explore the spatial variation, sources, and air-seawater exchange of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). Seawater Σ 16 PAH concentrations (particle + dissolved) ranged between 5107 and 294,624 pg L -1 , while Σ 41 PCB concentrations were in the range of 880-50,829 pg L -1 . Levels in sediments were highly variable ranging between 35.5-49,682 and 2.7-2450 μg kg -1 in dry weight for Σ 16 PAHs and Σ 41 PCBs, respectively. Atmospheric concentrations varied between 1791-274,974 and 104-20,083 pg m -3 for Σ 16 PAHs and Σ 41 PCBs, respectively. Sediment organic matter (OM) content and levels of Σ 16 PAHs and Σ 41 PCBs correlated weakly (r 2  = 0.19-0.23, p seawater, and sediment and factor analysis on the sediment levels pointed out that the major sources in the region are steel plants, petroleum refinery, petrochemical complex, ship breaking, loading/unloading activities at the ports, vehicular emissions, and fossil fuel combustion emissions. The direction of the air-seawater exchange was also explored by estimating seawater fugacity fractions of PAHs and PCBs. For PAHs, the number of cases implying deposition (43.0%) and volatilization (39.5%) was similar, while for PCBs, the number of cases implying volatilization (60.4%) was much higher compared to deposition (21.6%). Fugacity fractions were generally seawater and sediment levels were measured, implying that atmospheric deposition is an important mechanism affecting seawater and sediment PAH and PCB levels.

  8. Temperature profile data from surface seawater intake, bucket, and XBT casts in a world wide distribution from 1994-06-29 to 1996-06-08 (NODC Accession 9600120)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using surface seawater intake, bucket, and XBT casts from multiple vessels in a world wide distribution from June 29, 1994 to...

  9. Temperature profile data from surface seawater intake, bucket, and XBT casts in a world wide distribution from 1996-03-01 to 1997-01-03 (NODC Accession 9700036)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using surface seawater intake, bucket, and XBT casts from several vessels in a world wide distribution from March 1, 1996 to...

  10. Temperature profile data from surface seawater intake, bucket, and XBT casts in a world wide distribution from 1996-08-11 to 1997-07-16 (NODC Accession 9700213)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Temperature profile data were collected using surface seawater intake, bucket, and XBT casts in a world wide distribution by several vessels from August 11, 1996 to...

  11. Determination of iron in seawater by electrothermal atomic absorption spectrometry and atomic fluorescence spectrometry: A comparative study

    International Nuclear Information System (INIS)

    Cabon, J.Y.; Giamarchi, P.; Le Bihan, A.

    2010-01-01

    Two methods available for direct determination of total Fe in seawater at low concentration level have been examined: electrothermal atomization atomic absorption spectrometry (ETAAS) and electrothermal atomization laser excited atomic fluorescence spectrometry (ETA-LEAFS). In a first part, we have optimized experimental conditions of ETAAS (electrothermal program, matrix chemical modification) for the determination of Fe in seawater by minimizing the chemical interference effects and the magnitude of the simultaneous background absorption signal. By using the best experimental conditions, a detection limit of 80 ng L -1 (20 μL, 3σ) for total Fe concentration was obtained by ETAAS. Using similar experimental conditions (electrothermal program, chemical modification), we have optimized experimental conditions for the determination of Fe by LEAFS. The selected experimental conditions for ETA-LEAFS: excitation wavelength (296.69 nm), noise attenuation and adequate background correction led to a detection limit (3σ) of 3 ng L -1 (i.e. 54 pM) for total Fe concentration with the use a 20 μL seawater sample. For the two methods, concentration values obtained for the analysis of Fe in a NASS-5 (0.2 μg L -1 ) seawater sample were in good agreement with the certified values.

  12. Online preconcentration ICP-MS analysis of rare earth elements in seawater

    Science.gov (United States)

    Hathorne, Ed C.; Haley, Brian; Stichel, Torben; Grasse, Patricia; Zieringer, Moritz; Frank, Martin

    2012-01-01

    The rare earth elements (REEs) with their systematically varying properties are powerful tracers of continental inputs, particle scavenging intensity and the oxidation state of seawater. However, their generally low (˜pmol/kg) concentrations in seawater and fractionation potential during chemical treatment makes them difficult to measure. Here we report a technique using an automated preconcentration system, which efficiently separates seawater matrix elements and elutes the preconcentrated sample directly into the spray chamber of an ICP-MS instrument. The commercially available "seaFAST" system (Elemental Scientific Inc.) makes use of a resin with ethylenediaminetriacetic acid and iminodiacetic acid functional groups to preconcentrate REEs and other metals while anions and alkali and alkaline earth cations are washed out. Repeated measurements of seawater from 2000 m water depth in the Southern Ocean allows the external precision (2σ) of the technique to be estimated at mine water reference materials diluted with a NaCl matrix with recommended values in the literature. This makes the online preconcentration ICP-MS technique advantageous for the minimal sample preparation required and the relatively small sample volume consumed (7 mL) thus enabling large data sets for the REEs in seawater to be rapidly acquired.

  13. Numerical modeling of seawater intrusion in Zhoushuizi district of Dalian City, China

    Science.gov (United States)

    Zhao, J.; Lin, J.; Wu, J.

    2013-12-01

    A three-dimensional heterogeneous density-dependent numerical model was constructed to simulate the seawater intrusion process in coastal aquifers in Zhoushuizi Region, Dalian City. Model calibration was achieved through a prediction-correction method by adjusting the zonation and values of hydrogeologic parameters until the calculated heads and concentrations matched the observed values. Model validation results also showed that it was reasonable under current data conditions. Then the calibrated and validated model was applied to predict the dynamics and trend of seawater intrusion according to the current groundwater abstraction conditions in this study area 30 years after 2010. Prediction results showed that overall seawater intrusion in the future would be even more severe. Actually, with the growing of the population and development of the economy, the demand for ground water will be increasing continuously so that the problem of seawater intrusion may be more serious than that predicted by the modelin this study. Better strategies for reasonably governing exploitation of groundwater in the study area can be further developed by using this three-dimensional seawater intrusion model.

  14. High-precision measurements of seawater Pb isotope compositions by double spike thermal ionization mass spectrometry.

    Science.gov (United States)

    Paul, Maxence; Bridgestock, Luke; Rehkämper, Mark; van DeFlierdt, Tina; Weiss, Dominik

    2015-03-10

    A new method for the determination of seawater Pb isotope compositions and concentrations was developed, which combines and optimizes previously published protocols for the separation and isotopic analysis of this element. For isotopic analysis, the procedure involves initial separation of Pb from 1 to 2L of seawater by co-precipitation with Mg hydroxide and further purification by a two stage anion exchange procedure. The Pb isotope measurements are subsequently carried out by thermal ionization mass spectrometry using a (207)Pb-(204)Pb double spike for correction of instrumental mass fractionation. These methods are associated with a total procedural Pb blank of 28±21 pg (1sd) and typical Pb recoveries of 40-60%. The Pb concentrations are determined by isotope dilution (ID) on 50 mL of seawater, using a simplified version of above methods. Analyses of multiple aliquots of six seawater samples yield a reproducibility of about ±1 to ±10% (1sd) for Pb concentrations of between 7 and 50 pmol/kg, where precision was primarily limited by the uncertainty of the blank correction (12±4 pg; 1sd). For the Pb isotope analyses, typical reproducibilities (±2sd) of 700-1500 ppm and 1000-2000 ppm were achieved for (207)Pb/(206)Pb, (208)Pb/(206)Pb and (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)Pb, respectively. These results are superior to literature data that were obtained using plasma source mass spectrometry and they are at least a factor of five more precise for ratios involving the minor (204)Pb isotope. Both Pb concentration and isotope data, furthermore, show good agreement with published results for two seawater intercomparison samples of the GEOTRACES program. Finally, the new methods were applied to a seawater depth profile from the eastern South Atlantic. Both Pb contents and isotope compositions display a smooth evolution with depth, and no obvious outliers. Compared to previous Pb isotope data for seawater, the (206)Pb/(204)Pb ratios are well correlated

  15. The role of humic and fulvic acids in the phototransformation of phenolic compounds in seawater

    International Nuclear Information System (INIS)

    Calza, P.; Vione, D.; Minero, C.

    2014-01-01

    Humic substances (HS) are known to act as photosensitizers toward the transformation of pollutants in the surface layer of natural waters. This study focused on the role played by HS toward the transformation of xenobiotics in seawater, with the purpose of assessing the prevailing degradation routes. Phenol was chosen as model xenobiotic and its transformation was investigated under simulated sunlight in the presence of terrestrial or marine humic and fulvic acids, in pure water at pH 8, artificial seawater (ASW) or natural seawater (NSW). The following parameters were determined: (1) the phenol degradation rate; (2) the variation in HS concentration with irradiation time; (3) the production of transformation products; (4) the influence of iron species on the transformation process. Faster transformation of phenol was observed with humic acids (HA) compared to fulvic acids (SRFA), and transformation induced by both HA and SRFA was faster in ASW than that in pure water. These observations can be explained by assuming an interplay between different competing and sometimes opposite processes, including the competition between chloride, bromide and dissolved oxygen for reaction with HS triplet states. The analysis of intermediates formed in the different matrices under study showed the formation of several hydroxylated (hydroquinone, 1,4-benzoquinone, resorcinol) and condensed compounds (2,2′-bisphenol, 4,4′-bisphenol, 4-phenoxyphenol). Although 1,4-benzoquinone was the main transformation product, formation of condensed molecules was significant with both HA and SRFA. Experiments on natural seawater spiked with HS confirmed the favored formation of condensed products, suggesting a key role of humic matter in dimerization reactions occurring in saline water. - Highlights: • Phenol transformation in seawater can be photosensitized by humic substances. • Dimeric species are peculiar intermediates formed in the process. • Phenol degradation occurred faster with

  16. The role of humic and fulvic acids in the phototransformation of phenolic compounds in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Calza, P., E-mail: paola.calza@unito.it; Vione, D.; Minero, C.

    2014-09-15

    Humic substances (HS) are known to act as photosensitizers toward the transformation of pollutants in the surface layer of natural waters. This study focused on the role played by HS toward the transformation of xenobiotics in seawater, with the purpose of assessing the prevailing degradation routes. Phenol was chosen as model xenobiotic and its transformation was investigated under simulated sunlight in the presence of terrestrial or marine humic and fulvic acids, in pure water at pH 8, artificial seawater (ASW) or natural seawater (NSW). The following parameters were determined: (1) the phenol degradation rate; (2) the variation in HS concentration with irradiation time; (3) the production of transformation products; (4) the influence of iron species on the transformation process. Faster transformation of phenol was observed with humic acids (HA) compared to fulvic acids (SRFA), and transformation induced by both HA and SRFA was faster in ASW than that in pure water. These observations can be explained by assuming an interplay between different competing and sometimes opposite processes, including the competition between chloride, bromide and dissolved oxygen for reaction with HS triplet states. The analysis of intermediates formed in the different matrices under study showed the formation of several hydroxylated (hydroquinone, 1,4-benzoquinone, resorcinol) and condensed compounds (2,2′-bisphenol, 4,4′-bisphenol, 4-phenoxyphenol). Although 1,4-benzoquinone was the main transformation product, formation of condensed molecules was significant with both HA and SRFA. Experiments on natural seawater spiked with HS confirmed the favored formation of condensed products, suggesting a key role of humic matter in dimerization reactions occurring in saline water. - Highlights: • Phenol transformation in seawater can be photosensitized by humic substances. • Dimeric species are peculiar intermediates formed in the process. • Phenol degradation occurred faster with

  17. 238Pu concentrations in the marine environment at San Clemente Island

    International Nuclear Information System (INIS)

    Noshkin, V.E.; Brunk, J.L.; Jokela, T.A.; Wong, K.M.

    1981-01-01

    The concentration of plutonium and other radionuclides measured in samples of surface sediments, seawater and brown algae collected offshore from North Light Harbor Pier at San Clemente Island, CA, are presented. From 1967 to 1978, different forms of nuclear fuels used in operational or proposed SNAP (Systems for Nuclear Auxillary Power) devices were tested at this site to evaluate the effects of seawater on the heat sources. The principle radionuclide in the heat sources tested was 238 Pu. During these tests, small amounts of 238 Pu dissolved and migrated from the test chambers to the local marine environment. Currents dispersed this released 238 Pu so that at present a small increase in concentration above that of fallout background is evident in the surface 3.0-cm layer of near shore sediment that extends over a 3.0-km 2 area surrounding the pier. The 238 Pu associated with this sediment is slowly redissolving and can be taken up by marine algae. Except for a 0.025-km 2 region around the pier, the total plutonium ( 238 Pu + 239+240 Pu) in the surface 3.0-cm layer of sediment is within the range of total fallout plutonium reported in Atlantic and Pacific surface deposits from water depths less than 100 m. (author)

  18. Seawater mesocosm experiments in the Arctic uncover differential transfer of marine bacteria to aerosols.

    Science.gov (United States)

    Fahlgren, Camilla; Gómez-Consarnau, Laura; Zábori, Julia; Lindh, Markus V; Krejci, Radovan; Mårtensson, E Monica; Nilsson, Douglas; Pinhassi, Jarone

    2015-06-01

    Biogenic aerosols critically control atmospheric processes. However, although bacteria constitute major portions of living matter in seawater, bacterial aerosolization from oceanic surface layers remains poorly understood. We analysed bacterial diversity in seawater and experimentally generated aerosols from three Kongsfjorden sites, Svalbard. Construction of 16S rRNA gene clone libraries from paired seawater and aerosol samples resulted in 1294 sequences clustering into 149 bacterial and 34 phytoplankton operational taxonomic units (OTUs). Bacterial communities in aerosols differed greatly from corresponding seawater communities in three out of four experiments. Dominant populations of both seawater and aerosols were Flavobacteriia, Alphaproteobacteria and Gammaproteobacteria. Across the entire dataset, most OTUs from seawater could also be found in aerosols; in each experiment, however, several OTUs were either selectively enriched in aerosols or little aerosolized. Notably, a SAR11 clade OTU was consistently abundant in the seawater, but was recorded in significantly lower proportions in aerosols. A strikingly high proportion of colony-forming bacteria were pigmented in aerosols compared with seawater, suggesting that selection during aerosolization contributes to explaining elevated proportions of pigmented bacteria frequently observed in atmospheric samples. Our findings imply that atmospheric processes could be considerably influenced by spatiotemporal variations in the aerosolization efficiency of different marine bacteria. © 2015 Society for Applied Microbiology and John Wiley & Sons Ltd.

  19. Effect of medium-pressure UV-lamp treatment on disinfection by-products in chlorinated seawater swimming pool waters

    DEFF Research Database (Denmark)

    Cheema, Waqas Akram; Manasfi, Tarek; Kaarsholm, Kamilla Marie Speht

    2017-01-01

    Several brominated disinfection by-products (DBPs) are formed in chlorinated seawater pools, due to the high concentration of bromide in seawater. UV irradiation is increasingly employed in freshwater pools, because UV treatment photodegrades harmful chloramines. However, in freshwater pools it has...

  20. Aragonite coating solutions (ACS) based on artificial seawater

    Science.gov (United States)

    Tas, A. Cuneyt

    2015-03-01

    Aragonite (CaCO3, calcium carbonate) is an abundant biomaterial of marine life. It is the dominant inorganic phase of coral reefs, mollusc bivalve shells and the stalactites or stalagmites of geological sediments. Inorganic and initially precipitate-free aragonite coating solutions (ACS) of pH 7.4 were developed in this study to deposit monolayers of aragonite spherules or ooids on biomaterial (e.g., UHMWPE, ultrahigh molecular weight polyethylene) surfaces soaked in ACS at 30 °C. The ACS solutions of this study have been developed for the surface engineering of synthetic biomaterials. The abiotic ACS solutions, enriched with calcium and bicarbonate ions at different concentrations, essentially mimicked the artificial seawater composition and started to deposit aragonite after a long (4 h) incubation period at the tropical sea surface temperature of 30 °C. While numerous techniques for the solution deposition of calcium hydroxyapatite (Ca10(PO4)6(OH)2), of low thermodynamic solubility, on synthetic biomaterials have been demonstrated, procedures related to the solution-based surface deposition of high solubility aragonite remained uncommon. Monolayers of aragonite ooids deposited at 30 °C on UHMWPE substrates soaked in organic-free ACS solutions were found to possess nano-structures similar to the mortar-and-brick-type botryoids observed in biogenic marine shells. Samples were characterized using SEM, XRD, FTIR, ICP-AES and contact angle goniometry.

  1. Rapid and simultaneous determination of Strontium-89 and Strontium-90 in seawater.

    Science.gov (United States)

    Tayeb, Michelle; Dai, Xiongxin; Sdraulig, Sandra

    2016-03-01

    A rapid method has been developed for the direct determination of radiostrontium ((89)Sr and (90)Sr) released in seawater in the early phase of an accident. The method employs a fast and effective pre-concentration of radiostrontium by Sr-Ca co-precipitation followed by separation of radiostrontium using extraction chromatography technique. Radiostrontium is effectively separated in the presence of excessive dominant salts of seawater. Čerenkov and liquid scintillation assay (LSA) techniques are used to determine (89)Sr and (90)Sr. Sample preparation time is approximately 4 h for a set of 10 samples. The method was validated using spiked seawater samples at various activity ratios of (89)Sr:(90)Sr ranging from 1:10 to 9:1. The mean chemical recovery of Sr was 85 ± 3%. (90)Sr showed variable relative bias which enhanced with increasing ratio of (89)Sr:(90)Sr and was in the range ± 21%. The highest biases of (90)Sr determination were due to lower activity concentrations of (90)Sr and are regarded as acceptable in emergency situations with elevated levels of radiostrontium in the sample. The minimum detectable concentration (MDC) of (90)Sr and (89)Sr varied at different (89)Sr:(90)Sr ratios. For 0.1 L seawater and 15 min counting time on a low background Hidex liquid scintillation counter (LSC), the MDC of (90)Sr was in the range of 1.7-3.5 Bq L(-1) and MDC of (89)Sr was in the range 0.5-2.4 Bq L(-1). Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. [The effect of hypertonic seawater and isotonic seawater for nasal mucosa of allergic rhinitis mice model].

    Science.gov (United States)

    Deng, Zhifeng; Xu, Yu; Ou, Jin; Xiang, Rong; Tao, Zezhang

    2014-12-01

    To study the effect of hypertonic seawater and isotonic seawater for nasal mucosa of allergic rhinitis mice model, and explore the possible mechanism of nasal irrigation with seawater in treatment of allergic rhinitis. We used Der pl to make allergic rhinitis model of BALB/c mice, and divided them into three groups randomly. Nasal irrigation with hypertonic seawater (HS) or isotonic seawater (IS) in the treatment group 1-14 days after modeling, and black control (BC) group was given no treatment after modeling. Normal control (NC) group was given no treatment, the number of rubs and sneezings in each group were counted in 30 min after the last nasal irrigation. Mice were then killed 24 h after the last therapy. The noses of mice from each group were removed and fixed, then the slices were stained with hematoxylin and eosin, the others were observed by transmission electron microscope. Mice with hypertonic seawater and isotonic seawater were significantly improved in rubs and sneezings compared to the black control group (P 0. 05); Ciliated columnar epithelium cells in mucosal tissues of HS group and IS group were arranged trimly, better than that in the black control group. Morphology and microstructure in nasal mucosal of HS group was closer to the normal group than in IS group. The injury of nasal mucosa ciliated epithelium was significantly improved by nasal irrigation with hypertonic seawater and isotonic seawater, and the former is better than the latter, the mechanism of nasal irrigation with seawater in treatment of allergic rhinitis may rely on repairing the injured nasal mucosa ciliated epithelium, thereby the symptoms of nasal was reduced.

  3. A study of marine pollution caused by the release of metals into seawater following acid spills.

    Science.gov (United States)

    Cabon, Jean-Yves; Giamarchi, Philippe; Le Floch, Stephane

    2010-07-01

    This study examined the potential metal pollution induced by the accidental spill of different acids into seawater. The acids sink to the bottom according to their densities and subsequently react with marine sediments. The acids selected for this study were acetic, hydrochloric, nitric, sulfuric, and phosphoric acids; the metallic elements selected were Cr, Cu, Fe, Mn, Pb and Zn. The sediment was collected in Brest Harbour. The percentages of metals released from this sediment in the presence of various concentrations of acids in seawater were important; concentrations of approximately 7 mg L(-1) for Mn and 60 mg L(-1) for Zn were observed under our experimental conditions. We also examined the rate of release of these metals from the sediment into the seawater in the presence of the different acids and under different experimental conditions. We found that most of the metallic elements were released from the sediments into the seawater during the first fifteen minutes of exposure. After this time, a high degree of pollution was induced if acids leached into seawater were not rapidly diluted. Copyright 2010 Elsevier Ltd. All rights reserved.

  4. Determination of thorium in seawater by neutron activation analysis and mass spectrometry

    International Nuclear Information System (INIS)

    Huh, Chih-An.

    1987-01-01

    The recent development of neutron activation analysis and mass spectrometric methods for the determination of 232 Th in seawater has made possible rapid sampling and analysis of this long-lived, non-radiogenic thorium isotope on small-volume samples. The marine geochemical utility of 232 Th, whose concentration in seawater is extremely low, warrants the development of these sensitive techniques. The analytical methods and some results are presented and discussed in this article. 24 refs., 3 figs

  5. Contamination of the cement raw material in a quarry site by seawater intrusion, Darica-Turkey

    Science.gov (United States)

    Camur, M. Zeki; Doyuran, Vedat

    2008-02-01

    The open pit mining nearby shoreline is planned to be extended into below sea level in order to use additional reserves of the cement raw material (marl). The raw material is currently contaminated by seawater intrusion below a depth of 20 m up to the distance of 90 m from shoreline. Seawater intrusion related contamination of the material used for the cement production was investigated by means of diffusion process for the future two below sea level mining scenarios covering 43 years of period. According to the results, chloride concentrations higher than the tolerable limit of a cement raw material would be present in the material about 10-25 cm inward from each discontinuity surface, controlling groundwater flow, located between 170 and 300 m landward from the shoreline at below sea level mining depths of 0-30 m. The estimations suggest that total amounts of dilution required for the contaminated raw material to reduce its concentration level to the tolerance limit with uncontaminated raw material are about 113- to 124-fold for scenario I (13 years of below sea level mining after 30 years of above sea level mining) and about 126- to 138-fold for scenario II (43 years of simultaneous above and below sea level minings).

  6. Metagenomic survey of the taxonomic and functional microbial communities of seawater and sea ice from the Canadian Arctic.

    Science.gov (United States)

    Yergeau, Etienne; Michel, Christine; Tremblay, Julien; Niemi, Andrea; King, Thomas L; Wyglinski, Joanne; Lee, Kenneth; Greer, Charles W

    2017-02-08

    Climate change has resulted in an accelerated decline of Arctic sea ice since 2001 resulting in primary production increases and prolongation of the ice-free season within the Northwest Passage. The taxonomic and functional microbial community composition of the seawater and sea ice of the Canadian Arctic is not very well known. Bacterial communities from the bottom layer of sea ice cores and surface water from 23 locations around Cornwallis Island, NU, Canada, were extensively screened. The bacterial 16S rRNA gene was sequenced for all samples while shotgun metagenomics was performed on selected samples. Bacterial community composition showed large variation throughout the sampling area both for sea ice and seawater. Seawater and sea ice samples harbored significantly distinct microbial communities, both at different taxonomic levels and at the functional level. A key difference between the two sample types was the dominance of algae in sea ice samples, as visualized by the higher relative abundance of algae and photosynthesis-related genes in the metagenomic datasets and the higher chl a concentrations. The relative abundance of various OTUs and functional genes were significantly correlated with multiple environmental parameters, highlighting many potential environmental drivers and ecological strategies.

  7. The change of endotoxin, TNF-α, IL-6 and IL-8 in rats with open abdominal wound and seawater immersion

    International Nuclear Information System (INIS)

    Jiang Tao; Han Shanqiao; Hu Ming; Wang Dapeng; Chen Yongpeng; Chen Liang; Yu Jiyao

    2009-01-01

    Objective: To observe the change of endotoxin (lipopolysaccharide, LPS), tumor necrosis factor-α (TNF-α), IL-6, IL-8 in plasma in rats with open abdominal wound and seawater immersion. Method: One hundred and sixteen adult Wistar rats were randomly divided into 2 groups, ninety-six in the group of open abdominal wound with seawater immersion and 20 in open abdominal wound group (control group). LPS, TNF-α, IL-6 and IL-8 in plasma were examined at 0.5 h, 1 h, 2 h, 3 h and 4 h after open abdominal wound and seawater immersion by rapid microorganism-testing device and gamma detectors. All data were analyzed with statistic software. Results: Compared with the control group, the LPS level in plasma increased with significantly 2-4 hours after the open abdominal wound with seawater immersion (P<0.05), the concentrations of TNF-α significantly increased 4 hours after seawater immersion, and the IL-6 concentrations significantly increased 3-4 hours after seawater immersion. There was no statistical difference in IL-8 concentrations between the two groups. Conclusion: Closely related to the injury, the marked increase in LPS, TNF-α and IL-6 in plasma is one of the main fetal causes of toxic shock. (authors)

  8. Uranium in open ocean: concentration and isotopic composition

    International Nuclear Information System (INIS)

    Ku, T.L.; Knauss, K.G.; Mathieu, G.G.

    1977-01-01

    Uranium concentrations and 234 U/ 238 U activity ratios have been determined in 63 seawater samples (nine vertical profiles) from the Atlantic, and Pacific, and Arctic, and the Antarctic oceans, using the alpha-spectrometric method for their determinations. Correlation between uranium and salinity is well manifested by the data from the Arctic and the Antarctic oceans, but such a relation cannot be clearly defined with the +-(1 to 2)% precision of uranium measurements for the Atlantic and Pacific data. At the 95% confidence level: (1) the uranium/salinity ratio is (9.34 + - 0.56) x 10 -8 g/g for the seawater analyzed with salinity ranging from 30.3 to 36.2 per thousand; the uranium concentration of seawater of 35 per thousand salinity is 3.3 5 + - 0.2 μ g l -1 ; (2) the 234 U/ 238 U activity ratio is 1.14 +- 0.03. Uranium isotopes in interstitial waters of the Pacific surface sediments analyzed do not show large concentration differences across the sediment-water interface as suggested by previous measurements. Current estimations of the average world river uranium concentration (0.3 to 0.6 μ g l -1 ) and 234 U/ 238 U ratio (1.2 to 1.3) and of the diffusional 234 U influx from sediments 0.3 dpm cm -2 10 -3 yr -1 ) are essentially consistent with a model which depicts a steady state distribution of uranium in the ocean. However, the 0.3 to 0.6 μ g l -1 value for river uranium may be an upper limit estimate. (author)

  9. Distribution of lead-210 and polonium-210 between soluble and particulate phases in seawater

    International Nuclear Information System (INIS)

    Spencer, D.W.

    1975-01-01

    Results are reported from radiometric measurements of the distribution of 210 Pb and 210 Po in surface seawater and suspended particulate matter. Samples of plankton and sediments collected from some locations were also analyzed. Samples of seawater and suspended particulate matter were collected from stations located in the Gulf of Maine, the North Atlantic, and approximately 500 miles southwest of Gilbraltar. (U.S.)

  10. Intercomparison study of sampling methods for the determination of polychlorinated biphenyl (PCB) in seawater

    International Nuclear Information System (INIS)

    Schulz-Bull, D.E.

    1999-01-01

    The determination of organic pollutants in seawater is a serious problem, as their concentrations in the water column are typical in the fg - ng/L range. Available methods therefore includes extensive sampling and laboratory work. The development of simple sampling techniques for organochlorines (e.g. passive sampling with semipermeable membrane device (SPMD), mussel watch) is required. Three methods for the measurement of trace organochlorines in seawater were investigated: (1) the filtration (GF/F) and extraction (XAD-2 resin) of seawater with an in-situ pumping system, (2) biological-accumulation by mussels (mytilus edulis) and (3) passive sampling with SPMD

  11. Determination of iron in seawater by electrothermal atomic absorption spectrometry and atomic fluorescence spectrometry: a comparative study.

    Science.gov (United States)

    Cabon, J Y; Giamarchi, P; Le Bihan, A

    2010-04-07

    Two methods available for direct determination of total Fe in seawater at low concentration level have been examined: electrothermal atomization atomic absorption spectrometry (ETAAS) and electrothermal atomization laser excited atomic fluorescence spectrometry (ETA-LEAFS). In a first part, we have optimized experimental conditions of ETAAS (electrothermal program, matrix chemical modification) for the determination of Fe in seawater by minimizing the chemical interference effects and the magnitude of the simultaneous background absorption signal. By using the best experimental conditions, a detection limit of 80 ng L(-1) (20 microL, 3sigma) for total Fe concentration was obtained by ETAAS. Using similar experimental conditions (electrothermal program, chemical modification), we have optimized experimental conditions for the determination of Fe by LEAFS. The selected experimental conditions for ETA-LEAFS: excitation wavelength (296.69 nm), noise attenuation and adequate background correction led to a detection limit (3sigma) of 3 ng L(-1) (i.e. 54 pM) for total Fe concentration with the use a 20 microL seawater sample. For the two methods, concentration values obtained for the analysis of Fe in a NASS-5 (0.2 microg L(-1)) seawater sample were in good agreement with the certified values. Copyright 2010 Elsevier B.V. All rights reserved.

  12. Development of Novel Sorbents for Uranium Extraction from Seawater

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Wenbin [Univ. of Chicago, IL (United States); Taylor-Pashow, Kathryn [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2014-01-08

    As the uranium resource in terrestrial ores is limited, it is difficult to ensure a long-term sustainable nuclear energy technology. The oceans contain approximately 4.5 billion tons of uranium, which is one thousand times the amount of uranium in terrestrial ores. Development of technologies to recover the uranium from seawater would greatly improve the uranium resource availability, sustaining the fuel supply for nuclear energy. Several methods have been previously evaluated including solvent extraction, ion exchange, flotation, biomass collection, and adsorption; however, none have been found to be suitable for reasons such as cost effectiveness, long term stability, and selectivity. Recent research has focused on the amidoxime functional group as a promising candidate for uranium sorption. Polymer beads and fibers have been functionalized with amidoxime functional groups, and uranium adsorption capacities as high as 1.5 g U/kg adsorbent have recently been reported with these types of materials. As uranium concentration in seawater is only ~3 ppb, great improvements to uranium collection systems must be made in order to make uranium extraction from seawater economically feasible. This proposed research intends to develop transformative technologies for economic uranium extraction from seawater. The Lin group will design advanced porous supports by taking advantage of recent breakthroughs in nanoscience and nanotechnology and incorporate high densities of well-designed chelators into such nanoporous supports to allow selective and efficient binding of uranyl ions from seawater. Several classes of nanoporous materials, including mesoporous silica nanoparticles (MSNs), mesoporous carbon nanoparticles (MCNs), meta-organic frameworks (MOFs), and covalent-organic frameworks (COFs), will be synthesized. Selective uranium-binding liagnds such as amidoxime will be incorporated into the nanoporous materials to afford a new generation of sorbent materials that will be

  13. Development of Novel Sorbents for Uranium Extraction from Seawater

    International Nuclear Information System (INIS)

    Lin, Wenbin; Taylor-Pashow, Kathryn

    2014-01-01

    As the uranium resource in terrestrial ores is limited, it is difficult to ensure a long-term sustainable nuclear energy technology. The oceans contain approximately 4.5 billion tons of uranium, which is one thousand times the amount of uranium in terrestrial ores. Development of technologies to recover the uranium from seawater would greatly improve the uranium resource availability, sustaining the fuel supply for nuclear energy. Several methods have been previously evaluated including solvent extraction, ion exchange, flotation, biomass collection, and adsorption; however, none have been found to be suitable for reasons such as cost effectiveness, long term stability, and selectivity. Recent research has focused on the amidoxime functional group as a promising candidate for uranium sorption. Polymer beads and fibers have been functionalized with amidoxime functional groups, and uranium adsorption capacities as high as 1.5 g U/kg adsorbent have recently been reported with these types of materials. As uranium concentration in seawater is only ~3 ppb, great improvements to uranium collection systems must be made in order to make uranium extraction from seawater economically feasible. This proposed research intends to develop transformative technologies for economic uranium extraction from seawater. The Lin group will design advanced porous supports by taking advantage of recent breakthroughs in nanoscience and nanotechnology and incorporate high densities of well-designed chelators into such nanoporous supports to allow selective and efficient binding of uranyl ions from seawater. Several classes of nanoporous materials, including mesoporous silica nanoparticles (MSNs), mesoporous carbon nanoparticles (MCNs), meta-organic frameworks (MOFs), and covalent-organic frameworks (COFs), will be synthesized. Selective uranium-binding liagnds such as amidoxime will be incorporated into the nanoporous materials to afford a new generation of sorbent materials that will be

  14. In situ glass antifouling using Pt nanoparticle coating for periodic electrolysis of seawater

    Science.gov (United States)

    Xue, Yuxi; Zhao, Jin; Qiu, Ri; Zheng, Jiyong; Lin, Cunguo; Ma, Bojiang; Wang, Peng

    2015-12-01

    In situ electrochemical chlorination is a promising way to prohibit the biofouling on glass used for optical devices in seawater. To make this approach practical, a conductive glass should have low overpotential to generate Cl2, so that the electrical energy consumption, a critical issue for field application, will be low. Moreover, a long sustainability should also be taken into consideration from the application perspective. Following these criteria, we propose Pt/ITO surface to electrochemically generate Cl2, which immunizes biofouling for glass substrate. In this report, firstly, Pt nanoparticle/ITO is prepared via an electrodeposition approach. Secondly, electrocatalysis capability of Pt/ITO is elucidated, which shows the catalysis for Cl2 generation from NaCl solution and seawater has been sparked with Pt on the surface. Also, Pt/ITO is more sustainable and efficient than the bare ITO in natural seawater. Thirdly, the antifouling property is evaluated taking diatom as the target organism. Electrochemical chlorination on Pt/ITO can efficiently prevent the glass from fouling.

  15. Rapid determination of radium-224/226 in seawater sample by alpha spectrometry.

    Science.gov (United States)

    Song, Lijuan; Yang, Yonggang; Luo, Maoyi; Ma, Yan; Dai, Xiongxin

    2017-05-01

    A new radiochemical separation method has been developed for rapid determination of alpha-emitting radium isotopes in seawater samples. This method can be applied for the measurement of 226 Ra in seawater samples when 224 Ra is used as tracer for chemical recovery correction. Likewise, 226 Ra can also be added as tracer for the determination of 224 Ra in seawater sample. In the method, radium is first pre-concentrated with hydrous titanium oxide (HTiO) and is purified by combined anion/cation exchange column chromatographic separation. The radium in the eluate is then co-precipitated with HTiO, dissolved in 9 M H 2 SO 4 , and followed through a BaSO 4 micro-precipitation step to prepare a thin-layer counting source to determine the activities of 224 Ra/ 226 Ra by alpha spectrometry. Replicate spike and blank samples were measured to evaluate the performance of the procedure. The minimum detectable activity concentration was determined to be 0.5 mBq·L -1 for 226 Ra and 0.4 mBq·L -1 for 224 Ra in 1 L of seawater sample with a counting time of 48 h. The method is a promising candidate for rapid measurement for alpha-emitting Ra isotopes in a large population of environment water samples. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Potentiodynamic study of Al-Mg alloy with superhydrophobic coating in photobiologically active/not active natural seawater.

    Science.gov (United States)

    Benedetti, Alessandro; Cirisano, Francesca; Delucchi, Marina; Faimali, Marco; Ferrari, Michele

    2016-01-01

    Superhydrophobic coating technology is regarded as an attractive possibility for the protection of materials in a sea environment. DC techniques are a useful tool to characterize metals' behavior in seawater in the presence/absence of coatings and/or corrosion inhibitors. In this work, investigations concerning Al-5%Mg alloy with and without a sprayed superhydrophobic coating were carried out with potentiodynamic scans in photobiologically active and not active seawater (3 weeks of immersion). In not photobiologically active seawater, the presence of the superhydrophobic coating did not prevent pitting corrosion. With time, the coating underwent local exfoliations, but intact areas still preserved superhydrophobicity. In photobiologically active seawater, on samples without the superhydrophobic coating (controls) pitting was inhibited, probably due to the adsorption of organic compounds produced by the photobiological activity. After 3 weeks of immersion, the surface of the coating became hydrophilic due to diatom coverage. As suggested by intermediate observations, the surface below the diatom layer is suspected of having lost its superhydrophobicity due to early stages of biofouling processes (organic molecule adsorption and diatom attachment/gliding). Polarization curves also revealed that the metal below the coating underwent corrosion inhibiting phenomena as observed in controls, likely due to the permeation of organic molecules through the coating. Hence, the initial biofouling stages (days) occurring in photobiologically active seawater can both accelerate the loss of superhydrophobicity of coatings and promote corrosion inhibition on the underlying metal. Finally, time durability of superhydrophobic surfaces in real seawater still remains the main challenge for applications, where the early stages of immersion are demonstrated to be of crucial importance. Copyright © 2015 Elsevier B.V. All rights reserved.

  17. Electrochemical studies of biocorrosion of stainless steel in seawater (A summary of I.C.M.M. research in the field)

    International Nuclear Information System (INIS)

    Scotto, V.

    1989-01-01

    A summary of many years' research in the field is presented. This work has elucidated the mechanism by which a biofilm (slime layer) leads to corrosion of stainless steel in seawater. A layer of slime is deposited and grows on surfaces exposed in seawater. This slime causes the corrosion potential of stainless steel to increase with time of exposure to seawater, apparently because the slime catalyzes the cathodic reduction of oxygen in the water. This paper summarizes the evidence for this mechanism and also discusses the effects of water flow rate, temperature and surface cleaning

  18. Degradation of basalt fibre and glass fibre/epoxy resin composites in seawater

    International Nuclear Information System (INIS)

    Wei Bin; Cao Hailin; Song Shenhua

    2011-01-01

    Research highlights: → BFRP degradation process in seawater environment was first investigated. → The mass gain change includes two effects: absorption and extraction. → The interfacial adhesion of BFRP is bigger than GFRP. → After treated, the bending strength of BFRP is lower than GFRP. → Reducing the Fe 2+ in the basalt fibre could lead to a higher stability of BFRP. - Abstract: Epoxy resins reinforced, respectively, by basalt fibres and glass fibres were treated with a seawater solution for different periods of time. Both the mass gain ratio and the strength maintenance ratio of the composites were examined after the treatment. The fracture surfaces were characterized using scanning electron microscopy. The tensile and bending strengths of the seawater treated samples showed a decreasing trend with treating time. In general, the anti-seawater corrosion property of the basalt fibre reinforced composites was almost the same as that of the glass fibre reinforced ones. Based on the experimental results, possible corrosion mechanisms were explored, indicating that an effective lowering of the Fe 2+ content in the basalt fibre could lead to a higher stability for the basalt fibre reinforced composites in a seawater environment.

  19. Seawater predesalination with electrodialysis

    NARCIS (Netherlands)

    Galama, A.H.; Saakes, M.; Bruning, H.; Rijnaarts, H.H.M.; Post, J.W.

    2014-01-01

    The suitability of ED for seawater desalination was investigated and we quantified the energy losses that play a role in electrodialysis. The combination of electrodialysis (ED) and brackish water reverse osmosis (BWRO) is presented as an alternative desalination strategy for seawater reverse

  20. Anthropogenic 236U in Danish Seawater: Global Fallout versus Reprocessing Discharge

    DEFF Research Database (Denmark)

    Qiao, Jixin; Steier, Peter; Nielsen, Sven Poul

    2017-01-01

    This work focuses on the occurrence of 236U in seawater along Danish coasts, which is the sole water-exchange region between the North Sea-Atlantic Ocean and the Baltic Sea. Seawater collected in 2013 and 2014 were analyzed for 236U (as well as 238U and 137Cs). Our results indicate that 236U...... seawater. However, unexpectedly high 236U/238U ratios as well as high 236U concentrations were observed at low-salinity locations of the Baltic Sea. While this feature might be interpreted as a clue for another significant 236U input in the Baltic Sea, it may also be caused by the complexity of water...... currents or slow turnover rate....

  1. The strontium isotopic composition of seawater, and seawater-oceanic crust interaction

    International Nuclear Information System (INIS)

    Spooner, E.T.C.

    1976-01-01

    The 87 Sr/ 86 Sr ratio of seawater strontium (0.7091) is less than the 87 Sr/ 86 Sr ratio of dissolved strontium delivered to the oceans by continental run-off (approximately 0.716). Isotope exchange with strontium isotopically lighter oceanic crust during hydrothermal convection within spreading oceanic ridges can explain this observation. In quantitative terms, the current 87 Sr/ 86 Sr ratio of seawater (0.7091) may be maintained by balancing the continental run-off flux of strontium (0.59 x 10 12 g/yr) against a hydrothermal recirculation flux of 3.6 x 10 12 g/yr, during which the 87 Sr/ 86 Sr ratio of seawater drops by 0.0011. A concomitant mean increase in the 87 Sr/ 86 Sr ratio of the upper 4.5 km of oceanic crust of 0.0010 (0.7029-0.7039) should be produced. This required 87 Sr enrichment has been observed in hydrothermally metamorphosed ophiolitic rocks from the Troodos Massif, Cyprus. The post-Upper Cretaceous increase in the strontium isotopic composition of seawater (approximately 0.7075-0.7091) covaries smoothly with inferred increase in land area. This suggests that during this period the main factor which has caused variability in the 87 Sr/ 86 Sr ratio of seawater strontium could have been variation in the magnitude of the continental run-off flux caused by variation in land area. Variations in land area may themselves have been partly a consequence of variations in global mean sea-floor spreading rate. (Auth.)

  2. Behaviors and chemical forms of radionuclides in seawater

    International Nuclear Information System (INIS)

    Honda, Yoshihide

    1981-01-01

    Although the radionuclides introduced into the marine environment from various sources and routes are finally distributed among the components of the marine ecosystem, the residence time is one of the most useful measures of the reactivity of an element in the oceanic chemical system. Heavy metals such as Mn, Fe, Co and Zn which have shorter residence times, reveal more complicated behaviours in relation to marine radioecological interest than alkaline earth element such as Sr which has a longer residence time. The possible physico-chemical forms of radionuclides in the oceans are usually classified into three categories, that is, species in true solution, colloidal species, and particulate forms. The modeling to study the dispersion of radionuclides introduced into the marine environment can be approached with the aid of the knowledge of behaviors of their stable counterparts in seawater. The different physico-chemical forms between stable and radioactive nuclides in seawater may cause different biological concentration of the element. To realize the chemical speciation of radionuclides in the marine environment, it is also important in thermodynamical calculation to consider heterogeneous interfaces where cause raising the concentration of reactants in seawater, especially in the coastal waters. In the discussion on the primary factors that can affect the elemental distribution in the marine environment, primary productivity and bacterial activity are emphasized for the transformation of physicochemical states of radionuclides in the marine environment. Finally, the radioecological differences between radiocobalt in organic complexed and ionic forms were demonstrated in the experiments on the uptake and elimination of radiocobalt by mussels. (J.P.N.)

  3. Effect of seawater salinity on pore-size distribution on a poly(styrene)-based HP20 resin and its adsorption of diarrhetic shellfish toxins.

    Science.gov (United States)

    Fan, Lin; Sun, Geng; Qiu, Jiangbing; Ma, Qimin; Hess, Philipp; Li, Aifeng

    2014-12-19

    In the present study, okadaic acid (OA) and dinophysistoxin-1 (DTX1) were spiked into artificial seawater at low, medium and high estuarine salinities (9‰, 13.5‰ and 27‰). Passive samplers (HP20 resin) used for solid phase adsorption toxin tracking (SPATT) technology were exposed in these seawaters for 12-h periods. Adsorption curves well fitted a pseudo-secondary kinetics model. The highest initial sorption rates of both toxins occurred in the seawater of medium salinity, followed by seawater of low and high estuarine salinity. Pore volumes of micropores (seawater at high and low salinity but not in seawater at medium salinity, which demonstrated that the toxin molecules entered into micropores and mesopores (below 10nm in size) in seawaters of high and low salinity. More toxin or other matrix agglomerates were displayed on the surface of resin deployed in the seawater of medium salinity. Taking into consideration the pore-size distribution and surface images, it appears that intra-particle diffusion governs toxin adsorption in seawater at high salinity while film diffusion mainly controls the adsorption process in seawater at medium salinity. This is the first study to confirm that molecules of OA and DTX1 are able to enter into micropores (seawater with high salinity (∼27‰). Copyright © 2014 Elsevier B.V. All rights reserved.

  4. Performance and flow characteristics of MHD seawater thruster

    Energy Technology Data Exchange (ETDEWEB)

    Doss, E.D.

    1990-01-01

    The main goal of the research is to investigate the effects of strong magnetic fields on the electrical and flow fields inside MHD thrusters. The results of this study is important in the assessment of the feasibility of MHD seawater propulsion for the Navy. To accomplish this goal a three-dimensional fluid flow computer model has been developed and applied to study the concept of MHD seawater propulsion. The effects of strong magnetic fields on the current and electric fields inside the MHD thruster and their interaction with the flow fields, particularly those in the boundary layers, have been investigated. The results of the three-dimensional computations indicate that the velocity profiles are flatter over the sidewalls of the thruster walls in comparison to the velocity profiles over the electrode walls. These nonuniformities in the flow fields give rise to nonuniform distribution of the skin friction along the walls of the thrusters, where higher values are predicted over the sidewalls relative to those over the electrode walls. Also, a parametric study has been performed using the three-dimensional MHD flow model to analyze the performance of continuous electrode seawater thrusters under different operating parameters. The effects of these parameters on the fluid flow characteristics, and on the thruster efficiency have been investigated. Those parameters include the magnetic field (10--20 T), thruster diameter, surface roughness, flow velocity, and the electric load factor. The results show also that the thruster performance improves with the strength of the magnetic field and thruster diameter, and the efficiency decreases with the flow velocity and surface roughness.

  5. Sustainable and safe energy supply with seawater uranium fueled HTGR and its economy

    International Nuclear Information System (INIS)

    Fukaya, Y.; Goto, M.

    2017-01-01

    Highlights: • We discussed uranium resources with an energy security perspective. • We concluded seawater uranium is preferable for sustainability and energy security. • We evaluated electricity generation cost of seawater uranium fueled HTGR. • We concluded electricity generation with seawater uranium is reasonable. - Abstract: Sustainable and safe energy supply with High Temperature Gas-cooled Reactor (HTGR) fueled by uranium from seawater have been investigated and discussed. From the view point of safety feature of self-regulation with thermal reactor of HTGR, the uranium resources should be inexhaustible. The seawater uranium is expected to be alternative resources to conventional resources because it exists so much in seawater as a solute. It is said that 4.5 billion tons of uranium is dissolved in the seawater, which corresponds to a consumption of approximately 72 thousand years. Moreover, a thousand times of the amount of 4.5 trillion tU of uranium, which corresponds to the consumption of 72 million years, also is included in the rock on the surface of the sea floor, and that is also recoverable as seawater uranium because uranium in seawater is in an equilibrium state with that. In other words, the uranium from seawater is almost inexhaustible natural resource. However, the recovery cost with current technology is still expensive compared with that of conventional uranium. Then, we assessed the effect of increase in uranium purchase cost on the entire electricity generation cost. In this study, the economy of electricity generation of cost of a commercial HTGR was evaluated with conventional uranium and seawater uranium. Compared with ordinary LWR using conventional uranium, HTGR can generate electricity cheaply because of small volume of simple direct gas turbine system compared with water and steam systems of LWR, rationalization by modularizing, and high thermal efficiency, even if fueled by seawater uranium. It is concluded that the HTGR

  6. Cs-137 Concentration in Seawater from the Gulf of Thailand and the Andaman Sea and Radiation Doses in Marine Biota After the Fukushima Dai-ichi NPP Accident

    International Nuclear Information System (INIS)

    Tumnoi, Y.; Nakkaew, N.; Khrautongkieo, C.; Udomsomporn, S.

    2014-01-01

    Shortly after the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) was severely damaged in March 2011 by a large earthquake and subsequent tsunami, large amounts of radionuclides including 131 I, 134 Cs, 137 Cs and 90 Sr were released into the atmosphere and the marine environ- ment. These artificial radionuclides widely dispersed causing radioactive contaminations in several areas and concerns on the marine biota. In this study, a total of 52 seawater samples (10 stations) and 66 marine animals (9 stations) were collected from the Gulf of Thailand and the Andaman Sea between March 2012 and July 2013 for 137 Cs analysis. An ammonium molybdophosphate (AMP) method was used in conjunction with gammaspectrometry to measure 137 Cs in the seawater. 137 Cs was moreover extracted from the marine biota using a radiochemical technique followed by a measurement using low background proportional counters. The results showed 137 Cs concentrations in seawater ranging from 0.59 to 3.75 mBq/L (1.65±0.74 mBq/L). 137 Cs concentrations in benthic fish including Nemipterus hexodon and Saurida elongate were 0.06-1.23 Bq/kgww (0.24±0.26 Bq/kgww) and 0.07-0.64 Bq/kgww (0.16±0.12 Bq/kgww), respectively. Whereas, 137 Cs levels in squid (Loligo duvauceli) ranged between 0.03 and 0.15 Bq/kgww (0.08±0.04 Bq/kgww). An increase of 137 Cs concentrations in seawater and marine biota was not found when compared to those collected from the Gulf of Thailand and measured during 1989-1991. ERICA model was used to estimate radiation doses in the studied animals. Our results revealed that radiation doses of 137 Cs in N. hexodon and S. elongate were 0.7-4.2 nGy/hr (1.6±0.6 nGy/hr) and 0.7-3.4 nGy/hr (1.7±0.9 nGy/hr), respectively. While, a range of 0.7-3.2 nGy/hr (1.5±0.6 nGy/hr) was found in L. duvauceli. These radiation doses are well below the dose limit for aquatic organisms (10±Gy/hr). It can be concluded that Thai marine environment and animals have not been contaminated and not under a

  7. Seawater-sediment interaction at elevated temperatures and pressures: implications for the near field chemical environment

    International Nuclear Information System (INIS)

    Seyfried, W.E. Jr.; Thornton, E.C.; Janecky, D.R.

    1981-01-01

    Results of four experiments are reported which document chemical exchange and mineralogic modification during seawater-sediment interaction at 200 0 to 300 0 C, 500 bars. Sediments used for this study are from MPG-1 (central North Pacific). Experimental conditions (T, P, W/R) were chosen to be reasonably analogous to conditions which will characterize the near field environment; that is a zone within approximately 1 m of the buried waste canister. In general, the major element chemistry of seawater was similarly modified in all experiments. The aqueous concentrations of Ca, Mg, Sr, and SO 4 decreased and SiO 2 /sub (aq)/, Na, K, and ΣCO 2 increased relative to values in seawater prior to reaction with sediments. pH decreased and remained distinctly acid. Con comitantly significant concentrations of heavy metals entered seawater from the sediments during reaction. Dissolution of Mn-rich phases profoundly affected alteration processes. For example, reaction of MnO 2 components of the smectite-rich sediment (Pacific smectite) with seawater created an unusually oxidizing milieu (fO 2 = 10 -7 74 ), and resulted in dissolution of significant quantities of Au from the reaction cell. Although illite-quartz-Fe-chlorite (sediment B)-seawater interaction also created a relatively oxidizing environment, this environment was not capable of oxidizing Au. Thus, in this regard (oxidation potential) sediment mineralogy exerts a strong influence. Mineralogic modification of sediment B at 200 0 and 300 0 C was minor and characterized by partial dissolution of illite and exchange of Fe for Mg in chlorite. In contrast the smectite-rich sediment, which, prior to reaction with seawater contained a poorly crystalline smectite phase, clinoptilolite, and amorphous material, recrystallized totally to a well defined smectite mineral. Anhydrite was abundantly present amongst the alteration products of all experiments

  8. Precise determination of dissolved silica in seawater by ion-exclusion chromatography isotope dilution inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Nonose, Naoko; Cheong, Chikako; Ishizawa, Yukari; Miura, Tsutomu; Hioki, Akiharu

    2014-08-20

    Ion exclusion chromatograph (IEC) isotope dilution (ID) inductively coupled plasma mass spectrometry (ICP-MS) (IEC-ID-ICP-MS) was developed for measurement of dissolved silica in seawater, which was applied to production of certified reference materials (CRMs) of three concentration levels of nutrients (high, medium and low levels). IEC-ICP-MS has been employed to separate dissolved silica from seawater matrix. In the present study, in order to solve substantial problems due to spectral interference in ICP-MS and to improve the accuracy of IEC-ICP-MS beyond standard addition or conventional calibration methods, ID method was coupled with ICP-sector field mass spectrometry (operated under medium resolution,i.e., m/Δm=4000). In addition, effects of various operating parameters in ICP-MS on a silicon background level were also investigated to obtain lower background equivalent concentration (BEC). As a result, 3 ng g(-1) of the BEC and 0.5 % of relative standard uncertainties were achieved in the analyses of dissolved silica in seawater samples at concentration levels from 4.0 mg kg (-1) to 0.8 mg kg(-1) as silicon. The developed method was successfully validated by analyses of an artificial seawater containing a known amount of silicate and the seawater certified reference material MOOS-2 produced by the National Research Council Canada. Copyright © 2014 Elsevier B.V. All rights reserved.

  9. Adsorbent Alkali Conditioning for Uranium Adsorption from Seawater. Adsorbent Performance and Technology Cost Evaluation

    International Nuclear Information System (INIS)

    Tsouris, Costas; Mayes, Richard T.; Janke, Christopher James; Dai, Sheng; Das, S.; Liao, W.P.; Kuo, Li-Jung; Wood, Jordana; Gill, Gary; Byers, Maggie Flicker; Schneider, Eric

    2015-01-01

    The Fuel Resources program of the Fuel Cycle Research and Development program of the Office of Nuclear Energy (NE) is focused on identifying and implementing actions to assure that nuclear fuel resources are available in the United States. An immense source of uranium is seawater, which contains an estimated amount of 4.5 billion tonnes of dissolved uranium. This unconventional resource can provide a price cap and ensure centuries of uranium supply for future nuclear energy production. NE initiated a multidisciplinary program with participants from national laboratories, universities, and research institutes to enable technical breakthroughs related to uranium recovery from seawater. The goal is to develop advanced adsorbents to reduce the seawater uranium recovery technology cost and uncertainties. Under this program, Oak Ridge National Laboratory (ORNL) has developed a new amidoxime-based adsorbent of high surface area, which tripled the uranium capacity of leading Japanese adsorbents. Parallel efforts have been focused on the optimization of the physicochemical and operating parameters used during the preparation of the adsorbent for deployment. A set of parameters that need to be optimized are related to the conditioning of the adsorbent with alkali solution, which is necessary prior to adsorbent deployment. Previous work indicated that alkali-conditioning parameters significantly affect the adsorbent performance. Initiated in 2014, this study had as a goal to determine optimal parameters such as base type and concentration, temperature, and duration of conditioning that maximize the uranium adsorption performance of amidoxime functionalized adsorbent, while keeping the cost of uranium production low. After base-treatment at various conditions, samples of adsorbent developed at ORNL were tested in this study with batch simulated seawater solution of 8-ppm uranium concentration, batch seawater spiked with uranium nitrate at 75-100 ppb uranium, and continuous

  10. Adsorbent Alkali Conditioning for Uranium Adsorption from Seawater. Adsorbent Performance and Technology Cost Evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Tsouris, Costas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Mayes, Richard T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Janke, Christopher James [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Dai, Sheng [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Das, S. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Liao, W. -P. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Kuo, Li-Jung [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Wood, Jordana [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Gill, Gary [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Byers, Maggie Flicker [Univ. of Texas, Austin, TX (United States); Schneider, Eric [Univ. of Texas, Austin, TX (United States)

    2015-09-30

    The Fuel Resources program of the Fuel Cycle Research and Development program of the Office of Nuclear Energy (NE) is focused on identifying and implementing actions to assure that nuclear fuel resources are available in the United States. An immense source of uranium is seawater, which contains an estimated amount of 4.5 billion tonnes of dissolved uranium. This unconventional resource can provide a price cap and ensure centuries of uranium supply for future nuclear energy production. NE initiated a multidisciplinary program with participants from national laboratories, universities, and research institutes to enable technical breakthroughs related to uranium recovery from seawater. The goal is to develop advanced adsorbents to reduce the seawater uranium recovery technology cost and uncertainties. Under this program, Oak Ridge National Laboratory (ORNL) has developed a new amidoxime-based adsorbent of high surface area, which tripled the uranium capacity of leading Japanese adsorbents. Parallel efforts have been focused on the optimization of the physicochemical and operating parameters used during the preparation of the adsorbent for deployment. A set of parameters that need to be optimized are related to the conditioning of the adsorbent with alkali solution, which is necessary prior to adsorbent deployment. Previous work indicated that alkali-conditioning parameters significantly affect the adsorbent performance. Initiated in 2014, this study had as a goal to determine optimal parameters such as base type and concentration, temperature, and duration of conditioning that maximize the uranium adsorption performance of amidoxime functionalized adsorbent, while keeping the cost of uranium production low. After base-treatment at various conditions, samples of adsorbent developed at ORNL were tested in this study with batch simulated seawater solution of 8-ppm uranium concentration, batch seawater spiked with uranium nitrate at 75-100 ppb uranium, and continuous

  11. Impact of the surface roughness of AISI 316L stainless steel on biofilm adhesion in a seawater-cooled tubular heat exchanger-condenser.

    Science.gov (United States)

    García, Sergio; Trueba, Alfredo; Vega, Luis M; Madariaga, Ernesto

    2016-11-01

    The present study evaluated biofilm growth in AISI 316L stainless steel tubes for seawater-cooled exchanger-condensers that had four different arithmetic mean surface roughness values ranging from 0.14 μm to 1.2 μm. The results of fluid frictional resistance and heat transfer resistance regarding biofilm formation in the roughest surface showed increases of 28.2% and 19.1% respectively, compared with the smoothest surface. The biofilm thickness taken at the end of the experiment showed variations of up to 74% between the smoothest and roughest surfaces. The thermal efficiency of the heat transfer process in the tube with the roughest surface was 17.4% greater than that in the tube with the smoothest surface. The results suggest that the finish of the inner surfaces of the tubes in heat exchanger-condensers is critical for improving energy efficiency and avoiding biofilm adhesion. This may be utilised to reduce biofilm adhesion and growth in the design of heat exchanger-condensers.

  12. Impact of seawater [Ca

    NARCIS (Netherlands)

    Mewes, A.; Langer, G.; Thoms, S.; Nehrke, G.; Reichart, G.J.; de Nooijer, L.J.; Bijma, J.

    2015-01-01

    Mg / Ca ratios in foraminiferal tests are routinely used as paleotemperature proxies, but on long timescales, they also hold the potential to reconstruct past seawater Mg / Ca. The impact of both temperature and seawater Mg / Ca on Mg incorporation in Foraminifera has been quantified by a number of

  13. Cell Culture Isolation of Piscine Nodavirus (Betanodavirus) in Fish-Rearing Seawater.

    Science.gov (United States)

    Nishi, Shinnosuke; Yamashita, Hirofumi; Kawato, Yasuhiko; Nakai, Toshihiro

    2016-04-01

    Piscine nodavirus (betanodavirus) is the causative agent of viral nervous necrosis (VNN) in a variety of cultured fish species, particularly marine fish. In the present study, we developed a sensitive method for cell culture isolation of the virus from seawater and applied the method to a spontaneous fish-rearing environment. The virus in seawater was concentrated by an iron-based flocculation method and subjected to isolation with E-11 cells. A real-time reverse transcriptase PCR (RT-PCR) assay was used to quantify the virus in water. After spiking into seawater was performed, a betanodavirus strain (red spotted grouper nervous necrosis virus [RGNNV] genotype) was effectively recovered in the E-11 cells at a detection limit of approximately 10(5)copies (equivalent to 10(2)50% tissue culture infective doses [TCID50])/liter seawater. In an experimental infection of juvenile sevenband grouper (Epinephelus septemfasciatus) with the virus, the virus was isolated from the drainage of a fish-rearing tank when the virus level in water was at least approximately 10(5)copies/liter. The application of this method to seven band grouper-rearing floating net pens, where VNN prevailed, resulted in the successful isolation of the virus from seawater. No differences were found in the partial sequences of the coat protein gene (RNA2) between the clinical virus isolates of dead fish and the cell-cultured virus isolates from seawater, and the viruses were identified as RGNNV. The infection experiment showed that the virus isolates from seawater were virulent to seven band grouper. These results showed direct evidence of the horizontal transmission of betanodavirus via rearing water in marine aquaculture. Copyright © 2016, American Society for Microbiology. All Rights Reserved.

  14. Characterization of the corrosion behavior of different stainless steel alloys exposed to flowing fresh seawater, using E.I.S technique

    Energy Technology Data Exchange (ETDEWEB)

    Al Muhanna, K. [Petroleum Research and Studies Center, Kuwait Institute for Scientific Research, KISR, P.O.Box 24885, Safat 13109 Kuwait (Kuwait)

    2004-07-01

    E.I.S technique was used to characterize the corrosion behavior of UNS NO. S 31600 stainless steel, UNS NO. S 30400 stainless steel and UNS NO. S 62800 sanicro 28 exposed to continuous fresh Seawater. The total exposure time of the test was about 180 days. Two types of additives (4 ppm of Cl{sub 2} and 5 ppm of NH{sub 3}) were also added to the seawater to investigate their effect on the surfaces of these alloys. During the tests, no marine - macro fouling was observed on the surfaces of the tested alloys, as the seawater was filtrated at the Doha Desalination Research Center, where the study was carried out, but only a slimy layer spread on the whole surface of the alloys. The corrosion behavior of each alloy was monitored by the open circuit potential measurement, and the E.I.S technique using the EG and G 352 software and hardware instrument, where the resistance of the solution (R{sub sol}), the resistance of the surface of the tested alloy (R{sub p}), and the double layer capacitance (Cdl) was calculated. Under this study's experimental conditions, results indicated that the stainless steel alloys were highly resistant to marine fouling and corrosion in seawater, and were not affected by the aggressive additives, such as NH{sub 3}, and Cl{sub 2} in the seawater. (author)

  15. Simulation-Optimization Model for Seawater Intrusion Management at Pingtung Coastal Area, Taiwan

    Science.gov (United States)

    Huang, P. S.; Chiu, Y.

    2015-12-01

    In 1970's, the agriculture and aquaculture were rapidly developed at Pingtung coastal area in southern Taiwan. The groundwater aquifers were over-pumped and caused the seawater intrusion. In order to remedy the contaminated groundwater and find the best strategies of groundwater usage, a management model to search the optimal groundwater operational strategies is developed in this study. The objective function is to minimize the total amount of injection water and a set of constraints are applied to ensure the groundwater levels and concentrations are satisfied. A three-dimension density-dependent flow and transport simulation model, called SEAWAT developed by U.S. Geological Survey, is selected to simulate the phenomenon of seawater intrusion. The simulation model is well calibrated by the field measurements and replaced by the surrogate model of trained artificial neural networks (ANNs) to reduce the computational time. The ANNs are embedded in the management model to link the simulation and optimization models, and the global optimizer of differential evolution (DE) is applied for solving the management model. The optimal results show that the fully trained ANNs could substitute the original simulation model and reduce much computational time. Under appropriate setting of objective function and constraints, DE can find the optimal injection rates at predefined barriers. The concentrations at the target locations could decrease more than 50 percent within the planning horizon of 20 years. Keywords : Seawater intrusion, groundwater management, numerical model, artificial neural networks, differential evolution

  16. Fugacity analysis of polycyclic aromatic hydrocarbons between microplastics and seawater

    Science.gov (United States)

    Lee, Hwang; Chang, Sein; Kim, Seung-Kyu; Kwon, Jung-Hwan

    2017-03-01

    Recently, the accumulation of plastic debris in the marine environment has become a great concern worldwide. Although plastics are biologically and chemically inert, plastic debris has been suspected of causing adverse effects on ecosystems due to the increase in reactivity by size reduction and/or micropollutants associated with plastics. Because of the high sorption capacity of microplastics toward organic micropollutants, it is suspected that microplastics may play roles in the distribution and fate of micropollutants. In order to quantitatively evaluate the "net flow" of environmental contaminants in water-plastic-organism systems, a fugacity analysis was conducted using concentrations of polycyclic aromatic hydrocarbons (PAHs) in open oceans and in polyethylene as a representative material of plastic debris. Ratio of fugacity in polyethylene to that in seawater showed a decreasing trend with increasing partition coefficient between polyethylene and seawater (KPE/sw). This indicates that phase equilibrium between polyethylene and seawater is not attained for higher molecular weight PAHs. Disequilibrium of high molecular weight PAHs suggests that transfer from seawater to plastic debris is thermodynamically driven and the role of plastic debris as a vector to transfer them to living organisms would be minimal. However, additives may slowly migrate from plastics into the environment causing potentially serious effects on ecosystems.

  17. Sm-Nd in marine carbonates and phosphates: implications for Nd isotopes in seawater and crustal ages

    International Nuclear Information System (INIS)

    Shaw, H.F.; Wasserburg, G.J.

    1985-01-01

    This study explores the possibility of establishing Nd isotopic variations in seawater over geologic time. Calcite, aragonite and apatite are examined as possible phases recording seawater values of epsilonsubNd. Modern, biogenic and inorganically precipitated calcite and aragonite from marine environments were found to have Nd concentrations of from 0.2 to 70 ppb, showing that primary marine CaCO 3 contains little REE and that Nd/Ca is not greatly enhanced relative to seawater during carbonate precipitation. Very young marine limestone and dolomite containing no continental detritus have approx. 200 ppb Nd. All the carbonates are LREE enriched. Modern and very young Atlantic and Pacific carbonates have epsilonsub(Nd) in the range of shallow Atlantic and Pacific seawater respectively, implying that they derive their REE from local seawater. The Nd in well preserved carbonate fossils is 4 ppb, much greater than in their modern counterparts but like the high values found for carbonates in other studies. Results are also reported for apatite. They suggest that sedimentary apatite can be used to determine epsilonsub(Nd)(T) in ancient seawater. The seawater values so inferred range between -1.7 and -8.9 over the last 700 my and lie in the range of modern seawater, showing no evidence for drastic changes. (U.K.)

  18. Sorption isolation of strontium from seawater

    International Nuclear Information System (INIS)

    Avramenko, V.A.; Zheleznov, V.V.; Kaplun, E.V.; Sokol'nitskaya, T.A.; Yukhkam, A.A.

    2001-01-01

    Sorption isolation of strontium from seawater is considered and prospects of use of selective adsorbents for purification of seawater or liquid radioactive wastes mixed with seawater from 90 Sr are discussed. Comparative analysis of sorptive properties of adsorbents of different nature is done. It is shown that sorption-reagent materials developed by authors can to afford effective separation of 90 Sr from seawater. Possible mechanism of strontium sorption by these adsorbents is considered. The prospect of their use for purification of liquid radioactive wastes from strontium is shown [ru

  19. Development of radioactive seawater monitors, 1

    International Nuclear Information System (INIS)

    Fukushima, Masanori

    1989-01-01

    Applicability of some adsorptive materials to monitoring of radioactive seawater is generalized. Studied techniques that allow utilization of adsorptive materials in monitoring radioactive seawater are the substitute methods using sampled seawater or indicator plants such as gulfweed and the method using adsorptive materials for continuous monitoring of underwater radioactivity, the method using them for field measurement of under water radioactivity from a boat, and the method using an adsorptive material moored underwater for integration monitoring of underwater radioactivity. Selected adsorptive materials that were judged suitable for monitoring radioactive seawater is the one composed of some kind of adsorptive compound (manganese dioxide or ferrocyan cobalt potassium) fixed to crylic cellulose. This adsorptive material permits selective scavenging radioactive Cs, Mn, Co, Zn, Ce, Fe, Ru, Ra Th, Pu and Am from seawater. (aurhor)

  20. Viral lysis of photosynthesizing microbes as a mechanism for calcium carbonate nucleation in seawater

    Science.gov (United States)

    Lisle, John T.; Robbins, Lisa L.

    2016-01-01

    Removal of carbon through the precipitation and burial of calcium carbonate in marine sediments constitutes over 70% of the total carbon on Earth and is partitioned between coastal and pelagic zones. The precipitation of authigenic calcium carbonate in seawater, however, has been hotly debated because despite being in a supersaturated state, there is an absence of persistent precipitation. One of the explanations for this paradox is the geochemical conditions in seawater cannot overcome the activation energy barrier for the first step in any precipitation reaction; nucleation. Here we show that virally induced rupturing of photosynthetic cyanobacterial cells releases cytoplasmic-associated bicarbonate at concentrations ~23-fold greater than in the surrounding seawater, thereby shifting the carbonate chemistry toward the homogenous nucleation of one or more of the calcium carbonate polymorphs. Using geochemical reaction energetics, we show the saturation states (Ω) in typical seawater for calcite (Ω = 4.3), aragonite (Ω = 3.1), and vaterite (Ω = 1.2) are significantly elevated following the release and diffusion of the cytoplasmic bicarbonate (Ωcalcite = 95.7; Ωaragonite = 68.5; Ωvaterite = 25.9). These increases in Ω significantly reduce the activation energy for nuclei formation thresholds for all three polymorphs, but only vaterite nucleation is energetically favored. In the post-lysis seawater, vaterite's nuclei formation activation energy is significantly reduced from 1.85 × 10−17 J to 3.85 × 10−20 J, which increases the nuclei formation rate from highly improbable (seawater describes a mechanism through which the initial step in the production of carbonate sediments may proceed. It also presents an additional role of photosynthesizing microbes and their viruses in marine carbon cycles and reveals these microorganisms are a collective repository for concentrated and reactive dissolved inorganic carbon (DIC) that is currently not accounted for

  1. Role of H2O2 in the photo-transformation of phenol in artificial and natural seawater

    International Nuclear Information System (INIS)

    Calza, Paola; Campra, Laura; Pelizzetti, Ezio; Minero, Claudio

    2012-01-01

    In previous works, it was observed that phenol photo-induced transformation in natural seawater (NSW) mediated by natural photosensitizers occurs and leads to the formation of numerous hydroxylated, condensed, halogenated and nitroderivatives. Irradiation of NSW added with phenol and iron species had provided the enhanced formation of several halophenols, suggesting a central role played by iron species on the phenol halogenation in marine water. In this paper, we focus on hydrogen peroxide, another key photosensitizer, and its interaction with iron species. The ability of Fe(II)/Fe(III) and H 2 O 2 species to act as photo-sensitizers towards the transformation of organic compounds in seawater was investigated under simulated solar radiation. Light activation is necessary to induce the transformation of phenol, as no degradation occurs in the dark when either H 2 O 2 or iron/H 2 O 2 are initially added to artificial seawater (ASW). Fe(II) is easily transformed into Fe(III), assessing that a Fenton reaction (dark, Fe(II)/H 2 O 2 ) does not take place in marine environment, in favour of a photo-activated reaction involving Fe(III) and H 2 O 2 . When NSW is spiked with H 2 O 2 and Fe(III), halophenols' and nitrophenols' concentration decreases and completely disappears at high hydrogen peroxide concentration. Since Fe(II) and Fe(III) in spiked seawater induce an enhanced formation of haloderivatives, an excess of hydrogen peroxide act as scavenger towards the photo-produced chloro/bromo radicals, so hindering halogenation process in seawater. Hence, even if hydrogen peroxide efficiently induces the ·OH radical formation, and could then promote the phenol phototransformation, nevertheless it is negligibly involved in the production of the intermediates formed during phenol photolysis in seawater, whose formation is necessarily linked to other photosensitizer species. - Highlights: ► Hydrogen peroxide-mediated solar-driven transformations of pollutant in seawater are

  2. Roseovarius azorensis sp. nov., isolated from seawater at Espalamaca, Azores

    Digital Repository Service at National Institute of Oceanography (India)

    Rajasabapathy, R.; Mohandass, C; Dastager, S.G.; Liu, Q.; Khieu, T.-N.; Son, C; Li, W.-J; Colaco, A.

    A Gram-negative, motile, non-spore forming, rod shaped aerobic bacterium, designated strain SSW084T, was isolated from a surface seawater sample collected at Espalamaca (38°33`N; 28°39`W), Azores. Growth was found to occur from 15 to 40...

  3. A Method for Seawater Desalination via Squeezing Ionic Hydrogels.

    Science.gov (United States)

    Yu, Chi; Wang, Yanhong; Lang, Xuemei; Fan, Shuanshi

    2016-12-06

    In this study, mechanical force applied to squeeze poly(sodium acrylate-co-2-hydroxyethyl methacrylate) hydrogels that contained seawater in order to obtain fresh water. By incorporating ionic monomer sodium acrylate (SA) into hydrogels, the salt rejection was significantly enhanced from 27.62% to 64.57% (feed concentration 35.00g/L NaCl solution). As SA's concentration continuously increased, salt rejection declined due to the change in hydrogel's matrix structure. Therefore, water recovery raised as the current swelling degree increased. We also measured pore size distribution by applying mercury intrusion porosimetry on each hydrogel sample in the interest of finding out whether the sample SA5/HEMA15 owned multi pore structure, since the result could be good for the desalination performance. After 4 times reused, the hydrogel remained good desalination performance. Although compared to reverse osmosis (RO) and multistage flash distillation (MSF) & multiple effect distillation (MED) the salt rejection of this hydrogel (roughly 64%) seemed low, the hydrogels can be used for forward osmosis and reverse osmosis, as pretreatment of seawater to reduce the energy consumption for the downstream.

  4. Hydrogen evolution in enzymatic photoelectrochemical cell using modified seawater electrolytes produced by membrane desalination process

    Energy Technology Data Exchange (ETDEWEB)

    Joo, Hyunku; Yoon, Jaekyung [Hydrogen Energy Research Center, New and Renewable Energy Research Division, Korea Institute of Energy Research, 71-2 Jang-dong, Yuseong-gu, Daejeon 305-343 (Korea); Bae, Sanghyun [Department of Environmental Engineering, Yonsei University, 234 Maeji-ri, Hungub-myun, Wonju, Gangwon-do 220-710 (Korea); Kim, Chunghwan; Kim, Suhan [Korea Institute of Water and Environment, K-Water, 462-1 Jeonmin-dong, Yuseong-gu, Daejeon 305-730 (Korea)

    2009-09-15

    In the near future, potential water shortages are expected to occur all over the world and this problem will have a significant influence on the availability of water for water-splitting processes, such as photocatalysis and electrolysis, as well as for drinking water. For this reason, it has been suggested that seawater could be used as an alternative for the various water industries including hydrogen production. Seawater contains a large amount of dissolved ion components, thus allowing it to be used as an electrolyte in photoelectrochemical (PEC) systems for producing hydrogen. Especially, the concentrate (retentate) stream shows higher salinity than the seawater fed to the membrane desalination process, because purified water (fresh water) is produced as the permeate stream and the waste brine is more concentrated than the original seawater. In this study, we investigated the hydrogen evolution rate in a photoelectrochemical system, including the preparation and characterization of an anodized tubular TiO{sub 2} electrode (ATTE) as both the photoanode and the cathode with the assistance of an immobilized hydrogenase enzyme and an external bias (solar cell), and the use of various qualities of seawater produced by membrane desalination processes as the electrolyte. The results showed that the rate of hydrogen evolution obtained using the nanofiltration (NF) retentate in the PEC system is ca. 105 {mu}mol/cm{sup 2} h, showing that this is an effective seawater electrolyte for hydrogen production, the optimum amount of enzyme immobilized on the cathode is ca. 3.66 units per geometrical unit area (1 cm x 1 cm), and the optimum external external bias supplied by the solar cell is 2.0 V. (author)

  5. Desorption of radioactive cesium by seawater from the suspended particles in river water.

    Science.gov (United States)

    Onodera, Masaki; Kirishima, Akira; Nagao, Seiya; Takamiya, Kouichi; Ohtsuki, Tsutomu; Akiyama, Daisuke; Sato, Nobuaki

    2017-10-01

    In 2011, the accident at the Fukushima-Daiichi nuclear power plant dispersed radioactive cesium throughout the environment, contaminating the land, rivers, and sea. Suspended particles containing clay minerals are the transportation medium for radioactive cesium from rivers to the ocean because cesium is strongly adsorbed between the layers of clay minerals, forming inner sphere complexes. In this study, the adsorption and desorption behaviors of radioactive cesium from suspended clay particles in river water have been investigated. The radioactive cesium adsorption and desorption experiments were performed with two kinds of suspended particulate using a batch method with 137 Cs tracers. In the cesium adsorption treatment performed before the desorption experiments, simulated river water having a total cesium concentration ([ 133+137 Cs + ] total ) of 1.3 nM (10 -9  mol/L) was used. The desorption experiments were mainly conducted at a solid-to-liquid ratio of 0.17 g/L. The desorption agents were natural seawater collected at 10 km north of the Fukushima-Daiichi nuclear power plant, artificial seawater, solutions of NaCl, KCl, NH 4 Cl, and 133 CsCl, and ultrapure water. The desorption behavior, which depends on the preloaded cesium concentration in the suspended particles, was also investigated. Based on the cesium desorption experiments using suspended particles, which contained about 1000 ng/g loaded cesium, the order of cesium desorption ratios for each desorption agent was determined as 1 M NaCl (80%) > 470 mM NaCl (65%) > 1 M KCl (30%) ≈ seawater (natural seawater and Daigo artificial seawater) > 1 M NH 4 Cl (20%) > 1 M 133 CsCl (15%) ≫ ultrapure water (2%). Moreover, an interesting result was obtained: The desorption ratio in the 470 mM NaCl solution was much higher than that in seawater, even though the Na + concentrations were identical. These results indicate that the cesium desorption mechanism is not a simple ion exchange reaction

  6. Temporal mismatch between induction of superoxide dismutase and ascorbate peroxidase correlates with high H2O2 concentration in seawater from clofibrate-treated red algae Kappaphycus alvarezii.

    Science.gov (United States)

    Barros, Marcelo P; Granbom, Malena; Colepicolo, Pio; Pedersén, Marianne

    2003-12-01

    Algal cells have developed different strategies to cope with the common environmentally promoted generation of H(2)O(2), which include induction of catalase (CAT) and ascorbate peroxidase (APX), massive H(2)O(2) release in seawater, and synthesis of volatile halocarbons by specific peroxidases. The antioxidant adaptability of the economically important carrageenophyte Kappaphycus alvarezii (Doty) Doty (Gigartinales: Rhodophyta) was tested here against exposure to clofibrate (CFB), a known promoter of peroxisomal beta-oxidation in mammals and plants. Possibly as a consequence of CFB-induced H2O2 peroxisomal production, the maximum concentration of H(2)O(2) in the seawater of red algae cultures was found to occur (120+/-17 min) after the addition of CFB, which was followed by a significant decrease in the photosynthetic activity of PSII after 24 h. Interestingly, 4 h after the addition of CFB, the total SOD activity was about 2.5-fold higher than in the control, whereas no significant changes were observed in lipoperoxidation levels (TBARS) or in CAT and APX activities. The two H(2)O(2)-scavenging enzymes were only induced later (after 72 h), whereupon CAT showed a dose-dependent response with increasing concentrations of CFB. A more pronounced increase of TBARS concentration than in the controls was evidenced when a 50 microM Fe(2+/3+) solution (3:2 ratio) was added to CFB-treated cultures, suggesting that the combination of exacerbated H(2)O(2) levels in the seawater-in this work, caused by CFB exposure-and Fenton-reaction catalyst (ferric/ferrous ions), imposes harsh oxidative conditions on algal cultures. The bulk of data suggests that K. alvarezii possesses little ability to promptly induce CAT and APX compared to the immediately responsive antioxidant enzyme SOD and, to avoid harmful accumulation of H(2)O(2), the red alga presumably releases H(2)O(2) into the surrounding medium as an alternative mechanism.

  7. Sunlight-enhanced calcareous deposition on cathodic stainless steel in natural seawater

    Digital Repository Service at National Institute of Oceanography (India)

    Eashwar, M.; SathishKumar, P.; Ravishankar, R.; Subramanian, G.

    In replicate series of experiments in natural seawater, one in full darkness and the other in a 1:1 diurnal cycle with as little as 5 percent of natural solar illumination, sunlight promoted calcareous deposition on cathodic stainless steel surfaces...

  8. Physiological responses of coccolithophores to abrupt exposure of naturally low pH deep seawater.

    Science.gov (United States)

    Iglesias-Rodriguez, Maria Debora; Jones, Bethan M; Blanco-Ameijeiras, Sonia; Greaves, Mervyn; Huete-Ortega, Maria; Lebrato, Mario

    2017-01-01

    Upwelling is the process by which deep, cold, relatively high-CO2, nutrient-rich seawater rises to the sunlit surface of the ocean. This seasonal process has fueled geoengineering initiatives to fertilize the surface ocean with deep seawater to enhance productivity and thus promote the drawdown of CO2. Coccolithophores, which inhabit many upwelling regions naturally 'fertilized' by deep seawater, have been investigated in the laboratory in the context of ocean acidification to determine the extent to which nutrients and CO2 impact their physiology, but few data exist in the field except from mesocosms. Here, we used the Porcupine Abyssal Plain (north Atlantic Ocean) Observatory to retrieve seawater from depths with elevated CO2 and nutrients, mimicking geoengineering approaches. We tested the effects of abrupt natural deep seawater fertilization on the physiology and biogeochemistry of two strains of Emiliania huxleyi of known physiology. None of the strains tested underwent cell divisions when incubated in waters obtained from seawater from ~1,000 m (pH = 7.9; CO2 ~560 p.p.m.; 14-17 μM nitrate) and ~4,800 m (pH = 7.9; CO2 ~600 p.p.m.; 21 μM nitrate). Emiliania huxleyi strain CCMP 88E showed no differences in growth rate or in cellular content or production rates of particulate organic (POC) and inorganic (PIC) carbon and cellular particulate organic nitrogen (PON) between treatments using water from 1,000 m and 4,800 m. However, despite the N:P ratio of seawater being comparable in water from ~1,000 and ~4,800 m, the PON production rates were three times lower in one incubation using water from ~1,000 m compared to values observed in water from ~4,800 m. Thus, the POC:PON ratios were threefold higher in cells that were incubated in ~1,000 m seawater. The heavily calcified strain NZEH exhibited lower growth rates and PIC production rates when incubated in water from ~4,800 m compared to ~1,000 m, while cellular PIC, POC and PON were higher in water from 4,800 m

  9. Removal U(VI) from artificial seawater using facilely and covalently grafted polyacrylonitrile fibers with lysine

    Energy Technology Data Exchange (ETDEWEB)

    Li, Wenting; Liu, Qi; Liu, Jingyuan; Zhang, Hongsen; Li, Rumin; Li, Zhanshuang; Jing, Xiaoyan [Key Laboratory of Superlight Material and Surface Technology, Ministry of Education, Harbin Engineering University, Harbin 150001 (China); Wang, Jun, E-mail: zhqw1888@sohu.com [Key Laboratory of Superlight Material and Surface Technology, Ministry of Education, Harbin Engineering University, Harbin 150001 (China); Institute of Advanced Marine Materials, Harbin Engineering University, 150001 (China)

    2017-05-01

    Highlights: • Novel lysine modified fibrous adsorbents were prepared using a facile and green method. • PAN-Lys exhibited high adsorption activity and fast adsorption rate. • PAN-Lys significantly remove U(VI) from simulated seawater. - Abstract: Polyacrylonitrile fibers (PANF) covalently modified with lysine (PAN-Lys) was facilely synthesized and carefully characterized. The critical factors affecting U(VI) adsorption from aqueous solution were exploited, such as initial pH, contact time, concentration and temperature. The adsorption process is strongly dependent on solution pH. With excellent adsorption capacity and high affinity toward U(VI), the process for U(VI) is extremely rapid and the equilibrium can be reached within 20 min. The thermodynamics and kinetics were strictly evaluated. In addition, the hypothetical adsorption mechanisms were proposed. Moreover, the adsorption behavior at low concentrations (3–30 μg L{sup −1}) in simulated seawater was also investigated. Therefore, PAN-Lys can be potentially utilized for the efficient removal of U(VI) from seawater.

  10. 99Tc in seawater in the West Spitsbergen Current and adjacent areas

    International Nuclear Information System (INIS)

    Gerland, Sebastian; Lind, Bjoern; Dowdall, Mark; Karcher, M.; Kolstad, Anne Kathrine

    2003-01-01

    99 Tc levels were measured in seawater samples collected between 2000 and 2002 in the West Spitsbergen Current (WSC) and along the western coast of Svalbard or Spitzbergen and compared with available oceanographic 3-D modelling results for the late 1990s. Additional data from related regions are also presented in order to support the data interpretation. The seawater in the Arctic fjord Kongsfjorden on the western coast of Svalbard is influenced by the WSC, as shown by the 99 Tc levels in surface water. By means of the WSC, 99 Tc reaches the Eastern Fram Strait, where one branch of the WSC turns west into the East Greenland Current (EGC), and another branch continues northwards into the Arctic Ocean. Surface seawater collected in the central part of the WSC during a cruise on board the R/V 'Polarstern' in the summer of 2000, showed higher levels of 99 Tc than samples measured in Kongsfjorden in the spring of 2000. However, all levels measured in surface water are of the same order of magnitude. Data from sampling of deeper water in the WSC and EGC provide information pertaining to the lateral distribution of 99 Tc. In all vertical profiling surveys (conducted in spring and summer), the highest levels of 99 Tc were found in surface water. Comparison with oceanographic 3-D modelling indicates both significant seasonal variations in the lateral stratification of the WSC and variations with depth over shorter vertical distances. This information can be applied in sampling strategies, environmental monitoring, long-range transport of pollutants and physical oceanography

  11. Neodymium isotopic variations in seawater

    International Nuclear Information System (INIS)

    Piepgras, D.J.; Wasserburg, G.J.

    1980-01-01

    New data for the direct measurement of the isotopic composition of neodymium in Atlantic Ocean seawater are compared with previous measurements of Pacific Ocean seawater and ferromanganese sediments from major ocean basins. Data for Atlantic seawater are in excellent agreement with Nd isotopic measurements made on Atlantic ferromanganese sediments and are distinctly different from the observed compositions of Pacific samples. These results clearly demonstrate the existence of distinctive differences in the isotopic composition of Nd in the waters of the major ocean basins and are characteristic of the ocean basin sampled. The average epsilonsub(N)sub(d)(0) values for the major oceans as determined by data from seawater and ferromanganese sediments are as follows: Atlantic Ocean, epsilonsub(N)sub(d)(0) approx. equal to - 12 +- 2; Indian Ocean, epsilonsub(N)sub(d)(0) approx. equal to - 8 +- 2; Pacific Ocean, epsilonsub(N)sub(d)(0) approx. equal to -3 +- 2. These values are considerably less than epsilonsub(N)sub(d)(0) value sources with oceanic mantle affinities indicating that the REE in the oceans are dominated by continental sources. The difference in the absolute abundance of 143 Nd between the Pacific and Atlantic Oceans corresponds to approx. 10 6 atoms 143 Nd per gram of seawater. The correspondence between the 143 Nd/ 144 Nd in seawater and in the associated sediments suggests the possible application of this approach to paleo-oceanography. (orig./HAE)

  12. Estimation of surface area concentration of workplace incidental nanoparticles based on number and mass concentrations

    Science.gov (United States)

    Park, J. Y.; Ramachandran, G.; Raynor, P. C.; Kim, S. W.

    2011-10-01

    Surface area was estimated by three different methods using number and/or mass concentrations obtained from either two or three instruments that are commonly used in the field. The estimated surface area concentrations were compared with reference surface area concentrations (SAREF) calculated from the particle size distributions obtained from a scanning mobility particle sizer and an optical particle counter (OPC). The first estimation method (SAPSD) used particle size distribution measured by a condensation particle counter (CPC) and an OPC. The second method (SAINV1) used an inversion routine based on PM1.0, PM2.5, and number concentrations to reconstruct assumed lognormal size distributions by minimizing the difference between measurements and calculated values. The third method (SAINV2) utilized a simpler inversion method that used PM1.0 and number concentrations to construct a lognormal size distribution with an assumed value of geometric standard deviation. All estimated surface area concentrations were calculated from the reconstructed size distributions. These methods were evaluated using particle measurements obtained in a restaurant, an aluminum die-casting factory, and a diesel engine laboratory. SAPSD was 0.7-1.8 times higher and SAINV1 and SAINV2 were 2.2-8 times higher than SAREF in the restaurant and diesel engine laboratory. In the die casting facility, all estimated surface area concentrations were lower than SAREF. However, the estimated surface area concentration using all three methods had qualitatively similar exposure trends and rankings to those using SAREF within a workplace. This study suggests that surface area concentration estimation based on particle size distribution (SAPSD) is a more accurate and convenient method to estimate surface area concentrations than estimation methods using inversion routines and may be feasible to use for classifying exposure groups and identifying exposure trends.

  13. Estimation of surface area concentration of workplace incidental nanoparticles based on number and mass concentrations

    International Nuclear Information System (INIS)

    Park, J. Y.; Ramachandran, G.; Raynor, P. C.; Kim, S. W.

    2011-01-01

    Surface area was estimated by three different methods using number and/or mass concentrations obtained from either two or three instruments that are commonly used in the field. The estimated surface area concentrations were compared with reference surface area concentrations (SA REF ) calculated from the particle size distributions obtained from a scanning mobility particle sizer and an optical particle counter (OPC). The first estimation method (SA PSD ) used particle size distribution measured by a condensation particle counter (CPC) and an OPC. The second method (SA INV1 ) used an inversion routine based on PM1.0, PM2.5, and number concentrations to reconstruct assumed lognormal size distributions by minimizing the difference between measurements and calculated values. The third method (SA INV2 ) utilized a simpler inversion method that used PM1.0 and number concentrations to construct a lognormal size distribution with an assumed value of geometric standard deviation. All estimated surface area concentrations were calculated from the reconstructed size distributions. These methods were evaluated using particle measurements obtained in a restaurant, an aluminum die-casting factory, and a diesel engine laboratory. SA PSD was 0.7–1.8 times higher and SA INV1 and SA INV2 were 2.2–8 times higher than SA REF in the restaurant and diesel engine laboratory. In the die casting facility, all estimated surface area concentrations were lower than SA REF . However, the estimated surface area concentration using all three methods had qualitatively similar exposure trends and rankings to those using SA REF within a workplace. This study suggests that surface area concentration estimation based on particle size distribution (SA PSD ) is a more accurate and convenient method to estimate surface area concentrations than estimation methods using inversion routines and may be feasible to use for classifying exposure groups and identifying exposure trends.

  14. Sampling problems and the determination of mercury in surface water, seawater, and air

    International Nuclear Information System (INIS)

    Das, H.A.; van der Sloot, H.A.

    1976-01-01

    Analysis of surface water for mercury comprises the determination of both ionic and organically bound mercury in solution and that of the total mercury content of the suspended matter. Eventually, metallic mercury has to be determined too. Requirements for the sampling procedure are given. A method for the routine determination of mercury in surface water and seawater was developed and applied to Dutch surface waters. The total sample volume is 2500 ml. About 500 ml is used for the determination of the content of suspended matter and the total amount of mercury in the water. The sample is filtered through a bed of previously purified active charcoal at a low flow-rate. The main portion ca. 2000 ml) passes a flow-through centrifuge to separate the solid fraction. One liter is used to separate ''inorganic'' mercury by reduction, volatilization in an airstream and adsorption on active charcoal. The other liter is led through a column of active charcoal to collect all mercury. The procedures were checked with 197 Hg radiotracer both as an ion and incorporated in organic compounds. The mercury is determined by thermal neutron activation, followed by volatilization in a tube furnace and adsorption on a fresh carbon bed. The limit of determination is approximately equal to 1 ng 1 -1 . The rate of desorption from and adsorption on suspended material has been measured as a function of a pH of the solution for Hg +2 and various other ions. It can be concluded that only the procedure mentioned above does not disturb the equilibrium. The separation of mercury from air is obtained by suction of 1 m 3 through a 0.22 μm filter and a charcoal bed. The determination is then performed as in the case of the water samples

  15. Seawater-Soluble Pigments and Their Potential Use in Self-Polishing Antifouling Paints: Simulation-based Screening Tool

    DEFF Research Database (Denmark)

    Kiil, Søren; Dam-Johansen, Kim; Erik Weinell, Claus

    2002-01-01

    This work concerns the on-going development of efficient and environmentally friendly antifouling paints for biofouling control on large ocean-going ships. It is illustrated how a detailed mathematical model for a self-polishing antifouling paint exposed to seawater can be used as a product...... solubility and seawater diffusivity of dissolved pigment species have a significant influence on the polishing and leaching behaviour of a typical self-polishing paint system. The pigment size distribution, on the other hand, only has a minor influence on the paint-seawater interaction. Simulations also...... indicate that only compounds which are effective against biofouling at very low seawater concentrations are useful as active antifouling paint ingredients. The need for model verification and exploration of practical issues, subsequent a given pigment has been found of interest, is discussed. The model...

  16. A Simulation-Optimization Model for Seawater Intrusion Management at Pingtung Coastal Area, Taiwan

    Directory of Open Access Journals (Sweden)

    Po-Syun Huang

    2018-02-01

    Full Text Available The coastal regions of Pingtung Plain in southern Taiwan rely on groundwater as their main source of fresh water for aquaculture, agriculture, domestic, and industrial sectors. The availability of fresh groundwater is threatened by unsustainable groundwater extraction and the over-pumpage leads to the serious problem of seawater intrusion. It is desired to find appropriate management strategies to control groundwater salinity and mitigate seawater intrusion. In this study, a simulation–optimization model has been presented to solve the problem of seawater intrusion along the coastal aquifers in Pingtung Plain and the objective is using injection well barriers and minimizing the total injection rate based on the pre-determined locations of injection barriers. The SEAWAT code is used to simulate the process of seawater intrusion and the surrogate model of artificial neural networks (ANNs is used to approximate the seawater intrusion (SWI numerical model to increase the computational efficiency during the optimization process. The heuristic optimization scheme of differential evolution (DE algorithm is selected to identify the global optimal management solution. Two different management scenarios, one is the injection barriers located along the coast and the other is the injection barrier located at the inland, are considered and the optimized results show that the deployment of injection barriers at the inland is more effective to reduce total dissolved solids (TDS concentrations and mitigate seawater intrusion than that along the coast. The computational time can be reduced by more than 98% when using ANNs to replace the numerical model and the DE algorithm has been confirmed as a robust optimization scheme to solve groundwater management problems. The proposed framework can identify the most reliable management strategies and provide a reference tool for decision making with regard to seawater intrusion remediation.

  17. Effects of waterborne nitrite on hematological parameters and stress indicators in olive flounders, Paralichthys olivaceus, raised in bio-floc and seawater.

    Science.gov (United States)

    Kim, Jun-Hwan; Kim, Jin-Young; Lim, Lok-Ji; Kim, Su Kyoung; Choi, Hye Sung; Hur, Young Baek

    2018-06-11

    Juvenile olive flounders, Paralichthys olivaceus (mean weight 2.69 ± 0.31 g), were raised in bio-floc and seawater for six months, these P. olivaceus (mean weight 280.1 ± 10.5 g, mean length 28.37 ± 2.3 cm) were exposed to different concentrations of waterborne nitrite (0, 25, 50, 100, and 200 mg NO 2 - /L) for 7 days. None of the P. olivaceus individuals exposed to bio-floc and seawater containing waterborne nitrite concentrations of 200 mg/L for 7 days survived. Hematological parameters (hemoglobin and hematocrit) were significantly reduced by nitrite exposure. Regarding plasma components, the concentrations of glucose, glutamic oxalate transaminase (GOT), and glutamic pyruvate transaminase (GPT) increased significantly in response to nitrite exposure, whereas cholesterol concentrations significantly decreased. Stress indicators, including concentrations of plasma glucose, cortisol, and liver and gill concentrations of heat shock protein 70 (HSP70) were significantly increased by nitrite exposure. The results of the study indicate that nitrite exposure affected the hematological parameters and stress indicators of P. olivaceus raised in bio-floc and seawater, and these changes were more prominent in the P. olivaceus raised in seawater than those raised in bio-floc. Copyright © 2018 Elsevier Ltd. All rights reserved.

  18. Comparative decay of Catellicoccus marimmalium and enterococci in beach sand and seawater.

    Science.gov (United States)

    Brown, Kendra I; Boehm, Alexandria B

    2015-10-15

    Most studies characterize microbial source tracking (MST) target performance using sensitivity and specificity metrics. However, it is important to also consider the temporal stability of MST targets in relation to regulated microbial pollutants. Differences among bacterial target stabilities may lead to erroneous conclusions about sources of contamination. The present study evaluates the relative stability of MST targets and fecal indicator organisms using the gull/pigeon-associated Catellicoccus marimammalium (CAT) marker and enterococci (ENT). The decay rates of CAT and ENT measured by culture (cENT) and QPCR (tENT) were compared in sand and seawater laboratory microcosms under environmentally relevant conditions (subject to tidal wetting versus no wetting in sand, and sunlit versus dark conditions in seawater). Bacterial targets were more persistent in beach sand than in seawater with decay rates on the order of 0.01-0.1 per day and 1 to 10 per day, respectively. Targets were more persistent in unwetted compared to wetted sand, and dark compared to sunlit seawater. During the first 8 days of the sand experiment, the decay rate k of CAT was greater than that of cENT. The decay rates of CAT, tENT, and cENT were similar in sand after day 8 and in dark seawater. In sunlit seawater, the decay rates were different between targets with kcENT > kCAT > ktENT. The decay rates presented here are useful for fate and transport models and also inform the use of MST marker concentrations to infer ENT sources in the environment. Copyright © 2015 Elsevier Ltd. All rights reserved.

  19. Coulometric sodium chloride removal system with Nafion membrane for seawater sample treatment.

    Science.gov (United States)

    Grygolowicz-Pawlak, Ewa; Sohail, Manzar; Pawlak, Marcin; Neel, Bastien; Shvarev, Alexey; de Marco, Roland; Bakker, Eric

    2012-07-17

    Seawater analysis is one of the most challenging in the field of environmental monitoring, mainly due to disparate concentration levels between the analyte and the salt matrix causing interferences in a variety of analytical techniques. We propose here a miniature electrochemical sample pretreatment system for a rapid removal of NaCl utilizing the coaxial arrangement of an electrode and a tubular Nafion membrane. Upon electrolysis, chloride is deposited at the Ag electrode as AgCl and the sodium counterions are transported across the membrane. This cell was found to work efficiently at potentials higher than 400 mV in both stationary and flow injection mode. Substantial residual currents observed during electrolysis were found to be a result of NaCl back diffusion from the outer side of the membrane due to insufficient permselectivity of the Nafion membrane. It was demonstrated that the residual current can be significantly reduced by adjusting the concentration of the outer solution. On the basis of ion chromatography results, it was found that the designed cell used in flow injection electrolysis mode reduced the NaCl concentration from 0.6 M to 3 mM. This attempt is very important in view of nutrient analysis in seawater where NaCl is a major interfering agent. We demonstrate that the pretreatment of artificial seawater samples does not reduce the content of nitrite or nitrate ions upon electrolysis. A simple diffusion/extraction steady state model is proposed for the optimization of the electrolysis cell characteristics.

  20. Differential utility of the Bacteroidales DNA and RNA markers in the tiered approach for microbial source tracking in subtropical seawater.

    Science.gov (United States)

    Liu, Rulong; Cheng, Ken H F; Wong, Klaine; Cheng, Samuel C S; Lau, Stanley C K

    2015-07-01

    Source tracking of fecal pollution is an emerging component in water quality monitoring. It may be implemented in a tiered approach involving Escherichia coli and/or Enterococcus spp. as the standard fecal indicator bacteria (FIB) and the 16S rRNA gene markers of Bacteroidales as source identifiers. The relative population dynamics of the source identifiers and the FIB may strongly influence the implementation of such approach. Currently, the relative performance of DNA and RNA as detection targets of Bacteroidales markers in the tiered approach is not known. We compared the decay of the DNA and RNA of the total (AllBac) and ruminant specific (CF128) Bacteroidales markers with those of the FIB in seawater spiked with cattle feces. Four treatments of light and oxygen availability simulating the subtropical seawater of Hong Kong were tested. All Bacteroidales markers decayed significantly slower than the FIB in all treatments. Nonetheless, the concentrations of the DNA and RNA markers and E. coli correlated significantly in normoxic seawater independent of light availability, and in hypoxic seawater only under light. In hypoxic seawater without light, the concentrations of RNA but not DNA markers correlated with that of E. coli. Generally, the correlations between Enterococcus spp. and Bacteroidales were insignificant. These results suggest that either DNA or RNA markers may complement E. coli in the tiered approach for normoxic or hypoxic seawater under light. When light is absent, either DNA or RNA markers may serve for normoxic seawater, but only the RNA markers are suitable for hypoxic seawater.

  1. Optimal scheduling of biocide dosing for seawater-cooled power and desalination plants

    KAUST Repository

    Mahfouz, Abdullah Bin

    2011-02-13

    Thermal desalination systems are typically integrated with power plants to exploit the excess heat resulting from the power-generation units. Using seawater in cooling the power plant and the desalination system is a common practice in many parts of the world where there is a shortage of freshwater. Biofouling is one of the major problems associated with the usage of seawater in cooling systems. Because of the dynamic variation in the power and water demands as well as the changes in the characteristics of seawater and the process, there is a need to develop an optimal policy for scheduling biocide usage and cleaning maintenance of the heat exchangers. The objective of this article is to introduce a systematic procedure for the optimization of scheduling the dosing of biocide and dechlorination chemicals as well as cleaning maintenance for a power production/thermal desalination plant. A multi-period optimization formulation is developed and solved to determine: the optimal levels of dosing and dechlorination chemicals; the timing of maintenance to clean the heat-exchange surfaces; and the dynamic dependence of the biofilm growth on the applied doses, the seawater-biocide chemistry, the process conditions, and seawater characteristics for each time period. The technical, economic, and environmental considerations of the system are accounted for. A case study is solved to elucidate the applicability of the developed optimization approach. © 2011 Springer-Verlag.

  2. In situ experimental study for the optimization of chlorine dosage in seawater cooling systems

    Energy Technology Data Exchange (ETDEWEB)

    Nebot, E.; Casanueva, T.; Fernandez-Baston, M.M.; Sales, D. [Department of Chemical Engineering, Food Technology and Environmental Technologies, University of Cadiz (Spain); Casanueva, J.F. [Department of Thermal Engines, University of Cadiz (Spain)

    2006-11-15

    The paper details an in situ study for the evaluation of the evolution of fouling heat transfer resistance and to optimize the antifouling chlorine dosage at a 550MW power station. A portable pilot plant has been designed to simulate the steam surface condenser and used as an accurate fouling monitor that takes the seawater from the same intake point as the power station. This study includes fouling extraction and its characterization for different dosage patterns. The residual chlorine concentration at the cooling-water discharge from the power station is 0.2mg/l and has been considered appropriate for the prevention of the formation of fouling, because with this concentration approximately 90% reduction in the amount of fouling is obtained. Residual chlorine dosages lower than 0.2ppm could be effective in controlling fouling development if mechanical techniques of fouling control are also available. (author)

  3. New insight into the ternary complexes of uranyl carbonate in seawater.

    Science.gov (United States)

    Beccia, M R; Matara-Aho, M; Reeves, B; Roques, J; Solari, P L; Monfort, M; Moulin, C; Den Auwer, C

    2017-11-01

    Uranium is naturally present in seawater at trace levels and may in some cases be present at higher concentrations, due to anthropogenic nuclear activities. Understanding uranium speciation in seawater is thus essential for predicting and controlling its behavior in this specific environmental compartment and consequently, its possible impact on living organisms. The carbonato calcic complex Ca 2 UO 2 (CO 3 ) 3 was previously identified as the main uranium species in natural seawater, together with CaUO 2 (CO 3 ) 3 2- . In this work, we further investigate the role of the alkaline earth cation in the structure of the ternary uranyl-carbonate complexes. For this purpose, artificial seawater, free of Mg 2+ and Ca 2+ , using Sr 2+ as a spectroscopic probe was prepared. Combining TRLIF and EXAFS spectroscopy, together with DFT and theoretical thermodynamic calculations, evidence for the presence of Sr alkaline earth counter ion in the complex structure can be asserted. Furthermore, data suggest that when Ca 2+ is replaced by Sr 2+ , SrUO 2 (CO 3 ) 3 2- is the main complex in solution and it occurs with the presence of at least one monodentate carbonate in the uranyl coordination sphere. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Surface chemical characteristics of coal fly ash particles after interaction with seawater under natural deep sea conditions

    International Nuclear Information System (INIS)

    Brami, Y.; Shemesh, A.; Cohen, H.; Herut, B.

    1999-01-01

    The surface chemical characteristics of coal fly ash (CFA) before and after interaction with Mediterranean deep seawater was studied by X-ray photoelectron spectroscopy (XPS). Significantly lower values of Si, Ca, and S and higher values of Mg and Cl were found in the retrieved CFA as compared to fresh CFA. It is suggested that hydrolysis of the oxide matrixes results in an alkaline environment which rapidly leads to several chemical reactions. The two most important are (a) dissolution of the amorphous silicate and the calcium phases and (b) precipitation of Mg(OH) 2 -brucite. A depth profile of the retrieved CFA was measured by both line-shape analysis of the XPS spectra and by consecutive cycle of sputtering. The thickness of the brucite layer is estimated to be 1.3 nm

  5. Identification of distinct genes associated with seawater aspiration-induced acute lung injury by gene expression profile analysis

    Science.gov (United States)

    Liu, Wei; Pan, Lei; Zhang, Minlong; Bo, Liyan; Li, Congcong; Liu, Qingqing; Wang, Li; Jin, Faguang

    2016-01-01

    Seawater aspiration-induced acute lung injury (ALI) is a syndrome associated with a high mortality rate, which is characterized by severe hypoxemia, pulmonary edema and inflammation. The present study is the first, to the best of our knowledge, to analyze gene expression profiles from a rat model of seawater aspiration-induced ALI. Adult male Sprague-Dawley rats were instilled with seawater (4 ml/kg) in the seawater aspiration-induced ALI group (S group) or with distilled water (4 ml/kg) in the distilled water negative control group (D group). In the blank control group (C group) the rats' tracheae were exposed without instillation. Subsequently, lung samples were examined by histopathology; total protein concentration was detected in bronchoalveolar lavage fluid (BALF); lung wet/dry weight ratios were determined; and transcript expression was detected by gene sequencing analysis. The results demonstrated that histopathological alterations, pulmonary edema and total protein concentrations in BALF were increased in the S group compared with in the D group. Analysis of differential gene expression identified up and downregulated genes in the S group compared with in the D and C groups. A gene ontology analysis of the differential gene expression revealed enrichment of genes in the functional pathways associated with neutrophil chemotaxis, immune and defense responses, and cytokine activity. Kyoto Encyclopedia of Genes and Genomes analysis revealed that the cytokine-cytokine receptor interaction pathway was one of the most important pathways involved in seawater aspiration-induced ALI. In conclusion, activation of the cytokine-cytokine receptor interaction pathway may have an essential role in the progression of seawater aspiration-induced ALI, and the downregulation of tumor necrosis factor superfamily member 10 may enhance inflammation. Furthermore, IL-6 may be considered a biomarker in seawater aspiration-induced ALI. PMID:27509884

  6. Determination of rare earth elements in seawater by inductively coupled plasma-mass spectrometry

    International Nuclear Information System (INIS)

    Moeller, P.; Dulski, P.; Luck, J.

    1992-01-01

    Shortly after sampling, rare earth elements (REEs) from 11.5 l of seawater were concentrated in 35 ml solutions by ion exchange chromatography on board the German research vessel ''Sonne'' using Chelex 100 chelating resin for preconcentration. Two millilitres of a 0.2 μg g -1 Lu spike was added to the seawater samples (i) for monitoring the chemical yield which was always found to vary between 85 and 112% (mean: 100±6) and (ii) as an internal standard. Rare earth elements have been determined by ICP-MS, with REE concentrations ranging from 100 (La) to 1 (Eu) pmol kg -1 . La in blanks can be as high as 30 pmol kg -1 , but blank concentrations for other REEs range between 0.5 and 0.01 pmol kg -1 . The trend of the precision of relative response factors varies between 12% (La) and 4% (Yb). The accuracy is estimated to be about 10% with the exception of La and Ce. Methodology improvements are suggested. (author)

  7. Electrochemical corrosion of carbon steel exposed to biodiesel/simulated seawater mixture

    Energy Technology Data Exchange (ETDEWEB)

    Wang Wei [College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao 266100 (China); Department of Civil Engineering, University of Colorado Denver, Denver, CO 80217 (United States); Jenkins, Peter E. [Department of Mechanical Engineering, University of Colorado Denver, Denver, CO 80217 (United States); Ren Zhiyong, E-mail: zhiyong.ren@ucdenver.edu [Department of Civil Engineering, University of Colorado Denver, Denver, CO 80217 (United States)

    2012-04-15

    Highlights: Black-Right-Pointing-Pointer Characterized the unique corrosion behaviour of carbon steel in the biodiesel/seawater environment. Black-Right-Pointing-Pointer Illustrated the in situ anode and cathode distribution using a wire beam electrode approach. Black-Right-Pointing-Pointer Elucidated the corrosion mechanisms based on ion transfer and oxygen concentration gradient. - Abstract: The electrochemical corrosion of carbon steel exposed to a mixture of biodiesel and 3.5% NaCl solution simulated seawater was characterized using wire beam electrode (WBE) technique. Both optical images and in situ potential and current measurements showed that all the anodes and most cathodes formed in the water phase, but the cathodes were mainly located along the water/biodiesel interface. Due to oxygen concentration gradient and cross-phase ion transfer, low corrosion currents were also detected in biodiesel phase. Further anode reaction was partially blocked by iron rust, but the alkali residual in biodiesel may interact with corrosion and deteriorate biodiesel quality.

  8. Effect of different seawater Mg

    NARCIS (Netherlands)

    Mewes, A.; Langer, G.; de Nooijer, L.J.; Bijma, J.; Reichart, G.J.

    2014-01-01

    Magnesium, incorporated in foraminiferal calcite (Mg/CaCC), is used intensively to reconstruct past seawater temperatures but, in addition to temperature, the Mg/CaCC of foraminiferal tests also depends on the ratio of Mg and Ca in seawater (Mg/CaSW). The physiological mechanisms responsible for

  9. Seawater intrusion mapping using electrical resistivity tomography and hydrochemical data. An application in the coastal area of eastern Thermaikos Gulf, Greece

    Energy Technology Data Exchange (ETDEWEB)

    Kazakis, N., E-mail: kazanera@yahoo.com [Aristotle University of Thessaloniki, Department of Geology, Lab. of Engineering Geology & Hydrogeology, 54124 Thessaloniki (Greece); Pavlou, A. [Aristotle University of Thessaloniki, Department of Geology, Lab. of Engineering Geology & Hydrogeology, 54124 Thessaloniki (Greece); Vargemezis, G. [Aristotle University of Thessaloniki, Department of Geology, Lab. of Applied Geophysics, 54124 Thessaloniki (Greece); Voudouris, K.S.; Soulios, G. [Aristotle University of Thessaloniki, Department of Geology, Lab. of Engineering Geology & Hydrogeology, 54124 Thessaloniki (Greece); Pliakas, F. [Democritus University of Thrace, Department of Civil Engineering, Xanthi 67100 (Greece); Tsokas, G. [Aristotle University of Thessaloniki, Department of Geology, Lab. of Applied Geophysics, 54124 Thessaloniki (Greece)

    2016-02-01

    The aim of this study was to determine the extent and geometrical characteristics of seawater intrusion in the coastal aquifer of the eastern Thermaikos Gulf, Greece. Hydrochemical data and geoelectrical measurements were combined and supplemented to determine the hydrochemical regime of the study site in regard to seawater phenomena. Chemical analysis of groundwater was performed in 126 boreholes and fifteen electrical resistivity tomographies (ERT) were measured, whereas in two sites the ERT measurements were repeated following the wet season. The Cl{sup −} concentrations recorded reached 2240 mg/L indicating seawater intrusion which was also verified by ionic ratios. The ionic ratios were overlapped and a seawater intrusion map (SWIM) was produced. A significant part of the coastal aquifer (up to 150 km{sup 2}) is influenced by seawater intrusion. The areas with the most intensive salinization are located between Nea Kallikratia–Epanomi and Aggelochori–Peraia. According to the ERTs, in the influenced areas the salinization of the aquifer exceeds 1 km toward the mainland and its depth reaches 200 m. In the area surrounding Thessaloniki airport, the ERTs revealed salinization of the upper aquifer to depths of up to 40 m, whereas the lower aquifer is uninfluenced. This abnormal distribution of seawater intrusion demonstrates the value of geoelectrical methods in the study of seawater intrusion especially in areas with limited available hydrochemical data. - Highlights: • ERTs determined the geometrical characteristics of the saline aquifer. • An abnormal distribution of seawater intrusion was recorded. • Four ionic ratios overlapped and a seawater intrusion map was produced. • Cl{sup −} concentrations increased significantly from 2005 to 2010 by up to 1800 mg/L.

  10. Seawater intrusion mapping using electrical resistivity tomography and hydrochemical data. An application in the coastal area of eastern Thermaikos Gulf, Greece

    International Nuclear Information System (INIS)

    Kazakis, N.; Pavlou, A.; Vargemezis, G.; Voudouris, K.S.; Soulios, G.; Pliakas, F.; Tsokas, G.

    2016-01-01

    The aim of this study was to determine the extent and geometrical characteristics of seawater intrusion in the coastal aquifer of the eastern Thermaikos Gulf, Greece. Hydrochemical data and geoelectrical measurements were combined and supplemented to determine the hydrochemical regime of the study site in regard to seawater phenomena. Chemical analysis of groundwater was performed in 126 boreholes and fifteen electrical resistivity tomographies (ERT) were measured, whereas in two sites the ERT measurements were repeated following the wet season. The Cl"− concentrations recorded reached 2240 mg/L indicating seawater intrusion which was also verified by ionic ratios. The ionic ratios were overlapped and a seawater intrusion map (SWIM) was produced. A significant part of the coastal aquifer (up to 150 km"2) is influenced by seawater intrusion. The areas with the most intensive salinization are located between Nea Kallikratia–Epanomi and Aggelochori–Peraia. According to the ERTs, in the influenced areas the salinization of the aquifer exceeds 1 km toward the mainland and its depth reaches 200 m. In the area surrounding Thessaloniki airport, the ERTs revealed salinization of the upper aquifer to depths of up to 40 m, whereas the lower aquifer is uninfluenced. This abnormal distribution of seawater intrusion demonstrates the value of geoelectrical methods in the study of seawater intrusion especially in areas with limited available hydrochemical data. - Highlights: • ERTs determined the geometrical characteristics of the saline aquifer. • An abnormal distribution of seawater intrusion was recorded. • Four ionic ratios overlapped and a seawater intrusion map was produced. • Cl"− concentrations increased significantly from 2005 to 2010 by up to 1800 mg/L.

  11. Contribution of anthropic activities to the seawater pollution at the ...

    African Journals Online (AJOL)

    The high toxicity of seawater is due to the presence of lead and cadmium with concentrations exceeding 60 times the normal value (0.015 mg/l). Moreover, the deficit in D.O announces strong biological activities. This wild aggression is related to the industrial discharges in the port area. Keywords: marine pollution; heavy ...

  12. Microbial Degradation Behavior in Seawater of Polyester Blends Containing Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate (PHBHHx

    Directory of Open Access Journals (Sweden)

    Hitoshi Sashiwa

    2018-01-01

    Full Text Available The microbial degradation behavior of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate (PHBHHx and its compound with several polyesters such as poly(butylene adipate-co-telephtharate (PBAT, poly(butylene succinate (PBS, and polylactic acid (PLA in seawater was tested by a biological oxygen demand (BOD method. PHBHHx showed excellent biodegradation in seawater in this study. In addition, the biodegradation rate of several blends was much influenced by the weight ratio of PHBHHx in their blends and decreased in accordance with the decrement of PHBHHX ratio. The surface morphology of the sheet was important factor for controlling the biodegradation rate of PHBHHx-containing blends in seawater.

  13. Seawater reverse osmosis desalination and (harmful) algal blooms

    KAUST Repository

    Villacorte, Loreen O.; Tabatabai, S. Assiyeh Alizadeh; Anderson, Donald M.; Amy, Gary L.; Schippers, Jan Cornelis; Kennedy, Maria Dolores

    2015-01-01

    This article reviews the occurrence of HABs in seawater, their effects on the operation of seawater reverse osmosis (SWRO) plants, the indicators for quantifying/predicting these effects, and the pretreatment strategies for mitigating operational issues during algal blooms. The potential issues in SWRO plants during HABs are particulate/organic fouling of pretreatment systems and biological fouling of RO membranes, mainly due to accumulation of algal organic matter (AOM). The presence of HAB toxins in desalinated water is also a potential concern but only at very low concentrations. Monitoring algal cell density, AOM concentrations and membrane fouling indices is a promising approach to assess the quality of SWRO feedwater and performance of the pretreatment system. When geological condition is favourable, subsurface intake can be a robust pretreatment for SWRO during HABs. Existing SWRO plants with open intake and are fitted with granular media filtration can improve performance in terms of capacity and product water quality, if preceded by dissolved air flotation or sedimentation. However, the application of advanced pretreatment using ultrafiltration membrane with in-line coagulation is often a better option as it is capable of maintaining stable operation and better RO feed water quality during algal bloom periods with significantly lower chemical consumption.

  14. Seawater reverse osmosis desalination and (harmful) algal blooms

    KAUST Repository

    Villacorte, Loreen O.

    2015-03-01

    This article reviews the occurrence of HABs in seawater, their effects on the operation of seawater reverse osmosis (SWRO) plants, the indicators for quantifying/predicting these effects, and the pretreatment strategies for mitigating operational issues during algal blooms. The potential issues in SWRO plants during HABs are particulate/organic fouling of pretreatment systems and biological fouling of RO membranes, mainly due to accumulation of algal organic matter (AOM). The presence of HAB toxins in desalinated water is also a potential concern but only at very low concentrations. Monitoring algal cell density, AOM concentrations and membrane fouling indices is a promising approach to assess the quality of SWRO feedwater and performance of the pretreatment system. When geological condition is favourable, subsurface intake can be a robust pretreatment for SWRO during HABs. Existing SWRO plants with open intake and are fitted with granular media filtration can improve performance in terms of capacity and product water quality, if preceded by dissolved air flotation or sedimentation. However, the application of advanced pretreatment using ultrafiltration membrane with in-line coagulation is often a better option as it is capable of maintaining stable operation and better RO feed water quality during algal bloom periods with significantly lower chemical consumption.

  15. Effect of the scale inhibitor on ion content in reverse osmosis system for seawater desalination

    Science.gov (United States)

    Gao, Yuhua; Liu, Zhenfa; Zhang, Lihui; Li, Haihua

    2017-09-01

    A scale inhibitor was synthesized from polysuccinimide with 2-aminoethanesulfonic acid and aspartic acid. The effect of scale inhibitor on ion content in reverse osmosis system for seawater desalination was studied. The results showed that the ion content of permeate water is lower with the scale inhibitor added in RO system for seawater desalination than without scale inhibitor. On the contrary, the ion content of concentrate water is higher when with scale inhibitor in RO system.

  16. Electrochemical evaluation of the influence of pseudomonas sp on aluminium brass in seawater

    International Nuclear Information System (INIS)

    Frontini, Maria Alejandra; Rosso de Sanchez, Susana

    2004-01-01

    The development of a biofilm on metallic surfaces generates serious problems for the acceleration of corrosive processes. The control of the development of the biological film is important because its formation, among other effects, causes fouling of the surface where it has developed, producing differential aeration cells and aggressive metabolites. The influence of surface films was studied by applying electrochemical techniques in artificial seawater with and without bacteria, under different immersion times. Since the pitting potential (Epic) defines the metals' ability to resist pitting corrosion, a measure of susceptibility to pitting in aggressive solutions is considered. The pitting potential was studied in the systems being studied as well as the influence of seawater + ClO - ion biocides on the systems, since the biocides used was sodium hypochlorite (NaCIO). The material used was aluminum brass and a wild bacterial strain was used, which was isolated from the tubes by a heat exchanger from a thermoelectric plant (CW)

  17. Estimates of ikaite export from sea ice to the underlying seawater in a sea ice-seawater mesocosm

    Science.gov (United States)

    Geilfus, Nicolas-Xavier; Galley, Ryan J.; Else, Brent G. T.; Campbell, Karley; Papakyriakou, Tim; Crabeck, Odile; Lemes, Marcos; Delille, Bruno; Rysgaard, Søren

    2016-09-01

    The precipitation of ikaite and its fate within sea ice is still poorly understood. We quantify temporal inorganic carbon dynamics in sea ice from initial formation to its melt in a sea ice-seawater mesocosm pool from 11 to 29 January 2013. Based on measurements of total alkalinity (TA) and total dissolved inorganic carbon (TCO2), the main processes affecting inorganic carbon dynamics within sea ice were ikaite precipitation and CO2 exchange with the atmosphere. In the underlying seawater, the dissolution of ikaite was the main process affecting inorganic carbon dynamics. Sea ice acted as an active layer, releasing CO2 to the atmosphere during the growth phase, taking up CO2 as it melted and exporting both ikaite and TCO2 into the underlying seawater during the whole experiment. Ikaite precipitation of up to 167 µmol kg-1 within sea ice was estimated, while its export and dissolution into the underlying seawater was responsible for a TA increase of 64-66 µmol kg-1 in the water column. The export of TCO2 from sea ice to the water column increased the underlying seawater TCO2 by 43.5 µmol kg-1, suggesting that almost all of the TCO2 that left the sea ice was exported to the underlying seawater. The export of ikaite from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased vertical connectivity in sea ice due to the upward percolation of seawater and meltwater flushing during sea ice melt. Based on the change in TA in the water column around the onset of sea ice melt, more than half of the total ikaite precipitated in the ice during sea ice growth was still contained in the ice when the sea ice began to melt. Ikaite crystal dissolution in the water column kept the seawater pCO2 undersaturated with respect to the atmosphere in spite of increased salinity, TA and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying seawater can potentially hamper

  18. Physico-chemical behavior of radionuclides in seawater

    International Nuclear Information System (INIS)

    Kimura, Yuichiro; Ogawa, Yoshihiro; Honda, Yoshihide; Katsurayama, Kosuke.

    1980-01-01

    To elucidate the physico-chemical states of radionuclides in seawater in relation to uptake by the marine biosphere, the physicochemical behavior of radiocobalt, radioruthenium and radiocerium in seawater was investigated by electrodialysis, high-voltage paper electrophoresis, and also by paper chromatography for nitrosylruthenium complexes. Most of the radiocobalt in seawater behaved as dialytic cations. However, these cationic species were not necessarily simple divalent, because their electrophoretic bands were rather diffuse and showed two peaks temporarily. The electroneutral form also increased with aging in seawater. The radioruthenium in seawater showed relatively a number of well-defined species which could be readily classified into anionic, cationic, electroneutral, colloidal or particulate, non-dialytic and more or less adsorbable species. The radioruthenium in the chloro and nitratonitrosylruthenium complexes occurred mainly electroneutral and anionic species, while nitro and binuclear oxygen-bridged nitratonitrosylruthenium complexes showed dominant anionic species. The hydrolysis of higher nitro and nitratonitrosylruthenium complexes to lower ones was demonstrated with aging in seawater by paper chromatography. The radiocerium in seawater showed initially cationic species. However, the electroneutral and anionic species were revealed with aging by electrodialysis. The radiocerium were strongly adsorbed on filter paper at the starting band in paper electrophoresis, presumably because of the formation of strongly adsorbable or insoluble hydrolytic species or particle formation. (author)

  19. Viral lysis of photosynthesizing microbes as a mechanism for calcium carbonate nucleation in seawater

    Science.gov (United States)

    Lisle, John T.; Robbins, Lisa L.

    2016-01-01

    Removal of carbon through the precipitation and burial of calcium carbonate in marine sediments constitutes over 70% of the total carbon on Earth and is partitioned between coastal and pelagic zones. The precipitation of authigenic calcium carbonate in seawater, however, has been hotly debated because despite being in a supersaturated state, there is an absence of persistent precipitation. One of the explanations for this paradox is the geochemical conditions in seawater cannot overcome the activation energy barrier for the first step in any precipitation reaction; nucleation. Here we show that virally induced rupturing of photosynthetic cyanobacterial cells releases cytoplasmic-associated bicarbonate at concentrations ~23-fold greater than in the surrounding seawater, thereby shifting the carbonate chemistry toward the homogenous nucleation of one or more of the calcium carbonate polymorphs. Using geochemical reaction energetics, we show the saturation states (Ω) in typical seawater for calcite (Ω = 4.3), aragonite (Ω = 3.1), and vaterite (Ω = 1.2) are significantly elevated following the release and diffusion of the cytoplasmic bicarbonate (Ωcalcite = 95.7; Ωaragonite = 68.5; Ωvaterite = 25.9). These increases in Ω significantly reduce the activation energy for nuclei formation thresholds for all three polymorphs, but only vaterite nucleation is energetically favored. In the post-lysis seawater, vaterite's nuclei formation activation energy is significantly reduced from 1.85 × 10−17 J to 3.85 × 10−20 J, which increases the nuclei formation rate from highly improbable (nucleation of calcium carbonate in seawater describes a mechanism through which the initial step in the production of carbonate sediments may proceed. It also presents an additional role of photosynthesizing microbes and their viruses in marine carbon cycles and reveals these microorganisms are a collective repository for concentrated and reactive dissolved inorganic carbon (DIC

  20. Facile Preparation of Porous WO3 Film for Photoelectrochemical Splitting of Natural Seawater

    Science.gov (United States)

    Shi, Yonghong; Li, Yuangang; Wei, Xiaoliang; Feng, Juan; Li, Huajing; Zhou, Wanyi

    2017-12-01

    Sunlight-driven natural seawater splitting provides a promising way for large-scale conversion and storage of solar energy. Here, we develop a facile and low-cost method via a deposition-annealing technique to fabricate porous WO3 film and demonstrate its application as a photoanode for natural seawater splitting. The WO3 film yields a photocurrent density of 1.95 mA cm-2 and possesses excellent stability at 1.23 V (versus RHE), under the illumination of 100 mW cm-2 (AM 1.5G). The photoelectrochemical performance is ascribed to the large surface area and good permeation of the electrolyte into the porous film. Furthermore, the photocurrent density remains almost the same during 3 h continuous light irradiation. The evolution of chlorine gas from seawater splitting was determined with qualitative and quantitative analyses, with a Faradic efficiency of about 56%.

  1. Flow cytometric assessment of microbial abundance in the near-field area of seawater reverse osmosis concentrate discharge

    KAUST Repository

    Van Der Merwe, Riaan

    2014-06-01

    The discharge of concentrate and other process waters from seawater reverse osmosis (SWRO) plant operations into the marine environment may adversely affect water quality in the near-field area surrounding the outfall. The main concerns are the increase in salt concentration in receiving waters, which results in a density increase and potential water stratification near the outfall, and possible increases in turbidity, e.g., due to the discharge of filter backwash waters. Changes in ambient water quality may affect microbial abundance in the area, for example by hindering the photosynthesis process or disrupting biogenesis. It is widely accepted that marine biodiversity is lower in more extreme conditions, such as high salinity environments. As aquatic microbial communities respond very rapidly to changes in their environment, they can be used as indicators for monitoring ambient water quality. The objective of this study was to assess possible changes in microbial abundance as a result of concentrate discharge into the near-field area (<. 25. m) surrounding the outfall of the King Abdullah University of Science and Technology (KAUST) SWRO plant. Flow cytometric (FCM) analysis was conducted in order to rapidly determine microbial abundance on a single-cell level in 107 samples, taken by diving, from the discharge area, the intake area and two control sites. FCM analysis combined the measurement of distinct scatter of cells and particles, autofluorescence of cyanobacteria and algae, and fluorescence after staining of nucleic acids with SYBR® Green for a total bacterial count. The results indicate that changes in microbial abundance in the near-field area of the KAUST SWRO outfall are minor and appear to be the result of a dilution effect rather than a direct impact of the concentrate discharge. © 2014 Elsevier B.V.

  2. Seawater 234U/238U recorded by modern and fossil corals

    Science.gov (United States)

    Chutcharavan, Peter M.; Dutton, Andrea; Ellwood, Michael J.

    2018-03-01

    U-series dating of corals is a crucial tool for generating absolute chronologies of Late Quaternary sea-level change and calibrating the radiocarbon timescale. Unfortunately, coralline aragonite is susceptible to post-depositional alteration of its primary geochemistry. One screening technique used to identify unaltered corals relies on the back-calculation of initial 234U/238U activity (δ234Ui) at the time of coral growth and implicitly assumes that seawater δ234U has remained constant during the Late Quaternary. Here, we test this assumption using the most comprehensive compilation to date of coral U-series measurements. Unlike previous compilations, this study normalizes U-series measurements to the same decay constants and corrects for offsets in interlaboratory calibrations, thus reducing systematic biases between reported δ234U values. Using this approach, we reassess (a) the value of modern seawater δ234U, and (b) the evolution of seawater δ234U over the last deglaciation. Modern coral δ234U values (145.0 ± 1.5‰) agree with previous measurements of seawater and modern corals only once the data have been normalized. Additionally, fossil corals in the surface ocean display δ234Ui values that are ∼5-7‰ lower during the last glacial maximum regardless of site, taxon, or diagenetic setting. We conclude that physical weathering of U-bearing minerals exposed during ice sheet retreat drives the increase in δ234U observed in the oceans, a mechanism that is consistent with the interpretation of the seawater Pb-isotope signal over the same timescale.

  3. Progress in recovery technology for uranium from seawater

    International Nuclear Information System (INIS)

    Sugo, Takanobu; Saito, Kyoichi.

    1994-01-01

    By the facts that the research group in Japan improved the performance of amidoxime resin which is the adsorbent for collecting seawater uranium, proposed the method of mooring floating bodies utilizing sea current and waves as the adsorption system, and further, verified the results of laboratory basic experiment by marine experiment, the technology of collecting seawater uranium has progressed. After the oil crisis, various countries started the research on seawater uranium, but only Japan has continued the systematic study up to now. In this report, the research on seawater uranium collection carried out so far is summarized, and the characteristics of the adsorbent which was synthesized by radiation graft polymerization and the results of the uranium collection test using coastal seawater are reported. In seawater of 1 m 3 , the uranium of 3.3 mg is dissolved in the form of uranyl tricarbonate complex ions. In the total quantity of seawater, the dissolved uranium amounts to about 4.6 billion tons, about 1000 times of the uranium resources on land. The research on seawater uranium collection and the performance of uranium adsorption of synthesized amidoxime fibers are reported. (K.I.)

  4. Paleogene Seawater Osmium Isotope Records

    Science.gov (United States)

    Rolewicz, Z.; Thomas, D. J.; Marcantonio, F.

    2012-12-01

    Paleoceanographic reconstructions of the Late Cretaceous and early Cenozoic require enhanced geographic coverage, particularly in the Pacific, in order to better constrain meridional variations in environmental conditions. The challenge with the existing inventory of Pacific deep-sea cores is that they consist almost exclusively of pelagic clay with little existing age control. Pelagic clay sequences are useful for reconstructions of dust accumulation and water mass composition, but accurate correlation of these records to other sites requires improved age control. Recent work indicates that seawater Os isotope analyses provide useful age control for red clay sequences. The residence time of Os in seawater is relatively long compared to oceanic mixing, therefore the global seawater 187Os/188Os composition is practically homogeneous. A growing body of Late Cretaceous and Cenozoic data has constrained the evolution of the seawater Os isotopic composition and this curve is now a viable stratigraphic tool, employed in dating layers of Fe-Mn crusts (e.g., Klemm et al., 2005). Ravizza (2007) also demonstrated that the seawater Os isotopic composition can be extracted reliably from pelagic red clay sediments by analyzing the leached oxide minerals. The drawback to using seawater Os isotope stratigraphy to date Paleogene age sediments is that the compilation of existing data has some significant temporal gaps, notably between ~38 and 55 Ma. To improve the temporal resolution of the seawater Os isotope curve, we present new data from Ocean Drilling Program (ODP) Site 865 in the equatorial Pacific. Site 865 has excellent biostratigraphic age control over the interval ~38-55Ma. Preliminary data indicate an increase in the seawater composition from 0.427 at 53.4 Ma to 0.499 by 43 Ma, consistent with the apparent trend in the few existing data points. We also analyzed the Os isotopic composition recorded by oxide minerals at Integrated Ocean Drilling Program (IODP) Site U1370

  5. Impact of Seawater Nonlinearities on Nordic Seas Circulation

    Science.gov (United States)

    Helber, R. W.; Wallcraft, A. J.; Shriver, J. F.

    2017-12-01

    The Nordic Seas (Greenland, Iceland, and Norwegian Seas) form an ocean basin important for Arctic-mid-latitude climate linkages. Cold fresh water from the Arctic Ocean and warm salty water from the North Atlantic Ocean meet in the Nordic Seas, where a delicate balance between temperature and salinity variability results in deep water formation. Seawater non-linearities are stronger at low temperatures and salinities making high-latitude oceans highly subject to thermbaricity and cabbeling. This presentation highlights and quantifies the impact of seawater non-linearities on the Nordic Seas circulation. We use two layered ocean circulation models, the Hybrid Coordinate Ocean Model (HYOCM) and the Modular Ocean Model version 6 (MOM6), that enable accurate representation of processes along and across density or neutral density surfaces. Different equations-of-state and vertical coordinates are evaluated to clarify the impact of seawater non-linearities. Present Navy systems, however, do not capture some features in the Nrodic Seas vertical structure. For example, observations from the Greenland Sea reveal a subsurface temperature maximum that deepens from approximately 1500 m during 1998 to 1800 m during 2005. We demonstrate that in terms of density, salinity is the largest source of error in Nordic Seas Navy forecasts, regional scale models can represent mesoscale features driven by thermobaricity, vertical coordinates are a critical issue in Nordic Sea circulation modeling.

  6. Oxidative stress in the hydrocoral Millepora alcicornis exposed to CO2-driven seawater acidification

    Science.gov (United States)

    Luz, Débora Camacho; Zebral, Yuri Dornelles; Klein, Roberta Daniele; Marques, Joseane Aparecida; Marangoni, Laura Fernandes de Barros; Pereira, Cristiano Macedo; Duarte, Gustavo Adolpho Santos; Pires, Débora de Oliveira; Castro, Clovis Barreira e.; Calderon, Emiliano Nicolas; Bianchini, Adalto

    2018-06-01

    Global impacts are affecting negatively coral reefs' health worldwide. Ocean acidification associated with the increasing CO2 partial pressure in the atmosphere can potentially induce oxidative stress with consequent cellular damage in corals and hydrocorals. In the present study, parameters related to oxidative status were evaluated in the hydrocoral Millepora alcicornis exposed to three different levels of seawater acidification using a mesocosm system. CO2-driven acidification of seawater was performed until reaching 0.3, 0.6 and 0.9 pH units below the current pH of seawater pumped from the coral reef adjacent to the mesocosm. Therefore, treatments corresponded to control (pH 8.1), mild (pH 7.8), intermediate (pH 7.5) and severe (pH 7.2) seawater acidification. After 0, 16 and 30 d of exposure, hydrocorals were collected and the following parameters were analyzed in the holobiont: antioxidant capacity against peroxyl radicals (ACAP), total glutathione (GSHt) concentration, reduced (GSH) and oxidized (GSSG) glutathione ratio (GSH/GSSG), lipid peroxidation (LPO) and protein carbonyl group (PC) levels. ACAP was increased in hydrocorals after 16 d of exposure to intermediate levels of seawater acidification. GSHt and GSH/GSSG did not change over the experimental period. LPO was increased at any level of seawater acidification, while PC content was increased in hydrocorals exposed to intermediate and severe seawater acidification for 30 d. These findings indicate that the antioxidant defense system of M. alcicornis is capable of coping with acidic conditions for a short period of time (16 d). Additionally, they clearly show that a long-term (30 d) exposure to seawater acidification induces oxidative stress with consequent oxidative damage to lipids and proteins, which could compromise hydrocoral health.

  7. Numerical Study of Groundwater Flow and Salinity Distribution Cycling Controlled by Seawater/Freshwater Interaction in Karst Aquifer Using SEAWAT

    Science.gov (United States)

    Xu, Z.; Hu, B.

    2017-12-01

    The interest to predict seawater intrusion and salinity distribution in Woodville Karst Plain (WKP) has increased due to the huge challenge on quality of drinkable water and serious environmental problems. Seawater intrudes into the conduit system from submarine karst caves at Spring Creek Spring due to density difference and sea level rising, nowadays the low salinity has been detected at Wakulla Spring which is 18 km from coastal line. The groundwater discharge at two major springs and salinity distribution in this area is controlled by the seawater/freshwater interaction under different rainfall conditions: during low rainfall periods, seawater flow into the submarine spring through karst windows, then the salinity rising at the submarine spring leads to seawater further intrudes into conduit system; during high rainfall periods, seawater is pushed out by fresh water discharge at submarine spring. The previous numerical studies of WKP mainly focused on the density independent transport modeling and seawater/freshwater discharge at major karst springs, in this study, a SEAWAT model has been developed to fully investigate the salinity distribution in the WKP under repeating phases of low rainfall and high rainfall periods, the conduit system was simulated as porous media with high conductivity and porosity. The precipitation, salinity and discharge at springs were used to calibrate the model. The results showed that the salinity distribution in porous media and conduit system is controlled by the rainfall change, in general, the salinity distribution inland under low rainfall conditions is much higher and wider than the high rainfall conditions. The results propose a prediction on the environmental problem caused by seawater intrusion in karst coastal aquifer, in addition, provide a visual and scientific basis for future groundwater remediation.

  8. Determination of the total concentration and speciation of metal ions in river, estuarine and seawater samples.

    Science.gov (United States)

    Alberti, Giancarla; Biesuz, Raffaela; Pesavento, Maria

    2008-12-01

    Different natural water samples were investigated to determine the total concentration and the distribution of species for Cu(II), Pb(II), Al(III) and U(VI). The proposed method, named resin titration (RT), was developed in our laboratory to investigate the distribution of species for metal ions in complex matrices. It is a competition method, in which a complexing resin competes with natural ligands present in the sample to combine with the metal ions. In the present paper, river, estuarine and seawater samples, collected during a cruise in Adriatic Sea, were investigated. For each sample, two RTs were performed, using different complexing resins: the iminodiacetic Chelex 100 and the carboxylic Amberlite CG50. In this way, it was possible to detect different class of ligands. Satisfactory results have been obtained and are commented on critically. They were summarized by principal component analysis (PCA) and the correlations with physicochemical parameters allowed one to follow the evolution of the metals along the considered transect. It should be pointed out that, according to our findings, the ligands responsible for metal ions complexation are not the major components of the water system, since they form considerably weaker complexes.

  9. Impregnation/Agglomeration Laboratory Tests of Heavy Fuel from Prestige to Improve Its Manageability and Removal from Seawater Surface. (Physical Behaviour of Fuel Agglomates)

    International Nuclear Information System (INIS)

    Garcia Frutos, F. J.; Rodriguez, V.; Otero, J.

    2002-01-01

    The handling and removal problems showed by heavy fuel floating in seawater could be improved or solved by using materials that agglomerate it. These materials must fulfill the following conditions: be inert materials in marine environment, the agglomerated fuel/material should float and its application and removal should be done using simple technologies. Based on these requirements, clay minerals, pine chips, mineral coal and charcoal were selected. The preliminary/results on impregnation/agglomeration with the materials mentioned above of heavy fuel from Prestige at lab scale are presented in this paper. The results have shown that only hydrophobic materials, such as mineral coal and charcoal, are able to agglomerate with fuel, which is also a hydrophobic substance. Whereas the agglomerates fuel/mineral coal sink, the agglomerates fuel/charcoal keep floating on water surface. It can be concluded that the addition of charcoal on dispersed fuel in seawater could improve its handling and removal. In this sense, pilot scale and eventually controlled in situ tests to study the feasibility of the proposed solution should be performed. (Author) 2 refs

  10. 238U, 234U and 232Th in seawater

    International Nuclear Information System (INIS)

    Chen, J.H.; Edwards, R.L.; Wasserburg, G.J.

    1986-01-01

    We have developed techniques to determine 238 U, 234 U and 232 Th concentrations in seawater by isotope dilution mass spectrometry. Using these techniques, we have measured 238 U, 234 U and 232 Th in vertical profiles of unfiltered, acidified seawater from the Atlantic and 238 U and 234 U in vertical profiles from the Pacific. Determinations of 234 U/ 238 U at depths ranging from 0 to 4900 m in the Atlantic (7 0 44'N, 40 0 43'W) and the Pacific (14 0 41'N, 160 0 01'W) Oceans are the same within experimental error (±5per mille, 2σ). The average of these 234 U/ 238 U measurements is 144±2per mille (2σ) higher than the equilibrium ratio of 5.472 x 10 -5 . U concentrations, normalized to 35per mille salinity, range from 3.162 to 3.281 ng/g, a range of 3.8%. The average concentration of the Pacific samples (31 0 4'N, 159 0 1'W) is ∝1% higher than that of the Atlantic (7 0 44'N, 40 0 43'W and 31 0 49'N, 64 0 6'W). 232 Th concentrations from an Atlantic profile range from 0.092 to 0.145 pg/g. The observed constancy of the 234 U/ 238 U ratio is consistent with the predicted range of 234 U/ 238 U using a simple two-box model and the residence time of deep water in the ocean determined from 14 C. The variation in salinity-normalized U concentrations suggests that U may be much more reactive in the marine environment than previously thought. (orig./WB)

  11. Detection, occurrence and monthly variations of typical lipophilic marine toxins associated with diarrhetic shellfish poisoning in the coastal seawater of Qingdao City, China.

    Science.gov (United States)

    Li, Xin; Li, Zhaoyong; Chen, Junhui; Shi, Qian; Zhang, Rutan; Wang, Shuai; Wang, Xiaoru

    2014-09-01

    In recent years, related research has mainly examined lipophilic marine toxins (LMTs) in contaminated bivalves or toxic algae, whereas the levels of LMTs in seawater remain largely unexplored. Okadaic acid (OA), yessotoxin (YTX), and pectenotoxin-2 (PTX2) are three typical LMTs produced by certain marine algae that are closely linked to diarrhetic shellfish poisoning. In this study, a new method of solid phase extraction combined with liquid chromatography - electrospray ionization ion trap tandem mass spectrometry was developed to determine the presence of OA, YTX, and PTX2 in seawater simultaneously. Satisfactory sensitivity, repeatability (RSDseawater. OA and PTX2 were detected in all the seawater samples collected from eight locations along the coastline of Qingdao City, China on October 23, 2012, with concentration ranges of OA 4.24-9.64ngL(-1) and PTX2 0.42-0.74ngL(-1). Monthly concentrations of OA and PTX2 in the seawater of four locations were determined over the course of a year, with concentration ranges of OA 1.41-89.52ngL(-1) and PTX2 below detectable limit to 1.70ngL(-1). The peak values of OA and PTX2 in coastal seawater were observed in August and July, respectively. Our results suggest that follow-up research on the fate modeling and risk assessment of LMTs in coastal seawater should be implemented. Copyright © 2014 Elsevier Ltd. All rights reserved.

  12. Distribution and accumulation of organotin species in seawater, sediments and organisms collected from a Taiwan mariculture area.

    Science.gov (United States)

    Liu, Li-Lian; Wang, Jih-Terng; Chung, Kuo-Nan; Leu, Ming-Yih; Meng, Pei-Jie

    2011-01-01

    The present study was undertaken to evaluate the distribution and accumulation of tributyltin (TBT) and triphenyltin (TPhT) in seawater, sediments and selected organisms from a cage mariculture area in southern Taiwan, Hsiao Liouchiou Island. Our results show that ΣOTs were found in concentrations as high as 196 ng/L in seawater collected from the sites in Pai-Sa harbor, and up 1040 ng/g dry wt. in sediments dredged from sites within Da-Fu harbor. Also, ΣOTs concentrations of 859 ng/g dry wt. were observed in the liver of cobia (Rachycentron canadum) from mariculture cages. As most published studies have focused on the acute toxicity and bioaccumulation of organotins in mussels, the effects of organotins on cobia and other marine fauna are still poorly understood. This study highlights the significance of ΣBTs accumulation in cobia, as well as in the sediments and seawater surrounding their culture facilities. Copyright © 2011 Elsevier Ltd. All rights reserved.

  13. Determination of iridium in the Bering Sea and Arctic Ocean seawaters by anion exchange preconcentration-neutron activation analysis

    International Nuclear Information System (INIS)

    Li Shihong; Mao Xueying; Chai Zhifang

    2004-01-01

    Anion exchange method is investigated to separate and enrich iridium in seawater by radiotracer 192 Ir. The adsorption of Ir in the resin increases with the decreasing acidity in the 0.05-1.2 mol/L HCl media, The recovery of iridium in pH=1.5 seawater reaches 89% by a single anion-exchange column. The polyethylene container of acidity of pH=1.5 are suitable for storing trace Ir in seawater. An anion exchange preconcentration-neutron activation analysis procedure is developed to determine iridium in seawaters sampled from the Bering Sea and Arctic Ocean at different depth. The reagent blank value of the whole procedures is (0.18-0.20) x 10 -12 g Ir. The iridium concentrations in the Bering Sea and Arctic Ocean seawater samples are (0.85-3.58) x 10 -12 g/L (0-3504 m) and (1.26-1.97) x 10 -12 g/L (25-1900 m), respectively

  14. Kinetics of ikaite precipitation and dissolution in seawater-derived brines at sub-zero temperatures to 265 K

    Science.gov (United States)

    Papadimitriou, Stathys; Kennedy, Hilary; Kennedy, Paul; Thomas, David N.

    2014-09-01

    The kinetics of calcium carbonate hexahydrate (ikaite) precipitation and dissolution were investigated in seawater and seawater-derived brines at sub-zero temperatures using the constant addition experimental technique. The steady state rate of these two processes was found to be a function of the deviation of the solution from equilibrium with respect to ikaite and conformed to the same empirical rate law as the anhydrous CaCO3 polymorphs, calcite and aragonite. In addition to the saturation state of the brine with respect to ikaite, the salinity of the brine and the temperature of the reaction evidently exerted some control on the ikaite precipitation kinetics, while the dissolution kinetics of the polymorph were not noticeably influenced by these two parameters. The experimental salinity and temperature conditions were equivalent to those at thermal equilibrium between brine and ice in the sea ice cover of polar seas. Simple modelling of the CO2 system by extrapolation of the oceanic equivalent to sea ice brines showed that the physical concentration of seawater ions and the changes in ikaite solubility as a function of salinity and temperature, both inherent in the sea ice system, would be insufficient to drive the emergent brines to ikaite supersaturation and precipitation in sea ice down to -8 °C. The loss of dissolved inorganic carbon to the gas phase of sea ice and to sympagic autotrophs are two independent mechanisms which, in nature, could prompt the brine CO2 system towards ikaite supersaturation and precipitation. Under these conditions, the steady state precipitation rate of ikaite was found to be fast enough for rapid formation within short time scales (days to weeks) in sea ice. The observed ikaite dissolution kinetics were also found conducive to short turn-over time scales of a few hours to a few days in corrosive solutions, such as surface seawater.

  15. Direct measurement of uranium in seawater by inductively coupled plasma mass spectrometry

    DEFF Research Database (Denmark)

    Qiao, Jixin; Xu, Yihong

    2018-01-01

    samples taken from large volume of seawater stored in immovable containers for relatively long period (i.e., several months), the uranium concentration and salinity data showed slightly increasing trends with the increase of water depth in the container. Therefore, cautions need to be paid in sampling...

  16. Rapid determination of 90Sr in seawater

    International Nuclear Information System (INIS)

    Pavlotskaya, F.I.; Moskin, A.I.

    1994-01-01

    A method for determining 90 Sr in seawater that is based on direct isolation and radiochemical purification of daughter 90 Y is proposed. The analysis time is 6-8 h. The chemical yield of the Y-carrier during the 90 Sr determination from 35 liters of seawater varies in the range 37-69%. The analysis uncertainty is 90 Sr from seawater and subsequent isolation of 90 Y

  17. Enzymatic methods for the determination of pollution in seawater using salt resistant alkaline phosphatase from eggs of the sea urchin Strongylocentrotus intermedius

    International Nuclear Information System (INIS)

    Menzorova, Natalie I.; Seitkalieva, Alexandra V.; Rasskazov, Valery A.

    2014-01-01

    Highlights: • Alkaline phosphatase from eggs of the sea urchin (StAP) proved to be active in seawater. • Activity of StAP is inhibited by very low concentrations of heavy metal. • A test to assess sea and fresh water quality has been developed basing on StAP. • For the first time a salt resistant alkaline phosphatase has been found in eukaryote. - Abstract: A new salt resistant alkaline phosphatase from eggs of the sea urchin Strongylocentrotus intermedius (StAP) has been shown to have a unique property to hydrolyze substrate in seawater without loss of enzymatic activity. The enzyme has pH optimum at 8.0–8.5. Model experiments showed various concentrations of copper, zinc, cadmium and lead added to seawater or a standard buffer mixture to inhibit completely the enzyme activity at the concentrations of 15–150 μg/l. StAP sensitivity to the presence in seawater of metals, pesticides, detergents and oil products appears to be considerably less. Samples of seawater taken from aquatic areas of the Troitsy Bay of the Peter the Great Bay, Japan Sea have been shown to inhibit the enzyme activity; the same was shown for the samples of fresh waters. The phosphatase inhibition assay developed proved to be highly sensitive, technically easy-to use allowing to test a great number of samples

  18. Spatial and temporal distribution of tributyltin (TBT) in seawater, sediments and bivalves from coastal areas of Korea during 2001-2005.

    Science.gov (United States)

    Choi, Minkyu; Choi, Hee-Gu; Moon, Hyo-Bang; Kim, Gui-Young

    2009-04-01

    Tributyltin (TBT) concentrations were determined in seawater, sediments and bivalve samples collected from Korean coastal areas during 2001-2005, to investigate the levels and temporal variation in TBT contamination in relation to the timing of the imposition of regulations on TBT use in Korea. TBT concentrations ranged from TBT were found at locations close to intensive shipping traffic and industrial complexes, and the contamination at some hot spot areas was high enough to cause harmful effects on marine organisms. TBT concentrations and their occurrence in Korean coastal waters have been decreasing annually. In particular, TBT concentrations in seawater have dramatically decreased. This result is consistent with regulations and bans on the use of TBT in Korea.

  19. Influence of solution chemistry on the boron content in inorganic calcite grown in artificial seawater

    Science.gov (United States)

    Uchikawa, Joji; Harper, Dustin T.; Penman, Donald E.; Zachos, James C.; Zeebe, Richard E.

    2017-12-01

    The ratio of boron to calcium (B/Ca) in marine biogenic carbonates has been proposed as a proxy for properties of seawater carbonate chemistry. Applying this proxy to planktic foraminifera residing in the surface seawater largely in equilibrium with the atmosphere may provide a valuable handle on past atmospheric CO2 concentrations. However, precise controls on B/Ca in planktic foraminifera remain enigmatic because it has been shown to depend on multiple physicochemical seawater properties. To help establish a firm inorganic basis for interpreting the B/Ca records, we examined the effect of a suite of chemical parameters ([Ca2+], pH, [DIC], salinity and [PO43-]) on B/Ca in inorganic calcite precipitated in artificial seawater. These parameters were primarily varied individually while keeping all others constant, but we also tested the influence of pH and [DIC] at a constant calcite precipitation rate (R) by concurrent [Ca2+] adjustments. In the simple [Ca2+], pH and [DIC] experiments, both R and B/Ca increased with these parameters. In the pH-[Ca2+] and [DIC]-[Ca2+] experiments at constant R, on the other hand, B/Ca was invariant at different pH and decreased with [DIC], respectively. These patterns agree with the behavior of solution [BTotal/DIC] ratio such that, at a fixed [BTotal], it is independent of pH but decreases with [DIC]. Based on these results, R and [BTotal/DIC] ratio appear to be the primary controls on B/Ca in inorganic calcite, suggesting that both B(OH)4- and B(OH)3 are possibly involved in B incorporation. Moreover, B/Ca modestly increased with salinity and [PO43-]. Inorganic calcite precipitated at higher R and in the presence of oxyanions such as SO42- and PO43- in growth solutions often undergoes surface roughening due to formation of crystallographic defects, vacancies and, occasionally, amorphous/hydrous CaCO3. These non-lattice sites may provide additional space for B, particularly B(OH)3. Consequently, besides the macroscopic influence of

  20. Chemical Controls of Ozone Dry Deposition to the Sea Surface Microlayer

    Science.gov (United States)

    Carpenter, L.; Chance, R.; Tinel, L.; Saint, A.; Sherwen, T.; Loades, D.; Evans, M. J.; Boxhall, P.; Hamilton, J.; Stolle, C.; Wurl, O.; Ribas-Ribas, M.; Pereira, R.

    2017-12-01

    Oceanic dry deposition of atmospheric ozone (O3) is both the largest and most uncertain O3 depositional sink, and is widely acknowledged to be controlled largely by chemical reactions in the sea surface microlayer (SML) involving iodide (I-) and dissolved organic material (DOM). These reactions not only determine how quickly O3 can be removed from the atmosphere, but also result in emissions of trace gases including volatile organic compounds and may constitute a source of secondary organic aerosols to the marine atmosphere. Iodide concentrations at the sea surface vary by approximately an order of magnitude spatially, leading to more than fivefold variation in ozone deposition velocities (and volatile iodine fluxes). Sea-surface temperature is a reasonable predictor of [I-], however two recent parameterisations for surface I- differ by a factor of two at low latitudes. The nature and reactivity of marine DOM to O3 is almost completely unknown, although studies have suggested approximately equivalent chemical control of I- and DOM on ozone deposition. Here we present substantial new measurements of oceanic I- in both bulk seawater and the overlying SML, and show improved estimates of the global sea surface iodide distribution. We also present analyses of water-soluble DOM isolated from the SML and bulk seawater, and corresponding laboratory studies of ozone uptake to bulk and SML seawater, with the aim of characterizing the reactivity of O3 towards marine DOM.

  1. Multielement determination of major-to-ultratrace elements in deep-seawater salts by ICP-AES and ICP-MS

    International Nuclear Information System (INIS)

    Sakai, Takeshi; Nakagawa, Koji; Nakajima, Hiroshi; Itoh, Akihide; Ji, Shan; Haraguchi, Hiroki

    2002-01-01

    Major-to-ultratrace elements in deep-seawater salts were determined by ICP-AES and ICP-MS, after they were separated into the water-soluble, acid-soluble, and insoluble particle components. Deep-seawater salts were prepared from seawater collected at 344 m deep near the off-shore of Cape Muroto in Kochi Prefecture. The major and minor elements in salts were determined by ICP-AES after appropriate dilution with pure water. Trace and ultratrace elements in the water-soluble and acid-soluble components were preconcentrated by a chelating resin preconcentration method. In addition, the major to-ultratrace elements in the insoluble particle component were determined by ICP-AES and ICP-MS, after acid-digestion using HNO 3 /HF/HClO 4 . As a result, 21-35 elements in deep-seawater salts could be determined over the wide concentration range. It was found that the elements, such as Al, V, Fe, Mn, Co, Cu, Zn, and rare earth elements, were more abundant in the acid-soluble component of deep-seawater salts, which may play some essential roles in physiological effectiveness for intake of salt. (author)

  2. Seawater desalination with nuclear power

    International Nuclear Information System (INIS)

    2005-01-01

    Nuclear power helps reduce costs for energy-intensive processes such as seawater desalination. A new generation of innovative small and medium nuclear power plants could co-generate electricity and potable water from seawater, both safely and at competitive prices in today's market. The IAEA provides technical support to Member States facing water shortage problems, on assessing the viability of nuclear power in seawater desalination. The support, usually channelled through national Technical Cooperation (TC) projects, can take several forms, ranging from educational training and technical advice on feasibility studies to design and safety review of demonstration projects. The IAEA offers a software tool (DEEP) that can be used to evaluate the economics of the different desalination and heat source configurations, including nuclear and fossil options

  3. The clam (Chamelea gallina: evaluation of the effects of solids suspended in seawater on bivalve molluscs

    Directory of Open Access Journals (Sweden)

    Salvatora Angela Angioni

    2010-03-01

    Full Text Available The study was designed to evaluate the effects of solids in suspension in seawater on clams (Chamelea gallina. The aim was to investigate the possible correlation between the widespread deaths of clams in the coastal waters of the central and northern Adriatic in the last five years and increased concentrations of solids in suspension. The research involved conducting 96-hour tests on clams farmed in aquariums containing filtered seawater. The tests were preceded by a 7-day adaptation stage to allow the molluscs to acclimatise. During this period, the clams were fed on unicellular seaweed (Dunaliella tertiolecta. The molluscs were exposed to particles of solids in suspension consisting of pools of silica gel (SiO2 granules of various sizes, similar to those constituting silt, whose presence and suspension in the sea considerably increase after heavy rain and heavy seas. The study established that the number of deaths caused by solids suspended in seawater at the concentrations used in the tests was not statistically significant.

  4. Next generation in-situ optical Raman sensor for seawater investigations

    Science.gov (United States)

    Kolomijeca, A.; Kwon, Y.-H.; Ahmad, H.; Kronfeldt, H.-D.

    2012-04-01

    We introduce the next generation of optical sensors based on a combination of surfaced enhanced Raman scattering (SERS) and shifted excitation Raman difference spectroscopy (SERDS) suited for investigations of tiny concentrations of pollutions in the seawater. First field measurements were carried out in the Arctic area which is of global interest since it is more affected by global warming caused climatic changes than any other areas of our planet and it is a recipient for many toxic organic pollutants. A significant long-range atmospheric transport of pollutants to Svalbard is mainly originated from industrialized countries in Europe and North America during the last decades. Therefore, the main interest is to investigate the Arctic water column and also the sediments. Standard chemical methods for water/sediment analysis are extremely accurate but complex and time-consuming. The primary objective of our study was to develop a fast response in-situ optical sensor for easy to use and quick analysis. The system comprises several components: a handheld measurement head containing a 671 nm microsystem diode laser and the Raman optical bench, a laser driver electronics board, a custom-designed miniature spectrometer with an optical resolution of 8 cm-1 and a netbook to control the spectrometer as well as for data evaluation. We introduced for the first time the portable Raman sensor system on an Artic sea-trial during a three week cruise on board of the James Clark Ross research vessel in August 2011. Numerous Raman and SERS measurements followed by SERDS evaluations were taken around locations 78° N and 9° E. Different SERS substrates developed for SERS measurements in sea-water were tested for their capability to detect different substances (PAHs) in the water down to very small (nmol/l) concentrations. Stability tests of the substrates were carried out also for the applicability of our system e.g. on a mooring. Details of the in-situ Raman sensor were presented

  5. Analysis of lipophilic marine biotoxins by liquid chromatography coupled with high-resolution mass spectrometry in seawater from the Catalan Coast.

    Science.gov (United States)

    Bosch-Orea, Cristina; Sanchís, Josep; Farré, Marinella; Barceló, Damià

    2017-09-01

    Marine biotoxins regularly occur along the coast, with several consequences for the environment as well as the food industry. Monitoring of these compounds in seawater is required to assure the safety of marine resources for human consumption, providing a means for forecasting shellfish contamination events. In this study, an analytical method was developed for the detection of ten lipophilic marine biotoxins in seawater: azaspiracids 1, 2, 3, 4 and 5, classified as azaspiracid shellfish poisoning toxins, and pectenotoxin 2, okadaic acid and the related dinophysistoxin 1, yessotoxin and homoyessotoxin, classified as diarrheic shellfish poisoning toxins. The method is based on the application of solid-liquid ultrasound-assisted extraction and solid-phase extraction, followed by high-performance liquid chromatography coupled with high-resolution mass spectrometry. The limits of detection of this method are in the range of nanograms per litre and picograms per litre for most of the compounds, and recoveries range from 20.5% to 97.2%. To validate the effectiveness of this method, 36 samples of surface water from open coastal areas and marinas located along the Catalan coast on the Mediterranean Sea were collected and analysed. Eighty-eight per cent of these samples exhibited okadaic acid in particulate and aqueous phases in concentrations ranging from 0.11 to 560 μg/g and from 2.1 to 1780 ng/L respectively. Samples from open coastal areas exhibited higher concentrations of okadaic acid in particulate material, whereas in samples collected in sportive ports, the particulate material exhibited lower levels than the aqueous phase. Graphical Abstract Biotoxins investigated in seawater of the Catalan coast.

  6. Elution of Uranium and Transition Metals from Amidoxime-Based Polymer Adsorbents for Sequestering Uranium from Seawater

    Energy Technology Data Exchange (ETDEWEB)

    Pan, Horng-Bin; Kuo, Li-Jung; Wai, Chien M.; Miyamoto, Naomi; Joshi, Ruma; Wood, Jordana R.; Strivens, Jonathan E.; Janke, Christopher J.; Oyola, Yatsandra; Das, Sadananda; Mayes, Richard T.; Gill, Gary A.

    2015-11-30

    High-surface-area amidoxime and carboxylic acid grafted polymer adsorbents developed at Oak Ridge National Laboratory were tested for sequestering uranium in a flowing seawater flume system at the PNNL-Marine Sciences Laboratory. FTIR spectra indicate that a KOH conditioning process is necessary to remove the proton from the carboxylic acid and make the sorbent effective for sequestering uranium from seawater. The alkaline conditioning process also converts the amidoxime groups to carboxylate groups in the adsorbent. Both Na2CO3-H2O2 and hydrochloric acid elution methods can remove ~95% of the uranium sequestered by the adsorbent after 42 days of exposure in real seawater. The Na2CO3-H2O2 elution method is more selective for uranium than conventional acid elution. Iron and vanadium are the two major transition metals competing with uranium for adsorption to the amidoxime-based adsorbents in real seawater.

  7. Potential Effects of Desalinated Seawater on Arteriosclerosis in Rats.

    Science.gov (United States)

    Duan, Lian; Zhang, Li Xia; Zhang, Shao Ping; Kong, Jian; Zhi, Hong; Zhang, Ming; Lu, Kai; Zhang, Hong Wei

    2017-10-01

    To evaluate the potential risk of arteriosclerosis caused by desalinated seawater, Wistar rats were provided desalinated seawater over a 1-year period, and blood samples were collected at 0, 90, 180, and 360 days. Blood calcium, magnesium, and arteriosclerosis-related indicators were investigated. Female rats treated with desalinated seawater for 180 days showed lower magnesium levels than the control rats (P seawater for 360 days (P seawater, and no increase in risk of arteriosclerosis was observed. Copyright © 2017 The Editorial Board of Biomedical and Environmental Sciences. Published by China CDC. All rights reserved.

  8. Nitrogen fate in a subtropical mangrove swamp: Potential association with seawater-groundwater exchange.

    Science.gov (United States)

    Xiao, Kai; Wu, Jiapeng; Li, Hailong; Hong, Yiguo; Wilson, Alicia M; Jiao, Jiu Jimmy; Shananan, Meghan

    2018-04-18

    Coastal mangrove swamps play an important role in nutrient cycling at the land-ocean boundary. However, little is known about the role of periodic seawater-groundwater exchange in the nitrogen cycling processes. Seawater-groundwater exchange rates and inorganic nitrogen concentrations were investigated along a shore-perpendicular intertidal transect in Daya Bay, China. The intertidal transect comprises three hydrologic subzones (tidal creek, mangrove and bare mudflat zones), each with different physicochemical characteristics. Salinity and hydraulic head measurements taken along the transect were used to estimate the exchange rates between seawater and groundwater over a spring-neap tidal cycle. Results showed that the maximum seawater-groundwater exchange occurred within the tidal creek zone, which facilitated high-oxygen seawater infiltration and subsequent nitrification. In contrast, the lowest exchange rate found in the mangrove zone caused over-loading of organic matter and longer groundwater residence times. This created an anoxic environment conducive to nitrogen loss through the anammox and denitrification processes. Potential oxidation rates of ammonia and nitrite were measured by the rapid and high-throughput method and rates of denitrification and anammox were measured by the modified membrane inlet mass spectrometry (MIMS) with isotope pairing, respectively. In the whole transect, denitrification accounted for 90% of the total nitrogen loss, and anammox accounted for the remaining 10%. The average nitrogen removal rate was about 2.07g per day per cubic meter of mangrove sediments. Copyright © 2018 Elsevier B.V. All rights reserved.

  9. Dislocation behavior of surface-oxygen-concentration controlled Si wafers

    International Nuclear Information System (INIS)

    Asazu, Hirotada; Takeuchi, Shotaro; Sannai, Hiroya; Sudo, Haruo; Araki, Koji; Nakamura, Yoshiaki; Izunome, Koji; Sakai, Akira

    2014-01-01

    We have investigated dislocation behavior in the surface area of surface-oxygen-concentration controlled Si wafers treated by a high temperature rapid thermal oxidation (HT-RTO). The HT-RTO process allows us to precisely control the interstitial oxygen concentration ([O i ]) in the surface area of the Si wafers. Sizes of rosette patterns, generated by nano-indentation and subsequent thermal annealing at 900 °C for 1 h, were measured for the Si wafers with various [O i ]. It was found that the rosette size decreases in proportion to the − 0.25 power of [O i ] in the surface area of the Si wafers, which were higher than [O i ] of 1 × 10 17 atoms/cm 3 . On the other hand, [O i ] of lower than 1 × 10 17 atoms/cm 3 did not affect the rosette size very much. These experimental results demonstrate the ability of the HT-RTO process to suppress the dislocation movements in the surface area of the Si wafer. - Highlights: • Surface-oxygen-concentration controlled Si wafers have been made. • The oxygen concentration was controlled by high temperature rapid thermal oxidation. • Dislocation behavior in the surface area of the Si wafers has been investigated. • Rosette size decreased with increasing of interstitial oxygen atoms. • The interstitial oxygen atoms have a pinning effect of dislocations at the surface

  10. Dynamics of bacterial populations during bench-scale bioremediation of oily seawater and desert soil bioaugmented with coastal microbial mats.

    Science.gov (United States)

    Ali, Nidaa; Dashti, Narjes; Salamah, Samar; Sorkhoh, Naser; Al-Awadhi, Husain; Radwan, Samir

    2016-03-01

    This study describes a bench-scale attempt to bioremediate Kuwaiti, oily water and soil samples through bioaugmentation with coastal microbial mats rich in hydrocarbonoclastic bacterioflora. Seawater and desert soil samples were artificially polluted with 1% weathered oil, and bioaugmented with microbial mat suspensions. Oil removal and microbial community dynamics were monitored. In batch cultures, oil removal was more effective in soil than in seawater. Hydrocarbonoclastic bacteria associated with mat samples colonized soil more readily than seawater. The predominant oil degrading bacterium in seawater batches was the autochthonous seawater species Marinobacter hydrocarbonoclasticus. The main oil degraders in the inoculated soil samples, on the other hand, were a mixture of the autochthonous mat and desert soil bacteria; Xanthobacter tagetidis, Pseudomonas geniculata, Olivibacter ginsengisoli and others. More bacterial diversity prevailed in seawater during continuous than batch bioremediation. Out of seven hydrocarbonoclastic bacterial species isolated from those cultures, only one, Mycobacterium chlorophenolicum, was of mat origin. This result too confirms that most of the autochthonous mat bacteria failed to colonize seawater. Also culture-independent analysis of seawater from continuous cultures revealed high-bacterial diversity. Many of the bacteria belonged to the Alphaproteobacteria, Flavobacteria and Gammaproteobacteria, and were hydrocarbonoclastic. Optimal biostimulation practices for continuous culture bioremediation of seawater via mat bioaugmentation were adding the highest possible oil concentration as one lot in the beginning of bioremediation, addition of vitamins, and slowing down the seawater flow rate. © 2016 The Author. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.

  11. Seawater movement in the Japan Sea inferred from 14C measurement in seawater

    International Nuclear Information System (INIS)

    Otosaka, Shigeyoshi; Tanaka, Takayuki; Togawa, Orihiko; Amano, Hikaru; Aramaki, Takafumi

    2008-01-01

    Research Group for Environmental Science, JAEA has carried out oceanographic observations in the Japan Sea since 1997 to clarify the biogeochemical cycle in the Japan Sea. More than 3,000 seawater samples for measurement of radiocarbon were collected during the observations, and radiocarbon in the seawater samples was measured at AMS facility in JAEA Mutsu. In this paper, formation and circulation of water mass in the northern Japan Sea were discussed using analysis of radiocarbon and hydrographic data (e.g. salinity, temperature, nutrients). (author)

  12. Effect of medium-pressure UV-lamp treatment on disinfection by-products in chlorinated seawater swimming pool waters.

    Science.gov (United States)

    Cheema, Waqas A; Manasfi, Tarek; Kaarsholm, Kamilla M S; Andersen, Henrik R; Boudenne, Jean-Luc

    2017-12-01

    Several brominated disinfection by-products (DBPs) are formed in chlorinated seawater pools, due to the high concentration of bromide in seawater. UV irradiation is increasingly employed in freshwater pools, because UV treatment photodegrades harmful chloramines. However, in freshwater pools it has been reported that post-UV chlorination promotes the formation of other DBPs. To date, UV-based processes have not been investigated for DBPs in seawater pools. In this study, the effects of UV, followed by chlorination, on the concentration of three groups of DBPs were investigated in laboratory batch experiments using a medium-pressure UV lamp. Chlorine consumption increased following post-UV chlorination, most likely because UV irradiation degraded organic matter in the pool samples to more chlorine-reactive organic matter. Haloacetic acid (HAA) concentrations decreased significantly, due to photo-degradation, but the concentrations of trihalomethanes (THMs) and haloacetonitriles (HANs) increased with post-UV chlorination. Bromine incorporation in HAAs was significantly higher in the control samples chlorinated without UV irradiation but decreased significantly with UV treatment. Bromine incorporation was promoted in THM and HAN after UV and chlorine treatment. Overall, the accumulated bromine incorporation level in DBPs remained essentially unchanged in comparison with the control samples. Toxicity estimates increased with single-dose UV and chlorination, mainly due to increased HAN concentrations. However, brominated HANs are known in the literature to degrade following further UV treatment. Copyright © 2017 Elsevier B.V. All rights reserved.

  13. Occurrence and distribution of Polycyclic aromatic hydrocarbons (PAHs) in seawater, sediments and corals from Hainan Island, China.

    Science.gov (United States)

    Xiang, Nan; Jiang, Chunxia; Yang, Tinghan; Li, Ping; Wang, Haihua; Xie, Yanli; Li, Sennan; Zhou, Hailong; Diao, Xiaoping

    2018-05-15

    The levels of 16 US EPA priority polycyclic aromatic hydrocarbons (PAHs) were investigated in corals, ambient seawater and sediments of Hainan Island, China, using gas chromatography - mass spectrometry (GC-MS). The total PAHs (∑PAHs) concentrations ranged from 273.79 to 407.82ng/L in seawater. Besides, the concentrations of ∑PAHs in corals 333.88-727.03ng/g dw) were markedly (P corals. The highest concentration of ∑PAHs was detected at site S2 in Pavona decussate, which also bore the highest ∑PAHs levels in both seawater and sediments. The massive corals were more enriched with PAHs than the branching corals. Although 2 and 3-ring PAHs were predominant and accounted for 69.27-80.46% of the ∑PAHs in corals and ambient environment, the levels of high molecular weight (HMW) PAHs (4-6 ring) in corals also demonstrated their potential dangers for corals and organisms around coral reefs. Biota-sediment accumulation factor (BSAF) refers to an index of the pollutant absorbed by aquatic organisms from the surrounding sediments. The poor correlation between log BSAF and log K ow (hydrophobicity) indicated that PAHs in corals maybe not bioaccumulate from the ambient sediments but through pathways like absorbing from seawater, symbiosis, and feeding. Based on our data, long-term ecological monitoring in typical coral reef ecosystems combined with ecotoxicological tests of PAHs on corals is necessary to determine the impacts of PAHs on coral reefs. Copyright © 2018 Elsevier Inc. All rights reserved.

  14. Estimates of ikaite export from sea ice to the underlying seawater in a sea ice–seawater mesocosm

    Directory of Open Access Journals (Sweden)

    N.-X. Geilfus

    2016-09-01

    Full Text Available The precipitation of ikaite and its fate within sea ice is still poorly understood. We quantify temporal inorganic carbon dynamics in sea ice from initial formation to its melt in a sea ice–seawater mesocosm pool from 11 to 29 January 2013. Based on measurements of total alkalinity (TA and total dissolved inorganic carbon (TCO2, the main processes affecting inorganic carbon dynamics within sea ice were ikaite precipitation and CO2 exchange with the atmosphere. In the underlying seawater, the dissolution of ikaite was the main process affecting inorganic carbon dynamics. Sea ice acted as an active layer, releasing CO2 to the atmosphere during the growth phase, taking up CO2 as it melted and exporting both ikaite and TCO2 into the underlying seawater during the whole experiment. Ikaite precipitation of up to 167 µmolkg−1 within sea ice was estimated, while its export and dissolution into the underlying seawater was responsible for a TA increase of 64–66 µmolkg−1 in the water column. The export of TCO2 from sea ice to the water column increased the underlying seawater TCO2 by 43.5 µmolkg−1, suggesting that almost all of the TCO2 that left the sea ice was exported to the underlying seawater. The export of ikaite from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased vertical connectivity in sea ice due to the upward percolation of seawater and meltwater flushing during sea ice melt. Based on the change in TA in the water column around the onset of sea ice melt, more than half of the total ikaite precipitated in the ice during sea ice growth was still contained in the ice when the sea ice began to melt. Ikaite crystal dissolution in the water column kept the seawater pCO2 undersaturated with respect to the atmosphere in spite of increased salinity, TA and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying

  15. A new method for precise determination of iron, zinc and cadmium stable isotope ratios in seawater by double-spike mass spectrometry

    International Nuclear Information System (INIS)

    Conway, Tim M.; Rosenberg, Angela D.; Adkins, Jess F.; John, Seth G.

    2013-01-01

    Graphical abstract: ‘Metal-free’ seawater doped with varying concentrations of ‘zero’ isotope standards, processed through our simultaneous method, and then analyzed by double spike MC-ICPMS for Fe, Zn and Cd isotope ratios. All values were determined within 2 σ error (error bars shown) of zero. -- Highlights: •The first simultaneous method for isotopic analysis of Fe, Zn and Cd in seawater. •Designed for 1 L samples, a 1–20 fold improvement over previous methods. •Low blanks and high precision allow measurement of low concentration samples. •Small volume and fast processing are ideal for high-resolution large-scale studies. •Will facilitate investigation of marine trace-metal isotope cycling. -- Abstract: The study of Fe, Zn and Cd stable isotopes (δ 56 Fe, δ 66 Zn and δ 114 Cd) in seawater is a new field, which promises to elucidate the marine cycling of these bioactive trace metals. However, the analytical challenges posed by the low concentration of these metals in seawater has meant that previous studies have typically required large sample volumes, highly limiting data collection in the oceans. Here, we present the first simultaneous method for the determination of these three isotope systems in seawater, using Nobias PA-1 chelating resin to extract metals from seawater, purification by anion exchange chromatography, and analysis by double spike MC-ICPMS. This method is designed for use on only a single litre of seawater and has blanks of 0.3, 0.06 and <0.03 ng for Fe, Zn and Cd respectively, representing a 1–20 fold reduction in sample size and a 4–130 decrease in blank compared to previously reported methods. The procedure yields data with high precision for all three elements (typically 0.02–0.2‰; 1σ internal precision), allowing us to distinguish natural variability in the oceans, which spans 1–3‰ for all three isotope systems. Simultaneous extraction and purification of three metals makes this method ideal for high

  16. Non‐diluted seawater enhances nasal ciliary beat frequency and wound repair speed compared to diluted seawater and normal saline

    Science.gov (United States)

    Bonnomet, Arnaud; Luczka, Emilie; Coraux, Christelle

    2016-01-01

    Background The regulation of mucociliary clearance is a key part of the defense mechanisms developed by the airway epithelium. If a high aggregate quality of evidence shows the clinical effectiveness of nasal irrigation, there is a lack of studies showing the intrinsic role of the different irrigation solutions allowing such results. This study investigated the impact of solutions with different pH and ionic compositions, eg, normal saline, non‐diluted seawater and diluted seawater, on nasal mucosa functional parameters. Methods For this randomized, controlled, blinded, in vitro study, we used airway epithelial cells obtained from 13 nasal polyps explants to measure ciliary beat frequency (CBF) and epithelial wound repair speed (WRS) in response to 3 isotonic nasal irrigation solutions: (1) normal saline 0.9%; (2) non‐diluted seawater (Physiomer®); and (3) 30% diluted seawater (Stérimar). The results were compared to control (cell culture medium). Results Non‐diluted seawater enhanced the CBF and the WRS when compared to diluted seawater and to normal saline. When compared to the control, it significantly enhanced CBF and slightly, though nonsignificantly, improved the WRS. Interestingly, normal saline markedly reduced the number of epithelial cells and ciliated cells when compared to the control condition. Conclusion Our results suggest that the physicochemical features of the nasal wash solution is important because it determines the optimal conditions to enhance CBF and epithelial WRS thus preserving the respiratory mucosa in pathological conditions. Non‐diluted seawater obtains the best results on CBF and WRS vs normal saline showing a deleterious effect on epithelial cell function. PMID:27101776

  17. The airborne lava-seawater interaction plume at Kilauea Volcano, Hawai'i

    Science.gov (United States)

    Edmonds, M.; Gerlach, T.M.

    2006-01-01

    Lava flows into the sea at Kīlauea Volcano, Hawaiʻi, and generates an airborne gas and aerosol plume. Water (H2O), hydrogen chloride (HCl), carbon dioxide (CO2), nitrogen dioxide (NO2) and sulphur dioxide (SO2) gases were quantified in the plume in 2004–2005, using Open Path Fourier Transform infra-red Spectroscopy. The molar abundances of these species and thermodynamic modelling are used to discuss their generation. The range in molar HCl / H2O confirms that HCl is generated when seawater is boiled dry and magnesium salts are hydrolysed (as proposed by [T.M. Gerlach, J.L. Krumhansl, R.O. Fournier, J. Kjargaard, Acid rain from the heating and evaporation of seawater by molten lava: a new volcanic hazard, EOS (Trans. Am. Geophys. Un.) 70 (1989) 1421–1422]), in contrast to models of Na-metasomatism. Airborne droplets of boiled seawater brine form nucleii for subsequent H2O and HCl condensation, which acidifies the droplets and liberates CO2 gas from bicarbonate and carbonate. NO2 is derived from the thermal decomposition of nitrates in coastal seawater, which takes place as the lava heats droplets of boiled seawater brine to 350–400 °C. SO2 is derived from the degassing of subaerial lava flows on the coastal plain. The calculated mass flux of HCl from a moderate-sized ocean entry significantly increases the total HCl emission at Kīlauea (including magmatic sources) and is comparable to industrial HCl emitters in the United States. For larger lava ocean entries, the flux of HCl will cause intense local environmental hazards, such as high localised HCl concentrations and acid rain.

  18. A review of uranium extraction from seawater: Recent international research and development

    International Nuclear Information System (INIS)

    Nor Azillah Fatimah Othman; Jamaliah Sharif; Siti Fatahiyah Mohamad

    2012-01-01

    Radiation-induced grafting co-polymerization is widely used technique to produce high performance chemically active polymer materials for adsorption and separation processes on the basis of various commercial polymers available in different forms (films, fibers, resins, textiles, powders). The design and synthesis of polymer supported reagents that can selectively complex metal ions from multi-component solutions have been an important area of research during the last decades. Uranyl ions have been one of the target ions to be removed from aqueous systems. Despite the very low uranium concentration (3.3 ppb) in seawater, its total amount reaches 4 x 10 12 kg, that is equivalent to 1000 times of the mine uranium. To recover an economically significant quantity of uranium from seawater, an adsorption method using a suitable solid adsorbent seems to be feasible with regard to economical and environmental impacts. Extensive investigations of adsorbents capable of recovering uranium from seawater and aqueous systems have been carried out during the last two decades especially in Japan Atomic Energy Agency, Japan but until now, this method is not feasible for mass production. In this paper, recent international activities are summarized, on both the laboratory scale experiments and large scale marine experiments. Research and Development opportunities are discussed for improving the system performance and making the collection of uranium from seawater more economically competitive. (author)

  19. Evaluation of durability of SSCs injected with seawater

    International Nuclear Information System (INIS)

    2012-01-01

    At the units 1 to 4 in the Fukushima Daiichi Nuclear Power Plant, seawater was injected into reactor pressure vessels and spent fuel pools in order to cool down nuclear fuel is after the disaster of the 2011 off the Pacific Coast of Tohoku Earthquake and Tsunami. Therefore, for fuel cladding tubes exposed to seawater and piping items to pour seawater into a nuclear reactor, it was necessary to evaluate structural integrity under the seawater environment. And then, JNES carried out the safety research of 'Evaluation of Durability of SSCs injected with Seawater' in FY2011. The contents and the results obtained from the search are as follows; (1) For the pipes and nuclear reactor containment vessels, corrosion tests under high temperature seawater at 50degC and 80degC were carried out for the carbon steel that corrosion resistance was less. The data of relationship between a dipping time upto 1,500h and a corrosion rate were obtained as parameters at chloride ion (CI - ) content and the temperature of the seawater. As the results, the corrosion rate was almost 0.1 mm/y for the carbon steel SGV480. No significant influence of CT - content and the temperature of the seawater was confirmed. (2) Corrosion tests were carried out to obtain the relations of time and corrosion under different CI - content conditions for the simulated fuel rod specimens in seawater at 90degC for durations upto 1,200h. As the results, very little corrosion was observed on Zry-2 cladding tube. Brown rust was slightly appeared on the nut made of stainless steel and the lower tie plate made of cast stainless steel. Thinning and corrosion pit were not observed. (author)

  20. Improvement of seawater booster pump outlet check valve

    International Nuclear Information System (INIS)

    Li Xuning; Du Yansong; Huang Huimin

    2010-01-01

    Conventional island seawater booster pump set of QNPC 310 MWe unit are very important in the whole circulating cooling system, and the integrate function of seawater booster pump outlet check valve is the foundation of steady operation of the seawater booster pump set. The article mainly introduce that through the analyses to the reason to the problem that the seawater booster pump outlet check valve of QNPC 310 MWe unit appeared in past years by our team, and considering the influence of operation condition and circumstance, the team improve the seawater booster pump outlet check valve from swing check valve to shuttle check valve which operate more appropriately in the system. By the test of continuous practice, we make further modification to the inner structure of shuttle check valve contrapuntally, and therefore we solve the problem in seawater booster pump outlet check valve fundamentally which has troubled the security of system operation in past years, so we realize the aim of technical improvement and ensure that the system operate in safety and stability. (authors)

  1. An Engineering Scale Study on Radiation Grafting of Polymeric Adsorbents for Recovery of Heavy Metal Ions from Seawater

    International Nuclear Information System (INIS)

    Prasad, Tl; Saxena, Ak; Tewari, Pk; Sathiyamoorthy, D

    2009-01-01

    The ocean contains around eighty elements of the periodic table and uranium is also one among them, with a uniform concentration of 3.3 ppb and a relative abundance factor of 23. With a large coastline, India has a large stake in exploiting the 4 billion tonnes of uranium locked in seawater. The development of radiation grafting techniques, which are useful in incorporating the required functional groups, has led to more efficient adsorbent preparations in various geometrical configurations. Separation based on a polymeric adsorbent is becoming an increasingly popular technique for the extraction of trace heavy metals from seawater. Radiation grafting has provided definite advantages over chemical grafting. Studies related to thermally bonded non woven porous polypropylene fiber sheet substrate characterization and parameters to incorporate specific groups such as acrylonitrile (AN) into polymer back bones have been investigated. The grafted polyacrylonitrile chains were chemically modified to convert acrylonitrile group into an amidoxime group, a chelating group responsible for heavy metal uptake from seawater/brine. The present work has been undertaken to concentrate heavy metal ions from lean solutions from constant potential sources only. A scheme was designed and developed for investigation of the recovery of heavy metal ions such as uranium and vanadium from seawater

  2. Accurate Measurements of the Dielectric Constant of Seawater at L Band

    Science.gov (United States)

    Lang, Roger; Zhou, Yiwen; Utku, Cuneyt; Le Vine, David

    2016-01-01

    This paper describes measurements of the dielectric constant of seawater at a frequency of 1.413 GHz, the center of the protected band (i.e., passive use only) used in the measurement of sea surface salinity from space. The objective of the measurements is to accurately determine the complex dielectric constant of seawater as a function of salinity and temperature. A resonant cylindrical microwave cavity in transmission mode has been employed to make the measurements. The measurements are made using standard seawater at salinities of 30, 33, 35, and 38 practical salinity units over a range of temperatures from 0 degree C to 35 degree C in 5 degree C intervals. Repeated measurements have been made at each temperature and salinity. Mean values and standard deviations are then computed. The total error budget indicates that the real and imaginary parts of the dielectric constant have a combined standard uncertainty of about 0.3 over the range of salinities and temperatures considered. The measurements are compared with the dielectric constants obtained from the model functions of Klein and Swift and those of Meissner and Wentz. The biggest differences occur at low and high temperatures.

  3. Uptake of technetium from seawater by red abalone Haliotis rufescens

    International Nuclear Information System (INIS)

    Spies, R.B.

    1975-01-01

    Technetium accumulation from seawater by the abalone Haliotis rufescens was studied with 95 Tc. Concentration factors, uptake rates, steady state concentrations, and biological half-lives were determined experimentally for whole-body uptake. Whole-body concentration factors ranged from 135 to 205; biological half-life was 60 days. Changes in concentration factors were determined for six tissues during the uptake period. The highest activities were in the order of: digestive gland>gill>kidneys>heart>gonad>columnar muscle. Dead shells accumulated little activity compared to shells of living abalone. Gills and digestive system appear to be the routes of entry. Autoradiography shows that of the muscular tissues the outer edge of the foot and epipodium are the most active and the edible columnar muscle the least active. (author)

  4. Bacterial cell numbers and community structures of seawater biofilms depend on the attachment substratum

    KAUST Repository

    Yap, Scott A.

    2018-02-02

    Seawater is increasingly being used as a source for various industrial applications. For such applications, biofilm growth creates various problems including but not limited to pipe biocorrosion. In this study, it is hypothesized that the material type is preferred by certain bacterial populations in the seawater to attach and establish biofilms. By comparing differences in the total cell counts and microbial communities attached to high-density polyethylene (HDPE), polycarbonate, stainless steel (SS316) and titanium, the appropriate material can be used to minimize biofilm growth. All four materials have hydrophilic surfaces, but polycarbonate exhibits higher surface roughness. There were no significant differences in the cell numbers attached to polycarbonate, HDPE and titanium. Instead, there were significantly fewer cells attached to SS316. However, there was a higher relative abundance of genera associated with opportunistic pathogens on SS316. Copy numbers of genes representing Desulfobacteraceae and Desulfobulbaceae, both of which are sulfate-reducing bacteria (SRB), were approximately 10-fold higher in biofilms sampled from SS316. The enrichment of SRB in the biofilm associated with SS316 indicates that this material may be prone to biocorrosion. This study highlights the need for industries to consider the choice of material used in seawater applications to minimize microbial-associated problems.

  5. Bacterial cell numbers and community structures of seawater biofilms depend on the attachment substratum

    KAUST Repository

    Yap, Scott A.; Scarascia, Giantommaso; Hong, Pei-Ying

    2018-01-01

    Seawater is increasingly being used as a source for various industrial applications. For such applications, biofilm growth creates various problems including but not limited to pipe biocorrosion. In this study, it is hypothesized that the material type is preferred by certain bacterial populations in the seawater to attach and establish biofilms. By comparing differences in the total cell counts and microbial communities attached to high-density polyethylene (HDPE), polycarbonate, stainless steel (SS316) and titanium, the appropriate material can be used to minimize biofilm growth. All four materials have hydrophilic surfaces, but polycarbonate exhibits higher surface roughness. There were no significant differences in the cell numbers attached to polycarbonate, HDPE and titanium. Instead, there were significantly fewer cells attached to SS316. However, there was a higher relative abundance of genera associated with opportunistic pathogens on SS316. Copy numbers of genes representing Desulfobacteraceae and Desulfobulbaceae, both of which are sulfate-reducing bacteria (SRB), were approximately 10-fold higher in biofilms sampled from SS316. The enrichment of SRB in the biofilm associated with SS316 indicates that this material may be prone to biocorrosion. This study highlights the need for industries to consider the choice of material used in seawater applications to minimize microbial-associated problems.

  6. Experiences of corrosion and corrosion protection in seawater systems in the Nordic countries

    International Nuclear Information System (INIS)

    Henrikson, S.

    1985-01-01

    A summary is given of the experience of the corrosion resistance of pumps, heat exchangers, valves and pipings in different seawater cooling systems in Scandinavia, including power reactor cooling systems in Finland and Sweden. For pumps and heat exchangers the experience has been so extensive that a clear picture of today's standing can be given. Owing to scanty data concerning valves and pipes, the survey of the corrosion in these components is less well supported. Vertically extended centrifugal pumps are the pumps in general use in power plant cooling systems. To counteract corrosion on pump riser and pump casing having an organic surface coating, and on stainless steel shafts and impellers, these components should be provided with internal and external cathodic protection. For tube and plate type heat exchangers, titanium has proved to be the best material choice. Rubber-enclosed carbon steel pipings, or pipings having a thick coating of epoxy plastic, have shown very strong corrosion resistance in power plant seawater cooling systems. Valves in seawater systems have primarily been affected by corrosion due to poorly executed or damaged organic coating on cast iron. Different seawater-resistant bronzes (red bronze, tin bronze and aluminium bronze) are therefore preferable as valve materials

  7. Distributions of dissolved monosaccharides and polysaccharides in the surface microlayer and surface water of the Jiaozhou Bay and its adjacent area

    Science.gov (United States)

    Zhang, Yan-Ping; Yang, Gui-Peng; Lu, Xiao-Lan; Ding, Hai-Bing; Zhang, Hong-Hai

    2013-07-01

    Sea surface microlayer (SML) samples and corresponding bulk surface water (SW) samples were collected in the Jiaozhou Bay and its adjacent area in July and November 2008. The average concentrations of dissolved monosaccharides (MCHO) and polysaccharides (PCHO) revealed similar temporal variability, with higher concentrations during the green-tide period (in July) than during the non-green-tide period (in November). Average enrichment factors (EF) of MCHO and PCHO, defined as the ratio of the concentration in the SML to that in the SW, were 1.3 and 1.4 in July, respectively, while those values in November were 1.9 and 1.6. Our data also showed that the concentrations of MCHO and PCHO in the SML were strongly correlated with those in the SW, indicating that most of the organic materials in the SML came from the SW. The total dissolved carbohydrate concentrations (TDCHO) in the bulk surface water were closely correlated with salinity during the cruises (July: r=-0.580, n=18, P=0.01; November: r=-0.679, n=26, P<0.001), suggesting that riverine input had an important effect on the distribution of TDCHO in surface seawater of the study area.

  8. Evaluation of the leaching behavior of incineration bottom ash using seawater: A comparison with standard leaching tests.

    Science.gov (United States)

    Lin, Wenlin Yvonne; Heng, Kim Soon; Nguyen, Minh Quan; Ho, Jin Rui Ivan; Mohamed Noh, Omar Ahmad Bin; Zhou, Xue Dong; Liu, Alec; Ren, Fei; Wang, Jing-Yuan

    2017-04-01

    Batch and column tests were conducted on untreated incineration bottom ash (IBA) samples from two incineration plants in Singapore, using seawater as the leachant. The main objective of this study was to investigate the change in the leaching behavior of certain elements (i.e. As, Cd, Cr, Cu, Ni, Pb, Sb, Se and Zn) when IBA comes into contact with seawater. Such an investigation using seawater as leachant was not commonly carried out when investigating leaching behavior in IBA. The leaching tests were then carried out on the same IBA samples using DI water, as a comparison. Lower level of leaching was observed for Pb and Zn when seawater was used as the leachant. Cr and Sb showed significant cumulative release at Liquid-to-Solids (L/S) ratio 5 in the seawater column leaching. The influence of Dissolved Organic Carbon (DOC) on Cu leaching seems to decrease after L/S 2 when using seawater in the column test. Although the leaching behavior of IBA was affected when seawater was used, for the column test, there was no significant difference during the initial release when compared to DI water. The initial L/S fractions collected were important as the low L/S ratios represent the pore water concentration and the maximum output in an actual application. The results from this study would be useful for the future study on using IBA in marine applications. Copyright © 2016 Elsevier Ltd. All rights reserved.

  9. Proteolytic enzymes in seawater: contribution of prokaryotes and protists

    Science.gov (United States)

    Obayashi, Y.; Suzuki, S.

    2016-02-01

    Proteolytic enzyme is one of the major catalysts of microbial processing of organic matter in biogeochemical cycle. Here we summarize some of our studies about proteases in seawater, including 1) distribution of protease activities in coastal and oceanic seawater, 2) responses of microbial community and protease activities in seawater to organic matter amending, and 3) possible contribution of heterotrophic protists besides prokaryotes to proteases in seawater, to clarify cleared facts and remaining questions. Activities of aminopeptidases, trypsin-type and chymotrypsin-type proteases were detected from both coastal and oceanic seawater by using MCA-substrate assay. Significant activities were detected from not only particulate (cell-associated) fraction but also dissolved fraction of seawater, especially for trypsin-type and chymotrypsin-type proteases. Hydrolytic enzymes in seawater have been commonly thought to be mainly derived from heterotrophic prokaryotes; however, it was difficult to determine actual source organisms of dissolved enzymes in natural seawater. Our experiment with addition of dissolved protein to subtropical oligotrophic Pacific water showed drastically enhancement of the protease activities especially aminopeptidases in seawater, and the prokaryotic community structure simultaneously changed to be dominant of Bacteroidetes, indicating that heterotrophic bacteria were actually one of the sources of proteases in seawater. Another microcosm experiment with free-living marine heterotrophic ciliate Paranophrys marina together with an associated bacterium showed that extracellular trypsin-type activity was mainly attributed to the ciliate. The protist seemed to work in organic matter digestion in addition to be a grazer. From the results, we propose a system of organic matter digestion by prokaryotes and protists in aquatic environments, although their actual contribution in natural environments should be estimated in future studies.

  10. Sea-level rise impacts on seawater intrusion in coastal aquifers: Review and integration

    Science.gov (United States)

    Ketabchi, Hamed; Mahmoodzadeh, Davood; Ataie-Ashtiani, Behzad; Simmons, Craig T.

    2016-04-01

    Sea-level rise (SLR) influences groundwater hydraulics and in particular seawater intrusion (SWI) in many coastal aquifers. The quantification of the combined and relative impacts of influential factors on SWI has not previously been considered in coastal aquifers. In the present study, a systematic review of the available literature on this topic is first provided. Then, the potential remaining challenges are scrutinized. Open questions on the effects of more realistic complexities such as gradual SLR, parameter uncertainties, and the associated influences in decision-making models are issues requiring further investigation. We assess and quantify the seawater toe location under the impacts of SLR in combination with recharge rate variations, land-surface inundation (LSI) due to SLR, aquifer bed slope variation, and changing landward boundary conditions (LWBCs). This is the first study to include all of these factors in a single analysis framework. Both analytical and numerical models are used for these sensitivity assessments. It is demonstrated that (1) LSI caused by SLR has a significant incremental impact on the seawater toe location, especially in the flatter coasts and the flux-controlled (FC) LWBCs, however this impact is less than the reported orders of magnitude differences which were estimated using only analytical solutions; (2) LWBCs significantly influence the SLR impacts under almost all conditions considered in this study; (3) The main controlling factors of seawater toe location are the magnitudes of fresh groundwater discharge to sea and recharge rate. Regional freshwater flux entering from the landward boundary and the groundwater hydraulic gradient are the major contributors of fresh groundwater discharge to sea for both FC and head-controlled (HC) systems, respectively; (4) A larger response of the aquifer and larger seawater toe location changes are demonstrable for a larger ratio of the aquifer thickness to the aquifer length particularly in

  11. Determination of radioactive strontium in seawater

    International Nuclear Information System (INIS)

    Grahek, Zeljko; Rozmaric Macefat, Martina

    2005-01-01

    This paper describes the procedures of isolating strontium and yttrium from seawater that enable the determination of 89,90 Sr. In one procedure, strontium is directly isolated from seawater on the column filled with Sr resin by binding of strontium to the resin from 3 M HNO 3 in a seawater, and successive elution with HNO 3 . In others, strontium is precipitated from seawater with (NH 4 ) 2 CO 3 , followed by isolation on a Sr column or an anion exchange column. It is shown that strontium precipitation is optimal with concentration of 0.3 M (NH 4 ) 2 CO 3 at pH = 11. In these conditions, 100% Y, 78% Sr, 80% Ca and 50% Mg are precipitated. Strontium is bound on to Sr column from 5 to 8 M HNO 3 , separated from other elements by elution with 3 M HNO 3 and 0.05 M HNO 3 . Strontium and yttrium are bound on to anion exchange column from alcoholic solutions of nitric acid. The optimum mixture of alcohols for sample binding is a mixture of ethanol and methanol with the volume ratio 1:3. Strontium and yttrium are separated from Mg, Ca, K, and other elements by elution with 0.25 M HNO 3 in the mixture of ethanol and methanol. After the separation, yttrium and strontium are eluted from the column with water or methanol. In the procedure of direct isolation from 1 l of the sample, the average recovery of 50% was obtained. In the remaining two procedures, the strontium recovery was about 60% for the Sr column and 65% for anion exchange column. Recovery of yttrium is about 70% for the anion exchange column. It turned out that the procedure with the Sr resin (direct isolation and isolation after precipitation) is simpler and faster in the phase of the isolation on the column in comparison with the procedure with the anion exchanger. The procedure with the anion exchanger, however, enables the simultaneous isolation of yttrium and strontium and rapid determination of 89,90 Sr. These procedures were tested by determination of 89,90 Sr on liquid scintillation counter and Cherenkov

  12. Determination of diethylstilbestrol in seawater by molecularly imprinted solid-phase extraction coupled with high-performance liquid chromatography.

    Science.gov (United States)

    He, Xiuping; Mei, Xiaoqi; Wang, Jiangtao; Lian, Ziru; Tan, Liju; Wu, Wei

    2016-01-15

    An effective and highly selective molecularly imprinted material was prepared by suspension polymerization for the isolation and pre-concentration of synthetic estrogen diethylstilbestrol (DES) in seawater. The obtained MIPMs were proved to have more uniform size and porous structure, with maximum adsorption capacity of 8.43 mg g(-1) almost two times more than NIPMs (4.43 mg g(-1)). The MIPMs showed no significant deterioration of the adsorption capacity after five rounds of regeneration. An off-line molecularly imprinted solid phase extraction (MISPE) method followed by HPLC-DAD was proposed for the detection of DES in seawater, and recoveries were satisfactorily higher than 77%. Four seawater samples in aquaculture area were analyzed and 0.61 ng mL(-1) DES was detected in one sample. The result demonstrated that this method can be used for the rapid separation and clean up of trace residual of DES in seawater. Copyright © 2015 Elsevier Ltd. All rights reserved.

  13. Seawater-flooding events and impact on freshwater lenses of low-lying islands: Controlling factors, basic management and mitigation

    Science.gov (United States)

    Gingerich, Stephen B.; Voss, Clifford I.; Johnson, Adam G.

    2017-01-01

    An unprecedented set of hydrologic observations was collected after the Dec 2008 seawater-flooding event on Roi-Namur, Kwajalein Atoll, Republic of the Marshall Islands. By two days after the seawater flooding that occurred at the beginning of dry season, the observed salinity of water withdrawn by the island’s main skimming well increased to 100% seawater concentration, but by ten days later already decreased to only 10–20% of seawater fraction. However, the damaging impact on the potability of the groundwater supply (when pumped water had concentrations above 1% seawater fraction) lasted 22 months longer. The data collected make possible analyses of the hydrologic factors that control recovery and management of the groundwater-supply quality on Roi-Namur and on similar low-lying islands.With the observed data as a guide, three-dimensional numerical-model simulation analyses reveal how recovery is controlled by the island’s hydrology. These also allow evaluation of the efficacy of basic water-quality management/mitigation alternatives and elucidate how groundwater withdrawal and timing of the seawater-flooding event affect the length of recovery. Simulations show that, as might be expected, by adding surplus captured rainwater as artificial recharge, the freshwater-lens recovery period (after which potable groundwater may again be produced) can be shortened, with groundwater salinity remaining lower even during the dry season, a period during which no artificial recharge is applied. Simulations also show that the recovery period is not lengthened appreciably by groundwater withdrawals during recovery. Simulations further show that had the flooding event occurred at the start of the wet season, the recovery period would have been about 25% (5.5 months) shorter than actually occurred during the monitored flood that occurred at the dry-season start. Finally, analyses show that artificial recharge improves freshwater-lens water quality, making possible longer

  14. Seawater-flooding events and impact on freshwater lenses of low-lying islands: Controlling factors, basic management and mitigation

    Science.gov (United States)

    Gingerich, Stephen B.; Voss, Clifford I.; Johnson, Adam G.

    2017-08-01

    An unprecedented set of hydrologic observations was collected after the Dec 2008 seawater-flooding event on Roi-Namur, Kwajalein Atoll, Republic of the Marshall Islands. By two days after the seawater flooding that occurred at the beginning of dry season, the observed salinity of water withdrawn by the island's main skimming well increased to 100% seawater concentration, but by ten days later already decreased to only 10-20% of seawater fraction. However, the damaging impact on the potability of the groundwater supply (when pumped water had concentrations above 1% seawater fraction) lasted 22 months longer. The data collected make possible analyses of the hydrologic factors that control recovery and management of the groundwater-supply quality on Roi-Namur and on similar low-lying islands. With the observed data as a guide, three-dimensional numerical-model simulation analyses reveal how recovery is controlled by the island's hydrology. These also allow evaluation of the efficacy of basic water-quality management/mitigation alternatives and elucidate how groundwater withdrawal and timing of the seawater-flooding event affect the length of recovery. Simulations show that, as might be expected, by adding surplus captured rainwater as artificial recharge, the freshwater-lens recovery period (after which potable groundwater may again be produced) can be shortened, with groundwater salinity remaining lower even during the dry season, a period during which no artificial recharge is applied. Simulations also show that the recovery period is not lengthened appreciably by groundwater withdrawals during recovery. Simulations further show that had the flooding event occurred at the start of the wet season, the recovery period would have been about 25% (5.5 months) shorter than actually occurred during the monitored flood that occurred at the dry-season start. Finally, analyses show that artificial recharge improves freshwater-lens water quality, making possible longer use of

  15. A hybrid numerical model system of LCO2 and CO2 enriched seawater dynamics in the ocean induced by moving-ship releasing

    International Nuclear Information System (INIS)

    Chen, B.; Song, Y.; Ohsumi, T.; AIST, Ibaraki; Nishio, M.; Akai, M.

    2004-01-01

    A numerical modeling system has been developed, based on an engineering background, of the direct disposal of liquid carbon dioxide into the ocean by a moving-ship, to predict the physico-chemical dynamics of liquid carbon dioxide droplets and carbon dioxide enriched seawater in the ocean. This is a hybrid simulation model system consisting of a three-dimensional small-scale near-field model and a two-dimensional horizontal turbulent dispersion model. The dynamics near to release sites include double-plume creation, interaction, evolution, and coupling with ocean currents; these are described by using two-fluid large-eddy simulation technology. The further development of carbon dioxide enriched seawater, as a passive-inert scalar, in relatively larger spatial and time scales (28x28 km and up to 100 h) is then simulated by a horizontal turbulent dispersion model. For the case of liquid carbon dioxide release at a depth of 2000 m with mass flow rate of 100 kg/s and initial droplet diameter of 8.0 mm, and with ship speed of 3.0 m/s, the model predicts a vertically separated carbon dioxide enriched seawater plume, 330 m in height and 40 m in width at time about 1 h after release with a minimum pH of 6.20 corresponding to carbon dioxide concentration of 0.18 kg/m 3 , in the surrounding area. This carbon dioxide enriched seawater plume diffused turbulently in the horizontal surface to an area of 9.8x10.5 km 2 after 100 h. (author)

  16. Concentration and saturation effects of tethered polymer chains on adsorbing surfaces

    Science.gov (United States)

    Descas, Radu; Sommer, Jens-Uwe; Blumen, Alexander

    2006-12-01

    We consider end-grafted chains at an adsorbing surface under good solvent conditions using Monte Carlo simulations and scaling arguments. Grafting of chains allows us to fix the surface concentration and to study a wide range of surface concentrations from the undersaturated state of the surface up to the brushlike regime. The average extension of single chains in the direction parallel and perpendicular to the surface is analyzed using scaling arguments for the two-dimensional semidilute surface state according to Bouchaud and Daoud [J. Phys. (Paris) 48, 1991 (1987)]. We find good agreement with the scaling predictions for the scaling in the direction parallel to the surface and for surface concentrations much below the saturation concentration (dense packing of adsorption blobs). Increasing the grafting density we study the saturation effects and the oversaturation of the adsorption layer. In order to account for the effect of excluded volume on the adsorption free energy we introduce a new scaling variable related with the saturation concentration of the adsorption layer (saturation scaling). We show that the decrease of the single chain order parameter (the fraction of adsorbed monomers on the surface) with increasing concentration, being constant in the ideal semidilute surface state, is properly described by saturation scaling only. Furthermore, the simulation results for the chains' extension from higher surface concentrations up to the oversaturated state support the new scaling approach. The oversaturated state can be understood using a geometrical model which assumes a brushlike layer on top of a saturated adsorption layer. We provide evidence that adsorbed polymer layers are very sensitive to saturation effects, which start to influence the semidilute surface scaling even much below the saturation threshold.

  17. Methodological Considerations and Comparisons of Measurement Results for Extracellular Proteolytic Enzyme Activities in Seawater

    Directory of Open Access Journals (Sweden)

    Yumiko Obayashi

    2017-10-01

    Full Text Available Microbial extracellular hydrolytic enzymes that degrade organic matter in aquatic ecosystems play key roles in the biogeochemical carbon cycle. To provide linkages between hydrolytic enzyme activities and genomic or metabolomic studies in aquatic environments, reliable measurements are required for many samples at one time. Extracellular proteases are one of the most important classes of enzymes in aquatic microbial ecosystems, and protease activities in seawater are commonly measured using fluorogenic model substrates. Here, we examined several concerns for measurements of extracellular protease activities (aminopeptidases, and trypsin-type, and chymotrypsin-type activities in seawater. Using a fluorometric microplate reader with low protein binding, 96-well microplates produced reliable enzymatic activity readings, while use of regular polystyrene microplates produced readings that showed significant underestimation, especially for trypsin-type proteases. From the results of kinetic experiments, this underestimation was thought to be attributable to the adsorption of both enzymes and substrates onto the microplate. We also examined solvent type and concentration in the working solution of oligopeptide-analog fluorogenic substrates using dimethyl sulfoxide (DMSO and 2-methoxyethanol (MTXE. The results showed that both 2% (final concentration of solvent in the mixture of seawater sample and substrate working solution DMSO and 2% MTXE provide similarly reliable data for most of the tested substrates, except for some substrates which did not dissolve completely in these assay conditions. Sample containers are also important to maintain the level of enzyme activity in natural seawater samples. In a small polypropylene containers (e.g., standard 50-mL centrifugal tube, protease activities in seawater sample rapidly decreased, and it caused underestimation of natural activities, especially for trypsin-type and chymotrypsin-type proteases. In

  18. Non-diluted seawater enhances nasal ciliary beat frequency and wound repair speed compared to diluted seawater and normal saline.

    Science.gov (United States)

    Bonnomet, Arnaud; Luczka, Emilie; Coraux, Christelle; de Gabory, Ludovic

    2016-10-01

    The regulation of mucociliary clearance is a key part of the defense mechanisms developed by the airway epithelium. If a high aggregate quality of evidence shows the clinical effectiveness of nasal irrigation, there is a lack of studies showing the intrinsic role of the different irrigation solutions allowing such results. This study investigated the impact of solutions with different pH and ionic compositions, eg, normal saline, non-diluted seawater and diluted seawater, on nasal mucosa functional parameters. For this randomized, controlled, blinded, in vitro study, we used airway epithelial cells obtained from 13 nasal polyps explants to measure ciliary beat frequency (CBF) and epithelial wound repair speed (WRS) in response to 3 isotonic nasal irrigation solutions: (1) normal saline 0.9%; (2) non-diluted seawater (Physiomer®); and (3) 30% diluted seawater (Stérimar). The results were compared to control (cell culture medium). Non-diluted seawater enhanced the CBF and the WRS when compared to diluted seawater and to normal saline. When compared to the control, it significantly enhanced CBF and slightly, though nonsignificantly, improved the WRS. Interestingly, normal saline markedly reduced the number of epithelial cells and ciliated cells when compared to the control condition. Our results suggest that the physicochemical features of the nasal wash solution is important because it determines the optimal conditions to enhance CBF and epithelial WRS thus preserving the respiratory mucosa in pathological conditions. Non-diluted seawater obtains the best results on CBF and WRS vs normal saline showing a deleterious effect on epithelial cell function. © 2016 The Authors International Forum of Allergy & Rhinology, published by ARSAAOA, LLC.

  19. Rare Earth Element Distribution in the NE Atlantic: Evidence for Benthic Sources, Longevity of the Seawater Signal, and Biogeochemical Cycling

    Directory of Open Access Journals (Sweden)

    Kirsty C. Crocket

    2018-04-01

    Full Text Available Seawater rare earth element (REE concentrations are increasingly applied to reconstruct water mass histories by exploiting relative changes in the distinctive normalised patterns. However, the mechanisms by which water masses gain their patterns are yet to be fully explained. To examine this, we collected water samples along the Extended Ellett Line (EEL, an oceanographic transect between Iceland and Scotland, and measured dissolved REE by offline automated chromatography (SeaFAST and ICP-MS. The proximity to two continental boundaries, the incipient spring bloom coincident with the timing of the cruise, and the importance of deep water circulation in this climatically sensitive gateway region make it an ideal location to investigate sources of REE to seawater and the effects of vertical cycling and lateral advection on their distribution. The deep waters have REE concentrations closest to typical North Atlantic seawater and are dominated by lateral advection. Comparison to published seawater REE concentrations of the same water masses in other locations provides a first measure of the temporal and spatial stability of the seawater REE signal. We demonstrate the REE pattern is replicated for Iceland-Scotland Overflow Water (ISOW in the Iceland Basin from adjacent stations sampled 16 years previously. A recently published Labrador Sea Water (LSW dissolved REE signal is reproduced in the Rockall Trough but shows greater light and mid REE alteration in the Iceland Basin, possibly due to the dominant effect of ISOW and/or continental inputs. An obvious concentration gradient from seafloor sediments to the overlying water column in the Rockall Trough, but not the Iceland Basin, highlights release of light and mid REE from resuspended sediments and pore waters, possibly a seasonal effect associated with the timing of the spring bloom in each basin. The EEL dissolved oxygen minimum at the permanent pycnocline corresponds to positive heavy REE

  20. Direct determination of molybdenum in seawater by adsorption cathodic stripping square-wave voltammetry.

    Science.gov (United States)

    Sun, Y C; Mierzwa, J; Lan, C R

    2000-06-30

    A reliable and very sensitive procedure for the determination of trace levels of molybdenum in seawater is proposed. The complex of molybdenum with 8-hydroxyquinoline (Oxine) is analyzed by cathodic stripping square-wave voltammetry based on the adsorption collection onto a hanging mercury drop electrode (HMDE). This procedure of molybdenum determination was found to be more favorable than differential pulse cathodic stripping voltammetry because of inherently faster scan rate and much better linearity obtained through the one-peak (instead of one-of-two peaks) calibration. The variation of polarographic peak and peak current with a pH, adsorption time, adsorption potential, and some instrumental parameters such as scan rate and pulse height were optimized. The alteration of polarographic wave and its likely mechanism are also discussed. The relationship between peak current and molybdenum concentration is linear up to 150 mug l(-1). Under the optimal analytical conditions, the determination limit of 0.5 mug l(-1) Mo was reached after 60 s of the stirred collection. The estimated detection limit is better than 0.1 mug l(-1) of Mo. The applicability of this method to analysis of seawater was assessed by the determination of molybdenum in two certified reference seawater samples (CASS-2 and NASS-2) and the comparison of the analytical results for real seawater samples (study on a vertical distribution of Mo in the seawater column) with the results obtained by Zeeman-corrected electrothermal atomization atomic absorption spectrometry (Zeeman ETAAS). A good agreement between two used methods of molybdenum determination was obtained.

  1. Seawater sulfate reduction and sulfur isotope fractionation in basaltic systems: interaction of seawater with fayalite and magnetite at 200-3500C

    International Nuclear Information System (INIS)

    Shanks, W.C. III; Bischoff, J.L.; Rosenbauer, R.J.

    1981-01-01

    Sulfate reduction during seawater reaction with fayalite and with magnetite was rapid at 350 0 C, producing equilibrium assemblages of talc-pyrite-hematite-magnetite at low water/rock ratios and talc-pyrite-hematite-anhydrite at higher water/rock ratios. At 250 0 C, seawater reacting with fayalite produced detectable amounts of dissolved H 2 S. At 200 0 C, dissolved H 2 S was not detected, even after 219 days. Reaction stoichiometry indicates that sulfate reduction requires large amounts of H + , which, in subseafloor hydrothermal systems is provided by Mg metasomatism. Seawater contains sufficient Mg to supply all the H + necessary for quantitative reduction of seawater sulfate. Systematics of sulfur isotopes in the 250 and 350 0 C experiments indicate that isotopic equilibrium is reached and can be modeled as a Rayleigh distillation process. Isotopic composition of hydrothermally produced H 2 S in natural systems is strongly dependent upon the seawater/basalt ratio in the geothermal system, which controls the relative sulfide contributions from the two important sulfur sources, seawater sulfate and sulfide phases in basalt. Anhydrite precipitation during geothermal heating severely limits sulfate ingress into high temperature interaction zones. Quantitative sulfate reduction can thus be accomplished without producing strongly oxidized rocks and resultant sulfide sulfur isotope values represent a mixture of seawater and basaltic sulfur. (author)

  2. Silver Nanoparticle-Enhanced Resonance Raman Sensor of Chromium(III) in Seawater Samples.

    Science.gov (United States)

    Ly, Nguyễn Hoàng; Joo, Sang-Woo

    2015-04-29

    Tris(hydroxymethyl)aminomethane ethylenediaminetetraacetic acid (Tris-EDTA), upon binding Cr(III) in aqueous solutions at pH 8.0 on silver nanoparticles (AgNPs), was found to provide a sensitive and selective Raman marker band at ~563 cm-1, which can be ascribed to the metal-N band. UV-Vis absorption spectra also supported the aggregation and structural change of EDTA upon binding Cr(III). Only for Cr(III) concentrations above 500 nM, the band at ~563 cm-1 become strongly intensified in the surface-enhanced Raman scattering spectra. This band, due to the metal-EDTA complex, was not observed in the case of 50 mM of K+, Cd2+, Mg2+, Ca2+, Mn2+, Co2+, Na+, Cu2+, NH4+, Hg2+, Ni2+, Fe3+, Pb2+, Fe2+, and Zn2+ ions. Seawater samples containing K, Mg, Ca, and Na ion concentrations higher than 8 mM also showed the characteristic Raman band at ~563 cm-1 above 500 nM, validating our method. Our approach may be useful in detecting real water samples by means of AgNPs and Raman spectroscopy.

  3. Past seawater experience enhances seawater adaptability in medaka, Oryzias latipes.

    Science.gov (United States)

    Miyanishi, Hiroshi; Inokuchi, Mayu; Nobata, Shigenori; Kaneko, Toyoji

    2016-01-01

    During the course of evolution, fishes have acquired adaptability to various salinity environments, and acquirement of seawater (SW) adaptability has played important roles in fish evolution and diversity. However, little is known about how saline environments influence the acquirement of SW adaptability. The Japanese medaka Oryzias latipes is a euryhaline species that usually inhabits freshwater (FW), but is also adaptable to full-strength SW when transferred through diluted SW. In the present study, we examined how past SW experience affects hyposmoregulatory ability in Japanese medaka. For the preparation of SW-experienced fish, FW medaka were acclimated to SW after pre-acclimation to 1/2 SW, and the SW-acclimated fish were transferred back to FW. The SW-experienced fish and control FW fish (SW-inexperienced fish) were transferred directly to SW. Whereas control FW fish did not survive direct transfer to SW, 1/4 of SW-experienced fish adapted successfully to SW. Although there were no significant differences in blood osmolality and plasma Na(+) and Cl(-) concentrations between SW-experienced and control FW medaka in FW, increments in these parameters following SW transfer were lower in SW-experienced fish than in control FW fish. The gene expression of SW-type Na(+), K(+)-ATPase (NKA) in the gills of SW-experienced medaka increased more quickly after direct SW transfer compared with the expression in control FW fish. Prior to SW transfer, the density of NKA-immunoreactive ionocytes in the gills was higher in SW-experienced fish than in control FW fish. Ionocytes expressing CFTR Cl(-) channel at the apical membrane and those forming multicellular complexes, both of which were characteristic of SW-type ionocytes, were also increased in SW-experienced fish. These results indicate that past SW experience enhances the capacity of Na(+) and Cl(-) secretion in ionocytes and thus hypoosmoregulatory ability of Japanese medaka, suggesting the presence of epigenetic

  4. Pre-treatment of desalination feed seawater by Jordanian Tripoli, Pozzolana and Feldspar: batch experiments

    Directory of Open Access Journals (Sweden)

    AIMAN E. AL-RAWAJFEH

    2011-06-01

    Full Text Available In this research, composites of layered double hydroxide (LDH with three Jordanian natural raw materials: Tripoli (T, Pozzolana (P and Feldspar (F were prepared by co-precipitation and have been used for feed seawater pre-treatment. The data reveals that percent adsorption decreased with increase in initial concentration, but the actual amount of adsorbed ions per unit mass of LDH/T-P-F increased with increase in metal ion concentrations. The values of ΔG were negative and within 21 to 26 kJ/mol, while the values of and ΔS were positive, with ΔH within the range of 0.1 to 25 kJ/mol. The values of ΔH, ΔS and ΔG indicate the favorability of physisorption and show that the LDH/T-P-F composites have a considerable potential as adsorbents for the removal of ions from seawater.

  5. Inferring seawater temperature over the past 2,500 years in the Southern California Bight on the basis of brachiopods

    Science.gov (United States)

    Tomašových, Adam; Müller, Tamás; Kidwell, Susan M.

    2017-04-01

    Use of calcite δ18O in brachiopod shells in assessing past variations in seawater temperature remains poorly constrained in the absence of other methods due to vital effects and unknown variations in seawater density, salinity. Here, in order to evaluate past changes in seawater temperature of mainland shelf habitats off the Southern California Bight over the past 2,500 years, we analyze δ18O and Mg/Ca ratio of dead shells of the terebratulid brachiopod Laqueus erythraeus collected at 60-80 m water depths and age-dated by radiocarbon-calibrated amino acid racemization. These dead Holocene shells show excellent preservation (Mn concentrations < 10 ppm and Sr concentrations above 800 ppm). Although historical changes in sea-surface temperature in the southern California Bight were inferred on the basis of alkenones and δ18O in of planktonic foraminifers, temperature history of deeper shelf below storm wave base in this region remains unclear. First, we investigate thermal sensitivity of Mg/Ca ratio (using Laser Ablation Inductively Coupled Plasma Mass Spectrometry and wavelength-dispersive spectrometry) in the terebratulid brachiopod Laqueus erythraeus (collected in 1994 at Santa Catalina Island at 116 m water depth). At this depth, annual temperature range is relatively small (between 9-11°C), although at times of El Nino events in 1982-1983, 1986-1987, and 1992-1993, monthly temperature attained 13 °C. We find that δ18O measured along a growth profile of a shell precipitated in oxygen isotopic equilibrium with ambient seawater, and maxima in Mg/Ca ratio coincide with minima in δ18O, suggesting that fluctuations in Mg/Ca ratio trace temperature fluctuations, as observed also in other brachiopod species. Second, preliminary observations of Holocene shells show that Mg/Ca ratios show centennial-scale fluctuations but on average remain remarkably constant, with minima and maxima staying within intra-shell seasonal variations captured by extant specimens

  6. Comparison of marine dispersion model predictions with environmental radionuclide concentrations

    International Nuclear Information System (INIS)

    Johnson, C.E.; McKay, W.A.

    1988-01-01

    The comparison of marine dispersion model results with measurements is an essential part of model development and testing. The results from two residual flow models are compared with seawater concentrations, and in one case with concentrations measured in marine molluscs. For areas with short turnover times, seawater concentrations respond rapidly to variations in discharge rate and marine currents. These variations are difficult to model, and comparison with concentrations in marine animals provides an alternative and complementary technique for model validation with the advantages that the measurements reflect the mean conditions and frequently form a useful time series. (author)

  7. Uranium preconcentration from seawater using adsorptive membranes

    International Nuclear Information System (INIS)

    Das, Sadananda; Pandey, A.K.; Manchanda, V.K.; Athawale, A.A.

    2009-01-01

    Uranium recovery from bio-aggressive but lean feed like seawater is a challenging problem as it requires in situ preconcentration of uranium in presence of huge excess of competing ions with fast sorption kinetics. In our laboratory, widely used amidoxime membrane (AO-membrane) was evaluated for uranium sorption under seawater conditions. This study indicated that AO-membrane was inherently slow because of the complexation chemistry involved in transfer of U(VI) from (UO 2 (CO 3 ) 3 ) 4 - to AO sites in membrane. In order to search better options, several chemical compositions of membrane were scanned for their efficacy for uranium preconcentration from seawater, and concluded that EGMP-membrane offers several advantages over AO-membrane. In this paper, the comparison of EGMP-membrane with AO-membrane for uranium sorption under seawater conditions has been reviewed. (author)

  8. An Earth-Abundant Catalyst-Based Seawater Photoelectrolysis System with 17.9% Solar-to-Hydrogen Efficiency.

    Science.gov (United States)

    Hsu, Shao-Hui; Miao, Jianwei; Zhang, Liping; Gao, Jiajian; Wang, Hongming; Tao, Huabing; Hung, Sung-Fu; Vasileff, Anthony; Qiao, Shi Zhang; Liu, Bin

    2018-05-01

    The implementation of water splitting systems, powered by sustainable energy resources, appears to be an attractive strategy for producing high-purity H 2 in the absence of the release of carbon dioxide (CO 2 ). However, the high cost, impractical operating conditions, and unsatisfactory efficiency and stability of conventional methods restrain their large-scale development. Seawater covers 70% of the Earth's surface and is one of the most abundant natural resources on the planet. New research is looking into the possibility of using seawater to produce hydrogen through electrolysis and will provide remarkable insight into sustainable H 2 production, if successful. Here, guided by density functional theory (DFT) calculations to predict the selectivity of gas-evolving catalysts, a seawater-splitting device equipped with affordable state-of-the-art electrocatalysts composed of earth-abundant elements (Fe, Co, Ni, and Mo) is demonstrated. This device shows excellent durability and specific selectivity toward the oxygen evolution reaction in seawater with near 100% Faradaic efficiency for the production of H 2 and O 2 . Powered by a single commercial III-V triple-junction photovoltaic cell, the integrated system achieves spontaneous and efficient generation of high-purity H 2 and O 2 from seawater at neutral pH with a remarkable 17.9% solar-to-hydrogen efficiency. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. A comparison between evaporation ponds and evaporation surfaces as a source of the concentrated salt brine for salt gradient maintenance at Tajoura solar pond

    International Nuclear Information System (INIS)

    Ramadan, Abdulghani M.; Agha, Khairy R.; Abughres, M.

    2012-01-01

    One of the main problems that negatively affect the operation of salt gradient solar ponds and influence its thermal stability is the maintenance of salt gradient profile. Evaporation pond (EP) is designed to generate the salt which lost upward salt diffusion from the lower convective zone (LCZ) of the solar pond. Another attractive method is the evaporation surface facility (ES). Regions with moderate to high precipitation favor Evaporation Surface over Evaporation Ponds. Dry climates will generally favor Evaporation Ponds for the brine re-concentration. In previous studies [1-3], the authors have shown that the (EP) of Tajoura's Experimental Solar Pond (TESP) is under sized and can provide only about 30% of the salt required by a Salt Gradient Solar Pond (SGSP). The anticipated size of (EP) was estimated and presented in those studies under different design conditions, including Summer, Autumn and Spring designs, while the winter design was excluded due to the low rates of net evaporation during the winter season. In addition, the results presented were predicted for the first three years of operation. The daily variations of brine concentration in the (EP) of (TESP) and those based on different designs were predicted and discussed under different scenarios. The quantities of brine provided by the evaporation pond and that required by SGSP were predicted for both cases of surface water flushing (fresh water and sea-water) under the different design conditions as shown in Table 1. This paper investigates the differences between (EP) and (ES) both as a source for salt brine generation by evaporation. The effect of (EP) depth on the area ratio and daily variations of salt concentrations for three years of operation is shown. Results show that evaporation can be a reasonable method for salt brine generation. Reducing the depth of (EP) improves the capability of (EP) for brine re-concentration. It also increases the (EP) surface area for the same quantity of

  10. SOLUBILITIES AND PHYSICAL PROPERTIES OF SATURATED SOLUTIONS IN THE COPPER SULFATE + SULFURIC ACID + SEAWATER SYSTEM AT DIFFERENT TEMPERATURES

    OpenAIRE

    Justel, F. J.; Claros, M.; Taboada, M. E.

    2015-01-01

    Abstract In Chile, the most important economic activity is mining, concentrated in the north of the country. This is a desert region with limited water resources; therefore, the mining sector requires research and identification of alternative sources of water. One alternative is seawater, which can be a substitute of the limited fresh water resources in the region. This work determines the influence of seawater on the solid-liquid equilibrium for acid solutions of copper sulfate at different...

  11. Variations of surface ozone concentration across the Klang Valley, Malaysia

    Science.gov (United States)

    Latif, Mohd Talib; Huey, Lim Shun; Juneng, Liew

    2012-12-01

    Hourly air quality data covering the period 2004-2008 was obtained from the Air Quality Division, the Department of Environment (DOE) through long-term monitoring by Alam Sekitar Sdn. Bhd. (ASMA) were analysed to investigate the variations of surface ozone (O3) in the Klang Valley, Malaysia. A total of nine monitoring stations were selected for analysis in this study and the results show that there are distinct seasonal patterns in the surface O3 across the Klang Valley. A high surface O3 concentration is usually observed between January and April, while a low surface O3 concentration is found between June and August. Analysis of daily variations in surface O3 and the precursors - NO, NO2, CO, NMHC and UVb, indicate that the surface O3 photochemistry in this study area exhibits a positive response to the intensity and wavelength in UVb while being influenced by the concentration of NOx, particularly through tritration processes. Although results from our study suggested that NMHCs may influence the maximum O3 concentration, further investigation is required. Wind direction during different monsoons was found to influence the concentration of O3 around the Klang Valley. HYSPLIT back trajectories (-72 h) were used to indicate the air-mass transport patterns on days with high concentrations of surface O3 in the study area. Results show that 47% of the high O3 days was associated with the localized circulation. The remaining 32% and 22% were associated with mid-range and long-range transport across the South China Sea from the northeast.

  12. Primary biodegradation of petroleum hydrocarbons in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Comber, M.I.H.; Den Haan, K.H.; Djemel, N.; Eadsforth, C.V.; King, D.; Paumen, M.L.; Parkerton, T.; Dmytrasz, B.

    2012-12-15

    This report describes primary biodegradation experiments performed to determine the persistence of higher molecular weight petroleum hydrocarbons in seawater. Results from the biodegradation experiments show that the majority of tested petroleum hydrocarbons have half-lives in seawater less than 60 days.

  13. Seawater-cultured Botryococcus braunii for efficient hydrocarbon extraction.

    Directory of Open Access Journals (Sweden)

    Kenichi Furuhashi

    Full Text Available As a potential source of biofuel, the green colonial microalga Botryococcus braunii produces large amounts of hydrocarbons that are accumulated in the extracellular matrix. Generally, pretreatment such as drying or heating of wet algae is needed for sufficient recoveries of hydrocarbons from B. braunii using organic solvents. In this study, the Showa strain of B. braunii was cultured in media derived from the modified Chu13 medium by supplying artificial seawater, natural seawater, or NaCl. After a certain period of culture in the media with an osmotic pressure corresponding to 1/4-seawater, hydrocarbon recovery rates exceeding 90% were obtained by simply mixing intact wet algae with n-hexane without any pretreatments and the results using the present culture conditions indicate the potential for hydrocarbon milking.Seawater was used for efficient hydrocarbon extraction from Botryococcus braunii. The alga was cultured in media prepared with seawater or NaCl. Hydrocarbon recovery rate exceeding 90% was obtained without any pretreatment.

  14. Bacterial community structure and variation in a full-scale seawater desalination plant for drinking water production

    KAUST Repository

    Belila, Abdelaziz; El Chakhtoura, Joline; Otaibi, N.; Muyzer, G.; Gonzalez-Gil, Graciela; Saikaly, Pascal; van Loosdrecht, Mark C.M.; Vrouwenvelder, Johannes S.

    2016-01-01

    showed that bacterial species richness and diversity decreased during the seawater desalination process. The two-stage RO filtration strongly reduced the water conductivity (>99%), TOC concentration (98.5%) and total bacterial cell number (>99%), albeit

  15. Iron cycling at corroding carbon steel surfaces

    Science.gov (United States)

    Lee, Jason S.; McBeth, Joyce M.; Ray, Richard I.; Little, Brenda J.; Emerson, David

    2013-01-01

    Surfaces of carbon steel (CS) exposed to mixed cultures of iron-oxidizing bacteria (FeOB) and dissimilatory iron-reducing bacteria (FeRB) in seawater media under aerobic conditions were rougher than surfaces of CS exposed to pure cultures of either type of microorganism. The roughened surface, demonstrated by profilometry, is an indication of loss of metal from the surface. In the presence of CS, aerobically grown FeOB produced tight, twisted helical stalks encrusted with iron oxides. When CS was exposed anaerobically in the presence of FeRB, some surface oxides were removed. However, when the same FeOB and FeRB were grown together in an aerobic medium, FeOB stalks were less encrusted with iron oxides and appeared less tightly coiled. These observations suggest that iron oxides on the stalks were reduced and solubilized by the FeRB. Roughened surfaces of CS and denuded stalks were replicated with three culture combinations of different species of FeOB and FeRB under three experimental conditions. Measurements of electrochemical polarization resistance established different rates of corrosion of CS in aerobic and anaerobic media, but could not differentiate rate differences between sterile controls and inoculated exposures for a given bulk concentration of dissolved oxygen. Similarly, total iron in the electrolyte could not be used to differentiate treatments. The experiments demonstrate the potential for iron cycling (oxidation and reduction) on corroding CS in aerobic seawater media. PMID:24093730

  16. Influences of Scavenging and Removal of Surfactants by Bubble Processing on Primary Marine Aerosol Production from North Atlantic Seawater

    Science.gov (United States)

    Duplessis, P.; Chang, R.; Frossard, A. A.; Keene, W. C.; Maben, J. R.; Long, M. S.; Beaupre, S. R.; Kieber, D. J.; Kinsey, J. D.; Zhu, Y.; Lu, X.; Bisgrove, J.

    2017-12-01

    Primary marine aerosol particles (PMA) are produced by bursting bubbles from breaking waves at the air-sea interface and significantly modulate atmospheric chemical transformations and cloud properties. Surfactants in bulk seawater rapidly (seconds) adsorb onto fresh bubble surfaces forming organic films that influence size, rise velocity, bursting behavior, and associated PMA emissions. During a cruise on the R/V Endeavor in September and October 2016, PMA production from biologically productive and oligotrophic seawater was investigated at four stations in the western North Atlantic Ocean. PMA were produced in a high-capacity generator via turbulent mixing of seawater and clean air in a Venturi nozzle. When the flow of fresh seawater through the generator was turned off, surfactant depletion via bubble processing resulted in greater PMA mass production efficiencies per unit air detrained but had no consistent influence on number production efficiencies. The greater (factor of 3) production efficiencies of organic matter associated with PMA generated with the Venturi relative to those generated with frits during previous campaigns contributed to a faster depletion of surfactants from the seawater reservoir and corresponding divergence in response.

  17. Experimental investigation and modeling of dissolved organic carbon removal by coagulation from seawater.

    Science.gov (United States)

    Jeong, Sanghyun; Sathasivan, Arumugam; Kastl, George; Shim, Wang Geun; Vigneswaran, Saravanamuthu

    2014-01-01

    Coagulation removes colloidal matters and dissolved organic carbon (DOC) which can cause irreversible membrane fouling. However, how DOC is removed by coagulant is not well-known. Jar test was used to study the removal of hydrophobic and hydrophilic DOC fractions at various doses (0.5-8.0 mg-Fe(+3) L(-1)) of ferric chloride (FeCl3) and pH (5.0-9.0). Natural organic matter (NOM) in seawater and treated seawater were fractionated by liquid chromatography-organic carbon detector (LC-OCD). Compared to surface water, the removal of DOC in seawater by coagulation was remarkably different. Majority of DOC could be easily removed with very low coagulant dose (fraction (HB) was better removed at high pH while hydrophilic fraction (HF) was better removed at low pH. A modified model of Kastl et al. (2004) which assumed that the removal occurred by adsorption of un-dissociated compounds onto ferric hydroxide was formulated and successfully validated against the jar test data. Copyright © 2013 Elsevier Ltd. All rights reserved.

  18. The role of nitrite and nitrate ions as photosensitizers in the phototransformation of phenolic compounds in seawater

    Energy Technology Data Exchange (ETDEWEB)

    Calza, P., E-mail: paola.calza@unito.it [Universita degli Studi di Torino, Dipartimento di Chimica, Via P. Giuria 5, 10125 Torino (Italy); Vione, D. [Universita degli Studi di Torino, Dipartimento di Chimica, Via P. Giuria 5, 10125 Torino (Italy); Universita degli Studi di Torino, Centro Interdipartimentale NatRisk, Via Leonardo da Vinci 44, 10095 Grugliasco (Italy); Novelli, A. [Max Planck Institute for Chemistry, 55128 Mainz (Germany); Pelizzetti, E.; Minero, C. [Universita degli Studi di Torino, Dipartimento di Chimica, Via P. Giuria 5, 10125 Torino (Italy)

    2012-11-15

    Nitrite and nitrate are known to be involved in photochemical processes occurring in natural waters. In this study we have investigated the role played by these photosensitizers towards the transformation of xenobiotic organic matter in marine water, with the goal of assessing the typical transformation routes induced in seawater by irradiated nitrite/nitrate. For this purpose, phenol was chosen as model molecule. Phenol transformation was investigated under simulated solar radiation in the presence of nitrite (in the range of 1 Multiplication-Sign 10{sup -5}-1 Multiplication-Sign 10{sup -2} M) or nitrate ions, in pure water at pH 8, in artificial seawater (containing same dissolved salts as seawater but no organic matter), and in natural seawater. In all experiments, phenol degradation rate and formation of intermediates were assessed. As expected, phenol disappearance rate decreased with decreasing nitrite concentration and was slightly reduced by the presence of chloride. Other salts present in artificial seawater (e.g. HCO{sub 3}{sup -}, CO{sub 3}{sup 2-} and Br{sup -}) had a more marked effect on phenol transformation. Analysis of intermediates formed in the different matrices under study showed generation of hydroxyl-, nitro- and chloroderivatives of phenol, to a different extent depending on experimental conditions. 1,4-Benzoquinone prevailed in all cases, nitroderivatives were only formed with nitrite but were not detected in nitrate-spiked solutions. Competition was observed between halogenation and nitration of phenol, with variable outcome depending on nitrite concentration. The most likely reason is competition between nitrating and halogenating species for reaction with the phenoxyl radical. A kinetic model able to justify the occurrence of different intermediates under the adopted conditions is presented and discussed. -- Highlights: Black-Right-Pointing-Pointer Nitrite and nitrate-mediated solar-driven transformations of pollutant in seawater were

  19. The role of nitrite and nitrate ions as photosensitizers in the phototransformation of phenolic compounds in seawater

    International Nuclear Information System (INIS)

    Calza, P.; Vione, D.; Novelli, A.; Pelizzetti, E.; Minero, C.

    2012-01-01

    Nitrite and nitrate are known to be involved in photochemical processes occurring in natural waters. In this study we have investigated the role played by these photosensitizers towards the transformation of xenobiotic organic matter in marine water, with the goal of assessing the typical transformation routes induced in seawater by irradiated nitrite/nitrate. For this purpose, phenol was chosen as model molecule. Phenol transformation was investigated under simulated solar radiation in the presence of nitrite (in the range of 1 × 10 −5 –1 × 10 −2 M) or nitrate ions, in pure water at pH 8, in artificial seawater (containing same dissolved salts as seawater but no organic matter), and in natural seawater. In all experiments, phenol degradation rate and formation of intermediates were assessed. As expected, phenol disappearance rate decreased with decreasing nitrite concentration and was slightly reduced by the presence of chloride. Other salts present in artificial seawater (e.g. HCO 3 − , CO 3 2− and Br − ) had a more marked effect on phenol transformation. Analysis of intermediates formed in the different matrices under study showed generation of hydroxyl-, nitro- and chloroderivatives of phenol, to a different extent depending on experimental conditions. 1,4-Benzoquinone prevailed in all cases, nitroderivatives were only formed with nitrite but were not detected in nitrate-spiked solutions. Competition was observed between halogenation and nitration of phenol, with variable outcome depending on nitrite concentration. The most likely reason is competition between nitrating and halogenating species for reaction with the phenoxyl radical. A kinetic model able to justify the occurrence of different intermediates under the adopted conditions is presented and discussed. -- Highlights: ► Nitrite and nitrate-mediated solar-driven transformations of pollutant in seawater were studied. ► Phenol degradation rate and formation of intermediates were assessed

  20. Liquid chromatographic determination of uranium in seawater with coulometric detection

    International Nuclear Information System (INIS)

    Maekoya, Chiaki; Takata, Yoshinori

    1980-01-01

    A method of the separation with anion-exchange chromatography and of the coulometric detection of uranium in seawater was investigated. The size of the separation column used was 9 mm in inside diameter and 100 mm in length, and strong basic anion-exchange resin (Hitachi No. 2632) of carbonate form was packed in the column. A concentrator with two mini-columns in which the same resin was packed was applied for the preconcentration of uranium in seawater containing 20 g of potassium thiocyanate and 10 ml of hydrochloric acid per liter. Good result was obtained when a mixed solution of sodium carbonate (0.12 mol/l), sodium bicarbonate (0.08 mol/l), sodium bisulfite (0.03 mol/l) and sodium chloride (0.5 mol/l) was used as an eluent for the separation of uranium from vanadium. Sodium bisulfite was of use for dropping the background current based on an electrochemical reduction of dissolved oxygen. Sodium bicarbonate acted as an eliminator of an unknown peak by its bufferise effect. The optimum working electrode potential for the detection was -1.45 V vs. ferri-ferrocyanide. The detection limit was 3.2 x 10 -10 mol (80 ngU). The coefficient of variation at 3.0 ppb was about 4% (n=5) for seawater analysis. And the analysis time was approximately 1.5 hours. (author)

  1. Solid State Sensor for Simultaneous Measurement of Total Alkalinity and pH of Seawater.

    Science.gov (United States)

    Briggs, Ellen M; Sandoval, Sergio; Erten, Ahmet; Takeshita, Yuichiro; Kummel, Andrew C; Martz, Todd R

    2017-09-22

    A novel design is demonstrated for a solid state, reagent-less sensor capable of rapid and simultaneous measurement of pH and Total Alkalinity (A T ) using ion sensitive field effect transistor (ISFET) technology to provide a simplified means of characterization of the aqueous carbon dioxide system through measurement of two "master variables": pH and A T . ISFET-based pH sensors that achieve 0.001 precision are widely used in various oceanographic applications. A modified ISFET is demonstrated to perform a nanoliter-scale acid-base titration of A T in under 40 s. This method of measuring A T , a Coulometric Diffusion Titration, involves electrolytic generation of titrant, H + , through the electrolysis of water on the surface of the chip via a microfabricated electrode eliminating the requirement of external reagents. Characterization has been performed in seawater as well as titrating individual components (i.e., OH - , HCO 3 - , CO 3 2- , B(OH) 4 - , PO 4 3- ) of seawater A T . The seawater measurements are consistent with the design in reaching the benchmark goal of 0.5% precision in A T over the range of seawater A T of ∼2200-2500 μmol kg -1 which demonstrates great potential for autonomous sensing.

  2. Design Criteria, Operating Conditions, and Nickel-Iron Hydroxide Catalyst Materials for Selective Seawater Electrolysis.

    Science.gov (United States)

    Dionigi, Fabio; Reier, Tobias; Pawolek, Zarina; Gliech, Manuel; Strasser, Peter

    2016-05-10

    Seawater is an abundant water resource on our planet and its direct electrolysis has the advantage that it would not compete with activities demanding fresh water. Oxygen selectivity is challenging when performing seawater electrolysis owing to competing chloride oxidation reactions. In this work we propose a design criterion based on thermodynamic and kinetic considerations that identifies alkaline conditions as preferable to obtain high selectivity for the oxygen evolution reaction. The criterion states that catalysts sustaining the desired operating current with an overpotential seawater-mimicking electrolyte. The catalyst was synthesized by a solvothermal method and the activity, surface redox chemistry, and stability were tested electrochemically in alkaline and near-neutral conditions (borate buffer at pH 9.2) and under both fresh seawater conditions. The Tafel slope at low current densities is not influenced by pH or presence of chloride. On the other hand, the addition of chloride ions has an influence in the temporal evolution of the nickel reduction peak and on both the activity and stability at high current densities at pH 9.2. Faradaic efficiency close to 100 % under the operating conditions predicted by our design criteria was proven using in situ electrochemical mass spectrometry. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Corrosion and Protection of Metal in the Seawater Desalination

    Science.gov (United States)

    Hou, Xiangyu; Gao, Lili; Cui, Zhendong; Yin, Jianhua

    2018-01-01

    Seawater desalination develops rapid for it can solve water scarcity efficiently. However, corrosion problem in the seawater desalination system is more serious than that in normal water. So, it is important to pay attention to the corrosion and protection of metal in seawater desalination. The corrosion characteristics and corrosion types of metal in the seawater desalination system are introduced in this paper; In addition, corrosion protect methods and main influencing factors are stated, the latest new technologies about anti-corrosion with quantum energy assisted and magnetic inhibitor are presented.

  4. Simultaneous Extraction of Lithium and Hydrogen from Seawater

    Science.gov (United States)

    2011-08-22

    N00014-10-M-0234 20126083 0001AD Dr. Pyoungho Choi University of Central Florida/Florida Solar Energy Center 1679 Clearlake Road Cocoa FL 32922-5703...South America (Bolivia and Chile), Australia, and China. There have been debates as to whether the lithium supplies would meet the surging demand...extract the lithium in seawater should be developed [1]. Seawater is also the ultimate source of hydrogen. The production of hydrogen from seawater is

  5. Highly stable and magnetically separable alginate/Fe3O4 composite for the removal of strontium (Sr) from seawater.

    Science.gov (United States)

    Hong, Hye-Jin; Jeong, Hyeon Su; Kim, Byoung-Gyu; Hong, Jeongsik; Park, In-Su; Ryu, Taegong; Chung, Kang-Sup; Kim, Hyuncheol; Ryu, Jungho

    2016-12-01

    In this study, a highly stable alginate/Fe 3 O 4 composite was synthesized, and systematically investigated for the practical application of strontium (Sr) removal in complex media, such as seawater and radioactive wastewater. To overcome the drawbacks of the use of alginate microspheres, high contents of alginic acid and Fe 3 O 4 were used to provide a more rigid structure with little swelling and facile separation, respectively. The synthesized composite was optimized for particle sizes of seawater spiked with 50 mg/L of Sr, the alginate/Fe 3 O 4 composite showed 12.5 mg/g of Sr uptake, despite the highly concentrated ions in seawater. The adsorption experiment for radio-active 90 Sr revealed a removal efficiency of 67% in real seawater, demonstrating the reliability of the alginate/Fe 3 O 4 composite. Copyright © 2016 Elsevier Ltd. All rights reserved.

  6. Comparison of the partitioning behaviours of yttrium, rare earth elements, and titanium between hydrogenetic marine ferromanganese crusts and seawater

    Science.gov (United States)

    Bau, M.; Koschinsky, A.; Dulski, P.; Hein, J.R.

    1996-01-01

    In order to evaluate details of the partitioning behaviours of Y, rare earth elements (REEs), and Ti between inorganic metal oxide surfaces and seawater, we studied the distribution of these elements in hydrogenetic marine ferromanganese (Fe-Mn) crusts from the Central Pacific Ocean. Nonphosphatized Fe-Mn crusts display shale-normalized rare earths and yttrium (REYSN) patterns (Y inserted between Dy and Ho) that are depleted in light REEs (LREEs) and which show negative anomalies for YSN, and positive anomalies for LaSN, EuSN, GdSN, and in most cases, CeSN. They show considerably smaller Y/ Ho ratios than seawater or common igneous and clastic rocks, indicating that Y and Ho are fractionated in the marine environment. Compared to P-poor crusts, REYSN patterns of phosphatized Fe-Mn crusts are similar, but yield pronounced positive YSN anomalies, stronger positive LaSN anomalies, and enrichment of the HREEs relative to the MREEs. The data suggest modification of REY during phosphatization and indicate that studies requiring primary REY distributions or isotopic ratios should be restricted to nonphosphatized (layers of) Fe-Mn crusts. Apparent bulk coefficients, KMD, describing trace metal partitioning between nonphosphatized hydrogenetic Fe-Mn crusts and seawater, are similar for Pr to Eu and decrease for Eu to Yb. Exceptionally high values of KCeD, which are similar to those of Ti, result from oxidative scavenging of Ce and support previous suggestions that Ce(IV) is a hydroxide-dominated element in seawater. Yttrium and Gd show lower KD values than their respective neighbours in the REY series. Results of modelling the exchange equilibrium between REY dissolved in seawater and REY sorbed on hydrous Fe-Mn oxides corroborate previous studies that suggested the surface complexation of REY can be approximated by their first hydroxide binding constant. Negative "anomalies" occur for stabilities of bulk surface complexes of Gd, La, and particularly Y. The differences in

  7. Isotopic measurements in research on seawater ingression in the carbonate aquifer of the Salentine Peninsula, Southern Italy

    International Nuclear Information System (INIS)

    Cotecchia, V.; Tazioli, G.S.; Magri, G.

    1974-01-01

    Cretaceous calcareous and dolomitic rocks, bedded, jointed and karstified, and hence generally very permeable, form the basement of the Salentine Peninsula. These rocks constitute a huge aquifer with fresh and brackish groundwaters that float on groundwaters of marine origin. Sea level constitutes the base level of the ground waters. A basic outline is first given of the hydrogeology and the paleohydrogeology, so as to provide the necessary background information on the seawater intrusion phenomenon and to permit comparison of the results of the isotope data with those obtained by the classical methods of hydrogeological investigation. This is followed by presentation of the results of the isotopic measurements on 18 O, D, 13 C and 14 C. The δ 13 C contents indicate, in good agreement with the carbon dioxide and bicarbonate concentrations, that seawater ingression leads to the migration of carbon dioxide from the fresh and brackish waters towards the subjacent intrusive waters of marine origin. Along those stretches of coast where the seawaters are in direct communication with the groundwaters, all the isotope data point to very active renewal of groundwaters of marine origin by seawater. In the central parts of the peninsula and along those stretches of coast where direct communication between seawaters and groundwaters is impeded by impervious clays, the 14 C contents indicate that the seawater intrusion and consequently the migration of carbon dioxide are either very slow and continuous in time or that they occurred relatively rapidly in the past. Taking into consideration the paleohydrogeology of the peninsula, and the fact that the δ 18 O and δD values are higher than those of the present seawaters, leads to the belief that seawater intrusion may well have occurred during major variations in the sea level in the past, when climatic conditions were different from those now prevailing. (author)

  8. A new method for precise determination of iron, zinc and cadmium stable isotope ratios in seawater by double-spike mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Conway, Tim M., E-mail: conway.tm@gmail.com [Department of Earth and Ocean Sciences, University of South Carolina, Columbia, SC 29208 (United States); Rosenberg, Angela D. [Department of Earth and Ocean Sciences, University of South Carolina, Columbia, SC 29208 (United States); Adkins, Jess F. [California Institute of Technology, Division of Geological and Planetary Sciences, Pasadena, CA 91125 (United States); John, Seth G. [Department of Earth and Ocean Sciences, University of South Carolina, Columbia, SC 29208 (United States)

    2013-09-02

    Graphical abstract: ‘Metal-free’ seawater doped with varying concentrations of ‘zero’ isotope standards, processed through our simultaneous method, and then analyzed by double spike MC-ICPMS for Fe, Zn and Cd isotope ratios. All values were determined within 2 σ error (error bars shown) of zero. -- Highlights: •The first simultaneous method for isotopic analysis of Fe, Zn and Cd in seawater. •Designed for 1 L samples, a 1–20 fold improvement over previous methods. •Low blanks and high precision allow measurement of low concentration samples. •Small volume and fast processing are ideal for high-resolution large-scale studies. •Will facilitate investigation of marine trace-metal isotope cycling. -- Abstract: The study of Fe, Zn and Cd stable isotopes (δ{sup 56}Fe, δ{sup 66}Zn and δ{sup 114}Cd) in seawater is a new field, which promises to elucidate the marine cycling of these bioactive trace metals. However, the analytical challenges posed by the low concentration of these metals in seawater has meant that previous studies have typically required large sample volumes, highly limiting data collection in the oceans. Here, we present the first simultaneous method for the determination of these three isotope systems in seawater, using Nobias PA-1 chelating resin to extract metals from seawater, purification by anion exchange chromatography, and analysis by double spike MC-ICPMS. This method is designed for use on only a single litre of seawater and has blanks of 0.3, 0.06 and <0.03 ng for Fe, Zn and Cd respectively, representing a 1–20 fold reduction in sample size and a 4–130 decrease in blank compared to previously reported methods. The procedure yields data with high precision for all three elements (typically 0.02–0.2‰; 1σ internal precision), allowing us to distinguish natural variability in the oceans, which spans 1–3‰ for all three isotope systems. Simultaneous extraction and purification of three metals makes this method ideal

  9. Present status of uranium extraction from seawater

    International Nuclear Information System (INIS)

    Kusakabe, Katsuki; Morooka, Shigeharu

    1993-01-01

    For the research on the extraction of uranium from seawater, various processes have been examined, but the most promising process is adsorption. Its key point is the performance of the adsorbent. The system as compact as possible, in which a large quantity of seawater effectively contacts with the adsorbent, must be constructed economically. As the inorganic adsorbent, titanium oxide is the best, but organic amidoxime is superior to it. The present state of the development of the adsorbent, the rate of adsorption of the adsorbenbt, the seawater uranium adsorption system and the experiment in Imari Bay are reported. (K.I.)

  10. Acid-base responses to feeding and intestinal Cl- uptake in freshwater- and seawater-acclimated killifish, Fundulus heteroclitus, an agastric euryhaline teleost.

    Science.gov (United States)

    Wood, Chris M; Bucking, Carol; Grosell, Martin

    2010-08-01

    Marine teleosts generally secrete basic equivalents (HCO(3)(-)) and take up Na(+) and Cl(-) in the intestine so as to promote absorption of H(2)O. However, neither the integration of these functions with feeding nor the potential role of the gut in ionoregulation and acid-base balance in freshwater have been well studied. The euryhaline killifish (Fundulus heteroclitus) is unusual in lacking both an acid-secreting stomach and a mechanism for Cl(-) uptake at the gills in freshwater. Responses to a satiation meal were evaluated in both freshwater- and seawater-acclimated killifish. In intact animals, there was no change in acid or base flux to the external water after the meal, in accord with the absence of any post-prandial alkaline tide in the blood. Indeed, freshwater animals exhibited a post-prandial metabolic acidosis ('acidic tide'), whereas seawater animals showed no change in blood acid-base status. In vitro gut sac experiments revealed a substantially higher rate of Cl(-) absorption by the intestine in freshwater killifish, which was greatest at 1-3 h after feeding. The Cl(-) concentration of the absorbate was higher in preparations from freshwater animals than from seawater killifish and increased with fasting. Surprisingly, net basic equivalent secretion rates were also much higher in preparations from freshwater animals, in accord with the 'acidic tide'; in seawater preparations, they were lowest after feeding and increased with fasting. Bafilomycin (1 micromol l(-1)) promoted an 80% increase in net base secretion rates, as well as in Cl(-) and fluid absorption, at 1-3 h post-feeding in seawater preparations only, explaining the difference between freshwater and seawater fish. Preparations from seawater animals at 1-3 h post-feeding also acidified the mucosal saline, and this effect was associated with a marked rise in P(CO(2)), which was attenuated by bafilomycin. Measurements of chyme pH from intact animals confirmed that intestinal fluid (chyme) pH and

  11. Effects of seawater mixing on the mobility of trace elements in acid phosphogypsum leachates.

    Science.gov (United States)

    Papaslioti, Evgenia-Maria; Pérez-López, Rafael; Parviainen, Annika; Sarmiento, Aguasanta M; Nieto, José M; Marchesi, Claudio; Delgado-Huertas, Antonio; Garrido, Carlos J

    2018-02-01

    This research reports the effects of pH increase on contaminant mobility in phosphogypsum leachates by seawater mixing, as occurs with dumpings on marine environments. Acid leachates from a phosphogypsum stack located in the Estuary of Huelva (Spain) were mixed with seawater to achieve gradually pH7. Concentrations of Al, Fe, Cr, Pb and U in mixed solutions significantly decreased with increasing pH by sorption and/or precipitation processes. Nevertheless, this study provides insight into the high contribution of the phosphogypsum stack to the release of other toxic elements (Co, Ni, Cu, Zn, As, Cd and Sb) to the coastal areas, as 80-100% of their initial concentrations behaved conservatively in mixing solutions with no participation in sorption processes. Stable isotopes ruled out connexion between different phosphogypsum-related wastewaters and unveiled possible weathering inputs of estuarine waters to the stack. The urgency of adopting effective restoration measures in the study area is also stressed. Copyright © 2018 Elsevier Ltd. All rights reserved.

  12. Detection of silver nanoparticles in seawater at ppb levels using UV-visible spectrophotometry with long path cells.

    Science.gov (United States)

    Lodeiro, Pablo; Achterberg, Eric P; El-Shahawi, Mohammad S

    2017-03-01

    Silver nanoparticles (AgNPs) are emerging contaminants that are difficult to detect in natural waters. UV-visible spectrophotometry is a simple technique that allows detection of AgNPs through analysis of their characteristic surface plasmon resonance band. The detection limit for nanoparticles using up to 10cm path length cuvettes with UV-visible spectrophotometry is in the 0.1-10ppm range. This detection limit is insufficiently low to observe AgNPs in natural environments. Here we show how the use of capillary cells with an optical path length up to 200cm, forms an excellent technique for rapid detection and quantification of non-aggregated AgNPs at ppb concentrations in complex natural matrices such as seawater. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Seawater Carbonate Chemistry of Deep-sea Coral Beds off the Northwestern Hawaiian Islands

    Science.gov (United States)

    Brooks, J.; Shamberger, K.; Roark, E. B.; Miller, K.; Baco-Taylor, A.

    2016-02-01

    Many species of deep-sea octocorals produce calcium carbonate (CaCO3) skeletons and form coral beds that support diverse ecosystems crucial to fisheries. The geochemistry of deep-sea coral skeletons can provide valuable paleoceanographic information on ocean circulation and nutrient cycling. Deep-sea corals in the older bottom waters of the Pacific are naturally exposed to higher carbon dioxide (CO2) concentrations and lower pH than in the Atlantic where much of the previous deep-sea coral work has occurred. Therefore, some Pacific deep-sea corals may live and calcify in waters that are corrosive to their skeletons, but there have been few current seawater carbonate chemistry measurements of the waters surrounding deep-sea coral beds to assess this. The input of anthropogenic atmospheric CO2 known as ocean acidification (OA) lowers ocean pH and causes an expansion of these corrosive waters. Seawater carbonate chemistry must be characterized before accurate predictions can be made for the effects of OA on these important ecosystems. Total Alkalinity (TA) and Dissolved Inorganic Carbon (DIC) samples were collected in the fall of 2014 and 2015 from the surface to 1450 m depth off the Northwestern Hawaiian Island chain where deep-sea octocorals are found. The partial pressure of CO2 increased and pH, calcite saturation state (Ωca) and aragonite saturation state (Ωar) decreased with increasing latitude and depth. Notably, waters were undersaturated with respect to calcite and aragonite (Ωca and Ωar less than 1) below 800 m and 500 m, respectively. Therefore, deep-sea corals below these depths must calcify in waters that are thermodynamically favorable for CaCO3 dissolution. How deep-sea octocorals cope with such adverse seawater chemistry is critical to understanding future effects of OA. It is not known whether OA is currently negatively impacting deep-sea octocorals, but their naturally acidified environments could make them particularly susceptible to OA.

  14. Erythropoietin Pretreatment Attenuates Seawater Aspiration-Induced Acute Lung Injury in Rats.

    Science.gov (United States)

    Ji, Mu-Huo; Tong, Jian-Hua; Tan, Yuan-Hui; Cao, Zhen-Yu; Ou, Cong-Yang; Li, Wei-Yan; Yang, Jian-Jun; Peng, Y G; Zhu, Si-Hai

    2016-02-01

    Seawater drowning-induced acute lung injury (ALI) is a serious clinical condition characterized by increased alveolar-capillary permeability, excessive inflammatory responses, and refractory hypoxemia. However, current therapeutic options are largely supportive; thus, it is of great interest to search for alternative agents to treat seawater aspiration-induced ALI. Erythropoietin (EPO) is a multifunctional agent with antiinflammatory, antioxidative, and antiapoptotic properties. However, the effects of EPO on seawater aspiration-induced ALI remain unclear. In the present study, male rats were randomly assigned to the naive group, normal saline group, seawater group, or seawater + EPO group. EPO was administered intraperitoneally at 48 and 24 h before seawater aspiration. Arterial blood gas analysis was performed with a gas analyzer at baseline, 30 min, 1 h, 4 h, and 24 h after seawater aspiration, respectively. Histological scores, computed tomography scan, nuclear factor kappa B p65, inducible nitric oxide synthase, caspase-3, tumor necrosis factor-alpha, interleukin (IL)-1β, IL-6, IL-10, wet-to-dry weight ratio, myeloperoxidase activity, malondialdehyde, and superoxide dismutase in the lung were determined 30 min after seawater aspiration. Our results showed that EPO pretreatment alleviated seawater aspiration-induced ALI, as indicated by increased arterial partial oxygen tension and decreased lung histological scores. Furthermore, EPO pretreatment attenuated seawater aspiration-induced increase in the expressions of pulmonary nuclear factor kappa B p65, inducible nitric oxide synthase, caspase-3, tumor necrosis factor-alpha, IL-1β, myeloperoxidase activity, and malondialdehyde when compared with the seawater group. Collectively, our study suggested that EPO pretreatment attenuates seawater aspiration-induced ALI by down-regulation of pulmonary pro-inflammatory cytokines, oxidative stress, and apoptosis.

  15. Influence of seawater intrusion on microbial communities in groundwater.

    Science.gov (United States)

    Unno, Tatsuya; Kim, Jungman; Kim, Yumi; Nguyen, Son G; Guevarra, Robin B; Kim, Gee Pyo; Lee, Ji-Hoon; Sadowsky, Michael J

    2015-11-01

    Groundwater is the sole source of potable water on Jeju Island in the Republic of (South) Korea. Groundwater is also used for irrigation and industrial purposes, and it is severely impacted by seawater intrusion in coastal areas. Consequently, monitoring the intrusion of seawater into groundwater on Jeju is very important for health and environmental reasons. A number of studies have used hydrological models to predict the deterioration of groundwater quality caused by seawater intrusion. However, there is conflicting evidence of intrusion due to complicated environmental influences on groundwater quality. Here we investigated the use of next generation sequencing (NGS)-based microbial community analysis as a way to monitor groundwater quality and detect seawater intrusion. Pristine groundwater, groundwater from three coastal areas, and seawater were compared. Analysis of the distribution of bacterial species clearly indicated that the high and low salinity groundwater differed significantly with respect to microbial composition. While members of the family Parvularculaceae were only identified in high salinity water samples, a greater percentage of the phylum Actinobacteria was predominantly observed in pristine groundwater. In addition, we identified 48 shared operational taxonomic units (OTUs) with seawater, among which the high salinity groundwater sample shared a greater number of bacterial species with seawater (6.7%). In contrast, other groundwater samples shared less than 0.5%. Our results suggest that NGS-based microbial community analysis of groundwater may be a useful tool for monitoring groundwater quality and detect seawater intrusion. This technology may also provide additional insights in understanding hydrological dynamics. Copyright © 2015 Elsevier B.V. All rights reserved.

  16. Degradation of Organic UV filters in Chlorinated Seawater Swimming Pools: Transformation Pathways and Bromoform Formation.

    Science.gov (United States)

    Manasfi, Tarek; Coulomb, Bruno; Ravier, Sylvain; Boudenne, Jean-Luc

    2017-12-05

    Organic ultraviolet (UV) filters are used in sunscreens and other personal-care products to protect against harmful effects of exposure to UV solar radiation. Little is known about the fate of UV filters in seawater swimming pools disinfected with chlorine. The present study investigated the occurrence and fate of five commonly used organic UV filters, namely dioxybenzone, oxybenzone, avobenzone, 2-ethylhexyl-4-methoxycinnamate, and octocrylene, in chlorinated seawater swimming pools. Pool samples were collected to monitor the variation of UV filter concentrations during pool opening hours. Furthermore, laboratory-controlled chlorination experiments were conducted in seawater spiked with UV filters to investigate the reactivity of UV filters. Extracts of chlorination reaction samples were analyzed using high-resolution mass spectrometry and electron-capture detection to identify the potentially formed byproducts. In the collected pool samples, all the UV filters except dioxybenzone were detected. Chlorination reactions showed that only octocrylene was stable in chlorinated seawater. The four reactive UV filters generated brominated transformation products and disinfection byproducts. This formation of brominated products resulted from reactions between the reactive UV filters and bromine, which is formed rapidly when chlorine is added to seawater. Based on the identified byproducts, the transformation pathways of the reactive UV filters were proposed for the first time. Bromoform was generated by all the reactive UV filters at different yields. Bromal hydrate was also detected as one of the byproducts generated by oxybenzone and dioxybenzone.

  17. Corrosion Inhibition Study of Al-Cu-Ni Alloy in Simulated Sea-Water ...

    African Journals Online (AJOL)

    A study on the inhibition of Al-Cu-Ni alloy in simulated sea-water environment was investigated using Sodium Chromate as inhibitor. The inhibitor concentration was varied as control, 0.25, 0.5, 1.0, 1.5 and 2.0 Molar. Al-Cu-Ni alloy was sand cast into cylindrical bars of 20 mm x 300 mm dimension. The corrosion of the ...

  18. Mathematical modelling of a self-polishing antifouling paint exposed to seawater: A parameter study

    DEFF Research Database (Denmark)

    Kiil, Søren; Pedersen, M. S.; Dam-Johansen, Kim

    2002-01-01

    , and to suggest ways of controlling biocide release rates. A case study with an antifouling paint based on the well-known tributyltin self-polishing copolymer system showed that the rate of paint polishing was influenced, to various degrees, by the following parameters: seawater pH and concentration of Na...

  19. Natural Radionuclides and Heavy Metals Pollution in Seawater at Kuala Langat Coastal Area

    International Nuclear Information System (INIS)

    Sabarina Md Yunus; Zaini Hamzah; Ab Khalik Hj Wood; Ahmad Saat

    2015-01-01

    Rapid industrial developments along the Langat river basin play an important role in contributing to the increases of pollution loading at Kuala Langat coastal area. The major pollutant sources in this area may be originating from human activities such as industrial discharge, domestic sewage, construction, agriculture and pig farming near the tributaries that affects the water quality. In addition, Langat and Semenyih rivers flow through the mining and ex-mining area, which is related to the source of natural radionuclides contamination. Heavy metals in the aquatic environment and more likely to enter the food chain. This study is focusing to the levels of radionuclides and heavy metals in seawater. The samples were collected using appropriate water sampler, which is then acidified until pH 2 and filtered using cellulose acetate 0.45 μm. The concentration of these radionuclides and heavy metals were determined using Inductive Coupled Plasma Mass Spectrometer (ICPMS) after dilution. In general, the radionuclides and heavy metals concentrations are lower than Malaysia Marine Water Quality Standard (MMWQS) except for few locations where the concentration levels above the standards. The higher concentration of pollutant in the seawater may have a toxic effect on sensitive plants and living organisms. The results of pollution levels of these radionuclides and heavy metals were also compared with other studies. (author)

  20. Calibration of a degassing-emanation line for 222Rn determination in seawater samples

    International Nuclear Information System (INIS)

    Farias, Luciana Aparecida

    2002-01-01

    The purpose of this study is to calibrate a degassing-emanation line and to determine 222 Rn and 226 Ra activity concentrations in seawater samples. This methodology, also called Lucas method, consists in the extraction of radon (originally dissolved in seawater), collection of the gas in a liquid nitrogen cold trap and transfer from the trap to an alpha scintillation cell. Total extraction efficiencies of the 4 degassing-emanation systems were determined by measuring 226 Ra reference solutions. The efficiencies obtained for these 4 systems varied from 21 % to 62%. This work also presents preliminary results of a study carried out in a series of small embayements of Ubatuba, Sao Paulo State-Brazil: Flamengo Bay, Fortaleza Bay, Mar Virado Bay and Ubatuba Bay. Concentration of Rn in excess varied from 0,011 to 0,317 Bq/L for Flamengo Bay, from 0,009 to 0,130 Bq/L for Fortaleza Bay, from 0,018 to 0,050 Bq/L for Mar Virado Bay and from 0,004 to 0,120 Bq/L for Ubatuba Bay. The results obtained for the concentration of 222 Rn in excess in a transect at Flamengo Bay varied from 0,002 to 0,036 Bq/L. Higher concentrations of 222 Rn in excess were obtained in Flamengo Bay, Fortaleza Bay and Ubatuba bay. It was also observed that the concentration of 222 Rn in excess increases with depth, as expected. (author)

  1. Performance assessment of oxidants as a biocide for biofouling control in industrial seawater cooling towers

    KAUST Repository

    Al-Bloushi, Mohammed; Saththasivam, Jayaprakash; Jeong, Sanghyun; Amy, Gary L.; Leiknes, TorOve

    2017-01-01

    Biofouling can significantly hamper the efficiency of seawater cooling towers. The aim of this study was to investigate the effectiveness of alternative oxidants (i.e. ozone (O3) and chlorine dioxide (ClO2)) comparing with commonly being used chlorine in biofouling control. Effects of cycle of concentration, temperature and oxidant dosage along with residual decay and kinetics were studied. Even at lower oxidant dosage (total residual oxidant equivalent=0.1mg/L Cl2), ClO2 showed a better disinfection effect compared to chlorine and O3. Results of bench-scale studies will be helpful in the selection of appropriate oxidant for seawater cooling tower operation.

  2. Performance assessment of oxidants as a biocide for biofouling control in industrial seawater cooling towers

    KAUST Repository

    Al-Bloushi, Mohammed

    2017-10-14

    Biofouling can significantly hamper the efficiency of seawater cooling towers. The aim of this study was to investigate the effectiveness of alternative oxidants (i.e. ozone (O3) and chlorine dioxide (ClO2)) comparing with commonly being used chlorine in biofouling control. Effects of cycle of concentration, temperature and oxidant dosage along with residual decay and kinetics were studied. Even at lower oxidant dosage (total residual oxidant equivalent=0.1mg/L Cl2), ClO2 showed a better disinfection effect compared to chlorine and O3. Results of bench-scale studies will be helpful in the selection of appropriate oxidant for seawater cooling tower operation.

  3. Investigation of the strontium (Sr(II)) adsorption of an alginate microsphere as a low-cost adsorbent for removal and recovery from seawater.

    Science.gov (United States)

    Hong, Hye-Jin; Ryu, Jungho; Park, In-Su; Ryu, Taegong; Chung, Kang-Sup; Kim, Byuong-Gyu

    2016-01-01

    In this paper, we investigated alginate microspheres as a low-cost adsorbent for strontium (Sr(II)) removal and recovery from seawater. Alginate microspheres have demonstrated a superior adsorption capacity for Sr(II) ions (≈110 mg/g). A Freundlich isotherm model fits well with the Sr(II) adsorption of an alginate microsphere. The mechanism of Sr(II) adsorption is inferred as an ion exchange reaction with Ca(II) ions. The effects of the solution pH and co-existing ions in seawater are also investigated. Except for a pH of 1-2, Sr(II) adsorption capacity is not affected by pH. However, increasing the seawater concentration of metal cations seriously decreases Sr(II) uptake. In particular, highly concentrated (15,000 mg/L) Na(I) ions significantly interfere with Sr(II) adsorption. Sr(II) desorption was performed using 0.1 M HCl and CaCl2. Both regenerants show an excellent desorption efficiency, but the FTIR spectrum reveals that the chemical structure of the microsphere is destroyed after repeated use of HCl. Conversely, CaCl2 successfully desorbed Sr(II) without damage, and the Sr(II) adsorption capacity does not decrease after three repeated uses. The alginate microsphere was also applied to the adsorption of Sr(II) in a real seawater medium. Because of inhibition by co-existing ions, the Sr(II) adsorption capacity was decreased and the adsorption rate was retarded compared with D.I. water. Although the Sr(II) adsorption capacity was decreased, the alginate microsphere still exhibited 17.8 mg/g of Sr(II) uptake in the seawater medium. Considering its excellent Sr(II) uptake in seawater and its reusability, an alginate microsphere is an appropriate cost-effective adsorbent for the removal and recovery of Sr(II) from seawater. Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Mechanisms of Corrosion of Copper-Nickel Alloys in Sulfide-Polluted Seawater

    Science.gov (United States)

    1981-02-01

    anaerobic bacteria, which convert the natural sulfate content of the seawater into sulfides. Also, the putrefaction of organic compounds containing...corrosion rate bozause the Cu2 0 growth3 292 probably follows a parabolic rate law. The corrosion behavior at high oxygen concentrations (> 7.0 g/m ) is...determined using the rotating ring disk electrode method or SRI’s recently developed rotating cylinder- collector electrode.3 In these methods, the

  5. Extraction of uranium from seawater: a few facts

    Directory of Open Access Journals (Sweden)

    Guidez Joel

    2016-01-01

    Full Text Available Although uranium concentration in seawater is only about 3 micrograms per liter, the quantity of uranium dissolved in the world's oceans is estimated to amount to 4.5 billion tonnes of uranium metal (tU. In contrast, the current conventional terrestrial resource is estimated to amount to about 17 million tU. However, for a number of reasons the extraction of significant amounts of uranium from seawater remains today more a dream than a reality. Firstly, pumping the seawater to extract this uranium would need more energy than what could be produced with the recuperated uranium. Then if trying to use existing industrial flow rates, as for example on a nuclear power plant, it appears that the annual possible quantity remains very low. In fact huge quantities of water must be treated. To produce the annual world uranium consumption (around 65,000 tU, it would need at least to extract all uranium of 2 × 1013 tonnes of seawater, the volume equivalent of the entire North Sea. In fact only the great ocean currents are providing without pumping these huge quantities, and the idea is to try to extract even very partially this uranium. For example Japan, which used before the Fukushima accident about 8,000 tU by year, sees about 5.2 million tU passing every year, in the ocean current Kuro Shio in which it lies. A lot of research works have been published on the studies of adsorbents immersed in these currents. Then, after submersion, these adsorbents are chemically treated to recuperate the uranium. Final quantities remain very low in comparison of the complex and costly operations to be done in sea. One kilogram of adsorbent, after one month of submersion, yields about 2 g of uranium and the adsorbent can only be used six times due to decreasing efficiency. The industrial extrapolation exercise made for the extraction of 1,200 tU/year give with these values a very costly installation installed on more than 1000 km2 of sea with a

  6. Extraction of uranium from seawater: a few facts - 5025

    International Nuclear Information System (INIS)

    Guidez, J.; Gabriel, S.

    2015-01-01

    Although uranium concentration in seawater is only about 3 micrograms/liter, the quantity of uranium dissolved in the world's oceans is estimated to amount to 4.5 billions tonnes of uranium metal (tU). In contrast, the current conventional terrestrial resource is estimated to amount to about 17 million tU. However, for a number of reasons the extraction of significant amounts of uranium from seawater remains today more a dream than a reality. Firstly, pumping the seawater to extract this uranium would need more energy more energy than what could be produced with the recuperated uranium. Then if trying to use existing industrial flow rates, as for example on a nuclear power plant, it appears that the annual possible quantity remains very low. In fact huge quantities of water must be treated. To produce the annual world uranium consumption (around 65.000 tU), it would need at least to extract all uranium of 2*10 13 tonnes of water, the volume equivalent to the entire North Sea. In fact only the great ocean currents are providing without pumping huge quantities of seawater and the idea is to try to extract even very partially this uranium. A lot of research works have been published, on the studies of adsorbents immersed in these currents. Then, after immersion, these adsorbents are chemically treated to recuperate the uranium. Final quantities remain low in comparison of the complex and costly operations to be done in sea. One kilogram of adsorbent, after one month of immersion, yields about 2 g of uranium and the adsorbent can only be used 6 times due to decreasing efficiency. The industrial extrapolation exercise made for the extraction of 1.200 tU/year give with these values a very costly installation installed on more than 1000 km 2 of sea with a lot of boats for transportation and maintenance. The ecological management of this huge installation would present significant challenges. (authors)

  7. Green icebergs formed by freezing of organic-rich seawater to the base of Antarctic ice shelves

    Science.gov (United States)

    Warren, Stephen G.; Roesler, Collin S.; Morgan, Vincent I.; Brandt, Richard E.; Goodwin, Ian D.; Allison, Ian

    1993-01-01

    Although most icebergs are blue, green icebergs are seen occasionally in the Antarctic ocean. Chemical and isotopic analysis of samples from green icebergs indicate that the ice consists of desalinated frozen seawater, as does the basal ice from the Amery Ice Shelf. Spectral reflectance of a green iceberg measured near 67°S, 62°E, confirms that the color is inherent to the ice, not an artifact of the illumination. Pure ice appears blue owing to its absorption of red photons. Addition of a constituent that absorbs blue photons can shift the peak reflectance from blue to green. Such a constituent was identified by spectrophotometric analysis of core samples from this iceberg and from the Amery basal ice, and of seawater samples from Prydz Bay off the Amery Ice Shelf. Analysis of the samples by fluorescence spectroscopy indicates that the blue absorption, and hence the inherent green color, is due to the presence of marine-derived organic matter in the green iceberg, basal ice, and seawater. Thick accumulations of green ice, in icebergs and at the base of ice shelves, indicate that high concentrations of organic matter exist in seawater for centuries at the depth of basal freezing.

  8. An evaporated seawater origin for the ore-forming brines in unconformity-related uranium deposits (Athabasca Basin, Canada): Cl/Br and δ 37Cl analysis of fluid inclusions

    Science.gov (United States)

    Richard, Antonin; Banks, David A.; Mercadier, Julien; Boiron, Marie-Christine; Cuney, Michel; Cathelineau, Michel

    2011-05-01

    Analyses of halogen concentration and stable chlorine isotope composition of fluid inclusions from hydrothermal quartz and carbonate veins spatially and temporally associated with giant unconformity-related uranium deposits from the Paleoproterozoic Athabasca Basin (Canada) were performed in order to determine the origin of chloride in the ore-forming brines. Microthermometric analyses show that samples contain variable amounts of a NaCl-rich brine (Cl concentration between 120,000 and 180,000 ppm) and a CaCl 2-rich brine (Cl concentration between 160,000 and 220,000 ppm). Molar Cl/Br ratios of fluid inclusion leachates range from ˜100 to ˜900, with most values between 150 and 350. Cl/Br ratios below 650 (seawater value) indicate that the high salinities were acquired by evaporation of seawater. Most δ 37Cl values are between -0.6‰ and 0‰ (seawater value) which is also compatible with a common evaporated seawater origin for both NaCl- and CaCl 2-rich brines. Slight discrepancies between the Cl concentration, Cl/Br, δ 37Cl data and seawater evaporation trends, indicate that the evaporated seawater underwent secondary minor modification of its composition by: (i) mixing with a minor amount of halite-dissolution brine or re-equilibration with halite during burial; (ii) dilution in a maximum of 30% of connate and/or formation waters during its migration towards the base of the Athabasca sandstones; (iii) leaching of chloride from biotites within basement rocks and (iv) water loss by hydration reactions in alteration haloes linked to uranium deposition. The chloride in uranium ore-forming brines of the Athabasca Basin has an unambiguous dominantly marine origin and has required large-scale seawater evaporation and evaporite deposition. Although the direct evidence for evaporative environments in the Athabasca Basin are lacking due to the erosion of ˜80% of the sedimentary pile, Cl/Br ratios and δ 37Cl values of brines have behaved conservatively at the basin

  9. Satellite constraints on surface concentrations of particulate matter

    Science.gov (United States)

    Ford Hotmann, Bonne

    Because of the increasing evidence of the widespread adverse effects on human health from exposure to poor air quality and the recommendations of the World Health Organization to significantly reduce PM2.5 in order to reduce these risks, better estimates of surface air quality globally are required. However, surface measurements useful for monitoring particulate exposure are scarce, especially in developing countries which often experience the worst air pollution. Therefore, other methods are necessary to augment estimates in regions with limited surface observations. The prospect of using satellite observations to infer surface air quality is attractive; however, it requires knowledge of the complicated relationship between satellite-observed aerosol optical depth (AOD) and surface concentrations. This dissertation explores how satellite observations can be used in conjunction with a chemical transport model (GEOS-Chem) to better understand this relationship. First, we investigate the seasonality in aerosols over the Southeastern United States using observations from several satellite instruments (MODIS, MISR, CALIOP) and surface network sites (IMPROVE, SEARCH, AERONET). We find that the strong summertime enhancement in satellite-observed aerosol optical depth (factor 2-3 enhancement over wintertime AOD) is not present in surface mass concentrations (25-55% summertime enhancement). Goldstein et al. [2009] previously attributed this seasonality in AOD to biogenic organic aerosol; however, surface observations show that organic aerosol only accounts for ~35% of PM2.5 mass and exhibits similar seasonality to total surface PM2.5. The GEOS-Chem model generally reproduces these surface aerosol measurements, but under represents the AOD seasonality observed by satellites. We show that seasonal differences in water uptake cannot sufficiently explain the magnitude of AOD increase. As CALIOP profiles indicate the presence of additional aerosol in the lower troposphere

  10. Isolation and Screening of Diesel-Degrading Bacteria from the Diesel Contaminated Seawater at Kenjeran Beach, Surabaya

    Directory of Open Access Journals (Sweden)

    Pratiwi Putri Pranowo

    2016-07-01

    Full Text Available Samples of contaminated seawater by diesel were taken at Kenjeran Beach Surabaya using aseptic technique. Isolation was conducted using serial dilution and spread method on nutrient agar (NA media. The all bacteria colony were devided in to group based on with morphological characterization and gram staining. After that, those bacterial colonies were tested individually in NA media containing different concentration of diesel (2, 4, 6, 8, and 10% for up to 7 days at 30°C. The results showed that eight bacterial strains were isolated from diesel contaminated seawater in Kenjeran Beach Surabaya. Screening on diesel showed that all the isolation bacteria were capable of degrading diesel and bacteria with code of B and E haves highly percentage growth in compared to other bacterial isolation. In conclusion, bacteria with code of B and E have potential to be used in diesel bioremediation in contaminated seawater.

  11. Natural variability in the surface ocean carbonate ion concentration

    OpenAIRE

    N. S. Lovenduski; M. C. Long; K. Lindsay

    2015-01-01

    We investigate variability in the surface ocean carbonate ion concentration ([CO32−]) on the basis of a long control simulation with a fully-coupled Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical...

  12. Natural variability in the surface ocean carbonate ion concentration

    OpenAIRE

    Lovenduski, N. S.; Long, M. C.; Lindsay, K.

    2015-01-01

    We investigate variability in the surface ocean carbonate ion concentration ([CO32−]) on the basis of a~long control simulation with an Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical Pacific and ...

  13. Impregnation of sodium titanate onto DMAPAA-grafted fiber under mild reaction conditions and its strontium removal performance from seawater

    International Nuclear Information System (INIS)

    Katagiri, Mizuki; Kono, Michitaka; Goto, Shun-ichi; Kawai-Noma, Shigeko; Umeno, Daisuke; Saito, Kyoichi; Fujiwara, Kunio; Sugo, Takanobu

    2015-01-01

    Sodium titanate was impregnated onto a commercially available 6-nylon fiber by means of radiation-induced graft polymerization of dimethyaminopropyl acrylamide (DMAPAA) and subsequent chemical modifications. A peroxo complex of titanium anions was bound onto the DMAPAA-grafted fiber before the bound titanium species was converted to sodium titanate through precipitation with sodium hydroxide. Impregnation percentage of sodium titanate of the fiber was constant at 20% in the range of sodium hydroxide concentration in a mixture of methanol and water at a volume fraction of methanol of 80% of 0.001 to 1 M, whereas the removal percentage of strontium from seawater leveled off at 80% above a sodium hydroxide concentration in water of 0.1 M. Determination of adsorption isotherms in seawater demonstrates that the sodium-titanate-impregnated fiber with an impregnation percentage of 10% exhibited 2.6-fold higher amount of strontium adsorbed in seawater per g of sodium titanate (8.8 mg-Sr/g) than a commercially available granular adsorbent for strontium, SrTreat ® (3.4 mg-Sr/g). (author)

  14. Distribution and dynamics of radionuclides and stable elements in the coastal waters off Rokkasho Village, Japan, prior to the opening of a nuclear reprocessing facility. Part 3. Concentration levels of radionuclides in seawater off Rokkasho Village

    International Nuclear Information System (INIS)

    Kondo, K.; Kawabata, H.; Ueda, S.; Akata, N.; Inaba, J.; Ohmomo, Y.; Mitamura, O.; Seike, Y.

    2003-01-01

    A survey was conducted to determine the concentration levels of 3 H, 137 Cs, 90 Sr, 238,239+240 Pu, and 234,235,238 U in seawater off Rokkasho Village, Japan, before the start-up of a nuclear-fuel reprocessing plant. The level, fluctuation range and distribution characteristics of each radionuclide was determined. (author)

  15. Documentation of the seawater intrusion (SWI2) package for MODFLOW

    Science.gov (United States)

    Bakker, Mark; Schaars, Frans; Hughes, Joseph D.; Langevin, Christian D.; Dausman, Alyssa M.

    2013-01-01

    The SWI2 Package is the latest release of the Seawater Intrusion (SWI) Package for MODFLOW. The SWI2 Package allows three-dimensional vertically integrated variable-density groundwater flow and seawater intrusion in coastal multiaquifer systems to be simulated using MODFLOW-2005. Vertically integrated variable-density groundwater flow is based on the Dupuit approximation in which an aquifer is vertically discretized into zones of differing densities, separated from each other by defined surfaces representing interfaces or density isosurfaces. The numerical approach used in the SWI2 Package does not account for diffusion and dispersion and should not be used where these processes are important. The resulting differential equations are equivalent in form to the groundwater flow equation for uniform-density flow. The approach implemented in the SWI2 Package allows density effects to be incorporated into MODFLOW-2005 through the addition of pseudo-source terms to the groundwater flow equation without the need to solve a separate advective-dispersive transport equation. Vertical and horizontal movement of defined density surfaces is calculated separately using a combination of fluxes calculated through solution of the groundwater flow equation and a simple tip and toe tracking algorithm. Use of the SWI2 Package in MODFLOW-2005 only requires the addition of a single additional input file and modification of boundary heads to freshwater heads referenced to the top of the aquifer. Fluid density within model layers can be represented using zones of constant density (stratified flow) or continuously varying density (piecewise linear in the vertical direction) in the SWI2 Package. The main advantage of using the SWI2 Package instead of variable-density groundwater flow and dispersive solute transport codes, such as SEAWAT and SUTRA, is that fewer model cells are required for simulations using the SWI2 Package because every aquifer can be represented by a single layer of cells

  16. SOLUBILITIES AND PHYSICAL PROPERTIES OF SATURATED SOLUTIONS IN THE COPPER SULFATE + SULFURIC ACID + SEAWATER SYSTEM AT DIFFERENT TEMPERATURES

    Directory of Open Access Journals (Sweden)

    F. J. Justel

    2015-09-01

    Full Text Available AbstractIn Chile, the most important economic activity is mining, concentrated in the north of the country. This is a desert region with limited water resources; therefore, the mining sector requires research and identification of alternative sources of water. One alternative is seawater, which can be a substitute of the limited fresh water resources in the region. This work determines the influence of seawater on the solid-liquid equilibrium for acid solutions of copper sulfate at different temperatures (293.15 to 318.15 K, and its effect on physical properties (density, viscosity, and solubility. Knowledge of these properties and solubility data are useful in the leaching process and in the design of copper sulfate pentahydrate crystallization plants from the leaching process using seawater by means of the addition of sulfuric acid.

  17. The effect of artificial seawater on SERS spectra of amino acids-Ag colloids: An experiment of prebiotic chemistry

    Science.gov (United States)

    Nascimento, Fernanda C.; Carneiro, Cristine E. A.; Santana, Henrique de; Zaia, Dimas A. M.

    2014-01-01

    The large enhancement of signal observed in surface enhanced Raman spectroscopy (SERS) could be helpful for identifying amino acids on the surface of other planets, in particular for Mars, as well as in prebiotic chemistry experiments of interaction minerals/amino acids. This paper reports the effect of several substances (NaCl, MgCl2, KBr, CaSO4, K2SO4, MgSO4, KI, NH4Cl, SrCl2, CaCl2, Na2SO4, KOH, NaOH, H3BO3) on the SERS spectra of colloid of sodium citrate-CSC and colloid of sodium borohydride-CSB. The effect of four different artificial seawaters and these artificial seawaters plus amino acids (α-Ala-alanine, Gly-glycine, Cys-cysteine, AIB-2-aminoisobutiric acid) on SERS spectra using both CSC and CSB was also studied. For CSC, the effect of water, after dilution of the colloid, was the appearance of several absorption bands belonging to sodium citrate in the SERS spectrum. In general, artificial seawaters enhanced several bands in SERS spectra using CSC and CSB and CSC was more sensitive to those artificial seawaters than CSB. The identification of Gly, α-Ala and AIB using CSC or CSB was not possible because several bands belonging to artificial seawaters, sodium citrate or sodium borohydride were enhanced. On the other hand, artificial seawaters did not interfere in the SERS spectra of Cys using CSC or CSB, although the interaction of Cys with each colloid was different. For CSC the band at 2568 cm-1 (S-H stretching) of Cys vanished and for CSB the intensity of this band decreased, indicating the -SH of Cys was bonded to Ag to form -S-Ag. Thus SERS spectroscopy could be used for Cys detection on Mars soils using Mars land rovers as well as to study the interaction between Cys and minerals in prebiotic chemistry experiments.

  18. Control and Modelling of Seawater Desalination Using Solar Technology

    Energy Technology Data Exchange (ETDEWEB)

    Roca, L.; Yebra, L. J.; Berenguel, M.; Alarcon, D. C.

    2006-07-01

    Desalination plants play a fundamental role in fighting the shortage of fresh water in places with plentiful seawater resources. This paper briefly describes a solar desalination system designed, erected and operated in the AQUASOL project at the Plataforma Solar de Almeria (PSA), consisting basically of a CPC (Compound Parabolic Concentrator) solar collector field, two water storage tanks, a multi-effect distillation plant (MED) and a Double Effect Absorption Heat Pump (DEAHP). These subsystems have been modeled to estimate system behaviour and develop control techniques for maintaining optimal operating conditions. (Author)

  19. High Precision Seawater Sr/Ca Measurements in the Florida Keys by Inductively Coupled Plasma Atomic Emission Spectrometry: Analytical Method and Implications for Coral Paleothermometry

    Science.gov (United States)

    Khare, A.; Kilbourne, K. H.; Schijf, J.

    2017-12-01

    Standard methods of reconstructing past sea surface temperatures (SSTs) with coral skeletal Sr/Ca ratios assume the seawater Sr/Ca ratio is constant. However, there is little data to support this assumption, in part because analytical techniques capable of determining seawater Sr/Ca with sufficient accuracy and precision are expensive and time consuming. We demonstrate a method to measure seawater Sr/Ca using inductively coupled plasma atomic emission spectrometry where we employ an intensity ratio calibration routine that reduces the self- matrix effects of calcium and cancels out the matrix effects that are common to both calcium and strontium. A seawater standard solution cross-calibrated with multiple instruments is used to correct for long-term instrument drift and any remnant matrix effects. The resulting method produces accurate seawater Sr/Ca determinations rapidly, inexpensively, and with a precision better than 0.2%. This method will make it easier for coral paleoclimatologists to quantify potentially problematic fluctuations in seawater Sr/Ca at their study locations. We apply our method to test for variability in surface seawater Sr/Ca along the Florida Keys Reef Tract. We are collecting winter and summer samples for two years in a grid with eleven nearshore to offshore transects across the reef, as well as continuous samples collected by osmotic pumps at four locations adjacent to our grid. Our initial analysis of the grid samples indicates a trend of decreasing Sr/Ca values offshore potentially due to a decreasing groundwater influence. The values differ by as much as 0.05 mmol/mol which could lead to an error of 1°C in mean SST reconstructions. Future work involves continued sampling in the Florida Keys to test for seasonal and interannual variability in seawater Sr/Ca, as well as collecting data from small reefs in the Virgin Islands to test the stability of seawater Sr/Ca under different geologic, hydrologic and hydrographic environments.

  20. Determination of uranium in seawater by fluorescence spectrometry

    International Nuclear Information System (INIS)

    Kawashima, Toshi; Kawakubo, Senkichi; Minegishi, Hisako.

    1984-01-01

    A Fluorescence spectrometry for the determination of uranium in seawater has been developed. Anion exchange separation of uranium from seawater followed by preparation of NaF-carbonate cake and by spectrometry for ultraviolet ray excited fluorescence of uranium on the fluoride host provide the trace determinaton of uranium at the subnano gram level. Anion exchange behavior, excitation-emission behavior of the uranium on the host and effects of foreign ions to the fluorescence have been presented. Appling the method to 1 ml of seawater 3 ppb of uranium has been determined. (author)

  1. Ikaite solubility in seawater-derived brines at 1 atm and sub-zero temperatures to 265 K

    Science.gov (United States)

    Papadimitriou, Stathys; Kennedy, Hilary; Kennedy, Paul; Thomas, David N.

    2013-05-01

    The concentration-based (stoichiometric) equilibrium solubility product of ikaite (CaCO3·6H2O) in seawater and cryogenic seawater-derived brines was determined at 1 atm total pressure over the temperature range from -1.1 to -7.5 °C and the salinity range from 34 to 124 in temperature-salinity pairs representative of sea ice brines. The solubility measurements were obtained in solutions that were undersaturated and supersaturated with respect to ikaite by equilibration with CO2/N2 gas mixtures of known pCO2 (20-400 μatm). The solutions were then equilibrated with synthetic ikaite (seed) for up to 3 months in a closed system. Arrival of the solid-solution system at a long-term chemical equilibrium was indicated by attainment of constant chemical solution composition with respect to total dissolved calcium, total dissolved inorganic carbon, and total alkalinity. Using these measurements, the stoichiometric equilibrium solubility product of ikaite (Ksp,ikaite∗=[Ca][CO32-], in molkgsolution-2) was determined, with the carbonate ion concentration computed from the measured total alkalinity and total dissolved inorganic carbon concentrations. The computed carbonate ion concentration and, by extension, the Ksp,ikaite∗ are both contingent on solving the system of equations that describe the parameters of the CO2 system in seawater by extrapolation to the experimental salinity and temperature conditions. The results show that the pKsp,ikaite∗=-logKsp,ikaite∗ in seawater of salinity 34 at -1.1 °C was 5.362 ± 0.004 and that the pKsp,ikaite∗ in sea ice at the freezing point of brines of salinity greater than 34 can be described as a function of temperature (T, in K) by the equation, pKsp,ikaite∗=-15489.09608+623443.70216T-1+2355.14596lnT, in the temperature range of 265.15 K 1 month) approach to chemical equilibrium when incubated without seeding ikaite crystals. Simple modeling indicated that ikaite should not precipitate from sea ice brines evolving under

  2. Biologically mediated dissolution of volcanic glass in seawater

    NARCIS (Netherlands)

    Staudigel, H; Yayanos, A; Chastain, R; Davies, G.T.; Verdurmen, E.A Th; Schiffmann, P; Bourcier, R; de Baar, H.J.W.

    1998-01-01

    We studied the effects of biological mediation on the dissolution of basaltic glass in seawater. Experiments with typical seawater microbial populations were contrasted with a sterile control, and reactions were monitored chemically and isotopically. Biologically mediated experiments produce twice

  3. Metal distributions in complexes with Chlorella vulgaris in seawater and wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Pascucci, P.R.; Kowalak, A.D.

    1999-10-01

    Divalent cadmium (Cd), copper (Cu), iron (Fe), nickel (Ni), lead (Pb), and zinc (Zn) simultaneous complexes with an algal biomass Chlorella vulgaris were studied for bioremediation purposes in various aqueous media: distilled-deionized water (DDIW), seawater, nuclear-reactor pool water, and process wastewater. Reactions were monitored using various dry masses of algae at constant temperature and constant metal concentrations for reaction times ranging from 0 to 150 minutes. Complexes occurred within 30 minutes and reached a steady state after 80 to 120 minutes. Distribution constants (K{prime}{sub d}) were calculated for the complexes and relative orders of K{prime}{sub d} were reported. The K{prime}{sub d} are used to evaluate relative efficiency of metal remediation from waters. Lead, Cu, and Ni complexes had the greatest K{prime}{sub d} values and those metals were most efficiently removed from these waters. Zinc and Fe formed the most labile complexes. The order of K{prime}{sub d} values for complexes in DDIW was Pb > Cu > Cd > Zn, then Cu > Cd > Zn in seawater, Cd > Cu > Zn in reactor pool water, and Ni > Cd > Cu > Zn > Fe in wastewater. C. vulgaris biomass may potentially be used as an alternative to traditional water treatment methods for simultaneous extraction of metals from seawater, process wastewater, or drinking water.

  4. Neodymium isotopic variations in seawater

    Science.gov (United States)

    Piepgras, D. J.; Wasserburg, G. J.

    1980-01-01

    Direct measurement of the isotopic composition of Nd in the Atlantic agree with the Nd content in ferromanganese sediments and differ from the observed amounts in the Pacific samples. These data indicate the existence of distinctive differences in the isotopic composition of Nd in the waters of major oceans; the average values determined from seawater and ferromanganese sediments are considerably lower than in sources with oceanic mantle affinities showing that the REE in the oceans is dominated by continental sources. The Nd isotopic variations in seawater are applied to relate the residence time of Nd and mixing rates between the oceans.

  5. Seawater intrusion mapping using electrical resistivity tomography and hydrochemical data. An application in the coastal area of eastern Thermaikos Gulf, Greece.

    Science.gov (United States)

    Kazakis, N; Pavlou, A; Vargemezis, G; Voudouris, K S; Soulios, G; Pliakas, F; Tsokas, G

    2016-02-01

    The aim of this study was to determine the extent and geometrical characteristics of seawater intrusion in the coastal aquifer of the eastern Thermaikos Gulf, Greece. Hydrochemical data and geoelectrical measurements were combined and supplemented to determine the hydrochemical regime of the study site in regard to seawater phenomena. Chemical analysis of groundwater was performed in 126 boreholes and fifteen electrical resistivity tomographies (ERT) were measured, whereas in two sites the ERT measurements were repeated following the wet season. The Cl(-) concentrations recorded reached 2240 mg/L indicating seawater intrusion which was also verified by ionic ratios. The ionic ratios were overlapped and a seawater intrusion map (SWIM) was produced. A significant part of the coastal aquifer (up to 150 km(2)) is influenced by seawater intrusion. The areas with the most intensive salinization are located between Nea Kallikratia-Epanomi and Aggelochori-Peraia. According to the ERTs, in the influenced areas the salinization of the aquifer exceeds 1 km toward the mainland and its depth reaches 200 m. In the area surrounding Thessaloniki airport, the ERTs revealed salinization of the upper aquifer to depths of up to 40 m, whereas the lower aquifer is uninfluenced. This abnormal distribution of seawater intrusion demonstrates the value of geoelectrical methods in the study of seawater intrusion especially in areas with limited available hydrochemical data. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Application of micro-solid-phase extraction for the on-site extraction of heterocyclic aromatic amines in seawater.

    Science.gov (United States)

    Basheer, Chanbasha

    2018-04-01

    An efficient on-site extraction technique to determine carcinogenic heterocyclic aromatic amines in seawater has been reported. A micro-solid-phase extraction device placed inside a portable battery-operated pump was used for the on-site extraction of seawater samples. Before on-site applications, parameters that influence the extraction efficiency (extraction time, type of sorbent materials, suitable desorption solvent, desorption time, and sample volume) were investigated and optimized in the laboratory. The developed method was then used for the on-site sampling of heterocyclic aromatic amines determination in seawater samples close to distillation plant. Once the on-site extraction completed, the small extraction device with the analytes was brought back to the laboratory for analysis using high-performance liquid chromatography with fluorescence detection. Based on the optimized conditions, the calibration curves were linear over the concentration range of 0.05-20 μg/L with correlation coefficients up to 0.996. The limits of detection were 0.004-0.026 μg/L, and the reproducibility values were between 1.3 and 7.5%. To evaluate the extraction efficiency, a comparison was made with conventional solid-phase extraction and it was applied to various fortified real seawater samples. The average relative recoveries obtained from the spiked seawater samples varied in the range 79.9-95.2%. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. New Dielectric Measurement Data to Determine the Permittivity of Seawater at 1.4313 Hz

    Science.gov (United States)

    Lang, R.; Zhou, Y.; Utku, C.; Levine, D.

    2012-01-01

    This paper describes the new measurements - made in 2010-2011 - of the dielectric constant of seawater at 1.413 GHz using a resonant cavity technique. The purpose of these measurements is to develop an accurate relationship concerning the dependence of the dielectric constant of seawater on temperature and salinity for use by the Aquarius inversion algorithm. Aquarius is a NASA/CONAE satellite mission launched in June of 2011 with the primary mission of measuring global sea surface salinity with a 1.413 GHz radiometer to an accuracy of 0.2 psu. A brass microwave cavity resonant at 1.413 GHz has been used to measure the dielectric constant of seawater. The seawater is introduced into the cavity through a capillary glass tube having an inner diameter of 0.1 mm. The change of resonant frequency and the cavity Q value are used to determine the real and imaginary parts of the dielectric constant of seawater. Measurements are automated with Visual Basic software developed at the George Washington University. In this paper, new results from measurements made since September 2010 will be presented for salinities of 30, 35 and 38 psu with a temperature range of 0 C to 35 C in intervals of 5 C. These measurements are more accurate than earlier measurements made in 2008. The new results will be compared to the Klein-Swift (KS) and Meissner-Wentz (MW) model functions. The importance of an accurate model function will be illustrated by using these model functions to invert the Aquarius brightness temperature to retrieve the salinity values. The salinity values will be compared to co-located in situ data collected by Argo buoys.

  8. Factors affecting seawater-based pretreatment of lignocellulosic date palm residues

    DEFF Research Database (Denmark)

    Fang, Chuanji; Thomsen, Mette Hedegaard; Frankaer, Christian Grundahl

    2017-01-01

    Seawater-based pretreatment of lignocellulosic biomass is an innovative process at research stage. With respect to process optimization, factors affecting seawater-based pretreatment of lignocellulosic date palm residues were studied for the first time in this paper. Pretreatment temperature (180...... °C–210 °C), salinity of seawater (0 ppt–50 ppt), and catalysts (H2SO4, Na2CO3, and NaOH) were investigated. The results showed that pretreatment temperature exerted the largest influence on seawater-based pretreatment in terms of the enzymatic digestibility and fermentability of pretreated solids...

  9. Weekly variability of surface CO concentrations in Moscow

    Science.gov (United States)

    Sitnov, S. A.; Adiks, T. G.

    2014-03-01

    Based on observations of carbon monoxide (CO) concentrations at three Mosekomonitoring stations, we have analyzed the weekly cycle of CO in the surface air of Moscow in 2004-2007. At all stations the minimum long-term mean daily CO values are observed on Sunday. The weekly cycle of CO more clearly manifests itself at the center of Moscow and becomes less clear closer to the outskirts. We have analyzed the reproducibility of the weekly cycle of CO from one year to another, the seasonal dependence, its specific features at different times of day, and the changes in the diurnal cycle of CO during the week. The factors responsible for specific features of the evolution of surface CO concentrations at different observation stations have been analyzed. The empirical probability density functions of CO concentrations on weekdays and at week- end are presented. The regularity of the occurrence of the weekend effect in CO has been investigated and the possible reasons for breaks in weekly cycles have been analyzed. The Kruskal-Wallis test was used to study the statistical significance of intraweek differences in surface CO contents.

  10. Determination of Cobalt in Seawater Using Neutron Activation Analysis after Preconcentration by Adsorption onto γ-MnO2 Nanomaterial

    Directory of Open Access Journals (Sweden)

    Van-Phuc Dinh

    2018-01-01

    Full Text Available The γ-MnO2 nanomaterial has been used to adsorb cobalt in the seawater at Phan Thiet City, Binh Thuan Province, Vietnam. Its concentration is determined by using the neutron activation analysis (NAA method at the Dalat nuclear research reactor. Factors affecting the uptake of cobalt on the γ-MnO2 material such as the pH, adsorption time, and initial cobalt(II concentration are investigated. The irradiated experiment data are calculated using the K0-Dalat program. The results obtained show that the trace dissolved cobalt in Phan Thiet seawater is found equal to 0.25 ± 0.04 μg/L (n=5, P=95% with the adsorption efficiency being higher than 95% (n=4, P=95%.

  11. Analysis of molybdenum, tungsten, and vanadium in surface water of the Atlantic Ocean using solid phase extraction with 8-hydroxyquinoline and ICP MS determination

    Science.gov (United States)

    Rimskaya-Korsakova, M. N.; Berezhnaya, E. D.; Dubinin, A. V.

    2017-07-01

    An analytical technique is proposed to determine ultratrace concentrations of Mo, V, and W found in seawater using mass spectrometry with inductively coupled plasma (ICP MS) after preliminary concentration by solid-phase extraction of metal complexes with 8-hydroxyquinoline (8-HQ) on C18 octadecyl silica. The technique utilizes 150 mL of a water sample. A preconcentration factor 50 is obtained. The detection limits are 0.25 nmol/kg, 0.041 nmol/kg, and 5 pmol/kg for Mo, V, and W, respectively. Dissolved Mo, V, and Wconcentrations in surface seawater from Atlantic Ocean transect were determined. The concentrations ranges along the transect were: 91-108 nmol/kg for Mo, 28-35 nmol/kg for V, and 55-75 pmol/kg for W. The Mo/W ratio varied from 1300 to 1800.

  12. Analyzing the Propagation Behavior of a Gaussian Laser Beam through Seawater and Comparing with Atmosphere

    Directory of Open Access Journals (Sweden)

    F Dabbagh Kashani

    2013-12-01

    Full Text Available Study of the beam propagation behavior through oceanic media is a challenging subject. In this paper, based on generalized Collins integral, the mean irradiance profile of Gaussian laser beam propagation through ocean is investigated. Power In Special Bucket (PIB is calculated. Using analytical expressions and calculating seawater transmission, the effects of absorption and scattering on beam propagation are studied. Based on these formulae, propagation in ocean and atmosphere are compared. The effects of some optical and environmental specifications, such as divergence angle and chlorophyll concentration in seawater on beam propagation by using mean irradiance, PIB and analytical formula of oceanic transmission are studied. The calculated results are shown graphically.

  13. Isolation of microplastics in biota-rich seawater samples and marine organisms

    Science.gov (United States)

    Cole, Matthew; Webb, Hannah; Lindeque, Pennie K.; Fileman, Elaine S.; Halsband, Claudia; Galloway, Tamara S.

    2014-01-01

    Microplastic litter is a pervasive pollutant present in aquatic systems across the globe. A range of marine organisms have the capacity to ingest microplastics, resulting in adverse health effects. Developing methods to accurately quantify microplastics in productive marine waters, and those internalized by marine organisms, is of growing importance. Here we investigate the efficacy of using acid, alkaline and enzymatic digestion techniques in mineralizing biological material from marine surface trawls to reveal any microplastics present. Our optimized enzymatic protocol can digest >97% (by weight) of the material present in plankton-rich seawater samples without destroying any microplastic debris present. In applying the method to replicate marine samples from the western English Channel, we identified 0.27 microplastics m−3. The protocol was further used to extract microplastics ingested by marine zooplankton under laboratory conditions. Our findings illustrate that enzymatic digestion can aid the detection of microplastic debris within seawater samples and marine biota. PMID:24681661

  14. Tritium analysis in environmental samples around Nuclear Power Plants and nationwide surveillance of radionuclides in some environmental samples(meat and drinking water)

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Yong Woo; Han, Man Jung; Cho, Seong Won; Cho, Hong Jun; Oh, Hyeon Kyun; Lee, Jeong Min; Chang, Jae Sook [KORTIC, Taejon (Korea, Republic of)

    2001-12-15

    12 kind of environmental samples such as soil, underground water, seawater, etc. around the Nuclear Power Plants(NPP) and surface seawater around the Korea peninsula were sampled, For the samples of rain, pine-needle, air, seawater, underground water, chinese cabbage, grain of rice and milk sampled around NPP, and surface seawater and rain sampled all around country, tritium concentration was measured, The tritium concentration in the tap water and the gamma activity in the domestic and imported beef that were sampled at ward in the large city in Korea(Seoul, Pusan, Taegu, Taejun, Inchun, Kwangju) were analyzed for the meat and drinking waters. As the results of analyzing, tritium concentration in rain and tap water were very low all around country, but a little higher around the NPP than general surrounding. At the Wolsung NPP, tritium concentration was descend according to distance from the stack. Tritium activity of surface seawater around the Korea peninsula was also, very low. The measured radioactive elements in the beef is the same as the radioactive elements on the earth surface.

  15. Stability of cyanotoxins, microcystin-LR, microcystin-RR and nodularin in seawater and BG-11 medium of different salinity

    Directory of Open Access Journals (Sweden)

    Hanna Mazur

    2001-09-01

    Full Text Available Microcystins and nodularin are potent hepatotoxins produced by fresh and seawater cyanobacteria. The persistence of three hepatotoxins - microcystin-LR, microcystin-RR and nodularin - was investigated in sterile BG-11 medium of different salinity and in water collected from the Gulf of Gdansk. After 21 days of incubation at 17 ± 1oC and constant illumination of about 40 µmol photon m-2 s-1 the concentration of toxins decreased by about 30-37%. No significant changes in toxin concentration in the BG-11 media of different salinity were observed. When toxins were incubated in non-sterile seawater, their concentrations decreased markedly. It is likely that some strains of bacteria are responsible for the breakdown of the toxins. Nodularin turned out to be more resistant to biodegradation than the two microcystins. The influence of certain components of cyanobacteria cells on the accelerated rate of toxin degradation was also considered.

  16. Effectiveness of KNIFC-PAN Resin in Absorbing Radiocesium in Seawater

    International Nuclear Information System (INIS)

    Nurrul Assyikeen Mohd Jaffary; Abdul Kadir Ishak; Zal Uyun Wan Mahmood; Wo, Y.M.; Norfaizal Mohamed; Mohd Tarmizi Ishak

    2016-01-01

    The effectiveness of KNiFC-PAN absorber, potassium-nickel hexacyanoferrate (II) (KNiFC) bound into modified polyacrylonitrile (PAN) have been tested for capability in absorbing radiocesium in seawater samples. The efficiency of the KNiFC-PAN were measured by the different activity of the radiocesium measured using Hyper Pure Germanium Detector (HPGe) in initial spiked seawater and eluent seawater after passed through 5 ml of KNiFC absorber. Study showed 87 % effectiveness of the KNiFC-PAN in absorbing radiocesium. Further study conducted to illustrate relation between spiked seawater and activity measured for 5 ml of KniFC passed through spiked seawater in packed column. This study suggested this relative 15L cubitainer method can be used to monitor the radiocesium in emergency situation for the fast and reliable result. (author)

  17. Molecularly imprinted polymer for selective extraction of malachite green from seawater and seafood coupled with high-performance liquid chromatographic determination

    International Nuclear Information System (INIS)

    Lian Ziru; Wang Jiangtao

    2012-01-01

    Highlights: ► The malachite green molecularly imprinted polymer (MG-MIP) was prepared. ► The characteristics and regeneration property of MIP were studied. ► An off-line method for MG was developed using MIP as solid-phase extraction. ► The MG concentrations from seawater and seafood samples were determined. - Abstract: In this paper, a highly selective sample cleanup procedure combining molecular imprinting technique (MIT) and solid-phase extraction (SPE) was developed for the isolation of malachite green in seawater and seafood samples. The molecularly imprinted polymer (MIP) was prepared using malachite green as the template molecule, methacrylic acid as the functional monomer and ethylene glycol dimethacrylate as the cross-linking monomer. The imprinted polymer and non-imprinted polymer were characterized by scanning electron microscope and static adsorption experiments. The MIP showed a high adsorption capacity and was used as selective sorbent for the SPE of malachite green. An off-line molecularly imprinted solid-phase extraction (MISPE) method followed by high-performance liquid chromatography with diodearray detection for the analysis of malachite green in seawater and seafood samples was also established. Finally, five samples were determined. The results showed that malachite green concentration in one seawater sample was at 1.30 μg L −1 and the RSD (n = 3) was 4.15%.

  18. Ethanol fermentation with Kluyveromyces marxianus from Jerusalem artichoke grown in salina and irrigated with a mixture of seawater and freshwater.

    Science.gov (United States)

    Yuan, W J; Zhao, X Q; Ge, X M; Bai, F W

    2008-12-01

    To study fuel ethanol fermentation with Kluyveromyces marxianus ATCC8554 from Jerusalem artichoke (Helianthus tuberosus) grown in salina and irrigated with a mixture of seawater and freshwater. The growth and ethanol fermentation of K. marxianus ATCC8554 were studied using inulin as substrate. The activity of inulinase, which attributes to the hydrolysis of inulin, the main carbohydrate in Jerusalem artichoke, was monitored. The optimum temperatures were 38 degrees C for growth and inulinase production, and 35 degrees C for ethanol fermentation. Aeration was not necessary for ethanol fermentation with the K. marxianus from inulin. Then, the fresh Jerusalem artichoke tubers grown in salina and irrigated with 25% and 50% seawater were further examined for ethanol fermentation with the K. marxianus, and a higher ethanol yield was achieved for the Jerusalem artichoke tuber irrigated with 25% seawater. Furthermore, the dry meal of the Jerusalem artichoke tubers irrigated with 25% seawater was examined for ethanol fermentation at three solid concentrations of 200, 225 and 250 g l(-1), and the highest ethanol yield of 0.467, or 91.5% of the theoretical value of 0.511, was achieved for the slurry with a solid concentration of 200 g l(-1). Halophilic Jerusalem artichoke can be used for fuel ethanol production. Halophilic Jerusalem artichoke, not competing with grain crops for arable land, is a sustainable feedstock for fuel ethanol production.

  19. Effect of RuCl{sub 3} Concentration on the Lifespan of Insoluble Anode for Cathodic Protection on PCCP

    Energy Technology Data Exchange (ETDEWEB)

    Cho, H. W.; Kim, Y. S. [Materials Research Center for Energy and Clean Technology, School of Materials Science and Engineering, Andong National University, Andong (Korea, Republic of); Chang, H. Y.; Lim, B. T.; Park, H. B. [Power Engineering Research Institute, KEPCO Engineering and Construction Company, Seongnam (Korea, Republic of)

    2015-08-15

    Prestressed Concrete steel Cylinder Pipe (PCCP) is extensively used as seawater pipes for cooling in nuclear power plants. The internal surface of PCCP is exposed to seawater, while the external surface is in direct contact with underground soil. Therefore, materials and strategies that would reduce the corrosion of its cylindrical steel body and external steel wiring need to be employed. To prevent against the failure of PCCP, operators provided a cathodic protection to the pre-stressing wires. The efficiency of cathodic protection is governed by the anodic performance of the system. A mixed metal oxide (MMO) electrode was developed to meet criteria of low over potential and high corrosion resistance. Increasing coating cycles improved the performance of the anode, but cycling should be minimized due to high materials cost. In this work, the effects of RuCl{sub 3} concentration on the electrochemical properties and lifespan of MMO anode were evaluated. With increasing concentration of RuCl{sub 3}, the oxygen evolution potential lowered and polarization resistance were also reduced but demonstrated an increase in passive current density and oxygen evolution current density. To improve the electrochemical properties of the MMO anode, RuCl{sub 3} concentration was increased. As a result, the number of required coating cycles were reduced substantially and the MMO anode achieved an excellent lifespan of over 80 years. Thus, we concluded that the relationship between RuCl{sub 3} concentration and coating cycles can be summarized as follows: No. of coating cycle = 0.48{sup *}[RuCl{sub 3} concentration, M]{sup -0.97}.

  20. Impact of the Fukushima accident on tritium, radiocarbon and radiocesium levels in seawater of the western North Pacific Ocean: A comparison with pre-Fukushima situation.

    Science.gov (United States)

    Povinec, P P; Liong Wee Kwong, L; Kaizer, J; Molnár, M; Nies, H; Palcsu, L; Papp, L; Pham, M K; Jean-Baptiste, P

    2017-01-01

    Tritium, radiocarbon and radiocesium concentrations in water column samples in coastal waters offshore Fukushima and in the western North Pacific Ocean collected in 2011-2012 during the Ka'imikai-o-Kanaloa (KoK) cruise are compared with other published results. The highest levels in surface seawater were observed for 134 Cs and 137 Cs in seawater samples collected offshore Fukushima (up to 1.1 Bq L -1 ), which represent an increase by about three orders of magnitude when compared with the pre-Fukushima concentration. Tritium levels were much lower (up to 0.15 Bq L -1 ), representing an increase by about a factor of 6. The impact on the radiocarbon distribution was measurable, but the observed levels were only by about 9% above the global fallout background. The 137 Cs (and similarly 134 Cs) inventory in the water column of the investigated western North Pacific region was (2.7 ± 0.4) PBq, while for 3 H it was only (0.3 ± 0.2) PBq. Direct releases of highly contaminated water from the damaged Fukushima NPP, as well as dry and wet depositions of these radionuclides over the western North Pacific considerably changed their distribution patterns in seawater. Presently we can distinguish Fukushima labeled waters from global fallout background thanks to short-lived 134 Cs. However, in the long-term perspective when 134 Cs will decay, new distribution patterns of 3 H, 14 C and 137 Cs in the Pacific Ocean should be established for future oceanographic and climate change studies in the Pacific Ocean. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Greening Drylands with Seawater Easily and Naturally.

    Science.gov (United States)

    Moustafa, Khaled

    2017-03-01

    The sun and sea are inexhaustible sources of energy and water that could be used to transform drylands into more viable ecosystems. A sustainable and cost-effective approach is proposed for greening drylands and restoring wildlife and biodiversity in deserts using seawater desert-houses (or movable seawater ponds) that could offer important environmental advantages. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. Radioactive cesium removal from seawater using adsorptive fibers prepared by radiation-induced graft polymerization

    International Nuclear Information System (INIS)

    Goto, Shota; Kawai-Noma, Shigeko; Umeno, Daisuke; Saito, Kyoichi; Fujiwara, Kunio; Sugo, Takanobu; Kikuchi, Takahiro; Morimoto, Yasutomi

    2015-01-01

    The meltdown of three reactors of the TEPCO Fukushima Daiichi nuclear power station (NPS) caused by the Great East Japan Earthquake on March 11th 2011 resulted in the emission of radionuclides such as cesium-137 and strontium-90 to the environment. For example, radioactive cesium exceeding the legal discharge limit (90 Bq/L, 2×10 -13 M) was detected in the seawater of the seawater-intake area of the NPS at the end of September 2014. Adsorbents with a high selectivity for cesium ions over other alkali metal ions such as sodium and potassium ions are required for cesium removal from seawater because sodium and potassium ions dissolve respectively at much higher concentrations of 5×10 -1 and 1×10 -2 M than cesium ions (2×10 -9 M). In addition, the simple operations of the immersion in seawater and the recovery of the adsorbents from seawater are desirable at decontamination sites. We prepared a cobalt-ferrocyanide-impregnated fiber capable of specifically capturing cesium ions in seawater by radiation-induced graft polymerization and chemical modifications. First, a commercially available 6-nylon fiber was irradiated with γ-rays. Second, an epoxy-group-containing vinyl monomer, glycidyl methacrylate, was graft-polymerized onto the γ-ray-irradiated nylon fiber. Third, the epoxy ring of the grafted polymer chain was reacted with triethylenediamine to obtain an anion-exchange fiber. Fourth, ferrocyanide ions, [Fe(CN) 6 ] 4 - , were bound to the anion-exchange group of the polymer chains. Finally, the ferrocyanide-ion-bound-fiber was placed in contact with cobalt chloride to precipitate insoluble cobalt ferrocyanide onto the polymer chains. Insoluble cobalt ferrocyanide was immobilized at the periphery of the fiber. However, the impregnation structure remains unclear. Here, we clarified the structure of insoluble cobalt ferrocyanide impregnated onto the polymer chain grafted onto the fiber to ensure the chemical and physical stability of the adsorptive fiber in

  3. Sensitive and stable monitoring of lead and cadmium in seawater using screen-printed electrode and electrochemical stripping analysis

    International Nuclear Information System (INIS)

    Gueell, Raquel; Aragay, Gemma; Fontas, Claudia; Antico, Enriqueta; Merkoci, Arben

    2008-01-01

    Sensitive and stable monitoring of heavy metals in seawater using screen-printed electrodes (SPE) is presented. The analytical performance of SPE coupled with square wave anodic stripping voltammetry (SWASV) for the simultaneous determination of Pb and Cd in seawater samples, in the low μg L -1 range, is evaluated. The stripping response for the heavy metals following 2 min deposition was linear over the concentration range examined (10-2000 μg L -1 ) with detection limits of 1.8 and 2.9 μg L -1 for Pb and Cd, respectively. The accuracy of the method was validated by analyzing metal contents in different spiked seawater samples and comparing these results to those obtained with the well-established anodic stripping voltammetry using the hanging mercury drop electrode. Moreover, a certified reference material was also used and the results obtained were satisfactory

  4. Ionic liquid solvent bar micro-extraction of CdCln(n-2)- species for ultra-trace Cd determination in seawater.

    Science.gov (United States)

    Herce-Sesa, Belén; López-López, José A; Moreno, Carlos

    2018-02-01

    Water analysis of trace metals has been benefited by recent studies on sample preparation by liquid micro-extraction. However, there are still limitations for its application to seawater, such as the need of additives to preserve the sample or the availability of chemical extractants for the selective extraction from highly saline samples. In this work, a three phase solvent bar micro-extraction (3SBME) system containing the ionic liquid trioctylmethylammonium chloride (Aliquat ® 336) has been used for isolation and pre-concentration of Cd from seawater samples, due to its ability for ionic exchange of CdCl n (n-2)- . The system was optimized to work at the natural pH of seawater, and conditions for application to real samples were 0.18 M Aliquat ® 336 dissolved in kerosene with 0.25 M dodecan-1-ol as organic solution, 1.5 M HNO 3 as acceptor solution, 60 min extraction time, and 800 rpm stirring speed in the sample. Loss of organic solution into the sample during extraction was evaluated and revealed its dependence on stirring rate and extraction time. Under optimum conditions samples containing Cd 0.09-0.90 nM were pre-concentrated 65 times. GF-AAS was used for metal quantification with a limit of detection of 0.04 nM. Accuracy was successfully evaluated measuring Cd in a seawater certified reference material BCR-403. Copyright © 2017 Elsevier Ltd. All rights reserved.

  5. Assessment of seawater intrusion and nitrate contamination on the groundwater quality in the Korba coastal plain of Cap-Bon (North-east of Tunisia)

    Science.gov (United States)

    Zghibi, Adel; Tarhouni, Jamila; Zouhri, Lahcen

    2013-11-01

    In recent years, seawater intrusion and nitrate contamination of groundwater have become a growing concern for people in rural areas in Tunisia where groundwater is always used as drinking water. The coastal plain of Korba (north-east of Tunisia) is a typical area where the contamination of the aquifer in the form of saltwater intrusion and high nitrate concentrations is very developed and represents the major consequence of human activities. The objective of this study is to evaluate groundwater resource level, to determine groundwater quality and to assess the risk of NO3- pollution in groundwater using hydrogeochemical tools. Groundwater were sampled and analyzed for physic-chemical parameters: Ca2+, Mg2+, Na+, K+, Cl-, SO42-, HCO3-, NO3-, Total Dissolved Solid and of the physical parameters (pH, electrical conductivity and the temperature). The interpretation of the analytical results is shown numerically and graphically through the ionic deviations, Piper Diagram, seawater fractions and binary diagrams. Moreover, electrical conductivity investigations have been used to identify the location of the major intrusion plumes in this coastal area and to obtain new information on the spatial scales and dynamics of the fresh water-seawater interface. Those processes can be used as indicators of seawater intrusion progression. First, the hydrogeochemical investigation of this aquifer reveals the major sources of contamination, represented by seawater intrusion. Thus, the intensive extraction of groundwater from aquifer reduces freshwater outflow to the sea, creates several drawdown cones and lowering of the water table to as much as 12 m below mean sea level in the center part of the study area especially between Diarr El Hojjej and Tafelloun villages, causing seawater migration inland and rising toward the wells. Moreover, the results of this study revealed the presence of direct cation exchange linked to seawater intrusion and dissolution processes associated with

  6. Numerical Model of SO2 Scrubbing with Seawater Applied to Marine Engines

    Directory of Open Access Journals (Sweden)

    Lamas M. I.

    2016-04-01

    Full Text Available The present paper proposes a CFD model to study sulphur dioxide (SO2 absorption in seawater. The focus is on the treatment of marine diesel engine exhaust gas. Both seawater and distilled water were compared to analyze the effect of seawater alkalinity. The results indicate that seawater is more appropriate than distilled water due to its alkalinity, obtaining almost 100% cleaning efficiency for the conditions analyzed. This SO2 reduction meets the limits of SOx emission control areas (SECA when operating on heavy fuel oil. These numerical simulations were satisfactory validated with experimental tests. Such data are essential in designing seawater scrubbers and judging the operating cost of seawater scrubbing compared to alternative fuels.

  7. Modified montmorillonite clay microparticles for stable oil-in-seawater emulsions.

    Science.gov (United States)

    Dong, Jiannan; Worthen, Andrew J; Foster, Lynn M; Chen, Yunshen; Cornell, Kevin A; Bryant, Steven L; Truskett, Thomas M; Bielawski, Christopher W; Johnston, Keith P

    2014-07-23

    Environmentally benign clay particles are of great interest for the stabilization of Pickering emulsions. Dodecane-in-synthetic seawater (SSW) emulsions formed with montmorillonite (MMT) clay microparticles modified with bis(2-hydroxyethyl)oleylamine were stable against coalescence, even at clay concentrations down to 0.1% w/v. Remarkably, as little as 0.001% w/v surfactant lowered the hydrophilicity of the clay to a sufficient level for stabilization of oil-in-SSW emulsions. The favorable effect of SSW on droplet size reduction and emulsion stability enhancement is hypothesized to be due to reduced electrostatic repulsion between adsorbed clay particles and a consequent increase in the continuous phase (an aqueous clay suspension) viscosity. Water/oil (W/O) emulsions were inverted to O/W either by decreasing the mass ratio of surfactant-to-clay (transitional inversion) or by increasing the water volume fraction (catastrophic inversion). For both types of emulsions, coalescence was minimal and the sedimentation or creaming was highly correlated with the droplet size. For catastrophic inversions, the droplet size of the emulsions was smaller in the case of the preferred curvature. Suspensions of concentrated clay in oil dispersions in the presence of surfactant were stable against settling. The mass transfer pathways during emulsification of oil containing the clay particles were analyzed on the droplet size/stability phase diagrams to provide insight for the design of dispersant systems for remediating surface and subsurface oceanic oil spills.

  8. Boron Removal in Seawater Reverse Osmosis System

    KAUST Repository

    Rahmawati, Karina

    2011-07-01

    Reverse osmosis successfully proves to remove more than 99% of solute in seawater, providing fresh water supply with satisfied quality. Due to some operational constraints, however, some trace contaminants removal, such as boron, cannot be achieved in one pass system. The stringent criterion for boron from World Health Organization (WHO) and Saudi Arabia local standard (0.5 mg/l) is hardly fulfilled by single pass sea water reverse osmosis (SWRO) plants. Some design processes have been proposed to deal with boron removal, but they are not economically efficient due to high energy and chemical consumption. The objective of this study was to study boron removal by different reverse osmosis membranes in two pH conditions, with and without antiscalant addition. Thus, it was expected to observe the possibility of operating single pass system and necessity to operate two pass system using low energy membrane. Five membrane samples were obtained from two different manufacturers. Three types of feed water pH were used, pH 8, pH 10, and pH 10 with antiscalant addition. Experiment was conducted in parallel to compare membrane performance from two manufacturers. Filtration was run with fully recycle mode for three days. Sample of permeate and feed were taken every 12 hours, and analyzed for their boron and TDS concentration. Membrane samples were also tested for their surface charge. The results showed that boron rejection increases as the feed pH increases. This was caused by dissociation of boric acid to negatively charged borate ion and more negatively charged membrane surface at elevated pH which enhance boron rejection. This study found that single pass reverse osmosis system, with and without elevating the pH, may not be possible to be applied because of two reasons. First, permeate quality in term of boron, does not fulfill WHO and local Saudi Arabia regulations. Second, severe scaling occurs due to operation in alkaline condition, since Ca and Mg concentration are

  9. A portable multi-syringe flow system for spectrofluorimetric determination of iodide in seawater.

    Science.gov (United States)

    Frizzarin, Rejane M; Aguado, Enrique; Portugal, Lindomar A; Moreno, Daniel; Estela, José M; Rocha, Fábio R P; Cerdà, Victor

    2015-11-01

    A miniaturized analyzer encompassing a poly(methyl methacrylate) chip with integrated spectrofluorimetric detection and solutions propelling by a multi-syringe module is proposed. Iodide was determined through its catalytic effect on the reaction between Ce(IV) and As(III). Matrix isopotential synchronous fluorescence was explored to set the excitation and emission wavelengths. A two-level full factorial design allowed to evaluate the significance of variables (Ce(IV), As(III) and H2SO4 concentrations) and their interaction effects in the experimental domain. A Doehlert Matrix was applied to identify the critical values. The optimized procedure showed a linear response from 1 to 100 μg L(-1) (S=53.7+2.61C, in which S is the net fluorescence and C is iodide concentration in μg L(-1)). Detection limit, coefficient of variation (n=6) and sampling rate were estimated at 0.3 μg L(-1), 0.8% and 20 h(-1), respectively. Recoveries within 90-117% were estimated for iodide spiked to seawater samples. The proposed procedure stands out because of the portability, robustness, and simplicity for in-field analysis of iodide in seawater. Copyright © 2015 Elsevier B.V. All rights reserved.

  10. Multielement determination of trace elements in seawater by inductively coupled plasma mass spectrometry after tandem preconcentration with cooperation of chelating resin adsorption and lanthanum coprecipitation

    International Nuclear Information System (INIS)

    Yabutani, Tomoki; Chiba, Koichi; Haraguchi, Hiroki

    2001-01-01

    A tandem preconcentration method, in which chelating resin adsorption and La coprecipitation were cooperatively employed for preconcentration, was developed as a pretreatment method for simultaneous multielement determination of trace elements in seawater by ICP-MS. First, the seawater sample (250 ml) was treated with a chelating resin for preconcentration of trace elements, and then trace elements with good recoveries were determined by ICP-MS. Trace elements with the chemical properties of oxoanion- and hydride-formation, which were poorly recovered in the chelating resin preconcentration, were further subjected to preconcentration by La coprecipitation. As a result, more than 30 elements could be determined in the concentration range from 9.6 μg L -1 for Mo to 0.00018 μg L -1 for Tm, when the present tandem method was applied to the analysis of open seawater standard reference material (NASS-4). Furthermore, the analytical results for open seawater reference materials were compared with those for coastal seawater reference material as well as for coastal seawater collected in the Ise Bay. It was found that the multielement data for trace elements in these seawater samples clearly showed different elemental distributions, reflecting the different marine environments. (author)

  11. Liquid waveguide spectrophotometric measurement of nanomolar ammonium in seawater based on the indophenol reaction with o-phenylphenol (OPP).

    Science.gov (United States)

    Hashihama, Fuminori; Kanda, Jota; Tauchi, Ami; Kodama, Taketoshi; Saito, Hiroaki; Furuya, Ken

    2015-10-01

    We describe a highly sensitive colorimetric method for the determination of nanomolar concentrations of ammonium in seawater based on the indophenol reaction with o-phenylphenol [(1,1'-biphenyl)-2-ol, abbreviated as OPP]. OPP is available as non-toxic, stable flaky crystals with no caustic odor and has some advantages over phenol in practical use. The method was established by using a gas-segmented continuous flow analyzer equipped with two types of long path liquid waveguide capillary cell, LWCCs (100 cm and 200 cm) and an UltraPath (200 cm), which have inner diameters of 0.55 mm and 2 mm, respectively. The reagent concentrations, flow rates of the pumping tubes, and reaction path and temperature were determined on the basis of a manual indophenol blue method with OPP (Kanda, Water Res. 29 (1995) 2746-2750). The sample mixed with reagents that form indophenol blue dye was measured at 670 nm. Aged subtropical surface water was used as a blank, a matrix of standards, and the carrier. The detection limits of the analytical systems with a 100 cm LWCC, a 200 cm LWCC, and a 200 cm UltraPath were 6, 4, and 4 nM, respectively. These systems had high precision (<4% at 100 nM) and a linear dynamic range up to 200 nM. Non-linear baseline drift did not occur when using the UltraPath system. This is due to the elimination of cell clogging because of the larger inner diameter of the UltraPath compared to the LWCCs. The UltraPath system is thus more suitable for long-term measurements compared with the LWCC systems. The results of the proposed sensitive colorimetry and a conventional colorimetry for the determination of seawater samples showed no significant difference. The proposed analytical systems were applied to underway surface monitoring and vertical observation in the oligotrophic South Pacific. Copyright © 2015 Elsevier B.V. All rights reserved.

  12. Assessment of TBT and organic booster biocide contamination in seawater from coastal areas of South Korea.

    Science.gov (United States)

    Kim, Nam Sook; Shim, Won Joon; Yim, Un Hyuk; Hong, Sang Hee; Ha, Sung Yong; Han, Gi Myung; Shin, Kyung-Hoon

    2014-01-15

    Seawater samples from major enclosed bays, fishing ports, and harbors of Korea were analyzed to determine levels of tributyltin (TBT) and booster biocides, which are antifouling agents used as alternatives to TBT. TBT levels were in the range of not detected (nd) to 23.9 ng Sn/L. Diuron and Irgarol 1051, at concentration ranges of 35-1360 ng/L and nd to 14 ng/L, respectively, were the most common alternative biocides present in seawater, with the highest concentrations detected in fishing ports. Hot spots were identified where TBT levels exceeded environmental quality targets even 6 years after a total ban on its use in Korea. Diuron exceeded the UK environmental quality standard (EQS) value in 73% of the fishing port samples, 64% of the major bays, and 42% of the harbors. Irgarol 1051 levels were marginally below the Dutch and UK EQS values at all sites. Copyright © 2013 Elsevier Ltd. All rights reserved.

  13. Selective solid phase extraction and pre-concentration of heavy metals from seawater by physically and chemically immobilized 4-amino-3-hydroxy-2-(2-chlorobenzene)-azo-1-naphtalene sulfonic acid silica gel

    International Nuclear Information System (INIS)

    Mahmoud, M.E.; Soayed, A.A.; Hafez, O.F.

    2003-01-01

    4-Amino-3-hydroxy-2 - (2-chlorobenzene)-azo-l-naphthalene sulfonic acid (AHCANSA) was used as a chelating modifier to improve the reactivity of the silica gel surface in terms of selective binding and extraction of heavy metal ions. The surface cover-age values were found to be 0.488 and 0.473 mmol g -1 for the newly modified physically adsorbed silica gel phase (I) and chemically immobilized-AHCANSA phase (II), respectively. The modified silica gel phases (I, II) were tested for stability in different acidic buffer solutions (pH 1-6) and found to be highly resistant to hydrolysis and leaching by buffer solutions above pH 2. The application of these two phases as solid extractors for a series of mono-, di-, and tri-valent metal ions from aqueous solutions was also performed with different controlling factors such as the pH value of metal ion solutions and equilibrium shaking time. The mmol g -1 metal capacity values determined by silica gel phases (I, II) were found to confirm high affinity and selectivity characters for binding with heavy metal ions such as Cr 3+ , Ni 2+ , Cu 2+ , Zn 2+ , Cd 2+ and Pb 2+ in a range of 0.250-0.483. The tested alkali and alkaline earth metals, Na + , K + , Mg 2+ and Ca 2+ , were found to exhibit little interaction and binding ability with the modified silica gel phases. The selectivity characters incorporated into the modified silica gel phases were further utilized and applied in solid phase extraction and pre-concentration of trace concentration levels (∼1.0 μg mL -1 and 2.00-2.50 ng mL -1 ) from real seawater samples. The percentage recovery values determined for Cr 3+ , Cu 2+ , Zn 2+ , Cd 2+ and Pb 2+ were found to be in the range of 95.2-98.1 ± 2.0-5.0 %, and the pre-concentration recovery values for the same tested heavy metal ions were found to be in the range of 92.5-97.1 ± 3.0-6.0 % for the two newly modified silica gel phases with a pre-concentration factor of 500. Refs. 25 (author)

  14. Nucleation of metastable aragonite CaCO3 in seawater.

    Science.gov (United States)

    Sun, Wenhao; Jayaraman, Saivenkataraman; Chen, Wei; Persson, Kristin A; Ceder, Gerbrand

    2015-03-17

    Predicting the conditions in which a compound adopts a metastable structure when it crystallizes out of solution is an unsolved and fundamental problem in materials synthesis, and one which, if understood and harnessed, could enable the rational design of synthesis pathways toward or away from metastable structures. Crystallization of metastable phases is particularly accessible via low-temperature solution-based routes, such as chimie douce and hydrothermal synthesis, but although the chemistry of the solution plays a crucial role in governing which polymorph forms, how it does so is poorly understood. Here, we demonstrate an ab initio technique to quantify thermodynamic parameters of surfaces and bulks in equilibrium with an aqueous environment, enabling the calculation of nucleation barriers of competing polymorphs as a function of solution chemistry, thereby predicting the solution conditions governing polymorph selection. We apply this approach to resolve the long-standing "calcite-aragonite problem"--the observation that calcium carbonate precipitates as the metastable aragonite polymorph in marine environments, rather than the stable phase calcite--which is of tremendous relevance to biomineralization, carbon sequestration, paleogeochemistry, and the vulnerability of marine life to ocean acidification. We identify a direct relationship between the calcite surface energy and solution Mg:Ca [corrected] ion concentrations, showing that the calcite nucleation barrier surpasses that of metastable aragonite in solutions with Mg:Ca ratios consistent with modern seawater, allowing aragonite to dominate the kinetics of nucleation. Our ability to quantify how solution parameters distinguish between polymorphs marks an important step toward the ab initio prediction of materials synthesis pathways in solution.

  15. Productions of Volatile Organic Compounds (VOCs) in Surface Waters from Reactions with Atmospheric Ozone

    Science.gov (United States)

    Hopkins, Frances; Bell, Thomas; Yang, Mingxi

    2017-04-01

    Ozone (O3) is a key atmospheric oxidant, greenhouse gas and air pollutant. In marine environments, some atmospheric ozone is lost by reactions with aqueous compounds (e.g. dissolved organic material, DOM, dimethyl sulfide, DMS, and iodide) near the sea surface. These reactions also lead to formations of volatile organic compounds (VOCs). Removal of O3 by the ocean remains a large uncertainty in global and regional chemical transport models, hampering coastal air quality forecasts. To better understand the role of the ocean in controlling O3 concentrations in the coastal marine atmosphere, we designed and implemented a series of laboratory experiments whereby ambient surface seawater was bubbled with O3-enriched, VOC-free air in a custom-made glass bubble equilibration system. Gas phase concentrations of a range of VOCs were monitored continuously over the mass range m/z 33 - 137 at the outflow of the bubble equilibrator by a proton transfer reaction - mass spectrometer (PTR-MS). Gas phase O3 was also measured at the input and output of the equilibrator to monitor the uptake due to reactions with dissolved compounds in seawater. We observed consistent productions of a variety of VOCs upon reaction with O3, notably isoprene, aldehydes, and ketones. Aqueous DMS is rapidly removed from the reactions with O3. To test the importance of dissolved organic matter precursors, we added increasing (milliliter) volumes of Emiliania huxleyi culture to the equilibrator filled with aged seawater, and observed significant linear increases in gas phase concentrations of a number of VOCs. Reactions between DOM and O3 at the sea-air interface represent a potentially significant source of VOCs in marine air and a sink of atmospheric O3.

  16. Drinking water quality from the aspect of element concentrations

    International Nuclear Information System (INIS)

    Chiba, M.; Shinohara, A.; Sekine, M.; Hiraishi, S.

    2006-01-01

    Drinking water in developed countries is usually treated by the water-purification system, while in developing countries untreated natural water such as well water, river water, rain water, or pond water are used. On the other hand, many kinds of mineral water bottled in plastic containers are sold as drinking water with or without gas in urban areas in many countries. Seawater under hundreds meters from the surface is also bottled and sold as drinking water with advertising good mineral balance. Various element concentrations in water samples for drinking were analyzed, and then it was considered the effects of elements on human health. (author)

  17. Geophysical and Seawater intrusion models to distinguish Modern and Palaeo salinity in the Central Godvari Delta, Andhra Pradesh, India

    Science.gov (United States)

    Lagudu, S.; Nandan, M. J.; Durgaprasad, M.; Gurunadha Rao, V. V. S.

    2015-12-01

    Central Godavari Delta is located in the East coast of Andhra Pradesh along Bay of Bengal. Ample surface water is made available for irrigation and aqua culture through well distributed canals drawn from Godavari River since last 150 years. Groundwater in the area is highly saline though the groundwater levels are very shallow ranging from 1 to 3 m below ground level. Integrated Electrical Resistivity Tomograms (ERT), hydrochemical (pH, TDS, Ca2+, Mg2+, K+, F-, Cl-, SO42-, NO3-, HCO3- and CO3-), isotopic (Br- and δ18O ) and density dependant solute tranport (SEAWAT) modelling studies have been carried out for four years (2006, 2007, 2014 and 2015) to identify the salinity sources and to understand the possible extent of seawater intrusion. The integration of all these data sets revealed that coarse grained sands exhibits resistivity of 4-20 Ωm forming the surface layer, clay layer exhibits Na2++ K+) and (Ca2++Mg2+), (Na+-Cl- ) vs. Ca2++Mg2+-HCO3--SO42-)) and ionic ratios ( Na2+/Cl-, SO42-/Cl-, Mg2+/Ca2+, Mg2+/Cl- and Cl-/Br) and δ18O does not reflect any modern seawater signatures. These models indicated that salinity in the shallow wells is due to dissolution of evaporitic minerals and ion exchange processes. In the pumping wells the salinity is due to upconing of entrapped sea water that belongs to Palaeo origin and wells located near the coast and mudflats is due to physical mixing of marine water. The estimated regional groundwater balance using SEAWAT model indicate significant amount of submarine groundwater discharge as outfall to the Bay of Bengal. Assuming observed hydrological conditions, no considerable advance in seawater intrusion would be expected into the delta region.

  18. Hydraulic conductivity of some bentonites in artificial seawater

    International Nuclear Information System (INIS)

    Komine, Hideo; Murakami, Satoshi; Yasuhara, Kazuya

    2011-01-01

    A high-level radioactive waste disposal facility might be built in a coastal area in Japan from the viewpoint of feasible transportation of waste. Therefore, it is important to investigate the effects of seawater on a bentonite-based buffer. This study investigated the influence of seawater on hydraulic conductivity of three common sodium-types of bentonite and one calcium-type bentonite by the laboratory experiments. >From the results of laboratory experiment, this study discussed the influence of seawater on hydraulic conductivity of bentonites from the viewpoints of kinds of bentonite such as exchangeable-cation type and montmorillonite content and dry density of bentonite-based buffer. (author)

  19. Simulation of seawater intrusion in coastal aquifers: Some typical ...

    Indian Academy of Sciences (India)

    Springer Verlag Heidelberg #4 2048 1996 Dec 15 10:16:45

    Seawater intrusion; coastal aquifers; density-dependent flow and ... The seawater intrusion mechanism in coastal aquifers generally causes the occurrence of ... (4) The dynamic viscosity of the fluid does not change with respect to salinity and.

  20. One-dimensional self-sealing ability of bentonites in artificial seawater

    International Nuclear Information System (INIS)

    Komine, Hideo; Yasuhara, Kazuya; Murakami, Satoshi

    2009-01-01

    A high-level radioactive waste disposal facility might be built in a coastal area in Japan from the viewpoint of feasible transportation of waste. Therefore, it is important to investigate the effects of seawater on a bentonite-based buffer. This study investigated the influence of seawater on self-sealing ability of three common sodium-types of bentonite by the laboratory experiment and chemical analysis. From the results of laboratory experiment, suitable specifications were defined for a bentonite-based buffer that can withstand the effects of seawater. Furthermore, mechanism on filtration of seawater components in highly compacted bentonite was discussed by the results of chemical analysis. (author)

  1. An off-line automated preconcentration system with ethylenediaminetriacetate chelating resin for the determination of trace metals in seawater by high-resolution inductively coupled plasma mass spectrometry.

    Science.gov (United States)

    Minami, Tomoharu; Konagaya, Wataru; Zheng, Linjie; Takano, Shotaro; Sasaki, Masanobu; Murata, Rena; Nakaguchi, Yuzuru; Sohrin, Yoshiki

    2015-01-07

    A novel automated off-line preconcentration system for trace metals (Al, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb) in seawater was developed by improving a commercially available solid-phase extraction system SPE-100 (Hiranuma Sangyo). The utilized chelating resin was NOBIAS Chelate-PA1 (Hitachi High-Technologies) with ethylenediaminetriacetic acid and iminodiacetic acid functional groups. Parts of the 8-way valve made of alumina and zirconia in the original SPE-100 system were replaced with parts made of polychlorotrifluoroethylene in order to reduce contamination of trace metals. The eluent pass was altered for the back flush elution of trace metals. We optimized the cleaning procedures for the chelating resin column and flow lines of the preconcentration system, and developed a preconcentration procedure, which required less labor and led to a superior performance compared to manual preconcentration (Sohrin et al.). The nine trace metals were simultaneously and quantitatively preconcentrated from ∼120 g of seawater, eluted with ∼15 g of 1M HNO3, and determined by HR-ICP-MS using the calibration curve method. The single-step preconcentration removed more than 99.998% of Na, K, Mg, Ca, and Sr from seawater. The procedural blanks and detection limits were lower than the lowest concentrations in seawater for Mn, Ni, Cu, and Pb, while they were as low as the lowest concentrations in seawater for Al, Fe, Co, Zn, and Cd. The accuracy and precision of this method were confirmed by the analysis of reference seawater samples (CASS-5, NASS-5, GEOTRACES GS, and GD) and seawater samples for vertical distribution in the western North Pacific Ocean. Copyright © 2014 Elsevier B.V. All rights reserved.

  2. A Preliminary Study for Development of Amidoxime-functionalized Silica Adsorbents for Uranium(IV) Extraction from Seawater

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Minseok; Ryu, Ho Jin [KAIST, Daejeon (Korea, Republic of)

    2016-10-15

    4 billion tons of uranium, which can supply the electricity for tens of thousands of years, is contained in seawater. Therefore, development of techniques for uranium sequestering from the ocean has been regarded as a great challenging for making nuclear energy to be more economical and sustainable. Despite the inexhaustible uranium resource, it is still hard to produce uranium economically from seawater due to its extremely low level of concentration (3.0 μg/L) and stable complex chemical formation, UO{sub 2}(CO3)34-. Various methods for uranium extraction from seawater have been suggested such as precipitation, solvent extraction, ion exchange, adsorption and etc. The most preferred method for extracting uranium is adsorption due to ease of separation from the liquid phase, environment friendliness and cost-effectiveness. Organic or inorganic solids functionalized with amidoxime (AO, -R-C(NH2)=NOH) groups, which has high affinity to uranium species, is the one of candidate material for uranium adsorbents. For long-term nuclear power generation, developing uranium extraction technologies from seawater has been a crucial issue. AO-based adsorbent has been considered as the most effective methods for uranium extraction from seawater, and collaboration with nanotechnology has been tried to enhance the traditional adsorbents, recently. Despite the attempts, most AO-based adsorbents were suffered from complexation of uranyl ions with carbonate ions and under the effect of pH. To achieve more efficient uranium uptake, bi-functionalized mesoporous silica with AO group and acidic groups was chosen as a model for this study.

  3. Behaviour of stainless steel in natural seawater

    OpenAIRE

    Compere, Chantal; Le Bozec, Nathalie

    1997-01-01

    In this paper, investigations performed in natural and artificial seawater on stainless steels will be presented. They concerned studies on: biofilm formation, passive layers composition, electrochemical behaviour, localised corrosion and the evolution of these different parameters as a function of ageing time. According to literature surveys, the different aspects will be discussed. Some conclusions will be drawn concerning the actual knowledge on the behaviour of stainless steels in seawater.

  4. Sensitive and stable monitoring of lead and cadmium in seawater using screen-printed electrode and electrochemical stripping analysis

    Energy Technology Data Exchange (ETDEWEB)

    Gueell, Raquel [ICREA and Nanobioelectronics and Biosensors Group, Institut Catala de Nanotecnologia, Bellaterra, Barcelona (Spain); Department of Chemistry, Universitat Autonoma de Barcelona, Bellaterra, Barcelona (Spain); Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain); Aragay, Gemma [ICREA and Nanobioelectronics and Biosensors Group, Institut Catala de Nanotecnologia, Bellaterra, Barcelona (Spain); Department of Chemistry, Universitat Autonoma de Barcelona, Bellaterra, Barcelona (Spain); Fontas, Claudia; Antico, Enriqueta [Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona (Spain); Merkoci, Arben [ICREA and Nanobioelectronics and Biosensors Group, Institut Catala de Nanotecnologia, Bellaterra, Barcelona (Spain); Department of Chemistry, Universitat Autonoma de Barcelona, Bellaterra, Barcelona (Spain)], E-mail: arben.merkoci.icn@uab.es

    2008-10-10

    Sensitive and stable monitoring of heavy metals in seawater using screen-printed electrodes (SPE) is presented. The analytical performance of SPE coupled with square wave anodic stripping voltammetry (SWASV) for the simultaneous determination of Pb and Cd in seawater samples, in the low {mu}g L{sup -1} range, is evaluated. The stripping response for the heavy metals following 2 min deposition was linear over the concentration range examined (10-2000 {mu}g L{sup -1}) with detection limits of 1.8 and 2.9 {mu}g L{sup -1} for Pb and Cd, respectively. The accuracy of the method was validated by analyzing metal contents in different spiked seawater samples and comparing these results to those obtained with the well-established anodic stripping voltammetry using the hanging mercury drop electrode. Moreover, a certified reference material was also used and the results obtained were satisfactory.

  5. Study of the oxygen reduction reaction on stainless steel materials in natural seawater. Influence of the bio-film on corrosion processes

    International Nuclear Information System (INIS)

    Le Bozec, N.

    2000-01-01

    Bio-film development on stainless steels immersed in natural seawater can have prejudicial consequences on the resistance of these materials to corrosion. The goal of the present study was to get more precise information on the corrosion processes, and especially on the oxygen reduction reaction. As the reaction is linked to the stainless steel surface state, the characterisation of the oxides films (composition, structure, thickness...) is essential to understand the mechanisms and the oxygen reduction kinetic. The first aim of the study has been to correlate the oxygen reduction processes with the characteristics of the oxides layer as a function of the alloy surface treatment (mechanical polishing, electrochemical passivation and pre-reduction, chemical treatment with some acids or with hydrogen peroxide). The second stage has consisted in following the evolution of the oxygen reduction processes and of the characteristics of the oxides layer with the aging of stainless steels in natural and artificial sea-waters. One major bio-film effect appears to be the production of hydrogen peroxide at a concentration level which induces modifications of the oxides layers and, consequently, of the evolution of the oxygen reduction kinetics as well as of the open circuit potential. Electrochemical techniques (voltammetric analysis at rotating disk and ring-disk electrodes, coulometry) combined with a surface analytical method by X-ray photoelectron spectroscopy have been used. The characterisation of the bio-film required the use of microscopy (scanning electronic microscopy, epi-fluorescence microscopy) and microbiological methods (cultures). The in-situ detection of hydrogen peroxide formed inside the bio-film has been performed with a micro-electrode and the results were confirmed with enzymatic methods. (author)

  6. Durability of high performance concrete in seawater

    International Nuclear Information System (INIS)

    Amjad Hussain Memon; Salihuddin Radin Sumadi; Rabitah Handan

    2000-01-01

    This paper presents a report on the effects of blended cements on the durability of high performance concrete (HPC) in seawater. In this research the effect of seawater was investigated. The specimens were initially subjected to water curing for seven days inside the laboratory at room temperature, followed by seawater curing exposed to tidal zone until testing. In this study three levels of cement replacement (0%, 30% and 70%) were used. The combined use of chemical and mineral admixtures has resulted in a new generation of concrete called HPC. The HPC has been identified as one of the most important advanced materials necessary in the effort to build a nation's infrastructure. HPC opens new opportunities in the utilization of the industrial by-products (mineral admixtures) in the construction industry. As a matter of fact permeability is considered as one of the fundamental properties governing the durability of concrete in the marine environment. Results of this investigation indicated that the oxygen permeability values for the blended cement concretes at the age of one year are reduced by a factor of about 2 as compared to OPC control mix concrete. Therefore both blended cement concretes are expected to withstand in the seawater exposed to tidal zone without serious deterioration. (Author)

  7. The immune-related fatty acids are responsive to CO2 driven seawater acidification in a crustacean brine shrimp Artemia sinica.

    Science.gov (United States)

    Gao, Yan; Zheng, Shu-Cheng; Zheng, Chao-Qun; Shi, Yue-Chen; Xie, Xiao-Lu; Wang, Ke-Jian; Liu, Hai-Peng

    2018-04-01

    The gradual increase of CO 2 concentration in the atmosphere, absorbed by the ocean surface water through air to sea equilibration termed ocean acidification (OA), leads to the decline of pH in seawater. It is not clear so far how the composition of fatty acids, particular the immune-related, in marine crustacean and the subsequent energy supply in marine ecosystem are affected by OA. The brine shrimp Artemia sinica is an open and common feed that provide essential fatty acids for mariculture. In this study, the fatty acids profiles of brine shrimp cultured under different lower pH levels of CO 2 driven seawater were investigated. The results showed a significant reduction of the proportion of total saturated fatty acids under the pH7.6 within one week. Meanwhile, the percentage of total monounsaturated fatty acids was significantly decreased at day 14 under pH7.8, and this percentage gave a significant increase of proportion within one week under pH7.6. Furthermore, the relative content of total polyunsaturated fatty acids (PUFAs) was found to be clearly increased with exposure to different seawater acidification at day 1, suggesting that the brine shrimp immune response was likely to be affected by acidified seawater as the PUFAs have been well known to be involved in immunomodulatory effects through alterations on cell membrane fluidity/lipid mediators and gene expression of cell signaling pathways. Notably, eicosapentaenoic acid and docosahexaenoic acid, which have essential effect on various physiological processes such as inflammatory cytokines production and cell structural stability, were strongly increased under two lower pH treatments within one week and with the significant increase at day 1 under pH7.6. These data clearly supported the hypothesis that OA might affect fatty acids composition, likely also the innate immunity, in crustacean and the subsequent energy transfer by food-chain system in the marine ecosystem. Copyright © 2017 Elsevier Ltd. All

  8. The significance of oxygen as oxides and hydroxides in controlling the abundance and residence times of elements in seawater

    Digital Repository Service at National Institute of Oceanography (India)

    DileepKumar, M.

    A model is presented which signifies the role of oxygen (as oxides and hydroxides) in controlling the composition of seawater. respective concentration and residence times for the unknown elements can be estimated. Geometric and statistical indices...

  9. Diurnal variations in personal care products in seawater and mussels at three Mediterranean coastal sites.

    Science.gov (United States)

    Picot-Groz, Marina; Fenet, Hélène; Martinez Bueno, Maria Jesus; Rosain, David; Gomez, Elena

    2018-03-01

    The presence of personal care products (PCPs) in the marine environment is of major concern. PCPs, UV filters, and musks can enter the marine environment indirectly through wastewater or directly via recreational activities. We conducted this study to document patterns in the occurrence of seven PCPs at three coastal sites impacted by recreational activities during 1 day. The study focused on diurnal variations in these seven PCPs in seawater and indigenous mussels. In seawater, UV filters showed diurnal variations that mirrored variations in recreational activities at the sites. Ethylhexyl methoxycinnamate (EHMC) and octocrylene (OC) water concentrations increased from under the limit of quantification in the morning to 106 and 369 ng/L, respectively, when recreational activities were the highest. In mussels, diurnal variations in OC were observed, with the lowest concentrations recorded in the morning and then increasing throughout the day. As Mytilus spp. are widely used as sentinels in coastal pollution monitoring programs (mussel watch), our findings on diurnal variations could enhance sampling recommendations for recreational sites impacted by PCPs.

  10. Stability of the Cadmium Complex with the Bacterial Trihydroxamate Siderophore Desferrioxamine B at Seawater Ionic Strength

    Science.gov (United States)

    Christenson, E. A.; Schijf, J.

    2010-12-01

    The divalent transition metal cadmium occurs in seawater at ultra-trace levels. In the open ocean, dissolved Cd(II) displays a nutrient-like profile characterized by a strong gradient from low picomolar concentrations in surface waters to a mid-depth maximum of around 1 nM. Its vertical distribution is highly correlated with that of dissolved phosphate, seemingly at odds with the general perception that Cd is a very toxic element. On the other hand, in Zn-depleted waters Cd(II) has been found to replace Zn(II) or Co(II) in a functional, albeit less efficient form of carbonic anhydrase, a key enzyme enabling the assimilation of bicarbonate into organic matter. Considering these opposing roles, it is likely that phytoplankton regulates the toxicity and/or bioavailability of Cd(II) through the production of certain strong organic ligands, as it has been shown to do for example in the case of Cu(II). Siderophores are a fascinating class of organic ligands excreted by microorganisms to facilitate the acquisition of micronutrient Fe(III), preciously scarce due to its extremely low solubility in seawater. The linear trihydroxamic acid desferrioxamine B (DFOB) is naturally present in open ocean surface waters at picomolar concentrations and, because of its use as a pharmaceutical agent in the treatment of human iron overload disorders, the only purified siderophore commercially available in practicable quantities. The optimal spacing of three bidentate O-bearing functional groups along a flexible carbon frame allows the molecule to wrap around the Fe3+ ion in a polydentate heterocyclic structure that perfectly matches its ionic radius and preferred coordination. Despite its resultant exceptional affinity and selectivity for Fe3+ (β ~ 1031), DFOB also forms very stable complexes with an array of differently sized and charged cations. The only previous report on the stability constant of the Cd(II)-DFOB complex, dating from 1963, proposes a values of 108 at 0.1 M ionic

  11. Removal of I by adsorption with AgX (Ag-impregnated X Zeolite) from high-radioactive seawater waste

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Eil Hee; Lee, Keun Young; Kim, Kwang Wook; Kim, Hyung Ju; Kim, Ik Soo; Chung, Dong Yong; Moon, Jei Kwon; Choi, Jong Won [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2016-09-15

    This study aimed to the adsorption-removal of high- radioactive iodide (I) contained in the initially generated high-radioactive seawater waste (HSW), with the use of AgX (Ag-impregnated X zeolite). Adsorption of I by AgX (hereafter denoted as AgX-I adsorption) was increased by increasing the Ag-impregnated concentration in AgX, and its concentration was suitable at about 30 wt%. Because of AgCl precipitation by chloride ions contained in seawater waste, the leaching yields of Ag from AgX (Ag-impregnated concentration : about 30-35 wt%) was less than those in distilled water (< 1 mg/L). AgX-I adsorption was above 99% in the initial iodide concentration (Ci) of 0.01-10 mg/L at m/V (ratio of weight of adsorbent to solution volume)=2.5 g/L. This shows that efficient removal of I is possible. AgX-I adsorption was found to be more effective in distilled water than in seawater waste, and the influence of solution temperature was insignificant. Ag-I adsorption was better described by a Freundlich isotherm rather than a Langmuir isotherm. AgX-I adsorption kinetics can be expressed by a pseudo-second order rate equation. The adsorption rate constants (k2) decreased by increasing Ci, and conversely increased by increasing the ratio of m/V and the solution temperature. This time, the activation energy of AgX-I adsorption was about 6.3 kJ/mol. This suggests that AgX-I adsorption is dominated by physical adsorption with weaker bonds. The evaluation of thermodynamic parameters (a negative Gibbs free energy and a positive Enthalpy) indicates that AgX-I adsorption is a spontaneous reaction (forward reaction), and an endothermic reaction indicating that higher temperatures are favored.

  12. An optical biosensing film for biochemical oxygen demand determination in seawater with an automatic flow sampling system

    Science.gov (United States)

    Xin, Lingling; Wang, Xudong; Guo, Guangmei; Wang, Xiaoru; Chen, Xi

    2007-09-01

    An on-line roboticized apparatus, including an optical biosensing film with an automatic flow sampling system, has been developed for biochemical oxygen demand (BOD) determination of seawater. The sensing film employed in the apparatus consisted of an organically modified silicate (ORMOSIL) film embedded with tri(4,7-diphenyl-1,10-phenanthroline) ruthenium(II) perchlorate. Three species of microorganism cultivated from seawater were immobilized in an ORMOSIL-polyvinyl alcohol matrix. Possible factors affecting BOD determination were studied, including sampling frequency, temperature, pH and sodium chloride concentration. Based on measurements of the linear fluctuant coefficients and the reproducibility of its response to seawater, the BOD apparatus showed the advantages of high veracity and short response time. Generally, the linear fluctuant coefficient (R2) in the BOD range 0.2-40 mg l-1 was 0.9945 when using a glucose/glutamate (GGA) BOD standard solution. A reproducible response for the BOD sensing film of within ±2.8% could be obtained in the 2 mg l-1 GGA solution. The BOD apparatus was applied to the BOD determination of seawater, and the values estimated by this biosensing apparatus correlated well with those determined by the conventional 5 day BOD (BOD5) test.

  13. Mimicking Seawater For Culturing Marine Bacteria

    DEFF Research Database (Denmark)

    Rygaard, Anita Mac; Sonnenschein, Eva; Gram, Lone

    2015-01-01

    Only about 1% of marine bacteria have been brought into culture using traditional techniques. The purpose of this study was to investigate if mimicking the natural bacterial environment can increase culturability.We used marine substrates containing defined algal polymers or gellan gum as solidif......Only about 1% of marine bacteria have been brought into culture using traditional techniques. The purpose of this study was to investigate if mimicking the natural bacterial environment can increase culturability.We used marine substrates containing defined algal polymers or gellan gum...... as solidifying agents, and enumerated bacteria from seawater and algal exudates. We tested if culturability could be influenced by addition of quorum sensing signals (AHLs). All plates were incubated at 15°C. Bacterial counts (CFU/g) from algal exudates from brown algae were highest on media containing algal...... polymers. In general, bacteria isolated from algal exudates preferred more rich media than bacteria isolated from seawater. Overall, culturability ranged from 0.01 to 0.8% as compared to total cell count. Substitution of agar with gellan gum increased the culturability of seawater bacteria approximately...

  14. Endothelial Semaphorin 7A promotes inflammation in seawater aspiration-induced acute lung injury.

    Science.gov (United States)

    Zhang, Minlong; Wang, Li; Dong, Mingqing; Li, Zhichao; Jin, Faguang

    2014-10-28

    Inflammation is involved in the pathogenesis of seawater aspiration-induced acute lung injury (ALI). Although several studies have shown that Semaphorin 7A (SEMA7A) promotes inflammation, there are limited reports regarding immunological function of SEMA7A in seawater aspiration-induced ALI. Therefore, we investigated the role of SEMA7A during seawater aspiration-induced ALI. Male Sprague-Dawley rats were underwent seawater instillation. Then, lung samples were collected at an indicated time for analysis. In addition, rat pulmonary microvascular endothelial cells (RPMVECs) were cultured and then stimulated with 25% seawater for indicated time point. After these treatments, cells samples were collected for analysis. In vivo, seawater instillation induced lung histopathologic changes, pro-inflammation cytokines release and increased expression of SEMA7A. In vitro, seawater stimulation led to pro-inflammation cytokine release, cytoskeleton remodeling and increased monolayer permeability in pulmonary microvascular endothelial cells. In addition, knockdown of hypoxia-inducible factor (HIF)-1α inhibited the seawater induced increase expression of SEMA7A. Meanwhile, knockdown of SEMA7A by specific siRNA inhibited the seawater induced aberrant inflammation, endothelial cytoskeleton remodeling and endothelial permeability. These results suggest that SEMA7A is critical in the development of lung inflammation and pulmonary edema in seawater aspiration-induced ALI, and may be a therapeutic target for this disease.

  15. Direct seawater desalination by ion concentration polarization

    Science.gov (United States)

    Kim, Sung Jae; Ko, Sung Hee; Kang, Kwan Hyoung; Han, Jongyoon

    2010-04-01

    A shortage of fresh water is one of the acute challenges facing the world today. An energy-efficient approach to converting sea water into fresh water could be of substantial benefit, but current desalination methods require high power consumption and operating costs or large-scale infrastructures, which make them difficult to implement in resource-limited settings or in disaster scenarios. Here, we report a process for converting sea water (salinity ~500 mM or ~30,000 mg l-1) to fresh water (salinity water is divided into desalted and concentrated streams by ion concentration polarization, a phenomenon that occurs when an ion current is passed through ion-selective membranes. During operation, both salts and larger particles (cells, viruses and microorganisms) are pushed away from the membrane (a nanochannel or nanoporous membrane), which significantly reduces the possibility of membrane fouling and salt accumulation, thus avoiding two problems that plague other membrane filtration methods. To implement this approach, a simple microfluidic device was fabricated and shown to be capable of continuous desalination of sea water (~99% salt rejection at 50% recovery rate) at a power consumption of less than 3.5 Wh l-1, which is comparable to current state-of-the-art systems. Rather than competing with larger desalination plants, the method could be used to make small- or medium-scale systems, with the possibility of battery-powered operation.

  16. Uncertainties of retrospective radon concentration measurements by multilayer surface trap detector

    International Nuclear Information System (INIS)

    Bastrikov, V.; Kruzhalov, A.; Zhukovsky, M.

    2006-01-01

    The detector for retrospective radon exposure measurements is developed. The detector consists of the multilayer package of solid-state nuclear track detectors LR-115 type. Nitrocellulose films works both as α-particle detector and as absorber decreasing the energy of α-particles. The uncertainties of implanted 210 Pb measurements by two- and three-layer detectors are assessed in dependence on surface 210 Po activity and gross background activity of the glass. The generalized compartment behavior model of radon decay products in the room atmosphere was developed and verified. It is shown that the most influencing parameters on the value of conversion coefficient from 210 Po surface activity to average radon concentration are aerosol particles concentration, deposition velocity of unattached 218 Po and air exchange rate. It is demonstrated that with the use of additional information on surface to volume room ratio, air exchange rate and aerosol particles concentration the systematic bias of conversion coefficient between surface activity of 210 Po and average radon concentration can be decreased up to 30 %. (N.C.)

  17. Corrosion studies of a chromium steel in imitated seawater

    International Nuclear Information System (INIS)

    Lakatos-Varsanyi, M.; Meisel, W.

    2002-01-01

    A series of in-door experiments was performed to get some insight into the corrosion behavior of a commercial alloy Fe-12% Cr (3CR12) exposed to imitated seawater. Applying different analytical methods, the main corrosion process was found to be the formation of flakes on the surface which, peel off after they have reached a certain size. Some Cr is dissolved in the solution, its relative concentration with respect to Fe is higher than in the bulk material. The flakes consist mainly of mixed oxihydroxides of the type FeOOH containing some Cr and Mg. The oxidic layer on the interface is very thin, behaves essentially stationary with a slight growth of about 0.05 nm/day. It consists of Cr oxide with some inclusions of Fe and Mg and is not of a chromite type. Immediately below this oxidic layer, the metallic substrate exhibits a thin layer depleted in Cr and behaving like α-Fe (bcc). As compared with stainless steel, potentiostatic current vs. time records at anodic potentials below the pitting potential indicate a very different stability of the surface films for 3CR12. The kinetics of the passive layer formation on 3CR12 was found to follow a parabolic law initially and to change later (after 10...100 seconds in deaerated solution and even earlier in aerated solution) to a linear law. After some time, pitting corrosion and/or cracks due to internal stresses play the dominant role. Cr does not form a protective oxidic layer. The surface morphology of samples exposed at -200 mV for 20 and 80 minutes has been studied by scanning electron microscopy and scanning Auger microprobe. The results reflect the competing formation of oxidic layers and pitting, the participation of Cr in the dissolution process. It is also suggested that Mg, which is a component of the solution was incorporated into the rust and some Mg was also found on the metallic surface. (author)

  18. Effect of soil surface management on radiocesium concentrations in apple orchard and fruit

    International Nuclear Information System (INIS)

    Kusaba, Shinnosuke; Matsuoka, Kaori; Abe, Kazuhiro

    2016-01-01

    We investigated the effect of soil surface management on radiocesium accumulation in an apple orchard in Fukushima Prefecture over 4 years after Tokyo Electric Power Company’s Fukushima Daiichi nuclear power plant accident in mid-March 2011. Different types of soil surface management such as clean cultivation, intertillage management, intertillage with bark compost application, sod culture, and zeolite application were employed. The radiocesium concentrations in soil were higher in the surface layer (0–5 cm) than in the other layers. The radiocesium concentration in the surface layer soil with sod culture in 2014 increased non-significantly compared with that observed in 2011. The radiocesium concentration in the mid-layer soil (5–15 cm) managed with intertillage was higher than that in soil managed using other types of management. The radiocesium amount in the organic matter on the soil surface was the highest in sod culture, and was significantly lower in the management with intertillage. The radiocesium concentration in fruit decreased exponentially during the 4 years in each types of soil surface management. The decrease in radiocesium concentration showed similar trends with each type of soil surface management, even if the concentration in each soil layer varied according to the management applied. Furthermore, intertillage with bark compost application did not affect the radiocesium concentration in fruit. These results suggest that the soil surface management type that affected the radiocesium distribution in the soil or the compost application with conventional practice did not affect its concentration in fruit of apple trees for at least 4 years since the nuclear power plant accident, at a radiocesium deposition level similar to that recorded in Fukushima City. (author)

  19. Degradation of riverine dissolved organic matter by seawater bacteria

    NARCIS (Netherlands)

    Rochelle-Newall, E.J.; Pizay, M-D.; Middelburg, J.J.; Boschker, H.T.S.; Gattuso, J.P.

    2004-01-01

    The functional response of a seawater bacterial community transplanted into freshwater dissolved organic matter (DOM) was investigated together with the response of natural populations of bacteria to size-fractioned natural source water. Seawater bacteria were incubated over a period of 8 d in

  20. Corrosion of mild steel, copper and brass in crude oil / seawater mixture

    Digital Repository Service at National Institute of Oceanography (India)

    PrabhaDevi, S.; Sawant, S.S.; Wagh, A.B.

    Mild steel, copper and brass coupons were introduced in natural seawater containing varying amount of crude oil. Mild steel showed higher rate of corrosion in seawater containing oil and lower corrosion rate in natural as well as artificial seawater...