Sample records for maximum doc sorption

  1. Selective Sorption of Dissolved Organic Carbon Compounds by Temperate Soils

    Jagadamma, Sindhu [ORNL; Mayes, Melanie [ORNL; Phillips, Jana Randolph [ORNL


    Physico-chemical sorption of dissolved organic carbon (DOC) on soil minerals is one of the major processes of organic carbon (OC) stabilization in soils, especially in deeper layers. The attachment of C on soil solids is related to the reactivity of the soil minerals and the chemistry of the sorbate functional groups, but the sorption studies conducted without controlling microbial activity may overestimate the sorption potential of soil. This study was conducted to examine the sorptive characteristics of a diverse functional groups of simple OC compounds (D-glucose, L-alanine, oxalic acid, salicylic acid, and sinapyl alcohol) on temperate climate soil orders (Mollisols, Ultisols and Alfisols) with and without biological degradative processes. Equilibrium batch experiments were conducted using 0-100 mg C L-1 at a solid-solution ratio of 1:60 for 48 hrs and the sorption parameters were calculated by Langmuir model fitting. The amount of added compounds that remained in the solution phase was detected by high performance liquid chromatography (HPLC) and total organic C (TOC) analysis. Soil sterilization was performed by -irradiation technique and experiments were repeated to determine the contribution of microbial degradation to apparent sorption. Overall, Ultisols did not show a marked preference for apparent sorption of any of the model compounds, as indicated by a narrower range of maximum sorption capacity (Smax) of 173-527 mg kg soil-1 across compounds. Mollisols exhibited a strong preference for apparent sorption of oxalic acid (Smax of 5290 mg kg soil-1) and sinapyl alcohol (Smax of 2031 mg kg soil-1) over the other compounds. The propensity for sorption of oxalic acid is mainly attributed to the precipitation of insoluble Ca-oxalate due to the calcareous nature of most Mollisol subsoils and its preference for sinapyl alcohol could be linked to the polymerization of this lignin monomer on 2:2 mineral dominated soils. The reactivity of Alfisols to DOC was in

  2. Effect of precipitation, sorption and stable of isotope on maximum release rates of radionuclides from engineered barrier system (EBS) in deep repository.

    Malekifarsani, A; Skachek, M A


    shown that the concentrations of the following radionuclides are limited by solubility and precipitate around the waste and buffer: U, Np, Ra, Sm, Zr, Se, Tc, and Pd. The Sensitivity of maximum release rates in case precipitation shows that some nuclides such as Cs-135, Nb-94, Nb-93 m, Zr-93, Sn-126, Th-230, Pu-240, Pu-242, Pu-239, Cm-245, Am-243, Cm-245, U-233, Ac-227, Pb-210, Pa-231 and Th-229 are very little changed in case the maximum release rate from EBS corresponding to eliminate precipitation in buffer material. Some nuclides such as Se-79, Tc-99, Pd-107, Th-232, U-236, U-233, Ra-226, Np-237 U-235, U-234, and U-238 are virtually changed in the maximum release rate compared to case that taking account precipitation. In Sensitivity of maximum release rates in case to taking account stable isotopes (according to the table of inventory) there are only some nuclides with their stable isotopes in the vitrified waste. And calculation shows that Pd-107 and Se-79 are very increase in case eliminate stable isotope. The Sensitivity of maximum release rates in case retardation with sorption shows that some nuclides such as Pu-240, Pu-241, Pu-239, Cm-245, Am-241, Cm-246, and Am-243 are increased in some time in case maximum release rate from EBS corresponding to eliminate retardation in buffer material. Some nuclides such as U-235, U-233 and U-236 have a little decrease in case maximum release because their parents have short live and before decay to their daughter will released from the EBS. If the characteristic time taken for a nuclide to diffuse across the buffer exceeds its half-life, then the release rate of that nuclide from the EBS will be attenuated by radioactive decay. Thus, the retardation of the diffusion process due to sorption tends to reduce the release rates of short-lived nuclides more effectively than for the long-lived ones. For example, release rates of Pu-240, Cm-246 and Am-241, which are relatively short-lived and strongly sorbing, are very small

  3. Removal of dissolved organic carbon by aquifer material: Correlations between column parameters, sorption isotherms and octanol-water partition coefficient.

    Pradhan, Snigdhendubala; Boernick, Hilmar; Kumar, Pradeep; Mehrotra, Indu


    The correlation between octanol-water partition coefficient (KOW) and the transport of aqueous samples containing single organic compound is well documented. The concept of the KOW of river water containing the mixture of organics was evolved by Pradhan et al. (2015). The present study aims at determining the KOW and sorption parameters of synthetic aqueous samples and river water to finding out the correlation, if any. The laboratory scale columns packed with aquifer materials were fed with synthetic and river water samples. Under the operating conditions, the compounds in the samples did not separate, and all the samples that contain more than one organic compound yielded a single breakthrough curve. Breakthrough curves simulated from sorption isotherms were compared with those from the column runs. The sorption parameters such as retardation factor (Rf), height of mass transfer zone (HMTZ), rate of mass transfer zone (RMTZ), breakpoint column capacity (qb) and maximum column capacity (qx) estimated from column runs, sorption isotherms and models developed by Yoon-Nelson, Bohart-Adam and Thomas were in agreement. The empirical correlations were found between the KOW and sorption parameters. The transport of the organics measured as dissolved organic carbon (DOC) through the aquifer can be predicted from the KOW of the river water and other water samples. The novelty of the study is to measure KOW and to envisage the fate of the DOC of the river water, particularly during riverbank filtration. Statistical analysis of the results revealed a fair agreement between the observed and computed values.

  4. Diagnosis of Processes Controlling Dissolved Organic Carbon (DOC) Export in a Subarctic Region by a Dynamic Ecosystem Model

    Tang, J.


    Permafrost thawing in high latitudes allows more soil organic carbon (SOC) to become hydrologically accessible. This can increase dissolved organic carbon (DOC) exports and carbon release to the atmosphere as CO2 and CH4, with a positive feedback to regional and global climate warming. However, this portion of carbon loss through DOC export is often neglected in ecosystem models. In this paper, we incorporate a set of DOC-related processes (DOC production, mineralization, diffusion, sorption-desorption and leaching) into an Arctic-enabled version of the dynamic ecosystem model LPJ-GUESS (LPJ-GUESS WHyMe) to mechanistically model the DOC export, and to link this flux to other ecosystem processes. The extended LPJ-GUESS WHyMe with these DOC processes is applied to the Stordalen catchment in northern Sweden. The relative importance of different DOC-related processes for mineral and peatland soils for this region have been explored at both monthly and annual scales based on a detailed variance-based Sobol sensitivity analysis. For mineral soils, the annual DOC export is dominated by DOC fluxes in snowmelt seasons and the peak in spring is related to the runoff passing through top organic rich layers. Two processes, DOC sorption-desorption and production, are found to contribute most to the annual variance in DOC export. For peatland soils, the DOC export during snowmelt seasons is constrained by frozen soils and the processes of DOC production and mineralization, determining the magnitudes of DOC desorption in snowmelt seasons as well as DOC sorption in the rest of months, play the most important role in annual variances of DOC export. Generally, the seasonality of DOC fluxes is closely correlated with runoff seasonality in this region. The current implementation has demonstrated that DOC-related processes in the framework of LPJ-GUESS WHyMe are at an appropriate level of complexity to represent the main mechanism of DOC dynamics in soils. The quantified contributions

  5. AR DOC: Augmented reality documentaries

    Vistisen, Peter


    Augmented Reality Documentaries (AR DOC) er et ’lille’ Shareplay projekt (ansøgte midler augmented reality cross media løsninger, til at skabe engagerende publikumsformidling...... indenfor oplevelsesindustrien. Projektet har genereret ny viden omkring, hvordan fysisk og digital formidling kan understøttes via Augmented Reality som formidlingsformat....

  6. Freeze-thaw Effects on Sorption/Desorption of Dissolved Organic Carbon in Wetland Soils

    YU Xiaofei; ZHANG Yuxia; ZHAO Hongmei; LU Xianguo; WANG Guoping


    The effects of freeze-thaw cycles on sorption/desorption of dissolved organic carbon (DOC) in two wetland soils and one reclaimed wetland soil were investigated. DOC concentrations added were 0-600 mg/L. Laboratory in-cubations of sorption/desorption of DOC had been carried out at -15℃ for 10 h, and then at +5℃ for 13 h. Soil sam-ples were refrozen and thawed subsequently for 5 cycles. Initial Mass model was used to describe sorption behavior of DOC. The results indicate that freeze-thaw cycles can significantly increase the sorption capacity of DOC and reduce the desorption capacity of DOC in the three soils. The freeze-thaw effects on desorption of DOC in soils increase with the increasing freeze-thaw cycles. The conversion of natural wetlands to soybean farmland can decrease the sorption capacity and increase the desorption capacity of DOC in soils. Global wanning and reclamation may increase DOC re-lease, and subsequently increase the loss of carbon and the emission of greenhouse gas.

  7. Batch experiments of Cs, Co and Eu sorption onto cement with dissolved fibre mass UP2 in the liquid phase

    Holgersson, Stellan; Dubois, Isabelle; Boerstell, Lisa (Department of Chemical and Biochemical Engineering, Nuclear Chemistry, Chalmers University of Technology (Sweden))


    The potential effects of alkaline degradation products of the fibre mass UP2 on metal sorption onto fresh and degraded cement have been investigated. For this purpose, crushed cement have been leached to support material for the subsequent batch sorption experiments. Alkaline leaching of UP2 were also made, which gave leaching solutions of 30 ppm DOC after 300 days. These solutions were used in the batch experiments. Continued leaching shows that even higher concentrations can be expected: 45 ppm DOC in the leaching with a low-alkaline (pH 12.5) artificial cement pore-water and 150 ppm DOC with a high alkaline (pH 13.3) artificial pore-water. Batch sorption experiments with 134Cs and 60Co show no effects on metal sorption onto leached or fresh cement when the 30 ppm DOC leaching solutions of UP2 were used as liquid phase. The measured R{sub d} values were 10-3 m3/kg for Cs and in the range of 0.03-0.1 m3/kg for Co. Separate experiments with other organics ligands were also made: EDTA, ISA and citric acid with maximum concentrations of 500, 300 and 300 ppm DOC, respectively. Also here no effects on Cs and Co sorption onto leached and fresh cement were established. Batch experiments of 152Eu were not successful since results were above detection level of about 2-3 m3/kg. The addition of the aforementioned 30 ppm UP2 leaching solution or the other organic ligands did not affect the detection level. Measurements of background concentrations of total Eu show a peculiar result of Eu apparently increasing in batch experiments with cement to final values of about 5-10 nM. The underlying reason for this effect, whether real or artificial, could not be established. Background concentrations of Th were about 1 nM in both cement and blank samples. Background concentrations of Zr were about 100-700 nM in both cement and blank samples, the high values were measured acidic blanks, which suggests either acidic leaching from tube walls or contamination from the acid itself. No

  8. Dissolved organic carbon (DOC in Arctic ground ice

    M. Fritz


    Full Text Available Thermal permafrost degradation and coastal erosion in the Arctic remobilize substantial amounts of organic carbon (OC and nutrients which have been accumulated in late Pleistocene and Holocene unconsolidated deposits. Their vulnerability to thaw subsidence, collapsing coastlines and irreversible landscape change is largely due to the presence of large amounts of massive ground ice such as ice wedges. However, ground ice has not, until now, been considered to be a source of dissolved organic carbon (DOC, dissolved inorganic carbon (DIC and other elements, which are important for ecosystems and carbon cycling. Here we show, using geochemical data from a large number of different ice bodies throughout the Arctic, that ice wedges have the greatest potential for DOC storage with a maximum of 28.6 mg L−1 (mean: 9.6 mg L−1. Variation in DOC concentration is positively correlated with and explained by the concentrations and relative amounts of typically terrestrial cations such as Mg2+ and K+. DOC sequestration into ground ice was more effective during the late Pleistocene than during the Holocene, which can be explained by rapid sediment and OC accumulation, the prevalence of more easily degradable vegetation and immediate incorporation into permafrost. We assume that pristine snowmelt is able to leach considerable amounts of well-preserved and highly bioavailable DOC as well as other elements from surface sediments, which are rapidly stored in ground ice, especially in ice wedges, even before further degradation. In the Yedoma region ice wedges represent a significant DOC (45.2 Tg and DIC (33.6 Tg pool in permafrost areas and a fresh-water reservoir of 4172 km3. This study underlines the need to discriminate between particulate OC and DOC to assess the availability and vulnerability of the permafrost carbon pool for ecosystems and climate feedback upon mobilization.

  9. Sorption kinetics of hexadecyltrimethylammonium on natural clinoptilolite

    Li, Z.


    Sorption kinetics of hexadecyltrimethylammonium (HDTMA) chloride on a natural clinoptilolite was studied in this research. The amount of HDTMA sorbed is a function of the initial HDTMA input and the sorption time. When the initial HDTMA input is less than the external cation-exchange capacity of the clinoptilolite, the HDTMA sorption is fast and equilibrium can be established in 1 h. As the initial HDTMA input is greater than the external cation-exchange capacity of clinoptilolite, which will result in more than a monolayer HDTMA surface coverage, the time for HDTMA sorption to reach equilibrium increases exponentially. The HDTMA sorption maximum on clinoptilolite increases logarithmically with mixing time. The counterion solution concentration data suggest that at the initial stage HDTMA molecules sorb on the zeolite via micelle forms, which is manifested by a decrease in chloride solution concentration with time. When HDTMA solution concentration is depleted to less than its critical micelle concentration, the adsorbed micelles (admicelles) rearrange themselves to a more stable monolayer or bilayer configuration, which is reflected by an increase in counterion solution concentration due to the desorption of chloride from admicelles. The time required for the surface rearrangement increases exponentially as the HDTMA input increases. The data of HDTMA sorption kinetics were fitted to different kinetic models, and the parabolic diffusion model fits the data best for the HDTMA sorption, counterion sorption at the initial stage and counterion desorption at the rearrangement stage. Thus, the sorption of HDTMA on clinoptilolite surfaces is diffusion controlled. The results also indicate that it is incomplete to discuss surfactant sorption without counterion concentration data.

  10. Modelling impacts of temperature, and acidifying and eutrophying deposition on DOC trends

    Sawicka, Kasia; Rowe, Ed; Evans, Chris; Monteith, Don; Vanguelova, Elena; Wade, Andrew; Clark, Joanna


    Surface water dissolved organic carbon (DOC) concentrations in large parts of the northern hemisphere have risen over the past three decades, raising concern about enhanced contributions of carbon to the atmosphere and seas and oceans. The effect of declining acid deposition has been identified as a key control on DOC trends in soil and surface waters, since pH and ionic strength affect sorption and desorption of DOC. However, since DOC is derived mainly from recently-fixed carbon, and organic matter decomposition rates are considered sensitive to temperature, uncertainty persists regarding the extent to the relative importance of different drivers that affect these upward trends. We ran the dynamic model MADOC (Model of Acidity and Soil Organic Carbon) for a range of UK soils (podzols, gleysols and peatland), for which the time-series were available, to consider the likely relative importance of decreased deposition of sulphate and chloride, accumulation of reactive N, and higher temperatures, on DOC production in different soils. Modelled patterns of DOC change generally agreed favourably with measurements collated over 10-20 years, but differed markedly between sites. While the acidifying effect of sulphur deposition appeared to be the predominant control on the observed soil water DOC trends in all the soils considered other than a blanket peat, the model suggested that over the long term, the effects of nitrogen deposition on N-limited soils may have been sufficient to elevate the DOC recovery trajectory significantly. The second most influential cause of rising DOC in the model simulations was N deposition in ecosystems that are N-limited and respond with stimulated plant growth. Although non-marine chloride deposition made some contribution to acidification and recovery, it was not amongst the main drivers of DOC change. Warming had almost no effect on modelled historic DOC trends, but may prove to be a significant driver of DOC in future via its influence

  11. Temperature dependence of sorption of gases by coals and charcoals

    Sakurovs, Richard; Day, Stuart; Weir, Steve; Duffy, Greg (CSIRO Energy Technology PO Box 330 Newcastle 2300 Australia)


    Modelling the sorption properties of coals for carbon dioxide under supercritical conditions is necessary for accurate prediction of the sequestering ability of coals in seams. We present recent data for sorption curves of three dry Argonne Premium coals, for carbon dioxide, methane and nitrogen at two different temperatures at pressures up to 15 MPa. The sorption capacity of coals tends to decrease with increasing temperature. An investigation into literature values for sorption of nitrogen and methane by charcoal also show sorption capacities that decrease dramatically with increasing temperature. This is inconsistent with expectations from Langmuir models of coal sorption, which predict a sorption capacity that is independent of temperature. We have successfully fitted the isotherms using a modified Dubinin-Radushkevich equation that uses gas density rather than pressure. A simple pore-filling model that assumes there is a maximum pore width that can be filled in supercritical conditions and that this maximum pore width decreases with increasing temperature, can explain this temperature dependence of sorption capacity. It can also explain why different supercritical gases give apparently different surface sorption capacities on the same material. The calculated heat of sorption for these gases on these coals is similar to those found for these gases on activated carbon. (author)

  12. Quantification of DOC concentrations in relation with soil properties of soils in tundra and taiga of Northern European Russia

    M. R. Oosterwoud


    Full Text Available Potential mobilization and transport of Dissolved Organic Carbon (DOC in subarctic river basins towards the oceans is enormous, because 23–48% of the worlds Soil Organic Carbon (SOC is stored in northern regions. As climate changes, the amount and composition of DOC exported from these basins are expected to change. The transfer of organic carbon between soils and rivers results in fractionation of organic carbon compounds. The aim of this research is to determine the DOC concentrations, its fractions, i.e. humic (HA, fulvic (FA, and hydrophilic (HY acids, and soil characteristics that influence the DOC sorptive properties of different soil types within a tundra and taiga catchment of Northern European Russia. DOC in taiga and tundra soil profiles (soil solution consisted only of HY and FA, where HY became more abundant with increasing depth. Adsorption of DOC on mineral phases is the key geochemical process for release and removal of DOC from potentially soluble carbon pool. We found that adsorbed organic carbon may desorb easily and can release DOC quickly, without being dependent on mineralization and degradation. Although Extractable Organic Carbon (EOC comprise only a small part of SOC, it is a significant buffering pool for DOC. We found that about 80–90% of released EOC was previously adsorbed. Fractionation of EOC is also influenced by the fact that predominantly HA and FA adsorbed to soil and therefore also are the main compounds released when desorbed. Flowpaths vary between taiga and tundra and through seasons, which likely affects DOC concentration found in streams. As climate changes, also flowpaths of water through soils may change, especially in tundra caused by thawing soils. Therefore, adsorptive properties of thawing soils exert a major control on DOC leaching to rivers. To better understand the process of DOC ad- and de-sorption in soils, process based soil chemical modelling, which could bring more insight in solution

  13. Sorption of organic carbon compounds to the fine fraction of surface and Subsurface Soils

    Jagadamma, Sindhu [ORNL; Mayes, Melanie [ORNL; Zinn, Yuri [Federal University of Lavras, Brazil; Gisladottir, Gudrun [University of Iceland; Ann, Russell [Iowa State University


    Dissolved organic carbon (DOC) transported from the soil surface is stabilized in deeper soil profiles by physicochemical sorption processes. However, it is unclear how different forms of organic carbon (OC) compounds common in soil organic matter interact with soil minerals in the surface (A) and subsurface (B) horizons. We added four compounds (glucose, starch, cinnamic acid and stearic acid) to the silt- and clay-sized fraction (fine fraction) of A and B horizons of eight soils from varying climates (3 temperate, 3 tropical, 1 arctic and 1 sub-arctic). Equilibriumbatch experiments were conducted using 0 to 100 mg C L 1 of 14C-labeled compounds for 8 h. Sorption parameters (maximum sorption capacity, Qmax and binding coefficient, k) calculated by fitting sorption data to the Langmuir equation showed that Qmax of A and B horizons was very similar for all compounds. Both Qmax and k values were related to sorbate properties, with Qmax being lowest for glucose (20 500 mg kg 1), highest for stearic acid (20,000 200,000 mg kg 1), and intermediate for both cinnamic acid (200 4000 mg kg 1) and starch (400 6000 mg kg 1). Simple linear regression analysis revealed that physicochemical properties of the sorbents influenced the Qmax of cinnamic acid and stearic acid, but not glucose and starch. The sorbent properties did not show predictive ability for binding coefficient k. By using the fine fraction as sorbent, we found that the mineral fractions of A horizons are equally reactive as the B horizons irrespective of soil organic carbon content.

  14. Work Disability Benefits? Depends on the Doc

    ... Work Disability Benefits? Depends on the Doc International study found ... widely varying opinions about whether claimants for work disability benefits should get those benefits, researchers report. After ...

  15. Impact of exotic and inherent dissolved organic matter on sorption of phenanthrene by soils.

    Gao, Yanzheng; Xiong, Wei; Ling, Wanting; Wang, Xiaorong; Li, Qiuling


    The impacts of exotic and inherent dissolved organic matter (DOM) on phenanthrene sorption by six zonal soils of China, chosen so as to have different soil organic carbon (SOC) contents, were investigated using a batch technique. The exotic DOM was extracted from straw waste. In all cases, the sorption of phenanthrene by soils could be well described by the linear equation. The presence of inherent DOM in soils was found to impede phenanthrene sorption, since the apparent distribution coefficients (K(d)(*)) for phenanthrene sorption by deionized water-eluted soils were 3.13-21.5% larger than the distribution coefficients (K(d)) by control soils. Moreover, the enhanced sorption of phenanthrene by eluted versus control soils was in positive correlation with SOC contents. On the other hand, it was observed that the influence of exotic DOM on phenanthrene sorption was related to DOM concentrations. The K(d)(*) values for sorption of phenanthrene in the presence of exotic DOM increased first and decreased thereafter with increasing the added DOM concentrations (0-106mgDOC/L). The K(d)(*) values at a low exotic DOM concentration ( or =52mgDOC/L) of added exotic DOM clearly impeded the distribution of phenanthrene between soil and water. The effects of exotic and inherent DOM on phenanthrene sorption by soils may primarily be described as 'cumulative sorption', association of phenanthene with DOM in solution, and modified surface nature of soil solids due to DOM binding.

  16. DocSaludMental en netvibes

    Onís, Ricardo


    DocSaludMental es un escritorio virtual que, a partir de la plataforma netvibes, permite el acceso a información especializada y actualizada mediante la sindicación de contenidos a todos los profesionales de la red de salud mental en el Principado de Asturias DocSaludMental is a virtual desktop that allows access to expert information and updated from content syndication to all professionals in the mental health network in the Principality of Asturias

  17. DocSaludMental en netvibes

    Onís, Ricardo


    DocSaludMental es un escritorio virtual que, a partir de la plataforma netvibes, permite el acceso a información especializada y actualizada mediante la sindicación de contenidos a todos los profesionales de la red de salud mental en el Principado de Asturias DocSaludMental is a virtual desktop that allows access to expert information and updated from content syndication to all professionals in the mental health network in the Principality of Asturias

  18. Sorption of fibronectin to human root surfaces in vitro

    Mendieta, C.; Caravana, C.; Fine, D.H. (Columbia Univ., New York, NY (USA))


    The purpose of this study was to determine the conditions that favor the sorption and retention of human plasma fibronectin to cementum. Rectangular root segments prepared from teeth extracted for orthodontic reasons were mounted on a capillary pipette and immersed in solutions of {sup 125}I fibronectin for assay of cementum sorption under various conditions. Kinetic studies showed sorption to be rapid, with 77% of the maximum fibronectin sorption occurring within 1 minute. Fibronectin sorption was reduced when added in conjunction with serum and was inhibited by monovalent ions (such as sodium), but enhanced in the presence of divalent cations (such as calcium). Exposure of cementum to serum partially blocked subsequent sorption of fibronectin, while cementum bound fibronectin was eluted by subsequent exposure to serum. Treatment of cementum with citric acid pH 1.1 (4 minutes) followed by 5% sodium hypochlorite (5 minutes) caused a significant increase in fibronectin sorption with maximum retention upon subsequent exposure to serum (P less than 0.05). Fibronectin sorption to cementum was: rapid, electrostatic in nature, competitive, reversible, Ca+(+)-facilitated, and maximized by prior treatment of the root with citric acid and sodium hypochlorite. It is concluded that sorption of fibronectin to cementum can be achieved for clinical gain; however, conditions of application can significantly influence both accumulation and subsequent release of root sorbed material.

  19. Using polyacrylate-coated SPME fibers to quantify sorption of polar and ionic organic contaminants to dissolved organic carbon.

    Haftka, Joris J-H; Scherpenisse, Peter; Jonker, Michiel T O; Hermens, Joop L M


    A passive sampling method using polyacrylate-coated solid-phase microextraction (SPME) fibers was applied to determine sorption of polar and ionic organic contaminants to dissolved organic carbon (DOC). The tested contaminants included pharmaceuticals, industrial chemicals, hormones, and pesticides and represented neutral, anionic, and cationic structures. Prior to the passive sampler application, sorption of the chemicals to the fibers was characterized. This was needed in order to accurately translate concentrations measured in fibers to freely dissolved aqueous concentrations during the sorption tests with DOC. Sorption isotherms of neutral compounds to the fiber were linear, whereas isotherms of basic chemicals covered a nonlinear and a linear range. Sorption of acidic and basic compounds to the fiber was pH-dependent and was dominated by sorption of the neutral sorbate species. Fiber- and DOC-water partition coefficients of neutral compounds were both linearly related to octanol-water partition coefficients (log Kow). The results of this study show that polyacrylate fibers can be used to quantify sorption to DOC of neutral and ionic contaminants, having multiple functional groups and spanning a wide hydrophobicity range (log Kow = 2.5-7.5).


    L. E. Glagoleva


    Full Text Available The article presents information on the laws of the sorption of water to grow-negative polysaccharide complexes of the pumpkin and briar, deter-mined the rate constant of swelling as a function of temperature and pH, the maximum degree of swelling and limit the time to achieve it.

  1. Sorption of copper by chemically modified aspen wood fibers.

    Huang, Liyuan; Ou, Zhaoyang; Boving, Thomas B; Tyson, Julian; Xing, Baoshan


    Sorption of copper (Cu(2+)) by untreated and treated (bleaching and hydrolysis) aspen wood fibers, cellulose and lignin was examined to understand the Cu(2+) sorption behavior by these natural sorbents. All sorbents were characterized by solid-state (13)C NMR and FTIR. Bleaching broke up aromatic structures and increased hydrophilicity of the fibers, whereas hydrolysis decreased carbohydrate content, producing a more hydrophobic structure. Copper sorption was a function of pH; the percentage of Cu(2+) sorption steadily increased from pH 1.5 to 4.5 with a maximum sorption amount at around pH 5.5 for all the materials. All isotherms fitted well to the Langmuir equation. Bleached sample (BL) had a highest sorption capacity, followed by untreated (UTR), cellulose (CEL), and hydrolyzed (HHY), while lignin (LIG) had little Cu(2+) sorption under the studied conditions. The results suggested that carboxyl (-COOH) and hydroxyl (-CHOH) in carbohydrates are mainly responsible for Cu(2+) sorption, and that ion exchange may be a main sorption mechanism for the studied sorbents. Additionally, the sorption capacity for Cu(2+) on all sorbents decreased with the increase of the initial concentrations of Ca(2+), Na(+) or Al(3+). Copper sorption decreased rapidly at low initial concentrations of Ca(2+), Na(+) or Al(3+). However, the decline of Cu(2+) sorption slowed down when initial Na(+) and Ca(2+) concentration was higher than 0.05M or initial Al(3+) concentration was greater than 0.005M, indicating that specific adsorption may be taking place. Therefore, the majority of sorbed Cu(2+) to aspen wood fibers could be through ion exchange (especially, for UTR, BL and CEL), while a faction of sorbed Cu(2+) via inner-sphere complex (or specific adsorption).

  2. Sorption properties of wool

    Radetić Maja M.


    Full Text Available Strict ecological legislation, especially in highly developed countries, imposed requirements for the purification of industrial effluents and the need for efficient oil clean up after sea and inland water spills. Although numerous processes have been developed, the application of sorbents is still one of the most efficient methods to remove heavy metal ions, dyes and crude oil from water. Recently, special attention was paid to sorbents based on natural fibres. A review of studies concerning the sorption properties of wool is presented in this paper. The presence of various functional groups on the wool fibre surface contributes to the efficient sorption of heavy metal ions and dyes. A hydrophobic, scaly surface and fibre crimp strongly influence the high sorption capacity of wool for oil. Wool has great sorption potential even as a recycled material. Accordingly, it can be used as a viable substitute to commercially available synthetic sorbents that show poor biodegradab ility.

  3. Sorption of Pb(ll) by poly(hydroxamic acid) grafted oil palm empty fruit bunch.

    Haron, M J; Tiansin, M; Ibrahim, N A; Kassim, A; Wan Yunus, W M Z; Talebi, S M


    This paper describes the sorption of Pb(ll) from aqueous solution. Oil palm empty fruit bunch (OPEFB) fiber was first grafted with poly(methylacrylate) and then treated with hydroxylammonium chloride in alkaline medium to produce hydroxamic acid (PHA) grafted OPEFB. Sorption of Pb(ll) by PHA-OPEFB was maximum at pH 5. The sorption followed the Langmuir model with maximum capacityof 125.0 mg g-1 at 25 degrees C. The sorption process was exothermic, as shown by the negative value of enthalpy change, Delta H0. The free energy change (DeltaG0) for the sorption was negative, showing that the sorption process was spontaneous. A kinetic study showed that the Pb(ll) sorption followed a second order kinetic model.

  4. Sorption of roxarsone onto soils with different physicochemical properties.

    Fu, Qing-Long; He, Jian-Zhou; Blaney, Lee; Zhou, Dong-Mei


    Elevated roxarsone (ROX) concentrations in soils, caused by land application of ROX-bearing poultry litter, mandate investigation of ROX sorption onto soils. Equilibrium and kinetic studies of ROX sorption onto five soils were carried out to explore the relationship between sorption parameters and soil properties, and to reveal the effects of coexisting humic acid (HA), P(V), As(V), and As(III) on ROX transport. Experimental results indicated that ROX sorption reached equilibrium within 24 h, with pseudo-second order rate constants of 5.74-5.26 × 10(2) g/(mg h); film and intra-particle diffusion were the rate-limiting processes. ROX sorption to soils involved partitioning and adsorption phenomena; however, their relative contributions varied for different soils. The maximum ROX sorption varied with soil type, ranging from 0.59 to 4.12 mg/g. Results from correlation analysis and multiple linear regressions revealed that the maximum sorption capacities, partition coefficients, and desorption percentages were correlated with soil properties, especially iron content, total organic carbon, and dissolved organic carbon. ROX sorption to soils was affected more by soil pH than the initial pH of ROX-containing solutions. Carboxylic and amide functional groups were determined to be responsible for ROX sorption to soils. ROX sorption capacities decreased in the presence of HA, P(V), As(V), and As(III), indicating that ROX mobility in soils was facilitated by dissolved organic matter (DOM) and competing anions.

  5. Arsenic sorption onto laterite iron concretions: temperature effect.

    Partey, Frederick; Norman, David; Ndur, Samuel; Nartey, Robert


    We investigated arsenate and arsenite sorption onto laterite iron concretions (LIC) to test its suitability for use in the low-tech treatment of arsenic-bearing drinking water. Batch experiments on crushed LIC from Prestea, Ghana were conducted at a series of temperatures, ionic strengths, and pHs. The point of zero net charge on laterite iron concretion was determined by potentiometric titrations yielding an average pHp(ZNC) around 8.64. Experiments show that sorption capacity for both arsenite and arsenate increase with temperature. The equilibrium sorption capacity for arsenite was larger than that for arsenate over the 25 to 60 degrees C temperature range. A Langmuir model satisfactorily fits the arsenite and arsenate sorption isotherm data. Both arsenite and arsenate sorbed over the pH range of natural waters. Arsenite sorption increases with increasing solution pH to a maximum at pH 7, then decreases with further increase in solution pH. Arsenate sorption, on the other hand, shows little change with increasing solution pH. Increasing solution ionic strength 10-fold results in a slight increase in sorption. Ionic strength experiments show that an inner-sphere sorption mechanism is responsible for As (V) sorption on LIC, while As (III) sorption is by an outer-sphere mechanism. Gibbs free energy (DeltaG degrees) for arsenite and arsenate sorption onto LIC was calculated from Langmuir isotherms; the negative values agree with reaction spontaneity. The positive values of the standard enthalpy (DeltaH degrees) show the endothermic nature of arsenite and arsenate sorption onto LIC. Positive entropy (DeltaS degrees) values suggest the affinity of LIC for the arsenic species in solution. Analysis of the arsenic sorption data suggests that LIC can be used for low-tech natural-materials arsenic water treatment. Laterite iron concretions have a number of advantages for this use over commercial materials, including the ability to remove arsenic from waters with a wide


    Vasile Rusu


    Full Text Available Studies of the sorption capacity towards Cu2+ ions of diatomite from the Ghidirim location of RM, as well as of the extracted clay phase are presented. Separated clay fraction from diatomic material is clean enough, and especially is rich in montmorillonite. Maximum sorption capacity for studied clay fraction is achieved by rising the temperature of calcination treatment up to 200oC. At higher temperatures the lattice of montmorillonite is contracted and its sorption capacity towards Cu2+ ions decreases strongly.

  7. Competitive sorption of cadmium and lead in acid soils of central Spain

    Serrano, S.; Garrido, F.; Campbell, C.G.; Garcia-Gonzolez, Maria Teresa


    The bioavailability and ultimate fate of heavy metals in the environment are controlled by chemical sorption. To assess competitive sorption of Pb and Cd, batch equilibrium experiments (generating sorption isotherms) and kinetics sorption studies were performed using single and binary metal solutions in surface samples of four soils from central Spain. For comparisons between soils, as well as, single and binary metal solutions, soil chemical processes were characterized using the Langmuir equation, ionic strength, and an empirical power function for kinetic sorption. In addition, soil pH and clay mineralogy were used to explain observed sorption processes. Sorption isotherms were well described by the Langmuir equation and the sorption kinetics were well described by an empirical power function within the reaction times in this study. Soils with higher pH and clay content (characterized by having smectite) had the greatest sorption capacity as estimated by the maximum sorption parameter (Q) of the Langmuir equation. All soils exhibited greater sorption capacity for Pb than Cd and the presence of both metals reduced the tendency for either to be sorbed although Cd sorption was affected to a greater extent than that of Pb. The Langmuir binding strength parameter (k) was always greater for Pb than for Cd. However, these k values tended to increase as a result of the simultaneous presence of both metals, that may indicate competition for sorption sites promoting the retention of both metals on more specific sorption sites. The kinetic experiments showed that Pb sorption is initially faster than Cd sorption from both single and binary solutions although the simultaneous presence of both metals affected the sorption of Cd at short times while only a minor effect was observed on Pb. The estimated exponents of the kinetic function were in all cases smaller for Pb than for Cd, likely due to diffusion processes into micropores or interlayer space of the clay minerals which


    生秀杰; 周伟强; 姜莉; 张梅英; 王太一; 张学


    Objective: To detect the expression and the genomic sequence of Doc-1R gene in mice. Methods: The gene specific primers were designed and synthesized according to the eDNA sequence of Doc-1R gene. The sequence of Doc-1R gene was cloned by nested PCR. The expression of Doe-1R gene was examined by RT-PCR in thirteen kinds of tissues of mice. Results: The mouse Doc-1R gene has been obtained by two times genomic walking, which spans 2787bp and contains four exons and three introns. All of the splice donor/aeceptor site sequences are in accordance with the consensus "GT-AG" rule. There was expression of Doc-1R gene in the thirteen tissues. Conclusion: The mouse Doc-1R gene was cloned successfully. The expression pattern suggests that Doc-1R gene is a housekeeping gene,which is important to keep the function of tissues and organs.

  9. Enhancement of CO2 sorption uptake on hydrotalcite by impregnation with K2CO3.

    Lee, Jung Moo; Min, Yoon Jae; Lee, Ki Bong; Jeon, Sang Goo; Na, Jeong Geol; Ryu, Ho Jung


    The awareness of symptoms of global warming and its seriousness urges the development of technologies to reduce greenhouse gas emissions. Carbon dioxide (CO(2)) is a representative greenhouse gas, and numerous methods to capture and storage CO(2) have been considered. Recently, the technology to remove high-temperature CO(2) by sorption has received lots of attention. In this study, hydrotalcite, which has been known to have CO(2) sorption capability at high temperature, was impregnated with K(2)CO(3) to enhance CO(2) sorption uptake, and the mechanism of CO(2) sorption enhancement on K(2)CO(3)-promoted hydrotalcite was investigated. Thermogravimetric analysis was used to measure equilibrium CO(2) sorption uptake and to estimate CO(2) sorption kinetics. The analyses based on N(2) gas physisorption, X-ray diffractometry, Fourier transform infrared spectrometry, Raman spectrometry, transmission electron microscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy were carried out to elucidate the characteristics of sorbents and the mechanism of enhanced CO(2) sorption. The equilibrium CO(2) sorption uptake on hydrotalcite could be increased up to 10 times by impregnation with K(2)CO(3), and there was an optimal amount of K(2)CO(3) for a maximum equilibrium CO(2) sorption uptake. In the K(2)CO(3)-promoted hydrotalcite, K(2)CO(3) was incorporated without changing the structure of hydrotalcite and it was thermally stabilized, resulting in the enhanced equilibrium CO(2) sorption uptake and fast CO(2) sorption kinetics.

  10. Characteristics of Amine Surfactant Modified Peanut Shell and Its Sorption Property for Cr(VI)

    岳敏; 张猛; 刘斌; 许醒; 李小明; 岳钦艳; 马春元


    Modified peanut shell (MPS) was prepared by amination reaction with peanut shell (PS) as the starting material. The sorption of Cr(VI) oxyanions on MPS in static and column tests were investigated. In addition, the sorption isotherm and kinetic models were applied to confirm the sorption capacity and the sorption mechanisms. BET surface area analysis showed the physicochemical characteristics of the samples. The results of zeta potential, Fourier transform infrared (FT-IR) and Raman spectra analysis illustrated that chemical adsorption and ion ex-change are the potential sorption mechanism. The static sorption test showed that the maximum sorption capacity (qmax) of MPS for Cr(VI) increased with temperature, which indicated that the Cr(VI) sorption process was endo-thermic. The saturated sorption capacity of Cr(VI) in the column sorption test was 138.34 mg·g-1, which accounted for 93.9%of the qmax at 25 °C. The regeneration capacity of MPS was evaluated using HCl solution as an eluent. The high regeneration efficiency (82.6%) validated the dominance of the ion exchange mechanism in the Cr(VI) sorption process with Cl-ions displacing Cr(VI) oxyanion on MPS. The Langmuir isotherm model showed a higher correlation coefficient than the other adsorption isotherm models. And in the kinetic study, a pseudo-second-order model fit the data best.

  11. Sorption of cesium ions by nanostructured calcium aluminosilicates

    Gordienko, P. S.; Shabalin, I. A.; Yarusova, S. B.; Suponina, A. P.; Zhevtun, I. G.


    Data on the sorption properties of synthetic calcium aluminosilicates (CASes) with Al: Si ratios of 2: 2, 2: 6, and 2: 10, fabricated within the multicomponent system CaCl2-AlCl3-KOM-SiO2-H2O, are presented. Isotherms of the sorption of Cs+ ions from aqueous solutions with Cs+ concentrations of 0.2 to 6.0 mmol L-1 are analyzed. The CAS maximum sorption capacity and the Langmuir constants are determined. Kinetic data are obtained, and the energy of cation-exchange activation upon the sorption of Cs+ ions is determined. The effect of a salt background (1% KCl + 6% NaCl) has on the values of distribution coefficient ( K d) and the degree of Cs+ ion removal is established.

  12. Siderophore sorption to clays.

    Maurice, Patricia A; Haack, Elizabeth A; Mishra, Bhoopesh


    Siderophores are low molecular weight organic ligands exuded by some aerobic organisms and plants to acquire Fe under Fe-limited conditions. The hydroxamate siderophores may sorb to aluminosilicate clays through a variety of mechanisms depending upon the nature of the clay and of the siderophore along with solution conditions such as pH, ionic strength, and presence of metal cations. They may also affect metal binding to clays. Here, we review previous studies of siderophore sorption to aluminosilicate clays; briefly discuss how the techniques of X-ray diffractometry, Fourier-transform infrared spectroscopy, and X-ray absorption spectroscopy may be applied to such studies; review effects of siderophores on metal sorption to clays; and highlight some areas for future research.




    This report presents information and references to aid in the selection of 99Tc sorption media for feasibility studies regarding the removal of 99Tc from Hanford's low activity waste. The report contains literature search material for sorption media (including ion exchange media) for the most tested media to date, including SuperLig 639, Reillex HPQ, TAM (Kruion), Purolite A520E and A530E, and Dowex 1X8. The U.S. Department of Energy (DOE), Office of River Protection (ORP) is responsible for management and completion of the River Protection Project (RPP) mission, which comprises both the Hanford Site tank farms and the Waste Treatment and Immobilization Plant (WTP). The RPP mission is to store, retrieve and treat Hanford's tank waste; store and dispose of treated wastes; and close the tank farm waste management areas and treatment facilities in a safe, environmentally compliant, cost-effective and energy-effective manner.

  14. Changes in DOC treatability: Indications of compositional changes in DOC trends

    Worrall, F.; Burt, T. P.


    SummaryThis study considers long-term records of the nature of water colour and coincident water quality and quantity in order to test hypotheses about increases in release of dissolved organic carbon from peat soils across the northern hemisphere. The study focuses upon the treatment ratio, i.e. the ratio of the amount of coagulant dose required to the water colour of the incoming water, and compares this ratio to possible explanatory variables: pH, conductivity, water temperature, river flow and alkalinity. The study shows that: The annual average increase in treatment ratio is just less than 6.5% over a six year period. There is a long-term increase in the treatment ratio that is independent of changes in riverflow, pH, conductivity, water temperature and alkalinity and so a real change in DOC composition is occurring. There is a seasonal cycle in treatment ratio that is also independent of the available water and climate variables. The upward trend in treatment ratio is declining with time over the study period. The observed trends in DOC composition are consistent with an explanation of increasing DOC concentration and flux based upon changes in flow and temperature but is not consistent with present explanations based upon changes in atmospheric deposition or upon drought unless the effect of the drought are short-lived (1-2 years).

  15. Description of the phosphorus sorption and desorption processes in lowland peaty clay soils

    Schoumans, O.F.


    To determine phosphorus (P) losses from agricultural land to surface water, information is needed about the behavior of P in soils. In this study, the sorption and desorption characteristics of lowland peaty clay soils are described based on experimental laboratory studies. The maximum P sorption ca

  16. Sorption of actinides onto nanodiamonds

    Buchatskaya, Yulia; Romanchuk, Anna; Yakovlev, Ruslan; Kulakova, Inna [Lomonosov Moscow State Univ., Moscow (Russian Federation). Dept. of Chemistry; Shiryaev, Andrei [Russian Academy of Sciences, Moscow (Russian Federation). Frumkin Institute of Physical Chemistry and Electrochemistry; Russian Academy of Sciences, Moscow (Russian Federation). Inst. of Geology of Ore Deposits, Petrography, Mineralogy and Geochemistry; Kalmykov, Stepan [Lomonosov Moscow State Univ., Moscow (Russian Federation). Dept. of Chemistry; Russian Academy of Sciences, Moscow (Russian Federation). Frumkin Institute of Physical Chemistry and Electrochemistry; Russian Academy of Sciences, Moscow (Russian Federation). Vernadsky Institute of Geochemistry and Analytical Chemistry


    Detonation nanodiamonds (ND) present a significant part of nanocarbons group, which could be produced on commercial scale by detonation of explosives in a closed chamber. Their unique properties of high surface area, low weight and radiation resistance make ND a prospective candidate for applications in sorption processes in radiochemistry. To study the influence of surface chemistry on sorption properties, apristine sample of ND was treated with acids and hydrogen. The surface chemistry of the samples was characterised by infrared spectroscopy, X-ray photoelectron spectroscopy and Boehm titration. The sorption properties of ND were tested fordifferent radionuclides. The sorption capacity of ND was shown to be higher than those of commonly used radionuclide sorbents like activated carbon and compariable to other members of nanocarbon group like graphene oxide and carbon nanotubes. The sorption properties were shown to be influenced by the presence of oxygen-containing groups on the surface of ND. This represents an opportunity to increase the sorption capacity of ND.


    ZHANG Lei; SONG Feng-bin


    Four soils, phaeozem (PM), saline-alkali soil (SA), meadow albic bleached soil (MA) and dark brown forest soil (DB) from Northeast China were used to examine the sorption and desorption characteristics of Cd and pH influence on it. According to sorption experiment without pH control, the order of amount of absorbed Cd by soils was:SA>PM>DB>MA. The results from non-linear fitting method showed that Langmuir and Freundrich models were more adaptable than Temkin model in describing the sorption data. The maximum sorption amounts from Langmuir model were: PM>SA>MA>DB. Exponential equation for PM and SA and quadratic equation for MA and DB were suitable to fit the desorption data. The order of average desorption percentage was: MA>DB>PM>SA. The amounts of sorption by PM, DB and MA reached the maximum in pH 9.0, while sorption by SA was linearly increased in the experimental range of pH 3.3-11.4. In uniform pH, however, Cd sorption by SA was the minimum among four soils, which indicated that the more amounts of Cd absorbed by SA in isotherm sorption were ascribed to the higher soil pH. The higher sorption of Cd in PM resulted from the higher percentage of organic matter and clay components.

  18. A comparative study of phosphate sorption in lowland soils under oxic and anoxic conditions

    Heiberg, Lisa; Pedersen, Thomas Vils; Jensen, Henning S.;


    of 36 to 93% of the dithionite-extractable FeIII (FeBD). Langmuir fitted Pi sorption isotherms showed a Pi release of up to 1.1 mmol kg-1 in six soils when Pi concentrations in the matrix (Psol) were lower than 10 µM. Phosphate desorption was attributed to dissolution of amorphous iron oxides......Received for publication June 13, 2009. Phosphate (Pi) release due to FeIII oxide dissolution is well documented for soils undergoing reduction. The Pi sorption properties of soils in anoxic conditions are, however, still under consideration. In this investigation, Pi sorption to strictly anoxic...... FeII phosphates may have caused the higher sorption capacities. Use of maximum sorption capacity (Smax) is therefore misleading as a measure of Pi sorption at low Psol concentrations. The results demonstrate that none of the strongly anoxic soils, irrespective of the initial FeIII oxide content...

  19. Capacity and mechanisms of ammonium and cadmium sorption on different wetland-plant derived biochars

    Cui, Xiaoqiang [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); Hao, Hulin [Ningbo Raw Water Resource Research Academy, Ningbo (China); Zhang, Changkuan [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); He, Zhenli [Indian River Research and Education Center, Institute of Food and Agricultural Sciences, University of Florida, Fort Pierce, FL 34945 (United States); Yang, Xiaoe, E-mail: [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China)


    The objective of this study was to investigate the relationship between Cd{sup 2+}/NH{sub 4}{sup +} sorption and physicochemical properties of biochars produced from different wetland plants. Biochars from six species of wetland plants (i.e., Canna indica, Pennisetum purpureum Schum, Thalia dealbata, Zizania caduciflora, Phragmites australis and Vetiveria zizanioides) were obtained at 500 °C and characterized, and their sorption for ammonium and cadmium was determined. There were significant differences in elemental composition, functional groups and specific surface area among the biochars derived from different wetland plant species. Sorption of ammonium and cadmium on the biochars could be described by a pseudo second order kinetic model, and the simple Langmuir model fits the isotherm data better than the Freundlich or Temkin model. The C. indica derived biochar had the largest sorption capacity for NH{sub 4}{sup +} and Cd{sup 2+}, with a maximum sorption of 13.35 and 125.8 mg g{sup −1}, respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3 mg g{sup −1}) for Cd{sup 2+}. Ammonium sorption was mainly controlled by cation exchange, surface complexation with oxygen-containing functional groups and the formation of magnesium ammonium phosphate compounds, whereas for Cd{sup 2+} sorption, the formation of cadmium phosphate precipitates, cation exchange and binding to oxygen-containing groups were the major possible mechanisms. In addition, the sorption of ammonium and cadmium was not affected by surface area and microporosity of the biochars. - Highlights: • Biochars varied in physicochemical properties and adsorption capacity. • Canna indica derived biochar has a high sorption capacity for Cd{sup 2+}. • NH{sub 4}{sup +} and Cd{sup 2+} sorption on biochars fits a pseudo second order and Langmuir model. • Sorption mechanism is related to complexation, cation exchange and precipitation.

  20. Sorption product heat pump

    Antonini, G.; Francois, O.; Gendarme, J.P.; Guilleminot, J.J.; Meunier, F.


    A continuous operating, and thus with enhanced performance, heat pump is presented. In this heat pump, the heat transfer between the hot source and the output system or network is realized through a solid adsorbent-refrigerant couple having endothermal desorption properties and exothermal adsorption or absorption properties. The sorption products are carried in a closed cycle movement between the two parts of the reactor. Each side of the reactor is assuming always the same function and the thermal inertia have to be overcome only when starting the reactor.

  1. Influence of hydrological pulse on bacterial growth and DOC uptake in a clear-water Amazonian lake.

    Farjalla, Vinicius F; Azevedo, Debora A; Esteves, Francisco A; Bozelli, Reinaldo L; Roland, Fabio; Enrich-Prast, Alex


    This study was conducted to evaluate: (1) the bacterial growth and the dissolved organic carbon (DOC) uptake in an Amazonian lake (Lake Batata) at high-water and low-water periods of the flood pulse; (2) the influence of nitrogen and phosphorus (NP) additions on bacterial growth and DOC uptake in Lake Batata at two flood pulse periods; and (3) the bioavailability of the main DOC sources in Lake Batata. Lake Batata is a typical clear-water Amazonian lake, located in the watershed of Trombetas River, Central Amazon, Brazil. Bacterial batch cultures were set up with 90% 0.2-microm filtered water and 10% inoculum from Lake Batata. N-NH(4)NO(3) and P-KH(2)PO(4), with final concentrations of 50 and 5 microM, respectively, were added to the cultures, except for controls. Extra sources of DOC (e.g., algal lysate, plant leachates) were added to constitute six distinct treatments. Bacterial response was measured by maximum bacterial abundance and rates of bacterial production, respiration, DOC uptake, and bacterial growth efficiency (BGE). Bacterial growth and DOC uptake were higher in NP treatments than in controls, indicating a consistent nutrient limitation in Lake Batata. The composition of DOC also seems to be an important regulating factor of bacterial growth in Lake Batata. Seasonally, bacterial growth and DOC bioavailability were higher at low-water period, when the phytoplankton is a significant extra source of DOC, than at high-water period, when the forest is the main source of DOC. DOC bioavailability was better estimated based on the diversity and the diagenetic stage of carbon compounds than on single classes of labile compounds. Changes in BGE were better related to CNP stoichiometry in the water, and the "excess" of organic substrates was oxidized in catabolism, despite the quality of these compounds for bacterial growth. Finally, we conclude that bacterial growth and DOC uptake vary throughout the flood pulse in clear-water Amazonian ecosystems as a result

  2. CO2 Sorption to Subsingle Hydration Layer Montmorillonite Clay Studied by Excess Sorption and Neutron Diffraction Measurements

    Rother, Gernot; Ilton, Eugene S.; Wallacher, Dirk; Hauβ, Thomas; Schaef, Herbert T.; Qafoku, Odeta; Rosso, Kevin M.; Felmy, Andrew R.; Krukowski, Elizabeth G.; Stack, Andrew G.; Grimm, Nico; Bodnar, Robert J.


    Geologic storage of CO2 requires that the caprock sealing the storage rock is highly impermeable to CO2. Swelling clays, which are important components of caprocks, may interact with CO2 leading to volume change and potentially impacting the seal quality. The interactions of supercritical (sc) CO2 with Na saturated montmorillonite clay containing a subsingle layer of water in the interlayer region have been studied by sorption and neutron diffraction techniques. The excess sorption isotherms show maxima at bulk CO2 densities of ≈0.15 g/cm3, followed by an approximately linear decrease of excess sorption to zero and negative values with increasing CO2 bulk density. Neutron diffraction experiments on the same clay sample measured interlayer spacing and composition. The results show that limited amounts of CO2 are sorbed into the interlayer region, leading to depression of the interlayer peak intensity and an increase of the d(001) spacing by ca. 0.5 Å. The density of CO2 in the clay pores is relatively stable over a wide range of CO2 pressures at a given temperature, indicating the formation of a clay-CO2 phase. Finally, at the excess sorption maximum, increasing CO2 sorption with decreasing temperature is observed while the high-pressure sorption properties exhibit weak temperature dependence.

  3. Kinetic Model of the Sorption of Cu2+ and Pb2+ From Aqueous Solution Using Carbonized Treculia Africana Husk as Biomass

    , A.K. Asiagwu; , P.E Omuku; , J.I. Odiachi; , V.N. Okafor


    The sorption kinetics of model (Cu2+ and Pb“) from aqueous solution using carbonized Africana brad fruit (Treculia Africana) husk was investigated. The effect of contact time, variation in mass and particle size of adsorbent and adsorption isotherms were studied. The time-dependent experiment showed rapid sorption between 15-30 minutes with maximum sorption at 30mins, after which the rate of adsorption became almost constant. The sorption capacity is dependent on its particle size. A particle...

  4. 48 CFR 1329.203-70 - DOC Federal tax exemption.


    ... 48 Federal Acquisition Regulations System 5 2010-10-01 2010-10-01 false DOC Federal tax exemption. 1329.203-70 Section 1329.203-70 Federal Acquisition Regulations System DEPARTMENT OF COMMERCE GENERAL CONTRACTING REQUIREMENTS TAXES Federal Excise Taxes 1329.203-70 DOC Federal tax exemption. (a) The Office...

  5. 76 FR 9210 - Draft DOC National Aquaculture Policy


    ... DOC National Aquaculture Policy AGENCY: Commerce. ACTION: Notice of availability of draft aquaculture... draft national aquaculture policy that supports sustainable aquaculture in the United States. The intent of the policy is to guide DOC's actions and decisions on aquaculture and to provide a...

  6. Evaluation of terrestrial plants extracts for uranium sorption and characterization of potent phytoconstituents.

    Sharma, Sunita; Singh, Bikram; Thulasidas, S K; Kulkarni, Madhuri J; Natarajan, V; Manchanda, Vijay K


    Sorption capacity of four plants (Funaria hygrometrica, Musa acuminata, Brassica juncea and Helianthus annuus) extracts/fractions for uranium, a radionuclide was investigated by EDXRF and tracer studies. The maximum sorption capacity, i.e., 100% (complete sorption) was observed in case of Musa acuminata extract and fractions. Carbohydrate, proteins, phenolics and flavonoids contents in the active fraction (having maximum sorption capacity) were also determined. Further purification of the most active fraction provided three pure molecules, mannitol, sorbitol and oxo-linked potassium oxalate. The characterization of isolated molecules was achieved by using FTIR, NMR, GC-MS, MS-MS, and by single crystal-XRD analysis. Of three molecules, oxo-linked potassium oxalate was observed to have 100% sorption activity. Possible binding mechanism of active molecule with the uranyl cation has been purposed.

  7. Maximum Fidelity

    Kinkhabwala, Ali


    The most fundamental problem in statistics is the inference of an unknown probability distribution from a finite number of samples. For a specific observed data set, answers to the following questions would be desirable: (1) Estimation: Which candidate distribution provides the best fit to the observed data?, (2) Goodness-of-fit: How concordant is this distribution with the observed data?, and (3) Uncertainty: How concordant are other candidate distributions with the observed data? A simple unified approach for univariate data that addresses these traditionally distinct statistical notions is presented called "maximum fidelity". Maximum fidelity is a strict frequentist approach that is fundamentally based on model concordance with the observed data. The fidelity statistic is a general information measure based on the coordinate-independent cumulative distribution and critical yet previously neglected symmetry considerations. An approximation for the null distribution of the fidelity allows its direct conversi...

  8. Assessing the relative bioavailability of DOC in regional groundwater systems

    Chapelle, Francis H.; Bradley, Paul M.; Journey, Celeste; McMahon, Peter B.


    It has been hypothesized that the degree to which a hyperbolic relationship exists between concentrations of dissolved organic carbon (DOC) and dissolved oxygen (DO) in groundwater may indicate the relative bioavailability of DOC. This hypothesis was examined for 73 different regional aquifers of the United States using 7745 analyses of groundwater compiled by the National Water Assessment (NAWQA) program of the U.S. Geological Survey. The relative reaction quotient (RRQ), a measure of the curvature of DOC concentrations plotted versus DO concentrations and regressed to a decaying hyperbolic equation, was used to assess the relative bioavailability of DOC. For the basalt aquifer of Oahu, Hawaii, RRQ values were low (0.0013 mM−2), reflecting a nearly random relationship between DOC and DO concentrations. In contrast, on the island of Maui, treated sewage effluent injected into a portion of the basalt aquifer resulted in pronounced hyperbolic DOC-DO behavior and a higher RRQ (142 mM−2). RRQ values for the 73 aquifers correlated positively with mean concentrations of ammonia, dissolved iron, and manganese, and correlated negatively with mean pH. This indicates that greater RRQ values are associated with greater concentrations of the final products of microbial reduction reactions. RRQ values and DOC concentrations were negatively correlated with the thickness of the unsaturated zone (UNST) and depth to the top of the screened interval. Finally, RRQ values were positively correlated with mean annual precipitation (MAP), and the highest observed RRQ values were associated with aquifers receiving MAP rates ranging between 900 and 1300 mm/year. These results are uniformly consistent with the hypothesis that the hyperbolic behavior of DOC-DO plots, as quantified by the RRQ metric, can be an indicator of relative DOC bioavailability in groundwater systems.

  9. Sorption Behaviours of Exfoliated Graphite

    戴光泽; 伍川辉


    Exfoliated graphite (EG) is selected as a new kind of sorbent to sorb heavy oil spilled. In order to make use of EG more effectively, some basic experiments are performed to investigate its sorption properties,i.e., specific sorption, height of saturation layer, sorption time constant. In the present experiments, A-grade heavy oil is employed as a standard sorbate. It is concluded that 1) under the condition that the area of solid (filter bottom)-liquid (heavy oil) interface is a constant, specific sorption usually decreases when the amount of EG filled or the apparent bulk density increase; however, the specific sorption initially increases when the apparent bulk density is too low and the amount of EG filled is too much; 2) under the condition that the apparent bulk density of EG filled is a constant, the sorption time constant tends to increase when the amount of EG filled increases; however, for a constant amount of EG filled, the sorption time constant will decrease when the apparent bulk density increases.

  10. Sorption of sulphamethoxazole by the biochars derived from rice straw and alligator flag.

    Li, Tingqiang; Han, Xuan; Liang, Chengfeng; Shohag, M J I; Yang, Xiaoe


    The sorption ability of sulphamethoxazole (SMX) by biochar derived from rice straw (RS) and alligator flag (AF) at 600°C was studied to assess the ability of biochar as adsorbent to remove SMX from aqueous solution. The results indicated that sorption of SMX by biochars was well described using the Langmuir equation (R2>0.94), and the maximum sorption parameter (Q) of RS (3650 mg kg(-1)) was much higher than that of AF (1963 mg kg(-1)). Temperature had no effect on SMX sorption by biochars, while thermodynamics analysis indicated that the sorption of SMX on both biochars was a spontaneous physical process. The d 250 RS (diameter of RS sieved through 250 µm) and d 150 AF (diameter of AF sieved through 150 µm) showed excellent sorption ability for SMX. The sorption amount of RS was larger than that of AF when pH<7, whereas, the sorption amount of AF surpassed RS when pH≥7. The presence of Cu2+ and/or Cd2+ ion at low concentrations (20 mg L(-1)) significantly (P<0.05) increased the sorption of SMX on both RS and AF. Our study confirms that biochar derived from the wetland plants could be used as effective adsorbents to remove SMX from aqueous solution.

  11. Effect of dissolved organic matter on ammonium sorption kinetics and equilibrium to Chinese clinoptilolite.

    Zhang, Ying; Bi, Erping


    In the in-situ remediation of ammonium (NH4+) in groundwater by a sequential reactive barrier filled with zeolite, it is of great importance to understand the mechanisms of NH4+ sorption to zeolite. In this study, the effect of dissolved natural organic matter on NH4+ sorption to natural Chinese clinoptilolite was studied by batch experiments taking humic acid (HA) as a model substance. The surface of clinoptilolite was characterized by scanning electronic microscopy (SEM). A needle cluster of sorbed HA could be observed on the surface of the clinoptilolite. The negative effect of HA on NH4+ sorption is thought to be their competition for sorption sites, the surface coverage and blockage of the pores of clinoptilolite by HA. The fitting results of kinetic sorption data indicated that the rate-controlling step for NH4+ sorption by clinoptilolite in both NH4+ and NH4+ + HA systems is the heterogeneous chemisorption. The existence of HA (10 mg/L) significantly reduced the initial sorption rate of NH4+, but the effect of a further concentration increase of HA was slight. The effect of HA on maximum sorption capacity was found to be insignificant in the experiments. A high aqueous Ca2+ concentration can decrease the negative effect of HA on NH4+ sorption by precipitation of calcium humate.

  12. The biogeochemistry of carbon cycle in summer of the Prydz Bay,Antarctic Ⅰ :Characteristics of DOC distribution

    扈传昱; 潘建明; 刘小涯; 张海生


    The distributions and changes of dissolved organic carbon in the Prydz Bay and out open sea were investigated during CHINARE-15 ( the 15th Chinese National Antarctic Research Expedition). The results showed that the content of DOC was higher in the Prydz Bay and outer open sea compared to those typical of surface oceanic levels ( 70-80 μM) , average content of DOC in the surface water was 102.32 μM,the range was 68.23-125.92 μM. The vertical distribution of DOC in the water column was similar to many ocean sites, that is to say, the content of upper water is higher than deep water, a subsurface maximum persisted between 25-50 m. The DOC pool in the Prydz Bay were consisted with labile, semi-labile and refractory pools, in which refractory pools was mainly part. The concentration of refractory DOC was 92.34 and 76.89 μM in Prydz Bay and outer open sea, and account 77% and 82% for total DOC, respectively.

  13. Sorption isotherms and isosteric heats of sorption of Malaysian paddy.

    Mousa, Wael; Ghazali, Farinazleen Mohamad; Jinap, S; Ghazali, Hasanah Mohd; Radu, Son


    Understanding the water sorption characteristics of cereal is extremely essential for optimizing the drying process and ensuring storage stability. Water relation of rough rice was studied at 20, 30, 40 and 50 °C over relative humidity (RH.) between 0.113 and 0.976 using the gravimetric technique. The isotherms displayed the general sigmoid, Type II pattern and exhibited the phenomenon of hysteresis where it was more pronounced at lower temperatures. The sorption characteristics were temperature dependence where the sorption capacity of the paddy increased as the temperature was decreased at fixed (RH). Among the models assessed for their ability to fit the sorption data, Oswin equation was the best followed by the third order polynomial, GAB, Smith, Chung-Pfost, and Henderson models. The monolayer moisture content was higher for desorption than adsorption and tend to decrease with the increase in temperature. Given the temperature dependence of the sorption isotherms the isosteric heats of sorption were calculated using Claussius-Clapeyron equation. The net isosteric heats decreased as the moisture content was increased and heats of desorption were greater than that of adsorption.

  14. DOC-a file system cache to support mobile computers

    Huizinga, D. M.; Heflinger, K.


    This paper identifies design requirements of system-level support for mobile computing in small form-factor battery-powered portable computers and describes their implementation in DOC (Disconnected Operation Cache). DOC is a three-level client caching system designed and implemented to allow mobile clients to transition between connected, partially disconnected and fully disconnected modes of operation with minimal user involvement. Implemented for notebook computers, DOC addresses not only typical issues of mobile elements such as resource scarcity and fluctuations in service quality but also deals with the pitfalls of MS-DOS, the operating system which prevails in the commercial notebook market. Our experiments performed in the software engineering environment of AST Research indicate not only considerable performance gains for connected and partially disconnected modes of DOC, but also the successful operation of the disconnected mode.

  15. Too Few Women, Docs Understand Dangers of Heart Disease

    ... html Too Few Women, Docs Understand Dangers of Heart Disease It kills more than all cancers combined, but ... 22, 2017 THURSDAY, June 22, 2017 (HealthDay News) -- Heart disease is the leading killer of U.S. women, but ...

  16. Investigating Forest Harvest Effects on DOC Concentration and Quality: An In Situ, High Resolution Approach to Quantifying DOC Export Dynamics

    Jollymore, A. J.; Johnson, M. S.; Hawthorne, I.


    Justification: Forest harvest effects on water quality can signal alterations in hydrologic and ecologic processes incurred as a result of forest harvest activities. Organic matter (OM), specifically dissolved organic carbon (DOC), plays a number of important roles mediating UV-light penetration, redox reactivity and microbial activity within aquatic ecosystems. Quantification of DOC is typically pursued via grab sampling followed by chemical or spectrophotometric analysis, limiting the temporal resolution obtained as well as the accuracy of export calculations. The advent of field-deployable sensors capable of measuring DOC concentration and certain quality characteristics in situ provides the ability to observe dynamics at temporal scales necessary for accurate calculation of DOC flux, as well as the observation of dynamic changes in DOC quality on timescales impossible to observe through grab sampling. Methods: This study utilizes a field deployable UV-Vis spectrophotometer (spectro::lyzer, s::can, Austria) to investigate how forest harvest affects DOC export. The sensor was installed at an existing hydrologic monitoring site at the outlet of a headwater stream draining a small (91 hectare) second growth Douglasfir-dominated catchment near Campbell River on Vancouver Island, British Columbia. Measurement began late in 2009, prior to forest harvest and associated activities such as road building (which commenced in October 2010 and ended in early 2011), and continues to present. During this time - encompassing the pre, during and post-harvest conditions - the absorbance spectrum of stream water from 200 to 750 nm was measured. DOC concentration and spectroscopic indices related to DOC quality (including SUVA, which relates to the concentration of aromatic carbon, and spectral slope) were subsequently calculated for each spectra obtained at 30-minute intervals. Results and conclusions: High frequency measurements of DOC show that overall export of OM increased in

  17. Phosphate sorption-desorption characteristics in two Inceptisols and an Alfisol of Chattisgarh, India

    A. K. DOLUI; S. S. ROY


    Two Inceptisols and an Alfisol of the Indravati Catchment area in Chattisgarh, India, comprising several gradients in physical and chemical properties were studied to relate phosphate sorption and desorption to soil properties. From the P isotherm curve, the standard P requirement (SPR) of the soils was determined. Phosphate sorption data were also fitted both to the Langmuir and Freundlich Equations. The mean sorption maximum values for three different soil series were: Bastar > Geedam > Mosodi. The fraction of added phosphate sorbed for the 3 series followed this same trend as did SPR; the phosphate sorption maximum and the maximum phosphate buffering capacity, which were estimated by the Langmuir isotherm; and the Freundlich constant 1/n. However, phosphate desorption, as well as the maximum recovery percent did not follow this order. The phosphate affinity constant (K) was also different following the same progression for the 3 soil series as the Freundlich constant K′, which measured sorption strength. Meanwhile, an inverse order existed for K and K′ versus the percent desorbed relative to the sorbed as well as the maximum recovery percent. In addition,significant correlation coefficients among sorption parameters of P and soil factors were found.

  18. Modeling polychlorinated biphenyl sorption isotherms for soot and coal

    Jantunen, A.P.K.; Koelmans, A.A.; Jonker, M.T.O. [University of Utrecht, Utrecht (Netherlands)


    Sorption isotherms (pg-ng/L) were measured for 11 polychlorinated biphenyls (PCBs) of varying molecular planarity from aqueous solution to two carbonaceous geosorbents, anthracite coal and traffic soot. All isotherms were reasonably log-log-linear, but smooth for traffic soot and staircase-shaped for coal, to which sorption was stronger and more nonlinear. The isotherms were modeled using seven sorption models, including Freundlich, (dual) Langmuir, and Polanyi-Dubinin-Manes (PDM). PDM provided the best combination of reliability and mechanistically-interpretable parameters. The PDM normalizing factor Z appeared to correlate negatively with sorbate molecular volume, dependent on the degree of molecular planarity. The modeling results supported the hypothesis that maximum adsorption capacities (Q{sub max}) correlate positively with the sorbent's specific surface area. Q{sub max} did not decrease with increasing sorbate molecular size, and adsorption affinities clearly differed between the sorbents. Sorption was consistently stronger but not less linear for planar than for nonplanar PCBs, suggesting surface rather than pore sorption.

  19. Oil spill sorption using raw and acetylated sugarcane bagasse

    Reza Behnood; Bagher Anvaripour; Nematollah Jaafarzadeh; Masoome Farasati


    In the recent decades oil spills in the aquatic environments are one of the major sources of environmental pollutions, which are steadily growing with the increase in oil consumption. Adsorption is a rapid and cost effective processto minimize the environmental impacts of oil spills andcleanup these pollutants. In this work, the crude oil sorption capacity was examined with raw sugarcane bagasse and acetylated sugarcane bagasse. Results show that the acetylated bagasse was significantly more oleophilic than the raw bagasse and acetylation reaction can increase bagasse oil sorption ability by about 90%. The maximum sorption capacities of acetylated bagasse were obtained about 11.3 g and 9.1 g in dry system (crude oil sorption) and oil layer sorption, respectively. The physicochemical characteristics of the sorbents such as composition, water solubility, moisture content and density were measured according to ASTM standard methods. Also Fourier transform infrared spectroscopy (FTIR) of raw and acetylated bagasse was performed to investigate the effect of acetylation on sugarcane bagasse structure.

  20. Effect of DOC on evaporation from small Wisconsin lakes

    Watras, C. J.; Morrison, K. A.; Rubsam, J. L.


    Evaporation (E) dominates the loss of water from many small lakes, and the balance between precipitation and evaporation (P-E) often governs water levels. In this study, evaporation rates were estimated for three small Wisconsin lakes over several years using 30-min data from floating evaporation pans (E-pans). Measured E was then compared to the output of mass transfer models driven by local conditions over daily time scales. The three lakes were chosen to span a range of dissolved organic carbon (DOC) concentrations (3-20 mg L-1), a solute that imparts a dark, tea-stain color which absorbs solar energy and limits light penetration. Since the lakes were otherwise similar, we hypothesized that a DOC-mediated increase in surface water temperature would translate directly to higher rates of evaporation thereby informing climate response models. Our results confirmed a DOC effect on surface water temperature, but that effect did not translate to enhanced evaporation. Instead the opposite was observed: evaporation rates decreased as DOC increased. Ancillary data and prior studies suggest two explanatory mechanisms: (1) disproportionately greater radiant energy outflux from high DOC lakes, and (2) the combined effect of wind speed (W) and the vapor pressure gradient (es - ez), whose product [W(es - ez)] was lowest on the high DOC lake, despite very low wind speeds (changes in the variables that drive E can have measurable effects on water levels by shifting the balance between P and E.

  1. Modelling the fate of ciprofloxacin in activated sludge systems - The relevance of the sorption process

    Polesel, Fabio; Lehnberg, Kai; Dott, Wolfgang

    . In a previous study [1], a daily systematic reduction of ciprofloxacin removal in a full-scale WWTP (Bekkelaget, Norway) was associated to deteriorated sorption. Therefore, in this study we further investigated the sorption of ciprofloxacin onto activated sludge at laboratory- and full-scale. Targeted batch...... of ciprofloxacin in a full-scale activated sludge system. Sorption was described by linear kinetics and, in an extended version of ASM-X, using a Freundlich-based submodel. In the latter case, Freundlich parameter values estimated from the batch experiments were used for model calibration. The prediction accuracy...... was statistically evaluated in the two cases by comparing the model output with measured data. Batch experiments showed that maximum sorption capacity occurred at pH=7.4, corresponding to the isoelectric point of ciprofloxacin. A pH increase resulted in a significant reduction of sorption capacity as compared...

  2. Phosphorus sorption-desorption and effects of temperature, pH and salinity on phosphorus sorption in marsh soils from coastal wetlands with different flooding conditions.

    Bai, Junhong; Ye, Xiaofei; Jia, Jia; Zhang, Guangliang; Zhao, Qingqing; Cui, Baoshan; Liu, Xinhui


    Wetland soils act as a sink or source of phosphorus (P) to the overlaying water due to phosphorus sorption-desorption processes. Litter information is available on sorption and desorption behaviors of phosphorus in coastal wetlands with different flooding conditions. Laboratory experiments were conducted to investigate phosphorus sorption-desorption processes, fractions of adsorbed phosphorus, and the effects of salinity, pH and temperature on phosphorus sorption on soils in tidal-flooding wetlands (TW), freshwater-flooding wetlands (FW) and seasonal-flooding wetlands (SW) in the Yellow River Delta. Our results showed that the freshly adsorbed phosphorus dominantly exists in Occluded-P and Fe/AlP and their percentages increased with increasing phosphorus adsorbed. Phosphorus sorption isotherms could be better described by the modified Langmuir model than by the modified Freundlich model. A binomial equation could be properly used to describe the effects of salinity, pH, and temperature on phosphorus sorption. Phosphorus sorption generally increased with increasing salinity, pH, and temperature at lower ranges, while decreased in excess of some threshold values. The maximum phosphorus sorption capacity (Qmax) was larger for FW soils (256 mg/kg) compared with TW (218 mg/kg) and SW soils (235 mg/kg) (p < 0.05). The percentage of phosphorus desorption (Pdes) in the FW soils (7.5-63.5%) was much lower than those in TW (27.7-124.9%) and SW soils (19.2-108.5%). The initial soil organic matter, pH and the exchangeable Al, Fe and Cd contents were important factors influencing P sorption and desorption. The findings of this study indicate that freshwater restoration can contribute to controlling the eutrophication status of water bodies through increasing P sorption. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Residuejams and their effect on Infiltration, Runoff and Dissolved Organic Carbon (DOC) in Furrow Irrigation Systems

    Mailapalli, D. R.; Wallender, W. W.; Horwath, W.; Ma, S.; Lazicki, P.


    ), respectively. During the irrigation, the waterfront advance (for estimating infiltration), runoff and DOC concentration (at the tail end) were measured. After the irrigation, the location of the residuejams along the furrow and their dry weight were measured. Using the jam location data, the relative percentage spacing of the jams were estimated and found that it decreases down the furrow for all the cases. Hence, the number of residuejams increases down the furrow to a maximum at the tail end. Further, the number of jams is greater for NT followed by CC and ST. The infiltration and runoff data of these treatments were used for studying the effect of residuejams on these parameters. The water samples collected from these plots were analyzed for DOC concentration. Initially, DOC was high and then decreased with time in all cases. However, DOC was greater for NT followed by CC and ST. This may be due to more jams in NT followed by CC and ST. Hence, residuejams apparently affect DOC.

  4. Sorption of Arsenite onto Mackinawite Coated Sand

    Gallegos, T. J.; Hayes, K. F.; Abriola, L. M.


    Arsenic contamination of groundwater is a widespread problem affecting aquifers in the United States as well as abroad. Recent strengthening of the US EPA MCL for arsenic has prompted the need for technology capable of removing both arsenite and arsenate from solution. Arsenite, the more toxic form of arsenic, is more difficult to remove from anoxic zones in the subsurface. Studies by others have demonstrated the affinity of some types of iron sulfides for arsenite, such as troilite, pyrite, amorphous iron sulfide and mackinawite. However, these studies have not provided a comprehensive investigation of the macroscopic behavior of arsenite in the presence of crystalline mackinawite in a form that can be readily applied to real-world treatment technologies. This study examines the behavior of arsenite in the presence of mackinawite coated sand. PH edge results demonstrate that arsenite sorption onto mackinawite coated sand increases with increasing pH, reaching maximum removal at pH 10. Arsenite removal, albeit slight, occurring below pH 5 is independent of pH indicative of a different removal mechanism. Isotherm studies show that at low concentrations, removal is Langmuirian in nature. Arsenite sorption abruptly converts to linear behavior at high concentrations, possibly attributed to the saturation of the monolayer. Ionic strength effects were assessed by comparing pH edge data developed for three different concentrations of NaCl background electrolyte solution. Increases in ionic strength enhance the removal of arsenite from solution, suggesting possible inner-sphere surface complexation removal mechanisms. Information gathered in this study can be used to further develop surface complexation models to describe and predict reactivity of arsenite in the presence of mackinawite coated sands in anoxic regions. Mackinawite coated sands investigated here may provide a feasible reactive medium for implementation in above-ground sorption reactors or subsurface

  5. Sorption and desorption of pentachlorophenol to black carbon of three different origins.

    Luo, Ling; Lou, Liping; Cui, Xinyi; Wu, Binbin; Hou, Jiaai; Xun, Bei; Xu, Xinhua; Chen, Yingxu


    Rice straw charcoal, soot and fly ash (collectively termed "black carbon" or BC), which were found to widely exist in the environment and exhibit strong sorption of many organic compounds, were prepared for this study, and recorded as RC, SC, and FC, respectively. The characterization, sorption isotherm, and the effect of pH (from 3.0 to 9.0) on sorption capacity of each BC were investigated. It is demonstrated that RC possessed the largest surface area (234.9 m(2)/g), the highest porosity (0.4392 mL/g), and the largest amount of functional groups (2.995 mmol/g) of all. All the Freundlich, Langmuir and Dual-mode model can fit the sorption data of each BC well. The pH value could apparently affect the sorption capacity of pentachlorophenol (PCP) to BCs, which reached maximum value at pH 4.0. Furthermore, in order to validate the effect of pH on desorption capacity, we designed sorption-desorption cycle experiments at pH 9.0 and then pH 7.0, and found that the effect of pH on irreversible sorption and hysteresis effects were significant. As pH value decreasing from 9.0 to 7.0, the irreversible sorption capacities for RC, FC, and SC increased, and the desorption hysteresis index (H) values of PCP increased approximately 3 times for each BC.

  6. Effects of Common Ions on Zn Sorption in Some Calcareous Soils of Western Iran



    Zinc (Zn) is essential to plant growth and relatively mobile in soils.This study was conducted to assess the effect of common ions (Ca2+,K+,Na+,NH4+,Cl-,NO3-,and H2PO4-) on sorption of Zn in surface samples of ten calcareous soils from western Iran using 10 mmol L-1 KCl,KNO3,KH2PO4,Ca(NO3)2,NaNO3,and NH4NO3 solutions as background electrolytes.The results indicated that both NH4+,K+,and Ca2+ equally decreased Zn sorption as compared to Na+.Zinc sorption was decreased by H2PO4- as compared to NO3- and Cl-.The Langmuir and Freundlich equations fitted closely to the sorption data of all ions.The Langmuir maximum,bonding energy constant,and Freundlich distribution coefficient for Zn sorption differed among the various ionic background electrolytes.Langmuir sorption parameters showed that the presence of H2PO4- decreased the maximum Zn adsorbed,but increased the bonding energy.Although K+ and NH4+ equally influenced maximum Zn adsorbed,they differed in their effect on the distribution coefficient of Zn in soils.Values of saturation index calculated using Visual MINTEQ indicated that at the low Zn concentration,Zn solubility was controlled by sorption reactions and at the high Zn concentration,it was mainly controlled by sorption and mineral precipitation reactions,such as precipitation of Zn3 (PO4)2·4H2O,Zn5(OH)6(CO3)2,and ZnCO3.For most ionic background electrolytes,soil pH,CaCO3,and cation exchange capacity (CEC) were significantly correlated with sorption parameters.

  7. The Earth System Documentation (ES-DOC) Software Process

    Greenslade, M. A.; Murphy, S.; Treshansky, A.; DeLuca, C.; Guilyardi, E.; Denvil, S.


    Earth System Documentation (ES-DOC) is an international project supplying high-quality tools & services in support of earth system documentation creation, analysis and dissemination. It is nurturing a sustainable standards based documentation eco-system that aims to become an integral part of the next generation of exa-scale dataset archives. ES-DOC leverages open source software, and applies a software development methodology that places end-user narratives at the heart of all it does. ES-DOC has initially focused upon nurturing the Earth System Model (ESM) documentation eco-system and currently supporting the following projects: * Coupled Model Inter-comparison Project Phase 5 (CMIP5); * Dynamical Core Model Inter-comparison Project (DCMIP); * National Climate Predictions and Projections Platforms Quantitative Evaluation of Downscaling Workshop. This talk will demonstrate that ES-DOC implements a relatively mature software development process. Taking a pragmatic Agile process as inspiration, ES-DOC: * Iteratively develops and releases working software; * Captures user requirements via a narrative based approach; * Uses online collaboration tools (e.g. Earth System CoG) to manage progress; * Prototypes applications to validate their feasibility; * Leverages meta-programming techniques where appropriate; * Automates testing whenever sensibly feasible; * Streamlines complex deployments to a single command; * Extensively leverages GitHub and Pivotal Tracker; * Enforces strict separation of the UI from underlying API's; * Conducts code reviews.

  8. Kinetics and thermodynamics of basic dye sorption on phosphoric acid esterifying soybean hull with solid phase preparation technique.

    Gong, Renmin; Sun, Jin; Zhang, Demin; Zhong, Keding; Zhu, Guoping


    In this paper, the solid phase preparation method of a cationic sorbent, which bears hydroxyl groups of phosphoric acid derived from esterified soybean hull (ESH), was reported. The sorption kinetics and thermodynamics of two basic dyes, acridine orange (AO) and malachite green (MG), from aqueous solution onto ESH were investigated with a batch system. The isothermal data of dye sorptions followed the Langmuir model better than the Freundlich model. The maximum sorption capacity (Q(m)) of ESH for AO and MG was 238.1 mg/g and 178.57 mg/g, respectively. The dye sorption processes could be described by the pseudo-second-order kinetic model. The thermodynamic study indicated that the dye sorptions were spontaneous and exothermic. Lower temperatures were favorable for the sorption processes.

  9. Influence of porewater velocity and ionic strength on DOC concentrations in and losses from peat-sand mixtures

    Pfaffner, Nora; Tiemeyer, Bärbel; Fiedler, Sabine


    Organic soils play an important role in the global carbon cycle as they can act as a source or a sink for greenhouse gas emissions. The new IPCC Wetlands Supplement accounts for the first time for CO2 emissions from the decomposition of dissolved organic carbon (DOC). While there is a wealth of studies on "true" peat soils, knowledge on DOC losses from organic soils heavily disturbed by e.g. mixing with sand is fragmentary. Moreover, there are only a few studies on the influence of soil hydrological properties on DOC transport. This study investigates physico-chemical controls on the concentration and losses of DOC from a peat-sand mixture in a saturated column experiment with undisturbed columns. The soil originates from the study site "Grosses Moor" (Northern Germany) which is a former bog where peat layers remaining after peat mining were mixed with the underlying mineral soil. We studied the influence of the flow regime and the ionic strength of the irrigation solution on DOC concentrations and losses. Three different pumping rates and two different ionic strengths determined by different concentrations of a sodium chloride-calcium chloride mixture in the irrigation solution were applied. Transport properties of the soil were obtained by analyzing breakthrough curves (BTCs) of a conservative tracer (potassium bromide). For interpretation of the BTCs, the transport model STANMOD which is based on the two-region (mobile/immobile) non-equilibrium concept was fitted to the data. The shape of the BTCs and the STANMOD results showed that three of the four columns had a dual porosity structure, which affects the porewater velocity and the contact area. After a large initial peak, DOC concentrations equilibrated to nearly constant values. Increased porewater velocities decreased the concentration of DOC, but increased the losses. A new equilibrium concentration was reached after nearly all changes of the porewater velocity. At maximum pumping rates as determined from

  10. COLWRIT – Collaborative Online Writing in Google Docs

    Andreasen, Lars Birch; Winther, Frederikke; Hanghøj, Thorkild;

    The poster presents preliminary hypotheses and findings of an on-going research project at Aalborg University, Denmark, which explores university students’ uses of collaborative writing tools like Google Docs when doing collaborative project work. The research project has a special focus on the v......The poster presents preliminary hypotheses and findings of an on-going research project at Aalborg University, Denmark, which explores university students’ uses of collaborative writing tools like Google Docs when doing collaborative project work. The research project has a special focus...

  11. DOC-dynamics in a small headwater catchment as driven by redox fluctuations and hydrological flow paths - are DOC exports mediated by iron reduction/oxidation cycles?

    Knorr, K.-H.


    Dissolved organic carbon (DOC) exports from many catchments in Europe and North-America are steadily increasing. Several studies have sought to explain this observation. As possible causes, a decrease in acid rain or sulfate deposition, concomitant reductions in ionic strength and increasing temperatures were identified. DOC often originates from riparian wetlands; but here, despite higher DOC concentrations, ionic strength in pore waters usually exceeds that in surface waters. In the catchment under study, DOC concentrations were synchronous with dissolved iron concentrations in pore and stream water. This study aims at testing the hypothesis that DOC exports are mediated by iron reduction/oxidation cycles. Following the observed hydrographs, δ18O of water and DOC fluorescence, the wetlands were identified as the main source of DOC. Antecedent biogeochemical conditions, i.e., water table levels in the wetlands, influenced the discharge patterns of nitrate, iron and DOC during an event. The correlation of DOC with pH was positive in pore waters, but negative in surface waters; it was negative for DOC with sulfate in pore waters, but only weak in surface waters. Though, the positive correlation of DOC with iron was universal for pore and surface water. The decline of DOC and iron concentrations in transition from anoxic wetland pore water to oxic stream water suggests a flocculation of DOC with oxidising iron, leading to a drop in pH in the stream during high DOC fluxes. The pore water did not per se differ in pH. There is, thus, a need to consider processes more thoroughly of DOC mobilisation in wetlands when interpreting DOC exports from catchments. The coupling of DOC with iron fluxes suggested that increased DOC exports could at least, in part, be caused by increasing activities in iron reduction, possibly due to increases in temperature, increasing wetness of riparian wetlands, or by a shift from sulfate dominated to iron reduction dominated biogeochemical

  12. DOC-dynamics in a small headwater catchment as driven by redox fluctuations and hydrological flow paths – are DOC exports mediated by iron reduction/oxidation cycles?

    K.-H. Knorr


    Full Text Available Dissolved organic carbon (DOC exports from many catchments in Europe and North-America are steadily increasing. Several studies have sought to explain this observation. As possible causes, a decrease in acid rain or sulfate deposition, concomitant reductions in ionic strength and increasing temperatures were identified. DOC often originates from riparian wetlands; but here, despite higher DOC concentrations, ionic strength in pore waters usually exceeds that in surface waters. In the catchment under study, DOC concentrations were synchronous with dissolved iron concentrations in pore and stream water. This study aims at testing the hypothesis that DOC exports are mediated by iron reduction/oxidation cycles. Following the observed hydrographs, δ18O of water and DOC fluorescence, the wetlands were identified as the main source of DOC. Antecedent biogeochemical conditions, i.e., water table levels in the wetlands, influenced the discharge patterns of nitrate, iron and DOC during an event. The correlation of DOC with pH was positive in pore waters, but negative in surface waters; it was negative for DOC with sulfate in pore waters, but only weak in surface waters. Though, the positive correlation of DOC with iron was universal for pore and surface water. The decline of DOC and iron concentrations in transition from anoxic wetland pore water to oxic stream water suggests a flocculation of DOC with oxidising iron, leading to a drop in pH in the stream during high DOC fluxes. The pore water did not per se differ in pH. There is, thus, a need to consider processes more thoroughly of DOC mobilisation in wetlands when interpreting DOC exports from catchments. The coupling of DOC with iron fluxes suggested that increased DOC exports could at least, in part, be caused by increasing activities in iron reduction, possibly due to increases in temperature, increasing wetness of riparian wetlands, or by a shift from sulfate dominated to iron

  13. Sorption phenomena of PCBs in environment


    The relationship between the properties of PCBs and the behavior of soil and sediment is reviewed. The sorption phenomena of PCBs in the environment are described with different models. The research progress on the sorption mechanisms is also discussed.

  14. Sorption of Cs, Eu and U(VI) onto rock samples from Nizhnekansky massive

    Petrov, V.; Vlasova, I.; Kalmykov, S. [Lomonosov Moscow State University (Russian Federation); Kuzmenkova, N. [Vernadsky Institute of Geochemistry and Analytical Chemistry, Russian Academy of Science (Russian Federation); Petrov, V.; Poluektov, V. [Institute of Geology of Ore Deposits, Petrography, Mineralogy and Geochemistry, Russian Academy of Sciences - IGEM RAS (Russian Federation)


    The accepted in Russia concept for high level wastes (HLW) and spent nuclear fuel (SNF) disposal is based on their isolation into the deep underground crystalline rock formations. The 'Eniseysky' area (Nizhnekansky massive) is supposed as the most perspective location for the future HLW and SNF repository. Core materials from different areas of Nizhnekasnsky massive have been studied in terms of petrographic and mineralogical characterization; definition of filtration, elastic, petro-physical and strength properties; estimation of hydrothermal-metasomatic transformation of rocks. We used both undisturbed sliced cores and crushed material for the sorption experiments. Preliminary results of uranium sorption show some significant differences between used rock samples from different depth in sorption rate and pH-dependence. In all cases maximum sorption (more than 90%) is reached in 2-3 weeks. The pH-dependence of sorbed uranium fraction has typical hump-shape: increase of sorption percentage with increasing pH values to 6, plateau (90-98 % of uranium sorbed), decrease of sorption percentage with increasing pH values from 8 due to U(VI) hydrolysis. In the case of cesium the sorption maximum is reached within 10-12 days and in the case of europium - about 5 days. All radionuclides sorbed preferentially onto dark minerals. Local distribution and preferential sorption of cesium, europium and uranium (VI) onto different minerals within the sample were studied by radiography, SEM-EDX, etc. These data accompanying with rock sample composition will allow the development of quantitative model for Cs, Eu and U(VI) sorption onto investigated rocks. Document available in abstract form only. (authors)

  15. Impact of air-borne or canopy-derived dissolved organic carbon (DOC) on forest soil solution DOC in Flanders, Belgium

    Verstraeten, Arne; De Vos, Bruno; Neirynck, Johan; Roskams, Peter; Hens, Maarten


    Dissolved organic carbon (DOC) in the soil solution of forests originates from a number of biologically and/or biochemically mediated processes, including litter decomposition and leaching, soil organic matter mineralization, root exudation, mucilage and microbial activity. A variable amount of DOC reaches the forest floor through deposition, but limited information is available about its impact on soil solution DOC. In this study, trends and patterns of soil solution DOC were evaluated in relation to deposition of DOC over an 11-year period (2002-2012) at five ICP Forests intensive monitoring plots in Flanders, northern Belgium. Trend analysis over this period showed an increase of soil solution DOC concentrations for all observed depth intervals. Fluxes of DOC increased in the organic layer, but were nearly stable in the mineral soil. Annual leaching losses of DOC were higher in coniferous (55-61 kg C ha-1) compared to deciduous plots (19-30 kg C ha-1) but embody less than 0.05% of total 1-m soil organic C stocks. Temporal deposition patterns could not explain the increasing trends of soil solution DOC concentrations. Deposition fluxes of DOC were strongly correlated with soil solution fluxes of DOC, but their seasonal peaks were not simultaneous, which confirmed that air-borne or canopy-derived DOC has a limited impact on soil solution DOC.

  16. Sorption and desorption of silver ions by bentonite clays.

    Constantino, Leonel Vinicius; Quirino, Juliana Nunes; Monteiro, Alessandra Maffei; Abrão, Taufik; Parreira, Paulo Sérgio; Urbano, Alexandre; Santos, Maria Josefa


    Anthropogenic activities have increased the concentration of metal species in the environment. The toxicity of silver ions to aquatic and terrestrial organisms has required monitoring by analytical methods, besides actions to promote its control as pollutant. Sorption and desorption processes are directly related to the mobility and availability of metal ions in the environment. In this context, clay minerals can be used for pre-concentration, removal and recovery of silver ions from aqueous solution. Herein, two bentonite clays (BaVC-1 and SWy-2) were characterised and applied to investigate the sorption and desorption of silver ions. Isotherms were fitted to the dual-mode Langmuir-Freundlich model to qualify and quantify sorption sites and evaluate the mobilisation process. The maximum sorption capacity was 743 and 849 meq kg(-1) for BaVC-1 and SWy-2, respectively. Hysteresis index (HI) and mobilisation factor (MF) suggest that the desorption of silver ions in BaVC-1 is about four times more conducive compared to that in SWy-2, although both materials have demonstrated a great potential for Ag(+) pre-concentration from aqueous solutions.

  17. Soil Components Affecting Phosphate Sorption Parameters of Acid Paddy Soils in Guangdong Province


    Soil components affecting phosphate sorption parameters were studied using acid paddy soils derived from basalt, granite, sand-shale and the Pearl River Delta sediments, respectively, in Guangdong Province.For each soil, seven 2.50 g subsamples were equilibrated with 50 mL 0.02 mol L-1 (pH=7.0) of KCl containing 0, 5, 10, 15, 25, 50 and 100 ng P kg-1, respectively, in order to derive P sorption parameters (P sorption maximum, P sorption intensity factor and maximum buffer capacity) by Langmuir isotherm equation. It was shown that the main soil components influencing phosphate sorption maximum (Xm) included soil clay, pH,amorphous iron oxide (Feo) and amorphous aluminum oxide (Alo), with their effects in the order of Alo >Feo > pH > clay. Among these components, pH had a negative effect, and the others had a positive effect.Organic matter (OM) was the only soil component influencing P sorption intensity factor (K). The main components influencing maximum phosphate buffer capacity (MBC) consisted of soil clay, OM, pH, Feo and Alo, with their effects in the order of Alo > OM > pH > Feo > clay. Path analysis indicated that among the components with positive effects on maximum phosphate buffer capacity (MBC), the effect was in the order of Alo > Feo > Clay, while among the components with negative effects, OM > pH. OM played an important role in mobilizing phosphate in acid paddy soils mainly through decreasing the sorption intensity of phosphate by soil particles.

  18. Moisture Sorption in Porous Materials

    Nielsen, Lauge Fuglsang


    Abstract: Information on pore geometry is very important in any study of the mechanical and physical behavior of porous materials. Unfortunately pores are not very accessible for direct measurements. Indirect methods have to be used which involve impregnation (sorption) experiments from which...... in the subject considered this software is available on request to the author. Keywords: Porous materials, moisture, adsorption, desorption, BET-parameters....

  19. Oil sorption by lignocellulosic fibers

    Beom-Goo. Lee; James S. Han; Roger M. Rowell


    The oil sorption capacities of cotton fiber, kenaf bast fiber, kenaf core fiber, and moss fiber were compared after refining, extraction, and reduction in particle sizes. The tests were conducted on diesel oil in a pure form. Cotton fiber showed the highest capacity, followed by kenaf core and bast fibers. Wetting, extraction, and reduction in particle size all...

  20. Removal of basic (Methylene Blue) and acid (Egacid Orange) dyes from waters by sorption on chemically treated wood shavings.

    Janos, Pavel; Coskun, Sezen; Pilarová, Vera; Rejnek, Jaroslav


    Spruce wood shavings from Picea abies were used for an adsorptive removal of both basic as well as acid dyes from waters. The sorption properties of the sorbents were modified with HCl, Na(2)CO(3) and Na(2)HPO(4). The treatment of the wood sorbents with alkaline carbonate solution as well as with phosphate solution increased the sorption ability for the basic dye (Methylene Blue), whereas the treatment with mineral acid decreased the sorption ability for Methylene Blue to some extent. The opposite is true for the sorption of the acid dye--Egacid Orange. The maximum sorption capacities estimated from the Langmuir-Freundlich isotherms ranged from 0.060 to 0.165 mmol g(-1) for Methylene Blue, and from 0.045 to 0.513 mmol g(-1) for Egacid Orange. The basic dye sorption decreased at low pH values in accordance with a presupposed ion-exchange mechanism of the sorption. The sorption of acid dye, on the other hand, decreased with increasing pH. The presence of inorganic salts as well as surfactants exhibited only minor effects on the dye sorption.

  1. Characteristics of Lead Sorption on Clay Minerals in Relation to Metal Oxides


    Difference of montmorillonite (Mt), illite (It) and kaolinite (Kt) in lead sorption characteristics and the effects of amorphous Fe and Al oxide coatings on the haracteristics were experimentally studied with logistic model. The sorption curves had sigmoid feature due to use of acetate-type buffer solution. With the modelthe sorption process could be divided into four stages and the sorption characteristics at the stages were discussed. The results showed that, after Mt, It and Kt were coated by amorphous Fe oxide, their maximum sorption capacity (MSC) and percentage of high-SSC concentration scope (HCS) of Pb2+ increased markedly but the specific sorption capacity (SSC) decreased. With regard to effects of amorphous Al oxide coating,except for It+Al, the SSC of other samples showed a downtrend, despite that their MSC remained unchanged.Eventually, the gray correlation degrees to Pb2+ sorption for different physicochemical characteristics of the clay minerals were indicated to be higher for hydronium, zero point of surface charge and hydroxy, but lower for specific surface area, density of surface charge and amount of surface charges.

  2. Effect of Selected Organic Acids on Cadmium Sorption by Variable-and Permanent-Charge Soils

    HU Hong-Qing; LIU Hua-Liang; HE Ji-Zheng; HUANG Qiao-Yun


    Batch equilibrium experiments were conducted to investigate cadmium (Cd) sorption by two permanent-charge soils, a yellow-cinnamon soil and a yellow-brown soil, and two variable-charge soils, a red soil and a latosol, with addition of selected organic acids (acetate, tartrate, and citrate). Results showed that with an increase in acetate concentrations from 0 to 3.0 mmol L-1, Cd sorption percentage by the yellow-cinnamon soil, the yellow-brown soil, and the latosol decreased. The sorption percentage of Cd by the yellow-cinnamon soil and generally the yellow-brown soil (permanent-charge soils)decreased with an increase in tartrate concentration, but increased at low tartrate concentrations for the red soil and the latosol. Curves of percentage of Cd sorption for citrate were similar to those for tartrate. For the variable-charge soils with tartrate and citrate, there were obvious peaks in Cd sorption percentage. These peaks, where organic acids had maximum influence, changed with soil type, and were at a higher organic acid concentration for the variable-charge soils than for the permanent charge soils. Addition of cadmium after tartrate adsorption resulted in higher sorption increase for the variable-charge soils than permanent-charge soils. When tartrate and Cd solution were added together, sorption of Cd decreased with tartrate concentration for the yellow-brown soil, but increased at low tartrate concentrations and then decreased with tartrate concentration for the red soil and the latosol.

  3. Sorption of basic and acid dyes from aqueous solutions onto oxihumolite.

    Janos, Pavel; Sedivý, Pavel; Rýznarová, Milena; Grötschelová, Sylvie


    Naturally occurring kind of weathered and oxidised young brown coal called oxihumolite was used for an adsorptive removal of basic (Methylene Blue, Malachite Green) as well as acid (Egacid Orange, Midlon Black) dyes from waters. It was shown that both kinds of dyes can be sorbed onto oxihumolite. The maximum sorption capacities determined from the parameters of Langmuir isotherms ranged from 0.070 mmol g-1 (for Midlon Black) to 0.278 mmol g-1 (for Malachite Green) and did not differ significantly for basic and acid dyes. The dye sorption (except of Midlon Black) increased in the presence of inorganic salt. Non-ionic surfactants, and surfactants bearing the same charge as the dye exhibited only a minor effect on the dye sorption, whereas oppositely charged surfactants enhanced the dye sorption to a certain extent. The pH value of the aqueous phase exhibited rather pronounced effect on the sorption of acid dyes causing a suppression of the sorption with increasing pH. The sorption of basic dyes, on the other hand, remained almost unchanged in the examined pH range. Oxihumolite is recommended for the treatment of acid wastewaters because of its limited stability in alkaline aqueous solutions.

  4. Effects of Mo on the Microstructure and Hydrogen Sorption Properties of Ti-Mo Getters

    ZHOU Hong-guo; WEI Xiu-ying; MAO Chang-hui; XIONG Yu-hua; QIN Guang-rong


    The effects of Mo on the microstructure evolution, porosity and hydrogen sorption properties of Ti-Mo getters are investigated in this work. The results show that the addition of Mo prolongs the densification process of Ti-Mo getters and results in a significant amount of sintered pores. With the Mo content increasing, the porosity of getters firstly increases reaching the maximum value as it attains about 7.5wt.%, and then drops. At the room temperature, the hydrogen sorption property of getters increases progressively with the Mo content increasing, but the tendency is not very clear before its content lies below 2.5wt.%. When the Mo content achieves about7.5wt.%, the hydrogen sorption property proves to be the best. The discussion is made about the above mentioned phenomena inclusive of hydrogen sorption properties of getters under different activation conditions (from 500-750 ℃).

  5. G-DOC: A Systems Medicine Platform for Personalized Oncology

    Subha Madhavan


    Full Text Available Currently, cancer therapy remains limited by a “one-size-fits-all” approach, whereby treatment decisions are based mainly on the clinical stage of disease, yet fail to reference the individual's underlying biology and its role driving malignancy. Identifying better personalized therapies for cancer treatment is hindered by the lack of high-quality “omics” data of sufficient size to produce meaningful results and the ability to integrate biomedical data from disparate technologies. Resolving these issues will help translation of therapies from research to clinic by helping clinicians develop patient-specific treatments based on the unique signatures of patient's tumor. Here we describe the Georgetown Database of Cancer (G-DOC, a Web platform that enables basic and clinical research by integrating patient characteristics and clinical outcome data with a variety of high-throughput research data in a unified environment. While several rich data repositories for high-dimensional research data exist in the public domain, most focus on a single-data type and do not support integration across multiple technologies. Currently, G-DOC contains data from more than 2500 breast cancer patients and 800 gastrointestinal cancer patients, G-DOC includes a broad collection of bioinformatics and systems biology tools for analysis and visualization of four major “omics” types: DNA, mRNA, microRNA, and metabolites. We believe that G-DOC will help facilitate systems medicine by providing identification of trends and patterns in integrated data sets and hence facilitate the use of better targeted therapies for cancer. A set of representative usage scenarios is provided to highlight the technical capabilities of this resource.

  6. Leaching of DOC, DN, and inorganic constituents from scrap tires.

    Selbes, Meric; Yilmaz, Ozge; Khan, Abdul A; Karanfil, Tanju


    One concern for recycle and reuse of scrap tires is the leaching of tire constituents (organic and inorganic) with time, and their subsequent potential harmful impacts in environment. The main objective of this study was to examine the leaching of dissolved organic carbon (DOC), dissolved nitrogen (DN), and selected inorganic constituents from scrap tires. Different sizes of tire chips and crumb rubber were exposed to leaching solutions with pH's ranging from 3.0 to 10.0 for 28days. The leaching of DOC and DN were found to be higher for smaller size tire chips; however, the leaching of inorganic constituents was independent of the size. In general, basic pH conditions increased the leaching of DOC and DN, whereas acidic pH conditions led to elevated concentrations of metals. Leaching was minimal around the neutral pH values for all the monitored parameters. Analysis of the leaching rates showed that components associated with the rubbery portion of the tires (DOC, DN, zinc, calcium, magnesium, etc.) exhibited an initial rapid followed by a slow release. On the other hand, a constant rate of leaching was observed for iron and manganese, which are attributed to the metal wires present inside the tires. Although the total amounts that leached varied, the observed leaching rates were similar for all tire chip sizes and leaching solutions. Operation under neutral pH conditions, use of larger size tire chips, prewashing of tires, and removal of metal wires prior to application will reduce the impact of tire recycle and reuse. Copyright © 2015 Elsevier Ltd. All rights reserved.

  7. Effects of dissolved organic matter from sewage sludge on the atrazine sorption by soils

    LING Wanting; XU Jianming; GAO Yanzheng


    The effects of dissolved organic matter (DOM), water soluble organic matter derived from sewage sludge, on the sorption of atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-trazine) by soils were studied using a batch equilibrium technique. Six paddy soils, chosen so as to have different organic carbon contents, were experimented in this investigation. Atrazine sorption isotherms on soils were described by the linear equation, and the distribution coefficients without DOM (Kd) or with DOM (Kd*) were obtained. Generally, the values of Kd*/Kd initially insoil-solution system form. Critical concentrations of DOM (DOMnp) were obtained where the value of Kd* was equal to Kd. The presence of DOM with concentrations lower than DOMnp promoted atrazine sorption on soils (Kd* > Kd), whereas the presence of DOM with concentrations higher than DOMnp tended to inhibit atrazine sorption (Kd* < Kd). Interestingly, DOMnp for tested soils was negatively correlated to the soil organic carbon content, and the maximum of Kd*/Kd (i.e.Kmax) correlated positively with the maximum of DOM sorption on soil (Xmax). Further investigations showed that the presence of hydrophobic fraction of DOM evidently promoted the atrazine sorption on soils, whereas the presence of hydrophilic DOM fraction obviously tended to inhibit the atrazine sorption. Interactions of soil surfaces with DOM and its fractions were suggested to be the major processes determining atrazine sorption on soils. The results of this work provide a reference to the agricultural use of organic amendment such as sewage sludge for improving the availability of atrazine in soils.

  8. Sorption of dissolved organic matter and its effects on the atrazine sorption on soils

    LING Wan-ting; WANG Hai-zhen; XU Jian-ming; GAO Yan-zheng


    The dissolved organic matter(DOM), water soluble organic matter derived from sewage sludge was separated into hydrophobic fraction(Ho) and hydrophilic fraction(Hi). The sorption of DOM and its fractions on soils and the effects of DOM sorption on a nonionic pesticide(atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-trazine)) distribution between soil and water were investigated using a batch equilibrium technique. The total DOM sorption on soils described by the Langmuir equation reached saturation as the DOMconcentration increased. The sorption of Ho fit the Freundlich model. In contrast, a negative retention evidently occurred as adding Hi at higher level in tested soils. The sorption of Ho dominated the total DOM sorption and the release of soil organic matter(SOM). Effects of DOM on the atrazine sorption by soils were DOM-concentration dependent and dominated by the interaction of atrazine, DOM, and soil solids. Generally, the presence of DOM with lower concentration promoted atrazine sorption on soils, namely the apparent partitioning constant( K; ) for atrazine sorption in the presence of DOM was larger than the distribution constant ( Kd ) without DOM; whereas the presence of DOM with higher concentration inhibited atrazine sorption(i. e., K; < Kd ) . The overall effects of DOM on atrazine sorption in soils might be related to the DOM sorption and the release of soil intrinsic organic matter into aqueous solution. The sorption of Ho on soils promoted the atrazine sorption on soil, while the release of SOM by Hi and the competitive sorption between Hi and atrazine on soil surface led to a decrease of atrazine sorption. Information provided in this work may contribute to a better understanding of the DOM sorption and its impacts on the contaminant soil-water distribution.

  9. El editor de mapas conceptuales DigiDocMap The editor of conceptual maps, DigiDocMap

    Cristòfol Rovira Fontanals


    Full Text Available DigiDocMap es un editor freeware y open source para la creación de mapas conceptuales. Es el primer resultado de un proyecto de investigación orientado a la generación de herramientas para representar el conocimiento. Se han desarrollado tres versiones de este editor desde el año 2002. En el artículo se analizan las prestaciones de cada una de ellas y las razones que motivaron la incorporación de los principales cambios.DigiDocMap is freeware editor and open source for the creation of conceptual maps. It is the first product of a research project intended to generate tools for knowledge representation. Three versions of this editor have been created since 2002. The paper analyses each one of these and the reasons which motivated incorporation of the principal modifications.

  10. Reactive modelling of 1,2-DCA and DOC near the shoreline.

    Colombani, N; Pantano, A; Mastrocicco, M; Petitta, M


    1,2-Dichloroethane (1,2-DCA) was found to be the most abundant compound among chlorinated hydrocarbons detected in a petrochemical plant in southern Italy. This site is located near the coastline, and it is set above an unconfined coastal aquifer, where seawater intrusion is present. The presence of organic and inorganic contaminants at this site has required the implementation of remediation strategies, consisting of pumping wells (hydraulic barrier) and a horizontal flow barrier. The purpose of this work was to assess the influence of salt water intrusion on the degradation rate of 1,2-DCA. This was done on a three-dimensional domain relative to a limited portion of a well characterized field site, accounting for density-dependent flow and reactive transport modelling of 1,2-DCA and Dissolved Organic Carbon (DOC). The modelling procedure was performed employing SEAWAT-4.0 and PHT3D, to reproduce the complex three-dimensional flow and transport domain. In order to determine the fate of 1,2-DCA, detailed field investigations provided intensive depth profile information. Different, kinetically controlled degradation rates were simulated to explain the observed, selective degradation of pollutants in groundwater. Calibration of the model was accomplished by comparison with the two different sets of measurements obtained from the MLS devices and from pumping wells. With the calibrated model, it was possible to distinguish between dispersive non-reactive processes and bacterially mediated reactions. In the non-reactive model, 1,2-DCA sorption was simulated using linear sorption coefficient determined with field data and 1,2-DCA degradation was simulated using a first order decay coefficient using literature data as initial guess. Finally, on the reactive transport model, where a two-step approach with partial equilibrium approach was implemented, the effects of neglecting the cation exchange capacity, omitting density-dependent flow, and refining the vertical

  11. Indium Sorption to Iron Oxides

    White, S. J.; Sacco, S. A.; Hemond, H.; Hussain, F. A.; Runkel, R. L.; Walton-Day, K. E.; Kimball, B. A.; Shine, J. P.


    Indium is an increasingly important metal in semiconductors and electronics, and its use is growing rapidly as a semiconductive coating (as indium tin oxide) for liquid crystal displays (LCDs) and flat panel displays. It also has uses in important energy technologies such as light emitting diodes (LEDs) and photovoltaic cells. Despite its rapid increase in use, very little is known about the environmental behavior of indium, and concerns are being raised over the potential health effects of this emerging metal contaminant. One source of indium to the environment is acid mine drainage from the mining of lead, zinc, and copper sulfides. In our previous studies of a stream in Colorado influenced by acid mine drainage from lead and zinc mining activities, indium concentrations were found to be 10,000 times those found in uncontaminated rivers. However, the speciation and mobility of indium could not be reliably modeled because sorption constants to environmental sorbents have not been determined. In this study, we generate sorption constants for indium to ferrihydrite in the laboratory over a range of pHs, sorbent to sorbate ratios, and ionic strengths. Ferrihydrite is one of the most important sorbents in natural systems, and sorption to amorphous iron oxides such as ferrihydrite is thought to be one of the main removal mechanisms of metals from the dissolved phase in aqueous environments. Because of its relatively low solubility, we also find that indium hydroxide precipitation can dominate indium's partitioning at micromolar concentrations of indium. This precipitation may be important in describing indium's behavior in our study stream in Colorado, where modeling sorption to iron-oxides does not explain the complete removal of indium from the dissolved phase when the pH of the system is artificially raised to above 8. This study contributes much-needed data about indium's aqueous behavior, in order to better understand its fate, transport, and impacts in the

  12. Sorption Energy Maps of Clay Mineral Surfaces

    Cygan, Randall T.; Kirkpatrick, R. James


    A molecular-level understanding of mineral-water interactions is critical for the evaluation and prediction of the sorption properties of clay minerals that may be used in various chemical and radioactive waste disposal methods. Molecular models of metal sorption incorporate empirical energy force fields, based on molecular orbital calculations and spectroscopic data, that account for Coulombic, van der Waals attractive, and short-range repulsive energies. The summation of the non-bonded energy terms at equally-spaced grid points surrounding a mineral substrate provides a three dimensional potential energy grid. The energy map can be used to determine the optimal sorption sites of metal ions on the exposed surfaces of the mineral. By using this approach, we have evaluated the crystallographic and compositional control of metal sorption on the surfaces of kaolinite and illite. Estimates of the relative sorption energy and most stable sorption sites are derived based on a rigid ion approximation.

  13. Solubility and sorption of petroleum hydrocarbons in water and cosolvent systems

    CHEN Hong; CHEN Shuo; QUAN Xie; ZHAO Yazhi; ZHAO Huimin


    The solubility and sorption of oil by uncontaminated clay loam and silt loam soils were studied from water and cosolvent/watersolutions using batch techniques. The data obtained from the dissolution and sorption experinaents were used to evaluate theapplicability of the cosolvent theory to oil as a complex mixture. Aqueous solubility and soil-water distribution coefficients (Kd,w,L/kg) were estimated by extrapolating from cosolvent data, with a log-linear cosolvency model, to the volume fraction of cosolvent(fc) 0, and were compared with direct aqueous measurements. The extrapolated water solubility was 3.16 mg/L, in good agreementwith the directly measured value of 3.83 mg/L. Extrapolated values of Kd,w for the two soils were close to each other but consistentlyhigher than the values from direct aqueous measurements, because of the presence of dissolved organic carbon (DOC). The partitioncoefficient (KDOC) between the DOC and the reely dissolved phase and the OC-normalized sorption coefficient (KOC) were determined.The average values of logKDOC and logKoc were estimated as 4.34 and 3.32, respectively, giving insight into the possibility of oilbecoming mobilized and/or of the soil being remedied. This study revealed that the cosolvency model can be applied to a broader rangeof hydrophobic organic chemicals (HOCs) than has been previously thought. The results aided in a reliable determination of watersolubility and sorption coefficients and provide information about the fate of oil in solvent-contaminated environment.

  14. Manganese Nitride Sorption Joule-Thomson Refrigerator

    Jones, Jack A.; Phillips, Wayne M.


    Proposed sorption refrigeration system of increased power efficiency combines MnxNy sorption refrigeration stage with systems described in "Regenerative Sorption Refrigerator" (NPO-17630). Measured pressure-vs-composition isotherms for reversible chemisorption of N2 in MnxNy suggest feasibility to incorporate MnxNy chemisorption stage in Joule-Thomson cryogenic system. Discovery represents first known reversible nitrogen chemisorption compression system. Has potential in nitrogen-isotope separation, nitrogen purification, or contamination-free nitrogen compression.

  15. COLWRIT – Collaborative Online Writing in Google Docs

    Andreasen, Lars Birch; Winther, Frederikke; Hanghøj, Thorkild;


    Various online collaborative writing tools have emerged giving students new opportunities when co-producing texts. The aim of this work-in-progress paper is to present the preliminary hypotheses and findings of an on-going research project at Aalborg University, Denmark, which explores university...... students’ uses of collaborative writing tools like Google Docs when doing collaborative project work. The research project has a special focus on the various effects on the collaboration process of students’ various usage of the commenting functions of online writing tools....

  16. COLWRIT – Collaborative Online Writing in Google Docs

    Andreasen, Lars Birch; Winther, Frederikke; Hanghøj, Thorkild


    Various online collaborative writing tools have emerged giving students new opportunities when co-producing texts. The aim of this work-in-progress paper is to present the preliminary hypotheses and findings of an on-going research project at Aalborg University, Denmark, which explores university...... students’ uses of collaborative writing tools like Google Docs when doing collaborative project work. The research project has a special focus on the various effects on the collaboration process of students’ various usage of the commenting functions of online writing tools....

  17. Evaluation of Lagergren Kinetics Equation by Using Novel Kinetics Expression of Sorption of Zn2+ onto Horse Dung Humic Acid (HD-HA

    Bambang Rusdiarso


    Full Text Available Extraction and purification of humic acid from dry horse dung powder (HD-HA was performed successfully and the purified HD-HA was then applied as sorbent to adsorb Zn2+. Extraction and purification were performed based on procedure of Stevenson (1994 under atmospheric air. Parameters investigated in this work consist of effect of medium sorption acidity, sorption rate (ka and desorption rate constant (kd, Langmuir (monolayer and Freundlich (multilayer sorption capacities, and energy (E of sorption. The ka and kd were determined according to the kinetic model of second order sorption reaching equilibrium, monolayer sorption capacity (b and energy (E were determined according to Langmuir isotherm model, and multilayer sorption capacity (B was determined based on Freundlich isotherm model. Sorption of Zn2+ on purified HD-HA was maximum at pH 5.0. The novel kinetic expression resulted from proposed kinetic model has been shown to be more applicable than the commonly known Lagergren equation obtained from the pseudo-first order sorption model. The application of the equation revealed that the intercept of Lagergren equation, ln qe was more complex function of initial concentration of Zn2+ (a, Langmuir sorption capacity (b, and sorbed Zn2+ at equilibrium (xe.

  18. Dissolved organic carbon dynamics in a UK podzolic moorland catchment: linking storm hydrochemistry, flow path analysis and sorption experiments

    M. I. Stutter


    Full Text Available Better knowledge of spatial and temporal delivery of dissolved organic carbon (DOC in small catchments is required to understand the mechanisms behind reported long-term changes in C fluxes from some peatlands. We monitored two storms with contrasting seasons and antecedent conditions in a small upland UK moorland catchment. We examined DOC concentrations and specific UV absorbance (SUVA at 285 nm, together with solute concentrations required to undertake end-member mixing analyses to define dominant flow paths contributing to streamflow. This was combined with laboratory soil-solution equilibrations. We aimed to resolve how seasonal biogeochemical processing of DOC and flowpath changes in organo-mineral soils combine to affect DOC exported via the stream. An August storm following a dry period gave maximum DOC concentration of 10 mg l−1. Small DOC:DON ratios (16–28 and SUVA (2.7–3.6 l mg−1 m−1 was attributed to filtration of aromatic compounds associated with up to 53% B horizon flow contributions. This selective filtration of high SUVA DOC was reproduced in the experimental batch equilibration system. For a November storm, wetter antecedent soil conditions led to enhanced soil connectivity with the stream and seven times greater DOC stream-load (maximum concentration 16 mg l−1. This storm had a 63% O horizon flow contribution at its peak, limited B horizon buffering and consequently more aromatic DOC (SUVA 3.9–4.5 l mg−1 m−1 and DOC:DON ratio 35–43. We suggest that simple mixing of waters from different flow paths cannot alone explain the differences in DOC compositions between August and November and biogeochemical processing of DOC is required to fully explain the observed stream DOC dynamics. This preliminary evidence is in contrast to other studies proposing hydrological controls on the nature of DOC delivered to streams. Although our study is based only

  19. Dissolved organic carbon dynamics in a UK podzolic moorland catchment: linking storm hydrochemistry, flow path analysis and sorption experiments

    Stutter, M. I.; Dunn, S. M.; Lumsdon, D. G.


    Better knowledge of spatial and temporal delivery of dissolved organic carbon (DOC) in small catchments is required to understand the mechanisms behind reported long-term changes in C fluxes from some peatlands. We monitored two storms with contrasting seasons and antecedent conditions in a small upland UK moorland catchment. We examined DOC concentrations and specific UV absorbance (SUVA at 285 nm), together with solute concentrations required to undertake end-member mixing analyses to define dominant flow paths contributing to streamflow. This was combined with laboratory soil-solution equilibrations. We aimed to resolve how seasonal biogeochemical processing of DOC and flowpath changes in organo-mineral soils combine to affect DOC exported via the stream. An August storm following a dry period gave maximum DOC concentration of 10 mg l-1. Small DOC:DON ratios (16-28) and SUVA (2.7-3.6 l mg-1 m-1) was attributed to filtration of aromatic compounds associated with up to 53% B horizon flow contributions. This selective filtration of high SUVA DOC was reproduced in the experimental batch equilibration system. For a November storm, wetter antecedent soil conditions led to enhanced soil connectivity with the stream and seven times greater DOC stream-load (maximum concentration 16 mg l-1). This storm had a 63% O horizon flow contribution at its peak, limited B horizon buffering and consequently more aromatic DOC (SUVA 3.9-4.5 l mg-1 m-1 and DOC:DON ratio 35-43). We suggest that simple mixing of waters from different flow paths cannot alone explain the differences in DOC compositions between August and November and biogeochemical processing of DOC is required to fully explain the observed stream DOC dynamics. This preliminary evidence is in contrast to other studies proposing hydrological controls on the nature of DOC delivered to streams. Although our study is based only on two storms of very different hydrological and biogeochemical periods, this should promote wider

  20. Sorption of triclosan on electrospun fibrous membranes: Effects of pH and dissolved organic matter

    Jiangjie Xu


    Full Text Available Three hydrophobic and polyporous electrospun fibrous membranes (EFMs were prepared by electrospinning methoxy polyethylene glycol-poly(lactide-co-glycolide (MPEG-PLGA, poly(d,l-lactide-co-glycolide (PLGA and poly(d,l-lactide (PDLLA. The effects of pH and dissolved organic matter (DOM on triclosan (TCS sorption by EFMs in aqueous solution were investigated. The results indicated that hydrogen bonding, hydrophobic and π–π bonding interactions led to fast adsorption, which governed the adsorption rates of TCS onto EFMs. The maximum sorption capacities of MPEG-PLGA, PLGA and PDLLA reached 130, 93 and 99 mg g−1, respectively, which were in positive correlation with their pore volumes and influenced by pore filling processes. The solution pH could significantly influence the TCS sorption by EFMs. In acid condition, protonated TCS facilitated their sorption onto EFMs. No obvious sorption was observed in alkaline condition due to repulsive forces between negatively charged EFMs and deprotonated TCS (pKa = 7.9. The presence of DOM inhibited TCS sorption onto EFMs due to competitive adsorption. The results could be due to the occupation of the adsorption sites and the blockage of the pore entrance by DOM.

  1. 75 FR 12496 - Proposed Information Collection; Comment Request; DOC National Environmental Policy Act...


    ... Office of the Secretary Proposed Information Collection; Comment Request; DOC National Environmental Policy Act Environmental Questionnaire and Checklist AGENCY: Office of the Secretary, Office of... INFORMATION: I. Abstract The Department of Commerce (DOC) National Environmental Policy Act...

  2. Google Docs: an experience in collaborative work in the University



    Full Text Available The educational environment contains multiple reasons to make use of the new possibilities that Information and Communication Technologies (ICT as an educational resource offer. The educational experience presented here has been realized in the subject of New Technologies applied to Education, which forms part of the study plans for primary school teachers in the University of Burgos (UBU, and which has as its main goal to facilitate the acquisition of generic competences of ICT to work online. To reach this proposed goal, we have cultivated active learning of the students, from individual to collective learning. At first, they were given a text to work individually, to read and review. After that, groups were created to work on the document cooperatively, online, through the use of the office tool Google Docs. After sharing and editing the document, every group made a multimedia presentation in which all of their contributions are bundled. Finally, all of the presentations made by every one of the groups were made public. When the practical part of the course was done, the students answered a short questionnaire in which they were asked about their initial knowledge, and the level of dominion and didactic usefulness of the tool Google Docs. It is worth noting that 75% of the class did not know the application before the course and that, after using it, 92% say they would use it in the educational and professional future. This educational experience has been very satisfactory for students and professors alike.

  3. Plutonium sorption and desorption behavior on bentonite.

    Begg, James D; Zavarin, Mavrik; Tumey, Scott J; Kersting, Annie B


    Understanding plutonium (Pu) sorption to, and desorption from, mineral phases is key to understanding its subsurface transport. In this work we study Pu(IV) sorption to industrial grade FEBEX bentonite over the concentration range 10(-7)-10(-16) M to determine if sorption at typical environmental concentrations (≤10(-12) M) is the same as sorption at Pu concentrations used in most laboratory experiments (10(-7)-10(-11) M). Pu(IV) sorption was broadly linear over the 10(-7)-10(-16) M concentration range during the 120 d experimental period; however, it took up to 100 d to reach sorption equilibrium. At concentrations ≥10(-8) M, sorption was likely affected by additional Pu(IV) precipitation/polymerization reactions. The extent of sorption was similar to that previously reported for Pu(IV) sorption to SWy-1 Na-montmorillonite over a narrower range of Pu concentrations (10(-11)-10(-7) M). Sorption experiments with FEBEX bentonite and Pu(V) were also performed across a concentration range of 10(-11)-10(-7) M and over a 10 month period which allowed us to estimate the slow apparent rates of Pu(V) reduction on a smectite-rich clay. Finally, a flow cell experiment with Pu(IV) loaded on FEBEX bentonite demonstrated continued desorption of Pu over a 12 day flow period. Comparison with a desorption experiment performed with SWy-1 montmorillonite showed a strong similarity and suggested the importance of montorillonite phases in controlling Pu sorption/desorption reactions on FEBEX bentonite.

  4. [Effect of the Runoff-sediment Control of the Xiaolangdi Reservoir on DOC Transport].

    Zhang, Yong-ling; Wang, Ming-shi; Dong, Yu-long


    The sampling was carried out in Sanmenxia hydrological station, Xiaolangdi hydrological station and Huayuankou hydrological station from November 2011 to October 2012. The impact of the runoff-sediment control of the Xiaolangdi reservoir on DOC transport,was analyzed. The results were as follows. DOC contents in Sanmenxia station, Xiaolangdi station and Huayuankou station were 1.97-2.71 mg-L(-1), 1.87-2.76 mg x L(-1) and 2.07-2.93 mg x L(-1), respectively, during the normal operation period of Xiaolangdi Reservoir and Sanmenxia reservoir, and the DOC content in the three reservoirs had obvious seasonal change. DOC contents in the three stations were 2.14-3.32 mg x L(-1), 2.21-2.84 mg x L(-1) and 2.11-2.84 mg x L(-1), respectively, during the runoff-sediment control, and the DOC content in the sediment-releasing period of reservoir was higher than that in the water-releasing period of reservoir. DOC content had no significant correlation with TSS and flow either during the normal operation or during the water-sediment regulation of the reservoir. But the DOC content had significant correlation with water temperature during the normal operation of the reservoir. DOC flux in Sanmenxia station was similar to that in Xiaolangdi station from November to March. DOC flux in Sanmenxia station was obviously less than that in Xiaolangdi station from April to July. And the DOC flux in Sanmenxia station was much higher than that in Xiaolangdi station from August to October. The result showed that DOC was retained from August to October by Xiaolangdi reservoir and discharged from Xiaolangdi reservoir from April to July. The yearly DOC fluxes were 8.6 x 10(10), 9.0 x 10(10) and 9.7 x 10(10) g respectively in Sanmenxia station, Xiaolangdi station and Huayuankou station. The DOC flux of Sanmenxia station was the highest in September, which accounted for 22.0% of the yearly DOC flux, and the DOC flux of Xiaolangdi station was the highest in June, which accounted for 17.6% of the

  5. Sorption and desorption studies of a reactive azo dye on effective disposal of redundant material.

    Çelekli, Abuzer; Bozkurt, Hüseyin


    The effective disposal of redundant elephant dung (ED) is important for environmental protection and utilization of resource. The aim of this study was to remove a toxic-azo dye, Reactive Red (RR) 120, using this relatively cheap material as a new adsorbent. The FTIR-ATR spectra of ED powders before and after the sorption of RR 120 and zero point charge (pHzpc) of ED were determined. The sorption capacity of ED for removing of RR 120 were carried out as functions of particle size, adsorbent dose, pH, temperature, ionic strength, initial dye concentration, and contact time. Sorption isotherm, kinetic, activation energy, thermodynamic, and desorption parameters of RR 120 on ED were studied. The sorption process was found to be dependent on particle size, adsorbent dose, pH, temperature, ionic strength, initial dye concentration, and contact time. FTIR-ATR spectroscopy indicated that amine and amide groups have significant role on the sorption of RR 120 on ED. The pHzpc of ED was found to be 7.3. Sorption kinetic of RR 120 on ED was well described by sigmoidal Logistic model. The Langmuir isotherm was well fitted to the equilibrium data. The maximum sorption capacity was 95.71 mg g(-1). The sorption of RR 120 on ED was mainly physical and exothermic according to results of D-R isotherm, Arrhenius equation, thermodynamic, and desorption studies. The thermodynamic parameters showed that this process was feasible and spontaneous. This study showed that ED as a low-cost adsorbent had a great potential for the removal of RR 120 as an alternative eco-friendly process.

  6. Equilibrium, kinetic and thermodynamic studies for sorption of Ni (II) from aqueous solution using formaldehyde treated waste tea leaves


    The sorption characteristic of Ni (II) from aqueous solution using formaldehyde treated waste tea leaves as a low cost sorbent has been studied. The effect of pH, contact time, sorbent dose, initial metal ion concentration and temperature were investigated in batch experiments. The equilibrium data were fitted into four most common isotherm models; Freundlich, Langmuir, Tempkin and Dubinin–Radushkevich (D–R). The Langmuir model described the sorption isotherm best with maximum monolayer sorpt...

  7. Synthesis of Nano-sized Boehmites for Optimum Phosphate Sorption

    Watanabe, Yujiro; Kasama, Takeshi; Fukushi, Keisuke;


    Nano-sized boehmites with different crystallinity were synthesized at the temperature range of 25 to 200°C in order to produce phosphate absorbents with high capacity. The physicochemical property of boehmites was depended on the synthesis temperature: the particle size was increased and the surf......Nano-sized boehmites with different crystallinity were synthesized at the temperature range of 25 to 200°C in order to produce phosphate absorbents with high capacity. The physicochemical property of boehmites was depended on the synthesis temperature: the particle size was increased...... and the surface area showed the maximum for the boehmite at 50°C. The phosphate sorptions into boehmites were analyzed at room temperature in the phosphoric acid solutions as a model of wastewater at the concentration of 0.1 to 3.0 mmol l-1 and the pH of 3 to 7. The boehmite synthesized at 50°C exhibited...... the highest amount of phosphate sorption (1.73 mmol g-1 at pH 3.3) compared with Al-bearing materials. The reaction mechanism during phosphate sorption was described by the anion exchange reaction between phosphate ions in sodium phosphate solution and hydroxide ions on boehmite surfaces. Therefore...

  8. Google Docs in an Out-of-Class Collaborative Writing Activity

    Zhou, Wenyi; Simpson, Elizabeth; Domizi, Denise Pinette


    Google Docs, an online word processing application, is a promising tool for collaborative learning. However, many college instructors and students lack knowledge to effectively use Google Docs to enhance teaching and learning. Goals of this study include (1) assessing the effectiveness of using Google Docs in an out-of-class collaborative writing…

  9. Kinetics, mechanistic and thermodynamics of Zn(II) ion sorption: a modeling approach

    Mishra, Vishal; Balomajumder, Chandrajit; Agarwal, Vijay Kumar [Department of Chemical Engineering, Indian Institute of Technology, Roorkee (India)


    Biosorption potential of Cedrus deodara sawdust (CDS) in terms of sorption of Zn(II) ion across liquid phase has been evaluated in the present investigation. The surface of the CDS biomass before the sorption of Zn(II) ions seemed to be more porous, non-crystalline and heterogeneous. The maximum uptake capacity of CDS was 97.39 mg g{sup -1}. Sorption of Zn(II) ion on the surface of CDS sawdust was maximum at pH 5, temperature 45 C, initial concentration of Zn(II) ion 100 mg L{sup -1}, biomass dose 1 g L{sup -1}, contact time 150 min, and agitation rate 160 rpm. Pseudo second-order kinetics with the highest linear regression coefficient (R{sup 2} = 0.99), and lowest values of error functions, i.e., chi ({chi}{sup 2}) and sum of square errors (SSE) against pseudo first-order rate kinetics showed that the sorption of Zn(II) ion on the surface of CDS was mediated by chemosorptive forces of attraction rather than physical adsorption. Mechanistically, relatively higher proportion of sorption of Zn(II) ion in early phase of contact time was profoundly explained by Bangham's equation and film diffusivity (D{sup f}). Intraparticle or pore diffusion (D{sub p}) of Zn(II) ion inside the pores of CDS was rate limiting step at the later stage of contact time. Furthermore, the thermodynamic study on sorption of metal ion delineated the fact that the Zn(II) sorption on the surface of CDS was spontaneous, endothermic together with increased entropy at solid liquid interface. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Nitrate Sorption in an Agricultural Soil Profile

    Wissem Hamdi


    Full Text Available Increasing concentrations of in surface water and groundwater can cause ecological and public health effects and has come under increased scrutiny by both environmental scientists and regulatory agencies. For many regions though, including the Sahel of Tunisia, little is known about the sorption capacity of soils. In this project we measured sorption by a profile of an iso-humic soil from Chott Meriem, Tunisia. Soil samples were collected from four soil depths (0–25, 25–60, 60–90, and 90–120 cm on 1 June 2011, and their sorption capacity was determined using batch experiments under laboratory conditions. The effects of contact time, the initial concentration, and the soil-solution ratio on sorption were investigated. In general, the results suggested that was weakly retained by the Chott Meriem soil profile. The quantity of sorption increased with depth, contact time, initial concentration, and soil-solution ratios. To evaluate the sorption capacities of the soil samples at concentrations ranging between 25 and 150 mg L−1 experimental data were fitted to both Freundlich and Langmuir isotherm sorption models. The results indicated that Freundlich model was better for describing sorption in this soil profile.

  11. Surface complexation model of uranyl sorption on Georgia kaolinite

    Payne, T.E.; Davis, J.A.; Lumpkin, G.R.; Chisari, R.; Waite, T.D.


    The adsorption of uranyl on standard Georgia kaolinites (KGa-1 and KGa-1B) was studied as a function of pH (3-10), total U (1 and 10 ??mol/l), and mass loading of clay (4 and 40 g/l). The uptake of uranyl in air-equilibrated systems increased with pH and reached a maximum in the near-neutral pH range. At higher pH values, the sorption decreased due to the presence of aqueous uranyl carbonate complexes. One kaolinite sample was examined after the uranyl uptake experiments by transmission electron microscopy (TEM), using energy dispersive X-ray spectroscopy (EDS) to determine the U content. It was found that uranium was preferentially adsorbed by Ti-rich impurity phases (predominantly anatase), which are present in the kaolinite samples. Uranyl sorption on the Georgia kaolinites was simulated with U sorption reactions on both titanol and aluminol sites, using a simple non-electrostatic surface complexation model (SCM). The relative amounts of U-binding >TiOH and >AlOH sites were estimated from the TEM/EDS results. A ternary uranyl carbonate complex on the titanol site improved the fit to the experimental data in the higher pH range. The final model contained only three optimised log K values, and was able to simulate adsorption data across a wide range of experimental conditions. The >TiOH (anatase) sites appear to play an important role in retaining U at low uranyl concentrations. As kaolinite often contains trace TiO2, its presence may need to be taken into account when modelling the results of sorption experiments with radionuclides or trace metals on kaolinite. ?? 2004 Elsevier B.V. All rights reserved.

  12. Phenanthrene Sorption on Biochar-Amended Soils

    Kumari, K. G I D; Moldrup, Per; Paradelo, Marcos


    on their influences on the sorption of environmental contaminants. In a field-based study at two experimental sites in Denmark, we investigated the effect of birch wood-derived biochar (Skogans kol) on the sorption of phenanthrene in soils with different properties. The soil sorption coefficient, Kd (L kg-1......), of phenanthrene was measured on sandy loam and loamy sand soils which have received from zero up to 100 t ha-1 of biochar. Results show that birch wood biochar had a higher Kd compared to soils. Furthermore, the application of birch wood biochar enhanced the sorption of phenanthrene in agricultural soils...... carbon, while it negatively correlated with clay content. The results also revealed that biochar-mineral interactions play an important role in the sorption of phenanthrene in biochar-amended soil....

  13. Dissolved organic carbon dynamics in a UK podzolic moorland catchment: linking storm hydrochemistry, flow path analysis and sorption experiments

    M. I. Stutter


    Full Text Available Better knowledge of spatial and temporal delivery of dissolved organic Carbon (DOC in small catchments is required to understand the mechanisms behind reported long-term changes in C fluxes from some peatlands. We monitored two storms with contrasting seasons and antecedent conditions in a small upland UK moorland catchment. We examined DOC concentrations and specific UV absorbance (SUVA at 285 nm, together with solute concentrations required to undertake end member mixing analyses to define dominant flow paths contributing to streamflow. This was combined with laboratory soil-solution equilibrations. We aimed to resolve how seasonal biogeochemical processing of DOC and flowpath changes in organo-mineral soils combine to affect DOC exported via the stream. An August storm following a dry period gave maximum DOC concentration of 10 mg l−1. Small DOC:DON ratios (16–28 and SUVA (2.7–3.6 l mg−1 m−1 was attributed to filtration of aromatic compounds associated with up to 53% B horizon flow contributions. This selective filtration of high SUVA DOC was reproduced in the experimental batch equilibration system. For a November storm, wetter antecedent soil conditions led to enhanced soil connectivity with the stream and seven times greater DOC stream-load (maximum concentration 16 mg l−1. This storm had a 63% O horizon flow contribution at its peak, limited B horizon buffering and consequently more aromatic DOC (SUVA 3.9–4.5 l mg−1 m−1 and DOC:DON ratio 35–43. We suggest that simple mixing of waters from different flow paths cannot alone explain the differences in DOC compositions between August and November and biogeochemical processing of DOC is required to fully explain the observed stream DOC dynamics. This is in contrast to other studies proposing hydrological controls and provides evidence that DOC biogeochemistry must be incorporated in modelling to predict the

  14. The fate of silver nanoparticles in soil solution--Sorption of solutes and aggregation.

    Klitzke, Sondra; Metreveli, George; Peters, Andre; Schaumann, Gabriele E; Lang, Friederike


    Nanoparticles enter soils through various pathways. In the soil, they undergo various interactions with the solution and the solid phase. We tested the following hypotheses using batch experiments: i) the colloidal stability of Ag NP increases through sorption of soil-borne dissolved organic matter (DOM) and thus inhibits aggregation; ii) the presence of DOM suppresses Ag oxidation; iii) the surface charge of Ag NP governs sorption onto soil particles. Citrate-stabilized and bare Ag NPs were equilibrated with (colloid-free) soil solution extracted from a floodplain soil for 24h. Nanoparticles were removed through centrifugation. Concentrations of free Ag ions and DOC, the specific UV absorbance at a wavelength of 254 nm, and the absorption ratio α254/α410 were determined in the supernatant. Nanoparticle aggregation was studied using time-resolved dynamic light scattering (DLS) measurement following the addition of soil solution and 1.5mM Ca(2+) solution. To study the effect of surface charge on the adsorption of Ag NP onto soil particles, bare and citrate-stabilized Ag NP, differing in the zeta potential, were equilibrated with silt at a solid-to-solution ratio of 1:10 and an initial Ag concentration range of 30 to 320 μg/L. Results showed that bare Ag NPs sorb organic matter, with short-chained organic matter being preferentially adsorbed over long-chained, aromatic organic matter. Stabilizing effects of organic matter only come into play at higher Ag NP concentrations. Soil solution inhibits the release of Ag(+) ions, presumably due to organic matter coatings. Sorption to silt particles was very similar for the two particle types, suggesting that the surface charge does not control Ag NP sorption. Besides, sorption was much lower than in comparable studies with sand and glass surfaces. Copyright © 2014. Published by Elsevier B.V.

  15. Sorption of vanadium (V) onto natural soil colloids under various solution pH and ionic strength conditions.

    Luo, Xiuhua; Yu, Lin; Wang, Changzhao; Yin, Xianqiang; Mosa, Ahmed; Lv, Jialong; Sun, Huimin


    Batch sorption kinetics and isothermal characteristics of V(V) were investigated on three natural soil colloids (manual loessial soil colloid (MSC), aeolian sandy soil colloid (ASC), and cultivated loessial soil colloid (CSC)) under various solution pH and ionic strength (IS) conditions. Colloids were characterized by atomic force microscopy (AFM), X-ray diffraction (XRD), and fourier transform infrared spectroscopy (FTIR). AFM micrographs showed CSC with an aggregated shape with larger particle diameter as compared with ASC and MSC. XRD spectra revealed the presence of different minerals in natural soil colloids including biotite, kaolinite, calcite and quartz, which might contribute to sorption process. The sorption ability decreased with increase of colloidal particle size. The sorption was mainly attributed to complexation by active carboxylate and alcohol groups of colloidal components. Sorption kinetics and isotherms of V(V) onto natural soil colloids were best fitted with Pseudo-second-order and Freundlich models. Langmuir model indicated that sorption capacity of MSC and ASC was comparable (285.7 and 238.1 mg g(-1)); however, CSC exhibited the lowest sorption capacity (41.5 mg g(-1)) due to its larger particle diameter and aggregated shape. The maximum V(V) sorption capacity reached plateau values at a solution pH ranged between 5.0 and 9.0 for MSC and ASC, and 6.0-8.0 for CSC. Sorption capacity of V(V) onto natural soil colloids decreased with increasing IS. Based on result of this study we can conclude that sorption of V(V) onto natural soil colloids is pH- and IS-dependent. These findings provide insights on the remediation of vanadium-contaminated soils. Copyright © 2016 Elsevier Ltd. All rights reserved.

  16. Impacts of soil organic matter, pH and exogenous copper on sorption behavior of norfloxacin in three soils

    ZHANG Jie; LI Zhaojun; GE Gaofei; SUN Wanchun; LIANG Yongchao; WU Laosheng


    Norfloxacin (Nor) sorption and the factors (soil organic matter (SOM), pH, and exogenous copper (Cu) influencing the sorption were investigated in a black soil (soil B), a fluvo-aquic soil (soil F), and a red soil (soil R). With increasing of Nor concentrations, sorption amount of norfloxacin increased in both the bulk soils and their SOM-removed soils, but the sorption capacity in SOM-removed soils was higher than that of their corresponding bulk soils, indicating that the process of norfloxacin sorption in soil was influenced by the soil properties including SOM. The sorption data in all bulk soils and SOM-removed soils were fitted to Freundlich and Langmuir models. The correlation coefficients suggested that the experimental data fitted better to Freundlich equation than to Langmuir equation. Furthermore, the data from soil F and SOM-removed F could not be described by Langmuir equation. The norfloxacin sorption amount decreased in soil B and soil F, whereas it increased in soil R as solution pH increased. The maximum KD and KOC were achieved in soil R when the equilibrium solution pH was 6. And the norfloxacin sorption was also influenced by the exogenous Cu2+ ions, which depended on the soil types and Cu2+ concentrations. With increasing of Cu2+ concentrations in solution, generally, sorption amount, KD and KOC for norfloxacin in soils increased and were up to a peak at 100 mg/L Cu2+, and then the sorption amount decreased regardless of norfloxacin levels.

  17. Sorption kinetics of ofloxacin in soils and mineral particles.

    Pan, Bo; Wang, Peng; Wu, Min; Li, Jing; Zhang, Di; Xiao, Di


    The environmental behavior of antibiotics is not well known and the precise environmental risk assessment is not practical. This study investigated the sorption kinetics of ofloxacin, a widely used antibiotics, on soil particles with different organic carbon contents as well as soil components (a humic acid, ferric oxide and kaolinite). Two-compartment sorption kinetics were mathematically recognized (except ferric oxide because of its very fast sorption). The apparent sorption rate and the contribution of fast sorption compartment decreased with the increased organic carbon content with the exception of humic acid, suggesting that the slow sorption sites were partially located in organo-mineral complex. The OFL concentration-dependent sorption kinetics suggested that the slow sorption compartment was not controlled by diffusion process as indicated by slower sorption at higher OFL loading. The difference between OFL sorption kinetics and those of hydrophobic organic contaminants was discussed and possible mechanism of OFL two-compartment sorption was proposed.

  18. Link between DOC in near surface peat and stream water in an upland catchment.

    Clark, Joanna M; Lane, Stuart N; Chapman, Pippa J; Adamson, John K


    Hydrologic transport of dissolved organic carbon (DOC) from peat soils may differ to organo-mineral soils in how they responded to changes in flow, because of differences in soil profile and hydrology. In well-drained organo-mineral soils, low flow is through the lower mineral layer where DOC is absorbed and high flow is through the upper organic layer where DOC is produced. DOC concentrations in streams draining organo-mineral soils typically increase with flow. In saturated peat soils, both high and low flows are through an organic layer where DOC is produced. Therefore, DOC in stream water draining peat may not increase in response to changes in flow as there is no switch in flow path between a mineral and organic layer. To verify this, we conducted a high-resolution monitoring study of soil and stream water at an upland peat catchment in northern England. Our data showed a strong positive correlation between DOC concentrations at -1 and -5 cm depth and stream water, and weaker correlations between concentrations at -20 to -50 cm depth and stream water. Although near surface organic material appears to be the key source of stream water DOC in both peat and organo-mineral soils, we observed a negative correlation between stream flow and DOC concentrations instead of a positive correlation as DOC released from organic layers during low and high flow was diluted by rainfall. The differences in DOC transport processes between peat and organo-mineral soils have different implications for our understanding of long-term changes in DOC exports. While increased rainfall may cause an increase in DOC flux from peat due to an increase in water volume, it may cause a decrease in concentrations. This response is contrary to expected changes in DOC exports from organo-mineral soils, where increase rainfall is likely to result in an increase in flux and concentration.


    Hobbs, D.; Elvington, M.; Click, D.


    Inorganic, titanate-based sorbents are tested with respect to adsorption of a variety of sorbates under weakly acidic conditions (pH 3). Specifically, monosodium titanate (MST) and amorphous peroxotitanate (APT) sorption characteristics are initially probed through a screening process consisting of a pair of mixed metal solutions containing a total of 29 sorbates including alkali metals, alkaline earth metals, transition metals, metalloids and nonmetals. MST and APT sorption characteristics are further analyzed individually with chromium(III) and cadmium(II) using a batch method at ambient laboratory temperature, varying concentrations of the sorbents and sorbates and contact times. Maximum sorbate loadings are obtained from the respective adsorption isotherms.

  20. The Survey of Sorption Ion-Exchange Properties of Paleozoic Natural Minerals in the Static Conditions

    Germanova, T. V.; Nefedov, V. A.; Valieva, I. R.


    An experimental and exploring process’ results of iron’s ion, manganese and ammonium sodium extraction from aqueous solution by some Ural’s natural minerals in a static regime at certain physicochemical conditions: by the zeolite, montmorillonite and vermiculite in the static conditions. Values of maximum sorption capacity are estimated on a gram of natural sorbents for the present conditions. Comparison of the survey’s results shows that effective sorptions from exploring natural minerals can be used as a clinoptilolite and zeolite-mineral montmorillonite type.

  1. Sorption of chrysoidine by row cork and cork entrapped in calcium alginate beads

    Valeria M. Nurchi


    The influence on the sorption of pH, initial dye concentration, and particle size, as well as the efficiency of the entrapment, have been investigated. The maximum sorption was found for cork samples of fine particle size (FC, in both row and entrapped forms, at pH 7; conversely, at pH 4 the difference is significant (0.12 mmol/g for row cork and 0.20 mmol/g for entrapped cork, evoking a cooperation of alginate in binding the positively charged chrysoidine molecule.

  2. Sorption equilibria of ethanol on cork.

    Lequin, Sonia; Chassagne, David; Karbowiak, Thomas; Bellat, Jean-Pierre


    We report here for the first time a thermodynamic study of gaseous ethanol sorption on raw cork powder and plate. Our study aims at a better understanding of the reactivity of this material when used as a stopper under enological conditions, thus in close contact with a hydroethanolic solution, wine. Sorption−desorption isotherms were accurately measured by thermogravimetry at 298 K in a large range of relative pressures. Sorption enthalpies were determined by calorimetry as a function of loading. Sorption−desorption isotherms exhibit a hysteresis loop probably due to the swelling of the material and the absorption of ethanol. Surprisingly, the sorption enthalpy of ethanol becomes lower than the liquefaction enthalpy as the filling increases. This result could be attributed to the swelling of the material, which would generate endothermic effects. Sorption of SO₂ on cork containing ethanol was also studied. When the ethanol content in cork is 2 wt %, the amount of SO₂ sorbed is divided by 2. Thus, ethanol does not enhance the sorption rate for SO₂ but, on the contrary, decreases the SO₂ sorption activity onto cork, probably because of competitive sorption mechanisms.

  3. Sorption of melanoidin onto surfactant modified zeolite

    Onyango Maurice S.


    Full Text Available Melanoidin is responsible for the dark brown colour of distillery wastewater. Discharge of coloured wastewater has a major environmental impact on the biota of the receiving water body. Consequently, this study explores the removal of melanodin from aqueous solution. The equilibrium, kinetics and thermodynamics of melanoidin sorption are studied by varying initial solution pH, initial concentration, adsorbent dose and temperature. Kinetically, the melanoidin removal from solution by a surfactant modified zeolite is rapid and the amount adsorbed is dependent on pH, initial concentration, adsorbent dose and temperature. The equilibrium sorption data are fitted to the Freundlich and Langmuir models while the sorption, kinetics is described by the Ho pseudo-second order and Elovich models. The thermodynamic analysis indicates that the sorption is spontaneous and endothermic in nature. The FTIR spectra analyses show no new peaks or shift in peaks after sorption indicating that the melanoidin sorption may have occurred by a physical process. The results from desorption studies showed that melanoidin eluted back easily to the solution using distilled water which corroborates the physical sorption mechanism.

  4. Equilibrium, kinetic and thermodynamic studies for sorption of Ni (II from aqueous solution using formaldehyde treated waste tea leaves

    Jasmin Shah


    Full Text Available The sorption characteristic of Ni (II from aqueous solution using formaldehyde treated waste tea leaves as a low cost sorbent has been studied. The effect of pH, contact time, sorbent dose, initial metal ion concentration and temperature were investigated in batch experiments. The equilibrium data were fitted into four most common isotherm models; Freundlich, Langmuir, Tempkin and Dubinin–Radushkevich (D–R. The Langmuir model described the sorption isotherm best with maximum monolayer sorption capacity of 120.50 mg g−1. Four kinetic models, pseudo-first-order, pseudo-second-order, intraparticle diffusion and Elovich were employed to explain the sorption mechanism. The kinetics of sorption data showed that the pseudo-second-order model is the best with correlation coefficient of 0.9946. The spontaneous and exothermic nature of the sorption process was revealed from thermodynamic investigations. The effect of some common alkali and alkaline earth metal ions were also studied which showed that the presence of these ions have no effect on the sorption of Ni (II. The results showed that waste tea leaves have the potential to be used as a low cost sorbent for the removal of Ni (II from aqueous solutions.

  5. Alginate and Algal-Based Beads for the Sorption of Metal Cations: Cu(II) and Pb(II)

    Wang, Shengye; Vincent, Thierry; Faur, Catherine; Guibal, Eric


    Alginate and algal-biomass (Laminaria digitata) beads were prepared by homogeneous Ca ionotropic gelation. In addition, glutaraldehyde-crosslinked poly (ethyleneimine) (PEI) was incorporated into algal beads. The three sorbents were characterized by scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX): the sorption occurs in the whole mass of the sorbents. Sorption experiments were conducted to evaluate the impact of pH, sorption isotherms, and uptake kinetics. A special attention was paid to the effect of drying (air-drying vs. freeze-drying) on the mass transfer properties. For alginate, freeze drying is required for maintaining the porosity of the hydrogel, while for algal-based sorbents the swelling of the material minimizes the impact of the drying procedure. The maximum sorption capacities observed from experiments were 415, 296 and 218 mg Pb g−1 and 112, 77 and 67 mg Cu g−1 for alginate, algal and algal/PEI beads respectively. Though the sorption capacities of algal-beads decreased slightly (compared to alginate beads), the greener and cheaper one-pot synthesis of algal beads makes this sorbent more competitive for environmental applications. PEI in algal beads decreases the sorption properties in the case of the sorption of metal cations under selected experimental conditions. PMID:27598128

  6. ES-doc-errata: an issue tracker platform for CMIP6

    Ben Nasser, Atef; Levavasseur, Guillaume; Greenslade, Mark; Denvil, Sébastien


    In the context of overseeing the quality of data, and as a result of the inherent complexity of projects such as CMIP5/6, it is a mandatory task to keep track of the status of datasets and the version evolution they sustain in their life-cycle. The ESdoc-errata project aims to keep track of the issues affecting specific versions of datasets/files. It enables users to resolve the history tree of each dataset/file enabling a better choice of the data used in their work based on the data status. The ES-doc-errata project has been designed and built on top of the Parent-IDentifiers handle service that will be deployed in the next iteration of the CMIP project, by ensuring maximum usability of ESGF ecosystem and encapsulated in the ES-doc structure. Consuming PIDs from handle service is guided by a specifically built algorithm that extracts meta-data regarding the issues that may or may not affect the quality of datasets/files and cause newer version to be published replacing older deprecated versions. This algorithm is able to deduce the nature of the flaws to the file granularity, that is of high value to the end-user. This new platform has been designed keeping in mind usability by end-users specialized in the data publishing process or other scientists requiring feedback on reliability of data required for their work. To this end, a specific set of rules and a code of conduct has been defined. A validation process ensures the quality of this newly introduced errata meta-data , an authentication safe-guard was implemented to prevent tampering with the archived data, and a wide variety of tools were put at users disposal to interact safely with the platform including a command-line client and a dedicated front-end.

  7. Sorption of methylxanthines by different sorbents

    Dmitrienko, S. G.; Andreeva, E. Yu.; Tolmacheva, V. V.; Terent'eva, E. A.


    Sorption of caffeine, theophylline, theobromine, diprophylline, and pentoxyphylline on different sorbents (supercross-linked polystyrene, surface-modified copolymer of styrene and divinylbenzene Strata-X, and carbon nanomaterials Taunit and Diasorb-100-C16T) was studied in a static mode in an effort to find new sorbents suitable for sorption isolation and concentration of methylxanthines. The peculiarities of sorption of methylxanthines were explained in relation to the solution acidity, the nature of the sorbates and their concentration, the nature of the solvent, and the structural characteristics of the sorbents.


    James D. McSweeny


    Full Text Available Milled southern pine wood was modified with sequential treatments of sodium periodate and sodium hypobromite for the purpose of improving copper ion (Cu2+ sorption capacity of the wood when tested in 24-h equilibrium batch tests. The modified wood provided additional carboxyl groups to those in the native wood and substantially increased Cu2+ uptake over that of unmodified wood. Sorption capacity (qe measured with an unbuffered standard solution increased to a maximum of 7.8 mg Cu2+ ion per gram of wood (treated from 3.1 mg Cu2+ ion/g wood (untreated. Samples tested were first sodium ion exchanged to keep the pH of the standard solution from declining during the sorption test. The treatment necessary for maximum qe was 3% (w/v periodate for 24 h and 0.8% (w/v bromine (as hypobromite for 24 h; both treatments were at room temperature. These conditions corresponded to the maximum periodate concentration and treatment times tested. To further evaluate the efficacy of modification treatments, weight change after each treatment was determined. Weight loss after the periodate stage for any concentration and time used was minor, indicating the selective nature of this reaction. However, most of the weight loss was incurred after hypobromite treatment. Weight loss corresponding to the greatest increase in sorption capacity was 12.6% total from the combined periodate and hypobromite stages. The increase of carboxylate functional groups in the wood was monitored using FTIR/ATR spectroscopy.

  9. Characterization of sorption compressor for mixed refrigerant J-T cryocooler

    Mehta, Rohitkumar; Bapat, Shridhar; Atrey, Milind


    The requirement of a cryocooler with minimum vibrations for space borne system and highly sophisticated electronic devices for ground application, has led to the development of sorption compressor type J-T cryocooler. The adsorption capacity of any adsorbent material increases with an increase in pressure and decreases with an increase in temperature. In a Sorption compressor, adsorbed gases are desorbed in a confined volume by raising temperature of the sorption bed which results in increase in pressure of gas. A uniform temperature across the sorption bed ensures maximum discharge from the compressor amounting to higher flow rates and longer cycle time on account of reduced residual loading. In addition, it is also very important to determine the adsorption capacity of any material with respect to the gas or gases to be adsorbed as this varies with source of the adsorbent. The present work reports the characterization of a fully operational two-cell sorption compressor developed. The sorption compressor is characterized for discharge pressure variation with cycle time; this is essentially a function of a) the amount of adsorbent, b) the adsorption capacity for respective gas or gases, c) desorption temperature and its uniformity, and d) system dead volume. The present paper analyses these aspects theoretically and the results are compared with the experimental data obtained for individual gases as well as for gas mixtures. The effect of gas distribution on temperature uniformity across the bed and of heater power on high pressure generated is also studied. The paper also discusses the pressure profile obtained for a given amount of adsorbent for different gas or gas mixture. The work, based on the results obtained so far is being further extended for a four cell sorption compressor.

  10. Dynamics, chemical properties and bioavailability of DOC in an early successional catchment

    U. Risse-Buhl


    Full Text Available The dynamics of dissolved organic carbon (DOC have been intensively studied in mature ecosystems, but little is known about DOC dynamics and the significance of DOC as a substrate for microbial activity in early-successional catchments. We determined the concentration, chemical composition, source, radiocarbon age, and bioavailability of DOC along the hydrological flow path from soil solution to a downstream pond in a recently constructed catchment (Chicken Creek Catchment, Germany. Soil solution, upwelling ground water, stream water, subsurface water in an alluvial fan, and pond water all had high DOC concentrations (averages: 6.0–11.6 mg DOC L–1, despite small carbon stocks in both vegetation and soil of the catchment. Solid-state CPMAS 13C NMR of DOC in upwelling ground water revealed a higher proportion of aromatic compounds (32% and a lower proportion of carbohydrates (33% than in pond water (18% and 45%, respectively. The average 14C age of DOC in upwelling ground water was 2600 to 2900 yr, while organic matter of the Quaternary substrate of the catchment had a 14C age of 3000 to 16 000 yr. Both the 14C age data and 13C NMR spectra suggest that DOC partly derived from organic matter of the Quaternary substrate (about 40 to 90% of the C in the DOC, indicating that both recent and old C of the DOC can support microbial activity during early ecosystem succession. However, in a 70 day incubation experiment, only about 11% of the total DOC was found to be bioavailable. This proportion was irrespective of the water type. Origin of the microbial communities within the catchment (enriched from soil, stream sediment or pond water also had only a marginal effect on overall DOC utilization.

  11. Sorption of phenanthrene and benzene on differently structural kerogen: important role of micropore-filling.

    Zhang, Yulong; Ma, Xiaoxuan; Ran, Yong


    Shale was thermally treated to obtain a series of kerogen with varied maturation. Their chemical, structural and porous properties were related to the sorption and/or desorption behaviors of phenanthrene and benzene. As the treatment temperature increases, aliphatic and carbonyl carbon of the kerogen samples decrease, while their aromaticity and maturation increase. Meanwhile, the isothermal nonlinearity of phenanthrene and benzene increases whereas the sorption capacity and micropore adsorption volumes (Vo,d) initially increase and then decrease. The Vo,d of benzene is significantly correlated with, but higher than that of phenanthrene, suggesting similar micropore filling mechanism and molecular sieve effect. The benzene desorption exhibits hysteresis, which is related to the pore deformation of the kerogen and the entrapment of solute in the kerogen matrix. The Vo,d of phenanthrene and benzene on the kerogen samples accounts for 23-46% and 36-65% of the maximum sorption volumes, respectively, displaying the importance of the micropore filling.

  12. Bladder cancer documentation of causes: multilingual questionnaire, 'bladder cancer doc'.

    Golka, Klaus; Abreu-Villaca, Yael; Anbari Attar, Rowshanak; Angeli-Greaves, Miriam; Aslam, Muhammad; Basaran, Nursen; Belik, Rouslana; Butryee, Chaniphun; Dalpiaz, Orietta; Dzhusupov, Keneshbek; Ecke, Thorsten H; Galambos, Henrieta; Galambos, Henrieta; Gerilovica, Helena; Gerullis, Holger; Gonzalez, Patricia Casares; Goossens, Maria E; Gorgishvili-Hermes, Lela; Heyns, Chris F; Hodzic, Jasmin; Ikoma, Fumihiko; Jichlinski, Patrice; Kang, Boo-Hyon; Kiesswetter, Ernst; Krishnamurthi, Kannan; Lehmann, Marie-Louise; Martinova, Irina; Mittal, Rama Devi; Ravichandran, Beerappa; Romics, Imre; Roy, Bidyut; Rungkat-Zakaria, Fransiska; Rydzynski, Konrad; Scutaru, Cristian; Shen, Jianhua; Soufi, Maria; Toguzbaeva, Karlygash; Vu Duc, Trinh; Widera, Agata; Wishahi, Mohamed; Hengstler, Jan G


    There is a considerable discrepancy between the number of identified occupational-related bladder cancer cases and the estimated numbers particularly in emerging nations or less developed countries where suitable approaches are less or even not known. Thus, within a project of the World Health Organisation Collaborating Centres in Occupational Health, a questionnaire of the Dortmund group, applied in different studies, was translated into more than 30 languages (Afrikaans, Arabic, Bengali, Chinese, Czech, Dutch, English, Finnish, French, Georgian, German, Greek, Hindi, Hungarian, Indonesian, Italian, Japanese, Kannada, Kazakh, Kirghiz, Korean, Latvian, Malay, Persian (Farsi), Polish, Portuguese, Portuguese/Brazilian, Romanian, Russian, Serbo-Croatian, Slovak, Spanish, Spanish/Mexican, Tamil, Telugu, Thai, Turkish, Urdu, Vietnamese). The bipartite questionnaire asks for relevant medical information in the physician's part and for the occupational history since leaving school in the patient's part. Furthermore, this questionnaire is asking for intensity and frequency of certain occupational and non-occupational risk factors. The literature regarding occupations like painter, hairdresser or miner and exposures like carcinogenic aromatic amines, azo dyes, or combustion products is highlighted. The questionnaire is available on

  13. Docência na universidade: professores inovadores na USP

    Chamlian Helena Coharik


    Full Text Available O artigo trata de pesquisa realizada com um grupo de professores inovadores da Universidade de São Paulo tendo como objetivo procurar subsídios para a formação do professor universitário. Esses docentes foram entrevistados, solicitando que detalhassem melhor suas experiências inovadoras; explicassem as razões pelas quais haviam introduzido modificações em sua forma de trabalho; explicitassem as relações entre sua atividade de docência e de pesquisa, expressassem o papel que atribuíam ao ensino na universidade, bem como a forma pela qual sua trajetória acadêmica havia se cumprido até então. A diversidade de experiências relatadas e, ao mesmo tempo, a convergência de visões a respeito de suas funções de ensino e de pesquisa na universidade permitem-nos afirmar que, mais do que uma formação pedagógica específica, a sensibilização para as dificuldades do ensino e a valorização institucional dessa atividade consistiriam em grande avanço para a formação do professor.

  14. Computer simulation of molecular sorption in zeolites

    Calmiano, M D


    The work presented in this thesis encompasses the computer simulation of molecular sorption. In Chapter 1 we outline the aims and objectives of this work. Chapter 2 follows in which an introduction to sorption in zeolites is presented, with discussion of structure and properties of the main zeolites studied. Chapter 2 concludes with a description of the principles and theories of adsorption. In Chapter 3 we describe the methodology behind the work carried out in this thesis. In Chapter 4 we present our first computational study, that of the sorption of krypton in silicalite. We describe work carried out to investigate low energy sorption sites of krypton in silicalite where we observe krypton to preferentially sorb into straight and sinusoidal channels over channel intersections. We simulate single step type I adsorption isotherms and use molecular dynamics to study the diffusion of krypton and obtain division coefficients and the activation energy. We compare our results to previous experimental and computat...

  15. Optimization of isotherm models for pesticide sorption on biopolymer-nanoclay composite by error analysis.

    Narayanan, Neethu; Gupta, Suman; Gajbhiye, V T; Manjaiah, K M


    A carboxy methyl cellulose-nano organoclay (nano montmorillonite modified with 35-45 wt % dimethyl dialkyl (C14-C18) amine (DMDA)) composite was prepared by solution intercalation method. The prepared composite was characterized by infrared spectroscopy (FTIR), X-Ray diffraction spectroscopy (XRD) and scanning electron microscopy (SEM). The composite was utilized for its pesticide sorption efficiency for atrazine, imidacloprid and thiamethoxam. The sorption data was fitted into Langmuir and Freundlich isotherms using linear and non linear methods. The linear regression method suggested best fitting of sorption data into Type II Langmuir and Freundlich isotherms. In order to avoid the bias resulting from linearization, seven different error parameters were also analyzed by non linear regression method. The non linear error analysis suggested that the sorption data fitted well into Langmuir model rather than in Freundlich model. The maximum sorption capacity, Q0 (μg/g) was given by imidacloprid (2000) followed by thiamethoxam (1667) and atrazine (1429). The study suggests that the degree of determination of linear regression alone cannot be used for comparing the best fitting of Langmuir and Freundlich models and non-linear error analysis needs to be done to avoid inaccurate results.

  16. Modification of granular activated carbon surface by chitosan coating for geosmin removal: sorption performances.

    Vinitnantharat, S; Rattanasirisophon, W; Ishibashi, Y


    This study presents the results of the sorption performances for geosmin removal by sorption onto granular activated carbons (GAC) manufactured from different raw materials of coconut shell and bituminous coal. The surface of GAC was modified by chitosan coating. The 90% deacetylated chitosan flakes were used for coating on GAC with the GAC: chitosan ratio of 5:1. The surface of GAC was characterised by scanning electron microscope (SEM) analysis, Fourier transform infrared spectroscopy and measurement of the pH solution of GAC samples. The sorption of geosmin onto the chitosan for both uncoated and coated GACs could be described by the Freundlich adsorption model. Data revealed that the sequence of Freundlich constant (K(F)) was chitosan coated bitominous coal (CB) > uncoated bituminous coal (UB) > chitos approximately equal to an coated coconut shell (CC) approximately equal to uncoated coconut shell (UC). The bituminous coal based GAC with chitosan coating had a maximum capacity of 23.57 microg/g which was approximately two-fold of uncoated bituminous coal based GAC. Two simplified kinetic models, pseudo-first order and pseudo-second order, were tested to investigate the sorption mechanisms. It was found that the intraparticle diffusion was a rate controlling step for the sorption and followed the pseudo-second order equation.

  17. Sorption of Pyrene by Clay Minerals Coated with Dissolved Organic Matter (DOM from Landfill Leachate

    Pingxiao Wu


    Full Text Available Interactions of dissolved organic matter (DOM from landfill leachate with clays could affect significantly the fate of hydrophobic organic compounds (HOCs in soils. The complexes of montmorillonite (MT and kaolinite (KL with DOM extracted from landfill leachate were prepared under controlled conditions, termed CMT and CKL, respectively. The bare clays and their complexes were characterized by powder X-ray diffraction (XRD, Fourier transform infrared (FTIR, thermogravimetry (TG, differential scanning calorimetry (DSC, and scanning electron microscopy (SEM. Batch experiments were designed to investigate the sorption behavior of pyrene onto the clays in the presence of DOM. The maximum sorption capacities of pyrene on MT, CMT, KL, and CKL were 22.18, 38.96, 42.00, and 44.99 μg·g−1, respectively, at the initial concentration of 1000 ± 150 μg·L−1. The sorption isotherms of pyrene by the bare clays followed the Henry model well, whereas the Freundlich sorption isotherm provided a better fit to the equilibrium data of the sorption by the complexes. The role of montmorillonite and kaolinite complexes with DOM in the retention of pyrene in soils was different. This may be due to the different crystal structures between montmorillonite and kaolinite.

  18. Identifiability of sorption parameters in stirred flow-through reactor experiments and their identification with a Bayesian approach.

    Nicoulaud-Gouin, V; Garcia-Sanchez, L; Giacalone, M; Attard, J C; Martin-Garin, A; Bois, F Y


    This paper addresses the methodological conditions -particularly experimental design and statistical inference- ensuring the identifiability of sorption parameters from breakthrough curves measured during stirred flow-through reactor experiments also known as continuous flow stirred-tank reactor (CSTR) experiments. The equilibrium-kinetic (EK) sorption model was selected as nonequilibrium parameterization embedding the Kd approach. Parameter identifiability was studied formally on the equations governing outlet concentrations. It was also studied numerically on 6 simulated CSTR experiments on a soil with known equilibrium-kinetic sorption parameters. EK sorption parameters can not be identified from a single breakthrough curve of a CSTR experiment, because Kd,1 and k(-) were diagnosed collinear. For pairs of CSTR experiments, Bayesian inference allowed to select the correct models of sorption and error among sorption alternatives. Bayesian inference was conducted with SAMCAT software (Sensitivity Analysis and Markov Chain simulations Applied to Transfer models) which launched the simulations through the embedded simulation engine GNU-MCSim, and automated their configuration and post-processing. Experimental designs consisting in varying flow rates between experiments reaching equilibrium at contamination stage were found optimal, because they simultaneously gave accurate sorption parameters and predictions. Bayesian results were comparable to maximum likehood method but they avoided convergence problems, the marginal likelihood allowed to compare all models, and credible interval gave directly the uncertainty of sorption parameters θ. Although these findings are limited to the specific conditions studied here, in particular the considered sorption model, the chosen parameter values and error structure, they help in the conception and analysis of future CSTR experiments with radionuclides whose kinetic behaviour is suspected.

  19. Cobalt sorption in silica-pillared clays.

    Sampieri, A; Fetter, G; Bosch, P; Bulbulian, S


    Silicon pillared samples were prepared following conventional and microwave irradiation methods. The samples were characterized and tested in cobalt sorption. Ethylenediammine was added before cobalt addition to improve the amount of cobalt retained. The amount of cobalt introduced in the original clay in the presence of ethylenediammine was the highest. In calcined pillared clays the cobalt retention with ethylenediammine was lower (ca. 40%). In all cases the presence of ethylenediammine increased twice the amount of cobalt sorption measured for aqueous solutions.

  20. Enhanced fluoride sorption by mechanochemically activated kaolinites.

    Meenakshi, S; Sundaram, C Sairam; Sukumar, Rugmini


    Kaolinite clay obtained from the mines was processed and studied for its fluoride sorption capacity. The surface area of the clay mineral was increased from 15.11 m(2)/g (raw) to 32.43 m(2)/g (activated) by mechanochemical activation. Batch adsorption studies were conducted to optimize various equilibrating conditions like the effect of contact time, dosage, pH for both raw and micronized kaolinites (RK and MK). The effect of other interfering anions on the defluoridation capacity (DC) of the sorbents was studied. Sorption of fluoride by the sorbents was observed over a wide pH range of 3-11. The studies revealed there is an enhanced fluoride sorption on MK. FTIR and XRD were used for the characterization of the sorbent. The surface morphology of the clay material was observed using SEM. The adsorption of fluoride was studied at three different temperatures, viz., 303, 313 and 323 K. The sorption data obtained at optimized conditions were subjected to Freundlich and Langmuir isotherms. Sorption intensity (1/n) (0.770-0.810) has been evaluated using Freundlich isotherm, whereas the values of sorption capacity Q(0) (0.609, 0.714 and 0.782 mg/g) and binding energy b (0.158, 0.145 and 0.133 L/mg) at three different temperatures have been estimated using Langmuir isotherm. Adsorption process was found to be controlled by both Freundlich and Langmuir isotherms. Thermodynamic studies revealed that the sorption of fluoride on MK is endothermic and a spontaneous process. The kinetic studies indicate that the sorption of fluoride on MK follows pseudo-first-order and intraparticle diffusion models.

  1. Enhanced fluoride sorption by mechanochemically activated kaolinites

    Meenakshi, S. [Department of Chemistry, Gandhigram Rural University, Gandhigram 624302, Tamilnadu (India)], E-mail:; Sundaram, C. Sairam [Department of Science and Humanities, Karaikal Polytechnic College, Karaikal 609609, Puducherry (India); Sukumar, Rugmini [Chemical Sciences and Technologies, Regional Research Laboratory, Trivandrum 695019, Kerala (India)


    Kaolinite clay obtained from the mines was processed and studied for its fluoride sorption capacity. The surface area of the clay mineral was increased from 15.11 m{sup 2}/g (raw) to 32.43 m{sup 2}/g (activated) by mechanochemical activation. Batch adsorption studies were conducted to optimize various equilibrating conditions like the effect of contact time, dosage, pH for both raw and micronized kaolinites (RK and MK). The effect of other interfering anions on the defluoridation capacity (DC) of the sorbents was studied. Sorption of fluoride by the sorbents was observed over a wide pH range of 3-11. The studies revealed there is an enhanced fluoride sorption on MK. FTIR and XRD were used for the characterization of the sorbent. The surface morphology of the clay material was observed using SEM. The adsorption of fluoride was studied at three different temperatures, viz., 303, 313 and 323 K. The sorption data obtained at optimized conditions were subjected to Freundlich and Langmuir isotherms. Sorption intensity (1/n) (0.770-0.810) has been evaluated using Freundlich isotherm, whereas the values of sorption capacity Q{sup 0} (0.609, 0.714 and 0.782 mg/g) and binding energy b (0.158, 0.145 and 0.133 L/mg) at three different temperatures have been estimated using Langmuir isotherm. Adsorption process was found to be controlled by both Freundlich and Langmuir isotherms. Thermodynamic studies revealed that the sorption of fluoride on MK is endothermic and a spontaneous process. The kinetic studies indicate that the sorption of fluoride on MK follows pseudo-first-order and intraparticle diffusion models.

  2. Sorption of organophosphate esters by carbon nanotubes

    Yan, Wei; Yan, Li [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China); Duan, Jinming [School of Environmental and Municipal Engineering, Xi’an University of Architecture and Technology, Xi’an 710055 (China); Jing, Chuanyong, E-mail: [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085 (China)


    Graphical abstract: The interfacial interactions between the OPE molecules and CNTs. - Highlights: • Oxygen-containing groups on CNTs change the sorption property for OPEs. • Molecular configuration of OPEs has insignificant impact on their sorption. • Hydrophobic, π–π EDA and Brønsted acid–base interaction occurred between the CNTs and OPEs. - Abstract: Insights from the molecular-level mechanism of sorption of organophosphate esters (OPEs) on carbon nanotubes (CNTs) can further our understanding of the fate and transport of OPEs in the environment. The motivation for our study was to explore the sorption process of OPEs on multi-walled CNTs (MWCNTs), single-walled CNTs (SWCNTs) and their oxidized counterparts (O-MWCNTs and O-SWCNTs), and its molecular mechanism over a wide concentration range. The sorption isotherm results revealed that the hydrophobicity of OPEs dominated their affinities on a given CNT and the π–π electron donor–acceptor (EDA) interaction also played an important role in the sorption of aromatic OPEs. This π–π EDA interaction, verified with Raman and FT-IR spectroscopy, could restrict the radial vibration of SWCNTs and affect the deformation vibration γ(CH) bands of OPE molecules. The OPE surface coverage on CNTs, estimated using the nonlinear Dubinin–Ashtakhov model, indicated that the oxygen-containing functional groups on CNTs could interact with water molecules by H-bonding, resulting in a decrease in effective sorption sites. In addition, FTIR analysis also confirmed the occurrence of Brønsted acid–base interactions between OPEs and surface OH groups of SWCNTs. Our results should provide mechanistic insights into the sorption mechanism of OPE contaminants on CNTs.

  3. Peculiarities of sorption isotherm and sorption chemisms of caesium by mixed nickel-potassium ferrocyanide based on hydrated titanium dioxide

    Voronina, A. V.; Semenishchev, V. S.; Nogovitsyna, E. V.; Betenekov, N. D.


    Sorption isotherm of caesium from tap water by mixed nickel-potassium ferrocyanide based on hydrated titanium dioxide is obtained for a wide range of concentrations of caesium. It is shown that there are three types of specificity to caesium sorption sites in this sorbent. Sorption chemisms of caesium are studied, factors conditioned high sorption capacity of the sorbent are revealed. It is shown that occupation of sorption sites I and II is well approximated by Langmuir equilibrium and this ...

  4. Doc of prophage P1 is inhibited by its antitoxin partner Phd through fold complementation

    Garcia-Pino, Abel; Christensen-Dalsgaard, Mikkel; Wyns, Lode


    evolutionary origin for the phd/doc operon. Doc induces growth arrest of Escherichia coli cells in a reversible manner, by targeting the protein synthesis machinery. Moreover, Doc activates the endogenous E. coli RelE mRNA interferase but does not require this or any other known chromosomal toxin......Prokaryotic toxin-antitoxin modules are involved in major physiological events set in motion under stress conditions. The toxin Doc (death on curing) from the phd/doc module on phage P1 hosts the C-terminal domain of its antitoxin partner Phd (prevents host death) through fold complementation....... This Phd domain is intrinsically disordered in solution and folds into an alpha-helix upon binding to Doc. The details of the interactions reveal the molecular basis for the inhibitory action of the antitoxin. The complex resembles the Fic (filamentation induced by cAMP) proteins and suggests a possible...


    Tanja Nikolić


    Full Text Available The effect of periodate oxidation on the chemical and sorption properties of cotton yarn was investigated by determining aldehyde group content, moisture sorption, water retention and iodine sorption. Oxidation of cotton yarn was performed by varying concentration of sodium periodate solution and reaction time. To measure the aldehyde content present in the oxidized cotton, the aldehyde groups were selectively oxidized to carboxyl groups with sodium chlorite at pH 4-5, at room temperature for 48 h, and carboxyl group content was determined by modified calcium-acetate method. Differences in the sorption properties of untreated and oxidized cotton samples were obtained using conventional methods. The aldehyde groups were introduced into the oxidized cotton up to 99.2 µmol/g. Compared to the untreated fibers, oxidized cotton samples exhibited higher moisture sorption (up to 9% and lower water retention values (up to 19% and iodine sorption values (up to 31%. Based on the obtained results, it can be concluded that the crystalline structure of cellulose is not significantly changed by periodate oxidation, which is of great importance for textile material production.

  6. Dynamics, chemical properties and bioavailability of DOC in an early successional catchment

    U. Risse-Buhl


    Full Text Available The dynamics of dissolved organic carbon (DOC have been intensively studied in mature ecosystems, but little is known about DOC dynamics and the significance of DOC as a substrate for microbial activity in early-successional catchments. We determined the concentration, chemical composition, source, radiocarbon age, and bioavailability of DOC along the hydrological flow path from soil solution to a downstream pond in a recently constructed catchment (Chicken Creek Catchment, Germany. Soil solution, upwelling ground water, subsurface water in an alluvial fan, and pond water all had high DOC concentrations (averages of 6.0–11.6 mg DOC L−1, despite small carbon stocks in either vegetation or soil of the early-successional catchment. The mean 14C age of DOC in upwelling ground water was 2600 to 2800 yr. Solid-state CPMAS 13C NMR revealed a higher proportion of aromatic compounds (32% and a lower proportion of carbohydrates (33% in upwelling ground water than in pond water (18% and 45%, respectively. The 14C age and 13C NMR spectra suggest that DOC was partly mobilized from charred organic matter of the Quaternary substrate. In an experimental 70-days incubation experiment, 20% of the total DOC was found to be bioavailable, irrespective of the water type. Origin of microbial communities (enriched from soil, stream sediment or pond water had only marginal effects on overall DOC utilization. Overall, these data suggest that the old DOC can support microbial activity during early ecosystem succession to some extent, although the largest fraction is recalcitrant DOC that is exported from the catchment once it has been mobilized.

  7. Thermodynamics of cationic surfactant sorption onto natural clinoptilolite

    Sullivan, E.J.; Bowman, R.S. [New Mexico Inst. of Mining and Technology, Socorro, NM (United States); Carey, J.W. [Los Alamos National Lab., NM (United States)


    Sorption enthalpies of hexadecyltrimethylammonium bromide (HDTMA) as monomers and micelles and tetraethylammonium bromide (TEA) were used with surfactant, counterion, and co-ion sorption isotherms to infer the conformation, sorption mechanism, and relative stability of the sorbed surfactants on natural clinoptilolite. The average value of the sorption enthalpy was {minus}10.38 kJ/mol for monomers, {minus}11.98 kJ/mol for micelles, and +3.03 kJ/mol for TEA. Sorption of monomers produced a lower sorption plateau than equivalent micelle sorption (maxima 145 mmol/kg, 225 mmol/kg). Analysis of the sorption data demonstrated a change in the sorption mechanism at the external cation exchange capacity (ECEC) of clinoptilolite. Sorption data from below and above the ECEC were fit to a simple polynomial model and the Gibbs free energy of sorption ({Delta} G{sub m}{sup 0}) and sorption entropies were calculated. Resultant values of {Delta} G{sub m}{sup 0} were {minus}9.27 and {minus}14.38 kJ/mol for HDTMA monomers and micelles, respectively, for sorption below the ECEC, and {minus}16.11 and {minus}23.10 kJ/mol, respectively, for sorption above the ECEC. The value for TEA was {minus}1.04 kJ/mol, indicating weaker sorption than for HDTMA. Monomer sorption to clinoptilolite exceeded the ECEC, even when the solution concentration was below the critical micelle concentration. Hydrophobic (tail-tail) components of {Delta} G{sub m}{sup 0} were the driving force for sorption of HDTMA, both below and above the ECEC. A significant kinetic effect was observed in the sorption isotherms with a period of rapid sorption followed by slow equilibration requiring 7 days to achieve steady state for HDTMA; TEA equilibration occurred within 24 h.

  8. Maximum Autocorrelation Factorial Kriging

    Nielsen, Allan Aasbjerg; Conradsen, Knut; Pedersen, John L.


    This paper describes maximum autocorrelation factor (MAF) analysis, maximum autocorrelation factorial kriging, and its application to irregularly sampled stream sediment geochemical data from South Greenland. Kriged MAF images are compared with kriged images of varimax rotated factors from...

  9. Interactions between elevated CO2 and warming could amplify DOC exports from peatland catchments.

    Fenner, Nathalie; Freeman, Christopher; Lock, Maurice A; Harmens, Harry; Reynolds, Brian; Sparks, Tim


    Peatlands export more dissolved organic carbon (DOC) than any other biome, contributing 20% of all terrestrial DOC exported to the oceans. Both warming and elevated atmospheric CO2 (eCO2) can increase DOC exports, but their interaction is poorly understood. Peat monoliths were, therefore, exposed to eCO2, warming and eCO2 + warming (combined). The combined treatment produced a synergistic (i.e., significant interaction) rise in DOC concentrations available for export (119% higher than the control, interaction P exports from peatlands, with potentially widespread ramifications for aquatic processes in the receiving waters.

  10. Effects of biochar addition on the sorption of polar herbicides in paddy soils

    Garcia-Jaramillo, Manuel; Cox, Lucía; Hermosín, Mari Carmen; Helmus, Rick; Parsons, John R.; Kalbitz, Karsten


    Organic amendments, and their water soluble fraction, induce an important impact on pesticide dissipation in soils, affecting their adsorption and transport processes through various chemical interactions. Although in most cases addition of organic amendments increases sorption, leaching of the pesticides can be either reduced or promoted. Because of that, their effect on pesticide behavior must be assessed in order to optimize their use. The major objectives of this study were to investigate the impact of biochar and biochar water extractable substances (BWES) on the sorption behavior of two polar herbicides, azimsulfuron and penoxsulam, in two amended and unamended paddy soils under flooded conditions. The adsorption - desorption of these herbicides was studied in soils amended with fresh biochar and in soils amended with a washed version of the biochar, simulating the conditions of a soil recently amended and a soil where biochar was applied longer time before and most part of the BWES has been already removed because of the flooded conditions. Therefore, sorption on biochar was assessed before and after removing 80% of its water extractable substances, separately and in combination with each soil (at 2 and 5% w/w). BWES were analyzed by high resolution mass spectrometry. The most abundant fractions present in the high mass range were nitrogen-containing molecules. The aromatic character of the DOC-extracts of the unamended and amended soils, based on the specific UV absorbance at 280 nm (SUVA280), was increased with the amendment in all the conditions tested. Adsorption data of both herbicides fitted very well to the Freundlich equation, with R2 values higher than 0.9 in all the conditions tested. Sorption isotherms were in all cases nonlinear, with Nf values stress the importance of proper screening of biochar and soil characteristics before its application in combination with polar herbicides.

  11. Effects of Citrate and Arginine on Sorption of Nickel to Yazd Sepiolite and Calcite

    Ahmadreza Sheikhhosseini


    , and W was the mass (g of the sorbent. The Langmuir, Freundlich and linear isotherm models were fitted to sorption data using Graphpad prism 5.0. For kinetic study,30 mL of 0.01 M CaCl2 solution, with or without 0.1 mM citrate or arginine, containing Ni at a concentration corresponding to the maximum sorption capacity of each mineral (estimated from sorption isotherms were transferred into 50-ml polyethylene centrifuge tubes containing 0.3 g of sepiolite or calcite. The suspensions were shaken (180±2 rpm, 25 °C continuously and after 0.5, 1.5, 3, 6, 12, 18 and 24 hours, corresponding tubes were centrifuged (4000×g for 10 min and supernatants were analyzed for Ni concentration by atomic absorption spectrophotometer. Using Graphpad prism 5.0, kinetic data were fitted to Pseudo-first order, pseudo-second order and power function kinetic models. Results: With or without ligands, the Langmuir model was the best description of Ni sorption to sepiolite while the linear model was the best fit of calcite data showing the physical nature of Ni sorption by this mineral. Kinetics of Ni sorption to sepiolite and calcite were best described by power function model. In the presence of citrate, both capacity and rate of sorption of Ni to sepiolite decreased. There was no considerable change in sorption of Ni to calcite. In the presence of arginine, however, sorption capacity of minerals for Ni increased. Arginine enhanced the rate of Ni sorption on all three minerals. Citrate showed opposing effects on Ni sorption kinetics depending on the studied minerals. Totally, citrate and arginine had opposite effects on sorption of Ni to sepiolite and calcite. Conclusion: Organic ligands can change sorption characteristics of the minerals. It seems that citrate decreases sorption of Ni to sepiolite but its effect on Ni sorption to calcite is negligible, while arginine increases Ni sorption to both minerals. Our results suggested that presence of citrate and arginine in soil influence Ni

  12. Factors controlling spatial variability of DOC concentrations in soil solution at European level

    Camino Serrano, Marta; Janssens, Ivan; Luyssaert, Sebastiaan; Gielen, Bert; Guenet, Bertrand; De Vos, Bruno; Ciais, Philippe


    The lateral transport of dissolved organic carbon (DOC) is an important and not well-understood process linking terrestrial and aquatic ecosystems. Up to day very few Earth System Models (ESMs) represent explicitly this process despite its crucial role in the global carbon cycle. However, to be able to integrate DOC leaching in ESMs, more accurate information is needed in order to better understand and predict DOC dynamics. DOC concentrations mainly vary by geographical location, soil and vegetation types, topography, season and climate. Within this framework, a database was designed to compile data on DOC in soil solution at different depths in different ecosystems around the world, with special focus on European sites. The database contains information on 349 sites, with 304 being forest, gathered from published literature and datasets accessible on the internet. A substantial dataset was provided by International Co-operative Programme on Assessment and Monitoring of Air Pollution Effects on Forests (ICP Forests). The database also includes other meta-data related to the sites, such as land cover, soil properties, climate, annual water balance and other soil solution parameters. The analysis of the database has been focused on: 1) the study of the environmental and physical factors that are acting as drivers of DOC concentrations changes in soil solution across sites at European level , and 2) the DOC distribution through the soil profile and how this varies with different vegetation types and soil properties. The preliminary results show that variables related to biological processes (Dry weight of the organic layer, for example) are the most important in explaining the spatial distribution of the DOC concentration in soil solution at the European scale. However, the interactions between variables are complex and we will need further analysis in order to draw more robust conclusions. With regards to the vertical profile of DOC, we found that there is a

  13. Insights and issues with simulating terrestrial DOC loading of Arctic river networks

    Kicklighter, David W.; Hayes, Daniel J.; McClelland, James W.; Peterson, Bruce J.; McGuire, A. David; Melillo, Jerry M.


    Terrestrial carbon dynamics influence the contribution of dissolved organic carbon (DOC) to river networks in addition to hydrology. In this study, we use a biogeochemical process model to simulate the lateral transfer of DOC from land to the Arctic Ocean via riverine transport. We estimate that, over the 20th century, the pan-Arctic watershed has contributed, on average, 32 Tg C/yr of DOC to river networks emptying into the Arctic Ocean with most of the DOC coming from the extensive area of boreal deciduous needle-leaved forests and forested wetlands in Eurasian watersheds. We also estimate that the rate of terrestrial DOC loading has been increasing by 0.037 Tg C/yr2 over the 20th century primarily as a result of climate-induced increases in water yield. These increases have been offset by decreases in terrestrial DOC loading caused by wildfires. Other environmental factors (CO2 fertilization, ozone pollution, atmospheric nitrogen deposition, timber harvest, agriculture) are estimated to have relatively small effects on terrestrial DOC loading to Arctic rivers. The effects of the various environmental factors on terrestrial carbon dynamics have both offset and enhanced concurrent effects on hydrology to influence terrestrial DOC loading and may be changing the relative importance of terrestrial carbon dynamics on this carbon flux. Improvements in simulating terrestrial DOC loading to pan-Arctic rivers in the future will require better information on the production and consumption of DOC within the soil profile, the transfer of DOC from land to headwater streams, the spatial distribution of precipitation and its temporal trends, carbon dynamics of larch-dominated ecosystems in eastern Siberia, and the role of industrial organic effluents on carbon budgets of rivers in western Russia.

  14. Sorption of Ni(II) ions from aqueous solution by Lewatit cation-exchange resin.

    Dizge, Nadir; Keskinler, Bülent; Barlas, Hulusi


    Ion-exchange is an alternative process for uptake of heavy metals from aqueous solutions. In the present study, the sorption of nickel(II) ions from aqueous solution was investigated by using Lewatit MonoPlus SP 112 (strongly acidic, macroporous cation-exchange resin) in a batch adsorption system as a function of pH (2.0-8.0), initial nickel concentration (50-200 mg/L), resin dosage (0.5-2.0 g/L), contact time (0.5-3h), and temperatures (298-318K). The data were analyzed on the basis of Lagergren pseudo-first order, pseudo-second order (Types 1-5), Elovich and external, Weber-Morris intraparticle, pore-surface mass diffusion models. The experimental data showed that the maximum pH for efficient sorption of nickel(II) was 6.0. At the optimal conditions, nickel(II) ions sorption on the resin was decreased when the initial metal concentration increased. The results indicated that the resin dosage strongly affected the amount of nickel(II) ions removed from aqueous solution. The adsorption process was very fast due to 80% of nickel(II) sorption was occurred within 30 min and equilibrium was reached at about 90 min. Freundlich and Langmuir adsorption isotherm models were used for sorption equilibrium data and the maximum adsorption capacity (171 mg/g) of Lewatit MonoPlus SP 112 was obtained from Langmuir isotherm. The thermodynamic parameters (DeltaG degrees, free energy change; DeltaS degrees, enthalpy change; and DeltaH degrees, entropy change) for sorption of nickel(II) ions were evaluated. The rise in temperature caused a partly increase in the value of the equilibrium constant (K(c)) for the sorption of nickel(II) ions. Moreover, column flow adsorption study was also studied. Breakthrough curves were obtained from column flow studies by using both synthetic solution and rinsing bath water of filter industry. The column regeneration was carried out for two sorption-desorption cycles. The eluant used for regeneration of the cation-exchange resin was 7% (w/w) HCl. The

  15. [Sorption isotherms and sorption thermodynamics of faecal sterols on offshore sediment].

    Zhang, Xiao-Lei; Xue, Wen-Ping; Xu, Heng-Zhen; Ma, Xin-Dong


    Experiments of faecal sterols adsorption from aqueous solutions onto Dalian offshore sediment were done by a batch equilibrium method,and the sorption of 12 kinds of faecal sterols in sediment were investigated in this paper. It was shown that the adsorption equilibrium time was 24 h, and after 24 h the variation tendency of 5 kinds of fingerprint values was stable. It indicated that adsorption isothermal data was interpreted by the Henry, Freundlich, Langmuir, Duhinin-Radushkevich(D-R) and Temkin equations, and demonstrated that the other 4 isotherms provided stronger data fitting than the Langumir isotherm. It inferred that from D-R model the mean free energy of adsorption process of 12 kinds of faecal sterols was from 7 071.1 J x mol(-1) to 9 128.7 J x mol(-1), and concluded that it was mainly physical adsorption of the sorptive process of 12 kinds of faecal sterols in sediment. It discovered that from the Temkin model the value of K(f) of cholestanone was the maximum, and extrapolated that cholestanone was adsorbed most easily on sediment. It stated that the enthalpy and entropy change of the adsorption were both less than zero, and inferred that the adsorption process was exothermic and spontaneous.

  16. Sorption of Organic Compounds in Soil Organic Matter


    Soil organic matter (SOM)is the predominant component for sorption of hydrophobic organic compouds in soil and sorption by SOM ultimately affects chemical fate and availability in soil ,and the degree of remedia tion success of contaminated soils. This paper summarizes the latest development on sorption of organic com pounds in soil (natural) organic matter, addresses four sorption mechanisms: surface adsorption, solid - phase partitioning,dual-mode sorption,and fixed-pore sorption model ,and presents future research directions as well.

  17. Doc2b synchronizes secretion from chromaffin cells by stimulating fast and inhibiting sustained release

    da Silva Pinheiro, Paulo César; de Wit, Heidi; Walter, Alexander M;


    is still high. We conclude that Doc2b acts to inhibit vesicle priming during prolonged calcium elevations, thus protecting unprimed vesicles from fusing prematurely, and redirecting them to refill the readily releasable pool after relaxation of the calcium signal. In sum, Doc2b favors fast, synchronized...

  18. Keeping it simple: a conceptual model of DOC dynamics in a subarctic alpine catchment

    Lessels, J. S.; Tetzlaff, D.; Carey, S. K.; Soulsby, C.


    Understanding hydrological processes in subarctic alpine catchments characterised with discontinuous permafrost is important in order to understand carbon exports. Subarctic catchments have large storages of carbon in organic and permafrost soils. Active layer depth is one of the largest controlling factors of the release of dissolved organic carbon (DOC) due to its control on runoff pathways. Therefore, any change of this depth will affect the amount of DOC mobilised from these catchments. Simple low parameterised conceptual models offer the ability to characterise hydrological processes and linked DOC dynamics without introducing many of the uncertainties linked to high parameterised models. Lumped models can also be used to identify sources of DOC within catchments. Here, we investigate hydrological sources, flow pathways and consequently DOC dynamics in the Granger Basin, Canada, a subarctic alpine catchment using data collected from 2001 to 2008. The catchment is distinguished by aspect dependant discontinuous permafrost and seasonal frost, compounded further by differences in soil and vegetation types. Applying a simple low parameterised conceptual model allowed identification of the dominant flow paths of the main hydrological response units. The results showed that it was necessary to include active layer dynamics combined with aspect to represent the hydrological and DOC dynamics. The model provides information on the effect of climatic conditions on DOC releases. By identifying the key flow paths and relating these to spring freshet DOC exports over multiple years it is possible to gain an insight of the how climatic changes might affect hydrological processes within subarctic catchments.

  19. Sorption of small molecules in polymeric media

    Camboni, Federico; Sokolov, Igor M.


    We discuss the sorption of penetrant molecules from the gas phase by a polymeric medium within a model which is very close in spirit to the dual sorption mode model: the penetrant molecules are partly dissolved within the polymeric matrix, partly fill the preexisting voids. The only difference with the initial dual sorption mode situation is the assumption that the two populations of molecules are in equilibrium with each other. Applying basic thermodynamics principles we obtain the dependence of the penetrant concentration on the pressure in the gas phase and find that this is expressed via the Lambert W-function, a different functional form than the one proposed by dual sorption mode model. The Lambert-like isotherms appear universally at low and moderate pressures and originate from the assumption that the internal energy in a polymer-penetrant-void ternary mixture is (in the lowest order) a bilinear form in the concentrations of the three components. Fitting the existing data shows that in the domain of parameters where the dual sorption mode model is typically applied, the Lambert function, which describes the same behavior as the one proposed by the gas-polymer matrix model, fits the data equally well.

  20. Sorption of tylosin on clay minerals.

    Zhang, Qian; Yang, Chen; Huang, Weilin; Dang, Zhi; Shu, Xiaohua


    The equilibrium sorption of tylosin (TYL) on kaolinite and montmorillonite was measured at different solution pH using batch reactor systems. The results showed that all the sorption isotherms were nonlinear and that the nonlinearity decreased as the solution pH increased for a given clay. At a specific aqueous concentration, the single-point sorption distribution coefficient (KD) of TYL decreased rapidly as the solution pH increased. A speciation-dependent sorption model that accounted for the contributions of the cationic and neutral forms of TYL fit the data well, suggesting that the sorption may be dominated by both ion exchange and hydrophobic interactions. The isotherm data also fit well to a dual mode model that quantifies the contributions of a site-limiting Langmuir component (ion exchange) and a non-specific linear partitioning component (hydrophobic interactions). X-ray diffraction analyses revealed that the interlayers of montmorillonite were expanded due to the uptake of TYL. TYL molecules likely form a monolayer surface coverage.

  1. Influence of Calcite Solids and Dissolved Calcium on U(VI) Sorption and Desorption in Hanford Subsurface Sediments

    Dong, Wenming; Ball, William P.; Stone, Alan T.; Bai, Jing; Liu, Chongxuan; Wang, Zheming


    We have investigated U(VI) sorption and desorption with batch experiments conducted on core samples from the Hanford, WA, site as well as on sub-fractions of these materials and laboratory-grade calcite. In these studies, [U(VI)] was varied between 10- 7 and 10-5 and pH between 7.2 to 10, at constant I (=0.05) and constant PCO2 (10-3.5 atm), using water that was saturated with respect to calcite. A carbonate-free (acetic acid- treated) fraction of silt/clay material showed higher sorption than untreated material, suggesting that carbonates block access to higher affinity sites. Of particular interest was that U(VI) sorption on untreated material was maximum at pH=8.4, with substantially less sorption at lower and higher pH and in contrast to results from calcite free studies, which show strong sorption at pH {approx} 5 to 8. U(VI) speciation results suggest that aqueous-phase Ca2UO2(CO3)3 was the source of the otherwise unexpectedly low sorption at pH <8.4.

  2. Sorption of Uranium(VI and Thorium(IV by Jordanian Bentonite

    Fawwaz I. Khalili


    Full Text Available Purification of raw bentonite was done to remove quartz. This includes mixing the raw bentonite with water and then centrifuge it at 750 rpm; this process is repeated until white purified bentonite is obtained. XRD, XRF, FTIR, and SEM techniques will be used for the characterization of purified bentonite. The sorption behavior of purified Jordanian bentonite towards and Th4+ metal ions in aqueous solutions was studied by batch experiment as a function of pH, contact time, temperature, and column techniques at 25.0∘C and . The highest rate of metal ions uptake was observed after 18 h of shaking, and the uptake has increased with increasing pH and reached a maximum at . Bentonite has shown high metal ion uptake capacity toward uranium(VI than thorium(IV. Sorption data were evaluated according to the pseudo- second-order reaction kinetic. Sorption isotherms were studied at temperatures 25.0∘C, 35.0∘C, and 45.0∘C. The Langmuir, Freundlich, and Dubinin-Radushkevich (D-R sorption models equations were applied and the proper constants were derived. It was found that the sorption process is enthalpy driven for uranium(VI and thorium(IV. Recovery of uranium(VI and thorium(IV ions after sorption was carried out by treatment of the loaded bentonite with different concentrations of HNO3 1.0 M, 0.5 M, 0.1 M, and 0.01 M. The best percent recovery for uranium(VI and thorium(IV was obtained when 1.0 M HNO3 was used.

  3. Novel compact sorption generators for car air conditioning

    Tamainot-Telto, Z.; Metcalf, S.J.; Critoph, R.E. [School of Engineering, University of Warwick, Gibet Hill Road, Coventry CV4 7AL (United Kingdom)


    A prototype compact generator using the activated carbon-ammonia pair based on the plate heat exchanger concept has been designed and built at Warwick University. The novel generator has low thermal mass and good heat transfer. The heat exchanger uses nickel-brazed shims and spacers to create adsorbent layers only 4 mm thick between pairs of liquid flow channels of very low thermal mass. The prototype sorption generator manufactured was evaluated under EU car air conditioning test conditions. The prototype sorption generator is described and its experimental performance reported. While driven with waste heat from the engine coolant water (at 90 C), a pair of the current prototype generators (loaded with about 1 kg of activated carbon) operating out of phase has produced an average cooling power 1.6 kW with about 2 kW peaks. The typical average COP obtained is 0.22. (author) [French] Un prototype du generateur compact, base sur le concept des echangeurs de chaleur a plaques et utilisant la paire charbon actif-ammoniac, a ete concu et construit a l'Universite de Warwick. Le nouveau generateur a une faible inertie thermique et un excellent transfert de chaleur. L' echangeur utilise des plaques ayant des micro-canaux et des intercalaires brases au Nickel pour creer des couches d'adsorbant de 4 mm d'epaisseur entre les paires de plaques a l'interieur desquelles circule le fluide liquide. Le prototype du generateur a sorption ainsi fabrique a ete teste suivant des conditions prescrites par la Norme Europeenne de la Climatisation Automobile. Le prototype du generateur a sorption est decrit et ses performances experimentales presentees. Une paire dudit prototype (contenant chacun 1 kg the charbon actif), operant avec dephasage et ulisant des pertes thermiques en provenance de l'eau de refroidissement de moteur (a 90 C), a produit une puissance frigorifique moyenne de 1.6 kW avec une valeur maximum de 2 kW. La valeur typique du COP moyen est de

  4. Modeling nonlinear responses of DOC transport in boreal catchments in Sweden

    Kasurinen, Ville; Alfredsen, Knut; Ojala, Anne; Pumpanen, Jukka; Weyhenmeyer, Gesa A.; Futter, Martyn N.; Laudon, Hjalmar; Berninger, Frank


    Stream water dissolved organic carbon (DOC) concentrations display high spatial and temporal variation in boreal catchments. Understanding and predicting these patterns is a challenge with great implications for water quality projections and carbon balance estimates. Although several biogeochemical models have been used to estimate stream water DOC dynamics, model biases common during both rain and snow melt-driven events. The parsimonious DOC-model, K-DOC, with 10 calibrated parameters, uses a nonlinear discharge and catchment water storage relationship including soil temperature dependencies of DOC release and consumption. K-DOC was used to estimate the stream water DOC concentrations over 5 years for eighteen nested boreal catchments having total area of 68 km2 (varying from 0.04 to 67.9 km2). The model successfully simulated DOC concentrations during base flow conditions, as well as, hydrological events in catchments dominated by organic and mineral soils reaching NSEs from 0.46 to 0.76. Our semimechanistic model was parsimonious enough to have all parameters estimated using statistical methods. We did not find any clear differences between forest and mire-dominated catchments that could be explained by soil type or tree species composition. However, parameters controlling slow release and consumption of DOC from soil water behaved differently for small headwater catchments (less than 2 km2) than for those that integrate larger areas of different ecosystem types (10-68 km2). Our results emphasize that it is important to account for nonlinear dependencies of both, soil temperature, and catchment water storage, when simulating DOC dynamics of boreal catchments.

  5. Relative importance of multiple factors on terrestrial loading of DOC to Arctic river networks

    Kicklighter, David W. [Ecosystem Center, The; Hayes, Daniel J [ORNL; Mcclelland, James W [University of Texas; Peterson, Bruce [Marine Biological Laboratory; Mcguire, David [University of Alaska; Melillo, Jerry [Marine Biological Laboratory


    Terrestrial carbon dynamics influence the contribution of dissolved organic carbon (DOC) to river networks in addition to controlling carbon fluxes between the land surface and the atmosphere. In this study, we use a biogeochemical process model to simulate the lateral transfer of DOC from land to the Arctic Ocean via riverine transport. We estimate that the pan-arctic watershed has contributed, on average, 32 Tg C/yr of DOC to the Arctic Ocean over the 20th century with most coming from the extensive area of boreal deciduous needle-leaved forests and forested wetlands in Eurasian watersheds. We also estimate that the rate of terrestrial DOC loading has been increasing by 0.037 Tg C/yr2 over the 20th century primarily as a result of increases in air temperatures and precipitation. These increases have been partially compensated by decreases in terrestrial DOC loading caused by wildfires. Other environmental factors (CO2 fertilization, ozone pollution, atmospheric nitrogen deposition, timber harvest, agriculture) are estimated to have relatively small effects on terrestrial DOC loading to arctic rivers. The effects of the various environmental factors on terrestrial carbon dynamics have both compensated and enhanced concurrent effects on hydrology to influence terrestrial DOC loading. Future increases in riverine DOC concentrations and export may occur from warming-induced increases in terrestrial DOC production associated with enhanced microbial metabolism and the exposure of additional organic matter from permafrost degradation along with decreases in water yield associated with warming-induced increases in evapotranspiration. Improvements in simulating terrestrial DOC loading to pan-arctic rivers in the future will require better information on the spatial distribution of precipitation and its temporal trends, carbon dynamics of larch-dominated ecosystems in eastern Siberia, and the role of industrial organic effluents on carbon budgets of rivers in western

  6. Sorption of U(VI) in surfaces of SrTiO{sub 3}; Sorcion de U(VI) en superficies de SrTiO{sub 3}

    Ortiz O, H.B.; Ordonez R, E.; Fernandez V, S.M. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)


    In this work is presented the physico chemical characterization and evaluation of those surface properties and of sorption of U on the SrTiO{sub 3} like possible candidate for contention barrier in the deep geological confinement. The made studies showed that the SrTiO{sub 3} presents maximum levels of sorption of positive nature species (mainly UO{sub 2}{sup 2+} and UO{sub 2}NO{sub 3}{sup +}). (Author)

  7. Kinetic, equilibrium and thermodynamic modelling of the sorption of ...

    Kinetic, equilibrium and thermodynamic modelling of the sorption of metals ... Batch sorption studies were conducted to assess the potential of a ... negative Ea values, indicating their preference to bind to low-energy sites. ... Article Metrics.

  8. Removal of fluoride from aqueous phase by biosorption onto algal biosorbent Spirogyra sp.-IO2: Sorption mechanism elucidation

    Venkata Mohan, S. [Bioengineering and Environmental Centre, Indian Institute of Chemical Technology, Hyderabad 500007 (India)]. E-mail:; Ramanaiah, S.V. [Bioengineering and Environmental Centre, Indian Institute of Chemical Technology, Hyderabad 500007 (India); Rajkumar, B. [Bioengineering and Environmental Centre, Indian Institute of Chemical Technology, Hyderabad 500007 (India); Sarma, P.N. [Bioengineering and Environmental Centre, Indian Institute of Chemical Technology, Hyderabad 500007 (India)]. E-mail:


    This communication presents results pertaining to the adsorptive studies carried out on fluoride removal onto algal biosorbent (Spirogyra IO2). Batch sorption studies were performed and the results revealed that biosorbent demonstrated ability to adsorb the fluoride. Influence of varying the conditions for removal of fluoride, such as the fluoride concentration, the pH of aqueous solution, the dosage of adsorbent, the temperature on removal of fluoride, and the adsorption-desorption studies were investigated. Sorption interaction of fluoride on to algal species obeyed the pseudo first order rate equation. Experimental data showed good fit with the Langmuir's adsorption isotherm model. Fluoride sorption was found to be dependent on the aqueous phase pH and the uptake was observed to be greater at lower pH. Maximum fluoride sorption was observed at operating 30 deg. C operating temperature. Adsorption-desorption of fluoride into inorganic solutions and distilled water was observed and this indicated the combined effect of ion exchange and physical sorption phenomena. Significant changes in the FT-IR spectra was observed after fluoride sorption which is indicative of the participation of surface function groups associated with hydrogen atoms in the carboxylic groups in sorption interaction. From X-ray photoelectron spectroscopy (XPS) analysis a marginal increase in the area for the binding energy peak at 287.4 eV was observed which could be due to the formation of -C-F- bonds. Thermogravimetric (TGA) analysis of the fluoride loaded sorbent showed that the biosorbent underwent three steps decomposition process when heated from 25 to 100 deg. C. The maximum weight loss was observed to be between 200 and 400 deg. C and 700 and 800 deg. C.

  9. Trends in soil solution dissolved organic carbon (DOC) concentrations across European forests

    Camino-Serrano, Marta; Graf Pannatier, Elisabeth; Vicca, Sara; Luyssaert, Sebastiaan; Jonard, Mathieu; Ciais, Philippe; Guenet, Bertrand; Gielen, Bert; Peñuelas, Josep; Sardans, Jordi; Waldner, Peter; Etzold, Sophia; Cecchini, Guia; Clarke, Nicholas; Galić, Zoran; Gandois, Laure; Hansen, Karin; Johnson, Jim; Klinck, Uwe; Lachmanová, Zora; Lindroos, Antti-Jussi; Meesenburg, Henning; Nieminen, Tiina M.; Sanders, Tanja G. M.; Sawicka, Kasia; Seidling, Walter; Thimonier, Anne; Vanguelova, Elena; Verstraeten, Arne; Vesterdal, Lars; Janssens, Ivan A.


    Dissolved organic carbon (DOC) in surface waters is connected to DOC in soil solution through hydrological pathways. Therefore, it is expected that long-term dynamics of DOC in surface waters reflect DOC trends in soil solution. However, a multitude of site studies have failed so far to establish consistent trends in soil solution DOC, whereas increasing concentrations in European surface waters over the past decades appear to be the norm, possibly as a result of recovery from acidification. The objectives of this study were therefore to understand the long-term trends of soil solution DOC from a large number of European forests (ICP Forests Level II plots) and determine their main physico-chemical and biological controls. We applied trend analysis at two levels: (1) to the entire European dataset and (2) to the individual time series and related trends with plot characteristics, i.e., soil and vegetation properties, soil solution chemistry and atmospheric deposition loads. Analyses of the entire dataset showed an overall increasing trend in DOC concentrations in the organic layers, but, at individual plots and depths, there was no clear overall trend in soil solution DOC. The rate change in soil solution DOC ranged between -16.8 and +23 % yr-1 (median = +0.4 % yr-1) across Europe. The non-significant trends (40 %) outnumbered the increasing (35 %) and decreasing trends (25 %) across the 97 ICP Forests Level II sites. By means of multivariate statistics, we found increasing trends in DOC concentrations with increasing mean nitrate (NO3-) deposition and increasing trends in DOC concentrations with decreasing mean sulfate (SO42-) deposition, with the magnitude of these relationships depending on plot deposition history. While the attribution of increasing trends in DOC to the reduction of SO42- deposition could be confirmed in low to medium N deposition areas, in agreement with observations in surface waters, this was not the case in high N deposition areas. In

  10. Sorption Properties of Some Romanian Gingerbread

    Tulbure Anca


    Full Text Available Water activity of gingerbread is very important for keeping the product freshness and shelf life. Water activity is influenced by composition, water content and temperature. The water content of gingerbread could vary according with storage condition. i.e. rH. 11 gingerbread samples were analysed. The water content and water activity lies between 7.0 and 12.6% and respectively 0.590 and 0.715. The sorption isotherms were determined at 30°C by gravimetric method. The moisture sorption is influenced by composition, especially sweeteners and humectants. Honey and invert sugar have the same impact on gingerbread higroscopicity.

  11. A Sorption Hysteresis Model For Cellulosic Materials

    Frandsen, Henrik Lund; Damkilde, Lars


    The equilibrium concentration of adsorbed water in cellulosic materials is dependent on the history of the variations of vapor pressure in the ambient air, i.e. sorption hysteresis. Existing models to describe this phenomenon such as the independent domain theory have numerical drawbacks and....../or imply accounting for the entire history variations of every material point. This paper presents a sorption hysteresis model based on a state formulation and expressed in closed-form solutions, which makes it suitable for implementation into a numerical method....

  12. Gas Sorption and Storage Properties of Calixarenes

    Patil, Rahul S.; Banerjee, Debasis; Atwood, Jerry L.; Thallapally, Praveen K.


    Calixarenes, a class of organic macrocyclic molecules have shown interesting gas sorption properties towards industrially important gases such as carbon di-oxide, hydrogen, methane and acetylene. These macrocycles are involved in weak van der Waals interaction to form multidimensional supramolecular frameworks. The gas-diffusion and subsequent sorption occurs due to a cooperative behavior between neighboring macrocycles. Furthermore, the flexibility at the upper rim functional group also plays a key role in the overall gas uptake of calixarene. In this book chapter, we give a brief account of interaction and diffusion of gases in calixarene and selected derivatives.

  13. Tungstate and Carbonate Ions Sorption Using Anion Exchangers AV-17-8 and Purolite A400

    Chegrintsev S.


    Full Text Available The current paper shows the results of tungstate and carbonate ion sorption using strongly basic anion exchangers AV-17-8 and Purolite A400. It has been established that anion exchanger AV-17-8 in the chloride form with parameters of 168 g of tungstate ion and 157 g of carbonate ion per 1 kg of anion exchanger has the maximum capacity for the tungstate and carbonate ions.

  14. CO2, CH4, and DOC Flux During Long Term Thaw of High Arctic Tundra

    Stackhouse, B. T.; Vishnivetskaya, T. A.; Layton, A.; Bennett, P.; Mykytczuk, N.; Lau, C. M.; Whyte, L.; Onstott, T. C.


    rate of -196×12 (dark) nmol CH4 m-2 hr-1. Saturated cores occasionally acted as slight CH4 sources (17×17 nmol CH4 m-2 hr-1) but were generally found to still behave as CH4 sinks (maximum rate -93×56 nmol CH4 m-2 hr-1). Dissolved CH4 in the permafrost pore water immediately upon thaw was ~0.5 μM in all treatments, and remained at this concentration in the saturated cores. In in situ water saturation treatments, however, pore water CH4 concentrations decreased from 0.6×0.3 μM to 0.2×0.1 μM over the course of three weeks without release into the core headspace. This is likely due to aerobic methanotrophy, as the concentration of genomic sequences associated with methanotrophic bacteria was found to be 30 times greater in the upper 60 cm than in the permafrost. Sustained concentrations of CH4 in the deeper portion of saturated cores indicated that methanogenesis is occurring at depths near and below the permafrost table. Measurements of in situ DOC were 0.22×0.05 mmol L-1, whereas core DOC values increased to a maximum of >1.7 mmol L-1 (primarily acetate) during the course of the thawing experiment. These findings indicate that in a warming Arctic, even under various hydrological regimes, these soil types will be able to act as a sink of atmospheric CH4, a moderate source of CO2 and a potential source for DOC.

  15. Sorption of inorganic salts on carbon nanomaterials and magnetite

    Lyu, Sh. T.; Troshkina, I. D.; Rakov, E. G.


    Magnetic composites based on graphene oxides and functionalized carbon nanotubes containing magnetite nanoparticles are synthesized. The dispersing ability of these composites in water at different pH values is studied. It is shown that the solubility of Fe3O4 composites is constant in the pH range of 3.5-10, though these composites are unstable at both lower and higher pH values. Magnetic sorbents for extracting Ce(NO3)3 and La(NO3)3 from solutions are tested. Dependences of the volume on the sorbent's composition, pH value, and salt concentration in the solution are found. Maximum sorption capacity in relation to Ce3+ and La3+ at pH 7.5 and 8.5 are found to be 1040 and 920 mg/g respectively.

  16. An improved experimental and regression methodology for sorption isotherms

    Quirijns, E.J.; Boxtel, van A.J.B.; Loon, van W.K.P.; Straten, van G.


    Sorption isotherms of corn and starch cylinders with immobilised catalase are experimentally determined at different temperatures for use in drying models in optimal control studies. This application of the sorption isotherm requires an accurate prediction of the sorption data at different temperatu

  17. Sorption induced relaxations during water diffusion in S-PEEK

    Potreck, Jens; Uyar, Fuat; Sijbesma, Hylke; Nijmeijer, Kitty; Stamatialis, Dimitris; Wessling, Matthias


    This paper presents an analysis of the sorption kinetics of water vapor and liquid water in the glassy polymer sulfonated poly(ether ether ketone) (S-PEEK). Sorption isotherms are determined experimentally using a gravimetric sorption balance, and the relative contributions of Fickian diffusion and

  18. Using oxygen-18 to study DOC transport in a macroporous forest soil

    Dusek, Jaromir; Vogel, Tomas; Dohnal, Michal; Barth, Johannes A. C.; Sanda, Martin; Marx, Anne; Jankovec, Jakub


    Quantitative prediction of water movement and fluxes of dissolved substances such as organic carbon at both the hillslope and the catchment scales remains a challenge due to complex boundary conditions and soil spatial heterogeneity. In this study, water molecule 18O/16O ratios (expressed as δ18O) and dissolved organic carbon (DOC) concentrations in stormflow were analyzed using a physically-based modeling approach. A one-dimensional dual-continuum vertical flow and transport model was used to simulate the subsurface transport processes in a macroporous forest hillslope soil over a period of 2.5 years. The 18O isotope was used as a conservative natural tracer to contrast the behavior of DOC that undergoes complex transformations in the soil environment. The model was applied to describe the transformation of input signals of δ18O and DOC into output signals observed in the hillslope stormflow. To quantify uncertainty associated with the model parameterization, Monte Carlo analysis in conjunction with Latin hypercube sampling was performed. δ18O variations in hillslope discharge and in soil pore water were predicted reasonably well. Despite the complex nature of microbial transformations that caused uncertainty in model parameters and subsequent prediction of DOC transport, the simulated temporal patterns of DOC concentration in stormflow showed similar behavior to that reflected in the observed DOC fluxes. Due to preferential flow, the contribution of the hillslope DOC export was higher than the amounts that are usually found in the available literature.

  19. Controls upon DOC flux from UK rivers - flux at source and losses in stream.

    Worrall, Fred


    This study set out to examine the controls upon fluvial DOC flux from UK catchments. The study calculated the DOC flux from 180 catchments from throughout the UK for periods between 2001 and 2007. These catchments came from across the UK and included a range of soils and land uses, equally, the study considered catchments varying in scale from 40 to 10000 km2. For each of these catchments the soil, land use and hydrology were characterised and then multivariate statistics were used to assess controls upon the DOC flux. The study has found: i) Significant roles for: urban land, grazed land, organic soils, organo-mineral soil and mineral soils. ii) The approach is able to define an export equation that gave export coefficients for each land use and soil type found to be significant. iii) The modelling approach suggests that the flux of DOC from the UK is 0.9 Mtonnes C/yr. iv) The approach was able to estimate the loss of DOC flux with increased catchment area and suggests that in-stream losses of DOC across the UK were linear with increasing scale and amounted to 0.63 Mtonnes C/yr. v) The derived equations means that DOC export can be mapped across the country at the 1km2 scale. The study considered a separate set of peat-covered catchments at scales less than 40 km2 in order to assess linearity of losses across all scales.

  20. Evaluation of Compressive Strength and Sorption/Solubility of Four Luting Cements

    Tavangar MS


    Full Text Available Abstract: Statement of Problem: Compressive strength (CS and sorption/solubility of the luting cements are two associated factors. Searching a correlation between sorption/solubility and compressive strength of various luting cements is required. Objectives: To measure the water sorption/solubility, and compressive strength of three resin-based and one conventional glass ionomer (CGI luting cement after 1 and 24 h of immersion in distilled water and to determine if there is any correlation between those properties found. Materials and Methods: Four luting cements were investigated. For each material, 10 disc shaped specimens were prepared for measuring the sorption/solubility. The specimens were cured according to the manufacturer’s instructions, and the sorption/solubility were measured in accordance with the ISO 4049’s. For testing the compression strength, for each material 16 cylindrical specimens were prepared by insertion of cements into a stainless steel split mould. The specimens were cured, divided into groups of 8, and then stored in distilled water at (37 ± 1°C for 1 and 24 h. The test was performed using the universal testing machine, the maximum load was recorded and CS was calculated. The data were analysed using SPSS software version 18. One-way ANOVA, post-hoc Tukey’s test and Pearson’s correlation coefficient were performed. Results: G-CEM had the highest mean CS (153.60± 25.15 and CGI luting had the lowest CS (21.36±5.37 (p 0.05. The lowest mean sorption/solubility value was for RelyXTM U200 and Panavia F, and the highest for CGI luting (all p < 0.001. Conclusions: The compressive strength of all cements did not necessarily increase after 24 h and varied depending on the materials. There was a strong reverse correlation between sorption and CS values after both 1 and 24 h immersion. It may be practical for clinician to use those cements with the less sorption / solubility and more stable compression strength over

  1. Sorption of prioritized elements on montmorillonite colloids and their potential to transport radionuclides

    Wold, Susanna (Royal Inst. of Technology, Stockholm (Sweden). School of Chemical Science and Engineering, Nuclear Chemistry)


    Due to colloids potential to bind radionuclides (RN) and even mobilise sorbed RN, colloid transport of RN should be taken into account when modeling radionuclide transport in the scenario of a leaking canister in a deep bedrock repository of spent nuclear fuel. Colloids are always present in natural waters and the concentrations are controlled by the groundwater chemistry where specifically the ionic strength is of major importance. In many deep bedrock groundwaters, the ionic strength is fairly high (above the Critical Coagulation Concentration) and therefore colloids are not likely to be stable. In these types of groundwaters colloid concentrations up to 100 mug/l could be expected, and clay colloids organic degradation products and bacteria and viruses represent can be found. In a long time perspective cycles of glaciations can be expected in Sweden as in other Nordic countries. It can not be excluded that glacial melt water can intrude to repository depth with high flows. In this scenario the groundwater conditions may drastically change. In contact with dilute groundwater the bentonite barrier can start to propagate a bentonite gel and further release montmorillonite colloids into water bearing fractures. The concentration of colloids in vicinity of the bentonite barrier can then increase drastically. In contact with Grimsel groundwater types with [Na] and [Ca] of 0.001 and 0.0001 M respectively a montmorillonite concentration of a maximum of 20 mg/l is expected. Further, the groundwater chemistry of Grimsel seems to be representative for glacial meltwater when comparing with the water chemistry data on meltwaters from existing glaciers. A key to be able to model colloid transport of radionuclides is the sorption strength and the sorption reversibility. To facilitate this, a compilation of literature K{sub d}-values and an inventory of available sorption kinetic data has been composed for the prioritized elements Pu, Th, Am, Pb, Pa, Ra, Np, Cm, Ac, Tc, Cs, Nb

  2. Unified model for sorption, sequestration and degradation in soils and sediments

    Trapp, Stefan; Mayer, Philipp; Rein, Arno

    The objective of this study is to combine ad/desorption models for organic compounds with the growth and degradation kinetics of microbes in a mathematical simulation model. The goal is to interpret and predict observed effects, such as increasing persistence with time, decreasing degradation rates...... with concentration, and effects of amendments on sorption and degradation. A second objective is the mathematical definition of the terms “persistence”, “bioavailability”and “bioaccessibility”. A numerical model was set up that combines ad/desorption, microbial metabolism and the formation of non...... and degradation processes simultaneously and coupled together. By this, we hope to get a better understanding of aging and persistence in soil and of the formation of bound residues (better: non-extractable residues), but the goal is also the optimization of amendments, such as DOC, compost or charcoal...

  3. The effect of drought on dissolved organic carbon (DOC) release from peatland soil and vegetation sources

    Ritson, Jonathan P.; Brazier, Richard E.; Graham, Nigel J. D.; Freeman, Chris; Templeton, Michael R.; Clark, Joanna M.


    Drought conditions are expected to increase in frequency and severity as the climate changes, representing a threat to carbon sequestered in peat soils. Downstream water treatment works are also at risk of regulatory compliance failures and higher treatment costs due to the increase in riverine dissolved organic carbon (DOC) often observed after droughts. More frequent droughts may also shift dominant vegetation in peatlands from Sphagnum moss to more drought-tolerant species. This paper examines the impact of drought on the production and treatability of DOC from four vegetation litters (Calluna vulgaris, Juncus effusus, Molinia caerulea and Sphagnum spp.) and a peat soil. We found that mild droughts caused a 39.6 % increase in DOC production from peat and that peat DOC that had been exposed to oxygen was harder to remove by conventional water treatment processes (coagulation/flocculation). Drought had no effect on the amount of DOC production from vegetation litters; however large variation was observed between typical peatland species (Sphagnum and Calluna) and drought-tolerant grassland species (Juncus and Molinia), with the latter producing more DOC per unit weight. This would therefore suggest the increase in riverine DOC often observed post-drought is due entirely to soil microbial processes and DOC solubility rather than litter layer effects. Long-term shifts in species diversity may, therefore, be the most important impact of drought on litter layer DOC flux, whereas pulses related to drought may be observed in peat soils and are likely to become more common in the future. These results provide evidence in support of catchment management which increases the resilience of peat soils to drought, such as ditch blocking to raise water tables.

  4. Linking high-frequency DOC dynamics to the age of connected water sources

    Tunaley, C.; Tetzlaff, D.; Lessels, J.; Soulsby, C.


    We combined high-frequency dissolved organic matter fluorescence (FDOM) data with stable isotope observations to identify the sources and ages of runoff that cause temporal variability in dissolved organic carbon (DOC) within a peat-dominated Scottish catchment. FDOM was strongly correlated (r2 ˜ 0.8) with DOC, allowing inference of a 15 min time series. We captured 34 events over a range of hydrological conditions. Along with marked seasonality, different event responses were observed during summer depending on dry or wet antecedent conditions. The majority of events exhibited anticlockwise hysteresis as a result of the expansion of the riparian saturation zone, mobilizing previously unconnected DOC sources. Water ages from the main runoff sources were extracted from a tracer-aided hydrological model. Particularly useful were ages of overland flow, which were negatively correlated with DOC concentration. Overland flow age, which ranged between 0.2 and 360 days, reflected antecedent conditions, with younger water generally mobilizing the highest DOC concentrations in summer events. During small events with dry antecedent conditions, DOC response was proportionally higher due to the displacement and mixing of small volumes of previously unconnected highly concentrated riparian soil waters by new precipitation. During large events with wet antecedent conditions, the riparian saturation zone expands to organic layers on the hillslopes causing peaks in DOC. However, these peaks were limited by dilution and supply. This study highlights the utility of linking high-frequency DOC measurements with other tracers, allowing the effects of hydrologic connectivity and antecedent conditions on delivery of DOC to streams to be assessed.

  5. Hydration and sorption characteristics of a polyfunctional weak-base anion exchanger after the sorption of vanillin and ethylvanillin

    Rodionova, D. O.; Voronyuk, I. V.; Eliseeva, T. V.


    Features of the sorption of substituted aromatic aldehydes by a weak-base anion exchanger under equilibrium conditions are investigated using vanillin and ethylvanillin as examples. Analysis of the sorption isotherms of carbonyl compounds at different temperatures allows us to calculate the equilibrium characteristics of their sorption and assess the entropy and enthalpy contributions to the energy of the process. Hydration characteristics of the macroporous weak-base anion exchanger before and after the sorption of aromatic aldehydes are compared.

  6. Measurement of solubility and water sorption of dental nanocomposites light cured by argon laser.

    Mirsasaani, Seyed Shahabeddin; Ghomi, Farhad; Hemati, Mehran; Tavasoli, Tina


    Different parameters used for photoactivation process and also composition provide changes in the properties of dental composites. In the present work the effect of different power density of argon laser and filler loading on solubility (SL) and water sorption (WS) of light-cure dental nanocomposites was studied. The resin of nanocomposites was prepared by mixing bisphenol A glycol dimethacrylate (Bis-GMA) and triethylene glycol dimethacrylate (TEGDMA) with a mass ratio of 65/35. 20 wt.% and 25 wt.% of nanosilica fillers with a primary particle size of 10 nm were added to the resin. Camphorquinone (CQ) and DMAEMA were added as photoinitiator system. The nanocomposites were cured by applying the laser beam at the wavelength of 472 nm and power densities of 260 and 340 mW/cm(2) for 40 sec. Solubility and water sorption were then measured according to ISO 4049, which in our case, the maximums were 2.2% and 4.3% at 260 mW/cm(2) and 20% filler, respectively. The minimum solubility (1.2%) and water sorption (3.8%) were achieved for the composite containing 25% filler cured at 340 mW/cm(2). The results confirmed that higher power density and filler loading decreased solubility of unreacted monomers and water sorption and improved physico-mechanical properties of nanocomposites.

  7. Pentachlorophenol sorption in nylon fiber and removal by immobilized Rhizopus oryzae ENHE.

    León-Santiestebán, Hugo; Meraz, Mónica; Wrobel, Kazimierz; Tomasini, Araceli


    This study describes pentachlophenol (PCP) sorption in nylon fiber in which Rhizopus oryzae ENHE was immobilized to remove the chemical compound. The experimental sorption data were analyzed using the Langmuir, Freundlich, and Redlich-Peterson isotherm models using non-linear error functions to fit the experimental data to the three models. Results showed that the isotherm obtained from the data fitted the three models used. However, the g parameter from Redlich-Peterson model showed that the isotherm obtained approaches the Freundlich model. This support reached the sorption equilibrium concentration at 3mg PCPg(-1)nylon. To study PCP removal capability by R. oryzae ENHE and to eliminate the error caused by PCP sorbed by the nylon fiber during its quantification, nylon fiber at PCP equilibrium sorption concentration was used to immobilize R. oryzae ENHE. It was found that this fungus grew within nylon fiber cubes in presence or not of PCP, even when PCP caused growth inhibition. Maximum biomass accumulated into nylon cubes without PCP was of 32 mg biomass g(-1)nylon and into nylon cubes at PCP equilibrium concentration was of 18 mg g(-1)nylon. The results showed that R. oryzae ENHE immobilized into nylon fiber removed 88.6% and 92% of PCP in cultures with 12.5 and 25 mg PCPL(-1), as initial concentration, respectively. This is the first work to report that a zygomycete, such as R. oryzae ENHE, immobilized into nylon fiber kept its potential to remove PCP.

  8. Water sorption properties of HM-pectin and liposomes intended to alleviate dry mouth.

    Adamczak, Małgorzata I; Martinsen, Ørjan G; Smistad, Gro; Hiorth, Marianne


    Pharmaceutical formulations intended for treatment of xerostomia (dry mouth) should be able to keep the oral mucosa hydrated for a prolonged period of time. The products already existing on the market contain water-soluble polymers, however their ability to moisturize the oral mucosa for a longer period of time seems limited. In this paper the sorption properties of water vapor of high-methoxylated pectin (HM-pectin, a hydrophilic biopolymer) and phosphatidylcholine-based (Soya-PC) liposomes have been studied and compared using a gravimetric method. The kinetics of water desorption and sorption have been recorded over the relative humidity range RH=95-0-95%, at 35°C. The obtained isotherms were found to be well described by the n-layer Brunauer-Emmet-Teller (BET) adsorption model. The water isotherms on HM-pectin were Type II (IUPAC), while water isotherms on liposomes were Type III. The maximum water sorption capacity of liposomes (1.2mg water per mg of adsorbent at 95% RH) was found to be twice as high as for pectin. Due to the slower water release from the liposomes, as well as their high water sorption capacity, they seem to have great potential in relieving the symptoms of dry mouth syndrome.

  9. New insights into the sorption mechanism of cadmium on red mud.

    Luo, Lei; Ma, Chenyan; Ma, Yibing; Zhang, Shuzhen; Lv, Jitao; Cui, Mingqi


    Effectiveness and mechanism of cadmium (Cd) sorption on original, acidified and ball milling nano-particle red muds were investigated using batch sorption experiments, sequential extraction analysis and X-ray absorption near edge structure (XANES) spectroscopy. The maximum sorption capacity of Cd was 0.16, 0.19, and 0.21 mol/kg for the original, acidified, and nano-particle red muds at pH 6.5, respectively. Both acidification and ball-milling treatments significantly enhanced Cd sorption and facilitated transformation of Cd into less extractable fractions. The Cd LIII-edge XANES analysis indicated the formation of inner-sphere complexes of Cd similar to XCdOH (X represents surface groups on red mud) on the red mud surfaces although outer-sphere complexes of Cd were the primary species. This work shed light on the potential application of red mud to remediate Cd-contaminated soils and illustrated the promising tool of XANES spectroscopy for speciation of multicomponent systems of environmental relevance.

  10. Maximum Autocorrelation Factorial Kriging

    Nielsen, Allan Aasbjerg; Conradsen, Knut; Pedersen, John L.; Steenfelt, Agnete


    This paper describes maximum autocorrelation factor (MAF) analysis, maximum autocorrelation factorial kriging, and its application to irregularly sampled stream sediment geochemical data from South Greenland. Kriged MAF images are compared with kriged images of varimax rotated factors from an ordinary non-spatial factor analysis, and they are interpreted in a geological context. It is demonstrated that MAF analysis contrary to ordinary non-spatial factor analysis gives an objective discrimina...

  11. Sorption Recovery of Gold Thiosulphate Complexes

    A.G.Kholmogorov; O.N.Kononova; 等


    The gold sorption from thiosulphate solutions on carbon sorbents and on anion exchangers was studied. It was shown that the anion exchangers AV-17-10P and AP-100 are the most effective and selective at pH=5-8. These anion exchangers can be recommended for the gold recovery from the industrial solutions.

  12. Sorption of metals by Chlorobium spp.

    Garcia-Gil, J; Borrego, C


    The capacity of two species of green phototrophic sulfur bacteria, Chlorobium limicola and C. phaeobacteroides, to sorb several metal ions (Mn2+, Fe2+, Ni2+, Cu2+, Zn2+, Cd2+ and Pb2+) has been tested in laboratory batch cultures at increasing concentrations up to 2,000 mumol/l. Except for nickel--which was not sorbed to bacterial cells--the rest of metals tested were bound in a fast and passive process, which was mathematically described by means of Freundlich isotherms models. The sorption capacity of the two species studied were found to be dependent on the metal involved, whereas no differences were observed in the sorption intensity, suggesting that in all cases the sorption process proceeds in a similar way. Further, the comparison of the sorption intensity values as well as the metal recovery index (Ri), for both species, revealed that C. phaeobacteroides was more efficient that C. limicola to attach metal ions. The ecological significance of this ability in the water column of some stratified lakes, where coinciding maxima of ferrous iron and green photosynthetic sulfur bacteria are frequently found, is discussed.

  13. A Sorption Hysteresis Model For Cellulosic Materials

    Frandsen, Henrik Lund; Damkilde, Lars


    The equilibrium concentration of adsorbed water in cellulosic materials is dependent on the history of the variations of vapor pressure in the ambient air, i.e. sorption hysteresis. Existing models to describe this phenomenon such as the independent domain theory have numerical drawbacks and/or i...

  14. Enhancement of the bentonite sorption properties.

    Mockovciaková, Annamária; Orolínová, Zuzana; Skvarla, Jirí


    The almost monomineral fraction of bentonite rock-montmorillonite was modified by magnetic particles to enhance its sorption properties. The method of clay modification consists in the precipitation of magnetic nanoparticles, often used in preparing of ferrofluids, on the surface of clay. The influence of the synthesis temperature (20 and 85 degrees C) and the weight ratio of bentonite/iron oxides (1:1 and 5:1) on the composite materials properties were investigated. The obtained materials were characterized by the X-ray diffraction method and Mössbauer spectroscopy. Changes in the surface and pore properties of the magnetic composites were studied by the low nitrogen adsorption method and the electrokinetic measurements. The natural bentonite and magnetic composites were used in sorption experiments. The sorption of toxic metals (zinc, cadmium and nickel) from the model solutions was well described by the linearized Langmuir and Freundlich sorption model. The results show that the magnetic bentonite is better sorbent than the unmodified bentonite if the initial concentration of studied metals is very low. Copyright 2010 Elsevier B.V. All rights reserved.

  15. Sorption of pesticides to aquifer minerals

    Clausen, Liselotte; Fabricius, Ida Lykke


    This paper summarizes results from a work were the sorption of five pesticides on seven minerals were studied in order to quantify the adsorption to different mineral surfaces. Investigated mineral phases are: quartz, calcite, kaolinite, a-alumina, and three iron oxides (2-line ferrihydrite, goet...

  16. Sorption behavior of o-nitrophenol on marine sediment

    YANG Guipeng; WU Ping; KONG Dexin


    Systematic study on sorption behavior of o-nitrophenol on marine sediments was conducted.Isotherms of sorption of o-nitrophenol on marine sediments could be described by Freundlich model; and the isotherm of sorption of o-nitrophenol on HCl-treated sediment could be described by Langmuir model. The sorption behavior was affected by various factors including organic carbon content, aqueous solution salinity,temperature, and acidity. The sorption amount of o-nitrophenol increased when salinity and acidity of the aqueous solution increase, but decreased with increasing temperature. Organic carbon content in sediments had apparent effect on the behavior except for HCl-treated sediments.

  17. Implementation of sorption hysteresis in multi-Fickian moisture transport

    Frandsen, Henrik Lund; Svensson, Staffan


    represent this behavior. The multi-Fickian model describes the combined transport of bound water and vapor and their interaction through sorption. The bound-water concentration is also influenced by sorption hysteresis. In the worst case, sorption hysteresis may result in deviations of up to 30......-35% in moisture content. Hence, for a precise moisture content computation, sorption hysteresis must be taken into account. The present paper explains the relation between sorption hysteresis and multi-Fickian moisture transport, and clarifies how models for the two phenomena are coupled. To illustrate...

  18. Implementation of sorption hysteresis in multi-Fickian moisture transport

    Frandsen, Henrik Lund; Svensson, Staffan


    this behavior. The multi-Fickian model describes the combined transport of bound water and vapor and their interaction through sorption. The bound-water concentration is also influenced by sorption hysteresis. In the worst case, sorption hysteresis may result in deviations of up to 30-35% in moisture content....... Hence, for a precise moisture content computation, sorption hysteresis must be taken into account. The present paper explains the relation between sorption hysteresis and multi-Fickian moisture transport, and clarifies how models for the two phenomena are coupled. To illustrate the effects, a finite...

  19. Determination of {sup 60}Co sorption in natural clinoptilolite; Determinacion de la sorcion de {sup 60}Co en clinoptilolita natural

    Hernandez B, E.; Granados C, F. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)


    It was studied the clinoptilolite behavior coming from a deposit in Taxco, Guerrero in hydration and stabilization conditions with sodium for determining its sorption properties. The ion exchange process was carried out through gamma spectrometry using a CoCl{sub 2} solution marked with {sup 60} Co at p H 6.5 in different contact times. It was observed a maximum sorption of 0.408 m eq Co{sup +2}/g mineral, from 0.314 m eq Co{sup +2}/g mineral correspond at ion exchange. (Author)

  20. Modeling Fission Product Sorption in Graphite Structures

    Szlufarska, Izabela [University of Wisconsin, Madison, WI (United States); Morgan, Dane [University of Wisconsin, Madison, WI (United States); Allen, Todd [University of Wisconsin, Madison, WI (United States)


    The goal of this project is to determine changes in adsorption and desorption of fission products to/from nuclear-grade graphite in response to a changing chemical environment. First, the project team will employ principle calculations and thermodynamic analysis to predict stability of fission products on graphite in the presence of structural defects commonly observed in very high- temperature reactor (VHTR) graphites. Desorption rates will be determined as a function of partial pressure of oxygen and iodine, relative humidity, and temperature. They will then carry out experimental characterization to determine the statistical distribution of structural features. This structural information will yield distributions of binding sites to be used as an input for a sorption model. Sorption isotherms calculated under this project will contribute to understanding of the physical bases of the source terms that are used in higher-level codes that model fission product transport and retention in graphite. The project will include the following tasks: Perform structural characterization of the VHTR graphite to determine crystallographic phases, defect structures and their distribution, volume fraction of coke, and amount of sp2 versus sp3 bonding. This information will be used as guidance for ab initio modeling and as input for sorptivity models; Perform ab initio calculations of binding energies to determine stability of fission products on the different sorption sites present in nuclear graphite microstructures. The project will use density functional theory (DFT) methods to calculate binding energies in vacuum and in oxidizing environments. The team will also calculate stability of iodine complexes with fission products on graphite sorption sites; Model graphite sorption isotherms to quantify concentration of fission products in graphite. The binding energies will be combined with a Langmuir isotherm statistical model to predict the sorbed concentration of fission

  1. Sorption of niobium on boreal forest soil

    Soederlund, Mervi; Hakanen, Martti; Lehto, Jukka [Helsinki Univ. (Finland). Lab. of Radiochemistry


    The sorption of niobium (Nb) was investigated on humus and mineral soil samples taken from various depths of a four-metre deep forest soil pit on Olkiluoto Island, southwestern Finland. Mass distribution coefficients, K{sub d}, were determined in batch sorption tests. The steady state of Nb sorption was observed in the mineral soil samples already after one week of equilibration, and sorption decreased with depth from a very high value of 185000 mL/g at 0.7 m to 54000 mL/g at 3.4 m. The reason behind this decrease is probably the tenfold reduction in the specific surface area of the soil at the same depth range. Distribution coefficients were clearly lower in the humus layer (1000 mL/g). The K{sub d} values determined in pure water at a pH range of 4.7-6.5 were at a high level (above 55000 mL/g), but decreased dramatically above pH 6.5, corresponding to the change in the major Nb species from the neutral Nb(OH){sub 5} to the low-sorbing anionic Nb(OH){sub 6}{sup -} and Nb(OH){sub 7}{sup 2-}. However, the K{sub d} values in the model soil solution were in the slightly alkaline range an order of magnitude higher than in pure water, which is probably caused by the formation of calcium niobate surface precipitate or electrostatic interaction between surface-sorbed calcium and solute Nb. Among nine soil constituent minerals kaolinite performed best in retaining Nb in both pure water and model soil solution at pH 8, whereas potassium feldspar showed the poorest sorption. The K{sub d} value for kaolinite was above 500000 mL/g in both solutions, while the respective potassium feldspar values were in the range of 120-220 mL/g.

  2. Ionic strength and DOC determinations from various freshwater sources to the San Francisco Bay

    Hunter, Y.R.; Kuwabara, J.S.


    An exact estimation of dissolved organic carbon (DOC) within the salinity gradient of zinc and copper metals is significant in understanding the limit to which DOC could influence metal speciation. A low-temperature persulfate/oxygen/ultraviolet wet oxidation procedure was utilized for analyzing DOC samples adapted for ionic strength from major freshwater sources of the northern and southern regions of San Francisco Bay. The ionic strength of samples was modified with a chemically defined seawater medium up to 0.7M. Based on the results, a minimum effect of ionic strength on oxidation proficiency for DOC sources to the Bay over an ionic strength gradient of 0.0 to 0.7 M was observed. There was no major impacts of ionic strength on two Suwanee River fulvic acids. In general, the noted effects associated with ionic strength were smaller than the variances seen in the aquatic environment between high- and low-temperature methods.

  3. Variable relationships of DOC with oxygen in the northwestern Indian Ocean and their ecological implications

    Rajendran, A.; DileepKumar, M.; Ramaiah, N.; Ittekkot, V.; Desai, B.N.

    The relationships between DOC and AOU in the northwestern Indian Ocean regional variations reflecting the different biological characteristics dominanting the respective zones, resulting in the variable percentages of DOM respiration through nitrate...

  4. Don't Punish Pregnant Women for Opioid Use, Docs Say

    ... gov/news/fullstory_163680.html Don't Punish Pregnant Women for Opioid Use, Docs Say Better prevention ... action, should be the focus when dealing with pregnant women who use opioids, a leading pediatricians' group ...

  5. Addiction Drug Underused by Primary Care Docs in U.S.

    ... page: Addiction Drug Underused by Primary Care Docs in U.S. ... of a medication that can wean people off addiction to heroin and prescription painkillers, according to results ...

  6. Emergency medicine residents' beliefs about contributing to a Google DocsTM presentation: a survey protocol

    Patrick Archambault


    Conclusion To our knowledge, this study will be the first to use a theory based framework to identify healthcare trainees' salient beliefs concerning their decision whether to contribute to an online collaborative writing project using Google DocsTM.

  7. The eDoc-Server Project Building an Institutional Repository for the Max Planck Society

    Beier, Gerhard


    With the eDoc-Server the Heinz Nixdorf Center for Information Management in the Max Planck Society (ZIM) provides the research institutes of the Max Planck Society (MPS) with a platform to disseminate, store, and manage their scientific output. Moreover, eDoc serves as a tool to facilitate and promote open access to scientific information and primary sources. Since its introduction in October 2002 eDoc has gained high visibility within the MPS. It has been backed by strong institutional commitment to open access as documented in the 'Berlin Declaration on Open Access to the Data of the Sciences and Humanities', which was initiated by the MPS and found large support among major research organizations in Europe. This paper will outline the concept as well as the current status of the eDoc-Server, providing an example for the development and introduction of an institutional repository in a multi-disciplinary research organization.

  8. Sorption of triazoles to soil and iron minerals.

    Jia, Yu; Aagaard, Per; Breedveld, Gijs D


    Triazoles, additives in runway de-icers, are found in soil and groundwater at airport sites. To better understand the fate and transport of benzotriazole (BTA) and methylbenzotriazole (MeBTA) and to assess possible remediation options of contaminated groundwater, sorption to various soils and ferrous sorbents has been studied. In batch experiments, limited non-linear sorption of BTA to mineral subsoil from the Oslo International Airport, Gardermoen was observed. The sorption to soil could be described using a Freundlich isotherm. pH affected sorption of BTA to subsoil, although the effect was not strong. Increased sorption was observed to zerovalent iron (Fe(0)). MeBTA showed similar sorption behaviour as BTA although the sorption coefficient was generally higher. Sorption to Fe(0) seems to be controlled by multi-layer coverage. Our data suggest that sorption of triazoles to Fe(2)O(3) is negligible. However BTA sorption to 2-line and 6-line ferrihydrites showed strong sorption. The results demonstrate that triazoles are highly mobile in the subsurface environment, however zerovalent iron can be an effective medium for groundwater remediation. Without remediation, wide distribution of triazoles in the environment can be expected due to its extensive application and limited degradability.

  9. Sorption of Acid Dyes onto Silica Modified with Cetrltrimethylammonium Cations

    TahirImranQureshi; Dong-IkSong; 等


    The sorption behavior of acid dyes onto cetyltrimethylammonium bromide (CTAB)-modified silica as a function of pH in the aqueous medium was studied. Single-and multi-solute sorption equilibria of orange Ⅱ(OR), phenol red (PR) and Eriochrome Black T (EBT) were studied at pH 3, unbuffered water pH and pH 11. Sorption behavior of EBT could not be conducted at pH3 due to its aggregation in acidic medium. All the reaction conditions, experimental protocols and techniques remained the same throughout the sorption process. Sorption isotherms for single-solute system were fitted by the Langmuir model, while Langmuir competitive model (LCM) and the ideal adsorbed solution theory (IAST) coupled with Langmuir model (IAST/Langmuir) were used for the prediction of multisolute competitive sorption. Sorption affinities influenced by the factors like physical interactive forces between the molecules of CTA on silica and sorbate, structural limitations of the dyes based on their geometrical arrangement were investigated. Sorption affinity of OR was found to be higher than that of EBT and PR at all the pH values investigated. Magnitude of the sorption capacities was observed to be higher in acidic medium but lower in alkaline medium. Trends of the sorption affinities in multisolute system were simlar to those in single-solute system but magnitude of the sorption capacities was significantly reduced due to the prevailing competition among the sorbates.


    Md Jelas Haron


    Full Text Available This paper describes the preparation of chemically modified oil palm empty fruit bunch (OPEFB with hydroxamic acid functional group and its use for the sorption of Cu(II from aqueous solution. OPEFB was grafted with poly(methylacrylate (PMA, using H2O2/Fe2+ as initiator. The PMA grafted OPEFB (PMA-OPEFB was treated with hydroxylammonium chloride in alkaline medium to produce hydroxamic acid grafted fiber (PHA-OPEFB. The FTIR spectrum of OPEFB grafted with PMA showed an intense absorption band at 1734 cm-1 which is attributed to C=O vibration in the grafted ester. After hydroxylamine treatment, the intensity of absorption band at 1734 cm-1 decreased and new bands appeared at the 1640 cm-1 related to C=O vibration in hydroxamic acid and at the 1568 cm-1 related to the N-H amide. Sorption of Cu(II by PHA-OPEFB was effective over a pH range of 4 to 6. The sorption followed the Langmuir model with maximum capacities of 74.1 mg g-1 at 25 °C. The sorption process was exothermic, as shown by the negative value of enthalpy change, H. The free energy change (G for the sorption was negative, showing that the sorption process was spontaneous. A kinetic study showed that the Cu(II sorption followed a second order kinetic model.

  11. Sorption of aspartic and glutamic aminoacids on calcined hydrotalcite.

    Silvério, Fabiano; Dos Reis, Márcio José; Tronto, Jairo; Valim, João Barros


    Sorption of aspartic and glutamic aminoacids by regeneration of calcined hydrotalcite is reported. Hydrotalcite was synthesized by coprecipitation and calcined at 773 K. Sorption experiments were performed at 298 K and 310 K, and the results reveal that at low aminoacids equilibrium concentrations, intercalation of hydroxyl anions takes place while at high equilibrium concentrations, the sorption process occur by means re-hydration and aminoacids intercalation of hydrotalcite. The results also suggested that Asp and Glu sorption is a temperature dependent process. The amount of sorbed amino acid decreases as the temperature increase. The effect is more pronounced for Glu sorption probably due to its higher hydrophobic character, which makes the sorption more difficult in comparison with sorption of Asp at higher temperature.

  12. Quantifying tropical peatland dissolved organic carbon (DOC) using UV-visible spectroscopy

    Cook, Sarah; Peacock, Mike; Evans, Chris D.; Page, Susan E.; Whelan, Mick J.; Gauci, Vincent; Kho, Lip Khoon


    UV-visible spectroscopy has been shown to be a useful technique for determining dissolved organic carbon (DOC) concentrations. However, at present we are unaware of any studies in the literature that have investigated the suitability of this approach for tropical DOC water samples from any tropical peatlands, although some work has been performed in other tropical environments. We used water samples from two oil palm estates in Sarawak, Malaysia to: i) investigate the suitability of both sing...

  13. Z-DOC: a serious game for Z-plasty procedure training.

    Shewaga, Robert; Knox, Aaron; Ng, Gary; Kapralos, Bill; Dubrowski, Adam


    We present Z-DOC, a (prototype) serious game for training plastic surgery residents the steps comprising the Z-plasty surgical procedure. Z-DOC employs touch-based interactions and promotes competition amongst multiple players/users thus promote engagement and motivation. It is hypothesized that by learning the Z-plasty procedure in an interactive, engaging, and fun gaming environment, trainees will have a much better understanding of the procedure than by traditional learning modalities.

  14. Quantifying tropical peatland dissolved organic carbon (DOC) using UV-visible spectroscopy.

    Cook, Sarah; Peacock, Mike; Evans, Chris D; Page, Susan E; Whelan, Mick J; Gauci, Vincent; Kho, Lip Khoon


    UV-visible spectroscopy has been shown to be a useful technique for determining dissolved organic carbon (DOC) concentrations. However, at present we are unaware of any studies in the literature that have investigated the suitability of this approach for tropical DOC water samples from any tropical peatlands, although some work has been performed in other tropical environments. We used water samples from two oil palm estates in Sarawak, Malaysia to: i) investigate the suitability of both single and two-wavelength proxies for tropical DOC determination; ii) develop a calibration dataset and set of parameters to calculate DOC concentrations indirectly; iii) provide tropical researchers with guidance on the best spectrophotometric approaches to use in future analyses of DOC. Both single and two-wavelength model approaches performed well with no one model significantly outperforming the other. The predictive ability of the models suggests that UV-visible spectroscopy is both a viable and low cost method for rapidly analyzing DOC in water samples immediately post-collection, which can be important when working at remote field sites with access to only basic laboratory facilities. Copyright © 2017 The Authors. Published by Elsevier Ltd.. All rights reserved.

  15. Applicability of MIEX(®)DOC process for organics removal from NOM laden water.

    Karpinska, Anna M; Boaventura, Rui A R; Vilar, Vítor J P; Bilyk, Andrzej; Molczan, Marek


    The aim of this study was to evaluate applicability of ion exchange process for organics removal from Douro River surface water at the intake of Lever water treatment plant using magnetized ion exchange resin MIEX®. Qualitative analysis of the natural organic matter present in the surface water and prediction of its amenability to removal in conventional coagulation process were assessed. Results obtained in MIEX®DOC process kinetic batch experiments allowed determination of ion exchange efficiency in dissolved organic carbon (DOC), UV absorbing organics, and true color removal. The data were compared with the efficiencies of the conventional unit processes for organics removal at Lever WTP. MIEX®DOC process revealed to be more efficient in DOC removal than conventional treatment achieving the efficiencies in the range of 61-91 %, lowering disinfection by-products formation potential of the water. DOC removal efficiency at Lever WTP depends largely on the raw water quality and ranges from 28 % for water of moderated quality to 89 % of significantly deteriorated quality. In this work, MIEX®DOC process was also used as a reference method for the determination of contribution of anionic fraction to dissolved organic matter and selectivity of the unit processes at Lever WTP for its removal.

  16. Effect of light and nutrient availability on the release of dissolved organic carbon (DOC) by Caribbean turf algae

    Mueller, B.; den Haan, J.; Visser, P.M.; Vermeij, M.J.A.; van Duyl, F.C.


    Turf algae increasingly dominate benthic communities on coral reefs. Given their abundance and high dissolved organic carbon (DOC) release rates, turf algae are considered important contributors to the DOC pool on modern reefs. The release of photosynthetically fixed carbon as DOC generally, but not

  17. Phosphorus Changes and Sorption Characteristics in a Calcareous Soil Under Long-Term Fertilization

    GUO Sheng-Li; DANG Ting-Hui; HAO Ming-De


    Knowledge of phosphorus (P) behavior in long-term fertilized soils is essential for programming fertilization practices and for sustaining environmental quality.The long-term (1984-1997) effects of various fertilization treatments on P changes and sorption isotherms as well as the relationship of soil properties to P sorption and P forms were evaluated in an Ustic Isohumisol,a calcareous soil,on the Loess Plateau,China.Compared to 1984,after 13 years of crop production,total soil P in the no-P treatments (control and N treatment) decreased by 5%-7%,but in the phosphorus fertilizer alone (P),nitrogen and phosphorus fertilizers in combination (NP),manure alone (M),and nitrogen and phosphorus fertilizers and manure in combination (NPM) treatments,it increased by 22%,19%,28%,and 58%,respectively.Residual fertilizer P was found mainly in NH4Ac-soluble P (Cas-P),followed by NaHCO3-sohible P (NaHCO3-P),and NH4F-soluble P (Al-P).Phosphorus sorption in the soils with different fertilization practices fit the Langmuir equations.Phosphorus sorption capacity in the no-P treatments increased,whereas it decreased in the P-included treatments (P,NP,and NPM treatments).Phosphorus sorption maximum (Qm) was significantly and negatively correlated to inorganic P including Na4CO3-P,Cas-P,NaOH-Na2CO3-soluble P (Fe-P),and AI-P (P ≤ 0.01).Moreover,long-term fertilization increased soil organic carbon in the NP,M,and NPM treatments and decreased pH in the NP and NPM treatments.Thus,the ability of the soil to release sorbed P to the environment increased under long-term P fertilization.

  18. Dialysis experiments for assessing the pH-dependent sorption of sulfonamides to soil clay fractions.

    Anskjær, G G; Krogh, K A; Halling-Sørensen, B


    Equilibrium dialysis experiments, a novel approach for conducting soil/water distribution experiments in environmental samples, were found to be applicable for assessing pH-dependent partitioning and to quantify the sorption of three sulfonamides, sulfadiazine, sulfadoxine, and sulfacetamide. Clay fractions from two agricultural soils including both particulate and dissolved soil matter were used in the experiments to achieve a high sorption capacity when varying pH in a relevant environmental range. Stabilizing and controlling pH was done by using organic buffers. In two clay fractions, Kd for sulfadiazine was determined to be 43 and 129 L kg(-1), and 1.3 and 4.6 L kg(-1) at pH 4.0 and pH 9.0, respectively. This corresponded to Kd for the neutral and ionized form of sulfadiazine, respectively. The difference in sulfadiazine sorption between the two clay fractions could to some extent be related to the difference in the amount of organic carbon. Sorption experiments with sulfacetamide and sulfadoxine also exhibited decreasing sorption when increasing pH. At low pH, maximum Kd for sulfacetamide and sulfadoxine was determined to be 83 and 211 L kg(-1), respectively, while at high pH minimum Kd was 4.8 and 1.2 L kg(-1), respectively. Hence, compound speciation was important for the quantity of sorbed sulfonamide, which was confirmed by a correlation (R(2)) close to unity, when using the experimentally obtained Kd values with a simple model weighing the contribution from the neutral and the ionized compound, respectively.

  19. Sorption of cadmium to bacterial extracellular polymeric sediment coatings under estuarine conditions

    Schlekat, C.E.; Decho, A.W.; Chandler, G.T. [Univ. of South Carolina, Columbia, SC (United States). Dept. of Environmental Health Sciences


    Microbial extracellular polymeric substances (EPS) are ubiquitous features in aquatic environments. Produced by surface-adherent bacteria and microalgae, EPS are often present as coatings on surfaces of sediment particles and exhibit high affinities for divalent cationic metals. Thus, EPS sediment coatings may participate in the fate of potentially toxic metals. The authors coated particulate silica with EPS produced by NISC1, a bacterium isolated from estuarine sediments, in order to measure the metal binding characteristics of these coatings. They used the radioisotope {sup 109}Cd to measure effects of salinity, Cd concentration, and pH on Cd sorption to EPS-coated (EPS-silica) silica and to noncoated silica (NC-silica). Also, Cd sorption by NISC1 EPS coatings was compared to coatings of polymers formed by the bacterium, Alteromonas atlantica and the alga, Macrocystis porifera. Under all circumstances, EPS coatings increased the affinity of silica for Cd. Extracellular polymeric substance-particulate aggregates rapidly sorbed up to 90% of Cd from aqueous solution. Extracellular polymeric substance sediment coatings exhibited a maximum log distribution coefficient (K{sub d}) of 6.5 at 2.5%. Sorption of Cd to NC-silica was affected by salinity and metal concentration, whereas sorption of Cd to EPS-silica was only affected by salinity under high metal concentrations. Changes in pH had a dramatic effect on Cd sorption, with the proportion of free Cd to sorbed Cd changing from approximately 90% at pH 5 to 5% at pH 9. Desorption of Cd from EPS-silica was enhanced with increasing salinity. These experiments suggest that EPS coatings actively participate in binding dissolved overlying and pore-water metals in estuarine sediments.

  20. Defluoridation by Bacteriogenic Iron Oxides: Sorption Studies

    Evans, K.; Ferris, F.


    At concentrations above 1 mg/L, fluoride in drinking water can lead to dental and skeletal fluorosis, a disease that causes mottling of the teeth, calcification of ligaments, crippling bone deformities and many other physiological disorders that can, ultimately, lead to death. Conservative estimates are that fluorosis afflicts tens of millions of people worldwide. As there is no treatment for fluorosis, prevention is the only means of controlling the disease. While numerous defluoridation techniques have been explored, no single method has been found to be both effective and inexpensive enough to implement widely. Our research began in India, with a large-scale geochemical study of the groundwater in a fluoride-contaminated region of Orissa. Having developed a better understanding of the geochemical relationships that exist between fluoride and other parameters present in an affected area, as well as the complex relationships that arise among those parameters that can impact the presence of fluoride, we began investigating certain remediation scenarios involving iron oxides. A common approach to remediation involves the partitioning of fluoride from groundwater by sorption onto a variety of materials, one of the most effective of which is iron oxide whose surface area acts as a scavenger for fluoride. In the presence of iron oxidizing bacteria, the oxidation rate of iron has been shown to be ˜6 times greater than in their absence; fluoride should, therefore, be removed from an aqueous environment by bacteriogenic iron oxides (BIOS) much more quickly than by abiotic iron oxides. Most recently, sorption studies have been conducted using both BIOS and synthetic hydrous ferric oxides in order to compare the behavior between biotic and abiotic sorbents. These studies have provided sorption isotherms that allow comparison of fluoride removed by sorption to BIOS versus synthetic iron oxides. Sorption affinity constants have also been determined, which allow for the

  1. Maximum likely scale estimation

    Loog, Marco; Pedersen, Kim Steenstrup; Markussen, Bo


    A maximum likelihood local scale estimation principle is presented. An actual implementation of the estimation principle uses second order moments of multiple measurements at a fixed location in the image. These measurements consist of Gaussian derivatives possibly taken at several scales and/or ...

  2. Efficient sorption and reduction of U(VI) on zero-valent iron-polyaniline-graphene aerogel ternary composite.

    Chen, Lili; Feng, Shaojie; Zhao, Donglin; Chen, Shaohua; Li, Feifei; Chen, Changlun


    In this work, zero-valent iron-polyaniline-graphene aerogel composite (Fe-PANI-GA) was prepared and applied in the removal of U(VI) from aqueous solutions by batch sorption experiments. The experimental results showed that the Fe-PANI-GA composite had an excellent removal capacity for the removal of U(VI) in acidic solutions. The results also showed that the maximum removal capacity of the Fe-PANI-GA toward U(VI) was 350.47mg/g at pH 5.5. The sorption kinetics data were well-described by pseudo-second-order. The sorption isotherms of U(VI) fitted well with Langmuir isotherm and exhibited better removal efficiency with the increase of temperature. The thermodynamic parameters (ΔG, ΔS, ΔH) indicated that the sorption of U(VI) on the Fe-PANI-GA was an endothermic and spontaneous process. Moreover, removal mechanisms were studied based on the results of XRD, FTIR and XPS. Both U(VI) sorption and partially reductive precipitation of U(VI) to U(IV) contributed to the removal of U(VI) on Fe-PANI-GA. Therefore, Fe-PANI-GA was an economic and effective material for the removal of uranium from nuclear waste in practical application.

  3. Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

    Shubo DENG; Danmeng SHUAI; Qiang YU; Jun HUANG; Gang YU


    Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics,isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS On the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.

  4. Sorption kinetics and its effects on retention and leaching.

    de Wilde, Tineke; Mertens, Jan; Spanoghe, Pieter; Ryckeboer, Jaak; Jaeken, Peter; Springael, Dirk


    Sorption of pesticides to substrates used in biopurification systems is important as it controls the system's efficiency. Ideally, pesticide sorption should occur fast so that leaching of the pesticide in the biopurification system is minimized. Although modeling of pesticide transport commonly assumes equilibrium, this may not always be true in practice. Sorption kinetics have to be taken into account. This study investigated the batch sorption kinetics of linuron, isoproturon, metalaxyl, isoxaben and lenacil on substrates commonly used in a biopurification system, i.e. cow manure, straw, willow chopping, sandy loam soil, coconut chips, garden waste compost and peat mix. The first-order sorption kinetics model was fitted to the observed pesticide concentrations versus time resulting in an estimated kinetic rate constant alpha. Sorption appeared to be fast for the pesticides linuron and isoxaben, pesticides which were classified as immobile, while less mobile pesticides displayed an overall slower sorption. However, the substrate does not seem to be the main parameter influencing the sorption kinetics. Coconut chips, which is a substrate with a high organic matter content showed slow sorption for most of the pesticides. The effect of different estimated alpha values on the breakthrough of pesticides through a biopurification system was evaluated using the HYDRUS 1D model. Significant differences in leaching behavior were observed as a result of the obtained differences in sorption kinetics.

  5. Testosterone sorption and desorption: Effects of soil particle size

    Qi, Yong, E-mail: [Civil Engineering Dept., University of Nebraska-Lincoln at Omaha Campus, Omaha, NE 68182 (United States); Zhang, Tian C. [Civil Engineering Dept., University of Nebraska-Lincoln at Omaha Campus, Omaha, NE 68182 (United States); Ren, Yongzheng [School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China)


    Graphical abstract: - Highlights: • Smaller soil particles have higher sorption and lower desorption rates. • The sorption capacity ranks as clay > silt > sand. • Small particles like clays have less potential for desorption. • Colloids (clays) have high potential to facilitate the transport of hormones in soil–water environments. - Abstract: Soils contain a wide range of particles of different diameters with different mobility during rainfall events. Effects of soil particles on sorption and desorption behaviors of steroid hormones have not been investigated. In this study, wet sieve washing and repeated sedimentation methods were used to fractionate the soils into five ranges. The sorption and desorption properties and related mechanisms of testosterone in batch reactors filled with fractionated soil particles were evaluated. Results of sorption and desorption kinetics indicate that small soil particles have higher sorption and lower desorption rates than that of big ones. Thermodynamic results show the sorption processes are spontaneous and exothermal. The sorption capacity ranks as clay > silt > sand, depending mainly on specific surface area and surface functional groups. The urea control test shows that hydrogen bonding contributes to testosterone sorption onto clay and silt but not on sand. Desorption tests indicate sorption is 36–65% irreversible from clay to sand. Clays have highest desorption hysteresis among these five soil fractions, indicating small particles like clays have less potential for desorption. The results provide indirect evidence on the colloid (clay)-facilitated transport of hormones (micro-pollutants) in soil environments.

  6. Isotherm, kinetic, and thermodynamic study of ciprofloxacin sorption on sediments.

    Mutavdžić Pavlović, Dragana; Ćurković, Lidija; Grčić, Ivana; Šimić, Iva; Župan, Josip


    In this study, equilibrium isotherms, kinetics and thermodynamics of ciprofloxacin on seven sediments in a batch sorption process were examined. The effects of contact time, initial ciprofloxacin concentration, temperature and ionic strength on the sorption process were studied. The K d parameter from linear sorption model was determined by linear regression analysis, while the Freundlich and Dubinin-Radushkevich (D-R) sorption models were applied to describe the equilibrium isotherms by linear and nonlinear methods. The estimated K d values varied from 171 to 37,347 mL/g. The obtained values of E (free energy estimated from D-R isotherm model) were between 3.51 and 8.64 kJ/mol, which indicated a physical nature of ciprofloxacin sorption on studied sediments. According to obtained n values as measure of intensity of sorption estimate from Freundlich isotherm model (from 0.69 to 1.442), ciprofloxacin sorption on sediments can be categorized from poor to moderately difficult sorption characteristics. Kinetics data were best fitted by the pseudo-second-order model (R (2) > 0.999). Thermodynamic parameters including the Gibbs free energy (ΔG°), enthalpy (ΔH°) and entropy (ΔS°) were calculated to estimate the nature of ciprofloxacin sorption. Results suggested that sorption on sediments was a spontaneous exothermic process.

  7. Sorption of Phenanthrene on Agricultural Soils

    Soares, Antonio Alves; Møldrup, Per; Minh, Luong Nhat


    Polyaromatic hydrocarbon (PAH) sorption to soil is a key process deciding the transport and fate of PAH, and potential toxic impacts in the soil and groundwater ecosystems, for example in connection with atmospheric PAH deposition on soils. There are numerous studies on PAH sorption in relatively...... low organic porous media such as urban soils and groundwater sediments, but less attention has been given to cultivated soils. In this study, the phenanthrene partition coefficient, KD (liter per kilogram), was measured on 143 cultivated Danish soils (115 topsoils, 0–0.25-m soil depth and 28 subsoils...... (COC and NCOC, grams per gram). Multiple regression analyses showed that the NCOC-based phenanthrene partition coefficient (KNCOC) could be markedly higher than the COC-based partition coefficient (KCOC) for soils with a clay/OC ratio


    C.L. Cavalcante Jr.


    Full Text Available The sorption kinetics of some aromatics (toluene, p-xylene, o-xylene and p-diethylbenzene was studied experimentally with a high sensitivity microbalance (± 1µg at temperatures between 150 and 210oC and concentrations in the adsorbed phase of a maximum of 1 mmol/g. In general, the sorption rates decreased in the following order: toluene > p-xylene > o-xylene > p-diethylbenzene. Two diffusion models were tested against the experimental results. One model considers the mass transfer inside the zeolitic micropores as the controlling diffusion step. The other model supposes that resistance to mass transfer in the macropores (formed during pelletization of the crystals with the amorphous ligand is the limiting step. The results observed for both models are presented and analyzed

  9. Sorption of strontium on clinoptilolite and heulandite

    Chernyavskaya, N.B.


    The author investigates the sorption of strontium on the isostructural zeolites clinoptilolite and heulandite. In the Sr/Na/zeolite/H/sub 2/O system, clinoptilolite manifests selectivity for strontium, and heulandite for sodium. The role of the nature of the exchange ions is discussed. Modification of the clinoptilolite with acid, subsequently obtaining the Na, NH/sub 4/, or N/sub 2/H/sub 4/ form, increases the capacity for strontium by a factor of 2-4.

  10. Sorption dehumidification of natural gas exhaust

    Lazzarin, R.M.; Longo, G.A. (Padua Univ. (Italy)); Piccininni, F. (Politecnico di Bari (Italy). Ist. di Fisica Tecnica)


    The calorific value of natural gas can be fully utilized only if the water vapour in the exhaust gases is condensed. This can be achieved in condensing boilers. Another possibility is to dry the exhaust before discharge by sorption dehumidification. The sorbent can be regenerated directly by the boiler. The vapour developed in the regenerator can be condensed in a condenser with useful effect. Simulations given an efficiency higher than 97% with respect to the Gross Calorific value. (author).

  11. Maximum information photoelectron metrology

    Hockett, P; Wollenhaupt, M; Baumert, T


    Photoelectron interferograms, manifested in photoelectron angular distributions (PADs), are a high-information, coherent observable. In order to obtain the maximum information from angle-resolved photoionization experiments it is desirable to record the full, 3D, photoelectron momentum distribution. Here we apply tomographic reconstruction techniques to obtain such 3D distributions from multiphoton ionization of potassium atoms, and fully analyse the energy and angular content of the 3D data. The PADs obtained as a function of energy indicate good agreement with previous 2D data and detailed analysis [Hockett et. al., Phys. Rev. Lett. 112, 223001 (2014)] over the main spectral features, but also indicate unexpected symmetry-breaking in certain regions of momentum space, thus revealing additional continuum interferences which cannot otherwise be observed. These observations reflect the presence of additional ionization pathways and, most generally, illustrate the power of maximum information measurements of th...

  12. Sorption behavior of U(VI), 234U(VI) and 238U(VI) onto fracture-filling clays in Beishan granite, Gansu: Application to selecting the site of high-level radwaste repository in China

    MIN; Maozhong; LUO; Xingzhang; WANG; Ju; JIN; Yuanxin; WAN


    The first results of sorption experiments of U(VI), 234U(VI) and 238U(VI) onto original (unpurified) fracture-filling clays from No.1 monzonitic granite intrusion, Beishan area, Gansu Province, China are reported. The monzonitic granite intrusion is a potential location for a high-level radwaste (HLW) repository in China. The present experimental results show that the maximum U(VI) sorption reached 92% at near-neutral Ph and the distribution coefficient (Kd) was 1226 Ml/g. A high sorption capacity of the fracture-filling clays in host rock on radioactive elements is necessary for HLW deep geological disposal repository. No preferential sorption of 234U onto the clays was found. Finally, the sorption of U(VI) onto the clays was also modeled using a surface complexation model.

  13. DocOnto——一种基于本体的文本分类器%DocOnto: Ontology-based text classifier

    杨喜权; 孙娜; 张野; 孔德冉



  14. Sorption of BTEX mixtures to organobenonites

    SHEN Xue-you; LU Ying-ying; ZHU Li-zhong; LU Shu-yu


    Organobentonites synthesized by replacing the metal ions in bentonite with cetyltrimethylammonium(CTMA) or tetramethylammonium cation(TMA) were investigated for their behaviors to sorb benzene, toluene, p-xylene from water. The results served to distinguish the sorption mechanisms (adsorption or partition) of the twotypes of organobentonites. Bentonites modified with short-chain alkyl functional groups(e. g., TMA) sorb organiccontaminants primarily by an adsorption process, in which the sorbed amount decreases with increasing sterichindrance of the organic compound and the process exhibits a competitive effect because of steric hindrance in multi-solute systems. In contrast, the sorption of contaminants to organobentonites modified with long-chain alkyl groups(e. g., CTMA) occurs by partition process without exhibiting a competitive effect, and the additional organiccompounds may induce a cosorptive effect. In the latter case, the measured distribution coefficients of organiccompounds between organobentonites and water( log Kd ) are positively correlated with the octanol-water partitioncoefficients of the compounds (logKow) and the sorption process exhibits no competitive effect in multi-solutesystems.

  15. Sorption of sulfuryl fluoride by food commodities.

    Sriranjini, Venkata-rao; Rajendran, Somiahnadar


    The use of sulfuryl fluoride, a structural fumigant for termite and woodborer control, has recently been expanded to treating stored food commodities and food facilities. There is, however, a lack of data on the sorption of sulfuryl fluoride by food commodities. Knowledge about sorption is important in the context of effective treatment and residues. When sulfuryl fluoride was applied at a dose of 50 g m(-3) to various food commodities (total 68) with 300 g per replicate in 0.75 L gas wash bottles (fumigation chambers) at 25 +/- 1 degrees C, in most cases (81%) the gas concentrations in the free space of the commodities exceeded 50 g m(-3) (range 51-80 g m(-3)) at the end of 24 h exposure. In chambers without the substrate, an average concentration of 49.7 g m(-3) was recorded. About 54% of the commodities showed low-level ( 50%). The latter include white oats (terminal gas concentration 17.8 g m(-3)), some of the decorticated split pulses (24.0-29.3 g m(-3)), chickpea flour (26.3 g m(-3)), dried ginger (29.0 g m(-3)), refined wheat flour (30.3 g m(-3)) and coriander powder (40.5 g m(-3)). In unfumigated control commodities, owing to interfering volatiles, Fumiscope readings in the range 0-13 were noted. Sulfuryl fluoride has the advantage of a low or moderate level of sorption with the majority of the food commodities.

  16. Lead sorption-desorption from organic residues.

    Duarte Zaragoza, Victor M; Carrillo, Rogelio; Gutierrez Castorena, Carmen M


    Sorption and desorption are mechanisms involved in the reduction of metal mobility and bioavailability in organic materials. Metal release from substrates is controlled by desorption. The capacity of coffee husk and pulp residues, vermicompost and cow manure to adsorb Pb2+ was evaluated. The mechanisms involved in the sorption process were also studied. Organic materials retained high concentrations of lead (up to 36,000 mg L(-1)); however, the mechanisms of sorption varied according to the characteristics of each material: degree of decomposition, pH, cation exchange capacity and percentage of organic matter. Vermicompost and manure removed 98% of the Pb from solution. Lead precipitated in manure and vermicompost, forming lead oxide (PbO) and lead ferrite (PbFe4O7). Adsorption isotherms did not fit to the typical Freundlich and Langmuir equations. Not only specific and non-specific adsorption was observed, but also precipitation and coprecipitation. Lead desorption from vermicompost and cow manure was less than 2%. For remediation of Pb-polluted sites, the application of vermicompost and manure is recommended in places with alkaline soils because Pb precipitation can be induced, whereas coffee pulp residue is recommended for acidic soils where Pb is adsorbed.

  17. Absorption features of chromophoric dissolved organic matter (CDOM and tracing implication for dissolved organic carbon (DOC in Changjiang Estuary, China

    X. Y. Zhang


    Full Text Available Chromophoric dissolved organic matter (CDOM represents the light absorbing fraction of dissolved organic carbon (DOC. Studies have shown that the optical properties of CDOM can be used to infer the distribution and diffusion characteristics of DOC in the estuary and coastal zone. The inversion of DOC concentrations from remote sensing has been implemented in certain regions. In this study we investigate the potential of tracing DOC from CDOM by the measurement of DOC, absorption spectrum of CDOM, Chla concentration, suspended sediment (SS, and salinity from cruises in different seasons around the Changjiang estuary. Our results show that around the Changjiang estuary the absorption coefficients of CDOM in general have the similar spatial and temporal characteristics as that of DOC, but the strength of the correlation between CDOM and DOC varies locally and seasonally. The input of pollutants from outside the estuary, the bloom of phytoplankton in spring, re-suspension of deposited sediment, and light bleaching all contribute to the local and seasonal variation of the correlation between DOC and CDOM. An inversion model for the determination of DOC from CDOM is established, but the stability of model parameters and its application in different environments need further study. We find that relative to the absorption coefficient of CDOM, the fitted parameters of the absorption spectrum of DOM are better indictors for the composition of DOC. In addition, it is found that the terrestrial input of DOC to Changjiang estuary is a typical two-stage dilution process instead of a linear diffusion process.

  18. The influence of clay surface modification with berberine on the sorption of anthocyanins

    Chulkov, A. N.; Deineka, V. I.; Tikhova, A. A.; Vesentzev, A. I.; Deineka, L. A.


    The influence of preliminary sorption of berberine on the sorption of anthocyanins by bentonite clay was studied. The cation exchange sorption mechanism was found to be replaced by hydrophobic sorption of these compounds after clay modification with berberine. The enthalpy of sorption along the initial isotherm part changed from endothermic to exothermic.

  19. A statistical case against the use of the Langmuir model for describing P sorption data

    Sorption of P to soils is often investigated through batch experiments where sorption models are fit to the resultant sorption curve by least-squares regression. One of the most commonly used sorption models is the Langmuir model, a model which was originally developed for the study of gas sorption ...

  20. Plasmodium falciparum double C2 domain protein, PfDOC2, binds to calcium when associated with membranes.

    Jean, Sophonie; Zapata-Jenks, Mónica A; Farley, Julie M; Tracy, Erin; Mayer, D C Ghislaine


    The pathogenesis of malaria is strongly correlated with secretion of the micronemes, the apical organelles which contain the adhesins required for invasion of Plasmodium falciparum into human erythrocytes. A critical event in P. falciparum erythrocyte invasion is the production of calcium transients. After entering the cell, Ca(2+) binds to soluble Ca(2+)-binding proteins, such as the double C2 domains (DOC2). Recently, deletion of a P. falciparum DOC2 protein, PfDOC2, was shown to cause impairment in microneme secretion. However, PfDOC2 remains poorly characterized. Here, we report that PfDOC2 is expressed throughout the erythrocytic cycle and demonstrate that it is associated with membrane fractions and binds to calcium when it is part of these membranous structures. In summary, we show that PfDOC2 is a calcium lipid-binding protein of the protein kinase C type of DOC2 proteins.

  1. Automatisierte Artikelbestellverwaltung: Doctor-Doc – ein bibliothekarisches Verwaltungswerkzeug / Automation in Interlibrary Loan: Doctor-Doc – a tool for librarians

    Fischer, Markus


    Full Text Available Interlibrary loan has always been an important service to supplement own library holdings.To organize and standardize the order process of journal articles for 6 hospitals, we did create an online tool for the Solothurner Spitäler AG. The resulting application is available for libraries free of charge under The application is maintained and will be further developed by an association founded specially for this purpose. Doctor-Doc is not a supplier of articles, but rather a platform to organize orders at existing suppliers like Subito, British Library or any other supplying libraries. Doctor-Doc is OpenURL compliant and is able to resolve identifiers like PMIDs. In combination with an existing account from the german EZB, libraries can use the application as a linkresolver.The application has become an essential tool to efficiently manage interlibrary loan for the Solothurner Spitäler AG. The tool is also used by many libraries in Germany and Switzerland.

  2. Start-up performance of a full-scale riverbank filtration site regarding removal of DOC, nutrients, and trace organic chemicals.

    Regnery, Julia; Barringer, Jessica; Wing, Alexandre D; Hoppe-Jones, Christiane; Teerlink, Jennifer; Drewes, Jörg E


    The performance of a full-scale riverbank filtration facility in Colorado was evaluated from initial start-up over a period of seven years including the impact of seasonal variations to determine whether sustainable attenuation of various chemical constituents could be achieved. Both, annual and seasonal average concentrations were determined for several wastewater-derived constituents including dissolved organic carbon (DOC), ultraviolet absorbance at 254 nm, nitrate, phosphate for the years 2006, 2009, 2010, 2012, and trace organic chemicals (TOrC) for years 2009, 2010, and 2012. ANOVA analyses and Student's t-tests were performed to evaluate the consistency of contaminant attenuation at the site. Findings revealed no significant statistical differences for any of the bulk parameters with the exception of phosphate suggesting a highly reliable attenuation of DOC and nitrate from start-up to full-scale performance. Phosphate attenuation, however, exhibited a steady decline, which was likely attributed to exhaustion of sorption sites in the subsurface porous media. The river's flow regime influenced both occurrence levels and attenuation of TOrC during riverbank filtration, i.e. less river discharge resulted in higher TOrC concentrations and lower proportion of river water in the recovered groundwater. Differences in removal performance between annual data sets for caffeine, trimethoprim, sulfamethoxazole, and carbamazepine were caused by variations in the source; concentrations in riverbank filtrate remained similar over several years. The seasonal assessment for TOrC revealed steady or improving removal between winter and summer seasons based on the statistical analysis with atenolol being the only exception likely due to an increased microbial activity at elevated temperatures.

  3. Investigating DOC export dynamics using high-frequency instream concentration measurements

    Oosterwoud, Marieke; Keller, Toralf; Musolff, Andreas; Frei, Sven; Park, Ji-Hyung; Fleckenstein, Jan H.


    Being able to monitor DOC concentrations using in-situ high frequency measurements makes it possible to better understand concentration-discharge behavior under different hydrological conditions. We developed a UV-Vis probe setup for modified/adapted use under field conditions. The quasi mobile probe setup allows a more flexible probe deployment. New or existing monitoring sites can easily be equipped for quasi-continuous monitoring or measurements can be performed at changing locations, without the need for additional infrastructure. We were able to gather high frequency data on DOC dynamics for one year in two streams in the Harz mountains in Germany. It proved that obtaining accurate DOC concentrations from the UV-Vis probes required frequent maintenance and probe calibration. The advantage of the setup over standard monitoring protocols becomes evident when comparing net exports over a year. In addition to mass improved balance calculations the high-frequency measurements can reveal intricate hysteretic relationships between discharge and concentrations that can provide valuable insights into the hydrologic dynamics and mechanisms that govern the delivery of DOC to the receiving waters. Measurements with similar probes from two additional catchments in Southern Germany and South Korea will be used to illustrate different discharge-concentration relationships and what can be learned from them about the hydrologic mechanisms that control the dynamics of DOC export.

  4. Mathematical Modeling of Moisture Sorption Isotherms and Determination of Isosteric Heats of Sorption of Ziziphus Leaves

    Amel Saad


    Full Text Available Desorption and adsorption equilibrium moisture isotherms of Ziziphus spina-christi leaves were determined using the gravimetric-static method at 30, 40, and 50°C for water activity (aw ranging from 0.057 to 0.898. At a given aw, the results show that the moisture content decreases with increasing temperature. A hysteresis effect was observed. The experimental data of sorption were fitted by eight models (GAB, BET, Henderson-Thompson, modified-Chung Pfost, Halsey, Oswin, Peleg, and Adam and Shove. After evaluating the models according to several criteria, the Peleg and Oswin models were found to be the most suitable for describing the sorption curves. The net isosteric heats of desorption and adsorption of Ziziphus spina-christi leaves were calculated by applying the Clausius-Clapeyron equation to the sorption isotherms and an expression for predicting these thermodynamic properties was given.

  5. Sorption of dyes from aqueous solutions onto fly ash.

    Janos, Pavel; Buchtová, Hana; Rýznarová, Milena


    Brown coal fly ashes were tested as potentially low-cost sorbents for the removal of synthetic dyes from waters. It was shown that both basic (cationic) as well as acid (anionic) dyes can be sorbed onto the fly ash. The adsorption can be described by the multi-site Langmuir isotherm. The sorption capacities were in the range of 10(-1)-10(-3)mmol/g and did not differ significantly for basic and acid dyes. The dye sorption decreased in the presence of organic solvents (methanol, acetone). The presence of oppositely charged surfactants exhibited a pronounced effect on the dye sorption-low concentrations of the surfactant enhanced sorption, whereas high concentrations solubilized the dyes and kept them in solution. Inorganic salts exhibited only a minor effect on the dye sorption. The sorption of basic dyes increased at high pH values, whereas the opposite was true for acid dyes.

  6. Continuous cadmium removal from aqueous solutions by seaweed in a packed-bed column under consecutive sorption-desorption cycles

    Jafari, Seyed Ali; Jamali, Abbas [Persian Gulf Research Institute, Persian Gulf University, 75169, Bushehr (Iran, Islamic Republic of)


    Packed-bed column process efficiency for cadmium adsorption from aqueous solution was investigated under different bed heights (2.6 to 7.5 cm) and feed flow rates (15 to 30 ml min{sup -1}). The column was filled with brown seaweed, Sargassum angustifolium. Three simplified models, including Bed Depth Service Time, Thomas, and Yoon- Nelson were employed for describing the experimental breakthrough curves as well as achieving design parameters. Bed lifetime was also evaluated in several consecutive sorption-desorption cycles. Cadmium concentration of 0.005mg l−1, as a standard limit for potable water, was considered as the breakthrough concentration. The maximum column performance was achieved 81% at 7.5 cm bed length and flow rate of 15 ml min{sup -1}. Indeed, increasing the bed height increased the sorption performance and service time, while increasing the feed flow rate had a negative effect. Maximum sorption capacity value remained almost constant by the bed height changes; however, increase in the feed flow rate slightly decreased it. The modeling results revealed that the Yoon-Nelson model was more accurate than Thomas for describing the experimental breakthrough data, especially at low flow rates. Column service time predictions were surprisingly achieved using the Bed Depth Service Time model even at extrapolations. 20% reduction in column adsorption efficiency was observed at the end of four consecutive sorption-desorption cycles; however, desorption efficiencies were achieved more than 99% in each cycle.

  7. Sorption properties of modified potato starch

    Teresa Witczak


    Full Text Available Background. Starch is one of the biopolymers most commonly used in the food industry. In its native form its applications are limited. In contrast, its structure is relatively readily modified using various methods, producing starch derivatives of greatly diverse properties. The primary methods used to change characteristics of starch include acetylation and oxidation. Thus obtained raw materials are used as food additives. Stability of these raw materials and food products to a considerable extent depends on their composition and parameters characterizing storage facilities, i.e. relative humidity and temperature. One of the methods to specify adequate ambient conditions is based on water activity supplemented by sorption isotherms. As a result studies investigating correlations between water activity and moisture content are of importance for the optimization of storage conditions and design of certain food processing procedures. For this reason the aim of this study was to assess the effect of modification (oxidation, acetylation and their combination on sorption properties (described based on sorption isotherms of potato starch. Material and methods. Analyses were conducted on potato starch and its derivatives produced by acetylation, oxidation and co-modification (acetylation coupled with oxidation. Starch was oxidized using sodium chlorate (I, while acetylation was run using anhydrous acetic acid. Sorption isotherms were determined by the static desiccator method. Results were described applying selected mathematical methods equipped with physical interpretations (BET and GAB and empirical models (Halsey, Oswin, Henderson, Pelega, Lewicki, Blahovec-Yanniotis. Calculations were made using non-linear estimation. Results. The greatest water absorbability was found for native potato starch. Modifications caused a decrease in the amount of adsorbed water vapour, dependent on the applied modification. Acetylation resulted in significantly

  8. Pharmaceuticals' sorptions relative to properties of thirteen different soils.

    Kodešová, Radka; Grabic, Roman; Kočárek, Martin; Klement, Aleš; Golovko, Oksana; Fér, Miroslav; Nikodem, Antonín; Jakšík, Ondřej


    Transport of human and veterinary pharmaceuticals in soils and consequent ground-water contamination are influenced by many factors, including compound sorption on soil particles. Here we evaluate the sorption isotherms for 7 pharmaceuticals on 13 soils, described by Freundlich equations, and assess the impact of soil properties on various pharmaceuticals' sorption on soils. Sorption of ionizable pharmaceuticals was, in many cases, highly affected by soil pH. The sorption coefficient of sulfamethoxazole was negatively correlated to soil pH, and thus positively related to hydrolytic acidity and exchangeable acidity. Sorption coefficients for clindamycin and clarithromycin were positively related to soil pH and thus negatively related to hydrolytic acidity and exchangeable acidity, and positively related to base cation saturation. The sorption coefficients for the remaining pharmaceuticals (trimethoprim, metoprolol, atenolol, and carbamazepine) were also positively correlated with the base cation saturation and cation exchange capacity. Positive correlations between sorption coefficients and clay content were found for clindamycin, clarithromycin, atenolol, and metoprolol. Positive correlations between sorption coefficients and organic carbon content were obtained for trimethoprim and carbamazepine. Pedotransfer rules for predicting sorption coefficients of various pharmaceuticals included hydrolytic acidity (sulfamethoxazole), organic carbon content (trimethoprimand carbamazepine), base cation saturation (atenolol and metoprolol), exchangeable acidity and clay content (clindamycin), and soil active pH and clay content (clarithromycin). Pedotransfer rules, predicting the Freundlich sorption coefficients, could be applied for prediction of pharmaceutical mobility in soils with similar soil properties. Predicted sorption coefficients together with pharmaceutical half-lives and other imputes (e.g., soil-hydraulic, geological, hydro-geological, climatic) may be used for

  9. Hysteresis and Temperature Dependency of Moisture Sorption – New Measurements

    Rode, Carsten; Hansen, Kurt Kielsgaard


    It is well known that sorption characteristics of building materials exhibit hysteresis in the way the equilibrium curves develop between adsorption and desorption, and that the sorption curves are also somewhat temperature dependent. However, these two facts are most often neglected in models...... measurements of hysteresis and temperature dependency of the moisture sorption characteristics of three different porous building materials: aerated concrete, cement paste and spruce. Scanning curves are measured for all three materials where periods with adsorption and desorption interrupt each other...

  10. Competitive sorption of CO2 and CH4 on coals as a function of maturity and moisture content

    Merkel, Alexej; Gensterblum, Yves; Kroos, Bernhard; Littke, Ralf


    The competitive sorption of CH4 and CO2 from a two-component gas mixture on coals of different rank and moisture content has been studied at pressures up to 10 MPa. The aim of this study was to assess, the maximum sorption capacity as well as the selectivity of dry and moisturised coals of different rank with respect to sorption of CH4and CO2. The research addresses possible implications on Enhanced Coal Bed Methane (ECBM) recovery projects, where CO2is to be injected into coal seams to increase CH4production rates. The measurements were conducted using a manometric setup with continuous pressure and temperature recording and periodic analysis of gas compositions in the reference cell and the measuring cell throughout the duration of the experiment. Isotherms were determined with a gas mixture containing 70-80% CH4. Three isotherms were measured at three different moisture states for each of the three coal samples of different rank. A significant decrease of total excess sorption capacity was observed with increasing moisture content from the dry sample to the sample moisturised at 53% relative humidity (RH). The initial reduction of sorption capacity decreases with rank. Only a small further decrease occurred from 53% to the 97% RH moisturised coals. The effect of moisture on sorption capacity and selectivity is highly rank-dependent. In all cases the results show a preferential sorption of CO2from a binary CH4/CO2gas mixture at all three moisture states. Sorption capacity increases with rank for all but the dry state and in all cases the sample with the highest maturity shows the highest sorption capacity by far. Selectivity for CO2 decreases with increasing rank of the coal. The results of this study support that from the thermodynamic point of view coals have a tendency to selectively take up CO2under the conditions of ECBM recovery. The selectivity coefficients are important parameters for ECBM modelling and the design of production strategies.

  11. Maximum Likelihood Associative Memories

    Gripon, Vincent; Rabbat, Michael


    Associative memories are structures that store data in such a way that it can later be retrieved given only a part of its content -- a sort-of error/erasure-resilience property. They are used in applications ranging from caches and memory management in CPUs to database engines. In this work we study associative memories built on the maximum likelihood principle. We derive minimum residual error rates when the data stored comes from a uniform binary source. Second, we determine the minimum amo...

  12. Maximum likely scale estimation

    Loog, Marco; Pedersen, Kim Steenstrup; Markussen, Bo


    A maximum likelihood local scale estimation principle is presented. An actual implementation of the estimation principle uses second order moments of multiple measurements at a fixed location in the image. These measurements consist of Gaussian derivatives possibly taken at several scales and....../or having different derivative orders. Although the principle is applicable to a wide variety of image models, the main focus here is on the Brownian model and its use for scale selection in natural images. Furthermore, in the examples provided, the simplifying assumption is made that the behavior...... of the measurements is completely characterized by all moments up to second order....

  13. Functionalized macroporous copolymer of glycidyl methacrylate: The type of ligand and porosity parameters influence on Cu(II ion sorption from aqueous solutions

    Sandić Zvjezdana P.


    Full Text Available The removal of heavy metals from hydro-metallurgical and other industries' wastewaters, their safe storage and possible recovery from waste- water streams is one of the greater ecological problems of modern society. Conventional methods, like precipitation, adsorption and biosorption, electrowinning, membrane separation, solvent extraction and ion exchange are often ineffective, expensive and can generate secondary pollution. On the other hand, chelating polymers, consisting of crosslinked copolymers as a solid support and functional group (ligand, are capable of selectively loading different metal ions from aqueous solutions. In the relatively simple process, the chelating copolymer is contacted with the contaminated solution, loaded with metal ions, and stripped with the appropriate eluent. Important properties of chelating polymers are high capacity, high selectivity and fast kinetics combined with mechanical stability and chemical inertness. Macroporous hydrophilic copolymers of glycidyl methacrylate and ethylene glycol dimethacrylate modified by different amines show outstanding efficiency and selectivity for the sorption of precious and heavy metals from aqueous solutions. In this study poly(GMA-co-EGDMA copolymers were synthesized with different porosity parameters and functionalized in reactions with ethylene diamine (EDA, diethylene triamine (DETA and triethylene tetramine (TETA. Under non-competitive conditions, in batch experiments at room temperature, the rate of sorption of Cu(II ions from aqueous solutions and the influence of pH on it was determined for four samples of amino-functionalized poly(GMA-co-EGDMA. The sorption of Cu(II for both amino-functionalized samples was found to be very rapid. The sorption half time, t1/2, defined as the time required to reach 50% of the total sorption capacity, was between 1 and 2 min. The maximum sorption capacity for copper (2.80 mmol/g was obtained on SGE-10/12-deta sample. The sorption

  14. Dicyandiamide Sorption-Desorption Behavior on Soils and Peat Humus

    ZHANG Hai-Jun; WU Zhi-Jie; ZHOU Qi-Xing


    The sorption-desorption behavior of dicyandiamide (DCD) is an important chemical process that affects DCD fate and mobility in soils. Therefore, this study quantified DCD sorption-desorption on a phaeozem (Mollisol), a burozem (Alfisol), a soil with organic matter-removed and peat humus using the batch-equilibration procedure, and identified soil properties that influenced DCD sorption. The sorption on peat humus was higher than that on the phaeozem and the burozem, with much lower sorption observed on the soil with organic matter-removed, indicating that soil organic matter was the main carrier of DCD sorption. Due to its amphipathic property the DCD molecule sorption on the phaeozem and the burozem decreased as pH increased from about 2 to 5, but a further increase in pH led to a rise in DCD sorption.The DCD desorption hysteretic effect for peat humus was greater than that for the phaeozem and the burozem using 0.01 mol L-1 CaC12 as the background electrolyte, suggesting that the hydrophobic domains of organic matter may play an important role in DCD sorption.

  15. Sorption of radionuclides by cement-based barrier materials

    Li, Kefei, E-mail:; Pang, Xiaoyun


    This paper investigates the sorption of radionuclide ions, {sup 137}Cs{sup +} and {sup 90}Sr{sup 2+}, by cement-based barrier materials for radioactive waste disposal. A mortar with ternary binder is prepared and powder samples are ground from the hardened material following a predetermined granulometry. After pre-equilibrium with an artificial pore solution, the sorption behaviors of powder samples are investigated through single sorption and blended sorption. The results show that: (1) no systematic difference is observed for single and blended sorptions thus the interaction between {sup 137}Cs{sup +} and {sup 90}Sr{sup 2+} sorptions must be weak; (2) the sorption kinetics is rapid and all characteristic times are less than 1d; (3) the sorption capacity is enhanced by C–A–S–H hydrates and the measured K{sub d} values can be predicted from C–S–H sorption data with Ca/Si ratio equal to Ca/(Si + Al) ratio.

  16. Experimental study of strontium sorption on fissure filling material

    Eriksen, T.E.; Cui, Daqing [Royal Institute of Technology, Stockholm (Sweden). Dept. of Chemistry


    We have carried out a comparative study of sorption and desorption of strontium in groundwater on separated magnetic and size fractions of fissure filling material taken from natural fissures in granitic rock. Complete reversibility of the sorption process was demonstrated by identical Freundlich isotherms, isotopic exchangeability and pH dependence of the distribution coefficients Rd. The sorption was found to be strongly pH dependent in the range 3-11. The pH effect can be accommodated in the sorption model by considering the surface areas and surface charges of the minerals in the fissure filling material. 20 refs, 9 figs, 3 tabs.

  17. Determination of sorption of seventy five pharmaceuticals in sewage sludge

    Hörsing, Maritha; Ledin, Anna; Grabic, Roman


    Sorption of 75 active pharmaceutical ingredients (APIs) to three different types of sludge (primary sludge, secondary sludge with short and long sludge age respectively) were investigated. To obtain the sorption isotherms batch studies with the APIs mixture were performed in four nominal concentr......Sorption of 75 active pharmaceutical ingredients (APIs) to three different types of sludge (primary sludge, secondary sludge with short and long sludge age respectively) were investigated. To obtain the sorption isotherms batch studies with the APIs mixture were performed in four nominal...

  18. Nitrogen and dissolved organic carbon (DOC losses from an artificially drained grassland on organic soils

    B. Tiemeyer


    Full Text Available Nitrate-nitrogen (NO3-N as well as dissolved organic carbon (DOC and nitrogen (DON concentrations and losses were studied for three respectively two years in a small catchment dominated by a degraded peatland used as intensive grassland. Concentrations in the shallow groundwater were spatially and temporally very variable with NO3-N being the most dynamic component (7.3 ± 12.5 mg L–1. Average NO3-N concentrations of 10.3 ± 5.4 mg L–1 in the ditch draining the catchment and annual NO3-N losses of 19, 35 and 26 kg ha–1 confirmed drained peatlands as an important source of diffuse N pollution. The highest NO3-N losses occurred during the wettest year. Resulting from concentrations of 2.4 ± 0.8 mg L–1, DON added further 4.5 to 6.4 kg ha–1 to the N losses and thus formed a relevant component of the total N losses. Ditch DOC concentrations of 24.9 ± 5.9 mg L–1 resulted in DOC losses of 66 kg ha–1 in the wet year 2006/07 and 39 kg ha–1 in the dry year 2007/08. Both DOC and N concentrations were governed by hydrological conditions, but NO3-N reacted much faster and clearer on rising discharge rates than DOC which tended to be higher under dryer conditions. In the third year of the study, the superposition of a very wet summer and land use changes from grassland to arable land in a part of the catchment suggests that under re-wetting conditions with a high groundwater table in summer, NO3-N would diminish quickly, while DOC would remain on a similar level. Further intensification of the land use, on the other hand, would increase N losses to receiving water bodies.

  19. DOC Dynamics in Small Headwater Streams: the Role of Hydrology, Climate, and Land Management

    Lajtha, K.; Lee, B. S.; Jones, J. A.


    Dissolved organic carbon (DOC) is a critical component of the carbon (C) cycle of both terrestrial and aquatic systems. For small headwater allochthonous streams, terrestrial C delivery fuels the metabolism of receiving waters and significantly influences biotic diversity and function. While nutrient fluxes in streams have long been used as indicators of terrestrial ecosystem processes, less attention has been given to terrestrial controls on DOC export. We used the long-term stream chemistry records from the H.J. Andrews Forest LTER to examine forest management, climatic, and hydrologic controls on both seasonal and annual DOC fluxes. Within a watershed, annual DOC flux was highly related to annual discharge (Q), although considerable variability in higher discharge years suggested a role for indices of storminess, especially early in the water year. Among watersheds, younger, previously harvested watersheds generally had significantly lower DOC fluxes for a given Q than old-growth watersheds, even 4+ decades after harvest. The exception to this pattern was a harvested watershed that had significant downed wood retained on site, and had densities of coarse woody debris (CWD) close to that of the old-growth watersheds even though live tree biomass was similar to the other harvested watersheds. Other climatic factors did not appear to have significant roles in predicting either seasonal or annual fluxes of DOC. This is in sharp contrast to fluxes of nitrate at our site, which appears to be related most significantly to the presence of alder within the watershed. Taken together, our data suggest a persistent and cascading role for CWD in old-growth forest ecosystems.

  20. Natural Diet of Coral-Excavating Sponges Consists Mainly of Dissolved Organic Carbon (DOC)

    Mueller, Benjamin; de Goeij, Jasper M.; Vermeij, Mark J. A.; Mulders, Yannick; van der Ent, Esther; Ribes, Marta; van Duyl, Fleur C.


    Coral-excavating sponges are the most important bioeroders on Caribbean reefs and increase in abundance throughout the region. This increase is commonly attributed to a concomitant increase in food availability due to eutrophication and pollution. We therefore investigated the uptake of organic matter by the two coral-excavating sponges Siphonodictyon sp. and Cliona delitrix and tested whether they are capable of consuming dissolved organic carbon (DOC) as part of their diet. A device for simultaneous sampling of water inhaled and exhaled by the sponges was used to directly measure the removal of DOC and bacteria in situ. During a single passage through their filtration system 14% and 13% respectively of the total organic carbon (TOC) in the inhaled water was removed by the sponges. 82% (Siphonodictyon sp.; mean±SD; 13±17 μmol L−1) and 76% (C. delitrix; 10±12 μmol L−1) of the carbon removed was taken up in form of DOC, whereas the remainder was taken up in the form of particulate organic carbon (POC; bacteria and phytoplankton) despite high bacteria retention efficiency (72±15% and 87±10%). Siphonodictyon sp. and C. delitrix removed DOC at a rate of 461±773 and 354±562 μmol C h−1 respectively. Bacteria removal was 1.8±0.9×1010 and 1.7±0.6×1010 cells h−1, which equals a carbon uptake of 46.0±21.2 and 42.5±14.0 μmol C h−1 respectively. Therefore, DOC represents 83 and 81% of the TOC taken up by Siphonodictyon sp. and C. delitrix per hour. These findings suggest that similar to various reef sponges coral-excavating sponges also mainly rely on DOC to meet their carbon demand. We hypothesize that excavating sponges may also benefit from an increasing production of more labile algal-derived DOC (as compared to coral-derived DOC) on reefs as a result of the ongoing coral-algal phase shift. PMID:24587253

  1. Natural diet of coral-excavating sponges consists mainly of dissolved organic carbon (DOC.

    Benjamin Mueller

    Full Text Available Coral-excavating sponges are the most important bioeroders on Caribbean reefs and increase in abundance throughout the region. This increase is commonly attributed to a concomitant increase in food availability due to eutrophication and pollution. We therefore investigated the uptake of organic matter by the two coral-excavating sponges Siphonodictyon sp. and Cliona delitrix and tested whether they are capable of consuming dissolved organic carbon (DOC as part of their diet. A device for simultaneous sampling of water inhaled and exhaled by the sponges was used to directly measure the removal of DOC and bacteria in situ. During a single passage through their filtration system 14% and 13% respectively of the total organic carbon (TOC in the inhaled water was removed by the sponges. 82% (Siphonodictyon sp.; mean ± SD; 13 ± 17 μmol L(-1 and 76% (C. delitrix; 10 ± 12 μmol L(-1 of the carbon removed was taken up in form of DOC, whereas the remainder was taken up in the form of particulate organic carbon (POC; bacteria and phytoplankton despite high bacteria retention efficiency (72 ± 15% and 87 ± 10%. Siphonodictyon sp. and C. delitrix removed DOC at a rate of 461 ± 773 and 354 ± 562 μmol C h(-1 respectively. Bacteria removal was 1.8 ± 0.9 × 10(10 and 1.7 ± 0.6 × 10(10 cells h(-1, which equals a carbon uptake of 46.0 ± 21.2 and 42.5 ± 14.0 μmol C h(-1 respectively. Therefore, DOC represents 83 and 81% of the TOC taken up by Siphonodictyon sp. and C. delitrix per hour. These findings suggest that similar to various reef sponges coral-excavating sponges also mainly rely on DOC to meet their carbon demand. We hypothesize that excavating sponges may also benefit from an increasing production of more labile algal-derived DOC (as compared to coral-derived DOC on reefs as a result of the ongoing coral-algal phase shift.

  2. Natural diet of coral-excavating sponges consists mainly of dissolved organic carbon (DOC).

    Mueller, Benjamin; de Goeij, Jasper M; Vermeij, Mark J A; Mulders, Yannick; van der Ent, Esther; Ribes, Marta; van Duyl, Fleur C


    Coral-excavating sponges are the most important bioeroders on Caribbean reefs and increase in abundance throughout the region. This increase is commonly attributed to a concomitant increase in food availability due to eutrophication and pollution. We therefore investigated the uptake of organic matter by the two coral-excavating sponges Siphonodictyon sp. and Cliona delitrix and tested whether they are capable of consuming dissolved organic carbon (DOC) as part of their diet. A device for simultaneous sampling of water inhaled and exhaled by the sponges was used to directly measure the removal of DOC and bacteria in situ. During a single passage through their filtration system 14% and 13% respectively of the total organic carbon (TOC) in the inhaled water was removed by the sponges. 82% (Siphonodictyon sp.; mean ± SD; 13 ± 17 μmol L(-1)) and 76% (C. delitrix; 10 ± 12 μmol L(-1)) of the carbon removed was taken up in form of DOC, whereas the remainder was taken up in the form of particulate organic carbon (POC; bacteria and phytoplankton) despite high bacteria retention efficiency (72 ± 15% and 87 ± 10%). Siphonodictyon sp. and C. delitrix removed DOC at a rate of 461 ± 773 and 354 ± 562 μmol C h(-1) respectively. Bacteria removal was 1.8 ± 0.9 × 10(10) and 1.7 ± 0.6 × 10(10) cells h(-1), which equals a carbon uptake of 46.0 ± 21.2 and 42.5 ± 14.0 μmol C h(-1) respectively. Therefore, DOC represents 83 and 81% of the TOC taken up by Siphonodictyon sp. and C. delitrix per hour. These findings suggest that similar to various reef sponges coral-excavating sponges also mainly rely on DOC to meet their carbon demand. We hypothesize that excavating sponges may also benefit from an increasing production of more labile algal-derived DOC (as compared to coral-derived DOC) on reefs as a result of the ongoing coral-algal phase shift.

  3. Nitrogen and dissolved organic carbon (DOC) losses from an artificially drained grassland on organic soils

    Tiemeyer, B.; Kahle, P.


    Nitrate-nitrogen (NO3-N) as well as dissolved organic carbon (DOC) and nitrogen (DON) concentrations and losses were studied for three and two years, respectively, in a small catchment dominated by a degraded peatland used as intensive grassland. Concentrations in the shallow groundwater were spatially and temporally very variable, with NO3-N being the most dynamic component (7.3 ± 12.5 mg L-1) and ranging from 0 to 79.4 mg L-1. Average NO3-N concentrations of 10.3 ± 5.4 mg L-1 (0 to 25.5 mg L-1) in the ditch draining the catchment and annual NO3-N losses of 19, 35 and 26 kg ha-1 confirmed drained peatlands as an important source of diffuse N pollution. The highest NO3-N losses occurred during the wettest year. Resulting from concentration of 2.4 ± 0.8 mg L-1 (0.7 to 6.2 mg L-1), DON added a further 4.5 to 6.4 kg ha-1 to the N losses and thus formed a relevant (15%) component of the total N losses. Ditch DOC concentrations of 24.9 ± 5.9 mg L-1 (13.1 to 47.7 mg L-1) resulted in DOC losses of 66 kg ha-1 in the wet year of 2006/2007 and 39 kg ha-1 in the dry year of 2007/2008. Ditch DOC concentration were lower than the groundwater DOC concentration of 50.6 ± 15.2 mg L-1 (14.9 to 88.5 mg L-1). Both DOC and N concentrations were governed by hydrological conditions, but NO3-N reacted much faster and clearer on rising discharge rates than DOC, which tended to be higher under drier conditions. In the third year of the study, the superposition of a very wet summer and land use changes from grassland to arable land in a part of the catchment suggests that, under re-wetting conditions with a high groundwater table in summer, NO3-N would diminish quickly, while DOC would remain on a similar level. Further intensification of the land use, on the other hand, would increase N losses to receiving water bodies.

  4. Doc Tales

    Golden, Larry; Alamia, Jennifer; Baker, Ria; Chilson, Sally; Choucroun, Pierre; Cook, Katrina; de Vries-Kell, Sabina; Marbach, Christina; Peters, Scott


    Acceptance into a doctoral program is personally affirming and gives rise to optimism. It is also true that any change in the life of a person, even an apparently positive one, causes stress. The first cohort of students in a new doctoral program in counseling writes about the impact of embarking on a doctorate on themselves and their significant…

  5. High-efficient thermochemical sorption refrigeration driven by low-grade thermal energy

    LI TingXian; WANG RuZhu; WANG LiWei


    Thermochemical sorption refrigeration powered by low-grade thermal energy is one of the en ergy-saving and environment friendly green refrigeration technologies. The operation principle of sorption refrigeration system is based on the thermal effects of reversible physicochemical reaction processes between sorbents and refrigerants. This paper presents the developing study on the differ ent thermochemical sorption refrigeration cycles, and some representative high-efficient thermo chemical sorption refrigeration cycles were evaluated and analyzed based on the conventional single-effect sorption cycle. These advanced sorption refrigeration cycles mainly include the heat and mass recovery sorption cycle, double-effect sorption cycle, multi-effect sorption cycle, combined douhie-way sorption cycle, and double-effect and double-way sorption cycle with internal heat recovery.Moreover, the developing tendency of the thermochemical sorption refrigeration is also predicted in this paper.

  6. Determination of an organic-acid analog of DOC for use in copper toxicity studies on salmonids

    MacRae, R.K.; Meyer, J.S.; Hansen, J.A.; Bergman, H.L. [Univ. of Wyoming, Laramie, WY (United States); Maest, A.; Marr, J.; Beltman, D.; Lipton, J. [Hagler Bailly, Inc., Boulder, CO (United States)


    Concentrations of dissolved copper in streams draining mine sites often exceed concentrations shown to cause acute and chronic mortality in salmonids. However, toxicity and impaired behaviors may be modified by dissolved organic carbon (DOC) and other inorganic components present in the site water. The effects of DOC on copper speciation, and thus bioavailability and toxicity, were determined by titrating stream waters with copper, using a cupric ion-specific electrode to detect free copper concentrations. Effects of various competing cations (e.g., Ca{sup +2}, Co{sup +2}) on copper-DOC binding were also evaluated. Titration results were evaluated using Scatchard and non-linear regression analyses to quantify the strength and capacity of copper-DOC binding. Inorganic speciation was determined using the geochemical model MINEQL{sup +}. Results of these titrations indicated the presence of two or three distinct copper binding components in site water DOC. Three commercially available organic acids where then chosen to mimic the binding characteristics of natural DOC. This DOC-analog was used successfully in fish toxicity studies to evaluate the influence of DOC on copper bioavailability. Geochemical models were developed to predict copper speciation in both laboratory test waters and site waters, for any typical combination of water chemistry parameters (pH, alkalinity, [DOC], etc.). A combined interpretation of fish toxicity and modeling results indicate that some DOC-bound copper was bioavailable.

  7. Maximum Entropy Fundamentals

    F. Topsøe


    Full Text Available Abstract: In its modern formulation, the Maximum Entropy Principle was promoted by E.T. Jaynes, starting in the mid-fifties. The principle dictates that one should look for a distribution, consistent with available information, which maximizes the entropy. However, this principle focuses only on distributions and it appears advantageous to bring information theoretical thinking more prominently into play by also focusing on the "observer" and on coding. This view was brought forward by the second named author in the late seventies and is the view we will follow-up on here. It leads to the consideration of a certain game, the Code Length Game and, via standard game theoretical thinking, to a principle of Game Theoretical Equilibrium. This principle is more basic than the Maximum Entropy Principle in the sense that the search for one type of optimal strategies in the Code Length Game translates directly into the search for distributions with maximum entropy. In the present paper we offer a self-contained and comprehensive treatment of fundamentals of both principles mentioned, based on a study of the Code Length Game. Though new concepts and results are presented, the reading should be instructional and accessible to a rather wide audience, at least if certain mathematical details are left aside at a rst reading. The most frequently studied instance of entropy maximization pertains to the Mean Energy Model which involves a moment constraint related to a given function, here taken to represent "energy". This type of application is very well known from the literature with hundreds of applications pertaining to several different elds and will also here serve as important illustration of the theory. But our approach reaches further, especially regarding the study of continuity properties of the entropy function, and this leads to new results which allow a discussion of models with so-called entropy loss. These results have tempted us to speculate over

  8. Kinetic, equilibrium and thermodynamic studies on sorption of uranium and thorium from aqueous solutions by a selective impregnated resin containing carminic acid.

    Rahmani-Sani, Abolfazl; Hosseini-Bandegharaei, Ahmad; Hosseini, Seyyed-Hossein; Kharghani, Keivan; Zarei, Hossein; Rastegar, Ayoob


    In this work, the removal of uranium and thorium ions from aqueous solutions was studied by solid-liquid extraction using an advantageous extractant-impregnated resin (EIR) prepared by loading carminic acid (CA) onto Amberlite XAD-16 resin beads. Batch sorption experiments using CA/XAD-16 beads for the removal of U(VI) and Th(IV) ions were carried out as a function of several parameters, like equilibration time, metal ion concentration, etc. The equilibrium data obtained from the sorption experiments were adjusted to the Langmuir isotherm model and the calculated maximum sorption capacities in terms of monolayer sorption were in agreement with those obtained from the experiments. The experimental data on the sorption behavior of both metal ions onto the EIR beads fitted well in both Bangham and intra-particle diffusion kinetic models, indicating that the intra-particle diffusion is the rate-controlling step. The thermodynamic studies at different temperatures revealed the feasibility and the spontaneous nature of the sorption process for both uranium and thorium ions.

  9. Regularized maximum correntropy machine

    Wang, Jim Jing-Yan


    In this paper we investigate the usage of regularized correntropy framework for learning of classifiers from noisy labels. The class label predictors learned by minimizing transitional loss functions are sensitive to the noisy and outlying labels of training samples, because the transitional loss functions are equally applied to all the samples. To solve this problem, we propose to learn the class label predictors by maximizing the correntropy between the predicted labels and the true labels of the training samples, under the regularized Maximum Correntropy Criteria (MCC) framework. Moreover, we regularize the predictor parameter to control the complexity of the predictor. The learning problem is formulated by an objective function considering the parameter regularization and MCC simultaneously. By optimizing the objective function alternately, we develop a novel predictor learning algorithm. The experiments on two challenging pattern classification tasks show that it significantly outperforms the machines with transitional loss functions.

  10. Sorption of Lincomycin by Manure-Derived Biochars from Water.

    Liu, Cheng-Hua; Chuang, Ya-Hui; Li, Hui; Teppen, Brian J; Boyd, Stephen A; Gonzalez, Javier M; Johnston, Cliff T; Lehmann, Johannes; Zhang, Wei


    The presence of antibiotics in agroecosystems raises concerns about the proliferation of antibiotic-resistant bacteria and adverse effects to human health. Soil amendment with biochars pyrolized from manures may be a win-win strategy for novel manure management and antibiotics abatement. In this study, lincomycin sorption by manure-derived biochars was examined using batch sorption experiments. Lincomycin sorption was characterized by two-stage kinetics with fast sorption reaching quasi-equilibrium in the first 2 d, followed by slow sorption over 180 d. The fast sorption was primarily attributed to surface adsorption, whereas the long-term slow sorption was controlled by slow diffusion of lincomycin into biochar pore structures. Two-day sorption experiments were performed to explore effects of biochar particle size, solid/water ratio, solution pH, and ionic strength. Lincomycin sorption to biochars was greater at solution pH 6.0 to 7.5 below the dissociation constant of lincomycin (7.6) than at pH 9.9 to 10.4 above its dissociation constant. The enhanced lincomycin sorption at lower pH likely resulted from electrostatic attraction between the positively charged lincomycin and the negatively charged biochar surfaces. This was corroborated by the observation that lincomycin sorption decreased with increasing ionic strength at lower pH (6.7) but remained constant at higher pH (10). The long-term lincomycin sequestration by biochars was largely due to pore diffusion plausibly independent of solution pH and ionic composition. Therefore, manure-derived biochars had lasting lincomycin sequestration capacity, implying that biochar soil amendment could significantly affect the distribution, transport, and bioavailability of lincomycin in agroecosystems.

  11. Sorption separation of Eu and As from single-component systems by Fe-modified biochar. Kinetic and equilibrium study

    Fristak, Vladimir; Soja, Gerhard [Austrian Institute of Technology GmbH, Tulln (Austria). Energy Dept. Environmental Resources and Technologies; Michalekova-Richveisova, Barbora; Pipiska, Martin [Trnava Univ. (Slovakia). Dept. of Chemistry; Viglasova, Eva; Galambos, Michal [Comenius Univ., Bratislava (Slovakia). Dept. of Inorganic Chemistry; Duriska, Libor [Slovak Univ. of Technology in Bratislava, Trnava (Slovakia). Faculty of Materials Science and Technology; Moreno-Jimenez, Eduardo [Univ. Autonoma de Madrid (Spain). Dept. de Quimica Agricola y Bromatologia


    The utilization of carbonaceous materials in separation processes of radionuclides, heavy metals and metalloids represents a burning issue in environmental and waste management. The main objective of this study was to characterize the effect of chemical modification of corncob-derived biochar by Fe-impregnations on sorption efficiency of Eu and As as a model compounds of cationic lanthanides and anionic metalloids. The biochar sample produced in slow pyrolysis process at 500 C before (BC) and after (IBC) impregnation process was characterized by elemental, FTIR, SEM-EDX analysis to confirm the effectiveness of Fe-impregnation process. The basic physico-chemical properties showed differences in surface area and pH values of BC- and IBC-derived sorbents. Sorption processes of Eu and As by BC and IBC were characterized as a time- and initial concentration of sorbate-dependent processes. The sorption equilibrium was reached for both sorbates in 24 h of contact time. Batch equilibrium experiments revealed the increased maximum sorption capacities (Q{sub max}) of IBC for As about more than 20 times (Q{sub max} BC 0.11 and Q{sub max} IBC 2.26 mg g{sup -1}). Our study confirmed negligible effect of Fe-impregnation on sorption capacity of biochar for Eu (Q{sub max} BC 0.89 and Q{sub max} IBC 0.98 mg g{sup -1}). The iron-impregnation of biochar-derived sorbents can be utilized as a valuable treatment method to produce stable and more effective sorption materials for various xenobiotics separation from liquid wastes and aqueous solutions.

  12. panMetaDocs, eSciDoc, and DOIDB - an infrastructure for the curation and publication of file-based datasets for 'GFZ Data Services'

    Ulbricht, Damian; Elger, Kirsten; Bertelmann, Roland; Klump, Jens


    With the foundation of DataCite in 2009 and the technical infrastructure installed in the last six years it has become very easy to create citable dataset DOIs. Nowadays, dataset DOIs are increasingly accepted and required by journals in reference lists of manuscripts. In addition, DataCite provides usage statistics [1] of assigned DOIs and offers a public search API to make research data count. By linking related information to the data, they become more useful for future generations of scientists. For this purpose, several identifier systems, as ISBN for books, ISSN for journals, DOI for articles or related data, Orcid for authors, and IGSN for physical samples can be attached to DOIs using the DataCite metadata schema [2]. While these are good preconditions to publish data, free and open solutions that help with the curation of data, the publication of research data, and the assignment of DOIs in one software seem to be rare. At GFZ Potsdam we built a modular software stack that is made of several free and open software solutions and we established 'GFZ Data Services'. 'GFZ Data Services' provides storage, a metadata editor for publication and a facility to moderate minted DOIs. All software solutions are connected through web APIs, which makes it possible to reuse and integrate established software. Core component of 'GFZ Data Services' is an eSciDoc [3] middleware that is used as central storage, and has been designed along the OAIS reference model for digital preservation. Thus, data are stored in self-contained packages that are made of binary file-based data and XML-based metadata. The eSciDoc infrastructure provides access control to data and it is able to handle half-open datasets, which is useful in embargo situations when a subset of the research data are released after an adequate period. The data exchange platform panMetaDocs [4] makes use of eSciDoc's REST API to upload file-based data into eSciDoc and uses a metadata editor [5] to annotate the files

  13. Studies of anions sorption on natural zeolites.

    Barczyk, K; Mozgawa, W; Król, M


    This work presents results of FT-IR spectroscopic studies of anions-chromate, phosphate and arsenate - sorbed from aqueous solutions (different concentrations of anions) on zeolites. The sorption has been conducted on natural zeolites from different structural groups, i.e. chabazite, mordenite, ferrierite and clinoptilolite. The Na-forms of sorbents were exchanged with hexadecyltrimethylammonium cations (HDTMA(+)) and organo-zeolites were obtained. External cation exchange capacities (ECEC) of organo-zeolites were measured. Their values are 17mmol/100g for chabazite, 4mmol/100g for mordenite and ferrierite and 10mmol/100g for clinoptilolite. The used initial inputs of HDTMA correspond to 100% and 200% ECEC of the minerals. Organo-modificated sorbents were subsequently used for immobilization of mentioned anions. It was proven that aforementioned anions' sorption causes changes in IR spectra of the HDTMA-zeolites. These alterations are dependent on the kind of anions that were sorbed. In all cases, variations are due to bands corresponding to the characteristic Si-O(Si,Al) vibrations (occurring in alumino- and silicooxygen tetrahedra building spatial framework of zeolites). Alkylammonium surfactant vibrations have also been observed. Systematic changes in the spectra connected with the anion concentration in the initial solution have been revealed. The amounts of sorbed CrO4(2-), AsO4(3-) and PO4(3-) ions were calculated from the difference between their concentrations in solutions before (initial concentration) and after (equilibrium concentration) sorption experiments. Concentrations of anions were determined by spectrophotometric method.

  14. Humidity sorption on natural building stone

    Franzen, C.; Mirwald, P.


    processes, physical, chemical or biological, depend on the presence of water. Like most porous materials building stone respond on humidity by water uptake. The sorption isotherm represents the equilibrium moisture, specific for each material. The determination of the isotherm for stone of low and small porosity like marble is difficult. With the help of a newly developed water sorption analysis chamber [2], which allows the simultaneous measurement of 11 samples, good results on stone/rock samples have been obtained. Even at marble species with pore volumes lower than 0.4 % isotherms are measured. This analytical method offers new insights in the pore behaviour of low porosity materials. The advantages of this technique which supplements other techniques (e.g. BET, Hg-porosimetry) are: i) the testing agent is identical to the weathering agent, water; ii) the atmospheric parameters at the measurement reflect the natural conditions - thus no changes to the material properties have to be considered; iii) due to the small diameter of the water molecule (~0.28 nm), smaller pores are reached than e.g. with N2 (~0.31 nm). Sorption isotherms of sandstone (Baumberg, Obernkirchen, Groeden), granite (Brixen), and marble (Sterzing, Laas) are presented. Particular as to marbles the resolution is considerably higher. A previously observed negative hysteresis [3] seems an effect due to limited data resolution. [1] Snethlage, R. (1984) Steinkonservierung, Bayer. LA Denkmalpflege, Ah. 22, 203 S. [2] Griesser, U.J., Dillenz, J. (2002) Neuartiges, vollautomatisches Feuchtesorptionsprüfgerät mit hohem Probendurchsatz, Feuchtetag 2002, Weimar, 85-93. [3] Fimmel, R. (1996) Verwitterungsverhalten der alpinen Marmore von Laas und Sterzing, Diss. Univ. Ibk, 116 S.

  15. Thermodynamics of imidacloprid sorption in Croatian soils

    Milin, Čedomila; Broznic, Dalibor


    Neonicotinoids are increasingly replacing the organophosphate and methylcarbamate acetylcholinesterase inhibitors which are losing their effectiveness because of selection for resistant pest populations. Imidacloprid is the most important neonicotinoid with low soil persistence, high insecticidal potency and relatively low mammalian toxicity. In Croatia, imidacloprid is most commonly used in olive growing areas, including Istria and Kvarner islands, as an effective means of olive fruit fly infestation control. Sorption-desorption behavior of imidacloprid in six soils collected from five coastal regions in Croatia at 20, 30 and 40°C was investigated using batch equilibrium technique. Isothermal data were applied to Freundlich, Langmuir and Temkin equation, and the thermodynamic parameters ΔH°, ΔG°, ΔS° were calculated. The sorption isotherm curves were of non-linear and may be classified as L-type suggesting a relatively high sorption capacity for imidacloprid. Our results showed that the KFsor values decreased for all the tested soils as the temperature increases, indicating that the temperature strongly influence the sorption. Values of ΔG° were negative (-4.65 to -2.00 kJ/mol) indicating that at all experimental temperatures the interactions of imidacloprid with soils were spontaneous process. The negative and small ΔH° values (-19.79 to -8.89 kJ/mol) were in the range of weak forces, such as H-bonds, consistent with interactions and par¬titioning of the imidacloprid molecules into soil organic matter. The ΔS° values followed the range of -57.12 to -14.51 J/molK, suggesting that imidacloprid molecules lose entropy during transition from the solution phase to soil surface. It was found that imidacloprid desorption from soil was concentration and temperature dependent, i.e. at lower imidacloprid concentrations and temperature, lower desorption percentage occurred. Desorption studies revealed that hysteretic behavior under different temperature

  16. MEMS ion-sorption high vacuum pump

    Grzebyk, T.; Knapkiewicz, P.; Szyszka, P.; Gorecka-Drzazga, A.; Dziuban, J. A.


    In the article a miniature MEMS-type ion-sorption vacuum pump has been presented. The influence of electric and magnetic field, as well as horizontal and vertical dimensions of the micropump and type of material used for electrodes on the pump properties has been investigated. It has been found that the micropump works efficiently as long as the magnetic field is higher than 0.3 T, and pumping cell is larger than 1x1x1 mm3. The pump allows generating vacuum at the level of 10-7-10-9 hPa in 100 mm3 volume.

  17. Sorption of pesticides to aquifer minerals

    Clausen, Liselotte; Fabricius, Ida Lykke


    This paper summarizes results from a work were the sorption of five pesticides on seven minerals were studied in order to quantify the adsorption to different mineral surfaces. Investigated mineral phases are: quartz, calcite, kaolinite, a-alumina, and three iron oxides (2-line ferrihydrite, goet......, goethite, lepidocrocite). Selected pesticides are: atrazine, isoproturon, mecoprop, 2,4-D, and bentazone. The results demonstrate that pesticides adsorb to pure mineral surfaces. However, the size of the adsorption depends on the type of pesticide and the type of mineral....

  18. Water sorption and solubility of methacrylate resin-based root canal sealers.

    Donnelly, Adam; Sword, Jeremy; Nishitani, Yoshihiro; Yoshiyama, Masahiro; Agee, Kelli; Tay, Franklin R; Pashley, David H


    The water sorption and solubility characteristics of three contemporary methacrylate resin-based endodontic sealers, EndoREZ, Epiphany, and InnoEndo, were compared with those obtained from Kerr EWT, Ketac-Endo (positive control), GuttaFlow, and AH Plus (both negative controls). Ten disks of each material were dehydrated in Drierite for 24 h and weighed to constant dry mass. They were placed in water and weighed periodically until maximum water sorption was obtained. The disks were dehydrated again to determine their mass loss (solubility) at equilibrium. Epiphany exhibited the highest apparent water sorption (8%) followed by Ketac-Endo (6.2%), InnoEndo (3.4%), EndoREZ (3.0%), AH Plus (1.1%), GuttaFlow (0.4%), and Kerr EWT (0.3%). Significantly higher solubility (3.5-4%) were observed for all three methacrylate resin-based sealers and Kerr EWT (3.95%), compared with Ketac-Endo (1.6%), AH Plus (0.16%), and GuttaFlow (0.13%). American Dental Association specifications require<3% solubility for endodontic sealers. Only Ketac-Endo, AH Plus, and GuttaFlow met that criterion.

  19. Sorption of Pb2+ from Aqueous Solution unto Modified Rice Husk: Isotherms Studies

    A. O. Dada


    Full Text Available Investigation of the sorption potential of rice husk, an agricultural waste, as an adsorbent was carried out. The rice husk was modified with orthophosphoric acid and was used for adsorption of lead (II ions (Pb2+ from aqueous solution. Physicochemical properties of the modified rice husk were determined. Equilibrium sorption data were confirmed with Langmuir, Freundlich and Temkin adsorption isotherms. On the basis of adsorption isotherm graphs, R2 values were determined to be 0.995, 0.916, and 0.797 for Langmuir, Temkin, and Freundlich isotherms, respectively, indicating that the data fitted well into the adsorption isotherms, but Langmuir isotherm is a better model. The maximum monolayer coverage from Langmuir studies, Qmax=138.89 mg/g, Langmuir isotherm constant, KL=0.699 L/mg, and the separation factor, RL=1.41×10−2 at 100 mg/L of lead(II ions indicating that the sorption process, was favourable. The suitability of modified rice husk as an adsorbent for the removal of lead ions from aqueous solution and its potential for pollution control is established.

  20. Ammonium sorption from aqueous solutions by the natural zeolite Transcarpathian clinoptilolite studied under dynamic conditions.

    Sprynskyy, Myroslav; Lebedynets, Mariya; Terzyk, Artur P; Kowalczyk, Piotr; Namieśnik, Jacek; Buszewski, Bogusław


    The scope of this study is ammonium-ion uptake from synthetic aqueous solutions onto raw and pretreated forms of the natural zeolite Transcarpathian clinoptilolite under dynamic conditions. Hydrogen ions displaced exchangeable cations on the clinoptilolite in distilled water (sodium ions) and hydrochloric acid (sodium, potassium, and calcium ions) and destroyed the zeolite framework structure in the last case. Ammonium uptake onto the zeolite occurs by exchange with Na(+), Ca(2+), and K(+) ions. Although Na(+) ions were observed to be more easily exchanged for both hydrogen and ammonium ions, the role of Ca(2+) ions increased with zeolite saturation by NH(+)(4) ions. The maximum sorption capacity of the clinoptilolite toward NH(+)(4) ions, estimated under dynamic conditions, is significantly higher than that measured under static conditions; proximity of the values of a distribution coefficient and a retardation factor for different conditions (215-265 dm(3)/kg and 979-1107, respectively) allows us to use these parameters to model ammonium uptake onto the clinoptilolite. Slowing down or interruption in filtration resulted in the improvement of ammonium sorption properties of the zeolite. The ammonium removal improves with use of the finer fractions of the clinoptilolite up to 0.35 mm. A recycling study results confirmed the importance of external diffusion for ammonium sorption by the clinoptilolite. Preliminary treatment of the sorbent confirmed the predominant importance of the ion-exchange mechanism. The advantage of prior NaCl treatment of the clinoptilolite in improvement of ammonium removal over the other techniques was shown.

  1. Sorption of organic compounds to activated carbons. Evaluation of isotherm models

    Pikaar, I.; Koelmans, A.A.; van Noort, P.C.M. [RIZA, Lelystad (Netherlands). Inst. of Inland Water Management & Wastewater Treatment


    Sorption to 'hard carbon' (black carbon, coal, kerogen) in soils and sediments is of major importance for risk assessment of organic pollutants. We argue that activated carbon (AC) may be considered a model sorbent for hard carbon. Here, we evaluate six sorption models on a literature dataset for sorption of 12 compounds onto 12 ACs and one charcoal, at different temperatures (79 isotherms in total). A statistical analysis, accounting for differences in the number of fitting parameters, demonstrates that the dual Langmuir equation is in general superior and/or preferable to the single and triple Langmuir equation, the Freundlich equation, a Polanyi-Dubinin-Manes equation, and the Toth equation. Consequently, the analysis suggests the presence of two types of adsorption sites: a high-energy (HE) type of site and a low-energy (LE) type of site. Maximum adsorption capacities for the HE domain decreased with temperature while those for the LE domain increased. Average Gibbs free energies for adsorption from the hypothetical pure liquid state at 298 K were fairly constant at - 15 {+-} 4 and -5 {+-} 4 kJ mol{sup -1} for the HE and LE domain, respectively.

  2. The kinetics of fluoride sorption by zeolite: Effects of cadmium, barium and manganese

    Cai, Qianqian; Turner, Brett D.; Sheng, Daichao; Sloan, Scott


    Industrial wastewaters often consist of a complex chemical cocktail with treatment of target contaminants complicated by adverse chemical reactions. The impact of metal ions (Cd2 +, Ba2 + and Mn2 +) on the kinetics of fluoride removal from solution by natural zeolite was investigated. In order to better understand the kinetics, the pseudo-second order (PSO), Hill (Hill 4 and Hill 5) and intra-particle diffusion (IPD) models were applied. Model fitting was compared using the Akaike Information Criterion (AIC) and the Schwarz Bayesian Information Criterion (BIC). The Hill models (Hill 4 and Hill 5) were found to be superior in describing the fluoride removal processes due to the sigmoidal nature of the kinetics. Results indicate that the presence of Mn (100 mg L- 1) and Cd (100 mg L- 1) respectively increases the rate of fluoride sorption by a factor of 28.3 and 10.9, the maximum sorption capacity is increased by 2.2 and 1.7. The presence of Ba (100 mg L- 1) initially inhibited fluoride removal and very poor fits were obtained for all models. Fitting was best described with a biphasic sigmoidal model with the degree of inhibition decreasing with increasing temperature suggesting that at least two processes are involved with fluoride sorption onto natural zeolite in the presence of Ba.

  3. [Phosphate sorption characteristics onto sediments in the middle and lower reaches of the Yellow River].

    Wang, Xiao-li; Pan, Gang; Bao, Hua-ying; Zhang, Xian-wei; Chen, Hao; Guo, Bo-shu


    The equilibrium phosphate concentration (EPC0) of the Yellow River bed sediments has been measured, which was used to predict whether bed sediments are acting as a source or sink of soluble reactive phosphate (SRP). The modified Langmuir isotherm equation was used to describe phosphate (P) sorption on the Yellow River sediments. The maximum P sorption capacity (PAC) and P-binding energy constant (k) were obtained by the modified Langmuir isotherm model. Native adsorbed exchangeable phosphorus (NAP), the EPC0, and partitioning coefficients (Kp) were subsequently calculated by the corresponding formulae. The influence of pH values and ion strength were evaluated. All the EPC0 s are higher than the P concentration in the overlying water, indicating a potential source of phosphate from the sediments. PAC is linearly related to the contents of TOC of the sediment. The sorption capacity of P increased rapidly with pH below 6.0, and then reached a plateau between pH 6.0 to 9.7, and finally maintained at a slightly higher level from pH 9.7 to 12.0.The adsorption of P by the sediment decreased with the increase in Ca2+ ionic strength.

  4. Using Project-Based Learning and Google Docs to Support Diversity

    Leh, Amy


    A graduate course, ETEC543 ("Technology and Learning I"), was revised to better serve increasing new student population, international students, in an academic program. Project-based learning, Google Docs, and instructional strategies fostering diversity and critical thinking were incorporated into the course redesign. Observations,…

  5. Investigations of PAA degradation in aqueous solutions: Impacts of water hardness, salinity and DOC

    Peracetic acid (PAA) is used in aquaculture under various conditions for disinfection purposes. However, there is lack of information about its environmental fate. Therefore, the impact of water hardness, salinity, and dissolved organic carbon (DOC) on PAA-degradation within 5 hours was investigat...

  6. CTM4DOC : Electronic structure analysis from X-ray spectroscopy

    Delgado-Jaime, Mario Ulises; Zhang, Kaili; Vura-Weis, Josh; De Groot, Frank M F


    Two electronic structure descriptions, one based on orbitals and the other based on term symbols, have been implemented in a new Matlab-based program, CTM4DOC. The program includes a graphical user interface that allows the user to explore the dependence of details of electronic structure in transit

  7. TOC/DOC: "It Has Changed the Way I Do Science".

    Douglas, Kimberly; Roth, Dana L.


    Describes a user-based automated service developed at the California Institute of Technology that combines access to journal article databases with an in-house document delivery system. TOC/DOC (Tables of Contents/Document Delivery) has undergone a conceptual change from a catalog of locally-held journal articles to a broader, more retrospective…

  8. Exploring the Roles of Google.doc and Peer e-Tutors in English Writing

    Lin, Wen-Chuan; Yang, Shu Ching


    This study explored college students' experiences with and perceptions of integrating both the Google.doc and peer e-tutors into an English writing course. This socio-cultural study employed online collaborative learning mechanisms with an attempt to develop students' English writing skills and motivation over the course of one year. Participants…

  9. Surface Engineering of PAMAM-SDB Chelating Resin with Diglycolamic Acid (DGA) Functional Group for Efficient Sorption of U(VI) and Th(IV) from Aqueous Medium

    Ilaiyaraja, P.; Venkatraman, B., E-mail: [Radiological Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam (India); Deb, A.K. Singha [Chemical Engineering Division, Bhabha Atomic Research Centre, Mumbai (India); Ponraju, D. [Safety Engineering Division, Indira Gandhi Centre for Atomic Research, Kalpakkam (India); Ali, Sk. Musharaf [Chemical Engineering Division, Bhabha Atomic Research Centre, Mumbai (India)


    Highlights: • A new DGA-PAMAM-SDB chelating resin has been synthesized for actinide sorption. • Maximum sorption capacities of resin are 682 and 544.2 mg g{sup −1}for U(VI) and Th(IV). • DGA-PAMAM-SDB chelating resin could be regenerated and reused. • DFT calculation of actinides interaction with resin corroborates the experimental. • Resin is effective for sorption of actinides from both aqueous and HNO{sub 3} medium. - Abstract: A novel chelating resin obtained via growth of PAMAM dendron on surface of styrene divinyl benzene resin beads, followed by diglycolamic acid functionalization of the dendrimer terminal. Batch experiments were conducted to study the effects of pH, nitric acid concentration, amount of adsorbent, shaking time, initial metal ion concentration and temperature on U(VI) and Th(IV) adsorption efficiency. Diglycolamic acid terminated PAMAM dendrimer functionalized styrene divinylbenzene chelating resin (DGA-PAMAM-SDB) is found to be an efficient candidate for the removal of U(VI) and Th(IV) ions from aqueous (pH > 4) and nitric acid media (> 3 M). The sorption equilibrium could be reached within 60 min, and the experimental data fits with pseudo-second-order model. Langmuir sorption isotherm model correlates well with sorption equilibrium data. The maximum U(VI) and Th(IV) sorption capacity onto DGA-PAMAMG{sub 5}-SDB was estimated to be about 682 and 544.2 mg g{sup −1} respectively at 25 °C. The interaction of actinides and chelating resin is reversible and hence, the resin can be regenerated and reused. DFT calculation on the interaction of U(VI) and Th(IV) ions with chelating resin validates the experimental findings.

  10. Competitive sorption of heavy metals by water hyacinth roots.

    Zheng, Jia-Chuan; Liu, Hou-Qi; Feng, Hui-Min; Li, Wen-Wei; Lam, Michael Hon-Wah; Lam, Paul Kwan-Sing; Yu, Han-Qing


    Heavy metal pollution is a global issue severely constraining aquaculture practices, not only deteriorating the aquatic environment but also threatening the aquaculture production. One promising solution is adopting aquaponics systems where a synergy can be established between aquaculture and aquatic plants for metal sorption, but the interactions of multiple metals in such aquatic plants are poorly understood. In this study, we investigated the absorption behaviors of Cu(II) and Cd(II) in water by water hyacinth roots in both single- and binary-metal systems. Cu(II) and Cd(II) were individually removed by water hyacinth roots at high efficiency, accompanied with release of protons and cations such as Ca(2+) and Mg(2+). However, in a binary-metal arrangement, the Cd(II) sorption was significantly inhibited by Cu(II), and the higher sorption affinity of Cu(II) accounted for its competitive sorption advantage. Ionic exchange was identified as a predominant mechanism of the metal sorption by water hyacinth roots, and the amine and oxygen-containing groups are the main binding sites accounting for metal sorption via chelation or coordination. This study highlights the interactive impacts of different metals during their sorption by water hyacinth roots and elucidates the underlying mechanism of metal competitive sorption, which may provide useful implications for optimization of phytoremediation system and development of more sustainable aquaculture industry.

  11. Picloram and Aminopyralid Sorption to Soil and Clay Minerals

    Aminopyralid sorption data are lacking, and these data are needed to predict off-target transport and plant available herbicide in soil solution. The objective of this research was to determine the sorption of picloram and aminopyralid to five soils and three clay minerals and determine if the pote...

  12. Manometric determination of supercritical gas sorption in coal

    Van Hemert, P.


    The characteristics of the manometric method are investigated so that it can be used to obtain accurate data of sorption of supercritical gas in coal. Furthermore, data of the sorption of carbon dioxide, methane and nitrogen in coal at in situ conditions have been determined. Accurate data are req

  13. Molecular simulation of polycyclic aromatic hydrocarbon sorption to black carbon

    Haftka, J.J.H.; Parsons, J.R.; Govers, H.A.J.


    Strong sorption of hydrophobic organic contaminants to soot or black carbon (BC) is an important environmental process limiting the bioremediation potential of contaminated soils and sediments. Reliable methods to predict BC sorption coefficients for organic contaminants are therefore required. A co

  14. Using Weighted Least Squares Regression for Obtaining Langmuir Sorption Constants

    One of the most commonly used models for describing phosphorus (P) sorption to soils is the Langmuir model. To obtain model parameters, the Langmuir model is fit to measured sorption data using least squares regression. Least squares regression is based on several assumptions including normally dist...

  15. Effect of Animal Manure on Phosphorus Sorption to Soils

    In most phosphorus (P) sorption studies P is added as an inorganic salt to a pre-defined background solution such as CaCl2 or KCl; however, in many regions the application of P to agricultural fields is in the form of animal manure. The purpose of this study, therefore, was to compare the sorption b...

  16. Water Sorption and Transport in Dry, Crispy Bread Crust

    Meinders, M.B.J.; Nieuwenhuijzen, N.H. van; Tromp, R.H.; Hamer, R.J.; Vliet, T. van


    Water - sorption and dynamic properties of bread crust have been studied in gravimetric sorption experiments. Water uptake and loss were measured while relative humidity (RH) was stepwise increased or decreased (isotherm experiment) or varied between two adjusted values (oscillatory experiment). Exp

  17. Water sorption and transport in dry crispy bread crust

    Meinders, M.B.J.; Nieuwenhuijzen, van N.H.; Tromp, R.H.; Hamer, R.J.; Vliet, van T.


    Water sorption and dynamical properties of bread crust have been studied using gravimetric sorption experiments. Water uptake and loss were followed while relative humidity (RH) was stepwise in- or decreased (isotherm experiment) or varied between two adjusted values (oscillatory experiment). Experi


    Singano, J. J.; Mashauri, D. A.; Mtalo, F. W.;


    A series of sorption of fluoride on calcined magnesite are obtained from thermostatic pH-chemostat and jar test experiments. The fluoride removal is observed not to start instantly, as normal, but after a lag time of up to ½ an hour of contact time. A model for sorption kinetics is developed, bas...

  19. Liquid Chromatography Applications to Determination of Sorption on Aquifer Materials


    1985) observed a similar factor between column and batch sorption coefficients for nematicides on soils. They noted that this may be a consequence of...Development Branch, Norris, TN 37828 (1985). J. N. Bilkert and P. S. C. Rao. Sorption and leaching of three non-fumigant nematicides in soils. J

  20. Applied stress reduces the CO2 sorption capacity of coal

    Hol, S.; Peach, C.J.; Spiers, C.J.


    Though the adsorption of CO2 by coal has been extensively studied in experiments, few systematic studies have been done on the effects of the stress state within the coal on CO2 sorption. To investigate whether or not the CO2 sorption capacity of coal is influenced by the application of an effective

  1. Kinetics and reversibility of micropollutant sorption in sludge.

    Barret, Maialen; Carrère, Hélène; Patau, Mathieu; Patureau, Dominique


    The fate of micropollutants throughout wastewater treatment systems is highly dependent on their sorption interactions with sludge matter. In this study, both the sorption and desorption kinetics of polycyclic aromatic hydrocarbons (PAHs) in activated sludge were shown to be very rapid in comparison to biodegradation kinetics. It was concluded that PAH transfer does not limit their biodegradation and that their fate is governed by the sorption/desorption equilibrium state. The effect of contact time between sludge and PAHs was also investigated. It was shown that aging did not influence the sorption/desorption equilibrium although PAH losses during aging suggest that sequestration phenomena had occurred. This implies that for PAH sorption assessment within treatment processes there is no need to include a contact time dimension. As a consequence, thanks to an innovative approach taking into account sorption equilibria and sequestration, this work has demonstrated that studies in the literature which, in main, deal with micropollutant sorption in sewage sludge with only a short contact time can be extrapolated to real systems in which sorption, desorption and aging occur.

  2. Equalized near maximum likelihood detector


    This paper presents new detector that is used to mitigate intersymbol interference introduced by bandlimited channels. This detector is named equalized near maximum likelihood detector which combines nonlinear equalizer and near maximum likelihood detector. Simulation results show that the performance of equalized near maximum likelihood detector is better than the performance of nonlinear equalizer but worse than near maximum likelihood detector.

  3. Generalized Maximum Entropy

    Cheeseman, Peter; Stutz, John


    A long standing mystery in using Maximum Entropy (MaxEnt) is how to deal with constraints whose values are uncertain. This situation arises when constraint values are estimated from data, because of finite sample sizes. One approach to this problem, advocated by E.T. Jaynes [1], is to ignore this uncertainty, and treat the empirically observed values as exact. We refer to this as the classic MaxEnt approach. Classic MaxEnt gives point probabilities (subject to the given constraints), rather than probability densities. We develop an alternative approach that assumes that the uncertain constraint values are represented by a probability density {e.g: a Gaussian), and this uncertainty yields a MaxEnt posterior probability density. That is, the classic MaxEnt point probabilities are regarded as a multidimensional function of the given constraint values, and uncertainty on these values is transmitted through the MaxEnt function to give uncertainty over the MaXEnt probabilities. We illustrate this approach by explicitly calculating the generalized MaxEnt density for a simple but common case, then show how this can be extended numerically to the general case. This paper expands the generalized MaxEnt concept introduced in a previous paper [3].

  4. CNTs reinforced super-hydrophobic-oleophilic electrospun polystyrene oil sorbent for enhanced sorption capacity and reusability

    Wu, Jingya


    To meet the challenges of global oil spills and oil-water contamination, the development of a low-cost and reusable sorbents with good hydrophobicity and oleophilic nature is crucial. In this study, functionalized carbon nanotubes (CNTs) were wrapped in polystyrene (PS) polymer (PS-CNTs) and electrospun to create an effective and rigid sorbent for oil. Covalent modification and fluorination of CNTs improved their dispersibility and interfacial interaction with the polymer, resulting in a well-aligned CNTs configuration inside the porous fiber structure. Interestingly, the oil sorption process using PS-CNTs was observed to have two phases. First, the oil swiftly entered the membrane pores formed by interconnected nanofibers due to oleophilic properties of the micro-sized void. In the second phase, the oil not only moved to nano interior spaces of the fibers by capillary forces but also adsorbed on the surface of fibers where the latter was retained due to Van der Waals force. The sorption process fits well with the intra particle diffusion model. Maximum oil sorption capacity of the PS-CNTs sorbent for sunflower oil, peanut oil, and motor oils were 116, 123, and 112 g/g, respectively, which was 65% higher than that of the PS sorbent without CNTs. Overall, a significant increase in the porosity, surface area, water contact angle, and oleophilic nature was observed for the PS-CNTs composite sorbents. Not only did the PS-CNTs sorbents exhibited a promising oil sorption capacity but also showed potential for reusability, which is an important factor to be considered in determining the overall performance of the sorbent and its environmental impacts.

  5. Water properties in fern spores: sorption characteristics relating to water affinity, glassy states, and storage stability.

    Ballesteros, Daniel; Walters, Christina


    Ex situ conservation of ferns may be accomplished by maintaining the viability of stored spores for many years. Storage conditions that maximize spore longevity can be inferred from an understanding of the behaviour of water within fern spores. Water sorption properties were measured in spores of five homosporeous species of ferns and compared with properties of pollen, seeds, and fern leaf tissue. Isotherms were constructed at 5, 25, and 45 degrees C and analysed using different physicochemical models in order to quantify chemical affinity and heat (enthalpy) of sorption of water in fern spores. Fern spores hydrate slowly but dry rapidly at ambient relative humidity. Low Brunauer-Emmet-Teller monolayer values, few water-binding sites according to the D'Arcy-Watt model, and limited solute-solvent compatibility according to the Flory-Huggins model suggest that fern spores have low affinity for water. Despite the low water affinity, fern spores demonstrate relatively high values of sorption enthalpy (DeltaH(sorp)). Parameters associated with binding sites and DeltaH(sorp) decrease with increasing temperature, suggesting temperature- and hydration-dependent changes in volume of spore macromolecules. Collectively, these data may relate to the degree to which cellular structures within fern spores are stabilized during drying and cooling. Water sorption properties within fern spores suggest that storage at subfreezing temperatures will give longevities comparable with those achieved with seeds. However, the window of optimum water contents for fern spores is very narrow and much lower than that measured in seeds, making precise manipulation of water content imperative for achieving maximum longevity.

  6. Kinetics of phosphorus sorption in soils in the state of Paraíba¹

    Hemmannuella Costa Santos


    Full Text Available The soil P sorption capacity has been studied for many years, but little attention has been paid to the rate of this process, which is relevant in the planning of phosphate fertilization. The purpose of this experiment was to assess kinetics of P sorption in 12 representative soil profiles of the State of Paraíba (Brazil, select the best data fitting among four equations and relate these coefficients to the soil properties. Samples of 12 soils with wide diversity of physical, chemical and mineralogical properties were agitated in a horizontal shaker, with 10 mmo L-1 CaCl2 solution containing 6 and 60 mg L-1 P, for periods of 5, 15, 30, 45, 60, 90, 120, 420, 720, 1,020, and 1,440 min. After each shaking period, the P concentration in the equilibrium solution was measured and three equations were fitted based on the Freundlich equation and one based on the Elovich equation, to determine which soil had the highest sorption rate (kinetics and which soil properties correlated to this rate. The kinetics of P sorption in soils with high maximum P adsorption capacity (MPAC was fast for 30 min at the lower initial P concentration (6 mg L-1. No difference was observed between soils at the higher initial P concentration (60 mg L-1. The P adsorption kinetics were positively correlated with clay content, MPAC and the amount of Al extracted with dithionite-citrate-bicarbonate. The data fitted well to Freundlich-based equations equation, whose coefficients can be used to predict P adsorption rates in soils.

  7. Effect of light and nutrient availability on the release of dissolved organic carbon (DOC) by Caribbean turf algae.

    Mueller, Benjamin; den Haan, Joost; Visser, Petra M; Vermeij, Mark J A; van Duyl, Fleur C


    Turf algae increasingly dominate benthic communities on coral reefs. Given their abundance and high dissolved organic carbon (DOC) release rates, turf algae are considered important contributors to the DOC pool on modern reefs. The release of photosynthetically fixed carbon as DOC generally, but not always, increases with increased light availability. Nutrient availability was proposed as an additional factor to explain these conflicting observations. To address this proposed but untested hypothesis, we documented the interactive contributions of light and nutrient availability on the release of DOC by turf algae. DOC release rates and oxygen production were quantified in incubation experiments at two light levels (full and reduced light) and two nutrient treatments (natural seawater and enriched seawater). In natural seawater, DOC release at full light was four times higher than at reduced light. When nutrients were added, DOC release rates at both light levels were similar to the natural seawater treatment at full light. Our results therefore show that low light in combination with low nutrient availability reduces the release of DOC by turf algae and that light and nutrient availability interactively determine DOC release rates by this important component of Caribbean reef communities.

  8. Sorption of perfluoroalkyl substances to two types of minerals.

    Hellsing, Maja S; Josefsson, Sarah; Hughes, Arwel V; Ahrens, Lutz


    The sorption of perfluoroalkyl substances (PFASs) was investigated for two model soil mineral surfaces, alumina (Al2O3) and silica (SiO2), on molecular level using neutron scattering. The PFASs were selected (i.e. perfluorohexanoic acid (PFHxA), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorooctane sulfonic acid (PFOS)) to examine the role of hydrophobic chain length and hydrophilic functional group on their sorption behaviour. All four PFASs were found to sorb to alumina surface (positively charged) forming a hydrated layer consisting of 50% PFASs. The PFAS solubility limit, which decrease with chain length, was found to strongly influence the sorption behaviour. The sorbed PFAS layer could easily be removed by gentle rinsing with water, indicating release upon rainfall in the environment. No sorption was observed for PFOA and PFOS at silica surface (negatively charged), showing electrostatic interaction being the driving force in the sorption process.

  9. Characteristics of natural organic matter affect sorption of organic contaminants


    Several soil samples were used to study how the characteristics of natural organic matter (NOM) affect sorption of organic compounds. These soils contains different amounts and types of NOM. Aromaticity of NOM (percentage of aromatic carbons) was determined from solid-state CPMAS 13C NMR spectra and the soil effective polarity was computed from the equation developed by Xing et al. Naphthalene was used to examine the sorption characteristics of NOM. Both aromaticity and polarity of NOM strongly affected sorption of naphthalene. Old NOM showed higher affinity than that in the surface, young soils. Sorption increased with increasing aromaticity and decreasing polarity. Thus, the sorption coefficients of organic contaminants cannot be accurately predicted without some consideration of NOM characteristics.

  10. Sorption of chlorophenols onto fruit cuticles and potato periderm

    Yungui Li; Yingqing Deng; Baoliang Chen


    To better understand the interaction mechanisms of plant surfaces with polar organic compounds,sorption of 4-chlorophenol,2,4-dichlorophenol,and 2,4,6-trichlorophenol by fruit cuticles (i.e.,tomato,apple,and pepper),and potato tuber periderm were investigated.The roles of cuticular components (waxes,cutin,cutan and sugar) on sorption of chlorophenols are quantitatively compared.Cutin and waxes govern the sorption capacity of bulk apple cuticle by hydrophobic interactions.Potato periderm with highest sugar content exhibits the lowest sorption capability for the chlorophenols.With the increase of hydrophobicity (i.e.,Kow ) of sorbate,the relative contribution of lipophilic components (wax,cutin and cutan) on total sorption increases,however,the ratios of Koc to Kow decreases due to increasing ionization degree of sorbates.

  11. Uranium sorption on tezontle volcanic rock

    Lopez M, B. E.; Duran B, J. M.; Iturbe G, J. L.; Olguin G, M. T., E-mail: beatriz.lopez@inin.gob.m [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)


    It is described a study that demonstrates that hexavalent uranium ions were sorbed by the naturally occurring mineral using a batch technique. This mineral is found in abundant quantities in Mexico. Our study focused on the separation of U Vi from synthetic aqueous systems of both H{sub 2}O-UO{sub 2}(NO{sub 3}){sub 2}.6H{sub 2}O (acid) and H{sub 2}O-Na{sub 4}[UO{sub 2}(CO{sub 3}){sub 3}] (basic). The chemical speciation was performed by using high voltage electrophoresis, and the uranium content was determined by UV-Vis spectroscopy. The quantified U(Vi) sorption by tezontle from acidic and basic systems was 2.72 and 1.68 mumol/g, respectively, and the sorption behavior is discussed considering the surface charge of the tezontle at different ph values based on the point of zero charge characteristic of this material. (Author)

  12. Mechanism for Cu2+ Sorption on Palygorskite

    CHEN Tian-Hu; PENG Shu-Chuan; XU Hui-Fang; SHI Xiao-Li; HUANG Chuan-Hui


    A single-factor experiment of copper ion adsorption on pure palygorskite was carried out to understand the Cu2+ sorption of palygorskite-an important clay mineral in soil and sedimentary rock. In addition, pH of the solution and the surface microstructure of palygorskite were investigated before and after adsorption. The experimental results indicated that efficiency of Cu2+ removal was related to the oscillation rate of the specimen shaker, sorption time, initial pH value and the amount of adsorbent added. Palygorskite induced Cu2+ hydrolysis and interaction between copper hydroxide colloids and palygorskite surfaces, as observed with transmission electron microscopy (TEM), were the main contributions to palygorskite removal of Cu2+. This mechanism was different from adsorption at the mineral-water interface. It was proposed that surface hydrolysis of palygorskite raised the alkalinity of the palygorskite-water interface and suspension system. Thus, the induced pH of the solution was then high enough for Cu2+ hydrolysis on the mineral surface and in solution.

  13. Gas Sorption, Diffusion, and Permeation in Nafion

    Mukaddam, Mohsin Ahmed


    The gas permeability of dry Nafion films was determined at 2 atm and 35 °C for He, H2, N2, O2, CO2, CH4, C2H6, and C3H8. In addition, gas sorption isotherms were determined by gravimetric and barometric techniques as a function of pressure up to 20 atm. Nafion exhibited linear sorption uptake for low-solubility gases, following Henry’s law, and convex behavior for highly sorbing condensable gases, indicating rubber-like behavior at 35 °C. XRD results demonstrated that Nafion contains bimodal amorphous chain domains with average d-spacing values of 2.3 and 5.3 Å. Only helium and hydrogen showed relatively high gas permeability of 37 and 7 barrers, respectively; all other gases exhibited low permeability that decreased significantly as penetrant size increased. Dry Nafion was characterized by extraordinarily high selectivities: He/H2 = 5.2, He/CH4 = 445, He/C2H6 = 1275, He/C3H8 = 7400, CO2/CH4 = 28, CO2/C2H6 = 79, CO2/C3H8 = 460, H2/CH4 = 84, H2/C2H6 = 241, and H2/C3H8 = 1400. These high selectivities could make Nafion a potential candidate membrane material for dry feeds for helium recovery and carbon dioxide separation from natural gas and removal of higher hydrocarbons from hydrogen-containing refinery gases.

  14. Confinement of Mg-MgH2 systems into carbon nanotubes changes hydrogen sorption energetics.

    Liang, Jian-jie; Kung, W-C Paul


    The density functional theory (DFT) method was used to study the effect of nanoconfinement on the energetics of Mg-MgH2 systems. Varying levels of loading of the Mg/MgH2 particles into a (10,10) carbon nanotube were examined, and the corresponding energetics were computed. A clear trend was observed that, as the level of loading increases (increasing confinement), the net energy change in the hydrogen sorption/desorption processes decreases to a significant level when the loading approaches the maximum. The confinement was found not to depend on the tube length of the confining nanotubes.

  15. panMetaDocs, eSciDoc, and DOIDB—An Infrastructure for the Curation and Publication of File-Based Datasets for GFZ Data Services

    Damian Ulbricht


    Full Text Available The GFZ German Research Centre for Geosciences is the national laboratory for Geosciences in Germany. As part of the Helmholtz Association, providing and maintaining large-scale scientific infrastructures are an essential part of GFZ activities. This includes the generation of significant volumes and numbers of research data, which subsequently become source materials for data publications. The development and maintenance of data systems is a key component of GFZ Data Services to support state-of-the-art research. A challenge lies not only in the diversity of scientific subjects and communities, but also in different types and manifestations of how data are managed by research groups and individual scientists. The data repository of GFZ Data Services provides a flexible IT infrastructure for data storage and publication, including minting of digital object identifiers (DOI. It was built as a modular system of several independent software components linked together through Application Programming Interfaces (APIs provided by the eSciDoc framework. Principal application software are panMetaDocs for data management and DOIDB for logging and moderating data publications activities. Wherever possible, existing software solutions were integrated or adapted. A summary of our experiences made in operating this service is given. Data are described through comprehensive landing pages and supplementary documents, like journal articles or data reports, thus augmenting the scientific usability of the service.

  16. Characterization of natural zeolite clinoptilolite for sorption of contaminants

    Xingu-Contreras, E., E-mail:; García-Rosales, G., E-mail: [Instituto Tecnológico de Toluca (Mexico); García-Sosa, I., E-mail:; Cabral-Prieto, A., E-mail:; Solache-Ríos, M., E-mail: [Instituto Nacional de Investigaciones Nucleares, Departamento de Química (Mexico)


    The nanoparticles technology has received considerable attention for its potential applications in groundwater treatment for the removal of various pollutants as Cadmium. In this work, iron boride nanoparticles were synthesized in pure form and in presence of homo-ionized zeolite clinoptilolite, as support material. These materials were used for removing Cd (II) from aqueous solutions containing 10, 50, 100, 150, 200, 250, 300 and 400 mg/L. The characterization of these materials was made by using X-ray Diffraction, Scanning Electron Microscopy and Mössbauer Spectroscopy. Pure iron boride particles show a broad X-ray diffraction peak centered at 45{sup ∘} (2θ), inferring the presence of nanocrystals of Fe{sub 2}B as identified from Mössbauer Spectroscopy. The size of these Fe{sub 2}B particles was within the range of 50 and 120 nm. The maximum sorption capacities for Cd (II) of iron boride particles and supported iron boride particles in homo-ionized zeolitic material were nearly 100 %. For homo-ionized zeolite and homo-ionized zeolite plus sodium borohydride was ≥ 95 %.

  17. Characterization of natural zeolite clinoptilolite for sorption of contaminants

    Xingu-Contreras, E.; García-Rosales, G.; García-Sosa, I.; Cabral-Prieto, A.; Solache-Ríos, M.


    The nanoparticles technology has received considerable attention for its potential applications in groundwater treatment for the removal of various pollutants as Cadmium. In this work, iron boride nanoparticles were synthesized in pure form and in presence of homo-ionized zeolite clinoptilolite, as support material. These materials were used for removing Cd (II) from aqueous solutions containing 10, 50, 100, 150, 200, 250, 300 and 400 mg/L. The characterization of these materials was made by using X-ray Diffraction, Scanning Electron Microscopy and Mössbauer Spectroscopy. Pure iron boride particles show a broad X-ray diffraction peak centered at 45∘ (2 𝜃), inferring the presence of nanocrystals of Fe2B as identified from Mössbauer Spectroscopy. The size of these Fe2B particles was within the range of 50 and 120 nm. The maximum sorption capacities for Cd (II) of iron boride particles and supported iron boride particles in homo-ionized zeolitic material were nearly 100 %. For homo-ionized zeolite and homo-ionized zeolite plus sodium borohydride was ≥ 95 %.

  18. Irreversible Sorption of Contaminants During Ferrihydrite Transformation

    Anderson, H.L.; Arthur, S.E.; Brady, P.V.; Cygan, R.T.; Nagy, K.L.; Westrich, H.R.


    A better understanding of the fraction of contaminants irreversibly sorbed by minerals is necessary to effectively quantify bioavailability. Ferrihydrite, a poorly crystalline iron oxide, is a natural sink for sorbed contaminants. Contaminants may be sorbed/occluded as ferrihydrite precipitates in natural waters or as it ages and transforms to more crystalline iron oxides such as goethite or hematite. Laboratory studies indicate that Cd, Co, Cr, Cu, Ni, Np, Pb, Sr, U, and Zn are irreversibly sorbed to some extent during the aging and transformation of synthetic ferrihydrite. Barium, Ra and Sr are known to sorb on ferrihydrite in the pH range of 6 to 10 and sorb more strongly at pH values above its zero point of charge (pH> 8). We will review recent literature on metal retardation, including our laboratory and modeling investigation of Ba (as an analogue for Ra) and Sr adsorption/resorption, during ferrihydrite transformation to more crystalline iron oxides. Four ferrihydrite suspensions were aged at pH 12 and 50 °C with or without Ba in 0.01 M KN03 for 68 h or in 0.17 M KN03 for 3424 h. Two ferrihydrite suspensions were aged with and without Sr at pH 8 in 0.1 M KN03 at 70°C. Barium or Sr sorption, or resorption, was measured by periodically centrifuging suspension subsamples, filtering, and analyzing the filtrate for Ba or Sr. Solid subsamples were extracted with 0.2 M ammonium oxalate (pH 3 in the dark) and with 6 M HCl to determine the Fe and Ba or Sr attributed to ferrihydrite (or adsorbed on the goethite/hematite stiace) and the total Fe and Ba or Sr content, respectively. Barium or Sr occluded in goethite/hematite was determined by the difference between the total Ba or Sr and the oxalate extractable Ba or Sr. The percent transformation of ferrihydrite to goethite/hematite was estimated from the ratio of oxalate and HC1 extractable Fe. All Ba was retained in the precipitates for at least 20 h. Resorption of Ba reached a maximum of 7 to 8% of the Ba2+ added

  19. Characteristics of and sorption to biochars derived from waste material

    Sun, Huichao; Kah, Melanie; Sigmund, Gabriel; Hofmann, Thilo


    Biochars can exhibit a high sorption potential towards heavy metals and organic contaminants in various environmental matrices (e.g., water, soil). They have therefore been proposed for environmental remediation purposes to sequester contaminants. To date, most studies have focused on the physicochemical and sorption properties of mineral phases poor biochars, which are typically produced from plant residues. Only little knowledge is available for biochars derived from human and animal waste material, which are typically characterized by high mineral contents (e.g., sewage sludge, manure). Using human and animal waste as source material to produce biochars would support the development of attractive combined strategies for waste management and remediation. The potential impact of mineral phases on the physicochemical and sorption properties of biochars requires further studies so that the potential as sorbent material can be evaluated. With this purpose, different source material biochars were produced at 200°C, 350°C and 500°C, to yield a series of biochars representing a range of mineral content. The derived biochars from wood shavings (heavy metals and polycyclic aromatic hydrocarbons) of all materials were within the guidelines values proposed by the International Biochar Initiative, indicating their suitability for environmental application. Single point sorption coefficients for the model sorbate pyrene were measured to investigate the effect of mineral content, feedstock, pyrolysis temperature, particle size fractions and acid demineralization on sorption behavior. Overall, sorption of pyrene was strong for all materials (4 < Log Kd < 6.5 L/kg). Sorption generally increased with increasing pyrolysis temperature but there was no effect of particle size on sorption affinity. For mineral phase rich biochars, sorption generally increased after acid demineralization. When considering all materials together, the sorbent aromaticity (hydrogen-carbon ratio) was

  20. Sorption of polycyclic aromatic hydrocarbons (PAHs) on glass surfaces.

    Qian, Yuan; Posch, Tjorben; Schmidt, Torsten C


    Sorption of polycyclic aromatic hydrocarbons (PAHs) to glass commonly used in laboratories was studied. Sorption coefficients (Kd) of five selected PAHs to borosilicate glass surfaces were measured using column chromatography. A linear relationship between log Kd and the corresponding water solubility of the subcooled liquid (log Sw) of the investigated PAHs was observed. Based on the determined sorption coefficients our data revealed that mass loss caused by sorption on glass walls strongly depends on the ratio of solution volume to contacted surface area (V/S). The influence of solution chemistry such as ionic strength, solution pH, presence of cosolvent, and the influence of temperature on the sorption process were investigated. In the presence of ionic strength, sorption coefficients concurrently increased but less than a factor of 2 up to 0.005 M calcium chloride concentration. However, further increasing ionic strength had no influence on Kd. The cosolvent reduced sorption at a concentration of methanol in water above 0.5% (v/v); however, for benzo[a]pyrene even with 10% (v/v) methanol the mass loss would be still higher than 10% (with a V/S ratio less than 0.25). Significant effects of the solution pH and temperature were not observed. These results suggest that van der Waal's forces dominate the sorption process. In the analysis of highly hydrophobic PAHs in aqueous samples, mass loss due to sorption on glass walls should be accounted for in the final result if untreated glass is used. The presented relationship between log Kd and log Sw may help to decide if such a correction is necessary. Furthermore, the frequently used silanization of glass surfaces may not be sufficient to suppress sorption for large PAHs.

  1. Equilibrium modeling of mono and binary sorption of Cu(II and Zn(II onto chitosan gel beads

    Nastaj Józef


    Full Text Available The objective of the work are in-depth experimental studies of Cu(II and Zn(II ion removal on chitosan gel beads from both one- and two-component water solutions at the temperature of 303 K. The optimal process conditions such as: pH value, dose of sorbent and contact time were determined. Based on the optimal process conditions, equilibrium and kinetic studies were carried out. The maximum sorption capacities equaled: 191.25 mg/g and 142.88 mg/g for Cu(II and Zn(II ions respectively, when the sorbent dose was 10 g/L and the pH of a solution was 5.0 for both heavy metal ions. One-component sorption equilibrium data were successfully presented for six of the most useful three-parameter equilibrium models: Langmuir-Freundlich, Redlich-Peterson, Sips, Koble-Corrigan, Hill and Toth. Extended forms of Langmuir-Freundlich, Koble-Corrigan and Sips models were also well fitted to the two-component equilibrium data obtained for different ratios of concentrations of Cu(II and Zn(II ions (1:1, 1:2, 2:1. Experimental sorption data were described by two kinetic models of the pseudo-first and pseudo-second order. Furthermore, an attempt to explain the mechanisms of the divalent metal ion sorption process on chitosan gel beads was undertaken.

  2. The microbial impact on the sorption behaviour of selenite in an acidic, nutrient-poor boreal bog.

    Lusa, M; Bomberg, M; Aromaa, H; Knuutinen, J; Lehto, J


    (79)Se is among the most important long lived radionuclides in spent nuclear fuel and selenite, SeO3(2-), is its typical form in intermediate redox potential. The sorption behaviour of selenite and the bacterial impact on the selenite sorption in a 7-m-deep profile of a nutrient-poor boreal bog was studied using batch sorption experiments. The batch distribution coefficient (Kd) values of selenite decreased as a function of sampling depth and highest Kd values, 6600 L/kg dry weight (DW), were observed in the surface moss and the lowest in the bottom clay at 1700 L/kg DW. The overall maximum sorption was observed at pH between 3 and 4 and the Kd values were significantly higher in unsterilized compared to sterilized samples. The removal of selenite from solution by Pseudomonas sp., Burkholderia sp., Rhodococcus sp. and Paenibacillus sp. strains isolated from the bog was affected by incubation temperature and time. In addition, the incubation of sterilized surface moss, subsurface peat and gyttja samples with added bacteria effectively removed selenite from the solution and on average 65% of selenite was removed when Pseudomonas sp. or Burkholderia sp. strains were used. Our results demonstrate the important role of bacteria for the removal of selenite from the solution phase in the bog environment, having a high organic matter content and a low pH. Copyright © 2015 Elsevier Ltd. All rights reserved.

  3. Utilising conservative tracers and spatial surveys to identify controls on pathways and DOC exports in an Arctic catchment.

    Lessels, J. S.; Tetzlaff, D.; Dinsmore, K. J.; Street, L. E.; Dean, J.; Washbourne, I. J.; Billett, M. F.; Baxter, R.; Subke, J. A.; Wookey, P. A.


    Dissolved organic carbon (DOC) is typically the predominant form of carbon exported from headwater streams, it therefore represents a major carbon export from Arctic catchments. The projected deepening of thaw depth in permafrost regions, due to an increase in air temperature, may have a significant effect on the amount of DOC exported from these systems. However, quantification of the impacts of climate driven changes on DOC export are still highly uncertain. Understanding the processes controlling DOC export is therefore crucial in predicting the potential impact of projected environmental changes. The controls of DOC production and transport are heavily influenced by soil and vegetation, which are highly variable across the landscape. To completely understand these systems information regarding spatial variability of plants, soils and thaw depths must be taken into account. In this study sub-weekly sampling of DOC was undertaken throughout 2014 in a headwater (Canada. Spatial surveys of soil properties, active thaw depth and normalised difference vegetation index (NDVI) were collected and used in conjunction with conservative stable water isotopes tracers and major ions to understand sources, flow pathways and timing of DOC exports from the catchment. Stable isotope tracers act as fingerprints of water allowing sources and pathways to be assessed. Observations reveal changing DOC concentrations throughout the season as the active layer deepens and the connectivity of the soils to the stream network throughout the catchment increases. Linking the DOC data with the conservative tracer response improves the identification of carbon pathways and fluxes from the soils; preliminary analysis indicates DOC is being delivered via deeper more mineral soils later in the season. The results indicate that the active layer depth has a strong influence on the amount of DOC exported from the system, independent of the amount of carbon stored in these deeper soils.

  4. Sorption of Heavy Metal and Organic Pollutants on Modified Soils

    MENG Zhao-Fu; ZHANG Yi-Ping; WANG Guo-Dong


    Sorption characteristics of both an organic pollutant(phenol)and a heavy metal(cadmium ion)on the clay layer of a Lou soil(Eum-orthic Anthrosol in Chinese Soil Taxonomy)along with the sorption mechanism were investigated using three soil treatments:modification with a cationic surfactant cetyltrimethylammonium bromide added at an amount equivalent to 50%and 100%of the soil CEC (50%CB and 100%CB),modification with an amphoteric surface-modifying agent dodecyldimethylbetaine(commercially known as BS-12)added at an amount equivalent to 50%and 100%of the soil CEC(50%BS and 100%BS),and an unmodified control(CK).Results showed that the BS soil treatments increased sorption of both the heavy metal Cd2+ and the organic pollutant phenol.The equilibrium sorption amount of Cd2+decreased in the order:50%BS>100%BS>CK>50%CB>100%CB,with the BS soil treatments being about 1.3 to 1.8 times higher and the CB soil treatments about 23%to 41%lower than CK.Both the single-site and two-site Langmuir models could be applied to describe the sorption of Cd2+ in each soil treatment.The equilibrium sorption amount of phenol on the soil samples decreased in the order:100%CB>50%CB>100%BS>50%BS>CK,with the CB soil treatments being 41.0 to 79.6 times higher and the BS soil treatments 4.0 to 8.3 times higher than CK.The Freundlich equation could also be used to describe the sorption characteristics of phenol.In the BS soil treatments,both an organophobic long carbon chain and hydrophilic charged groups resulted in a relatively strong sorption ability for both heavy metals and organic pollutants.In addition.the sorption ratio K,the ratio of phenol sorption amount of the modified soil to that of CK,increased initially and decreased later with the amount of phenol added,and the critical sorption ratio Kc,the peak value of the sorption ratio curve plotted against the added phenol concentration.was a good index for evaluating the sorption ability of phenol in the soil.

  5. Scaling effects of riparian peatlands on stable isotopes in runoff and DOC mobilisation

    Tunaley, C.; Tetzlaff, D.; Soulsby, C.


    We combined 13 months of daily isotope measurements in stream water with daily DOC and 15 min FDOM (fluorescent component of dissolved organic matter) data at three nested scales to identify how riparian peatlands generate runoff and influence DOC dynamics in streams. We investigated how runoff generation processes in a small, riparian peatland-dominated headwater catchment (0.65 km2) propagate to larger scales (3.2 km2 and 31 km2) with decreasing percentage of riparian peatland coverage. Isotope damping was most pronounced in the 0.65 km2 headwater catchment due to high water storage in the organic soils encouraging tracer mixing. At the largest scale, stream flow and water isotope dynamics showed a more flashy response. The isotopic difference between the sites was most pronounced in the summer months when stream water signatures were enriched. During the winter months, the inter-site difference reduced. The isotopes also revealed evaporative fractionation in the peatland dominated catchment, in particular during summer low flows, which implied high hydrological connectivity in the form of constant seepage from the peatlands sustaining high baseflows at the headwater scale. This connectivity resulted in high DOC concentrations at the peatland site during baseflow (∼5 mg l-1). In contrast, at the larger scales, DOC was minimal during low flows (∼2 mg l-1) due to increased groundwater influence and the disconnection between DOC sources and the stream. High frequency data also revealed diel variability during low flows. Insights into event dynamics through the analysis of hysteresis loops showed slight dilution on the rising limb, the strong influence of dry antecedent conditions and a quick recovery between events at the riparian peatland site. Again, these dynamics are driven by the tight coupling and high connectivity of the landscape to the stream. At larger scales, the disconnection between the landscape units increases and the variable connectivity

  6. Sorption of cesium in young till soils

    Lusa, Merja; Lempinen, Janne; Ahola, Hanna; Soederlund, Mervi; Lehto, Jukka [Helsinki Univ. (Finland). Laboratory of Radiochemistry; Lahdenperae, Anne-Maj [Saanio and Riekkola Oy, Consulting Engineers, Helsinki (Finland); Ikonen, Ari T.K. [Posiva Oy, Eurajoki (Finland)


    Soil samples from three forest soil pits were examined down to a depth of approximately three metres using 1 M ammonium acetate extraction and microwave-assisted extraction with concentrated nitric acid (HNO{sub 3}), to study the binding of cesium (Cs) at Olkiluoto Island, southern Finland. Ammonium acetate was used to extract the readily exchangeable Cs fractions roughly representing the Cs fraction in soil which is available for plants. Microwave-assisted HNO{sub 3} extraction dissolves various minerals, e.g. carbonates, most sulphides, arsenides, selenides, phosphates, molybdates, sulphates, iron (Fe) and manganese (Mn) oxides and some silicates (olivine, biotite, zeolite), and reflects the total Cs concentrations. Cs was mostly found in the strongly bound fraction obtained through HNO{sub 3} extraction. The average Cs concentrations found in this fraction were 3.53 ± 0.30 mg/kg (d.w.), 3.06 ± 1.86 mg/kg (d.w.) and 1.83 ± 0.42 mg/kg (d.w.) in the three soil pits, respectively. The average exchangeable Cs found in the ammonium acetate extraction in all three sampling pits was 0.015 ± 0.008 mg/kg (d.w.). In addition, Cs concentrations in the soil solution were determined and in situ distribution coefficients (K{sub d}) for Cs were calculated. Furthermore, the in situ K{sub d} data was compared with the Cs K{sub d} data obtained using the model batch experiments. The in situ K{sub d} values were observed to fairly well follow the trend of batch sorption data with respect to soil depth, but on average the batch distribution coefficients were almost an order of magnitude higher than the in situ K{sub d} data. In situ Cs sorption data could be satisfactory fitted with the Langmuir sorption isotherm, but the Freundlich isotherm failed to fit the data. Finally, distribution coefficients were calculated by an ion exchange approach using soil solution data, the cation exchange capacity (CEC) as well as Cs to sodium (Na) and Cs to potassium (K) ion exchange selectivity

  7. Sorption and deformation of coals in liquid and gas medium

    S.A. Aipshtein; D.L. Shirochin; V.I. Minaev; A.V. Bunin; A.A. Belyi [Moscow State University of Mining (MSMU), Moscow (Russian Federation)


    The collection of coals from Kuznetsk and Donetsk basins was selected with the following criteria: a) different rank; b) different genetic types. Sorption and deformation of coals have been investigated in the medium of carbonic gas and at interaction with dimethylformaldehyde (DMFA). The experimental data on the gas sorption were obtained through a laser method. Such method allows to measure the dependence of adsorption values {zeta} and sorption deformations x (t) simultaneously on the same sample in wide interval of gas pressure P (from 10{sup 2} Pa up to 10 MPa). Sorption processes of carbon dioxide on different rank coals of identical genotypes were investigated. The influence of rank on coal sorption and deformation was established. Differences in structures of isometamorphic coals of different genetic types were established. Using the independent analytical methods with investigation of sorption DMFA by coals have been allowed to establish feature of structure of isometamorphic coals of different genotype types. It was established, the sorption DMFA by coals of 'a'- genotype led to essential transformation coals' organic substance. 8 refs., 5 figs., 5 tabs.

  8. Study on sorption of D155 resin for gadolinium

    XIONG Chunhua


    The sorption behavior and mechanism of a Macroporous weak acid resin,(D155 resin,)for Gd(III) were investigated. The statically saturated sorption capacity is 283 mg/g resin at 298 K in HAc-NaAc medium. The Gd(III) adsorbed on macroporous weak acid resin,(D155 resin,)could be reductively eluted with the mixed solution of HCl and NaCl, and the elution percentage was as high as 100%. The resin could be regenerated and reused without remarkable decrease in sorption capacity. The apparent sorption rate constant was k298=1.98×10-5 s-1. The apparent activation energy was Ea=2.78 kJ/mol. The sorption behavior of D155 resin for Gd(III) obeyed the Langmuir isotherm. The thermodynamic sorption parameters were (H=33.0 kJ/mol, (S=192 J/mol/K, and (G298=-24.3 kJ/mol. The sorption mechanism of D155 resin for Gd(III) was examined by using chemical method and IR spectrometry. The coordination compound was formed between oxygen atoms in the functional group of D155 resin and Gd (III).

  9. Water vapor sorption thermodynamics of the Nafion ionomer membrane.

    Wadsö, Lars; Jannasch, Patric


    The water interactions of polymer electrolyte membranes are of significant interest when these materials are used in, for example, fuel cells. We have therefore studied the sorption thermodynamics of Nafion with a sorption calorimeter that simultaneously measures the sorption isotherm and the mixing (sorption) enthalpy. This unique method is suitable for investigating the sorption thermodynamics of ionic polymers. The measurements were made at 25 °C on a series of samples dried at different temperatures from 25 to 120 °C. The sorption isotherms indicate that the samples dried at 120 °C lost about 0.8 more water molecules per sulfonic group during the drying than did the samples dried at 25 °C, and this result was verified gravimetrically. The mixing enthalpies showed several peaks or plateaus for the samples dried at 60-120 °C. This behavior was seen up to about 2 water molecules per sulfonic group. As these peaks were not directly related to any feature in the sorption isotherm, they probably have their origin in a secondary process, such as a reorganization of the polymer.

  10. Dissolved organic carbon (DOC) concentrations in UK soils and the influence of soil, vegetation type and seasonality.

    van den Berg, Leon J L; Shotbolt, Laura; Ashmore, Mike R


    Given the lack of studies which measured dissolved organic carbon (DOC) over long periods, especially in non-forest habitat, the aim of this study was to expand the existing datasets with data of mainly non-forest sites that were representative of the major soil and habitat types in the UK. A further aim was to predict DOC concentrations from a number of biotic and abiotic explanatory variables such as rainfall, temperature, vegetation type and soil type in a multivariate way. Pore water was sampled using Rhizon or Prenart samplers at two to three week intervals for 1 year. DOC, pH, organic carbon, carbon/nitrogen (C:N) ratios of soils and slope were measured and data on vegetation, soil type, temperature and precipitation were obtained. The majority of the variation in DOC concentrations between the UK sites could be explained by simple empirical models that included annual precipitation, and soil C:N ratio with precipitation being negatively related to DOC concentrations and C:N ratio being positively related to DOC concentrations. Our study adds significantly to the data reporting DOC concentrations in soils, especially in grasslands, heathlands and moorlands. Broad climatic and site factors have been identified as key factors influencing DOC concentrations.

  11. Soil C:N ratio as a predictor of annual riverine DOC flux at local and global scales

    Aitkenhead, J. A.; McDowell, W. H.


    Dissolved organic carbon (DOC) is important in a wide variety of chemical, physical, and biological processes in surface waters. We examined the relationship between DOC flux and soil C:N ratio on a biome basis. DOC fluxes for 164 rivers were subdivided into 15 biome types including tropical rain forest, coniferous forests, peatland, deciduous forests, mixed forests, and grasslands. A database of soil C:N ratios was constructed and subdivided into biome types. At a global scale, mean soil C:N ratio of a biome accounts for 99.2% of the variance in annual riverine DOC flux among biomes. The relationship between soil C:N ratio and DOC flux at the biome scale was used to predict annual riverine DOC flux at the watershed scale for three test watersheds not included in the original model. Predicted flux of each watershed was within 4.5% of the actual DOC flux. Using the C:N model, we estimated the total export of carbon from land to the oceans to be 3.6×1014 g yr-1. This empirical model should be useful in predicting changes in DOC flux under changing climatic conditions.

  12. Contribution to the study of sorption mechanisms at solid-liquid interfaces: application to the cases of apatites and oxy-hydroxides; Contribution a l'etude des mecanismes de sorption aux interfaces solide-liquide: application aux cas des apatites et des oxy-hydroxydes

    Duc, M


    Sorption-desorption phenomena play an important role in the transport of toxic and radioactive elements in surface and underground water in contact with solid matter. Selenium, which is one of the long-lived radionuclides present in radioactive waste, is characterized by several oxidation states and by anionic species in aqueous solutions. In order to predict its transport, we need a good knowledge of its sorption processes. We have studied the sorption of Se(IV) and Se(VI) on two types of solids present in natural media or which have been proposed as additives to active barriers: hydroxy-apatites, fluoro-apatite and iron oxi-hydroxides (goethite and hematite). Sorption mechanisms have been studied through an approach including several different and complementary methods: titrimetry, zeta-metry, scanning and transmission electron microscopy, infrared spectroscopy, X-ray diffraction, X-ray photo electron spectroscopy, etc... Results showed that Se(VI) is much less sorbed than Se(VI) on both types of solids. For Se(IV) the sorption mechanisms are different for iron oxides and apatites. On oxides, sorption increases when pH decreases. It can be interpreted by a surface complexation model, essentially through an inner sphere complex (monodentate or bidentate). Modelling of Se sorption curves was performed after the determination of acido-basic properties of oxides. However, the determination of the intrinsic properties of oxides is disturbed by several parameters identified as impurities, evolution of the solid in solution, kinetic and solubility of the solid. For apatites, selenium sorption proceeds by exchange with superficial groups, with a maximum of fixation at approximately pH 8. Thanks to XPS measurements and the elaboration of a mathematical model, we could determine the depth of penetration of both selenium and cadmium on apatites. (author)

  13. Characterisation of DOC and its relation to the deep terrestrial biosphere

    Vieth, Andrea; Vetter, Alexandra; Sachse, Anke; Horsfield, Brian


    The deep subsurface is populated by a large number of microorganisms playing a pivotal role in the carbon cycling. The question arises as to the origin of the potential carbon sources that support deep microbial communities and their possible interactions within the deep subsurface. As the carbon sources need to be dissolved in formation fluids to become available to microorganisms, the dissolved organic carbon (DOC) needs further characterisation as regards concentration, structural as well as molecular composition and origin. The Malm carbonates in the Molasse basin of southern Germany are of large economic potential as they are targets for both hydrocarbon and geothermal exploration (ANDREWS et al., 1987). Five locations that differ in their depth of the Malm aquifer between 220 m and 3445 m below surface have been selected for fluid sampling. The concentration and the isotopic composition of the DOC have been determined. To get a better insight into the structural composition of the DOC, we also applied size exclusion chromatography and quantified the amount of low molecular weight organic acids (LMWOA) by ion chromatography. With increasing depth of the aquifer the formation fluids show increasing salinity as chloride concentrations increase from 2 to 300 mg/l and also the composition of the DOC changes. Water samples from greater depth (>3000 m) showed that the DOC mainly consists of LMWOA (max. 83 %) and low percentages of neutral compounds (alcohols, aldehyde, ketones, amino acids) as well as "building blocks". Building blocks have been described to be the oxidation intermediates from humic substances to LMWOA. With decreasing depth of the aquifer, the DOC of the fluid becomes increasingly dominated by neutral compounds and the percentage of building blocks increases to around 27%. The fluid sample from 220 m depth still contains a small amount of humic substances. The DOC of formation fluids in some terrestrial sediments may originate from organic

  14. Sorption of phenanthrene in agricultural soils

    Soares, António Carlos Alves; Minh, Luong Nhat; Vendelboe, Anders Lindblad

    the saturation line as defined by Dexter. Top soils and subsoils showed different sorption behavior, with typically higher Koc for topsoils, likely due to different organic matter quality related to soil management and hydrological impact. Topsoils generally exhibited Koc values between the traditionally applied...... for predicting average Koc for agricultural topsoils. Subsoils mostly followed Abdul, in agreement with that this model was developed for deeper soils and groundwater sediments lower in organic carbon (0.4 - 2%). This study only concerns solid-liquid partioning and thus the probability for PAH adsorption onto...... assumingly non-mobile soil particles. In perspective, the combined risk of dissolved PAH leaching and colloid-facilitated PAH leaching from cultivated land areas should be considered....

  15. Sorption of aromatic hydrocarbons onto montmorillonite as affected by norfloxacin

    Pei, Zhiguo, E-mail: [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, PO Box 2871, Beijing 100085 (China); Kong, Jingjing [School of Chemistry and Materials, Fujian Normal University, Fuzhou 350007 (China); Shan, Xiao-quan; Wen, Bei [State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, PO Box 2871, Beijing 100085 (China)


    Graphical abstract: {sup 1}H NMR spectrum provided direct evidence for {pi}-{pi} and cation-{pi} complexation between PAHs and Nor{sup +} by ring-current-induced upfield chemical shifts of the amino group and methylene group of Nor{sup +}. Highlights: Black-Right-Pointing-Pointer Nor decreases 1,3-DNB sorption, and increases NAPH, PHEN and PYR sorption on montmorillonite. Black-Right-Pointing-Pointer Nor{sup {+-}} increased PHEN and PYR sorption more pronounced than Nor{sup +} and Nor{sup -}. Black-Right-Pointing-Pointer The corresponding mechanisms were described by FTIR and {sup 1}H NMR. - Abstract: Effect of norfloxacin (Nor) on the sorption of 1,3-dinitrobenzene (1,3-DNB), and PAHs (naphthalene (NAPH), phenanthrene (PHEN) and pyrene (PYR)) to K{sup +}-montmorillonite was studied. Nor suppressed 1,3-DNB sorption due to their competition for the same sorption sites. 1,3-DNB was sorbed on K{sup +}-montmorillonite surface via cation-polar interaction and n-{pi} electron donor-acceptor interaction. Nor also was sorbed on these sites through cation exchange, cation bridging and/or surface complexation. Nor increased three PAHs sorption on montmorillonite and the enhanced magnitude was positively correlated with the {pi}-donor strength of three PAHs. The enhanced sorption of PAHs by Nor was primarily attributed to {pi}-{pi} interaction between {pi}-electron-depleted quinoline ring of Nor and {pi}-electron-rich PAHs. Compared with cation (Nor{sup +}) and anion (Nor{sup -}), zwitterion (Nor{sup {+-}}) of Nor increased PHEN and PYR sorption more pronounced due to additional cation-{pi} interaction between the sorbed Nor{sup {+-}} and PAHs. {sup 1}H NMR spectrum provided direct evidence for {pi}-{pi} and cation-{pi} complexation between PAHs and Nor{sup +} in solution by ring-current-induced upfield chemical shifts of amino group and methylene group of Nor{sup +}.

  16. TogoDoc server/client system: smart recommendation and efficient management of life science literature.

    Iwasaki, Wataru; Yamamoto, Yasunori; Takagi, Toshihisa


    In this paper, we describe a server/client literature management system specialized for the life science domain, the TogoDoc system (Togo, pronounced Toe-Go, is a romanization of a Japanese word for integration). The server and the client program cooperate closely over the Internet to provide life scientists with an effective literature recommendation service and efficient literature management. The content-based and personalized literature recommendation helps researchers to isolate interesting papers from the "tsunami" of literature, in which, on average, more than one biomedical paper is added to MEDLINE every minute. Because researchers these days need to cover updates of much wider topics to generate hypotheses using massive datasets obtained from public databases or omics experiments, the importance of having an effective literature recommendation service is rising. The automatic recommendation is based on the content of personal literature libraries of electronic PDF papers. The client program automatically analyzes these files, which are sometimes deeply buried in storage disks of researchers' personal computers. Just saving PDF papers to the designated folders makes the client program automatically analyze and retrieve metadata, rename file names, synchronize the data to the server, and receive the recommendation lists of newly published papers, thus accomplishing effortless literature management. In addition, the tag suggestion and associative search functions are provided for easy classification of and access to past papers (researchers who read many papers sometimes only vaguely remember or completely forget what they read in the past). The TogoDoc system is available for both Windows and Mac OS X and is free. The TogoDoc Client software is available at, and the TogoDoc server is available at

  17. TogoDoc server/client system: smart recommendation and efficient management of life science literature.

    Wataru Iwasaki

    Full Text Available In this paper, we describe a server/client literature management system specialized for the life science domain, the TogoDoc system (Togo, pronounced Toe-Go, is a romanization of a Japanese word for integration. The server and the client program cooperate closely over the Internet to provide life scientists with an effective literature recommendation service and efficient literature management. The content-based and personalized literature recommendation helps researchers to isolate interesting papers from the "tsunami" of literature, in which, on average, more than one biomedical paper is added to MEDLINE every minute. Because researchers these days need to cover updates of much wider topics to generate hypotheses using massive datasets obtained from public databases or omics experiments, the importance of having an effective literature recommendation service is rising. The automatic recommendation is based on the content of personal literature libraries of electronic PDF papers. The client program automatically analyzes these files, which are sometimes deeply buried in storage disks of researchers' personal computers. Just saving PDF papers to the designated folders makes the client program automatically analyze and retrieve metadata, rename file names, synchronize the data to the server, and receive the recommendation lists of newly published papers, thus accomplishing effortless literature management. In addition, the tag suggestion and associative search functions are provided for easy classification of and access to past papers (researchers who read many papers sometimes only vaguely remember or completely forget what they read in the past. The TogoDoc system is available for both Windows and Mac OS X and is free. The TogoDoc Client software is available at, and the TogoDoc server is available at

  18. Italian-Russian Glossary of DOP-IGP-DOC foods from Emilia Romagna

    Perini, Francesca


    This glossary is addressed to Russian students and operators who are interested in the Italian food culture. It includes terms about eight DOP, IGP and DOC foods from the region Emilia Romagna. It is a linguistic tool because it gives: - the translation of the terms from Italian into Russian; - the definition of the terms in Russian language; - information about the context in which the terms can occur; - synonyms of the terms. It is a reliable marketing tool because it desc...

  19. Fido, a novel AMPylation domain common to fic, doc, and AvrB.

    Lisa N Kinch

    Full Text Available BACKGROUND: The Vibrio parahaemolyticus type III secreted effector VopS contains a fic domain that covalently modifies Rho GTPase threonine with AMP to inhibit downstream signaling events in host cells. The VopS fic domain includes a conserved sequence motif (HPFx[D/E]GN[G/K]R that contributes to AMPylation. Fic domains are found in a variety of species, including bacteria, a few archaea, and metazoan eukaryotes. METHODOLOGY/PRINCIPAL FINDINGS: We show that the AMPylation activity extends to a eukaryotic fic domain in Drosophila melanogaster CG9523, and use sequence and structure based computational methods to identify related domains in doc toxins and the type III effector AvrB. The conserved sequence motif that contributes to AMPylation unites fic with doc. Although AvrB lacks this motif, its structure reveals a similar topology to the fic and doc folds. AvrB binds to a peptide fragment of its host virulence target in a similar manner as fic binds peptide substrate. AvrB also orients a phosphate group from a bound ADP ligand near the peptide-binding site and in a similar position as a bound fic phosphate. CONCLUSIONS/SIGNIFICANCE: The demonstrated eukaryotic fic domain AMPylation activity suggests that the VopS effector has exploited a novel host posttranslational modification. Fic domain-related structures give insight to the AMPylation active site and to the VopS fic domain interaction with its host GTPase target. These results suggest that fic, doc, and AvrB stem from a common ancestor that has evolved to AMPylate protein substrates.

  20. Long-term trends in dissolved iron and DOC concentration linked to nitrate depletion in riparian soils

    Musolff, Andreas; Selle, Benny; Fleckenstein, Jan H.; Oosterwoud, Marieke R.; Tittel, Jörg


    The instream concentrations of dissolved organic carbon (DOC) are rising in many catchments of the northern hemisphere. Elevated concentrations of DOC, mainly in the form of colored humic components, increase efforts and costs of drinking water purification. In this study, we evaluated a long-term dataset of 110 catchments draining into German drinking water reservoirs in order to assess sources of DOC and drivers of a potential long-term change. The average DOC concentrations across the wide range of different catchments were found to be well explained by the catchment's topographic wetness index. Higher wetness indices were connected to higher average DOC concentrations, which implies that catchments with shallow topography and pronounced riparian wetlands mobilize more DOC. Overall, 37% of the investigated catchments showed a significant long-term increase in DOC concentrations, while 22% exhibited significant negative trends. Moreover, we found that increasing trends in DOC were positively correlated to trends in dissolved iron concentrations at pH≤6 due to remobilization of DOC previously sorbed to iron minerals. Both, increasing trends in DOC and dissolve iron were found to be connected to decreasing trends and low concentrations of nitrate (below ~6 mg/L). This was especially observed in forested catchments where atmospheric N-depositions were the major source for nitrate availability. In these catchments, we also found long-term increases of phosphate concentrations. Therefore, we argue that dissolved iron, DOC and phosphate were jointly released under iron-reducing conditions when nitrate as a competing electron acceptor was too low in concentrations to prevent the microbial iron reduction. In contrast, we could not explain the observed increasing trends in DOC, iron and phosphate concentrations by the long-term trends of pH, sulfate or precipitation. Altogether this study gives strong evidence that both, source and long-term increases in DOC are

  1. What drove Dissolved Organic Carbon (DOC) concentration variability in the River Thames (UK) between 1884 and 2014?

    Noacco, Valentina; Wagener, Thorsten; Howden, Nicholas; Duffy, Christopher


    Climate and atmospheric circulation patterns influence the variability of basin hydrochemistry, therefore understanding their influence is essential to put short-term water quality trends into the right context and to predict future hydrochemistry responses in the face of climate change. We investigate the drivers of DOC concentration variability in the Thames basin over 130 years. Our previous work has shown that increased urbanization since the 1880s in the Thames basin was the major driver for the increase in riverine DOC, but it does not explain DOC variability. Our current work investigates the links between hydro-climatic variability (temperature, precipitation and runoff) and teleconnections (ENSO and NAO), and the variability in DOC concentration. Moreover we compare the impact of hydro-climatic variability on riverine DOC, to the impact of land-use change and population increase. We use singular spectrum analysis to identify and then compare the dominant oscillatory components of hydro-climatic and hydro-biogeochemical variables. We use phase-plane trajectories of the noise-free, intra-annual to inter-annual reconstructed components to elucidate the biogeochemical and hydro-climatic dynamics of the system. This allows us to elucidate the links between the variability of hydro-climatic variables and DOC. Moreover they enable the identification of points in time where the dynamics of the system have changed, e.g. due to anthropogenic influences. Further, lag-correlations between teleconnections, DOC and flow are explored, to consider the hydrological memory of the catchment due to the permeable geology present. We show that the high seasonal to inter-annual variability in DOC concentration is linked to the variability of precipitation and runoff, rather than temperature. The dominant inter-annual modes of variability in DOC are connected to the ENSO oscillatory components. During strong El Niño and La Niña years there is statistically significant positive

  2. Control of the extraction procedures on the response of DOC concentration and composition to soil temperature increase

    Lambert, Thibault; Pierson-Wickmann, Anne-Catherine; Gruau, Gérard; Jaffrézic, Anne; Jeanneau, Laurent; Racape, Armelle


    Dissolved organic carbon (DOC) leached from soils is a crucial component of the terrestrial C cycling and a major source for DOC export at the landscape scale by stream and river waters. In the context of global warming, it is necessary to understand how changes in soil temperature will impact the DOC dynamic in soils, but this remains a matter of debate. We conducted a series of experiments in order to study both biological and physical processes involved in soil DOC production and mobilisation at different temperatures. Two experiments of DOC extraction were conducted at different temperatures: (i) soil solution percolation through a soil column and (ii) soil solution agitation in jars, which are both commonly used in the literature. The organo-mineral horizon of a wetland soil was incubated during 14 days at temperature ranging from 4 to 30 ° C. Along with DOC concentrations, changes in DOC composition were assessed by monitoring the natural stable carbon isotopic composition of (δ13C) and the specific ultra violet absorbance (SUVA) of DOC. The results showed strong differences between the two extraction procedures in term of DOC response to temperature rise, both in concentration and composition. DOC released by percolation through soil column displayed a strong concentration increase with increasing temperature. Whatever the temperature, a low SUVA and relatively high δ13C values indicated a release of molecules with lower aromaticity and lower molecular weight the two first days than after. On the contrary, DOC extracted by agitation in jars showed minor changes in both concentrations and composition along the incubation. The difference observed between soil leaching and batch incubation can mainly be explained by the extraction procedures. Indeed, the percolation procedure favors transfer from the micro-porosity to the macro-porosity pool between two successive leaching, whereas agitation procedure releases DOC produced and accumulated in the whole soil


    A. G. Savvina


    Full Text Available The widespread use of aromatic acids (benzoic acid, salicylic as preservatives necessitates their qualitative and quantitative determination in food. Effective and common way to separation and concentration of aromatic acids liquid extraction. Biphasic system of water-soluble polymers based on (poly-N-vinyl pyrrolidone, and poly-N-vinylcaprolactam satisfy the requirements of the extraction system. When sorption concentration improved definition of the metrological characteristics, comply with the requirements for sensitivity and selectivity definition appears possible, use of inexpensive and readily available analytical equipment. When studying the adsorption of benzoic acid used as a sorbent crosslinked polymer based on N-vinyl pyrrolidone, obtained by radical polymerisation of a functional monomer and crosslinker. In the extraction of benzoic acid to maximize the allocation of water and the organic phase of the polymer used salt solutions with concentrations close to saturation. Regardless of the nature of the anion salt is used as salting-out agent, aromatic acids sorption increases with the size of the cations. In the experiment the maximum recovery rate (80% benzoic acid obtained in the PVP (0.2 weight%. Ammonium sulphate. The dependence stepepni benzoic acid extraction from time sorption sorbent mass and the pH of the aqueous phase. To establish equilibrium in the system, for 20 minutes. The dependence of the degree of extraction of the acid pH indicates that the acid is extracted into the molecular form. The maximum adsorption is reached at pH 3,5, with its efficiency decreases symbatically reduce the amount of undissociated acid molecules in solution.

  4. Memoriais escolares e processos de iniciação à docência

    Maria Aparecida Bergamaschi


    Full Text Available Neste texto, nos debruçamos sobre as narrativas de memória de 14 estudantes do curso de Pedagogia, bolsistas do Programa Institucional de Bolsas de Iniciação à Docência - PIBID. Os memoriais, que compõem o livro Iniciação à docência em Pedagogia: memórias que contam histórias, são analisados na perspectiva de compreendê-los como parte importante no processo formativo dos bolsistas que integram o programa, que desde o presente miram o passado e constroem memórias que revelam, principalmente, seus percursos escolares. Relendo cada memorial, retomamos também o processo de elaboração dos mesmos e o significado que adquiriram na formação de cada bolsista, destacando o que, coletivamente, apresentam como aspectos marcantes nas trajetórias de vida: a infância e a família, as experiências escolares e, por fim, a escolha da docência e o estar professor no PIBID.

  5. [Effect of reclamation on the vertical distribution of SOC and retention of DOC].

    Huo, Li-Li; Zou, Yuan-Chun; Guo, Jia-Wei; Lü, Xian-Guo


    Contents and density of soil organic carbon (SOC) in soil profiles and dissolved organic carbon (DOC) of soil solution in different soil depths in wetland, soybean and paddy field reclaimed from the wetland around Xingkai Lake were determined to investigate how reclamation of wetland for soybean and rice farming impacts vertical distribution of SOC and retention of DOC. SOC contents in 0-40 cm soil layers were significantly influenced. SOC contents in 0-10, 10-20, 20-30 and 30-40 cm soil layers in soybean and paddy field were 79.07% and 82.01%, 79.01% and 82.28%, 79.86% and 92.90%, 37.49% and 78.05% respectively lower than those in wetland. Before and after reclamation, SOC contents in soil layers deeper than 40 cm were not significantly different. SOC densities in soybean and paddy field were 25.50% and 47.35% respectively lower than those in wetland. However, either in wetland or farm land, most of the SOC storage in 0-100 cm soil layer was stored in 0-50 cm soil layer. The relationships between SOC content and soil depth in wetland and two farm lands all could be described by exponential functions; cultivation did not change the variation of SOC content with soil depth. The retention of DOC was more obvious for soybean farming than wetland and rice farming, and that was roughly the same for wetland as rice farming.

  6. Sorption of lanthanum ions by natural clinoptilolite tuff

    Dampilova, B. V.; Zonkhoeva, E. L.


    The equilibrium and kinetics of sorption of lanthanum ions on natural clinoptilolite tuff are studied. It is demonstrated that sorption of lanthanum ions from diluted solutions occurs in micropores of clinoptilolite, and from concentrated solutions in the mesoporous structure of tuff. The main capacity of zeolite tuff is found in the secondary porous structure. The sorption of lanthanum ions is limited by diffusion in tuff grains. Lanthanum ions are regularly distributed in the tuff phase and interact with the Brønsted centers of large clinoptilolite cavities.

  7. Kinetics of sorption of oil products by hydroxide precipitates

    Petrova, N.A.; Dubrovskaya, G.E.; Berezyuk, V.G.; Pushkarev, V.V.


    Study of the kinetics of sorption of oils (palm and coriander oils, Genrex-26, Emulsol E-2(B)) under static conditions by aluminum and iron hydroxide precipitates (with FeSO/sub 4/, FeCl/sub 3/, and AlCl/sub 3/ as coagulants) showed that an increase of temperature to 40 to 50/sup 0/C raises the sorption rate substantially. The kinetic relations can be represented by equations for first-order reactions. The calculated rate constants and the values of the empirical activation energies are evidence of physical sorption with diffusion as the controlling step.

  8. Sorption Properties of Steam Treated Wood and Plant Fibres

    Hoffmeyer, Preben; Jensen, Signe Kamp; Jones, Dennis;


    mechanism may be the gradual filling of such micropores by lignin made to flow by further steam treatment. As a result of these counteractive mechanisms, sorption at high RH in steam treated fibres was seen to first grow, then drop and ultimately settle at a level corresponding to pure sorption at primary...... sorption sites. The annual plant fibres proved less susceptible than wood fibres to chemical breakdown from steam treatment. The component most susceptible to chemical breakdown was hemicellulose. Beech, wheat and hemp showed only a modest decrease of cellulose content, even at high temperatures, whereas...

  9. Arsenic Sorption on Mechanically Activated Magnetite and Olivine

    Zdenka Bujňáková


    Full Text Available Arsenic sorption on mechanically activated minerals such as magnetite Fe3O4 (Kiruna, Sweden and olivine (Mg,Fe2SiO4 (Ǻheim,Norway has been studied and compared in this work. Experiments were carried out with non-activated and mechanically activatedsamples. The activation of both minerals was performed in a planetary mill at different milling conditions. The specific surface areaand consequent sorption activity were enhanced by mechanical activation. The using of olivine seems to be better than magnetite fromthe point of view of milling time, which is necessary for achievement of the same sorption effect.

  10. Designing a Dynamic Data Driven Application System for Estimating Real-Time Load of DOC in a River

    Ouyang, Y.; None


    Understanding the dynamics of naturally occurring dissolved organic carbon (DOC) in a river is central to estimating surface water quality, aquatic carbon cycling, and climate change. Currently, determination of DOC in surface water is primarily accomplished by manually collecting samples for laboratory analysis, which requires at least 24 hours. In other words, no effort has been devoted to monitoring real-time variations of DOC in a river due to the lack of suitable and/or cost-effective wireless sensors. However, when considering human health, carbon footprints, and effects of urbanization, industry, and agriculture on water resource supply, timely DOC information may be critical. We have developed here a new paradigm, a dynamic data driven application system (DDDAS), for estimating the real-time load of DOC into a river. This DDDAS consisted of the following four components: (1) a Visual Basic (VB) program for downloading US Geological Survey real-time chlorophyll and discharge data; (2) a STELLA model for evaluating real-time DOC load based on the relationship between chlorophyll a, DOC, and river discharge; (3) a batch file for linking the VB program and STELLA model; and (4) a Microsoft Windows Scheduled Tasks wizard for executing the model and displaying output on a computer screen at selected times. Results show that the real-time load of DOC into the St. Johns River basin near Satsuma, Putnam County, Florida, USA varied over a range from -13,143 to 29,248 kg/h at the selected site in Florida, USA. The negative loads occurred because of the back flow in the estuarine reach of the river. The cumulative load of DOC in the river for the selected site at the end of the simulation (178 hours) was about 1.2 tons. Our results support the utility of the DDDAS developed in this study for estimating the real-time variations of DOC in river ecosystems.

  11. Direct analysis of δ13C and concentration of dissolved organic carbon (DOC) in environmental samples by TOC-IRMS

    Kirkels, Frédérique; Cerli, Chiara; Federherr, Eugen; Kalbitz, Karsten


    Dissolved organic carbon (DOC) plays an important role in carbon cycling in terrestrial and aquatic systems. Stable isotope analysis (delta 13C) of DOC could provide valuable insights in its origin, fluxes and environmental fate. Precise and routine analysis of delta 13C and DOC concentration are therefore highly desirable. A promising, new system has been developed for this purpose, linking a high-temperature combustion TOC analyzer trough an interface with a continuous flow isotope ratio mass spectrometer (Elementar group, Hanau, Germany). This TOC-IRMS system enables simultaneous stable isotope (bulk delta 13C) and concentration analysis of DOC, with high oxidation efficiency by high-temperature combustion for complex mixtures as natural DOC. To give delta 13C analysis by TOC-IRMS the necessary impulse for broad-scale application, we present a detailed evaluation of its analytical performance for realistic and challenging conditions inclusive low DOC concentrations and environmental samples. High precision (standard deviation, SD predominantly memory effects, no concentration/volume effects and a wide linearity. Low DOC concentrations (highlighted by automated, online analysis, a variable injection volume, high throughput and no extensive maintenance. Sample analysis is simple, using small aliquots and with minimal sample preparation. Further investigations should focus on complex, saline matrices and very low DOC concentrations, to achieve a potential lower limit of 0.2 mgC/L. High-resolution, routine delta 13C analysis of DOC by TOC-IRMS offers opportunities for wide-scale application in terrestrial, freshwater and marine research to elucidate the role of DOC in biogeochemical processes and ecosystem functioning.

  12. Development of a Self-Consistent Model of Plutonium Sorption: Quantification of Sorption Enthalpy and Ligand-Promoted Dissolution

    Powell, Brian [Clemson Univ., SC (United States); Kaplan, Daniel I [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Arai, Yuji [Univ. of Illinois, Urbana-Champaign, IL (United States); Becker, Udo [Univ. of Michigan, Ann Arbor, MI (United States); Ewing, Rod [Stanford Univ., CA (United States)


    This university lead SBR project is a collaboration lead by Dr. Brian Powell (Clemson University) with co-principal investigators Dan Kaplan (Savannah River National Laboratory), Yuji Arai (presently at the University of Illinois), Udo Becker (U of Michigan) and Rod Ewing (presently at Stanford University). Hypothesis: The underlying hypothesis of this work is that strong interactions of plutonium with mineral surfaces are due to formation of inner sphere complexes with a limited number of high-energy surface sites, which results in sorption hysteresis where Pu(IV) is the predominant sorbed oxidation state. The energetic favorability of the Pu(IV) surface complex is strongly influenced by positive sorption entropies, which are mechanistically driven by displacement of solvating water molecules from the actinide and mineral surface during sorption. Objectives: The overarching objective of this work is to examine Pu(IV) and Pu(V) sorption to pure metal (oxyhydr)oxide minerals and sediments using variable temperature batch sorption, X-ray absorption spectroscopy, electron microscopy, and quantum-mechanical and empirical-potential calculations. The data will be compiled into a self-consistent surface complexation model. The novelty of this effort lies largely in the manner the information from these measurements and calculations will be combined into a model that will be used to evaluate the thermodynamics of plutonium sorption reactions as well as predict sorption of plutonium to sediments from DOE sites using a component additivity approach.

  13. A comparative study for the sorption of Cd(II) by K-feldspar and sepiolite as soil components, and the recovery of Cd(II) using rhamnolipid biosurfactant.

    Aşçi, Y; Nurbaş, M; Açikel, Y Sağ


    This study investigated the sorption characteristics and recovery of selected heavy metal Cd(II) from K-feldspar and sepiolite, representative soil components, using rhamnolipid biosurfactant. Although the proposed technique was classified as a soil bioremediation process, it can also be applied to treatment of waste waters containing Cd(II) ions with minor modifications. The effect of initial Cd(II) concentration on sorption capacity was characterized by determining the sorption isotherms. Of the four models examined, the Freundlich model showed the best fit for the sorption of Cd(II) on K-feldspar, whereas the Langmuir-model was used successfully to characterize the sorption of Cd(II) on sepiolite. Although a high Cd(II) uptake of 7.49 mmol/kg by K-feldspar was obtained, sepiolite was a superior Cd(II) accumulater, with a maximum Cd(II) uptake of 24.66 mmol Cd(II)/kg. The presence of Cd(II) in the sepiolite or K-feldspar prior to addition of the rhamnolipid generally resulted in less rhamnolipid sorption to sepiolite or K-feldspar. The maximum Cd(II) desorption efficiency by rhamnolipid from K-feldspar was substantially higher than that of sepiolite and determined to be 96% of the sorbed Cd(II), whereas only 10.1% of the sorbed Cd(II) from sepiolite was recovered by rhamnolipid solution.

  14. Sorption of Th(IV) onto ZnO nanoparticles and diatomite-supported ZnO nanocomposite. Kinetics, mechanism and activation parameters

    Yusan, Sabriye; Aslani, Mahmut A.A.; Aytas, Sule [Ege Univ., Izmir (Turkey). Inst. of Nuclear Sciences; Bampaiti, Anastasia; Noli, Fotini [Aristotle University of Thessaloniki (Greece). Dept. of Chemistry; Erenturk, Sema [Istanbul Technical Univ., Ayazaga Campus, Maslak-Istanbul (Turkey). Energy Inst.


    In this study, for the first time ZnO nanoparticles and diatomite-supported ZnO nanocomposite have been utilized as adsorbent for the removal of Th(IV) ions from aqueous solutions under different experimental conditions. The Langmuir, Freundlich, Temkin and Dubinin- Radushkevich (D-R) isotherms were used to analyze the equilibrium data. The sorption equilibrium data were fitted well to the Langmuir isotherm with maximum sorption capacities values was found to be 1.105 mmol/g and 0.320 mmol/g for ZnO nanoparticles and diatomite supported ZnO nanocomposite, respectively. Pseudo-first and pseudo-second order equations, Intraparticle diffusion and Bangham's models were considered to evaluate the rate parameters and sorption mechanism. Sorption kinetics were better reproduced by the pseudo-second order model (R{sup 2} > 0.999), with an activation energy (E{sub a}) of +99.74 kJ/mol and +62.95 kJ/mol for ZnO nanoparticles and diatomite-supported ZnO nanocomposite, respectively. In order to specify the type of sorption reaction, thermodynamic parameters were also determined. The evaluated ΔG* and ΔH* indicate the non-spontaneous and endothermic nature of the reactions. The results of this work suggest that both of the used materials are fast and effective adsorbents for removing Th(IV) from aqueous solutions and chemical sorption plays a role in controlling the sorption rate.

  15. Transformation and sorption of illicit drug biomarkers in sewer biofilms

    Ramin, Pedram; Brock, Andreas Libonati; Causanilles Llanes, Ana


    , 16 drug biomarkers were selected, including the major human metabolites of mephedrone, methadone, cocaine, heroin, codeine and tetrahydrocannabinol (THC). Transformation and sorption of these substances were assessed in targeted batch experiments using laboratory-scale biofilm reactors operated under...

  16. Sorption kinetics and mechanism of various oils into kapok assembly.

    Dong, Ting; Wang, Fumei; Xu, Guangbiao


    Sorption rates of kapok fibers on different oils, such as diesel, cooking oil, used motor oil, and motor oil, were quantitatively evaluated by using a wicking method. Kapok fibers absorbing different oils exhibited large differences in terms sorption coefficients. Microscopic observations of oil wetting on a single kapok showed that the four oils had varying wettability and adhesiveness to kapok, but that all of them penetrated into kapok lumens quickly because of the fiber's low surface energy, which was 40.64 mN/m, and extreme hydrophobicity, with a water contact angle up to 151°. After treatment with chloroform, there were slight changes in oil absorbencies to kapok, but the sorption coefficients for the four oils increased markedly. SEM demonstrated that chloroform treatments caused the smooth surface of the kapok fibers to become highly roughened, with densely vertical grooves that provided more available surface and a larger driving force for oil sorption through the fiber assembly.

  17. Sorption of caesium in soils from various regions of Libya

    Shenber, M.A.; Johanson, K.J. (Dept. of Radioecology, Swedish Univ. of Agricultural Sciences, Uppsala (Sweden))


    The sorption characteristics of caesium in some common Libyan soils from various regions of Libya were studied using batch techniques. The influences of clay content, contact time and various concentrations of Cs[sup +], K[sup +], and NH[sub 4][sup +] in the solution on the sorption ratio for Cs[sup +] were determined by using tracer [sup 134]Cs. All experiments were carried out in the presence of a supporting electrolyte (0.01 N CaCl[sub 2]). An apparent steady state was reached in 4 - 7 days. Important parameters influencing the sorption were clay content, pH, and the concentrations of other cations, in particular K[sup +] and NH[sub 4][sup +] which compete with Cs[sup +] for the sorption sites. (orig.).

  18. Moisture sorption isotherms of castor beans. Part 2: Thermodynamic properties

    André L. D. Goneli

    Full Text Available ABSTRACT Knowledge on the water sorption within agricultural products is extremely important for decision making during post-harvest procedures. In order to improve this knowledge, thermodynamic properties regarding water sorption provide useful data. Thermodynamic properties of castor beans, related to sorption, were determined. Static gravimetric technique under different conditions of temperature (25, 35, 45 and 55 ± 1 °C was used. Saturated salt solutions in the range of 37-87% ± 2% were utilized to create the required controlled humidity environment. After the sorption procedure, differential enthalpy, differential entropy and Gibbs free energy of this process were calculated and decreased with increased values of equilibrium moisture content.

  19. suitability of murram for phosphorus sorption in constructed wetlands


    significantly influence phosphorus sorption on 1-2mm grain. Moshi Pumice has high ... properties of the substrate (Fe, Mg, Al-, Ca-minerals, specific surface area and .... incubator (WTB binder type, model 720, German) for twenty-four hours.

  20. Synthesis and characterization of poly(maleic acid)-grafted crosslinked chitosan nanomaterial with high uptake and selectivity for Hg(II) sorption.

    Ge, Huacai; Hua, Tingting


    Chitosan-poly(maleic acid) nanomaterial (PMACS) with the size of 400-900nm was synthesized by grafting poly(maleic acid) onto chitosan and then crosslinking with glutaraldehyde. The synthesis conditions were optimized. The structure and morphology of PMACS were characterized by FT-IR, XRD, SEM and TGA. PMACS was used to adsorb some heavy metal ions such as Hg(II), Pb(II), Cu(II), Cd(II), Co(II), and Zn(II). The results indicated that PMACS had selectivity for Hg(II) sorption. The effects of various variables for sorption of Hg(II) were further explored. The maximum capacity for Hg(II) sorption was found to be 1044mgg(-1) at pH 6.0, which could compare with the maximal value of the recently reported other sorbents. The sorption followed the pseudo-second-order kinetics and Langmuir isotherm models. The rising of temperature benefited the uptake and the sorption was a spontaneous chemical process. The sorbent could be reused with EDTA. Hence, the nanomaterial would be used as a selective and high uptake sorbent in the removal of Hg(II) from effluents. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Optimization, equilibrium, kinetic, thermodynamic and desorption studies on the sorption of Cu(II) from an aqueous solution using marine green algae: Halimeda gracilis.

    Jayakumar, R; Rajasimman, M; Karthikeyan, C


    The aptitude of marine green algae Helimeda gracilis for sorption of Cu(II) ions from an aqueous solution was studied in batch experiments. The effect of relevant parameters such as function of pH, sorbent dosage, agitation speed and contact time was evaluated by using Response surface methodology (RSM). A maximum percentage removal of Cu (II) by Halimeda gracilis occurs at pH-4.49, sorbent dosage-1.98g/L, agitation speed-119.43rpm and contact time-60.21min. Further, the sorbent was characterized by using Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron microscope (SEM) analysis. Experimental data were analyzed in terms of pseudo-first order, pseudo-second order, intraparticle diffusion, power function and elovich kinetic models. The results showed that the sorption process of Cu(II) ions followed well pseudo-second order kinetics. The sorption data of Cu(II) ions at 308.15K are fitted to Langmuir, Freundlich, Dubinin-Radushkevich (D-R), Temkin, Sips and Toth isotherms. Sorption of Cu(II) onto marine green algae Helimeda gracilis followed the Langmuir and Toth isotherm models (R(2)=0.998 and R(2)=0.999) with the maximum sorption capacity of 38.46 and 38.07mg/g. The calculated thermodynamic parameters such as ΔG°, ΔH° and ΔS° showed that the sorption of Cu(II) ions onto Helimeda gracilis biomass was feasible, spontaneous and endothermic. Desorption study shows that the sorbent could be regenerated using 0.2M HCl solution, with up to 89% recovery. Copyright © 2015 Elsevier Inc. All rights reserved.

  2. Understanding mechanisms to predict and optimize biochar for agrochemical sorption

    Hall, Kathleen; Gámiz, Beatriz; Cox, Lucia; Spokas, Kurt; Koskinen, William


    The ability of biochars to bind various organic compounds has been widely studied due to the potential effects on pesticide fate in soil and interest in the adoption of biochar as a "low-cost" filter material. However, the sorptive behaviors of biochars are extremely variable and much of the reported data is limited to specific biochar-chemical interactions. The lack of knowledge regarding biochar sorption mechanisms limits our current ability to predict and optimize biochar's use. This work unveils mechanistic drivers of organic pesticide sorption on biochars through targeted alteration of biochar surface chemistry. Changes in the quantity and type of functional groups on biochars and other black carbon materials were achieved through treatments with H2O2, and CO2, and characterized using Fourier transform infrared spectroscopy and scanning electron microscope (SEM/EDX). The sorption capacities of these treated biochars were subsequently measured to evaluate the effects of different surface moieties on the binding of target herbicides cyhalofop acid ((R)-2-[4-(4-cyano-2-fluorophenoxy)phenoxy]propionic acid) and clomazone (2-[(2-chlorophenyl)methyl]-4,4-dimethyl-1,2-oxazolidin-3-one). Sorption of both herbicides on the studied biochars increased following H2O2 activation; however, the influence of the H2O2 activation on sorption was more pronounced for cyhalofop acid (pKa = 3.9) than clomazone, which is non-ionizable. Increased cyhalofop acid sorption on H2O2 treated biochars can be attributed to the increase in oxygen containing functional groups as well as the decrease in biochar pH. In contrast, CO2 activation reduced the sorption of cyhalofop acid compared to untreated biochar. FTIR data suggest the reduced sorption on CO2 -treated biochar was due to the removal of surface carboxyl groups, further supporting the role of specific functionality in the sorption of ionizable herbicides. Results from this work offer insight into the mechanisms of sorption and

  3. Efficient sorption of Cu(2+) by composite chelating sorbents based on potato starch-graft-polyamidoxime embedded in chitosan beads.

    Dragan, Ecaterina Stela; Apopei Loghin, Diana Felicia; Cocarta, Ana Irina


    Ionic composites based on cross-linked chitosan (CS) as matrix and poly(amidoxime) grafted on potato starch (AOX) as entrapped chelating resin were prepared as beads, for the first time in this work, by two strategies: (1) thorough mixing of previously prepared AOX in the CS solution followed by the bead formation and (2) thorough mixing of the potato starch-g-poly(acrylonitrile) (PS-g-PAN) copolymer in the initial CS solution, followed by bead formation, the amidoximation of the nitrile groups taking place inside the beads. Ionotropic gelation in tripolyphosphate was used to obtain the composite beads, and in situ covalent cross-linking by epichlorohydrin was carried out to stabilize the beads in the acidic pH range. Fourier transform infrared spectroscopy and the swelling ratio values in the acidic pH range confirmed the influence of the synthesis strategy on the structure of the CS/AOX composites. Scanning electron microscopy was employed to reveal the morphology of the novel composites, both before and after their loading with Cu(2+). The binding capacity of Cu(2+) ions as a function of sorbent composition, synthesis strategy, pH, sorbent dose, contact time, initial concentration of Cu(2+), and temperature was examined in batch mode. The main difference between the composites prepared with the two strategies consisted of the higher sorption capacity and the much faster settlement of the equilibrium sorption for the composite prepared by the in situ amidoximation of PS-g-PAN. The Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, and Sips isotherms were applied to fit the sorption equilibrium data. The maximum equilibrium sorption capacity, qm, evaluated by the Langmuir model at 25 °C was 133.15 mg Cu(2+)/g for the CS/AOX composite beads prepared with the first strategy and 238.14 mg Cu(2+)/g for the CS/AOX composite beads prepared with the second strategy, at the same AOX content. The pseudo-second order kinetic model well fitted the sorption kinetics data

  4. Sorption, Desorption and Diffusion of Tc Under Anaerobic Conditions


    The sorption and diffusion of Tc on granite under anaerobic conditions were investigated. Influencesof pH values, ferrous minerals(reduced iron powder or magnetite), bentonite, concentration of cations andanion (Fe3+, Fe2+ and CO32-) on the distribution coefficient, Kd, were studied. The sorption mechanism of99Tc on granite was analyzed by the desorption method of adding H2O2 into desorption solvent. Based on

  5. Sorption heat engines: simple inanimate negative entropy generators

    Muller, Anthonie W. J.; Schulze-Makuch, Dirk


    The name 'sorption heat engines' is proposed for simple negative entropy generators that are driven by thermal cycling and work on alternating adsorption and desorption. These generators are in general not explicitly recognized as heat engines. Their mechanism is applicable to the fields of engineering, physics, chemistry, geology, and biology, in particular the origin of life. Four kinds of sorption heat engines are distinguished depending on the occurrence of changes in the adsorbent or ads...

  6. Groundwater transport modeling with nonlinear sorption and intraparticle diffusion

    Singh, Anshuman; Allen-King, Richelle M.; Rabideau, Alan J.


    Despite recent advances in the mechanistic understanding of sorption in groundwater systems, most contaminant transport models provide limited support for nonideal sorption processes such as nonlinear isotherms and/or diffusion-limited sorption. However, recent developments in the conceptualization of "dual mode" sorption for hydrophobic organic contaminants have provided more realistic and mechanistically sound alternatives to the commonly used Langmuir and Freundlich models. To support the inclusion of both nonlinear and diffusion-limited sorption processes in groundwater transport models, this paper presents two numerical algorithms based on the split operator approach. For the nonlinear equilibrium scenario, the commonly used two-step split operator algorithm has been modified to provide a more robust treatment of complex multi-parameter isotherms such as the Polanyi-partitioning model. For diffusion-limited sorption, a flexible three step split-operator procedure is presented to simulate intraparticle diffusion in multiple spherical particles with different sizes and nonlinear isotherms. Numerical experiments confirmed the accuracy of both algorithms for several candidate isotherms. However, the primary advantages of the algorithms are: (1) flexibility to accommodate any isotherm equation including "dual mode" and similar expressions, and (2) ease of adapting existing grid-based transport models of any dimensionality to include nonlinear sorption and/or intraparticle diffusion. Comparisons are developed for one-dimensional transport scenarios with different isotherms and particle configurations. Illustrative results highlight (1) the potential influence of isotherm model selection on solute transport predictions, and (2) the combined effects of intraparticle diffusion and nonlinear sorption on the plume transport and flushing for both single-particle and multi-particle scenarios.

  7. Sorption properties of greenwaste biochar for two triazine pesticides.

    Zheng, Wei; Guo, Mingxin; Chow, Teresa; Bennett, Douglas N; Rajagopalan, Nandakishore


    Biochar is a carbon-rich product generated from biomass through pyrolysis. This study evaluated the ability of an unmodified biochar to sorb two triazine pesticides - atrazine and simazine, and thereby explored potential environmental values of biochar on mitigating pesticide pollution in agricultural production and removing contaminants from wastewater. A greenwaste biochar was produced by heating waste biomass under the oxygen-limited condition at 450 degrees C. The effects of several experimental parameters, including biochar particle size, contact time, solid/solution ratio, and solution pH on the sorption of atrazine and simazine were comprehensively investigated. The biochar with small particle size needed less time to reach sorption equilibrium. The sorption affinity of the biochar for the two pesticides increased with decreasing solid/solution ratio. The sorbed amounts (C(s)) of atrazine and simazine increased from 451 to 1158 mg/kg and 243 to 1066 mg/kg, respectively, when the solid/solution ratio decreased from 1:50 to 1:1000 (g/mL). The sorption of the biochar for both pesticides was favored by low pH. The sorption isotherms of atrazine and simazine on the biochar are nonlinear and follow a Freundlich model. When atrazine and simazine co-existed, a competitive sorption occurred between these two pesticides on the biochar, reflecting a decrease in sorption capacity (K(f)) from 435 to 286 for atrazine and from 514 to 212 for simazine. Combined adsorption and partition mechanisms well depicted sorption of atrazine and simazine on carbonized and noncarbonized fractions of the biochar in the single-solute and co-solute systems.


    B. Kristoffer Segerholm,


    Full Text Available Moisture sorption in wood-plastic composites (WPCs affects their durability and dimensional stability. In certain outdoor exposures, the moisture properties of WPCs are altered due to e.g. cracks induced by swelling and shrinkage of the components, as well as UV degradation or biological attack. The aim of this work was to study the effect of different artificial ageing routes on the moisture sorption properties of WPCs. Extruded WPCs were prepared with either unmodified or acetylated wood and recycled high-density polyethylene (HDPE. The WPC samples were artificially aged involving water soaking, artificial weathering, and white- or brown-rot decay in different combinations. After the ageing, the samples were conditioned in either 65% or 90% relative humidity (RH until equilibrium moisture content was reached. A dynamic moisture sorption analyzer was used to monitor the sorption rate of samples subjected to a climate change from 65% to 90% RH. Scanning electron microscopy was used to study the surface morphology of the aged composites. Results showed that the artificial weathering caused cracking of the HDPE matrix at the composite surface, as well as a wood-matrix debonding, resulting in an increased moisture sorption rate. The WPC samples subjected to white-rot decay showed the highest moisture sorption rate.

  9. Surface complexation modeling of americium sorption onto volcanic tuff.

    Ding, M; Kelkar, S; Meijer, A


    Results of a surface complexation model (SCM) for americium sorption on volcanic rocks (devitrified and zeolitic tuff) are presented. The model was developed using PHREEQC and based on laboratory data for americium sorption on quartz. Available data for sorption of americium on quartz as a function of pH in dilute groundwater can be modeled with two surface reactions involving an americium sulfate and an americium carbonate complex. It was assumed in applying the model to volcanic rocks from Yucca Mountain, that the surface properties of volcanic rocks can be represented by a quartz surface. Using groundwaters compositionally representative of Yucca Mountain, americium sorption distribution coefficient (Kd, L/Kg) values were calculated as function of pH. These Kd values are close to the experimentally determined Kd values for americium sorption on volcanic rocks, decreasing with increasing pH in the pH range from 7 to 9. The surface complexation constants, derived in this study, allow prediction of sorption of americium in a natural complex system, taking into account the inherent uncertainty associated with geochemical conditions that occur along transport pathways.

  10. Patterns of dissolved organic carbon (DOC) and nitrogen (DON) fluxes in deciduous and coniferous forests under historic high nitrogen deposition

    Sleutel, S.; Vandenbruwane, J.; de Schrijver, A.; Wuyts, K.; Moeskops, B.; Verheyen, K.; de Neve, S.


    Numerous recent studies have indicated that dissolved organic carbon (DOC) and nitrogen (DON) play an important role in C and N cycling in natural ecosystems, and have shown that N deposition alters the concentrations and fluxes of dissolved organic substances and may increase leaching losses from forests. Our study was set up to accurately quantify concentrations and flux patterns of DOC, DON and dissolved inorganic nitrogen (DIN) in deciduous and coniferous forest in Flanders under historical high nitrogen deposition. We measured DOC, DON and DIN concentrations at two weekly intervals in a silver birch (SB) stand, a corsican pine (CP) stand and a pine stand with higher N deposition (CPN), and used the SWAP model (calibrated with PEST) for generating accurate water and matter fluxes. The input with precipitation was an important source of DON, but not for DOC. Release of DOC from the forest floor was minimally affected by forest type, but higher N deposition (CPN stand) caused an 82% increase of DOC release from the forest floor. Adsorption to mineral soil material rich in iron and/or aluminum oxyhydroxides was suggested to be the most important process removing DOC from the soil solution, responsible for substantial retention (67-84%) of DOC entering the mineral soil profile with forest floor leachate. Generally, DON was less reactive (i.e. less removal from the soil solution) than DOC, resulting in decreasing DOC/DON ratios with soil depth. We found increased DOC retention in the mineral soil as a result of higher N deposition (84 kg N ha-1 yr-1 additional DOC retention in CPN compared to CP). Overall DON leaching losses were 2.2, 3.3 and 5.0 kg N ha-1 yr-1 for SB, CP and CPN, respectively, contributing between 9-28% to total dissolved N (TDN) leaching. DON loss from SB and CP was not much higher than from unpolluted forests, and its relative contribution to TDN leaching was mainly determined by (large) differences in DIN leaching. The large TDN leaching losses

  11. Patterns of dissolved organic carbon (DOC and nitrogen (DON fluxes in deciduous and coniferous forests under historic high nitrogen deposition

    S. Sleutel


    Full Text Available Numerous recent studies have indicated that dissolved organic carbon (DOC and nitrogen (DON play an important role in C and N cycling in natural ecosystems, and have shown that N deposition alters the concentrations and fluxes of dissolved organic substances and may increase leaching losses from forests. Our study was set up to accurately quantify concentrations and flux patterns of DOC, DON and dissolved inorganic nitrogen (DIN in deciduous and coniferous forest in Flanders under historical high nitrogen deposition. We measured DOC, DON and DIN concentrations at two weekly intervals in a silver birch (SB stand, a corsican pine (CP stand and a pine stand with higher N deposition (CPN, and used the SWAP model (calibrated with PEST for generating accurate water and matter fluxes. The input with precipitation was an important source of DON, but not for DOC. Release of DOC from the forest floor was minimally affected by forest type, but higher N deposition (CPN stand caused an 82% increase of DOC release from the forest floor. Adsorption to mineral soil material rich in iron and/or aluminum oxyhydroxides was suggested to be the most important process removing DOC from the soil solution, responsible for substantial retention (67–84% of DOC entering the mineral soil profile with forest floor leachate. Generally, DON was less reactive (i.e. less removal from the soil solution than DOC, resulting in decreasing DOC/DON ratios with soil depth. We found increased DOC retention in the mineral soil as a result of higher N deposition (84 kg N ha−1 yr−1 additional DOC retention in CPN compared to CP. Overall DON leaching losses were 2.2, 3.3 and 5.0 kg N ha−1 yr−1 for SB, CP and CPN, respectively, contributing between 9–28% to total dissolved N (TDN leaching. DON loss from SB and CP was not much higher than from unpolluted forests, and its relative contribution to TDN leaching was mainly determined by

  12. Concentration, UV-spectroscopic characteristics and fractionation of DOC in stormflow from an urban stream, Southern California, USA

    Izbicki, J.A.; Pimentel, I.M.; Johnson, R.; Aiken, G.R.; Leenheer, J.


    The composition of dissolved organic carbon (DOC) in stormflow from urban areas has been greatly altered, both directly and indirectly, by human activities and there is concern that there may be public health issues associated with DOC, which has unknown composition from different sources within urban watersheds. This study evaluated changes in the concentration and composition of DOC in stormflow in the Santa Ana River and its tributaries between 1995 and 2004 using a simplified approach based on the differences in the optical properties of DOC and using operationally defined differences in molecular weight and solubility. The data show changes in the composition of DOC in stormflow during the rainy season and differences associated with runoff from different parts of the basin, including extensive upland areas burned prior to the 2004 rainy season. Samples were collected from the Santa Ana River, which drains ???6950 km2 of the densely populated coastal area of southern California, during 23 stormflows between 1995 and 2004. Dissolved organic carbon (DOC) concentrations during the first stormflows of the ?winter' (November to March) rainy season increased rapidly with streamflow and were positively correlated with increased faecal indicator bacteria concentrations. DOC concentrations were not correlated with streamflow or with other constituents during stormflows later in the rainy season and DOC had increasing UV absorbance per unit carbon as the rainy season progressed. DOC concentrations in stormflow from an urban drain tributary to the river also increased during stormflow and were greater than concentrations in the river. DOC concentrations in stormflow from a tributary stream, draining urban and agricultural land that contained more than 320 000 animals, mostly dairy cows, were higher than concentrations in stormflow from the river and from the urban drain. Fires that burned large areas of the basin before the 2004 rainy season did not increase DOC

  13. Sorption of organic water pollutants on dead vegetable biomass; Sorption organischer Wasserschadstoffe an abgestorbene pflanzliche Biomasse

    Kraeuter, A.


    Hemp-derived biological sorption agents were produced, and their physical, chemical and sorptive characteristics were tested in batch and filter tests. The experiments were accompanied by model calculations. In the natural state, the sorption agents had a kation exchange capacity of 0.1-0.3 mmol/g, modified sorption agents had about 2 mmol/g. Kationized hemp had values of 0.34 mmol/g and thermally modified hemp absorption agents absorbed more than 1.2 mmol/g of dichlorophenol. In the case of a liquid effluent from a textile dyeing plant, only a discoloration effect was achieved. The absorption agents can be regenerated, combusted or composted after use. [German] Im Rahmen dieser Arbeit wurden naturbelassene und modifizierte Billig-Biosorbentien aus Hanfschaeben zur Entfernung organischer Schadstoffe aus Waessern hergestellt und ihre physikalischen, chemischen und sorptiven Eigenschaften in Batch- und Filterversuchen untersucht. Wegen der Komplexheit des Systems ''Biosorption organischer Wasserschadstoffe'' wurden die ermittelten Sorptionsisothermen mit den Ansaetzen nach Langmuir und Freundlich beschrieben. Die Sorptionskinetik und das Durchbruchsverhalten wurde ebenfalls mit einfachen Ansaetzen modelliert. Naturbelassene Hanfschaeben erreichten Kationenaustauschkapazitaeten von 0,1-0,3 mmol/g, entsprechend modifizierte Hanfschaeben ca. 2 mmol/g. Kationisierte Hanfschaeben dagegen erreichten Anionenaustauschkapazitaeten von 0,34 mmol/g und thermisch modifizierte Hanfschaeben sorbierten bis ueber 1,2 mmol/g Dichlorphenol. Bei der Behandlung eines Abwassers aus einer Textilfaerberei beschraenkte sich die Reinigungsleistung der hergestellten Biosorbentien auf eine Entfaerbung. Nach Schadstoffbeladung koennen die Hanfschaeben regeneriert, thermisch verwertet oder kompostiert werden. (orig.)

  14. Effect of Colloids on the Calculation of Distribution Coefficients in Studies of Metal Sorption on Organic Matter

    Straka, A. M.; Schijf, J.


    organic ligand released, as monitored by DOC concentrations, is nearly identical in each case. All sorption edges were satisfactorily modeled with an appropriate pH-dependent complexation model. At 0.05 M ionic strength, distribution coefficients calculated from the 0.22 μm filtrates show an unexpected inversion around pH 5 to decreasing sorption with increasing pH, most prominently for the MREEs, clearly reflecting the erroneous omission of YREE colloids from the particulate fraction. This feature could be completely reversed by using the modeled colloidal contributions to correct the measurements. A similar correction of the 0.5 and 5.0 M data revealed a more insidious effect on both absolute and relative distribution coefficients that was not otherwise apparent from their pH-dependent behavior. Failure to account for colloid-bound metals can ostensibly lead to a substantial misinterpretation of experimental results, an issue that is not sufficiently acknowledged or addressed in many metal sorption studies.

  15. Colaboración del alumnado en la nube: una experiencia con Google Docs

    Arufe Martínez, María Isabel; Moreno Brea, Manuela de Jesús; Arellano López, Juana Mª; Albendín García, Gemma


    En este trabajo presentamos el análisis de una actividad colaborativa basada en Google Docs. La experiencia de innovación docente se ha diseñado en el marco de la asignatura Toxicología Ambiental y Ecotoxicología, materia troncal de 4º curso de la Licenciatura en Ciencias Ambientales. El trabajo se enmarca en el proyecto "Estrategias digitales para fomentar el aprendizaje y el trabajo colaborativo" (Código PI2_12_043), dentro de la Convocatoria de Proyectos y Mejora Docente del curso 2011/...

  16. Exploring the potential of DOC fluorescence as proxy for groundwater contamination by pesticides

    Farlin, Julien; Gallé, Tom; Bayerle, Michael; Pittois, Denis; Huck, viola


    Of the different water quality surrogates the fluorescence of dissolved organic content (FDOC) appears particularly promising due to its sensitivity and specificity. A complete spectrum of FDOC can be obtained using bench top instruments scanning a spectral space going from short wavelength UV to visible blue, yielding a so-called an excitation-emission matrix (EEM). The raw EEM can be either used directly for correlation analysis with the variable of interest, or first decomposed into underlying elements corresponding to different groups of organic compounds displaying similar properties using multiway techniques such as Parallel factor analysis (PARAFAC). Fluorescence spectroscopy has up to now only rarely been applied specifically to groundwater environments. The objective of the project was to explore systematically the possibilities offered by FDOC and PARAFAC for the assessment of groundwater contamination by pesticides, taking into account the transit time from the pesticide source to the groundwater outlet. Three sites corresponding to different transit times were sampled: -one spring regularly contaminated by surface water from a nearby stream (sub-daily to daily response to fast-flow generating storm events) -one spring displaying a weekly to monthly response to interflow -sampling along a flowline consisting of a series of springs and an observation well situated upgradient with mean transit times difference of several years Preliminary results show that a three component PARAFAC model is sufficient to decompose the raw EEMs, which is less than the seven or eight component models often encountered in surface water studies. For the first site, one component in the protein-like region 275(excitation)/310 (emission) nm measured in the stream samples was filtrered completely by the aquifer and did not appear in the spring samples. The other two components followed roughly the trend of the DOC and pesticide breakthrough. For the second site, soil sampling of

  17. Production and decomposition of new DOC by marine plankton communities: carbohydrates, refractory components and nutrient limitation

    Kragh, T.; Søndergaard, Morten


    The accumulation and biodegradation of dissolved organic carbon (DOC) and dissolved and particulate combined neutral sugars (DCNS, PCNS) were followed during a period of 22 days in experimental marine phytoplankton incubations. Five different growth regimes were established in 11 m(3) coastal mes...... driven towards the most severe P limitation both with and without silicate. This shows that RDOC can be produced directly by the phytoplankton or indirectly in food web processes during the later stages of a bloom where the phytoplankton is P limited...

  18. Moisture sorption characteristics of microalgae Spirulina platensis

    E. G. Oliveira


    Full Text Available In recent times, the microalgae Spirulina platensis has been used as a functional ingredient in several food applications; its process involving drying and storage steps. Moisture equilibrium data for adsorption isotherms of microalgae Spirulina were investigated at 10, 20 and 30ºC and for desorption, at 40, 50 and 60ºC, using the gravimetric static method. The experimental data were analyzed by GAB and BET models. The GAB equation showed the best fitting to the experimental data with R² ≈ 99% and MRE < 10%. The water surface area values calculated by GAB and BET models were very similar. The isosteric heats were determined by application of Clausius-Clapeyron equation to sorption isotherms obtained from the best-fitting equation. The isosteric heat and the entropy of desorption isotherm presented similar behavior, with a sharp change in an equilibrium moisture content of 10%. The enthalpy-entropy compensation theory was applied to the isotherms, indicating that they are enthalpy-controlled.

  19. Vertical barriers with increased sorption capacities

    Bradl, H.B. [Bilfinger + Berger Bauaktiengesellschaft, Mannheim (Germany)


    Vertical barriers are commonly used for the containment of contaminated areas. Due to the very small permeability of the barrier material which is usually in the order of magnitude of 10-10 m/s or less the advective contaminant transport can be more or less neglected. Nevertheless, there will always be a diffusive contaminant transport through the barrier which is caused by the concentration gradient. Investigations have been made to increase the sorption capacity of the barrier material by adding substances such as organoclays, zeolites, inorganic oxides and fly ashes. The contaminants taken into account where heavy metals (Pb) and for organic contaminants Toluole and Phenantrene. The paper presents results of model calculations and experiments. As a result, barrier materials can be designed {open_quotes}tailor-made{close_quotes} depending on the individual contaminant range of each site (e.g. landfills, gasworks etc.). The parameters relevant for construction such as rheological properties, compressive strength and permeability are not affected by the addition of the sorbents.

  20. Measurement of Sorption-Induced Strain

    Eric P. Robertson; Richard L. Christiansen


    Strain caused by the adsorption of gases was measured in samples of subbituminous coal from the Powder River basin of Wyoming, U.S.A. and high-volatile bituminous coal from east-central Utah, U.S.A. using an apparatus developed jointly at the Idaho National Laboratory (Idaho Falls, Idaho, U.S.A.) and Colorado School of Mines (Golden, Colorado, U.S.A.). The apparatus can be used to measure strain on multiple small coal samples based on the optical detection of the longitudinal strain instead of the more common usage of strain gauges, which require larger samples and longer equilibration times. With this apparatus, we showed that the swelling and shrinkage processes were reversible and that accurate strain data could be obtained in a shortened amount of time. A suite of strain curves was generated for these coals using gases that included carbon dioxide, nitrogen, methane, helium, and various mixtures of these gases. A Langmuir-type equation was applied to satisfactorily model the strain data obtained for pure gases. The sorption-induced strain measured in the subbituminous coal was larger than the high-volatile bituminous coal for all gases tested over the range of pressures used in the experimentation, with the CO2-induced strain for the subbituminous coal over twice as great at the bituminous coal.

  1. Surface complexation modeling of inositol hexaphosphate sorption onto gibbsite.

    Ruyter-Hooley, Maika; Larsson, Anna-Carin; Johnson, Bruce B; Antzutkin, Oleg N; Angove, Michael J


    The sorption of Inositol hexaphosphate (IP6) onto gibbsite was investigated using a combination of adsorption experiments, (31)P solid-state MAS NMR spectroscopy, and surface complexation modeling. Adsorption experiments conducted at four temperatures showed that IP6 sorption decreased with increasing pH. At pH 6, IP6 sorption increased with increasing temperature, while at pH 10 sorption decreased as the temperature was raised. (31)P MAS NMR measurements at pH 3, 6, 9 and 11 produced spectra with broad resonance lines that could be de-convoluted with up to five resonances (+5, 0, -6, -13 and -21ppm). The chemical shifts suggest the sorption process involves a combination of both outer- and inner-sphere complexation and surface precipitation. Relative intensities of the observed resonances indicate that outer-sphere complexation is important in the sorption process at higher pH, while inner-sphere complexation and surface precipitation are dominant at lower pH. Using the adsorption and (31)P MAS NMR data, IP6 sorption to gibbsite was modeled with an extended constant capacitance model (ECCM). The adsorption reactions that best described the sorption of IP6 to gibbsite included two inner-sphere surface complexes and one outer-sphere complex: ≡AlOH + IP₆¹²⁻ + 5H⁺ ↔ ≡Al(IP₆H₄)⁷⁻ + H₂O, ≡3AlOH + IP₆¹²⁻ + 6H⁺ ↔ ≡Al₃(IP₆H₃)⁶⁻ + 3H₂O, ≡2AlOH + IP₆¹²⁻ + 4H⁺ ↔ (≡AlOH₂)₂²⁺(IP₆H₂)¹⁰⁻. The inner-sphere complex involving three surface sites may be considered to be equivalent to a surface precipitate. Thermodynamic parameters were obtained from equilibrium constants derived from surface complexation modeling. Enthalpies for the formation of inner-sphere surface complexes were endothermic, while the enthalpy for the outer-sphere complex was exothermic. The entropies for the proposed sorption reactions were large and positive suggesting that changes in solvation of species play a major role in driving

  2. Sorption and biodegradation of propylparaben in greywater by aerobic attached-growth biomass.

    Song, Haihong; Alfiya, Yuval; Dubowski, Yael; Friedler, Eran


    Greywater (GW) is becoming an important alternative water source for non-potable purposes, but requires treatment to remove contaminants, including micropollutants that in GW mainly originate from personal care products. Biofilters are commonly used for onsite GW treatment, but there are still significant knowledge gaps regarding their ability and mechanism of micropollutants removal. This study investigates the removal of propylparaben (PPB) by aerobic attached-growth biomass, quantifying the kinetics and the interplay between sorption and biodegradation. The ability of biomass, collected from a pilot scale biofilter treating real GW, to eliminate PPB from both synthetic greywater (SGW) and deionized (DI) water was studied in laboratory batch experiments. Elimination of PPB was found to proceed via sorption to biomass followed by biodegradation. Sorption of PPB by biomass in SGW and in DI water exhibited similar kinetics, fitting Langmuir isotherm with the maximum adsorbed amount of 9.8mgPPB gbiomass(-1). PPB biodegradation exhibited first-order kinetics in both SGW and DI water, with a 30h lag-phase in SGW and no lag-phase in DI water. This difference is attributed to presence of readily-biodegradable organic matter in the SGW. Actual PPB degradation rate in both cases (excluding the lag phase in SGW) was very similar, 62mgPPB gbiomass(-1)d(-1), yielding almost full mineralization. These findings show the relative contribution of the major processes involved in PPB elimination by biofilters and can be applied for designing GW treatment units. Copyright © 2017 Elsevier B.V. All rights reserved.

  3. Energetic features of copper and lead sorption by innovative aminoalcohol-functionalized cobalt phyllosilicates.

    Melo, Maurício Alves; Airoldi, Claudio


    Inorganic-organic cobalt phyllosilicate hybrids were synthesized by the sol-gel procedure under mild non-hydrothermal conditions with a silicon precursor, formed through individual reactions between the silane 3-glycidoxypropyltriethoxysilane and the aminoalcohols ethanol- or diethanolamine. These procedures generated talc-like phyllosilicates containing pendant organic chains with nitrogen and oxygen basic centres located in the interlamellar region. For organofunctionalized phyllosilicates the lamellar structure obtained through the sol-gel method was confirmed by X-ray powder diffraction, while elemental analysis indicated that the densities of the organic groups attached to the new matrices were 3.31 ± 0.05 and 3.08 ± 0.07 mmol g(-1) for hybrids functionalized with ethanol- and diethanolamines, respectively. Infrared spectroscopy and nuclear magnetic resonance in the solid state for (13)C and (29)Si showed that the organic groups are indeed covalently bonded to the inorganic structures and the process of functionalization did not affect the original structures of the silylating agents employed. The thermally stable hybrids presented well-formed particles with a homogeneous distribution of cobalt and nitrogen atoms. Their abilities for copper removal from aqueous solutions gave maximum capacities of sorption of 2.01 ± 0.11 and 2.55 ± 0.15 mmol g(-1) for phyllosilicates containing ethanol- and diethanolamine groups, respectively. For lead sorption the values of 2.59 ± 0.11 and 2.43 ± 0.12 mmol g(-1) were found for this same sequence. These sorption data were adjusted to the non-linear regression of the Langmuir equation. Energetic features related to the interactions between the cations and the pendant basic centres were determined through calorimetric titrations. The acid-basic interactions reflect the spontaneity of the reactions, which are also enthalpically and entropically favourable for these chelating processes at the solid-liquid interface.

  4. Utilizing surfactants to control the sorption, desorption, and biodegradation of phenanthrene in soil-water system.

    Jin, Haiwei; Zhou, Wenjun; Zhu, Lizhong


    An integrative technology including the surfactant enhanced sorption and subsequent desorption and biodegradation of phenanthrene in the soil-water system was introduced and tested. For slightly contaminated agricultural soils, cationic-nonionic mixed surfactant-enhanced sorption of organic contaminants onto soils could reduce their transfer to plants, therefore safe-guarding agricultural production. After planting, residual surfactants combined with added nonionic surfactant could also promote the desorption and biodegradation of residual phenanthrene, thus providing a cost-effective pollution remediation technology. Our results showed that the cationic-nonionic mixed surfactants dodecylpyridinium bromide (DDPB) and Triton X-100 (TX100) significantly enhanced soil retention of phenanthrene. The maximum sorption coefficient Kd of phenanthrene for contaminated soils treated by mixed surfactants was about 24.5 times that of soils without surfactant (Kd) and higher than the combined effects of DDPB and TX100 individually, which was about 16.7 and 1.5 times Kd, respectively. On the other hand, TX100 could effectively remove phenanthrene from contaminated soils treated by mixed surfactants, improving the bioavailability of organic pollutants. The desorption rates of phenanthrene from these treated soils were greater than 85% with TX100 concentration above 2000 mg/L and approached 100% with increasing TX100 concentration. The biodegradation rates of phenanthrene in the presence of surfactants reached over 95% in 30 days. The mixed surfactants promoted the biodegradation of phenanthrene to some extent in 10-22 days, and had no obvious impact on phenanthrene biodegradation at the end of the experiment. Results obtained from this study provide some insight for the production of safe agricultural products and a remediation scheme for soils slightly contaminated with organic pollutants.

  5. Impact of changing DOC concentrations on the potential distribution of acid sensitive biota in a boreal stream network

    H. Laudon


    Full Text Available DOC concentrations have increased in many surface waters in Europe and North America over the past few decades. As DOC exerts a strong influence on pH this DOC increase could have detrimental effects on acid sensitive biota in many streams and lakes. To investigate the potential implications of changes in the DOC concentration on stream water biota, we have used a mesoscale boreal stream network in northern Sweden as a case study. The network was sampled for stream water chemistry at 60 locations during both winter base flow and spring flood periods, representing the extremes experienced annually in these streams both in terms of discharge and acidity. The effect of changing DOC on pH was modeled for all sampling locations using an organic acid model, with input DOC concentrations for different scenarios adjusted by between –30% and +50% from measured present concentrations. The resulting effect on pH was then used to quantify the proportion of stream length in the catchment with pH below the acid thresholds of pH 5.5 and pH 5.0. The results suggest that a change in stream water DOC during base flow would have only a limited effect on pH and hence on the stream length with pH below the acid thresholds. During the spring flood on the other hand a change in DOC would strongly influence pH and the stream length with pH below the acid thresholds. For example an increase in DOC concentration of 30% at all sites would increase the proportion of stream length with pH below 5.5 from 37% to 65%, and the proportion of stream length with pH below 5.0 would increase from 18% to 27%. The results suggest that in poorly-buffered high DOC waters, even a marginal change in the DOC concentration could impact acid sensitive biota in a large portion of the aquatic landscape.

  6. Impact of changing DOC concentrations on the potential distribution of acid sensitive biota in a boreal stream network

    H. Laudon


    Full Text Available DOC concentrations have increased in many surface waters in Europe and North America over the past few decades. As DOC exudes a strong influence on pH this DOC increase could have detrimental effects on acid sensitive biota in many streams and lakes. To investigate the potential implications of changes in the DOC concentration on stream water biota, we have used a mesoscale boreal stream network in northern Sweden as a case study. The network was sampled for stream water chemistry at 60 locations during both winter base flow and spring flood periods, representing the extremes experienced annually in these streams both in terms of discharge and acidity. The effect of changing DOC on pH was modeled for all sampling locations using an organic acid model, with input DOC concentrations for different scenarios adjusted by between −30% and +50% from measured present concentrations. The resulting effect on pH was then used to quantify the proportion of stream length in the catchment with pH below the acid thresholds of pH 5.5 and pH 5.0. The results suggest that a change in stream water DOC during base flow would have only a limited effect on pH and hence on the stream length with pH below the acid thresholds. During the spring flood on the other hand a change in DOC would strongly influence pH and the stream length with pH below the acid thresholds. For example an increase in DOC concentration of 30% at all sites would increase the proportion of stream length with pH below 5.5 from 37% to 65%, and the proportion of stream length with pH below 5.0 would increase from 18% to 27%. The results suggest that in high DOC waters, even a marginal change in the DOC concentration could impact acid sensitive biota in a large portion of the aquatic landscape.

  7. Water sorption and solubility of polyamide denture base materials.

    Nguyen, Long G; Kopperud, Hilde M; Øilo, Marit


    Purpose: Some patients experience adverse reactions to poly(methyl methacrylate)-based (PMMA) dentures. Polyamide (PA) as an alternative to PMMA has, however, not been well documented with regard to water sorption and water solubility. The aim of this in vitro study was to measure water sorption and water solubility of two PA materials compared with PMMA, and to evaluate the major components released from the PA materials and the effect on hardness of the materials. Methods: Ten discs (40.0 mm diameter, 2.0 mm thick) of each material (PA: Valplast and Breflex; PMMA: SR Ivocap HIP) were prepared according to manufacturers' recommendations. The specimens were tested for water sorption and water solubility, according to a modification of ISO 20795-1:2008. Released substances were analysed by gas chromatography/mass spectrometry (GC/MS). Results: There were statistically significant differences among the materials regarding water sorption, water solubility and time to water saturation. Breflex had the highest water sorption (30.4 μg/mm(3)), followed by PMMA-material (25.8 μg/mm(3)) and Valplast (13.6 μg/mm(3)). Both PA materials had statistically significant lower water solubility than the PMMA. Both PA had a net increase in weight. Analysis by GC/MS identified release of the compound 12-aminododecanolactam from the material Valplast. No release was found from the Breflex material. Conclusions: The PA denture materials show differences in water sorption and solubility, but within the limits of the standard requirements. The PA showed a net increase in weight after long-term water sorption. The clinical implications of the findings are not elucidated.

  8. Sorption of tylosin and sulfamethazine on solid humic acid.

    Guo, Xuetao; Tu, Bei; Ge, Jianhua; Yang, Chen; Song, Xiaomei; Dang, Zhi


    Tylosin (TYL) and sulfamethazine (SMT) are ionizable and polar antimicrobial compounds, which have seeped into the environment in substantial amounts via fertilizing land with manure or sewage. Sorption of TYL and SMT onto humic acid (HA) may affect their environmental fate. In this study, the sorption of TYL and SMT on HA at different conditions (pH, ionic strength) was investigated. All sorption isotherms fitted well to the Henry and Freundlich models and they were highly nonlinear with values of n between 0.5 and 0.8, which suggested that the HA had high heterogeneity. The sorption of TYL and SMT on HA decreased with increasing pH (2.0-7.5), implying that the primary sorption mechanism could be due to cation exchange interactions between TYL(+)/SMT(+) species and the functional groups of HA. Increasing ionic strength resulted in a considerable reduction in the Kd values of TYL and SMT, hinting that interactions between H bonds and π-π EDA might be an important factor in the sorption of TYL and SMT on HA. Results of Fourier transform infrared (FT-IR) and (13)C-nuclear magnetic resonance (NMR) analysis further demonstrated that carboxyl groups and O-alkyl structures in the HA could interact with TYL and SMT via ionic interactions and H bonds, respectively. Overall, this work gives new insights into the mechanisms of sorption of TYL and SMT on HA and hence aids us in assessing the environmental risk of TYL and SMT under diverse conditions. Copyright © 2015. Published by Elsevier B.V.

  9. Catalytic gasification of biomass (Miscanthus) enhanced by CO2 sorption.

    Zamboni, I; Debal, M; Matt, M; Girods, P; Kiennemann, A; Rogaume, Y; Courson, C


    The main objective of this work concerns the coupling of biomass gasification reaction and CO2 sorption. The study shows the feasibility to promote biomass steam gasification in a dense fluidized bed reactor with CO2 sorption to enhance tar removal and hydrogen production. It also proves the efficiency of CaO-Ca12Al14O33/olivine bi-functional materials to reduce heavy tar production. Experiments have been carried out in a fluidized bed gasifier using steam as the fluidizing medium to improve hydrogen production. Bed materials consisting of CaO-based oxide for CO2 sorption (CaO-Ca12Al14O33) deposited on olivine for tar reduction were synthesized, their structural and textural properties were characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), and temperature-programmed reduction (TPR) methods, and the determination of their sorption capacity and stability analyzed by thermogravimetric analysis (TGA). It appears that this CaO-Ca12Al14O33/olivine sorbent/catalyst presents a good CO2 sorption stability (for seven cycles of carbonation/decarbonation). Compared to olivine and Fe/olivine in a fixed bed reactor for steam reforming of toluene chosen as tar model compound, it shows a better hydrogen production rate and a lower CO2 selectivity due to its sorption on the CaO phase. In the biomass steam gasification, the use of CaO-Ca12Al14O33/olivine as bed material at 700 °C leads to a higher H2 production than olivine at 800 °C thanks to CO2 sorption. Similar tar concentration and lighter tar production (analyzed by HPLC/UV) are observed. At 700 °C, sorbent addition allows to halve tar content and to eliminate the heaviest tars.

  10. Sorption of 1-naphthol by plant cuticular fractions


    The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment, but sorption mechanism is still not fully understood. In this study,sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction. Toward this end, cuticular materials were isolated from the fruits of tomato by chemical method. The tomato cuticle sheet consisted of waxes(6.5 wt%), cuticular monomer (69.5 wt%), and polysaccharide (24.0 wt%). Isotherms of 1-naphthol to the cuticular fractions were nonlinear (N value (0.82 - 0.90)) at the whole tested concentration ranges. The Koc/Kow ratios for bulk cuticle (TC1), dewaxed cuticle(TC2), cutin (TC4), and desugared cuticle (TC5) were larger than unity, suggested that tomato bulk cuticle and cutin are much powerful sorption medium. Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3). The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions.Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material. There was a linear negative trend between Koc values and the amount of polysaccharides or fraction's polarities((N+O)/C); while a linear positive relationship between Koc values and the content of cutin monomer (linear R2 = 0.993) was observed for present in the cuticular fractions. Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer, contributing to 91.7% of the total sorption of tomato bulk cuticle.

  11. Natural minerals and synthetic materials for sorption of radioactive anions

    Kang, Mun Ja; Chun, Kwan Sik; Kim, Seung Soo


    Technetium-99 and iodine-129 are fission products with long half-lives, and exist as highly soluble anionic species. Studies on natural and synthetic materials sorbing TcO{sub 4} and/or I have been performed by several researchers. The application of these materials as an additive in the high-level waste disposal has been considered. The iron- or sulfide-containing minerals such as metal iron, iron powder, stibnite and pyrrhotite show a high capacity for TcO{sub 4} sorption. And the small amounts of activated carbon are reported to have high distribution coefficients recently. In the iodine sorption studies, sulfide-, copper-, lead- or mercury-containing minerals can be a candidate. Pyrite, chalcopyrite, galena, Cu{sub 2}S and CuS reveal a high capacity for I sorption. The synthetic materials were found to have high sorption capacity and compensate the defects of natural minerals, which contain hydrous oxides such as zirconium oxide, aluminium oxide and mercarbide. The mercarbide has the high distribution coefficients for the sorption of TcO{sub 4} and I. Recently it was proposed that the synthetic clay, hydrotalcite, could be useful for the fixation of anion. However, to determine the applicability of those natural and synthetic materials as an additive to a buffer or backfill material for sorption of TcO{sub 4} and/or I, the sorption behavior of the anions on those materials under the repository conditions should be identified. (author). 32 refs., 21 tabs., 10 figs

  12. Long-term environmental drivers of DOC fluxes: Linkages between management, hydrology and climate in a subtropical coastal estuary

    Regier, Peter; Briceño, Henry; Jaffé, Rudolf


    Urban and agricultural development of the South Florida peninsula has disrupted historic freshwater flow in the Everglades, a hydrologically connected ecosystem stretching from central Florida to the Gulf of Mexico, USA. Current system-scale restoration efforts aim to restore natural hydrologic regimes to reestablish pre-drainage ecosystem functioning through increased water availability, quality and timing. Aquatic transport of carbon in this ecosystem, primarily as dissolved organic carbon (DOC), plays a critical role in biogeochemical cycling and food-web dynamics, and will be affected both by water management policies and climate change. To better understand DOC dynamics in South Florida estuaries and how hydrology, climate and water management may affect them, 14 years of monthly data collected in the Shark River estuary were used to examine DOC flux dynamics in a broader environmental context. Multivariate statistical methods were applied to long-term datasets for hydrology, water quality and climate to untangle the interconnected environmental drivers that control DOC export at monthly and annual scales. DOC fluxes were determined to be primarily controlled by hydrology but also by seasonality and long-term climate patterns and episodic weather events. A four-component model (salinity, rainfall, inflow, Atlantic Multidecadal Oscillation) capable of predicting DOC fluxes (R2 = 0.84, p < 0.0001, n = 155) was established and applied to potential climate change scenarios for the Everglades to assess DOC flux response to climate and restoration variables. The majority of scenario runs indicated that DOC export from the Everglades is expected to decrease due to future changes in rainfall, water management and salinity.

  13. Trends in Drought Frequency. The Fate of DOC Export From British Peatlands

    Worrall, F. [Department of Geological Sciences, Science Laboratories, South Road, Durham, DH1 3LE (United Kingdom); Burt, T.P. [Department of Geography, Science Laboratories, South Road, Durham, DH1 3LE (United Kingdom); Adamson, J.K. [Environmental Change Network, Centre for Ecology and Hydrology, Merlewood, Windermere Road, Grange over Sands, Cumbria, LA11 6JU (United Kingdom)


    There is increasing evidence that drought is leading to increased loss of dissolved organic carbon (DOC) from upland peats. Therefore, this study endeavours to understand the severity and frequency of the scale of drought responsible for driving the observed changes; and, by reconstructing climatic records, to understand whether such droughts are increasing in severity and frequency. The study suggests that there are two levels of drought severity important in the peatlands: a hydrological drought that causes hydrophobic effects in the upper peat profile lasting 3-4 years in duration, and a more severe biogeochemical drought that triggers new mechanisms of DOC production and decade-long effects. The study uses long term climate data from Central England and Northern England to reconstructs depth to water table for an upland peat catchment back to 1766 and shows that hydrological drought has a return period of 25 years and that biogeochemical drought has a return period of 15.5 years. Statistical modelling of the time series of annual droughts shows only weak evidence for an increasing frequency of severe droughts since 1766, but stronger evidence for the recent past. The return period of drought of sufficient severity to cause biogeochemical response is coming close to the length of effect such a drought would have, i.e. trends in drought frequency mean that peatlands may no longer be resilient to the impact of drought, with dire consequences for the storage of carbon in these environments.

  14. Impact of Biodiesel Impurities on the Performance and Durability of DOC, DPF and SCR Technologies: Preprint

    Williams, A.; McCormick, R.; Luecke, J.; Brezny, R.; Geisselmann, A.; Voss, K.; Hallstrom, K.; Leustek, M.; Parsons, J.; Abi-Akar, H.


    An accelerated durability test method determined the potential impact of biodiesel ash impurities, including engine testing with multiple diesel particulate filter substrate types, as well as diesel oxidation catalyst and selective catalyst reduction catalysts. The results showed no significant degradation in the thermo-mechanical properties of a DPF after exposure to 150,000-mile equivalent biodiesel ash and thermal aging. However, exposure to 435,000-mile equivalent aging resulted in a 69% decrease in thermal shock resistance. A decrease in DOC activity was seen after exposure to 150,000-mile equivalent aging, resulting in higher hydrocarbon slip and a reduction in NO2 formation. The SCR catalyst experienced a slight loss in activity after exposure to 435,000-mile equivalent aging. The SCR catalyst, placed downstream of the DPF and exposed to B20 exhaust suffered a 5% reduction in overall NOx conversion activity over the HDDT test cycle. It is estimated that the additional ash from 150,000 miles of biodiesel use would also result in a moderate increases in exhaust backpressure for a DPF. The results of this study suggest that long-term operation with B20 at the current specification limits for alkali and alkaline earth metal impurities will adversely impact the performance of DOC, DPF and SCR systems.

  15. Enseñanza individual a través de Skype y Google Docs

    Agata Łazor


    Full Text Available El artículo presenta ideas para clases on-line utilizando Google Docs y Skype. En la parte teórica se explica el concepto de enseñanza virtual asincrónica y sincrónica. Se comentan las ventajas e inconvenientes de ambos modos de enseñanza.Los ejercicios prácticos utilizan sobre todo los métodos y herramientas sincrónicos y tienen el propósito de utilizar varias aplicaciones de Google Docs. Todas las tareas se adaptan a diferentes estilos de aprendizaje. La primera está relacionada con recordar y repetir colocaciones y expresiones. En el segundo ejercicio se utiliza una fotografía y se la etiqueta aprovechando la opción dada por Google Drawing. En la tercera tarea se aplican tanto las estrategias de e-learning sincrónico como asincrónico y consiste en la corrección on-line de una tarea previamente escrita. La última tarea implica la búsqueda en internet de una página web y la simulación de un intercambio de e-mails con el propietario de un piso.

  16. Sorption of acetaminophen, 17alpha-ethynyl estradiol, nalidixic acid, and norfloxacin to silica, alumina. and a hydrophobic medium.

    Lorphensri, Oranuj; Intravijit, Jittipong; Sabatini, David A; Kibbey, Tohren C G; Osathaphan, Khemarath; Saiwan, Chintana


    Two pure minerals and a hydrophobic medium were selected to study sorption of pharmaceuticals. The sorption of four pharmaceuticals, acetaminophen (analgesic), 17alpha-ethynyl estradiol (synthetic hormone), nalidixic acid (antibiotic), and norfloxacin (antibiotic), was evaluated with silica, alumina, and Porapak P (a hydrophobic medium). Alumina and silica were selected to represent positively charged and negatively charged aquifer mineral surfaces at neutral pH, respectively, while Porapak P was selected to represent the hydrophobic organic content of an aquifer medium. At neutral pH, acetaminophen, the least hydrophobic pharmaceutical, showed no significant sorption to any of the media, while 17alpha-ethynyl estradiol, the most hydrophobic pharmaceutical, showed significant sorption to Porapak P. Nalidixic acid, which has a carboxyl functional group that is anionic at neutral pH, showed significant adsorption to the positively charged alumina. Norfloxacin, with both a carboxyl (anionic) and a piperazynyl (cationic) group, can exist in four forms (neutral, cationic, anionic, and zwitterionic) depending on the aqueous pH. Norfloxacin also showed significant adsorption than nalidixic acid. Both nalidixic acid and norfloxacin adsorbed to silica and Porapak P to a much lower extent. The pH dependence of nalidixic acid and norfloxacin adsorption to silica and alumina was also studied by varying the pH between 4 and 11. The maximum adsorption of nalidixic acid to alumina occurred near its pKa (pH approximately 6), where the combination of cationic alumina and anionic nalidixic produced maximum adsorption. The maximum adsorption of norfloxacin to alumina was observed at pH approximately 7, which was the region where the zwitterionic form dominated. This research demonstrates that the adsorption of ionizable pharmaceuticals is strongly dependent on the system pH, the pharmaceutical properties (pKa and hydrophobicity), and the nature of the surface charge (point of zero


    XiongChunhua; ChenYiyong; 等


    The influences of Medium pH,sorption temperature,sorption time,etc.on the sorption capacity of macroporous phosphonic acid resin for La3+ were determined.The sorption rate constant was k298=7.64×10-5 s-1. The complex ratio of phosphonic groups of the resin to La3+ was 3:1.The basic sorption parameters were determined. The sorption mechanism of macroporous phosphonic acid resin for La3+ was examined by chemical analysis and IR-spectrometry.

  18. Linking High Frequency Variations in Stream Water DOC to Ages of Water Sources in Peat-Dominated Montane Watersheds

    Tunaley, C.; Tetzlaff, D.; Lessels, J. S.; Soulsby, C.


    We combined time series of inferred DOC (from optical sensors) and stable isotopes in streams and watershed source areas to assess the link between water age and C fluxes. We monitored temporal dynamics of FDOM for 2 yrs at nested scales (0.9, 3.0 and 30km2) in a montane Scottish watershed. FDOM was strongly correlated (r2 ~ 0.8) with DOC allowing inference of 15 min timeseries. Marked seasonality was observed, with highest DOC concentrations (~25 mg l-1) in summer events and lower concentrations (~5mg l-1) in winter. During events, anticlockwise hysteresis was observed; consistent with expansion of the riparian saturation zone, increasing hydrological connectivity across peat soils and mobilizing DOC. Lag times for peak discharge and DOC were 1-12 hrs depending on event characteristics and antecedent conditions. Isotope time series from precipitation, streams and catchment source waters (overland flow and hillslope drainage) were also generated. These allowed us to model the non-stationary characteristics of their ages. Stream water age ranges from 3 months at high flows when overland flow dominates runoff to 4 yrs under baseflow. Overland flow age was a dominant influence on DOC transport. Highest concentrations occurred in small summer events with relatively young (strategies.

  19. Oxygen dynamics in a boreal lake responds to long-term changes in climate, ice phenology, and DOC inputs

    Couture, Raoul-Marie; Wit, Heleen A.; Tominaga, Koji; Kiuru, Petri; Markelov, Igor


    Boreal lakes are impacted by climate change, reduced acid deposition, and changing loads of dissolved organic carbon (DOC) from catchments. We explored, using the process-based lake model MyLake, how changes in these pressures modulate ice phenology and the dissolved oxygen concentrations (DO) of a small boreal humic lake. The model was parametrized against year-round time series of water temperature and DO from a lake buoy. Observed trends in air temperature (+0.045°C yr-1) and DOC concentration (0.11 mg C L-1 yr-1, +1% annually) over the past 40 years were used as model forcings. A backcast of ice freezing and breakup dates revealed that ice breakup occurred on average 8 days earlier in 2014 than in 1974. The earlier ice breakup enhanced water column ventilation resulting in higher DO in the spring. Warmer water in late summer led to longer anoxic periods, as microbial DOC turnover increased. A long-term increase in DOC concentrations caused a decline in lake DO, leading to 15% more hypoxic days (climate warming and increasing DOC loads are antagonistic with respect to their effect on DO availability. The model suggests that DOC is a stronger driver of DO consumption than temperature. The browning of lakes may thus cause reductions in the oxythermal habitat of fish and aquatic biota in boreal lakes.

  20. Heat cascading regenerative sorption heat pump

    Jones, Jack A. (Inventor)


    A simple heat cascading regenerative sorption heat pump process with rejected or waste heat from a higher temperature chemisorption circuit (HTCC) powering a lower temperature physisorption circuit (LTPC) which provides a 30% total improvement over simple regenerative physisorption compression heat pumps when ammonia is both the chemisorbate and physisorbate, and a total improvement of 50% or more for LTPC having two pressure stages. The HTCC contains ammonia and a chemisorbent therefor contained in a plurality of canisters, a condenser-evaporator-radiator system, and a heater, operatively connected together. The LTPC contains ammonia and a physisorbent therefor contained in a plurality of compressors, a condenser-evaporator-radiator system, operatively connected together. A closed heat transfer circuit (CHTC) is provided which contains a flowing heat transfer liquid (FHTL) in thermal communication with each canister and each compressor for cascading heat from the HTCC to the LTPC. Heat is regenerated within the LTPC by transferring heat from one compressor to another. In one embodiment the regeneration is performed by another CHTC containing another FHTL in thermal communication with each compressor. In another embodiment the HTCC powers a lower temperature ammonia water absorption circuit (LTAWAC) which contains a generator-absorber system containing the absorbent, and a condenser-evaporator-radiator system, operatively connected together. The absorbent is water or an absorbent aqueous solution. A CHTC is provided which contains a FHTL in thermal communication with the generator for cascading heat from the HTCC to the LTAWAC. Heat is regenerated within the LTAWAC by transferring heat from the generator to the absorber. The chemical composition of the chemisorbent is different than the chemical composition of the physisorbent, and the absorbent. The chemical composition of the FHTL is different than the chemisorbent, the physisorbent, the absorbent, and ammonia.

  1. Improved hydrogen sorption kinetics in wet ball milled Mg hydrides

    Meng, Li


    In this work, wet ball milling method is used in order to improve hydrogen sorption behaviour due to its improved microstructure of solid hydrogen materials. Compared to traditional ball milling method, wet ball milling has benefits on improvement of MgH{sub 2} microstructure and further influences on its hydrogen sorption behavior. With the help of solvent tetrahydrofuran (THF), wet ball milled MgH{sub 2} powder has much smaller particle size and its specific surface area is 7 times as large as that of dry ball milled MgH{sub 2} powder. Although after ball milling the grain size is decreased a lot compared to as-received MgH{sub 2} powder, the grain size of wet ball milled MgH{sub 2} powder is larger than that of dry ball milled MgH{sub 2} powder due to the lubricant effect of solvent THF during wet ball milling. The improved particle size and specific surface area of wet ball milled MgH{sub 2} powder is found to be determining its hydrogen sorption kinetics especially at relatively low temperatures. And it also shows good cycling sorption behavior, which decides on its industrial applicability. With three different catalysts MgH{sub 2} powder shows improved hydrogen sorption behavior as well as the cyclic sorption behavior. Among them, the Nb{sub 2}O{sub 5} catalyst is found to be the most effective one in this work. Compared to the wet ball milled MgH{sub 2} powder, the particle size and specific surface area of the MgH{sub 2} powder with catalysts are similar to the previous ones, while the grain size of the MgH{sub 2} with catalysts is much finer. In this case, two reasons for hydrogen sorption improvement are suggested: one is the reduction of the grain size. The other may be as pointed out in some literatures that formation of new oxidation could enhance the hydrogen sorption kinetics, which is also the reason why its hydrogen capacity is decreased compared to without catalysts. After further ball milling, the specific surface area of wet ball milled Mg

  2. OECD Maximum Residue Limit Calculator

    With the goal of harmonizing the calculation of maximum residue limits (MRLs) across the Organisation for Economic Cooperation and Development, the OECD has developed an MRL Calculator. View the calculator.

  3. Sorption of polycyclic aromatic hydrocarbons to polystyrene nanoplastic.

    Liu, Lijing; Fokkink, Remco; Koelmans, Albert A


    Microplastic has become an emerging contaminant of global concern. Bulk plastic can degrade to form smaller particles down to the nanoscale (nanoplastics. Because of their high surface area, nanoplastic may bind hydrophobic chemicals very effectively, increasing their hazard when such nanoplastics are taken up by biota. The present study reports distribution coefficients for sorption of polycyclic aromatic hydrocarbons (PAHs) to 70 nm polystyrene in freshwater, and PAH adsorption isotherms spanning environmentally realistic aqueous concentrations of 10(-5)  μg/L to 1 μg/L. Nanopolystyrene aggregate state was assessed using dynamic light scattering. The adsorption isotherms were nonlinear, and the distribution coefficients at the lower ends of the isotherms were very high, with values up to 10(9) L/kg. The high and nonlinear sorption was explained from π-π interactions between the planar PAHs and the surface of the aromatic polymer polystyrene and was higher than for micrometer-sized polystyrene. Reduction of nanopolystyrene aggregate sizes had no significant effect on sorption, which suggests that the PAHs could reach the sorption sites on the pristine nanoparticles regardless of the aggregation state. Pre-extraction of the nanopolystyrene with C18 polydimethylsiloxane decreased sorption of PAHs, which could be explained by removal of the most hydrophobic fraction of the nanopolystyrene. Environ Toxicol Chem 2016;35:1650-1655. © 2015 SETAC.

  4. Sorption of Emerging Organic Wastewater Contaminants to Four Soils

    Sarah Roberts


    Full Text Available Conventional onsite wastewater treatment system design relies on a septic tank and soil treatment unit (STU for treatment of wastewater and integration of the final effluent into the environment. Organic water contaminants (OWCs, chemicals found in pharmaceutical drugs, detergents, surfactants, and other personal care and cleaning products, have been observed in septic tank effluent and the environment. Sorption of OWC mass to soil is a key mechanism in the removal and retardation of many of these chemicals in effluent as it travels through an STU. The primary purpose of this study was to investigate the relationship between the fraction of organic carbon of soil and the equilibrium sorption partitioning coefficient of a selected group of relevant and diverse OWCs. A secondary goal is to evaluate current methods of modeling the sorption of selected OWCs in soil. Five point Freundlich isotherms were constructed from equilibrium sorption batch tests for target OWCs with four different soils. For soils with organic carbon fraction between 0.021 and 0.054, Kd values were calculated between 60 and 185 for 4-nonylphenol, 75 to 260 for triclosan, 115 to 270 for bisphenol-A, 3 to 255 for 17β-estradiol, 40 to 55 for 17α-ethynylestradiol, and 28 to 70 for estrone. An empirically derived, direct relationship between foc and Kd may be a useful approach to estimating sorption for a soil based on organic carbon content.

  5. Sorption-desorption behavior of polybrominated diphenyl ethers in soils

    Olshansky, Yaniv; Polubesova, Tamara [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100 (Israel); Vetter, Walter [Institute of Food Chemistry (170b), University of Hohenheim, Garbenstr. 28, D-70599 Stuttgart (Germany); Chefetz, Benny, E-mail: [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100 (Israel)


    Polybrominated diphenyl ethers (PBDEs) are flame retardants that are commonly found in commercial and household products. These compounds are considered persistent organic pollutants. In this study, we used 4,4'-dibromodiphenyl ether (BDE-15) as a model compound to elucidate the sorption and desorption behavior of PBDEs in soils. The organic carbon-normalized sorption coefficient (K{sub OC}) of BDE-15 was more than three times higher for humin than for bulk soils. However, pronounced desorption hysteresis was obtained mainly for bulk soils. For humin, increasing concentration of sorbed BDE-15 resulted in decreased desorption. Our data illustrate that BDE-15 and probably other PBDEs exhibit high sorption affinity to soils. Moreover, sorption is irreversible and thus PBDEs can potentially accumulate in the topsoil layer. We also suggest that although humin is probably a major sorbent for PBDEs in soils, other humic materials are also responsible for their sequestration. - Highlights: > BDE-15 exhibited pronounced desorption hysteresis. > BDE-15 sowed higher sorption affinity to humin as compared to the bulk soils. > Sequestration of PBDEs depends on soil organic matter constitutes other than humin. - Pronounced desorption hysteresis was observed for BDE-15 in natural soils.


    Pingping Su,


    Full Text Available Sorption of metal ions from aqueous solutions to birch wood and spruce heartwood and sapwood has been studied. Functional groups in wood were determined by acid-base titrations. The sorption of metal ions to wood of the different tree species was investigated by a column chromatographic technique. The mechanism of sorption is mainly ion exchange by complexation of metal ions to the functional groups, e.g. carboxyl groups and phenolic hydroxyl groups, in the wood phase. By combination of the sorption experiments with four different metal ion mixtures, the following affinity order was established for spruce sapwood particles: Fe3+>>Pb2+>>Cu2+>>Fe2+>Cd2+>Zn2+>Ni2+>Mn2+≥Ca2+≥Sr2+≥Ba2+>>Mg2+>>K+>Na+≈Li+. For all three types of stemwood studied, the affinity orders were almost the same. The ion exchange properties of wood were comparable to those of a weakly acid cation exchanger. The affinity order obtained for the synthetic resin was quite similar to the order given above for wood. The metal sorption properties of wood materials imply that they could be a potential material for removal of metal ions from aqueous solutions.

  7. Ethylene oxide removal by sorption on aluminium oxide

    Arsenijević Zorana Lj.


    Full Text Available The dynamics of ethylene oxide sorption and desorption on Al2O3 sorbent were investigated. The investigations of ethylene oxide sorption on Al2O3 show that significant sorption appeared above 125°C. The removal of sorbed ethylene oxide from Al2O3 was achieved by continuous increasing of the temperature up to 450°C in air stream. The analysis of desorbed products show that 90% of adsorbed ethylene oxide is converted to CO2 and the rest consists of the three derivatives of ethylene oxide. The exact composition of desorbed organic products will be determined in further investigation. The desorption temperature profiles point out the presence of two exothermic picks, as was confirmed by detection of CO2 and derivates of ethylene oxide at these temperatures. Investigation of textural characteristics and thermal stability of Al2O3 sorbent show that there are no changes of any characteristics of Al2O3 in sorption/desorption operating temperatures regimes. Only at 700°C the specific surface area of Al2O3 decreases of about 10%. This indicates that the investigated Al2O3 is convenient material for removal of ethylene oxide by sorption.

  8. Moisture sorption characteristics of freeze-dried human platelets

    Meng-jie XU; Guang-ming CHEN; Ju-li FAN; Jin-hui LIU; Xian-guo XU; Shao-zhi ZHANG


    Freeze-drying is a promising method for a long-term storage of human platelets. The moisture sorption characteristics of freeze-dried human platelets (FDHPs) were studied in this paper. The moisture sorption isotherms of FDHPs and freeze-dried lyophilization buffer (FDLB) were measured at 4, 25, and 37 ℃. The experimental data were fitted to Brunauer-Emmett-Teller (BET) and Guggenheim-Anderson-de Boer (GAB) equations. There were no significant statistical differences (P>0.05) between the sorption characteristics of FDHPs and FDLB at 4 and 25 ℃, while FDHPs absorbed more water at 37 ℃. The net isosteric heat of sorption was derived. The heat for FDHPs showed an abnormal negative value at low moisture contents when 25 and 37 ℃ data were used. Dynamic sorption experiments were carried out at 25 ℃ with environmental water activity controlled at 0.75, 0.85, and 0.90. The moisture diffusion coefficient was fitted to be 8.24x 10-12 m2/s when experimental data at initial time were used. These results would be helpful in choosing prehydration and storage condition for FDHPs.

  9. Sorption of pharmaceuticals and personal care products to polyethylene debris.

    Wu, Chenxi; Zhang, Kai; Huang, Xiaolong; Liu, Jiantong


    Presence of plastic debris in marine and freshwater ecosystems is increasingly reported. Previous research suggested plastic debris had a strong affiliation for many pollutants, such as polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and heavy metals. In this study, the sorption behavior of pharmaceuticals and personal care products (PPCPs), including carbamazepine (CBZ), 4-methylbenzylidene camphor (4MBC), triclosan (TCS), and 17α-ethinyl estradiol (EE2), to polyethylene (PE) debris (250 to 280 μm) was investigated. The estimated linear sorption coefficients (K d) are 191.4, 311.5, 5140, and 53,225 L/kg for CBZ, EE2, TCS, and 4MBC, and are related to their hydrophobicities. Increase of salinity from 0.05 to 3.5 % did not affect the sorption of 4MBC, CBZ, and EE2 but enhanced the sorption of TCS, likely due to the salting-out effect. Increase of dissolved organic matter (DOM) content using Aldrich humic acid (HA) as a proxy reduced the sorption of 4MBC, EE2, and TCS, all of which show a relatively strong affiliation to HA. Results from this work suggest that microplastics may play an important role in the fate and transport of PPCPs, especially for those hydrophobic ones.

  10. A study of dyes sorption on biobased cryogels

    Dobritoiu, Rodica; Patachia, Silvia, E-mail:


    Three types of biopolymers based materials were synthesized and tested as adsorbents for the dyes from aqueous solutions. Blends based on poly (vinyl alcohol) [PVA] and scleroglucan [Scl], cellulose micro-fibres [cel] and zein, respectively, have been prepared by repeated freezing–thawing cycles. Methylene blue [MB] was selected as a model dye in order to evaluate the capacity of the prepared materials to remove the dyes from aqueous solutions. The effects of the initial dye concentration, contact time and the composition of materials on the kinetic and thermodynamic parameters of sorption were discussed. The pseudo-second-order kinetics was found to better fit the experimental data thus being able to consistently predict the amount of dye adsorbed over the entire sorption period. The sorption equilibrium data obey Freundlich isotherm. Sorption capacity was evaluated both by dye solution and cryogel analysis by using VIS spectrometry and image analysis with CIELAB system. The sorption of monomer or aggregated dye molecules was identified and correlated with the type and morphology of the gel. The highest efficiency in MB removal was obtained for Scl/PVA cryogels in 1:9 weight ratio (9.5279 mg/g MB for an initial concentration by 8 × 10{sup −5} mol/L in MB). These materials are suitable as sorbents for the advanced removal of dyes from waste water.

  11. Thermodynamics of selenium sorption on alumina and montmorillonite

    Jean-Pierre Morel


    Full Text Available The effect of pH and temperature on the thermodynamics of selenium sorption on alumina and montmorillonite was investigated. The equilibrium constants were obtained from batch experiments carried out at 25 and 40°C, under acidic and near to neutral conditions. Microcalorimetry was used to measure directly the enthalpy change upon sorption. These data were analysed by taking into account the different reactions that occur during the sorption process (the acid–base equilibria in the bulk solution on the one hand and the complexation equilibria between surface sites of the solid and solution species on the other hand. This was done using a simple surface model which assumes that the thermodynamic properties of the aluminol surface sites of both alumina and montmorillonite are identical. Two of the considered reactions were found to predominate, one under acidic conditions and one at near neutral pH. The microcalorimetric data allowed to check that the temperature effect on selenium sorption on alumina and montmorillonite can be correctly predicted simply using the above assumption concerning the sorption sites and by applying van’t Hoff relation both to the homogeneous and heterogeneous reactions.

  12. Sorption and transport of atrazine in an agricultural soil

    Hakan Akyol, Nihat


    Sorption and transport of atrazine in an agricultural soil Atrazine is one of the most commonly used herbicides in large quantity worldwide. The objective of this study was to perform some batch and column experiments to examine the transport of atrazine in an agricultural soil from Turkey. Batch experiments indicated that sorption isotherm was nonlinear with a freundlich isotherm over a range of concentration (0.2-10 mg/L) examined. Column experiments showed that transport of atrazine in the soil was moderately retarded compared to non-reactive tracer (R = 2.9-4.0). The degree of retardation decreased with increasing atrazine concentration and residance time had negligable impact on degree of sorption. Flow interruption tests in the column experiments indicated that the rate-limited desorption of atrazine mainly controlled the non-ideal transport of atrazine due to the presence of organic matter fraction (0.83 %) in the soil. Sorption and desorption behavior of atrazine in such soils could have important impacts for risk assessment of atrazine-contaminated soil and should be taken into account in the regulation, management, and remediation of atrazine-contaminated sites. Keywords: Atrazine, Agricultural soil, Batch, Column, Desorption, Rate-limited desorption, Sorption, Transport.

  13. The Response of Artificial Aging to Sorption Properties of Biochar for Potentially Toxic Heavy Metals

    Frišták Vladimír


    Full Text Available This paper evaluates the effect of simulated conditions of artificial aging on sorption capacity of two types of biochar. These were produced by slow pyrolysis from different feedstock - beech wood chips (BC A and garden green waste residues (BC B. Cadmium served as a model for potentially toxic metals. Twenty freeze-thaw cycles were used to simulate physical aging. The determination of biochar physicochemical properties showed main changes in CEC and SA values of aged sorbents. The maximum sorption capacities of aged BC A sorbent were higher by about 26 % and aged BC B sorbent by about 20% compared to Qmax of non-aged biochar. Qmax of aged BC B peaked at 9.4 mg g-1 whereas BC A sorbed significantly less Cd. FT-IR analyses confirmed the changes in structural composition and content of functional groups on biochar surfaces. The artificial physical aging model was assessed as an efficient tool for investigation of natural weathering conditions.

  14. Sorption of methylene blue on treated agricultural adsorbents: equilibrium and kinetic studies

    Tiwari, D. P.; Singh, S. K.; Sharma, Neetu


    Agricultural adsorbents are reported to have a remarkable performance for adsorption of dyes. In the present study, formaldehyde and sulphuric acid treated two agricultural adsorbents; potato peel and neem bark are used to adsorb methylene blue. On the whole, the acid-treated adsorbents are investigated to have high sorption efficiency compared to HCHO treated adsorbents. The percentage removal efficiency of H2SO4 treated potato peel (APP) increases considerably high from 75 to 100 % with increase in adsorbent dose, whereas the removal efficiency of H2SO4 treated neem bark (ANB) is found to be 98 % after adding the first dose only. The monolayer sorption behaviour of HCHO treated potato peel (PP) and APP is well defined by Langmuir, whereas the chemisorptions behaviour of HCHO treated neem bark (NB) and ANB is suggested by Temkin's isotherm model. The maximum adsorption capacity measured is highest in ANB followed by NB, PP and APP with the values of 1000, 90, 47.62 and 40.0 mg/g, respectively. The pseudo-second-order kinetic model fitted well with the observed data of all the four adsorbents. The results obtained reveal that NB and ANB both are good adsorbents compared to PP and APP.

  15. Impact of operating conditions on cooling capacity for sorption systems using water as refrigerant

    Tremeac, Brice; Giraud, Florine; Vallon, Pierrick


    The implementation of compact heat exchanger in sorption systems is a key factor to allow the development of these systems. The aim of this paper is to develop a statistical model with a design of experiment (DOE) methodology and use dimensionless number to evaluate and understand the influence of the height of refrigerant liquid and secondary fluid inlet temperature on cooling capacity of a compact pate-type evaporator for sorption systems working near vacuum pressure. For this purpose, an experimental campaign was conducted on a small adsorption test bench using 13X/water as working couple. Cooling capacities from 640 to 2000 W were measured. The DOE is a Doelhert type with two parameters: the inlet secondary fluid temperature (from 10 to 21 °C) and the filing level of refrigerant in the evaporator (from 6 to 24 cm). Thanks to the exploitation of the mathematical model obtained, optimal points under different constraints were found. A maximum cooling capacity of 2021 +/-75 W in the entire experimental field was predicted for a secondary fluid inlet temperature of 25°C and a height of liquid level of 19.2 cm. Bond number and modified Jacob number per the ratio Psat/Ptriple were analyzed. The dimensionless numbers are correlated to the cooling capacity as a first step for designing compact plate-type evaporator for adsorption systems using water as refrigerant.

  16. A hybrid sorption - Spectrometric method for determination of synthetic anionic dyes in foodstuffs.

    Tikhomirova, Tatyana I; Ramazanova, Gyulselem R; Apyari, Vladimir V


    A sorption-spectrometric method for determination of the anionic synthetic dyes based on their sorption on silica sorbent modified with hexadecyl groups (C16) followed by measuring the diffuse reflectance spectra on the surface of the sorbent has been proposed. Adsorption of sulfonated azo dyes Tartrazine (E102), Sunset Yellow FCF (E110), Ponceau 4R (E124) reaches maximum in acidic medium (1M HCl - pH 1). For the quinophthalone type dye Quinoline Yellow (E104), the adsorption is also maximal in an acidic medium (1M HCl - pH 2). The triphenylmethane dye Fast Green FCF (E143) is absorbed in the wider area of pH (1M HCl - pH 6). Increasing concentration of the dyes in a solution led to the increase in absorption band intensity in diffuse reflectance spectra of the adsorbent, which was used for their direct determination. The proposed method was applied to the determination of dyes in beverages and pharmaceuticals.

  17. Climatic and chemical drivers of trends in DOC in northern surface waters in Europa and North America

    de Wit, Heleen A.; Monteith, Don T.; Stoddard, John L.


    Concentrations of DOC in boreal surface waters have increased to levels that create challenges for water treatment plants, and that potentially impact lake habitat through increased anoxia and thermal mixing, and productivity. Aquatic transport of DOC from land to oceans is likely to increase, even if runoff patterns would remain stable. Reduced acid deposition appears to be a dominant driver behind the increase in DOC concentrations, through increasing organic matter solubility. We hypothesize that the higher solubility of organic matter makes DOC more susceptible to climate change. Here, we present trends in DOC from circa 500 lakes and streams in subarctic, boreal and temperate headwater catchments in Europe (UK, Fennoscandia, Czech Republic, Slovakia) and North America (Northeastern US, Ontario, Atlantic Canada) from 1990 until 2012; an extension of the trend analysis presented in Monteith et al. (2007). The water chemical data stem from national monitoring networks, assembled by the ICP Waters network. Sampling frequencies vary from 1 to 52 samples per year. Climate data were obtained from Climate Research Unit in the UK. Trends were calculated using the Mann-Kendall test and the Sen-slope estimator. We test 1) if DOC responds to changes in the rate of decline in acid deposition, and 2) if trends in temperature and precipitation affect trends and variability in DOC. Positive trends dominate: the median (±2.5% quartile) of the absolute and relative DOC trends is +0.06 (+0.36 to -0.02) mg C L-1 yr-1 and +1.4 (+4.7 to -0.9) % yr-1, respectively. Overall, the trends do not level off when comparing 1990-2004, and 1998-2012, except in the UK and Atlantic Canada. These two regions are strongly impacted by seasalt deposition but may also experience stronger warming than elsewhere. The response of DOC to changes in SO4 (expressed as trend ratios) is stronger in 1998-2012 than in 1990-2004. We will explore whether this changing relates to increasing dominance of

  18. Cementitious near-field sorption data bases for performance assessment of a L/ILW repository in a Palfris marl host rock. CEM-94: update I, June 1997

    Bradbury, M.H.; Loon, L.R. van [Paul Scherrer Inst. (PSI), Villigen (Switzerland)


    This report is an update on an earlier cementitious sorption data base (SDB) prepared by Bradbury and Sarott (1994). The aim is to review any new information or data which have become available in the intervening time and modify the existing SDB appropriately. Discussions will be confined predominantly to areas which have led to significant changes to or reappraisals of the data/values or procedures for obtaining/modifying them. From this point of view this update and the previous SDB are closely related and belong together. The complexation of radionuclides with organic ligands from the chemical degradation of cellulose, and the subsequent negative effects on sorption properties, were identified as being processes of great importance. Since 1994 significant progress has been made in this field and a major part of this work is devoted to a reassessment of the impact of `organics` on near-field sorption. In particular, the very conservative assumptions which had been made previously because of the general lack of good quality data available at that time, could be replaced by realistic parameter estimates based on new knowledge. For example, maximum likely concentrations of cellulose degradation products and cement additives in the cement pore waters could be calculated allowing the potential effects of these organic ligands on sorption to be bounded. Sorption values for safety relevant radionuclides corresponding to the three broad stages of cement/concrete degradation during the lifetime of the repository are presented in tabulated form. The influence of the wide variety of organic ligands existing in the different waste categories, SMA-1 to SMA-4, is quantified in terms of sorption reduction factors. In the compilation of this cement SDB update, radionuclide uptake onto the vast quantities of aggregate materials and corrosion products from iron/steel was not taken into account. (author) 10 figs., 8 tabs., refs.

  19. Extremely High Phosphate Sorption Capacity in Cu-Pb-Zn Mine Tailings.

    Huang, Longbin; Li, Xiaofang; Nguyen, Tuan A H


    Elevated inorganic phosphate (Pi) concentrations in pore water of amended tailings under direct revegetation may cause toxicity in some native woody species but not native forbs or herb species, all of which are key constituents in target native plant communities for phytostabilizing base metal mine tailings. As a result, Pi sorption capacity has been quantified by a conventional batch procedure in three types of base metal mine tailings sampled from two copper (Cu)-lead (Pb)-zinc (Zn) mines, as the basis for Pi-fertiliser addition. It was found that the Pi-sorption capacity in the tailings and local soil was extremely high, far higher than highly weathered agricultural soils in literature, but similar to those of volcanic ash soils. The Langmuir P-sorption maximum was up to 7.72, 4.12, 4.02 and 3.62 mg P g-1 tailings, in the fresh tailings of mixed Cu-Pb-Zn streams (MIMTD7), the weathered tailings of mixed Cu-Pb-Zn streams (MIMTD5), EHM-TD (fresh Cu-stream, high magnetite content) and local soil (weathered shale and schist), respectively. Physicochemical factors highly correlated with the high Pi-sorption in the tailings were fine particle distribution, oxalate and dithionite-citrate-bicarbonate extractable Fe (FeO and Fed), oxalate-extractable Al and Mn, and the levels of soluble Cd and Zn, and total S and Fe. Large amounts of amorphous Fe oxides and oxyhydroxides may have been formed from the oxidation of pyritic materials and redox cycles of Fe-minerals (such as pyrite (FeS2), ankerite (Ca(Fe Mg)(CO3)2 and siderite (FeCO3), as indicated by the extractable FeO values. The likely formation of sparingly soluble Zn-phosphate in the Pb-Zn tailings containing high levels of Zn (from sphalerite ((Zn,Fe)S, ZnS, (Zn,Cd)S)) may substantially lower soluble Zn levels in the tailings through high rates of Pi-fertiliser addition. As a result, the possibility of P-toxicity in native plant species caused by the addition of soluble phosphate fertilizers would be minimal.

  20. Cd2+ and Zn2+ sorption on apatite in the presence of EDTA and humic substance

    Viipsi K.


    Full Text Available The sorption of Cd2+ and Zn2+ on hydroxyapatite [HAP- Ca10(PO46(OH2] and fluorapatite [FAP- Ca10( PO46(F2] with different specific surface area and stoichiometry was investigated in batch experiments in the pH range 4 to 11 (25 ◦C; 0.1 M KNO3. The impact of different conditions was concerned: solution pH, the presence of complexing ligands (EDTA and humic substance and competing metal ions, as well as reaction kinetic and equilibrium conditions. To evaluate the reversibility of Cd2+ sorption onto HAP, desorption characteristics in water, Ca, EDTA, and HUM-solutions were determined. Additionally to solution analysis the surface composition of solid phases was analysed by X-Ray Photoelectron Spectroscopy XPS. The information from the chemical analyses was used to design an equilibration model that takes into account dissolution, surface potential, solution and surface complexation, as well as possible phase transformations. It was revealed that apatites effectively sorb Cd2+ and Zn2+ by ion exchange reactions on surface by formation of new surface phases. Using XPS the formation of a Me-enriched HAP surface was found, which was interpreted as the formation of a solid solution with the general formula: Ca8.4-xMex(HPO41.6(PO44.4(OH0.4. In a binary solution (Cd+Zn the competition of metals reduced individual sorbed amount compared with the single component solutions but the total adsorption maximum was approximately constant. The presence of EDTA reduces the metal sorption on apatite due to [CdEDTA]2- and [ZnEDTA]2- complexes and increases apatite solubility due to [CaEDTA]2- complex formation. The dissolved humic substance was bound on apatite in suspensions but the amount of Cd2+ bound was not changed. The results showed that the solution pH and the presence of complexing ligands have a significant effect on heavy metal sorption on apatite and must be considered if apatites are used as remediation agent. The proposed model can be used to predict

  1. C-MORE Professional Development Training Program for Graduate Students and Post-Docs

    Bruno, B. C.; DeLeo, F.; Bottjer, D.; Jungbluth, S.; Burkhardt, B.; Hawco, N.; Boiteau, R.


    The Center for Microbial Oceanography: Research and Education (C-MORE) is a National Science Foundation-sponsored Science and Technology Center. C-MORE comprises six partner institutions: University of Hawaii (headquarters), Massachusetts Institute of Technology, Woods Hole Oceanographic Institution, Oregon State University, University of California at Santa Cruz and Monterey Bay Aquarium Research Institute. C-MORE's Professional Development Training Program is aimed at equipping graduate students and post-docs at all six institutions with the skills and experiences needed to maximize their potential and succeed in their professional careers. This program is administered through the C-MORE Education Office and was developed in close collaboration with graduate students, post-docs, and faculty. This program has formal but flexible requirements. There is only one required module (Outreach). The seven optional modules include: Science Communication, Leadership, Mentoring, Teaching, Research Exchange, Diversity and Proposal Writing. Masters students choose three optional modules; Ph.D. students and post-docs choose five. Most modules consist of a training component, followed by a practical component. All participants will are expected to complete program evaluations. Below are some examples of program offerings: Science Communication Module In partnership with the Communication Partnership for Science and the Sea, C-MORE organized three Science Communication workshops at the University of Hawaii, Monterey Bay Aquarium Research Institute and Massachusetts Institute of Technology. These workshops train participants to distill their research into language that is free of jargon and accessible to a general audience. After the training, participants are asked to produce a communication product based on their research, such as a magazine article, press release, podcast or a blog. Diversity Module To date, C-MORE has organized three teleconferences on diversity, attended by

  2. 'Ike Wai Professional Development Model for Students and Post-docs

    Bruno, B. C.


    'Ike Wai: Securing Hawaii's Water Future, funded by NSF EPSCoR, is an interdisciplinary research collaboration among geophysicists, geochemists, engineers, microbiologists, computational modelers, data scientists and social scientists. Key questions include: How much water is there? How does it flow? How long will it last? Undergraduate students, graduate students and post-docs are actively involved in the research, and their professional development is a key part of the project. An underlying principle is that students assume responsibility for their own learning and professional development. Based on the model created by the NSF Center for Microbial Oceanography: Research and Education (C-MORE) (Bruno et al, 2008; Guannel et al 2014, Bottjer et al 2014), the 'Ike Wai professional development program includes (1) Leadership. Each student and post-doc creates an Individualized Professional Development plan, which includes leadership training (provided by external facilitators) and assuming leadership roles (such as developing and implementing trainings for their peers). (2) EDventures. Based on the C-MORE model, EDventures combines proposal-writing training with the incentive of seed money. Rather than providing training a priori, the EDventures model encourages students and post-docs to write a proposal based on guidelines provided. Training occurs during a two-stage review stage: proposers respond to panel reviews and resubmit their proposal within a single review cycle. C-MORE EDventures alumni self-report statistically significant confidence gains on all questions posed. Their subsequent proposal success is envious: of the 12 proposals submitted by to NSF, 50% were funded. (Wood Charlson & Bruno, 2015) (3) Layered Mentoring Network. All ´Ike Wai participants serve as both mentor and mentee. Students are matched with a non-research mentor in addition to their advisor to promote a holistic approach to career development. They will also serve as mentors to more

  3. Effects of biochar and clay amendment on nutrient sorption of an Arenosol in semi-arid NE-Brazil

    Beusch, Christine; Kaupenjohann, Martin


    In the semi-arid Northeast of Brazil nutrient-poor Arenosol with a low capacity to retain water and nutrients is the predominant soil type. Our aim is to provide a long-term melioration of the soils with locally available and inexpensive materials. We hypothesize an increase in nutrient sorption by the addition of biochar and clay. We conducted adsorption experiments according to OECD 106 batch equilibrium method in order to test this hypothesis. Sandy Arenosol, locally produced pyrolized biochar made of Prosopis juliflora, and a clayey Vertisol with a clay content of 69.8 %, all from our project area in Pernambuco, NE-Brazil, were used. The percentage of biochar and Vertisol added were 0 % (pure Arenosol), 1 %, 2.5 %, 5 %, 10 %, 100 % (pure biochar respectively Vertisol). Samples were shaken for 24 hours in a 1:5 solid-solution ratio in six different concentrations of Ammonium-N, Nitrate-N (0 - 25 mg L-1 each), Phosphorus (0 - 19.8 mg L-1) and Potassium (0 - 50 mg L-1). These concentrations were chosen to represent a common range of nutrients in a prevalent quaternary fertilization scheme of N:P:K of 1:0.4:1, with half NH4-N and NO3-N each. Then, where possible, sorption isotherms according to Langmuir were derived. Addition of biochar and Vertisol only showed marginal effects on Ammonium sorption. We detected a high loss of Ammonium with pure biochar, we assume loss of gaseous NH3. High rates of biochar addition caused Nitrate retention. Biochar increased P sorption with a maximum adsorption capacity (qmax) of 27.35 mg kg-1 for the 5 % amendment, although some P was leached out (up to 1.58 mg kg-1 for the 10 % addition). Phosphate sorption on Vertisol was even higher with a qmax for the 5 % addition of 60.77 mg kg-1. Potassium did not sorb to biochar, but was strongly leached out (84.19 mg kg-1 out of the 5 % addition). For Vertisol we observed a strong Potassium sorption that is linear within the concentration range we tested. A possible enhancement of nutrient

  4. Sorption of pure N2O to biochars and other organic and inorganic materials under anhydrous conditions

    Cornelissen, Gerard; Rutherford, David W.; Arp, Hans Peter H.; Dorsch, Peter; Kelly, Charlene N.; Rostad, Colleen E.


    Suppression of nitrous oxide (N2O) emissions from soil is commonly observed after amendment with biochar. The mechanisms accounting for this suppression are not yet understood. One possible contributing mechanism is N2O sorption to biochar. The sorption of N2O and carbon dioxide (CO2) to four biochars was measured in an anhydrous system with pure N2O. The biochar data were compared to those for two activated carbons and other components potentially present in soils—uncharred pine wood and peat—and five inorganic metal oxides with variable surface areas. Langmuir maximum sorption capacities (Qmax) for N2O on the pine wood biochars (generated between 250 and 500 °C) and activated carbons were 17–73 cm3 g–1 at 20 °C (median 51 cm3 g–1), with Langmuir affinities (b) of 2–5 atm–1 (median 3.4 atm–1). Both Qmaxand b of the charred materials were substantially higher than those for peat, uncharred wood, and metal oxides [Qmax 1–34 cm3 g–1 (median 7 cm3 g–1); b 0.4–1.7 atm–1 (median 0.7 atm–1)]. This indicates that biochar can bind N2O more strongly than both mineral and organic soil materials. Qmax and b for CO2 were comparable to those for N2O. Modeled sorption coefficients obtained with an independent polyparameter—linear free-energy relationship matched measured data within a factor 2 for mineral surfaces but underestimated by a factor of 5–24 for biochar and carbonaceous surfaces. Isosteric enthalpies of sorption of N2O were mostly between −20 and −30 kJ mol–1, slightly more exothermic than enthalpies of condensation (−16.1 kJ mol–1). Qmax of N2O on biochar (50000–130000 μg g–1 biochar at 20 °C) exceeded the N2O emission suppressions observed in the literature (range 0.5–960 μg g–1 biochar; median 16 μg g–1) by several orders of magnitude. Thus, the hypothesis could not be falsified that sorption of N2O to biochar is a mechanism of N2O emission suppression.

  5. The sensitivity of peat soil and peatland vegetation to drought: release of dissolved organic carbon (DOC) on rewetting

    Ritson, Jonathan; Graham, Nigel; Templeton, Michael; Freeman, Christopher; Clark, Joanna


    Organic rich peat soils are a major store of carbon worldwide. Their existence is predicated on high year-round water tables which create an anoxic environment, thus limiting decay, and also to the recalcitrance of plant litter (dead plant material) commonly found in peatland areas. Climate change threatens the stability of peat soils by altering the biogeochemical cycles which control plant decay, lowering water tables so that oxic degradation can occur and by changing habitat niches such that less recalcitrant species can thrive in peatlands. One of the major fluxes of carbon from peatlands is through dissolved organic carbon (DOC) in surface waters. As peatland areas in the UK are often used as source waters for drinking water supply this presents a problem to water utilities as DOC must be effectively removed to limit colour, odour and the formation of potentially carcinogenic by-products on disinfection. Changes in catchment vegetation may occur due to climate change, nutrient deposition and changing bioclimatic envelopes. How different peatland vegetation contribute to DOC flux and how this may change in the future is therefore of interest. A six week laboratory simulation was performed on typical peatland litter (Sphagnum spp., Calluna vulgaris, Molinea caerulea, Juncus effusus) and a peat soil collected from Exmoor National Park, UK. The simulation monitored DOC flux from the decaying litter/soil and considered the impact of different drought severities using the 50th, 25th, 10th and 5th percentiles of the mean July/August monthly rainfall for Exmoor. On rewetting following the drought, all sources produced significantly different amounts of DOC (Tukey HSD pJuncus>Calluna>Sphagnum>peat. The source also had a significant (ANOVA pdrinking water treatment, with Juncus DOC proving the easiest to remove whilst Sphagnum DOC was the most difficult. Sphagnum DOC had the lowest ratio of humic-like to protein-like fluorescence, which is indicative of DOC which is

  6. Biosorption kinetics, thermodynamics and isosteric heat of sorption of Cu(II) onto Tamarindus indica seed powder.

    Chowdhury, Shamik; Saha, Papita Das


    Biosorption of Cu(II) by Tamarindus indica seed powder (TSP) was investigated as a function of temperature in a batch system. The Cu(II) biosorption potential of TSP increased with increasing temperature. The rate of the biosorption process followed pseudo second-order kinetics while the sorption equilibrium data well fitted to the Langmuir and Freundlich isotherm models. The maximum monolayer Cu(II) biosorption capacity increased from 82.97 mg g(-1) at 303 K to 133.24 mg g(-1) at 333 K. Thermodynamic study showed spontaneous and endothermic nature of the sorption process. Isosteric heat of sorption, determined using the Clausius-Clapeyron equation increased with increase in surface loading showing its strong dependence on surface coverage. The biosorbent was characterized by scanning electron microscopy (SEM), surface area and porosity analyzer, X-ray diffraction (XRD) spectrum and Fourier transform infrared (FTIR) spectroscopy. The results of FTIR analysis of unloaded and Cu(II)-loaded TSP revealed that -NH(2), -OH, -C=O and C-O functional groups on the biosorbent surface were involved in the biosorption process. The present study suggests that TSP can be used as a potential, alternative, low-cost biosorbent for removal of Cu(II) ions from aqueous media.

  7. Removal of arsenate from aqueous solution by nanocrystalline Mg/Al layered double hydroxide: sorption characteristics, prospects, and challenges.

    Goh, K H; Lim, T T; Dong, Z L


    Removal of arsenate (As(V)) from aqueous solution using both nanocrystalline and coprecipitated Mg/Al layered double hydroxides (LDHs) was examined under different sorption/desorption conditions. The surface area, pore volume, and pore size of the nanocrystalline LDH were significantly higher than those of the coprecipitated LDH, thus resulting in a higher As(V) sorption maximum than the coprecipitated LDH. The calculated activation energy (E(a)) value was 24.7 kJ/mol, suggesting the occurrence of anion exchange process for As(V) removal by the nanocrystalline LDH. The predominance of anion exchange process was further supported by the investigation of ionic strength effect, and XRD and FTIR analyses. The effect of aqueous matrix on As(V) sorption by the nanocrystalline LDH was found to increase in the order of nitrate nanocrystalline LDH besides the predominant anion exchange process. Prospects and challenges for practical application of the nanocrystalline LDH were also discussed in the latter part of this study.

  8. Sorption behavior of Eu(III) from an aqueous solution onto modified hydroxyapatite: kinetics, modeling and thermodynamics.

    Gad, H M H; Youssef, M A


    Nano-pore hydroxyapatite (HAP) was prepared using physical activation of raw and chemically modified [using Acid; HNO3 (HAPA) or Base; NaOH (HAPB)] bone char (BC) by heating at 900°C for 1 hr to obtain HAP9, HAPA9 and HAPB9, respectively. Investigation the effects of thermal and chemical treatment of prepared nano-hydroxyapatite on elemental analysis, FTIR, scanning electron microscopy, surface area and consequently, the sorption behavior of Eu (III) ions onto the prepared nano-pore hydroxyapatite. Batch adsorption technique was used and the obtained results revealed that the optimum pH = 5.0. The % removal of europium (III) using HAPA9 and HAPB9 reach to 100% within 15 min, while HAP9 after 180 min and the pseudo-second-order was found to be fit to the experimental data. According to Langmuir model, the maximum sorption capacities (qm) were 123.8, 384.9 and 74.2 mg g(-1) for HAP9, HAPA9 and HAPB9, respectively. The reaction is spontaneous according to ΔG° value. HCl (0.5 M) was the most efficient desorbing agent for recovery of Eu(III) and regeneration of adsorbents. Finally, nano-pore hydroxyapatite (HAP) was low cost and very effective adsorbent for sorption or recovery of Eu(III) from aqueous solutions and remediation of environmental pollution.

  9. Sorption isotherm studies of Cd(II) ions using living cells of the marine microalga Tetraselmis suecica (Kylin) Butch.

    Pérez-Rama, M; Torres, E; Suárez, C; Herrero, C; Abalde, J


    The present work reports the use of living cells of the marine microalga Tetraselmis suecica for the biosorption of cadmium ions. For a better understanding of the biosorption characteristics, three fractions of removed cadmium (total, bioadsorbed and intracellular) were measured in the cells after 24 and 72 h of exposure to different initial cadmium concentrations (0.6-45 mg L(-1)). Both the Langmuir and Freundlich models were suitable for describing the sorption of cadmium ions by this microalga. The maximum sorption capacity was estimated to be 40.22 mg Cd g(-1) after 72 h using the Langmuir sorption model. In the lower cadmium concentrations, metal removed intracellularly was higher than that removed on the microalgal cell surface. Therefore, the intracellular fraction contributed more to the total removed cadmium than the fraction bioadsorbed to the cellular surface. The results showed that the cadmium removal capacity using living biomass could be much more effective than with non-living biomass due to the intracellular bioaccumulation. According to the microorganism selected and its tolerance to the toxic effect of the metal, the cadmium content in the intracellular fraction can become very significant, just like it happened with Tetraselmis.

  10. Novel experimental methods for assessment of hydrogen storage capacity and modelling of sorption in Cu-BTC

    Khvostikova, O. [IFW Dresden, Institute for Complex Materials, P.O. Box 27 01 16, D-01171 Dresden (Germany); Institut fuer Werkstoffwissenschaft, TU Dresden, Helmholtzstr. 7, D-01069 Dresden (Germany); Assfour, B.; Seifert, G. [Institut fuer Physikalische Chemie, TU Dresden, Bergstr. 66b, D-01062 Dresden (Germany); Hermann, H.; Horst, A.; Ehrenberg, H. [IFW Dresden, Institute for Complex Materials, P.O. Box 27 01 16, D-01171 Dresden (Germany)


    Novel experimental procedures for hydrogen adsorption studies are presented. The methods provide an important advantage: pure material sorption behaviour can be directly determined without the use of equations of state (EOS) at low temperatures. The storage properties of Cu-BTC [Cu{sub 3}(BTC){sub 2}, BTC - 1,3,5-benzenetricarboxylate] were investigated under different thermodynamic conditions. The maximum hydrogen uptake of 4.6 wt% was observed at 25 K. We compared the results obtained in this work with previously reported experimental data to prove the validity of the novel methods for the hydrogen sorption measurements. The experimental data of the present work show a good agreement with the results reported in the literature. Additionally, the modelling of the hydrogen sorption processes in Cu-BTC was carried out. The simulations were performed in the form of isotherms and isobars. Fairly good agreement with experimental data has been achieved. Uncertainties in MOF-H{sub 2} interactions are most likely the major reasons for the remaining difference between simulations and experiments. (author)

  11. Investigation into the sorption of nitroglycerin and diazepam into PVC tubes and alternative tube materials during application.

    Treleano, Anna; Wolz, Gerd; Brandsch, Rainer; Welle, Frank


    Plastic bags and tubes are increasingly used for the storage and application of pharmaceutical formulations. The most common polymer material for drug application sets is plasticized poly(vinylchloride) (PVC). During application of pharmaceutical drug solution through PVC tubes, the polymer and the contact media interact which leads to leaching out of polymer additives or sorption of ingredients of the drug solution. Whereas the discussion of leaching of plasticizers is focussed on the toxicological properties of a drug packaging system, the sorption of drug formulation compounds has an influence on the dosage of the active pharmaceutical ingredient resulting in a reduced drug delivery to the patient. Therefore sorption has an influence on the effectiveness and success of the therapy. Within the study, the concentration profiles of nitroglycerin and diazepam solutions were determined after pumping the solutions through infusion administration sets. The study includes plasticized PVC tubes with different plasticizers (DEHP, DEHA, DEHT, TEHTM, DINCH, poly adipate), PVC (DEHP) tubes with different shore hardness as well as alternative polymer materials like EVA, TPE, PUR, silicone, LDPE and PP. From the experimental concentration curves it could be shown, that in the first minutes of the application of the drug solution the sorption of the active compound is at its maximum, resulting in the lowest concentration in the applied pharmaceutical solution. For a PVC tube with DEHP as plasticizer and a shore hardness of 80 only about 57% of the initial nitroglycerin concentration in the solution is applied to the patient in the first minutes of the application. For PVC tube (DEHP, shore 80) the experimental data were simulated using mathematical diffusion models. The concentration profiles during application could be well simulated using the partition coefficient K=50 (nitroglycerin) and K=300 (diazepam), respectively. However, the experimental results indicate, that the

  12. In situ sorption of technetium using activated carbon

    Holm, E. E-mail:; Gaefvert, T.; Lindahl, P.; Roos, P


    The sorption of technetium in pertechnetate form on carbon has been investigated. The sorption is pH dependent with maximal distribution coefficients, K{sub d}, in the order of 10{sup 6} at pH 2-4 for activated carbon with a grain size {<=}100 {mu}m. The equilibrium time to reach such distribution coefficient was about 5 h at room temperature. The exact mechanisms for the sorption are not fully understood but reduction of Tc by the carbon might be an important process. Technetium can effectively and rapidly (5 l min{sup -1}) be sorbed from very large volumes (several hundred liters) of environmental waters on commercial cartridge filters impregnated with activated carbon. After incineration, the filters can be analyzed for {sup 99}Tc by conventional methods.

  13. Rapid and fully automated Measurement of Water Vapor Sorption Isotherms

    Arthur, Emmanuel; Tuller, Markus; Møldrup, Per


    Eminent environmental challenges such as remediation of contaminated sites, the establishment and maintenance of nuclear waste repositories, or the design of surface landfill covers all require accurate quantification of the soil water characteristic at low water contents. Furthermore, several...... essential but difficult-to-measure soil properties such as clay content and specific surface area are intimately related to water vapor sorption. Until recently, it was a major challenge to accurately measure detailed water vapor sorption isotherms within an acceptable time frame. This priority...... and pesticide volatilization, toxic organic vapor sorption kinetics, and soil water repellency are illustrated. Several methods to quantify hysteresis effects and to derive soil clay content and specific surface area from VSA-measured isotherms are presented. Besides above mentioned applications, potential...

  14. Carbon dioxide sorption capacities of coal gasification residues.

    Kempka, Thomas; Fernández-Steeger, Tomás; Li, Dong-Yong; Schulten, Marc; Schlüter, Ralph; Krooss, Bernhard M


    Underground coal gasification is currently being considered as an economically and environmentally sustainable option for development and utilization of coal deposits not mineable by conventional methods. This emerging technology in combination with carbon capture and sorptive CO2 storage on the residual coke as well as free-gas CO2 storage in the cavities generated in the coal seams after gasification could provide a relevant contribution to the development of Clean Coal Technologies. Three hard coals of different rank from German mining districts were gasified in a laboratory-scale reactor (200 g of coal at 800 °C subjected to 10 L/min air for 200 min). High-pressure CO2 excess sorption isotherms determined before and after gasification revealed an increase of sorption capacity by up to 42%. Thus, physical sorption represents a feasible option for CO2 storage in underground gasification cavities.

  15. Radionuclide and metal sorption on cement and concrete

    Ochs, Michael; Wang, Lian


    Cementitious materials are being widely used as solidification/stabilisation and barrier materials for a variety of chemical and radioactive wastes, primarily due to their favourable retention properties for metals, radionuclides and other contaminants. The retention properties result from various mineral phases in hydrated cement that possess a high density and diversity of reactive sites for the fixation of contaminants through a variety of sorption and incorporation reactions. This book presents a state of the art review and critical evaluation of the type and magnitude of the various sorption and incorporation processes in hydrated cement systems for twenty-five elements relevant for a broad range of radioactive and industrial wastes. Effects of cement evolution or ageing on sorption/incorporation processes are explicitly evaluated and quantified. While the immobilisation of contaminants by mixing-in during hydration is not explicitly addressed, the underlying chemical processes are similar. A quantitativ...

  16. Aroma compound sorption by oak wood in a model wine.

    Ramirez Ramirez, G; Lubbers, S; Charpentier, C; Feuillat, M; Voilley, A; Chassagne, D


    Oak wood used for wine barrels was immersed into a model wine containing eight aroma compounds (e.g., aromatic and terpene alcohols, ethyl esters, and aldehyde), for which activity coefficients in water and model wine were determined using the mutual solubility measurement. A mass balance of these volatiles considering their reactivity in model wine was established. For most of the studied aroma compounds, and mainly for linalool and ethyl octanoate, a sorption behavior into wood was reported for the first time. This phenomenon was selective and could not be related to the solubilities in model wine and hydrophobicities of the studied aroma compounds, suggesting that acid-base and polar characteristics of wood were more involved in this sorption mechanism. This study has also shown that the level of sorption is a function of the ratio of wood surface area/solution volume.

  17. Comparative sorption properties of metal(III) phosphates

    Mustafa, S.; Naeem, A.; Murtaza, S.; Rehana, N.; Samad, H.Y.


    Sorption behavior of metal(III) phosphates toward Zn{sup 2+} was investigated using different concentrations, pHs, and temperatures. Ion exchange between protons from the surface and metal cations from solutions was found to be responsible for metal sorption by metal(III) phosphates. Dissociation constants of metal(III) phosphates and binding constants of the Zn{sup 2+} with metal(III) phosphates were determined using Henderson-Hasselbach and modified Langmuir equations, respectively. The sorption process in all the three metal phosphates was found to be endothermic in nature while the dissociation process was observed to be endothermic in AlPO{sub 4} and FePO{sub 4} and exothermic in CrPO{sub 4}.

  18. Theory of Sorption Hysteresis in Nanoporous Solids: II. Molecular condensation

    Bazant, Martin Z


    Motivated by the puzzle of sorption hysteresis in Portland cement concrete or cement paste, we develop in Part II of this study a general theory of vapor sorption and desorption from nanoporous solids, which attributes hysteresis to hindered molecular condensation with attractive lateral interactions. The classical mean-field theory of van der Waals is applied to predict the dependence of hysteresis on temperature and pore size, using the regular solution model and gradient energy of Cahn and Hilliard. A simple "hierarchical wetting" model for thin nanopores is developed to describe the case of strong wetting by the first monolayer, followed by condensation of nanodroplets and nanobubbles in the bulk. The model predicts a larger hysteresis critical temperature and enhanced hysteresis for molecular condensation across nanopores at high vapor pressure than within monolayers at low vapor pressure. For heterogeneous pores, the theory predicts sorption/desorption sequences similar to those seen in molecular dynami...

  19. Responses of CO2 emission and pore water DOC concentration to soil warming and water table drawdown in Zoige Peatlands

    Yang, Gang; Wang, Mei; Chen, Huai; Liu, Liangfeng; Wu, Ning; Zhu, Dan; Tian, Jianqing; Peng, Changhui; Zhu, Qiuan; He, Yixin


    Peatlands in Zoige Plateau contains more than half of peatland carbon stock in China. This part of carbon is losing with climate change through dissolved organic carbon (DOC) export and carbon dioxide (CO2) emissions, both of which are vulnerable to the environmental changes, especially on the Zoige Plateau with a pace of twice the observed rate of global climate warming. This research aimed to understand how climate change including soil warming, rainfall reduction and water table change affect CO2 emissions and whether the trends of changes in CO2 emission are consistent with those of pore water DOC concentration. A mesocosm experiment was designed to investigate the CO2 emission and pore water DOC during the growing seasons of 2009-2010 under scenarios of passive soil warming, 20% rainfall reduction and changes to the water table levels. The results showed a positive relationship between CO2 emission and DOC concentration. For single factor effect, we found no significant relationship between water table and CO2 emission or DOC concentration. However, temperature at 5 cm depth was found to have positive linear relationship with CO2 emission and DOC concentration. The combined effect of soil warming and rainfall reduction increased CO2 emission by 96.8%. It suggested that the drying and warming could stimulate potential emission of CO2. Extending this result to the entire peatland area in Zoige Plateau translates into 0.45 Tg CO2 emission per year over a growing season. These results suggested that the dryer and warmer Zoige Plateau will increase CO2 emission. We also found the contribution rate of DOC concentration to CO2 emission was increased by 12.1% in the surface layer and decreased by 13.8% in the subsurface layer with combined treatment of soil warming and rainfall reduction, which indicated that the warmer and dryer environmental conditions stimulate surface peat decomposition process.

  20. Investigation of sorption and migration of {sup 90}Sr on clinoptilolite and mordenite

    Minglu Ye; Lu shi jun; Chenkou Quin; Lihong Xu; Adi He; Zhihua Tang [Fudan Univ., Shanghai (China). Dept. of Nuclear Science; Guoqing Xu; Xuanlin Fan; Jifang Gu; Zhichao Du [Beijing Research Inst. of Uranium Geology (BRIUG), BJ (China)


    In this work the behaviors of sorption and migration of radioactive strontium on clinoptilolite and mordenite in simulated groundwater has been investigated by both batch technique and column experiment. The sorption ratios (Rd) and the sorption equilibrium time were determined. The effects of particle size of samples, water-to-rock ratios, pH values of simulated groundwater and concentration of strontium in the simulated groundwater on the sorption ratios of Sr were studied. The sorption capacity and sorption isotherm of Sr were determined. The behaviors of sorption and migration of Sr in clinoptilolite column were studied. The migration velocity of Sr was calculated. The results show that sorption abilities of clinoptilolite and mordenite for Sr were very strong. (orig.)

  1. Sorption of polycyclic aromatic hydrocarbons (PAHs) to lignin: effects of hydrophobicity and temperature.

    Zhang, Ming; Ahmad, Mahtab; Lee, Sang Soo; Xu, Li Heng; Ok, Yong Sik


    The study of the sorption of contaminants to lignin is significant for understanding the migration of contaminants in the environment as well as developing low cost sorbent. In this study, sorption of three polycyclic aromatic hydrocarbons (PAHs), naphthalene, acenaphthene and phenanthrene, to lignin was investigated. Sorption isotherms were well described by both linear and Freundlich sorption models. Sorption coefficients of PAHs to lignin from water obtained from regression of both linear model (K d) and Freundlich model (K f) were highly positively correlated with hydrophobicity of PAHs. The amorphous structure of lignin provided sufficient sorption domain for partitioning of PAHs, and the attraction between PAHs molecules and aromatic fractions in lignin via π-π electron-donor-acceptor (π-π EDA) interaction is hypothesized to provide a strong sorption force. Thermodynamic modeling revealed that sorption of PAHs to lignin was a spontaneous and exothermic process.

  2. Effect of soil pH on sorption of salinomycin in clay and sandy soils


    Full Length Research Paper. Effect of ... In this study, sorption of salinomycin was measured in four agricultural soils, a clay soil with low organic ... Key words: Salinomycin, sorption, pH, desorption, environmental pollution, phosphate buffer.


    Cadmium sorption and desorption experiments were conducted on different fractions of soils amended with different biosolids with varying chemical properties and unamended soil (control). Biosolids addition increased the slope of the Cd sorption isotherms compared to the control s...

  4. Sorption of Enrofloxacin and Ciprofloxacin in Agricultural Soils: Effect of Organic Matter

    Teixidó, Marc; Medeiros, Joana; Beltrán, José L; Prat, Maria-Dolors; Granados, Mercè


    ...), an organic matter (OM) surrogate, to the sorption of FQs in natural soils. Sorption of enrofloxacin and ciprofloxacin was studied in two completely different Spanish agricultural soils with similar pH...

  5. Bio—Rad公司:VersaDocTM 4000成像系统



  6. Performance e Educação: configurações parateatrais da docência

    Marcelo de Andrade Pereira


    Full Text Available texto procura discutir a docência como performance parateatral. Para tanto, parte-se da contribuição dos Estudos da Performance e das discussões contemporâneas da Educação, introduzindo conceitos como cotidiano, performatividade, prática docente. Problematiza-se a natureza e a função do ato docente em sua teatralidade. As figuras do clown, do bufão e do dândi são convocadas para servirem de apoio por intermédio do qual a performance e a teatralidade do ato docente encontram termo.

  7. CTM4DOC: electronic structure analysis from X-ray spectroscopy

    Delgado-Jaime, Mario Ulises; Zhang, Kaili; Vura-Weis, Josh; de Groot, Frank M. F.


    Two electronic structure descriptions, one based on orbitals and the other based on term symbols, have been implemented in a new Matlab-based program, CTM4DOC. The program includes a graphical user interface that allows the user to explore the dependence of details of electronic structure in transition metal systems, both in the ground and core-hole excited states, on intra-atomic electron–electron, crystal-field and charge-transfer interactions. The program can also track the evolution of electronic structure features as the crystal-field parameters are systematically varied, generating Tanabe–Sugano-type diagrams. Examples on first-row transition metal systems are presented and the implications on the interpretation of X-ray spectra and on the understanding of low-spin, high-spin and mixed-spin systems are discussed. PMID:27577785

  8. Current status of bacteriological parameters and DOC/POC in Xiamen coastal waters

    Khalid Maskaoui; Tianling Zheng; Huasheng Hong; Zhiming Yu; Zhong Hu; Yun Tian; Lizhe Cai


    The surface and bottom waters samples were collected from six locations in Xiamen west-em sea. The quantified estimation of bacterial production (3H-thymidine method) and observation ofbacterial heterotrophic activity (14C-glucose method) have been made in order to have a better under-standing of the role of marine bacteria and their activities. The results showed that the mean value ofbacterial heterotrophic activity was 9 × 108 cells/(L. h) in the surface waters and 2.6 × 108 cells/( L. h)in the bottom waters. The mean value of bacterial production was 38 × 108 cells/( L. h) in the surfacewaters and 7.1 × 108 cells/(L.h) in the bottom waters. The relationship between bacterial production,heterotrophic activity, POC and DOC measured during this survey were discussed. The good under-standing of the relationship between bacteria activity and total coliform was addressed.

  9. Temperature, DOC level and basin interactions explain the declining oxygen concentrations in the Bothnian Sea

    Ahlgren, Joakim; Grimvall, Anders; Omstedt, Anders; Rolff, Carl; Wikner, Johan


    Hypoxia and oxygen deficient zones are expanding worldwide. To properly manage this deterioration of the marine environment, it is important to identify the causes of oxygen declines and the influence of anthropogenic activities. Here, we provide a study aiming to explain the declining oxygen levels in the deep waters of the Bothnian Sea over the past 20 years by investigating data from environmental monitoring programmes. The observed decline in oxygen concentrations in deep waters was found to be primarily a consequence of water temperature increase and partly caused by an increase in dissolved organic carbon (DOC) in the seawater (R2Adj. = 0.83) as well as inflow from the adjacent sea basin. As none of the tested eutrophication-related predictors were significant according to a stepwise multiple regression, a regional increase in nutrient inputs to the area is unlikely to explain a significant portion of the oxygen decline. Based on the findings of this study, preventing the development of anoxia in the deep water of the Bothnian Sea is dependent on the large-scale measures taken to reduce climate change. In addition, the reduction of the nutrient load to the Baltic Proper is required to counteract the development of hypoxic and phosphate-rich water in the Baltic Proper, which can form deep water in the Bothnian Sea. The relative importance of these sources to oxygen consumption is difficult to determine from the available data, but the results clearly demonstrate the importance of climate related factors such as temperature, DOC and inflow from adjacent basins for the oxygen status of the sea.

  10. Assessment of long-term outcomes for the STRokE DOC telemedicine trial.

    Meyer, Brett C; Raman, Rema; Ernstrom, Karin; Tafreshi, Gilda M; Huisa, Branko; Stemer, Andrew B; Hemmen, Thomas M


    Telemedicine can provide stroke evaluations in locations with limited available expertise. The reliability of telestroke has been established. Decision making efficacy has been shown in the National Institutes of Health's STRokE DOC trial. No prospective trial has assessed long-term telestroke outcomes, however. In an institutional review board-approved trial (NCT00936455), we contacted patients originally enrolled in the STRokE DOC trial. A telephone script was used to verify consent. Patients were asked standardized questions regarding disposition, modified Rankin Scale (mRS) score, mortality, and recurrent stroke for 2 retrospective time points (6 and 12 months postevent) and one current time point. Blind was maintained. Primary outcome measures of mortality and percent mRS score of 0-1 [%mRS(0-1)] at 6 months are reported. Wilcoxon's rank-sum test was used for continuous variables, and Fisher's exact was used for categorical variables. Of the original 222 participants, 75 patients or surrogates could be contacted. Mean time from enrollment was 3.96 ± 1.0 years (range, 2.33-5.45 years). Mean National Institutes of Health Stroke Scale (NIHSS) score was 8 ± 7 (5 ± 8 for telephone; 12 ± 8 for telemedicine; P = .002). The rate of intravenous recombinant tissue plasminogen activator (rt-PA) use was 31%. Six-month %mRS(0-1) outcome was not different, at 42%. Mortality after imputation to the entire study sample also was not different, at 18%. There was no difference in the rate of recurrent stroke (P = .61). Some 85% of patients were home at 6 months. This study reports a good 6-month outcome for stroke patients evaluated by telemedicine or telephone. This design is limited by the time since original enrollment and resultant inability to contact participants. Although these findings can add to the limited data on telemedicine outcomes, a prospective trial is needed.

  11. Sorption and desorption of carbamazepine from water by smectite clays.

    Zhang, Weihao; Ding, Yunjie; Boyd, Stephen A; Teppen, Brian J; Li, Hui


    Carbamazepine is a prescription anticonvulsant and mood stabilizing pharmaceutical administered to humans. Carbamazepine is persistent in the environment and frequently detected in water systems. In this study, sorption and desorption of carbamazepine from water was measured for smectite clays with the surface negative charges compensated with K+, Ca2+, NH4+, tetramethylammonium (TMA), trimethylphenylammonium (TMPA) and hexadecyltrimethylammonium (HDTMA) cations. The magnitude of sorption followed the order: TMPA-smectite≥HDTMA-smectite>NH4-smectite>K-smectite>Ca-smectite⩾TMA-smectite. The greatest sorption of carbamazepine by TMPA-smectite is attributed to the interaction of conjugate aromatic moiety in carbamazepine with the phenyl ring in TMPA through π-π interaction. Partitioning process is the primary mechanism for carbamazepine uptake by HDTMA-smectite. For NH4-smectite the urea moiety in carbamazepine interacts with exchanged cation NH4+ by H-bonding hence demonstrating relatively higher adsorption. Sorption by K-, Ca- and TMA-smectites from water occurs on aluminosilicate mineral surfaces. These results implicate that carbamazepine sorption by soils occurs primarily in soil organic matter, and soil mineral fractions play a secondary role. Desorption of carbamazepine from the sorbents manifested an apparent hysteresis. Increasing irreversibility of desorption vs. sorption was observed for K-, Ca-, TMA-, TMPA- and HDTMA-clays as aqueous carbamazepine concentrations increased. Desorption hysteresis of carbamazepine from K-, Ca-, NH4-smectites was greater than that from TMPA- and HDTMA-clays, suggesting that the sequestrated carbamazepine molecules in smectite interlayers are more resistant to desorption compared to those sorbed by organic phases in smectite clays.

  12. Sorption of 2,4-dinitroanisole (DNAN) on lignin

    Rabih Saad; Zorana Radovic-Hrapovic; Behzad Ahvazi; Sonia Thiboutot; Guy Ampleman; Jalal Hawari


    The present study describes the use of two commercially available lignins,namely,alkali and organosolv lignin,for the removal of 2,4-dinitroanisole (DNAN),a chemical widely used by the military and the dye industry,from water.Sorption of DNAN on both lignins reached equilibrium within 10 hr and followed pseudo second-order kinetics with sorption being faster with alkali than with organosolv lignin,i.e.k2 10.3 and 0.3 g/(,respectively.In a separate study we investigated sorption of DNAN between 10 and 40℃ and found that the removal of DNAN by organosolv lignin increased from 0.8 to 7.5 mg/g but reduced slightly from 8.5 to 7.6 mg/g in the case of alkali lignin.Sorption isotherms for either alkali or organosolv lignin best fitted Freundlich equation with enthalpy of formation,△H0 equaled to 14 or 80 kJ/mol.To help understand DNAN sorption mechanisms we characterized the two lignins by elemental analysis,BET nitrogen adsorption-desorption and 31p NMR.Variations in elemental compositions between the two lignins indicated that alkali lignin should have more sites (O- and S-containing functionalities) for H-bonding.The BET surface area and calculated total pore volume of alkali lignin were almost 10 times greater than that of organosolv lignin suggesting that alkali lignin should provide more sites for sorption.31p NMR showed that organosolv lignin contains more phenolic -OH groups than alkali lignin,i.e.,70% and 45%,respectively.The variations in the type of OH groups between the two lignins might have affected the strength of H-bonding between DNAN and the type of lignin used.

  13. Sorption of 2,4-dinitroanisole (DNAN) on lignin.

    Saad, Rabih; Radovic-Hrapovic, Zorana; Ahvazi, Behzad; Thiboutot, Sonia; Ampleman, Guy; Hawari, Jalal


    The present study describes the use of two commercially available lignins, namely, alkali and organosolv lignin, for the removal of 2,4-dinitroanisole (DNAN), a chemical widely used by the military and the dye industry, from water. Sorption of DNAN on both lignins reached equilibrium within 10 hr and followed pseudo second-order kinetics with sorption being faster with alkali than with organosolv lignin, i.e. k2 10.3 and 0.3 g/(mg x hr), respectively. In a separate study we investigated sorption of DNAN between 10 and 40 degrees C and found that the removal of DNAN by organosolv lignin increased from 0.8 to 7.5 mg/g but reduced slightly from 8.5 to 7.6 mg/g in the case of alkali lignin. Sorption isotherms for either alkali or organosolv lignin best fitted Freundlich equation with enthalpy of formation, deltaH0 equaled to 14 or 80 kJ/mol. To help understand DNAN sorption mechanisms we characterized the two lignins by elemental analysis, BET nitrogen adsorption-desorption and 31P NMR. Variations in elemental compositions between the two lignins indicated that alkali lignin should have more sites (O- and S-containing functionalities) for H-bonding. The BET surface area and calculated total pore volume of alkali lignin were almost 10 times greater than that of organosolv lignin suggesting that alkali lignin should provide more sites for sorption. 31P NMR showed that organosolv lignin contains more phenolic -OH groups than alkali lignin, i.e., 70% and 45%, respectively. The variations in the type of OH groups between the two lignins might have affected the strength of H-bonding between DNAN and the type of lignin used.

  14. Partially-irreversible sorption of formaldehyde in five polymers

    Ye, Wei; Cox, Steven S.; Zhao, Xiaomin; Frazier, Charles E.; Little, John C.


    Due to its environmental ubiquity and concern over its potential toxicity, the mass-transfer characteristics of formaldehyde are of critical importance to indoor air quality research. Previous studies have suggested that formaldehyde mass transfer in polymer is partially irreversible. In this study, mechanisms that could cause the observed irreversibility were investigated. Polycarbonate and four other polymeric matrices were selected and subjected to formaldehyde sorption/desorption cycles. Mass transfer of formaldehyde was partially irreversible in all cases, and three potential mechanisms were evaluated. First, attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) analysis was used to investigate possible formaldehyde polymerization on polymer surfaces. ATR-FTIR showed no detectable paraformaldehyde or formaldehyde on the film surfaces that had been exposed to formaldehyde and air. ATR-FTIR did detect aliphatic acids suggesting oxidation had occurred on film surfaces as a result of exposure to formaldehyde. However, additional study suggested that air is not the primary cause for irreversibility. Second, statistical physics theory was tested as a possible explanation. According to this theory, reversible and irreversible sorption could be taking place simultaneously. The irreversible fraction should be constant during sorption and the fraction could be determined by performing a complete sorption/desorption test. The sorption/desorption data was consistent with this theory. Third, chemisorption was considered as another possible cause for irreversibility. Extraction/fluorimetry testing of post-sorption and post-desorption polymer films showed measurable quantities of formaldehyde suggesting that some of the chemisorbed formaldehyde was reversible at the higher extraction temperature. Further quantitative study on chemical reaction products is needed.

  15. Water sorption/solubility of dental adhesive resins.

    Malacarne, Juliana; Carvalho, Ricardo M; de Goes, Mario F; Svizero, Nadia; Pashley, David H; Tay, Franklin R; Yiu, Cynthia K; Carrilho, Marcela Rocha de Oliveira; de Oliveira Carrilho, Marcela Rocha


    This study evaluated the water sorption, solubility and kinetics of water diffusion in commercial and experimental resins that are formulated to be used as dentin and enamel bonding agents. Four commercial adhesives were selected along with their solvent-monomer combination: the bonding resins were of Adper Scotchbond Multi-Purpose (MP) and Clearfil SE Bond (SE) systems, and the "one-bottle" systems, Adper Single Bond (SB) and Excite (EX). Five experimental methacrylate-based resins of known hydrophilicities (R1, R2, R3, R4 and R5) were used as reference materials. Specimen disks were prepared by dispensing the uncured resin into a mould (5.8mm x 0.8mm). After desiccation, the cured specimens were weighed and then stored in distilled water for evaluation of the water diffusion kinetics over a 28-day period. Resin composition and hydrophilicity (ranked by their Hoy's solubility parameters) influenced water sorption, solubility and water diffusion in both commercial and experimental dental resins. The most hydrophilic experimental resin, R5, showed the highest water sorption, solubility and water diffusion coefficient. Among the commercial adhesives, the solvated systems, SB and EX, showed water sorption, solubility and water diffusion coefficients significantly greater than those observed for the non-solvated systems, MP and SE (p<0.05). In general, the extent and rate of water sorption increased with the hydrophilicity of the resin blends. The extensive amount of water sorption in the current hydrophilic dental resins is a cause of concern. This may affect the mechanical stability of these resins and favor the rapid and catastrophic degradation of resin-dentin bonds.

  16. Maximum margin Bayesian network classifiers.

    Pernkopf, Franz; Wohlmayr, Michael; Tschiatschek, Sebastian


    We present a maximum margin parameter learning algorithm for Bayesian network classifiers using a conjugate gradient (CG) method for optimization. In contrast to previous approaches, we maintain the normalization constraints on the parameters of the Bayesian network during optimization, i.e., the probabilistic interpretation of the model is not lost. This enables us to handle missing features in discriminatively optimized Bayesian networks. In experiments, we compare the classification performance of maximum margin parameter learning to conditional likelihood and maximum likelihood learning approaches. Discriminative parameter learning significantly outperforms generative maximum likelihood estimation for naive Bayes and tree augmented naive Bayes structures on all considered data sets. Furthermore, maximizing the margin dominates the conditional likelihood approach in terms of classification performance in most cases. We provide results for a recently proposed maximum margin optimization approach based on convex relaxation. While the classification results are highly similar, our CG-based optimization is computationally up to orders of magnitude faster. Margin-optimized Bayesian network classifiers achieve classification performance comparable to support vector machines (SVMs) using fewer parameters. Moreover, we show that unanticipated missing feature values during classification can be easily processed by discriminatively optimized Bayesian network classifiers, a case where discriminative classifiers usually require mechanisms to complete unknown feature values in the data first.

  17. Maximum Entropy in Drug Discovery

    Chih-Yuan Tseng


    Full Text Available Drug discovery applies multidisciplinary approaches either experimentally, computationally or both ways to identify lead compounds to treat various diseases. While conventional approaches have yielded many US Food and Drug Administration (FDA-approved drugs, researchers continue investigating and designing better approaches to increase the success rate in the discovery process. In this article, we provide an overview of the current strategies and point out where and how the method of maximum entropy has been introduced in this area. The maximum entropy principle has its root in thermodynamics, yet since Jaynes’ pioneering work in the 1950s, the maximum entropy principle has not only been used as a physics law, but also as a reasoning tool that allows us to process information in hand with the least bias. Its applicability in various disciplines has been abundantly demonstrated. We give several examples of applications of maximum entropy in different stages of drug discovery. Finally, we discuss a promising new direction in drug discovery that is likely to hinge on the ways of utilizing maximum entropy.

  18. Hydrogen peroxide modified sodium titanates with improved sorption capabilities

    Nyman, May D.; Hobbs, David T.


    The sorption capabilities (e.g., kinetics, selectivity, capacity) of the baseline monosodium titanate (MST) sorbent material currently being used to sequester Sr-90 and alpha-emitting radioisotopes at the Savannah River Site are significantly improved when treated with hydrogen peroxide; either during the original synthesis of MST, or, as a post-treatment step after the MST has been synthesized. It is expected that these peroxide-modified MST sorbent materials will have significantly improved sorption capabilities for non-radioactive cations found in industrial processes and waste streams.

  19. Natural composites: Strength, packing ability and moisture sorption of cellulose fibres, and the related performance of composites

    Lilholt, Hans; Madsen, Bo


    Biobased materials are becoming of increasing interest as potential structural materials for the future. A useful concept in this context is the fibre reinforcement of materials by stiff and strong fibres. The bio-resources can contribute with cellulose fibres and (bio) polymers from hemicellulos...... in stiffness, on the packing ability of cellulose fibres and the related maximum fibre volume fraction in composites, on the moisture sorption of cellulose fibres and the related mass increase and (large) hygral strains induced, and on the mechanical performance of composites....

  20. Sorption of Uranium Ions from Their Aqueous Solution by Resins Containing Nanomagnetite Particles

    Mahmoud O. Abd El-Magied


    Full Text Available Magnetic amine resins composed of nanomagnetite (Fe3O4 core and glycidyl methacrylate (GMA/N,N′-methylenebisacrylamide (MBA shell were prepared by suspension polymerization of glycidyl methacrylate with N,N′-methylenebisacrylamide in the presence of nanomagnetite particles and immobilized with different amine ligands. These resins showed good magnetic properties and could be easily retrieved from their suspensions using an external magnetic field. Adsorption behaviors of uranium ions on the prepared resins were studied. Maximum sorption capacities of uranium ions on R-1 and R-2 were found to be 92 and 158 mg/g. Uranium was extracted successfully from three granite samples collected from Gabal Gattar pluton, North Eastern Desert, Egypt. The studied resins showed good durability and regeneration using HNO3.

  1. Combination volumetric and gravimetric sorption instrument for high accuracy measurements of methane adsorption

    Burress, Jacob; Bethea, Donald; Troub, Brandon


    The accurate measurement of adsorbed gas up to high pressures (˜100 bars) is critical for the development of new materials for adsorbed gas storage. The typical Sievert-type volumetric method introduces accumulating errors that can become large at maximum pressures. Alternatively, gravimetric methods employing microbalances require careful buoyancy corrections. In this paper, we present a combination gravimetric and volumetric system for methane sorption measurements on samples between ˜0.5 and 1 g. The gravimetric method described requires no buoyancy corrections. The tandem use of the gravimetric method allows for a check on the highest uncertainty volumetric measurements. The sources and proper calculation of uncertainties are discussed. Results from methane measurements on activated carbon MSC-30 and metal-organic framework HKUST-1 are compared across methods and within the literature.

  2. DOC, Color and Disinfection By-Product Precursor Dynamics along an Urbanization Gradient, Croton Water Supply System, New York, USA

    Hassett, J. M.; Mitchell, M. J.; Burns, D. A.; Heisig, P. M.


    Hydrologic processes in suburban watersheds and their effects on water quality warrant investigation. Biweekly and storm samples were collected and analyzed for base cations, selected anions, and DOC over a one-year period at the outlet of three small (37 - 55 ha) watersheds (one forested, two with different degrees of suburban development) in the Croton Watershed, southeastern New York. Less frequent sampling for Pt/Co color and disinfection by-product precursors (DBPs) were also conducted. Median baseflow concentrations (>3 days since rainfall) of DOC were similar, ranging from 2.1 to 1.8 to 1.7 mg L -1 for the most urbanized to the forested watershed, respectively. On a unit area load basis (kg ha-1 yr-1), the range was from 8.9 to 6.4 to 5.1, again from most urbanized to forested watershed. All three watersheds showed similar storm responses, with evidence for a flushing mechanism in that DOC concentration increased with increasing discharge. Pt/Co color and DBPs (determined as both total trihalomethane and total haloacetic acid formation potentials) showed similar storm behavior, although the range of response was greater than observed for DOC, suggesting a labile DOC fraction was mobilized during storm events. The more urbanized watersheds tended to favor brominated over chlorinated forms of DBPs; the reasons for this are unclear.

  3. Sorption of V and VI group metalloids (As, Sb, Te on modified peat sorbents

    Ansone-Bertina Linda


    Full Text Available The present work investigates arsenic, antimony and tellurium sorption using iron modified peat. The results were obtained using batch tests and the sorption was studied as a function of initial metalloid concentration, pH and sorption time, as well as the presence of competing substances. The obtained results indicate that modification of peat with Fe compounds significantly enhances the sorption capacity of the sorbents used for sorption of arsenic, antimony and tellurium. The optimal pH interval for the sorption of Sb(III is 6.5–9 and for As(V and Sb(V – 3–6, while As(III and tellurium sorption using Fe-modified peat is favourable in a wider interval of 3–9. The presence of competing ions as well as HA affect sorption of metalloids on Fe-modified peat. A minor impact on the reduction of metalloid sorption was detected in the presence of nitrate, sulphate, carbonate and tartrate ions, while in the presence of phosphate and HA the sorption ability of metalloids can be considerably reduced. The obtained results of kinetic experiments indicate that sorption of metalloids on Fe-modified peat mainly occurs relying on mechanisms of physical sorption processes.

  4. Using proper regression methods for fitting the Langmuir model to sorption data

    The Langmuir model, originally developed for the study of gas sorption to surfaces, is one of the most commonly used models for fitting phosphorus sorption data. There are good theoretical reasons, however, against applying this model to describe P sorption to soils. Nevertheless, the Langmuir model...

  5. Mechanism and kinetics of aluminum dissolution during copper sorption by acidity paddy soil in South China.

    Liu, Peiya; Li, Yujiao; Wen, Qinliang; Dong, Changxun; Pan, Genxing


    Soil aggregates were prepared from a bulk soil collected from paddy soil in the Taihu Lake region and aluminum (Al) dissolution, solution pH changes during copper (Cu(2+)) sorption were investigated with static sorption and magnetic stirring. Kinetics of Cu(2+) sorption and Al dissolution were also studied by magnetic stirring method. No Al dissolution was observed until Cu(2+) sorption was greater than a certain value, which was 632, 450, 601 and 674 mg/kg for sand, clay, silt, and coarse silt fractions, respectively. Aluminum dissolution increased with increasing Cu(2+) sorption and decreasing solution pH. An amount of dissolved Al showed a significant positive correlation with non-specific sorption of Cu(2+) (R(2)>0.97), and it was still good under different pH values (R(2)>0.95). Copper sorption significantly decreased solution pH. The magnitude of solution pH decline increased as Cu(2+) sorption and Al dissolution increased. The sand and clay fraction had a less Al dissolution and pH drop due to the higher ferric oxide, Al oxide and organic matter contents. After sorption reaction for half an hour, the Cu(2+) sorption progress reached more than 90% while the Al dissolution progress was only 40%, and lagged behind the Cu(2+) sorption. It indicated that aluminum dissolution is associated with non-specific sorption.

  6. A Discussion of Reversible and Irreversible Sorption for Sr, Cs, Np, and Pu

    Carroll, Susan [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Tinnacher, Ruth [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kersting, Annie [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)


    Here we discuss the possibility that fission product and actinide sorption is reversible when thermodynamic and kinetic factors are accounted for in predictive models. We do this by reviewing the sorption behavior of Sr, Cs, Np, and Pu, and by reviewing our ability to model their sorption behavior.

  7. Present status of developments in physical sorption cooling for space applications

    Benthem, B.; Doornink, J.; Boom, E.; Holland, Herman J.; Lerou, P.P.P.M.; Burger, Johannes Faas; ter Brake, Hermanus J.M.


    A sorption cooler uses the Joule–Thomson effect for cooling a gas by expanding it through a flow restriction. The flow of gas is sustained by a compressor consisting of one or more sorption cells, which cyclically adsorb and desorb gas according to the fully reversible process of physical sorption.

  8. Present status of developments in physical sorption cooling for space applications

    Benthem, B.; Doornink, J.; Boom, E.; Holland, H.J.; Lerou, P.P.P.M.; Burger, J.F.; Brake, ter H.J.M.


    A sorption cooler uses the Joule–Thomson effect for cooling a gas by expanding it through a flow restriction. The flow of gas is sustained by a compressor consisting of one or more sorption cells, which cyclically adsorb and desorb gas according to the fully reversible process of physical sorption.

  9. Groundwater flow and sorption processes in fractured rocks (I)

    Kim, Won Young; Woo, Nam Chul; Yum, Byoung Woo; Choi, Young Sub; Chae, Byoung Kon; Kim, Jung Yul; Kim, Yoo Sung; Hyun, Hye Ja; Lee, Kil Yong; Lee, Seung Gu; Youn, Youn Yul; Choon, Sang Ki [Korea Institute of Geology Mining and Materials, Taejon (Korea, Republic of)


    This study is objected to characterize groundwater flow and sorption processes of the contaminants (ground-water solutes) along the fractured crystalline rocks in Korea. Considering that crystalline rock mass is an essential condition for using underground space cannot be overemphasized the significance of the characterizing fractured crystalline rocks. the behavior of the groundwater contaminants is studied in related to the subsurface structure, and eventually a quantitative technique will be developed to evaluate the impacts of the contaminants on the subsurface environments. The study has been carried at the Samkwang mine area in the Chung-Nam Province. The site has Pre-Cambrian crystalline gneiss as a bedrock and the groundwater flow system through the bedrock fractures seemed to be understandable with the study on the subsurface geologic structure through the mining tunnels. Borehole tests included core logging, televiewer logging, constant pressure fixed interval length tests and tracer tests. The results is summarized as follows; 1) To determine the hydraulic parameters of the fractured rock, the transient flow analysis produce better results than the steady - state flow analysis. 2) Based on the relationship between fracture distribution and transmissivities measured, the shallow part of the system could be considered as a porous and continuous medium due to the well developed fractures and weathering. However, the deeper part shows flow characteristics of the fracture dominant system, satisfying the assumptions of the Cubic law. 3) Transmissivities from the FIL test were averaged to be 6.12 x 10{sup -7}{sub m}{sup 2}{sub /s}. 4) Tracer tests result indicates groundwater flow in the study area is controlled by the connection, extension and geometry of fractures in the bedrock. 5) Hydraulic conductivity of the tracer-test interval was in maximum of 7.2 x 10{sup -6}{sub m/sec}, and the effective porosity of 1.8 %. 6) Composition of the groundwater varies

  10. Groundwater flow and sorption processes in fractured rocks (I)

    Kim, Won Young; Woo, Nam Chul; Yum, Byoung Woo; Choi, Young Sub; Chae, Byoung Kon; Kim, Jung Yul; Kim, Yoo Sung; Hyun, Hye Ja; Lee, Kil Yong; Lee, Seung Gu; Youn, Youn Yul; Choon, Sang Ki [Korea Institute of Geology Mining and Materials, Taejon (Korea, Republic of)


    This study is objected to characterize groundwater flow and sorption processes of the contaminants (ground-water solutes) along the fractured crystalline rocks in Korea. Considering that crystalline rock mass is an essential condition for using underground space cannot be overemphasized the significance of the characterizing fractured crystalline rocks. the behavior of the groundwater contaminants is studied in related to the subsurface structure, and eventually a quantitative technique will be developed to evaluate the impacts of the contaminants on the subsurface environments. The study has been carried at the Samkwang mine area in the Chung-Nam Province. The site has Pre-Cambrian crystalline gneiss as a bedrock and the groundwater flow system through the bedrock fractures seemed to be understandable with the study on the subsurface geologic structure through the mining tunnels. Borehole tests included core logging, televiewer logging, constant pressure fixed interval length tests and tracer tests. The results is summarized as follows; 1) To determine the hydraulic parameters of the fractured rock, the transient flow analysis produce better results than the steady - state flow analysis. 2) Based on the relationship between fracture distribution and transmissivities measured, the shallow part of the system could be considered as a porous and continuous medium due to the well developed fractures and weathering. However, the deeper part shows flow characteristics of the fracture dominant system, satisfying the assumptions of the Cubic law. 3) Transmissivities from the FIL test were averaged to be 6.12 x 10{sup -7}{sub m}{sup 2}{sub /s}. 4) Tracer tests result indicates groundwater flow in the study area is controlled by the connection, extension and geometry of fractures in the bedrock. 5) Hydraulic conductivity of the tracer-test interval was in maximum of 7.2 x 10{sup -6}{sub m/sec}, and the effective porosity of 1.8 %. 6) Composition of the groundwater varies

  11. Experimental studies of Cs, Sr, Ni, and Eu sorption on Na-illite and the modelling of Cs sorption

    Poinssot, C.; Baeyens, B.; Bradbury, M.H.


    A natural illite (illite du Puy) was purified and converted to the homo-ionic Na-form. The conditioned Na-illite was characterised in terms of its mineralogy, chemical inventory and physico-chemical properties. The structural formula was determined from energy dispersive spectroscopic analyses (SEM/TEM-EDS) and bulk chemistry measurements. A cation exchange capacity of 127 meq kg{sup -1} was determined by the {sup 22}Na isotope dilution method at neutral pH. The Na-CEC was also measured as a function of pH. The stability of Na-illite as a function of pH in the range between 3 and 6 was investigated. At low pH values partial dissolution of the illite occurs releasing the structural elements Al, Si, Mg, and K into solution. The presence of Ca and Sr in solution was interpreted as being due to desorption from cation exchange sites. All of these elements are also present at neutral pH but at considerably lower levels. Such effects cannot be avoided and must be considered in the interpretation of the sorption measurements. The main focus of the experimental work presented here is on the sorption behaviour of Cs, Sr, Ni and Eu on conditioned Na-illite as a function of NaClO{sub 4} background electrolyte concentration (0.1 and 0.01 M), nuclide concentration and pH in the range between 3 and 11. Sorption edge data (R{sub d} versus pH) and sorption isotherms (quantity of nuclide sorbed versus equilibrium nuclide concentration) are presented for these four elements. Prior to beginning these experiments, sorption kinetics were measured. The broad based pool of sorption measurements generated from this work will provide the source data sets for subsequent modelling. So far only the Cs sorption measurements have been modelled. A two site cation exchange model was developed to describe the sorption of Cs over the whole range of experimental conditions. The two site types were termed 'frayed edge sites' (FES, high affinity/low capacity) and 'type II sites

  12. Solar-aided air conditioning through sorption. Final report. Phase 2; Solar unterstuetzte Klimatisierung ueber Sorption. Endbericht zur Phase 2

    Laevemann, E.; Kessling, W.; Peltzer, M.


    The present article reports on possibilities of using solar energy for cooling buildings. It contains the following chapters: Current state of research and development; room air conditioning; planning and results of the studies; theory; experimental studies on the sorption dehumidifier; development of exchange surfaces; development of solution distributors; cooling of exchange surfaces; construction of a sorption dehumidifier. (HW) [Deutsch] Die Arbeit berichtet ueber Moeglichkeiten der Anwendung von Solarenergie zur Kuehlung von Gebaeuden. Die Arbeit enthaelt folgende Kapitel: - Stand der Forschung und Entwicklung - Raumklimatisierung - Planung und Ergebnis der Untersuchungen - Theorie - Experimentelle Untersuchungen am Sorptionsentfeuchter - Entwicklung von Austauschflaechen - Entwicklung von Loesungsverteilern - Kuehlung von Austauschflaechen - Konstruktion eines Sorptionsentfeuchters. (HW)

  13. The Maximum Density of Water.

    Greenslade, Thomas B., Jr.


    Discusses a series of experiments performed by Thomas Hope in 1805 which show the temperature at which water has its maximum density. Early data cast into a modern form as well as guidelines and recent data collected from the author provide background for duplicating Hope's experiments in the classroom. (JN)

  14. Abolishing the maximum tension principle

    Dabrowski, Mariusz P


    We find the series of example theories for which the relativistic limit of maximum tension $F_{max} = c^2/4G$ represented by the entropic force can be abolished. Among them the varying constants theories, some generalized entropy models applied both for cosmological and black hole horizons as well as some generalized uncertainty principle models.

  15. Abolishing the maximum tension principle

    Mariusz P. Da̧browski


    Full Text Available We find the series of example theories for which the relativistic limit of maximum tension Fmax=c4/4G represented by the entropic force can be abolished. Among them the varying constants theories, some generalized entropy models applied both for cosmological and black hole horizons as well as some generalized uncertainty principle models.

  16. Arsenate uptake and arsenite simultaneous sorption and oxidation by Fe-Mn binary oxides: influence of Mn/Fe ratio, pH, Ca2+, and humic acid.

    Zhang, Gaosheng; Liu, Huijuan; Qu, Jiuhui; Jefferson, William


    Arsenate retention, arsenite sorption and oxidation on the surfaces of Fe-Mn binary oxides may play an important role in the mobilization and transformation of arsenic, due to the common occurrence of these oxides in the environment. However, no sufficient information on the sorption behaviors of arsenic on Fe-Mn binary oxides is available. This study investigated the influences of Mn/Fe molar ratio, solution pH, coexisting calcium ions, and humic acids have on arsenic sorption by Fe-Mn binary oxides. To create Fe-Mn binary oxides, simultaneous oxidation and co-precipitation methods were employed. The Fe-Mn binary oxides exhibited a porous crystalline structure similar to 2-line ferrihydrite at Mn/Fe ratios 1:3 and below, whereas exhibited similar structures to δ-MnO(2) at higher ratios. The As(V) sorption maximum was observed at a Mn/Fe ratio of 1:6, but As(III) uptake maximum was at Mn/Fe ratio 1:3. However, As(III) adsorption capacity was much higher than that of As(V) at each Mn/Fe ratio. As(V) sorption was found to decrease with increasing pH, while As(III) sorption edge was different, depending on the content of MnO(2) in the binary oxides. The presence of Ca(2+) enhanced the As(V) uptake under alkaline pH, but did not significantly influence the As(III) sorption by 1:9 Fe-Mn binary oxide; whereas the presence of humic acid slightly reduced both As(V) and As(III) uptake. These results indicate that As(III) is more easily immobilized than As(V) in the environment, where Fe-Mn binary oxides are available as sorbents and they represent attractive adsorbents for both As(V) and As(III) removal from water and groundwater. Copyright © 2011 Elsevier Inc. All rights reserved.

  17. Degradation of soil-sorbed trichloroethylene by stabilized zero valent iron nanoparticles: Effects of sorption, surfactants, and natural organic matter

    Zhang, Man [Auburn University, Auburn, Alabama; He, Feng [ORNL; Zhao, Dongye [Auburn University, Auburn, Alabama; Hao, Xiaodi [Beijing University of Civil Engineering and Architecture


    Zero valent iron (ZVI) nanoparticles have been studied extensively for degradation of chlorinated solvents in the aqueous phase, and have been tested for in-situ remediation of contaminated soil and groundwater. However, little is known about its effectiveness for degrading soil-sorbed contaminants. This work studied reductive dechlorination of trichloroethylene (TCE) sorbed in two model soils (a potting soil and Smith Farm soil) using carboxymethyl cellulose (CMC) stabilized Fe-Pd bimetallic nanoparticles. Effects of sorption, surfactants and dissolved organic matter (DOC) were determined through batch kinetic experiments. While the nanoparticles can effectively degrade soil-sorbed TCE, the TCE degradation rate was strongly limited by desorption kinetics, especially for the potting soil which has a higher organic matter content of 8.2%. Under otherwise identical conditions, {approx}44% of TCE sorbed in the potting soil was degraded in 30 h, compared to {approx}82% for Smith Farm soil (organic matter content = 0.7%). DOC from the potting soil was found to inhibit TCE degradation. The presence of the extracted SOM at 40 ppm and 350 ppm as TOC reduced the degradation rate by 34% and 67%, respectively. Four prototype surfactants were tested for their effects on TCE desorption and degradation rates, including two anionic surfactants known as SDS (sodium dodecyl sulfate) and SDBS (sodium dodecyl benzene sulfonate), a cationic surfactant hexadecyltrimethylammonium (HDTMA) bromide, and a non-ionic surfactant Tween 80. All four surfactants were observed to enhance TCE desorption at concentrations below or above the critical micelle concentration (cmc), with the anionic surfactant SDS being most effective. Based on the pseudo-first-order reaction rate law, the presence of 1 x cmc SDS increased the reaction rate by a factor of 2.5 when the nanoparticles were used for degrading TCE in a water solution. SDS was effective for enhancing degradation of TCE sorbed in Smith Farm

  18. Dissolution and sorption of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and 2,4,6-trinitrotoluene (TNT) residues from detonated mineral surfaces.

    Jaramillo, Ashley M; Douglas, Thomas A; Walsh, Marianne E; Trainor, Thomas P


    Composition B (Comp B) is a commonly used military formulation composed of the toxic explosive compounds 2,4,6-trinitrotoluene (TNT), and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX). Numerous studies of the temporal fate of explosive compounds in soils, surface water and laboratory batch reactors have been conducted. However, most of these investigations relied on the application of explosive compounds to the media via aqueous addition and thus these studies do not provide information on the real world loading of explosive residues during detonation events. To address this we investigated the dissolution and sorption of TNT and RDX from Comp B residues loaded to pure mineral phases through controlled detonation. Mineral phases included nontronite, vermiculite, biotite and Ottawa sand (quartz with minor calcite). High Performance Liquid Chromatography and Attenuated Total Reflectance Fourier Transform Infrared spectroscopy were used to investigate the dissolution and sorption of TNT and RDX residues loaded onto the mineral surfaces. Detonation resulted in heterogeneous loading of TNT and RDX onto the mineral surfaces. Explosive compound residues dissolved rapidly (within 9 h) in all samples but maximum concentrations for TNT and RDX were not consistent over time due to precipitation from solution, sorption onto mineral surfaces, and/or chemical reactions between explosive compounds and mineral surfaces. We provide a conceptual model of the physical and chemical processes governing the fate of explosive compound residues in soil minerals controlled by sorption-desorption processes. Published by Elsevier Ltd.

  19. Reversible Second Order Kinetics of Sorption-Desorption of Cr(VI Ion on Activated Carbon from Palm Empty Fruit Bunches

    Iip Izul Falah


    Full Text Available Activated carbon (AC from palm empty fruit bunches has been prepared, and this material was then used to adsorb Cr(VI from a solution. Characterization of the AC was conducted by detection of its functional groups, determination of total volatile compounds (VC content and its iodine number. Study on sorption-desorption kinetics was conducted by comparing results of evaluations of several models with proposed reversible second order model using the data produced in this work. Results of the works showed that the AC had similar characters compared with the AC produced by previous researchers. Application of the kinetics models on sorption Cr(VI onto the AC showed that nearly all of the models gave a good linearity. However, only the proposed model had a good relation with Langmuir isotherm, with respectively sorption (ks and desorption (kd constants were 5.75 x 10-4‑1.min-1 and 2.20 x 10-3 min-1; maximum sorption capacity, qm = 20.00 mg.g-1; and equilibrium constant, K from kinetics experiment (0.261 was comparable with the result from the isotherm experiment (0.269 Hence, using this model, kinetics and Langmuir parameters can probably be determined from a single kinetics data experiment.

  20. Cadmium sorption in solution by a chitin: effect of pH; Sorption du cadmium en solution par une chitine: effet du pH

    Benguella, B.; Benaissa, H. [Universtie de Tlemcen, Lab. de Materiaux Sorbants et Traitement des Eaux, Dept. de Chimie, Faculte des Sciences, Tlemcen (Algeria)


    The pH is an essential factor to take into consideration in the sorption mechanisms of metals: it acts both on the metal speciation in solution and on the chemical behaviour of the surface of the sorbing material, and thus indirectly on the sorption mechanism. The effect of the initial pH of the solution on the cadmium sorption by raw state chitin has been studied in static conditions. The approach used is the determination of the sorption kinetics and equilibria for different values of initial pH (pH < 7-7.5). An increase of the initial pH value of the solution leads to an increase of the cadmium sorption capacity by chitin at the equilibrium. The Langmuir model has revealed to be convenient for a mathematical description of the sorption isotherms obtained. (J.S.)

  1. Sorption of untreated and humic acid coated silver nanoparticles to environmental and model surfaces

    Abraham, Priya M.; Baumann, Thomas; Schaumann, Gabriele E.


    The environmental fate of engineered nanoparticles is controlled their colloidal stability and their interaction with different environmental surfaces. Little is known about sorption of nanoparticles to environmental surfaces under quasi-equilibrium conditions. Nevertheless, sorption isotherms may also be a valuable means of studying nanoparticle-sorbent interactions. We investigated sorption of engineered silver nanoparticles (nAg) from stable and unstable suspensions in presence and absence of natural organic matter (NOM) to model surfaces (sorbents with specific chemical functional groups) and environmental materials (plant leaves and sand). Morphology and nanomechanical parameters of the surfaces covered with nanoparticles were assessed using atomic force microscopy (AFM) and scanning electron microscopy (SEM). The sorption of nAg from stable suspensions and in absence of NOM was non-linear and best described by a Langmuir model, where Langmuir coefficients varied with sorbent surface chemistry, which suggests monolayer sorption (Abraham et al. 2013). For nAg sorption from an unstable suspension, the sorption isotherms did not follow any classical sorption models, suggesting interplay between aggregation and sorption (Abraham et al. 2013). In contrast, sorption was strongly suppressed and exhibited linear sorption isotherms in the presence of NOM. The difference in sorption isotherms suggests predominance of different sorption mechanisms depending on presence or absence of NOM, which can be only partly explained by the NOM coating alone. On the basis of the current results, a partial release of NOM coating for sorption of certain surfaces cannot be excluded. The validity of the Langmuir isotherm suggests monolayer sorption, which can be explained by the blocking effect due to electrostatic repulsion of individual nanoparticles. In unstable suspensions, aggregates are instead formed in suspension, formed on the surface and then sorbed, or formed in both ways

  2. ICF-DOC: the ICF dedicated checklist for evaluating functioning and disability in people with disorders of consciousness.

    Leonardi, Matilde; Covelli, Venusia; Giovannetti, Ambra M; Raggi, Alberto; Sattin, Davide


    Clinicians need a comprehensive description of patients' functioning state to capture the complex interaction between symptoms and environmental factors, and to determine the actual level of functioning in patients in a vegetative state or a minimally conscious state. The aim of this study is to develop an International Classification of Functioning, Disability, and Health (ICF) checklist for patients with disorders of consciousness (DOC) so as to capture and describe, with a tailored list of categories, the most common health, disability, and functioning issues of adult patients with DOC. The WHO ICF checklist was used as a basis for collecting data. This was an observational, cross-sectional, multicenter study conducted in 69 Italian centers. Specific methodological procedures were used to identify the most appropriate categories for DOC patients to be added to or deleted from the ICF checklist so as to develop the ICF-DOC checklist. A total of 566 adult patients were enrolled: 398 in a vegetative state and 168 in a minimally conscious state. A total of 127 ICF categories reached the threshold of 20% concerning the presence of a problem: 37 categories from the body functions chapter, 13 from the body structures chapter, 46 from the activities and participations chapter, and 31 from the environmental factors chapter. ICF categories identified in this study can be useful guidelines for clinicians and researchers to collect data on functioning and disability of adult patients with DOC. The new ICF-DOC checklist allows monitoring of the effects of interventions on functional areas and possible changes in each patient in follow-up studies.

  3. Aminosilane-Functionalized Cellulosic Polymer for Increased Carbon Dioxide Sorption

    Pacheco, Diana M.


    Improvement in the efficiency of CO 2 separation from flue gases is a high-priority research area to reduce the total energy cost of carbon capture and sequestration technologies in coal-fired power plants. Efficient CO 2 removal from flue gases by adsorption systems requires the design of novel sorbents capable of capturing, concentrating, and recovering CO 2 on a cost-effective basis. This paper describes the preparation of an aminosilane-functionalized cellulosic polymer sorbent with enhanced CO 2 sorption capacity and promising performance for use in postcombustion carbon capture via rapid temperature-swing adsorption systems. The introduction of aminosilane functionalities onto the backbone of cellulose acetate was achieved by the anhydrous grafting of N-(2-aminoethyl)-3- aminoisobutyldimethylmethoxysilane. The dry sorption capacity of the modified cellulosic polymer reached 27 cc (STP) CO 2/cc sorbent (1.01 mmol/g sorbent) at 1 atm and 39 cc (STP) CO 2/cc sorbent (1.46 mmol/g sorbent) at 5 atm and 308 K. The amine loading achieved was 5.18 mmol amine(nitrogen)/g sorbent. Exposure to water vapor after the first dry sorption cycle increased the dry sorption capacity of the sorbent by 12% at 1 atm, suggesting its potential for rapid cyclic adsorption processes under humid feed conditions. The CO 2 sorbent was characterized in terms of chemical composition, density changes, molecular structure, thermal stability, and surface morphology. © 2011 American Chemical Society.

  4. Sorption of perfluorinated compounds from contaminated water to activated carbon

    Hansen, Mona C.; Boerresen, Marion H. [Norwegian Geotechnical Inst. (NGI), Oslo (Norway); Schlabach, Martin [Norwegian Inst. for Air Research, Kjeller (Norway); Cornelissen, Gerard [Norwegian Geotechnical Inst. (NGI), Oslo (Norway); Dept. of Applied Environmental Sciences (ITM), Stockholm Univ. (Sweden)


    Introduction: Perfluorinated compounds (PFC) are toxic and bioaccumulative compounds that are ubiquitous in the environment. It is important to develop effective techniques to remove PFC from water. This study is the first to investigate sorption of PFC to activated carbon (AC) at environmentally relevant nanogram per liter concentrations. Methods: Batch AC sorption isotherms were measured for water from a contaminated groundwater well, for three perfluorosulfonates and five perfluoroacetic acids. Results: For perfluorooctane sulfonate and perfluorooctanoic acid Freundlich sorption coefficients, log K{sub iF} for powdered activated carbon (PAC) were 4.0 and 3.8 (ng/g)(ng/L){sup -n}, respectively, and for granular activated carbon (GAC) were 2.7 and 2.3 (ng/g)(ng/L){sup -n}, respectively. Sorption was nonlinear, with Freundlich n coefficients generally around 0.5. The K{sub iF} on both GAC and PAC were PFC chain-length dependant, with increasing number of carbon yielding increasing K{sub iF}. This chain-length dependence appeared stronger for perfluorosulfonates than for perfluoroacetic acids. Tests with short (10 min) adsorption times still yielded substantial PFC removal (20-40% for GAC, 60-90% for PAC) and revealed that AC is probably suitable for PFC removal in flow-through systems. A perfluorinated polymer, Teflon, was also tested as a PFC removal agent but proved not to be effective for PFC-contaminated water purification. (orig.)

  5. Polycyclic aromatic hydrocarbons (PAHs) removal by sorption: A review.

    Lamichhane, Shanti; Bal Krishna, K C; Sarukkalige, Ranjan


    Polycyclic aromatic hydrocarbons (PAHs) are organic micro pollutants which are persistent compounds in the environment due to their hydrophobic nature. Concerns over their adverse effects in human health and environment have resulted in extensive studies on various types of PAHs removal methods. Sorption is one of the widely used methods as PAHs possess a great sorptive ability into the solid media and their low aqueous solubility property. Several adsorbent media such as activated carbon, biochar, modified clay minerals have been largely used to remove PAHs from aqueous solution and to immobilise PAHs in the contaminated soils. According to the past studies, very high removal efficiency could be achieved using the adsorbents such as removal efficiency of activated carbon, biochar and modified clay mineral were 100%, 98.6% and >99%, respectively. PAHs removal efficiency or adsorption/absorption capacity largely depends on several parameters such as particle size of the adsorbent, pH, temperature, solubility, salinity including the production process of adsorbents. Although many studies have been carried out to remove PAHs using the sorption process, the findings have not been consolidated which potentially hinder to get the correct information for future study and to design the sorption method to remove PAHs. Therefore, this paper summarized the adsorbent media which have been used to remove PAHs especially from aqueous solutions including the factor affecting the sorption process reported in 142 literature published between 1934 and 2015.

  6. Sorption Behavior of Radionuclide Iodine on Organic and Inorganic sorbents

    Kim, Min Kyoung; Chang, See Un; Choung, Sung Wook; Um, Woo Yong [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)


    Radioactive iodine ({sup 125/129/131}I) has been released into the environment as a result of nuclear testing, nuclear fuel processing, and nuclear accidents such as Chernobyl and Fukushima. The released iodine radioisotopes are harmful to human and ecological system due to their high toxicity. In particular, long half-life of {sup 129}I (t{sub 1/2} = 1.6 x 10{sup 7} years) leads to contamination of soils, sediments, and groundwater surrounding nuclear facilities. Prior studies have suggested that the transport behavior of iodine in environment depends on the iodine speciation, based on different chemical reaction for individual iodine species. Iodate (IO{sub 3}{sup -}) and certain organo-iodine (OI) species are strongly affected by sorption processes, while iodide (I{sup -}) is not. The sorption characteristics of iodine species are also differentiated by the properties and composition of soils and sediments. However, contribution of mineral and organic matter types in soils/sediments on the sorption behavior was not properly evaluated. As the first step of systematical research, the objective of this study is to investigate the sorption behavior of iodine species, especially, IO{sub 3}{sup -}, on different types of natural inorganic and organic sorbents in soils/sediments

  7. Sorption and desorption of 1,4-dichlorobenzene on peat


    Sorption and desorption of 1,4-dichlorobenzene (DCB) on peat (>92% organic matter)display large-scale hysteresis and nonlinearity. The magnitude of desorption hysteresis decreases in the order: untreated Pahokee peat (P)>acid treated peat (FP)>humin (TP). The desorption percentages are lower than 28% of the sorbed 1, 4-DCB after desorbing for 6 days. The sorption and desorption isotherms are well fitted to Freundlich equation, whose parameter 1/n ranges from 0.055 to 0.527. Moreover, the parameter 1/n of the desorption isotherm is significantly lower than that of the sorption isotherm, but the parameter IogK increases on contrary to 1/n. The desorption isotherms are very well fitted to Langmuir equation, whose Qm decreases in the order: TP>FP>P.The apparent partition coefficients (Kp) increase with increasing sorption time or decreasing aqueous equilibrium concentration of DCB. And Kp of P is significantly higher than that of FP or TP.

  8. Sorption equilibrium of mercury onto ground-up tree fern

    Ho, Y.-S. [Department of Chemical Engineering, I-Shou University, No. 1, Section 1, Hsueh-Cheng Road, Ta-Hsu Hsiang, Kaohsiung County 840, Taiwan (China)], E-mail:; Wang, C.-C. [Department of Chemical Engineering, I-Shou University, No. 1, Section 1, Hsueh-Cheng Road, Ta-Hsu Hsiang, Kaohsiung County 840, Taiwan (China)


    The sorption behavior of mercury at different temperatures onto ground-up tree fern was investigated. The experimental results were fitted to two two-parameter isotherms, the Freundlich and Langmuir isotherms, as well as to two three-parameter isotherms, the Redlich-Peterson and Sips isotherms to obtain the characteristic parameters of each model. A comparison of best-fitting was performed using the coefficient of determination and Chi-square test. Both the Langmuir and Redlich-Peterson isotherms were found to well represent the measured sorption data. According to the evaluation using the Langmuir equation, the saturated monolayer sorption capacity of mercury ions onto ground-up tree fern was 26.5 mg/g at 298 K. It was noted that an increase in temperature resulted in a higher mercury ion loading per unit weight of the tree fern. In addition, various thermodynamic parameters, such as {delta}G{sup o}, {delta}H{sup o}, and {delta}S{sup o}, were calculated and compared with the sorption of mercury by other sorbents.

  9. The effect of inositol hexaphosphate on cadmium sorption to gibbsite.

    Ruyter-Hooley, Maika; Larsson, Anna-Carin; Johnson, Bruce B; Antzutkin, Oleg N; Angove, Michael J


    Oxides, hydrous oxides and hydroxides of aluminium and iron are important in determining the availability of trace and heavy metals in soil systems. The presence of complexing anions is also known to affect the binding of these metals in soils. Since organophosphates, such as inositol hexaphosphate (IP6), are present in most soil systems they are expected to affect the nature of the interaction between metal ions and metal (hyr)oxides. Both adsorption edge and isotherm experiments were conducted on Cd(II)-gibbsite and Cd(II)-IP6-gibbsite systems. In addition, solid-state (31)P MAS NMR measurements were performed on the ternary system. All results were used to develop Extended Constant Capacitance surface complexation models of both the Cd(II)-gibbsite and IP6-Cd(II)-gibbsite sorption systems. The presence of IP6 significantly increased sorption of Cd(II) to gibbsite below pH 8 especially at higher concentrations of Cd(II) and IP6. The (31)P MAS NMR spectra, together with surface complexation modeling, indicated the presence of two outer-sphere ternary complexes with the first, [(SOH2)3(3+)(LHCd)(9-)](6-), important at relatively low concentrations, while the second, [SLH3(8-)Cd(2+)](6-), dominated sorption at higher sorbate concentrations. Thus the presence of organophosphates in soil systems increases sorption and may therefore decrease the availability of trace and heavy metals to plants. Copyright © 2016 Elsevier Inc. All rights reserved.

  10. Better Gas-Gap Thermal Switches For Sorption Compressors

    Bhandari, Pradeep; Rodriguez, Jose


    Gas-gap thermal switches associated with sorption compressors of some heat pumps and cryogenic systems designed for higher performance, according to proposal, by introducing controlled turbulent flows into gas gaps. Utilizes convection in turbulent flow to transfer heat at greater rate. Design takes advantage of flow of working fluid. Working fluid also serve as heat transfer medium in gas gap.

  11. Modeling Heavy Metal Sorption Kinetics Using Fractional Calculus

    V. C. Friesen


    Full Text Available Heavy metals are commonly regarded as environmentally aggressive and hazardous to human health. Among the different metals, lead plays an important economic role due to its large use in the automotive industry, being an essential component of batteries. Different approaches have been reported in the literature aimed at lead removal, and among them a very successful one considers the use of water hyacinths for sorption-based operation. The modeling of the metal sorption kinetics is a fundamental step towards in-depth studies and proper separation equipment design and optimization. Fractional calculus represents a novel approach and a growing research field for process modeling, which is based on the successful use of derivatives of arbitrary order. This paper reports the modeling of the kinetics of lead sorption by water hyacinths (Eichhornia crassipes using a fractional calculus. A general procedure on error analysis is also employed to prove the actual fractional nature of the proposed model by the use of parametric variance analysis, which was carried out using two different approaches (with the complete Hessian matrix and with a simplified Hessian matrix. The joint parameter confidence regions were generated, allowing to successfully show the fractional nature of the model and the sorption process.

  12. Bio-sorption of neptunium(V) by Pseudomonas fluorescens

    Songkasiri, W. [Dept. of Civil Engineering, Northwestern Univ., Evanston, IL (United States); Chemical Technology Div., Argonne National Lab., Argonne, IL (United States); Reed, D.T. [Chemical Technology Div., Argonne National Lab., Argonne, IL (United States); Rittmann, B.E. [Dept. of Civil Engineering, Northwestern Univ., Evanston, IL (United States)


    The bio-sorption of neptunyl (NpO{sub 2}{sup +}) by Pseudomonas fluorescens was investigated. The overall goals of this research are to identify key interactions between neptunium and soil bacteria and to model these effects under subsurface-related conditions. Neptunyl, which is generally thought to be non-sorptive, was significantly sorbed under all conditions studied. At initial neptunyl concentrations of 4.75 {mu}M and pH = 7, as much as 85% of the neptunium was sorbed under aerobic conditions. Kinetic studies show that neptunyl was sorbed rapidly within the first 15 minutes. The extent of sorption also increased with pH. In all cases, the sorbed neptunium was shown to be NpO{sub 2}{sup +} by X-ray absorption near edged spectroscopy (XANES) analysis, confirming that there was no reduction to Np(IV) under the conditions of our experiment. The sorption data were modeled using Langmuir and Freundlich isotherms. A comparison of the two approaches showed a significantly better fit for the Freundlich isotherm, and the Freundlich parameter values suggest interactions between sorbed NpO{sub 2}{sup +} molecules. These data show that bio-sorption, even for neptunyl, has a significant role in defining the speciation of neptunium and, hence, its overall mobility in the subsurface. (orig.)

  13. Sorption of benzotriazoles under the conditions of RP HPLC

    Dzhabieva, S. A.; Kurbatova, S. V.; Belousova, Z. P.


    The results of a chromatographic study of sorption of several benzotriazole derivatives on octadecyl silica gel were reported. The physicochemical and electronic parameters of benzotriazoles were calculated. The effect of the structure of analyte molecules and eluent composition on chromatographic retention of these substances was analyzed.

  14. Modeling polychlorinated biphenyl sorption isotherms for soot and coal

    Jantunen, A.P.K.; Koelmans, A.A.; Jonker, M.T.O.


    Sorption isotherms (pg-ng/L) were measured for 11 polychlorinated biphenyls (PCBs) of varying molecular planarity from aqueous solution to two carbonaceous geosorbents, anthracite coal and traffic soot. All isotherms were reasonably log-log-linear, but smooth for traffic soot and staircase-shaped

  15. Performance of chromatographic systems to model soil-water sorption.

    Hidalgo-Rodríguez, Marta; Fuguet, Elisabet; Ràfols, Clara; Rosés, Martí


    A systematic approach for evaluating the goodness of chromatographic systems to model the sorption of neutral organic compounds by soil from water is presented in this work. It is based on the examination of the three sources of error that determine the overall variance obtained when soil-water partition coefficients are correlated against chromatographic retention factors: the variance of the soil-water sorption data, the variance of the chromatographic data, and the variance attributed to the dissimilarity between the two systems. These contributions of variance are easily predicted through the characterization of the systems by the solvation parameter model. According to this method, several chromatographic systems besides the reference octanol-water partition system have been selected to test their performance in the emulation of soil-water sorption. The results from the experimental correlations agree with the predicted variances. The high-performance liquid chromatography system based on an immobilized artificial membrane and the micellar electrokinetic chromatography systems of sodium dodecylsulfate and sodium taurocholate provide the most precise correlation models. They have shown to predict well soil-water sorption coefficients of several tested herbicides. Octanol-water partitions and high-performance liquid chromatography measurements using C18 columns are less suited for the estimation of soil-water partition coefficients.

  16. Sorption rate and thermal barriers in a gas-zeolite system: investigation of n-hexane sorption in MFI-type zeolite.

    Wloch, J; Kornatowski, J


    The nonequilibrium gravimetric sorption method was used to determine diffusion coefficient values for n-hexane in MFI-type materials. Improvements in the measurement device and experimental conditions resulted in high values of the corrected diffusion coefficient, which are comparable to the literature data obtained by the methods of pulsed field gradient nuclear magnetic resonance (PFG NMR) and frequency response (FR). The results indicate that thermal effects of sorption affect practically neither the rate of the sorption nor the diffusion coefficient.

  17. Sorption and speciation of selenium in boreal forest soil.

    Söderlund, Mervi; Virkanen, Juhani; Holgersson, Stellan; Lehto, Jukka


    Sorption and speciation of selenium in the initial chemical forms of selenite and selenate were investigated in batch experiments on humus and mineral soil samples taken from a 4-m deep boreal forest soil excavator pit on Olkiluoto Island, on the Baltic Sea coast in southwestern Finland. The HPLC-ICP-MS technique was used to monitor any possible transformations in the selenium liquid phase speciation and to determine the concentrations of selenite and selenate in the samples for calculation of the mass distribution coefficient, Kd, for both species. Both SeO3(2-) and SeO4(2-) proved to be resistant forms in the prevailing soil conditions and no changes in selenium liquid phase speciation were seen in the sorption experiments in spite of variations in the initial selenium species, incubation time or conditions, pH, temperature or microbial activity. Selenite sorption on the mineral soil increased with time in aerobic conditions whilst the opposite trend was seen for the anaerobic soil samples. Selenite retention correlated with the contents of organic matter and weakly crystalline oxides of aluminum and iron, solution pH and the specific surface area. Selenate exhibited poorer sorption on soil than selenite and on average the Kd values were 27-times lower. Mineral soil was more efficient in retaining selenite and selenate than humus, implicating the possible importance of weakly crystalline aluminum and iron oxides for the retention of oxyanions in Olkiluoto soil. Sterilization of the soil samples decreased the retention of selenite, thus implying some involvement of soil microbes in the sorption processes or a change in sample composition, but it produced no effect for selenate. There was no sorption of selenite by quartz, potassium feldspar, hornblende or muscovite. Biotite showed the best retentive properties for selenite in the model soil solution at about pH 8, followed by hematite, plagioclase and chlorite. The Kd values for these minerals were 18, 14, 8 and 7

  18. Meta-analysis of pesticide sorption in subsoils

    Jarvis, Nicholas


    It has been known for several decades that sorption koc values tend to be larger in soils that are low in organic carbon (i.e. subsoils). Nevertheless, in a regulatory context, the models used to assess leaching of pesticides to groundwater still rely on a constant koc value, which is usually measured on topsoil samples. This is mainly because the general applicability of any improved model approach that is also simple enough to use for regulatory purposes has not been demonstrated. The objective of this study was therefore first to summarize and generalize available literature data in order to assess the magnitude of any systematic increase of koc values in subsoil and to test an alternative model of subsoil sorption that could be useful in pesticide risk assessment and management. To this end, a database containing the results of batch sorption experiments for pesticides was compiled from published studies in the literature, which placed at least as much emphasis on measurements in subsoil horizons as in topsoil. The database includes 967 data entries from 46 studies and for 34 different active substances (15 non-ionic compounds, 13 weak acids, 6 weak bases). In order to minimize pH effects on sorption, data for weak acids and bases were only included if the soil pH was more than two units larger than the compound pKa. A simple empirical model, whereby the sorption constant is given as a power law function of the soil organic carbon content, gave good fits to most data sets. Overall, the apparent koc value, koc(app), for non-ionic compounds and weak bases roughly doubled as the soil organic carbon content decreased by a factor of ten. The typical increase in koc(app) was even larger for weak acids: on average koc(app) increased by a factor of six as soil organic carbon content decreased by a factor of ten. These results suggest the koc concept currently used in leaching models should be replaced by an alternative approach that gives a more realistic

  19. Resiliência: necessidade e possibilidade de problematização em contextos de docência

    Timm, Edgar Zanini; Mouriño Mosquera, Juan José; Stobäus, Claus Dieter


    O artigo revê o conceito de resiliência no contexto do mal-estar que alcança a docência. Não se limitando à constatação da condição do mal-estar na contemporaneidade, afirma a possibilidade de o professor conseguir chegar a realizar-se no magistério tendo resiliência e uma vez que considere como fundamental o cuidado de si em seu projeto existencial. Descritores – Resiliência; mal-estar; bem-estar; docência; auto-imagem; auto-estima; cuidado de si; projeto existencial.

  20. Automatic publishing ISO 19115 metadata with PanMetaDocs using SensorML information

    Stender, Vivien; Ulbricht, Damian; Schroeder, Matthias; Klump, Jens


    create ISO 19115 compliant metadata. The resulting metadata file is stored in the GFZ Potsdam data infrastructure. The publishing workflow for file based research datasets at GFZ Potsdam is based on the eSciDoc infrastructure, using PanMetaDocs (PMD) as the graphical user interface. PMD is a collaborative, metadata based data and information exchange platform [1]. Besides SWE, metadata are also syndicated by PMD through an OAI-PMH interface. In addition, metadata from other observatories, projects or sensors in TERENO can be accessed through the TERENO Northeast data portal. [1]