Water Column Sonar Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — The collection and analysis of water column sonar data is a relatively new avenue of research into the marine environment. Primary uses include assessing biological...

Water hammer with column separation : a historical review

NARCIS (Netherlands)

Bergant, A.; Simpson, A.R.; Tijsseling, A.S.

2006-01-01

Column separation refers to the breaking of liquid columns in fully filled pipelines. This may occur in a water-hammer event when the pressure in a pipeline drops to the vapor pressure at specific locations such as closed ends, high points or knees (changes in pipe slope). The liquid columns are

Preconcentration and determination of heavy metals in water, sediment and biological samples

Directory of Open Access Journals (Sweden)

Shirkhanloo Hamid

2011-01-01

Full Text Available In this study, a simple, sensitive and accurate column preconcentration method was developed for the determination of Cd, Cu and Pb ions in river water, urine and sediment samples by flame atomic absorption spectrometry. The procedure is based on the retention of the analytes on a mixed cellulose ester membrane (MCEM column from buffered sample solutions and then their elution from the column with nitric acid. Several parameters, such as pH of the sample solution, volume of the sample and eluent and flow rates of the sample were evaluated. The effects of diverse ions on the preconcentration were also investigated. The recoveries were >95 %. The developed method was applied to the determination of trace metal ions in river water, urine and sediment samples, with satisfactory results. The 3δ detection limits for Cu, Pb and Cd were found to be 2, 3 and 0.2 μg dm−3, respectively. The presented procedure was successfully applied for determination of the copper, lead and cadmium contents in real samples, i.e., river water and biological samples.

Speciation of arsenic in water samples by high-performance liquid chromatography-hydride generation-atomic absorption spectrometry at trace levels using a post-column reaction system

Energy Technology Data Exchange (ETDEWEB)

Stummeyer, J. [Bundesanstalt fuer Geowissenschaften und Rohstoffe, Hannover (Germany); Harazim, B. [Bundesanstalt fuer Geowissenschaften und Rohstoffe, Hannover (Germany); Wippermann, T. [Bundesanstalt fuer Geowissenschaften und Rohstoffe, Hannover (Germany)

1996-02-01

Anion-exchange HPLC has been combined with hydride generation - atomic absorption spectrometry (HG-AAS) for the routine speciation of arsenite, arsenate, monomethylarsenic acid and dimethylarsinic acid. The sensitivity of the AAS-detection was increased by a post-column reaction system to achieve complete formation of volatile arsines from the methylated species and arsenate. The system allows the quantitative determination of 0.5 {mu}g/l of each arsenic compound in water samples. The stability of synthetical and natural water containing arsenic at trace levels was investigated. To preserve stored water samples, a method for quantitative separation of arsenate at high pH-values with the basic anion-exchange resin Dowex 1 x 8 was developed. (orig.)

Enrichment of heavy water in thermal-diffusion columns connected in series

International Nuclear Information System (INIS)

Yeh, Ho-Ming; Chen, Liu Yi

2009-01-01

The separation equations for enrichment of heavy water from water isotope mixture by thermal diffusion in multiple columns connected in series, have been derived based on one column design developed in previous work. The improvement in separation is achievable by operating in a double-column device, instead of in a single-column device, with the same total column length. It is also found that further improvement in separation is obtainable if a triple-column device is employed, except for operating under small total column length and low flow rate.

Comparison of Passive Samplers for Monitoring Dissolved Organic Contaminants in Water Column Deployments NAC/SETAC 2012

Science.gov (United States)

Nonionic organic contaminants (NOCs) are difficult to measure in the water column due to their inherent chemical properties resulting in low water solubility and high particle activity. Traditional sampling methods require large quantities of water to be extracted and interferen...

Denitrification in the water column of the central Baltic Sea

DEFF Research Database (Denmark)

Dalsgaard, Tage; De Brabandere, Loreto; Hall, Per O. J.

2013-01-01

Removal of fixed nitrogen in the water column of the eastern Gotland Basin, central Baltic Sea, was studied during two cruises in September 2008 and August 2010. The water column was stratified with anoxic sulfidic bottom water meeting oxic nitrate containing water at the oxic–anoxic interface......3 or sulfide concentrations were converted to in situ rates using the measured water column concentrations of NO3 and sulfide and the actual measured relations between NO3 and sulfide concentrations and enitrification rates. In situ denitrification ranged from 0.24 to 15.9 nM N2 h1. Assuming...... area. Even with an active denitrification layer of 3–6 m thickness the pelagic denitrification per unit area clearly exceeded sediment denitrification rates elsewhere in the Baltic Sea. When extrapolated to the entire Baltic Proper (BP) denitrification in the water column was in the range of 132...

Water column methanotrophy controlled by a rapid oceanographic switch

NARCIS (Netherlands)

Steinle, L.; Graves, C.A.; Treude, T.; Ferré, B.; Biastoch, A.; Bussmann, I.; Berndt, C.; Krastel, S.; James, R.H.; Behrens, E.; Böning, C.W.; Greinert, J.; Sapart, C.-J.; Scheinert, M.; Sommer, S.; Lehmann, M.F.; Niemann, H.

2015-01-01

From the seabed to the water column, where it may be consumed by aerobic methanotrophic bacteria. The size and activity of methanotrophic communities, which determine the amount of methane consumed in the water column,are thought to be mainly controlled by nutrient and redoxdynamics3–7. Here, we

Process for prevention of water build-up in cryogenic distillation column

International Nuclear Information System (INIS)

Hopewell, R.B.

1988-01-01

In a process for the separation of a hydrocarbon and acid gas containing feed stream in a cryogenic distillation column, a zone of the column which is operated at a temperature of 60 0 F or less, wherein free water accumulates or forms hydrates in the column from water vapor in the feed stream during the cryogenic process, and which process comprises separating the feed stream in the column into an overhead stream and a bottom stream, this patent describes the improvement which comprises: withdrawing a hydrocarbon and acid gas vapor stream which stream is enriched in water vapor with respect to the feed stream, thereby preventing the excess accumulation of free water or the formation of hydrates in the cryogenic column

EX0904 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0904: Water Column Exploration Field...

Mobility of arsenic, cadmium and zinc in a multi-element contaminated soil profile assessed by in-situ soil pore water sampling, column leaching and sequential extraction

International Nuclear Information System (INIS)

Beesley, Luke; Moreno-Jimenez, Eduardo; Clemente, Rafael; Lepp, Nicholas; Dickinson, Nicholas

2010-01-01

Three methods for predicting element mobility in soils have been applied to an iron-rich soil, contaminated with arsenic, cadmium and zinc. Soils were collected from 0 to 30 cm, 30 to 70 cm and 70 to 100 cm depths in the field and soil pore water was collected at different depths from an adjacent 100 cm deep trench. Sequential extraction and a column leaching test in the laboratory were compared to element concentrations in pore water sampled directly from the field. Arsenic showed low extractability, low leachability and occurred at low concentrations in pore water samples. Cadmium and zinc were more labile and present in higher concentrations in pore water, increasing with soil depth. Pore water sampling gave the best indication of short term element mobility when field conditions were taken into account, but further extraction and leaching procedures produced a fuller picture of element dynamics, revealing highly labile Cd deep in the soil profile. - Mobility of arsenic, cadmium and zinc in a polluted soil can be realistically interpreted by in-situ soil pore water sampling.

Seasonal and Water Column Trends of the Relative Role of Nitrate and Nitrite as ·OH Sources in Surface Waters

International Nuclear Information System (INIS)

Vione, D.; Minero, C.; Maurino, V.; Pelizzetti, E.

2007-01-01

Based on literature data of sunlight spectrum, photolysis quantum yields, and absorption spectra, the relative role of nitrite and nitrate as ·OH sources in surface waters was assessed, and its dependence on the season and the depth of the water column studied. In the majority of surface water samples (river, lake and seawater) nitrite is expected to play a more important role as ·OH source compared to nitrate, in spite of the usually lower [NO 2 - ] values. Interestingly, under the hypothesis of a constant ratio of the concentrations of nitrate and nitrite (to be corrected later on for the actual concentration ratio in a given sample), the relative role of nitrite compared to nitrate would be minimum in summer, at noon, in the surface layer of natural waters. Any decrease in the sunlight intensity that can be experienced in the natural environment (different season than summer, water column absorption, time of the day other than the solar noon), with its associated influence on the sunlight spectrum, would increase the relative role of nitrite compared to nitrate

HPLC determination of betamethasone and prednisolone in urine samples using monolithic column

International Nuclear Information System (INIS)

Abro, K.; Memon, N.; Bhanger, M.I.

2011-01-01

A fast and reliable HPLC method is reported for the separation and quantification of betamethasone and prednisolone in urine samples using Chromolith at the rate of Performance RP-l8e (100 mm x 4.6 mm) column. The separation and detection was achieved using an isocratic mobile phase composed of methanol:water (44:56 v/v) at 2.0 mL/min and wavelength of 254 nm. After successful optimisation of method parameters, it was applied to the urine samples. Solid phase extraction technique was used to clean the sample before analysis. The developed method was validated for the system suitability, precision and accuracy. The limits of defection for the prednisolone and betamethasone are 0.11 ng and 0.075 ng/10 macro L injection, respectively allowing their determination in human urine samples. Recovery for spiked urine samples was in the range of 97-103 %. The method offers a valuable alternative to the methodologies currently employed for separation and quantification of prednisolone and betamethasone in urine samples. A fast and reliable HPLC method is reported for the separation and quantification of betamethasone and prednisolone in urine samples using Chromolith at the rate of Performance RP-l8e (100 mm x 4.6 mm) column. The separation and detection was achieved using an isocratic mobile phase composed of methanol:water (44:56 v/v) at 2.0 mL/min and wavelength of 254 nm. After successful optimisation of method parameters, it was applied to the urine samples. Solid phase extraction technique was used to clean the sample before analysis. The developed method was validated for the system suitability, precision and accuracy. The limits of defection for the prednisolone and betamethasone are 0.11 ng and 0.075 ng/10 macro L injection, respectively allowing their determination in human urine samples. Recovery for spiked urine samples was in the range of 97-103 %. The method offers a valuable alternative to the methodologies currently employed for separation and quantification

Flow of gasoline-in-water microemulsion through water-saturated soil columns

International Nuclear Information System (INIS)

Ouyang, Y.; Mansell, R.S.; Rhue, R.D.

1995-01-01

Much consideration has been given to the use of surfactants to clean up nonaqueous phase liquids (NAPLs) from contaminated soil and ground water. Although this emulsification technique has shown significant potential for application in environmental remediation practices, a major obstacle leading to low washing efficiency is the potential formation of macroemulsion with unfavorable flow characteristics in porous media. This study investigated influences of the flow of leaded-gasoline-in-water (LG/W) microemulsion upon the transport of gasoline and lead (Pb) species in water-saturated soil columns. Two experiments were performed: (1) the immiscible displacement of leaded gasoline and (2) the miscible displacement of LG/W microemulsion through soil columns, followed by sequentially flushing with NaCl solution and a water/surfactant/cosurfactant (W/S/CoS) mixture. Comparison of breakthrough curves (BTC) for gasoline between the two experiments shows that about 90% of gasoline and total Pb were removed from the soil columns by NaCl solution in the LG/W microemulsion experiment as compared to 40% removal of gasoline and 10% removal of total Pb at the same process in the leaded gasoline experiment. Results indicate that gasoline and Pb species moved much more effectively through soil during miscible flow of LG/W microemulsion than during immiscible flow of leaded gasoline. In contrast to the adverse effects of macroemulsion on the transport of NAPLs, microemulsion was found to enhance the transport of gasoline through water-saturated soil. Mass balance analysis shows that the W/S/CoS mixture had a high capacity for removing residual gasoline and Pb species from contaminated soil. Comparison of water-pressure differences across the soil columns for the two experiments indicates that pore clogging by gasoline droplets was greatly minimized in the LG/W microemulsion experiment

Water column velocimeter for NSRR experiment. Characteristics and data processing procedure

International Nuclear Information System (INIS)

Sugiyama, Tomoyuki; Fuketa, Toyoshi

2000-11-01

In order to clarify fuel behavior under reactivity initiated accident (RIA) conditions, pulse irradiation experiments on fuel rods are carried out in the Nuclear Safety Research Reactor (NSRR). One of concerns at fuel failure is mechanical energy generation in the reactor vessel. The mechanical energy is generated by a water hammer or a pressure impact occurred at fuel failure, and has possibility to damage reactor structures. Thus, the amount of generated mechanical energy is critical information for the safety evaluation of power reactor. In the NSRR experiments, the mechanical energy due to the water hammer is evaluated as the kinetic energy of the jumping water column at fuel failure, and the velocity of the water column is measured by the float type water column velocimeter. This report presents characteristics of the water column velocimeter and the procedure of data processing in the NSRR experiments. (author)

Insights into head-column field-amplified sample stacking: Part II. Study of the behavior of the electrophoretic system after electrokinetic injection of cationic compounds across a short water plug

Czech Academy of Sciences Publication Activity Database

Šesták, Jozef; Thormann, W.

2017-01-01

Roč. 1512, AUG (2017), s. 124-132 ISSN 0021-9673 Institutional support: RVO:68081715 Keywords : head-column field-amplified sample stacking * capillary electrophoresis * water plug Subject RIV: CB - Analytical Chemistry, Separation OBOR OECD: Analytical chemistry Impact factor: 3.981, year: 2016

Insights into head-column field-amplified sample stacking: Part II. Study of the behavior of the electrophoretic system after electrokinetic injection of cationic compounds across a short water plug

Czech Academy of Sciences Publication Activity Database

Šesták, Jozef; Thormann, W.

2017-01-01

Roč. 1512, AUG (2017), s. 124-132 ISSN 0021-9673 Institutional support: RVO:68081715 Keywords : head- column field-amplified sample stacking * capillary electrophoresis * water plug Subject RIV: CB - Analytical Chemistry, Separation OBOR OECD: Analytical chemistry Impact factor: 3.981, year: 2016

Water column conditions in a coastal lagoon near Jeddah, Red Sea

Directory of Open Access Journals (Sweden)

Alaa M. A. Albarakati

2012-11-01

Full Text Available Water column conditions in a lagoon near Jeddah are investigated on the basisof changes in potential energy. Three major factors including balance ofsurface heat at the air-sea interface, wind and tidal mixing are considered.A negative potential energy change dv/dt will developstratification, whereas positive dv/dt will tend to mix the watercolumn. The tidal effect is greater in summer with wind mixing showing nogreat variations. The buoyancy effect of the heat balance at the surface isnegative from April to October. This negative buoyancy effect will tend to developstratification but the positive contributions of wind and tide counteract this andthe water column remains mixed except in September and October, when a weakstratification may develop. Generally, the water column remains practically mixedthroughout the year. The change in heat content of the water column from mid-Aprilto mid-September is about 3.3 × 108 J. During this period the netheat input at the air interface is about 2.0 × 108 J, which isabout 40% less than the heat content of the water column, showing that the heat is advected towards the central area from the shallower periphery of the lagoon.

Quantifying the Benthic Source of Nutrients to the Water Column of Upper Klamath Lake, Oregon

Science.gov (United States)

Kuwabara, James S.; Lynch, Dennis D.; Topping, Brent R.; Murphy, Fred; Carter, James L.; Simon, Nancy S.; Parcheso, Francis; Wood, Tamara M.; Lindenberg, Mary K.; Wiese, Katryn; Avanzino, Ronald J.

2007-01-01

Executive Summary Five sampling trips were coordinated in April, May and August 2006, and May and July 2007 to sample the water column and benthos of Upper Klamath Lake, OR (Fig. 1; Table 1), before, during and after the annual cyanophyte bloom of Aphanizomenon flos-aquae (AFA). A pore-water profiler was designed and fabricated to obtain the first high-resolution (centimeter-scale) estimates of the vertical concentration gradients for diffusive-flux determinations. Estimates based on molecular diffusion may underestimate benthic flux because solute transport across the sediment-water interface can be enhanced by processes including bioturbation, bioirrigation and ground-water advection. Water-column and benthic samples were also collected to help interpret spatial and temporal trends in diffusive-flux estimates. Data from these samples complement geochemical analyses of bottom-sediments taken from Upper Klamath Lake (UKL) in 2005. This ongoing study provides information necessary for developing process-interdependent solute-transport models for the watershed (that is, models integrating physical, geochemical and biological processes), and supports efforts to evaluate remediation or load-allocation strategies. To augment studies funded by the U.S. Bureau of Reclamation (USBR), the Department of Interior supported an additional full deployment of pore-water profilers in July 2007, during the summer AFA bloom. Results from this recent field trip are not fully completed. Data not presented herein will be included in a subsequent publication, scheduled for March 2009.

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides in water columns from the Pearl River and the Macao harbor in the Pearl River Delta in South China.

Science.gov (United States)

Luo, Xiaojun; Mai, Bixian; Yang, Qingshu; Fu, Jiamo; Sheng, Guoying; Wang, Zhishi

2004-06-01

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) were measured in suspended particles and dissolved phase from the Baiertang water column and the Macao water column samples as collected from the Guangzhou channel of the Pearl River and the Macao harbor, where the sediments were heavily contaminated with organic pollutants. Total OCPs concentration varies from 23.4 to 61.7 ng/l in Baiertang water column and from 25.2 to 67.8 ng/l in Macao column, while total PAHs concentration varies from 987.1 to 2878.5 ng/l in the Baiertang water column and from 944.0 to 6654.6 ng/l in the Macao column. The vertical distribution profiles of pollutants and the partition of pollutants between particles and dissolved phases indicate that the sediments in Baiertang act as an important source of selected pollutants, and the pollutants in water of this region were mainly originated from the release and re-suspension of contaminants residing in the sediments. The sediments in Macao harbor act as a reservoir for organochlorine pesticides, such as DDTs mainly introduced by river inflow from Xijiang and PAHs input by brackish water from the Lingdingyang estuary. Combustion of fossil fuels and petroleum input are the main sources of PAHs in the Macao water column, while combustion of fossil fuels and coal is responsible for the PAHs in the Baiertang water column. The ratios of DDT/(DDD+DDE) for the Macao water column samples demonstrate that such chemicals were input into this region in recent times.

Water column correction for coral reef studies by remote sensing.

Science.gov (United States)

Zoffoli, Maria Laura; Frouin, Robert; Kampel, Milton

2014-09-11

Human activity and natural climate trends constitute a major threat to coral reefs worldwide. Models predict a significant reduction in reef spatial extension together with a decline in biodiversity in the relatively near future. In this context, monitoring programs to detect changes in reef ecosystems are essential. In recent years, coral reef mapping using remote sensing data has benefited from instruments with better resolution and computational advances in storage and processing capabilities. However, the water column represents an additional complexity when extracting information from submerged substrates by remote sensing that demands a correction of its effect. In this article, the basic concepts of bottom substrate remote sensing and water column interference are presented. A compendium of methodologies developed to reduce water column effects in coral ecosystems studied by remote sensing that include their salient features, advantages and drawbacks is provided. Finally, algorithms to retrieve the bottom reflectance are applied to simulated data and actual remote sensing imagery and their performance is compared. The available methods are not able to completely eliminate the water column effect, but they can minimize its influence. Choosing the best method depends on the marine environment, available input data and desired outcome or scientific application.

Water column separation in power plant circulating water systems

International Nuclear Information System (INIS)

Papadakis, C.N.

1977-01-01

Power plant circulating water system condensers operate with a siphon. Column separation is a common occurence in such condensers during low pressure transients. The assumptions that no gas evolves from solution leads to very conservative values of maximum pressures upon rejoining of separated column. A less conservative method led to the development of a macroscopic mathematical model including the presence of air and vapor in a cavity which forms at the top of the condenser. The method of characteristics is used to solve the equations. A case study is analyzed to illustrate the applicability of the developed mathematical model and to provide comparisons of the results obtained

Tritium isotope separation by water distillation column packed with silica-gel beads

International Nuclear Information System (INIS)

Fukada, Satoshi

2004-01-01

Tritium enrichment or depletion by water distillation was investigated using a glass column of 32cm in height packed with silica-gel beads of 3.4mm in average diameter. The total separation factor of the silica-gel distillation column, α H-T , was compared with those of an open column distillation tower and of a column packed with stainless-steel Dixon rings. Depletion of the tritium activity in the distillate was enhanced by isotopic exchange with water absorbed on silica-gel beads that have a higher affinity for HTO than for H 2 O. The value of α H-T -1 of the silica-gel distillation column was about four times larger than that of a column without any packing and about two times larger than that of the Dixon-ring column. The improvement of α H-T by the silica-gel adsorbent indicated that the height of the distillation-adsorption column becomes shorter than that of the height of conventional distillation columns. (author)

Influence of bioassay volume, water column height, and octanol-water partition coefficient on the toxicity of pesticides to rainbow trout.

Science.gov (United States)

Altinok, Ilhan; Capkin, Erol; Boran, Halis

2011-06-01

Effects of water volume and water column height on toxicity of cypermethrin, carbaryl, dichlorvos, tetradifon, maneb, captan, carbosulfan endosulfan and HgCl₂ to juvenile rainbow trout (Oncorhynchus mykiss, 3.2 ± 0.7 g) were evaluated in different glass aquaria under static conditions. When fish were exposed to the chemical compounds in 23 cm water column height (25 L), their mortality ranged between 0% and 58%. At the same water volume, but lower water column height (9 cm), mortality of fish increased significantly and was in a range from 60% to 95%. At the same water column height, toxic effects of chemicals were significantly higher in 25 L water volume than that of 8.5 L, water except maneb which has lowest (-0.45) octanol-water partition coefficient value. Mortality rates ratio of 9 and 23 cm water column height ranged between 1.12 and 90 while mortality rates ratio of 9 and 25 L water volume ranged between 1.20 and 4.0. Because actual exposure concentrations were not affected by either water volume or water column height, we propose that increased pesticides' toxicity was related to an increase in bioassay volume, since more pesticide molecules were able to interact with or accumulate the fish. However, there seem to be no relationship between the effects of water volume, water column height and Kow value of chemicals with regard to toxicity in juvenile rainbow trout.

Gradient HPLC of antibiotics in urine, ground water, chicken muscle, hospital wastewater, and pharmaceutical samples using C-18 and RP-amide columns.

Science.gov (United States)

Kumar, Ashwini; Kumar Malik, Ashok; Kumar Tewary, Dhananjay; Singh, Baldev

2008-02-01

A simple and highly sensitive high pressure liquid chromatographic (HPLC-UV) method has been developed for the determination of ofloxacin, lomefloxacin, cinoxacin, and nalidixic acid, in mobile phase citrate buffer (0.001 M) of pH 4.5 prepared in water (X), methanol (Y), and ACN (Z) using gradient at a flow rate of 1.0 mL/min by direct UV absorbance detection at lambda = 280 nm. Separation of analytes was studied on the C-18 and RP-amide columns and best results were observed on the RP-amide column with LODs (3.3 x S/m) 0.89, 0.55, 0.67, and 1.41 ng/mL for ofloxacin, lomefloxacin, cinoxacin, and nalidixic acid, respectively, and better RSD than the C-18 column. The recovery of Fluoroquinolones (FQs) in urine, ground water, hospital wastewater, and chicken muscle using this method is more than 90%. The method was successfully applied to the analysis of ofloxacin, lomefloxacin, cinoxacin, and nalidixic acid in urine, ground water, pharmaceutical dosage forms, hospital wastewater, and chicken muscle.

A device for fresh water sampling before radioactive measurements

International Nuclear Information System (INIS)

Maubert, Henri; Picat, Philippe.

1982-06-01

On account of the many field operations carried out by the laboratory, a water sampling device has been developed. This portable autonomous device performs in situ water filtration and concentration on ion exchange resins and activated carbon columns. The device is described and the trapping performance for 8 radionuclides is given. A comparison is made with the so-called evaporation method. The effects of the treatment of the filtrating elements on the radioactive results are studied. This sampling method is very sensitive [fr

Methane seepage along the Hikurangi Margin of New Zealand : geochemical and physical data from the water column, sea surface and atmosphere

OpenAIRE

Faure, Kevin; Greinert, Jens; Schneider, Jens; McGinnis, Daniel; Kipfer, Rolf; Linke, Peter

2010-01-01

The concentration and carbon isotope values of dissolved methane were measured in the water column at Rock Garden, Omakere Ridge and Wairarapa areas in the first dedicated cold seep investigation along the Hikurangi Margin of New Zealand. These measurements provide a high resolution impression of the methane distribution in the water column and show that these seep sites are actively venting methane with varying intensity. The highest concentrations (up to 3500 nM) measured in water samples o...

Water Column Correction for Coral Reef Studies by Remote Sensing

Directory of Open Access Journals (Sweden)

Maria Laura Zoffoli

2014-09-01

Full Text Available Human activity and natural climate trends constitute a major threat to coral reefs worldwide. Models predict a significant reduction in reef spatial extension together with a decline in biodiversity in the relatively near future. In this context, monitoring programs to detect changes in reef ecosystems are essential. In recent years, coral reef mapping using remote sensing data has benefited from instruments with better resolution and computational advances in storage and processing capabilities. However, the water column represents an additional complexity when extracting information from submerged substrates by remote sensing that demands a correction of its effect. In this article, the basic concepts of bottom substrate remote sensing and water column interference are presented. A compendium of methodologies developed to reduce water column effects in coral ecosystems studied by remote sensing that include their salient features, advantages and drawbacks is provided. Finally, algorithms to retrieve the bottom reflectance are applied to simulated data and actual remote sensing imagery and their performance is compared. The available methods are not able to completely eliminate the water column effect, but they can minimize its influence. Choosing the best method depends on the marine environment, available input data and desired outcome or scientific application.

Water Column Correction for Coral Reef Studies by Remote Sensing

Science.gov (United States)

Zoffoli, Maria Laura; Frouin, Robert; Kampel, Milton

2014-01-01

Human activity and natural climate trends constitute a major threat to coral reefs worldwide. Models predict a significant reduction in reef spatial extension together with a decline in biodiversity in the relatively near future. In this context, monitoring programs to detect changes in reef ecosystems are essential. In recent years, coral reef mapping using remote sensing data has benefited from instruments with better resolution and computational advances in storage and processing capabilities. However, the water column represents an additional complexity when extracting information from submerged substrates by remote sensing that demands a correction of its effect. In this article, the basic concepts of bottom substrate remote sensing and water column interference are presented. A compendium of methodologies developed to reduce water column effects in coral ecosystems studied by remote sensing that include their salient features, advantages and drawbacks is provided. Finally, algorithms to retrieve the bottom reflectance are applied to simulated data and actual remote sensing imagery and their performance is compared. The available methods are not able to completely eliminate the water column effect, but they can minimize its influence. Choosing the best method depends on the marine environment, available input data and desired outcome or scientific application. PMID:25215941

Recycling of drinking water treatment residue as an additional medium in columns for effective P removal from eutrophic surface water.

Science.gov (United States)

Wang, Changhui; Wu, Yu; Bai, Leilei; Zhao, Yaqian; Yan, Zaisheng; Jiang, Helong; Liu, Xin

2018-07-01

This study assesses the feasibility of recycling drinking water treatment residue (DWTR) to treat eutrophic surface water in a one-year continuous flow column test. Heat-treated DWTR was used as an additional medium (2%-4%) in columns in case excessive organic matter and N were released from the DWTR to surface water. The results indicated that with minimal undesirable effects on other water properties, DWTR addition substantially enhanced P removal, rendering P concentrations in treated water oligotrophic and treated water unsuitable for Microcystis aeruginosa breeding. Long-term stable P removal by DWTR-column treatment was mainly attributed to the relatively low P levels in raw water (cycles and multiple pollution control (e.g., Dechloromonas, Geobacter, Leucobacter, Nitrospira, Rhodoplanes, and Sulfuritalea); an apparent decrease in Mycobacterium with potential pathogenicity was observed in DWTR-columns. Regardless, limited denitrification of DWTR-columns was observed as a result of low bioavailability of C in surface water. This finding indicates that DWTR can be used with other methods to ensure denitrification for enhanced treatment effects. Overall, the use of DWTR as an additional medium in column systems can potentially treat eutrophic surface water. Copyright © 2018 Elsevier Ltd. All rights reserved.

46 CFR 52.01-110 - Water-level indicators, water columns, gauge-glass connections, gauge cocks, and pressure gauges...

Science.gov (United States)

2010-10-01

... § 52.01-110 Water-level indicators, water columns, gauge-glass connections, gauge cocks, and pressure... 46 Shipping 2 2010-10-01 2010-10-01 false Water-level indicators, water columns, gauge-glass connections, gauge cocks, and pressure gauges (modifies PG-60). 52.01-110 Section 52.01-110 Shipping COAST...

Qualilty, isotopes, and radiochemistry of water sampled from the Upper Moenkopi Village water-supply wells, Coconino County, Arizona

Science.gov (United States)

Carruth, Rob; Beisner, Kimberly; Smith, Greg

2013-01-01

water with a major ion composition of calcium and sulfate. There is no significant vertical distribution of ion concentrations in the samples collected from the upper and lower portion of the water column within the two wells. The samples collected at MSW-3 are higher in sodium and lower in calcium than the samples collected from MSW-1 and MSW-2, and contain a similar sulfate-ion percentage. There is a vertical distribution of ion concentrations in the samples collected from the upper and lower portion of the water column in MSW-3. Groundwater samples from the three water-supply wells analyzed for oxygen-18 and deuterium stable isotopes plot on a local water line that is approximately parallel to the global meteoric water line. Tritium concentrations in samples from MSW-1 and MSW-3 were equal to or less than laboratory detection limits and were interpreted to contain no modern (post-1952) water. Tritium concentration in a sample from the top of the water column at MSW-2 was 0.41 tritium units, indicating that the composition is primarily pre-bomb (pre-1952) water, but may contain a small fraction of post-bomb modern water. The calculated carbon-14 ages of groundwater in MSW-1 and MSW-2, both completed about 140 feet into the Navajo Sandstone, are about 3,000 years before present. The calculated carbon-14 age of groundwater in MSW-3, completed about 240 feet into the Kayenta Formation-Navajo Sandstone transition zone is about 5,000 years before present in the upper portion of the water column and about 8,500 years before present in the lower portion of the water column. The gross alpha radioactivity of samples collected from the three water-supply wells ranged from 5.1 to 9.8 picocuries per liter-less than the U.S. Environmental Protection Agency primary drinking water standard of 15 picocuries per liter. The gross beta radioactivity of samples collected from the wells ranged from 0.9 to 2.8 picocuries per liter and are not considered elevated relative to the U

Water table fluctuations and soil biogeochemistry: An experimental approach using an automated soil column system

Science.gov (United States)

Rezanezhad, F.; Couture, R.-M.; Kovac, R.; O'Connell, D.; Van Cappellen, P.

2014-02-01

Water table fluctuations significantly affect the biological and geochemical functioning of soils. Here, we introduce an automated soil column system in which the water table regime is imposed using a computer-controlled, multi-channel pump connected to a hydrostatic equilibrium reservoir and a water storage reservoir. The potential of this new system is illustrated by comparing results from two columns filled with 45 cm of the same homogenized riparian soil. In one soil column the water table remained constant at -20 cm below the soil surface, while in the other the water table oscillated between the soil surface and the bottom of the column, at a rate of 4.8 cm d-1. The experiment ran for 75 days at room temperature (25 ± 2 °C). Micro-sensors installed at -10 and -30 cm below the soil surface in the stable water table column recorded constant redox potentials on the order of 600 and -200 mV, respectively. In the fluctuating water table column, redox potentials at the same depths oscillated between oxidizing (∼700 mV) and reducing (∼-100 mV) conditions. Pore waters collected periodically and solid-phase analyses on core material obtained at the end of the experiment highlighted striking geochemical differences between the two columns, especially in the time series and depth distributions of Fe, Mn, K, P and S. Soil CO2 emissions derived from headspace gas analysis exhibited periodic variations in the fluctuating water table column, with peak values during water table drawdown. Transient redox conditions caused by the water table fluctuations enhanced microbial oxidation of soil organic matter, resulting in a pronounced depletion of particulate organic carbon in the midsection of the fluctuating water table column. Denaturing Gradient Gel Electrophoresis (DGGE) revealed the onset of differentiation of the bacterial communities in the upper (oxidizing) and lower (reducing) soil sections, although no systematic differences in microbial community structure

On-line immunoaffinity column-liquid chromatography-tandem mass spectrometry method for trace analysis of diuron in wastewater treatment plant effluent sample.

Science.gov (United States)

Zhang, Xiuli; Martens, Dieter; Krämer, Petra M; Kettrup, Antonius A; Liang, Xinmiao

2006-11-10

An on-line immunoaffinity column with liquid chromatography/tandem mass spectrometry (IAC-LC-MS/MS) method for the determination of diuron in water matrices was described. This method used a sol-gel immunoaffinity column (20 mm x 4 mm I.D.) for on-line sample cleanup and enrichment, a monolithic analytical column (100 mm x 4.6 mm I.D.) for separation, and a triple quadrupole mass spectrometer for quantitation. The major challenges for the on-line set-up were discussed. The optimized on-line protocol was emphasized by the fact that low limit of quantitation (LOQ) of 1.0 ng/L was achieved with only 2.5-mL sample. In addition, a satisfactory accuracy ( approximately 90% of recovery) and precision (effect, the on-line IAC-LC-MS/MS analysis method can reliably determine diuron in wastewater treatment plant effluent sample.

Distinct Iron-binding Ligands in the Upper Water Column at Station ALOHA

Science.gov (United States)

Bundy, R.; Boiteau, R.; Repeta, D.

2016-02-01

The distribution and chemical properties of iron-binding organic ligands at station ALOHA were examined using a combination of solid phase extraction (SPE) followed by high pressure liquid chromatography-inductively coupled plasma mass spectrometry (HPLC-ICPMS). HPLC-ICPMS ligand measurements were complemented by competitive ligand exchange adsorptive cathodic stripping voltammetry (CLE-ACSV) analysis using salicylaldoxime as the added ligand. By HPLC-ICPMS, we find enhanced concentrations of distinct naturally-occurring polar iron-binding ligands present at the surface and in the chlorophyll maximum. Lower concentrations were found in the subsurface, where a suite of non-polar ligands was detected. Siderophores were present at the deepest depths sampled at station ALOHA, down to 400m. Incubation studies provided evidence for the production of iron-binding ligands associated with nutrient amended phytoplankton growth in surface waters, and as a result of microbial particle remineralization in the subsurface water column. Ligands classes identified via SPE were then compared to CLE-ACSV ligand measurements, as well as the conditional stability constants measured from model polar and non-polar siderophores, yielding insight to the sources of iron-binding ligands throughout the water column at station ALOHA.

Comparison of Granular Activated Carbon, Natural Clinoptilolite Zeolite, and Anthracite Packed Columns in Removing Mercury from Drinking Water

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Mohammad Taghi Samadi

2010-01-01

Full Text Available Development of effective methods for the removal of such pollutants as heavy metals (e.g., mercury from surface and ground water resources introduced by municipal and industrial wastewaters seems to be inevitable, especially in the face of the importance of water reuse in combating water shortages, limited availability of water resources, and imminent risks of a water crisis in Iran. A number of methods are already available for the removal of mercury from water resources. However, these techniques must be investigated for their practicability and economy, in addition to their not only effectiveness. In this research, granular activated carbon, natural zeolite, and anthracite packed-columns were investigated as cheap and effective adsorbents for the removal of mercury. Moreover, the effects of changes in pH (6-8, influent mercury concentrations (0.25, 0.5, 0.75, and 1 ppm, contact time (0.5, 1, 2, 3 hr were investigated. Mercury concentration in the samples was determined using a ditizon indicator and spectrophotometry at 492 nm. Results showed that decreasing influent mercury concentration from 1 ppm to 0.25 ppm (under constant conditions increased the removal efficiencies of anthracite, granular activated carbon, and zeolite columns from22%, 63%, and 55% to 28%, 72%, and 64%, respectively. Increasing contact time from 0.5 hr to 3 hr caused the removal efficiencies of these columns to increase from 22%, 56%, and 54% to 42%, 86%, and 82%, respectively. Also, increasing pH level led to increased removal efficiencies of the studied columns. It was found that contact time played a more effective role in enhancing mercury removal efficiency in the granular activated carbon column than in the other two columns. The ranges of mercury removal efficiency obtained for the granular activated carbon, natural zeolite, and anthracite columns under various conditions were (51%-92%, (42%-88%, and (16%-52%, respectively. Based on these results, granular

Slow physics: recording the ascent and descent of a water column

Science.gov (United States)

Lindén, Johan; Källman, Kjell-Mikael; Holm, Erik

2018-07-01

A glass filled with carbon dioxide gas upside down on a plate of water constitutes an excellent demonstration of the solubility of gases. If the water level on the plate is maintained the CO2 will slowly dissolve and the column of water will rise inside the glass, without quite reaching the ceiling, before an opposite process sets in: the water level will even more slowly begin to sink in a process which will take several years. We followed the process for several months, recording images of the water column with 10 min to 1 h intervals. The physics of the process is discussed and modeled quantitatively.

Mitigating oil spills in the water column

International Nuclear Information System (INIS)

Barry, Edward; Libera, Joseph A.; Mane, Anil University; Avila, Jason R.; DeVitis, David

2017-01-01

The scale and scope of uncontrolled oil spills can be devastating. Diverse marine environments and fragile ecologies are some of the most susceptible to the many ill effects, while the economic costs can be crippling. A notoriously difficult challenge with no known technological solution is the successful removal of oil dispersed in the water column. Here, we address this problem through cheap and reusable oil sorbents based on the chemical modification of polymer foams. Interfacial chemistry was optimized and subsequently tested in a simulated marine environment at the National Oil Spill Response Research & Renewable Energy Test Facility, Ohmsett. We find favorable performance for surface oil mitigation and, for the first time, demonstrate the advanced sorbent's efficiency and efficacy at pilot scale in extraction of crude oil and refined petroleum products dispersed in the water column. As a result, this is a potentially disruptive technology, opening a new field of environmental science focused on sub-surface pollutant sequestration.

Ion Chromatographic Analyses of Sea Waters, Brines and Related Samples

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Nataša Gros

2013-06-01

Full Text Available This review focuses on the ion chromatographic methods for the analyses of natural waters with high ionic strength. At the beginning a natural diversity in ionic composition of waters is highlighted and terminology clarified. In continuation a brief overview of other review articles of potential interest is given. A review of ion chromatographic methods is organized in four sections. The first section comprises articles focused on the determination of ionic composition of water samples as completely as possible. The sections—Selected Anions, Selected Cations and Metals—follow. The most essential experimental conditions used in different methods are summarized in tables for a rapid comparison. Techniques encountered in the reviewed articles comprise: direct determinations of ions in untreated samples with ion- or ion-exclusion chromatography, or electrostatic ion chromatography; matrix elimination with column-switching; pre-concentration with a chelation ion chromatography and purge-and-trap pre-concentration. Different detection methods were used: non-suppressed conductometric or suppressed conductometric, direct spectrometric or spectrometric after a post-column derivetization, and inductively coupled plasma in combination with optical emission or mass spectrometry.

Absolute measurement of the isotopic ratio of a water sample with very low deuterium content

International Nuclear Information System (INIS)

Hagemann, R.; Nief, G.; Roth, E.

1968-01-01

The presence of H 3+ ions which are indistinguishable from HD + ions presents the principal difficulty encountered in the measurement of isotopic ratios of water samples with very low deuterium contents using a mass spectrometer. Thus, when the sample contains no deuterium, the mass spectrometer does not indicate zero. By producing, in situ, from the sample to be measured, water vapor with an isotopic ratio very close to zero using a small distilling column, this difficulty is overcome. This column, its operating parameters, as well as the way in which the measurements are made are described. An arrangement is employed in which the isotopic ratios can be measured with a sensitivity better than 0.01 x 10 -6 . The method is applied to the determination of the isotopic ratios of three low deuterium content water samples. The results obtained permit one to assign to the sample with the lowest deuterium content an absolute value equal to 1.71 ± 0.03 ppm. This water sample is a primary standard from which is determined the isotopic ratio of a natural water sample which serves as the laboratory standard. (author) [fr

Gas Chromatograph Method Optimization Trade Study for RESOLVE: 20-meter Column v. 8-meter Column

Science.gov (United States)

Huz, Kateryna

2014-01-01

RESOLVE is the payload on a Class D mission, Resource Prospector, which will prospect for water and other volatile resources at a lunar pole. The RESOLVE payload's primary scientific purpose includes determining the presence of water on the moon in the lunar regolith. In order to detect the water, a gas chromatograph (GC) will be used in conjunction with a mass spectrometer (MS). The goal of the experiment was to compare two GC column lengths and recommend which would be best for RESOLVE's purposes. Throughout the experiment, an Inficon Fusion GC and an Inficon Micro GC 3000 were used. The Fusion had a 20m long column with 0.25mm internal diameter (Id). The Micro GC 3000 had an 8m long column with a 0.32mm Id. By varying the column temperature and column pressure while holding all other parameters constant, the ideal conditions for testing with each column length in their individual instrument configurations were determined. The criteria used for determining the optimal method parameters included (in no particular order) (1) quickest run time, (2) peak sharpness, and (3) peak separation. After testing numerous combinations of temperature and pressure, the parameters for each column length that resulted in the most optimal data given my three criteria were selected. The ideal temperature and pressure for the 20m column were 95 C and 50psig. At this temperature and pressure, the peaks were separated and the retention times were shorter compared to other combinations. The Inficon Micro GC 3000 operated better at lower temperature mainly due to the shorter 8m column. The optimal column temperature and pressure were 70 C and 30psig. The Inficon Micro GC 3000 8m column had worse separation than the Inficon Fusion 20m column, but was able to separate water within a shorter run time. Therefore, the most significant tradeoff between the two column lengths was peak separation of the sample versus run time. After performing several tests, it was concluded that better

The annual cycle of plutonium in the water column of a warm, monomictic reservoir

International Nuclear Information System (INIS)

Pinder, J.E. III; Alberts, J.J.; Bowling, J.W.; Nelson, D.M.; Orlandini, K.A.

1992-01-01

An annual cycle occurs in the 239,240 Pu inventories of the water column of Pond B, an 87-ha warm monomictic reservoir on the US Department of Energy's Savannah River Site in Barnwell Co., South Carolina. The pond has elevated concentrations of 238 Pu and 239,240 Pu in sediments due to releases from former reactor operations and continues to receive additional Pu input from atmospheric deposition. For surface waters, the 239,240 Pu inventory increases following turnover in November to a maximum in March followed by a decline until later summer when minimum inventories occur. For deeper waters, the 239,240 Pu inventories increase rapidly following turnover and reach maximum values in March. The inventories in deeper waters remain large from March until turnover. Maximum inventories for the entire water column occur in March with minimum inventories at turnover in October and November. Turnover results in a redistribution of Pu across water depth but no measurable Pu loss from the water column. Ratios of 238 Pu: 239,240 Pu indicate that the cycle involves primarily Pu from sediment sources with little influence from atmospheric sources. Thus, the cycle represents net remobilization of 239,240 Pu from the sediments to the water column during the oxic, holomictic portion of the year followed by a net loss of Pu from the water column once stratification occurs. (author)

A rapid and simple separation method of Tc-99 in water samples

International Nuclear Information System (INIS)

Uchida, Shigeo; Tagami, Keiko

1999-01-01

Technetium-99 ( 99 Tc) is one of the important elements on safety evaluation of reprocessing plant and waste disposal plant, because it is a long half-life nuclide and large fission yield (about 6%) from 235 U and 239 Pu. We studied in this work a rapid and simple separation method of 99 Tc in water samples by ICP-MS. Tc in 2 litre of inland water or 1.5 litre of sea water sample solutions was condensed and separated by mini-column resin (TEVA·Spec resin) (Eichrom Co., Ltd.). The experimental results showed the best conditions as followed that 1) after controlling 0.1M nitric acid sample solution, passed it through the column, 2) then the inhibitory elements such as Ru are removed by 40 ml of 2M nitric acid solution, and 3) Tc was recovered by 4 ml of 8M nitric acid solution. 95% or more recovery of Tc was obtained. 100% Ru, an inhibited element of ICP-MS, was removed. The elute obtained from 4 ml of 8M nitric acid solution was diluted ten times with pure water and 99 Tc was measured by ICP-MS. The limit of detection of 2 litre inland water and 1.5 litre sea water were 3 mBql -1 and 4 mBql -1 , respectively. The organic compounds were not removed before running to column, because the concentration of organic compounds was not so large. When large amounts of them are contained, they should be removed. If suspended materials absorb Tc, Tc should be changed to TcO 4 - . (S.Y.)

In situ quantitative characterisation of the ocean water column using acoustic multibeam backscatter data

Science.gov (United States)

Lamarche, G.; Le Gonidec, Y.; Lucieer, V.; Lurton, X.; Greinert, J.; Dupré, S.; Nau, A.; Heffron, E.; Roche, M.; Ladroit, Y.; Urban, P.

2017-12-01

Detecting liquid, solid or gaseous features in the ocean is generating considerable interest in the geoscience community, because of their potentially high economic values (oil & gas, mining), their significance for environmental management (oil/gas leakage, biodiversity mapping, greenhouse gas monitoring) as well as their potential cultural and traditional values (food, freshwater). Enhancing people's capability to quantify and manage the natural capital present in the ocean water goes hand in hand with the development of marine acoustic technology, as marine echosounders provide the most reliable and technologically advanced means to develop quantitative studies of water column backscatter data. This is not developed to its full capability because (i) of the complexity of the physics involved in relation to the constantly changing marine environment, and (ii) the rapid technological evolution of high resolution multibeam echosounder (MBES) water-column imaging systems. The Water Column Imaging Working Group is working on a series of multibeam echosounder (MBES) water column datasets acquired in a variety of environments, using a range of frequencies, and imaging a number of water-column features such as gas seeps, oil leaks, suspended particulate matter, vegetation and freshwater springs. Access to data from different acoustic frequencies and ocean dynamics enables us to discuss and test multifrequency approaches which is the most promising means to develop a quantitative analysis of the physical properties of acoustic scatterers, providing rigorous cross calibration of the acoustic devices. In addition, high redundancy of multibeam data, such as is available for some datasets, will allow us to develop data processing techniques, leading to quantitative estimates of water column gas seeps. Each of the datasets has supporting ground-truthing data (underwater videos and photos, physical oceanography measurements) which provide information on the origin and

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides in water columns from the Pearl River and the Macao harbor in the Pearl River Delta in South China

Energy Technology Data Exchange (ETDEWEB)

Luo, X.J.; Mai, B.X.; Yang, Q.S.; Fu, J.M.; Sheng, G.Y.; Wang, Z.S. [Chinese Academy of Science, Guangzhou (China)

2004-06-01

Polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) were measured in suspended particles and dissolved phase from the Baiertang water column and the Macao water column samples as collected from the Guangzhou channel of the Pearl River and the Macao harbor, where the sediments were heavily contaminated with organic pollutants. Total OCPs concentration varies from 23.4 to 61.7 ng/l in Baiertang water column and from 25.2 to 67.8 ng/l in Macao column, while total PAHs concentration varies from 987.1 to 2878.5 ng/l in the Baiertang water column and from 944.0 to 6654.6 ng/l in the Macao column. The vertical distribution profiles of pollutants and the partition of pollutants between particles and dissolved phases indicate that the sediments in Baiertang act as an important source of selected pollutants, and the pollutants in water of this region were mainly originated from the release and re-suspension of contaminants residing in the sediments. The sediments in Macao harbor act as a reservoir for organochlorine pesticides, such as DDTs mainly introduced by river inflow from Xijiang and PAHs input by brackish water from the Lingdingyang estuary. Combustion of fossil fuels and petroleum input are the main sources of PAHs in the Macao water column, while combustion of fossil fuels and coal is responsible for the PAHs in the Baiertang water column.

Estimation of polycyclic aromatic hydrocarbon concentrations in the water column based on tissue residues in mussels and salmon: An equilibrium partitioning approach

International Nuclear Information System (INIS)

Neff, J.M.; Burns, W.A.

1996-01-01

Equilibrium partitioning was used to estimate concentrations of dissolved polycyclic aromatic hydrocarbons (PAHs) in the water column from PAH residues in tissues of mussels and juvenile pink salmon collected from coastal marine waters affected by the Exxon Valdez oil spill. Estimated concentrations were within factors of 2 to 5 for fish and 5 to 10 for mussels of average total dissolved and particulate PAHs measured in concurrent water samples. Temporal trends of estimated and measured water-column PAH concentrations were comparable. Water-column PAH concentrations estimated from residues in tissues of mussels (Mytilus trossulus) were higher than estimates based on residues in tissues of juvenile pink salmon (Oncorhynchus gorbuscha). Possible reasons for this difference include seasonal variations in mussel lipid content, differences in PAH uptake and depuration rates between fish and mussels, differences in how fish and mussels interact with particulate oil, and possible short exposure times for juvenile pink salmon. All of these factors may play a role. In any event, estimates of dissolved PAHs in the water column, based on PAH residues in either fish or mussel tissue, confirm that PAH concentrations generally did not exceed water quality standards for protection of marine life

Transient behavior of enrichment of tritium water in adsorption-distillation column

International Nuclear Information System (INIS)

Fukada, Satoshi

2006-01-01

Enrichment of tritium in an adsorption-distillation column was experimentally investigated under the two processes of simple distillation and total-reflux distillation. Adsorption of water on silica-gel pellets enhanced the total isotope separation factor in the water distillation column. The transient behavior of tritium enrichment was analyzed using material balance equations of tritium and water in each cell with a height corresponding to HETP. The experimental transient behavior was well simulated by the material balance equations with additional assumptions on vapor and liquid flow rates regardless of the different processes of simple distillation and total-reflux distillation. (author)

Performance of a hydrostatic sampler for collecting samples at the water-sediment interface in lakes

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Fernando PEDROZO

2008-02-01

Full Text Available The water-sediment interface plays a significant role in the determination of the trophic degree of a waterbody. Numerous redox reactions take place there, resulting in the release of contaminants from the sediments to the water column. The aim of the present work was to develop an equipment for collecting samples from the water-sediment interface. Such equipment was to have a simple design, low construction cost, no depth limitations, and high levels of personal safety and to be reliable in the collection of samples. The performance of the hydrostatic sampler thus developed was tested against samples collected either remotely with a corer or directly with syringes by autonomous divers. The hydrostatic sampler permits access to depths where the costs of the traditional diving methodology are expensive, and where working conditions are dangerous for the diver. The hydrostatic sampler provides an additional means of collecting samples from the water-sediment interface, which together with pore-water samples, facilitates the investigation and understanding of chemical mechanisms in lakes, for instance, those that control the P release from sediment to the water column.

Numerical Simulation of a Dual-Chamber Oscillating Water Column Wave Energy Converter

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Dezhi Ning

2017-09-01

Full Text Available The performance of a dual-chamber Oscillating Water Column (OWC Wave Energy Converter (WEC is considered in the present study. The device has two sub-chambers with a shared orifice. A two-dimensional (2D fully nonlinear numerical wave flume based on the potential-flow theory and the time-domain higher-order boundary element method (HOBEM is applied for the simulation. The incident waves are generated by using the immerged sources and the air-fluid coupling influence is considered with a simplified pneumatic model. In the present study, the variation of the surface elevation and the water column volume in the two sub-chambers are investigated. The effects of the chamber geometry (i.e., the draft and breadth of two chambers on the surface elevation and the air pressure in the chamber are investigated, respectively. It is demonstrated that the surface elevations in the two sub-chambers are strongly dependent on the wave conditions. The larger the wavelength, the more synchronous motion of the two water columns in the two sub-chambers, thus, the lager the variation of the water column volume.

Vertical distribution of zooplankton in the water column of Lago Amapá, Rio Branco, Acre, Brazil

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Erlei Cassiano Keppeler

2004-06-01

Full Text Available The aim of investigation was to study the model of vertical distribution in Lago Amapá, taking into consideration the seasonality of its zooplanktonic composition. Lago Amapá (10º2'36"S and 67º50'24"W is located in the floodplain of the Rio Acre. Samplings were conducted at three different depths of the water column, to study the vertical distribution of zooplankton populations and determine some physico-chemical and biological parameters of Lago Amapá. Weekly samples were taken with a Van Dorn sampler. The species showed greater concentrations at the by means of water column. Thirty-eight zooplankton species were found in the samples represented by Rotifera (30, Cladocera (5 and Cyclopoida (3. The temperature of the water column showed a tendency toward relatively high values (about 30ºC with little variation, consequently resulting in low viscosity. Based of Jaccard's index, it was seen that during the low-water phase, S1 and S3 of the three sampling stations studied, had greater similarity (Cj = 0.7058 in the middle of the water column. Lago Amapá showed characteristics in line with the intermediate disturbance hypothesis model, favoring colonization by opportunistic species such as rotifers.O objetivo desta investigação foi observar a distribuição vertical da comunidade do zooplâncton no Lago Amapá (10º2'36"S e 67º50'24"W, localizado na planície de inundação do Rio Acre. Amostragens foram conduzidas em três diferentes profundidades da coluna da água, considerando aspectos sazonais do zooplâncton, parâmetros físicos, químicos e biológicos. Coletas foram realizadas semanalmente com Garrafa de Van Dorn. As espécies apresentaram maiores concentrações no meio da coluna da água. Foram encontradas 38 espécies, assim distribuídas: Rotifera (30, Cladocera (5 e Cyclopoida (3. A temperatura da coluna da água em geral apresentou-se alta, em torno de 30ºC, com pequena variação, resultando em baixa viscosidade. O �

Spinal column damage from water ski jumping.

Science.gov (United States)

Horne, J; Cockshott, W P; Shannon, H S

1987-01-01

We conducted a radiographic survey of 117 competitive water ski jumpers to determine whether this sport can cause spinal column damage and, if so, whether damage is more likely to occur in those who participate during the period of spinal growth and development (age 15 years or younger). We found a high prevalence of two types of abnormality: Scheuermann (adolescent) spondylodystrophy (present in 26% of the skiers) and vertebral body wedging (present in 34%). The prevalence of adolescent spondylodystrophy increased with the number of years of participation in the sport before age 15 years or less. Of those in this age group who had skied for 5 years or more, 57 showed adolescent spondylodystrophy; of those in the same age group who had skied for 9 years or more, 100% were affected. Wedged vertebrae increased as time of participation increased, regardless of the age at which exposure began. We conclude that competitive water ski jumping may damage the spinal column and that consideration should be given to regulating this sport, particularly for children.

Spinal column damage from water ski jumping

International Nuclear Information System (INIS)

Horne, J.; Cockshott, W.P.; Shannon, H.S.

1987-01-01

We conducted a radiographic survey of 117 competitive water ski jumpers to determine whether this sport can cause spinal column damage and, if so, whether damage is more likely to occur in those who participate during the period of spinal growth and development (age 15 years or younger). We found a high prevalence of two types of abnormality: Scheuermann (adolescent) spondylodystrophy (present in 26% of the skiers) and vertebral body wedging (present in 34%). The prevalence of adolescent spondylodystrophy increased with the number of years of participation in the sport before age 15 years or less. Of those in this age group who had skied for 5 years or more, 57 showed adolescent spondylodystrophy; of those in the same age group who had skied for 9 years or more, 100% were affected. Wedged vertebrae increased as time of participation increased, regardless of the age at which exposure began. We conclude that competitive water ski jumping may damage the spinal column and that consideration should be given to regulating this sport, particularly for children. (orig.)

Spinal column damage from water ski jumping

Energy Technology Data Exchange (ETDEWEB)

Horne, J.; Cockshott, W.P.; Shannon, H.S.

1987-11-01

We conducted a radiographic survey of 117 competitive water ski jumpers to determine whether this sport can cause spinal column damage and, if so, whether damage is more likely to occur in those who participate during the period of spinal growth and development (age 15 years or younger). We found a high prevalence of two types of abnormality: Scheuermann (adolescent) spondylodystrophy (present in 26% of the skiers) and vertebral body wedging (present in 34%). The prevalence of adolescent spondylodystrophy increased with the number of years of participation in the sport before age 15 years or less. Of those in this age group who had skied for 5 years or more, 57 showed adolescent spondylodystrophy; of those in the same age group who had skied for 9 years or more, 100% were affected. Wedged vertebrae increased as time of participation increased, regardless of the age at which exposure began. We conclude that competitive water ski jumping may damage the spinal column and that consideration should be given to regulating this sport, particularly for children. (orig.)

Monitoring changes in soil water content on adjustable soil slopes of a soil column using time domain reflectometry (TDR) techniques

International Nuclear Information System (INIS)

Wan Zakaria Wan Muhd Tahir; Lakam Anak Mejus; Johari Abdul Latif

2004-01-01

Time Domain Reflectometry (TDR) is one of non-destructive methods and widely used in hydrology and soil science for accurate and flexible measurement of soil water content The TDR technique is based on measuring the dielectric constant of soil from the propagation of an electromagnetic pulse traveling along installed probe rods (parallel wire transmission line). An adjustable soil column i.e., 80 cm (L) x 35 cm (H) x 44 cm (W) instrumented with six pairs of vertically installed CS615 reflectometer probes (TDR rods) was developed and wetted under a laboratory simulated rainfall and their sub-surface moisture variations as the slope changes were monitored using TDR method Soil samples for gravimetric determination of water content, converted to a volume basis were taken at selected times and locations after the final TDR reading for every slope change made of the soil column Comparisons of water contents by TDR with those from grawmetric samples at different slopes of soil column were examined. The accuracy was found to be comparable and to some extent dependent upon the variability of the soil. This study also suggests that the response of slope (above 20 degrees) to the gradual increase in water content profile may cause soil saturation faster and increased overland flow (runoff especially on weak soil conditions

Chapter 2: Optical Properties of the Water Column

Science.gov (United States)

Kiefer, D. A.; Collins, D. J.

1994-01-01

In this chapter, and in chapter 29, the basic inter-relationship between the flux of radiant energy through the water column and the fixation of carbon by the phytoplankton in the ocean through processes of photosynthesis or primary production will be discussed.

Simulation of water column separation in Francis pump-turbine draft tube

International Nuclear Information System (INIS)

Nicolet, C; Alligne, S; Bergant, A; Avellan, F

2012-01-01

The paper presents the modelling, simulation and analysis of the transient behaviour of a 340 MW pump-turbine in case of emergency shutdown in turbine mode with focus on possible draft tube water column separation. The model of a pumped storage power plant with simplified layout is presented. This model includes a penstock feeding one 340MW pump-turbine with the related rotating inertia and a tailrace tunnel. The model of the tailrace tunnel allowing for water column separation simulation is introduced. The simulation results of the transient behaviour of the pump-turbine in case of emergency shutdown in generating mode, with and without downstream water column separation model are presented for different degree of severity triggered by the submergence and the tailrace tunnel length. The amplitudes of the pressure peaks induced by the cavity collapse are analysed with respect to the pressure drop magnitude and tailrace dimensions. The maximum and minimum pressure amplitudes obtained along the tailrace tunnel are analysed for different test case conditions.

Interaction of the heavy metals (Cr +6, Cd, Pb, Ni) between the silt and the water column in the case study of Bogota River

International Nuclear Information System (INIS)

Pinzon U, L.F.; Rodriguez, J.A.; Giraldo, E.

1993-01-01

For the present study the Bogota River it uses as framework, this river has a course of 255 km., in it pathway through 26 municipalities, including the Western area of the District Capital (Bogota). In the District Capital area, some significant sampling points were founded, due to their localization on the bed and that industrial activities of grateful polluting function are developed. Silt samples were extracted and it dilutes for chemical-physical analysis and study to scale; these samples were implanted in columns or reactors; one of characteristic totally anaerobic and another of characteristic aerobic. Of equal forms it procedure is repeated, but replacing the river water for dilution water; every third day the extracted samples are been about agreement with the metal to analyze Chromium IV for the waters, Total Chromium for the silts, Cadmium, Lead and Total Nickel in the column of water and silts to be analyzed by means of Absorption Atomic Spectrophotometry. The object is the one of establishing that exchange type is presented between the polluted water and the water free of contaminants

Solid-phase extraction of polar pesticides from environmental water samples on graphitized carbon and Empore-activated carbon disks and on-line coupling to octadecyl-bonded silica analytical columns.

Science.gov (United States)

Slobodník, J; Oztezkizan, O; Lingeman, H; Brinkman, U A

1996-10-25

The suitability of Empore-activated carbon disks (EACD), Envi-Carb graphitized carbon black (GCB) and CPP-50 graphitized carbon for the trace enrichment of polar pesticides from water samples was studied by means of off-line and on-line solid-phase extraction (SPE). In the off-line procedure, 0.5-2 l samples spiked with a test mixture of oxamyl, methomyl and aldicarb sulfoxide were enriched on EnviCarb SPE cartridges or 47 mm diameter EACD and eluted with dichloromethane-methanol. After evaporation, a sample was injected onto a C18-bonded silica column and analysed by liquid chromatography with ultraviolet (LC-UV) detection. EACD performed better than EnviCarb cartridges in terms of breakthrough volumes (> 2 l for all test analytes), reproducibility (R.S.D. of recoveries, 4-8%, n = 3) and sampling speed (100 ml/min); detection limits in drinking water were 0.05-0.16 microgram/l. In the on-line experiments, 4.6 mm diameter pieces cut from original EACD and stacked onto each other in a 9 mm long precolumn, and EnviCarb and CPP-50 packed in 10 x 2.0 mm I.D. precolumn, were tested, and 50-200 ml spiked water samples were preconcentrated. Because of the peak broadening caused by the strong sorption of the analytes on carbon, the carbon-packed precolumns were eluted by a separate stream of 0.1 ml/min acetonitrile which was mixed with the gradient LC eluent in front of the C18 analytical column. The final on-line procedure was also applied for the less polar propoxur, carbaryl and methiocarb. EnviCarb could not be used due to its poor pressure resistance. CPP-50 provided less peak broadening than EACD: peak widths were 0.1-0.3 min and R.S.D. of peak heights 4-14% (n = 3). In terms of analyte trapping efficiency on-line SPE-LC-UV with a CPP-50 precolumn also showed better performance than when Bondesil C18/OH or polymeric PLRP-S was used, but chromatographic resolution was similar. With the CPP-50-based system, detection limits of the test compounds were 0.05-1 microgram

An all-glass solid sampling device for open tubular columns in gas chromatography

NARCIS (Netherlands)

Cox, T.P.H.; vd Berg, P.M.J.

1972-01-01

An all-glass system for direct sample-introduction of high-boiling compounds onto open tubular columns is described. The standard deviation for quantitative measurements is less than 2.7%. The loss in resolving power of capillary columns, due to this injection system is negligible. The system is

Glufosinate ammonium clean-up procedure from water samples using SPE

Science.gov (United States)

Tayeb M., A.; Ismail B., S.; Mardiana-Jansar, K.; Ta, Goh Choo; Agustar, Hani Kartini

2015-09-01

For the determination of glufosinate ammonium residue in soil and water samples, different solid phase extraction (SPE) sorbent efficiency was studied. Four different SPE sorbents i.e.: CROMABOND PS-H+, CROMABOND PS-OH-, ISOLUTE ENV+, Water Sep-Pak and OASIS HLB were used. Sample clean-up performance was evaluated using high performance liquid chromatography (Agilent 1220 infinity LC) with fluorescence detector. Detection of FMO-derivatives was done at λ ex = 260 nm and λ em= 310 nm. OASIS HLB column was the most suitable for the clean-up in view of the overall feasibility of the analysis.

Laser incising of wood: Impregnation of columns with water-soluble dye

International Nuclear Information System (INIS)

Hattori, N.; Ando, K.; Kitayama, S.; Nakamura, Y.

1994-01-01

To know whether or not laser incising is a useful pre-treatment technique in impregnating a chemical fluid into lumber, pin holes were made in columns of hinoki (Chamaecyparis obtusa Endl.), sugi (Cryptomeria japonica D. Don), karamatsu (Larix leptolepis Gordon) and douglas-fir (Pseudo-tsuga menziesii Franco) with 1.7 kW CO2 laser, and a water-soluble dye was impregnated into these columns with a local pressure impregnation device. Retentions, and lengths and widths of penetrations from each hole were measured quantitatively. Referring to the results of the preparatory experiment mentioned above, incising patterns for sugi and douglas-fir were designed, and the same water-soluble dye was impregnated into the laser-incised columns as well as into non-incised ones with the vacuum-pressure method to obtain penetrated layers with the target depths completely. As a result, a retention of 200 kg/m3 of dye could be achieved for a column of douglas-fir even if it is a species difficult to impregnate. The penetrated layer also could be formed completely at the depth of the laser incision. Therefore, it is concluded that laser incising can be used for the pre-treatment before impregnation of wood columns. (author)

Synoptic Bi-monthly and Storm Response Water Quality Sampling in Southern Kaneohe Bay, HI 2005-2007 (NODC Accession 0060061)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Synoptic sampling including water column profiles and collected surface water samples was conducted on a bi-monthly basis throughout the rainy season(October-May)...

Mathematical simulation of water distillation column for decreasing volume of tritiated water

International Nuclear Information System (INIS)

Kinoshita, Masahiro; Naruse, Yuji

1981-12-01

Water distillation is an attractive method for decreasing volume of the tritiated water produced by operation of tritium facilities. The tritiated water is continuously fed to a column and it is separated into two streams. The top stream is discarded to the environment after addition of sufficient amount of uncontaminated water. The bottom stream is further treated for solidification and capsulation. The tridiagonal matrix method proved to provide surprisingly rapid convergences of the calculations. The concentration of deuterium naturally contained in the tritiated water is higher than the tritium concentration, but it was verified that presence of HDO can be ignored in the calculation. (author)

An alternative procedure for uranium analysis in drinking water using AQUALIX columns: application to varied French bottled waters.

Science.gov (United States)

Bouvier-Capely, C; Bonthonneau, J P; Dadache, E; Rebière, F

2014-01-01

The general population is chronically exposed to uranium ((234)U, (235)U, and (238)U) and polonium ((210)Po) mainly through day-to-day food and beverage intake. The measurement of these naturally-occurring radionuclides in drinking water is important to assess their health impact. In this work the applicability of calix[6]arene-derivatives columns for uranium analysis in drinking water was investigated. A simple and effective method was proposed on a specific column called AQUALIX, for the separation and preconcentration of U from drinking water. This procedure is suitable for routine analysis and the analysis time is considerably shortened (around 4h) by combining the separation on AQUALIX with fast ICP-MS measurement. This new method was tested on different French bottled waters (still mineral water, sparkling mineral water, and spring water). Then, the case of simultaneous presence of uranium and polonium in water was considered due to interferences in alpha spectrometry measurement. A protocol was proposed using a first usual step of spontaneous deposition of polonium on silver disc in order to separate Po, followed by the uranium extraction on AQUALIX column before alpha spectrometry counting. © 2013 Published by Elsevier B.V.

Treatment of arsenic contaminated water in a laboratory scale up-flow bio-column reactor

International Nuclear Information System (INIS)

Mondal, P.; Majumder, C.B.; Mohanty, B.

2008-01-01

The present paper describes the observations on the treatment of arsenic contaminated synthetic industrial effluent in a bio-column reactor. Ralstonia eutropha MTCC 2487 has been immobilized on the granular activated carbon (GAC) bed in the column reactor. The synthetic water sample containing As(T) (As(III):As(V) = 1:1), Fe, Mn, Cu and Zn at the initial concentrations of 25, 10, 2, 5, 10 ppm, respectively, was used. Concentrations of all the elements have been found to be reduced below their permissible limits in the treated water. The significant effect of empty bed contact time (EBCT) and bed height on the arsenic removal was observed in the initial stage. However, after some time of operation (approximately 3-4 days) no such effect was observed. Removal of As(III) and As(V) was almost similar after ∼2 days of operation. However, at the initial stage As(V) removal was slightly more than that of As(III). In absence of washing, after ∼4-5 days of operation, the bio-column reactor was observed to act as a GAC column reactor based on physico-chemical adsorption. Like arsenic, the percent removals of Fe, Mn, Cu and Zn also attained minimum after ∼1 day and increased significantly to the optimum value within 3-4 days of operation. Dissolved oxygen (DO) has been found to decrease along with the increasing bed height from the bottom. The pH of the solution in the reactor has increased slightly and oxidation-reduction potential (ORP) has decreased with the time of operation

A purge-and-trap capillary column gas chromatographic method for the measurement of halocarbons in water and air

Energy Technology Data Exchange (ETDEWEB)

Happell, J.D.; Wallace, D.W.R.; Wills, K.D.; Wilke, R.J.; Neill, C.C.

1996-06-01

This report describes an automated, accurate, precise and sensitive capillary column purge- and -trap method capable of quantifying CFC-12, CFC-11, CFC-113, CH{sub 3}CCL{sub 3}, and CCL{sub 4} during a single chromatographic analysis in either water or gas phase samples.

Protozoan Bacterivory in the Ice and the Water Column of a Cold Temperate Lagoon.

Science.gov (United States)

Sime-Ngando; Demers; Juniper

1999-02-01

> Abstract Bacterial abundance and bacterivorous protist abundance and activity were examined in ice-brine and water column communities of a cold temperate Japanese lagoon (Saroma-Ko Lagoon, Hokkaido, 44 degreesN, 144 degreesE), during the late winter phase of ice community development (February-March 1992). Bacterial abundance averaged 6 and 1 x 10(5) cells ml-1 in the ice-brine and plankton samples, respectively, and generally decreased during the sampling period. Bacterivorous protists, identified based on direct observation of short-term (Protist abundance averaged 4 x 10(3) and 8.1 cells ml-1 in the ice-brine and 0.3 x 10(3) and 1.2 cells ml-1 in the plankton, for flagellates and ciliates, respectively. In contrast to bacteria, the abundance of protists generally increased throughout the sampling period, indicating predator-prey interactions. Protistan bacterivory, measured from the rate of FLB disappearance over 24 h, averaged 36% (ice) and 24% (plankton) of bacterial standing stock and exhibited the same seasonal pattern as for protist abundance. The calculated specific clearance (range, 2-67 nl protozoa-1 h-1) and ingestion (protists" on nonbacterial food items were also provided. Although alternative sources of bacterial loss are likely to be of importance, this study provides evidence for the potential of protozoan assemblages as bacterial grazers in both sea ice-brine biota and water column at the southern limit of sea ice in the northern hemisphere.

The use of a chelating resin column for preconcentration of trace elements from sea-water in their determination by neutron-activation analysis

International Nuclear Information System (INIS)

Lee, C.; Kim, N.B.; Lee, I.C.; Chung, K.S.

1977-01-01

A Chelex-100 resin column has been employed for the preliminary concentration of trace elements in water samples before their determination by neutron-activation analysis. The column filled with a 1 : 1 mixture of the resin (50 to 100 mesh) and Pyrex glass powder of the same mesh size, is shown to maintain a constant flow-rate and give reproducible results. By a combination of preconcentration and neutron-activation analysis it is possible to determine Ba, Ca, Cd, Ce, Co, Cr, Cu, Fe, La, Mg, Mn, Sc, U, V and Zn in sea-water and/or fresh water simultaneously at the parts per milliard level. (author)

Transport of perfluoroalkyl acids in a water-saturated sediment column investigated under near-natural conditions

International Nuclear Information System (INIS)

Vierke, Lena; Möller, Axel; Klitzke, Sondra

2014-01-01

The aim of this study was to gain an understanding of the transport of C 4–10 perfluoroalkyl carboxylic acids (PFCAs) and C 4,6,8 perfluoroalkyl sulfonic acids (PFSAs) in a water-saturated sediment column representing a riverbank filtration scenario under near-natural conditions. Short-chain PFCAs and PFSAs with up to six C-atoms showed complete tracer-like breakthrough. Longer chain ones were retarded due to sorption to the sediment or due to other processes in the aqueous phase. The study reports the first column derived sediment–water partition coefficients ranging from 0.01 cm 3 g −1 to 0.41 cm 3 g −1 for C 4,6 PFSAs and from 0.0 cm 3 g −1 to 6.5 cm 3 g −1 for C 4,5,6,8,9 PFCAs. The results clearly indicate that short-chain PFCAs and PFSAs may pose a problem if contaminated surface waters are used for drinking water production via riverbank filtration. Highlights: • Transport of per- and polyfluorinated compounds in a riverbank filtration scenario. • Investigations under near-natural conditions with a water-saturated sediment column. • Processes in water and sediment control the transport of analytes. • Short chain PFCAs and PFSAs are not retarded in the water-saturated sediment column. • First column derived sediment–water partition coefficients. -- Quantification of breakthrough of perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs) under conditions simulating a riverbank filtration scenario

A review of oscillating water columns.

Science.gov (United States)

Heath, T V

2012-01-28

This paper considers the history of oscillating water column (OWC) systems from whistling buoys to grid-connected power generation systems. The power conversion from the wave resource through to electricity via pneumatic and shaft power is discussed in general terms and with specific reference to Voith Hydro Wavegen's land installed marine energy transformer (LIMPET) plant on the Scottish island of Islay and OWC breakwater systems. A report on the progress of other OWC systems and power take-off units under commercial development is given, and the particular challenges faced by OWC developers reviewed.

Water-Column Stratification Observed along an AUV-Tracked Isotherm

Science.gov (United States)

Zhang, Y.; Messié, M.; Ryan, J. P.; Kieft, B.; Stanway, M. J.; Hobson, B.; O'Reilly, T. C.; Raanan, B. Y.; Smith, J. M.; Chavez, F.

2016-02-01

Studies of marine physical, chemical and microbiological processes benefit from observing in a Lagrangian frame of reference, i.e. drifting with ambient water. Because these processes can be organized relative to specific density or temperature ranges, maintaining observing platforms within targeted environmental ranges is an important observing strategy. We have developed a novel method to enable a Tethys-class long-range autonomous underwater vehicle (AUV) (which has a propeller and a buoyancy engine) to track a target isotherm in buoyancy-controlled drift mode. In this mode, the vehicle shuts off its propeller and autonomously detects the isotherm and stays with it by actively controlling the vehicle's buoyancy. In the June 2015 CANON (Controlled, Agile, and Novel Observing Network) Experiment in Monterey Bay, California, AUV Makai tracked a target isotherm for 13 hours to study the coastal upwelling system. The tracked isotherm started from 33 m depth, shoaled to 10 m, and then deepened to 29 m. The thickness of the tracked isotherm layer (within 0.3°C error from the target temperature) increased over this duration, reflecting weakened stratification around the isotherm. During Makai's isotherm tracking, another long-range AUV, Daphne, acoustically tracked Makai on a circular yo-yo trajectory, measuring water-column profiles in Makai's vicinity. A wave glider also acoustically tracked Makai, providing sea surface measurements on the track. The presented method is a new approach for studying water-column stratification, but requires careful analysis of the temporal and spatial variations mingled in the vehicles' measurements. We will present a synthesis of the water column's stratification in relation to the upwelling conditions, based on the in situ measurements by the mobile platforms, as well as remote sensing and mooring data.

Foliar uptake of 137Cs from the water column by aquatic macrophytes

International Nuclear Information System (INIS)

Kelly, M.S.; Pinder, J.E. III

1996-01-01

A transplant experiment was performed to determine the relative importances of root uptake from the sediments and foliar uptake from the water column in determining the accumulation of 137 Cs by aquatic macrophytes. Uncontaminated individuals of three species, Brasenia schreberi, Nymphaea odorata and Nymphoides cordata, were transplanted into pots containing either contaminated sediments (i.e. 1.2 Bq 137 Cs g -1 dry mass) or uncontaminated sediments (i.e. -1 dry mass) and immersed in Pond B, a former reactor cooling pond where 137 Cs concentrations in surface waters range from 0.4 to 0.8 Bq liter -1 . The plants is uncontaminated sediments rapidly accumulated 137 Cs from the water column and after 35 days of immersion had 137 Cs concentrations in leaves that were: (1) not statistically significantly different from those for plants in contaminated sediments; and (2) similar to those for the same species growing naturally in Pond B. The similarity in 137 Cs concentrations between naturally-occurring plants and those in pots with uncontaminated sediments suggests that foliar uptake from the water column is the principal mode of Cs accumulation by these species in Pond B. (author)

Microbial methane production in oxygenated water column of an oligotrophic lake

Science.gov (United States)

Grossart, Hans-Peter; Frindte, Katharina; Dziallas, Claudia; Eckert, Werner; Tang, Kam W.

2011-01-01

The prevailing paradigm in aquatic science is that microbial methanogenesis happens primarily in anoxic environments. Here, we used multiple complementary approaches to show that microbial methane production could and did occur in the well-oxygenated water column of an oligotrophic lake (Lake Stechlin, Germany). Oversaturation of methane was repeatedly recorded in the well-oxygenated upper 10 m of the water column, and the methane maxima coincided with oxygen oversaturation at 6 m. Laboratory incubations of unamended epilimnetic lake water and inoculations of photoautotrophs with a lake-enrichment culture both led to methane production even in the presence of oxygen, and the production was not affected by the addition of inorganic phosphate or methylated compounds. Methane production was also detected by in-lake incubations of lake water, and the highest production rate was 1.8–2.4 nM⋅h−1 at 6 m, which could explain 33–44% of the observed ambient methane accumulation in the same month. Temporal and spatial uncoupling between methanogenesis and methanotrophy was supported by field and laboratory measurements, which also helped explain the oversaturation of methane in the upper water column. Potentially methanogenic Archaea were detected in situ in the oxygenated, methane-rich epilimnion, and their attachment to photoautotrophs might allow for anaerobic growth and direct transfer of substrates for methane production. Specific PCR on mRNA of the methyl coenzyme M reductase A gene revealed active methanogenesis. Microbial methane production in oxygenated water represents a hitherto overlooked source of methane and can be important for carbon cycling in the aquatic environments and water to air methane flux. PMID:22089233

Mitigation of Oil in Water Column: Mitigation Prototype Tests

Science.gov (United States)

2017-06-01

designed with an open end to allow aquatic animals to escape. After the treated foam becomes saturated with submerged oil, the net would be lifted...needed openings to allow the frame to pass through the water column without causing severe drag resistance . However, this also allows oil to flow...to the water and should only help the regions of hypoxia caused by microbial degradation of the oil. However, the proposed field set up with

EX0802 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0802: Operation Halloween Shakedown...

EX0801 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0801: Mapping Operations Shakedown...

EX1204 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1204: Northeastern Canyons and...

EX1702 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1702: American Samoa Expedition:...

Synoptic Bi-monthly and Storm Response Water Quality Sampling in Southern Kaneohe Bay, HI November 2007 - April 2009 (NODC Accession 0062644)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Synoptic sampling including water column profiles and collected surface water samples was conducted on a bi-monthly basis throughout the rainy season(October-May)...

Chromatographic enrichment of isotopes in hydrogen and water samples on palladium

International Nuclear Information System (INIS)

Andreev, B.M.; Polevoi, A.S.; Perevezentsev, A.N.

1987-01-01

Data on the isotopic enrichment of hydrogen and water samples by chromatography on palladium have been analyzed. Experimental data on the effect of temperature, hydrogen flow, volume of the enriched fraction, and length of the chromatographic column on the degree of separation attainable in the column have been obtained. It has been shown that the maximum separation achievable (regardless of the type of the isotope mixture) at 273 K falls with increase of hydrogen flow and volume of the enriched gas fraction recoverable from the column. A separation degree of ∼ 1040 has been achieved for a mixture of protium and deuterium in a 10-mm wide and 0.6-m long chromatographic column packed with palladium black with a grain size of 0.2-0.5 mm at 273 K and a specific hydrogen flow of 1.22 mole/m 2 x sec. For a protium-tritium mixture a separation degree of ∼ 90 has been reached in a similar column at 273 K and a specific hydrogen flow of 0.4 mole/m 2 x sec

EX1602 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1602: Mission System Shakedown/CAPSTONE...

EX1203 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1203: Florida Escarpment and Straits...

EX1604 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1604: CAPSTONE Wake Island PRIMNM...

EX1701 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1701: Kingman/Palmyra, Jarvis (Mapping)...

EX1303 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1303: New England Seamount Chain...

EX1104 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1104: Mid-Cayman Rise Exploration...

EX1705 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1705: American Samoa, Kingman/Palmyra,...

Potential of capillary-column-switching liquid chromatography-tandem mass spectrometry for the quantitative trace analysis of small molecules. Application to the on-line screening of drugs in water.

Science.gov (United States)

Pitarch, Elena; Hernandez, Felix; ten Hove, Jan; Meiring, Hugo; Niesing, Willem; Dijkman, Ellen; Stolker, Linda; Hogendoorn, Elbert

2004-03-26

We have investigated the potential of capillary-column-switching liquid chromatography coupled to tandem mass spectrometry (cLC-MS-MS) for the quantitative on-line trace analysis of target compounds in aqueous solutions. The technical design of the nano-scale cLC system developed at our Institute for peptide and protein identification has been tested and evaluated for the direct trace analysis of drugs in water samples. Sulphametoxazole, bezafibrate, metoprolol, carbamazepine and bisoprolol occurring frequently in Dutch waters, were selected as test compounds. Adequate conditions for trapping, elution and MS-MS detection were investigated by employing laboratory made 200 microm i.d. capillary columns packed with 5 microm aqua C18 material. In the final cLC-MS-MS conditions, a 1 cm length trapping column and a 4 cm length analytical column were selected. Under these conditions, the target compounds could be directly determined in water down to a level of around 50 ng/l employing only 25 microl of water sample. Validation was done by recovery experiments in ground-, surface- and drinking-water matrices as well as by the analysis of water samples with incurred residues and previously analyzed with a conventional procedure involving off-line solid-phase extraction and narrow-bore LC with MS-MS detection. The new methodology provided recoveries (50-500 ng/l level) between 50 and 114% with RSDs (n = 3, each level) below 20% for most of the compounds. Despite the somewhat less analytical performance in comparison to the conventional procedure, the on-line approach of the new methodology is very suitable for screening of drugs in aqueous samples.

High sensitivity and selectivity in quantitative analysis of drugs in biological samples using 4-column multidimensional micro-UHPLC-MS enabling enhanced sample loading capacity.

Science.gov (United States)

de Vries, Ronald; Vereyken, Liesbeth; François, Isabelle; Dillen, Lieve; Vreeken, Rob J; Cuyckens, Filip

2017-10-09

Sensitivity is often a critical parameter in quantitative bioanalyses in drug development. For liquid-chromatography-based methods, sensitivity can be improved by reducing the column diameter, but practical sensitivity gains are limited by the reduced sample loading capacity on small internal diameter (I.D.) columns. We developed a set-up that has overcome these limitations in sample loading capacity. The set-up uses 4 columns with gradually decreasing column diameters along the flow-path (2.1 → 1 → 0.5 → 0.15 mm). Samples are pre-concentrated on-line on a 2.1 mm I.D. trapping column and back flushed to a 1 mm I.D. UHPLC analytical column and separated. The peak(s) of interest are transferred using heartcutting to a second trapping column (0.5 mm I.D.), which is back-flushed to a 0.15 mm I.D. micro-UHPLC analytical column for orthogonal separation. The proof of concept of the set-up was demonstrated by the simultaneous analysis of midazolam and 1'-hydroxy midazolam in plasma by injection of 80 μL of protein precipitated plasma. The 4-column funnel set-up proved to be robust and resulted in a 10-50 times better sensitivity compared to a trap-elute approach and 250-500 fold better compared to direct micro-UHPLC analysis. A lower limit of quantification of 100 fg/mL in plasma was obtained for both probe compounds. Copyright © 2017 Elsevier B.V. All rights reserved.

Performance of passive samplers for monitoring estuarine water column concentrations: 2. Emerging contaminants.

Science.gov (United States)

Perron, Monique M; Burgess, Robert M; Suuberg, Eric M; Cantwell, Mark G; Pennell, Kelly G

2013-10-01

Measuring dissolved concentrations of emerging contaminants, such as polybrominated diphenyl ethers (PBDEs) and triclosan, can be challenging due to their physicochemical properties resulting in low aqueous solubilities and association with particles. Passive sampling methods have been applied to assess dissolved concentrations in water and sediments primarily for legacy contaminants. Although the technology is applicable to some emerging contaminants, the use of passive samplers with emerging contaminants is limited. In the present study, the performance of 3 common passive samplers was evaluated for sampling PBDEs and triclosan. Passive sampling polymers included low-density polyethylene (PE) and polyoxymethylene (POM) sheets, and polydimethylsiloxane (PDMS)-coated solid-phase microextraction (SPME) fibers. Dissolved concentrations were calculated using measured sampler concentrations and laboratory-derived partition coefficients. Dissolved tri-, tetra-, and pentabrominated PBDE congeners were detected at several of the study sites at very low pg/L concentrations using PE and POM. Calculated dissolved water concentrations of triclosan ranged from 1.7 ng/L to 18 ng/L for POM and 8.8 ng/L to 13 ng/L for PE using performance reference compound equilibrium adjustments. Concentrations in SPME were not reported due to lack of detectable chemical in the PDMS polymer deployed. Although both PE and POM were found to effectively accumulate emerging contaminants from the water column, further research is needed to determine their utility as passive sampling devices for emerging contaminants. © 2013 SETAC.

EX1603 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1603: Hohonu Moana: Exploring the Deep...

EX1302 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1302: Ship Shakedown, Patch Test and...

EX1005 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1005: Guam to Honolulu, HI Transit...

EX1102 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1102: ROV and Camera Sled Integration...

EX1403 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1403: East Coast Mapping and Exploration...

EX1607 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1607: CAPSTONE Wake Island PRI MNM...

EX1003 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1003: Transit from Hawaii to Guam...

EX0905 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0905: Mapping Field Trials II Mendocino...

EX1704 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1704: American Samoa and Cook Islands...

EX1301 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1301: Ship Shakedown and Patch Test...

Analisa Kinerja Pneumatic Wave Energy Converter (WEC Dengan Menggunakan Oscillating Water Column(OWC

Directory of Open Access Journals (Sweden)

Rico Ary Sona

2014-03-01

Full Text Available Sistem konversi energi gelombang laut merupakan sistem yang menangkap energi gelombang laut untuk dikonversi menjadi energi lain seperti energi listrik. Salah satu jenis wave energy converter (WEC yang banyak digunakan diantaranya yaitu Oscillating Water Columnatau OWC. Prinsip kerja sistem WEC ini ialah mengubah pergerakan naik turunnya gelombang pada silinder kolom udara untuk menghasilkan udara bertekanan yang selanjutnya digunakan untuk menggerakkan turbin dan generator listrik. Penelitian ini ditujukan untuk dapat mengetahui kinerja dari Oscillating Water Column (OWC dalam menangkap energi gelombang laut. Untuk dapat melakukan penelitian ini diperlukan beberapa perlatan yaitu pembuatan konfigurasi peralatan pembuat dan penangkapan gelombang yang terdiri dari pelampung dan silinder Oscillating Water Column (OWC. Percobaan ini dilakukan dengan cara memvariasikan panjang dan tinggi gelombang pada flow water channel dengan mengatur bukaan pada pneumatic speed control. Dari hasil percobaan diperoleh bahwa kinerja paling efektif diperoleh pada panjang gelombang 0.9 m dan tinggi gelombang 0.23m. Pada karakteristik gelombang tersebut diperoleh tekanan, kecepatan dan volume pada silinder Oscillating Water Column (OWC sebesar  1.11 bar, 39.39 m/s dan 0.0057 m3. Dari hasil percobaan juga diperoleh waktu pengisian Pressure Vessel selama 100 menit dengan tekanan 3 Psi.

Slow Physics: Recording the Ascent and Descent of a Water Column

Science.gov (United States)

Lindén, Johan; Källman, Kjell-Mikael; Holm, Erik

2018-01-01

A glass filled with carbon dioxide gas upside down on a plate of water constitutes an excellent demonstration of the solubility of gases. If the water level on the plate is maintained the CO[subscript 2] will slowly dissolve and the column of water will rise inside the glass, without quite reaching the ceiling, before an opposite process sets in:…

EX1006 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1006: Hawaii to San Francisco Transit to...

EX1105 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1105: Field Trials of EM302 Multibeam...

Synoptic Bi-monthly and storm response water quality sampling in Southern Kaneohe Bay, Hawaii, from November 2007 - April 2009 (NODC Accession 0062644)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Synoptic sampling including water column profiles and collected surface water samples was conducted on a bi-monthly basis throughout the rainy season (October-May)...

Predicting pollutant concentrations in the water column during dredging operations: Implications for sediment quality criteria

International Nuclear Information System (INIS)

Wasserman, Julio Cesar; Wasserman, Maria Angélica V.; Barrocas, Paulo Rubens G.; Almeida, Aline Mansur

2016-01-01

The development of new dredging techniques that can reduce, or at least predict, the environmental impacts, is in high demand by governments in developing countries. In the present work, a new methodology was developed, to evaluate the level of metals contamination (i.e. cadmium, lead and zinc) of the water column, during a dredging operation. This methodology was used to evaluate the impacts of the construction of a new maritime terminal in Sepetiba Bay, Brazil. The methodology quantifies the amount of resuspended sediments and calculates the expected contaminants concentrations in the water column. The results indicated that sediment quality criteria were not compatible with water quality criteria, because the dredging of contaminated sediments does not necessarily yield contaminated water. It is suggested that the use of sediment quality criteria for dredging operations might be abandoned, and the methodology presented in this study applied to assess dredging's environmental impacts, predicting water contamination levels. - Graphical abstract: A graphic model showing transference of contaminants from the sediments to the water column. The dark sediment area represents the dredged sediments and the arrows emerging from them represent the resuspended sediments affecting the water column. - Highlights: •Developing countries demand for new dredging projects. •A new model evaluates concentrations of metals in the water, caused by dredging. •The model shows that water and sediment quality criteria are not compatible. •Local hydrodynamics have a strong influence on the contamination of the water. •Management of dredging operations reduces environmental contamination.

Water hammer with column separation : a review of research in the twentieth century

NARCIS (Netherlands)

Bergant, A.; Simpson, A.R.; Tijsseling, A.S.

2004-01-01

Column separation refers to the breaking of liquid columns in fully filled pipelines. This may occur in a water hammer event when the pressure drops to the vapor pressure at specific locations such as closed ends, high points or knees (changes in pipe slope). A vapor cavity, driven by the inertia of

Ether lipids of planktonic archae in the marine water column

NARCIS (Netherlands)

Sinninghe Damsté, J.S.; Hoefs, M.J.L.; Schouten, S.; King, L.L.; Wakeham, S.G.; Leeuw, J.W. de

1997-01-01

Acyclic and cyclic biphytanes derived from the membrane ether lipids of archaea were found in water column particulate and sedimentary organic matter from several oxic and anoxic marine environments. Compound-specific isotope analyses of the carbon skeletons suggest that planktonic archaea utilize

Measurement of capacity coefficient of inclined liquid phase catalytic exchange column for tritiated water processing

International Nuclear Information System (INIS)

Yamai, Hideki; Konishi, Satoshi; Yamanishi, Toshihiko; Okuno, Kenji

1994-01-01

Liquid phase catalytic exchange (LPCE) is effective method for enrichment and removal of tritium from tritiated water. Capacity coefficients of operating LPCE column that are essential to evaluate column performance were measured. Experiments were performed with short catalyst packed columns and effect of inclination was studied. Method for evaluation of capacity coefficients was established from measurement of isotope concentration of liquid, vapor, gas phases at the two ends of the column. The capacity coefficients were measured under various superficial gas velocities. Feasibility study of helical columns with roughened inner surface was performed with short inclined columns. The column performance was not strongly affected by the inclination. The result indicates technological feasibility of helical LPCE column, that is expected to have operation stability and reduced height

Determination of zearalenone content in cereals and feedstuffs by immunoaffinity column coupled with liquid chromatography.

Science.gov (United States)

Fazekas, B; Tar, A

2001-01-01

The zearalenone content of maize, wheat, barley, swine feed, and poultry feed samples was determined by immunoaffinity column cleanup followed by liquid chromatography (IAC-LC). Samples were extracted in methanol-water (8 + 2, v/v) solution. The filtered extract was diluted with distilled water and applied to immunoaffinity columns. Zearalenone was eluted with methanol, dried by evaporation, and dissolved in acetonitrile-water (3 + 7, v/v). Zearalenone was separated by isocratic elution of acetonitrile-water (50 + 50, v/v) on reversed-phase C18 column. The quantitative analysis was performed by fluorescence detector and confirmation was based on the UV spectrum obtained by a diode array detector. The mean recovery rate of zearalenone was 82-97% (RSD, 1.4-4.1%) on the original (single-use) immunoaffinity columns. The limit of detection of zearalenone by fluorescence was 10 ng/g at a signal-to-noise ratio of 10:1 and 30 ng/g by spectral confirmation in UV. A good correlation was found (R2 = 0.89) between the results obtained by IAC-LC and by the official AOAC-LC method. The specificity of the method was increased by using fluorescence detection in parallel with UV detection. This method was applicable to the determination of zearalenone content in cereals and other kinds of feedstuffs. Reusability of immunoaffinity columns was examined by washing with water after sample elution and allowing columns to stand for 24 h at room temperature. The zearalenone recovery rate of the regenerated columns varied between 79 and 95% (RSD, 3.2-6.3%). Columns can be regenerated at least 3 times without altering their performance and without affecting the results of repeated determinations.

Rapid determination of glyphosate in cereal samples by means of pre-column derivatisation with 9-fluorenylmethyl chloroformate and coupled-column liquid chromatography with fluorescence detection.

Science.gov (United States)

Hogendoorn, E A; Ossendrijver, F M; Dijkman, E; Baumann, R A

1999-02-12

A rapid procedure for the determination of glyphosate in cereals has been developed. Convenient sample pretreatment is carried out by (i) a overnight standing extraction of 1.0 g homogenized sample with 20 ml of water, (ii) centrifugation of the samples, (iii) a passing of 2.5 ml of the clear layer through a 100 mg C18 solid-phase extraction cartridge and (iv) collection of the last 1.5 ml of the eluent into a calibrated tube. For the instrumental analysis, the efficient approach developed earlier for environmental water samples [J.V. Sancho, F. Hernández, F.J. LUpez, E.A. Hogendoorn, E. Dijkman, P. van Zoonen, J. Chromatogr. A, 737 (1996) 75] was successfully adopted for the determination of glyphosate in the obtained cereal extracts. The procedure includes a 15 min derivatisation step of the analyte with 9-fluorenylmethyl chloroformate and a 16 times dilution step prior to instrumental analysis employing coupled-column LC with fluorescence detection. The developed procedure has a sample throughput of more than 25 samples per day and a limit of quantification of 0.5 mg/kg. The method was validated by analyzing freshly spiked cereal samples and samples with aged residues at levels between 1.0 and 10 mg/kg. The overall recovery of the freshly spiked samples was 86% (n = 10) with a repeatability of 6.5% and a reproducibility of 9.5%. For samples with aged residues recoveries performed at different time intervals (range 80-150 days) did not differ significantly; the overall recovery (n = 10) was 74% with a repeatability and reproducibility of 14 and 20%, respectively.

Uranium Series Radionuclides in the Water Column of the Northeast Atlantic Ocean

Energy Technology Data Exchange (ETDEWEB)

Carvalho, F. P. [Nuclear and Technological Institute, Department of Radiological Protection and Nuclear Safety, Sacavem (Portugal)

2013-07-15

Naturally occurring radionuclides, namely {sup 238}U, {sup 234}U, {sup 230}Th, {sup 226}Ra, {sup 210}Pb, {sup 210}Po and {sup 232}Th, were analysed in water samples from ocean vertical profiles in three major abyssal basins of the NE Atlantic (Porcupine, Iberia and Tejo Basins), from the surface to the deep sea water layer. Concentrations were determined in the dissolved and particulate phases. The profiles of uranium isotopes in the water column, mostly in dissolved phase, showed nearly homogenized concentrations with {sup 238}U averaging 37{+-}4 mBq/Land {sup 234}U/{sup 238}U activity ratios averaging 1.13{+-}0.04, while {sup 226}Ra concentrations were 2-3 times higher in the bottom than at the ocean surface. {sup 230}Th activity concentrations were four orders of magnitude lower than {sup 234}U, confirming rapid Th scavenging from solution by the particulate matter. {sup 210}Pb and {sup 210}Po activity concentrations in the soluble phase were much lower than dissolved {sup 226}Ra. Modelling the distribution of these radionuclides in the water column leads to an average residence time of dissolved {sup 210}Pb and {sup 210}Po in the upper layer of 5 a and 1 a, respectively, and 0.6 a in the particulate phase for both radionuclides. In the deep water layer, soluble {sup 210}Pb and {sup 210}Po mean residence times were 42{+-}20 a and 2 a, respectively. The calculated {sup 210}Pb deposition flux at the abyssal sea floor is comparable with the flux derived from the {sup 210}Pb-excess inventory measured in sediments, and about 100 Bq.m-2.a{sup -1}. The {sup 210}Pb atmospheric deposition flux at the ocean surface in this region was estimated at about 74 Bq.m{sup -2}a{sup -1} and the {sup 210}Pb sink in the Northeast Atlantic is discussed. (author)

Modeling and Circumventing the Effect of Sediments and Water Column on Receiver Functions

Science.gov (United States)

Audet, P.

2017-12-01

Teleseismic P-wave receiver functions are routinely used to resolve crust and mantle structure in various geologic settings. Receiver functions are approximations to the Earth's Green's functions and are composed of various scattered phase arrivals, depending on the complexity of the underlying Earth structure. For simple structure, the dominant arrivals (converted and back-scattered P-to-S phases) are well separated in time and can be reliably used in estimating crustal velocity structure. In the presence of sedimentary layers, strong reverberations typically produce high-amplitude oscillations that contaminate the early part of the wave train and receiver functions can be difficult to interpret in terms of underlying structure. The effect of a water column also limits the interpretability of under-water receiver functions due to the additional acoustic wave propagating within the water column that can contaminate structural arrivals. We perform numerical modeling of teleseismic Green's functions and receiver functions using a reflectivity technique for a range of Earth models that include thin sedimentary layers and overlying water column. These modeling results indicate that, as expected, receiver functions are difficult to interpret in the presence of sediments, but the contaminating effect of the water column is dependent on the thickness of the water layer. To circumvent these effects and recover source-side structure, we propose using an approach based on transfer function modeling that bypasses receiver functions altogether and estimates crustal properties directly from the waveforms (Frederiksen and Delayney, 2015). Using this approach, reasonable assumptions about the properties of the sedimentary layer can be included in forward calculations of the Green's functions that are convolved with radial waveforms to predict vertical waveforms. Exploration of model space using Monte Carlo-style search and least-square waveform misfits can be performed to

Dynamics of thraustochytrid protists in the water column of the Arabian Sea

Digital Repository Service at National Institute of Oceanography (India)

Raghukumar, S.; Ramaiah, N.; Raghukumar, C.

). Thraustochytrids were present in substantial numbers throughout the 150 m water column in all the stations investigated during the end of the biologically productive summer and winter monsoons (0 to 1313 x 10 sup(3) and 3.7 to 183 x 10 sup(3) cells l sup(-1) water...

Lake Mixing Regime Influences Arsenic Transfer from Sediments into the Water Column and Uptake in Plankton

Science.gov (United States)

Gawel, J.; Barrett, P. M.; Hull, E.; Burkart, K.; McLean, J.; Hargrave, O.; Neumann, R.

2017-12-01

The former ASARCO copper smelter in Ruston, WA, now a Superfund site, contaminated a large area of the south-central Puget Sound region with arsenic over its almost 100-year history. Arsenic, a priority Superfund contaminant and carcinogen, is a legacy pollutant impacting aquatic ecosystems in urban lakes downwind of the ASARCO emissions stack. We investigated the impact of lake mixing regime on arsenic transfer from sediments into lake water and aquatic biota. We regularly collected water column and plankton samples from four study lakes for two years, and deployed sediment porewater peepers and sediment traps to estimate arsenic flux rates to and from the sediments. In lakes with strong seasonal stratification, high aqueous arsenic concentrations were limited to anoxic hypolimnetic waters while low arsenic concentrations were observed in oxic surface waters. However, in polymictic, shallow lakes, we observed elevated arsenic concentrations throughout the entire oxic water column. Sediment flux estimates support higher rates of arsenic release from sediments and vertical transport. Because high arsenic in oxic waters results in spatial overlap between arsenate, a phosphate analog, and lake biota, we observed enhanced trophic transfer of arsenic in polymictic, shallow study lakes, with higher arsenic accumulation (up to an order of magnitude) in both phytoplankton and zooplankton compared to stratified lakes. Chemical and physical mechanisms for higher steady-state arsenic concentrations will be explored. Our work demonstrates that physical mixing processes coupled with sediment/water redox status exert significant control over bioaccumulation, making shallow, periodically-mixed urban lakes uniquely vulnerable to environmental and human health risks from legacy arsenic contamination.

Formation of well-mixed warm water column in central Bohai Sea during summer: Role of high-frequency atmospheric forcing

Science.gov (United States)

Ma, Weiwei; Wan, Xiuquan; Wang, Zhankun; Liu, Yulong; Wan, Kai

2017-12-01

The influence of high-frequency atmospheric forcing on the formation of a well-mixed summer warm water column in the central Bohai Sea is investigated comparing model simulations driven by daily surface forcing and those using monthly forcing data. In the absence of high-frequency atmospheric forcing, numerical simulations have repeatedly failed to reproduce this vertically uniform column of warm water measured over the past 35 years. However, high-frequency surface forcing is found to strongly influence the structure and distribution of the well-mixed warm water column, and simulations are in good agreement with observations. Results show that high frequency forcing enhances vertical mixing over the central bank, intensifies downward heat transport, and homogenizes the water column to form the Bohai central warm column. Evidence presented shows that high frequency forcing plays a dominant role in the formation of the well-mixed warm water column in summer, even without the effects of tidal and surface wave mixing. The present study thus provides a practical and rational way of further improving the performance of oceanic simulations in the Bohai Sea and can be used to adjust parameterization schemes of ocean models.

Ciliated protists from the nepheloid layer and water column of sites affected by the Deepwater Horizon oil spill in the Northeastern Gulf of Mexico

Science.gov (United States)

Moss, Joseph A.; McCurry, Chelsea; Tominack, Sarah; Romero, Isabel C.; Hollander, David; Jeffrey, Wade H.; Snyder, Richard A.

2015-12-01

Benthic marine protists have been well documented from shallow marine benthic habitats but remain understudied in deeper habitats on continental shelves and slopes, particularly in the Northeastern Gulf of Mexico (NEGOM). This region was affected by a deep water oil well failure (BP-Deepwater Horizon, 2010). The combination of a lack of information on deep sea microbenthic communities and the potential for benthic microbial petroleum mineralization prompted this investigation. Water column and nepheloid layer samples were obtained via Niskin bottles and a multicorer respectively at stations across the NEGOM to: (1) determine whether nepheloid and water column communities are distinct and (2) assess benthic species richness relative to sediment PAH contamination. Phylum specific 18S rRNA gene amplification was used to construct clone libraries of ciliate assemblages. BLAST searches in the NCBI database indicated that a majority (~75%) of the clone sequences corresponded (94-100% similarity) with listed, yet unclassified sequences. Several putative species were common at most site locations and depths. Many known benthic ciliates, such as Uronychia transfuga, Uronychia setigera, and Spirotrachelostyla tani, were common in the nepheloid layer samples and not recovered in water column samples. Ciliated protist species richness increased with PAH levels found in surface sediments, suggesting a positive microbial response to petroleum enrichment of the benthos. The presence of previously unknown microbenthic communites in the nephaloid layer over oceanic clay-silt muds alters our view of microbial processes in the deep sea and merits investigation of the microbial processes and rates of microbial mineralization and biomass production important to global biogeochemistry.

Insights into head-column field-amplified sample stacking: Part II. Study of the behavior of the electrophoretic system after electrokinetic injection of cationic compounds across a short water plug.

Science.gov (United States)

Šesták, Jozef; Thormann, Wolfgang

2017-08-25

Part I on head-column field-amplified sample stacking comprised a detailed study of the electrokinetic injection of a weak base across a short water plug into a phosphate buffer at low pH. The water plug is converted into a low conductive acidic zone and cationic analytes become stacked at the interface between this and a newly formed phosphoric acid zone. The fundamentals of electrokinetic processes occurring thereafter were studied experimentally and with computer simulation and are presented as part II. The configuration analyzed represents a discontinuous buffer system. Computer simulation revealed that the phosphoric acid zone at the plug-buffer interface becomes converted into a migrating phosphate buffer plug which corresponds to the cationically migrating system zone of the phosphate buffer system. Its mobility is higher than that of the analytes such that they migrate behind the system zone in a phosphate buffer comparable to the applied background electrolyte. The temporal behaviour of the current and the conductivity across the water plug were monitored and found to reflect the changes in the low conductivity plug. Determination of the buffer flow in the capillary revealed increased pumping caused by the mismatch of electroosmosis within the low conductivity plug and the buffer. This effect becomes elevated with increasing water plug length. For plug lengths up to 1% of the total column length the flow quickly drops to the electroosmotic flow of the buffer and simulations with experimentally determined current and flow values predict negligible band dispersion and no loss of resolution for both low and large molecular mass components. Copyright © 2017 Elsevier B.V. All rights reserved.

Differentiating leucine incorporation of Archaea and Bacteria throughout the water column of the eastern Atlantic using metabolic inhibitors

NARCIS (Netherlands)

Yokokawa, Taichi; Sintes, Eva; de Corte, Daniele; Olbrich, Kerstin; Herndl, Gerhard J.

2012-01-01

The abundance (based on catalyzed reporter deposition-fluorescence in situ hybrid ization, CARD-FISH) and leucine incorporation rates of Archaea and Bacteria were determined throughout the water column in the eastern Atlantic. Bacteria dominated throughout the water column, although their

Oscillating water column structural model

Energy Technology Data Exchange (ETDEWEB)

Copeland, Guild [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Bull, Diana L [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Jepsen, Richard Alan [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Gordon, Margaret Ellen [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

2014-09-01

An oscillating water column (OWC) wave energy converter is a structure with an opening to the ocean below the free surface, i.e. a structure with a moonpool. Two structural models for a non-axisymmetric terminator design OWC, the Backward Bent Duct Buoy (BBDB) are discussed in this report. The results of this structural model design study are intended to inform experiments and modeling underway in support of the U.S. Department of Energy (DOE) initiated Reference Model Project (RMP). A detailed design developed by Re Vision Consulting used stiffeners and girders to stabilize the structure against the hydrostatic loads experienced by a BBDB device. Additional support plates were added to this structure to account for loads arising from the mooring line attachment points. A simplified structure was designed in a modular fashion. This simplified design allows easy alterations to the buoyancy chambers and uncomplicated analysis of resulting changes in buoyancy.

Improved Design Tools for Surface Water and Standing Column Well Heat Pump Systems (DE-EE0002961)

Energy Technology Data Exchange (ETDEWEB)

Spitler, J. D.; Culling, J. R.; Conjeevaram, K.; Ramesh, M.; Selvakumar, M.

2012-11-30

Ground-source heat pump (GSHP) systems are perhaps the most widely used “sustainable” heating and cooling systems, with an estimated 1.7 million installed units with total installed heating capacity on the order of 18 GW. They are widely used in residential, commercial, and institutional buildings. Standing column wells (SCW) are one form of ground heat exchanger that, under the right geological conditions, can provide excellent energy efficiency at a relatively low capital cost. Closed-loop surface water heat pump (SWHP) systems utilize surface water heat exchangers (SWHE) to reject or extract heat from nearby surface water bodies. For building near surface water bodies, these systems also offer a high degree of energy efficiency at a low capital cost. However, there have been few design tools available for properly sizing standing column wells or surface water heat exchangers. Nor have tools for analyzing the energy consumption and supporting economics-based design decisions been available. The main contributions of this project lie in providing new tools that support design and energy analysis. These include a design tool for sizing surface water heat exchangers, a design tool for sizing standing column wells, a new model of surface water heat pump systems implemented in EnergyPlus and a new model of standing column wells implemented in EnergyPlus. These tools will better help engineers design these systems and determine the economic and technical feasibility.

A Review of Protist Grazing Below the Photic Zone Emphasizing Studies of Oxygen-Depleted Water Columns and Recent Applications of In situ Approaches

Directory of Open Access Journals (Sweden)

Virginia P. Edgcomb

2017-04-01

Full Text Available Little is still known of the impacts of protist grazing on bacterioplankton communities in the dark ocean. Furthermore, the accuracy of assessments of in situ microbial activities, including protist grazing, can be affected by sampling artifacts introduced during sample retrieval and downstream manipulations. Potential artifacts may be increased when working with deep-sea samples or samples from chemically unique water columns such as oxygen minimum zones (OMZs. OMZs are oxygen-depleted regions in the ocean, where oxygen concentrations can drop to <20 μM. These regions are typically located near eastern boundary upwelling systems and currently occur in waters occupying below about 8% of total ocean surface area, representing ~1% of the ocean's volume. OMZs have a profound impact not only on the distribution of marine Metazoa, but also on the composition and activities of microbial communities at the base of marine food webs. Here we present an overview of current knowledge of protist phagotrophy below the photic zone, emphasizing studies of oxygen-depleted waters and presenting results of the first attempt to implement new technology for conducting these incubation studies completely in situ (the Microbial Sampling- Submersible Incubation Device, MS-SID. We performed 24-h incubation experiments in the Eastern Tropical South Pacific (ETSP OMZ. This preliminary study shows that up to 28% of bacterial biomass may be consumed by protists in waters where oxygen concentrations were down to ~4.8 μM and up to 13% at a station with nitrite accumulation where oxygen concentrations were undetectable. Results also show that shipboard measurements of grazing rates were lower than rates measured from the same water using the MS-SID, suggesting that in situ experiments help to minimize artifacts that may be introduced when conducting incubation studies using waters collected from below the photic zone, particularly from oxygen-depleted regions of the water

Green rust formation controls nutrient availability in a ferruginous water column

DEFF Research Database (Denmark)

Zegeye, Asfaw; Bonneville, Steeve; Benning, Liane G.

2013-01-01

a mechanism for reconstructing ancient ocean chemistry. Such reconstructions depend, however, on precise knowledge of the iron minerals formed in the water column. Here, we combine mineralogical and geochemical analyses to demonstrate formation of the mixed-valence iron mineral, green rust, in ferruginous...

Characterization of Bubble Size Distributions within a Bubble Column

OpenAIRE

Shahrouz Mohagheghian; Brian R. Elbing

2018-01-01

The current study experimentally examines bubble size distribution (BSD) within a bubble column and the associated characteristic length scales. Air was injected into a column of water via a single injection tube. The column diameter (63–102 mm), injection tube diameter (0.8–1.6 mm) and superficial gas velocity (1.4–55 mm/s) were varied. Large samples (up to 54,000 bubbles) of bubble sizes measured via 2D imaging were used to produce probability density functions (PDFs). The PDFs were used to...

Cost effectiveness of detritiating water with resin columns

International Nuclear Information System (INIS)

Drake, R.H.; Williams, D.S.

1997-10-01

There are technologies in use for cleaning up concentrated tritiated process water. These are not cost effective for tritiated water with low concentrations of tritium. There are currently no cost-effective technologies for cleaning up low-tritium-concentration tritiated water, such as most tritiated groundwater, spent fuel storage basin water, or underground storage tank water. Resin removal of tritium from tritiated water at low concentrations (near the order of magnitude of drinking water standard maximums) is being tested on TA-SO (Los Alamos National Laboratory's Liquid Radioactive Waste Treatment Facility) waste streams. There are good theoretical and test indications that this may be a technologically effective means of removing tritium from tritiated water. Because of likely engineering design similarity, it is reasonable to anticipate that a resin column system's costs will be similar to some common commercial water treatment systems. Thus, the potential cost effectiveness of a resin treatment system offers hope for treating tritiated water at affordable costs. The TA-50 resin treatment cost projection of $18 per 1,000 gallons is within the same order of magnitude as cost data for typical commercial groundwater cleanup projects. The prospective Los Alamos National Laboratory (LANL) resin treatment system at $18 per 1,000 gallons appears to have a likely cost advantage of at least an order of magnitude over the competing, developmental, water detritiation technologies

Effects of salt pond restoration on benthic flux: Sediment as a source of nutrients to the water column

Science.gov (United States)

Topping, Brent R.; Kuwabara, James S.; Carter, James L.; Garrettt, Krista K.; Mruz, Eric; Piotter, Sarah; Takekawa, John Y.

2016-01-01

Understanding nutrient flux between the benthos and the overlying water (benthic flux) is critical to restoration of water quality and biological resources because it can represent a major source of nutrients to the water column. Extensive water management commenced in the San Francisco Bay, Beginning around 1850, San Francisco Bay wetlands were converted to salt ponds and mined extensively for more than a century. Long-term (decadal) salt pond restoration efforts began in 2003. A patented device for sampling porewater at varying depths, to calculate the gradient, was employed between 2010 and 2012. Within the former ponds, the benthic flux of soluble reactive phosphorus and that of dissolved ammonia were consistently positive (i.e., moving out of the sediment into the water column). The lack of measurable nitrate or nitrite concentration gradients across the sediment-water interface suggested negligible fluxes for dissolved nitrate and nitrite. The dominance of ammonia in the porewater indicated anoxic sediment conditions, even at only 1 cm depth, which is consistent with the observed, elevated sediment oxygen demand. Nearby openestuary sediments showed much lower benthic flux values for nutrients than the salt ponds under resortation. Allochthonous solute transport provides a nutrient advective flux for comparison to benthic flux. For ammonia, averaged for all sites and dates, benthic flux was about 80,000 kg/year, well above the advective flux range of −50 to 1500 kg/year, with much of the variability depending on the tidal cycle. By contrast, the average benthic flux of soluble reactive phosphorus was about 12,000 kg/year, of significant magnitude, but less than the advective flux range of 21,500 to 30,000 kg/year. These benthic flux estimates, based on solute diffusion across the sediment-water interface, reveal a significant nutrient source to the water column of the pond which stimulates algal blooms (often autotrophic). This benthic source may be

Simultaneous determination of iodide and iodate in soil solution samples by HPLC with electrochemical detection and post-column reaction method

Energy Technology Data Exchange (ETDEWEB)

Takeda, Akira; Takaku, Yuichi; Hisamatsu, Shun' ichi [Department of Radioecology, Institute for Environmental Sciences, Aomori 039-3212 (Japan); Tsukada, Hirofumi [Department of Radioecology, Institute for Environmental Sciences, Aomori 039-3212 (Japan); Institute of Environmental Radioactivity, Fukushima University, Fukushima 960-1196 (Japan)

2014-07-01

Iodine-129 (half-life 1.6 x 10{sup 7} y) discharged into the atmosphere from nuclear facilities (e.g., a nuclear fuel reprocessing plant) is partly deposited on land and introduced into soil. Stable iodine ({sup 127}I) can be used as a natural analogue to predict the long-term behavior of {sup 129}I in the terrestrial environment. Iodine in soil mainly exists as I{sup -}, IO{sub 3}{sup -}, and organic iodine. Because the mobilities of these species in soil are quite different, iodine speciation in soil solution is a key for predicting the behavior of iodine in soil. We developed a new speciation method suitable for routine analysis of many soil solution samples, and successfully applied the method to real samples. The method involves determining the concentration of total iodine and then separately measuring the I{sup -} and IO{sub 3}{sup -} concentrations with an HPLC system. The HPLC system (Nano-space SI-2; Shiseido, Tokyo, Japan) consisted of a UV/Vis spectrometer and an electrochemical (amperometric) detector (50 mV Ag/AgCl). Two reverse-phase columns (2.0 x 50 mm Capcel Pak DD C8 and 2.0 x 250 mm Capcel Pak MGII C18; Shiseido) were serially connected, and a switching valve was set between them. I{sup -} and IO{sub 3}{sup -} in the sample solution were separated from each other in the DD C8 column. IO{sub 3}{sup -} eluted first from the column, while I{sup -} was retained. After IO{sub 3}{sup -} was further separated from other halogen acids with the C18 column, IO{sub 3}{sup -} was reacted with KBr and o-dianisidine in a thermos-reactor (90 deg. C), and absorption at 450 nm was measured with the UV/Vis spectrometer. The concentration of I{sup -} eluted from the first column was determined with the electrochemical detector. To determine the concentration of total iodine in the sample solution, organic iodine was decomposed by UV irradiation (UV digester 705; Metrohm AG, Herisau, Switzerland) for 30 min at 20 deg. C. The iodine in the solution was reduced to I

Physicochemical and biological factors controlling water column metabolism in Sundarbans estuary, India.

Science.gov (United States)

Chaudhuri, Kaberi; Manna, Suman; Sarma, Kakoli Sen; Naskar, Pankaj; Bhattacharyya, Somenath; Bhattacharyya, Maitree

2012-10-19

Sundarbans is the single largest deltaic mangrove forest in the world, formed at estuarine phase of the Ganges - Brahmaputra river system. Primary productivity of marine and coastal phytoplankton contributes to 15% of global oceanic production. But unfortunately estuarine dynamics of tropical and subtropical estuaries have not yet received proper attention in spite of the fact that they experience considerable anthropogenic interventions and a baseline data is required for any future comparison. This study is an endeavor to this end to estimate the primary productivity (gross and net), community respiration and nitrification rates in different rivers and tidal creeks around Jharkhali island, a part of Sundarbans estuary surrounded by the mangrove forest during a period of three years starting from November'08 to October'11. Various physical and chemical parameters of water column like pH, temperature, conductivity, dissolved oxygen, turbidity, suspended particulate matter, secchi disc index, tidal fluctuation and tidal current velocity, standing crop and nutrients were measured along with water column productivity. Relationship of net water column productivity with algal biomass (standing crop), nutrient loading and turbidity were determined experimentally. Correlations of bacterial abundance with community respiration and nitrification rates were also explored. Annual integrated phytoplankton production rate of this tidal estuary was estimated to be 151.07 gC m-2 y-1. Gross primary productivity showed marked inter annual variation being lowest in monsoon and highest in postmonsoon period. Average primary production was a function of nutrient loading and light penetration in the water column. High aquatic turbidity, conductivity and suspended particulate matter were the limiting factors to attenuate light penetration with negative influence on primary production. Community respiration and nitrification rates of the estuary were influenced by the bacterial abundance

Physicochemical and biological factors controlling water column metabolism in Sundarbans estuary, India

Science.gov (United States)

2012-01-01

Background Sundarbans is the single largest deltaic mangrove forest in the world, formed at estuarine phase of the Ganges - Brahmaputra river system. Primary productivity of marine and coastal phytoplankton contributes to 15% of global oceanic production. But unfortunately estuarine dynamics of tropical and subtropical estuaries have not yet received proper attention in spite of the fact that they experience considerable anthropogenic interventions and a baseline data is required for any future comparison. This study is an endeavor to this end to estimate the primary productivity (gross and net), community respiration and nitrification rates in different rivers and tidal creeks around Jharkhali island, a part of Sundarbans estuary surrounded by the mangrove forest during a period of three years starting from November’08 to October’11. Results Various physical and chemical parameters of water column like pH, temperature, conductivity, dissolved oxygen, turbidity, suspended particulate matter, secchi disc index, tidal fluctuation and tidal current velocity, standing crop and nutrients were measured along with water column productivity. Relationship of net water column productivity with algal biomass (standing crop), nutrient loading and turbidity were determined experimentally. Correlations of bacterial abundance with community respiration and nitrification rates were also explored. Annual integrated phytoplankton production rate of this tidal estuary was estimated to be 151.07 gC m-2 y-1. Gross primary productivity showed marked inter annual variation being lowest in monsoon and highest in postmonsoon period. Conclusion Average primary production was a function of nutrient loading and light penetration in the water column. High aquatic turbidity, conductivity and suspended particulate matter were the limiting factors to attenuate light penetration with negative influence on primary production. Community respiration and nitrification rates of the estuary were

EX1103L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1103: Exploration and Mapping, Galapagos...

Experience from the application of an aerated trickle column to the removal of volatile organic substances and radon from water

International Nuclear Information System (INIS)

Broz, Z.; Kuthan, K.

1991-01-01

Experience from the use of aerated trickle columns containing oriented polypropylene netting is described. The columns are applied to the removal of chlorinated hydrocarbons and petroleum substances from polluted ground water and to the elimination of radon from drinking water in water treatment plants. One column has been in continuous use since 1989 in open space to remove petroleum substances, another has been in use in a water treatment plant since 1990 to eliminate radon. The facility features high reliability. (M.D.). 5 tabs., 5 figs., 12 refs

Design of a Cryogenic Distillation Column for JET Water Detritiation System for Tritium Recovery

International Nuclear Information System (INIS)

Parracho, A.I.; Camp, P.; Dalgliesh, P.; Hollingsworth, A.; Lefebvre, X.; Lesnoj, S.; Sacks, R.; Shaw, R.; Smith, R.; Wakeling, B.

2015-01-01

A Water Detritiation System (WDS) is currently being designed and manufactured to be installed in the Active Gas Handling System (AGHS) of JET, currently the largest magnetic fusion experiment in the world. JET has been designed and built to study fusion operating conditions with the plasma fuelling done by means of a deuterium-tritium gas mixture. AGHS is a plant designed and built to safely process gas mixtures and impurities containing tritium recovered from the JET torus exhaust gases. Tritium is removed from these gas mixtures and recycled. Tritium depleted gases are sent to Exhaust Detritiation System (EDS) for final tritium removal prior to discharge into the environment. In EDS, tritium and tritiated species are catalytically oxidized into water, this tritiated water is then adsorbed onto molecular sieve beds (MSB). After saturation the MSBs are heated and the water is desorbed and collected for tritium recovery. The WDS facility is designed to recover tritium from water with an average activity of 1.9 GBq/l, and is able to process water with activities of 85 GBq/l and higher. Tritiated water is filtered and supplied to the electrolyser where the water is converted into gaseous oxygen and tritiated hydrogen. The hydrogen stream is first purified by selective diffusion through membranes of palladium alloy and then is fed to two cryogenic distillation columns (CD). These operate in parallel or in series depending on the water activity. In the CD columns, hydrogen isotopes containing tritium are recovered as the bottom product and hydrogen, the top product, is safely discarded to a stack. The CD columns are foreseen to have a throughput between 200 and 300 mole/h of hydrogen isotopes vapour and they operate at approximately ≈21.2K and 105 kPa. The design of the CD columns will be presented in this work. This work has been carried out within the framework of the Contract for the Operation of the JET Facilities and has received funding from the European Union�

EX0909L4 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0909L4: Mapping Field Trials -...

EX1004L3 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1004L3: Exploration Indonesia - Bitung...

EX1004L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1004L2: Exploration Indonesia - Bitung...

EX1205L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1205L1: Exploration, Blake Plateau...

EX1502L3 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1502L3: Caribbean Exploration (ROV)...

EX1502L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1502L1: Caribbean Exploration (Mapping)...

EX1502L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1502L2: Caribbean Exploration (Mapping)...

EX1504L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1504L1: CAPSTONE NWHI & Johnston...

EX1202L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1202: Gulf of Mexico Exploration between...

EX1503L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1503L1: Tropical Exploration (Mapping I)...

EX0909L3 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0909L3: Mapping Field Trials - Hawaiian...

EX1304L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1304L2: Northeast U.S. Canyons...

EX1004L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1004L1: Exploration Indonesia - Guam to...

EX1202L3 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1202L3: Gulf of Mexico Exploration...

EX1504L4 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1504L4: Campaign to Address Pacific...

EX0909L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX0909L2: Mapping Field Trials - Necker...

Small zeolite column tests for removal of cesium from high radioactive contaminated water in Fukushima Daiichi Nuclear Power Station

International Nuclear Information System (INIS)

Hijikata, Takatoshi; Uozumi, Koichi; Tukada, Takeshi; Koyama, Tadafumi; Ishikawa, Keiji; Ono, Shoichi; Suzuki, Shunichi; Denton, Mark; Raymont, John

2011-01-01

After the earthquake on March 11th 2011, a large amount (more than 0.12 million m 3 ) of highly radioactive contaminated water had pooled in Fukushima Daiichi nuclear power station. As an urgent issue, highly radioactive nuclides should be removed from this contaminated water to reduce radioactivity in the turbine buildings and nuclear reactor buildings. Removal of Cs from this contaminated water is a key issue, because 134 Cs and 137 Cs are highly radioactive γ-emitting nuclides. The zeolite column system was used for Cs and Sr removal from the radioactive water of Three-Mile Island Unit 2, and modified columns were then developed as a Cs removal method for high-level radioactive water in US national laboratories (WRSC, ORNL, PNNL, Hanford, etc.). In order to treat Fukushima's highly contaminated water with a similar system, it was necessary to understand the properties of zeolite to remove Cs from sea salt as well as the applicability of the column system to a high throughput of around 1200 m 3 /d. The kinetic characteristics of the column were another property to be understood before actual operation. Hence, a functional small-scale zeolite column system was installed in CRIEPI for conducting the experiments to understand decontamination behaviors. Each column has a 2- or 3-cm inner diameter and a 12-cm height, and 12 g of zeolite-type media was packed into the column. The column experiments were carried out with Kurion-zeolite, Herschelite, at different feed rates of simulated water with different concentrations of Cs and sea salt. As for the water with 4 ppm Cs and 0 ppm sea salt, only a 10% Cs concentration was observed in the effluent after 20,000 bed volumes were fed at a rate of 33 cm/min, which corresponds to the actual system. On the other hand, a 40% Cs concentration was observed in the effluent after only 50 bed volumes were passed for water with 2 ppm Cs and 3.4 wt.% sea salt at a feed rate of 34 cm/min. As the absorption of Cs is hampered by the

Assessing the removal of turbidity and coliform transport through canal-bed sediment at lab-scale: column experiments

International Nuclear Information System (INIS)

Kandhar, I.; Sahito, A.R.

2017-01-01

This study was conducted at lab scale to determine the performance of the canal-bed for the removal of turbidity and microorganisms TC (Total Coliforms) from surface water. The canal-bed sediments were collected and analyzed for the characteristics of sediments for grain size distribution, hydraulic conductivity and the POM (Particulate Organic Matter) percent. Canal-bed sediments were containing fine particles<0.075mm in the range of 40-58%, with hydraulic conductivity averaged 7ft/day, and the POM 2.75%. The water samples collected from the canal-water have shown average POM 3.6%. Theremoval-reduction in turbidity and TC were determined through the column experiments on the canal-bed sediments. Three columns were prepared at lab-scale by using prepared canal-bed sediment as a filter-bed in the columns for the filtration of raw water samples. Fine particles of the canal-bed grain size D10 0.2 and D10 0.1mm were selected for the filter-bed formation. The prepared concentrated and diluted influent water samples containing turbidity and TC were passed through the washed filter-bed into the columns for 8-weeks filter run. The frequency of sampling and analysis were followedafter the interval of one-week run, the influent (raw water) and effluent (filtered) water samples were collected and analyzed for the turbidity and TC concentrations. The performance of the grain size D10 0.1mm have shown 95-99.95% reduction in turbidity and TC compared to the larger grain size having D10 0.2mm particles. (author)

Trends of total water vapor column above the Arctic from satellites observations

Science.gov (United States)

Alraddawi, Dunya; Sarkissian, Alain; Keckhut, Philippe; Bock, Olivier; Claud, Chantal; Irbah, Abdenour

2016-04-01

Atmospheric water vapor (H2O) is the most important natural (as opposed to man-made) greenhouse gas, accounting for about two-thirds of the natural greenhouse effect. Despite this importance, its role in climate and its reaction to climate change are still difficult to assess. Many details of the hydrological cycle are poorly understood, such as the process of cloud formation and the transport and release of latent heat contained in the water vapor. In contrast to other important greenhouse gases like carbon dioxide (CO2) and methane, water vapor has a much higher temporal and spatial variability. Total precipitable water (TPW) or the total column of water vapor (TCWV) is the amount of liquid water that would result if all the water vapor in the atmospheric column of unit area were condensed. TCWV distribution contains valuable information on the vigor of the hydrological processes and moisture transport in the atmosphere. Measurement of TPW can be obtained based on atmospheric water vapor absorption or emission of radiation in the spectral range from UV to MW. TRENDS were found over the terrestrial Arctic by means of TCWV retrievals (using Moderate Resolution Imaging Spectro-radiometer (MODIS) near-infrared (2001-2015) records). More detailed approach was made for comparisons with ground based instruments over Sodankyla - Finland (TCWV from: SCIAMACHY 2003-2011, GOME-2A 2007-2011, SAOZ 2003-2011, GPS 2003-2011, MODIS 2003-2011)

Water flow induced transport of Pseudomonas fluorescens cells through soil columns as affected by inoculant treatment

NARCIS (Netherlands)

Hekman, W.E.; Heijnen, C.E.; Trevors, J.T.; Elsas, van J.D.

1994-01-01

Water flow induced transport of Pseudomonas fluorescens cells through soil columns was measured as affected by the inoculant treatment. Bacterial cells were introduced into the topsoil of columns, either encapsulated in alginate beads of different types or mixed with bentonite clay in concentrations

EX1605L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1605L2: CAPSTONE CNMI and Mariana Trench...

EX1402L1 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1402L1: Gulf of Mexico Mapping and...

EX1402L2 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1402L2: Gulf of Mexico Mapping and...

EX1504L3 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1504L3: CAPSTONE Leg III: Main Hawaiian...

Diversity of active aerobic methanotrophs along depth profiles of arctic and subarctic lake water column and sediments

Science.gov (United States)

He, Ruo; Wooller, Matthew J.; Pohlman, John W.; Quensen, John; Tiedje, James M.; Leigh, Mary Beth

2012-01-01

Methane (CH4) emitted from high-latitude lakes accounts for 2–6% of the global atmospheric CH4 budget. Methanotrophs in lake sediments and water columns mitigate the amount of CH4 that enters the atmosphere, yet their identity and activity in arctic and subarctic lakes are poorly understood. We used stable isotope probing (SIP), quantitative PCR (Q-PCR), pyrosequencing and enrichment cultures to determine the identity and diversity of active aerobic methanotrophs in the water columns and sediments (0–25 cm) from an arctic tundra lake (Lake Qalluuraq) on the north slope of Alaska and a subarctic taiga lake (Lake Killarney) in Alaska's interior. The water column CH4 oxidation potential for these shallow (~2m deep) lakes was greatest in hypoxic bottom water from the subarctic lake. The type II methanotroph, Methylocystis, was prevalent in enrichment cultures of planktonic methanotrophs from the water columns. In the sediments, type I methanotrophs (Methylobacter, Methylosoma and Methylomonas) at the sediment-water interface (0–1 cm) were most active in assimilating CH4, whereas the type I methanotroph Methylobacter and/or type II methanotroph Methylocystis contributed substantially to carbon acquisition in the deeper (15–20 cm) sediments. In addition to methanotrophs, an unexpectedly high abundance of methylotrophs also actively utilized CH4-derived carbon. This study provides new insight into the identity and activity of methanotrophs in the sediments and water from high-latitude lakes.

Tidal variability of CO2 and CH4 emissions from the water column within a Rhizophora mangrove forest (New Caledonia).

Science.gov (United States)

Jacotot, Adrien; Marchand, Cyril; Allenbach, Michel

2018-08-01

We performed a preliminary study to quantify CO 2 and CH 4 emissions from the water column within a Rhizophora spp. mangrove forest. Mean CO 2 and CH 4 emissions during the studied period were 3.35±3.62mmolCm -2 h -1 and 18.30±27.72μmolCm -2 h -1 , respectively. CO 2 and CH 4 emissions were highly variable and mainly driven by tides (flow/ebb, water column thickness, neap/spring). Indeed, an inverse relationship between the magnitude of the emissions and the thickness of the water column above the mangrove soil was observed. δ 13 CO 2 values ranged from -26.88‰ to -8.6‰, suggesting a mixing between CO 2 -enriched pore waters and lagoon incoming waters. In addition, CO 2 and CH 4 emissions were significantly higher during ebb tides, mainly due to the progressive enrichment of the water column by diffusive fluxes as its residence time over the forest floor increased. Eventually, we observed higher CO 2 and CH 4 emissions during spring tides than during neap tides, combined to depleted δ 13 CO 2 values, suggesting a higher contribution of soil-produced gases to the emissions. These higher emissions may result from higher renewable of the electron acceptor and enhanced exchange surface between the soil and the water column. This study shows that CO 2 and CH 4 emissions from the water column were not negligible and must be considered in future carbon budgets in mangroves. Copyright © 2018 Elsevier B.V. All rights reserved.

Prolongation of the deployment and monitoring of a multiple oscillating water column wave energy converter

Energy Technology Data Exchange (ETDEWEB)

Johnson, F.; Chudley, J.; Dai, Y.M.

2003-07-01

This report summarises the findings of a project to prolong the sea trials of a multiple oscillating water column wave energy converter (MOWC) device for another 12 months to obtain further data. The objectives of the project include the evaluation of the ability of the MOWC to generate reliable energy to produce electricity, the estimation of the conversion efficiency, and the identification of improvements to increase the conversion efficiency, Details are given of the analysis of the sea trials data, and the performance of the broadband oscillating water column prototype.

EX1402L3 Water Column Summary Report and Profile Data Collection

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — A complete set of water column profile data and CTD Summary Report (if generated) generated by the Okeanos Explorer during EX1402L3: Gulf of Mexico Mapping and ROV...

Solid-phase microextraction of phthalate esters in water sample using different activated carbon-polymer monoliths as adsorbents.

Science.gov (United States)

Lirio, Stephen; Fu, Chung-Wei; Lin, Jhih-Yun; Hsu, Meng-Ju; Huang, Hsi-Ya

2016-07-13

In this study, the application of different activated carbon-polymer (AC-polymer) monoliths as adsorbents for the solid-phase microextraction (SPME) of phthalate esters (PAEs) in water sample were investigated. The activated carbon (AC) was embedded in organic polymers, poly(butyl methacrylate-co-ethylene dimethacrylate) (poly(BMA-EDMA)) or poly(styrene-co-divinylbenzene) (poly(STY-DVB)), via a 5-min microwave-assisted or a 15-min water bath heating polymerization. Preliminary investigation on the performance of the native poly(BMA-EDMA) and poly(STY-DVB) demonstrated remarkable adsorption efficiencies for PAEs. However, due to the strong hydrophobic, π-π, and hydrogen bonding interactions between the analytes and polymers, low extraction recoveries were achieved. In contrast, the presence of AC in native polymers not only enhanced the adsorption efficiencies but also assisted the PAE desorption, especially for AC-poly(STY-DVB) with extraction recovery ranged of 76.2-99.3%. Under the optimized conditions, the extraction recoveries for intra-, inter-day and column-to-column were in the range of 76.5-100.8% (<3.7% RSDs), 77.2-97.6% (<5.6% RSDs) and 75.5-99.7% (<6.2% RSDs), respectively. The developed AC-poly(STY-DVB) monolithic column showed good mechanical stability, which can be reused for more than 30 extraction times without any significant loss in the extraction recoveries of PAEs. The AC-poly(STY-DVB) monolithic column was successfully applied in SPME of PAEs in water sample with extraction recovery ranged of 78.8%-104.6% (<5.5% RSDs). Copyright © 2016 Elsevier B.V. All rights reserved.

Variations in Microbial Community Structure through the Stratified Water Column in the Tyrrhenian Sea (Central Mediterranean

Directory of Open Access Journals (Sweden)

Francesco Smedile

2015-08-01

Full Text Available The central Mediterranean Sea is among the most oligotrophic habitats in the marine environment. In this study, we investigated the abundance, diversity and activity of prokaryoplankton in the water column (25–3000-m depth at Station Vector (Tyrrhenian Sea, 39°32.050′ N; 13°22.280′ E. This specific water column consists of three different water masses (Modified Atlantic Water (MAW, Levantine Intermediate Water (LIW and Tyrrhenian Deep Water (TDW, possessing a typical stratification of the Central Mediterranean basin. CARD-FISH showed that the metabolically-active fraction of bacterial populations exceeded the archaeal fraction along the whole water column, except at the deepest water masses. 16S rDNA and 16S rRNA clone libraries obtained from each type of water mass were used to analyse the prokaryoplankton community structure and to distinguish between active and “less active” microbial fractions. Our results showed that the rRNA-derived bacterial libraries seemed to be more depth specific compared to 16S rDNA-derived counterparts. Major differences were detected between the active fractions of bacterioplankton thriving in photic (25 m, MAW and aphotic layers (500–3000 m, LIW and TDW respectively, whereas no statistically-significant differences were detected within the deep, aphotic layers (500–3000 m, LIW and TDW. Archaeal communities possessed more depth-specific distribution patterns with both total and active fractions showing depth stratification. Cyanobacteria and Marine Group II MAGII of Euryarchaea dominated the MAW prokaryoplankton. A notable fraction of Geitlerinema-related cyanobacteria was detected among the metabolically-active bacterial population recovered from the mesopelagic (500 m, LIW aphotic layer, which is indicative of their mixotrophic behaviour. Heterotrophic Gammaproteobacteria and members of Marine Group 1.1a and the PSL12-related ALOHA group of Thaumarchaeota were both abundant in the aphotic layers

Mass transfer model liquid phase catalytic exchange column simulation applicable to any column composition profile

Energy Technology Data Exchange (ETDEWEB)

Busigin, A. [NITEK USA Inc., Ocala, FL (United States)

2015-03-15

Liquid Phase Catalytic Exchange (LPCE) is a key technology used in water detritiation systems. Rigorous simulation of LPCE is complicated when a column may have both hydrogen and deuterium present in significant concentrations in different sections of the column. This paper presents a general mass transfer model for a homogenous packed bed LPCE column as a set of differential equations describing composition change, and equilibrium equations to define the mass transfer driving force within the column. The model is used to show the effect of deuterium buildup in the bottom of an LPCE column from non-negligible D atom fraction in the bottom feed gas to the column. These types of calculations are important in the design of CECE (Combined Electrolysis and Catalytic Exchange) water detritiation systems.

Tropical intercontinental optical measurement network of aerosol, precipitable water and total column ozone

Science.gov (United States)

Holben, B. N.; Tanre, D.; Reagan, J. A.; Eck, T. F.; Setzer, A.; Kaufman, Y. A.; Vermote, E.; Vassiliou, G. D.; Lavenu, F.

1992-01-01

A new generation of automatic sunphotometers is used to systematically monitor clear sky total column aerosol concentration and optical properties, precipitable water and total column ozone diurnally and annually in West Africa and South America. The instruments are designed to measure direct beam sun, solar aureole and sky radiances in nine narrow spectral bands from the UV to the near infrared on an hourly basis. The instrumentation and the algorithms required to reduce the data for subsequent analysis are described.

Identification and quantification of flavonoids in human urine samples by column switching liquid chromatography coupled to atmospheric pressure chemical ionization mass spectrometry

DEFF Research Database (Denmark)

Nielsen, S. E.; Freese, R.; Cornett, Claus

2000-01-01

A rapid and sensitive high-performance liquid chromatographic mass spectrometric (HPLC-MS) method is described for the determination and quantification of 12 dietary flavonoid glycosides and aglycons in human urine samples. Chromatographic separation of the analytes of interest was achieved...... by column-switching, using the first column (a Zorbax 300SB C-3 column) for sample cleanup and eluting the heart-cut flavonoid fraction onto the second column (a Zorbax SE C-18 column) for separation and detection by ultraviolet and atmospheric pressure chemical ionization MS using single ion monitoring...... of variation for the analysis of the 12 different flavonoids in quality control urine samples were 12.3% on average (range 11.0-13.7%, n = 24, reproducibility) and the repeatability of the assay were 5.0% (mean, range 0.1-14.8%, it = 12). A subset of 10 urine samples from a human dietary intervention study...

Evaluation of an in-situ x-ray fluorescence analyzer for inorganic pollutants in sediments and water columns

International Nuclear Information System (INIS)

Wogman, N.A.

1979-09-01

The applicability of an energy dispersive x-ray fluorescence spectrometer for measurement of trace elements in sediments and in water columns from Coast Guard vessels has been investigated. This investigation was conducted in both freshwater and saltwater areas and included Puget Sound, Lake Washington, Lake Union, and the ship canal in the State of Washington. The spectrometer system consisted of a solid cryogen-cooled Si(Li) detector and a 109 Cd excitation source. Sediments and water columns were viewed through a 0.2 mm Be window. This study showed the feasibility of measuring trace elements at concentrations ranging from 20 to about 100 ppM. Measurements of this sensitivity with a 100 mCi 109 Cd source are possible for time intervals as short as 5 minutes. This in-situ measurement capability permits the on-site mapping of pollution and avoids the problem of sediment disturbance which is inherent in the collection of grab samples of the sediment surface. Recommendations for an improved analyzer system included a detector assembly which could be towed, or allow continuous sediment surface analysis thereby recording the average composition of a large area

Carbon dioxide degassing in fresh and saline water I: Degassing performance of a cascade column

DEFF Research Database (Denmark)

Moran, Damian

2010-01-01

A study was undertaken to measure carbon dioxide degassing in a cascade column operating with both fresh (0‰) and saline water (35‰ NaCl) at 15 °C. The cascade column contained bio-block type packing material, was 1.7 m long in each dimension, and was tested both with and without countercurrent a...

Sedimentary deposition and reflux of phosphorus (P in the Eastern Gotland Basin and their coupling with P concentrations in the water column

Directory of Open Access Journals (Sweden)

Sven Hille

2005-12-01

Full Text Available In order to describe the role of sedimentary processes for the phosphorus (P cycle in the open Baltic Proper, P deposition and reflux were quantified for the predominately anoxic sediments of the Eastern Gotland Basin. The study is based on investigations of 53 surface sediment samples and pore water samples from 8 sediment cores. The average P deposition rate was estimated at 0.20 g ± 0.18 g -2 yr-1, the fluctuation being due to variable bulk sediment deposition rates. P refluxes were estimated by applying Fick's First Law of Diffusion. A fairly good positive correlation between sedimentary P deposition and P release was obtained. P release from sediments by diffusion exceeds net P deposition by a factor of 2. This suggests that 2/3 of the deposited gross P is recycled in the sediments and released back into the water column; only 1/3 remains in the sediment permanently. A budget calculation demonstrates that the released dissolved inorganic phosphorus (DIP accounts for the observed increase in DIP concentrations in the deep water during periods of stagnation, which is noticeable even at the surface P concentrations. Under such conditions and with the present remediation conditions it is not possible to freely manage P concentrations in the water column on short time scales.

A column switching ultrahigh-performance liquid chromatography-tandem mass spectrometry method to determine anandamide and 2-arachidonoylglycerol in plasma samples.

Science.gov (United States)

Marchioni, Camila; de Souza, Israel Donizeti; Grecco, Caroline Fernandes; Crippa, José Alexandre; Tumas, Vitor; Queiroz, Maria Eugênia Costa

2017-05-01

This study reports a fast, sensitive, and selective column switching ultrahigh-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method to determine the endocannabinoids (eCBs), anandamide (AEA), and 2-arachidonoylglycerol (2-AG) in plasma samples. This bidimensional system used a restricted access media column (RP-8 ADS, 25 mm × 4 mm × 25 μM) in the first dimension and a core-shell Kinetex C18 (100 mm × 2, 1.7 mm × 1 μM) column in the second dimension, followed by detection in a mass spectrometer triple quadrupole (multiple reactions monitoring mode) operating in the positive mode. RP-8 ADS was used for trace enrichment of eCBs (reverse phase partitioning) and macromolecular matrix size exclusion; the core-shell column was used for the chromatographic separation. The column switching UHPLC-MS/MS method presented a linear range spanning from 0.1 ng mL -1 (LOQ) to 6 ng mL -1 for AEA and from 0.04 ng mL -1 (LOQ) to 10 ng mL -1 for 2-AG. Excluding the LLOQ values, the precision assays provided coefficients of variation lower than 8% and accuracy with relative standard error values lower than 14%. Neither carryover nor matrix effects were detected. This high-throughput column switching method compared to conventional methods is time saving as it involves fewer steps, consumes less solvent, and presents lower LLOQ. The column switching UHPLC-MS/MS method was successfully applied to determine AEA and 2-AG in plasma samples obtained from Alzheimer's disease patients. Graphical abstract A column switching ultra high-performance liquid chromatography-tandem mass spectrometry method using RP-8 ADS column and core shell column to determine endocannabinoids in plasma samples.

JGOFS IV. Subproject: natural radionuclides as tracers for particle dynamics in the water column. Final report

International Nuclear Information System (INIS)

Scholten, J.C.; Fietzke, J.; Mangini, A.; Stoffers, P.

2000-01-01

As part of the German JOINT GLOBAL OCEAN FLUX STUDY (JGOFS) the aim of the project was to investigate the particle dynamics in the water column, especially to estimate the trapping efficiencies of sediment traps deployed in the eastern North Atlantic (L1: 33 N 21 W; L2: 47 N 19.5 W; L3: 54,4 N 21,1 W; ESTOC: 29,07 N 15,25 W; OMEX: 49 N 12,5 W). This investigation was based on measurements of the distribution of natural radionuclides in the water column and in sediment traps. In the upper water column (≤1000 m) the 230 Th concentrations are similar at all locations investigated and a reversible scavenging model was able to describe the 230 Th distribution. In the deep water-column at L2 and L3 the 230 Th concentrations were significantly lower than predicted from the reversible scavenging model. The 230 Th concentrations here could be described by a scavenging-mixing model which assumes an advection of 230 Th depleted water masses and a rapid ventilation between 3 and 25 years. Based on two models, a mass balance for 230 Th and 231 Pa and a constant removal model, sediment trap efficiencies were calculated to be between 9% and 143%. The lowest efficiencies (9%-36%) were determined in the 500 m and 1000 m traps and no direct relation between water currents velocities and trapping biases were observed. The correction for trapping biases were found to be important for the understanding of the regional differences in the particle flux in the eastern north Atlantic. (orig.) [de

A new type separation column for the water-hydrogen isotope catalytic exchange process

International Nuclear Information System (INIS)

Fedorchenko, O.A.; Alekseev, I.A.; Trenin, V.D.

2001-01-01

The catalytic water/hydrogen isotope exchange process is by right considered the most attractive for the solution a number of urgent problems of hydrogen isotope separation. A new type exchange reaction column is described and studied in details by computer simulation and with the help of McCabe-Thiele diagrams. It is shown that the new column in comparison with a traditional one needs less catalyst quantity and a smaller diameter for the solving of the same separation tasks. Generalized calculation data are presented in graphical form

Understanding and diminishing the extra-column band broadening effects in supercritical fluid chromatography.

Science.gov (United States)

De Pauw, Ruben; Shoykhet Choikhet, Konstantin; Desmet, Gert; Broeckhoven, Ken

2015-07-17

Supercritical fluid chromatography, where a low-viscosity mobile phase such as carbon dioxide is used, proves to be an excellent technique for fast and efficient separations, especially when sub-2μm particles are used. However, to achieve high velocities when using these small particles, and in order to stay within the flow rate range of current SFC-instruments, narrow columns (e.g. 2.1mm ID) must be used. Unfortunately, state-of-the-art instrumentation is limiting the full separation power of these narrower columns due to significant extra-column band broadening effects. The present work identifies and quantifies the different contributions to extra-column band broadening in SFC such as the influence of the sample solvent, injection volume, extra-column volumes and detector cell volume/design. When matching the sample solvent to the mobile phase in terms of elution strength and polarity (e.g. using hexane/ethanol/isopropanol 85/10/5vol%) and lowering the injection volume to 0.4μL, the plate count can be increased from 7600 to 21,300 for a low-retaining compound (k'=2.3) on a 2.1mm×150mm column (packed with 1.8μm particles). The application of a water/acetonitrile mixture as sample solvent was also investigated. It was found that when the volumetric ratio of water/acetonitrile was optimized, only a slightly lower plate count was measured compared to the hexane-based solvent when minimizing injection and extra-column volume. This confirms earlier results that water/acetonitrile can be used if water-soluble samples are considered or when a less volatile solvent is preferred. Minimizing the ID of the connection capillaries from 250 to 65μm, however, gives no further improvement in obtained efficiency for early-eluting compounds when a standard system configuration with optimized sample solvent was used. When switching to a state-of-the-art detector design with reduced (dispersion) volume (1.7-0.6μL), an increase in plate count is observed (from 11,000 to 14

Par Pond refill water quality sampling

International Nuclear Information System (INIS)

Koch, J.W. II; Martin, F.D.; Westbury, H.M.

1996-08-01

This study was designed to document anoxia and its cause in the event that the anoxia caused a fish kill. However, no fish kill was observed during this study, and dissolved oxygen and nutrient concentrations generally remained within the range expected for southeastern reservoirs. Par Pond water quality monitoring will continue during the second summer after refill as the aquatic macrophytes become reestablished and nutrients in the sediments are released to the water column

Modelling soil water content variations under drought stress on soil column cropped with winter wheat

Directory of Open Access Journals (Sweden)

Csorba Szilveszter

2014-12-01

Full Text Available Mathematical models are effective tools for evaluating the impact of predicted climate change on agricultural production, but it is difficult to test their applicability to future weather conditions. We applied the SWAP model to assess its applicability to climate conditions, differing from those, for which the model was developed. We used a database obtained from a winter wheat drought stress experiment. Winter wheat was grown in six soil columns, three having optimal water supply (NS, while three were kept under drought-stressed conditions (S. The SWAP model was successfully calibrated against measured values of potential evapotranspiration (PET, potential evaporation (PE and total amount of water (TSW in the soil columns. The Nash-Sutcliffe model efficiency coefficient (N-S for TWS for the stressed columns was 0.92. For the NS treatment, we applied temporally variable soil hydraulic properties because of soil consolidation caused by regular irrigation. This approach improved the N-S values for the wetting-drying cycle from -1.77 to 0.54. We concluded that the model could be used for assessing the effects of climate change on soil water regime. Our results indicate that soil water balance studies should put more focus on the time variability of structuredependent soil properties.

Ion Chromatographic Method with Post-Column Fuchsin Reaction for Measurement of Bromate in Chlorinated Water

Directory of Open Access Journals (Sweden)

Homer C. Genuino

2009-06-01

Full Text Available An ion chromatographic method that employs a post-column reaction with fuchsin and spectrophotometric detection was optimized for measuring bromate (BrO3- in water. BrO3- is converted to Br2 by sodium metabisulfite and then reacted with acidic fuchsin to form a red-colored product that strongly absorbs at 530 nm. The reaction of BrO3- and fuchsin reagent is optimum at pH 3.5 and 65 oC. The method has a limit of quantitation of 4.5 µg L-1 and is linear up to 150 µg L-1 BrO3-. Recoveries from spiked samples were high ranging from 95 to 102 % using external standard calibration and 87 to 103 % using standard addition method. Intra-batch and inter-batch reproducibility studies of the method resulted to RSD values ranging from 0.62 to 2.01 % and percent relative error of 0.12 to 2.94 % for BrO3- concentrations of 10 µg L-1 and 50 µg L-1. This method is free of interferences from common inorganic anions at levels typically found in chlorinated tap drinking water without preconcentration. The optimized method can be applied to trace analysis of bromate in chlorinated tap drinking water samples.

Fixed bed column study for Cu (II) removal from aqueous solution using water hyacinth (Eichornia crassipes) biomass.

Science.gov (United States)

Gandhimathi, R; Ramesh, S T; Yadu, Anubhav; Bharathi, K S

2013-07-01

This paper reports the results of the study on the performance of low-cost biosorbent water hyacinth (WH) in removing Cu (II) from aqueous solution. The adsorbent material adopted was found to be an efficient media for the removal of Cu (II) in continuous mode using fixed bed column. The column studies were conducted with 10 mg/L metal solution with a flow rate of 10 mL/min with different bed depths such as 10, 20 and 30 cm. The column design parameters like adsorption rate constant, adsorption capacity and minimum bed depth were calculated. It was found that, the adsorption capacity of copper ions by water hyacinth increased by increasing the bed depth and the contact time.

Synoptic bi-monthly and storm response water quality sampling in Southern Kaneohe Bay, HI, 2005-2007 in support of the Coral Reef Instrumented Monitoring Platform (CRIMP) (NODC Accession 0060061)

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Synoptic sampling including water column profiles and collected surface water samples was conducted on a bi-monthly basis throughout the rainy season (October-May)...

Testing the Role of Microbial Ecology, Redox-Mediated Deep Water Production and Hypersalinity on TEX86: Lipids and 16s Sequences from Archaea and Bacteria in the Water Column and Sediments of Orca Basin

Science.gov (United States)

Warren, C.; Romero, I.; Ellis, G.; Goddard, E.; Krishnan, S.; Nigro, L. M.; Super, J. R.; Zhang, Y.; Zhuang, G.; Hollander, D. J.; Pagani, M.

2014-12-01

Mesophilic marine archaea and bacteria are known to substantially contribute to the oceanic microbial biomass and play critical roles in global carbon, nitrogen and nutrient cycles. The Orca Basin, a 2400 meter deep bathymetric depression on the continental slope of the north-central Gulf of Mexico, is an ideal environment to examine how redox-dependent biochemical processes control the input and cycling of bacterial and archaea-derived lipid compounds from formation in near-surface water, through secondary recycling processes operating at the redox-transition in the water column, to sedimentary diagenetic processes operating in oxic to anoxic zones within the basin. The lowermost 180 meters of the Orca Basin is characterized by an anoxic, hypersaline brine that is separated from the overlying oxic seawater by a well-defined redox sequence associated with a systematic increasing in salinity from 35 - 250‰. While surface water conditions are viewed as normal marine with a seasonally productive water column, the sub-oxic to anoxic transition zones within the deep-water column and the sediment spans over 200 m allowing the unique opportunity for discrete sampling of resident organisms and lipids. Here we present 16s rRNA sequence data of Bacteria and Archaea collected parallel to GDGT lipid profiles and in situ environmental measurements from the sediment and overlying water column in the intermediate zone of the basin, where movements of chemical transition zones are preserved. We evaluated GDGTs and corresponding taxa across the surface water, chlorophyll maximum, thermocline, and the deep redox boundary, including oxygenation, denitrification, manganese, iron and sulfate reduction zones, to determine if GDGTs are being produced under these conditions and how surface-derived GDGT lipids and the TEX86 signal may be altered. The results have implications for the application of the TEX86 paleotemperature proxy.

Admittance Scanning for Whole Column Detection.

Science.gov (United States)

Stamos, Brian N; Dasgupta, Purnendu K; Ohira, Shin-Ichi

2017-07-05

Whole column detection (WCD) is as old as chromatography itself. WCD requires an ability to interrogate column contents from the outside. Other than the obvious case of optical detection through a transparent column, admittance (often termed contactless conductance) measurements can also sense changes in the column contents (especially ionic content) from the outside without galvanic contact with the solution. We propose here electromechanically scanned admittance imaging and apply this to open tubular (OT) chromatography. The detector scans across the column; the length resolution depends on the scanning velocity and the data acquisition frequency, ultimately limited by the physical step resolution (40 μm in the present setup). Precision equal to this step resolution was observed for locating an interface between two immiscible liquids inside a 21 μm capillary. Mechanically, the maximum scanning speed was 100 mm/s, but at 1 kHz sampling rate and a time constant of 25 ms, the highest practical scan speed (no peak distortion) was 28 mm/s. At scanning speeds of 0, 4, and 28 mm/s, the S/N for 180 pL (zone length of 1.9 mm in a 11 μm i.d. column) of 500 μM KCl injected into water was 6450, 3850, and 1500, respectively. To facilitate constant and reproducible contact with the column regardless of minor variations in outer diameter, a double quadrupole electrode system was developed. Columns of significant length (>1 m) can be readily scanned. We demonstrate its applicability with both OT and commercial packed columns and explore uniformity of retention along a column, increasing S/N by stopped-flow repeat scans, etc. as unique applications.

Rapid column extraction method for actinides and strontium in fish and other animal tissue samples

International Nuclear Information System (INIS)

Maxwell III, S.L.; Faison, D.M.

2008-01-01

The analysis of actinides and radiostrontium in animal tissue samples is very important for environmental monitoring. There is a need to measure actinide isotopes and strontium with very low detection limits in animal tissue samples, including fish, deer, hogs, beef and shellfish. A new, rapid separation method has been developed that allows the measurement of plutonium, neptunium, uranium, americium, curium and strontium isotopes in large animal tissue samples (100-200 g) with high chemical recoveries and effective removal of matrix interferences. This method uses stacked TEVA Resin R , TRU Resin R and DGA Resin R cartridges from Eichrom Technologies (Darien, IL, USA) that allows the rapid separation of plutonium (Pu), neptunium (Np), uranium (U), americium (Am), and curium (Cm) using a single multi-stage column combined with alphaspectrometry. Strontium is collected on Sr Resin R from Eichrom Technologies (Darien, IL, USA). After acid digestion and furnace heating of the animal tissue samples, the actinides and 89/90 Sr are separated using column extraction chromatography. This method has been shown to be effective over a wide range of animal tissue matrices. Vacuum box cartridge technology with rapid flow rates is used to minimize sample preparation time. (author)

Acoustic reflections in the water column of Krishna-Godavari offshore basin, Bay of Bengal

Digital Repository Service at National Institute of Oceanography (India)

Sinha, S.K.; Dewangan, P.; Sain, K.

reflection seismic data. Remarkable similarities between the reflection seismic and the salinity profile in the upper thermocline suggest the importance of salinity variations on the water column reflection. Furthermore, impedance inversion...

Economic optimization of heat pump-assisted distillation columns in methanol-water separation

International Nuclear Information System (INIS)

Shahandeh, Hossein; Jafari, Mina; Kasiri, Norollah; Ivakpour, Javad

2015-01-01

Finding efficient alternative to CDiC (Conventional Distillation Column) for methanol-water separation has been an attractive field of study in literature. In this work, five heat pump-assisted schemes are proposed and compared to each other to find the optimal one; (1) VRC (Vapor Recompression Column), (2) external HIDiC (Heat-Integrated Distillation Column), (3) intensified HIDiC with feed preheater, (4) double compressor intensified HIDiC-1, and (5) double compressor intensified HIDiC-2. GA (Genetic Algorithm) is then implemented for optimization of the schemes when TAC (Total Annual Cost) is its objective function. During optimization, two new variables are added for using only appropriate amount of the overhead stream in VRC and double compressor intensified HIDiCs, and another new binary variable is also used for considering feed preheating. Although TAC of the intensified HIDiC with feed preheater is found higher than CDiC by 25.0%, all optimal VRC, external HIDiC, double compressor intensified HIDiCs schemes are reached lower optimal TAC by 3.1%, 27.2%, 24.4%, and 34.2%. Introduced for the first time, the optimal scheme is the double compressor intensified HIDiC-2 with 34.2% TAC saving, 70.4% TEC (Total Energy Consumption) reduction with payback period of 3.30 years. - Highlights: • Study of an industrial distillation unit in methanol-water separation. • Optimization of different heat pump-assisted distillation columns. • Implementation of genetic algorithm during optimization. • Economic and thermodynamic comparisons of optimal results with the industrial case

Effect of IX column maintenance on carbon-14 concentration in moderator systems

International Nuclear Information System (INIS)

Gallagher, C.L.; Tripple, A.W.

2006-01-01

The radionuclide 14 C is produced in CANDU reactors primarily by the (n,α) reaction with 17 O. Because of high neutron fluxes in the core, the majority of the 14 C (94.5%) is produced in the moderator. In the moderator system, 14 C is present mainly as CO 2 in the cover gas in dynamic equilibrium with dissolved carbonates, bicarbonates and CO 2 in the moderator water. Emissions of 14 C from reactors occur through venting or leakage of the cover gas. By controlling the dissolved carbonates in the moderator water with an ion exchange (IX) purification system, the amount of 14 C in the cover gas is minimized and thus the emissions of 14 C can be reduced. A study was conducted to measure the 14 C concentrations in the moderator system at Gentilly 2 in order to determine the effectiveness of the purification system in removing 14 C. Moderator water samples were obtained from the inlet and outlet of the purification system from 2004 January 14 to July 12, covering the operation of two IX columns (IX-1 and IX-3). The moderator water samples contained high levels of tritium (∼2 TBq·L -1 ). As both tritium and 14 C are β-radiation emitters, direct counting of moderator water for 14 C is impossible as the signal due to tritium dominates over that of other β-emitters. Therefore, a procedure developed by Caron et al. was used in this study, which involved acidifying the sample to release the dissolved 14 CO 2 as gas and collecting the 14 CO 2 in a base (NaOH), which could then be measured by liquid scintillation counting to determine the 14 C concentration. Both of the IX columns started with 14 C removal efficiencies of about 95%. The efficiency began to decrease almost immediately with the IX-1 column dropping to 80% efficiency after ∼1115 hours. This drop in efficiency also led to an increase in the inlet concentration over time. IX-1 column was removed from service after ∼1745 hours with a 14 C removal efficiency of ∼31%. IX-3 column was then placed in service

USE OF COMPOSITE DATA SETS FOR SOURCE-TRACKING ENTEROCCOCCI IN THE WATER COLUMN AND SHORELINE INTERSTITIAL WATERS ON PENSACOLA BEACH, FL

Science.gov (United States)

Genthner, Fred J., Joseph B. James, Diane F. Yates and Stephanie D. Friedman. Submitted. Use of Composite Data Sets for Source-Tracking Enterococci in the Water Column and Shoreline Interstitial Waters on Pensacola Beach Florida. Mar. Pollut. Bull. 33 p. (ERL,GB 1212). So...

Uranium facilitated transport by water-dispersible colloids in field and soil columns

Energy Technology Data Exchange (ETDEWEB)

Crancon, P.; Pili, E. [CEA Bruyeres-le-Chatel, DIF, 91 (France); Charlet, L. [Univ Grenoble 1, Lab Geophys Interne and Tectonophys LGIT OSUG, CNRS, UJF, UMR5559, F-38041 Grenoble 9 (France)

2010-07-01

The transport of uranium through a sandy podsolic soil has been investigated in the field and in column experiments. Field monitoring, numerous years after surface contamination by depleted uranium deposits, revealed a 20 cm deep uranium migration in soil. Uranium retention in soil is controlled by the {<=} 50 {mu}m mixed humic and clayey coatings in the first 40 cm i.e. in the E horizon. Column experiments of uranium transport under various conditions were run using isotopic spiking. After 100 pore volumes elution, 60% of the total input uranium is retained in the first 2 cm of the column. Retardation factor of uranium on E horizon material ranges from 1300 (column) to 3000 (batch). In parallel to this slow uranium migration, we experimentally observed a fast elution related to humic colloids of about 1-5% of the total-uranium input, transferred at the mean pore-water velocity through the soil column. In order to understand the effect of rain events, ionic strength of the input solution was sharply changed. Humic colloids are retarded when ionic strength increases, while a major mobilization of humic colloids and colloid-borne uranium occurs as ionic strength decreases. Isotopic spiking shows that both {sup 238}U initially present in the soil column and {sup 233}U brought by input solution are desorbed. The mobilization process observed experimentally after a drop of ionic strength may account for a rapid uranium migration in the field after a rainfall event, and for the significant uranium concentrations found in deep soil horizons and in groundwater, 1 km downstream from the pollution source. (authors)

Coastal circulation and water-column properties in the National Park of American Samoa, February–July 2015

Science.gov (United States)

Storlazzi, Curt; Cheriton, Olivia; Rosenberger, Kurt; Logan, Joshua; Clark, Timothy B.

2017-06-06

There is little information on the oceanography in the National Park of American Samoa (NPSA). The transport pathways for potentially harmful constituents of land-derived runoff, as well as larvae and other planktonic organisms, are driven by nearshore circulation patterns. To evaluate the processes affecting coral reef ecosystem health, it is first necessary to understand the oceanographic processes driving nearshore circulation, residence times, exposure rates, and transport pathways. Information on how the NPSA’s natural resources may be affected by anthropogenic sources of pollution, sediment runoff, larval transport, or modifications to the marine protected areas is critical to NPSA resource managers for understanding and ultimately managing coastal and marine resources. To address this need, U.S. Geological Survey and U.S. National Park Service researchers conducted a collaborative study in 2015 to determine coastal circulation patterns and water-column properties along north-central Tutuila, American Samoa, in an area focused on NPSA’s Tutuila Unit and its coral reef ecosystem. The continuous measurements of waves, currents, tides, and water-column properties from these instrument deployments over 150 days, coupled with available meteorological measurements of wind and rainfall, provide information on nearshore circulation and the variability in these hydrodynamic properties for NPSA’s Tutuila Unit. In general, circulation was strongly driven by regional winds at longer (greater than day) timescales and by tides at shorter (less than day) timescales. Flows were primarily directed along shore, with current speeds faster offshore to the north and slower closer to shore, especially in embayments. Water-column properties exhibit strong seasonality coupled to the shift from non-trade wind season to trade wind season. During the non-trade wind season that was characterized by variable winds and larger waves in the NPSA, waters were warmer, slightly more

The hyperturbid state of the water column in estuaries and rivers: the importance of hindered settling

Science.gov (United States)

Dijkstra, Yoeri M.; Schuttelaars, Henk M.; Winterwerp, Johan C.

2018-03-01

Over the last few decades, some estuaries have undergone a transition to a hyperturbid state, characterised by suspended sediment concentrations of several grammes per litre averaged over the water column. To improve our understanding of this transition and of naturally hyperturbid estuaries, we systematically identify the processes allowing for high suspended sediment concentrations using a water column (1DV) model. Under a range of realistic forcing conditions, the state of the water column can be characterised by one of two equilibrium states. The first is an erosion-limited state, in which there still is sediment available for erosion at the bed. We find that this state only occurs with relatively low concentrations. The second is a supply-limited state, in which all erodable sediment is in suspension. The concentration in this state depends entirely on the amount of sediment in the system and can potentially be very high. We identify the conditions under which the state of the water column can jump from a low to a high concentration and identify hysteresis in the transition between the two states. The mechanism responsible for this hysteresis is hindered settling. It thus follows that hyperturbidity is only possible in a supply-limited state. From this observation we derive a necessary condition for an estuarine system to make the transition from low turbidity to hyperturbidity in a 1DV context. This is an important step towards understanding why some estuaries are hyperturbid and assessing the risk that particular estuaries may become hyperturbid in the future.

Simultaneous preconcentration of Co(II), Ni(II), Cu(II), and Cd(II) from environmental samples on Amberlite XAD-2000 column and determination by FAAS

International Nuclear Information System (INIS)

Duran, Celal; Senturk, Hasan Basri; Elci, Latif; Soylak, Mustafa; Tufekci, Mehmet

2009-01-01

A new method for the preconcentration of some trace metals (Co, Ni, Cu, and Cd) as complexed with ammonium pyrrolidynedithiocarbamate (APDC) was developed using a mini-column filled with Amberlite XAD-2000 resin. Metal contents were determined by flame atomic absorption spectrometry (FAAS) after the metal complexes accumulated on the resin were eluted with 1 M HNO 3 in acetone. The effects of the analytical parameters such as sample pH, quantity of complexing agent, eluent type, resin quantity, sample volume, sample flow rate, and matrix ions were investigated on the recovery of the metals from aqueous solutions. The relative standard deviation (R.S.D.) of the method was <6%. The validation of the method was confirmed using two certified reference materials (CRM TMDW-500 Drinking Water and CRM SA-C Sandy Soil C). The method was successfully applied to some stream waters and mushroom samples from Eastern Black Sea Region (Trabzon city) of Turkey

4SM: A Novel Self-Calibrated Algebraic Ratio Method for Satellite-Derived Bathymetry and Water Column Correction

Directory of Open Access Journals (Sweden)

Yann G. Morel

2017-07-01

Full Text Available All empirical water column correction methods have consistently been reported to require existing depth sounding data for the purpose of calibrating a simple depth retrieval model; they yield poor results over very bright or very dark bottoms. In contrast, we set out to (i use only the relative radiance data in the image along with published data, and several new assumptions; (ii in order to specify and operate the simplified radiative transfer equation (RTE; (iii for the purpose of retrieving both the satellite derived bathymetry (SDB and the water column corrected spectral reflectance over shallow seabeds. Sea truth regressions show that SDB depths retrieved by the method only need tide correction. Therefore it shall be demonstrated that, under such new assumptions, there is no need for (i formal atmospheric correction; (ii conversion of relative radiance into calibrated reflectance; or (iii existing depth sounding data, to specify the simplified RTE and produce both SDB and spectral water column corrected radiance ready for bottom typing. Moreover, the use of the panchromatic band for that purpose is introduced. Altogether, we named this process the Self-Calibrated Supervised Spectral Shallow-sea Modeler (4SM. This approach requires a trained practitioner, though, to produce its results within hours of downloading the raw image. The ideal raw image should be a “near-nadir” view, exhibit homogeneous atmosphere and water column, include some coverage of optically deep waters and bare land, and lend itself to quality removal of haze, atmospheric adjacency effect, and sun/sky glint.

4SM: A Novel Self-Calibrated Algebraic Ratio Method for Satellite-Derived Bathymetry and Water Column Correction.

Science.gov (United States)

Morel, Yann G; Favoretto, Fabio

2017-07-21

All empirical water column correction methods have consistently been reported to require existing depth sounding data for the purpose of calibrating a simple depth retrieval model; they yield poor results over very bright or very dark bottoms. In contrast, we set out to (i) use only the relative radiance data in the image along with published data, and several new assumptions; (ii) in order to specify and operate the simplified radiative transfer equation (RTE); (iii) for the purpose of retrieving both the satellite derived bathymetry (SDB) and the water column corrected spectral reflectance over shallow seabeds. Sea truth regressions show that SDB depths retrieved by the method only need tide correction. Therefore it shall be demonstrated that, under such new assumptions, there is no need for (i) formal atmospheric correction; (ii) conversion of relative radiance into calibrated reflectance; or (iii) existing depth sounding data, to specify the simplified RTE and produce both SDB and spectral water column corrected radiance ready for bottom typing. Moreover, the use of the panchromatic band for that purpose is introduced. Altogether, we named this process the Self-Calibrated Supervised Spectral Shallow-sea Modeler (4SM). This approach requires a trained practitioner, though, to produce its results within hours of downloading the raw image. The ideal raw image should be a "near-nadir" view, exhibit homogeneous atmosphere and water column, include some coverage of optically deep waters and bare land, and lend itself to quality removal of haze, atmospheric adjacency effect, and sun/sky glint.

Differentiating leucine incorporation of Archaea and Bacteria throughout the water column of the eastern Atlantic using metabolic inhibitors

OpenAIRE

Yokokawa, Taichi; Sintes, Eva; de Corte, Daniele; Olbrich, Kerstin; Herndl, Gerhard J.

2012-01-01

The abundance (based on catalyzed reporter deposition-fluorescence in situ hybrid ization, CARD-FISH) and leucine incorporation rates of Archaea and Bacteria were determined throughout the water column in the eastern Atlantic. Bacteria dominated throughout the water column, although their contribution to total prokaryotic abundance in the bathypelagic layer (1000 to 4000 m depth) was lower than in the surface and mesopelagic layers (0 to 1000 m depth). While marine Crenarchaeota Group I (MCG ...

Liquid-chromatographic analysis for cyclosporine with use of a microbore column and small sample volume.

Science.gov (United States)

Annesley, T; Matz, K; Balogh, L; Clayton, L; Giacherio, D

1986-07-01

This liquid-chromatographic assay requires 0.2 to 0.5 mL of whole blood, avoids the use of diethyl ether, and consumes only 10 to 20% of the solvents used in prior methods. Sample preparation involves an acidic extraction with methyl-t-butyl ether, performed in a 13 X 100 mm disposable glass tube, then a short second extraction of the organic phase with sodium hydroxide. After evaporation of the methyl-t-butyl ether, chromatography is performed on an "Astec" 2.0-mm (i.d.) octyl column. We compared results by this procedure with those by use of earlier larger-scale extractions and their respective 4.6-mm (i.d.) columns; analytical recoveries of cyclosporins A and D were comparable with previous findings and results for patients' specimens were equivalent, but the microbore columns provided greatly increased resolution and sensitivity.

Nitrification and the ammonia-oxidizing communities in the central Baltic Sea water column

Science.gov (United States)

Jäntti, Helena; Ward, Bess B.; Dippner, Joachim W.; Hietanen, Susanna

2018-03-01

The redoxclines that form between the oxic and anoxic water layers in the central Baltic Sea are sites of intensive nitrogen cycling. To gain better understanding of nitrification, we measured the biogeochemical properties along with potential nitrification rates and analyzed the assemblages of ammonia-oxidizing bacteria and archaea using functional gene microarrays. To estimate nitrification in the entire water column, we constructed a regression model for the nitrification rates and applied it to the conditions prevailing in the area in 2008-2012. The highest ammonia oxidation rates were found in a thin layer at the top of the redoxcline and the rates quickly decreased below detection limit when oxygen was exhausted. This is probably because extensive suboxic layers, which are known to harbor pelagic nitrification, are formed only for short periods after inflows in the Baltic Sea. The nitrification rates were some of the highest measured in the water columns, but the thickness of the layer where conditions were favorable for nitrification, was very small and it remained fairly stable between years. However, the depth of the nitrification layer varied substantially between years, particularly in the eastern Gotland Basin (EGB) due to turbulence in the water column. The ammonia oxidizer communities clustered differently between the eastern and western Gotland Basin (WGB) and the composition of ammonia-oxidizing assemblages correlated with the environmental variables. The ammonia oxidizer community composition was more even in the EGB, which may be related to physical instability of the redoxcline that does not allow predominance of a single archetype, whereas in the WGB, where the position of the redoxcline is more constant, the ammonia-oxidizing community was less even. Overall the ammonia-oxidizing communities in the Baltic Sea redoxclines were very evenly distributed compared to other marine environments where microarrays have been applied previously.

Artificial neural network modelling of retention of pesticides in various octadecylsiloxane-bonded reversed-phase columns and water-acetonitrile mobile phase

Energy Technology Data Exchange (ETDEWEB)

D' Archivio, Angelo Antonio, E-mail: angeloantonio.darchivio@univaq.it [Dipartimento di Chimica, Ingegneria Chimica e Materiali, Universita degli Studi di L' Aquila, Via Vetoio, 67010 Coppito, L' Aquila (Italy); Maggi, Maria Anna; Mazzeo, Pietro; Ruggieri, Fabrizio [Dipartimento di Chimica, Ingegneria Chimica e Materiali, Universita degli Studi di L' Aquila, Via Vetoio, 67010 Coppito, L' Aquila (Italy)

2009-07-30

Previously, retention of 26 pesticides in the reversed-phase column Gemini (Phenomenex) and water-acetonitrile mobile phase was modelled using a feed-forward artificial neural network (ANN) learned by error back-propagation, accounting for both the effect of solute structure and mobile phase composition. To this end, log K{sub ow} of solutes and four quantum chemical molecular descriptors (the dipole moment, the mean polarizability, the anisotropy of the polarizability and an hydrogen-bonding descriptor based on the atomic charges located on the acid and basic functional groups) and acetonitrile % (v/v) in the eluent (%ACN) were used as ANN inputs. The above ANN-based approach is here tested on further five similar octadecylsiloxane-bonded columns in water-acetonitrile mobile phase within the %ACN range 30-70%. A quite good predictive performance evaluated on three external solutes in the whole %ACN range is observed, prediction errors being lower than {+-}0.1 log k units or slightly higher although still within {+-}0.15 log k units. On the other hand, multilinear regression used in place of ANN provides a more diffuse and non-uniform residual distribution for all the investigated columns. ANN multiple-column retention prediction is attempted by adding to the above variables a column descriptor defined as the average retention of calibration solutes extrapolated to 100% water. This more general model is built using 16 solutes and five 5-{mu}m columns in calibration, while its predictive performance is tested on the remaining 10 compounds. Under these conditions, prediction errors are generally within {+-}0.2 log k units regardless of the kind of column. The possibility of cross-column prediction is evaluated by column leave-one-out cross-validation within the five 5-{mu}m stationary phases and on a 4-{mu}m external column. This analysis reveals that accuracy of retention prediction for unknown solutes in unknown columns is acceptable provided that the external

Artificial neural network modelling of retention of pesticides in various octadecylsiloxane-bonded reversed-phase columns and water-acetonitrile mobile phase

International Nuclear Information System (INIS)

D'Archivio, Angelo Antonio; Maggi, Maria Anna; Mazzeo, Pietro; Ruggieri, Fabrizio

2009-01-01

Previously, retention of 26 pesticides in the reversed-phase column Gemini (Phenomenex) and water-acetonitrile mobile phase was modelled using a feed-forward artificial neural network (ANN) learned by error back-propagation, accounting for both the effect of solute structure and mobile phase composition. To this end, log K ow of solutes and four quantum chemical molecular descriptors (the dipole moment, the mean polarizability, the anisotropy of the polarizability and an hydrogen-bonding descriptor based on the atomic charges located on the acid and basic functional groups) and acetonitrile % (v/v) in the eluent (%ACN) were used as ANN inputs. The above ANN-based approach is here tested on further five similar octadecylsiloxane-bonded columns in water-acetonitrile mobile phase within the %ACN range 30-70%. A quite good predictive performance evaluated on three external solutes in the whole %ACN range is observed, prediction errors being lower than ±0.1 log k units or slightly higher although still within ±0.15 log k units. On the other hand, multilinear regression used in place of ANN provides a more diffuse and non-uniform residual distribution for all the investigated columns. ANN multiple-column retention prediction is attempted by adding to the above variables a column descriptor defined as the average retention of calibration solutes extrapolated to 100% water. This more general model is built using 16 solutes and five 5-μm columns in calibration, while its predictive performance is tested on the remaining 10 compounds. Under these conditions, prediction errors are generally within ±0.2 log k units regardless of the kind of column. The possibility of cross-column prediction is evaluated by column leave-one-out cross-validation within the five 5-μm stationary phases and on a 4-μm external column. This analysis reveals that accuracy of retention prediction for unknown solutes in unknown columns is acceptable provided that the external column is not very

Development of a numerical model for calculating exposure to toxic and nontoxic stressors in the water column and sediment from drilling discharges.

Science.gov (United States)

Rye, Henrik; Reed, Mark; Frost, Tone Karin; Smit, Mathijs G D; Durgut, Ismail; Johansen, Øistein; Ditlevsen, May Kristin

2008-04-01

Drilling discharges are complex mixtures of chemical components and particles which might lead to toxic and nontoxic stress in the environment. In order to be able to evaluate the potential environmental consequences of such discharges in the water column and in sediments, a numerical model was developed. The model includes water column stratification, ocean currents and turbulence, natural burial, bioturbation, and biodegradation of organic matter in the sediment. Accounting for these processes, the fate of the discharge is modeled for the water column, including near-field mixing and plume motion, far-field mixing, and transport. The fate of the discharge is also modeled for the sediment, including sea floor deposition, and mixing due to bioturbation. Formulas are provided for the calculation of suspended matter and chemical concentrations in the water column, and burial, change in grain size, oxygen depletion, and chemical concentrations in the sediment. The model is fully 3-dimensional and time dependent. It uses a Lagrangian approach for the water column based on moving particles that represent the properties of the release and an Eulerian approach for the sediment based on calculation of the properties of matter in a grid. The model will be used to calculate the environmental risk, both in the water column and in sediments, from drilling discharges. It can serve as a tool to define risk mitigating measures, and as such it provides guidance towards the "zero harm" goal.

Study on the breakwater caisson as oscillating water column facility

Science.gov (United States)

Huang, Yan; Shi, Hongda; Liu, Defu; Liu, Zhen

2010-09-01

The Oscillating Water Column (OWC) wave energy convertor with the advantage of its simple geometrical construction and excellent stability is widely employed. Recently, perforated breakwaters have been often used as they can effectively reduce the wave reflection from and wave forces acting on the structures. Considering the similarity between the compartment of perforated caisson and the air chamber of OWC wave energy convertor, a new perforated caisson of breakwater is designed in this paper. The ordinary caisson is modified by installing facilities similar to the air chamber of OWC converter, but here they are utilized to dissipate the wave energy inside the caisson. Such an arrangement improves the stability of the caisson and reduces the construction cost by using the compartment of perforated caisson like using an air chamber. This innovation has both academic significance and important engineering value. For a new type of caisson, reliability analysis of the structure is necessary. Linear potential flow theory is applied to calculate the horizontal wave force acting on the caisson. The calculated results are compared with experimental data, showing the feasibility of the method. The Importance Sampling Procedure (ISP) is used to analyse the reliability of this caisson breakwater.

Water-column mass losses during the emptying of a large-scale pipeline by pressurized air

NARCIS (Netherlands)

Laanearu, J.; Hou, Q.; Annus, I.; Tijsseling, A.S.

2015-01-01

In many industrial applications the liquid trapped inside long pipelines can cause a number of problems. Intrusion of the pressurized air on top of the water column inside the horizontal pipeline can result in a less or more mixed stratified flow. The dynamics of a moving air–water front during the

Considerations regarding design of ion exchange columns for applications in heavy water nuclear reactors- a comprehensive review

International Nuclear Information System (INIS)

Joginder Kumar; Nema, M.K.

2000-01-01

In nuclear reactor applications the principal role of the purification system is to maintain a satisfactory chemistry of moderator and coolant which are different at various stages of reactor operations e.g. during reactor start up, for removal of neutron poison from the moderator, the purification flows are much different compared to steady state operation of the reactor. In order to cater to varying requirements regarding purification load, optimisation in connection with ion exchange column design plays an important role and becomes very challenging in Heavy Water Nuclear Reactors mainly due to the fact that heavy water is very very expensive. In this paper a comprehensive review is made for various designs adopted so far regarding IX column in Indian PHWRs of 220 MWe size for normal operations. Design and operating experience regarding large size IX column used for occasional needs during dilute chemical decontamination of 220 MWe PHWRs is also discussed. The experience regarding development testing of the proposed design of ion exchange column for 500 MWe PHWRs is also discussed

Environmental surveillance master sampling schedule

International Nuclear Information System (INIS)

Bisping, L.E.

1995-02-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the U.S. Department of Energy (DOE). This document contains the planned 1994 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP), Drinking Water Project, and Ground-Water Surveillance Project. Samples are routinely collected for the SESP and analyzed to determine the quality of air, surface water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. The responsibility for monitoring onsite drinking water falls outside the scope of the SESP. PNL conducts the drinking water monitoring project concurrent with the SESP to promote efficiency and consistency, utilize expertise developed over the years, and reduce costs associated with management, procedure development, data management, quality control, and reporting. The ground-water sampling schedule identifies ground-water sampling .events used by PNL for environmental surveillance of the Hanford Site. Sampling is indicated as annual, semi-annual, quarterly, or monthly in the sampling schedule. Some samples are collected and analyzed as part of ground-water monitoring and characterization programs at Hanford (e.g. Resources Conservation and Recovery Act (RCRA), Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), or Operational). The number of samples planned by other programs are identified in the sampling schedule by a number in the analysis column and a project designation in the Cosample column. Well sampling events may be merged to avoid redundancy in cases where sampling is planned by both-environmental surveillance and another program

Environmental surveillance master sampling schedule

Energy Technology Data Exchange (ETDEWEB)

Bisping, L.E.

1995-02-01

Environmental surveillance of the Hanford Site and surrounding areas is conducted by the Pacific Northwest Laboratory (PNL) for the U.S. Department of Energy (DOE). This document contains the planned 1994 schedules for routine collection of samples for the Surface Environmental Surveillance Project (SESP), Drinking Water Project, and Ground-Water Surveillance Project. Samples are routinely collected for the SESP and analyzed to determine the quality of air, surface water, soil, sediment, wildlife, vegetation, foodstuffs, and farm products at Hanford Site and surrounding communities. The responsibility for monitoring onsite drinking water falls outside the scope of the SESP. PNL conducts the drinking water monitoring project concurrent with the SESP to promote efficiency and consistency, utilize expertise developed over the years, and reduce costs associated with management, procedure development, data management, quality control, and reporting. The ground-water sampling schedule identifies ground-water sampling .events used by PNL for environmental surveillance of the Hanford Site. Sampling is indicated as annual, semi-annual, quarterly, or monthly in the sampling schedule. Some samples are collected and analyzed as part of ground-water monitoring and characterization programs at Hanford (e.g. Resources Conservation and Recovery Act (RCRA), Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), or Operational). The number of samples planned by other programs are identified in the sampling schedule by a number in the analysis column and a project designation in the Cosample column. Well sampling events may be merged to avoid redundancy in cases where sampling is planned by both-environmental surveillance and another program.

Hydraulic conductivity of indeformed soil columns determination by gamma ray transmission

International Nuclear Information System (INIS)

Moreira, Anderson Camargo; Moraes Cavalcante, Fabio Henrique de; Rocha, Marcos Correa da; Filho, Otavio Portezan; Quinones, Fernando Rodolfo Espinosa; Appoloni, Carlos Roberto

2000-01-01

The spatial variation of the soil structure influences the water movement through its porous geometry, which could cause problems in the development of agricultural cultures and also accelerate processes of soil erosion. The gamma ray transmission method has established efficiency for the non-destructive measurement of moisture temporal and space evolution, and consequently in the determination of the hydraulic conductivity of the soil, K(θ). Columns of undisturbed soil (approximately 0.11 x 0.06 x 0.60 m) were removed from a trench in the Campus of Londrina State University. The used soil was classified like distrophic dark red soil (LRd). The indeformed soil columns were wrapped up with paraffin and gauze and were fixed on the table of measurement. The water vertical infiltration in the soil was accomplished by maintaining a water layer of approximately 0.01 m over an area of soil of 75 x 10 -4 m 2 . Layers of filter papers and foam controlled the flow of water in the soil surface. After the conclusion of the infiltration, began the process of redistribution of the water in the soil column, with the objective to determine the function K(θ) in relation to the depth in the column. The moisture profiles θ(z,t) are obtained using a radioactive source of 241 Am (3.7 x 10 9 Bq; 0.0596 MeV), spectrometric electronic chain, a 2x2'' NaI(Tl) detector and a measurements table , which allows the sample to move vertically. The hydraulic conductivity function was determined, applying the Sisson model , at 10 levels in the soil column and the results exhibit an increase of K(θ) with depth. (author)

Impacts of Saharan dust on downward irradiance and photosynthetically available radiation in the water column

Directory of Open Access Journals (Sweden)

T. Ohde

2012-09-01

Full Text Available A semi-empirical approach was used to quantify the modification of the underwater light field in amplitude (magnitude effect and spectral distribution (spectral effect by different atmospheric conditions altering the incident light. The approach based on an optical model in connection with radiation measurements in the area off Northwest Africa. Key inputs of the model were parameterized magnitude and spectral effects. Various atmospheric conditions were considered: clear sky, dusty sky without clouds, cloudy sky without dust and skies with different ratios of dust and clouds. Their impacts were investigated concerning the modification of the downward irradiance and photosynthetically available radiation in the water column. The impact on downward irradiance depended on the wavelength, the water depth, the optical water properties, the dust and cloud properties, and the ratio of clouds to dust. The influence of clouds on the amplitude can be much higher than that of dust. Saharan dust reduced the photosynthetically available radiation in the water column. Ocean regions were more influenced than coastal areas. Compensations of the magnitude and spectral effects were observed at special water depths in ocean regions and at atmospheric conditions with definite cloud to dust ratios.

Microbial ecology of the stratified water column of the Black Sea as revealed by a comprehensive biomarker study

DEFF Research Database (Denmark)

Wakeham, Stuart G.; Amann, Rudi; Freemann, Katherine H.

2007-01-01

The stratified water column of the Black Sea is partitioned into oxic, suboxic, and euxinic zones, each characterized by different biogeochemical processes and by distinct microbial communities. In 2003, we collected particulate matter by large volume in situ filtration at the highest resolution...... reduction, and sulfide oxidation at the chemocline, and bacterial sulfate reduction and anaerobic oxidation of methane by archaea in the anoxic zone. Cell densities for archaea and sulfate reducing bacteria are estimated based on water column biomarker concentrations and compared with CARD-FISH results....

Seabed gallery intakes: Investigation of the water pretreatment effectiveness of the active layer using a long-term column experiment

KAUST Repository

Dehwah, Abdullah; Missimer, Thomas M.

2017-01-01

) in improving raw water quality was conducted by using a long-term bench-scale columns experiment. Two different media types, silica and carbonate sand, were tested in 1 m columns to evaluate the effectiveness of media type in terms of algae, bacteria, Natural

Novel design for centrifugal counter-current chromatography: VI. Ellipsoid column.

Science.gov (United States)

Gu, Dongyu; Yang, Yi; Xin, Xuelei; Aisa, Haji Akber; Ito, Yoichiro

2015-01-01

A novel ellipsoid column was designed for centrifugal counter-current chromatography. Performance of the ellipsoid column with a capacity of 3.4 mL was examined with three different solvent systems composed of 1-butanol-acetic acid-water (4:1:5, v/v) (BAW), hexane-ethyl acetate-methanol-0.1 M HCl (1:1:1:1, v/v) (HEMH), and 12.5% (w/w) PEG1000 and 12.5% (w/w) dibasic potassium phosphate in water (PEG-DPP) each with suitable test samples. In dipeptide separation with BAW system, both stationary phase retention (Sf) and peak resolution (Rs) of the ellipsoid column were much higher at 0° column angle (column axis parallel to the centrifugal force) than at 90° column angle (column axis perpendicular to the centrifugal force), where elution with the lower phase at a low flow rate produced the best separation yielding Rs at 2.02 with 27.8% Sf at a flow rate of 0.07 ml/min. In the DNP-amino acid separation with HEMW system, the best results were obtained at a flow rate of 0.05 ml/min with 31.6% Sf yielding high Rs values at 2.16 between DNP-DL-glu and DNP-β-ala peaks and 1.81 between DNP-β-ala and DNP-L-ala peaks. In protein separation with PEG-DPP system, lysozyme and myolobin were resolved at Rs of 1.08 at a flow rate of 0.03 ml/min with 38.9% Sf. Most of those Rs values exceed those obtained from the figure-8 column under similar experimental conditions previously reported.

Reactor water sampling device

International Nuclear Information System (INIS)

Sakamaki, Kazuo.

1992-01-01

The present invention concerns a reactor water sampling device for sampling reactor water in an in-core monitor (neutron measuring tube) housing in a BWR type reactor. The upper end portion of a drain pipe of the reactor water sampling device is attached detachably to an in-core monitor flange. A push-up rod is inserted in the drain pipe vertically movably. A sampling vessel and a vacuum pump are connected to the lower end of the drain pipe. A vacuum pump is operated to depressurize the inside of the device and move the push-up rod upwardly. Reactor water in the in-core monitor housing flows between the drain pipe and the push-up rod and flows into the sampling vessel. With such a constitution, reactor water in the in-core monitor housing can be sampled rapidly with neither opening the lid of the reactor pressure vessel nor being in contact with air. Accordingly, operator's exposure dose can be reduced. (I.N.)

Determination of trihalomethanes in water samples: A review

Energy Technology Data Exchange (ETDEWEB)

Perez Pavon, Jose Luis [Departamento de Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias Quimicas, Universidad de Salamanca, 37008 Salamanca (Spain)], E-mail: jlpp@usal.es; Herrero Martin, Sara; Garcia Pinto, Carmelo; Moreno Cordero, Bernardo [Departamento de Quimica Analitica, Nutricion y Bromatologia, Facultad de Ciencias Quimicas, Universidad de Salamanca, 37008 Salamanca (Spain)

2008-11-23

This article reviews the most recent literature addressing the analytical methods applied for trihalomethanes (THMs) determination in water samples. This analysis is usually performed with gas chromatography (GC) combined with a preconcentration step. The detectors most widely used in this type of analyses are mass spectrometers (MS) and electron capture detectors (ECD). Here, we review the analytical characteristics, the time required for analysis, and the simplicity of the optimised methods. The main difference between these methods lies in the sample pretreatment step; therefore, special emphasis is placed on this aspect. The techniques covered are direct aqueous injection (DAI), liquid-liquid extraction (LLE), headspace (HS), and membrane-based techniques. We also review the main chromatographic columns employed and consider novel aspects of chromatographic analysis, such as the use of fast gas chromatography (FGC). Concerning the detection step, besides the common techniques, the use of uncommon detectors such as fluorescence detector, pulsed discharge photoionization detector (PDPID), dry electrolytic conductivity detector (DELCD), atomic emission detector (AED) and inductively coupled plasma-mass spectrometry (ICP-MS) for this type of analysis is described.

Recruitment of benthic Microcystis (Cyanophyceae) to the water column: internal buoyancy changes or resuspension?

NARCIS (Netherlands)

Verspagen, J.M.H.; Snelder, E.O.F.M.; Visser, P.M.; Huisman, J.; Mur, L.R.; Ibelings, B.W.

2004-01-01

In some lakes, large amounts of the potentially toxic cyanobacterium Microcystis overwinter in the sediment. This overwintering population might inoculate the water column in spring and promote the development of dense surface blooms of Microcystis during summer. In the Dutch Lake Volkerak, we found

Quantifying Methane Flux from a Prominent Seafloor Crater with Water Column Imagery Filtering and Bubble Quantification Techniques

Science.gov (United States)

Mitchell, G. A.; Gharib, J. J.; Doolittle, D. F.

2015-12-01

Methane gas flux from the seafloor to atmosphere is an important variable for global carbon cycle and climate models, yet is poorly constrained. Methodologies used to estimate seafloor gas flux commonly employ a combination of acoustic and optical techniques. These techniques often use hull-mounted multibeam echosounders (MBES) to quickly ensonify large volumes of the water column for acoustic backscatter anomalies indicative of gas bubble plumes. Detection of these water column anomalies with a MBES provides information on the lateral distribution of the plumes, the midwater dimensions of the plumes, and their positions on the seafloor. Seafloor plume locations are targeted for visual investigations using a remotely operated vehicle (ROV) to determine bubble emission rates, venting behaviors, bubble sizes, and ascent velocities. Once these variables are measured in-situ, an extrapolation of gas flux is made over the survey area using the number of remotely-mapped flares. This methodology was applied to a geophysical survey conducted in 2013 over a large seafloor crater that developed in response to an oil well blowout in 1983 offshore Papua New Guinea. The site was investigated by multibeam and sidescan mapping, sub-bottom profiling, 2-D high-resolution multi-channel seismic reflection, and ROV video and coring operations. Numerous water column plumes were detected in the data suggesting vigorously active vents within and near the seafloor crater (Figure 1). This study uses dual-frequency MBES datasets (Reson 7125, 200/400 kHz) and ROV video imagery of the active hydrocarbon seeps to estimate total gas flux from the crater. Plumes of bubbles were extracted from the water column data using threshold filtering techniques. Analysis of video images of the seep emission sites within the crater provided estimates on bubble size, expulsion frequency, and ascent velocity. The average gas flux characteristics made from ROV video observations is extrapolated over the number

Properties of the Water Column and Bottom Derived from AVIRIS Data

Science.gov (United States)

Lee, Zhong-Ping; Carder, Kendall L.; Chen, F. Robert; Peacock, Thomas G.

2001-01-01

Using AVIRIS data as an example, we show in this study that the optical properties of the water column and bottom of a large, shallow area can be adequately retrieved using a model-driven optimization technique. The simultaneously derived properties include bottom depth, bottom albedo, and water absorption and backscattering coefficients, which in turn could be used to derive concentrations of chlorophyll, dissolved organic matter, and suspended sediments. The derived bottom depths were compared with a bathymetry chart and a boat survey and were found to agree very well. Also, the derived bottom-albedo image shows clear spatial patterns, with end members consistent with sand and seagrass. The image of absorption and backscattering coefficients indicates that the water is quite horizontally mixed. These results suggest that the model and approach used work very well for the retrieval of sub-surface properties of shallow-water environments even for rather turbid environments like Tampa Bay, Florida.

New techniques for analysis of organic pollutants in drinking water

Energy Technology Data Exchange (ETDEWEB)

Kissinger, L.D.

1979-01-01

An abstractor packing prepared by coating Chromosorb G AW/DMCS with copper(II) chloride was effective for removal of amines from gas-chromatographic streams, but it did not affect the chromatographic behavior of nonamine compounds. By using pre-columns packed with the abstractor packing, solventless chromatograms were obtained for samples in pyridine. A method was developed for determining haloforms in drinking water by sorption of the haloforms on columns packed with acetylated XAD-2. A pre-column of the abstractor packing was used to remove the pyridine solvent from the samples containing the haloforms concentrated from waters. Detection limits for the four chloro-, bromo- haloforms in a 100-ml water sample using an electron capture detector were below 1 ppB. Addition of ascorbic acid to chlorinated waters was effective for stopping the production of haloforms. Design of the inlet allowed samples to be introduced to the capillary column in a Tracor model 550 gas chromatograph with or without splitting of the carrier-gas stream. An exit splitter was implemented that carried the effluent from the capillary column to two detectors. The capillary-column system was applied to the analysis of trace components in complex mixtures. Small columns packed with Florisil were used to fractionate mixtures of organic compounds by gravity-flow liquid chromatography. Three fractions of organic compounds were collected from the Florisil columns. The recovery and elution behavior of many organic compounds was investigated. Organic compounds from fifteen waters were fractionated on Florisil.

Temporal structure of an electric signal produced upon interaction of radiation from a HF laser with the bottom surface of a water column

International Nuclear Information System (INIS)

Andreev, Sergei N; Kazantsev, S Yu; Kononov, I G; Pashinin, Pavel P; Firsov, K N

2009-01-01

Generation of an electric signal is investigated when a HF-laser pulse interacts with the lower surface of a water column in a cell with a bottom transparent to laser radiation, while the upper surface of the water column remains open. The electric signal exhibits a temporal structure of two spikes spaced by time τ which is linearly dependent on the laser output energy. It is found that the value of τ (up to 1.3 ms) is an order of magnitude greater than the time during which the vapour pressure in a cavity produced due to the volume explosive boiling of water in the exposed area is greater than the atmospheric pressure. The second spike was determined to appear upon the collapse of the vapour cavity. A mathematical model is constructed that explains the motion of the water column above the vapour cavity taking into account the temporal evolution of the vapour pressure above it. It is shown that the prolonged lifetime of the vapour cavity after the decrease in the vapour pressure down to the atmospheric value is caused by the inertial motion of the water column acquiring the velocity at the initial stage of the cavity expansion. The calculated time of the water column motion agrees well with the experimental time interval between the spikes of an electric signal. (interaction of laser radiation with matter)

Studies on the liquid-liquid phase distribution equilibria of selenium and its measurement in water using extraction plant with a pulsation column

International Nuclear Information System (INIS)

Iskanderani, F.; Sobhi, K.M.; Ejaz, M.

1989-01-01

Normal heptane, xylene and a 0.01 molar solution of 4-(5-nonyl)pyridine in toluene were investigated as extractants for selenium(IV) from nitric acid media in potassium iodide. Various parameters affecting the distribution of the element are investigated. Extraction at high aqueous to organic phase volume ratio was studied, using a liquid-liquid extraction plant with a pulsation column. The results were employed to measure selenium in spiked water samples. (author) 24 refs.; 8 figs

Mesoscale changes in the water column in response to fish farming zones in three coastal areas in the Eastern Mediterranean Sea

Science.gov (United States)

Pitta, P.; Apostolaki, E. T.; Giannoulaki, M.; Karakassis, I.

2005-11-01

The hypothesis that the presence of fish farming zones affects the water quality and plankton communities at large spatial scales was investigated through sampling carried out in three regions of the Aegean Sea during May and September. In each region, two sub-areas were sampled: one with fish farming zones (within 2-3 nm) and one without fish farms ('reference site', more than 20 nm). Replicated water samples at different depths were taken in each sub-area for each of the investigated regions. Samples were analysed for nutrients, chlorophyll a, phaeopigments, POC and PON as well as for heterotrophic bacteria, cyanobacteria, flagellates and ciliates. Statistically significant changes in some nutrient species were found during September, which is in the period of maximal supply of feed to caged fish and nutrient loss to a highly stratified oligotrophic environment. Most of the significant changes of nutrients as well as chlorophyll a or PON were found at the deepest layer of the water column below the thermocline, indicating that it is related to the remineralization of benthic organic material. The data support previously published results in this area indicating that there is a rapid transfer of nutrients up the food web. This study also showed the need for studying the effects of fish farms on water quality at larger spatial scales.

Circulation, retention, and mixing of waters within the Weddell-Scotia Confluence, Southern Ocean: The role of stratified Taylor columns

Science.gov (United States)

Meredith, Michael P.; Meijers, Andrew S.; Naveira Garabato, Alberto C.; Brown, Peter J.; Venables, Hugh J.; Abrahamsen, E. Povl; Jullion, Loïc.; Messias, Marie-José

2015-01-01

The waters of the Weddell-Scotia Confluence (WSC) lie above the rugged topography of the South Scotia Ridge in the Southern Ocean. Meridional exchanges across the WSC transfer water and tracers between the Antarctic Circumpolar Current (ACC) to the north and the subpolar Weddell Gyre to the south. Here, we examine the role of topographic interactions in mediating these exchanges, and in modifying the waters transferred. A case study is presented using data from a free-drifting, intermediate-depth float, which circulated anticyclonically over Discovery Bank on the South Scotia Ridge for close to 4 years. Dimensional analysis indicates that the local conditions are conducive to the formation of Taylor columns. Contemporaneous ship-derived transient tracer data enable estimation of the rate of isopycnal mixing associated with this column, with values of O(1000 m2/s) obtained. Although necessarily coarse, this is of the same order as the rate of isopycnal mixing induced by transient mesoscale eddies within the ACC. A picture emerges of the Taylor column acting as a slow, steady blender, retaining the waters in the vicinity of the WSC for lengthy periods during which they can be subject to significant modification. A full regional float data set, bathymetric data, and a Southern Ocean state estimate are used to identify other potential sites for Taylor column formation. We find that they are likely to be sufficiently widespread to exert a significant influence on water mass modification and meridional fluxes across the southern edge of the ACC in this sector of the Southern Ocean.

Ultrasonic testing device having an adjustable water column

Science.gov (United States)

Roach, Dennis P.; Neidigk, Stephen O.; Rackow, Kirk A.; Duvall, Randy L.

2015-09-01

An ultrasonic testing device having a variable fluid column height is disclosed. An operator is able to adjust the fluid column height in real time during an inspection to to produce optimum ultrasonic focus and separate extraneous, unwanted UT signals from those stemming from the area of interest.

Denitrification in the water column of the central Baltic Sea

DEFF Research Database (Denmark)

Dalsgaard, Tage; De Brabandere, Loreto; Hall, Per

2013-01-01

denitrification ranged from 0.24 to 15.9 nM N2 h−1. Assuming that these rates were valid throughout the anoxic View the MathML source containing zone, depth integrated in situ denitrification rates of 0.06–2.11 mmol N m−2 d−1 were estimated. The thickness of this zone was generally 3–6 m, which is probably what...... View the MathML source or sulfide concentrations were converted to in situ rates using the measured water column concentrations of View the MathML source and sulfide and the actual measured relations between View the MathML source and sulfide concentrations and denitrification rates. In situ...... can be maintained through regular turbulent mixing induced by internal waves at the oxic–anoxic interface. However, layers of up to 55 m thickness with low O2 water (Math...

Responses of Water and Salt Parameters to Groundwater Levels for Soil Columns Planted with Tamarix chinensis

Science.gov (United States)

Xia, Jiangbao; Zhao, Ximei; Chen, Yinping; Fang, Ying; Zhao, Ziguo

2016-01-01

Groundwater is the main water resource for plant growth and development in the saline soil of the Yellow River Delta in China. To investigate the variabilities and distributions of soil water and salt contents at various groundwater level (GL), soil columns with planting Tamarix chinensis Lour were established at six different GL. The results demonstrated the following: With increasing GL, the relative soil water content (RWC) declined significantly, whereas the salt content (SC) and absolute soil solution concentration (CS) decreased after the initial increase in the different soil profiles. A GL of 1.2 m was the turning point for variations in the soil water and salt contents, and it represented the highest GL that could maintain the soil surface moist within the soil columns. Both the SC and CS reached the maximum levels in these different soil profiles at a GL of 1.2 m. With the raise of soil depth, the RWC increased significantly, whereas the SC increased after an initial decrease. The mean SC values reached 0.96% in the top soil layer; however, the rates at which the CS and RWC decreased with the GL were significantly reduced. The RWC and SC presented the greatest variations at the medium (0.9–1.2 m) and shallow water levels (0.6 m) respectively, whereas the CS presented the greatest variation at the deep water level (1.5–1.8 m).The RWC, SC and CS in the soil columns were all closely related to the GL. However, the correlations among the parameters varied greatly within different soil profiles, and the most accurate predictions of the GL were derived from the RWC in the shallow soil layer or the SC in the top soil layer. A GL at 1.5–1.8 m was moderate for planting T. chinensis seedlings under saline groundwater conditions. PMID:26730602

Responses of Water and Salt Parameters to Groundwater Levels for Soil Columns Planted with Tamarix chinensis.

Science.gov (United States)

Xia, Jiangbao; Zhao, Ximei; Chen, Yinping; Fang, Ying; Zhao, Ziguo

2016-01-01

Groundwater is the main water resource for plant growth and development in the saline soil of the Yellow River Delta in China. To investigate the variabilities and distributions of soil water and salt contents at various groundwater level (GL), soil columns with planting Tamarix chinensis Lour were established at six different GL. The results demonstrated the following: With increasing GL, the relative soil water content (RWC) declined significantly, whereas the salt content (SC) and absolute soil solution concentration (CS) decreased after the initial increase in the different soil profiles. A GL of 1.2 m was the turning point for variations in the soil water and salt contents, and it represented the highest GL that could maintain the soil surface moist within the soil columns. Both the SC and CS reached the maximum levels in these different soil profiles at a GL of 1.2 m. With the raise of soil depth, the RWC increased significantly, whereas the SC increased after an initial decrease. The mean SC values reached 0.96% in the top soil layer; however, the rates at which the CS and RWC decreased with the GL were significantly reduced. The RWC and SC presented the greatest variations at the medium (0.9-1.2 m) and shallow water levels (0.6 m) respectively, whereas the CS presented the greatest variation at the deep water level (1.5-1.8 m).The RWC, SC and CS in the soil columns were all closely related to the GL. However, the correlations among the parameters varied greatly within different soil profiles, and the most accurate predictions of the GL were derived from the RWC in the shallow soil layer or the SC in the top soil layer. A GL at 1.5-1.8 m was moderate for planting T. chinensis seedlings under saline groundwater conditions.

Responses of Water and Salt Parameters to Groundwater Levels for Soil Columns Planted with Tamarix chinensis.

Directory of Open Access Journals (Sweden)

Jiangbao Xia

Full Text Available Groundwater is the main water resource for plant growth and development in the saline soil of the Yellow River Delta in China. To investigate the variabilities and distributions of soil water and salt contents at various groundwater level (GL, soil columns with planting Tamarix chinensis Lour were established at six different GL. The results demonstrated the following: With increasing GL, the relative soil water content (RWC declined significantly, whereas the salt content (SC and absolute soil solution concentration (CS decreased after the initial increase in the different soil profiles. A GL of 1.2 m was the turning point for variations in the soil water and salt contents, and it represented the highest GL that could maintain the soil surface moist within the soil columns. Both the SC and CS reached the maximum levels in these different soil profiles at a GL of 1.2 m. With the raise of soil depth, the RWC increased significantly, whereas the SC increased after an initial decrease. The mean SC values reached 0.96% in the top soil layer; however, the rates at which the CS and RWC decreased with the GL were significantly reduced. The RWC and SC presented the greatest variations at the medium (0.9-1.2 m and shallow water levels (0.6 m respectively, whereas the CS presented the greatest variation at the deep water level (1.5-1.8 m.The RWC, SC and CS in the soil columns were all closely related to the GL. However, the correlations among the parameters varied greatly within different soil profiles, and the most accurate predictions of the GL were derived from the RWC in the shallow soil layer or the SC in the top soil layer. A GL at 1.5-1.8 m was moderate for planting T. chinensis seedlings under saline groundwater conditions.

Prediction of E. coli release from streambed to water column during base flow periods using SWAT model

Science.gov (United States)

Microbial water quality in streams is of importance for recreation, irrigation, and other uses. The streambed sediment has been shown to harbor large fecal indicator bacteria (FIB) population that can be released to water column during high-flow events when sediments are resuspended. There have been...

Properties of the water column and bottom derived from Airborne Visible Infrared Imaging Spectrometer (AVIRIS) data

Science.gov (United States)

Lee, Zhongping; Carder, Kendall L.; Chen, Robert F.; Peacock, Thomas G.

2001-06-01

Using Airborne Visible Infrared Imaging Spectrometer (AVIRIS) data as an example, we show in this study that the properties of the water column and bottom of a large, shallow area can be adequately retrieved using a model-driven optimization technique. The simultaneously derived properties include bottom depth, bottom albedo, and water absorption and backscattering coefficients, which in turn could be used to derive concentrations of chlorophyll, dissolved organic matter, and suspended sediments in the water column. The derived bottom depths were compared with a bathymetry chart and a boat survey and were found to agree very well. Also, the derived bottom albedo image shows clear spatial patterns, with end-members consistent with sand and seagrass. The image of absorption and backscattering coefficients indicates that the water is quite horizontally mixed. Without bottom corrections, chlorophyll a retrievals were ˜50 mg m-3, while the retrievals after bottom corrections were tenfold less, approximating real values. These results suggest that the model and approach used work very well for the retrieval of subsurface properties of shallow-water environments even for rather turbid environments like Tampa Bay, Florida.

Comparison of two sample preparation procedures for HPLC determination of ochratoxin A

Directory of Open Access Journals (Sweden)

Vuković Gorica L.

2009-01-01

Full Text Available In preparation of samples for chromatographic determination of ochratoxin A, two types of columns were used for sample cleanup (SPE and immunoaffinity columns. The first method consisted of liquid-liquid extraction with a mixture of chloroform and phosphoric acid, followed by ion-exchange cleanup on Waters Oasis MAX columns. The sec­ond method consisted of extraction with a mixture of water and methanol, followed by LCTech OtaCLEAN immunoaf­finity column cleanup. Recoveries of the methods were determined at three levels in three repetitions for maize flour, and they were 84% (%RSD = 19.2 for the first method of sample preparation and 101% (%RSD = 2.2 for the second method. Values of LOQ for OTA were 0.25 and 1.00 μg/kg for the IAC and SPE clean-up procedures, respectively. Both methods comply with present regulations, but the MAX sample clean-up procedure should be used as an alternative, since the immunoaffinity column clean-up procedure is characterized by better reproducibility, accuracy, and efficiency.

Developing Water Sampling Standards

Science.gov (United States)

Environmental Science and Technology, 1974

1974-01-01

Participants in the D-19 symposium on aquatic sampling and measurement for water pollution assessment were informed that determining the extent of waste water stream pollution is not a cut and dry procedure. Topics discussed include field sampling, representative sampling from storm sewers, suggested sampler features and application of improved…

Deuterium used as artificial tracer in column studies under saturated water flow conditions

Science.gov (United States)

Koeniger, P.; Geiges, M.; Leibundgut, Ch.

2003-04-01

In contrast to numerous investigations using deuterium as an environmental tracer, hydrological investigations with deuterium-labelled water are rather rare. Currently applications in groundwater studies are restricted due to increasing costs of spiking large water quantities but an application as intelligent tracer might be of advantage especially in combination with other tracers and under distinct environmental conditions. Therefore deuterium was applied as artificial tracer in column experiments that are well proved as a tool to characterise tracer behaviour in recent studies. Deuterium was tested in comparison to the more familiar conservative tracer fluorescein. Varying experimental conditions, e.g. column length (0.5, 1.0, 1.5 m), initial tracer concentration (0.01, 0.02, 0.2 mg) and flow velocity (1.5 to 6.0 m/d) were used to investigate tracer behaviour under saturated water flow conditions. Deuterium was analysed using an H/Device with chrome reduction connected to an isotope ratio mass spectrometer and expressed in relative concentrations [per mill V-SMOW]. Theoretical tracer breakthrough curves were calculated using a one dimensional dispersion model. The results indicate higher mean transport velocities and smaller dispersion for deuterium in all experiments. Due to different molecule properties that also determine the interaction of soil substrate and tracer, deuterium indicates a more conservative transport behaviour. Deuterium is non-toxic, completely soluble, chemically and biologically stable and not subject to light-influenced decay. Furthermore, it shows promise for investigations of water flow in the unsaturated zone, and of interactions of water in soil-plant-atmosphere systems. A further discussion of problems, together with possibilities for applying deuterium as an artificial tracer, will be presented.

Numerical prediction of the natural frequency of an Oscillating Water Column operating under resonant conditions

Directory of Open Access Journals (Sweden)

Marco Torresi

2016-12-01

Full Text Available Among the different technologies developed in order to harness wave energy, the Oscillating Water Column devices are the most accredited for an actual diffusion. Recently, Boccotti has patented the REWEC1 (REsonant sea Wave Energy Converter solution 1, a submerged breakwater that performs an active coast protection, embedding an Oscillating Water Column device, which is capable of operating under resonant conditions with that sea state, which gives the highest yearly energy contribution. The REWEC1 dynamic behavior can be approximated by means of a mass-spring-damper system. According to this approximation, a criterion for evaluating the oscillating natural frequency of the REWEC1 has been derived. This criterion has been validated against both experimental results and computational fluid dynamics simulations, performed on a REWEC1 laboratory-scale model. The numerical simulations have shown a good agreement between measurements and predictions.

The analysis of scaling mechanism for water-injection pipe columns in the Daqing Oilfield

OpenAIRE

Jing, Guolin; Tang, Shan; Li, Xiaoxiao; Wang, Huaiyuan

2013-01-01

Although water-injection in mature reservoirs is a promising low-cost method of enhanced oil recovery (EOR), in the process of development in the oilfield, scale has been produced in water-injection pipe columns. The ability to prevent and control the deposition of scale is critical to the efficient recovery of crude oil from hard environments, as part of the broader discipline of “flow assurance” in the petroleum industry. To this end laboratory-scale deposition tests have been useful to und...

Study on two phase flow characteristics in annular pulsed extraction column with different ratio of annular width to column diameter

International Nuclear Information System (INIS)

Qin Wei; Dai Youyuan; Wang Jiading

1994-01-01

Annular pulsed extraction column can successfully provide large throughput and can be made critically safe for fuel reprocessing. This investigation is to study the two phase flow characteristics in annular pulsed extraction column with four different annular width. 30% TBP (in kerosene)-water is used (water as continuous phase). Results show that modified Pratt correlation is valid under the experimental operation conditions for the annular pulsed extraction column. The characteristic velocity U K decreased with the increase of energy input and increased with the increase of the ratio of annular width to column diameter. Flooding velocity correlation is suggested. The deviation of the calculated values from the experimental data is within +20% for four annular width in a pulsed extraction column

Application of immunoaffinity columns for different food item samples preparation in micotoxins determination

Directory of Open Access Journals (Sweden)

Ćurčić Marijana

2016-01-01

Full Text Available In analytical methods used for monitoring of what special attention is paid to sample preparation. Therefore, the objective of this study was testing the efficiency of immunoaffinity columns (IAC that are based on solid phase extraction principles used for samples preparation in determining aflatoxins and ochratoxins. Aflatoxins and ochratoxins concentrations were determined in totally 56 samples of food items: wheat, corn, rice, barley and other grains (19 samples, flour and flour products from grain and additives for the bakery industry (7 samples, fruits and vegetables (3 samples, hazelnut, walnut, almond, coconut flour (4 samples, roasted cocoa beans, peanuts, tea, coffee (16 samples, spices (4 samples and meat and meat products (4 samples. Obtained results indicate advantage of IAC use for sample preparation based on enhanced specificity due to binding of extracted molecules to incorporated specific antibodies and rinsing the rest molecules from sample which could interfere with further analysis. Additional advantage is the usage of small amount of organic solvents and consequently decreased exposure of staff who conduct micotoxins determination. Of special interest is increase in method sensitivity since limit of quantification for aflatoxins and ochratoxins determination method is lower than maximal allowed concentration of these toxines prescribed by national rule book.

Capillary ion chromatography with on-column focusing for ultra-trace analysis of methanesulfonate and inorganic anions in limited volume Antarctic ice core samples.

Science.gov (United States)

Rodriguez, Estrella Sanz; Poynter, Sam; Curran, Mark; Haddad, Paul R; Shellie, Robert A; Nesterenko, Pavel N; Paull, Brett

2015-08-28

Preservation of ionic species within Antarctic ice yields a unique proxy record of the Earth's climate history. Studies have been focused until now on two proxies: the ionic components of sea salt aerosol and methanesulfonic acid. Measurement of the all of the major ionic species in ice core samples is typically carried out by ion chromatography. Former methods, whilst providing suitable detection limits, have been based upon off-column preconcentration techniques, requiring larger sample volumes, with potential for sample contamination and/or carryover. Here, a new capillary ion chromatography based analytical method has been developed for quantitative analysis of limited volume Antarctic ice core samples. The developed analytical protocol applies capillary ion chromatography (with suppressed conductivity detection) and direct on-column sample injection and focusing, thus eliminating the requirement for off-column sample preconcentration. This limits the total sample volume needed to 300μL per analysis, allowing for triplicate sample analysis with Application to composite ice-core samples is demonstrated, with coupling of the capillary ion chromatograph to high resolution mass spectrometry used to confirm the presence and purity of the observed methanesulfonate peak. Copyright © 2015 Elsevier B.V. All rights reserved.

Multi-column adsorption systems with condenser for tritiated water vapor removal

International Nuclear Information System (INIS)

Kotoh, Kenji; Kudo, Kazuhiko

1996-01-01

Two types of multi-column adsorption system are proposed as the system for removal of tritiated moisture from tritium process gases or/and handling room atmospheres. The types are of recycle use of adsorption columns, and are composed of twin or triplet columns and one condenser which is used for collecting the adsorbed moisture from columns in desorption process. The systems utilize the dry gas from a working column as the purge gas for regenerating a saturated column and appropriate an active column for recovery of the tritiated moisture passing through the condenser. Each column hence needs the additional amount of adsorbent for collecting the moisture from the condenser. In the modeling and design of an adsorption column, it is primary to estimate the necessary amount of a candidate adsorbent for its packed-bed. The performance of the proposed systems is examined here by analyzing the dependence of the necessary amount of adsorbent for their columns on process operational conditions and adsorbent moisture-adsorption characteristics. The result shows that the necessary amount is sensitive to the types of adsorption isotherm, and suggests that these systems should employ adsorbents which exhibit the Langmuir-type isotherms. (author)

Column-Parallel Single Slope ADC with Digital Correlated Multiple Sampling for Low Noise CMOS Image Sensors

NARCIS (Netherlands)

Chen, Y.; Theuwissen, A.J.P.; Chae, Y.

2011-01-01

This paper presents a low noise CMOS image sensor (CIS) using 10/12 bit configurable column-parallel single slope ADCs (SS-ADCs) and digital correlated multiple sampling (CMS). The sensor used is a conventional 4T active pixel with a pinned-photodiode as photon detector. The test sensor was

RETENTION TIME EFFECT ON METAL REMOVAL BY PEAT COLUMNS

Energy Technology Data Exchange (ETDEWEB)

Nelson, E

2007-02-28

The potential use of a peat bed to treat the H-12 Outfall discharge to bring it to new compliance limits was previously investigated and reported utilizing a 7 hour retention time. The influence of retention time (contact time) of water with peat moss on the removal of copper from the water was investigated under laboratory conditions using vertical flow peat moss columns. Reduction of the necessary retention time has a large influence on the design sizing of any peat bed that would be constructed to treat the H-12 discharge on a full scale basis. Retention times of 5 hours, 3 hours and 1 hour were tested to determine the copper removal by the peat columns using vertical flow. Water samples were collected after 4, 8, 12, and 16 water volumes had passed through the columns and analyzed for a suite of metals, with quantitative emphasis on copper. Laboratory results indicated that copper removal was very high at each of the 3 retention times tested, ranging from 99.6 % removal at 5 and 3 hours to 98.8% removal at 1 hour. All these values are much lower that the new compliance limit for the outfall. The results also indicated that most divalent metals were removed to their normal reporting detection limit for the analytical methods used, including zinc. Lead levels in the H-12 discharge used in this study were below PQL in all samples analyzed. While each of the retention times studied removed copper very well, there were indications that 1 hour is probably too short for an operational, long-term facility. At that retention time, there was about 6% compaction of the peat in the column due to the water velocity, and this may affect long term hydraulic conductivity of the peat bed. At that retention time, copper concentration in the effluent was higher than the other times tested, although still very low. Because of the potential compacting and somewhat reduced removal efficiency at a 1 hour retention time, it would be prudent to design to at least a 3 hour retention

Combined impact of water column oxygen and temperature on internal oxygen status and growth of Zostera marina seedlings and adult shoots

DEFF Research Database (Denmark)

Raun, Ane-Marie Løvendahl; Borum, Jens

2013-01-01

Eelgrass (Zostera marina L.) occasionally experiences severe die-offs during warm summer periods with variable water column oxygen partial pressures (pO). Eelgrass is known to be very intolerant to tissue anoxia with reduced growth and increasing mortality after ≤12h anoxia in the dark...... at temperatures of ≥25°C. In the present study we experimentally examine the impact of combined water column oxygen and temperature on oxygen dynamics in leaf meristems of seedlings and adult shoots to better understand how stressful environmental conditions affect eelgrass oxygen dynamics and subsequent growth...... and mortality. There was a strong interaction between water column oxygen and temperature on meristem pO implying that eelgrass is rather resistant to unfavorable oxygen conditions in winter but becomes increasingly vulnerable in summer, especially at high temperatures. At 25°C meristems became anoxic...

Diagnostic-Photographic Determination of Drag/Lift/Torque Coefficients of High Speed Rigid Body in Water Column

National Research Council Canada - National Science Library

Chu, Peter C; Fan, Chenwu; Gefken, Paul R

2008-01-01

Prediction of rigid body falling through water column with a high speed (such as Mk-84 bomb) needs formulas for drag/lift and torque coefficients, which depend on various physical processes such as supercavitation and bubbles...

Determination of physical and dynamic properties of suspended particles in water column with ultrasonic scanning in between the water surface and stable sediment layer.

Science.gov (United States)

Acar, Dursun; Alpar, Bedri; Ozeren, Sinan; Cagatay, Namık; Sari, Erol; Vardar, Denizhan; Eris, Kadir

2015-04-01

The behavior of seafloor sediment with its water column should be known against any occurrences of anoxic or oxic conditions. The most important ones of these conditions are possible leakage of natural gas or escape of liquids from sediment. On the basis of combined solid/liquid flow dynamics in sedimentation, such kind of events can change, even in an effective manner, the dynamic movements of molecules and their cumulative mass of particules, i.e. the suspended materials. The deployment of suitable sediment traps or ultrasonic transducers somewhere in the water column are not easy attempts in order to obtain useful information about the state of suspended materials during sedimentation. These are usually bulky instruments; therefore they may behave like an anti-move suppresser on the particles moving in the float direction, in oxic and anoxic manner. These instruments, on the other hand, may cover the effects of diffusive flow or bubble formed gas and fluid escape from the sediment surface into the water column. Ultrasonic scanners, however, are able to make observations in a remote manner, without affecting such artificial events. Our field trials were successfully completed at the historical estuary called Halic of Marmara sea . The physical properties; such as the velocity of particles, their travel directions, their dimensions and the ability to observe anti-compositor crushes of shock waves of the bubbles are only a few of these observations in natural ambience. The most important problem solved about water pressure during 3 atmosphere . The sensor has been tested successfully few times. We used the ''High voltage electric isolator oil filling'' to the inside of the scanner for pressure equalization between outer side and inner body of probe at a depth of (20 meters) beneath the sea surface . The transmitted signals by the planar crystal of the transducer become weaker under the pressure of overlying water column in depths. Our efforts are now focused on the

Marine Group II Dominates Planktonic Archaea in Water Column of the Northeastern South China Sea

Directory of Open Access Journals (Sweden)

Haodong Liu

2017-06-01

Full Text Available Temperature, nutrients, and salinity are among the important factors constraining the distribution and abundance of microorganisms in the ocean. Marine Group II (MGII belonging to Euryarchaeota commonly dominates the planktonic archaeal community in shallow water and Marine Group I (MGI, now is called Thaumarchaeota in deeper water in global oceans. Results of quantitative PCR (qPCR and 454 sequencing in our study, however, showed the dominance of MGII in planktonic archaea throughout the water column of the northeastern South China Sea (SCS that is characterized by strong water mixing. The abundance of ammonia-oxidizing archaea (AOA representing the main group of Thaumarchaeota in deeper water in the northeastern SCS was significantly lower than in other oceanic regions. Phylogenetic analysis showed that the top operational taxonomic units (OTUs of the MGII occurring predominantly below 200 m depth may be unique in the northeastern SCS based on the observation that they are distantly related to known sequences (identity ranging from 90–94%. The abundance of MGII was also significantly correlated with total bacteria in the whole column, which may indicate that MGII and bacteria may have similar physiological or biochemical properties or responses to environmental variation. This study provides valuable information about the dominance of MGII over AOA in both shallow and deep water in the northeastern SCS and highlights the need for comprehensive studies integrating physical, chemical, and microbial oceanography.

Method of analyzing the shipping inspection water in nuclear fuels

International Nuclear Information System (INIS)

Ishikawa, Tatsuo; Izumoji, Yoshiaki.

1984-01-01

Purpose: To automatically perform radioactive-corrosion-products removing operation and thereby automatic analysis for shipping inspection water. Method: An radioactive-corrosion-product removing device has a column filled with a chelate resin layer. Shipping-inspection water as a specimen is injected from a sample-water inlet to the column, passes through the chelate resin layer, issues through the sample-water exit and is then stored once in a sample collector. The shipping inspection water sampled in the sampling collector is sent to an inspection port in an on-line or off-line manner and gamma-ray determination is made by a gamma-ray spectrum analyzer. (Horiuchi, T.)

A Simple Method for Automated Solid Phase Extraction of Water Samples for Immunological Analysis of Small Pollutants.

Science.gov (United States)

Heub, Sarah; Tscharner, Noe; Kehl, Florian; Dittrich, Petra S; Follonier, Stéphane; Barbe, Laurent

2016-01-01

A new method for solid phase extraction (SPE) of environmental water samples is proposed. The developed prototype is cost-efficient and user friendly, and enables to perform rapid, automated and simple SPE. The pre-concentrated solution is compatible with analysis by immunoassay, with a low organic solvent content. A method is described for the extraction and pre-concentration of natural hormone 17β-estradiol in 100 ml water samples. Reverse phase SPE is performed with octadecyl-silica sorbent and elution is done with 200 µl of methanol 50% v/v. Eluent is diluted by adding di-water to lower the amount of methanol. After preparing manually the SPE column, the overall procedure is performed automatically within 1 hr. At the end of the process, estradiol concentration is measured by using a commercial enzyme-linked immune-sorbent assay (ELISA). 100-fold pre-concentration is achieved and the methanol content in only 10% v/v. Full recoveries of the molecule are achieved with 1 ng/L spiked de-ionized and synthetic sea water samples.

Studying, Determining The Radionuclide Of Tritum In The Water Samples (Rain, Surface Water) By Using Liquid Scintillation Counting (TRi-carb 3180TR/SL)

International Nuclear Information System (INIS)

Nguyen Thi Linh; Nguyen Dinh Tung; Truong Y; Le Nhu Sieu; Nguyen Van Phuc; Nguyen Van Phu; Nguyen Kim Thanh

2014-01-01

Tritium in the environment is of natural or man-made origin. Tritium is a radioactive isotope that occurs in the environment and is associated with the interaction of cosmic ray in the atmosphere. However, the most significant sources of tritium in the environment results from nuclear weapons testing in the atmosphere carried out during the late 1950s and early 1960s. Today, the most important new sources of tritium in the environments, such as power stations, processing and using of isotopes released the local tritium. The objective of this study is the application of the liquid scintillation technique to tritium analysis in water samples (rain, and surface waters). Following the Eichrom Tritium Column technique, an aliquot of the passed tritium resin sample (10 mL) is mixed with 10 mL of scintillation cocktail (Ultima Gold LLT, Packard) in 20-mL plastic- container vials and the sample activity is determined using a liquid scintillation spectrometer, Tri-carb 3180TR/SL. Counting efficiency is evaluated with internal standards. The tritium concentrations of water samples that were collected from DaLat, Lamdong range between 0 to 36.2 TU. (author)

Ground improvement using soil–cement columns: Experimental investigation

Directory of Open Access Journals (Sweden)

Ahmed Farouk

2013-12-01

Full Text Available The construction of heavy structures on soils of low relative density is a challenging task. The inclusion of soil–cement columns produced by the deep mixing method is one of the soil stabilizing techniques that could be applied successfully to overcome this challenge. Nevertheless, this technique did not receive a considerable attention in Egypt yet. In the first part of this study, two different natural silty sand soils extracted from the Delta of the River Nile were mixed with cement to prepare samples of different cement doses and different water cement ratios. After curing, the hardened samples were tested and their unconfined compressive strength was investigated. The second part of this study investigates the interaction between a strip footing model and Nile deltaic soil improved by a group of soil–cement columns. Results of the first part of this study showed that the compressive strength of the investigated Nile delta soils could be increased even at lower values of cement doses. Results extracted from the second part of this study showed that a considerable settlement reduction up to 80% could be achieved depending on both the number and the length of the soil–cement columns that is used to improve the soil.

Fate of polychlorinated biphenyls in a contaminated lake ecosystem: combining equilibrium passive sampling of sediment and water with total concentration measurements of biota.

Science.gov (United States)

Mäenpää, Kimmo; Leppänen, Matti T; Figueiredo, Kaisa; Mayer, Philipp; Gilbert, Dorothea; Jahnke, Annika; Gil-Allué, Carmen; Akkanen, Jarkko; Nybom, Inna; Herve, Sirpa

2015-11-01

Equilibrium sampling devices can be applied to study and monitor the exposure and fate of hydrophobic organic chemicals on a thermodynamic basis. They can be used to determine freely dissolved concentrations and chemical activity ratios and to predict equilibrium partitioning concentrations of hydrophobic organic chemicals in biota lipids. The authors' aim was to assess the equilibrium status of polychlorinated biphenyls (PCBs) in a contaminated lake ecosystem and along its discharge course using equilibrium sampling devices for measurements in sediment and water and by also analyzing biota. The authors used equilibrium sampling devices (silicone rubber and polyethylene [PE]) to determine freely dissolved concentrations and chemical activities of PCBs in the water column and sediment porewater and calculated for both phases the corresponding equilibrium concentrations and chemical activities in model lipids. Overall, the studied ecosystem appeared to be in disequilibrium for the studied phases: sediment, water, and biota. Chemical activities of PCBs were higher in sediment than in water, which implies that the sediment functioned as a partitioning source of PCBs and that net diffusion occurred from the sediment to the water column. Measured lipid-normalized PCB concentrations in biota were generally below equilibrium lipid concentrations relative to the sediment (CLip ⇌Sed ) or water (CLip ⇌W ), indicating that PCB levels in the organisms were below the maximum partitioning levels. The present study shows the application versatility of equilibrium sampling devices in the field and facilitates a thermodynamic understanding of exposure and fate of PCBs in a contaminated lake and its discharge course. © 2015 SETAC.

Preconcentration of trace manganese from natural waters by complexation with dithiocarbamate and adsorption onto C18-solid phase extraction column for neutron activation analysis

International Nuclear Information System (INIS)

Sarmani, S.B.; Abdullah, M.P.; Bobaker, A.M.

2004-01-01

A method was developed for the preconcentration and separation of trace manganese from natural water samples by complexation with dithiocarbamate followed by adsorption onto C 18 -solid phase extraction column prior to irradiation. The Mn recovery was better than 99.8% without interference from iron(III) at 5 mg x l -1 , copper(II), zinc(II), aluminum(III) and cobalt(II) at 0.5 mg x l -1 and sodium(I), potassium(I), magnesium(II) and calcium(II) at 1 mg x l -1 . The separation factor was 100 and the detection limit was 0.01 μg x l -1 with good precision and accuracy with a relative error lower than 3%. The method was applied to the determination of Mn in tap, well, river and treated water samples. (author)

Photogeneration of reactive transient species upon irradiation of natural water samples: Formation quantum yields in different spectral intervals, and implications for the photochemistry of surface waters.

Science.gov (United States)

Marchisio, Andrea; Minella, Marco; Maurino, Valter; Minero, Claudio; Vione, Davide

2015-04-15

Chromophoric dissolved organic matter (CDOM) in surface waters is a photochemical source of several transient species such as CDOM triplet states ((3)CDOM*), singlet oxygen ((1)O2) and the hydroxyl radical (OH). By irradiation of lake water samples, it is shown here that the quantum yields for the formation of these transients by CDOM vary depending on the irradiation wavelength range, in the order UVB > UVA > blue. A possible explanation is that radiation at longer wavelengths is preferentially absorbed by the larger CDOM fractions, which show lesser photoactivity compared to smaller CDOM moieties. The quantum yield variations in different spectral ranges were definitely more marked for (3)CDOM* and OH compared to (1)O2. The decrease of the quantum yields with increasing wavelength has important implications for the photochemistry of surface waters, because long-wavelength radiation penetrates deeper in water columns compared to short-wavelength radiation. The average steady-state concentrations of the transients ((3)CDOM*, (1)O2 and OH) were modelled in water columns of different depths, based on the experimentally determined wavelength trends of the formation quantum yields. Important differences were found between such modelling results and those obtained in a wavelength-independent quantum yield scenario. Copyright © 2015 Elsevier Ltd. All rights reserved.

Development of a fully automated open-column chemical-separation system—COLUMNSPIDER—and its application to Sr-Nd-Pb isotope analyses of igneous rock samples

Science.gov (United States)

Miyazaki, Takashi; Vaglarov, Bogdan Stefanov; Takei, Masakazu; Suzuki, Masahiro; Suzuki, Hiroaki; Ohsawa, Kouzou; Chang, Qing; Takahashi, Toshiro; Hirahara, Yuka; Hanyu, Takeshi; Kimura, Jun-Ichi; Tatsumi, Yoshiyuki

A fully automated open-column resin-bed chemical-separation system, named COLUMNSPIDER, has been developed. The system consists of a programmable micropipetting robot that dispenses chemical reagents and sample solutions into an open-column resin bed for elemental separation. After the initial set up of resin columns, chemical reagents, and beakers for the separated chemical components, all separation procedures are automated. As many as ten samples can be eluted in parallel in a single automated run. Many separation procedures, such as radiogenic isotope ratio analyses for Sr and Nd, involve the use of multiple column separations with different resin columns, chemical reagents, and beakers of various volumes. COLUMNSPIDER completes these separations using multiple runs. Programmable functions, including the positioning of the micropipetter, reagent volume, and elution time, enable flexible operation. Optimized movements for solution take-up and high-efficiency column flushing allow the system to perform as precisely as when carried out manually by a skilled operator. Procedural blanks, examined for COLUMNSPIDER separations of Sr, Nd, and Pb, are low and negligible. The measured Sr, Nd, and Pb isotope ratios for JB-2 and Nd isotope ratios for JB-3 and BCR-2 rock standards all fall within the ranges reported previously in high-accuracy analyses. COLUMNSPIDER is a versatile tool for the efficient elemental separation of igneous rock samples, a process that is both labor intensive and time consuming.

Adsorptive removal of heavy metals from water using sodium titanate nanofibres loaded onto GAC in fixed-bed columns.

Science.gov (United States)

Sounthararajah, D P; Loganathan, P; Kandasamy, J; Vigneswaran, S

2015-04-28

Heavy metals are serious pollutants in aquatic environments. A study was undertaken to remove Cu, Cd, Ni, Pb and Zn individually (single metal system) and together (mixed metals system) from water by adsorption onto a sodium titanate nanofibrous material. Langmuir adsorption capacities (mg/g) at 10(-3)M NaNO3 ionic strength in the single metal system were 60, 83, 115 and 149 for Ni, Zn, Cu, and Cd, respectively, at pH 6.5 and 250 for Pb at pH 4.0. In the mixed metals system they decreased at high metals concentrations. In column experiments with 4% titanate material and 96% granular activated carbon (w/w) mixture at pH 5.0, the metals breakthrough times and adsorption capacities (for both single and mixed metals systems) decreased in the order Pb>Cd, Cu>Zn>Ni within 266 bed volumes. The amounts adsorbed were up to 82 times higher depending on the metal in the granular activated carbon+titanate column than in the granular activated carbon column. The study showed that the titanate material has high potential for removing heavy metals from polluted water when used with granular activated carbon at a very low proportion in fixed-bed columns. Copyright © 2015 Elsevier B.V. All rights reserved.

Water calibration measurements for neutron radiography: Application to water content quantification in porous media

Energy Technology Data Exchange (ETDEWEB)

Kang, M., E-mail: kangm@ornl.gov [Department of Earth and Planetary Sciences, University of Tennessee, Knoxville, TN (United States); Chemical and Engineering Materials Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Bilheux, H.Z., E-mail: bilheuxhn@ornl.gov [Chemical and Engineering Materials Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Voisin, S. [Computational Sciences and Engineering Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Cheng, C.L.; Perfect, E. [Department of Earth and Planetary Sciences, University of Tennessee, Knoxville, TN (United States); Horita, J. [Department of Geosciences, Texas Tech University, Lubbock, TX (United States); Warren, J.M. [Environmental Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States)

2013-04-21

Using neutron radiography, the measurement of water thickness was performed using aluminum (Al) water calibration cells at the High Flux Isotope Reactor (HFIR) Cold-Guide (CG) 1D neutron imaging facility at Oak Ridge National Laboratory, Oak Ridge, TN, USA. Calibration of water thickness is an important step to accurately measure water contents in samples of interest. Neutron attenuation by water does not vary linearly with thickness mainly due to beam hardening and scattering effects. Transmission measurements for known water thicknesses in water calibration cells allow proper correction of the underestimation of water content due to these effects. As anticipated, strong scattering effects were observed for water thicknesses greater than 0.2 cm when the water calibration cells were positioned close to the face of the detector/scintillator (0 and 2.4 cm away, respectively). The water calibration cells were also positioned 24 cm away from the detector face. These measurements resulted in less scattering and this position (designated as the sample position) was used for the subsequent experimental determination of the neutron attenuation coefficient for water. Neutron radiographic images of moist Flint sand in rectangular and cylindrical containers acquired at the sample position were used to demonstrate the applicability of the water calibration. Cumulative changes in the water volumes within the sand columns during monotonic drainage determined by neutron radiography were compared with those recorded by direct reading from a burette connected to a hanging water column. In general, the neutron radiography data showed very good agreement with those obtained volumetrically using the hanging water-column method. These results allow extension of the calibration equation to the quantification of unknown water contents within other samples of porous media.

Biological nitrogen removal using soil columns for the reuse of reclaimed water: Performance and microbial community analysis.

Science.gov (United States)

Sun, Jiaji; Chen, Lei; Rene, Eldon R; Hu, Qian; Ma, Weifang; Shen, Zhenyao

2018-07-01

The main aim of this study was to remove nitrogen compounds from reclaimed water and reuse the water in semi-arid riverine lake systems. In order to assess the nitrogen removal efficiencies in different natural environments, laboratory scale column experiments were performed using sterilized soil (SS), silty clay (SC), soil with submerged plant (SSP) and biochar amendment soil (BCS). The initial concentration of NO 3 - -N and the flow rate was maintained constant at 15 mg L -1 and 0.6 ± 0.1 m d -1 , respectively. Among the tested columns, both SSP and BCS were able to achieve NO 3 - -N levels <0.2 mg L -1 in the treated reclaimed water. The results from bacterial community structure analysis, using 454 pyrosequencing of 16s rRNA genes, showed that the dominant denitrifier was Bacillus at the genera level. Copyright © 2018 Elsevier Ltd. All rights reserved.

Carbon and oxygen dynamics on the Louisiana continental shelf: role of water column primary production and respiration

Science.gov (United States)

We conducted a multi-year study of the Louisiana continental shelf (LCS) to better understand the linkages between water column net metabolism and the formation of hypoxia (dissolved oxygen respiration (R) and primary p...

Water Column Exploration Field Trial I (EX0904, EM302) aboard the NOAA Ship Okeanos Explorer in the Gorda Ridge, off the coasts of Oregon and California

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — This cruise is a water column exploration field trial cruise, designed to test and refine operations for conducting water column exploration using NOAA Ship Okeanos...

Fate of parabens and 4-hydroxybenzoic acid in aquifer materials columns during step experiments with fresh and sea waters

Science.gov (United States)

López-Ortiz, C. M.; Boluda-Botella, N.; Prats-Rico, D.; Sentana-Gadea, I.

2018-02-01

Coastal areas submitted to seawater intrusion and with discharges from urban and industrial wastewaters, municipal landfill leachates, rivers, recreational waters and other sources are sensitive to be polluted with parabens. Understanding the fate of these compounds in environmental studies, it requires previously the knowledge of the reactive processes in controlled conditions. In this research, laboratory columns experiments were carried out with a group of parabens (methyl-, ethyl-, propyl- and butylparaben) and their main degradation compound (4-hydroxybenzoic acid) to study mainly the dynamic sorption processes in different aquifer materials (100% sand and heterogeneous: 81% sand, 9% silt and 10% clay) and with fresh and sea waters, the end members of seawater intrusions. To the column hydrodynamic characterization, tracer assays with increase and decrease of salinity were performed, to obtain the mean residence time of each column and other transport parameters which allow us to compare parabens' sorption in different conditions. The results of the adsorption and desorption of parabens in the sand column demonstrated be fast and simultaneous, with a short delay and without influence of the water salinity. Very different results were found in the column experiments with heterogeneous material, where the presence of clay and organic matter increase the time of adsorption/desorption as the length of the alkyl chain paraben increased, according with their hydrophobicity. It should be noted that despite the quick desorption of the major quantities of parabens, the elution of their trace concentrations was very slow (for the seawater, the buthylparaben required a dimensionless time of 800). Planning the restoration of a coastal aquifer with freshwater, and in the conditions of the studied sand column experiment, it will need a dimensionless time of 160. However, it is necessary to take into account that the studied parabens and 4-hydroxybenzoic acid are

Seabed gallery intakes: Investigation of the water pretreatment effectiveness of the active layer using a long-term column experiment

KAUST Repository

Dehwah, Abdullah

2017-05-11

Seabed gallery intake systems used for seawater reverse osmosis facilities employ the same principle of water treatment as slow sand filtration in freshwater systems. An investigation concerning the effectiveness of the active layer (top layer) in improving raw water quality was conducted by using a long-term bench-scale columns experiment. Two different media types, silica and carbonate sand, were tested in 1 m columns to evaluate the effectiveness of media type in terms of algae, bacteria, Natural Organic Matter (NOM) and Transparent Exopolymer Particles (TEP) removal over a period of 620 days. Nearly all algae in the silica sand column, 87% (σ = 0.04) of the bacteria, 59% (σ = 0.11) of the biopolymer fraction of NOM, 59% (σ = 0.16) of particulate and 32% (σ = 0.25) of colloidal TEP were removed during the last 330 days of the experiment. Total removal was observed in the carbonate sand column for algal concentration, while the bacterial removal was lower at 74% (σ = 0.08). Removal of biopolymers, particulate and colloidal TEP were higher in the carbonate column during the last 330 days with 72% (σ = 0.15), 66% (σ = 0.08) and 36% (σ = 0.12) removed for these organics respectively. Removal of these key organics through the 1 m thick column, representing the active layer, will likely reduce the rate of biofouling, reduce chemical usage and minimize operating cost in SWRO systems. The data show that the media will require several months at the beginning of operation to reach equilibrium so that high organic removal rates can be achieved. No development of a “schmutzdecke” layer occurred. The experimental results suggest that unlike freshwater slow sand filtration wherein most water treatment occurs in the upper 10 cm, in seawater systems treatment occurs throughout the full active layer depth of 1 m. The results of this study will help in designing and operating seabed gallery intake systems in varied geological conditions.

Differentiating leucine incorporation of Archaea and Bacteria throughout the water column of the eastern Atlantic using metabolic inhibitors

OpenAIRE

Yokokawa, T.; Sintes, E.; de Corte, D.; Olbrich, K.; Herndl, G.J.

2012-01-01

The abundance (based on catalyzed reporter deposition-fluorescence in situ hybrid ization, CARD-FISH) and leucine incorporation rates of Archaea and Bacteria were determined throughout the water column in the eastern Atlantic. Bacteria dominated throughout the water column, although their contribution to total prokaryotic abundance in the bathypelagic layer (1000 to 4000 m depth) was lower than in the surface and mesopelagic layers (0 to 1000 m depth). While marine Crenarchaeota Group I (MCG ...

[Preparation and applications of a supported liquid-liquid extraction column with a composite diatomite material].

Science.gov (United States)

Bao, Jianmin; Ma, Zhishuang; Sun, Ying; Wang, Yongzun; Li, Youxin

2012-08-01

A rapid and special supported liquid-liquid extraction (SLE) column was developed with a composite diatomite material. The SLE column was evaluated by high performance liquid chromatography (HPLC) with acidic, neutral and alkaline compounds dissolved in water. Furthermore, some real complex samples were also analyzed by HPLC with the SLE method. The recoveries of benzoic acid (acidic), p-nitroaniline (alkaline) and 4-hydroxy-benzoic methyl ester (neutral) treated by the SLE column were 90.6%, 98.1% and 97.7%. However, the recoveries of the three compounds treated by traditional liquid-liquid extraction (LLE) method were 71.9%, 81.9% and 83.9%. The results showed that the SLE technique had higher recoveries than the traditional LLE method. The spiked recoveries of the complex samples, such as benzoic acid in Sprite and dexamethasone acetate, chlorphenamine maleate, indomethacin in bovine serum, were between 80% and 110% and the relative standard deviations (RSDs) were less than 15%. For biological specimen, the results could be accepted. Meantime, many disadvantages associated with traditional LLE method, such as emulsion formation, didn't occur using SLE column. The SLE column technique is a good sample preparation method with many advantages, such as rapid, simple, robust, easily automated, high recovery and high-throughput, which would be widely used in the future.

Simultaneous determination of palladium, platinum and rhodium by on-line column enrichment and HPLC with 2,4-dihydroxybenzylidenethiorhodanine as pre-column derivatization reagent

Directory of Open Access Journals (Sweden)

Dong Xuechang

2006-01-01

Full Text Available A new method for the simultaneous determination of palladium, platinum and rhodium ions as metal-DHBTR chelates was developed. The palladium, platinum and rhodium ions were pre-column derivatized with 2,4-dihydroxybenzylidenethiorhodanine (DHBTR to form colored chelates. The Pd-DHBTR, Pt-DHBTR and Rh-DHBTR chelates can be absorbed onto the front of the enrichment column when they were injected into the injector and sent to the enrichment column with a 0.05 mol L-1 sodium acetate-acetic acid buffer solution (pH 3.5 as mobile phase. After the enrichment had finished, by switching the six ports switching valve, the retained chelates were back-flushed by mobile phase and traveling towards the analytical column. These chelates separation on the analytical column was satisfactory with 62% (v/v acetonitrile (containing 0.05 mol L-1 of pH 3.5 sodium acetate-acetic acid buffer salt and 0.1% (m/v of tritonX-100 as mobile phase. The Limits of detection of palladium, platinum and rhodium are 3.6 ng L-1, 3.2 ng L-1 and 4.5 ng L-1, respectively. This method was applied to the determination of palladium, platinum and rhodium in water, urine and soil samples with good results.

Heat Transfer Analysis for a Fixed CST Column

International Nuclear Information System (INIS)

Lee, S.Y.

2004-01-01

In support of a small column ion exchange (SCIX) process for the Savannah River Site waste processing program, a transient two-dimensional heat transfer model that includes the conduction process neglecting the convection cooling mechanism inside the crystalline silicotitanate (CST) column has been constructed and heat transfer calculations made for the present design configurations. For this situation, a no process flow condition through the column was assumed as one of the reference conditions for the simulation of a loss-of-flow accident. A series of the modeling calculations has been performed using a computational heat transfer approach. Results for the baseline model indicate that transit times to reach 130 degrees Celsius maximum temperature of the CST-salt solution column are about 96 hours when the 20-in CST column with 300 Ci/liter heat generation source and 25 degrees Celsius initial column temperature is cooled by natural convection of external air as a primary heat transfer mechanism. The modeling results for the 28-in column equipped with water jacket systems on the external wall surface of the column and water coolant pipe at the center of the CST column demonstrate that the column loaded with 300 Ci/liter heat source can be maintained non-boiling indefinitely. Sensitivity calculations for several alternate column sizes, heat loads of the packed column, engineered cooling systems, and various ambient conditions at the exterior wall of the column have been performed under the reference conditions of the CST-salt solution to assess the impact of those parameters on the peak temperatures of the packed column for a given transient time. The results indicate that a water-coolant pipe at the center of the CST column filled with salt solution is the most effective one among the potential design parameters related to the thermal energy dissipation of decay heat load. It is noted that the cooling mechanism at the wall boundary of the column has significant

Measuring and modeling three-dimensional water uptake of a growing faba bean (Vicia faba) within a soil column

Science.gov (United States)

Huber, Katrin; Koebernick, Nicolai; Kerkhofs, Elien; Vanderborght, Jan; Javaux, Mathieu; Vetterlein, Doris; Vereecken, Harry

2014-05-01

A faba bean was grown in a column filled with a sandy soil, which was initially close to saturation and then subjected to a single drying cycle of 30 days. The column was divided in four hydraulically separated compartments using horizontal paraffin layers. Paraffin is impermeable to water but penetrable by roots. Thus by growing deeper, the roots can reach compartments that still contain water. The root architecture was measured every second day by X-ray CT. Transpiration rate, soil matric potential in four different depths, and leaf area were measured continously during the experiment. To investigate the influence of the partitioning of available soil water in the soil column on water uptake, we used R-SWMS, a fully coupled root and soil water model [1]. We compared a scenario with and without the split layers and investigated the influence on root xylem pressure. The detailed three-dimensional root architecture was obtained by reconstructing binarized root images manually with a virtual reality system, located at the Juelich Supercomputing Centre [2]. To verify the properties of the root system, we compared total root lengths, root length density distributions and root surface with estimations derived from Minkowski functionals [3]. In a next step, knowing the change of root architecture in time, we could allocate an age to each root segment and use this information to define age dependent root hydraulic properties that are required to simulate water uptake for the growing root system. The scenario with the split layers showed locally much lower pressures than the scenario without splits. Redistribution of water within the unrestricted soil column led to a more uniform distribution of water uptake and lowers the water stress in the plant. However, comparison of simulated and measured pressure heads with tensiometers suggested that the paraffin layers were not perfectly hydraulically isolating the different soil layers. We could show compensation efficiency of

Diversity of nitrite reductase genes (nirS) in the denitrifying water column of the coastal Arabian Sea

Digital Repository Service at National Institute of Oceanography (India)

Jayakumar, D.A.; Francis, C.A.; Naqvi, S.W.A.; Ward, B.B.

Denitrification often occurs in the water column, underlying zones of intense productivity and decomposition in upwelling regions. In the denitrifying zone off the southwest coast of India, high concentrations of nitrite (greater than 15 mu M...

Analysis of s-triazine herbicides in model systems and samples of groundwater by gas and liquid chromatography

Directory of Open Access Journals (Sweden)

Kostadinović Ljiljana

2010-01-01

Full Text Available In this paper, residues of s-triazine herbicides (Simazine, Atrazine, Amethrine, Promethrine and Azyprothrine have been determined in samples of model systems and real groundwater samples by gas-chromatography and high performance liquid chromatography. S-triazine herbicides were isolated from water samples by chloroform-methanol mixture (1:1, followed by purification of extract on the Al2O3 column. Gas-chromatographic determination the residues of s-triazines is performed on parallel capilar columns ULTRA I and ULTRA II, using specific NP detector. Liquid-chromatographic determination the s-triazines was performed on the column TSK ODS-120 A 5 mm 'LKB', using the mobile phase methanol-water (60:40. Total concentration of s-triazines in samples of Danube water was 3.54 mg dm-3. .

The Inter Facility Testing of a Standard Oscillating Water Column (OWC) Type Wave Energy Converter (WEC)

DEFF Research Database (Denmark)

Andersen, Morten Thøtt; Thomsen, Jonas Bjerg

This report describes the behavior and preliminary performance of a simplified standard oscillating water column (OWC) wave energy converter (WEC). The same tests will be conducted at different scales at 6 different test facilities and the results obtained will be used for comparison. This project...

Determination of lead and nickel in environmental samples by flame atomic absorption spectrometry after column solid-phase extraction on Ambersorb-572 with EDTA

Energy Technology Data Exchange (ETDEWEB)

Baytak, Sitki [Department of Chemistry, Faculty of Science and Arts, Harran University, 63100 Sanliurfa (Turkey); Tuerker, A. Rehber [Department of Chemistry, Faculty of Science and Arts, Gazi University, 06500 Ankara (Turkey)]. E-mail: aturker@gazi.edu.tr

2006-02-28

Lead and nickel were preconcentrated as their ethylenediaminetetraacedic acid (EDTA) complexes from aqueous sample solutions using a column containing Ambersorb-572 and determined by flame atomic absorption spectrometry (FAAS). pH values, amount of solid phase, elution solution and flow rate of sample solution have been optimized in order to obtain quantitative recovery of the analytes. The effect of interfering ions on the recovery of the analytes has also been investigated. The recoveries of Pb and Ni under the optimum conditions were 99 {+-} 2 and 97 {+-} 3%, respectively, at 95% confidence level. Seventy-five-fold (using 750 mL of sample solution and 10 mL of eluent) and 50-fold (using 500 mL of sample solution and 10 mL of eluent) preconcentration was obtained for Pb and Ni, respectively. Time of analysis is about 4.5 h (for obtaining enrichment factor of 75). By applying these enrichment factors, the analytical detection limits of Pb and Ni were found as 3.65 and 1.42 ng mL{sup -1}, respectively. The capacity of the sorbent was found as 0.17 and 0.21 mmol g{sup -1} for Pb and Ni, respectively. The interferences of some cations, such as Mn{sup 2+}, Co{sup 2+}, Fe{sup 3+}, Al{sup 3+}, Zn{sup 2+}, Cd{sup 2+}, Ca{sup 2+}, Mg{sup 2+}, K{sup +} and Na{sup +} usually present in water samples were also studied. This procedure was applied to the determination of lead and nickel in parsley, green onion, sea water and waste water samples. The accuracy of the procedure was checked by determining Pb and Ni in standard reference tea leaves sample (GBW-07605). The results demonstrated good agreement with the certified values.

Observation of Mountain Lee Waves with MODIS NIR Column Water Vapor

Science.gov (United States)

Lyapustin, A.; Alexander, M. J.; Ott, L.; Molod, A.; Holben, B.; Susskind, J.; Wang, Y.

2014-01-01

Mountain lee waves have been previously observed in data from the Moderate Resolution Imaging Spectroradiometer (MODIS) "water vapor" 6.7 micrometers channel which has a typical peak sensitivity at 550 hPa in the free troposphere. This paper reports the first observation of mountain waves generated by the Appalachian Mountains in the MODIS total column water vapor (CWV) product derived from near-infrared (NIR) (0.94 micrometers) measurements, which indicate perturbations very close to the surface. The CWV waves are usually observed during spring and late fall or some summer days with low to moderate CWV (below is approx. 2 cm). The observed lee waves display wavelengths from3-4 to 15kmwith an amplitude of variation often comparable to is approx. 50-70% of the total CWV. Since the bulk of atmospheric water vapor is confined to the boundary layer, this indicates that the impact of thesewaves extends deep into the boundary layer, and these may be the lowest level signatures of mountain lee waves presently detected by remote sensing over the land.

An inexpensive and stable LED Sun photometer for measuring the water vapor column over South Texas from 1990 to 2001

Science.gov (United States)

Mims, Forrest M.

2002-07-01

A Sun photometer that uses near-infrared light-emitting diodes (LEDs) as spectrally-selective photodetectors has measured total column water vapor in South Texas since February 1990. The 12 years of solar noon observations to date are correlated with upper air soundings at Del Rio, Texas (r2 = 0.75), and highly correlated with measurements by a Microtops II filter Sun photometer (r2 = 0.94). LEDs are inexpensive and have far better long term stability than the interference filters in conventional Sun photometers. The LED Sun photometer therefore provides an inexpensive, stable and portable means for measuring column water vapor.

Chromatographic properties PLOT multicapillary columns.

Science.gov (United States)

Nikolaeva, O A; Patrushev, Y V; Sidelnikov, V N

2017-03-10

Multicapillary columns (MCCs) for gas chromatography make it possible to perform high-speed analysis of the mixtures of gaseous and volatile substances at a relatively large amount of the loaded sample. The study was performed using PLOT MCCs for gas-solid chromatography (GSC) with different stationary phases (SP) based on alumina, silica and poly-(1-trimethylsilyl-1-propyne) (PTMSP) polymer as well as porous polymers divinylbenzene-styrene (DVB-St), divinylbenzene-vinylimidazole (DVB-VIm) and divinylbenzene-ethylene glycol dimethacrylate (DVB-EGD). These MCCs have the efficiency of 4000-10000 theoretical plates per meter (TP/m) and at a column length of 25-30cm can separate within 10-20s multicomponent mixtures of substances belonging to different classes of chemical compounds. The sample amount not overloading the column is 0.03-1μg and depends on the features of a porous layer. Examples of separations on some of the studied columns are considered. Copyright © 2017 Elsevier B.V. All rights reserved.

Comparison of various liquid chromatographic methods involving UV and atmospheric pressure chemical ionization mass spectrometric detection for the efficient trace analysis of phenylurea herbicides in various types of water samples.

Science.gov (United States)

van der Heeft, E; Dijkman, E; Baumann, R A; Hogendoorn, E A

2000-05-19

The performance of mass spectrometric (MS) detection and UV detection in combination with reversed-phase liquid chromatography without and with the use of coupled column RPLC (LC-LC) has been compared for the trace analysis of phenylurea herbicides in environmental waters. The selected samples of this comparative study originated from an inter-laboratory study. For both detection modes, a 50 mm x 4.6 mm I.D. column and a 100 mm x 4.6 mm I.D. column packed with 3 microm C18 were used as the first (C-1) and second (C-2) column, respectively. Atmospheric pressure chemical ionization mass spectrometry was performed on a magnetic sector instrument. The LC-LC-MS analysis was carried out on-line by means of direct large volume (11.7 ml) injection (LVI). The performance of both on-line (LVI, 4 ml of sample) and off-line LC-LC-UV (244 nm) analysis was investigated. The latter procedure consisted of a solid-phase extraction (SPE) of 250 ml of water sample on a 500 mg C18 cartridge. The comparative study showed that LC-LC-MS is more selective then LC-LC-UV and, in most cases, more sensitive. The LVI-LC-LC-MS approach combines direct quantification and confirmation of most of the analytes down to a level of 0.01 microg/l in water samples in less then 30 min. As regards LC-LC-UV, the off-line method appeared to be a more viable approach in comparison with the on-line procedure. This method allows the screening of phenylurea's in various types of water samples down to a level of at least 0.05 microg/l. On-line analysis with LVI provided marginal sensitivity (limits of detection of about 0.1 microg/l) and selectivity was sometimes less in case of surface water samples. Both the on-line LVI-LC-LC-MS method and the LC-LC-UV method using off-line SPE were validated by analysing a series of real-life reference samples. These samples were part of an inter-laboratory test and contained residues of herbicides ranging from 0.02 to 0.8 microg/l. Beside good correlation between the methods

A novel fiber-packed column for on-line preconcentration and speciation analysis of chromium in drinking water with flame atomic absorption spectrometry.

Science.gov (United States)

Monasterio, Romina P; Altamirano, Jorgelina C; Martínez, Luis D; Wuilloud, Rodolfo G

2009-02-15

A novel on-line preconcentration and determination system based on a fiber-packed column was developed for speciation analysis of Cr in drinking water samples prior to its determination by flame atomic absorption spectrometry (FAAS). All variables involved in the development of the preconcentration method including, pH, eluent type, sample and eluent flow rates, interfering effects, etc., were studied in order to achieve the best analytical performance. A preconcentration factor of 32 was obtained for Cr(VI) and Cr(III). The levels of Cr(III) species were calculated by difference of total Cr and Cr(VI) levels. Total Cr was determined after oxidation of Cr(III) to Cr(VI) with hydrogen peroxide. The calibration graph was linear with a correlation coefficient of 0.999 at levels near the detection limit and up to at least 50 microg L(-1). The relative standard deviation (R.S.D.) was 4.3% (C=5 microg L(-1) Cr(VI), n=10, sample volume=25 mL). The limit of detection (LOD) for both Cr(III) and Cr(VI) species was 0.3 microg L(-1). Verification of the accuracy was carried out by the analysis of a standard reference material (NIST SRM 1643e "Trace elements in natural water"). The method was successfully applied to the determination of Cr(III) and Cr(VI) species in drinking water samples.

Beryllium-10 concentrations in water samples of high northern latitudes

Energy Technology Data Exchange (ETDEWEB)

Strobl, C.; Eisenhauer, A.; Schulz, V.; Baumann, S.; Mangini, A. [Heidelberger Akademie der Wissenschaften, Heildelberg (Germany); Kubik, P.W. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1997-09-01

{sup 10}Be concentrations in the water column of high northern latitudes were not available so far. We present different {sup 10}Be profiles from the Norwegian-Greenland Sea, the Arctic Ocean, and the Laptev Sea. (author) 3 fig., 3 refs.

Strengthening and Stabilization of the Weak Water Saturated Soils Using Stone Columns

Directory of Open Access Journals (Sweden)

Sinyakov Leonid

2016-01-01

Full Text Available The article considers innovative modern materials and structures for strengthening of weak soils. In this paper describes a method of strengthening of weak saturated soils using stone columns. The method of calculating the physical-mechanical characteristics of reinforced soil mass is presented. Two approaches to determining the stress-strain state and timeframe of consolidation of strengthened soil foundation using the finite element technique in two-dimensional formulation are proposed. The first one approach it is a modeling of reinforced soil mass, where each pile is represented as a separate 2D stripe. The second approach is to the simulation of the strengthened mass the equivalent composite block with improved physical-mechanical characteristics. The use of the equivalent composite block can significantly reduce the time spent on the preparation of a design scheme. The results of calculations were compared. They show the allowable divergence of results of calculation by two methods were presented, and the efficiency of the strengthening of weak water saturated soils by stone column is proved.

Simultaneous multi-mycotoxin determination in nutmeg by ultrasound-assisted solid-liquid extraction and immunoaffinity column clean-up coupled with liquid chromatography and on-line post-column photochemical derivatization-fluorescence detection.

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Kong, Wei-Jun; Liu, Shu-Yu; Qiu, Feng; Xiao, Xiao-He; Yang, Mei-Hua

2013-05-07

A simple and sensitive analytical method based on ultrasound-assisted solid-liquid extraction and immunoaffinity column clean-up coupled with high performance liquid chromatography and on-line post-column photochemical derivatization-fluorescence detection (USLE-IAC-HPLC-PCD-FLD) has been developed for simultaneous multi-mycotoxin determination of aflatoxins B1, B2, G1, G2 (AFB1, AFB2, AFG1, AFG2) and ochratoxin A (OTA) in 13 edible and medicinal nutmeg samples marketed in China. AFs and OTA were extracted from nutmeg samples by ultrasonication using a methanol : water (80 : 20, v/v) solution, followed by an IAC clean-up step. Different USL extraction conditions, pre-processing ways for nutmeg sample and clean-up columns for mycotoxins, as well as HPLC-PCD-FLD parameters (mobile phase, column temperature, elution procedure, excitation and emission wavelengths) were optimized. This method, which was appraised for analyzing nutmeg samples, showed satisfactory results with reference to limits of detection (LODs) (from 0.02 to 0.25 μg kg(-1)), limits of quantification (LOQs) (from 0.06 to 0.8 μg kg(-1)), linear ranges (up to 30 ng mL(-1) for AFB1, AFG1 and OTA and 9 ng mL(-1) for AFB2 and AFG2), intra- and inter-day variability (all application of developed method in nutmeg samples have elucidated that four samples were detected with contamination of AFs and one with OTA. AFB1 was the most frequently found mycotoxin in 30.8% of nutmeg samples at contamination levels of 0.73-16.31 μg kg(-1). At least two different mycotoxins were co-occurred in three samples, and three AFs were simultaneously detected in one sample.

Zoolankton distribution in neuston and water column along west coast of India from Goa to Gujarat

Digital Repository Service at National Institute of Oceanography (India)

Padmavati, G.; Goswami, S.C.

) . Zooplankton biomass (ml.m sup(-3)) and population density (no.m sup(-3)) were higher in the water column (av = 0.5,592) than in the upper neustonic layer (av = 0.3,245). Copepods were dominant (51.8 to 71.6%). The other important groups were ostracods...

Development and optimization of the determination of pharmaceuticals in water samples by SPE and HPLC with diode-array detection.

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Pavlović, Dragana Mutavdžić; Ašperger, Danijela; Tolić, Dijana; Babić, Sandra

2013-09-01

This paper describes the development, optimization, and validation of a method for the determination of five pharmaceuticals from different therapeutic classes (antibiotics, anthelmintics, glucocorticoides) in water samples. Water samples were prepared using SPE and extracts were analyzed by HPLC with diode-array detection. The efficiency of 11 different SPE cartridges to extract the investigated compounds from water was tested in preliminary experiments. Then, the pH of the water sample, elution solvent, and sorbent mass were optimized. Except for optimization of the SPE procedure, selection of the optimal HPLC column with different stationary phases from different manufacturers has been performed. The developed method was validated using spring water samples spiked with appropriate concentrations of pharmaceuticals. Good linearity was obtained in the range of 2.4-200 μg/L, depending on the pharmaceutical with the correlation coefficients >0.9930 in all cases, except for ciprofloxacin (0.9866). Also, the method has revealed that low LODs (0.7-3.9 μg/L), good precision (intra- and interday) with RSD below 17% and recoveries above 98% for all pharmaceuticals. The method has been successfully applied to the analysis of production wastewater samples from the pharmaceutical industry. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Occurence of antibiotic compounds found in the water column and bottom sediments from a stream receiving two waste water treatment plant effluents in northern New Jersey, 2008

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Gibs, Jacob; Heckathorn, Heather A.; Meyer, Michael T.; Klapinski, Frank R.; Alebus, Marzooq; Lippincott, Robert

2013-01-01

An urban watershed in northern New Jersey was studied to determine the presence of four classes of antibiotic compounds (macrolides, fluoroquinolones, sulfonamides, and tetracyclines) and six degradates in the water column and bottom sediments upstream and downstream from the discharges of two wastewater treatment plants (WWTPs) and a drinking-water intake (DWI). Many antibiotic compounds in the four classes not removed by conventional WWTPs enter receiving waters and partition to stream sediments. Samples were collected at nine sampling locations on 2 days in September 2008. Two of the nine sampling locations were background sites upstream from two WWTP discharges on Hohokus Brook. Another background site was located upstream from a DWI on the Saddle River above the confluence with Hohokus Brook. Because there is a weir downstream of the confluence of Hohokus Brook and Saddle River, the DWI receives water from Hohokus Brook at low stream flows. Eight antibiotic compounds (azithromycin (maximum concentration 0.24 μg/L), ciprofloxacin (0.08 μg/L), enrofloxacin (0.015 μg/L), erythromycin (0.024 μg/L), ofloxacin (0.92 μg/L), sulfamethazine (0.018 μg/L), sulfamethoxazole (0.25 μg/L), and trimethoprim (0.14 μg/L)) and a degradate (erythromycin-H2O (0.84 μg/L)) were detected in the water samples from the sites downstream from the WWTP discharges. The concentrations of six of the eight detected compounds and the detected degradate compound decreased with increasing distance downstream from the WWTP discharges. Azithromycin, ciprofloxacin, ofloxacin, and trimethoprim were detected in stream-bottom sediments. The concentrations of three of the four compounds detected in sediments were highest at a sampling site located downstream from the WWTP discharges. Trimethoprim was detected in the sediments from a background site. Pseudo-partition coefficients normalized for streambed sediment organic carbon concentration were calculated for azithromycin, ciprofloxacin, and

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

Application of column tests and electrical resistivity methods for leachate transport monitoring

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Wychowaniak Dorota

2015-09-01

Full Text Available Development of the human civilization leads to the pollution of environment. One of the contamination which are a real threat to soil and groundwater are leachates from landfills. In this paper the solute transport through soil was considered. For this purpose, the laboratory column tests of chlorides tracer and leachates transport on two soil samples have been carried out. Furthermore, the electrical resistivity method was applied as auxiliary tool to follow the movements of solute through the soil column what allowed to compare between the results obtained with column test method and electrical resistivity measurements. Breakthrough curves obtained by conductivity and resistivity methods represents similar trends which leads to the conclusion about the suitability of electrical resistivity methods for contamination transport monitoring in soil-water systems.

Temperature-assisted On-column Solute Focusing: A General Method to Reduce Pre-column Dispersion in Capillary High Performance Liquid Chromatography

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Groskreutz, Stephen R.; Weber, Stephen G.

2014-01-01

Solvent-based on-column focusing is a powerful and well known approach for reducingthe impact of pre-column dispersion in liquid chromatography. Here we describe an orthogonal temperature-based approach to focusing called temperature-assisted on-column solute focusing (TASF). TASF is founded on the same principles as the more commonly used solvent-based method wherein transient conditions are created thatlead to high solute retention at the column inlet. Combining the low thermal mass of capillary columns and the temperature dependence of solute retentionTASF is used effectivelyto compress injection bands at the head of the column through the transient reduction in column temperature to 5 °C for a defined 7 mm segment of a 6 cm long 150 μm I.D. column. Following the 30 second focusing time, the column temperature is increased rapidly to the separation temperature of 60 °C releasing the focused band of analytes. We developed a model tosimulate TASF separations based on solute retention enthalpies, focusing temperature, focusing time, and column parameters. This model guides the systematic study of the influence of sample injection volume on column performance.All samples have solvent compositions matching the mobile phase. Over the 45 to 1050 nL injection volume range evaluated, TASF reducesthe peak width for all soluteswith k’ greater than or equal to 2.5, relative to controls. Peak widths resulting from injection volumes up to 1.3 times the column fluid volume with TASF are less than 5% larger than peak widths from a 45 nL injection without TASF (0.07 times the column liquid volume). The TASF approach reduced concentration detection limits by a factor of 12.5 relative to a small volume injection for low concentration samples. TASF is orthogonal to the solvent focusing method. Thus, it canbe used where on-column focusing is required, but where implementation of solvent-based focusing is difficult. PMID:24973805

Selective solid-phase extraction of Ni(II) by an ion-imprinted polymer from water samples

International Nuclear Information System (INIS)

Saraji, Mohammad; Yousefi, Hamideh

2009-01-01

A new ion-imprinted polymer (IIP) material was synthesized by copolymerization of 4-vinylpyridine as monomer, ethyleneglycoldimethacrylate as crosslinking agent and 2,2'-azobis-sobutyronitrile as initiator in the presence of Ni-dithizone complex. The IIP was used as sorbent in a solid-phase extraction column. The effects of sampling volume, elution conditions, sample pH and sample flow rate on the extraction of Ni ions form water samples were studied. The maximum adsorption capacity and the relative selectivity coefficients of imprinted polymer for Ni(II)/Co(II), Ni(II)/Cu(II) and Ni(II)/Cd(II) were calculated. Compared with non-imprinted polymer particles, the IIP had higher selectivity for Ni(II). The relative selectivity factor (α r ) values of Ni(II)/Co(II), Ni(II)/Cu(II) and Ni(II)/Cd(II) were 21.6, 54.3, and 22.7, respectively, which are greater than 1. The relative standard deviation of the five replicate determinations of Ni(II) was 3.4%. The detection limit for 150 mL of sample was 1.6 μg L -1 using flame atomic absorption spectrometry. The developed method was successfully applied to the determination of trace nickel in water samples with satisfactory results.

Controlling factors of harmful microalgae distribution in water column, biofilm and sediment in shellfish production area (South of Sfax, Gulf of Gabes) from southern Tunisia

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Loukil-Baklouti, Amira; Feki-Sahnoun, Wafa; Hamza, Asma; Abdennadher, Moufida; Mahfoudhi, Mabrouka; Bouain, Abderrahmen; Jarboui, Othman

2018-01-01

The aim of this study was to investigate the spatio-temporal distribution of harmful microalgae coupled with environmental factors in the most important area for natural stocks of the grooved carpet shell Ruditapes decussatus in southern Tunisia. Sampling was performed monthly from May 2010 to April 2011 in five stations through the Tunisian National Monitoring Stations Network of Phytoplankton and Phycotoxins along the southern coasts of Sfax (Gulf of Gabes). The presence of harmful microalgae species was explored in three compartments: water column, biofilm and sediment. Our results revealed fourteen species were identified belonging to dinoflagellates and diatoms with higher densities during the summer period. The co-inertia plot analysis exhibited that the seasonal fluctuations of these species were controlled by the temperature as well as the nutrients (particularly nitrogenous). Ternary diagrams showed that biofilm was the most colonized compartment by toxic benthic dinoflagellates species, namely Amphidinium carterae, Prorocentrum rathymum, Prorocentrum concavum, Prorocentrum lima, Ostreopsis cf. ovata and Coolia monotis. In addition, these species were recorded simultaneously in the water column and the sediment, a fact that could be explained by the resuspension of these benthic dinoflagellates from the biofilm by hydrodynamics. The data suggest that harmful microalgae could be the source of toxins in the studied stations, which provide support to the implication of these results on the future sampling strategy of harmful microalgae in shellfish collecting areas in Tunisia.

Water born pollutants sampling using porous suction samples

International Nuclear Information System (INIS)

Baig, M.A.

1997-01-01

The common standard method of sampling water born pollutants in the vadoze zone is core sampling and it is followed by extraction of pore fluid. This method does not allow sampling at the same location next time and again later on. There is an alternative approach for sampling fluids (water born pollutants) from both saturated and unsaturated regions of vadose zone using porous suction samplers. There are three types of porous suction samplers, vacuum-operated, pressure-vacuum lysimeters, high pressure vacuum samples. The suction samples are operated in the range of 0-70 centi bars and usually consist of ceramic and polytetrafluorethylene (PTFE). The operation range of PTFE is higher than ceramic cups. These samplers are well suited for in situ and repeated sampling form the same location. This paper discusses the physical properties and operating condition of such samplers to the utilized under our environmental sampling. (author)

The design of a new concept chromatography column.

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Camenzuli, Michelle; Ritchie, Harald J; Ladine, James R; Shalliker, R Andrew

2011-12-21

Active Flow Management is a new separation technique whereby the flow of mobile phase and the injection of sample are introduced to the column in a manner that allows migration according to the principles of the infinite diameter column. A segmented flow outlet fitting allows for the separation of solvent or solute that elutes along the central radial section of the column from that of the sample or solvent that elutes along the wall region of the column. Separation efficiency on the analytical scale is increased by 25% with an increase in sensitivity by as much as 52% compared to conventional separations.

Vertical transport of particulate-associated plutonium and americium in the upper water column of the Northeast Pacific

International Nuclear Information System (INIS)

Fowler, S.W.; Ballestra, S.; La Rosa, J.; Fukai, R.

1983-01-01

Concentrations of plutonium (Pu) and americium (Am) were determined in seawater, suspended particulate matter, sediment trap samples, and biogenic material collected at the VERTEX I site in the North Pacific off central California. From a vertical profile taken over the upper 1500 m, the presence of sub-surface maxima of sup(239+240)Pu and 241 Am were identified between 100 to 750 m and 250 to 750 m, respectively. A large fraction (32%) of the filterable sup(239+240)Pu in surface waters was associated with cells during a phytoplankton bloom; Pu:Am activity ratios in surface water and the suspended particles indicated that Pu was concentrated by the cells to a greater degree than Am. However, similar measurements beneath the surface layer showed an overall enrichment of Am over Pu on fine suspended particles with depth. Freshly produced zooplankton fecal pellets and large, fast sinking particles collected in PITS contained relatively high concentrations of Pu and Am. Both transuranic concentrations in trapped particles and transuranic flux tended to increase with depth down to 750 m, suggesting that their scavenging is in the upper water column. Am appeared to be scavenged by sinking biogenic particles to a greater extent than Pu. The results are discussed. (author)

Application of a simple column-switching ion chromatography technique for removal of matrix interferences and sensitive fluorescence determination of acidic compounds (pharmaceutical drugs) in complex samples.

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Muhammad, Nadeem; Subhani, Qamar; Wang, Fenglian; Guo, Dandan; Zhao, Qiming; Wu, Shuchao; Zhu, Yan

2017-09-15

This work illustrates the introduction of a simple, rugged and flexible column-switching ion chromatography (IC) technique for an automated on-line QuEChERS extracted samples extracts washing followed by sensitive fluorescence (FLD) determination of five acidic pharmaceutical drugs namely; clofibric acid (CLO), ibuprofen (IBU), aspirin (ASP), naproxen (NAP) and flurobrofen (FLU) in three complex samples (spinach, apple and hospital sewage sludge). An old anion exchange column IonPac ® AS11-HC was utilized as a pre-treatment column for on-line washing of inorganic and organic interferences followed by isocratic separation of five acidic drugs with another anion exchange IonPac ® AS12A analytical column by exploiting the column-switching technique. This novel method exhibited good linearity with correlation coefficients (r 2 ) for all drugs were in the range 0.976-0.996. The limit of detection and quantification of all five acidic drugs were in the range 0.024μg/kg to 8.70μg/kg and 0.082μg/kg to 0.029mg/kg, respectively, and better recoveries in the range 81.17-112.5% with percentage relative standard deviations (RSDs) less than 17.8% were obtained. This on-line sample pre-treatment method showed minimum matrix effect in the range of 0.87-1.25 except for aspirin. This simple rugged and flexible column-switching system required only 28min for maximum elimination of matrices and interferences in three complex samples extracts, isocratic separation of five acidic drugs and for the continuous regeneration of pre-treatment column prior to every subsequent analysis. Finally, this simple automated IC system was appeared so rugged and flexible, which can eliminate and wash out most of interference, impurities and matrices in complex samples, simply by adjusting the NaOH and acetonitrile concentration in washing mobile phase with maximum recoveries of acidic analytes of interest. Copyright © 2017. Published by Elsevier B.V.

Managed aquifer recharge: the fate of pharmaceuticals from infiltrated treated wastewater investigated through soil column experiments

Science.gov (United States)

Silver, Matthew; Selke, Stephanie; Balsaa, Peter; Wefer-Roehl, Annette; Kübeck, Christine; Schüth, Christoph

2017-04-01

The EU FP7 project MARSOL addresses water scarcity challenges in arid regions, where managed aquifer recharge (MAR) is an upcoming technology to recharge depleted aquifers using alternative water sources. Within this framework, column experiments were conducted to investigate the fate of pharmaceuticals when secondary treated wastewater (TWW) is infiltrated through a natural soil (organic matter content 6.8%) being considered for MAR. Three parallel experiments were run under conditions of continuous infiltration (one column) and wetting-drying cycles (two columns, with different analytes) over a 16 month time period. The pharmaceuticals diclofenac, ibuprofen, carbamazepine, naproxen, gemfibrozil, and fenoprofen, as well as the antibiotics doxycycline, sulfadimidine, and sulfamethoxazole, are commonly present in treated wastewater in varying concentrations. For the experiments, concentration variability was reduced by spiking the column inflow water with these compounds. Concentrations were periodically analyzed at different depths in each column and the mass passing each depth over the duration of the experiment was calculated. At the end of the experiments, sorbed pharmaceuticals were extracted from soil samples collected from different depths. A pressurized liquid extraction method was developed and resulted in recoveries from spiked post-experiment soil samples ranging from 64% (gemfibrozil) to 82% (carbamazepine) for the six non-antibiotic compounds. Scaling results by these recovery rates, the total mass of pharmaceuticals sorbed to the soil in the columns was calculated and compared to the calculated attenuated mass (i.e. mass that left the water phase). The difference between the attenuated mass and the sorbed mass is considered to be mass that degraded. Results for continuous infiltration conditions indicate that for carbamazepine and diclofenac, sorption is the primary attenuation mechanism, with missing (i.e. degraded) mass lying within the propagated

A Comparison of Soil-Water Sampling Techniques

Science.gov (United States)

Tindall, J. A.; Figueroa-Johnson, M.; Friedel, M. J.

2007-12-01

The representativeness of soil pore water extracted by suction lysimeters in ground-water monitoring studies is a problem that often confounds interpretation of measured data. Current soil water sampling techniques cannot identify the soil volume from which a pore water sample is extracted, neither macroscopic, microscopic, or preferential flowpath. This research was undertaken to compare values of extracted suction lysimeters samples from intact soil cores with samples obtained by the direct extraction methods to determine what portion of soil pore water is sampled by each method. Intact soil cores (30 centimeter (cm) diameter by 40 cm height) were extracted from two different sites - a sandy soil near Altamonte Springs, Florida and a clayey soil near Centralia in Boone County, Missouri. Isotopically labeled water (O18? - analyzed by mass spectrometry) and bromide concentrations (KBr- - measured using ion chromatography) from water samples taken by suction lysimeters was compared with samples obtained by direct extraction methods of centrifugation and azeotropic distillation. Water samples collected by direct extraction were about 0.25 ? more negative (depleted) than that collected by suction lysimeter values from a sandy soil and about 2-7 ? more negative from a well structured clayey soil. Results indicate that the majority of soil water in well-structured soil is strongly bound to soil grain surfaces and is not easily sampled by suction lysimeters. In cases where a sufficient volume of water has passed through the soil profile and displaced previous pore water, suction lysimeters will collect a representative sample of soil pore water from the sampled depth interval. It is suggested that for stable isotope studies monitoring precipitation and soil water, suction lysimeter should be installed at shallow depths (10 cm). Samples should also be coordinated with precipitation events. The data also indicate that each extraction method be use to sample a different

Rapid determination of amino acids in biological samples using a monolithic silica column.

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Song, Yanting; Funatsu, Takashi; Tsunoda, Makoto

2012-05-01

A high-performance liquid chromatography method in which fluorescence detection is used for the simultaneous determination of 21 amino acids is proposed. Amino acids were derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F) and then separated on a monolithic silica column (MonoClad C18-HS, 150 mm×3 mm i.d.). A mixture of 25 mM citrate buffer containing 25 mM sodium perchlorate (pH 5.5) and acetonitrile was used as the mobile phase. We found that the most significant factor in the separation was temperature, and a linear temperature gradient from 30 to 49°C was used to control the column temperature. The limits of detection and quantification for all amino acids ranged from 3.2 to 57.2 fmol and 10.8 to 191 fmol, respectively. The calibration curves for the NBD-amino acid had good linearity within the range of 40 fmol to 40 pmol when 6-aminocaproic acid was used as an internal standard. Using only conventional instruments, the 21 amino acids could be analyzed within 10 min. This method was found to be suitable for the quantification of the contents of amino acids in mouse plasma and adrenal gland samples.

Communities of nirS-type denitrifiers in the water column of the oxygen minimum zone in the eastern South Pacific.

Science.gov (United States)

Castro-González, Maribeb; Braker, Gesche; Farías, Laura; Ulloa, Osvaldo

2005-09-01

The major sites of water column denitrification in the ocean are oxygen minimum zones (OMZ), such as one in the eastern South Pacific (ESP). To understand the structure of denitrifying communities in the OMZ off Chile, denitrifier communities at two sites in the Chilean OMZ (Antofagasta and Iquique) and at different water depths were explored by terminal restriction fragment length polymorphism analysis and cloning of polymerase chain reaction (PCR)-amplified nirS genes. NirS is a functional marker gene for denitrification encoding cytochrome cd1-containing nitrite reductase, which catalyses the reduction of nitrite to nitric oxide, the key step in denitrification. Major differences were found between communities from the two geographic locations. Shifts in community structure occurred along a biogeochemical gradient at Antofagasta. Canonical correspondence analysis indicated that O2, NO3-, NO2- and depth were important environmental factors governing these communities along the biogeochemical gradient in the water column. Phylogenetic analysis grouped the majority of clones from the ESP in distinct clusters of genes from presumably novel and yet uncultivated denitrifers. These nirS clusters were distantly related to those found in the water column of the Arabian Sea but the phylogenetic distance was even higher compared with environmental sequences from marine sediments or any other habitat. This finding suggests similar environmental conditions trigger the development of denitrifiers with related nirS genotypes despite large geographic distances.

Investigative studies on water contamination in Bangladesh. Primary treatment of water samples at the sampling site

International Nuclear Information System (INIS)

Sera, K.; Islam, Md. Shafiqul; Takatsuji, T.; Nakamura, T.; Goto, S.; Takahashi, C.; Saitoh, Y.

2010-01-01

Arsenic concentration in 13 well waters, 9 pond waters, 10 agricultural waters and a coconut juice taken in Comilla district, Bangladesh, where the problem of arsenic pollution is the most severe, was investigated. High-level arsenic is detected even in the well water which has been kept drinking by the people. Relatively high arsenic concentration was detected for some pond and farm waters even though the sampling was performed just after the rainy season and the waters were expected to be highly diluted. Clear relationship was observed in elemental compositions between the pond water and the coconut juice collected at the edge of the water. These results are expected to become the basic information for evaluating the risk of individual food such as cultured fishes, shrimps and farm products, and for controlling total intakes of arsenic. In order to solve the problem of transportation of water samples internationally, a simple method of target preparation performed at the sampling site was established and its validity was confirmed. All targets were prepared at the sampling sites in this study on the basis of this method. (author)

Flooding characteristics of pulsed-sieve plate column. Contributed Paper ED-09

International Nuclear Information System (INIS)

Vishnu Anand, P.; Pandey, N.K.; Rajeev, R.; Joyakin, C.V.; Kamachi Mudali, U.; Natarajan, R.

2014-01-01

Successful design of a pulsed sieve plate extraction column relies on profound understanding of its hydrodynamic and mass transfer characteristics. Present work outlines a comprehensive study of flooding velocity, a hydrodynamic parameter, as a function of various operating conditions of the column. Experimental studies were carried out using water-normal paraffin hydrocarbon system, under no mass transfer condition, in a pilot plant pulsed sieve plate column equipped with standard plate cartridges. Flooding velocity is characterized here as a function of phase flow ratio and pulse velocity with the aid of characteristic velocity concept together with an exponential function. Flooding points were experimentally identified with satisfactory accuracy using a quantitative method and dispersed phase hold-up was measured by online sampling. To verify the extent of applicability of some of the reported generalized flooding correlations from a design perspective, an analysis was done using our precisely generated experimental flooding data. (author)

Coastal circulation and water column properties off Kalaupapa National Historical Park, Molokai, Hawaii, 2008-2010

Science.gov (United States)

Storlazzi, Curt D.; Presto, Katherine; Brown, Eric K.

2011-01-01

More than 2.2 million measurements of oceanographic forcing and the resulting water-column properties were made off U.S. National Park Service's Kalaupapa National Historical Park on the north shore of Molokai, Hawaii, between 2008 and 2010 to understand the role of oceanographic processes on the health and sustainability of the area's marine resources. The tides off the Kalaupapa Peninsula are mixed semidiurnal. The wave climate is dominated by two end-members: large northwest Pacific winter swell that directly impacts the study site, and smaller, shorter-period northeast trade-wind waves that have to refract around the peninsula, resulting in a more northerly direction before propagating over the study site. The currents primarily are alongshore and are faster at the surface than close to the seabed; large wave events, however, tend to drive flow in a more cross-shore orientation. The tidal currents flood to the north and ebb to the south. The waters off the peninsula appear to be a mix of cooler, more saline, deeper oceanic waters and shallow, warmer, lower-salinity nearshore waters, with intermittent injections of freshwater, generally during the winters. Overall, the turbidity levels were low, except during large wave events. The low overall turbidity levels and rapid return to pre-event background levels following the cessation of forcing suggest that there is little fine-grained material. Large wave events likely inhibit the settlement of fine-grained sediment at the site. A number of phenomena were observed that indicate the complexity of coastal circulation and water-column properties in the area and may help scientists and resource managers to better understand the implications of the processes on marine ecosystem health.

Intense molybdenum accumulation in sediments underneath a nitrogenous water column and implications for the reconstruction of paleo-redox conditions based on molybdenum isotopes

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Scholz, Florian; Siebert, Christopher; Dale, Andrew W.; Frank, Martin

2017-09-01

The concentration and isotope composition of molybdenum (Mo) in sediments and sedimentary rocks are widely used proxies for anoxic conditions in the water column of paleo-marine systems. While the mechanisms leading to Mo fixation in modern restricted basins with anoxic and sulfidic (euxinic) conditions are reasonably well constrained, few studies have focused on Mo cycling in the context of open-marine anoxia. Here we present Mo data for water column particulate matter, modern surface sediments and a paleo-record covering the last 140,000 years from the Peruvian continental margin. Mo concentrations in late Holocene and Eemian (penultimate interglacial) shelf sediments off Peru range from ∼70 to 100 μg g-1, an extent of Mo enrichment that is thought to be indicative of (and limited to) euxinic systems. To investigate if this putative anomaly could be related to the occasional occurrence of sulfidic conditions in the water column overlying the Peruvian shelf, we compared trace metal (Mo, vanadium, uranium) enrichments in particulate matter from oxic, nitrate-reducing (nitrogenous) and sulfidic water masses. Coincident enrichments of iron (Fe) (oxyhydr)oxides and Mo in the nitrogenous water column as well as co-variation of dissolved Fe and Mo in the sediment pore water suggest that Mo is delivered to the sediment surface by Fe (oxyhydr)oxides. Most of these precipitate in the anoxic-nitrogenous water column due to oxidation of sediment-derived dissolved Fe with nitrate as a terminal electron acceptor. Upon reductive dissolution in the surface sediment, a fraction of the Fe and Mo is re-precipitated through interaction with pore water sulfide. The Fe- and nitrate-dependent mechanism of Mo accumulation proposed here is supported by the sedimentary Mo isotope composition, which is consistent with Mo adsorption onto Fe (oxyhydr)oxides. Trace metal co-variation patterns as well as Mo and nitrogen isotope systematics suggest that the same mechanism of Mo delivery

Investigating geochemical aspects of managed aquifer recharge by column experiments with alternating desalinated water and groundwater.

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Ronen-Eliraz, Gefen; Russak, Amos; Nitzan, Ido; Guttman, Joseph; Kurtzman, Daniel

2017-01-01

Managed aquifer recharge (MAR) events are occasionally carried out with surplus desalinated seawater that has been post-treated with CaCO 3 in infiltration ponds overlying the northern part of the Israeli Coastal Aquifer. This water's chemical characteristics differ from those of any other water recharged to the aquifer and of the natural groundwater. As the MAR events are short (hours to weeks), the sediment under the infiltration ponds will intermittently host desalinated and natural groundwater. As part of comprehensive research on the influence of those events, column experiments were designed to simulate the alternation of the two water types: post-treated desalinated seawater (PTDES) and natural groundwater (GW). Each experiment included three stages: (i) saturation with GW; (ii) inflow of PTDES; (iii) inflow of GW. Three runs were conducted, each with different sediments extracted from the field and representing a different layer below the infiltration pond: (i) sand (<1% CaCO 3 ), (ii) sand containing 7% CaCO 3 , and (iii) crushed calcareous sandstone (35% CaCO 3 ). The results from all columns showed enrichment of K + and Mg 2+ (up to 0.4meq/L for 20 pore volumes) when PTDES replaced GW, whereas an opposite trend of Ca 2+ depletion (up to 0.5meq/L) was observed only in the columns that contained a high percentage of CaCO 3 . When GW replaced PTDES, depletion of Mg 2+ and K + was noted. The results indicated that adsorption/desorption of cations are the main processes causing the observed enrichment/depletion. It was concluded that the high concentration of Ca 2+ (relative to the total concentration of cations) and the low concentration of Mg 2+ in the PTDES relative to natural GW are the factors controlling the main sediment-water interaction. The enrichment of PTDES with Mg 2+ may be viewed as an additional post-treatment. Copyright © 2016 Elsevier B.V. All rights reserved.

Analytical procedures for determining Pb and Sr isotopic compositions in water samples by ID-TIMS

Directory of Open Access Journals (Sweden)

Veridiana Martins

2008-01-01

Full Text Available Few articles deal with lead and strontium isotopic analysis of water samples. The aim of this study was to define the chemical procedures for Pb and Sr isotopic analyses of groundwater samples from an urban sedimentary aquifer. Thirty lead and fourteen strontium isotopic analyses were performed to test different analytical procedures. Pb and Sr isotopic ratios as well as Sr concentration did not vary using different chemical procedures. However, the Pb concentrations were very dependent on the different procedures. Therefore, the choice of the best analytical procedure was based on the Pb results, which indicated a higher reproducibility from samples that had been filtered and acidified before the evaporation, had their residues totally dissolved, and were purified by ion chromatography using the Biorad® column. Our results showed no changes in Pb ratios with the storage time.

Characterization of Bubble Size Distributions within a Bubble Column

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Shahrouz Mohagheghian

2018-02-01

Full Text Available The current study experimentally examines bubble size distribution (BSD within a bubble column and the associated characteristic length scales. Air was injected into a column of water via a single injection tube. The column diameter (63–102 mm, injection tube diameter (0.8–1.6 mm and superficial gas velocity (1.4–55 mm/s were varied. Large samples (up to 54,000 bubbles of bubble sizes measured via 2D imaging were used to produce probability density functions (PDFs. The PDFs were used to identify an alternative length scale termed the most frequent bubble size (dmf and defined as the peak in the PDF. This length scale as well as the traditional Sauter mean diameter were used to assess the sensitivity of the BSD to gas injection rate, injector tube diameter, injection tube angle and column diameter. The dmf was relatively insensitive to most variation, which indicates these bubbles are produced by the turbulent wakes. In addition, the current work examines higher order statistics (standard deviation, skewness and kurtosis and notes that there is evidence in support of using these statistics to quantify the influence of specific parameters on the flow-field as well as a potential indicator of regime transitions.

Determination of 210Pb and 210Po in water samples

International Nuclear Information System (INIS)

Ayranov, M.; Tosheva, Z.; Kies, A.

2004-01-01

Lead-210 and Polonium-210 are naturally occurring members of the Uranium-238 decay series. They could be found in various environmental samples, such as groundwater, fish and shellfish, contributing an important component of the human natural radiation background. For this reason the development of a fast, reproducible and sensitive method for determination of 210 Pb and 210 Po is of a great concern. The aims of our study were to adopt procedures for radiochemical separation of these radionuclides and radioanalytical methods for their determination. The combination of electrochemical deposition, co-precipitation and extraction chromatography gives the opportunity for fast and effective radiochemical separation of the analytes. Polonium was spontaneously plated on copper disk from the stock solution. Lead was co-precipitated with Fe(OH) 3 and further purified by extraction chromatography on Sr Spec columns. Alpha spectra of polonium were collected on Canberra PIPS detectors with 900 mm 2 active surface. The activities of lead were determined by LSC (Gardian Wallac Oy). The minimum detectable activities for sample size 1000 mL and chemical yield of 88 % for the polonium and 85 % for the lead are presented. The proposed method proved to be fast, accurate and reproducible for routine determination of lead and polonium in environmental water samples. (authors)

Comparative proteomics and activity of a green sulfur bacterium across the water column of Lake Cadagno, Switzerland

DEFF Research Database (Denmark)

Habicht, Kirsten S.; Miller, Mette; Cox, Raymond P.

2011-01-01

.8-fold over the summer. Cells from four positions in the water column were used for comparative analysis of the Chl. clathratiforme proteome in order to investigate changes in protein composition in response to the chemical and physical gradient in their environment, with special focus on how...

Sulfur geochemistry of hydrothermal waters in Yellowstone National Park, Wyoming, USA. III. An anion-exchange resin technique for sampling and preservation of sulfoxyanions in natural waters

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Ball James W

2003-06-01

Full Text Available A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad™ AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site IC analysis (U.S. Geological Survey mobile lab and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan. Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad™ AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns.

Determination of rare earth elements in water ore and grass sample around monazite dressing plant by high performance liquid chromatography

International Nuclear Information System (INIS)

Laoharojanaphand, S.

1993-01-01

High performance liquid chromatography technique for the analysis of rare earth elements; yttrium, cerium and lanthanum, was developed. A comparison of two mobile phases between α-hydroxy isobutyric acid and mandelic acid was carried out using C 1 8 column for separation and the amount of the rare earth elements were detected by post column complex formation with Arsenazo III. It was found that α-hydroxy isobutyric acid had higher efficiency in separation of the rare earth elements than mandelic acid when 1-octanesulfonic acid was used as an organic modifier. The optimum conditions of the mobile phase were comprised of the p H of 3.65, a flow rate of 1 ml/min which resulted in the values of resolution to be 13.62 between yttrium and cerium and 3.49 between cerium and lanthanum. Standard curves of yttrium and lanthanum yielded linear range of 0.1-45 and 1-60 ppm whereas the cerium curve was in the range of 1-100 ppm. The analyses of water, ore and grass samples collected around the monazite dressing plants from Prachuap Khiri Khan and Phuket showed that none of the rare earth elements was detected in all samples from Prachuap Khiri Khan. But 0.5 ppm of yttrium and 1.5 ppm of lanthanum were found in the water samples from Phuket while in the grass samples contained yttrium and cerium in the amounts of 2 ppm and 14 ppm whereas none was detected in the ore samples by this technique under the previous conditions

Tritium Isotope Separation Using Adsorption-Distillation Column

International Nuclear Information System (INIS)

Fukada, Satoshi

2005-01-01

In order to miniaturize the height of a distillation tower for the detritiation of waste water from fusion reactors, two experiments were conducted: (1) liquid frontal chromatography of tritium water eluting through an adsorption column and (2) water distillation using a column packed with adsorbent particles. The height of the distillation tower depends on the height equivalent to a theoretical plate, HETP, and the equilibrium isotope separation factor, α H-T equi . The adsorption action improved not only HETP but also α H-T equi . Since the adsorption-distillation method proposed here can shorten the tower height with keeping advantages of the distillation, it may bring an excellent way for miniaturizing the distillation tower to detritiate a large amount of waste water from fusion reactors

Retrieval of water vapor column abundance and aerosol properties from ChemCam passive sky spectroscopy

Science.gov (United States)

McConnochie, Timothy H.; Smith, Michael D.; Wolff, Michael J.; Bender, Steve; Lemmon, Mark; Wiens, Roger C.; Maurice, Sylvestre; Gasnault, Olivier; Lasue, Jeremie; Meslin, Pierre-Yves; Harri, Ari-Matti; Genzer, Maria; Kemppinen, Osku; Martínez, Germán M.; DeFlores, Lauren; Blaney, Diana; Johnson, Jeffrey R.; Bell, James F.

2018-06-01

We derive water vapor column abundances and aerosol properties from Mars Science Laboratory (MSL) ChemCam passive mode observations of scattered sky light. This paper covers the methodology and initial results for water vapor and also provides preliminary results for aerosols. The data set presented here includes the results of 113 observations spanning from Mars Year 31 Ls = 291° (March 30, 2013) to Mars Year 33 Ls= 127° (March 24, 2016). Each ChemCam passive sky observation acquires spectra at two different elevation angles. We fit these spectra with a discrete-ordinates multiple scattering radiative transfer model, using the correlated-k approximation for gas absorption bands. The retrieval proceeds by first fitting the continuum of the ratio of the two elevation angles to solve for aerosol properties, and then fitting the continuum-removed ratio to solve for gas abundances. The final step of the retrieval makes use of the observed CO2 absorptions and the known CO2 abundance to correct the retrieved water vapor abundance for the effects of the vertical distribution of scattering aerosols and to derive an aerosol scale height parameter. Our water vapor results give water vapor column abundance with a precision of ±0.6 precipitable microns and systematic errors no larger than ±0.3 precipitable microns, assuming uniform vertical mixing. The ChemCam-retrieved water abundances show, with only a few exceptions, the same seasonal behavior and the same timing of seasonal minima and maxima as the TES, CRISM, and REMS-H data sets that we compare them to. However ChemCam-retrieved water abundances are generally lower than zonal and regional scale from-orbit water vapor data, while at the same time being significantly larger than pre-dawn REMS-H abundances. Pending further analysis of REMS-H volume mixing ratio uncertainties, the differences between ChemCam and REMS-H pre-dawn mixing ratios appear to be much too large to be explained by large scale circulations and thus

Column-to-column packing variation of disposable pre-packed columns for protein chromatography.

Science.gov (United States)

Schweiger, Susanne; Hinterberger, Stephan; Jungbauer, Alois

2017-12-08

In the biopharmaceutical industry, pre-packed columns are the standard for process development, but they must be qualified before use in experimental studies to confirm the required performance of the packed bed. Column qualification is commonly done by pulse response experiments and depends highly on the experimental testing conditions. Additionally, the peak analysis method, the variation in the 3D packing structure of the bed, and the measurement precision of the workstation influence the outcome of qualification runs. While a full body of literature on these factors is available for HPLC columns, no comparable studies exist for preparative columns for protein chromatography. We quantified the influence of these parameters for commercially available pre-packed and self-packed columns of disposable and non-disposable design. Pulse response experiments were performed on 105 preparative chromatography columns with volumes of 0.2-20ml. The analyte acetone was studied at six different superficial velocities (30, 60, 100, 150, 250 and 500cm/h). The column-to-column packing variation between disposable pre-packed columns of different diameter-length combinations varied by 10-15%, which was acceptable for the intended use. The column-to-column variation cannot be explained by the packing density, but is interpreted as a difference in particle arrangement in the column. Since it was possible to determine differences in the column-to-column performance, we concluded that the columns were well-packed. The measurement precision of the chromatography workstation was independent of the column volume and was in a range of±0.01ml for the first peak moment and±0.007 ml 2 for the second moment. The measurement precision must be considered for small columns in the range of 2ml or less. The efficiency of disposable pre-packed columns was equal or better than that of self-packed columns. Copyright © 2017 The Author(s). Published by Elsevier B.V. All rights reserved.

Radon measurement in Malaysia water samples

International Nuclear Information System (INIS)

Ibrahim, A.B.; Rosli Mahat; Yusof Md Amin

1995-01-01

This paper reported the results of the measurement of radon in local water. The water samples collected were rainwater, river water, seawater, well water or ground water at area of State of Selangor and Kuala Lumpur. The samples were collected in scintillation cell ZnS(Ag) through Radon Degassing Unit RDU 200. Alpha activity was counted with scintillation counters RD 200 at energy 5.5 MeV. (author)

HPLC determination of chlorine in air and water samples following precolumn derivatization to 4-bromoacetanilide

Energy Technology Data Exchange (ETDEWEB)

Jain, A. (Rani Durgavati Univ., Jabalpur (India). Dept. of Chemistry); Verma, K.K. (Rani Durgavati Univ., Jabalpur (India). Dept. of Chemistry)

1993-11-01

Chlorine has been determined in air and water samples by a rapid and sensitive method entailing precolumn derivatization to 4-bromoacetanilide. A mixed potassium bromide - acetanilide reagent was used as a trapping agent for chlorine in air, and for its derivatization. The 4-bromoacetanilide formed was determined by reversed-phase HPLC on an ODS column, using methanol-water, 65:35 (v/v) as mobile phase; detection was at 240 nm. A rectilinear calibration graph was obtained for the range 0.1-30 [mu]g mL[sup -1] chlorine; the limit of detection found to be 0.01 [mu]g mL[sup -1]. The precolumn derivative has been found to have a shelf-life of at least 21 days; this enables the use of the method for samples transported from the field to the analytical laboratory, or the testing of a variety of conditions for chlorine scrubbing studies without the need for immediate analysis of samples. Humic substances do not cause any interference with the proposed method and the presence of nitrite does not lead to artificially high results and consequent misleading conclusions of the presence of high levels of chlorine. (orig.)

HPLC determination of chlorine in air and water samples following precolumn derivatization to 4-bromoacetanilide

International Nuclear Information System (INIS)

Jain, A.; Verma, K.K.

1993-01-01

Chlorine has been determined in air and water samples by a rapid and sensitive method entailing precolumn derivatization to 4-bromoacetanilide. A mixed potassium bromide - acetanilide reagent was used as a trapping agent for chlorine in air, and for its derivatization. The 4-bromoacetanilide formed was determined by reversed-phase HPLC on an ODS column, using methanol-water, 65:35 (v/v) as mobile phase; detection was at 240 nm. A rectilinear calibration graph was obtained for the range 0.1-30 μg mL -1 chlorine; the limit of detection found to be 0.01 μg mL -1 . The precolumn derivative has been found to have a shelf-life of at least 21 days; this enables the use of the method for samples transported from the field to the analytical laboratory, or the testing of a variety of conditions for chlorine scrubbing studies without the need for immediate analysis of samples. Humic substances do not cause any interference with the proposed method and the presence of nitrite does not lead to artificially high results and consequent misleading conclusions of the presence of high levels of chlorine. (orig.)

Methane concentration in water column and in pore water of a coastal lagoon (Cabiúnas lagoon, Macaé, RJ, Brazil

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André Luiz dos Santos Fonseca

2004-06-01

Full Text Available The aim of this study was to evaluate methane concentration in water column and pore water at limnetic and littoral regions of a coastal lagoon. At the littoral region samples were taken from three monospecific macrophytes stands (Typha domingensis, Eleocharis interstincta and Potamogeton stenostachys. The methane concentration in the pore water at the littoral region was higher than the concentration found at the limnetic region in each fraction of the sediment. The higher methane concentration in the superficial fraction of the sediment (0-2 cm was shown at the P. stenostachys stand (3.7 mM. It was the only significantly different (p0.05. It could be concluded that there was a high influence of aquatic macrophytes on the pore water methane concentration.O objetivo dessa pesquisa foi determinar a concentração de metano na coluna d'água e na água intersticial do sedimento nas regiões limnética e litorânea de uma lagoa costeira (Lagoa Cabiúnas, Macaé, RJ. Na região litorânea as amostras foram coletadas em três estandes de macrófitas (Typha domingensis, Eleocharis interstincta e Potamogeton stenostachys. A concentração de metano na água intersticial na região litorânea foi maior do que aquela encontrada na região limnética em cada fração do sedimento. A maior concentração de metano na fração superficial do sedimento (0-2 cm foi observada no estande de P. stenostachys (3.7 mM. Este resultado foi o único significativamente diferente (p0.05. Os resultados sugerem que há uma considerável influência das macrófitas aquáticas estudadas na concentração de metano na água intersticial do sedimento.

Recovery of deuterium from H-D gas mixture by thermal diffusion in a multi-concentric-tube column device of fixed total sum of column heights with transverse sampling streams

International Nuclear Information System (INIS)

Yeh, H.-M.

2010-01-01

The effect of the increment in the number of concentric-tube thermal diffusion columns on the recovery of deuterium from H 2 -HD-D 2 system with fixed total sum of column heights, has been investigated. The equations for predicting the degrees of separation in single-column, double-column and triple-column devices have been derived. Considerable improvement in recovery can be achieved if a multi-column device with larger number of column is employed, instead of a single-column device with column height equal to the same total sum of column heights, especially for the case of higher flow-rate operation and larger total sum of column heights.

Analysis of an industrial process simulator column using third-generation computed tomography

International Nuclear Information System (INIS)

Kirita, Rodrigo; Carvalho, Diego Vergacas de Sousa; Mesquita, Carlos Henrique de; Vasquez, Pablo Antonio S.; Hamada, Margarida Mizue

2011-01-01

The CT methodology must be tested using a simulator column in the laboratory before applying it in the industrial plants. In this work, using the third-generation industrial computed tomography developed at the IPEN, a gas absorption column, used as a simulator column for industrial process was evaluated. It is a glass cylindrical tube of 90 mm diameter and 1400 mm height constituted the following parts: random packed column, liquid circuit (water), gas circuit and analysis was used as a simulator column. Gamma ray tomography experiments were carried out, using this simulator column empty and filled with water. In this work the scanner was setting for 90 views and 19 projections for each detector totalizing 11970 projections. The resulting images describe the presence of liquid or gas phases and are possible to evaluate the linear attenuation coefficients inside the column. In this case, linear attenuation coefficient for water was 0.0813 cm-1. It was established that the newly developed third-generation fan-beam arrangement gamma scanner unit has a good spatial resolution acceptable given the size of the column used in this study. (author)

Subnanogram proteomics: Impact of LC column selection, MS instrumentation and data analysis strategy on proteome coverage for trace samples

Energy Technology Data Exchange (ETDEWEB)

Zhu, Ying; Zhao, Rui; Piehowski, Paul D.; Moore, Ronald J.; Lim, Sujung; Orphan, Victoria J.; Paša-Tolić, Ljiljana; Qian, Wei-Jun; Smith, Richard D.; Kelly, Ryan T.

2018-04-01

One of the greatest challenges for mass spectrometry (MS)-based proteomics is the limited ability to analyze small samples. Here we investigate the relative contributions of liquid chromatography (LC), MS instrumentation and data analysis methods with the aim of improving proteome coverage for sample sizes ranging from 0.5 ng to 50 ng. We show that the LC separations utilizing 30-µm-i.d. columns increase signal intensity by >3-fold relative to those using 75-µm-i.d. columns, leading to 32% increase in peptide identifications. The Orbitrap Fusion Lumos mass spectrometer significantly boosted both sensitivity and sequencing speed relative to earlier generation Orbitraps (e.g., LTQ-Orbitrap), leading to a ~3× increase in peptide identifications and 1.7× increase in identified protein groups for 2 ng tryptic digests of bacterial lysate. The Match Between Runs algorithm of open-source MaxQuant software further increased proteome coverage by ~ 95% for 0.5 ng samples and by ~42% for 2 ng samples. The present platform is capable of identifying >3000 protein groups from tryptic digestion of cell lysates equivalent to 50 HeLa cells and 100 THP-1 cells (~10 ng total proteins), respectively, and >950 proteins from subnanogram bacterial and archaeal cell lysates. The present ultrasensitive LC-MS platform is expected to enable deep proteome coverage for subnanogram samples, including single mammalian cells.

Water sampling techniques for continuous monitoring of pesticides in water

Directory of Open Access Journals (Sweden)

Šunjka Dragana

2017-01-01

Full Text Available Good ecological and chemical status of water represents the most important aim of the Water Framework Directive 2000/60/EC, which implies respect of water quality standards at the level of entire river basin (2008/105/EC and 2013/39/EC. This especially refers to the control of pesticide residues in surface waters. In order to achieve the set goals, a continuous monitoring program that should provide a comprehensive and interrelated overview of water status should be implemented. However, it demands the use of appropriate analysis techniques. Until now, the procedure for sampling and quantification of residual pesticide quantities in aquatic environment was based on the use of traditional sampling techniques that imply periodical collecting of individual samples. However, this type of sampling provides only a snapshot of the situation in regard to the presence of pollutants in water. As an alternative, the technique of passive sampling of pollutants in water, including pesticides has been introduced. Different samplers are available for pesticide sampling in surface water, depending on compounds. The technique itself is based on keeping a device in water over a longer period of time which varies from several days to several weeks, depending on the kind of compound. In this manner, the average concentrations of pollutants dissolved in water during a time period (time-weighted average concentrations, TWA are obtained, which enables monitoring of trends in areal and seasonal variations. The use of these techniques also leads to an increase in sensitivity of analytical methods, considering that pre-concentration of analytes takes place within the sorption medium. However, the use of these techniques for determination of pesticide concentrations in real water environments requires calibration studies for the estimation of sampling rates (Rs. Rs is a volume of water per time, calculated as the product of overall mass transfer coefficient and area of

The effects of carbide column to swelling potential and Atterberg limit on expansive soil with column to soil drainage

Science.gov (United States)

Muamar Rifa'i, Alfian; Setiawan, Bambang; Djarwanti, Noegroho

2017-12-01

The expansive soil is soil that has a potential for swelling-shrinking due to changes in water content. Such behavior can exert enough force on building above to cause damage. The use of columns filled with additives such as Calcium Carbide is done to reduce the negative impact of expansive soil behavior. This study aims to determine the effect of carbide columns on expansive soil. Observations were made on swelling and spreading of carbides in the soil. 7 Carbide columns with 5 cm diameter and 20 cm height were installed into the soil with an inter-column spacing of 8.75 cm. Wetting is done through a pipe at the center of the carbide column for 20 days. Observations were conducted on expansive soil without carbide columns and expansive soil with carbide columns. The results showed that the addition of carbide column could reduce the percentage of swelling by 4.42%. Wetting through the center of the carbide column can help spread the carbide into the soil. The use of carbide columns can also decrease the rate of soil expansivity. After the addition of carbide column, the plasticity index value decreased from 71.76% to 4.3% and the shrinkage index decreased from 95.72% to 9.2%.

Alpha spetrometric determination of 226Ra in water samples by using ion exchanger MnO2-PAN

International Nuclear Information System (INIS)

Gardonova, V.; Dulanska, S.; Matel, L.; Bilohuscin, J.; Horvathova, B.; Sebesta, F.

2014-01-01

A method for 226 Ra preconcentration and separation from water samples using MnO 2 -PAN (polyacrylonitrile) ion absorber composite was proposed, optimized and verified. The optimization was focused on prevention of the destruction of MnO 2 -PAN composite absorber during radium elution from the column, testing of multiple use of the resin, influence of calcium concentration on radiochemical yields and application of the method for various types of water samples. Absorber was produced at Czech Technical University in Prague and now is also commercially available from Triskem International, France as MnO 2 -PAN Resin.This absorber with grain size (0.1-0.3) mm was used for 226 Ra preconcentration from various types of water samples at pH = (6.5-7.0). Radium was eluted from the ion exchanger MnO 2 -PAN with 20 mL of 6.5 mol/L HCl at flow rate of 1.5 mL/min. Samples were precipitated with Ba 2+ to form Ba(Ra)SO 4 microprecipitate for alpha spectrometry counting..The proposed method was applied to samples of natural mineral, mountain spring, drinking and natural healing waters from Slovakia, Slovenia and Czech Republic. Radium radiochemical recoveries were monitored by non-isotopic tracer 133 Ba and they were in the range of (92 - 100) %. The obtained 226 Ra activities in the analyzed samples were compared with the limit values set in Edict 528 of the Ministry of Health of the Slovak Republic in 2007 and no limit was exceeded. (authors)

Infiltration of water in disturbed soil columns as affected by clay dispersion and aggregate slaking

OpenAIRE

Amezketa, E.; Aragües, R.; Gazol, R.

2004-01-01

Soil crusting negatively affects the productivity and sustainability of irrigated agriculture, reducing water infiltration and plant emergence, and enhancing surface runoff and erosion. Clay dispersion and slaking of the aggregates at the soil surface are the main processes responsible for crusting. The infiltration rates (IR) of ten arid-zone soils in disturbed soil columns were measured and their relative susceptibilities to dispersion and slaking were determined. It was also examined wheth...

Influence of pressure on the properties of chromatographic columns. II. The column hold-up volume.

Science.gov (United States)

Gritti, Fabrice; Martin, Michel; Guiochon, Georges

2005-04-08

The effect of the local pressure and of the average column pressure on the hold-up column volume was investigated between 1 and 400 bar, from a theoretical and an experimental point of view. Calculations based upon the elasticity of the solids involved (column wall and packing material) and the compressibility of the liquid phase show that the increase of the column hold-up volume with increasing pressure that is observed is correlated with (in order of decreasing importance): (1) the compressibility of the mobile phase (+1 to 5%); (2) in RPLC, the compressibility of the C18-bonded layer on the surface of the silica (+0.5 to 1%); and (3) the expansion of the column tube (columns packed with the pure Resolve silica (0% carbon), the derivatized Resolve-C18 (10% carbon) and the Symmetry-C18 (20% carbon) adsorbents, using water, methanol, or n-pentane as the mobile phase. These solvents have different compressibilities. However, 1% of the relative increase of the column hold-up volume that was observed when the pressure was raised is not accounted for by the compressibilities of either the solvent or the C18-bonded phase. It is due to the influence of the pressure on the retention behavior of thiourea, the compound used as tracer to measure the hold-up volume.

Fate of polychlorinated biphenyls in a contaminated lake ecosystem: Combining equilibrium passive sampling of sediment and water with total concentration measurements of biota

DEFF Research Database (Denmark)

Mäenpää, Kimmo; Leppänen, Matti T.; Figueiredo, Kaisa

2015-01-01

Equilibrium sampling devices can be applied to study and monitor the exposure and fate of hydrophobic organic chemicals on a thermodynamic basis. They can be used to determine freely dissolved concentrations and chemical activity ratios and to predict equilibrium partitioning concentrations...... of hydrophobic organic chemicals in biota lipids. The authors' aim was to assess the equilibrium status of polychlorinated biphenyls (PCBs) in a contaminated lake ecosystem and along its discharge course using equilibrium sampling devices for measurements in sediment and water and by also analyzing biota....... The authors used equilibrium sampling devices (silicone rubber and polyethylene [PE]) to determine freely dissolved concentrations and chemical activities of PCBs in the water column and sediment porewater and calculated for both phases the corresponding equilibrium concentrations and chemical activities...

Do pharmaceuticals, pathogens, and other organic waste water compounds persist when waste water is used for recharge?

Science.gov (United States)

Cordy, Gail E.; Duran, Norma L.; Bouwer, Herman; Rice, Robert C.; Furlong, Edward T.; Zaugg, Steven D.; Meyer, Michael T.; Barber, Larry B.; Kolpin, Dana W.

2004-01-01

A proof-of-concept experiment was devised to determine if pharmaceuticals and other organic waste water compounds (OWCs), as well as pathogens, found in treated effluent could be transported through a 2.4 m soil column and, thus, potentially reach ground water under recharge conditions similar to those in arid or semiarid climates. Treated effluent was applied at the top of the 2.4 m long, 32.5 cm diameter soil column over 23 days, Samples of the column inflow were collected from the effluent storage tank at the beginning (Tbegin) and end (Tend) of the experiment, and a sample of the soil column drainage at the base of the column (Bend) was collected at the end of the experiment. Samples were analyzed for 131 OWCs including veterinary and human antibiotics, other prescription and nonprescription drugs, widely used household and industrial chemicals, and steroids and reproductive hormones, as well as the pathogens Salmonella and Legionella. Analytical results for the two effluent samples taken at the beginning (Tbegin) and end (Tend) of the experiment indicate that the number of OWCs detected in the column inflow decreased by 25% (eight compounds) and the total concentration of OWCs decreased by 46% while the effluent was in the storage tank during the 23-day experiment. After percolating through the soil column, an additional 18 compounds detected in Tend (67% of OWCs) were no longer detected in the effluent (Bend) and the total concentration of OWCs decreased by more than 70%. These compounds may have been subject to transformation (biotic and abiotic), adsorption, and (or) volatilization in the storage tank and during travel through the soil column. Eight compounds—carbamazapine; sulfamethoxazole; benzophenone; 5-methyl-1H-benzotriazole; N,N-diethyltoluamide; tributylphosphate; tri(2-chloroethyl) phosphate; and cholesterol—were detected in all three samples indicating they have the potential to reach ground water under recharge conditions similar to those in

HPLC-CUPRAC post-column derivatization method for the determination of antioxidants: a performance comparison between porous silica and core-shell column packing.

Science.gov (United States)

Haque, Syed A; Cañete, Socrates Jose P

2018-01-01

An HPLC method employing a post-column derivatization strategy using the cupric reducing antioxidant capacity reagent (CUPRAC reagent) for the determining antioxidants in plant-based materials leverages the separation capability of regular HPLC approaches while allowing for detection specificity for antioxidants. Three different column types, namely core-shell and porous silica including two chemically different core-shell materials (namely phenyl-hexyl and C18), were evaluated to assess potential improvements that could be attained by changing from a porous silica matrix to a core-shell matrix. Tea extracts were used as sample matrices for the evaluation specifically looking at catechin and epigallocatechin gallate (EGCG). Both the C18 and phenyl-hexyl core-shell columns showed better performance compared to the C18 porous silica one in terms of separation, peak shape, and retention time. Among the two core-shell materials, the phenyl-hexyl column showed better resolving power compared to the C18 column. The CUPRAC post-column derivatization method can be improved using core-shell columns and suitable for quantifying antioxidants, exemplified by catechin and EGCG, in tea samples.

Simple, specific analysis of organophosphorus and carbamate pesticides in sediments using column extraction and gas chromatography

Science.gov (United States)

Belisle, A.A.; Swineford, D.M.

1988-01-01

A simple, specific procedure was developed for the analysis of organophosphorus and carbamate pesticides in sediment. The wet soil was mixed with anhydrous sodium sulfate to bind water and the residues were column extracted in acetone:methylene chloride (1:l,v/v). Coextracted water was removed by additional sodium sulfate packed below the sample mixture. The eluate was concentrated and analyzed directly by capillary gas chromatography using phosphorus and nitrogen specific detectors. Recoveries averaged 93 % for sediments extracted shortly after spiking, but decreased significantly as the samples aged.

Novel amide polar-embedded reversed-phase column for the fast liquid chromatography-tandem mass spectrometry method to determine polyether ionophores in environmental waters.

Science.gov (United States)

Herrero, P; Borrull, F; Pocurull, E; Marcé, R M

2012-11-09

A fast chromatographic method has been developed that takes less than 5 min per run to determine five polyether ionophores with a novel amide polar-embedded reversed-phase column coupled to a triple quadrupole mass spectrometer. A comparison between Oasis HLB and Oasis MAX sorbents for the solid-phase extraction was done. Oasis HLB sorbent gave recoveries close to 90% and the repeatability (%RSD, 25-100 ng/L, n=3) of the method was less than 7% for all compounds in all matrices. The presence of polyether ionophores in environmental waters such as river water and sewage was investigated. Monensin and narasin were frequently determined in influent and effluent sewage at concentrations from 10 ng/L to 47 ng/L in influents and from 6 ng/L to 34 ng/L in effluents. In river waters, polyether ionophores were not detected in any sample. Copyright © 2012 Elsevier B.V. All rights reserved.

Organics in water contamination analyzer, phase 1

Science.gov (United States)

1986-01-01

The requirements which would result in identifying the components of an automatic analytical system for the analysis of specific organic compounds in the space station potable water supply are defined. The gas chromatographic system for such an analysis is limited to commercially available off-the-shelf hardware and includes the sample inlet, an ionization detector, capillary columns as well as computerized compound identification. The sampling system will be a special variation of the purge and trap Tenax mode using six-port valves and a 500 microliter water sample. Capillary columns used for the separating of contaminants will be bonded phase fused silica with a silicone stationary phase. Two detectors can be used: photoionization and far ultraviolet, since they are sensitive and compatible with capillary columns. A computer system evaluation and program with the principle of compound identification based on the retention index is presented.

The Design of Sample Driver System for Gamma Irradiator Facility at Thermal Column of Kartini Reactor

International Nuclear Information System (INIS)

Suyamto; Tasih Mulyono; Setyo Atmojo

2007-01-01

The design and construction of sample driver system for gamma irradiator facility at thermal column of Kartini reactor post operation has been carried out. The design and construction is based on the space of thermal column and the sample speed rotation which has to as low as possible in order the irradiation process can be more homogeneity. The electrical and mechanical calculation was done after fixation the electrical motor and transmission system which will be applied. By the assumption that the maximum sample weight is 50 kg, the electric motor specification is decided due to its rating i.e. single phase induction motor, run capacitor type, 0.5 HP; 220 V; 3.61 A, CCW and CW, rotation speed 1430 rpm. To achieve the low load rotation speed, motor speed was reduced twice using the conical reduction gear with the reduction ratio 3.9 and thread reduction gear with the reduction ratio 60. From the calculation it is found that power of motor is 118.06 watt, speed rotation of load sample is 6.11 rpm due to the no load rotation of motor 1430 rpm. From the test by varying weight of load up to 75 kg it is known that the device can be operated in a good condition, both in the two direction with the average speed of motor 1486 rpm and load 6.3 rpm respectively. So that the slip is 0.268 % and 0.314 % for no load and full load condition. The difference input current to the motor during no load and full load condition is relative small i.e. 0.14 A. The safety factor of motor is 316 % which is correspond to the weight of load 158 kg. (author)

Sulfur geochemistry of hydrothermal waters in Yellowstone National Park, Wyoming, USA. III. An anion-exchange resin technique for sampling and preservation of sulfoxyanions in natural waters

Science.gov (United States)

Druschel, G.K.; Schoonen, M.A.A.; Nordstorm, D.K.; Ball, J.W.; Xu, Y.; Cohn, C.A.

2003-01-01

A sampling protocol for the retention, extraction, and analysis of sulfoxyanions in hydrothermal waters has been developed in the laboratory and tested at Yellowstone National Park and Green Lake, NY. Initial laboratory testing of the anion-exchange resin Bio-Rad??? AG1-X8 indicated that the resin was well suited for the sampling, preservation, and extraction of sulfate and thiosulfate. Synthetic solutions containing sulfate and thiosulfate were passed through AG1-X8 resin columns and eluted with 1 and 3 M KCl, respectively. Recovery ranged from 89 to 100%. Comparison of results for water samples collected from five pools in Yellowstone National Park between on-site IC analysis (U.S. Geological Survey mobile lab) and IC analysis of resin-stored sample at SUNY-Stony Brook indicates 96 to 100% agreement for three pools (Cinder, Cistern, and an unnamed pool near Cistern) and 76 and 63% agreement for two pools (Sulfur Dust and Frying Pan). Attempts to extract polythionates from the AG1-X8 resin were made using HCl solutions, but were unsuccessful. Bio-Rad??? AG2-X8, an anion-exchange resin with weaker binding sites than the AG1-X8 resin, is better suited for polythionate extraction. Sulfate and thiosulfate extraction with this resin has been accomplished with KCl solutions of 0.1 and 0.5 M, respectively. Trithionate and tetrathionate can be extracted with 4 M KCl. Higher polythionates can be extracted with 9 M hydrochloric acid. Polythionate concentrations can then be determined directly using ion chromatographic methods, and laboratory results indicate recovery of up to 90% for synthetic polythionate solutions using AG2-X8 resin columns. ?? The Royal Society of Chemistry and the Division of Geochemistry of the American Chemical Society 2003.

Column treatment of brewery wastewater using clay fortified with stone-pebbles

International Nuclear Information System (INIS)

Oladoja, N.A.; Ademoroti, C.M.A.; Idiaghe, J.A.; Oketola, A.A.

2006-01-01

The study aimed at providing a low-cost treatment for brewery wastewater, which was achieved by mixing clay with stone-pebbles to improve the low permeability of water through clay beds. The combination (clay/stone-pebbles) was used in columns for the treatment of brewery wastewater. The crystal chemistry of the clay samples was studied using X-ray diffractometer. Three principal clay minerals (kaolin, illite and smectite) were detected in the samples. Atomic absorption spectrophotometer was used to study the geochemistry of the clay samples. The results of the geochemical studies showed that all the samples were hydrated aluminosilicates. Performance efficiency studies were conducted to determine the best combination ratio of clay to stone-pebbles, which showed that combination ratio 3:1 (clay/stone pebbles, w/w) performed better. The flow-rate studies showed that brewery wastewater had longer residence time in non fortified clay than in fortified clay. The flow-rate of the wastewater in the percolating media varied from one medium to another. Two modes of treatment (batch and continuous) were used. The effluent passed through the continuous treatment mode had better quality characteristics as compared with the effluent passed through the batch treatment mode. The effect of repeated use of the fortified column on the performance efficiency was also studied. The pH, total solids, and the chemical oxygen demand (COD) of the effluent was monitored over time. The results of the COD monitored over time were analysed using breakthrough curves. The different columns were found to have different bed volumes at both the break through and exhaustion points. (author)

Biogeochemical controls on the oxygen, nitrogen and sulfur distributions in the water column of Golfo Dulce: an anoxic basin on the Pacific coast of Costa Rica revisited

International Nuclear Information System (INIS)

Ferdelman, Timothy G.; Thamdrup, Bo; Canfield, Donald E.; Noehr Glud, Ronnie; Kuever, Jan; Lillebaek, Rolf; Birger Ramsing, Niels; Wawer, Cathrin

2006-01-01

Chemical distributions, respiration rates, and bacterial distributions were measured in 1994 in the water column and sediments of a small, tropical, anoxic basin (Golfo Dulce, Pacific coast of Costa Rica) to examine the biogeochemical controls on anoxia, sulfide, dissolved inorganic nitrogen, and organic carbon consumption. As reported previously, the deepest 100 m of the water column were anoxic, and sulfide concentrations in the bottom waters were less than 7 μM and then only transiently. Both free-swimming sulfide-oxidizing bacteria and Beggiatoa sp. (containing large vacuoles) were observed in the anoxic bottom waters or at the sediment-water interface. Aerobic respiration dominated the decomposition of organic matter in the surface waters and pycnocline, whereas sulfate reduction was principally restricted to the sediments. Bacteria were distributed in discrete zones and exhibited the highest densities where oxygen decreased below 1 μM around 100 m depth, and near the sediment-water interface. The sub-oxic, sub-pycnocline water column was characterized by a dissolved inorganic nitrogen (DIN) deficit of 2.9 mole m -2 . With a water residence time of 35 - 57 d, estimated from a salt balance, this deficit corresponded to a DIN loss of 51 - 85 mmol m -2 d -1 , comparable to the sub-pycnocline oxygen consumption. Sulfide in the water column was maintained at low concentrations by frequent inputs of oxygenated water from the Pacific Ocean. Sulfide production in the sediments due to bacterial sulfate reduction was scavenged by frequent deposition of iron-rich turbidites. Based on 210 Pb distributions, the most recent emplacement of a turbidite in the basin sediments was determined to have occurred between 1989 and 1992. (author) [es

Gyrokinetic-water-bag modeling of low-frequency instabilities in a laboratory magnetized plasma column

Science.gov (United States)

Gravier, E.; Klein, R.; Morel, P.; Besse, N.; Bertrand, P.

2008-12-01

A new model is presented, named collisional-gyro-water-bag (CGWB), which describes the collisional drift waves and ion-temperature-gradient (ITG) instabilities in a plasma column. This model is based on the kinetic gyro-water-bag approach recently developed [P. Morel et al., Phys. Plasmas 14, 112109 (2007)] to investigate ion-temperature-gradient modes. In CGWB electron-neutral collisions have been introduced and are now taken into account. The model has been validated by comparing CGWB linear analysis with other models previously proposed and experimental results as well. Kinetic effects on collisional drift waves are investigated, resulting in a less effective growth rate, and the transition from collisional drift waves to ITG instability depending on the ion temperature gradient is studied.

Analytical Methods for Malachite Green : Completion Report : Malachite Green Analysis in Water.

Energy Technology Data Exchange (ETDEWEB)

Allen, John L.; Gofus, Jane E.; Meinertz, Jeffery R.

1991-06-01

Malachite green is a known teratogen and therefore its use is limited to nonfood fish under an Investigational New Animal Drug permit (INAD), number 2573. Although a charcoal adsorption column was developed to remove malachite green from hatchery water, INAD compliance requires that the malachite green residue concentrations in any effluent from hatcheries using the chemical be quantified. Therefore, we developed a method for the analysis of malachite green residues in water. Enrichment of the residues of malachite green in water on a diol column followed by High Performance Liquid Chromatographic (HPLC) analysis gives a minimum sensitivity of less than 10 ppb for the chemical. When combined with post-column oxidation using a lead oxide post-column reactor, the procedure can be used for the simultaneous analysis of malachite green in its leuco form, a decomposition product of the dye, as well as its chromatic form. Recovery of the leuco form is pH dependent and water samples should be adjusted to pH 6 to optimize recovery of this form. Water samples spiked with malachite green were concentrated on a diol column followed by elution with 0.05 M p-toluene sulfonic acid in methanol. The methanol elutes were analyzed by HPLC. Pond water samples spiked with malachite green and leuco malachite green yielded average recoveries of 95.4% for malachite green and 57.3% for leuco malachite green. Tap water samples spiked with the carbinol form of malachite green gave average recoveries of 98.6%. The method is very sensitive and is capable of detecting malachite green residues in water at less than 10 ppb. Fish culturists, who cannot find an effective replacement for malachite green, can utilize the method to ensure that their effluents comply with INAD regulations. 13 refs., 2 figs., 7 tabs.

Water-quality assessment of the Rio Grande Valley, Colorado, New Mexico, and Texas; occurrence and distribution of selected pesticides and nutrients at selected surface-water sites in the Mesilla Valley, 1994-95

Science.gov (United States)

Healy, D.F.

1996-01-01

The Rio Grande Valley study unit of the U.S. Geological Survey National Water-Quality Assessment Program conducted a two-phase synoptic study of the occurrence and distribution of pesticides and nutrients in the surface water of the Mesilla Valley, New Mexico and Texas. Phase one, conducted in April-May 1994 during the high-flow irrigation season, consisted of a 6-week time- series sampling event during which 17 water-column samples were collected at 3 main-stem sites on the Rio Grande and a synoptic irrigation-run sampling event during which 19 water-column samples were collected at 7 main-stem sites, 10 drain sites, and 2 sites at the discharges of wastewater-treatment plants. Three samples are included in both the time-series and irrigation-run events. Phase two, conducted in January 1995 during the low-flow non-irrigation season, consisted of a non-irrigation synoptic sampling event during which 18 water-column samples were collected at seven main-stem sites, nine drain sites, and two sites at the discharges of wastewater-treatment plants and a bed- material sampling event during which 6 bed-material samples were collected at six sites near the mouths of drains that discharge to the Rio Grande. The 51 water-column samples were analyzed for 78 pesticides and metabolites and 8 nutrients along with other constituents. The six bed-material samples were analyzed for 21 pesticides and metabolites, gross polychlorinated biphenyls, and gross polychlorinated naphthalenes. The presence of dissolved pesticides in the surface water of the Mesilla Valley is erratic. A total of 100 detections of 17 different pesticides were detected in 44 of the water-column samples. As many as 38 percent of these detections may be attributed to pesticide use upstream from the valley or to nonagricultural pesticide use within the valley. There were 29 detections of 10 different pesticides in 17 samples during the irrigation run and 41 detections of 13 pesticides in 16 samples during the non

Aluminum based metal-organic framework-polymer monolith in solid-phase microextraction of penicillins in river water and milk samples.

Science.gov (United States)

Lirio, Stephen; Liu, Wan-Ling; Lin, Chen-Lan; Lin, Chia-Her; Huang, Hsi-Ya

2016-01-08

In this study, aluminum based metal-organic framework (Al-MOF)-organic polymer monoliths were prepared via microwave-assisted polymerization of ethylene dimethacrylate (EDMA), butyl methacrylate (BMA) with different weight percentages of Al-MOF (MIL-53; 37.5-62.5%) and subsequently utilized as sorbent in solid-phase microextraction (SPME) of penicillins (penicillin G, penicillin V, oxacillin, cloxacillin, dicloxacillin, nafcillin). The Al-MOF-polymer was characterized using Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM) and SEM-energy-dispersive X-ray spectroscopy (SEM-EDS) to clarify the retained crystalline structure well as the homogeneous dispersion of Al-MOF (MIL-53) in polymer monolith. The developed Al-MOF-polymer (MIL-53) monolithic column was evaluated according to its extraction recovery of penicillins. Several parameters affecting the extraction recoveries of penicillins using fabricated Al-MOF-polymer (MIL-53) monolithic column including different MIL-53 weight percentages, column length, pH, desorption solvent, and mobile phase flow rate were investigated. For comparison, different Al-based MOFs (MIL-68, CYCU-4 and DUT-5) were fabricated using the optimized condition for MIL-53-polymer (sample matrix at pH 3, 200μL desorption volume using methanol, 37.5% of MOF, 4-cm column length at 0.100mLmin(-1) flow rate). Among all the Al-MOF-polymers, MIL-53(Al)-polymer still afforded the best extraction recovery for penicillins ranging from 90.5 to 95.7% for intra-day with less than 3.5% relative standard deviations (RSDs) and inter-day precision were in the range of 90.7-97.6% with less than 4.2% RSDs. Meanwhile, the recoveries for column-to-column were in the range of 89.5-93.5% (<3.4% RSDs) while 88.5-90.5% (<5.8% RSDs) for batch-to-batch (n=3). Under the optimal conditions, the limit of detections were in the range of 0.06-0.26μgL(-1) and limit of quantifications between 0.20 and 0.87�

Autonomous gliders reveal features of the water column associated with foraging by adelie penguins.

Science.gov (United States)

Kahl, L Alex; Schofield, Oscar; Fraser, William R

2010-12-01

Despite their strong dependence on the pelagic environment, seabirds and other top predators in polar marine ecosystems are generally studied during their reproductive phases in terrestrial environments. As a result, a significant portion of their life history is understudied which in turn has led to limited understanding. Recent advances in autonomous underwater vehicle (AUV) technologies have allowed satellite-tagged Adélie penguins to guide AUV surveys of the marine environment at the Palmer Long-Term Ecological Research (LTER) site on the western Antarctic Peninsula. Near real-time data sent via Iridium satellites from the AUVs to a centralized control center thousands of miles away allowed scientists to adapt AUV sampling strategies to meet the changing conditions of the subsurface. Such AUV data revealed the water masses and fine-scale features associated with Adélie penguin foraging trips. During this study, the maximum concentration of chlorophyll was between 30 and 50 m deep. Encompassing this peak in the chlorophyll concentration, within the water-column, was a mixture of nutrient-laden Upper Circumpolar Deep (UCDW) and western Antarctic Peninsula winter water (WW). Together, data from the AUV survey and penguin dives reveal that 54% of foraging by Adélie penguins occurs immediately below the chlorophyll maximum. These data demonstrate how bringing together emerging technologies, such as AUVs, with established methods such as the radio-tagging of penguins can provide powerful tools for monitoring and hypothesis testing of previously inaccessible ecological processes. Ocean and atmosphere temperatures are expected to continue increasing along the western Antarctic Peninsula, which will undoubtedly affect regional marine ecosystems. New and emerging technologies such as unmanned underwater vehicles and individually mounted satellite tracking devices will provide the tools critical to documenting and understanding the widespread ecological change

Separation, preconcentration and determination of silver ion from water samples using silica gel modified with 2,4,6-trimorpholino-1,3,5-triazin

International Nuclear Information System (INIS)

Madrakian, Tayyebeh; Afkhami, Abbas; Zolfigol, Mohammad Ali; Solgi, Mohammad

2006-01-01

A new modified silica gel using 2,4,6-trimorpholino-1,3,5-triazin was used for separation, preconcentration and determination of silver ion in natural water by atomic absorption spectrometry (AAS). This new bonded silica gel was used as an effective sorbent for the solid-phase extraction (SPE) of silver ion from aqueous solutions. Experimental conditions for effective adsorption of trace levels of silver ion were optimized with respect to different experimental parameters in column process. Common coexisting ions did not interfere with the separation and determination of silver at pH 3.5 so that silver ion completely adsorbed on the column. The preconcentration factor is 130 (1 mL elution volume for a 130 mL sample volume). The relative standard deviation (R.S.D.) under optimum conditions is 3.03% (n = 5). The accuracy of the method was estimated by using spring and tap water samples that were spiked with different amounts of silver ion. The adsorption isotherm of silver ion was obtained. The capacity of the sorbent at optimum conditions has been found to be 384 μg of silver per gram of sorbent

Leaching of Uranium from pit-water application to soil columns. Effect of vegetation, phosphate fertilizer and amendment

International Nuclear Information System (INIS)

Bonetto, Juan P.

2006-01-01

Pit-water accumulated in the San Rafael uranium (U) Mining and Processing Facility (CMFSR) poses a risk of contaminant dispersion and hinders mining labours in the flooded pits. Soil application of the pit-water may be a way of eliminating it through evapotranspiration, but it requires minimization of U migration to the subsurface water courses in order to be considered an adequate disposal practice. The pH > 7 and carbonate content of the soil may induce the formation of uranyl-carbonate complexes, which have high mobility in soils. Furthermore, its physical and chemical characteristics suggest low metal retention capabilities. A 30 cm long soil column experiment was carried out irrigating pit-water on CMFSR soil with the aim of knowing its U retention capacity, as well as the effect of a phosphate fertilizer, an organic amendment and of vegetation cover on such retention. It was concluded that soil alone was able to retain 60 % of the applied U mass in its first 3 centimeters, leaching 0,6 %. Plant presence enhanced U mobility. However, reduced leachate volume caused by higher evapotranspiration rates balanced this mobility, producing a decrease in the mass of leached U. Phosphate fertilizer incorporated to the soil increased U retention in tits upper centimeters. It also increased vegetation growth, and, accordingly, evapotranspiration in the columns. On the contrary, the use of ground plant material as soil amendment increased U migration. (author) [es

Transport of Cryptosporidium parvum oocysts in soil columns following applications of raw and separated liquid slurry

DEFF Research Database (Denmark)

Petersen, Heidi Huus; Enemark, Heidi L.; Olsen, Annette

2012-01-01

to determine the effectiveness of different slurry separation technologies to remove oocysts and other pathogens, as well as whether application of separated liquid slurry to agricultural land may represent higher risks for ground water contamination as compared to application of raw slurry.......The potential for transport of viable Cryptosporidium parvum oocysts through soil to land drains and groundwater was studied using simulated rainfall and intact soil columns which were applied raw slurry or separated liquid slurry. Following irrigation and weekly samplings over a four week period......, C. parvum oocysts were detected from all soil columns regardless of slurry type and application method although recovery rates were low (liquid slurry leached 73% and 90% more oocysts compared with columns with injected and surface applied raw slurry, respectively...

Study of hydrodynamic and mass transfer parameters in pulsed sieve-plate columns

International Nuclear Information System (INIS)

Safdari, J.

2001-01-01

One of the most important liquid-liquid extractor in industry is pulsed column. The pulsed columns are generally classified into the following categories: 1-Pulsed perforated-plate column. 2- Pulsed packed column. The pulsed plate column is differential contactor with the application of mechanical energy and is used for a diverse range of processes. Probably its best known application has been in the nuclear fuel industry. The pulsed plate column consists of a cylindrical shell with settling zones at the top and the bottom of the column. The liquids are fed continuously to the column (flowing counter-currently) and are removed continuously from opposite ends of the column. In this work using a pilot pulsed plate column and two different chemical systems (toluene/acetone/water and n-butyl acetate/acetone/water) various experiments are carried out. In each experiment direction of mass transfer is from organic phase (dispersed phase) into aqueous phase (continuous phase) and the continuous phase is water. The main objects of this thesis are as follow: a- Investigation of effect of operating parameters on dispersed phase hold up, volumetric overall mass transfer coefficients based on dispersed and continuous phase, extraction efficiency, pressure drop of column and flooding velocities (maximum column capacities). Obtained results in this part show that if the calorimetric flow rate of aqueous phase or pulsation intensity increase, hold up, volumetric overall mass transfer coefficients based on both two phases and extraction efficiency will increase and flooding velocities will decrease. Also results show that if volumetric flow rate of organic phase increase, hold up, volumetric mass transfer coefficients based on both two phases and pressure drop will increase and extraction efficiency and flooding velocities will decrease. b- Investigation of effect of internal circulation inside drops in designing pulsed perforated-plate column

Cosmogenic 22Na and 26Al in samples of lunar ground from a drill column of Moon-24

International Nuclear Information System (INIS)

Lavrukhina, A.K.; Povinets, P.; Ustinova, G.K.

1984-01-01

The method of low background (β-γ-γ)-spectrometry without destruction of the sample has been used to measure 22 Na and 26 Al radioactivity in samples of lunar ground 24118.4-4, 24143.4-4 apd 24184.4-4 from the ''Luna-24'' drilling column. Equilibrium radioactivity of these cosmoqenic isotopes is calculated by the analytic method. The analysis of theoretical and experimental data shows that at depths lower than approximately 40 cm from the lunar surface the drilling process did not bring about ground mixing in the drilling column. For the last million of years the regolite surface layer in the place of ''Luna-24'' landing remained pracically unchanged, i. e. has not been subjected to intensive effect of some mechanic processes on lunar surface. The average intensity of galactic cosmic rays with the rigidity > 0.5 GV for the last million years within the limits of approximtaely 20% remained stable and corresponded to their modern medium intensity 0.24 particlesxcm -2 xc -1 xsr -1 . The average spectrum of galactic cosmic rays for a million years approximately corresponds to the average spectrum for 1962 or 1971

Using CF11 cellulose columns to inexpensively and effectively remove human DNA from Plasmodium falciparum-infected whole blood samples

Directory of Open Access Journals (Sweden)

Venkatesan Meera

2012-02-01

Full Text Available Abstract Background Genome and transcriptome studies of Plasmodium nucleic acids obtained from parasitized whole blood are greatly improved by depletion of human DNA or enrichment of parasite DNA prior to next-generation sequencing and microarray hybridization. The most effective method currently used is a two-step procedure to deplete leukocytes: centrifugation using density gradient media followed by filtration through expensive, commercially available columns. This method is not easily implemented in field studies that collect hundreds of samples and simultaneously process samples for multiple laboratory analyses. Inexpensive syringes, hand-packed with CF11 cellulose powder, were recently shown to improve ex vivo cultivation of Plasmodium vivax obtained from parasitized whole blood. This study was undertaken to determine whether CF11 columns could be adapted to isolate Plasmodium falciparum DNA from parasitized whole blood and achieve current quantity and purity requirements for Illumina sequencing. Methods The CF11 procedure was compared with the current two-step standard of leukocyte depletion using parasitized red blood cells cultured in vitro and parasitized blood obtained ex vivo from Cambodian patients with malaria. Procedural variations in centrifugation and column size were tested, along with a range of blood volumes and parasite densities. Results CF11 filtration reliably produces 500 nanograms of DNA with less than 50% human DNA contamination, which is comparable to that obtained by the two-step method and falls within the current quality control requirements for Illumina sequencing. In addition, a centrifuge-free version of the CF11 filtration method to isolate P. falciparum DNA at remote and minimally equipped field sites in malaria-endemic areas was validated. Conclusions CF11 filtration is a cost-effective, scalable, one-step approach to remove human DNA from P. falciparum-infected whole blood samples.

Resuspension of polychlorinated biphenyl-contaminated field sediment: release to the water column and determination of site-specific K DOC.

Science.gov (United States)

Friedman, Carey L; Lohmann, Rainer; Burgess, Robert M; Perron, Monique M; Cantwell, Mark G

2011-02-01

Sediments from the New Bedford Harbor (NBH) U.S. Environmental Protection Agency (U.S. EPA) Superfund site (Massachusetts, USA), contaminated with polychlorinated biphenyls (PCBs), were resuspended under different water column redox conditions: untreated, oxidative, and reductive. The partitioning of PCBs to the overlying water column was measured with polyethylene samplers and compared to partitioning without resuspension. Greater concentrations of total aqueous (freely dissolved + dissolved organic carbon (DOC)-associated) PCBs were found in all resuspended treatments for PCBs with mid-range K(OW)s, but no difference was observed in total aqueous concentrations among different redox conditions. The magnitude of increased concentrations depended on resuspension time and congener K(OW), but ranged from approximately one to eight times those found without resuspension. In a parallel study, DOC was flocculated and removed from smaller-scale NBH sediment resuspensions. In situ K(DOC)s were determined and used to calculate freely dissolved and DOC-associated fractions of the increase in total aqueous PCB concentrations due to resuspension. The importance of DOC-associated PCBs increased with increasing K(OW). In situ K(DOC)s were approximately one to two orders of magnitude greater than those calculated with a commonly used linear free energy relationship (LFER). The present study demonstrates that resuspension of contaminated sediments releases PCBs to the water column, of which a significant fraction are DOC-associated (e.g., 28, 65, and 90% for PCBs 28, 66, and 110, respectively). Results also imply that site-specific PCB K(DOC)s are superior to those calculated with generic LFERs. © 2010 SETAC.

Evaluation and application of static headspace-multicapillary column-gas chromatography-ion mobility spectrometry for complex sample analysis.

Science.gov (United States)

Denawaka, Chamila J; Fowlis, Ian A; Dean, John R

2014-04-18

An evaluation of static headspace-multicapillary column-gas chromatography-ion mobility spectrometry (SHS-MCC-GC-IMS) has been undertaken to assess its applicability for the determination of 32 volatile compounds (VCs). The key experimental variables of sample incubation time and temperature have been evaluated alongside the MCC-GC variables of column polarity, syringe temperature, injection temperature, injection volume, column temperature and carrier gas flow rate coupled with the IMS variables of temperature and drift gas flow rate. This evaluation resulted in six sets of experimental variables being required to separate the 32 VCs. The optimum experimental variables for SHS-MCC-GC-IMS, the retention time and drift time operating parameters were determined; to normalise the operating parameters, the relative drift time and normalised reduced ion mobility for each VC were determined. In addition, a full theoretical explanation is provided on the formation of the monomer, dimer and trimer of a VC. The optimum operating condition for each VC calibration data was obtained alongside limit of detection (LOD) and limit of quantitation (LOQ) values. Typical detection limits ranged from 0.1ng bis(methylthio)methane, ethylbutanoate and (E)-2-nonenal to 472ng isovaleric acid with correlation coefficient (R(2)) data ranging from 0.9793 (for the dimer of octanal) through to 0.9990 (for isobutyric acid). Finally, the developed protocols were applied to the analysis of malodour in sock samples. Initial work involved spiking an inert matrix and sock samples with appropriate concentrations of eight VCs. The average recovery from the inert matrix was 101±18% (n=8), while recoveries from the sock samples were lower, that is, 54±30% (n=8) for sock type 1 and 78±24% (n=6) for sock type 2. Finally, SHS-MCC-GC-IMS was applied to sock malodour in a field trial based on 11 volunteers (mixed gender) over a 3-week period. By applying the SHS-MCC-GC-IMS database, four VCs were

Performance of zeolite scavenge column in Xe monitoring system

International Nuclear Information System (INIS)

Wang Qian; Wang Hongxia; Li Wei; Bian Zhishang

2010-01-01

In order to improve the performance of zeolite scavenge column, its ability of removal of humidity and carbon dioxide was studied by both static and dynamic approaches. The experimental results show that various factors, including the column length and diameter, the mass of zeolite, the content of water in air, the temperature rise during adsorption, and the activation effectiveness all effect the performance of zeolite column in scavenging humanity and carbon dioxide. Based on these results and previous experience, an optimized design of the zeolite column is made for use in xenon monitoring system. (authors)

Remote sensing of water vapour profiles in the framework of the Total Carbon Column Observing Network (TCCON

Directory of Open Access Journals (Sweden)

M. Schneider

2010-12-01

Full Text Available We show that the near infrared solar absorption spectra recorded in the framework of the Total Carbon Column Observing Network (TCCON can be used to derive the vertical distribution of tropospheric water vapour. The resolution of the TCCON spectra of 0.02 cm⁻¹ is sufficient for retrieving lower and middle/upper tropospheric water vapour concentrations with a vertical resolution of about 3 and 8 km, respectively. We document the good quality of the remotely-sensed profiles by comparisons with coincident in-situ Vaisala RS92 radiosonde measurements. Due to the high measurement frequency, the TCCON water vapour profile data offer novel opportunities for estimating the water vapour variability at different timescales and altitudes.

Analysis of {sup 210}Pb in water samples with plastic scintillation resins

Energy Technology Data Exchange (ETDEWEB)

Lluch, E.; Barrera, J. [Department of Analytical Chemistry, University of Barcelona, Martí i Franqués, 1-11, E-08028, Barcelona (Spain); Tarancón, A., E-mail: alex.tarancon@ub.edu [Department of Analytical Chemistry, University of Barcelona, Martí i Franqués, 1-11, E-08028, Barcelona (Spain); Bagán, H. [Department of Pure and Applied Biochemistry, Lund University, Getingevägen 60, Hus II, 22100 SE, Lund (Sweden); García, J.F. [Department of Analytical Chemistry, University of Barcelona, Martí i Franqués, 1-11, E-08028, Barcelona (Spain)

2016-10-12

{sup 210}Pb is a radioactive lead isotope present in the environment as member of the {sup 238}U decay chain. Since it is a relatively long-lived radionuclide (T{sub 1/2} = 22.2 years), its analysis is of interest in radiation protection and the geochronology of sediments and artwork. Here, we present a method for analysing {sup 210}Pb using plastic scintillation resins (PSresins) packaged in solid-phase extraction columns (SPE cartridge). The advantages of this method are its selectivity, the low limit of detection, as well as reductions in the amount of time and reagents required for analysis and the quantity of waste generated. The PSresins used in this study were composed of a selective extractant (4′,4″(5″)-Di-tert-butyldicyclohexano-18-crown-6 in 1-octanol) covering the surface of plastic scintillation microspheres. Once the amount of extractant (1:1/4) and medium of separation (2 M HNO{sub 3}) were optimised, PSresins in SPE cartridges were calibrated with a standard solution of {sup 210}Pb. {sup 210}Pb could be fully separated from its daughters, {sup 210}Bi and {sup 210}Po, with a recovery value of 91(3)% and detection efficiency of 44(3)%. Three spiked water samples (one underground and two river water samples) were analysed in triplicates with deviations lower than 10%, demonstrating the validity of the PS resin method for {sup 210}Pb analysis. - Highlights: • A plastic scintillation resin for selective analysis of {sup 210}Pb has been developed. • A commercial SPE cartridge has been use for separation and scintillation counting. • {sup 210}Pb separation from {sup 210}Bi and {sup 210}Po is achieved with a 91(3)% of recovery. • The method is valid for analysis of {sup 210}Pb in river water samples.

Automation of column-based radiochemical separations. A comparison of fluidic, robotic, and hybrid architectures

Energy Technology Data Exchange (ETDEWEB)

Grate, J.W.; O' Hara, M.J.; Farawila, A.F.; Ozanich, R.M.; Owsley, S.L. [Pacific Northwest National Laboratory, Richland, WA (United States)

2011-07-01

Two automated systems have been developed to perform column-based radiochemical separation procedures. These new systems are compared with past fluidic column separation architectures, with emphasis on using disposable components so that no sample contacts any surface that any other sample has contacted, and setting up samples and columns in parallel for subsequent automated processing. In the first new approach, a general purpose liquid handling robot has been modified and programmed to perform anion exchange separations using 2 mL bed columns in 6 mL plastic disposable column bodies. In the second new approach, a fluidic system has been developed to deliver clean reagents through disposable manual valves to six disposable columns, with a mechanized fraction collector that positions one of four rows of six vials below the columns. The samples are delivered to each column via a manual 3-port disposable valve from disposable syringes. This second approach, a hybrid of fluidic and mechanized components, is a simpler more efficient approach for performing anion exchange procedures for the recovery and purification of plutonium from samples. The automation architectures described can also be adapted to column-based extraction chromatography separations. (orig.)

Inert carriers for column extraction chromatography

International Nuclear Information System (INIS)

Katykhin, G.S.

1978-01-01

Inert carriers used in column extraction chromatography are reviewed. Such carriers are devided into two large groups: hydrophilic carriers which possess high surface energy and are well wetted only with strongly polar liquids (kieselguhrs, silica gels, glasses, cellulose, Al 2 O 3 ) and water-repellent carriers which possess low surface energy and are well wetted with various organic solvents (polyethylene, polytetrafluorethylene polytrifluorochlorethylene). Properties of various carriers are presented: structure, chemical and radiation stability, adsorption properties, extracting agent capacity. The effect of structure and sizes of particles on the efficiency of chromatography columns is considered. Ways of immovable phase deposition on the carrier and the latter's regeneration. Peculiarities of column packing for preparative and continuous chromatography are discussed

Vibration of an Offshore Structure Having the Form of a Hollow Column Partially Filled with Multiple Fluids and Immersed in Water

OpenAIRE

Lin, Hsien-Yuan; Lee, Jeng-Nan; Sung, Wen-Hao

2012-01-01

This paper employs the numerical assembly method (NAM) to determine the exact frequency-response amplitudes of an offshore structure such as piles or towers having the form of a hollow column filled with multiple fluids, immersed in water, carrying an eccentric tip mass supported by a translational spring and/or a rotational spring, and subjected to a harmonic force. The hollow column is modeled as a Bernoulli-Euler cantilever beam fixed at the bottom. For the case of zero harmonic force, the...

Estimation of tritium trapped in the used ion exchange column resins using water as scavenger

International Nuclear Information System (INIS)

Kumaravel, S.; Ramakrishna, V.; Nair, B.S.K.; Ganesh, G.; Tripathi, R.M.

2018-01-01

Estimation of Tritium trapped in the used resins of Ion exchange (IX) columns apart from the gross beta activity in heavy water systems of Pressurised Heavy Water Reactors (PHWR) is mandatory before their disposal as radioactive waste. The gross beta activity is estimated by Gieger- Muller (GM) counter and by using gamma spectrometer. Accurate estimation of tritium activity of the resin without compromising the counting efficiency is a challenging task because, if a fixed quantity of the resin is directly added to the scintillation solution and counted on a liquid scintillation analyser (LSA), it is prone to interfere with counting efficiency drastically and results in unquantifiable errors and other practical difficulties. In this study a standard technique using light water as scavenger medium to precisely quantify the total activity of tritium trapped in the resin by a systematic approach was carried out

Aluminum-based water treatment residual use in a constructed wetland for capturing urban runoff phosphorus: Column study

Science.gov (United States)

Aluminum-based water treatment residuals (Al-WTR) have a strong affinity to sorb phosphorus. In a proof-of-concept greenhouse column study, Al-WTR was surface-applied at 0, 62, 124, and 248 Mg/ha to 15 cm of soil on top of 46 cm of sand; Al-WTR rates were estimated to capture 0, 10, 20, and 40 year...

Geographic variability in amoeboid protists and other microbial groups in the water column of the lower Hudson River Estuary (New York, USA)

Science.gov (United States)

Juhl, Andrew R.; Anderson, O. Roger

2014-12-01

In comparison to other groups of planktonic microorganisms, relatively little is known about the role of amoeboid protists (amebas) in planktonic ecosystems. This study describes the first geographic survey of the abundance and biomass of amebas in an estuarine water column. Samples collected in the lower Hudson River Estuary were used to investigate relationships between ameba abundance and biomass and hydrographic variables (temperature, salinity, and turbidity), water depth (surface and near bottom), distance from mid-channel to shore, phytoplankton biomass (chlorophyll fluorescence) and the occurrence of other heterotrophic microbial groups (heterotrophic bacteria, nanoflagellates, and ciliates) in the plankton. Although salinity increased significantly towards the mouth of the estuary, there were no significant differences in the abundance or biomass of any microbial group in surface samples collected at three stations separated by 44 km along the estuary's mid-channel. Peak biomass values for all microbial groups were found at the station closest to shore, however, cross-channel trends in microbial abundance and biomass were not statistically significant. Although ameba abundance and biomass in most samples were low compared to other microbial groups, clear patterns in ameba distribution were nevertheless found. Unlike other microbial groups examined, ameba numbers and biomass greatly increased in near bottom water compared to surface samples. Ameba abundance and biomass (in surface samples) were also strongly related to increasing turbidity. The different relationships of ameba abundance and biomass with turbidity suggest a rising contribution of large amebas in microbial communities of the Hudson estuary when turbidity increases. These results, emphasizing the importance of particle concentration as attachment and feeding surfaces for amebas, will help identify the environmental conditions when amebas are most likely to contribute significantly to estuarine

Separation of rate processes for isotopic exchange between hydrogen and liquid water in packed columns 10

International Nuclear Information System (INIS)

Butler, J.P.; Hartog, J. den; Goodale, J.W.; Rolston, J.H.

1977-01-01

Wetproofed platinum catalysts in packed columns promote isotopic exchange between counter-current streams of hydrogen saturated with water vapour and liquid water. The net rate of deuterium transfer from isotopically enriched hydrogen has been measured and separated into two rate processes involving the transfer of deuterium from hydrogen to water vapour and from water vapour to liquid. These are compared with independent measurements of the two rate processes to test the two-step successive exchange model for trickle bed reactors. The separated transfer rates are independent of bed height and characterize the deuterium concentrations of each stream along the length of the bed. The dependences of the transfer rates upon hydrogen and liquid flow, hydrogen pressure, platinum loading and the effect of dilution of the hydrophobic catalyst with inert hydrophilic packing are reported. The results indicate a third process may be important in the transfer of deuterium between hydrogen and liquid water. (author)

Influence of pycnocline topography and water-column structure on marine distributions of alcids (Aves: Alcidae) in Anadyr Strait, Northern Bering Sea, Alaska

Science.gov (United States)

Haney, J. Christopher

1991-01-01

Systematic ship-board surveys were used to simultaneously record seabird abundances and resolve coarse-scale (3 to 10 km) horizontal and fine-scale (1 to 10 m) vertical variability in water-column structure and bathymetry for portions of the coastal zone in Anadyr Strait near western St. Lawrence Island, northern Bering Sea, Alaska, during August and September 1987. Three plankton-feeding alcids, parakeet (Cyclorrhynchus psittacula), crested (Aethia cristatella) and least (A. pusilla) auklets, each exhibited distinct associations for different pycnocline characteristics. Least auklets were more abundant in mixed water, but they also occurred within stratified water where the pycnocline and upper-mixed layer were shallow (≤8 m) and thin (≤10 m), respectively. Low body mass (85 g), high buoyancy, and relatively poor diving ability may have restricted this auklet to areas where water-column strata nearly intersected the surface, or to areas from which strata were absent altogether due to strong vertical mixing. Parakeet and crested auklets, which are larger-bodied (ca. 260 g) planktivores with presumably greater diving ability, were more abundant in stratified water, and both species exhibited less specific affinities for water-column characteristic at intermediate and shallow levels. All three auklets avoided locations with strong pycnocline gradients (≤0.22σtm−1), a crude index of the strong, subsurface shear in water velocities characteristic of this region. Auklet distributions in Anadyr Strait were consistent with: (1) strata accessibility, as estimated from relationships between body mass and relative diving ability, (2) possible avoidance of strong subsurface water motions, and (3) habits and distributions of plankton prey. In contrast, largebodied (>450 g) alcids [i.e., common (Uria aalge) and thick-billed (U. lomvia) murres, pigeon guillemots (Cephus columba), tufted (Fratercula cirrhata), and horned (F. corniculata) puffins feeding on fish or

Heat storage in the Hettangian aquifer in Berlin - results from a column experiment

Science.gov (United States)

Milkus, Chri(Sch)augott

2015-04-01

Aquifer Thermal Energy Storage (ATES) is a sustainable alternative for storage and seasonal availability of thermal energy. However, its impact on the subsurface flow regime is not well known. In Berlin (Germany), the Jurassic (Hettangian) sandstone aquifer with highly mineralized groundwater (TDS 27 g/L) is currently used for heat storage. The aim of this study was to examine the hydrogeochemical changes that are caused by the induced temperature shift and its effects on the hydraulic permeability of the aquifer. Column experiments were conducted, in which stainless steel columns were filled with sediment from the aquifer and flushed with native groundwater for several weeks. The initial temperature of the experiment was 20°C, comparable to the in-situ conditions within the aquifer. After reaching equilibrium between sediment and water, the temperature was increased to simulate heating of the aquifer. During the experiment, physical and chemical parameters (pH, ORP, dissolved oxygen and dissolved carbon dioxide) were measured at the outflow of the column and the effluent water was sampled. Using a Scanning Electron Microscope, the deposition of precipitated minerals and biofilm on sediment grains was analyzed. Changes in hydraulic properties of the sediment were studied by the use of tracer tests with Uranin.

Technical Note: Detection of gas bubble leakage via correlation of water column multibeam images

Science.gov (United States)

Schneider von Deimling, J.; Papenberg, C.

2012-03-01

Hydroacoustic detection of natural gas release from the seafloor has been conducted in the past by using singlebeam echosounders. In contrast, modern multibeam swath mapping systems allow much wider coverage, higher resolution, and offer 3-D spatial correlation. Up to the present, the extremely high data rate hampers water column backscatter investigations and more sophisticated visualization and processing techniques are needed. Here, we present water column backscatter data acquired with a 50 kHz prototype multibeam system over a period of 75 seconds. Display types are of swath-images as well as of a "re-sorted" singlebeam presentation. Thus, individual and/or groups of gas bubbles rising from the 24 m deep seafloor clearly emerge in the acoustic images, making it possible to estimate rise velocities. A sophisticated processing scheme is introduced to identify those rising gas bubbles in the hydroacoustic data. We apply a cross-correlation technique adapted from particle imaging velocimetry (PIV) to the acoustic backscatter images. Temporal and spatial drift patterns of the bubbles are assessed and are shown to match very well to measured and theoretical rise patterns. The application of this processing to our field data gives clear results with respect to unambiguous bubble detection and remote bubble rise velocimetry. The method can identify and exclude the main source of misinterpretations, i.e. fish-mediated echoes. Although image-based cross-correlation techniques are well known in the field of fluid mechanics for high resolution and non-inversive current flow field analysis, we present the first application of this technique as an acoustic bubble detector.

Technical Note: Detection of gas bubble leakage via correlation of water column multibeam images

Directory of Open Access Journals (Sweden)

J. Schneider von Deimling

2012-03-01

Full Text Available Hydroacoustic detection of natural gas release from the seafloor has been conducted in the past by using singlebeam echosounders. In contrast, modern multibeam swath mapping systems allow much wider coverage, higher resolution, and offer 3-D spatial correlation. Up to the present, the extremely high data rate hampers water column backscatter investigations and more sophisticated visualization and processing techniques are needed. Here, we present water column backscatter data acquired with a 50 kHz prototype multibeam system over a period of 75 seconds. Display types are of swath-images as well as of a "re-sorted" singlebeam presentation. Thus, individual and/or groups of gas bubbles rising from the 24 m deep seafloor clearly emerge in the acoustic images, making it possible to estimate rise velocities. A sophisticated processing scheme is introduced to identify those rising gas bubbles in the hydroacoustic data. We apply a cross-correlation technique adapted from particle imaging velocimetry (PIV to the acoustic backscatter images. Temporal and spatial drift patterns of the bubbles are assessed and are shown to match very well to measured and theoretical rise patterns. The application of this processing to our field data gives clear results with respect to unambiguous bubble detection and remote bubble rise velocimetry. The method can identify and exclude the main source of misinterpretations, i.e. fish-mediated echoes. Although image-based cross-correlation techniques are well known in the field of fluid mechanics for high resolution and non-inversive current flow field analysis, we present the first application of this technique as an acoustic bubble detector.

Commissioning and operation of distillation column at Madras Atomic Power Station (Paper No. 1.10)

International Nuclear Information System (INIS)

Neelakrishnan, G.; Subramanian, N.

1992-01-01

In Madras Atomic Power Station (MAPS), an upgrading plant based on vacuum distillation was constructed to upgrade the downgraded heavy water collected in vapor recovery dryers. There are two distillation columns and each having a capacity of 77.5 tonne per annum of reactor grade heavy water with average feed concentration of 30% IP. The performance of the distillation columns has been very good. The column I and column II have achieved an operating factor of 92% and 90% respectively. The commissioning activities, and subsequent improvements carried out in the distillation columns are described. (author)

Multi-residue analysis method for analysis of pharmaceuticals using liquid chromatography-time of flight/mass spectrometry (LC-TOF/MS) in water sample

Science.gov (United States)

Al-Qaim, Fouad Fadhil; Abdullah, Md Pauzi; Othman, Mohamed Rozali

2013-11-01

In this work, a developed method using solid - phase extraction (SPE) followed by liquid chromatography - time of flight mass spectrometry (LC-ESI-TOF/MS) was developed and validated for quantification and confirmation of eleven pharmaceuticals with different therapeutic classes in water samples, Malaysia. These compounds are caffeine (CAF), prazosin (PRZ), enalapril (ENL), carbamazepine (CBZ), nifedipine (NFD), levonorgestrel (LNG), simvastatin (SMV), hydrochlorothiazide (HYD), gliclazide (GLIC), diclofenac-Na (DIC-Na) and mefenamic acid (MEF). LC was performed on a Dionex Ultimate 3000/LC 09115047 (USA) system. Chromatography was performed on a Thermo Scientific C18 (250 mm × 2.1 mm, i.d.: 5μm) column. Several parameters were optimised such as; mobile phase, gradient elution, collision energy and solvent elution for extraction of compounds from water. The recoveries obtained ranged from 30-148 % in river water. Five pharmaceutical compounds were detected in the surface water samples: caffeine, prazosin, enalpril, diclofenac-Na and mefenamic acid. The developed method is precise and accepted recoveries were got. In addition, this method is suitable to identify and quantify trace concentrations of pharmaceuticals in surface water.

Elastic oscillations of water column in the 2003 Tokachi-oki tsunami source: in-situ measurements and 3-D numerical modelling

Directory of Open Access Journals (Sweden)

M. A. Nosov

2007-01-01

Full Text Available During the 2003 Tokachi-Oki tsunamigenic earthquake the real-time JAMSTEC observatory obtained records which provided a unique opportunity to have a look deep inside the tsunami source. Considering water column as a compressible medium we processed the bottom pressure records in order to estimate amplitude, duration and velocity of bottom displacement. Spectral analysis of the records revealed a clear manifestation of the low-frequency elastic oscillations of water column. We also presented 3-D finite-difference numerical model developed in the framework of linear potential theory of ideal compressible fluid to better understand dynamical processes in the tsunami source. The model reproduces position of the main spectral maximum rather correctly. However, due to neglecting of crust elasticity and to lack of exact knowledge of spatiotemporal laws of bottom motion, there is an essential difference between in-situ observed and computed spectra.

Evaluation of the boundary condition influence on PAH concentrations in the water column during the sediment dredging of a port.

Science.gov (United States)

Cutroneo, L; Castellano, M; Carbone, C; Consani, S; Gaino, F; Tucci, S; Magrì, S; Povero, P; Bertolotto, R M; Canepa, G; Capello, M

2015-12-30

The mobilisation of sediments and related contaminants connected to dredging activities is one of the most critical issues to the environmental risk and exposure assessment of a dredging project. The aim of this paper was an investigation of the mobilisation of polycyclic aromatic hydrocarbons (PAHs) due to the dredging of the Port of Genoa (Italy) to identify the temporal and spatial extent of the contaminant transport, and the influence of the dredging and the boundary conditions on it. The results showed relatively low background PAH concentrations in the water column and confirmed the dredging as the primary rising factor of concentrations in the water column, but also showed a complex scenario in which the different environmental and dredging factors forced the concentrations at different levels and moments. The post dredging phase showed PAH values close to the background conditions and the concentrations remained relatively high only for a few PAHs.

Removal of cadmium, copper, nickel, cobalt and mercury from water by Apatite IITM: Column experiments

International Nuclear Information System (INIS)

Oliva, Josep; De Pablo, Joan; Cortina, Jose-Luis; Cama, Jordi; Ayora, Carlos

2011-01-01

Highlights: → The efficiency of Apatite II TM increases as the acidity decreases, then the application of apatite-based materials for metal removal treatments should be restricted to slightly acid to neutral waters. → Because of the preferred process of using phosphate ions to form metal-phosphate precipitates, the mixture with other sources of alkalinity, such as limestone, is proposed to extend the duration of Apatite II TM . → Compared with other reactive materials such as limestone and caustic magnesia that exhibit a reduction of porosity Apatite II TM showed stable hydraulic performance. → The extrapolation of the column durabilities to a 1-m-thick passive treatment suggests that the Apatite II TM filling can be active between 5 and 10 years for an inflow pH exceeding 5. - Abstract: Apatite II TM , a biogenic hydroxyapatite, was evaluated as a reactive material for heavy metal (Cd, Cu, Co, Ni and Hg) removal in passive treatments. Apatite II TM reacts with acid water by releasing phosphates that increase the pH up to 6.5-7.5, complexing and inducing metals to precipitate as metal phosphates. The evolution of the solution concentration of calcium, phosphate and metals together with SEM-EDS and XRD examinations were used to identify the retention mechanisms. SEM observation shows low-crystalline precipitate layers composed of P, O and M. Only in the case of Hg and Co were small amounts of crystalline phases detected. Solubility data values were used to predict the measured column experiment values and to support the removal process based on the dissolution of hydroxyapatite, the formation of metal-phosphate species in solution and the precipitation of metal phosphate. Cd 5 (PO 4 ) 3 OH(s), Cu 2 (PO 4 )OH(s), Ni 3 (PO 4 ) 2 (s), Co 3 (PO 4 ) 2 8H 2 O(s) and Hg 3 (PO 4 ) 2 (s) are proposed as the possible mineral phases responsible for the removal processes. The results of the column experiments show that Apatite II TM is a suitable filling for permeable

Time-series measurements of bubble plume variability and water column methane distribution above Southern Hydrate Ridge, Oregon

Science.gov (United States)

Philip, Brendan T.; Denny, Alden R.; Solomon, Evan A.; Kelley, Deborah S.

2016-03-01

An estimated 500-2500 gigatons of methane carbon is sequestered in gas hydrate at continental margins and some of these deposits are associated with overlying methane seeps. To constrain the impact that seeps have on methane concentrations in overlying ocean waters and to characterize the bubble plumes that transport methane vertically into the ocean, water samples and time-series acoustic images were collected above Southern Hydrate Ridge (SHR), a well-studied hydrate-bearing seep site ˜90 km west of Newport, Oregon. These data were coregistered with robotic vehicle observations to determine the origin of the seeps, the plume rise heights above the seafloor, and the temporal variability in bubble emissions. Results show that the locations of seep activity and bubble release remained unchanged over the 3 year time-series investigation, however, the magnitude of gas release was highly variable on hourly time scales. Bubble plumes were detected to depths of 320-620 m below sea level (mbsl), in several cases exceeding the upper limit of hydrate stability by ˜190 m. For the first time, sustained gas release was imaged at the Pinnacle site and in-between the Pinnacle and the Summit area of venting, indicating that the subseafloor transport of fluid and gas is not restricted to the Summit at SHR, requiring a revision of fluid-flow models. Dissolved methane concentrations above background levels from 100 to 300 mbsl are consistent with long-term seep gas transport into the upper water column, which may lead to the build-up of seep-derived carbon in regional subsurface waters and to increases in associated biological activity.

New hybrid materials as Zn(II) sorbents in water samples

International Nuclear Information System (INIS)

Perez-Quintanilla, Damian; Sanchez, Alfredo; Hierro, Isabel del; Fajardo, Mariano; Sierra, Isabel

2010-01-01

Mesoporous silicas have been chemically modified with 5-mercapto-1-methyltetrazole (MTTZ) obtaining hybrid materials denominated MTTZ-MSU-2 and MTTZ-HMS. These materials were employed as Zn(II) sorbents from aqueous media at room temperature. The effect of several variables (stirring time, pH, presence of other metals) has been studied using batch and column techniques. Flame atomic absorption spectrometry (FAAS) was used to determinate Zn(II) concentration in the filtrate or in the eluted solution after the adsorption process. The results indicate that under pH 8, the maximum adsorption value was 0.94 ± 0.01 and 0.72 ± 0.01 mmol Zn(II)/g for MTTZ-MSU-2 and MTTZ-HMS, respectively. In tap water samples, a preconcentration factor of 200 was obtained. On the basis of these results, it can be concluded that it is possible to modify chemically MSU-2 and HMS with 5-mercapto-1-methyltetrazole and to use the resulting modified mesoporous silica as an effective adsorbent for Zn(II) in aqueous media.

Water sampling device for fuel rod failure monitoring

International Nuclear Information System (INIS)

Oogami, Hideaki; Echigoya, Hironori; Matsuoka, Tesshi.

1991-01-01

The device of the present invention accurately samples coolants in a channel box as sampling water even if the upper end of the channel box of a fuel assembly is positioned at the same height or lower than the upper end of an upper lattice plate. An existent device comprises an outer cap, an inner cap, an air supply pipe and a water sampling tube. In addition, the device of the present invention comprises a sealing material disposed at the end of the outer cap for keeping liquid sealing with the upper lattice plate and a water level monitoring pipe extended to lower than the inner cap passing through the liquid sealing of the outer cap for sucking the atmosphere in the outer cap. Pressurized air is sent through the air supply pipe, to lower the water level of the coolants in the outer cap and the water level monitoring pipe sucks the pressurized air, by which the inside and the outside of the channel box are partitioned. Subsequently, if the sample water is sampled by a sampling tube, sampling water which enables accurate evaluation for radioactivity concentration in the fuel assembly can be obtained. (I.S.)

Numerical study of the air-flow in an oscillating water column wave energy converter

Energy Technology Data Exchange (ETDEWEB)

Paixao Conde, J.M. [Department of Mechanical and Industrial Engineering, Faculty of Sciences and Technology, New University of Lisbon, Monte de Caparica, 2829-516 Caparica (Portugal); IDMEC, Instituto Superior Tecnico, Technical University of Lisbon, 1049-001 Lisboa (Portugal); Gato, L.M.C. [IDMEC, Instituto Superior Tecnico, Technical University of Lisbon, 1049-001 Lisboa (Portugal)

2008-12-15

The paper presents a numerical study of the air-flow in a typical pneumatic chamber geometry of an oscillating water column (OWC)-type wave energy converter (WEC), equipped with two vertical-axis air turbines, asymmetrically placed on the top of the chamber. Outwards and inwards, steady and periodic, air-flow calculations were performed to investigate the flow distribution at the turbines' inlet sections, as well as the properties of the air-jet impinging on the water free-surface. The original design of the OWC chamber is likely to be harmful for the operation of the turbines due to the possible air-jet-produced water-spray at the water free-surface subsequently ingested by the turbine. A geometry modification of the air chamber, using a horizontal baffle-plate to deflect the air from the turbines, is proposed and proved to be very effective in reducing the risk of water-spray production from the inwards flow. The flow distribution at the turbines' inlet sections for the outwards flow was found to be fairly uniform for the geometries considered, providing good inlet flow conditions for the turbines. Steady flow was found to be an acceptable model to study the air-flow inside the pneumatic chamber of an OWC-WEC. (author)

STURM: Resuspension mesocosms with realistic bottom shear stress and water column turbulence for benthic-pelagic coupling studies: Design and Applications

Science.gov (United States)

Sanford, L. P.; Porter, E.; Porter, F. S.; Mason, R. P.

2016-02-01

Shear TUrbulence Resuspension Mesocosm (STURM) tanks, with high instantaneous bottom shear stress and realistic water column mixing in a single system, allow more realistic benthic-pelagic coupling studies that include sediment resuspension. The 1 m3 tanks can be programmed to produce tidal or episodic sediment resuspension over extended time periods (e.g. 4 weeks), over muddy sediments with or without infaunal organisms. The STURM tanks use a resuspension paddle that produces uniform bottom shear stress across the sediment surface while gently mixing a 1 m deep overlying water column. The STURM tanks can be programmed to different magnitudes, frequencies, and durations of bottom shear stress (and thus resuspension) with proportional water column turbulence levels over a wide range of mixing settings for benthic-pelagic coupling experiments. Over eight STURM calibration settings, turbulence intensity ranged from 0.55 to 4.52 cm s-1, energy dissipation rate from 0.0032 to 2.65 cm2 s-3, the average bottom shear stress from 0.0068 to 0.19 Pa, and the instantaneous bottom shear stress from 0.07 to 2.0 Pa. Mixing settings can be chosen as desired and/or varied over the experiment, based on the scientific question at hand. We have used the STURM tanks for four 4-week benthic-pelagic coupling ecosystem experiments with tidal resuspension with or without infaunal bivalves, for stepwise erosion experiments with and without infaunal bivalves, for experiments on oyster biodeposit resuspension, to mimic storms overlain on tidal resuspension, and for experiments on the effects of varying frequency and duration of resuspension on the release of sedimentary contaminants. The large size of the tanks allows water quality and particle measurements using standard oceanographic instrumentation. The realistic scale and complexity of the contained ecosystems has revealed indirect feedbacks and responses that are not observable in smaller, less complex experimental systems.

Spectrophotometric Determination of Boron in Environmental Water Samples

International Nuclear Information System (INIS)

San San; Khin Win Kyi; Kwaw Naing

2002-02-01

The present paper deals with the study on the methods for the determination of boron in the environmental water samples. The standard methods which are useful for this determination are discussed thoroughly in this work. Among the standard methods approved by American Public Health Association, the carmine method was selected for this study. Prior to the determination of boron in the water samples, the precision and accuracy of the methods of choice were examined by using standard boron solutions. The determination of Boron was carried out by using water samples, waste water from Aquaculture Research Centre, University of Yangon, the Ayeyarwady River water near Magway Myathalon Pagoda in Magway Division, ground water from Sanchaung Township, and tap water from Universities' Research Centre, University of Yangon. Analyses of these water samples were done and statistical treatment of the results was carried out. (author)

HILIC separation and quantitation of water-soluble vitamins using diol column.

Science.gov (United States)

Karatapanis, Andreas E; Fiamegos, Yiannis C; Stalikas, Constantine D

2009-04-01

Hydrophilic interaction liquid-chromatography (HILIC) in conjunction with diode array detection has been applied for the separation of selected-water-soluble vitamins using an end-capped HILIC-diol column. Vitamins with significant biological importance, such as thiamine (B(1)), riboflavin (B(2)), nicotinic acid (B(3)), nicotinamide (B(3)), pyridoxine (B(6)), folic acid (B(9)), cyanocobalamin (B(12)) and ascorbic acid (vitamin C) were simultaneously separated. Chromatographic conditions including type and percentage of organic modifier in the mobile phase, pH, type and concentration of buffer salt and flow rate were investigated. ACN was shown to offer superior separation for the compounds tested as compared to methanol, isopropanol and THF. Isocratic separation and analysis were achieved for six vitamins (B(1), B(2), nicotinic acid/nicotinamide, B(6) and C) at ACN-H(2)O 90:10, containing ammonium acetate 10 mM, triethylamine 20 mM, pH 5.0, using a flow rate of 0.8 mL/min, while a gradient was necessary to resolve a mixture of all eight water-soluble vitamins. The HILIC method was validated and successfully applied to the analysis of a pharmaceutical formulation and an energy drink negating the need for time consuming clean-up steps.

High-Accuracy Measurements of Total Column Water Vapor From the Orbiting Carbon Observatory-2

Science.gov (United States)

Nelson, Robert R.; Crisp, David; Ott, Lesley E.; O'Dell, Christopher W.

2016-01-01

Accurate knowledge of the distribution of water vapor in Earth's atmosphere is of critical importance to both weather and climate studies. Here we report on measurements of total column water vapor (TCWV) from hyperspectral observations of near-infrared reflected sunlight over land and ocean surfaces from the Orbiting Carbon Observatory-2 (OCO-2). These measurements are an ancillary product of the retrieval algorithm used to measure atmospheric carbon dioxide concentrations, with information coming from three highly resolved spectral bands. Comparisons to high-accuracy validation data, including ground-based GPS and microwave radiometer data, demonstrate that OCO-2 TCWV measurements have maximum root-mean-square deviations of 0.9-1.3mm. Our results indicate that OCO-2 is the first space-based sensor to accurately and precisely measure the two most important greenhouse gases, water vapor and carbon dioxide, at high spatial resolution [1.3 x 2.3 km(exp. 2)] and that OCO-2 TCWV measurements may be useful in improving numerical weather predictions and reanalysis products.

Comparison of neptunium sorption results using batch and column techniques

International Nuclear Information System (INIS)

Triay, I.R.; Furlano, A.C.; Weaver, S.C.; Chipera, S.J.; Bish, D.L.

1996-08-01

We used crushed-rock columns to study the sorption retardation of neptunium by zeolitic, devitrified, and vitric tuffs typical of those at the site of the potential high-level nuclear waste repository at Yucca Mountain, Nevada. We used two sodium bicarbonate waters (groundwater from Well J-13 at the site and water prepared to simulate groundwater from Well UE-25p No. 1) under oxidizing conditions. It was found that values of the sorption distribution coefficient, Kd, obtained from these column experiments under flowing conditions, regardless of the water or the water velocity used, agreed well with those obtained earlier from batch sorption experiments under static conditions. The batch sorption distribution coefficient can be used to predict the arrival time for neptunium eluted through the columns. On the other hand, the elution curves showed dispersivity, which implies that neptunium sorption in these tuffs may be nonlinear, irreversible, or noninstantaneous. As a result, use of a batch sorption distribution coefficient to calculate neptunium transport through Yucca Mountain tuffs would yield conservative values for neptunium release from the site. We also noted that neptunium (present as the anionic neptunyl carbonate complex) never eluted prior to tritiated water, which implies that charge exclusion does not appear to exclude neptunium from the tuff pores. The column experiments corroborated the trends observed in batch sorption experiments: neptunium sorption onto devitrified and vitric tuffs is minimal and sorption onto zeolitic tuffs decreases as the amount of sodium and bicarbonate/carbonate in the water increases

Uranium facilitated transport by water-dispersible colloids in field and soil columns

Energy Technology Data Exchange (ETDEWEB)

Crancon, P., E-mail: pierre.crancon@cea.fr [CEA, DAM, DIF, F-91297 Arpajon (France); Pili, E. [CEA, DAM, DIF, F-91297 Arpajon (France); Charlet, L. [Laboratoire de Geophysique Interne et Tectonophysique (LGIT-OSUG), University of Grenoble-I, UMR5559-CNRS-UJF, BP53, 38041 Grenoble cedex 9 (France)

2010-04-01

The transport of uranium through a sandy podzolic soil has been investigated in the field and in column experiments. Field monitoring, numerous years after surface contamination by depleted uranium deposits, revealed a 20 cm deep uranium migration in soil. Uranium retention in soil is controlled by the < 50 {mu}m mixed humic and clayey coatings in the first 40 cm i.e. in the E horizon. Column experiments of uranium transport under various conditions were run using isotopic spiking. After 100 pore volumes elution, 60% of the total input uranium is retained in the first 2 cm of the column. Retardation factor of uranium on E horizon material ranges from 1300 (column) to 3000 (batch). In parallel to this slow uranium migration, we experimentally observed a fast elution related to humic colloids of about 1-5% of the total-uranium input, transferred at the mean porewater velocity through the soil column. In order to understand the effect of rain events, ionic strength of the input solution was sharply changed. Humic colloids are retarded when ionic strength increases, while a major mobilization of humic colloids and colloid-borne uranium occurs as ionic strength decreases. Isotopic spiking shows that both {sup 238}U initially present in the soil column and {sup 233}U brought by input solution are desorbed. The mobilization process observed experimentally after a drop of ionic strength may account for a rapid uranium migration in the field after a rainfall event, and for the significant uranium concentrations found in deep soil horizons and in groundwater, 1 km downstream from the pollution source.

The role of sedimentation in the removal of radiocaesium from water column on an example of the lake Svyatskoe

International Nuclear Information System (INIS)

Derengovskaya, R.A.; Ostapenya, A.P.

2002-01-01

The contribution of sedimentation processes to the removal of radiocaesium from water column was determined in mesotrophic Lake Svyatskoe. During the period April till October 19,3 tons dry weight of the particle matter was precipitated on the lake bottom, which corresponds to 0,97*10 9 Bk radiocaesium associated with suspended matter

Mathematical modeling of alcohol distillation columns

Directory of Open Access Journals (Sweden)

Ones Osney Pérez

2011-04-01

Full Text Available New evaluation modules are proposed to extend the scope of a modular simulator oriented to the sugar cane industry, called STA 4.0, in a way that it can be used to carry out x calculation and analysis in ethanol distilleries. Calculation modules were developed for the simulation of the columns that are combined in the distillation area. Mathematical models were supported on materials and energy balances, equilibrium relations and thermodynamic properties of the ethanol-water system. Ponchon-Savarit method was used for the evaluation of the theoretical stages in the columns. A comparison between the results using Ponchon- Savarit method and those obtained applying McCabe-Thiele method was done for a distillation column. These calculation modules for ethanol distilleries were applied to a real case for validation.

Methods of Analysis by the U.S. Geological Survey National Water Quality Laboratory - Determination of Moderate-Use Pesticides and Selected Degradates in Water by C-18 Solid-Phase Extraction and Gas Chromatography/Mass Spectrometry

Science.gov (United States)

Sandstrom, Mark W.; Stroppel, Max E.; Foreman, William T.; Schroeder, Michael P.

2001-01-01

A method for the isolation and analysis of 21 parent pesticides and 20 pesticide degradates in natural-water samples is described. Water samples are filtered to remove suspended particulate matter and then are pumped through disposable solid-phase-extraction columns that contain octadecyl-bonded porous silica to extract the analytes. The columns are dried by using nitrogen gas, and adsorbed analytes are eluted with ethyl acetate. Extracted analytes are determined by capillary-column gas chromatography/mass spectrometry with selected-ion monitoring of three characteristic ions. The upper concentration limit is 2 micrograms per liter (?g/L) for most analytes. Single-operator method detection limits in reagent-water samples range from 0.00 1 to 0.057 ?g/L. Validation data also are presented for 14 parent pesticides and 20 degradates that were determined to have greater bias or variability, or shorter holding times than the other compounds. The estimated maximum holding time for analytes in pesticide-grade water before extraction was 4 days. The estimated maximum holding time for analytes after extraction on the dry solid-phase-extraction columns was 7 days. An optional on-site extraction procedure allows for samples to be collected and processed at remote sites where it is difficult to ship samples to the laboratory within the recommended pre-extraction holding time. The method complements existing U.S. Geological Survey Method O-1126-95 (NWQL Schedules 2001 and 2010) by using identical sample preparation and comparable instrument analytical conditions so that sample extracts can be analyzed by either method to expand the range of analytes determined from one water sample.

UMTRA project water sampling and analysis plan, Maybell, Colorado

International Nuclear Information System (INIS)

1994-06-01

This water sampling and analysis plan (WSAP) describes planned water sampling activities and provides the regulatory and technical basis for ground water sampling in 1994 at the US Department of Energy's (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project site in Maybell, Colorado. The WSAP identifies and justifies sampling locations, analytical parameters, and sampling frequencies at the site. The ground water data will be used for site characterization and risk assessment. The regulatory basis for the ground water and surface water monitoring activities is derived from the EPA regulations in 40 CFR Part 192 (1993) and the proposed EPA standards of 1987 (52 FR 36000). Sampling procedures are guided by the UMTRA Project standard operating procedures (SOP) (JEG, n.d.), the Technical Approach Document (TAD) (DOE, 1989), and the most effective technical approach for the site. This WSAP also includes a summary and the results of water sampling activities from 1989 through 1992 (no sampling was performed in 1993)

Estimating cyclopoid copepod species richness and geographical distribution (Crustacea across a large hydrographical basin: comparing between samples from water column (plankton and macrophyte stands

Directory of Open Access Journals (Sweden)

Gilmar Perbiche-Neves

2014-06-01

Full Text Available Species richness and geographical distribution of Cyclopoida freshwater copepods were analyzed along the "La Plata" River basin. Ninety-six samples were taken from 24 sampling sites, twelve sites for zooplankton in open waters and twelve sites for zooplankton within macrophyte stands, including reservoirs and lotic stretches. There were, on average, three species per sample in the plankton compared to five per sample in macrophytes. Six species were exclusive to the plankton, 10 to macrophyte stands, and 17 were common to both. Only one species was found in similar proportions in plankton and macrophytes, while five species were widely found in plankton, and thirteen in macrophytes. The distinction between species from open water zooplankton and macrophytes was supported by nonmetric multidimensional analysis. There was no distinct pattern of endemicity within the basin, and double sampling contributes to this result. This lack of sub-regional faunal differentiation is in accordance with other studies that have shown that cyclopoids generally have wide geographical distribution in the Neotropics and that some species there are cosmopolitan. This contrasts with other freshwater copepods such as Calanoida and some Harpacticoida. We conclude that sampling plankton and macrophytes together provided a more accurate estimate of the richness and geographical distribution of these organisms than sampling in either one of those zones alone.

Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of semivolatile organic compounds in bottom sediment by solvent extraction, gel permeation chromatographic fractionation, and capillary-column gas chromatography/mass spectrometry