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Sample records for equilibrium sorption isotherm

  1. Cosolvent effects on sorption isotherm linearity.

    PubMed

    Bouchard, Dermont C

    2002-06-01

    Sorption-desorption hysteresis, slow desorption kinetics, and other nonideal phenomena have been attributed to the differing sorptive characteristics of the natural organic polymers associated with soils and sediments. In this study, aqueous and mixed solvent systems were used to investigate the effects of a cosolvent, methanol, on sorption isotherm linearity with natural organic matter (NOM), and to evaluate whether these results support, or weaken, the rubbery/glassy polymer conceptualization of NOM. All of the sorption isotherms displayed some nonlinear character. Our data indicates that all of the phenanthrene and atrazine isotherms were nonlinear up to the highest equilibrium solution concentration to solute solubility in water or cosolvent ratios (Ce/Sw,c) used, approximately 0.018 and 0.070, respectively. Isotherm linearity was also observed to increase with volumetric methanol content (fc). This observation is consistent with the NOM rubbery/glassy polymer conceptualization: the presence of methanol in NOM increased isotherm linearity as do solvents in synthetic polymers, and suggests that methanol is interacting with the NOM, enhancing its homogeneity as a sorptive phase so that sorption is less bimodal as fc increases. When the equilibrium solution concentration was normalized for solute solubility in water or methanol-water solutions, greater relative sorption magnitude was observed for the methanol-water treatments. This observation, in conjunction with the faster sorption kinetics observed in the methanol-water sediment column systems, indicates that the increase in relative sorption magnitude with fc may be attributed to the faster sorption kinetics in the methanol-water systems, and hence, greater relative sorptive uptake for the rubbery polymer fraction of NOM at similar time scales.

  2. Thermodynamic analysis of sorption isotherms of cassava (Manihot esculenta).

    PubMed

    Koua, Blaise Kamenan; Koffi, Paul Magloire Ekoun; Gbaha, Prosper; Toure, Siaka

    2014-09-01

    Sorption isotherms of cassava were determined experimentally using a static gravimetric method at 30, 45 and 60 °C and within the range of 0.10-0.90 water activity. At a constant water activity, equilibrium moisture content decreased with increasing temperature. The equilibrium moisture content increased with increasing water activity at a given temperature. The experimental results were modelled using seven sorption models using non-linear regression technique. Results demonstrated that the GAB model adequately predicted equilibrium moisture content of cassava for the range of temperatures and water activities studied. The thermodynamic functions such as net isosteric heat of sorption, differential entropy of sorption, net integral enthalpy and entropy were evaluated to provide an understanding of the properties of water and energy requirements associated with the sorption behaviour. Net isosteric heat and differential entropy decreased with increasing equilibrium moisture content. The net integral enthalpy decreased while net integral entropy increased with increasing equilibrium moisture content. Net integral entropy was negative in value. All thermodynamic functions were adequately characterised by a power law model. The point of maximum stability was found between 0.053 and 0.154 kg water/kg db for cassava. PMID:25190827

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

    PubMed

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

    2014-10-01

    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. PMID:25328208

  4. Thermodynamic properties of water sorption isotherms of grape seed

    NASA Astrophysics Data System (ADS)

    Majd, Kamran Maleki; Karparvarfard, Seyed H.; Farahnaky, Asgar; Ansari, Sara

    2014-03-01

    In this study the moisture sorption isotherm of grape seed was determined by using a static gravimetric method at 35-65°C and 0.108-0.821 water activity range. The sorption isotherms were found to be typical sigmoid shape of most food materials. Five models including the Brunauer-Emmett-Teller (2-parameter), Guggenheim, Anderson and De Boer (3-parameter), Oswin (2-parameter), Ferro-Fontan (3-parameter) and Peleg (4-parameter) models were considered to fit the experimental data. The Ferro- Fontan and Peleg equations (at three temperatures 35, 45, 65°C) having R2 greater than 0.97 and lower values of standard error of estimate and deviation modulus gave the best fit of the experimental data throughout the entire range of water activity. The net isosteric heat of sorption, calculated by Calusius-Clapeyron equation on experimental data, was found to be a polynomial and exponential function of equilibrium moisture content within the temperature range investigated.

  5. Column Chromatography To Obtain Organic Cation Sorption Isotherms.

    PubMed

    Jolin, William C; Sullivan, James; Vasudevan, Dharni; MacKay, Allison A

    2016-08-01

    Column chromatography was evaluated as a method to obtain organic cation sorption isotherms for environmental solids while using the peak skewness to identify the linear range of the sorption isotherm. Custom packed HPLC columns and standard batch sorption techniques were used to intercompare sorption isotherms and solid-water sorption coefficients (Kd) for four organic cations (benzylamine, 2,4-dichlorobenzylamine, phenyltrimethylammonium, oxytetracycline) with two aluminosilicate clay minerals and one soil. A comparison of Freundlich isotherm parameters revealed isotherm linearity or nonlinearity was not significantly different between column chromatography and traditional batch experiments. Importantly, skewness (a metric of eluting peak symmetry) analysis of eluting peaks can establish isotherm linearity, thereby enabling a less labor intensive means to generate the extensive data sets of linear Kd values required for the development of predictive sorption models. Our findings clearly show that column chromatography can reproduce sorption measures from conventional batch experiments with the benefit of lower labor-intensity, faster analysis times, and allow for consistent sorption measures across laboratories with distinct chromatography instrumentation. PMID:27379799

  6. Column Chromatography To Obtain Organic Cation Sorption Isotherms.

    PubMed

    Jolin, William C; Sullivan, James; Vasudevan, Dharni; MacKay, Allison A

    2016-08-01

    Column chromatography was evaluated as a method to obtain organic cation sorption isotherms for environmental solids while using the peak skewness to identify the linear range of the sorption isotherm. Custom packed HPLC columns and standard batch sorption techniques were used to intercompare sorption isotherms and solid-water sorption coefficients (Kd) for four organic cations (benzylamine, 2,4-dichlorobenzylamine, phenyltrimethylammonium, oxytetracycline) with two aluminosilicate clay minerals and one soil. A comparison of Freundlich isotherm parameters revealed isotherm linearity or nonlinearity was not significantly different between column chromatography and traditional batch experiments. Importantly, skewness (a metric of eluting peak symmetry) analysis of eluting peaks can establish isotherm linearity, thereby enabling a less labor intensive means to generate the extensive data sets of linear Kd values required for the development of predictive sorption models. Our findings clearly show that column chromatography can reproduce sorption measures from conventional batch experiments with the benefit of lower labor-intensity, faster analysis times, and allow for consistent sorption measures across laboratories with distinct chromatography instrumentation.

  7. Effect of temperature on sorption isotherms of Brussels sprout.

    PubMed

    Irzyniec, Zbigniew; Klimczak, Jolanta

    2003-02-01

    The effect of temperature (0, 20 and 40 degrees C) on the sorptivity of freeze-dried Brussels sprout was studied. It was checked which of the sorption isotherm equations that included temperature was the best to estimate experimental data. The surface area of a monolayer and isosteric heat of sorption was calculated. From the tested equations the Guggenheim-Anderson-de Boer (GAB) and Oswin equations appeared to be the best for describing sorption isotherms of freeze-dried Brussels sprout. The Clausius-Clapeyron equation was found suitable for the calculation of pure isosteric heat of sorption.

  8. Equilibrium sorption of cobalt, cesium, and strontium on Bandelier Tuff: analysis of alternative mathematical modeling

    SciTech Connect

    Polzer, W.L.; Fuentes, H.R.; Essington, E.H.; Roensch, F.R.

    1985-01-01

    Sorption isotherms are derived from batch equilibrium data for cobalt, cesium and strontium on Bandelier Tuff. Experiments were conducted at an average temperature of 23/sup 0/C and equilibrium was defined at 48 hours. The solute concentrations ranged from 0 to 500 mg/L. The radioactive isotopes /sup 60/Co, /sup 137/Cs, and /sup 85/Sr were used to trace the sorption of the stable solutes. The Linear, Langmuir, Freundlich and a Modified Freundlich isotherm equations are evaluated. The Modified Freundlich isotherm equation is validated as a preferred general mathematical tool for representing the sorption of the three solutes. The empirical constants derived from the Modified Freundlich isotherm equation indicate that under dynamic flow conditions strontium will move most rapidly and cobalt least rapidly. On the other hand, chemical dispersion will be greatest for cesium and least for strontium. Hill Plots of the sorption data suggest that in the region of low saturation sorption of all three solutes is impeded by interactions among sorption sites; cobalt exhibits the greatest effect of interactions and strontium shows only a minimal effect. In the saturation region of 50% or more, sorption of cobalt is enhanced slightly by interactions among sorption sites whereas sorption of cesium and strontium appears to be independent of site interactions. 9 references, 4 figures, 2 tables.

  9. COSOLVENT EFFECTS ON SORPTION ISOTHERM LINEARITY

    EPA Science Inventory

    Sorption-desorption hysteresis, slow desorption kinetics, and other nonideal phenomena have been attributed to the differing sorptive characteristics of the natural organic polymers associated with soils and sediments. In this study, aqueous and mixed solvent systems were used t...

  10. CEC-normalized clay-water sorption isotherm

    NASA Astrophysics Data System (ADS)

    Woodruff, W. F.; Revil, A.

    2011-11-01

    A normalized clay-water isotherm model based on BET theory and describing the sorption and desorption of the bound water in clays, sand-clay mixtures, and shales is presented. Clay-water sorption isotherms (sorption and desorption) of clayey materials are normalized by their cation exchange capacity (CEC) accounting for a correction factor depending on the type of counterion sorbed on the mineral surface in the so-called Stern layer. With such normalizations, all the data collapse into two master curves, one for sorption and one for desorption, independent of the clay mineralogy, crystallographic considerations, and bound cation type; therefore, neglecting the true heterogeneity of water sorption/desorption in smectite. The two master curves show the general hysteretic behavior of the capillary pressure curve at low relative humidity (below 70%). The model is validated against several data sets obtained from the literature comprising a broad range of clay types and clay mineralogies. The CEC values, derived by inverting the sorption/adsorption curves using a Markov chain Monte Carlo approach, are consistent with the CEC associated with the clay mineralogy.

  11. ISOT_Calc: A versatile tool for parameter estimation in sorption isotherms

    NASA Astrophysics Data System (ADS)

    Beltrán, José L.; Pignatello, Joseph J.; Teixidó, Marc

    2016-09-01

    Geochemists and soil chemists commonly use parametrized sorption data to assess transport and impact of pollutants in the environment. However, this evaluation is often hampered by a lack of detailed sorption data analysis, which implies further non-accurate transport modeling. To this end, we present a novel software tool to precisely analyze and interpret sorption isotherm data. Our developed tool, coded in Visual Basic for Applications (VBA), operates embedded within the Microsoft Excel™ environment. It consists of a user-defined function named ISOT_Calc, followed by a supplementary optimization Excel macro (Ref_GN_LM). The ISOT_Calc function estimates the solute equilibrium concentration in the aqueous and solid phases (Ce and q, respectively). Hence, it represents a very flexible way in the optimization of the sorption isotherm parameters, as it can be carried out over the residuals of q, Ce, or both simultaneously (i.e., orthogonal distance regression). The developed function includes the most usual sorption isotherm models, as predefined equations, as well as the possibility to easily introduce custom-defined ones. Regarding the Ref_GN_LM macro, it allows the parameter optimization by using a Levenberg-Marquardt modified Gauss-Newton iterative procedure. In order to evaluate the performance of the presented tool, both function and optimization macro have been applied to different sorption data examples described in the literature. Results showed that the optimization of the isotherm parameters was successfully achieved in all cases, indicating the robustness and reliability of the developed tool. Thus, the presented software tool, available to researchers and students for free, has proven to be a user-friendly and an interesting alternative to conventional fitting tools used in sorption data analysis.

  12. The sorption of sulfamethazine on soil samples: isotherms and error analysis.

    PubMed

    Mutavdžić Pavlović, Dragana; Ćurković, Lidija; Blažek, Dijana; Župan, Josip

    2014-11-01

    In this paper, batch sorption of sulfamethazine on eight soil samples (six from Croatia and two from Bosnia and Hercegovina) with different organic matter contents ranging from 1.52 to 12.8% was investigated. The effects of various parameters such as agitation time, initial concentration, and ionic strength on the sulfamethazine sorption were studied. The experimental data were analysed using a one-parameter model, Linear isotherm, and two two-parameter models, the Freundlich and Dubinin-Radushkevich isotherms. The goodness of fit was measured using the linear regression and the determination coefficient (R(2)) value. Also, the equilibrium data of the two-parameter models were analysed using the residual root mean square error (RMSE), the sum of squares of errors (ERRSQ), and a composite fractional error function (HYBRID). Non-linear regression has better characteristics for analysing experimental data. The obtained sorption coefficients Kd (from 0.25 to 8.10 mL/g) and the Freundlich sorption coefficients KF (from 1.16 to 7.99 (μg/g)(mL/μg)(1/n)) exhibited quite low values, which indicated that sulfamethazine is weakly adsorbed on the evaluated soils, is highly mobile, and has a great potential to penetrate and pollute the ground water. The Dubinin-Radushkevich isotherm was used to estimate the apparent free energy of sorption. PMID:25163651

  13. The sorption of sulfamethazine on soil samples: isotherms and error analysis.

    PubMed

    Mutavdžić Pavlović, Dragana; Ćurković, Lidija; Blažek, Dijana; Župan, Josip

    2014-11-01

    In this paper, batch sorption of sulfamethazine on eight soil samples (six from Croatia and two from Bosnia and Hercegovina) with different organic matter contents ranging from 1.52 to 12.8% was investigated. The effects of various parameters such as agitation time, initial concentration, and ionic strength on the sulfamethazine sorption were studied. The experimental data were analysed using a one-parameter model, Linear isotherm, and two two-parameter models, the Freundlich and Dubinin-Radushkevich isotherms. The goodness of fit was measured using the linear regression and the determination coefficient (R(2)) value. Also, the equilibrium data of the two-parameter models were analysed using the residual root mean square error (RMSE), the sum of squares of errors (ERRSQ), and a composite fractional error function (HYBRID). Non-linear regression has better characteristics for analysing experimental data. The obtained sorption coefficients Kd (from 0.25 to 8.10 mL/g) and the Freundlich sorption coefficients KF (from 1.16 to 7.99 (μg/g)(mL/μg)(1/n)) exhibited quite low values, which indicated that sulfamethazine is weakly adsorbed on the evaluated soils, is highly mobile, and has a great potential to penetrate and pollute the ground water. The Dubinin-Radushkevich isotherm was used to estimate the apparent free energy of sorption.

  14. Effect of plasticizer on moisture sorption isotherm of sugar palm (Arenga Pinnata) starch film

    NASA Astrophysics Data System (ADS)

    Jatmiko, Tri Hadi; Poeloengasih, Crescentiana D.; Prasetyo, Dwi Joko; Rosyida, Vita Taufika

    2016-02-01

    The effect of plasticizer type (glycerol, sorbitol) and plasticizer concentrations (30, 35, 40, 45% w/w polymer) on the moisture sorption isotherm characteristics of sugar palm (Arenga pinnata) starch films were investigated. Moisture affinity of sugar palm starch films was influenced by the plasticizer type and plasticizer concentration. The affinity of the glycerol plasticized film is stronger than that of sorbitol plasticized film. Sugar palm starch film with a higher concentration of glycerol absorbs more moisture with higher initial absorption rate than that of with sorbitol. Films with higher plasticizer concentration of glycerol and sorbitol show higher equilibrium moisture contents at the given relative humidity. The moisture sorption isotherm characteristic of sugar palm starch films can be described very well with the semi empirical 4 parameter Peleg's model.

  15. Sorption isotherms of brominated diphenyl ethers on natural soils with different organic carbon fractions.

    PubMed

    Liu, WenXin; Li, WeiBo; Xing, BaoShan; Chen, JiangLin; Tao, Shu

    2011-10-01

    Sorption isotherms of BDE-28 and BDE-47 on natural soils with different contents of soil organic matter (SOM) were investigated. Due to low water solubility of BDEs and resulted narrow ranges of aqueous equilibrium concentration, the linear distribution model showed similar and good fitting efficiency to the linear portion of nonlinear Freundlich curve. For the same sample, the linear and nonlinear model fitting sorption coefficients were close. At the statistically significant level of 0.05 or 0.1, significant relationships of total organic carbon fraction (fOC) with the fitting sorption coefficients can be observed. As for BDE-28, the relationships of fOC and SOM fractions with the single point partition coefficients at different aqueous concentrations of BDEs were significant; while for BDE-47, the relationships became less significant or insignificant, especially at higher aqueous concentrations. The findings in this study may facilitate more understanding on transport and fate of studied BDEs in soil systems. PMID:21752501

  16. Determination of the Moisture-Sorption Isotherms and Isosteric Heat of Henna Leaves

    NASA Astrophysics Data System (ADS)

    Bennaceur, S.; Draoui, B.; Touati, B.; Benseddik, A.; Saad, A.; Bennamoun, L.

    2015-01-01

    Equilibrium moisture desorption and adsorption isotherms of Lawsonia inermis L. (commonly known as henna) leaves at temperatures of 30, 40 and 50°C with a water activity ranging from 0.057 to 0.898 were obtained by the gravimetric-static method. It was established that when the temperature of these leaves increases, their moisture content increases too with a hysteresis effect. The experimental data on the sorption of the indicated leaves were compared with the corresponding calculation data obtained with the use of the GAB, modified BET, Henderson-Thompson, modified Halsey, modified Oswin, and Peleg models. Evaluation of these models on the basis of statistical processing of the data obtained with them, including the calculus of the standard error and the correlation coefficient, has shown that the GAB and Peleg models represent sorption curves more adequately. The net isosteric heats of desorption and adsorption of henna leaves were determined by the sorption isotherms constructed using the Clausius-Clapeyron equation. An expression for predicting these thermodynamic properties of plants is proposed.

  17. Metals sorption from aqueous solutions by Kluyveromyces marxianus: process optimization, equilibrium modeling and chemical characterization.

    PubMed

    Pal, Rama; Tewari, Saumyata; Rai, Jai P N

    2009-10-01

    The dead Kluyveromyces marxianus biomass, a fermentation industry waste, was used to explore its sorption potential for lead, mercury, arsenic, cobalt, and cadmium as a function of pH, biosorbent dosage, contact time, agitation speed, and initial metal concentration. The equilibrium data fitted the Langmuir model better for cobalt and cadmium, but Freundlich isotherm for all metals tested. At equilibrium, the maximum uptake capacity (Qmax) was highest for lead followed by mercury, arsenic, cobalt, and cadmium. The RL values ranged between 0-1, indicating favorable sorption of all test metals by the biosorbent. The maximum Kf value of Pb showed its efficient removal from the solution. However, multi-metal analysis depicted that sorption of all metals decreased except Pb. The potentiometric titration of biosorbent revealed the presence of functional groups viz. amines, carboxylic acids, phosphates, and sulfhydryl group involved in heavy metal sorption. The extent of contribution of functional groups and lipids to biosorption was in the order: carboxylic>lipids>amines>phosphates. Blocking of sulfhydryl group did not have any significant effect on metal sorption.

  18. ISOFIT - A PROGRAM FOR FITTING SORPTION ISOTHERMS TO EXPERIMENTAL DATA

    EPA Science Inventory

    Isotherm expressions are important for describing the partitioning of contaminants in environmental systems. ISOFIT (ISOtherm FItting Tool) is a software program that fits isotherm parameters to experimental data via the minimization of a weighted sum of squared error (WSSE) obje...

  19. SORPTION OF VOLATILE ORGANIC SOLVENTS FROM AQUEOUS SOLUTION ONTO SUBSURFACE SOLIDS

    EPA Science Inventory

    Sorption isotherms for tetrachloroethene on low-carbon subsurface core samples were linear to equilibrium solution concentrations of 2 mg L−1. Concentrations above this value produced pronounced curvature in the sorption isotherms. Sorption of tetrachloroethene, benzene, trichlor...

  20. Computer model of one-dimensional equilibrium controlled sorption processes

    USGS Publications Warehouse

    Grove, D.B.; Stollenwerk, K.G.

    1984-01-01

    A numerical solution to the one-dimensional solute-transport equation with equilibrium-controlled sorption and a first-order irreversible-rate reaction is presented. The computer code is written in FORTRAN language, with a variety of options for input and output for user ease. Sorption reactions include Langmuir, Freundlich, and ion-exchange, with or without equal valance. General equations describing transport and reaction processes are solved by finite-difference methods, with nonlinearities accounted for by iteration. Complete documentation of the code, with examples, is included. (USGS)

  1. Effect of drying methods on the moisture sorption isotherms and thermodynamic properties of mint leaves.

    PubMed

    Dalgıç, Ali Coşkun; Pekmez, Hatice; Belibağlı, Kadir Bülent

    2012-08-01

    Mint leaves were dried by three different types of dryers, namely; tray, freeze and distributed (indirect)-type solar dryer. Sorption isotherms of fresh, solar, tray and freeze dried mint were determined at temperatures of 15 °C, 25 °C and 35 °C over a range of relative humidities (10-90%). The effect of drying method on the water sorption isotherms of dried mint samples was evaluated. Experimental data were used to determine the best models for predicting the moisture sorption content of mint. Among nine sorption models tested, Peleg, GAB, Lewicki and modified Mizrahi equations gave the best fit to experimental data. The sorption data were analyzed for determination of monolayer moisture content, density of sorbed water, number of adsorbed monolayers, percent bound water, and surface area of adsorbance. The experimental data were also used to determine some thermodynamic properties of mint. PMID:23904652

  2. Sorption: Equilibrium partitioning and QSAR development using molecular predictors

    SciTech Connect

    Means, J.C.

    1994-12-31

    Sorption of chemical contaminants to sediments and soils has long been a subject of intensive investigation and QSAR development. Progressing the development of organic carbon-normalized, equilibrium partition constants (Koc) have greatly advanced the prediction of environmental fate. Integration of observed experimental results with thermodynamic modeling of compound behavior, based upon concepts of phase activities and fugacity have placed these QSARs on a firm theoretical base. An increasing spectrum of compound properties such as solubility, chemical activity, molecular surface area and other molecular topological indices have been evaluated for their utility as predictors of sorption properties. Questions concerning the effects of nonequilibrium states, hysteresis or irreversibility in desorption kinetics and equilibria, and particle-concentrations effects upon equilibrium constants as they affect fate predictions remain areas of contemporary investigation. These phenomena are considered and reviewed. The effects of modifying factors such as the effects of salinity or the presence of co-solvents may alter predicted fate of a compound. Competitive sorption with mobile microparticulate or colloidal phases may also impact OSAR predictions. Research on the role of both inorganic and organic-rich colloidal phases as a modifying influence on soil/sediment equilibrium partitioning theory is summarized.

  3. Kinetics and Equilibrium Sorption Models: Fitting Plutonium, Strontium, Uranium and Neptunium Loading on Monosodium Titanate (MST)

    SciTech Connect

    Fondeur, F

    2006-03-08

    The Dubinin-Astashov (DA) isotherm parameters for U, Pu, Sr and Np have been updated to include additional data obtained since the original derivation. The DA isotherms were modified to include a kinetic function derived by Rahn to describe sorbate loading from the beginning of sorption up to steady state. The final functions describe both kinetic and thermodynamic sorption.

  4. Kinetics, equilibrium and thermodynamics of the sorption of p-nitrophenol on two variable charge soils of Southern China

    NASA Astrophysics Data System (ADS)

    Zhang, Jiyang; Wu, Chunde; Jia, Aiyin; Hu, Bing

    2014-04-01

    The sorption of p-nitrophenol (PNP) on two variable charge soils was studied under a series of batch experimental conditions of solution pH, contact time, and temperature. Their kinetic and equilibrium parameters were assessed. The optimum pH for sorption of PNP was 5.0 for Xuwen soil and 5.4 for Guangzhou soil, respectively. Langmuir and Freundlich models were successfully used to describe the sorption isotherms. Results implied that monolayer sorption and heterogeneous energetic distribution of active sites on the surface of the soils were possible. The kinetic data were fitted with pseudo-first-order, pseudo-second-order, and intra-particle diffusion models. The sorption process was well described by pseudo-second-order kinetic model, and the intra-particle diffusion was not the sole rate-controlling step. The negative standard Gibbs free energy (ΔrGm0) values of the sorption implied that the sorption of PNP on soils was spontaneous, and the changes of the standard enthalpy (ΔrHm0) showed that the sorption as endothermic. In addition, the soils were characterized by surface area, X-ray diffraction (XRD) spectrum and Fourier transform infrared (FTIR) spectroscopy.

  5. Evaluation of theoretical and empirical water vapor sorption isotherm models for soils

    NASA Astrophysics Data System (ADS)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per; de Jonge, Lis W.

    2016-01-01

    The mathematical characterization of water vapor sorption isotherms of soils is crucial for modeling processes such as volatilization of pesticides and diffusive and convective water vapor transport. Although numerous physically based and empirical models were previously proposed to describe sorption isotherms of building materials, food, and other industrial products, knowledge about the applicability of these functions for soils is noticeably lacking. We present an evaluation of nine models for characterizing adsorption/desorption isotherms for a water activity range from 0.03 to 0.93 based on measured data of 207 soils with widely varying textures, organic carbon contents, and clay mineralogy. In addition, the potential applicability of the models for prediction of sorption isotherms from known clay content was investigated. While in general, all investigated models described measured adsorption and desorption isotherms reasonably well, distinct differences were observed between physical and empirical models and due to the different degrees of freedom of the model equations. There were also considerable differences in model performance for adsorption and desorption data. While regression analysis relating model parameters and clay content and subsequent model application for prediction of measured isotherms showed promise for the majority of investigated soils, for soils with distinct kaolinitic and smectitic clay mineralogy predicted isotherms did not closely match the measurements.

  6. Determination of low levels of amorphous content in inhalation grade lactose by moisture sorption isotherms.

    PubMed

    Vollenbroek, Jasper; Hebbink, Gerald A; Ziffels, Susanne; Steckel, Hartwig

    2010-08-16

    Alpha-lactose monohydrate is widely used as an excipient in dry powder inhalers, and plays a very important role in the efficiency of the drug delivery. Due to the processing, low levels of amorphous lactose could be present in the blends. Varying amounts could have a strong effect on the efficiency of drug delivery of the powder blends. Therefore, the accurate measurement of low levels of amorphous lactose content is very important. A new method was developed to measure the amorphous content, based on dynamic vapour sorption (DVS). In contrast to the traditional re-crystallization approach of amorphous lactose, the new method is based on moisture sorption isotherms. Moisture sorption isotherms of blends of crystalline alpha-lactose and freeze-dried or spray-dried amorphous lactose were measured. By fitting the data with a Brunauer, Emmett, and Teller (BET) isotherm, a linear correlation was found between measured and actual amorphous content for the whole range of 0.1-100%. Differences between freeze-dried and spray-dried lactose, due to different molecular arrangements, could be removed by a preconditioning the samples at 35% RH prior to the isotherm measurement. It was shown that accurate determination of very low concentrations of amorphous lactose content is possible using moisture sorption isotherm analyses. PMID:20493937

  7. Soft computing modelling of moisture sorption isotherms of milk-foxtail millet powder and determination of thermodynamic properties.

    PubMed

    Simha, H V Vikram; Pushpadass, Heartwin A; Franklin, Magdaline Eljeeva Emerald; Kumar, P Arun; Manimala, K

    2016-06-01

    Moisture sorption isotherms of spray-dried milk-foxtail millet powder were determined at 10, 25 and 40 °C. Sorption data was fitted using classical and soft-computing approaches. The isotherms were of type II, and equilibrium moisture content (EMC) was temperature dependent. The BET monolayer moisture content decreased from 3.30 to 2.67 % as temperature increased from 10 to 40 °C. Amongst the classical models, Ferro-Fontan gave the best fit of EMC-aw data. However, the Sugeno-type adaptive neuro-fuzzy inference system (ANFIS) with generalized bell-shaped membership function performed better than artificial neural network and classical models with RMSE as low as 0.0099. The isosteric heat of sorption decreased from 150.32 kJ mol(-1) at 1 % moisture content to 44.11 kJ mol(-1) at 15 % moisture. The enthalpy-entropy compensation theory was validated, and the isokinetic and harmonic mean temperatures were determined as 333.1 and 297.5 K, respectively. PMID:27478226

  8. Equilibrium Sequences and Gravitational Instability of Rotating Isothermal Rings

    NASA Astrophysics Data System (ADS)

    Kim, Woong-Tae; Moon, Sanghyuk

    2016-09-01

    Nuclear rings at the centers of barred galaxies exhibit strong star formation activities. They are thought to undergo gravitational instability when they are sufficiently massive. We approximate them as rigidly rotating isothermal objects and investigate their gravitational instability. Using a self-consistent field method, we first construct their equilibrium sequences specified by two parameters: α corresponding to the thermal energy relative to gravitational potential energy, and {\\widehat{R}}{{B}} measuring the ellipticity or ring thickness. Unlike in the incompressible case, not all values of {\\widehat{R}}{{B}} yield an isothermal equilibrium, and the range of {\\widehat{R}}{{B}} for such equilibria shrinks with decreasing α. The density distributions in the meridional plane are steeper for smaller α, and well approximated by those of infinite cylinders for slender rings. We also calculate the dispersion relations of non-axisymmetric modes in rigidly rotating slender rings with angular frequency Ω0 and central density {ρ }c. Rings with smaller α are found more unstable with a larger unstable range of the azimuthal mode number. The instability is completely suppressed by rotation when Ω0 exceeds the critical value. The critical angular frequency is found to be almost constant at ∼ 0.7{(G{ρ }c)}1/2 for α ≳ 0.01 and increases rapidly for smaller α. We apply our results to a sample of observed star-forming rings and confirm that rings without a noticeable azimuthal age gradient of young star clusters are indeed gravitationally unstable.

  9. Methods for determining the CO2 sorption capacity of coal: Experimental and theoretical high pressure isotherms

    NASA Astrophysics Data System (ADS)

    Weishauptová, Zuzana; Přibyl, Oldřich

    2016-04-01

    One way to reduce CO2 emissions discharged into the atmosphere is by trapping it and storing it in suitable repositories, including coal-bearing strata. The history of coal mining in the Czech Republic is very rich but most of the mines have been closed down in recent years. However, the unmined coal seams are interesting for the purposes of CO2 storage, especially due the opportunities they offer for recovering coal-bed methane. Mine structures of this kind can be found in large parts of the Upper Silesian Basin, where the total storage capacity has been estimated at about 380 Mt CO2. This is an interesting storage potential. In order to identify a suitable high-capacity locality for CO2 storage within a coal seam, it is necessary to study not only the geological conditions within the seam, but also the textural properties of the coal, which control the mechanism and the extent of the storage. The major storage mechanism is by sorption processes that take place in the coal porous system (adsorption in micropores and on the surface of meso/macropores, and absorption in the macromolecular structure). The CO2 sorption capacity is generally indirectly determined in a laboratory by measuring the amount of carbon dioxide captured in a coal sample at a pressure and temperature corresponding to the in situ conditions, using high pressure sorption techniques. The low pressure sorption technique can be used, by setting the partial volumes of CO2 according to its binding and storage mode. The sorption capacity is determined by extrapolation to the saturation pressure as the sum of the individual partially sorbed volumes. The aim of the study was to determine the partial volumes of CO2 bound by different mechanisms in the individual parts of the porous system of the coal, and to compare the sum with the results obtained by the high pressure isotherm. The study was carried out with 3 samples from a borehole survey in the Czech part of the Upper Silesian Basin. A high pressure

  10. Moisture sorption isotherms and thermodynamic properties of Oak wood (Quercus robur and Quercus canariensis): optimization of the processing parameters

    NASA Astrophysics Data System (ADS)

    Bahar, Rim; Azzouz, Soufien; Remond, Romain; Ouertani, Sahbi; Elaieb, Mohamed Taher; El Cafci, Mohamed Afif

    2016-09-01

    The aim of this paper was to determine the moisture desorption isotherms and essentials thermodynamic properties of two Oak wood varieties. Desorption isotherms were measured using a static gravimetric method at 50, 60, 70 and 80 °C within the range of 5-90 % relative humidity. The equilibrium moisture content decreased with increasing temperature and decreased with decreasing relative humidity at a constant temperature. The `Thermodynamic' sorption equation was found to be the best for describing the experimental moisture sorption isotherms of woods within the range of temperature and water activity investigated. The Fiber saturation point, deduced from the `Thermodynamic' model parameters, depends on the temperature and varying from 22.6 to 54.4 (% kg water/kg dry matter). Isosteric heat of desorption and differential entropy were calculated by applying Clausius-Clapeyron equation to the desorption data fitted by the `Thermodynamic' model. The isosteric heat of desorption and the differential entropy decreased with increasing moisture content according to an exponential law equation and varying from 2.03 to 31.14 kJ/mol and from 73.98 to 4.34 J/(mol K), respectively. The linear relationship between differential enthalpy and entropy satisfied the enthalpy-entropy compensation theory. The sign of Gibbs free energy was found to be positive (+283 J/mol) and (+97 J/mol) for Quercus robur and Quercus canariensis, respectively. The isokinetic temperature was found to be greater than the harmonic temperature. Based on the enthalpy-entropy compensation theory, it could be concluded that the moisture desorption isotherm of Oak wood is a non-spontaneous and enthalpy-controlled process.

  11. Equilibrium, kinetics and mechanism modeling and simulation of basic and acid dyes sorption onto jute fiber carbon: Eosin yellow, malachite green and crystal violet single component systems.

    PubMed

    Porkodi, K; Vasanth Kumar, K

    2007-05-01

    Batch experiments were carried out for the sorption of eosin yellow, malachite green and crystal violet onto jute fiber carbon (JFC). The operating variables studied are the initial dye concentration, initial solution pH, adsorbent dosage and contact time. Experimental equilibrium data were fitted to Freundlich, Langmuir and Redlich-Peterson isotherm by non-linear regression method. Langmuir isotherm was found to be the optimum isotherm for eosin yellow/JFC system and Freundlich isotherm was found to be the optimum isotherm for malachite green/JFC and crystal violet/JFC system at equilibrium conditions. The sorption capacities of eosin yellow, malachite green and crystal violet onto JFC according to Langmuir isotherm were found to 31.49 mg/g, 136.58 mg/g, 27.99 mg/g, respectively. A single stage batch adsorber was designed for the adsorption of eosin yellow, malachite green and crystal violet onto JFC based on the optimum isotherm. A pseudo second order kinetic model well represented the kinetic uptake of dyes studied onto JFC. The pseudo second order kinetic model successfully simulated the kinetics of dye uptake process. The dye sorption process involves both surface and pore diffusion with predominance of surface diffusion at earlier stages. A Boyd plot confirms the external mass transfer as the rate limiting step in the dye sorption process. The influence of initial dye concentration on the dye sorption process was represented in the form of dimensionless mass transfer numbers (Sh/Sc(0.33)) and was found to be agreeing with the expression:

  12. Equilibrium studies of sorption of lead(II) ions by different pectin compounds.

    PubMed

    Khotimchenko, Maxim; Kovalev, Valeri; Khotimchenko, Yuri

    2007-11-19

    The adsorption of Pb(II) ions from aqueous solution by different pectin compounds was studied in a batch sorption system. Water-soluble low- and high-esterified pectins and insoluble calcium pectate beads were investigated. The lead-binding capacity of all pectin compounds was highest within the pH range from 7 to 8. The binding capacities and rates of Pb(II) ions by pectin compounds were evaluated. The Langmuir, Freundlich and BET sorption models were applied to describe the isotherms and isotherm constants. Sorption isothermal data could be well interpreted by the Langmuir model. These results obtained through the study suggest that pectin compounds are favorable sorbers. The largest amount of Pb(II) ions were bound by pectin with the low degree of esterfication. Therefore, pectin substances may be considered as perspective for sorption and removal of Pb(II) ions from wastewaters.

  13. Modeling of sorption isotherms of dried vegetable wastes from wholesale market

    SciTech Connect

    Lopez, A.; Iguaz, A.; Esnoz, A.; Virseda, P.

    2000-05-01

    The moisture sorption isotherms of dried vegetable wastes (based on green leaves and fruits) from wholesale market were determined at 25, 40, 60 and 90 C by the static gravimetric method. Experimental data were fit by using several mathematical models. The G.A.B. and the Halsey model gave the minimum mean square error. G.A.B. parameters were related with temperature by Arrhenius expressions.

  14. Comparison of high-pressure CO2 sorption isotherms on Eastern and Western US coals

    SciTech Connect

    Romanov, V; Hur, T -B; Fazio, J; Howard, B

    2013-10-01

    Accurate estimation of carbon dioxide (CO2) sorption capacity of coal is important for planning the CO2 sequestration efforts. In this work, we investigated sorption and swelling behavior of several Eastern and Western US coal samples from the Central Appalachian Basin and from San Juan Basin. The CO2 sorption isotherms have been completed at 55°C for as received and dried samples. The role of mineral components in coal, the coal swelling, the effects of temperature and moisture, and the error propagation have been analyzed. Changes in void volume due to dewatering and other factors such as temporary caging of carbon dioxide molecules in coal matrix were identified among the main factors affecting accuracy of the carbon dioxide sorption isotherms. The (helium) void volume in the sample cells was measured before and after the sorption isotherm experiments and was used to build the volume-corrected data plots.

  15. Sorption equilibrium of emerging and traditional organic contaminants in leafy rape, Chinese mustard, lettuce and Chinese cabbage.

    PubMed

    Yang, Chien-Ying; Chang, Meei-Ling; Wu, Siang Chen; Shih, Yang-Hsin

    2016-07-01

    Emerging and petroleum contaminants could transfer into food chains by plant uptake, potentially causing food security problems. To build a prediction model, the sorption equilibrium and uptake kinetics of toluene, p-xylene, naphthalene, bisphenol A, and 4-bromo-diphenyl ether in some common leafy vegetables including leafy rape, Chinese mustard, lettuce and Chinese cabbage were examined. The kinetic experiments revealed that high sorption rates were observed for these plants that had high lipid contents. For two emerging contaminants with polar functional groups, their resulting isotherms were strongly linear (R(2) = 0.92 to 1.00), indicating that the sorption was dominated by partitioning. Moreover, regression correlation showed that log Klip, the lipid-water partition coefficient, and log Kow, the octanol-water coefficient, for these organic chemicals were strongly linear-related, following the equation: log Klip = 0.894 × log Kow+0.219 (R(2) = 0.953). The correlation equation allows the prediction of the sorption capacity of plant species for an organic compound when the plant composition and the log Kow of the chemical are determined. This improved model containing different organic chemicals with a wide range of log Kow (2.73-4.80) and including emerging contaminants was established, which shows further utilization for predicting the sorption of organic contaminants by plants.

  16. Sorption equilibrium of emerging and traditional organic contaminants in leafy rape, Chinese mustard, lettuce and Chinese cabbage.

    PubMed

    Yang, Chien-Ying; Chang, Meei-Ling; Wu, Siang Chen; Shih, Yang-Hsin

    2016-07-01

    Emerging and petroleum contaminants could transfer into food chains by plant uptake, potentially causing food security problems. To build a prediction model, the sorption equilibrium and uptake kinetics of toluene, p-xylene, naphthalene, bisphenol A, and 4-bromo-diphenyl ether in some common leafy vegetables including leafy rape, Chinese mustard, lettuce and Chinese cabbage were examined. The kinetic experiments revealed that high sorption rates were observed for these plants that had high lipid contents. For two emerging contaminants with polar functional groups, their resulting isotherms were strongly linear (R(2) = 0.92 to 1.00), indicating that the sorption was dominated by partitioning. Moreover, regression correlation showed that log Klip, the lipid-water partition coefficient, and log Kow, the octanol-water coefficient, for these organic chemicals were strongly linear-related, following the equation: log Klip = 0.894 × log Kow+0.219 (R(2) = 0.953). The correlation equation allows the prediction of the sorption capacity of plant species for an organic compound when the plant composition and the log Kow of the chemical are determined. This improved model containing different organic chemicals with a wide range of log Kow (2.73-4.80) and including emerging contaminants was established, which shows further utilization for predicting the sorption of organic contaminants by plants. PMID:27085315

  17. Phosphate sorption by three potential filter materials as assessed by isothermal titration calorimetry.

    PubMed

    Lyngsie, Gry; Penn, Chad J; Hansen, Hans C B; Borggaard, Ole K

    2014-10-01

    Phosphorus eutrophication of lakes and streams, coming from drained farmlands, is a serious problem in areas with intensive agriculture. Installation of phosphate (P) sorbing filters at drain outlets may be a solution. The aim of this study was to improve the understanding of reactions involved in P sorption by three commercial P sorbing materials, i.e. Ca/Mg oxide-based Filtralite-P, Fe oxide-based CFH-12 and Limestone in two particle sizes (2-1 mm and 1-0.5 mm), by means of isothermal titration calorimetry (ITC), sorption isotherms, sequential extractions and SEM-EDS. The results indicate that P retention by CFH is due to surface complexation by rapid formation of strong Fe-P bonds. In contrast, retention of P by Filtralite-P and Limestone strongly depends on pH and time and is interpreted due to formation of calcium phosphate precipitate(s). Consequently, CFH can unambiguously be recommended as P retention filter material in drain outlets, whereas the use of Filtralite-P and Limestone has certain (serious) limitations. Thus, Filtralite-P has high capacity to retain P but only at alkaline pH (pH ≥ 10) and P retention by Limestone requires long-time contact and a high ratio between sorbent and sorbate.

  18. Isothermal Adsorption Measurement for the Development of High Performance Solid Sorption Cooling System

    NASA Astrophysics Data System (ADS)

    Saha, Bidyut Baran; Koyama, Shigeru; Alam, K. C. Amanul; Hamamoto, Yoshinori; Akisawa, Atsushi; Kashiwagi, Takao; Ng, Kim Choon; Chua, Hui Tong

    Interest in low-grade thermal heat powered solid sorption system using natural refrigerants has been increased. However, the drawbacks of these adsorption systems are their poor performance. The objective of this paper is to improve the performance of thermally powered adsorption cooling system by selecting new adsorbent-refrigerant pairs. Adsorption capacity of adsorbent-refrigerant pair depends on the thermophysical properties (pore size, pore volume and pore diameter) of adsorbent and isothermal characteristics of the adsorbent-refrigerant pair. In this paper, the thermophysical properties of three types of silica gels and three types of pitch based activated carbon fibers are determined from the nitrogen adsorption isotherms. The standard nitrogen gas adsorption/desorption measurements on various adsorbents at liquid nitrogen of temperature 77.4 K were performed. Surface area of each adsorbent was determined by the Brunauer, Emmett and Teller (BET) plot of nitrogen adsorption data. Pore size distribution was measured by the Horvath and Kawazoe (HK) method. Adsorption/desorption isotherm results showed that all three carbon fibers have no hysteresis and had better adsorption capacity in comparison with those of silica gels.

  19. Idealized Shale Sorption Isotherm Measurements to Determine Pore Volume, Pore Size Distribution, and Surface Area

    NASA Astrophysics Data System (ADS)

    Holmes, R.; Wang, B.; Aljama, H.; Rupp, E.; Wilcox, J.

    2014-12-01

    One method for mitigating the impacts of anthropogenic CO2-related climate change is the sequestration of CO2 in depleted gas and oil reservoirs, including shale. The accurate characterization of the heterogeneous material properties of shale, including pore volume, surface area, pore size distributions (PSDs) and composition is needed to understand the interaction of CO2 with shale. Idealized powdered shale sorption isotherms were created by varying incremental amounts of four essential components by weight. The first two components, organic carbon and clay, have been shown to be the most important components for CO2 uptake in shales. Organic carbon was represented by kerogen isolated from a Silurian shale, and clay groups were represented by illite from the Green River shale formation. The rest of the idealized shale was composed of equal parts by weight of SiO2 to represent quartz and CaCO3 to represent carbonate components. Baltic, Eagle Ford, and Barnett shale sorption measurements were used to validate the idealized samples. The idealized and validation shale sorption isotherms were measured volumetrically using low pressure N2 (77K) and CO2 (273K) adsorbates on a Quantachrome Autosorb IQ2. Gravimetric isotherms were also produced for a subset of these samples using CO2 and CH4adsorbates under subsurface temperature and pressure conditions using a Rubotherm magnetic suspension balance. Preliminary analyses were inconclusive in validating the idealized samples. This could be a result of conflicting reports of total organic carbon (TOC) content in each sample, a problem stemming from the heterogeneity of the samples and different techniques used for measuring TOC content. The TOC content of the validation samples (Eagle Ford and Barnett) was measured by Rock-Eval pyrolysis at Weatherford Laboratories, while the TOC content in the Baltic validation samples was determined by LECO TOC. Development of a uniform process for measuring TOC in the validation samples is

  20. Mono-component versus binary isotherm models for Cu(II) and Pb(II) sorption from binary metal solution by the green alga Pithophora oedogonia.

    PubMed

    Kumar, Dhananjay; Singh, Alpana; Gaur, J P

    2008-11-01

    The sorption of Cu(II) and Pb(II) by Pithophora markedly decreased as the concentration of the secondary metal ion, Cu(II) or Pb(II), increased in the binary metal solution. However, the test alga showed a greater affinity to sorb Cu(II) than Pb(II) from the binary metal solution. Mono-component Freundlich, Langmuir, Redlich-Peterson and Sips isotherms successfully predicted the sorption of Cu(II) and Pb(II) from both single and binary metal solutions. None of the tested binary sorption isotherms could realistically predict Cu(II) and Pb(II) sorption capacity and affinity of the test alga for the binary metal solutions of varying composition, which mono-component isotherms could very well accomplish. Hence, mono-component isotherm modeling at different concentrations of the secondary metal ion seems to be a better option than binary isotherms for metal sorption from binary metal solution.

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

    PubMed

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

    2015-04-01

    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. PMID:25576783

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

    PubMed

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

    2015-04-01

    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.

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

    NASA Astrophysics Data System (ADS)

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

    2016-07-01

    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.

  4. Kinetics and equilibrium of the sorption of bisphenol A by carbon nanotubes from wastewater.

    PubMed

    Bohdziewicz, J; Kamińska, G

    2013-01-01

    The aim of this study was to determine the sorption potential of carbon nanotubes (CNTs) to bisphenol A (BPA) contained in synthetic wastewater whose composition corresponds to biologically treated effluents. These nanotubes differed in their outer diameter, the number of graphene layers and the presence of modifying functional groups. Based on the nitrogen adsorption-desorption isotherms, mensuration of the specific surface area and pore size distribution was undertaken. The porous structure of the CNTs was bidispersive; the majority consisted of micropores, there was an average fraction of mesopores, and macropores did not occur. On the basis of common kinetics models (pseudo-first-order and pseudo-second-order models), a trial of modelling the kinetics of BPA sorption onto nanotubes was undertaken. The experimental data were well fitted only to the pseudo-second-order models. The kinetics study indicated that adsorption of BPA on CNTs proceeded very fast, with the majority of the adsorbate being adsorbed in the first few seconds. The sorption capacity of nanotubes to BPA was the highest for single-walled CNTs. A decrease in the sorption potential of the nanotubes for higher pH values occurred as a result of the deprotonation of the BPA and formation of bisphenolate anions, consequently leading to a decrease of π-π (hydrophobic) interaction and enhancing electrostatic repulsion. Overall, these results unequivocally confirm the ideal performance and potential of nanotubes for removal of micropollutants from synthetic wastewater. Replicating the conditions occurring in real wastewater allows us to expect a high sorption of BPA in real competitive sorption systems. PMID:24056428

  5. Kinetics and equilibrium of the sorption of bisphenol A by carbon nanotubes from wastewater.

    PubMed

    Bohdziewicz, J; Kamińska, G

    2013-01-01

    The aim of this study was to determine the sorption potential of carbon nanotubes (CNTs) to bisphenol A (BPA) contained in synthetic wastewater whose composition corresponds to biologically treated effluents. These nanotubes differed in their outer diameter, the number of graphene layers and the presence of modifying functional groups. Based on the nitrogen adsorption-desorption isotherms, mensuration of the specific surface area and pore size distribution was undertaken. The porous structure of the CNTs was bidispersive; the majority consisted of micropores, there was an average fraction of mesopores, and macropores did not occur. On the basis of common kinetics models (pseudo-first-order and pseudo-second-order models), a trial of modelling the kinetics of BPA sorption onto nanotubes was undertaken. The experimental data were well fitted only to the pseudo-second-order models. The kinetics study indicated that adsorption of BPA on CNTs proceeded very fast, with the majority of the adsorbate being adsorbed in the first few seconds. The sorption capacity of nanotubes to BPA was the highest for single-walled CNTs. A decrease in the sorption potential of the nanotubes for higher pH values occurred as a result of the deprotonation of the BPA and formation of bisphenolate anions, consequently leading to a decrease of π-π (hydrophobic) interaction and enhancing electrostatic repulsion. Overall, these results unequivocally confirm the ideal performance and potential of nanotubes for removal of micropollutants from synthetic wastewater. Replicating the conditions occurring in real wastewater allows us to expect a high sorption of BPA in real competitive sorption systems.

  6. Humidity scanning quartz crystal microbalance with dissipation monitoring setup for determination of sorption-desorption isotherms and rheological changes.

    PubMed

    Björklund, Sebastian; Kocherbitov, Vitaly

    2015-05-01

    A new method to determine water sorption-desorption isotherms with high resolution in the complete range of water activities (relative humidities) is presented. The method is based on quartz crystal microbalance with dissipation monitoring (QCM-D). The QCM-D is equipped with a humidity module in which the sample film is kept in air with controlled humidity. The experimental setup allows for continuous scanning of the relative humidity from either dry to humid conditions or vice versa. The amount of water sorbed or desorbed from the sample is determined from the resonance frequencies of the coated quartz sensor, via analysis of the overtone dependence. In addition, the method allows for characterization of hydration induced changes of the rheological properties from the dissipation data, which is closely connected to the viscoelasticity of the film. The accuracy of the humidity scanning setup is confirmed in control experiments. Sorption-desorption isotherms of pig gastric mucin and lysozyme, obtained by the new method, show good agreement with previous results. Finally, we show that the deposition technique used to coat the quartz sensor influences the QCM-D data and how this issue can be used to obtain further information on the effect of hydration. In particular, we demonstrate that spin-coating represents an attractive alternative to obtain sorption-desorption isotherms, while drop-coating provides additional information on changes of the rheological properties during hydration. PMID:26026556

  7. Humidity scanning quartz crystal microbalance with dissipation monitoring setup for determination of sorption-desorption isotherms and rheological changes

    SciTech Connect

    Björklund, Sebastian Kocherbitov, Vitaly

    2015-05-15

    A new method to determine water sorption-desorption isotherms with high resolution in the complete range of water activities (relative humidities) is presented. The method is based on quartz crystal microbalance with dissipation monitoring (QCM-D). The QCM-D is equipped with a humidity module in which the sample film is kept in air with controlled humidity. The experimental setup allows for continuous scanning of the relative humidity from either dry to humid conditions or vice versa. The amount of water sorbed or desorbed from the sample is determined from the resonance frequencies of the coated quartz sensor, via analysis of the overtone dependence. In addition, the method allows for characterization of hydration induced changes of the rheological properties from the dissipation data, which is closely connected to the viscoelasticity of the film. The accuracy of the humidity scanning setup is confirmed in control experiments. Sorption-desorption isotherms of pig gastric mucin and lysozyme, obtained by the new method, show good agreement with previous results. Finally, we show that the deposition technique used to coat the quartz sensor influences the QCM-D data and how this issue can be used to obtain further information on the effect of hydration. In particular, we demonstrate that spin-coating represents an attractive alternative to obtain sorption-desorption isotherms, while drop-coating provides additional information on changes of the rheological properties during hydration.

  8. Humidity scanning quartz crystal microbalance with dissipation monitoring setup for determination of sorption-desorption isotherms and rheological changes

    NASA Astrophysics Data System (ADS)

    Björklund, Sebastian; Kocherbitov, Vitaly

    2015-05-01

    A new method to determine water sorption-desorption isotherms with high resolution in the complete range of water activities (relative humidities) is presented. The method is based on quartz crystal microbalance with dissipation monitoring (QCM-D). The QCM-D is equipped with a humidity module in which the sample film is kept in air with controlled humidity. The experimental setup allows for continuous scanning of the relative humidity from either dry to humid conditions or vice versa. The amount of water sorbed or desorbed from the sample is determined from the resonance frequencies of the coated quartz sensor, via analysis of the overtone dependence. In addition, the method allows for characterization of hydration induced changes of the rheological properties from the dissipation data, which is closely connected to the viscoelasticity of the film. The accuracy of the humidity scanning setup is confirmed in control experiments. Sorption-desorption isotherms of pig gastric mucin and lysozyme, obtained by the new method, show good agreement with previous results. Finally, we show that the deposition technique used to coat the quartz sensor influences the QCM-D data and how this issue can be used to obtain further information on the effect of hydration. In particular, we demonstrate that spin-coating represents an attractive alternative to obtain sorption-desorption isotherms, while drop-coating provides additional information on changes of the rheological properties during hydration.

  9. Humidity scanning quartz crystal microbalance with dissipation monitoring setup for determination of sorption-desorption isotherms and rheological changes.

    PubMed

    Björklund, Sebastian; Kocherbitov, Vitaly

    2015-05-01

    A new method to determine water sorption-desorption isotherms with high resolution in the complete range of water activities (relative humidities) is presented. The method is based on quartz crystal microbalance with dissipation monitoring (QCM-D). The QCM-D is equipped with a humidity module in which the sample film is kept in air with controlled humidity. The experimental setup allows for continuous scanning of the relative humidity from either dry to humid conditions or vice versa. The amount of water sorbed or desorbed from the sample is determined from the resonance frequencies of the coated quartz sensor, via analysis of the overtone dependence. In addition, the method allows for characterization of hydration induced changes of the rheological properties from the dissipation data, which is closely connected to the viscoelasticity of the film. The accuracy of the humidity scanning setup is confirmed in control experiments. Sorption-desorption isotherms of pig gastric mucin and lysozyme, obtained by the new method, show good agreement with previous results. Finally, we show that the deposition technique used to coat the quartz sensor influences the QCM-D data and how this issue can be used to obtain further information on the effect of hydration. In particular, we demonstrate that spin-coating represents an attractive alternative to obtain sorption-desorption isotherms, while drop-coating provides additional information on changes of the rheological properties during hydration.

  10. A gel probe equilibrium sampler for measuring arsenic porewater profiles and sorption gradients in sediments: I. Laboratory development

    USGS Publications Warehouse

    Campbell, K.M.; Root, R.; O'Day, P. A.; Hering, J.G.

    2008-01-01

    A gel probe equilibrium sampler has been developed to study arsenic (As) geochemistry and sorption behavior in sediment porewater. The gels consist of a hydrated polyacrylamide polymer, which has a 92% water content. Two types of gels were used in this study. Undoped (clear) gels were used to measure concentrations of As and other elements in sediment porewater. The polyacrylamide gel was also doped with hydrous ferric oxide (HFO), an amorphous iron (Fe) oxyhydroxide. When deployed in the field, HFO-doped gels introduce a fresh sorbent into the subsurface thus allowing assessment of in situ sorption. In this study, clear and HFO-doped gels were tested under laboratory conditions to constrain the gel behavior prior to field deployment. Both types of gels were allowed to equilibrate with solutions of varying composition and re-equilibrated in acid for analysis. Clear gels accurately measured solution concentrations (??1%), and As was completely recovered from HFO-doped gels (??4%). Arsenic speciation was determined in clear gels through chromatographic separation of the re-equilibrated solution. For comparison to speciation in solution, mixtures of As(III) and As(V) adsorbed on HFO embedded in gel were measured in situ using X-ray absorption spectroscopy (XAS). Sorption densities for As(III) and As(V) on HFO embedded in gel were obtained from sorption isotherms at pH 7.1. When As and phosphate were simultaneously equilibrated (in up to 50-fold excess of As) with HFO-doped gels, phosphate inhibited As sorption by up to 85% and had a stronger inhibitory effect on As(V) than As(III). Natural organic matter (>200 ppm) decreased As adsorption by up to 50%, and had similar effects on As(V) and As(III). The laboratory results provide a basis for interpreting results obtained by deploying the gel probe in the field and elucidating the mechanisms controlling As partitioning between solid and dissolved phases in the environment. ?? 2008 American Chemical Society.

  11. Metal-anion sorption by chitosan beads: Equilibrium and kinetic studies

    SciTech Connect

    Guibal, E.; Milot, C.; Tobin, J.M.

    1998-04-01

    Chitosan is a well-known biopolymer, whose high nitrogen content confers remarkable ability for the sorption of metal ions from dilute effluents. However, its sorption performance in both equilibrium and kinetic terms is controlled by diffusion processes. Gel bead formation allows an expansion of the polymer network, which improves access to the internal sorption sites and enhances diffusion mechanisms. Molybdate and vanadate recovery using glutaraldehyde cross-linked chitosan beads reaches uptake capacities as high as 7--8 mmol/g, depending on the pH. The optimum pH (3--3.5) corresponded to the predominance range of hydrolyzed polynuclear metal forms and optimum electrostatic attraction. While for beads, particle size does not influence equilibrium, for flakes, increasing sorbent radius significantly decreases uptake capacities to 1.5 mmol/g. Sorption kinetics are mainly controlled by intraparticle diffusion for beads, while for flakes the controlling mechanisms are both external and intraparticle diffusion. The gel conditioning increases the intraparticle diffusivity by 3 orders of magnitude: intraparticle diffusivities range between 10{sup {minus}13} and 10{sup {minus}10} m{sup 2}/min, depending on the sorbent size and the conditioning.

  12. Sorption of boron trifluoride by activated carbons

    SciTech Connect

    Polevoi, A.S.; Petrenko, A.E.

    1988-01-10

    The sorption of born trifluoride on AG-3, SKT, SKT-3, SKT-7, SKT-4A, SKT-6A, and SKT-2B carbons was investigated. The sorption isotherms for both vapors and gas were determined volumetrically. The coefficients of two equations described the sorption of BF/sub 3/ in the sorption of BF/sub 3/ on active carbons. Heats of sorption of BF/sub 3/ on the activated carbons are shown and the sorption isotherms and temperature dependences of the equilibrium pressure of BF/sub 3/ for activated carbons were presented. The values of the heats of sorption indicated the weak character of the reaction of BF/sub 3/ with the surface of the carbons. The equations can be used for calculating the phase equilibrium of BF/sub 3/ on carbons in a wider range of temperatures and pressures.

  13. Relation of organic contaminant equilibrium sorption and kinetic uptake in plants

    USGS Publications Warehouse

    Li, H.; Sheng, G.; Chiou, C.T.; Xu, O.

    2005-01-01

    Plant uptake is one of the environmental processes that influence contaminant fate. Understanding the magnitude and rate of plant uptake is critical to assessing potential crop contamination and the development of phytoremediation technologies. We determined (1) the partition-dominated equilibrium sorption of lindane (LDN) and hexachlorobenzene (HCB) by roots and shoots of wheat seedlings, (2) the kinetic uptake of LDN and HCB by roots and shoots of wheat seedlings, (3) the kinetic uptake of HCB, tetrachloroethylene (PCE), and trichloroethylene (TCE) by roots and shoots of ryegrass seedlings, and (4) the lipid, carbohydrate, and water contents of the plants. Although the determined sorption and the plant composition together suggest the predominant role of plant lipids for the sorption of LDN and HCB, the predicted partition with lipids of LDN and HCB using the octanol-water partition coefficients is notably lower than the measured sorption, due presumably to underestimation of the plant lipid contents and to the fact that octanol is less effective as a partition medium than plant lipids. The equilibrium sorption or the estimated partition can be viewed as the kinetic uptake limits. The uptakes of LDN, PCE, and TCE from water at fixed concentrations increased with exposure time in approach to steady states. The uptake of HCB did not reach a plateau within the tested time because of its exceptionally high partition coefficient. In all of the cases, the observed uptakes were lower than their respective limits, due presumably to contaminant dissipation in and limited water transpiration by the plants. ?? 2005 American Chemical Society.

  14. Modification of a method-of-characteristics solute-transport model to incorporate decay and equilibrium-controlled sorption or ion exchange

    USGS Publications Warehouse

    Goode, D.J.; Konikow, L.F.

    1989-01-01

    The U.S. Geological Survey computer model of two-dimensional solute transport and dispersion in ground water (Konikow and Bredehoeft, 1978) has been modified to incorporate the following types of chemical reactions: (1) first-order irreversible rate-reaction, such as radioactive decay; (2) reversible equilibrium-controlled sorption with linear, Freundlich, or Langmuir isotherms; and (3) reversible equilibrium-controlled ion exchange for monovalent or divalent ions. Numerical procedures are developed to incorporate these processes in the general solution scheme that uses method-of- characteristics with particle tracking for advection and finite-difference methods for dispersion. The first type of reaction is accounted for by an exponential decay term applied directly to the particle concentration. The second and third types of reactions are incorporated through a retardation factor, which is a function of concentration for nonlinear cases. The model is evaluated and verified by comparison with analytical solutions for linear sorption and decay, and by comparison with other numerical solutions for nonlinear sorption and ion exchange.

  15. The effects of sugars on moisture sorption isotherm and functional properties of cold water fish gelatin films.

    PubMed

    Hazaveh, Parham; Mohammadi Nafchi, Abdorreza; Abbaspour, Hossein

    2015-08-01

    Sugars were incorporated into CWFG solutions at different ratios (0%, 2%, 4%, and 6% w/w). Functional properties of the modified films were characterized following American standard test methods, and moisture sorption isotherm was characterized by polynomial and GAB models. Permeation to water vapor and oxygen of the modified films decreased compared to that of the control CWFG films. Moisture content, solubility, and monolayer water content of CWFG films decreased with the increase of sugar content. The addition of sugars significantly increased the Tensile strength of CWFG films from 30 to 40 MPa for ribose, and 30 to 35 MPa for fructose whereas elongation at the breaks decreased from 60% to 30% for ribose, and from 60% to 45% for that which incorporated fructose sugars. Moisture sorption isotherm curve significantly shifted to lower moisture content in aw<0.6. In aw>0.6, ribose-incorporated CWFG films, had similar function to hydrogel materials. In all the characterizations, the effects of ribose were significantly higher than those of fructose. Results of this research can be explored for commercial use, depending on the application for either packaging purposes or in the cosmetics industries.

  16. Sorption of methylene blue on treated agricultural adsorbents: equilibrium and kinetic studies

    NASA Astrophysics Data System (ADS)

    Tiwari, D. P.; Singh, S. K.; Sharma, Neetu

    2015-03-01

    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.

  17. Sorption of water alkalinity and hardness from high-strength wastewater on bifunctional activated carbon: process optimization, kinetics and equilibrium studies.

    PubMed

    Amosa, Mutiu K

    2016-08-01

    Sorption optimization and mechanism of hardness and alkalinity on bifunctional empty fruit bunch-based powdered activation carbon (PAC) were studied. The PAC possessed both high surface area and ion-exchange properties, and it was utilized in the treatment of biotreated palm oil mill effluent. Batch adsorption experiments designed with Design Expert(®) were conducted in correlating the singular and interactive effects of the three adsorption parameters: PAC dosage, agitation speed and contact time. The sorption trends of the two contaminants were sequentially assessed through a full factorial design with three factor interaction models and a central composite design with polynomial models of quadratic order. Analysis of variance revealed the significant factors on each design response with very high R(2) values indicating good agreement between model and experimental values. The optimum operating conditions of the two contaminants differed due to their different regions of operating interests, thus necessitating the utility of desirability factor to get consolidated optimum operation conditions. The equilibrium data for alkalinity and hardness sorption were better represented by the Langmuir isotherm, while the pseudo-second-order kinetic model described the adsorption rates and behavior better. It was concluded that chemisorption contributed majorly to the adsorption process.

  18. Sorption of water alkalinity and hardness from high-strength wastewater on bifunctional activated carbon: process optimization, kinetics and equilibrium studies.

    PubMed

    Amosa, Mutiu K

    2016-08-01

    Sorption optimization and mechanism of hardness and alkalinity on bifunctional empty fruit bunch-based powdered activation carbon (PAC) were studied. The PAC possessed both high surface area and ion-exchange properties, and it was utilized in the treatment of biotreated palm oil mill effluent. Batch adsorption experiments designed with Design Expert(®) were conducted in correlating the singular and interactive effects of the three adsorption parameters: PAC dosage, agitation speed and contact time. The sorption trends of the two contaminants were sequentially assessed through a full factorial design with three factor interaction models and a central composite design with polynomial models of quadratic order. Analysis of variance revealed the significant factors on each design response with very high R(2) values indicating good agreement between model and experimental values. The optimum operating conditions of the two contaminants differed due to their different regions of operating interests, thus necessitating the utility of desirability factor to get consolidated optimum operation conditions. The equilibrium data for alkalinity and hardness sorption were better represented by the Langmuir isotherm, while the pseudo-second-order kinetic model described the adsorption rates and behavior better. It was concluded that chemisorption contributed majorly to the adsorption process. PMID:26752149

  19. Sorption of Ochratoxin A from aqueous solutions using beta-cyclodextrin-polyurethane polymer

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The ability of a cyclodextrin-polyurethane polymer to remove ochratoxin A from aqueous solutions, including wine, was examined by batch rebinding assays and equilibrium sorption isotherms. The results were fit to two parameter models. Freundlich analysis of the sorption isotherm indicates the polyme...

  20. Numerical simulation of advective-dispersive multisolute transport with sorption, ion exchange and equilibrium chemistry

    USGS Publications Warehouse

    Lewis, F.M.; Voss, C.I.; Rubin, Jacob

    1986-01-01

    A model was developed that can simulate the effect of certain chemical and sorption reactions simultaneously among solutes involved in advective-dispersive transport through porous media. The model is based on a methodology that utilizes physical-chemical relationships in the development of the basic solute mass-balance equations; however, the form of these equations allows their solution to be obtained by methods that do not depend on the chemical processes. The chemical environment is governed by the condition of local chemical equilibrium, and may be defined either by the linear sorption of a single species and two soluble complexation reactions which also involve that species, or binary ion exchange and one complexation reaction involving a common ion. Partial differential equations that describe solute mass balance entirely in the liquid phase are developed for each tenad (a chemical entity whose total mass is independent of the reaction process) in terms of their total dissolved concentration. These equations are solved numerically in two dimensions through the modification of an existing groundwater flow/transport computer code. (Author 's abstract)

  1. Mild hydration of didecyldimethylammonium chloride modified DNA by 1H-nuclear magnetic resonance and by sorption isotherm

    NASA Astrophysics Data System (ADS)

    Harańczyk, H.; Kobierski, J.; Nizioł, J.; Hebda, E.; Pielichowski, J.; Zalitacz, D.; Marzec, M.; El-Ghayoury, A.

    2013-01-01

    The gaseous phase hydration of deoxyribonucleic acid and didecyldimethylammonium chloride (C19H42ClN) complexes (DNA-DDCA) was observed using hydration kinetics, sorption isotherm, and high power nuclear magnetic resonance. Three bound water fractions were distinguished: (i) a very tightly bound water not removed by incubation over silica gel, (ii) a tightly bound water saturating with the hydration time t1h = (0.59 ± 0.04) h, and a loosely bound water fraction, (iii) with the hydration time t2h = (20.9 ± 1.3) h. Proton free induction decay was decomposed into the signal associated with the solid matrix of DNA-DDCA complex (T2S∗≈ 30 μs) and two liquid signal components coming from tightly bound (T2L1∗≈ 100 μs) and from loosely bound water fraction (T2L2∗≈ 1000 μs).

  2. Monte-Carlo sorption and neutron diffraction study of the filling isotherm in clathrate hydrates

    SciTech Connect

    Klapproth, Alice; Kuhs, Werner F.; Chazallon, Bertrand

    1999-06-15

    We are interested in the thermodynamics of the gas filling of clathrate hydrates. In order to determine the pressure-dependent filling of the cages, neutron powder diffraction experiments on N{sub 2} and CO{sub 2} clathrates were performed. Interaction potentials were refined by comparing the experimentally determined fillings with those generated by MC-sorption calculations. Unsatisfactory agreement between experiment and simulation is observed when using the widely employed SPC water-water interaction potential.

  3. [Sorption mechanism of ofloxacin by carbon nanotubes].

    PubMed

    Zhao, Xing-Xing; Yu, Shui-Li; Wang, Zhe

    2014-02-01

    Sorption of ofloxacin (OFL) by carbon nanotubes is an effective method to control its fate in aquatic environment. The sorption process of OFL by mixed acid-treated and non-treated multi-walled carbon nanotubes was discussed. Sorption kinetics, sorption isotherm, desorption, sorption thermodynamics and effect of pH were investigated. The results indicated that the sorption kinetics followed the pseudo-second order kinetics model. The equilibrium sorption capacity of OFL on MWCNTs-O was higher. The sorption isotherm could be fitted by both the Langmuir and Freundlich models. The equilibrium sorption capacity dropped when the pH of aqueous solution was in the range of 6.0 to 10.0. Obvious desorption hysteresis was observed during the desorption experiments, especially on MWCNTs-O. Sorption thermodynamics analysis showed that the interactions between the OFL and sorbents were mainly between molecules. More oxygen-containing functional groups introduced on MWCNTs provided OFL molecules with more sorptive sites, which facilitated the generation of hydrogen bonds, a relatively strong interaction. The hydrogen bonds dominated the sorption process of OFL by MWCNTs/MWCNTs-O, explaining the experimental phenomena.

  4. Moisture sorption isotherms and thermodynamic properties of mexican mennonite-style cheese.

    PubMed

    Martinez-Monteagudo, Sergio I; Salais-Fierro, Fabiola

    2014-10-01

    Moisture adsorption isotherms of fresh and ripened Mexican Mennonite-style cheese were investigated using the static gravimetric method at 4, 8, and 12 °C in a water activity range (aw) of 0.08-0.96. These isotherms were modeled using GAB, BET, Oswin and Halsey equations through weighed non-linear regression. All isotherms were sigmoid in shape, showing a type II BET isotherm, and the data were best described by GAB model. GAB model coefficients revealed that water adsorption by cheese matrix is a multilayer process characterized by molecules that are strongly bound in the monolayer and molecules that are slightly structured in a multilayer. Using the GAB model, it was possible to estimate thermodynamic functions (net isosteric heat, differential entropy, integral enthalpy and entropy, and enthalpy-entropy compensation) as function of moisture content. For both samples, the isosteric heat and differential entropy decreased with moisture content in exponential fashion. The integral enthalpy gradually decreased with increasing moisture content after reached a maximum value, while the integral entropy decreased with increasing moisture content after reached a minimum value. A linear compensation was found between integral enthalpy and entropy suggesting enthalpy controlled adsorption. Determination of moisture content and aw relationship yields to important information of controlling the ripening, drying and storage operations as well as understanding of the water state within a cheese matrix. PMID:25328178

  5. Moisture sorption isotherms and thermodynamic properties of mexican mennonite-style cheese.

    PubMed

    Martinez-Monteagudo, Sergio I; Salais-Fierro, Fabiola

    2014-10-01

    Moisture adsorption isotherms of fresh and ripened Mexican Mennonite-style cheese were investigated using the static gravimetric method at 4, 8, and 12 °C in a water activity range (aw) of 0.08-0.96. These isotherms were modeled using GAB, BET, Oswin and Halsey equations through weighed non-linear regression. All isotherms were sigmoid in shape, showing a type II BET isotherm, and the data were best described by GAB model. GAB model coefficients revealed that water adsorption by cheese matrix is a multilayer process characterized by molecules that are strongly bound in the monolayer and molecules that are slightly structured in a multilayer. Using the GAB model, it was possible to estimate thermodynamic functions (net isosteric heat, differential entropy, integral enthalpy and entropy, and enthalpy-entropy compensation) as function of moisture content. For both samples, the isosteric heat and differential entropy decreased with moisture content in exponential fashion. The integral enthalpy gradually decreased with increasing moisture content after reached a maximum value, while the integral entropy decreased with increasing moisture content after reached a minimum value. A linear compensation was found between integral enthalpy and entropy suggesting enthalpy controlled adsorption. Determination of moisture content and aw relationship yields to important information of controlling the ripening, drying and storage operations as well as understanding of the water state within a cheese matrix.

  6. Graphical representation for isothermal kinetics of non-equilibrium grain-boundary segregation

    SciTech Connect

    Wang Kai; Xu Tingdong; Song Shenhua; Shao Chong

    2011-06-15

    A model of non-equilibrium grain-boundary segregation of solute is expressed with graphs for the isothermal aging at various temperatures after quenching from a solution temperature. It is found from the graphical representations that when the samples are aged for a certain time at various temperatures there is a maximum value in the segregation concentration at a certain temperature. The aging time is equal or close to the critical time of non-equilibrium segregation corresponding to this temperature. This finding is experimentally confirmed with sulfur in an Ni-base superalloy with the aid of Auger electron spectroscopy. As an application of the new finding, a mechanism for intermediate temperature embrittlement of alloys is suggested and identified experimentally with tension tests of the superalloy. - Research Highlights: {yields} A peak of solute segregation emerges at a temperature when aging for a certain time at various temperatures after quenching. {yields} The aging time is equal or close to the critical time of segregation at this temperature. {yields} This finding is experimentally confirmed in an Ni-Cr-Fe superalloy. {yields} A mechanism for intermediate temperature embrittlement of alloys is proposed.

  7. Interaction of removal Ethidium Bromide with Carbon Nanotube: Equilibrium and Isotherm studies

    PubMed Central

    2014-01-01

    Drinking water resources may be contaminated with Ethidium Bromide (EtBr) which is commonly used in molecular biology laboratories for DNA identification in electrophoresis. Carbon nanotubes are expected to play an important role in sensing, pollution treatment and separation techniques. In this study adsorption of Ethidium Bromide on single-walled carbon nanotubes (SWCNTs) and carboxylate group functionalized single-walled carbon nanotube (SWCNT-COOH) surfaces have been investigated by UV–vis spectrophotometer. The effect of contact time, initial concentration and temperature were investigated. The adsorbents exhibits high efficiency for EtBr adsorption and equilibrium can be achieved in 6 and 3 min for SWCNTs and SWCNT-COOH, respectively. The effect of temperature on adsorption of EtBr by toward adsorbents shows the process in this research has been endothermic. The results showed that the equilibrium data were well described by the Langmuir isotherm model, with a maximum adsorption capacity of 0.770 and 0.830 mg/g for SWCNTs and SWCNT-COOH, respectively. The adsorption of EtBr on SWCNT-COOH is more than SWCNTs surfaces. A comparison of kinetic models was evaluated for the pseudo first-order, pseudo second-order models. Pseudo second-order was found to agree well with the experimental data. PMID:24401790

  8. Biosorption of food dyes onto Spirulina platensis nanoparticles: equilibrium isotherm and thermodynamic analysis.

    PubMed

    Dotto, G L; Lima, E C; Pinto, L A A

    2012-01-01

    The biosorption of food dyes FD&C red no. 40 and acid blue 9 onto Spirulina platensis nanoparticles was studied at different conditions of pH and temperature. Four isotherm models were used to evaluate the biosorption equilibrium and the thermodynamic parameters were estimated. Infra red analysis (FT-IR) and energy dispersive X-ray spectroscopy (EDS) were used to verify the biosorption behavior. The maximum biosorption capacities of FD&C red no. 40 and acid blue 9 were found at pH 4 and 298 K, and the values were 468.7 mg g(-1) and 1619.4 mg g(-1), respectively. The Sips model was more adequate to fit the equilibrium experimental data (R2>0.99 and ARE<5%). Thermodynamic study showed that the biosorption was exothermic, spontaneous and favorable. FT-IR and EDS analysis suggested that at pH 4 and 298 K, the biosorption of both dyes onto nanoparticles occurred by chemisorption.

  9. Solute transport with equilibrium aqueous complexation and either sorption or ion exchange: Simulation methodology and applications

    USGS Publications Warehouse

    Lewis, F.M.; Voss, C.I.; Rubin, J.

    1987-01-01

    Methodologies that account for specific types of chemical reactions in the simulation of solute transport can be developed so they are compatible with solution algorithms employed in existing transport codes. This enables the simulation of reactive transport in complex multidimensional flow regimes, and provides a means for existing codes to account for some of the fundamental chemical processes that occur among transported solutes. Two equilibrium-controlled reaction systems demonstrate a methodology for accommodating chemical interaction into models of solute transport. One system involves the sorption of a given chemical species, as well as two aqueous complexations in which the sorbing species is a participant. The other reaction set involves binary ion exchange coupled with aqueous complexation involving one of the exchanging species. The methodology accommodates these reaction systems through the addition of nonlinear terms to the transport equations for the sorbing species. Example simulation results show (1) the effect equilibrium chemical parameters have on the spatial distributions of concentration for complexing solutes; (2) that an interrelationship exists between mechanical dispersion and the various reaction processes; (3) that dispersive parameters of the porous media cannot be determined from reactive concentration distributions unless the reaction is accounted for or the influence of the reaction is negligible; (4) how the concentration of a chemical species may be significantly affected by its participation in an aqueous complex with a second species which also sorbs; and (5) that these coupled chemical processes influencing reactive transport can be demonstrated in two-dimensional flow regimes. ?? 1987.

  10. Moisture adsorption isotherms and glass transition temperature of pectin.

    PubMed

    Basu, Santanu; Shivhare, U S; Muley, S

    2013-06-01

    The moisture adsorption isotherms of low methoxyl pectin were determined at 30-70°C and water activity ranging from 0.11 to 0.94. The moisture adsorption isotherms revealed that the equilibrium moisture content increased with water activity. Increase in temperature, in general, resulted in decreased equilibrium moisture content. However in some cases, equilibrium moisture content values increased with temperature at higher water activities. Selected sorption models (GAB, Halsey, Henderson, Oswin, modified Oswin) were tested for describing the adsorption isotherms. Parameters of each sorption models were determined by nonlinear regression analysis. Oswin model gave the best fit for pectin sorption behaviour. Isosteric heat of sorption decreased with increase in moisture content and varied between 14.607 and 0.552 kJ/mol. Glass transition temperature decreased with increase in moisture content of pectin. PMID:24425957

  11. Impact of kerogen heterogeneity on sorption of organic pollutants. 2. Sorption equilibria

    SciTech Connect

    Yang, C.; Yu, Z.Q.; Xiao, B.H.; Huang, W.L.; Fu, J.M.; Dang, Z.

    2009-08-15

    Phenanthrene and naphthalene sorption isotherms were measured for three different series of kerogen materials using completely mixed batch reactors. Sorption isotherms were nonlinear for each sorbate-sorbent system, and the Freundlich isotherm equation fit the sorption data well. The Freundlich isotherm linearity parameter n ranged from 0.192 to 0.729 for phenanthrene and from 0.389 to 0.731 for naphthalene. The n values correlated linearly with rigidity and aromaticity of the kerogen matrix, but the single-point, organic carbon-normalized distribution coefficients varied dramatically among the tested sorbents. A dual-mode sorption equation consisting of a linear partitioning domain and a Langmuir adsorption domain adequately quantified the overall sorption equilibrium for each sorbent-sorbate system. Both models fit the data well, with r{sup 2} values of 0.965 to 0.996 for the Freundlich model and 0.963 to 0.997 for the dual-mode model for the phenanthrene sorption isotherms. The dual-mode model fitting results showed that as the rigidity and aromaticity of the kerogen matrix increased, the contribution of the linear partitioning domain to the overall sorption equilibrium decreased, whereas the contribution of the Langmuir adsorption domain increased. The present study suggested that kerogen materials found in soils and sediments should not be treated as a single, unified, carbonaceous sorbent phase.

  12. Batch sorption dynamics and equilibrium for the removal of lead ions from aqueous phase using activated carbon developed from coffee residue activated with zinc chloride.

    PubMed

    Boudrahem, F; Aissani-Benissad, F; Aït-Amar, H

    2009-07-01

    Lignocellulosic materials are good precursors for the production of activated carbon. In this work, coffee residue has been used as raw material in the preparation of powder activated carbon by the method of chemical activation with zinc chloride for the sorption of Pb(II) from dilute aqueous solutions. The influence of impregnation ratio (ZnCl2/coffee residue) on the physical and chemical properties of the prepared carbons was studied in order to optimize this parameter. The optimum experimental condition for preparing predominantly microporous activated carbons with high pore surface area (890 m2/g) and micropore volume (0.772 cm3/g) is an impregnation ratio of 100%. The developed activated carbon shows substantial capability to sorb lead(II) ions from aqueous solutions and for relative impregnation ratios of 75 and 100%, the maximum uptake is practically the same. Thus, 75% represents the optimal impregnation ratio. Batch experiments were conducted to study the effects of the main parameters such as contact time, initial concentration of Pb(II), solution pH, ionic strength and temperature. The maximum uptake of lead(II) at 25 degrees C was about 63 mg/g of adsorbent at pH 5.8, initial Pb(II) concentration of 10 mg/L, agitation speed of 200 rpm and ionic strength of 0.005 M. The kinetic data were fitted to the models of pseudo-first order and pseudo-second order, and follow closely the pseudo-second order model. Equilibrium sorption isotherms of Pb(II) were analyzed by the Langmuir, Freundlich and Temkin isotherm models. The Freundlich model gives a better fit than the others. Results from this study suggest that activated carbon produced from coffee residue is an effective adsorbent for the removal of lead from aqueous solutions and that ZnCl2 is a suitable activating agent for the preparation of high-porosity carbons. PMID:19447542

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

    PubMed

    Zhang, Ying; Bi, Erping

    2012-01-01

    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.

  14. Batch removal of malachite green from aqueous solutions by adsorption on oil palm trunk fibre: equilibrium isotherms and kinetic studies.

    PubMed

    Hameed, B H; El-Khaiary, M I

    2008-06-15

    Oil palm trunk fibre (OPTF)--an agricultural solid waste--was used as low-cost adsorbent to remove malachite green (MG) from aqueous solutions. The operating variables studied were contact time, initial dye concentration, and solution pH. Equilibrium adsorption data were analyzed by three isotherms, namely the Freundlich isotherm, the Langmuir isotherm, and the multilayer adsorption isotherm. The best fit to the data was obtained with the multilayer adsorption. The monolayer adsorption capacity of OPTF was found to be 149.35 mg/g at 30 degrees C. Adsorption kinetic data were modeled using the Lagergren pseudo-first-order, Ho's pseudo-second-order and Elovich models. It was found that the Lagergren's model could be used for the prediction of the system's kinetics. The overall rate of dye uptake was found to be controlled by external mass transfer at the beginning of adsorption, then for initial MG concentrations of 25, 50, 100, 150, and 300 mg/L the rate-control changed to intraparticle diffusion at a later stage, but for initial MG concentrations 200 and 250 mg/L no evidence was found of intraparticle diffusion at any period of adsorption. It was found that with increasing the initial concentration of MG, the pore-diffusion coefficient increased while the film-diffusion coefficient decreased. PMID:18022316

  15. Moisture sorption isotherms and glass transition temperature of elecampe (Inula helenium L.) and burdock (Arctium lappa L.) roots at 25°C.

    PubMed

    Cervenka, L; Kubínová, J; Juszczak, L; Witczak, M

    2012-02-01

    Sorption isotherms of elecampe (Inula helenium L.) and burdock (Arctium lappa L.) root samples were obtained at 25 °C. Elecampe exhibited hysteresis loop in the range of 0.35-0.90 a(w) , whereas burdock roots showed significant differences between adsorption and desorption isotherms from 0.65 to 0.80 a(w) . Blahovec-Yanniotis was considered to give the best fit over the whole range of a(w) tested. Various parameters describing the properties of sorbed water derived from GAB, Henderson and Blahovec-Yanniotis models have been discussed. Differential scanning calorimetric method was used to measure the glass transition temperature (T (g)) of root samples in relation to water activity. The safe moisture content was determined in 12.01 and 14.96 g/100 g d. b. for burdock and elecampe root samples at 25 °C, respectively. Combining the T (g) line with sorption isotherm in one plot, it was found that the glass transition temperature concept overestimated the temperature stability for both root samples.

  16. [Sorption behaviors of BDE-28 on natural soils].

    PubMed

    Liu, Wen-Xin; Ling, Xi; Chen, Jiang-Lin; Li, Wei-Bo; Dou, Han; Tao, Shu

    2011-03-01

    The sorption kinetics and isotherms of BDE-28 on three natural soils with different soil organic matter fractions (f(oc)) were investigated. The results indicated that a two (fast and slow)-compartment first-order model was more appropriate for describing the sorption kinetic data, compared to a one-compartment first-order model, especially in the initial sorption stage within 25 h. The fast sorption was predominant during the whole sorption process from beginning to the apparent sorption equilibrium; while the contribution of the slow sorption to the total sorption amount gradually increased and then achieved a plateau at 49 h or 55 h. The approaching time to the individual sorption capacity for the fast sorption was much shorter than that for the slow sorption. The contribution of the fast sorption to the increase in the total sorption amount of BDE-28 was prevailing at the beginning of sorption process from 2.5 h to 4.5 h; whereas the fraction of the slow sorption became primary at the subsequent stage of sorption process. The fitting results by the Dubinin-Ashtakhov (DA) model were comparable with those by the Freundlich model in the range of apparent equilibrium concentration studied. As for the Freundlich model, the nonlinear exponent (n) values of BDE-28 for the two samples with lower f(oc) (0.72%) or higher f(oc) (7.90%) approached to 1.0 (1.03 +/- 0.05 and 1.00 +/- 0.05, respectively), suggesting the linear sorption characteristics in the studied range of apparent equilibrium concentrations of BDE-28; while the nonlinear behavior of BDE-28 for the left sample with medium f(oc) (4.42%) was indicated by its n value less than 1.0 (0.89 +/- 0.04). PMID:21634174

  17. Use of ramping and equilibrium water vapor sorption methods to determine the critical relative humidity at which the glassy to rubbery transition occurs in polydextrose.

    PubMed

    Li, Qingruisi E; Schmidt, Shelly J

    2011-01-01

    Recent research has demonstrated that the critical relative humidity (RHc) values, obtained using automatic water vapor sorption instruments, can be used to detect the glassy to rubbery transition. However, reported time dependency of these RHc values suggests that additional research be carried out using equilibrium water vapor sorption methods. Thus, the objectives of this study were to: (1) determine the RHc for amorphous polydextrose at various temperatures using both instrumental (Dynamic Vapor Sorption [DVS] ramping and equilibrium) and saturated salt slurry methods, and (2) compare the RHc values obtained via sorption methods to the glass transition temperature (Tg) values obtained via differential scanning calorimetry (DSC). When plotted as a "glass curve" on a state diagram, the RHc values (plotted as a function of temperature) were found to be similar to the Tg values (plotted as a function of relative humidity). Of the 3 sorption methods employed, at 25 °C, the saturated salt slurry exhibited the lowest RHc value (34.3%), followed by the DVS equilibrium method (41.7%), and the DVS ramping method (49.9%). The RHc DVS equilibrium method was closest to the calculated DSC Tg onset RHc value (41.6% at 25 °C). These water sorption methods show promise as practical tools for predicting the quality and stability attributes of amorphous materials by being able to routinely determine the location of the glassy to rubbery transition. Future research applying these sorption methods to more complex amorphous food systems is suggested. Practical Application: Despite its extreme usefulness, the Tg, a key element of the Food Polymer Science approach, remains a challenging parameter to routinely measure in amorphous food materials. Recent research has demonstrated that the RHc values can be used to detect the glassy to rubbery transition. However, reported time dependency of these RHc values suggests that additional research be carried out using equilibrium water vapor

  18. Sorption of untreated and humic acid coated silver nanoparticles to environmental and model surfaces

    NASA Astrophysics Data System (ADS)

    Abraham, Priya M.; Baumann, Thomas; Schaumann, Gabriele E.

    2014-05-01

    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

  19. Water absorption of freeze-dried meat at different water activities: a multianalytical approach using sorption isotherm, differential scanning calorimetry, and nuclear magnetic resonance.

    PubMed

    Venturi, Luca; Rocculi, Pietro; Cavani, Claudio; Placucci, Giuseppe; Dalla Rosa, Marco; Cremonini, Mauro A

    2007-12-26

    Hydration of freeze-dried chicken breast meat was followed in the water activity range of aw=0.12-0.99 by a multianalytical approach comprising of sorption isotherm, differential scanning calorimetry (DSC), and nuclear magnetic resonance (NMR). The amount of frozen water and the shape of the T2-relaxogram were evaluated at each water content by DSC and NMR, respectively. Data revealed an agreement between sorption isotherm and DSC experiments about the onset of bulk water (aw=0.83-0.86), and NMR detected mobile water starting at aw=0.75. The origin of the short-transverse relaxation time part of the meat NMR signal was also reinvestigated through deuteration experiments and proposed to arise from protons belonging to plasticized matrix structures. It is proved both by D2O experiments and by gravimetry that the extra protons not contributing to the water content in the NMR experiments are about 6.4% of the total proton NMR CPMG signal of meat.

  20. Water absorption of freeze-dried meat at different water activities: a multianalytical approach using sorption isotherm, differential scanning calorimetry, and nuclear magnetic resonance.

    PubMed

    Venturi, Luca; Rocculi, Pietro; Cavani, Claudio; Placucci, Giuseppe; Dalla Rosa, Marco; Cremonini, Mauro A

    2007-12-26

    Hydration of freeze-dried chicken breast meat was followed in the water activity range of aw=0.12-0.99 by a multianalytical approach comprising of sorption isotherm, differential scanning calorimetry (DSC), and nuclear magnetic resonance (NMR). The amount of frozen water and the shape of the T2-relaxogram were evaluated at each water content by DSC and NMR, respectively. Data revealed an agreement between sorption isotherm and DSC experiments about the onset of bulk water (aw=0.83-0.86), and NMR detected mobile water starting at aw=0.75. The origin of the short-transverse relaxation time part of the meat NMR signal was also reinvestigated through deuteration experiments and proposed to arise from protons belonging to plasticized matrix structures. It is proved both by D2O experiments and by gravimetry that the extra protons not contributing to the water content in the NMR experiments are about 6.4% of the total proton NMR CPMG signal of meat. PMID:18047277

  1. Transport and sorption of volatile organic compounds and water vapor in porous media

    SciTech Connect

    Lin, Tsair-Fuh

    1995-07-01

    To gain insight on the controlling mechanisms for VOC transport in porous media, the relations among sorbent properties, sorption equilibrium and intraparticle diffusion processes were studied at the level of individual sorbent particles and laboratory columns for soil and activated carbon systems. Transport and sorption of VOCs and water vapor were first elucidated within individual dry soil mineral grains. Soil properties, sorption capacity, and sorption rates were measured for 3 test soils; results suggest that the soil grains are porous, while the sorption isotherms are nonlinear and adsorption-desorption rates are slow and asymmetric. An intragranular pore diffusion model coupled with the nonlinear Freundlich isotherm was developed to describe the sorption kinetic curves. Transport of benzene and water vapor within peat was studied; partitioning and sorption kinetics were determined with an electrobalance. A dual diffusion model was developed. Transport of benzene in dry and moist soil columns was studied, followed by gaseous transport and sorption in activated carbon. The pore diffusion model provides good fits to sorption kinetics for VOCs to soil and VOC to granular activated carbon and activated carbon fibers. Results of this research indicate that: Intraparticle diffusion along with a nonlinea sorption isotherm are responsible for the slow, asymmetric sorption-desorption. Diffusion models are able to describe results for soil and activated carbon systems; when combined with mass transfer equations, they predict column breakthrough curves for several systems. Although the conditions are simplified, the mechanisms should provide insight on complex systems involving transport and sorption of vapors in porous media.

  2. Equilibrium studies of copper ion adsorption onto palm kernel fibre.

    PubMed

    Ofomaja, Augustine E

    2010-07-01

    The equilibrium sorption of copper ions from aqueous solution using a new adsorbent, palm kernel fibre, has been studied. Palm kernel fibre is obtained in large amounts as a waste product of palm oil production. Batch equilibrium studies were carried out and system variables such as solution pH, sorbent dose, and sorption temperature were varied. The equilibrium sorption data was then analyzed using the Langmuir, Freundlich, Dubinin-Radushkevich (D-R) and Temkin isotherms. The fit of these isotherm models to the equilibrium sorption data was determined, using the linear coefficient of determination, r(2), and the non-linear Chi-square, chi(2) error analysis. The results revealed that sorption was pH dependent and increased with increasing solution pH above the pH(PZC) of the palm kernel fibre with an optimum dose of 10g/dm(3). The equilibrium data were found to fit the Langmuir isotherm model best, with a monolayer capacity of 3.17 x 10(-4)mol/g at 339K. The sorption equilibrium constant, K(a), increased with increasing temperature, indicating that bond strength between sorbate and sorbent increased with temperature and sorption was endothermic. This was confirmed by the increase in the values of the Temkin isotherm constant, B(1), with increasing temperature. The Dubinin-Radushkevich (D-R) isotherm parameter, free energy, E, was in the range of 15.7-16.7kJ/mol suggesting that the sorption mechanism was ion exchange. Desorption studies showed that a high percentage of the copper was desorbed from the adsorbent using acid solutions (HCl, HNO(3) and CH(3)COOH) and the desorption percentage increased with acid concentration. The thermodynamics of the copper ions/palm kernel fibre system indicate that the process is spontaneous and endothermic. PMID:20346574

  3. Equilibrium studies of copper ion adsorption onto palm kernel fibre.

    PubMed

    Ofomaja, Augustine E

    2010-07-01

    The equilibrium sorption of copper ions from aqueous solution using a new adsorbent, palm kernel fibre, has been studied. Palm kernel fibre is obtained in large amounts as a waste product of palm oil production. Batch equilibrium studies were carried out and system variables such as solution pH, sorbent dose, and sorption temperature were varied. The equilibrium sorption data was then analyzed using the Langmuir, Freundlich, Dubinin-Radushkevich (D-R) and Temkin isotherms. The fit of these isotherm models to the equilibrium sorption data was determined, using the linear coefficient of determination, r(2), and the non-linear Chi-square, chi(2) error analysis. The results revealed that sorption was pH dependent and increased with increasing solution pH above the pH(PZC) of the palm kernel fibre with an optimum dose of 10g/dm(3). The equilibrium data were found to fit the Langmuir isotherm model best, with a monolayer capacity of 3.17 x 10(-4)mol/g at 339K. The sorption equilibrium constant, K(a), increased with increasing temperature, indicating that bond strength between sorbate and sorbent increased with temperature and sorption was endothermic. This was confirmed by the increase in the values of the Temkin isotherm constant, B(1), with increasing temperature. The Dubinin-Radushkevich (D-R) isotherm parameter, free energy, E, was in the range of 15.7-16.7kJ/mol suggesting that the sorption mechanism was ion exchange. Desorption studies showed that a high percentage of the copper was desorbed from the adsorbent using acid solutions (HCl, HNO(3) and CH(3)COOH) and the desorption percentage increased with acid concentration. The thermodynamics of the copper ions/palm kernel fibre system indicate that the process is spontaneous and endothermic.

  4. Sorption of microconstituents onto primary sludge.

    PubMed

    Ying, Zhu; Droste, R L

    2015-01-01

    The presence of microconstituents (MCs) in the environment has become an emerging concern to scientists and engineers. Sorption is one of the important removal mechanisms for MCs in wastewater treatment plants (WWTPs) since there is significant sludge production. The purpose of this study is to explore sorption kinetics and isotherms of MCs onto primary sludge. Three MCs, bisphenol-A (BPA), 17-α-ethinylestradiol (EE2) and triclosan (TCS), were chosen for this study. They are hydrophobic and have low vapor pressure, which makes sorption a potential removal mechanism. Both sorption kinetics and isotherm experiments were conducted using primary sludge collected from a local municipal WWTP. The time to equilibrium was around 7 h for all chosen MCs. A pseudo second-order rate model was better at describing the sorption rate than a pseudo first-order rate model. Linear sorption isotherm models were found to fit the experimental data, and the solid-liquid partitioning coefficients for BPA, EE2 and TCS were 81, 728 and 6,407 L/kg. PMID:26287837

  5. The determination of equilibrium constants, DeltaG, DeltaH and DeltaS for vapour interaction with a pharmaceutical drug, using gravimetric vapour sorption.

    PubMed

    Willson, Richard J; Beezer, Anthony E

    2003-06-01

    The application of gravimetric vapour sorption (GVS) to the characterisation of pharmaceutical drugs is often restricted to the study of gross behaviour such as a measure of hygroscopicity. Although useful in early development of a drug substance, for example, in salt selection screening exercises, such types of analysis may not contribute to a fundamental understanding of the properties of the material. This paper reports a new methodology for GVS experimentation that will allow specific sorption parameters to be calculated; equilibrium constant (K), van't Hoff enthalpy change (DeltaH(v)), Gibbs free energy for sorption (DeltaG) and the entropy change for sorption (DeltaS). Unlike other reports of such type of analysis that require the application of a specific model, this method is model free. The analysis does require that over the narrow temperature range of the study DeltaH(v) is constant and there is no change in interaction mechanism.

  6. Using a Gel Probe Equilibrium Sampler to Measure Arsenic Mobilization and Sorption Gradients in Haiwee Reservoir Sediments

    NASA Astrophysics Data System (ADS)

    Campbell, K. M.; Root, R.; O'Day, P. A.; Hering, J. G.

    2005-12-01

    Sediment deposited at Haiwee Reservoir (Olancha, CA, USA) is enriched in arsenic and iron as a result of a large-scale water treatment process to remove naturally occurring arsenic from the Los Angeles Aqueduct (LAA). A poorly crystalline iron oxyhydroxide floc is precipitated in the aqueduct to adsorb dissolved arsenic, removing it from the water column. The iron/arsenic floc then settles in the inlet channel into Haiwee Reservoir. Previous studies at this site indicate that a fraction of the total arsenic is released into the sediment porewaters at depth, most likely as a result of bacterial reductive dissolution of the iron oxyhydroxide. A gel probe equilibrium sampler was used to measure gradients in porewater concentrations and arsenic sorption chemistry in situ in Haiwee Reservoir sediments. The gels were composed of an inert polyacrylamide matrix (92% water). They were inserted into a ladder-like Plexiglas holder, and covered with a 0.45μm membrane filter. The probe was allowed to equilibrate for 24 hours with the sediment porewaters. Two types of gels were deployed simultaneously in the probe: undoped (clear) gels to measure porewater composition, and hydrous ferric oxide (HFO)-doped gels to determine arsenic sorption behavior as a function of porewater composition. Upon removal from the sediments, the gels were re-equilibrated in acid, and a suite of metals and metalloids were measured using ICP-MS. In addition, arsenic speciation was measured in the clear gels using LC-ICP-MS. X-ray absorption spectroscopy was used to determine the oxidation state of arsenic sorbed onto HFO in the doped gels as well as arsenic in sediment cores collected when the gel probes were deployed. Arsenic in the sediment cores was reduced from As(V) to As(III) by a depth of 10 cm, but mixed oxidation states were observed in the porewaters as arsenic was mobilized into the dissolved phase, typically at depths greater than 10 cm. Dissolved arsenic was correlated to iron in the

  7. Magnetohydrostatic equilibrium structure and mass of filamentary isothermal cloud threaded by lateral magnetic field

    SciTech Connect

    Tomisaka, Kohji

    2014-04-10

    Herschel observations have recently revealed that interstellar molecular clouds consist of many filaments. Polarization observations in optical and infrared wavelengths indicate that the magnetic field often runs perpendicular to the filament. In this article, we study the magnetohydrostatic configuration of isothermal gas in which the thermal pressure and the Lorentz force are balanced against the self-gravity, and the magnetic field is globally perpendicular to the axis of the filament. The model is controlled by three parameters: center-to-surface density ratio (ρ {sub c}/ρ {sub s}), plasma β of surrounding interstellar gas (β{sub 0}), and the radius of the hypothetical parent cloud normalized by the scale-height (R{sub 0}{sup ′}), although there remains freedom in how the mass is distributed against the magnetic flux (mass loading). In the case where R{sub 0}{sup ′} is small enough, the magnetic field plays a role in confining the gas. However, the magnetic field generally has the effect of supporting the cloud. There is a maximum line-mass (mass per unit length) above which the cloud is not supported against gravity. Compared with the maximum line-mass of a nonmagnetized cloud (2c{sub s}{sup 2}/G, where c{sub s} and G represent, respectively, the isothermal sound speed and the gravitational constant), that of the magnetized filament is larger than the nonmagnetized one. The maximum line-mass is numerically obtained as λ{sub max}≃0.24Φ{sub cl}/G{sup 1/2}+1.66c{sub s}{sup 2}/G, where Φ{sub cl} represents one half of the magnetic flux threading the filament per unit length. The maximum mass of the filamentary cloud is shown to be significantly affected by the magnetic field when the magnetic flux per unit length exceeds Φ{sub cl} ≳ 3 pc μG (c{sub s} /190 m s{sup –1}){sup 2}.

  8. Groundwater transport modeling with nonlinear sorption and intraparticle diffusion

    NASA Astrophysics Data System (ADS)

    Singh, Anshuman; Allen-King, Richelle M.; Rabideau, Alan J.

    2014-08-01

    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.

  9. Optimization, equilibrium, kinetic, thermodynamic and desorption studies on the sorption of Cu(II) from an aqueous solution using marine green algae: Halimeda gracilis.

    PubMed

    Jayakumar, R; Rajasimman, M; Karthikeyan, C

    2015-11-01

    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.

  10. Application of green seaweed biomass for MoVI sorption from contaminated waters. Kinetic, thermodynamic and continuous sorption studies.

    PubMed

    Bertoni, Fernando A; Medeot, Anabela C; González, Juan C; Sala, Luis F; Bellú, Sebastián E

    2015-05-15

    Spongomorpha pacifica biomass was evaluated as a new sorbent for Mo(VI) removal from aqueous solution. The maximum sorption capacity was found to be 1.28×10(6)±1×10(4) mg kg(-1) at 20°C and pH 2.0. Sorption kinetics and equilibrium studies followed pseudo-first order and Langmuir adsorption isotherm models, respectively. FTIR analysis revealed that carboxyl and hydroxyl groups were mainly responsible for the sorption of Mo(VI). SEM images show that morphological changes occur at the biomass surface after Mo(VI) sorption. Activation parameters and mean free energies obtained with Dubinin-Radushkevich isotherm model demonstrate that the mechanism of sorption process was chemical sorption. Thermodynamic parameters demonstrate that the sorption process was spontaneous, endothermic and the driven force was entropic. The isosteric heat of sorption decreases with surface loading, indicating that S. pacifica has an energetically non-homogeneous surface. Experimental breakthrough curves were simulated by Thomas and modified dose-response models. The bed depth service time (BDST) model was employed to scale-up the continuous sorption experiments. The critical bed depth, Z0 was determined to be 1.7 cm. S.pacifica biomass showed to be a good sorbent for Mo(VI) and it can be used in continuous treatment of effluent polluted with molybdate ions.

  11. Application of green seaweed biomass for MoVI sorption from contaminated waters. Kinetic, thermodynamic and continuous sorption studies.

    PubMed

    Bertoni, Fernando A; Medeot, Anabela C; González, Juan C; Sala, Luis F; Bellú, Sebastián E

    2015-05-15

    Spongomorpha pacifica biomass was evaluated as a new sorbent for Mo(VI) removal from aqueous solution. The maximum sorption capacity was found to be 1.28×10(6)±1×10(4) mg kg(-1) at 20°C and pH 2.0. Sorption kinetics and equilibrium studies followed pseudo-first order and Langmuir adsorption isotherm models, respectively. FTIR analysis revealed that carboxyl and hydroxyl groups were mainly responsible for the sorption of Mo(VI). SEM images show that morphological changes occur at the biomass surface after Mo(VI) sorption. Activation parameters and mean free energies obtained with Dubinin-Radushkevich isotherm model demonstrate that the mechanism of sorption process was chemical sorption. Thermodynamic parameters demonstrate that the sorption process was spontaneous, endothermic and the driven force was entropic. The isosteric heat of sorption decreases with surface loading, indicating that S. pacifica has an energetically non-homogeneous surface. Experimental breakthrough curves were simulated by Thomas and modified dose-response models. The bed depth service time (BDST) model was employed to scale-up the continuous sorption experiments. The critical bed depth, Z0 was determined to be 1.7 cm. S.pacifica biomass showed to be a good sorbent for Mo(VI) and it can be used in continuous treatment of effluent polluted with molybdate ions. PMID:25660712

  12. Kinetics of cadmium ion sorption on ion exchange and chelating resins

    SciTech Connect

    Bilba, D.; Bilba, N.; Albu, M.

    1999-11-01

    Cadmium sorption from aqueous solutions on sulfonic (C-150) and iminodiacetic (S-930) Purolite macroporous resins was investigated. The influence of operating variables such as initial pH, Cd(II) concentration, time and temperature on the equilibrium parameters was measured. The ion preference and sorption ability of resins, i.e., binding constant (b) and saturation capacity (x{sub m}), derived from sorption isotherm, depend on the functional group structure. The Cd(II) uptake is only particle diffusion controlled. The kinetic parameters, i.e., t{sub 1/2} values for 50% attainment of equilibrium sorption, rate constant ({bar K}) and diffusion coefficient ({bar D}) are higher on the sulfonic resin. The moving boundary particle diffusion model fits the entire ion sorption process on chelating resin, but only the initial sorption on the sulfonic resin, confirming the difference in chemistry between chelation and ion exchange.

  13. EPSP synthase: binding studies using isothermal titration microcalorimetry and equilibrium dialysis and their implications for ligand recognition and kinetic mechanism.

    PubMed

    Ream, J E; Yuen, H K; Frazier, R B; Sikorski, J A

    1992-06-23

    Isothermal titration calorimetry measurements are reported which give important new binding constant (Kd) information for various substrate and inhibitor complexes of Escherichia coli EPSP synthase (EPSPS). The validity of this technique was first verified by determining Kd's for the known binary complex with the substrate, shikimate 3-phosphate (S3P), as well as the herbicidal ternary complex with S3P and glyphosate (EPSPS.S3P.glyphosate). The observed Kd's agreed very well with those from previous independently determined kinetic and fluorescence binding measurements. Further applications unequivocally demonstrate for the first time a fairly tight interaction between phosphoenolpyruvate (PEP) and free enzyme (Kd = 390 microM) as well as a correspondingly weak affinity for glyphosate (Kd = 12 mM) alone with enzyme. The formation of the EPSPS.PEP binary complex was independently corroborated using equilibrium dialysis. These results strongly suggest that S3P synergizes glyphosate binding much more effectively than it does PEP binding. These observations add important new evidence to support the hypothesis that glyphosate acts as a transition-state analogue of PEP. However, the formation of a catalytically productive PEP binary complex is inconsistent with the previously reported compulsory binding order process required for catalysis and has led to new studies which completely revise the overall EPSPS kinetic mechanism. A previously postulated ternary complex between S3P and inorganic phosphate (EPSPS.S3P.Pi, Kd = 4 mM) was also detected for the first time. Quantitative binding enthalpies and entropies were also determined for each ligand complex from the microcalorimetry data. These values demonstrate a clear difference in thermodynamic parameters for recognition at the S3P site versus those observed for the PEP, Pi, and glyphosate sites.

  14. Sorption behavior of fluoride ions from aqueous solutions by hydroxyapatite.

    PubMed

    Jiménez-Reyes, M; Solache-Ríos, M

    2010-08-15

    The effects of pH, contact time, fluoride-ion concentration, and the dose of sorbent on the sorption of fluoride ions by hydroxyapatite were studied. Equilibrium was reached in 16 h of contact time and the maximum sorption of fluoride ions was in the pH(eq) range between 5 and 7.3. The highest efficiency in the sorption system was determined by using 0.01 g of hydroxyapatite and 25 mL of solution. The pseudo-second order model described the kinetic sorption processes, and the Freundlich model, the sorption isotherm process. These results indicated that the mechanism was chemisorption on a heterogeneous material. Fluoride ions were partially desorbed using an alkaline solution.

  15. Moisture sorption characteristics of freeze dried whey-grape beverage mix.

    PubMed

    Varghese, K Shiby; Radhakrishna, K; Bawa, A S

    2014-10-01

    Moisture sorption isotherms of freeze dried whey-grape beverage powder were determined at 20, 30 and 40 °C. A gravimetric static method was used under 0.11-0.85 water activity range and the sorption isotherms were found to be Type II. Various mathematical models were fitted to experimental data and it was found that Peleg model suits best in describing the equilibrium moisture content-equilibrium relative humidity relationships of instant whey-grape beverage mix over the range of temperatures studied. The net isosteric heat of sorption varied between 5.22 and 1.12 KJ/mol at moisture level varying between 1 and 9 % db. At moisture content below 1 % (db) the isosteric heat of sorption increased sharply for freeze dried whey-grape beverage powder and value of 49.08 KJ/mol was estimated. PMID:25328219

  16. Sorption isotherms, thermodynamic properties and glass transition temperature of mucilage extracted from chia seeds (Salvia hispanica L.).

    PubMed

    Velázquez-Gutiérrez, Sandra Karina; Figueira, Ana Cristina; Rodríguez-Huezo, María Eva; Román-Guerrero, Angélica; Carrillo-Navas, Hector; Pérez-Alonso, César

    2015-05-01

    Freeze-dried chia mucilage adsorption isotherms were determined at 25, 35 and 40°C and fitted with the Guggenheim-Anderson-de Boer model. The integral thermodynamic properties (enthalpy and entropy) were estimated with the Clausius-Clapeyron equation. Pore radius of the mucilage, calculated with the Kelvin equation, varied from 0.87 to 6.44 nm in the temperature range studied. The point of maximum stability (minimum integral entropy) ranged between 7.56 and 7.63kg H2O per 100 kg of dry solids (d.s.) (water activity of 0.34-0.53). Enthalpy-entropy compensation for the mucilage showed two isokinetic temperatures: (i) one occurring at low moisture contents (0-7.56 kg H2O per 100 kg d.s.), controlled by changes in water entropy; and (ii) another happening in the moisture interval of 7.56-24 kg H2O per 100 kg d.s. and was enthalpy driven. The glass transition temperature Tg of the mucilage fluctuated between 42.93 and 57.93°C.

  17. Sorption isotherms, thermodynamic properties and glass transition temperature of mucilage extracted from chia seeds (Salvia hispanica L.).

    PubMed

    Velázquez-Gutiérrez, Sandra Karina; Figueira, Ana Cristina; Rodríguez-Huezo, María Eva; Román-Guerrero, Angélica; Carrillo-Navas, Hector; Pérez-Alonso, César

    2015-05-01

    Freeze-dried chia mucilage adsorption isotherms were determined at 25, 35 and 40°C and fitted with the Guggenheim-Anderson-de Boer model. The integral thermodynamic properties (enthalpy and entropy) were estimated with the Clausius-Clapeyron equation. Pore radius of the mucilage, calculated with the Kelvin equation, varied from 0.87 to 6.44 nm in the temperature range studied. The point of maximum stability (minimum integral entropy) ranged between 7.56 and 7.63kg H2O per 100 kg of dry solids (d.s.) (water activity of 0.34-0.53). Enthalpy-entropy compensation for the mucilage showed two isokinetic temperatures: (i) one occurring at low moisture contents (0-7.56 kg H2O per 100 kg d.s.), controlled by changes in water entropy; and (ii) another happening in the moisture interval of 7.56-24 kg H2O per 100 kg d.s. and was enthalpy driven. The glass transition temperature Tg of the mucilage fluctuated between 42.93 and 57.93°C. PMID:25659716

  18. Mechanistic understanding and performance of biosorption of metal ions by grapefruit peel using FTIR spectroscopy, kinetics and adsorption isotherms modeling, alkali and alkaline metal displacement and EDX analysis

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The performance and mechanism of the sorptive removal of Ni2+ and Zn2+ from aqueous solution using grapefruit peel (GFP) as a new sorbent was investigated. The sorption process was fast, equilibrium was established in 60 min. The equilibrium process was described well by the Langmuir isotherm model,...

  19. Sorption of tylosin on clay minerals.

    PubMed

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

    2013-11-01

    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.

  20. Equilibrium isotherm and kinetic studies for the simultaneous removal of phenol and cyanide by use of S. odorifera (MTCC 5700) immobilized on coconut shell activated carbon

    NASA Astrophysics Data System (ADS)

    Singh, Neetu; Balomajumder, Chandrajit

    2016-09-01

    In this study, simultaneous removal of phenol and cyanide by a microorganism S. odorifera (MTCC 5700) immobilized onto coconut shell activated carbon surface (CSAC) was studied in batch reactor from mono and binary component aqueous solution. Activated carbon was derived from coconut shell by chemical activation method. Ferric chloride (Fecl3), used as surface modification agents was applied to biomass. Optimum biosorption conditions were obtained as a function of biosorbent dosage, pH, temperature, contact time and initial phenol and cyanide concentration. To define the equilibrium isotherms, experimental data were analyzed by five mono component isotherm and six binary component isotherm models. The higher uptake capacity of phenol and cyanide onto CSAC biosorbent surface was 450.02 and 2.58 mg/g, respectively. Nonlinear regression analysis was used for determining the best fit model on the basis of error functions and also for calculating the parameters involved in kinetic and isotherm models. The kinetic study results revealed that Fractal-like mixed first second order model and Brouser-Weron-Sototlongo models for phenol and cyanide were capable to offer accurate explanation of biosorption kinetic. According to the experimental data results, CSAC with immobilization of bacterium S. odorifera (MTCC 5700) seems to be an alternative and effective biosorbent for the elimination of phenol and cyanide from binary component aqueous solution.

  1. Sorption of carbamazepine from water by magnetic molecularly imprinted polymers based on chitosan-Fe₃O₄.

    PubMed

    Zhang, Ya-Lei; Zhang, Juan; Dai, Chao-Meng; Zhou, Xue-Fei; Liu, Shu-Guang

    2013-09-12

    A novel magnetic-molecularly imprinted polymer (MMIP) based on chitosan-Fe₃O₄ has been synthesized for fast separation of carbamazepine (CBZ) from water. During polymerization, the modified chitosan-Fe₃O₄ was used not only as supporter but also as functional monomer. The properties of obtained MMIP were characterized by scanning electron and transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectra, thermo-gravimetric analysis and so on. The sorption equilibrium data was well described by Freundlich isotherm model and the increase in the temperature generated an increase in the sorption amount, indicating endothermic nature of adsorption process. Sorption kinetics followed the pseudo-second-order model. The feasibility of selective sorption of CBZ from real water by the MMIP was analyzed by using spiked real water samples. The result showed that the sorption capacity of MMIP has no obvious decrease in different water samples whereas there was obvious decline in the sorption amount of the MNIP.

  2. Sorption behavior of dibutyl phthalate and dioctyl phthalate by aged refuse.

    PubMed

    Fang, Cheng-ran; Long, Yu-yang; Shen, Dong-sheng

    2014-06-01

    Sorption is a fundamental process controlling the transformation, fate, degradation, and biological activity of hydrophobic organic contaminants in the environment. We investigated the kinetics, isotherms, and potential mechanisms for the sorption of two phthalic acid esters (PAEs), dibutyl phthalate (DBP) and dioctyl phthalate (DOP), on aged refuse. A two-compartment first-order model performed better than a one-compartment first-order model in describing the kinetic sorption of PAEs, with a fast sorption process dominating. Both the Freundlich and Dubinin-Astakhov (DA) models fit the sorption isotherms of DBP and DOP, with the DA model being of a better fit over the range of apparent equilibrium concentrations. The values of the fitting parameters (n, b, E) of the PAEs suggest nonlinear sorption characteristics. Higher predicted partition coefficient values and saturated sorption capacity existed in refuse containing larger quantities of organic matter. The sorption capacity of DOP was significantly higher than that of DBP. PAE sorption was dependent on liquid phase pH. Desorption hysteresis occurred in PAE desorption experiments, especially for the long-chain DOP. PAEs may therefore be a potential environmental risk in landfill.

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

    SciTech Connect

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

    2004-01-30

    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

  4. Sorption equilibria of CO2/CH4 mixture on activated carbon in presence of water.

    PubMed

    Sun, Yan; Xue, Quanmin; Zhou, Yaping; Zhou, Li

    2008-06-01

    The sorption isotherms of CO2 + CH4 mixtures on an activated carbon were collected in the presence of water at a temperature suitable for hydrate formation. The equilibrium composition of both phases was determined. The initial concentration of CO2 in mixtures was set at 33, 38 and 42%, and the total pressure was up to 10 MPa. CO2 hydrates were firstly formed following the increase of total pressure, and CO2 dominates the sorbed phase composition. CO2 concentration in the sorbed phase begins to decrease when the partial pressure of methane allows for the formation of methane hydrates. Competition for hydrate cavities was observed between CO2 and CH4 as reflected in the isotherm shape and phase composition at equilibrium. The formation pressure of hydrates is lower for mixtures than for pure gases, and the highest sorption capacity of each gas decreased in the mixture sorption either.

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

    PubMed

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

    2008-05-15

    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

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

    PubMed

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

    2008-05-15

    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

  7. Sorption of aromatic organic pollutants to grasses from water

    USGS Publications Warehouse

    Barbour, J.P.; Smith, J.A.; Chiou, C.T.

    2005-01-01

    The influence of plant lipids on the equilibrium sorption of three aromatic solutes from water was studied. The plant-water sorption isotherms of benzene, 1,2-dichlorobenzene, and phenanthrene were measured over a large range of solute concentrations using sealed vessels containing water, dried plant material, and solute. The plant materials studied include the shoots of annual rye, tall fescue, red fescue, and spinach as well as the roots of annual rye. Seven out of eight sorption isotherms were linear with no evidence of competitive effects between the solutes. For a given plant type, the sorption coefficient increased with decreasing solute water solubility. For a given solute, sorption increased with increasing plant lipid content. The estimated lipid-water partition coefficients of individual solutes were found to be significantly greater than the corresponding octanol-water partition coefficients. This indicates that plant lipids are a more effective partition solvent than octanol for the studied aromatic compounds. As expected, the solute lipid-water partition coefficients were log-linearly related to the respective water solubilities. For the compounds studied, partitioning into the lipids is believed to be the primary sorption mechanism. ?? 2005 American Chemical Society.

  8. Sorption kinetics and equilibrium of the herbicide diuron to carbon nanotubes or soot in absence and presence of algae.

    PubMed

    Schwab, Fabienne; Camenzuli, Louise; Knauer, Katja; Nowack, Bernd; Magrez, Arnaud; Sigg, Laura; Bucheli, Thomas D

    2014-09-01

    Carbon nanotubes (CNT) are strong sorbents for organic micropollutants, but changing environmental conditions may alter the distribution and bioavailability of the sorbed substances. Therefore, we investigated the effect of green algae (Chlorella vulgaris) on sorption of a model pollutant (diuron, synonyms: 3-(3,4-Dichlorophenyl)-1,1-dimethylurea, DCMU) to CNT (multi-walled purified, industrial grade, pristine, and oxidized; reference material: Diesel soot). In absence of algae, diuron sorption to CNT was fast, strong, and nonlinear (Freundlich coefficients: 10(5.79)-10(6.24) μg/kgCNT·(μg/L)(-n) and 0.62-0.70 for KF and n, respectively). Adding algae to equilibrated diuron-CNT mixtures led to 15-20% (median) diuron re-dissolution. The relatively high amorphous carbon content slowed down ad-/desorption to/from the high energy sorption sites for both industrial grade CNT and soot. The results suggest that diuron binds readily, but - particularly in presence of algae - partially reversibly to CNT, which is of relevance for environmental exposure and risk assessment. PMID:24949853

  9. Thermodynamics of Cadmium Sorption on Different Soils of West Bengal, India

    PubMed Central

    Paul, Ranjit Kumar; Das, D. K.; Boruah, Romesh K.; Sonar, Indira

    2014-01-01

    A sorption study was conducted on different soils collected from five agroecological zones of West Bengal, India, to understand the soil environmental behavior and fate of cadmium. For this purpose batch adsorption experiments were carried out at the native soil pH and at three different temperatures (25°C, 35°C, and 45°C). The adsorption data fitted by a linear least squares technique to the different sorption isotherms. Most data obtained give the good fit to both Freundlich and modified Langmuir isotherms, but they are not consistent with the linear Langmuir adsorption model. Thermodynamic parameters, namely, thermodynamics equilibrium constant at a particular temperature T  (KT0), Gibbs free energy at a particular temperature T  (ΔGT0), and change of enthalpy (ΔH0) and change of entropy at temperature T  (ΔST0), were also determined by applying sorption value and concentrations of Cd in equilibrium solution within the temperature range. The thermodynamic parameters revealed that Cd sorption increases as the values of KT0, ΔGT0, ΔH0, and ΔST0 were increased on reaction temperatures. The spontaneous sorption reaction can be concluded due to high values of ΔGT0. The positive values of ΔH0 indicated that the Cd sorption is an endothermic one. Under these present conditions, the soil and its components possibly supply a number of sites having different adsorption energies for cadmium sorption. PMID:24683322

  10. [Sorption Characteristics of Phenanthrene and 1, 1-Dichloroethene onto Reed Straw Biochar in Aquatic Solutions].

    PubMed

    Wu, Qing-wen; Meng, Liang; Zhang, Zhi-hao; Luo, Qi-shi; Yang, Jie

    2016-02-15

    The purpose of this study was to investigate the sorption characteristics of phenanthrene (PHE) and 1, 1-dichloroethene (1, 1-DCE) onto reed straw biochar at 500 degrees C in aquatic solutions. The sorption mechanisms and effects of solution pH and biochar mass on sorption intensity were discussed. The results showed that the time required to reach sorption equilibrium was 60 min and 480 min for PHE and 1, 1-DCE, respectively, with maximum removal rates of 81, 87% and 90.18%. The sorption kinetics of both PHE and 1, 1-DCE fitted the pseudo-second-order model well, but the pseudo-second-order reaction rate of PHE was higher than that of 1, 1-DCE. Furthermore, the sorption processes were controlled by both membrane diffusion and intra-particle diffusion, and the latter was found to be the rate-controlling step. Sorption isotherms of the two organic pollutants fitted well with the Freundlich equation, and the sorption affinity of 1, 1-DCE onto biochar was greater than that of PHE. The total sorption mechanism of biochar was the combination of partition and adsorption, and dominated by adsorption. The adsorption capacity of 1, 1-DCE was greater than that of PHE, but its partition capacity was much smaller, indicating that pollutants' molecular volume and relative polarity would mainly affect the total sorption. Analysis of Fourier transform infrared spectroscopy (FTIR) demonstrated that oxygen- and hydrogen-containing functional groups and pi--pi interaction were important for PHE and 1, 1-DCE sorption onto biochar. The solution pH value had no significant effect on the sorption intensity of PHE and 1, 1-DCE, however, with biochar mass increasing from 5 mg to 50 mg, the equilibrium sorption amount of PHE and 1, 1-DCE decreased by 6.78 times and 2.18 times, and the removal rate increased by 20.21% and 15.78%, respectively. PMID:27363160

  11. A Gel Probe Equilibrium Sampler for Measuring Arsenic Porewater Profiles And Sorption Gradients in Sediments: Ii. Field Application to Haiwee Reservoir Sediment

    SciTech Connect

    Campbell, K.M.; Root, R.; O'Day, P.A.; Hering, J.G.

    2009-05-12

    Arsenic (As) geochemistry and sorption behavior were measured in As- and iron (Fe)-rich sediments of Haiwee Reservoir by deploying undoped (clear) polyacrylamide gels and hydrous ferric oxide (HFO)-doped gels in a gel probe equilibrium sampler, which is a novel technique for directly measuring the effects of porewater composition on As adsorption to Fe oxides phases in situ. Arsenic is deposited at the sediment surface as As(V) and is reduced to As(III) in the upper layers of the sediment (0-8 cm), but the reduction of As(V) does not cause mobilization into the porewater. Dissolved As and Fe concentrations increased at depth in the sediment column driven by the reductive dissolution of amorphous Fe(III) oxyhydroxides and conversion to a mixed Fe(II, III) green rust-type phase. Adsorption of As and phosphorous (P) onto HFO-doped gels was inhibited at intermediate depths (10-20 cm), possibly due to dissolved organic or inorganic carbon, indicating that dissolved As concentrations were at least partially controlled by porewater composition rather than surface site availability. In sediments that had been recently exposed to air, the region of sorption inhibition was not observed, suggesting that prior exposure to air affected the extent of reductive dissolution, porewater chemistry, and As adsorption behavior. Arsenic adsorption onto the HFO-doped gels increased at depths >20 cm, and the extent of adsorption was most likely controlled by the competitive effects of dissolved phosphate. Sediment As adsorption capacity appeared to be controlled by changes in porewater composition and competitive effects at shallower depths, and by reductive dissolution and availability of sorption sites at greater burial depths.

  12. A gel probe equilibrium sampler for measuring arsenic porewater profiles and sorption gradients in sediments: II. Field application to Haiwee reservoir sediment

    USGS Publications Warehouse

    Campbell, K.M.; Root, R.; O'Day, P. A.; Hering, J.G.

    2008-01-01

    Arsenic (As) geochemistry and sorption behavior were measured in As- and iron (Fe)-rich sediments of Haiwee Reservoir by deploying undoped (clear) polyacrylamide gels and hydrous ferric oxide (HFO)-doped gels in a gel probe equilibrium sampler, which is a novel technique for directly measuring the effects of porewater composition on As adsorption to Fe oxides phases in situ. Arsenic is deposited at the sediment surface as As(V) and is reduced to As(III) in the upper layers of the sediment (0-8 cm), but the reduction of As(V) does not cause mobilization into the porewater. Dissolved As and Fe concentrations increased at depth in the sediment column driven by the reductive dissolution of amorphous Fe(III) oxyhydroxides and conversion to a mixed Fe(II, III) green rust-type phase. Adsorption of As and phosphorous (P) onto HFO-doped gels was inhibited at intermediate depths (10-20 cm), possibly due to dissolved organic or inorganic carbon, indicating that dissolved As concentrations were at least partially controlled by porewater composition rather than surface site availability. In sediments that had been recently exposed to air, the region of sorption inhibition was not observed, suggesting that prior exposure to air affected the extent of reductive dissolution, porewater chemistry, and As adsorption behavior. Arsenic adsorption onto the HFO-doped gels increased at depths >20 cm, and the extent of adsorption was most likely controlled by the competitive effects of dissolved phosphate. Sediment As adsorption capacity appeared to be controlled by changes in porewater composition and competitive effects at shallower depths, and by reductive dissolution and availability of sorption sites at greater burial depths. ?? 2008 American Chemical Society.

  13. Rapid Adsorption of Copper(II) and Lead(II) by Rice Straw/Fe3O4 Nanocomposite: Optimization, Equilibrium Isotherms, and Adsorption Kinetics Study

    PubMed Central

    Khandanlou, Roshanak; Ahmad, Mansor B.; Fard Masoumi, Hamid Reza; Shameli, Kamyar; Basri, Mahiran; Kalantari, Katayoon

    2015-01-01

    Rice straw/magnetic nanocomposites (RS/Fe3O4-NCs) were prepared via co-precipitation method for removal of Pb(II) and Cu(II) from aqueous solutions. Response surface methodology (RSM) was utilized to find the optimum conditions for removal of ions. The effects of three independent variables including initial ion concentration, removal time, and adsorbent dosage were investigated on the maximum adsorption of Pb (II) and Cu (II). The optimum conditions for the adsorption of Pb(II) and Cu(II) were obtained (100 and 60 mg/L) of initial ion concentration, (41.96 and 59.35 s) of removal time and 0.13 g of adsorbent for both ions, respectively. The maximum removal efficiencies of Pb(II) and Cu(II) were obtained 96.25% and 75.54%, respectively. In the equilibrium isotherm study, the adsorption data fitted well with the Langmuir isotherm model. The adsorption kinetics was best depicted by the pseudo-second order model. Desorption experiments showed adsorbent can be reused successfully for three adsorption-desorption cycles. PMID:25815470

  14. Rapid adsorption of copper(II) and lead(II) by rice straw/Fe₃O₄ nanocomposite: optimization, equilibrium isotherms, and adsorption kinetics study.

    PubMed

    Khandanlou, Roshanak; Ahmad, Mansor B; Fard Masoumi, Hamid Reza; Shameli, Kamyar; Basri, Mahiran; Kalantari, Katayoon

    2015-01-01

    Rice straw/magnetic nanocomposites (RS/Fe3O4-NCs) were prepared via co-precipitation method for removal of Pb(II) and Cu(II) from aqueous solutions. Response surface methodology (RSM) was utilized to find the optimum conditions for removal of ions. The effects of three independent variables including initial ion concentration, removal time, and adsorbent dosage were investigated on the maximum adsorption of Pb (II) and Cu (II). The optimum conditions for the adsorption of Pb(II) and Cu(II) were obtained (100 and 60 mg/L) of initial ion concentration, (41.96 and 59.35 s) of removal time and 0.13 g of adsorbent for both ions, respectively. The maximum removal efficiencies of Pb(II) and Cu(II) were obtained 96.25% and 75.54%, respectively. In the equilibrium isotherm study, the adsorption data fitted well with the Langmuir isotherm model. The adsorption kinetics was best depicted by the pseudo-second order model. Desorption experiments showed adsorbent can be reused successfully for three adsorption-desorption cycles.

  15. Statistical Thermodynamics of an "Open" Hard Sphere System on the Equilibrium Fluid Isotherm: Study of Properties of the Freezing Transition Without Direct Involvement of the Equilibrium Solid Phase

    NASA Astrophysics Data System (ADS)

    Reiss, Howard; Manzanares, José A.

    2016-09-01

    Using several theoretical toolsldots (i) the nucleation theorem, (ii) an equivalent cavity, (iii) the reversible work of adding a cavity to an open hard sphere system, and (iv) the theory of "stability"... the authors estimated the density at which the hard sphere freezing transition occurs. No direct involvement of the equilibrium solid phase is involved. The reduced density \\uppi a^3ρ _f/6 (where a is the hard sphere diameter and ρ _f is the actual density at which freezing occurs) is found to be 0.4937 while the value obtained by computer simulation is 0.494. The agreement is good, but the new method still contains some approximation. However, the approximation is based on the idea that at a density just below ρ _f the fluid adopts a distorted structure resembling the solid, but different enough so that long-range order vanishes. Initial loss of stability may not be involved in every fluid-solid transition, but it may be an early step in the hard sphere and related systems.

  16. Equilibrium, Thermodynamics, and Kinetic Sorption Studies for the Removal of Coomassie Brilliant Blue on Wheat Bran as a Low-Cost Adsorbent

    PubMed Central

    Ata, Sadia; Imran Din, Muhammad; Rasool, Atta; Qasim, Imran; Ul Mohsin, Ijaz

    2012-01-01

    The sorption studies of coomassie brilliant blue (CBB) from aqueous solution have been carried out on wheat bran (WB). Coomassie brilliant blue on wheat bran was used to study the adsorption behavior under various parameters such as pH, dosage amount, and contact time. It was observed that under optimized conditions up to 95.70% dye could be removed from solution onto WB. Langmuir and Freundlich adsorption isotherms were used to elaborate the results. Freundlich model was found to be fitted well and favored multilayer adsorption. The Freundlich constants n and KF were determined as 0.53 and 2.5 × 10−4. Thermodynamic parameters such as ΔG, ΔH, and ΔS studied were taking into account, showed spontaneous and favorable reaction for coomassie brilliant blue on wheat bran. The maximum adsorption capacity qm was found to be 6.410 mg/g. The investigations show that non treated WB is a low-cost adsorbent for the removal of dyes from textile industry effluents. PMID:22567559

  17. Least-Squares Analysis of Phosphorus Soil Sorption Data with Weighting from Variance Function Estimation: A Statistical Case for the Freundlich Isotherm

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Phosphorus sorption data for soil of the Pembroke classification are recorded at high replication — 10 experiments at each of 7 initial concentrations — for characterizing the data error structure through variance function estimation. The results permit the assignment of reliable weights for the su...

  18. Sorption of sulfisoxazole onto soil--an insight into different influencing factors.

    PubMed

    Maszkowska, Joanna; Białk-Bielińska, Anna; Mioduszewska, Katarzyna; Wagil, Marta; Kumirska, Jolanta; Stepnowski, Piotr

    2015-08-01

    Although sulfonamides (SAs) are among the most commonly used veterinary drugs and their presence in the environment is well documented, knowledge of their fate and behavior in the soil environment is still limited, especially for sulfisoxazole (SSX) which is characterized by the lowest (among other SAs) pK a value associated with acid-base equilibrium of sulfonamide group. Thus, this work was focused on determining the sorption potential of SSX onto natural soils differing in physicochemical properties. All the results were modeled using linear, Freundlich, Langmuir, Dubinin-Radushkevich, and Temkin sorption isotherms. The established sorption coefficients (K(d)) for SSX were quite low (from 0.27 to 0.95 L kg(-1)), which indicated that this substance is highly mobile and has the potential to run off into surface waters and/or infiltrate ground water. The sorption data of SSX is well fitted to the Freundlich isotherm model (R(2) > 0.968). Moreover, we assessed the sorption mechanism of these compounds in the edaphic environment with respect to organic matter (OM) content, pH, and ionic strength. To clarify the current state of knowledge, these factors were examined much more thoroughly than in previous investigations concerning other SAs. The wide range of ionic strength examined showed positive correlation of this factor and sorption of SAs. The results also yielded new insight into dependency of sorption of SAs on organic matter content in soil. PMID:25893618

  19. [Surface Property and Sorption Characteristics of Phosphorus onto Surface Sediments in Sanggou Bay].

    PubMed

    Zhu, Jia-mei; Cao, Xiao-yan; Liu, Su-mei; Wang, Li-sha; Yang, Gui-peng; Ge, Cheng-feng; Lu, Min

    2016-02-15

    Kinetic curves and isotherms were investigated to study the sorption mechanism of phosphorus onto the sediments of Sanggou Bay, together with the surface charge properties of sediments and the forms of phosphorus studied. The results showed that the sorption including a fast process and a slow one, and could be described by a two-compartment first order equation. The thermodynamic isotherms were well fitted with a modified Langmuir equation. The maximum adsorption capacity was larger in summer than in spring, and the smaller particle size was favorable to the sorption. The maximum adsorption capacities (Qm) were 0.0471-0.1230 mg x g(-1), and the zero equilibrium phosphorus concentration (EPC0) of the sediments ranged from 0.0596 mg x L(-1) to 0.1927 mg x L(-1), which indicated that the sediments from Sanggou Bay were sources of phosphorus. Inorganic phosphorus (IP) was the main form of total phosphorus (TP). The contents of exchangeable or loosely absorbed P and Fe-bound P increased significantly in the samples after sorption. The sorption process involved physical sorption and chemical sorption, with the former being the predominant.

  20. Silica coated magnetic particles using microwave synthesis for removal of dyes from natural water samples: Synthesis, characterization, equilibrium, isotherm and kinetics studies

    NASA Astrophysics Data System (ADS)

    Ahmed, Salwa A.; Soliman, Ezzat M.

    2013-11-01

    Monitoring pollutants in water samples is a challenge to analysts. So, the removal of Napthol blue black (NBB) and Erichrome blue black R (EBBR) from aqueous solutions was investigated using magnetic chelated silica particles. Magnetic solids are widely used in detection and analytical systems because of the performance advantages they offer compared to similar solids that lack magnetic properties. In this context, a fast, simple and clean method for modification of magnetic particles (Fe3O4) with silica gel was developed using microwave technique to introduce silica gel coated magnetic particles (SG-MPs) sorbent. The magnetic sorbent was characterized by the FT-IR, X-ray diffraction (XRD), and scan electron microscope (SEM) analyses. The effects of pH, time, weight of sorbent and initial concentration of dye were evaluated. It was interesting to find from results that SG-MPs exhibits high percentage extraction of the studied dyes (100% for NBB and 98.75% for EBBR) from aqueous solutions. The Freundlich isotherm with r2 = 0.973 and 0.962 and Langmuir isotherms with r2 = 0.993 and 0.988 for NBB and EBBR, respectively were used to describe adsorption equilibrium. Also, adsorption kinetic experiments have been carried out and the data have been well fitted by a pseudo-second-order equation r2 = 1.0 for NBB and 0.999 for EBBR. The prepared sorbent with rapid adsorption rate and separation convenience was applied for removal of NBB and EBBR pollutants from natural water samples with good precision (RSD% = 0.05-0.3%).

  1. Non-equilibrium zinc uptake onto compost particles from synthetic stormwater.

    PubMed

    Al-Mashaqbeh, Othman; McLaughlan, Robert G

    2012-11-01

    Zinc uptake onto different particle size compost was evaluated in batch and column studies using a synthetic stormwater to quantify sorption capacity and kinetics. The results showed that the pseudo equilibrium time for uptake increased from 2h to greater than 120h as the particle size of compost increased from 75μm to 6.75mm. This was due to intra-particle diffusion becoming a rate limiting process as the particle size increased. Column effluent data with 1.18mm particles could be fitted by Freundlich isotherm while that from the 4.75mm particles and a mixed particle size columns showed rate limited sorption with tailing and could not be adequately fitted using an equilibrium based isotherm. The results have established rate-limited sorption in amended filtration media due to larger particles under these flow conditions. This needs to be accounted for in the design of these filtration media and during performance modelling.

  2. Searching the best equilibrium moisture equation for lettuce seeds using measures of curvature and bias.

    PubMed

    Bortolotti, Carolina T; Barrozo, Marcos A S

    2013-11-01

    In the present work, we performed a discrimination analysis of the nonlinear equations used to describe sorption isotherms of the lettuce seeds. The equilibrium data were obtained by the static method using saturated salt solutions. The best model to describe the equilibrium moisture of lettuce seeds was selected using measures of curvature and bias. The obtained results showed that the Copace equation was the best model in terms of nonsignificance for bias and nonlinearity measures. PMID:24804051

  3. Searching the best equilibrium moisture equation for lettuce seeds using measures of curvature and bias

    PubMed Central

    Bortolotti, Carolina T; Barrozo, Marcos A S

    2013-01-01

    In the present work, we performed a discrimination analysis of the nonlinear equations used to describe sorption isotherms of the lettuce seeds. The equilibrium data were obtained by the static method using saturated salt solutions. The best model to describe the equilibrium moisture of lettuce seeds was selected using measures of curvature and bias. The obtained results showed that the Copace equation was the best model in terms of nonsignificance for bias and nonlinearity measures. PMID:24804051

  4. Competitive sorption between 17alpha-ethinyl estradiol and bisphenol A/4-n-nonylphenol by soils.

    PubMed

    Li, Jianzhong; Jiang, Lu; Xiang, Xi; Xu, Shuang; Wen, Rou; Liu, Xiang

    2013-06-01

    The sorption of 17alpha-ethinyl estradiol (EE2), bisphenol A (BPA), and 4-n-nonylphenol (NP) in single systems and the sorption of EE2 with different initial aqueous concentrations of BPA or NP were examined using three soils. Results showed that all sorption isotherms were nonlinear and fit the Freundlich model. The degree of nonlinearity was in the order BPA (0.537-0.686) > EE2 (0.705-0.858) > NP (0.875-0.0.951) in single systems. The isotherm linearity index of EE2 sorption calculated by the Freundlich model for Loam, Silt Loam and Silt increased from 0.758, 0.705 and 0.858, to 0.889, 0.910 and 0.969, respectively, when BPA concentration increased from 0 to 1000 microg/L, but the effect of NP was comparably minimal. Additionally, EE2 significantly suppressed the sorption of BPA, but insignificantly suppressed that of NP. These findings can be attributed to the difference of sorption affinity of EE2, NP and BPA on the hard carbon (e.g., black carbon) of soil organic matter that dominated the sorption in the low equilibrium aqueous concentration range of endocrine-disrupting chemicals (EDCs). Competitive sorption among EDCs presents new challenges for predicting the transport and fate of EDCs under the influence of co-solutes.

  5. Sorption of biodegradation end products of nonylphenol polyethoxylates onto activated sludge.

    PubMed

    Hung, Nguyen Viet; Tateda, Masafumi; Ike, Michihiko; Fujita, Masanori; Tsunoi, Shinji; Tanaka, Minoru

    2004-01-01

    Nonylphenol(NP), nonylphenoxy acetic acid (NP1EC), nonylphenol monoethoxy acetic acid (NP2EC), nonylphenol monoethoxylate (NP1EO) and nonylphenol diethoxylate (NP2EO) are biodegradation end products (BEPs) of nonionic surfactant nonylphenolpolyethoxylates (NPnEO). In this research, sorption of these compounds onto model activated sludge was characterized. Sorption equilibrium experiments showed that NP, NP1EO and NP2EO reached equilibrium in about 12 h, while equilibrium of NP1EC and NP2EC were reached earlier, in about 4 h. In sorption isotherm experiments, obtained equilibrium data at 28 degrees C fitted well to Freundlich sorption model for all investigated compounds. For NP1EC, in addition to Freundlich, equilibrium data also fitted well to Langmuir model. Linear sorption model was also tried, and equilibrium data of all NP, NP1EO, NP2EO and NP2EC except NP1EC fitted well to this model. Calculated Freundlich coefficient (K(F)) and linear sorption coefficient (K(D)) showed that sorption capacity of the investigated compounds were in order NP > NP2EO > NP1EO > NP1EC approximately NP2EC. For NP, NP1EO and NP2EO, high values of calculated K(F) and K(D) indicated an easy uptake of these compounds from aqueous phase onto activated sludge. Whereas, NP1EC and NP2EC with low values of K(F) and K(D) absorbed weakly to activated sludge and tended to preferably remain in aqueous phase. PMID:15495957

  6. Enhanced molar sorption ratio for naphthalene through the impregnation of surfactant into chitosan hydrogel beads.

    PubMed

    Chatterjee, Sudipta; Lee, Dae S; Lee, Min W; Woo, Seung H

    2010-06-01

    Surfactants in their impregnated forms in chitosan beads (CBs) were used for sorption of naphthalene (NAP) from aqueous solutions. Three different surfactants, Triton X-100 (TX100), cetyltrimethyl ammonium bromide (CTAB) and sodium dodecyl sulfate (SDS), were selected for this study. The results showed that surfactant-impregnated CS beads (SICBs) in the form of a separate phase surfactant were very effective for NAP sorption. The calculated molar sorption ratio (MSR(B) mol NAP/mol surfactant) of the surfactant impregnated into SICBs was much greater than the intrinsic molar solubilization ratio (MSR) in liquid phase. The high MSR(B) value could be explained by favorable configurations of surfactants in beads, such as micelles in sorbed form. The equilibrium isotherm did not follow Langmuir or Freundlich models, but followed Chapman sigmoidal equation, indicating co-operative sorption of solutes. Using SICBs as a separate phase surfactant may be a valuable tool for remediation of groundwater contaminated with hydrophobic organic compounds.

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

    PubMed

    Çelekli, Abuzer; Bozkurt, Hüseyin

    2013-07-01

    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.

  8. Characterization of U(VI) Sorption-Desorption Processes and Model Upscaling

    SciTech Connect

    Bai, Jing; Dong, Wenming; Ball, William P.

    2006-10-12

    (VI) diffusion in silt/clay layers. Batch isotherm experiments were first used to confirm sorption isotherms under the intended test conditions and diffusion cell experiments were then conducted to explore the diffusion hypotheses. Important new information was obtained about the role of aqueous calcium and solid calcium carbonate in controlling sorption equilibrium with Hanford sediments. The retarded interparticle diffusion model with local sorption equilibrium was shown to very successfully simulate diffusion at high aqueous concentration of U(VI). By contrast, however, diffusion data obtained at low concentration suggested nonequilibrium of sorption even at diffusion time scales. Such nonequilibrium effects at low concentration are likely to be the result of sorption retarded intraparticle diffusion, and strong U(VI) sorption in the low concentration range.

  9. [Sorption behavior of Triton X-100 on loess and affecting factors].

    PubMed

    Zhong, Jin-Kui; Zhao, Bao-Wei; Zhu, Kun; Qian, Xiao-Long; Zhang, Jie-Xi

    2013-03-01

    Batch experiments involving soil-aqueous systems were conducted to determine sorption of Triton X-100 onto natural loess as a function of equilibrium time, Triton X-100 concentration, ionic strength, and pH value. The results showed that the equilibration time for sorption of Triton X-100 onto loess was about 30 min. The sorption kinetics of Triton X-100 fitted well to the pseudo-first-order kinetic model and the corresponding parameters Q(e), k1, and r2 were 3.041 mg x g(-1), 0.102 min(-1), and 0.9934, respectively. Sorption isotherm was found to be distinctly nonlinear. The Sips model provided the best fitting to the experimental data among the four isothermal models tested. Q(max) and r2 of Sips model were 3.202 mg x g(-1) and 0.998 7, respectively. It was found that the ionic strength and the pH of the solution had a significant influence on the sorption of Triton X-100 onto loess. The amount of Triton X-100 sorbed onto the loess increased significantly with increasing concentration of NaCl. Sorption of Triton X-100 onto loess was influenced greatly by pH, the amount of Triton X-100 sorbed decreased as the pH increased.

  10. Sorption and dissipation of testosterone, estrogens, and their primary transformation products in soils and sediment.

    PubMed

    Lee, Linda S; Strock, Troy J; Sarmah, Ajit K; Rao, P Suresh C

    2003-09-15

    Concern over the potential negative ecological effects of steroid hormones from human- and animal-derived wastes has resulted in an increased interest regarding the mobility and persistence of these compounds in the environment. Batch experiments were conducted to examine the simultaneous sorption and dissipation of three reproductive hormones (testosterone, 17beta-estradiol, and 17alpha-ethynyl estradiol) in four midwestern U.S. soils and one freshwater sediment. Sorption isotherms were generated by measuring aqueous concentrations and by extracting the sorbed parent chemical or transformation products (e.g., estrone, androstenedione). Apparent sorption equilibrium is reached within a few hours. Measured sorption isotherms for the three parent chemicals and their principal transformation products were generally linear. Average organic carbon normalized sorption coefficients (K(oc)) resulted in standard deviations of less than 0.2 log units and were consistent with reported aqueous solubilites and octanol-water partition coefficients, indicating hydrophobic partitioning as the dominant sorption mechanism. Large log K(oc) values (approximately 3-4) suggest that leaching from soils will be limited, runoff of soil- and land-applied biosolids are the most likely inputs into surface waters, and that a significant fraction of these compounds will be associated with sediments. Half-lives for hormone dissipation in the aerobic soil and sediment slurries estimated assuming pseudo first-order processes ranged from a few hours to a few days with testosterone having the shortest half-life.

  11. Determination of soil–water sorption coefficients of volatile methylsiloxanes

    PubMed Central

    Kozerski, Gary E; Xu, Shihe; Miller, Julie; Durham, Jeremy

    2014-01-01

    The sorption behaviors of 4 cyclic and linear volatile methyl siloxane (VMS) compounds between water and organic matter in 3 United Kingdom soils were studied by a batch equilibrium method using13C-enriched sorbates. Sorption and desorption kinetics and isotherms were determined for octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5), octamethyltrisiloxane (L3), and decamethyltetrasiloxane (L4). Concentrations of [13C]-VMS in the soil and aqueous phases were measured directly by extraction and gas chromatography–mass spectrometry techniques. All VMS compounds were sorbed rapidly, reaching constant distributions in all soils by 24 h. Desorption kinetics were very rapid, with reattainment of equilibrium within 1 h. In the main, linear isotherms were observed for aqueous concentrations at or below 4% of the solubility limits. The average sorption organic carbon partition coefficient (log KOC) values across soils were 4.23 for D4, 5.17 for D5, 4.32 for L3, and 5.13 for L4, with standard deviations of 0.09 to 0.34. Desorption KOC values were systematically greater by 0.1 log units to 0.3 log units. The linear isotherms and low variation in KOC values across soils suggested partitioning-dominated sorption of the VMS. Compared with traditional hydrophobic organic compounds, KOC values for the VMS compounds were significantly lower than expected on the basis of their octanol–water partition coefficients. A linear free energy relationship analysis showed that these differences could be rationalized quantitatively in terms of the inherent characteristics of the VMS compounds, combined with the differences in solvation properties of organic matter and octanol. Environ Toxicol Chem 2014; 33:1937–1945. PMID:24862578

  12. Sorption-desorption and biosorption of bisphenol A, triclosan, and 17α-ethinylestradiol to sewage sludge.

    PubMed

    Banihashemi, Bahman; Droste, Ronald L

    2014-07-15

    To better understand the fate of microconstituents (MCs) in an activated sludge (AS) system, sorption, biosorption, and desorption studies were investigated at μg/L range for 17α-ethinylestradiol (EE2), bisphenol A (BPA), and triclosan (TCS). Batch experiments with activated and deactivated sludge originating from continuous flow porous pot reactors operating at solid retention times (SRTs) of 5, 10, and 15 days were conducted in order to investigate the sorption kinetics and distinguish physicochemical sorption and biosorption. The effect of SRT and the biomass concentration on sorption kinetics were also studied. Selected MCs showed high sorption affinity to the non-viable biomass during the first 30 min of the experiment, which was gradually reduced until equilibrium was reached. Desorption results showed two distinct stages, a very rapid desorption within 20 min followed by a slow desorption stage. Biosorption study indicated that the soluble concentrations of target compounds decreased rapidly for selected MCs similar to the sorption study; however, the soluble and solid phase concentrations continued to decrease slowly during the length of the experiment which indicates the possible biodegradation of these compounds in both phases. Finally, mathematical models were applied to describe the sorption mechanism and Freundlich sorption isotherms with values of 1/n close to 1 were found to best fit the results which demonstrate that all tested concentrations result on the linear part of the Freundlich isotherm. Calculation of the Freundlich constant, KF and distribution coefficient, Kd exhibited the greater tendency of EE2 and TCS for sorption, compared to BPA. The results of this study indicated that the SRT had a clear effect on the sorption kinetics where the highest sorption rate constant was achieved for a SRT of 10 days for all three target substances. This could be due to change of the morphology of the biomass from reactors operating at different SRTs

  13. Analysis of moisture desorption isotherms of eggplant (Solanum melongena).

    PubMed

    Moreira, R; Chenlo, F; Torres, M D; Vallejo, N

    2010-10-01

    Sorption isotherms of eggplant were determined employing, as experimental technique, a static gravimetric method, using saturated salt solutions to achieve the equilibrium. The experiments were carried out at different temperatures (20, 35, 50 and 65 °C). The sorption isotherms can be classified, according to Brunauer's classification, as type II or III depending on temperature. Equilibrium moisture content data were correlated by two models usually applied to foodstuffs (Brunauer--Emmet--Teller (BET) and Halsey). BET model was employed to determine monolayer moisture content (0.121 kg/kg d.b.). Halsey model was selected by the goodness of fitting. Experimental data were analyzed by a thermodynamic approach to obtain some properties as net isosteric heat, equilibrium heat and differential and net integral entropy. The differential enthalpy and entropy decreased with increasing moisture content and satisfied the compensation theory. The net integral enthalpy and entropy showed maximum values (≈31 kJ/mol and ≈88 J/mol.K) at 0.093 (kg/kg d.b.) of moisture content.

  14. The batch study of Sr(2+) sorption by bone char.

    PubMed

    Smiciklas, I; Dimovic, S; Sljivic, M; Plecas, I

    2008-02-01

    Considering the excellent sorption properties of synthetic calcium hydroxyapatite (HAP) towards many divalent cations, the potential application of bone char, the natural source of HAP, for sequestering Sr(2+)ions from aqueous solutions has been studied in batch conditions. Contact time, initial solution pH and initial Sr(2+) concentrations were varied to examine the effect of these process parameters on the amount of Sr(2+) sorbed. The kinetics of Sr(2+) sorption was found to be a 2-step process, with contact time of 24 h required for attaining equilibrium. The sorption isotherm was well fitted with Langmuir and DKR theoretical models. Sorption of Sr(2+) on bone char was found to be a favorable, thermodynamically feasible and spontaneous process, with the maximum sorption capacity of 0.271 mmol/g and sorption energy of 11.09 kJ/mol. The sorption was pH-independent in the initial pH range 4-10, as a result of excellent buffering properties of bone char (constant final pH), while for pH > 10 sorbed amounts of Sr(2+) increased due to attractive electrostatic forces between negatively charged sorbent surface and positively charged metal ions. On the basis of the amount of Ca(2+) released and final pH decrease in respect to the point of zero charge of bone char (pH(PZC)), two possible mechanisms of Sr(2+) sorption were identified: ion-exchange and the formation of complex compounds with HAP and carbon active surface sites. The amounts of Sr(2+) leached from bone char increased with the increase of Ca(2+) content and the decrease of solution pH. In comparison with synthetic HAP, bone char represents a cost-effective alternative for Sr(2+) sequestering. PMID:18172814

  15. Nonlinear Chlorinated Solvent Sorption Impedes Remediation in Sedimentary Aquifers

    NASA Astrophysics Data System (ADS)

    Allen-King, R. M.; Rabideau, A. J.; Merlo, A.; Salvado i Estivill, J. A.; Barbarosa, V.; Matott, L. S.

    2014-12-01

    A 'tailing' pattern of rapid initial contaminant concentration decline followed by sustained release at a lower concentration is commonly produced by active remediation strategies. The ability of aquitard layers to cause this pattern is recognized. However, we hypothesize that nonlinear sorption combined with intragranular diffusion and mass storage within coarse, porous grains, can also cause tailing. Our project combines laboratory measurements of the equilibrium sorption isotherm for trichloroethene (TCE), release measurements from granular samples, and simulations of retarded intragranular diffusion. A novel aspect of our study is that we are examining a sample containing condensed kerogen as the primary form of organic matter on the impact of TCE mass storage, uptake and release rates. The kerogen-containing marine sedimentary rock used in our study is representative of the source rock of the surficial glacial aquifers in the southern Ontario, Canada region. The fact that energy producing shale units occur within the regional stratigraphic sequences indicates the high level of thermal maturation of the kerogen that comprises the sorbent for TCE in these samples. The equilibrium sorption isotherm spans nearly five orders of magnitude in aqueous concentration and is nonlinear. Preliminary comparisons between the mass release curve for grains equilibrated with a high TCE aqueous concentration (ca. 1000 mg/L) show that the physically-based model, which represents release controlled by intragranular diffusion with nonlinear local equilibrium sorption, provides a reasonable fit to the observed data with modest adjustment of the independently determined parameters. Additional experiments documenting TCE release from samples equilibrated at different initial aqueous concentrations and of different grain sizes will also be evaluated using the model and the results compared. Through extending simulations to the field scale, our results will contribute to a general

  16. Thermodynamics of cadmium sorption on different soils of West Bengal, India.

    PubMed

    Karak, Tanmoy; Paul, Ranjit Kumar; Das, D K; Boruah, Romesh K; Sonar, Indira

    2014-01-01

    A sorption study was conducted on different soils collected from five agroecological zones of West Bengal, India, to understand the soil environmental behavior and fate of cadmium. For this purpose batch adsorption experiments were carried out at the native soil pH and at three different temperatures (25°C, 35°C, and 45°C). The adsorption data fitted by a linear least squares technique to the different sorption isotherms. Most data obtained give the good fit to both Freundlich and modified Langmuir isotherms, but they are not consistent with the linear Langmuir adsorption model. Thermodynamic parameters, namely, thermodynamics equilibrium constant at a particular temperature T (K T (0)), Gibbs free energy at a particular temperature T (ΔG T (0)), and change of enthalpy (ΔH (0)) and change of entropy at temperature T (ΔS T (0)), were also determined by applying sorption value and concentrations of Cd in equilibrium solution within the temperature range. The thermodynamic parameters revealed that Cd sorption increases as the values of K T (0), ΔG T (0), ΔH (0), and ΔS T (0) were increased on reaction temperatures. The spontaneous sorption reaction can be concluded due to high values of ΔG T (0). The positive values of ΔH (0) indicated that the Cd sorption is an endothermic one. Under these present conditions, the soil and its components possibly supply a number of sites having different adsorption energies for cadmium sorption. PMID:24683322

  17. Thermodynamics of cadmium sorption on different soils of West Bengal, India.

    PubMed

    Karak, Tanmoy; Paul, Ranjit Kumar; Das, D K; Boruah, Romesh K; Sonar, Indira

    2014-01-01

    A sorption study was conducted on different soils collected from five agroecological zones of West Bengal, India, to understand the soil environmental behavior and fate of cadmium. For this purpose batch adsorption experiments were carried out at the native soil pH and at three different temperatures (25°C, 35°C, and 45°C). The adsorption data fitted by a linear least squares technique to the different sorption isotherms. Most data obtained give the good fit to both Freundlich and modified Langmuir isotherms, but they are not consistent with the linear Langmuir adsorption model. Thermodynamic parameters, namely, thermodynamics equilibrium constant at a particular temperature T (K T (0)), Gibbs free energy at a particular temperature T (ΔG T (0)), and change of enthalpy (ΔH (0)) and change of entropy at temperature T (ΔS T (0)), were also determined by applying sorption value and concentrations of Cd in equilibrium solution within the temperature range. The thermodynamic parameters revealed that Cd sorption increases as the values of K T (0), ΔG T (0), ΔH (0), and ΔS T (0) were increased on reaction temperatures. The spontaneous sorption reaction can be concluded due to high values of ΔG T (0). The positive values of ΔH (0) indicated that the Cd sorption is an endothermic one. Under these present conditions, the soil and its components possibly supply a number of sites having different adsorption energies for cadmium sorption.

  18. Sorption-desorption of imidacloprid onto a lacustrine Egyptian soil and its clay and humic acid fractions.

    PubMed

    Kandil, Mahrous M; El-Aswad, Ahmed F; Koskinen, William C

    2015-01-01

    Sorption-desorption of the insecticide imidacloprid 1-[(6-chloro-3-pyridinyl)-methyl]-N-nitro-2-imidazolidinimine onto a lacustrine sandy clay loam Egyptian soil and its clay and humic acid (HA) fractions was investigated in 24-h batch equilibrium experiments. Imidacloprid (IMDA) sorption-desorption isotherms onto the three sorbents were found to belong to a non-linear L-type and were best described by the Freundlich model. The value of the IMDA adsorption distribution coefficient, Kd(ads), varied according to its initial concentration and was ranged 40-84 for HA, 14-58 for clay and 1.85-4.15 for bulk soil. Freundlich sorption coefficient, Kf(ads), values were 63.0, 39.7 and 4.0 for HA, clay and bulk soil, respectively. The normalized soil Koc value for imidacloprid sorption was ∼800 indicating its slight mobility in soils. Nonlinear sorption isotherms were indicated by 1/n(ads) values <1 for all sorbents. Values of the hysteresis index (H) were <1, indicating the irreversibility of imidacloprid sorption process with all tested sorbents. Gibbs free energy (ΔG) values indicated a spontaneous and physicosorption process for IMDA and a more favorable sorption to HA than clay and soil. In conclusion, although the humic acid fraction showed the highest capacity and affinity for imidacloprid sorption, the clay fraction contributed to approximately 95% of soil-sorbed insecticide. Clay and humic acid fractions were found to be the major two factors controlling IMDA sorption in soils. The slight mobility of IMDA in soils and the hysteresis phenomenon associated with the irreversibility of its sorption onto, mainly, clay and organic matter of soils make its leachability unlikely to occur.

  19. Investigation of sulfonated aromatic compound (SAC) modification to nylon film. 2. Study of SAC sorption isotherm and atomic force microscopic characterization of nylon surfaces

    SciTech Connect

    Zhang, J.; Watson, B.A.; Keown, R.W.; Malone, C.P.; Barteau, M.A.

    1995-08-01

    Nylon 6 and nylon 66 films have been treated with aqueous sulfonated aromatic compound (SAC) solutions at concentrations ranging from 0.005 to 1.0 wt%. SAC uptakes at different treatment concentrations were measured and found to follow a BET isotherm. The surface morphologies of nylon film samples, including the original and SAC-treated films, have been characterized by atomic force microscopy (AFM). For untreated nylon 6 and nylon 66 films, AFM images show a randomly distributed fibrillar surface structure. Characteristic widths of fibrils in the nylon 66 and 6 films were 150-225 and 75-150 nm, respectively. For SAC-treated nylon films, the AFM images revealed that the surfaces of the films became covered with nodule-like features having a diameter range of 25-60 nm. AFM analysis provides evidence that SAC treatment deposited a surface coating on nylon films. AFM images of SAC-treated nylon films suggest a mechanism for stain resistance in which the SAC first forms a thin coating on the nylon via bondings between attractive groups in the SAC and nylon polymers. After treatment at increased SAC concentration, the surface is covered with nodule-like deposits which likely serve as a physical barrier to dye permeation. 20 refs., 8 figs.

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

    NASA Astrophysics Data System (ADS)

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

    2012-03-01

    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.

  1. Sorption mechanism of Cd(II) from water solution onto chicken eggshell

    NASA Astrophysics Data System (ADS)

    Flores-Cano, Jose Valente; Leyva-Ramos, Roberto; Mendoza-Barron, Jovita; Guerrero-Coronado, Rosa María; Aragón-Piña, Antonio; Labrada-Delgado, Gladis Judith

    2013-07-01

    The mechanism and capacity of eggshell for sorbing Cd(II) from aqueous solution was examined in detail. The eggshell was characterized by several techniques. The eggshell was mainly composed of Calcite (CaCO3). The surface charge distribution was determined by acid-base titration and the point of zero charge (PZC) of the eggshell was found to be 11.4. The sorption equilibrium data were obtained in a batch adsorber, and the adsorption isotherm of Langmuir fitted the data quite well. The sorption capacity of eggshell increased while raising the pH from 4 to 6, this tendency was attributed to the electrostatic interaction between the Cd2+ in solution and the surface of the eggshell. Furthermore, the sorption capacity was augmented by increasing the temperature from 15 to 35 °C because the sorption was endothermic. The sorption of Cd(II) occurred mainly onto the calcareous layer of the eggshell, but slightly on the membrane layer. It was demonstrated that the sorption of Cd(II) was not reversible, and the main sorption mechanisms were precipitation and ion exchange. The precipitation of (Cd,Ca)CO3 on the surface of the eggshell was corroborated by SEM and XRD analysis.

  2. Silica gel modified with N-(3-propyl)-O-phenylenediamine: functionalization, metal sorption equilibrium studies and application to metal enrichment prior to determination by flame atomic absorption spectrometry.

    PubMed

    Akl, Magda Ali Abd-elAziz; Kenawy, Ibraheim Mohamed; Lasheen, Rabab Ramadan

    2005-08-01

    The use of the chemically modified silica gel N-(3-propyl)-O-phenylenediamine (SiG-NPPDA) adsorbent, for the preconcentration and separation of trace heavy metals, was described. SiG-NPPDA sorbs quantitatively (90-100% recovery) trace amounts of nine heavy metals, viz., Cd(II), Zn(II), Fe(III), Cu(II), Pb(II), Mn(II), Cr(III), Co(II) and Ni(II) at pH 7-8. The sorption capacity varies from 350 to 450 micromol g(-1). Desorption was found to be quantitative with 1-2 M HNO3 or 0.05 M Na2EDTA. The distribution coefficient, Kd and the percentage concentration of the investigated metal ions on the adsorbent at equilibrium, C(M,eqm)% (Recovery, R%), were studied as a function of experimental parameters. The logarithmic values of the distribution coefficient, log Kd, ranges between 4.0 and 6.4. Some foreign ions caused little interference in the preconcentration and determination of the investigated nine metals by flame atomic absorption spectrometry (AAS). The adsorbent and its formed metal chelates were characterized by IR (absorbance and/or reflectance), potentiometric titrations and thermogravimetric analysis (TGA and DTG). The mode of chelation between the SiG-NPPDA adsorbent and the investigated metal ions is proposed to be due to the reaction of the investigated metal ions with the two nitrogen atoms of the SiG-NPPDA adsorbent. The present adsorbent coupled with flame AAS has been used to enrich and determine the nine metal ions in natural aqueous systems and in certified reference materials (RSD < or = 5%). The copper, iron, manganese and zinc present in some pharmaceutical vitamin samples were also preconcentrated on SiG-NPPDA adsorbent and determined by flame AAS (RSD < or = 4.2%). Nanogram concentrations (0.07-0.14 ng ml(-1)) of Cd(II), Zn(II), Fe(III), Pb(II), Cr(III), Mn(II), Cu(II), Co(II) and Ni(II) can be determined reliably with a preconcentration factor of 100.

  3. The Influence of Temperature on the Sorption and Permeability of CO2 in poly(fluoroalkoxyphosphazene) membranes

    SciTech Connect

    Mayur Ostwal; JOshua M. Lau; Christopher J. Orme; Frederick F. Stewart; J. Douglas Way

    2009-11-01

    This paper reports the transport and sorption properties of poly(fluoroalkoxyphosphazene) (PFAP) membranes for carbon dioxide and nitrogen in both pure and mixed gas experiments. The CO2 permeability decreased from 336 to 142 Barrers with an increase in the CO2/N2 ideal separation factor from 12 to 21 as the membrane temperature was decreased from 303 K to 258 K at feed pressure of 2.9 bars. At lower feed pressure (1.5 bars) the CO2 permeability decreased from 327 to 140 Barrers, while the CO2/N2 ideal separation factor increased from 13 to 22 over the same temperature range. CO2 sorption isotherms were measured using the pressure decay equilibrium method. Solubility of CO2 was determined using the sorption isotherms and the diffusion coefficients were calculated from CO2 permeabilities and solubilities. Sorption isotherms were linear at each temperature for the pressure range studied and the enthalpy of sorption was -5.8 kcal/mol. The solubility coefficient values for CO2 increased from 0.95 to 5.43 cm3 CO2(STP)/cm3 polymer.atm whereas the diffusion coefficient decreased from 2.71 X 10-6 to 0.19 X 10-6 cm2/sec as the temperature decreased from 303 K to 258 K.

  4. Remediation of Rare Earth Element Pollutants by Sorption Process Using Organic Natural Sorbents.

    PubMed

    Butnariu, Monica; Negrea, Petru; Lupa, Lavinia; Ciopec, Mihaela; Negrea, Adina; Pentea, Marius; Sarac, Ionut; Samfira, Ionel

    2015-09-01

    The effects of the sorption of environmental applications by various source materials of natural organic matter, i.e., bone powder, was examined. Sorption capacities and subsequent rare earth element retention characteristics of all metals tested were markedly increased by ionic task-specific. In this study, the abilities of three models' isotherms widely were used for the equilibrium sorption data: Langmuir, Freundlich and Redlich-Peterson. For all studied metal ions the maximum adsorption capacity is close to those experimentally determined. The characteristic parameters for each isotherm and related coefficients of determination have been determined. The experimental data achieved excellent fits within the following isotherms in the order: Langmuir > Redlich-Peterson > Freundlich, based on their coefficient of determination values. The bone powder has developed higher adsorption performance in the removal process of Nd(III), Eu(III), La(III) from aqueous solutions than in the case of the removal process of Cs(I), Sr(II) and Tl(I) from aqueous solutions. The described relationships provide direct experimental evidence that the sorption-desorption properties of bone powder are closely related to their degree of the type of the metal. The results suggest a potential for obtaining efficient and cost-effective engineered natural organic sorbents for environmental applications. PMID:26378553

  5. Remediation of Rare Earth Element Pollutants by Sorption Process Using Organic Natural Sorbents.

    PubMed

    Butnariu, Monica; Negrea, Petru; Lupa, Lavinia; Ciopec, Mihaela; Negrea, Adina; Pentea, Marius; Sarac, Ionut; Samfira, Ionel

    2015-09-10

    The effects of the sorption of environmental applications by various source materials of natural organic matter, i.e., bone powder, was examined. Sorption capacities and subsequent rare earth element retention characteristics of all metals tested were markedly increased by ionic task-specific. In this study, the abilities of three models' isotherms widely were used for the equilibrium sorption data: Langmuir, Freundlich and Redlich-Peterson. For all studied metal ions the maximum adsorption capacity is close to those experimentally determined. The characteristic parameters for each isotherm and related coefficients of determination have been determined. The experimental data achieved excellent fits within the following isotherms in the order: Langmuir > Redlich-Peterson > Freundlich, based on their coefficient of determination values. The bone powder has developed higher adsorption performance in the removal process of Nd(III), Eu(III), La(III) from aqueous solutions than in the case of the removal process of Cs(I), Sr(II) and Tl(I) from aqueous solutions. The described relationships provide direct experimental evidence that the sorption-desorption properties of bone powder are closely related to their degree of the type of the metal. The results suggest a potential for obtaining efficient and cost-effective engineered natural organic sorbents for environmental applications.

  6. Sorption of copper(II) ions in the biomass of alga Spirogyra sp.

    PubMed

    Rajfur, Małgorzata; Kłos, Andrzej; Wacławek, Maria

    2012-10-01

    Sorption of copper ions by the alga Spirogyra sp. was investigated to determine the influence of experimental conditions and the methods of sample preparation on the process. The experiments were carried out both under the static and the dynamic conditions. Kinetics and equilibrium parameters of the sorption were evaluated. In addition, the influence was studied of the algae preparation methods on the conductivity of demineralized water in which the algae samples were immersed. The static experiments showed that the sorption of Cu(2+) ions reached equilibrium in about 30 min, with approximately 90% of the ions adsorbed in the initial 15 min. The sorption capacity determined from the Langmuir isotherms appeared highly uncertain (SD=±0.027 mg/g dry mass or ±11%, for the live algae). Under static conditions, the slopes of the Langmuir isotherms depended on the ratio of the alga mass to the volume of solution. The conductometric measurements were proven to be a simple and fast way to evaluate the quality of algae used for the experiments.

  7. Effects of resident water and non-equilibrium adsorption on the primary and enhanced coalbed methane gas recovery

    NASA Astrophysics Data System (ADS)

    Jahediesfanjani, Hossein

    The major part of the gas in coalbed methane and shale gas reservoirs is stored as the adsorbed gas in the coal and organic materials of the black shale internal surfaces. The sorption sites in both reservoirs are composed of several macropores that contain very small pore sizes. Therefore, the adsorption/desorption is very slow process and follows a non-equilibrium trend. The time-dependency of the sorption process is further affected by the reservoir resident water. Water can diffuse into the matrix and adsorption sites, plug the pores and affect the reservoir gas production. This study presents an experimental and theoretical procedure to investigate the effects of the resident water and time-dependency of the sorption process on coalbed and shale gas primary and enhanced recovery by simultaneous CO 2/N2 injection. Series of the experiments are conducted to construct both equilibrium and non-equilibrium single and multi-component isotherms with the presence of water. A novel and rapid data interpretation technique is developed based on the nonequilibrium adsorption/desorption thermodynamics, mass conservation law, and volume filling adsorption theory. The developed technique is implemented to construct both equilibrium and non-equilibrium multi-component multi-phase isotherms from the early time experimental measurements. The non-equilibrium isotherms are incorporated in the coalbed methane/shale gas reservoir simulations to account for the time-dependency of the sorption process. The experimental results indicate that the presence of water in the sorption system reduces both carbon dioxide and nitrogen adsorption rates. Reduction in the adsorption rate for carbon dioxide is more than nitrogen. The results also indicate that the resident water reduces the adsorption ability of low rank coals more than high rank ones. The results of the multi-component sorption tests indicate that increasing the initial mole fraction of the nitrogen gas in the injected CO2/N2

  8. Isotope studies to the sorption behavior of atmospheric sulfate in humus layers of scots pine ecosystems.

    PubMed

    Schulz, H; Neue, H-U

    2005-03-01

    The sorption potential for SO4(2-) in humus layer samples from field sites along a deposition gradient was determined experimentally in batch experiments. The Freundlich equation was used to quantify the sorption of added SO4(2-) in humus layer samples and to determine site-dependent sorption parameters. SO4(2-) sorption in humus layers is a concentration-dependent process. The linearity of isotherms reveals that SO4(2-) is reversibly bound in the organic surface layer, as long as soil solution concentrations remain above 26 to 44 mg SO4(2-) L(-1). Natural isotope variations of sulfur in SO4(2-) were analysed to investigate the degree of sorption of dissolved atmospheric and added SO4(2-). Both sulfate species differed significantly in their isotope composition. The pattern of delta34S values for SO4(2-) in all equilibrium solutions confirm the findings from sorption isotherms, showing a close relationship between the sulfur isotope ratios of SO4(2-) in soil solutions and the amount of SO4(2-) sorbed at the humus layer matrix. Stored atmospheric SO4(2-) in humus layers is released at sites where sulfate concentration in throughfall drops below 26 mg SO4(2-) L(-1). Concentration of soluble Fe decreased with increasing sulfate sorption, thus supporting the assumption that active Fe for example is important. Iron probably stabilizes the reactive surface of humus complexes and therefore has a positive influence on the SO4(2-) sorption in humus layers.

  9. Thermodynamic study on dynamic water vapor sorption in Sylgard-184.

    PubMed

    Harley, Stephen J; Glascoe, Elizabeth A; Maxwell, Robert S

    2012-12-01

    The dynamic and equilibrium water vapor sorption properties of Sylgard-184, a commercially available poly(dimethylsiloxane) elastomer (PDMS), were determined via gravimetric analysis from 30 to 70 °C. Described here is a methodology for quantitatively assessing how water vapor diffuses and ad/absorbs into polymeric materials that are traditionally considered hydrophobic. PDMS materials are frequently chosen for their moisture barrier properties; our results, however, demonstrate that moisture is able to penetrate the material over a range of temperatures and humidities. The sorption values measured here ranged from ca. 0.1 to 1.4 cm(3) (STP) H(2)O/g Sylgard. The isotherms exhibited sigmoidal character and were fit to a triple mode sorption model. Asymptotic behavior at low water activities was characterized using a Langmuir type adsorption model, linear behavior was fit to a Henry's law type dependence, and the convex portion at higher activities was fit with good agreement to Park's equation for pooling or clustering. The thermal dependence of these sorption modes was also explored and reported. The dynamics of the sorption process were fit to a Fickian model and effective diffusivities are reported along with corresponding activation energies. The diffusivity values measured here ranged from ca. 0.5 to 3.5 × 10(-5) cm(2)/s depending on the temperature and relative humidity. The concentration dependence of the diffusivity showed a direct correlation with the three modes of uptake obtained from the isotherms. Corrections to the diffusivities were calculated using existing models that take into account adsorption and pooling. PMID:23153278

  10. Thermodynamic study on dynamic water vapor sorption in Sylgard-184.

    PubMed

    Harley, Stephen J; Glascoe, Elizabeth A; Maxwell, Robert S

    2012-12-01

    The dynamic and equilibrium water vapor sorption properties of Sylgard-184, a commercially available poly(dimethylsiloxane) elastomer (PDMS), were determined via gravimetric analysis from 30 to 70 °C. Described here is a methodology for quantitatively assessing how water vapor diffuses and ad/absorbs into polymeric materials that are traditionally considered hydrophobic. PDMS materials are frequently chosen for their moisture barrier properties; our results, however, demonstrate that moisture is able to penetrate the material over a range of temperatures and humidities. The sorption values measured here ranged from ca. 0.1 to 1.4 cm(3) (STP) H(2)O/g Sylgard. The isotherms exhibited sigmoidal character and were fit to a triple mode sorption model. Asymptotic behavior at low water activities was characterized using a Langmuir type adsorption model, linear behavior was fit to a Henry's law type dependence, and the convex portion at higher activities was fit with good agreement to Park's equation for pooling or clustering. The thermal dependence of these sorption modes was also explored and reported. The dynamics of the sorption process were fit to a Fickian model and effective diffusivities are reported along with corresponding activation energies. The diffusivity values measured here ranged from ca. 0.5 to 3.5 × 10(-5) cm(2)/s depending on the temperature and relative humidity. The concentration dependence of the diffusivity showed a direct correlation with the three modes of uptake obtained from the isotherms. Corrections to the diffusivities were calculated using existing models that take into account adsorption and pooling.

  11. Inhibitory effect on the uptake and diffusion of Cd(2+) onto soybean hull sorbent in Cd-Pb binary sorption systems.

    PubMed

    Módenes, Aparecido N; Espinoza-Quiñones, Fernando R; Colombo, Andréia; Geraldi, Claudinéia L; Trigueros, Daniela E G

    2015-05-01

    The uptake of Cd(2+) and Pb(2+) ions by a soybean hull (SH) biosorbent in single and binary systems has been investigated. Sorption tests regarding SH in natura and chemically treated were carried out testing a suitable value range of solution pH, sorption temperature and shaking velocity. Sorption capacity is improved at pH 4, 30 °C temperature and 100 rpm. When a strong base is applied, a related-to-untreated SH increasing of 20% in the sorption capacity of Pb(2+) ions was observed, but with poor results for Cd(2+) uptake. Additionally, a relatively strong decreasing in both sorption capacities of Pb(2+) and Cd(2+) ions was evidenced for all acidic treatments. Regarding untreated SH, kinetic sorption data of both metals were well-interpreted by a pseudo second-order model and a rate-limiting step on the basis of an intra-particle diffusion model was suggested to occur. An inhibitory effect of Pb(2+) diffusion over Cd(2+) one was observed, limiting to reach the obtained maximum sorption capacity in single system. Maximum adsorption capacities of 0.49 and 0.67mequivg(-1) for Cd(2+) and Pb(2+), respectively, were predicted by the Langmuir isotherm model that reproduced well the equilibrium sorption data for single systems. The inhibitory effect of one metal over the other one was verified in equilibrium sorption data for binary systems interpreted on the basis of a modified extended Langmuir isotherm model, predicting changes in metal affinity onto the SH surface. Finally, SH is an alternative biosorbent with a great potential for the wastewater treatment containing cadmium and lead ions.

  12. Sorption of selected veterinary antibiotics onto dairy farming soils of contrasting nature.

    PubMed

    Srinivasan, Prakash; Sarmah, Ajit K; Manley-Harris, Merilyn

    2014-02-15

    The sorption potential for three sulfonamides (SAs), sulfamethoxazole (SMO), sulfachloropyridazine (SCP) and sulfamethazine (SM) and a macrolide, tylosin tartrate (TT) was assessed on six New Zealand dairy farming soils of contrasting physico-chemical properties. Kinetics studies showed that the sorption was rapid in the first few hours of the contact time (0-2h for SA and 0-4h for TT) and thereafter apparent equilibrium was achieved. Batch sorption isotherm data revealed that the degree of isotherm linearity (N) for SCP and SM varied between 0.50 and 1.08 in the six soils. Isotherms of both TT and SMO were mostly non-linear with the degree of non-linearity for TT (N=0.38-0.71) being greater than for SMO (0.42-0.75) in all soils except Manawatu (TT) and Te Kowhai (SMO) where a linear pattern was observed. Concentration-dependent effective distribution coefficient (Kd(eff)) values for the SMO, SCP and SM antibiotics in the soils ranged from 0.85 to 16.35 L kg(-1), while that for TT was 1.6 to 1,042 L kg(-1). The sorption affinity for all soils followed an order: TT>SCP>SM>SMO. Remarkable high sorption for tylosin in Matawhero soil as compared to other soils was attributed to the presence of oxygen containing acidic polar functional groups as evident in the FT-IR spectra of the soil. Furthermore, it was hypothesised that sorption of TT onto soils was mostly driven by metal oxide-surface mediated transformations whereas for sulfonamides it was primarily due to hydrophobic interactions. PMID:24326064

  13. Manganese Nitride Sorption Joule-Thomson Refrigerator

    NASA Technical Reports Server (NTRS)

    Jones, Jack A.; Phillips, Wayne M.

    1992-01-01

    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.

  14. Trihalomethane formation potential of aquatic and terrestrial fulvic and humic acids: Sorption on activated carbon.

    PubMed

    Abouleish, Mohamed Y Z; Wells, Martha J M

    2015-07-15

    Humic substances (HSs) are precursors for the formation of hazardous disinfection by-products (DBPs) during chlorination of water. Various surrogate parameters have been used to investigate the generation of DBPs by HS precursors and the removal of these precursors by activated carbon treatment. Dissolved organic carbon (DOC)- and ultraviolet absorbance (UVA254)-based isotherms are commonly reported and presumed to be good predictors of the trihalomethane formation potential (THMFP). However, THMFP-based isotherms are rarely published such that the three types of parameters have not been compared directly. Batch equilibrium experiments on activated carbon were used to generate constant-initial-concentration sorption isotherms for well-characterized samples obtained from the International Humic Substances Society (IHSS). HSs representing type (fulvic acid [FA], humic acid [HA]), origin (aquatic, terrestrial), and geographical source (Nordic, Suwannee, Peat, Soil) were examined at pH6 and pH9. THMFP-based isotherms were generated and compared to determine if DOC- and UVA254-based isotherms were good predictors of the THMFP. The sorption process depended on the composition of the HSs and the chemical nature of the activated carbon, both of which were influenced by pH. Activated carbon removal of THM-precursors was pH- and HS-dependent. In some instances, the THMFP existed after UVA254 was depleted.

  15. Sorption and biodegradation characteristics of the selected pharmaceuticals and personal care products onto tropical soil.

    PubMed

    Foolad, Mahsa; Hu, Jiangyong; Tran, Ngoc Han; Ong, Say Leong

    2016-01-01

    In the present study, the sorption and biodegradation characteristics of five pharmaceutical and personal care products (PPCPs), including acetaminophen (ACT), carbamazepine (CBZ), crotamiton (CTMT), diethyltoluamide (DEET) and salicylic acid (SA), were studied in laboratory-batch experiments. Sorption kinetics experimental data showed that sorption systems under this study were more appropriately described by the pseudo second-order kinetics with a correlation coefficient (R2)>0.98. Sorption equilibrium data of almost all target compounds onto soil could be better described by the Freundlich sorption isotherm model. The adsorption results showed higher soil affinity for SA, following by ACT. Results also indicated a slight effect of pH on PPCP adsorption with lower pH causing lower adsorption of compounds onto the soil except for SA at pH 12. Moreover, adsorption of PPCPs onto the soil was influenced by natural organic matter (NOM) since the higher amount of NOM caused lower adsorption to the soil. Biodegradation studies of selected PPCPs by indigenous microbial community present in soil appeared that the removal rates of ACT, SA and DEET increased with time while no effect had been observed for the rest. This study suggests that the CBZ and CTMT can be considered as suitable chemical sewage indicators based on their low sorption affinity and high resistance to biodegradation.

  16. Sorption and biodegradation characteristics of the selected pharmaceuticals and personal care products onto tropical soil.

    PubMed

    Foolad, Mahsa; Hu, Jiangyong; Tran, Ngoc Han; Ong, Say Leong

    2016-01-01

    In the present study, the sorption and biodegradation characteristics of five pharmaceutical and personal care products (PPCPs), including acetaminophen (ACT), carbamazepine (CBZ), crotamiton (CTMT), diethyltoluamide (DEET) and salicylic acid (SA), were studied in laboratory-batch experiments. Sorption kinetics experimental data showed that sorption systems under this study were more appropriately described by the pseudo second-order kinetics with a correlation coefficient (R2)>0.98. Sorption equilibrium data of almost all target compounds onto soil could be better described by the Freundlich sorption isotherm model. The adsorption results showed higher soil affinity for SA, following by ACT. Results also indicated a slight effect of pH on PPCP adsorption with lower pH causing lower adsorption of compounds onto the soil except for SA at pH 12. Moreover, adsorption of PPCPs onto the soil was influenced by natural organic matter (NOM) since the higher amount of NOM caused lower adsorption to the soil. Biodegradation studies of selected PPCPs by indigenous microbial community present in soil appeared that the removal rates of ACT, SA and DEET increased with time while no effect had been observed for the rest. This study suggests that the CBZ and CTMT can be considered as suitable chemical sewage indicators based on their low sorption affinity and high resistance to biodegradation. PMID:26744934

  17. Competitive sorption of persistent organic pollutants onto microplastics in the marine environment.

    PubMed

    Bakir, Adil; Rowland, Steven J; Thompson, Richard C

    2012-12-01

    Plastics are known to sorb persistent organic pollutants from seawater. However, studies to quantify sorption rates have only considered the affinity of chemicals in isolation, unlike the conditions in the environment where contaminants are present as complex mixtures. Here we examine whether phenanthrene and 4,4'-DDT, in a mixture, compete for sorption sites onto PVC with no added additives (unplasticised PVC or uPVC) and Ultra-High Molecular Weight polyethylene. Interactions were investigated by exposing particles of uPVC and UHMW PE to mixtures of 3H and 14C radiolabelled Phe and DDT. Changes in sorption capacity were modelled by applying a Freundlich binding sorption isotherms. An Extended Langmuir Model and an Interaction Factor Model were also applied to predict equilibrium concentrations of pollutants onto plastic. This study showed that in a bi-solute system, DDT exhibited no significantly different sorption behaviour than in single solute systems. However, DDT did appear to interfere with the sorption of Phe onto plastic, indicating an antagonistic effect.

  18. [Effects of soil compositions on sorption and desorption behavior of tetrachloroethylene in soil].

    PubMed

    Hu, Lin; Qiu, Zhao-Fu; He, Long; Dou, Ying; Lü, Shu-Guang; Sui, Qian; Lin, Kuang-Fei

    2013-12-01

    Sorption and desorption play an important role in the transport and the fate of tetrachloroethylene (PCE) in soil. In order to examine influences of different soil compositions on PCE sorption-desorption, equilibrium batch experiments were carried out using four sorbents (natural soil with 2.23% total organic carbon (TOC), H2O2-treated soil, 375 degrees C-treated soil and 600 degrees C-treated soil) with different initial PCE liquid concentrations (c0). The effects of main parameters (TOC, soft carbon, hard carbon, minerals, c0) on PCE sorption-desorption were investigated. At 16 degrees C, when c0 was increased from 5 to 80 mg x L(-1), the results showed that sorption and desorption isotherms of PCE on four sorbents can be best described by the Freundlich model (r2 > 0.96). The sorption contribution rate of SOM was higher than 60% in natural soil, and hard carbon was the main influencing factor,while the desorption contribution rate of SOM was close to that of minerals in natural soil, and soft carbon accounted for more than 80% in the total desorption contribution rate of SOM. In addition, the higher the c0, the higher the sorption contribution rate of PCE in hard carbon and desorption contribution rate of PCE in soft carbon and minerals were. Moreover, desorption of PCE from four sorbents exhibited hysteresis, and hard carbon played a remarkable role in the hysteresis of natural soil.

  19. Competitive sorption of persistent organic pollutants onto microplastics in the marine environment.

    PubMed

    Bakir, Adil; Rowland, Steven J; Thompson, Richard C

    2012-12-01

    Plastics are known to sorb persistent organic pollutants from seawater. However, studies to quantify sorption rates have only considered the affinity of chemicals in isolation, unlike the conditions in the environment where contaminants are present as complex mixtures. Here we examine whether phenanthrene and 4,4'-DDT, in a mixture, compete for sorption sites onto PVC with no added additives (unplasticised PVC or uPVC) and Ultra-High Molecular Weight polyethylene. Interactions were investigated by exposing particles of uPVC and UHMW PE to mixtures of 3H and 14C radiolabelled Phe and DDT. Changes in sorption capacity were modelled by applying a Freundlich binding sorption isotherms. An Extended Langmuir Model and an Interaction Factor Model were also applied to predict equilibrium concentrations of pollutants onto plastic. This study showed that in a bi-solute system, DDT exhibited no significantly different sorption behaviour than in single solute systems. However, DDT did appear to interfere with the sorption of Phe onto plastic, indicating an antagonistic effect. PMID:23044032

  20. Sorption and desorption of alcohol sulfate surfactants in an agricultural soil.

    PubMed

    Fernández-Ramos, Carolina; Ballesteros, Oscar; Zafra-Gómez, Alberto; Blanc-García, Rosario; Navalón, Alberto; Crovetto, Sara Isabel; Oliver-Rodríguez, Bartolomé; García-Delgado, Rafael Antonio; Vílchez, José Luís

    2014-03-01

    Alcohol sulfates are one of the most important types of commercial anionic surfactants and may pose serious environmental problems. The present study examines the sorption behavior of alcohol sulfates in an agricultural soil using a batch reactor and column experiments. Kinetics and equilibrium isotherms of the sorption and desorption processes of the following alcohol sulfate homologues have been determined: AS-C12, AS-C14, AS-C16 , and AS-C18. Sorption and desorption occurred rapidly, and equilibrium was achieved in approximately 1 h. The sorbed mass percentages were 35.1% AS-C12 , 67.2% AS-C14 , and 100% for both AS-C16 and AS-C18. A pseudo-first-order kinetic model provided an adequate fit of data. Sorption and desorption equilibrium data were fitted into 1) a linear model, with r(2) values in the ranges 0.712 to 0.988 and 0.736 to 0.983, respectively, and 2) a Freundlich model, with r(2) values in the ranges 0.956 to 0.991 and 0.891 to 0.981, respectively. Continuous-flow experiments in soil columns were carried out to obtain the breakthrough curves for each compound. The present study provides basic theoretical concepts and key parameters for developing mathematical models that simulate the migration of alcohol sulfate into agricultural soils.

  1. Sorption and transformation of the reactive tracers resazurin and resorufin in natural river sediments

    NASA Astrophysics Data System (ADS)

    Lemke, D.; González-Pinzón, R.; Liao, Z.; Wöhling, T.; Osenbrück, K.; Haggerty, R.; Cirpka, O. A.

    2014-08-01

    Resazurin (Raz) and its reaction product resorufin (Rru) have increasingly been used as reactive tracers to quantify metabolic activity and hyporheic exchange in streams. Previous work has indicated that these compounds undergo sorption in stream sediments. We present laboratory experiments on Raz and Rru transport, sorption, and transformation, consisting of 4 column and 72 batch tests using 2 sediments with different physicochemical properties under neutral (pH = 7) and alkaline (pH = 9) conditions. The study aimed at identifying the key processes of reactive transport of Raz and Rru in streambed sediments and the experimental setup best suited for their determination. Data from column experiments were simulated by a travel-time-based model accounting for physical transport, equilibrium and kinetic sorption, and three first-order reactions. We derived the travel-time distributions directly from the breakthrough curve (BTC) of the conservative tracer, fluorescein, rather than from fitting an advective-dispersive transport model, and inferred from those distributions the transfer functions of Raz and Rru, which provided conclusive approximations of the measured BTCs. The most likely reactive transport parameters and their uncertainty were determined by a Markov chain-Monte Carlo approach. Sorption isotherms of both compounds were obtained from batch experiments. We found that kinetic sorption dominates sorption of both Raz and Rru, with characteristic timescales of sorption in the order of 12 to 298 min. Linear sorption models for both Raz and Rru appeared adequate for concentrations that are typically applied in field tracer tests. The proposed two-site sorption model helps to interpret transient tracer tests using the Raz-Rru system.

  2. Use of lipophilic ion adsorption isotherms to determine the surface area and the monolayer capacity of a chromatographic packing, as well as the thermodynamic equilibrium constant for its adsorption.

    PubMed

    Cecchi, T

    2005-04-29

    A method that champions the approaches of two independent research groups, to quantitate the chromatographic stationary phase surface available for lipophilic ion adsorption, is presented. For the first time the non-approximated expression of the electrostatically modified Langmuir adsorption isotherm was used. The non approximated Gouy-Chapman (G-C) theory equation was used to give the rigorous surface potential. The method helps model makers, interested in ionic interactions, determine whether the potential modified Langmuir isotherm can be linearized, and, accordingly, whether simplified retention equations can be properly used. The theory cultivated here allows the estimates not only of the chromatographically accessible surface area, but also of the thermodynamic equilibrium constant for the adsorption of the amphiphile, the standard free energy of its adsorption, and the monolayer capacity of the packing. In addition, it establishes the limit between a theoretical and an empirical use of the Freundlich isotherm to determine the surface area. Estimates of the parameters characterising the chromatographic system are reliable from the physical point of view, and this greatly validates the present comprehensive approach.

  3. Production of activated carbon from biodiesel solid residues: An alternative for hazardous metal sorption from aqueous solution.

    PubMed

    Ribeiro, Rita F L; Soares, Vitor C; Costa, Letícia M; Nascentes, Clésia C

    2015-10-01

    In this study, the potential for the sorption of Pb(2+) and Cd(2+) from aqueous solutions using HNO3-treated activated carbon (TAC) obtained from radish press cake (Raphanus sativus L.), a solid residue from biodiesel production, was investigated. Activated carbon (AC) was obtained by physical activation with CO2(g). Chemical modification with HNO3 was employed to increase the sorption capability of the AC. The sorption of Pb(2+) and Cd(2+) was studied in monometallic systems in equilibrium with different metal-ion concentrations (10-400 mg L(-1)). The experimental sorption equilibrium data were fit to the Langmuir and Freundlich isotherm models. The maximum sorption capacity (qmax) obtained for AC from the Langmuir isotherm was 45.5 mg g(-1) for Cd(2+) and 250 mg g(-1) for Pb(2+). Moreover, TAC presented qmax of 166.7 mg g(-1) (1.48 mmol g(-1)) for Cd(2+) and 500.0 mg g(-1) (2.41 mmol g(-1)) for Pb(2+)showing the effect of chemical modification. Sorption-desorption studies showed that the interaction between metals and TAC is reversible and this sorbent can be reused for several consecutive cycles. Furthermore, the sorption of Cd(2+) and Pb(2+) by TAC was not affected by the presence of competing ions. The experimental data obtained in this study indicated that this solid residue is viable for the production of sorbents that remove metals, such as cadmium and lead, from wastewaters and thereby contribute to the sustainable development of the production of biodiesel.

  4. Linearised and non-linearised isotherm models optimization analysis by error functions and statistical means.

    PubMed

    Subramanyam, Busetty; Das, Ashutosh

    2014-01-01

    In adsorption study, to describe sorption process and evaluation of best-fitting isotherm model is a key analysis to investigate the theoretical hypothesis. Hence, numerous statistically analysis have been extensively used to estimate validity of the experimental equilibrium adsorption values with the predicted equilibrium values. Several statistical error analysis were carried out. In the present study, the following statistical analysis were carried out to evaluate the adsorption isotherm model fitness, like the Pearson correlation, the coefficient of determination and the Chi-square test, have been used. The ANOVA test was carried out for evaluating significance of various error functions and also coefficient of dispersion were evaluated for linearised and non-linearised models. The adsorption of phenol onto natural soil (Local name Kalathur soil) was carried out, in batch mode at 30 ± 20 C. For estimating the isotherm parameters, to get a holistic view of the analysis the models were compared between linear and non-linear isotherm models. The result reveled that, among above mentioned error functions and statistical functions were designed to determine the best fitting isotherm. PMID:25018878

  5. Typical agricultural diffuse herbicide sorption with agricultural waste-derived biochars amended soil of high organic matter content.

    PubMed

    Ouyang, Wei; Zhao, Xuchen; Tysklind, Mats; Hao, Fanghua

    2016-04-01

    Biochar application has been identified as the effective soil amendment and the materials to control the diffuse herbicide pollution. The atrazine was selected as the typical diffuse herbicide pollutant as the dominant proportion in applications. The biochar treated from four types of crops biomass were added to soil with high organic matter content. The basic sorption characteristics of biocahrs from corn cob (CC), corn stalk (CS), soybean straw (SS), rice straw (RS) and corn stalk paralyzed with 5% of ammonium dihydrogen phosphate (ACS) were analyzed, along with the comparison of the sorption difference of the raw soil and soil amended with biochars at four levels of ratio (0.5%, 1.0%, 3.0% and 5.0%). It was found that the linear distribution isotherm of raw soil was much effective due to the high organic matter background concentration. The addition of five types of biochars under two kinds of initial atrazine concentration (1 mg/L and 20 mg/L) demonstrated the sorption variances. Results showed the soil amended with RS and CS biochar had the biggest removal rate in four regular biochars and the removal rate of the ACS was the biggest. The sorption coefficient and the normalized sorption coefficient from Freundlich modeling presented the isothermal sorption characteristics of atrazine with soil of high organic matter content. The normalized sorption coefficient increased with the equilibrium concentration decreased in the biochar amended soil, which indicated the sorption performance will be better due to the low atrazine concentration in practice. Results showed that biochar amendment is the effective way to prevent leakage of diffuse herbicide loss.

  6. Typical agricultural diffuse herbicide sorption with agricultural waste-derived biochars amended soil of high organic matter content.

    PubMed

    Ouyang, Wei; Zhao, Xuchen; Tysklind, Mats; Hao, Fanghua

    2016-04-01

    Biochar application has been identified as the effective soil amendment and the materials to control the diffuse herbicide pollution. The atrazine was selected as the typical diffuse herbicide pollutant as the dominant proportion in applications. The biochar treated from four types of crops biomass were added to soil with high organic matter content. The basic sorption characteristics of biocahrs from corn cob (CC), corn stalk (CS), soybean straw (SS), rice straw (RS) and corn stalk paralyzed with 5% of ammonium dihydrogen phosphate (ACS) were analyzed, along with the comparison of the sorption difference of the raw soil and soil amended with biochars at four levels of ratio (0.5%, 1.0%, 3.0% and 5.0%). It was found that the linear distribution isotherm of raw soil was much effective due to the high organic matter background concentration. The addition of five types of biochars under two kinds of initial atrazine concentration (1 mg/L and 20 mg/L) demonstrated the sorption variances. Results showed the soil amended with RS and CS biochar had the biggest removal rate in four regular biochars and the removal rate of the ACS was the biggest. The sorption coefficient and the normalized sorption coefficient from Freundlich modeling presented the isothermal sorption characteristics of atrazine with soil of high organic matter content. The normalized sorption coefficient increased with the equilibrium concentration decreased in the biochar amended soil, which indicated the sorption performance will be better due to the low atrazine concentration in practice. Results showed that biochar amendment is the effective way to prevent leakage of diffuse herbicide loss. PMID:26852289

  7. Neptunium and Plutonium Sorption to Snake River Plain, Idaho Soil

    SciTech Connect

    Mincher, Bruce Jay; Fox, Robert Vincent; Cooper, David Craig; Groenewold, Gary Steven

    2003-07-01

    The behavior of Np and Pu on soil collected from the subsurface disposal area at the Idaho National Engineering and Environmental Laboratory was investigated by performing short-duration, sorption experiments to measure sorption isotherms. Neptunium sorption can be described with a Freundlich isotherm; however, Pu sorption can only be described in this fashion as a conservative estimate of minimum sorption. Geochemical modeling predictions suggest that initial sorption of Np is controlled predominantly by surface complexation on clay minerals, while Pu is controlled by a competition between complexation with iron oxyhydroxides and the precipitation of hydrolysis products. Longer-term sorption is governed by the transformation of these species to oxide minerals. Solution ionic strength and carbonate alkalinity did not significantly affect Np or Pu soil sorption.

  8. Sorption kinetics of Cs and Sr in sediments of a Savannah River Site reservoir

    SciTech Connect

    Stephens, J.A.

    1997-07-01

    Laboratory measurements of the sorption and desorption of {sup 134}Cs and {sup 85}Sr to sediments were conducted. These sediments were sampled from the profundal zone of Par Pond at the Savannah River Site, Aiken, South Carolina. The isotopes {sup 134}Cs and {sup 85}Sr were used to trace the sorption properties of the main contaminants found in the reservoir which are {sup 137}Cs and {sup 90}Sr respectively. The sorption behavior of these two elements was studied using spiked sediment/water slurries of a known mass to volume ratio. The results reveal that Sr undergoes significant reversible sorption while a fraction of Cs irreversibly sorbs to the sediment. The calculated distribution coefficient Kd at equilibrium was (3 {+-} 0.6) x 10{sup 3} for {sup 134}Cs after 60 d and (1 {+-} 0.2) x 10{sup 3} for {sup 85}Sr after 7 d at pH {approx} 6 and slurry ratio of 1:1000 g/ml. The K{sub d} for {sup 134}Cs ranged from 2 x 10{sup 2} to 3 x 10{sup 4} depending on pH and conductivity. The {sup 85}Sr reached equilibrium in a few days, while {sup 134}Cs reached an apparent equilibrium in 1--2 months. The K{sub d} for {sup 134}Cs was a function of the slurry ratio, pH, conductivity, and contact time. These factors were interrelated since the sediments released ions to the slurry mixture which decreased the pH and increased the conductivity. A sorption isotherm measured for {sup 134}Cs was linear at water concentrations from 60 mBq/ml to 20 Bq/ml. A kinetic model was proposed to describe the basic sorption of {sup 134}Cs to Par Pond sediments under homogeneous laboratory conditions.

  9. Sorption kinetic studies of ammonium from aqueous solution on different inorganic and organic media.

    PubMed

    Kucić, Dajana; Cosić, Ivana; Vuković, Marija; Briski, Felicita

    2013-01-01

    In this study, the sorption of ammonium from aqueous solution onto activated carbon, natural zeolite, peat and potting soil was studied by performing batch kinetic sorption experiments. The activated carbon wasn't efficiently removing ammonium at concentrations higher than 50 mg L(-1). Sorption isotherms of ammonium on zeolite, peat and potting soil were determined at 25 degrees C and 200 rpm with the initial concentration of 50-7000 mg L(-1). Equilibrium data were fitted by Freundlich, Langmuir and Temkin isotherm and parameters were evaluated according these models. Langmuir model gives better fit to experimental data than Freundlich and Temkin models. Maximum adsorption capacities were for activated carbon 0.631 mg g(-1), zeolite 58 mg g(-1), peat 595 mg g(-1) and for potting soil 575 mg g(-1). The equilibrium kinetic data were analyzed using adsorption kinetic models: the pseudo-first and second-order equations and were found to follow the pseudo-second-order kinetic model. A comparison between linear and non-linear regression method for estimating the adsorption and kinetics parameters was examined. The obtained results showed that non-linear method may be a better way to determine the kinetic parameters. Thermodynamic studies showed exothermic and endothermic nature of the adsorption of NH4(+) on inorganic and organic adsorbents, respectively. From present results it can be seen that zeolite, peat and potting soil are good adsorbents for removal ammonium from aqueous solution.

  10. Sorption of bentazone, dichlorprop, MCPA, and propiconazole in reference soils from Norway.

    PubMed

    Thorstensen, C W; Lode, O; Eklo, O M; Christiansen, A

    2001-01-01

    Sorption-desorption kinetic and isotherm studies were performed by the batch equilibrium technique in three Norwegian soils. The soils were a fine sandy loam, a loam, and a soil of highly decomposed organic material. Two commercially formulations were used, Triagran-P and Tilt, containing either a mixture of bentazone [3-isopropyl-1H-2, 1,3-benzothiadiazin-4(3H)-one 2,2-dioxide], dichlorprop [(R)-2-(2, 4-dichlorophenoxy)-propionic acid], and MCPA [(4-chloro-2-methylphenoxy)acetic acid], or propiconazole [(+/-)1-(2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl)-1H-1,2,4-triazole] alone. Sorption-desorption equilibrium occurred within 10 h for all pesticides. The Freundlich isotherms indicated nonlinear sorption of bentazone, dichlorprop, MCPA, and propiconazole. For all pesticides the highest Freundlich adsorption coefficient (K(F)) values were in the soil with highest organic content and lowest pH. For the fine sandy loam and loam, which are representative Norwegian agricultural soils, the results indicate that bentazone, dichlorprop, and MCPA are mobile with KF values ranging from 0.07 to 1.50 mg1-1/n kg(-1) L1/n. Propiconazole is much less mobile with KF values ranging from 27.00 to 36.02 mg1-1/n kg(-1) L1/n in the agricultural soils.

  11. Thermodynamics of imidacloprid sorption in Croatian soils

    NASA Astrophysics Data System (ADS)

    Milin, Čedomila; Broznic, Dalibor

    2015-04-01

    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

  12. Thermodynamics of Water Sorption in High Performance Glassy Thermoplastic Polymers

    NASA Astrophysics Data System (ADS)

    Mensitieri, Giuseppe; Scherillo, Giuseppe; Petretta, Mauro; Galizia, Michele; La Manna, Pietro; Musto, Pellegrino

    2014-05-01

    Sorption thermodynamics of water in two glassy polymers, polyetherimide (PEI) and polyetheretherketone (PEEK), is investigated by coupling gravimetry and on line FTIR spectroscopy in order to gather information on the total amount of sorbed water as well as on the different species of water molecules absorbed within the polymers, addressing the issue of cross- and self-interactions occurring in the polymer/water systems. Water sorption isotherms have been determined at temperatures ranging fro 30 to 70°C while FTIR spectroscopy has been performed only at 30°C. The experimental analysis provided information on the groups present on the polymer backbones involved in hydrogen bonding interactions with absorbed water molecules. Moreover, it also supplied qualitative indications about the different’populations’ of water molecules present within the PEEK and a quantitative assessment of these ‘populations’ in the case of PEI.The results of the experimental analysis have been interpreted using an equation of state theory based on a compressible lattice fluid model for the Gibbs energy of the polymer-water mixture, developed by extending to the case of out of equilibrium glassy polymers a previous model intended for equilibrium rubbery polymers. The model accounts for the non equilibrium nature of glassy poymers as well as for mean field and for hydrogen bonding interactions, providing a satisfactory quantitative interpretation of the experimental data.

  13. Influence of soil properties on heavy metal sequestration by biochar amendment: 2. Copper desorption isotherms.

    PubMed

    Uchimiya, Minori; Klasson, K Thomas; Wartelle, Lynda H; Lima, Isabel M

    2011-03-01

    Contaminant desorption constrains the long-term effectiveness of remediation technologies, and is strongly influenced by dynamic non-equilibrium states of environmental and biological media. Information is currently lacking in the influence of biochar and activated carbon amendments on desorption of heavy metal contaminants from soil components. In this study, copper sorption-desorption isotherms were obtained for clay-rich, alkaline San Joaquin soil with significant heavy metal sorption capacity, and eroded, acidic Norfolk sandy loam soil having low capacity to retain copper. Acidic pecan shell-derived activated carbon and basic broiler litter biochar were employed in desorption experiments designed to address both leaching by rainfall and toxicity characteristics. For desorption in synthetic rain water, broiler litter biochar amendment diminished sorption-desorption hysteresis. In acetate buffer (pH 4.9), significant copper leaching was observed, unless acidic activated carbon (pH(pzc)=3.07) was present. Trends observed in soluble phosphorus and zinc concentrations for sorption and desorption equilibria suggested acid dissolution of particulate phases that can result in a concurrent release of copper and other sorbed elements. In contrast, sulfur and potassium became depleted as a result of supernatant replacements only when amended carbon (broiler litter biochar) or soil (San Joaquin) contained appreciable amounts. A positive correlation was observed between the equilibrium aluminum concentration and initial copper concentration in soils amended with acidic activated carbon but not basic biochar, suggesting the importance of cation exchange mechanism, while dissolution of aluminum oxides cannot be ruled out.

  14. EFFECTS OF BIOSOLIDS ON SORPTION AND DESORPTION BEHAVIOR OF CADMIUM IN BIOSOLIDS-AMENDED SOILS

    EPA Science Inventory

    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...

  15. USING METHANOL-WATER SYSTEMS TO INVESTIGATE PHENANTHRENE SORPTION-DESORPTION ON SEDIMENT

    EPA Science Inventory

    Sorption isotherm nonlinearity, sorption-desorption hysteresis, slow desorption kinetics, and other nonideal phenomena have been attributed to the differing sorptive characteristics of the natural organic matter (NOM) polymers associated with soils and sediments. A conceptualizat...

  16. Thermodynamics of cationic surfactant sorption onto natural clinoptilolite

    SciTech Connect

    Sullivan, E.J.; Bowman, R.S.; Carey, J.W.

    1998-10-15

    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.

  17. Abamectin in soils: Analytical methods, kinetics, sorption and dissipation.

    PubMed

    Dionisio, Andreza Camilotti; Rath, Susanne

    2016-05-01

    Abamectin is a broad-spectrum antiparasitic agent that has been widely employed in veterinary medicine and has also been used as a pesticide in agriculture. Veterinary drugs may reach the soil and may be transported to surface and ground waters, posing risks to terrestrial and aquatic organisms. Sorption, transformation and transport processes are primarily responsible for the fate of these substances in the environment. In this study, the sorption and the aerobic dissipation of abamectin in Brazilian soils (sand, clay and sandy-clay) were evaluated. For sorption studies, batch equilibrium experiments were performed. Sorption and desorption isotherms were fitted to the Freundlich model. Abamectin showed a high affinity to soil particles, with Freundlich sorption and desorption coefficients ranging from 44 to 138 μg(1-1/n) (cm(3))(1/n) g(-1) and from 89 to 236 μg(1-1/n) (cm(3))(1/n) g(-1), respectively. Dissipation of abamectin was evaluated in sterile and non-sterile soils in an aerobic and dark environment under controlled temperature and humidity. The time required for a 50% reduction of the amount of abamectin present in non-sterile soils was up to 4 days, and the time period for 90% dissipation was up to 12 days. In sterilized soils, there was no reduction in the concentration of abamectin over 37 days of exposure, suggesting that aerobic microbial degradation must have been the primary mechanism responsible for the dissipation of abamectin in soils. PMID:26923238

  18. Sorption of phenol and 4-chlorophenol onto pumice treated with cationic surfactant.

    PubMed

    Akbal, Feryal

    2005-02-01

    In this study the sorption of phenol and 4-chlorophenol on pumice modified with the cationic surfactants hexadecyltrimethyl ammonium bromide (HDTMA) and benzyldimethyl tetradecylammonium chloride (BDTDA) was investigated. Experimental studies indicate that HDTMA-pumice and BDTDA-pumice have the capability to remove phenol and 4-chlorophenol from aqueous solution. The influence of initial concentration and adsorbent dosage was studied. The adsorption of phenol and 4-chlorophenol increased with increasing initial concentration and decreased with increasing amount of adsorbent used. The Freundlich adsorption isotherm was found to describe well the equilibrium adsorption data. The parameters of the Freundlich model have been determined using the adsorption data.

  19. Plutonium(IV) and (V) Sorption to Goethite at Sub-Femtomolar to Micromolar Concentrations: Redox Transformations and Surface Precipitation.

    PubMed

    Zhao, Pihong; Begg, James D; Zavarin, Mavrik; Tumey, Scott J; Williams, Ross; Dai, Zurong R; Kips, Ruth; Kersting, Annie B

    2016-07-01

    Pu(IV) and Pu(V) sorption to goethite was investigated over a concentration range of 10(-15)-10(-5) M at pH 8. Experiments with initial Pu concentrations of 10(-15) - 10(-8) M produced linear Pu sorption isotherms, demonstrating that Pu sorption to goethite is not concentration-dependent across this concentration range. Equivalent Pu(IV) and Pu(V) sorption Kd values obtained at 1 and 2-week sampling time points indicated that Pu(V) is rapidly reduced to Pu(IV) on the goethite surface. Further, it suggested that Pu surface redox transformations are sufficiently rapid to achieve an equilibrium state within 1 week, regardless of the initial Pu oxidation state. At initial concentrations >10(-8) M, both Pu oxidation states exhibited deviations from linear sorption behavior and less Pu was adsorbed than at lower concentrations. NanoSIMS and HRTEM analysis of samples with initial Pu concentrations of 10(-8) - 10(-6) M indicated that Pu surface and/or bulk precipitation was likely responsible for this deviation. In 10(-6) M Pu(IV) and Pu(V) samples, HRTEM analysis showed the formation of a body centered cubic (bcc) Pu4O7 structure on the goethite surface, confirming that reduction of Pu(V) had occurred on the mineral surface and that epitaxial distortion previously observed for Pu(IV) sorption occurs with Pu(V) as well. PMID:27268262

  20. Isothermal Calorimeter

    NASA Technical Reports Server (NTRS)

    Rowlette, John J.

    1990-01-01

    Pressure-feedback signal indicates rate of heating. Improved isothermal calorimeter measures rate of heating in object under test. Called "isothermal" because chamber holding object and its environment maintained at or near constant temperature to minimize spurious tranfers of heat introducing errors into measurements. When item under test generates heat, rate of boiling and pressure in inner chamber increase. Servo-valve opens wider to maintain preset differential pressure. Valve-control voltage used as measure of rate of heating.

  1. Removal of Direct Red 12B by garlic peel as a cheap adsorbent: Kinetics, thermodynamic and equilibrium isotherms study of removal

    NASA Astrophysics Data System (ADS)

    Asfaram, A.; Fathi, M. R.; Khodadoust, S.; Naraki, M.

    2014-06-01

    The removal of dyes from industrial waste is very important from health and hygiene point of view and for environmental protection. In this work, efficiency and performance of garlic peel (GP) adsorbent for the removal of Direct Red 12B (DR12B) from wastewater was investigated. The influence of variables including pH, concentration of the dye and amount of adsorbent, particle size, contact time and temperature on the dye removal has been investigated. It was observed that the pseudo-second-order kinetic model fits better with good correlation coefficient and the equilibrium data fitted well with the Langmuir model. More than 99% removal efficiency was obtained within 25 min at adsorbent dose of 0.2 g per 50 ml for initial dye concentration of 50 mg L-1. Calculation of various thermodynamic parameters such as, Gibb's free energy, entropy and enthalpy of the on-going adsorption process indicate feasibility and endothermic nature of DR12B adsorption.

  2. Freundlich and dual Langmuir isotherm models for predicting 137Cs binding on Savannah River Site soils.

    PubMed

    Goto, Momoko; Rosson, Robert; Wampler, J Marion; Elliott, W Crawford; Serkiz, Steven; Kahn, Bernd

    2008-01-01

    Distribution of 137Cs and stable cesium between aqueous solution and near-surface soil samples from five locations at the Savannah River Site was measured in order to develop a predictive model for 137Cs uptake by the soils. Sorption of 137Cs in these soils appears to be mostly by hydroxy-interlayered vermiculite. Batch sorption studies with 4 d for equilibration were conducted at three cesium concentrations and at two backing electrolyte (NaNO3) concentrations. The soil-solution mixtures were pH-adjusted to evaluate the effects of pH on cesium sorption. Sorbed cesium was related to the equilibrium aqueous cesium concentrations by a Freundlich isotherm model. Model fits on logarithmic scales have a common slope of 0.60 +/- 0.03 for acidic mixtures and 0.69 +/- 0.04 for neutralized mixtures but have unique intercepts that are influenced by backing electrolyte concentration and pH. An ion-exchange model is proposed that pertains to all five soils and relates the Freundlich isotherms to the cation exchange capacity of soil and the aqueous concentrations of cesium, sodium, and a third ionic species that was hydrogen in the acidic mixtures and potassium in the neutralized mixtures. Model fits are consistent with Kd values in the entire range of 5-2,300 L kg(-1) determined for the five soil types. As an alternate model, dual Langmuir isotherms were fitted to the data. The results suggest cesium sorption by (1) relatively few interlayer-wedge sites, highly selective for cesium, and (2) much more abundant but less selective sites on internal and external planar surfaces.

  3. Equilibrium uptake, sorption dynamics, process optimization, and column operations for the removal and recovery of malachite green from wastewater using activated carbon and activated slag

    SciTech Connect

    Gupta, V.K.; Srivastava, S.K.; Mohan, D.

    1997-06-01

    The waste slurry generated in fertilizer plants and slag (blast furnace waste) have been converted into low-cost adsorbents, activated carbon and activated slag, respectively, and these are utilized for the removal of malachite green (a basic dye) from wastewater. In the batch experiments, parameters studied include the effect of pH, sorbent dosage, adsorbate concentration, temperature, and contact time. Kinetic studies have been performed to have an idea of the mechanistic aspects and to obtain the thermodynamic parameters of the process. The uptake of the dye is greater on carbonaceous material than on activated slag. Sorption data have been correlated with both Langmuir and Freundlich adsorption models. The presence of anionic surfactants does not affect the uptake of dye significantly. The mass transfer kinetic approach has been applied for the determination of various parameters necessary for the designing of fixed-bed contactors. Chemical regeneration has been achieved with acetone in order to recover the loaded dye and restore the column to its original capacity without dismantling the same.

  4. Water adsorption isotherms of carboxymethyl cellulose, guar, locust bean, tragacanth and xanthan gums.

    PubMed

    Torres, María D; Moreira, Ramón; Chenlo, Francisco; Vázquez, María J

    2012-06-20

    Water adsorption isotherms of carboxymethyl cellulose (CMC), guar gum (GG), locust bean gum (LBG), tragacanth gum (TG) and xanthan gum (XG) were determined at different temperatures (20, 35, 50, and 65°C) using a gravimetric method. Several saturated salt solutions were selected to obtain different water activities in the range from 0.09 to 0.91. Water adsorption isotherms of tested hydrocolloids were classified like type II isotherms. In all cases, equilibrium moisture content decreased with increasing temperature at each water activity value. Three-parameter Guggenheim-Anderson-de Boer (GAB) model was employed to fit the experimental data in the water activity range and statistical analysis indicated that this model gave satisfactory results. CMC and GG were the most and the least hygroscopic gums, respectively. Sorption heats decreased with increasing moisture content. Monolayer moisture content evaluated with GAB model was consistent with equilibrium conditions of maximum stability calculated from thermodynamic analysis of net integral entropy. Values of equilibrium relative humidity at 20°C are proposed to storage adequately the tested gums.

  5. Effects of plasticizers on sorption and optical properties of gum cordia based edible film.

    PubMed

    Haq, Muhammad Abdul; Jafri, Feroz Alam; Hasnain, Abid

    2016-06-01

    The present study aimed to characterize a biodegradable film produced from the polysaccharide of an indigenous plant Cordia myxa. Effect of plasticizer type (Glycerol, Sorbitol, PEG200 and PEG 400) and concentration (0-30 %) was studied on sorption and optical properties of the casted film. Increase in plasticizer concentration resulted in increase in equilibrium moisture content of the film and was supported by GAB model of sorption indicating that isotherms were of Type II. The monolayer value increased with the increase in plasticizer concentration with a peak of 0.93 g.g-1 for glycerol. Addition of plasticizers improved the total color (ΔE) with glycerol showing the highest effects. All films showed resistance to UV light in the range of 280-200 nm. The polysaccharide of the fruit of C.myxa can be used to prepare an edible film with improved properties as compared to other available edible coatings. PMID:27478216

  6. Reversibility of strontium sorption on fracture fillings

    SciTech Connect

    Cui, D.; Eriksen, T.E.

    1995-12-31

    Granite has been chosen by several countries as a major candidate for deep geologic disposal of radioactive waste. The authors have carried out a comparative study of sorption and desorption of strontium in groundwater on separated size and magnetic fractions of fracture fillings from deep granite. Complete reversibility of the sorption process was demonstrated by identical Freundlich isotherms, isotopic exchangeability and pH dependence of the distribution coefficient R{sub d}.

  7. Enhanced fluoride sorption by mechanochemically activated kaolinites.

    PubMed

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

    2008-05-01

    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.

  8. SORPTION ON WASTEWATER SOLIDS: ELIMINATION OF BIOLOGICAL ACTIVITY

    EPA Science Inventory

    Sorption was found to be greatly affected by the biological activity in wastewater solids. wo experimental techniques, cyanide treatment and pasteurization, were developed for eliminating the biological activity during isotherm measurements. oth methods are effective; however, pa...

  9. Effect of solution ionic strength and iron coatings on mineral grains on the sorption of bacterial cells to quartz sand.

    PubMed

    Mills, A L; Herman, J S; Hornberger, G M; Dejesús, T H

    1994-09-01

    Understanding the interaction between bacterial cells and solid surfaces is essential to our attempts to quantify and predict the transport of microbes in groundwater aquifers, whether from the point of view of contamination or from that of bioremediation. The sorption of bacterial cells suspended in groundwater to porous medium grains was examined in batch studies. Bacterial sorption to clean quartz sand yielded equilibrium, linear, adsorption isotherms that varied with the bacterial strain used and the ionic strength of the aqueous solution. Values of K(d) (the slope of the linear sorption isotherm) ranged from 0.55 to 6.11 ml g, with the greatest sorption observed for the highest groundwater ionic strength. These findings are consistent with the interpretation that an increasingly compressed electrical double layer results in stronger adsorption between the like-charged mineral surface and the bacterial cells. When iron-oxyhydroxide-coated sand was used, however, all of the added bacteria were adsorbed up to a threshold of 6.93 x 10 cells g of coated sand, beyond which no further adsorption occurred. The irreversible, threshold adsorption is the result of a strong electrostatic attraction between the sesquioxide coating and the bacterial cells. Experimental results of adsorption in mixtures of quartz and Fe(III)-coated sand were successfully predicted by a simple additive model for sorption by the two substrate phases. Even small amounts of Fe(III)-coated sand in a mixture influenced the extent of adsorption of bacterial cells. A quantitative description of adsorption in the mixtures can be realized by using a linear isotherm for reversible adsorption to the quartz grains with a y intercept that represents the number of cells irreversibly adsorbed to the Fe(III)-coated sand.

  10. Simultaneous sorption and mechanical entrapment during polymer flow through porous media

    NASA Astrophysics Data System (ADS)

    Farajzadeh, R.; Bedrikovetsky, P.; Lotfollahi, M.; Lake, L. W.

    2016-03-01

    Physical adsorption and mechanical entrapment are two major causes of polymer retention in porous media. Physical adsorption is considered an equilibrium process and is often modeled by assuming a Langmuir isotherm. The outcome is a steady state pressure response because the permeability reduction is also accounted for by adsorption. However, some experimental data show gradual increase of pressure with time, implying that polymer retention is a time-dependent process. We discuss simultaneous effect of sorption and mechanical entrapment on the polymer retention in porous media. An exact solution for 1-D flow problem for the case of constant filtration coefficient and Langmuir-sorption isotherm, including explicit formulae for breakthrough concentration and pressure drop across the core is derived. The general model with a varying filtration coefficient was successfully matched with experimental data confirming the occurrence of simultaneous sorption with deep-bed filtration during polymer flow in porous media. In the absence of mechanical entrapment, the physical adsorption causes delay in the polymer front and does not affect the polymer concentration behind the front. Addition of mechanical entrapment results in slow recovery of the injected concentration at the outlet (for a varying filtration coefficient) or reaching to a steady state concentration, which is only a fraction of the injected concentration (for a constant filtration coefficient). Accurate assessment and quantification of the polymer retention requires both pressure and effluent concentration data at the outlet of the porous medium.

  11. Advances in Understanding Sorption and Transport Processes Affecting the Fate of Environmental Pollutants in the Subsurface

    NASA Astrophysics Data System (ADS)

    Karapanagioti, H. K.; Werner, D.; Werth, C.

    2012-04-01

    The results of a call for a special issue that is now in press by the Journal of Contaminant Hydrology will be presented. This special issue is edited by the authors and is entitled "Sorption and Transport Processes Affecting the Fate of Environmental Pollutants in the Subsurface". A short abstract of each paper will be presented along with the most interesting results. Nine papers were accepted. Pollutants studied include: biocolloids, metals (arsenic, chromium, nickel), organic compounds such as hydrocarbons, chlorinated hydrocarbons, micropollutants (PAHs, PCBs), pesticides (glyphosate, 2,4-D). Findings presented in the papers include a modified batch reactor system to study equilibrium-reactive transport problems of metals. Column studies along with theoretical approximations evaluate the combined effects of grain size and pore water velocity on the transport in water saturated porous media of three biocolloids. A polluted sediment remediation method is evaluated considering site-specific conditions through monitoring results and modelling. A field study points to glogging and also sorption as mechanisms affecting the effectiveness of sub-surface flow constructed wetlands. A new isotherm model combining modified traditionally used isotherms is proposed that can be used to simulate pH-dependent metal adsorption. Linear free energy relationships (LFERs) demonstrate ability to predict slight isotope shifts into the groundwater due to sorption. Possible modifications that improve the reliability of kinetic models and parameter values during the evaluation of experiments that assess the sorption of pesticides on soils are tested. Challenges in selecting groundwater pollutant fate and transport models that account for the effect of grain-scale sorption rate limitations are evaluated based on experimental results and are discussed based on the Damköhler number. Finally, a thorough review paper presents the impact of mineral micropores on the transport and fate of

  12. Removal of divalent heavy metals (Cd, Cu, Pb, and Zn) and arsenic(III) from aqueous solutions using scoria: kinetics and equilibria of sorption.

    PubMed

    Kwon, Jang-Soon; Yun, Seong-Taek; Lee, Jong-Hwa; Kim, Soon-Oh; Jo, Ho Young

    2010-02-15

    Kinetic and equilibrium sorption experiments were conducted on removal of divalent heavy metals (Pb(II), Cu(II), Zn(II), Cd(II)) and trivalent arsenic (As(III)) from aqueous solutions by scoria (a vesicular pyroclastic rock with basaltic composition) from Jeju Island, Korea, in order to examine its potential use as an efficient sorbent. The removal efficiencies of Pb, Cu, Zn, Cd, and As by the scoria (size=0.1-0.2mm, dose=60gL(-1)) were 94, 70, 63, 59, and 14%, respectively, after a reaction time of 24h under a sorbate concentration of 1mM and the solution pH of 5.0. A careful examination on ionic concentrations in sorption batches suggested that sorption behaviors of heavy metals onto scoria are mainly controlled by cation exchange. On the other hand, arsenic appeared to be sensitive to specific sorption onto hematite (a minor constituent of scoria). Equilibrium sorption tests indicated that the removal efficiency for heavy metals increases with increasing pH of aqueous solutions, which is resulted from precipitation as hydroxides. Similarly, multi-component systems containing heavy metals and arsenic showed that the arsenic removal increases with increasing pH of aqueous solutions, which can be attributed to coprecipitation with metal hydroxides. The empirically determined sorption kinetics were well fitted to a pseudo-second order model, while equilibrium sorption data for heavy metals and arsenic onto scoria were consistent with the Langmuir and Freundlich isotherms, respectively. Natural scoria studied in this work is an efficient sorbent for concurrent removal of divalent heavy metals and arsenic.

  13. Kinetics and equilibrium adsorption of nano-TiO 2 particles on synthetic biofilm

    NASA Astrophysics Data System (ADS)

    Sahle-Demessie, Endalkachew; Tadesse, Haregewine

    2011-07-01

    Understanding the environmental behavior of nanoparticles includes their interaction with biofilms, which is a covering on the surface of a living or nonliving substrate composed of microorganisms. This study focuses on nano-TiO2 sorption mechanism by synthetic biofilm that was prepared as superporous spherical beads from agarose, using batch stirred flasks kept at room temperature. The pH plays an important part in these phenomena, by its influence on the nanoparticles and biofilm chemistry, where the biofilm nanoTiO2 uptake at neutral pH was enhanced over acidic conditions. Hydroxylation of TiO2 nanoparticles, dependent on pH and the salinity of the solution, influences the stability of colloids, the sorption kinetics via the nature of limiting phases: diffusion through the boundary layer or intrabiofilm mass transfer and the sorption mechanism. The sorption follows pseudo first-order adsorption kinetics with estimated average rate constants of 2.2 (min- 1). Equilibrium isotherms were evaluated using Langmuir and Freundlich isotherms to obtain the maximum uptake at different solution pH and the free energy of the adsorption. The adsorption is apparently irreversible because biofilm limits diffusion of particles out of the pores and the complexation active binding sites on the surface hydrated biofilm to the hydrophilic TiO2 nanoparticles.

  14. Heterogeneous carbonaceous matter in sedimentary rock lithocomponents causes significant trichloroethylene (TCE) sorption in a low organic carbon content aquifer/aquitard system.

    PubMed

    Choung, Sungwook; Zimmerman, Lisa R; Allen-King, Richelle M; Ligouis, Bertrand; Feenstra, Stanley

    2014-10-15

    This study evaluated the effects of heterogeneous thermally altered carbonaceous matter (CM) on trichloroethylene (TCE) sorption for a low fraction organic carbon content (foc) alluvial sedimentary aquifer and aquitard system (foc=0.046-0.105%). The equilibrium TCE sorption isotherms were highly nonlinear with Freundlich exponents of 0.46-0.58. Kerogen+black carbon was the dominant CM fraction extracted from the sediments and accounted for >60% and 99% of the total in the sands and silt, respectively. Organic petrological examination determined that the kerogen included abundant amorphous organic matter (bituminite), likely of marine origin. The dark calcareous siltstone exhibited the greatest TCE sorption among aquifer lithocomponents and accounted for most sorption in the aquifer. The results suggest that the source of the thermally altered CM, which causes nonlinear sorption, was derived from parent Paleozoic marine carbonate rocks that outcrop throughout much of New York State. A synthetic aquifer-aquitard unit system (10% aquitard) was used to illustrate the effect of the observed nonlinear sorption on mass storage potential at equilibrium. The calculation showed that >80% of TCE mass contained in the aquifer was sorbed on the aquifer sediment at aqueous concentration <1000 μgL(-1). These results show that sorption is likely a significant contributor to the persistence of a TCE groundwater plume in the aquifer studied. It is implied that sorption may similarly contribute to TCE persistence in other glacial alluvial aquifers with similar geologic characteristics, i.e., comprised of sedimentary rock lithocomponents that contain thermally altered CM.

  15. Heterogeneous carbonaceous matter in sedimentary rock lithocomponents causes significant trichloroethylene (TCE) sorption in a low organic carbon content aquifer/aquitard system.

    PubMed

    Choung, Sungwook; Zimmerman, Lisa R; Allen-King, Richelle M; Ligouis, Bertrand; Feenstra, Stanley

    2014-10-15

    This study evaluated the effects of heterogeneous thermally altered carbonaceous matter (CM) on trichloroethylene (TCE) sorption for a low fraction organic carbon content (foc) alluvial sedimentary aquifer and aquitard system (foc=0.046-0.105%). The equilibrium TCE sorption isotherms were highly nonlinear with Freundlich exponents of 0.46-0.58. Kerogen+black carbon was the dominant CM fraction extracted from the sediments and accounted for >60% and 99% of the total in the sands and silt, respectively. Organic petrological examination determined that the kerogen included abundant amorphous organic matter (bituminite), likely of marine origin. The dark calcareous siltstone exhibited the greatest TCE sorption among aquifer lithocomponents and accounted for most sorption in the aquifer. The results suggest that the source of the thermally altered CM, which causes nonlinear sorption, was derived from parent Paleozoic marine carbonate rocks that outcrop throughout much of New York State. A synthetic aquifer-aquitard unit system (10% aquitard) was used to illustrate the effect of the observed nonlinear sorption on mass storage potential at equilibrium. The calculation showed that >80% of TCE mass contained in the aquifer was sorbed on the aquifer sediment at aqueous concentration <1000 μgL(-1). These results show that sorption is likely a significant contributor to the persistence of a TCE groundwater plume in the aquifer studied. It is implied that sorption may similarly contribute to TCE persistence in other glacial alluvial aquifers with similar geologic characteristics, i.e., comprised of sedimentary rock lithocomponents that contain thermally altered CM. PMID:25168960

  16. Sorption equilibria of ethanol on cork.

    PubMed

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

    2013-06-01

    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.

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

    PubMed Central

    Jagadamma, Sindhu; Mayes, Melanie A.; Phillips, Jana R.

    2012-01-01

    Background Physico-chemical sorption onto soil minerals is one of the major processes of dissolved organic carbon (OC) stabilization in deeper soils. The interaction of DOC on soil solids is related to the reactivity of soil minerals, the chemistry of sorbate functional groups, and the stability of sorbate to microbial degradation. This study was conducted to examine the sorption of diverse OC compounds (D-glucose, L-alanine, oxalic acid, salicylic acid, and sinapyl alcohol) on temperate climate soil orders (Mollisols, Ultisols and Alfisols). Methodology Equilibrium batch experiments were conducted using 0–100 mg C L−1 at a solid-solution ratio of 1∶60 for 48 hrs on natural soils and on soils sterilized by γ-irradiation. The maximum sorption capacity, Qmax and binding coefficient, k were calculated by fitting to the Langmuir model. Results Ultisols appeared to sorb more glucose, alanine, and salicylic acid than did Alfisols or Mollisols and the isotherms followed a non-linear pattern (higher k). Sterile experiments revealed that glucose and alanine were both readily degraded and/or incorporated into microbial biomass because the observed Qmax under sterile conditions decreased by 22–46% for glucose and 17–77% for alanine as compared to non-sterile conditions. Mollisols, in contrast, more readily reacted with oxalic acid (Qmax of 886 mg kg−1) and sinapyl alcohol (Qmax of 2031 mg kg−1), and no degradation was observed. The reactivity of Alfisols to DOC was intermediate to that of Ultisols and Mollisols, and degradation followed similar patterns as for Ultisols. Conclusion This study demonstrated that three common temperate soil orders experienced differential sorption and degradation of simple OC compounds, indicating that sorbate chemistry plays a significant role in the sorptive stabilization of DOC. PMID:23209742

  18. Linearity of iodine sorption and sorption capacities for seven soils

    SciTech Connect

    Sheppard, M.I.; Hawkins, J.L.; Smith, P.A.

    1996-11-01

    Iodine, a soluble and prevalent element in spent nuclear fuel and a pivotal element in the assessment of Canada`s nuclear fuel waste disposal option, sorbs to soils rich in organics and hydrous oxides. Biotic factors, such as microbes, enzymes and plant exudates, have been implicated in the retention of I to soils. Anion exchange of I{sup {minus}} or IO{sub 3}{sup {minus}} and chemical or biological oxidation to I{sub 2} followed by reactions with the soil organic matter are possible retention mechanisms. We have carried out sorption and desorption studies across a wide range of soil solution concentrations (10{sup {minus}7} to 10{sup 5} mg I/L, 10{sup {minus}12} to 1 M) for seven soils typical of upland and lowland soils of the Canadian Precambrian Shield. Soil solid-liquid partition values (K{sub d}), required for impact assessments, varied from 60 to 1800 L/kg and were significantly correlated with extractable Al oxide content, and background I and organic matter content. Freundlich isotherm fits show that sorption of I across our intentionally large concentration range is nonlinear; however, sorption of I across our intentionally large concentration range is nonlinear; however, sorption of I at environmental concentrations (<0.1 mg I/L soil solution) is linear and can be described by the K{sub d} model. Sorption of I was not related to peroxidase enzyme activity. Desorption percentages were small implying sorption was not easily reversed, even with a strong electrolyte, KNO{sub 3}. Desorption results and simple correlations of I sorption to soil properties suggest that the oxidation of I{sup {minus}} to I{sub 2} and complexation to organic functional groups or oxides are the major processes for I retention in Shield soils. 52 refs., 2 figs., 2 tabs.

  19. The sorption characteristics of mercury as affected by organic matter content and/or soil properties

    NASA Astrophysics Data System (ADS)

    Šípková, Adéla; Šillerová, Hana; Száková, Jiřina

    2014-05-01

    The determination and description of the mercury sorption extend on soil is significant for potential environmental toxic effects. The aim of this study was to assess the effectiveness of mercury sorption at different soil samples and vermicomposts. Mercury interactions with soil organic matter were studied using three soils with different physical-chemical properties - fluvisol, cambisol, and chernozem. Moreover, three different vermicomposts based on various bio-waste materials with high organic matter content were prepared in special fermentors. First was a digestate, second was represented by a mixture of bio-waste from housing estate and woodchips, and third was a garden bio-waste. In the case of vermicompost, the fractionation of organic matter was executed primarily using the resin SuperliteTM DAX-8. Therefore, the representation of individual fractions (humic acid, fulvic acid, hydrophilic compounds, and hydrophobic neutral organic matter) was known. The kinetics of mercury sorption onto materials of interest was studied by static sorption experiments. Samples were exposed to the solution with known Hg concentration of 12 mg kg-1 for the time from 10 minutes to 24 hours. Mercury content in the solutions was measured by the inductively coupled plasma mass spectrometry (ICP-MS). Based on this data, the optimum conditions for following sorption experiments were chosen. Subsequently, the batch sorption tests for all soil types and vermicomposts were performed in solution containing variable mercury concentrations between 1 and 12 mg kg-1. Equilibrium concentration values measured in the solution after sorption and calculated mercury content per kilogram of the soil or the vermi-compost were plotted. Two basic models of sorption isotherm - Langmuir and Freundlich, were used for the evaluation of the mercury sorption properties. The results showed that the best sorption properties from studied soil were identified in chernozem with highest cation exchange

  20. Competitive sorption of organic contaminants in chalk

    NASA Astrophysics Data System (ADS)

    Graber, E. R.; Borisover, M.

    2003-12-01

    In the Negev desert, Israel, a chemical industrial complex is located over fractured Eocene chalk formations where transfer of water and solutes between fracture voids and matrix pores affects migration of contaminants in the fractures due to diffusion into the chalk matrix. This study tests sorption and sorption competition between contaminants in the chalk matrix to make it possible to evaluate the potential for contaminant attenuation during transport in fractures. Single solute sorption isotherms on chalk matrix material for five common contaminants ( m-xylene, ametryn, 1,2-dichloroethane, phenanthrene, and 2,4,6-tribromophenol) were found to be nonlinear, as confirmed in plots of Kd versus initial solution concentration. Over the studied concentration ranges, m-xylene Kd varied by more than a factor of 100, ametryn Kd by a factor of 4, 1,2-dichloroethane Kd by more than a factor of 3, phenanthrene Kd by about a factor of 2, and 2,4,6-tribromophenol Kd by a factor of 10. It was earlier found that sorption is to the organic matter component of the chalk matrix and not to the mineral phases (Chemosphere 44 (2001) 1121). Nonlinear sorption isotherms indicate that there is at least some finite sorption domain. Bi-solute competition experiments with 2,4,6-tribromophenol as the competitor were designed to explore the nature of the finite sorption domain. All of the isotherms in the bi-solute experiments are more linear than in the single solute experiments, as confirmed by smaller variations in Kd as a function of initial solution concentration. For both m-xylene and ametryn, there is a small nonlinear component or domain that was apparently not susceptible to competition by 2,4,6-tribromophenol. The nonlinear sorption domain(s) is best expressed at low solution concentrations. Inert-solvent-normalized single and bi-solute sorption isotherms demonstrate that ametryn undergoes specific force interactions with the chalk sorbent. The volume percent of phenanthrene

  1. Sorption kinetics and leachability of heavy metal from the contaminated soil amended with immobilizing agent (humus soil and hydroxyapatite).

    PubMed

    Chaturvedi, Pranav Kumar; Seth, Chandra Shekhar; Misra, Virendra

    2006-08-01

    Release of heavy metals onto the soil as a result of agricultural and industrial activities may pose a serious threat to the environment. This study investigated the kinetics of sorption of heavy metals on the non-humus soil amended with (1:3) humus soil and 1% hydroxyapatite used for in situ immobilization and leachability of heavy metals from these soils. For this, a batch equilibrium experiment was performed to evaluate metal sorption in the presence of 0.05 M KNO(3) background electrolyte solutions. The Langmuir isotherms applied for sorption studies showed that the amount of metal sorbed on the amended soil decreased in the order of Pb(2+)>Zn(2+)>Cd(2+). The data suggested the possibility of immobilization of Pb due to sorption process and immobilization of Zn and Cd by other processes like co-precipitation and ion exchange. The sorption kinetics data showed the pseudo-second-order reaction kinetics rather than pseudo-first-order kinetics. Leachability study was performed at various pHs (ranging from 3 to 10). Leachability rate was slowest for the Pb(2+) followed by Zn(2+) and Cd(2+). Out of the metal adsorbed on the soil only 6.1-21.6% of Pb, 7.3-39% of Zn and 9.3-44.3% of Cd leached out from the amended soil.

  2. Synthesis of assorted metal ions anchored alginate bentonite biocomposites for Cr(VI) sorption.

    PubMed

    Gopalakannan, Venkatrajan; Periyasamy, Soodamani; Viswanathan, Natrayasamy

    2016-10-20

    Biocomposites were synthesized by dispersing bentonite (Bent) clay in a biopolymer namely alginate (Alg) and cross-linked with bi (Ca(2+)), tri (Ce(3+)) and tetravalent (Zr(4+)) metal ions viz., Ca@AlgBent, Ce@AlgBent and Zr@AlgBent composites respectively. The synthesized biocomposites were characterized by various instrumental techniques like FTIR, SEM and EDAX. Cr(VI) sorption capacities (SCs) of the biocomposites Ca@AlgBent, Ce@AlgBent and Zr@AlgBent were examined by batch process. Various adsorption influencing factors viz., contact time, dosage of the sorbent, pH of the medium, temperature, presence of common co-ions and initial Cr(VI) concentration were studied. Freundlich, Langmuir and Dubinin-Radushkevich (D-R) isotherm models were adopted to examine the adsorption equilibrium. Kinetics of the sorption process was carried out by pseudo-first-order and pseudo-second-order models. The nature of the sorption process was explained using thermodynamic parameters like ΔS°, ΔG° and ΔH° and a possible mechanism for the sorption of Cr(VI) onto the biocomposites was given. The application of the biocomposites at field conditions was also examined by testing it with industrial water. The regeneration studies were carried to know about the reusability of the biocomposites.

  3. Synthesis of assorted metal ions anchored alginate bentonite biocomposites for Cr(VI) sorption.

    PubMed

    Gopalakannan, Venkatrajan; Periyasamy, Soodamani; Viswanathan, Natrayasamy

    2016-10-20

    Biocomposites were synthesized by dispersing bentonite (Bent) clay in a biopolymer namely alginate (Alg) and cross-linked with bi (Ca(2+)), tri (Ce(3+)) and tetravalent (Zr(4+)) metal ions viz., Ca@AlgBent, Ce@AlgBent and Zr@AlgBent composites respectively. The synthesized biocomposites were characterized by various instrumental techniques like FTIR, SEM and EDAX. Cr(VI) sorption capacities (SCs) of the biocomposites Ca@AlgBent, Ce@AlgBent and Zr@AlgBent were examined by batch process. Various adsorption influencing factors viz., contact time, dosage of the sorbent, pH of the medium, temperature, presence of common co-ions and initial Cr(VI) concentration were studied. Freundlich, Langmuir and Dubinin-Radushkevich (D-R) isotherm models were adopted to examine the adsorption equilibrium. Kinetics of the sorption process was carried out by pseudo-first-order and pseudo-second-order models. The nature of the sorption process was explained using thermodynamic parameters like ΔS°, ΔG° and ΔH° and a possible mechanism for the sorption of Cr(VI) onto the biocomposites was given. The application of the biocomposites at field conditions was also examined by testing it with industrial water. The regeneration studies were carried to know about the reusability of the biocomposites. PMID:27474660

  4. Sorption of chromium(VI) from aqueous solution by cassava (Manihot sculenta Cranz.) waste biomass.

    PubMed

    Horsfall, Michael; Ogban, Fred; Akporhonor, Eyitemi Emmanuel

    2006-02-01

    The sorption of highly toxic Cr(VI) ions by cassava waste biomass was quantitatively investigated. The sorption was found to be influenced by several physico-chemical factors such as agitation speed, temperature, contact time, pH, and sorbent/sorbate ratio. The adsorption data at equilibrium were fitted to Freundlich and Langmuir isotherms. The monolayer sorption capacity was found to be 61.79 mg of Cr(VI) per gram of biomass. The kinetics of Cr(VI) adsorption to pure cassava-tuber-bark wastes were determined based on a pseudo-second-order-rate model using the batch-sorption technique at a temperature of 30 degrees. The kinetics data suggest that the adsorption process is exothermic, and that the rate-limiting step is physisorption. Negative DeltaG(ads) values indicate that the adsorption is spontaneous and exothermic in nature. Also, under optimal conditions (in agitated 1M H(2)SO(4) at 30 degrees), the cassava waste biomass appears to be recyclable.

  5. Pectin-rich fruit wastes as biosorbents for heavy metal removal: equilibrium and kinetics.

    PubMed

    Schiewer, Silke; Patil, Santosh B

    2008-04-01

    Biosorption can be used as a cost effective and efficient technique for the removal of toxic heavy metals from wastewater. Waste materials from industries such as food processing and agriculture may act as biosorbents. This study investigates the removal of cadmium by fruit wastes (derived from several citrus fruits, apples and grapes). Citrus peels were identified as the most promising biosorbent due to high metal uptake in conjunction with physical stability. Uptake was rapid with equilibrium reached after 30-80 min depending on the particle size (0.18-0.9 mm). Sorption kinetics followed a second-order model. Sorption equilibrium isotherms could be described by the Langmuir model in some cases, whereas in others an S-shaped isotherm was observed, that did not follow the Langmuir isotherm model. The metal uptake increased with pH, with uptake capacities ranging between 0.5 and 0.9 meq/g of dry peel. Due to their low cost, good uptake capacity, and rapid kinetics, citrus peels are a promising biosorbent material warranting further study. PMID:17540559

  6. SORPTION OF ARSENATE AND ARSENITE ON RUO2.XH2O: A SPECTROSCOPIC AND MACROSCOPIC STUDY

    EPA Science Inventory

    The sorption of arsenate (As(V)) and arsenite (As(III)) on RuO2 xH2O was examined using macroscopic and microscopic techniques. Constant solid:solution ratio isotherms were constructed from batch sorption experiments to study the sorption of the inorganic arsenic species on RuO2...

  7. Fractionation of aquatic natural organic matter upon sorption to goethite and kaolinite

    USGS Publications Warehouse

    Meier, M.; Namjesnik-Dejanovic, K.; Maurice, P.A.; Chin, Y.-P.; Aiken, G.R.

    1999-01-01

    Natural organic matter (NOM) consists of a complex mixture of organic molecules; previous studies have suggested that preferential sorption of higher molecular weight, more hydrophobic, and more aromatic components may lead to fractionation of the NOM pool upon passage through porous media. Our work expands upon previous studies by quantifying the change in solution-phase weight average molecular weight (M(w)) upon sorption of bulk (rather than isolated) surface water NOM from the Suwannee River (SR) and the Great Dismal Swamp (GDS) to goethite and kaolinite at different sorption densities and at pH 4, 22??C. High pressure size exclusion chromatography (HPSEC) was used to quantify changes in M(w) upon sorption, and molar absorptivities at ?? = 280 nm were used to approximate changes in solution NOM aromaticity. Two SR water samples were used, with M(w) = 2320 and 2200 Da; a single GDS sample was used, with M(w) = 1890 Da. The SR NOM was slightly more hydrophobic and aromatic. These differences were reflected in greater sorption of SR NOM than GDS NOM. Both surface water NOMs showed a much greater affinity for goethite than for kaolinite. HPSEC analysis of the NOM remaining in solution after 24 h reaction time with geothite revealed that the largest changes in solution phase M(w)s (decreases by 900-1700 Da) occurred at relatively low equilibrium sorbate concentrations (approximately 5-20 mg C 1-1); the decrease in solution M(w) suggested that reactive surface sites were occupied disproportionately by large and intermediate size NOM moieties. At higher equilibrium NOM concentrations (>20 mg C 1-1), as percent adsorption decreased, M(w) in solution was similar to original samples. A smaller decrease in solution NOM M(w) (300-500 Da at 10-20 mg C 1-1 ~ 100 Da at > 20 mg) also occurred upon sorption to kaolinite. Overall, our results showed that factors (as related to NOM composition, clay mineral surface properties, and position along the sorption isotherm) which

  8. Sorption of strontium onto bacteriogenic iron oxides.

    PubMed

    Langley, Sean; Gault, Andrew G; Ibrahim, Alexandre; Takahashi, Yoshio; Renaud, Rob; Fortin, Danielle; Clark, Ian D; Ferris, F Grant

    2009-02-15

    Bacteriogenic iron oxides (BIOS) were obtained from a dilute, circumneutral groundwater seep, characterized with respect to mineralogy, and examined for their ability to sorb aqueous Sr2+. BIOS were composed of microbial sheaths encrusted in 2-line ferrihydrite. Sorption experiments indicated that Sr remained completely unbound at pH < 4.5, but sorption increased with increasing pH (maximum of 95% at pH > 7.6). EXAFS analysis of Sr-loaded BIOS failed to elucidate whether Sr sorption occurred on sites specific to the mineral or microbial fraction, but indicated that sorption likely occurred by outer-sphere complexation between BIOS and hydrated Sr2+. Sorption experiments showed that at low ionic strength (I = 0.001 M), sorption followed a Langmuir isotherm (S(max) = 3.41 mol Sr (g of Fe)(1-), K(ads) = 1.26). At higher ionic strength (I = 0.1 M), there was significant inhibition of Sr sorption (S(max) = 1.06 mol Sr (g of Fe)(1-), K(ads) = 1.23), suggesting that sorption to BIOS occurs by outer-sphere complexation. The results suggest that, under dilute circumneutral conditions, BIOS deposits should efficiently sorb dissolved Sr from groundwater flow systems where such deposits exist. This finding has particular relevance to sites impacted by radioactive 90Sr groundwater contamination. PMID:19320150

  9. Sorption of strontium onto bacteriogenic iron oxides.

    PubMed

    Langley, Sean; Gault, Andrew G; Ibrahim, Alexandre; Takahashi, Yoshio; Renaud, Rob; Fortin, Danielle; Clark, Ian D; Ferris, F Grant

    2009-02-15

    Bacteriogenic iron oxides (BIOS) were obtained from a dilute, circumneutral groundwater seep, characterized with respect to mineralogy, and examined for their ability to sorb aqueous Sr2+. BIOS were composed of microbial sheaths encrusted in 2-line ferrihydrite. Sorption experiments indicated that Sr remained completely unbound at pH < 4.5, but sorption increased with increasing pH (maximum of 95% at pH > 7.6). EXAFS analysis of Sr-loaded BIOS failed to elucidate whether Sr sorption occurred on sites specific to the mineral or microbial fraction, but indicated that sorption likely occurred by outer-sphere complexation between BIOS and hydrated Sr2+. Sorption experiments showed that at low ionic strength (I = 0.001 M), sorption followed a Langmuir isotherm (S(max) = 3.41 mol Sr (g of Fe)(1-), K(ads) = 1.26). At higher ionic strength (I = 0.1 M), there was significant inhibition of Sr sorption (S(max) = 1.06 mol Sr (g of Fe)(1-), K(ads) = 1.23), suggesting that sorption to BIOS occurs by outer-sphere complexation. The results suggest that, under dilute circumneutral conditions, BIOS deposits should efficiently sorb dissolved Sr from groundwater flow systems where such deposits exist. This finding has particular relevance to sites impacted by radioactive 90Sr groundwater contamination.

  10. Equilibrium, kinetic and thermodynamic studies of acid Orange 52 dye biosorption by Paulownia tomentosa Steud. leaf powder as a low-cost natural biosorbent.

    PubMed

    Deniz, Fatih; Saygideger, Saadet D

    2010-07-01

    The biosorption of Acid Orange 52 onto the leaf powder of Paulownia tomentosa Steud. was studied in a batch adsorption system to estimate the equilibrium, kinetic and thermodynamic parameters as a function of solution pH, biosorbent concentration, dye concentration, biosorbent size, temperature and contact time. The Langmuir, Freundlich and Temkin isotherm models were used for modeling the biosorption equilibrium. The experimental equilibrium data could be well interpreted by the Temkin and Langmuir isotherms with maximum adsorption capacity of 10.5 mg g(-1). In order to state the sorption kinetics, the fits of pseudo-first order, pseudo-second order, Elovich and intraparticle diffusion kinetic models were investigated. It was obtained that the biosorption process followed the pseudo-second order rate kinetics. Thermodynamic studies indicated that this system was exothermic process. The results revealed that P. tomentosa leaf powder could be an efficient biosorbent for the treatment of wastewater containing Acid Orange 52. PMID:20194017

  11. Unified water isotherms for clayey porous materials

    NASA Astrophysics Data System (ADS)

    Revil, A.; Lu, N.

    2013-09-01

    We provide a unified model for the soil-water retention function, including the effect of bound and capillary waters for all types of soils, including clayey media. The model combines a CEC-normalized isotherm describing the sorption of the bound water (and the filling of the trapped porosity) and the van Genuchten model to describe the capillary water sorption retention but ignore capillary condensation. For the CEC-normalized isotherm, we tested both the BET and Freundlich isotherms, and we found that the Freundlich is more suitable than the BET isotherm in fitting the data. It is also easier to combine the Freundlich isotherm with the van Genuchten model. The new model accounts for (1) the different types of clay minerals, (2) the different types of ions sorbed in the Stern layer and on the basal planes of 2:1 clays, and (3) the pore size distribution. The model is validated with different data sets, including mixtures of kaolinite and bentonite. The model parameters include two exponents (the pore size exponent of the van Genuchten model and the exponent of the Freundlich isotherm), the capillary entry pressure, and two critical water contents. The first critical water content is the water content at saturation (porosity), and the second is the maximum water content associated with adsorption forces, including the trapped nonbound water.

  12. Impact of long-term wastewater irrigation on sorption and transport of atrazine in Mexican agricultural soils.

    PubMed

    Müller, K; Duwig, C; Prado, B; Siebe, C; Hidalgo, C; Etchevers, J

    2012-01-01

    In the Mezquital Valley, Mexico, crops have been irrigated with untreated municipal wastewater for more than a century. Atrazine has been applied to maize and alfalfa grown in the area for weed control for 15 years. Our objectives were to analyse (i) how wastewater irrigation affects the filtering of atrazine, and (ii) if the length of irrigation has a significant impact. We compared atrazine sorption to Phaeozems that have been irrigated with raw wastewater for 35 (P35) and 85 (P85) years with sorption to a non-irrigated (P0) Phaeozem soil under rainfed agriculture. The use of bromide as an inert water tracer in column experiments and the subsequent analysis of the tracers' breakthrough curves allowed the calibration of the hydrodynamic parameters of a two-site non equilibrium convection-dispersion model. The quality of the irrigation water significantly altered the soils' hydrodynamic properties (hydraulic conductivity, dispersivity and the size of pores that are hydraulically active). The impacts on soil chemical properties (total organic carbon content and pH) were not significant, while the sodium adsorption ratio was significantly increased. Sorption and desorption isotherms, determined in batch and column experiments, showed enhanced atrazine sorption and reduced and slower desorption in wastewater-irrigated soils. These effects increased with the length of irrigation. The intensified sorption-desorption hysteresis in wastewater-irrigated soils indicated that the soil organic matter developed in these soils had fewer high-energy, easily accessible sorption sites available, leading to lower and slower atrazine desorption rates. This study leads to the conclusion that wastewater irrigation decreases atrazine mobility in the Mezquital valley Phaeozems by decreasing the hydraulic conductivity and increasing the soil's sorption capacity.

  13. Heterogeneity of chlorinated hydrocarbon sorption properties in a sandy aquifer.

    PubMed

    Zhao, Xianda; Wallace, Roger B; Hyndman, David W; Dybas, Michael J; Voice, Thomas C

    2005-08-01

    Hydraulic conductivity and sorption coefficients for chlorinated hydrocarbons (chloroform, carbon tetrachloride and tetrachloroethylene) were evaluated for 216 sediment samples collected across a 15 m transect and a 21 m depth interval in a contaminated aquifer near Schoolcraft, Michigan. Relationships between hydraulic conductivity, linear sorption partition coefficients, grain size classes, and spatial location were investigated using linear regression analysis and geostatistical techniques. Clear evidence of layering was found in sorption properties, hydraulic conductivity and grain sizes. Conductivity correlated well with grain size, as expected, but sorption varied inversely with grain size, contrary to some previous reports. No significant correlation was found between sorption properties and hydraulic conductivity. This is likely due to the unexpected presence of small amounts of highly sorptive coal-like solids, which dominate the sorption behavior but have little effect on conductivity. The results demonstrate that recent findings regarding the high sorption capacity of coal materials found in soils can exert a controlling influence on contaminant transport. Designers of in situ remediation systems should be cautioned that 1) it is not reasonable to assume that sorption capacity and hydraulic conductivity are related, 2) sorption capacity and hydraulic conductivity are critical measurements for contaminant site characterization and subsequent transport modeling, 3) estimating sorption capacity from organic carbon measurement may lead to greater errors than performing sorption isotherms, and 4) it is more important to characterize vertical heterogeneity rather than horizontal heterogeneity because both sorption and hydraulic conductivity are correlated across longer distances in the horizontal plane.

  14. Equilibrium and kinetic aspects of sodium cromoglycate adsorption on chitosan: mass uptake and surface charging considerations.

    PubMed

    de Lima, C R M; Pereira, M R; Fonseca, J L C

    2013-09-01

    Chitosan has more and more been suggested as a material for use as adsorbent in the treatment of effluents as well as in the synthesis of drug-loaded nanoparticles for controlled release. In both cases, a good understanding of the process of adsorption, both kinetically and in terms of equilibrium, has an importance of its own. In this manuscript we study the interaction between sodium cromoglycate, a drug used in asthma treatment, and chitosan. Equilibrium experiments showed that Sips (or Freundlich-Langmuir) isotherm described well the resultant data and adsorption possibly occurred as in multilayers. A model based on ordinary reaction-rate theory, compounded of two processes, each one with a correlated velocity constant, described the kinetics of sorption. Kinetic and equilibrium data suggested the possibility of surface rearrangement, favored by the increase of temperature.

  15. Sorption and Transport of Ranitidine in Natural Soils

    NASA Astrophysics Data System (ADS)

    Gaynor, A. J.; Vulava, V. M.

    2013-12-01

    Increasing levels of pharmaceuticals and their degradants are being discovered in natural water systems all over the world. These chemicals are reported to be discharged from wastewater treatment plants, sewage overflow, and leaking septic tanks. Ranitidine is an example of one such pharmaceutical chemical found in municipal drinking water, streams, and streambed sediments. It is a histamine H2-receptor antagonist, which inhibits the production of stomach acid and is commonly used to treat peptic ulcers and gastro esophageal reflux disease. Ranitidine is a complex organic compound; it is acidic, highly polar, and has two pKa values of approximately 8.2 and 2.7 because of the amine functional groups. When administered orally 25 - 30% of unchanged ranitidine has been shown to expel through urine. The objective of this research is to establish sorption and transport patterns of ranitidine in natural soils and to determine which soil properties influence these patterns the most. Laboratory experiments were preformed on A-horizon and B-horizon soil samples collected from the relatively undisturbed Francis Marion National Forest, a managed forest near Charleston, SC. The soils were characterized for chemical and physical properties: ranges of clay content = 6-20%, total organic content = 1-8%, and pH = 3.6-4.9. Kinetic reaction rates and equilibrium sorption isotherms were measured using batch experiments, whereas column experiments were used to quantify transport behavior. The reaction rates were -0.22/day and -0.33/day for organic-rich and clay-rich soils, respectively. The kinetic reaction rates were used to determine equilibration times for further equilibrium batch reactor experiments, which have soil solutions spiked with concentrations of ranitidine ranging from 0.1 mg/L to 100 mg/L. The concentration remaining in solution (C, mg/L) was plotted against the concentration in the soil (q, mg/kg) to create sorption isotherms. Ranitidine was more strongly sorbed to B

  16. Adsorption of Pb(II) ions from aqueous solution by native and activated bentonite: kinetic, equilibrium and thermodynamic study.

    PubMed

    Kul, Ali Riza; Koyuncu, Hülya

    2010-07-15

    In this study, the adsorption kinetics, equilibrium and thermodynamics of Pb(II) ions on native (NB) and acid activated (AAB) bentonites were examined. The specific surface areas, pore size and pore-size distributions of the samples were fully characterized. The adsorption efficiency of Pb(II) onto the NB and AAB was increased with increasing temperature. The kinetics of adsorption of Pb(II) ions was discussed using three kinetic models, the pseudo-first-order, the pseudo-second-order and the intra-particle diffusion model. The experimental data fitted very well the pseudo-second-order kinetic model. The initial sorption rate and the activation energy were also calculated. The activation energy of the sorption was calculated as 16.51 and 13.66 kJ mol(-1) for NB and AAB, respectively. Experimental results were also analysed by the Langmuir, Freundlich and Dubinin-Redushkevich (D-R) isotherm equations at different temperatures. R(L) separation factor for Langmuir and the n value for Freundlich isotherm show that Pb(II) ions are favorably adsorbed by NB and AAB. Thermodynamic quantities such as Gibbs free energy (DeltaG), the enthalpy (DeltaH) and the entropy change of sorption (DeltaS) were determined as about -5.06, 10.29 and 0.017 kJ mol(-1) K(-1), respectively for AAB. It was shown that the sorption processes were an endothermic reactions, controlled by physical mechanisms and spontaneously.

  17. Pyrolytic temperatures impact lead sorption mechanisms by bagasse biochars.

    PubMed

    Ding, Wenchuan; Dong, Xiaoling; Ime, Inyang Mandu; Gao, Bin; Ma, Lena Q

    2014-06-01

    The characteristics and mechanisms of Pb sorption by biochars produced from sugarcane bagasse at 250, 400, 500, and 600 °C were examined. The Pb sorption isotherms, kinetics and desorption were investigated. All biochars were effective in Pb sorption and were well described by Langmuir isotherm model and pseudo-second-order kinetic model. The maximum sorption capacity decreased from 21 to 6.1 mg g(-1) as temperature increased from 250 to 600 °C. The Pb sorption was rapid initially, probably controlled by cation exchange and complexation and then slowed down, which might be due to intraparticle diffusions. FTIR data and kinetic models suggested that oxygen functional groups were probably responsible for the high Pb sorption onto low temperature biochars (250 and 400 °C) whereas intraparticle diffusion was mainly responsible for low Pb sorption onto high temperature biochars (500 and 600 °C). Decreased phosphorus concentration indicated that P-induced Pb precipitation was also responsible for Pb sorption. Pyrolysis temperature significantly affected biochar properties and played an important role in Pb sorption capacity and mechanisms by biochars. PMID:24393563

  18. Sorption of triazoles to soil and iron minerals.

    PubMed

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

    2007-02-01

    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.

  19. Impact of Sequential Ammonia Fiber Expansion (AFEX) Pretreatment and Pelletization on the Moisture Sorption Properties of Corn Stover

    SciTech Connect

    Bonner, Ian J.; Thompson, David N.; Teymouri, Farzaneh; Campbell, Timothy; Bals, Bryan; Tumuluru, Jaya Shankar

    2015-05-01

    Combining ammonia fiber expansion (AFEX™) pretreatment with a depot processing facility is a promising option for delivering high-value densified biomass to the emerging bioenergy industry. However, because the pretreatment process results in a high moisture material unsuitable for pelleting or storage (40% wet basis), the biomass must be immediately dried. If AFEX pretreatment results in a material that is difficult to dry, the economics of this already costly operation would be at risk. This work tests the nature of moisture sorption isotherms and thin-layer drying behavior of corn (Zea mays L.) stover at 20°C to 60°C before and after sequential AFEX pretreatment and pelletization to determine whether any negative impacts to material drying or storage may result from the AFEX process. The equilibrium moisture content to equilibrium relative humidity relationship for each of the materials was determined using dynamic vapor sorption isotherms and modeled with modified Chung-Pfost, modified Halsey, and modified Henderson temperature-dependent models as well as the Double Log Polynomial (DLP), Peleg, and Guggenheim Anderson de Boer (GAB) temperature-independent models. Drying kinetics were quantified under thin-layer laboratory testing and modeled using the Modified Page's equation. Water activity isotherms for non-pelleted biomass were best modeled with the Peleg temperature-independent equation while isotherms for the pelleted biomass were best modeled with the Double Log Polynomial equation. Thin-layer drying results were accurately modeled with the Modified Page's equation. The results of this work indicate that AFEX pretreatment results in drying properties more favorable than or equal to that of raw corn stover, and pellets of superior physical stability in storage.

  20. Understand rotating isothermal collapses yet

    SciTech Connect

    Tohline, J.E.

    1985-01-01

    A scalar virial equation is used to describe the dynamic properties of equilibrium gas clouds, taking into account the relative effects of surface pressure, rotation, self gravity and internal isothermal pressure. Details concerning the internal structure of the clouds are ignored in order to obtain a globalized analytical expression. The obtained solution to the equation is found to agree with the surface-pressure-dominated model of Stahler (1983), and the rotation-dominated model of Hayashi, Narita, and Miyama (1982). On the basis of the analytical expression of virial equilibrium in the clouds, some of the limiting properties of isothermal clouds are described, and a realistic starting model for cloud collapse is proposed. 18 references.

  1. Investigating the moisture sorption behavior of amorphous sucrose using a dynamic humidity generating instrument.

    PubMed

    Yu, X; Kappes, S M; Bello-Perez, L A; Schmidt, S J

    2008-01-01

    The moisture sorption behavior of freeze-dried amorphous sucrose was investigated using a dynamic humidity generating instrument, the Dynamic Vapor Sorption (DVS) instrument. The kinetic moisture sorption profiles of freeze-dried amorphous sucrose samples with 29% crystalline content were obtained using the DVS instrument at 9 relative humidity (RH) values, ranging from 10% to 90%, at 25 degrees C. Moisture-induced crystallization was observed for %RH values between 40% and 80%, where the crystallization onset time decreased as %RH increased. The moisture sorption behavior of freeze-dried amorphous sucrose with 3 crystalline contents, 23%, 29%, and 80%, was also compared, revealing that the crystalline content had a significant impact on the pseudo-sorption isotherm of freeze-dried amorphous sucrose. In general, for %RH values below 90%, samples that had a lower percent crystalline content had a higher pseudo-equilibrium moisture content, with the difference becoming most pronounced for the 60% to 80% RH values. The moisture-induced crystallization results as a function of %RH obtained in this study were compared to those previously reported in the literature, leading to an extensive discussion of both the experimental protocols used and the hypothesized mechanisms governing the long-term stability of amorphous materials. The hypothesized mechanisms discussed included the glass transition temperature boundary, the zero mobility temperature, and the hydration limit. Based on the dissimilarity in these hypothesized mechanisms, additional theoretical and experimental exploration is still merited in order to adequately predict the conditions (for example, moisture content, %RH, and temperature) required to ensure long-term stability of amorphous solids.

  2. Plutonium sorption and desorption behavior on bentonite.

    PubMed

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

    2015-03-01

    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. PMID:25574607

  3. Plutonium sorption and desorption behavior on bentonite.

    PubMed

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

    2015-03-01

    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. Phosphorus sorption and buffering mechanisms in suspended sediments from the Yangtze Estuary and Hangzhou Bay, China

    NASA Astrophysics Data System (ADS)

    Li, M.; Whelan, M. J.; Wang, G. Q.; White, S. M.

    2013-05-01

    The adsorption isotherm and the mechanism of the buffering effect are important controls on phosphorus (P) behaviors in estuaries and are important for estimating phosphate concentrations in aquatic environments. In this paper, we derive phosphate adsorption isotherms in order to investigate sediment adsorption and buffering capacity for phosphorus discharged from sewage outfalls in the Yangtze Estuary and Hangzhou Bay near Shanghai, China. Experiments were also carried out at different temperatures in order to explore the buffering effects for phosphate. The results show that P sorption in sediments with low fine particle fractions was best described using exponential equations. Some P interactions between water and sediment may be caused by the precipitation of CaHPO4 from Ca2+ and HPO42- when the phosphate concentration in the liquid phase is high. Results from the buffering experiments suggest that the Zero Equilibrium Phosphate Concentrations (EPC0) vary from 0.014 mg L-1 to 0.061 mg L-1, which are consistent with measured phosphate concentrations in water samples collected at the same time as sediment sampling. Values of EPC0 and linear sorption coefficients (K) in sediments with high fine particle and organic matter contents are relatively high, which implies that they have high buffering capacity. Both EPC0 and K increase with increasing temperature, indicating a higher P buffering capacity at high temperatures.

  5. Phosphorus sorption and buffering mechanisms in suspended sediments from the Yangtze Estuary and Hangzhou Bay, China

    NASA Astrophysics Data System (ADS)

    Li, M.; Whelan, M. J.; Wang, G.; White, S. M.

    2012-12-01

    The adsorption isotherm and the mechanism of the buffering effect are important controls on phosphorus behaviors in estuaries and are important for estimating phosphate concentrations in aquatic environments. In this paper, we derive phosphate adsorption isotherms in order to investigate sediment adsorption and buffering capacity for phosphorus discharged from sewage outfalls in the Yangtze Estuary and Hangzhou Bay near Shanghai, China. Experiments were also carried out at different temperatures in order to explore the buffering effects for phosphate. The results show that P sorption in sediments with low fine particle fractions was best described using exponential equations. Some P interactions between water and sediment may be caused by the precipitation of CaHPO4 from Ca2+ and HPO42- when the phosphate concentration in the liquid phase is high. Results from the buffering experiments suggest that the Zero Equilibrium Phosphate Concentrations (EPC0) vary from 0.014 mg l-1 to 0.061 mg l-1, which are consistent with measured phosphate concentrations in water samples collected at the same time as sediment sampling. Values of EPC0 and linear sorption coefficients (K) in sediments with high fine particle and organic matter contents are relatively high, which implies that they have high buffering capacity. Both EPC0 and K increase with increasing temperature, indicating a higher P buffering capacity at high temperatures.

  6. Moisture sorption curves of fruit and nut cereal bar prepared with sugar and sugar substitutes.

    PubMed

    Pallavi, Byrappa Vasu; Chetana, Ramakrishna; Ravi, Ramaswamy; Reddy, Sunkireddy Yella

    2015-03-01

    Low sugar, low fat, dry fruit and nut cereal bars without sugar were prepared using cereals, nuts, and sugar substitutes. The sorption characteristics of the bars prepared with sugar substitutes in comparison with that of sugar were studied by keeping the bars at water activity (aw) from 0.1 to 0.9. The sorption isotherms of low sugar bars were practically identical below aw of 0.5 but above aw of 0.5, a clear differentiation in the isotherms could be observed compared to that of sugar counterpart. A sharp increase in moisture content was observed in the bars prepared with alternative sweeteners, above aw 0.6, whereas a gradual increase in aw was observed in the case of bar prepared with sugar. The ERH (Equilibrium relative humidity) value for bar with sugar was 50 %, and for bars prepared with alternative sweeteners, it was about 60 %. Low sugar cereal bar prepared with sorbitol + maltitol (SM) syrup scored higher sensory quality compared to other product prepared with sorbitol + nutriose (SN) as the former retained softness and chewiness on storage. Thus, it was observed that bars with alternative sweeteners will be more stable as their ERH is closer to normal ambient conditions compared to that prepared with sugar. PMID:25745238

  7. Sorption of uranium(VI) ions from hydrochloric acid and ammonium chloride solutions by anion exchangers

    SciTech Connect

    Pakholkov, V.S.; Denisova, L.A.; Rychkov, V.N.; Kurnosenko, N.A.

    1988-01-01

    The sorption of macroscopic quantities of uranium from solutions of UO/sub 2/Cl/sub 2/ containing HCl and NH/sub 4/Cl in concentrations from 0.0 to 6.0 M by the AV-17 x 8, AV-16G, EDE-10P, AN-31, AN-2F, AN22, and AN-251 anion exchangers has been investigated under static conditions. The sorption isotherms are described by an equation similar to Freundlich's equation: K/sub d/ = K tilde x C/sub eq/sup 1/z/ or log K/sub d/ = log K tilde + 1/z x log C/sub eq/. Equations describing the dependence of the sorbability (or K/sub d/) on the equilibrium concentration of uranium in the solution have been obtained with the aid of the least-squares method. Conclusions regarding the chemistry of the exchange of uranium ions on anion exchangers in chloride solutions have been drawn on the basis of the UV spectra of the original solutions and the IR spectra of the ion exchangers obtained in this work, as well as the established general laws governing sorption.

  8. Efficient sorption of Cu(2+) by composite chelating sorbents based on potato starch-graft-polyamidoxime embedded in chitosan beads.

    PubMed

    Dragan, Ecaterina Stela; Apopei Loghin, Diana Felicia; Cocarta, Ana Irina

    2014-10-01

    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

  9. Efficient sorption of Cu(2+) by composite chelating sorbents based on potato starch-graft-polyamidoxime embedded in chitosan beads.

    PubMed

    Dragan, Ecaterina Stela; Apopei Loghin, Diana Felicia; Cocarta, Ana Irina

    2014-10-01

    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

  10. Sorption-desorption of aminocyclopyrachlor in selected Brazilian soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Aminocyclopyrachlor sorption and desorption was investigated in 14 soils from Brazil, representing a range of pH, and organic carbon (OC) and clay contents. Sorption kinetics demonstrated that soil-solution equilibrium was attained in a 24-h period. Freundlich equation adequately described behavior ...

  11. Sorption-desorption of indaziflam in selected agricultural soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Sorption and desorption of indaziflam in 6 soils from Brazil and 3 soils from the USA, with different physical chemical properties, were investigated using the batch equilibration method. Sorption kinetics demonstrated that soil-solution equilibrium was attained in a 24-h period. The Freundlich equa...

  12. Sorption and Transport of Diphenhydramine in Natural Soils

    NASA Astrophysics Data System (ADS)

    Rutherford, C. J.; Vulava, V. M.

    2013-12-01

    Pharmaceutical and related chemicals have been detected in streams and ground water sources throughout the world, as a result of sewage overflows, runoff, or sewage treatment facilities unequipped to remove trace levels of pharmaceuticals. Diphenhydramine- an antihistamine that is used to treat allergy and common cold symptoms, induce sleep, suppress cough, and treat motion sickness- is prominent among them. Diphenhydramine has a complex, highly polar organic structure including two benzene rings and an amine functional group. It has a solubility of 3.06 g/L and a pKa of 8.98. Recent studies have shown that diphenhydramine in streams disrupts the ecology by affecting the algal and bacterial biofilms present on the streambed. In streams, photosynthesis has been found to decrease by up to 99% and plant respiration has been inhibited. Diphenhydramine has also altered the types and numbers of bacteria found in streams. Its presence in contaminated stream bodies can result in contact with soils and sediment in the stream floodplain. The objective of this study is to measure sorption and transport behavior of diphenhydramine in natural soils and determine reactivity of soil components. These studies were conducted in the laboratory using natural soil collected from the Francis Marion National Forrest. Soil samples from A and B horizons of several soil series were characterized for physical and chemical properties: organic matter content ranged between 0.6-7.6%, clay content between 6-20%, and soil pH between 3.7-4.9. The B-horizon soils contain a higher amount of clay than the organic-rich A-horizon soils. Equilibrium sorption isotherms and reaction kinetic rates were measured using batch reactor experiments and chromatographic column experiments were conducted to measure transport behavior. Kinetic experiments showed that diphenhydramine sorbed more strongly to the clay-rich soils and reached equilibrium after seven days, compared to ten days in organic-rich soils. The

  13. Sorption of paracetamol onto biomaterials.

    PubMed

    Ferchichi, Maroua; Dhaouadi, Hatem

    2016-01-01

    Pharmaceutical residues released into the environment are posing more and more public health problems. It is worthwhile to study the retention of pharmaceuticals residues by adsorption on solid supports. Batch sorption experiments are intended to identify the adsorption isotherms of the pharmaceutically active ingredient on the biomaterials. The results obtained in this study have shown that the retention possibilities of these compounds by bio-adsorbents (clay and sand) are not significant. The negligible sorption for these media is explained by the low hydrophobicity of paracetamol (Log K(ow) = 0.46). The retention of paracetamol on the dehydrated sewage sludge and on Posidonia oceanica showed a relatively significant adsorption with a maximal quantity of 0.956 mg g(-1) and 1.638 mg g(-1) for the dehydrate sludge and P. oceanica, respectively. On the other hand, the study of paracetamol retention on the powdered activated carbon showed a high adsorption capacity of about 515.27 mg g(-1). Isotherm data show a good fit with Langmuir's model. An infrared analysis is carried out. It shows identical bands before and after adsorption, with some modifications. PMID:27387007

  14. Evaluating phenanthrene sorption on various wood chars

    USGS Publications Warehouse

    James, G.; Sabatini, D.A.; Chiou, C.T.; Rutherford, D.; Scott, A.C.; Karapanagioti, H.K.

    2005-01-01

    A certain amount of wood char or soot in a soil or sediment sample may cause the sorption of organic compounds to deviate significantly from the linear partitioning commonly observed with soil organic matter (SOM). Laboratory produced and field wood chars have been obtained and analyzed for their sorption isotherms of a model solute (phenanthrene) from water solution. The uptake capacities and nonlinear sorption effects with the laboratory wood chars are similar to those with the field wood chars. For phenanthrene aqueous concentrations of 1 ??gl-1, the organic carbon-normalized sorption coefficients (log Koc) ranging from 5.0 to 6.4 for field chars and 5.4-7.3 for laboratory wood chars, which is consistent with literature values (5.6-7.1). Data with artificial chars suggest that the variation in sorption potential can be attributed to heating temperature and starting material, and both the quantity and heterogeneity of surface-area impacts the sorption capacity. These results thus help to corroborate and explain the range of log Koc values reported in previous research for aquifer materials containing wood chars. ?? 2004 Elsevier Ltd. All rights reserved.

  15. Relations between environmental black carbon sorption and geochemical sorbent characteristics.

    PubMed

    Cornelissen, Gerard; Kukulska, Zofia; Kalaitzidis, Stavros; Christanis, Kimon; Gustafsson, Orjan

    2004-07-01

    Pyrogenic carbon particles in sediments (soot and charcoal, collectively termed "black carbon" or BC) appear to be efficient sorbents of many hydrophobic organic compounds, so they may play an important role in the fate and toxicity of these substances. To properly model toxicant sorption behavior, it is important to (i) quantify the magnitude of the role of BC in sorption and (ii) elucidate which geochemical BC characteristics determine the strength of environmental BC sorption. Sorption isotherms of d10-phenanthrene (d10-PHE) were determined over a wide concentration range (0.0003-20 microg/L), for five sediments with widely varying characteristics. From the sorption isotherms, we determined Freundlich coefficients of environmental BC sorption, K(F,BCenv. These varied from 10(4.7) to 10(5.5). From the data, it could be deduced that BC was responsible for 49-85% of the total d10-PHE sorption at a concentration of 1 ng/L. At higher concentrations, the importance of BC for the sorption process diminished to <20% at 1 microg/L and 0-1% at 1 mg/L. There were no significant relationships between BC sorption strength and the tested geochemical BC characteristics [the fraction of small (<38 microm) BC particles, the BC resistance to high-temperature oxidation, the fraction of biomass-derived BC, the native polycyclic aromatic hydrocarbon and total organic carbon contents]. Because of the limited variation in BC sorption strength with widely varying BC characteristics, the presented BC sorption coefficients may putatively be used as generic starting points for environmental modeling purposes. PMID:15296315

  16. Modeling Fission Product Sorption in Graphite Structures

    SciTech Connect

    Szlufarska, Izabela; Morgan, Dane; Allen, Todd

    2013-04-08

    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

  17. Sorption of acid red 57 from aqueous solution onto sepiolite.

    PubMed

    Alkan, Mahir; Demirbaş, Ozkan; Celikçapa, Sermet; Doğan, Mehmet

    2004-12-10

    Sepiolite, a highly porous mineral, is becoming widely used as an alternative material in areas where sorptive, catalytic and rheological applications are required. High ion exchange capacity and high surface area and more importantly its relatively cheap price make it an attractive adsorbent. In this study, the adsorption of acid red 57 by natural mesoporous sepiolite has been examined in order to measure the ability of this mineral to remove coloured textile dyes from wastewater. For this purpose, a series of batch adsorption tests of acid red 57 from aqueous sepiolite solutions have been systematically investigated as a function of parameters such as pH, ionic strength and temperature. Adsorption equilibrium was reached within 1h. The removal of acid red 57 decreases with pH from 3 to 9 and temperature from 25 to 55 degrees C, whereas it increases with ionic strength from 0 to 0.5 mol L(-1). Adsorption isotherms of acid red on sepiolite were determined and correlated with common isotherm equations such as Langmuir and Freundlich models. It was found that the Langmuir model appears to fit the isotherm data better than the Freundlich model. The physical properties of this adsorbent were consistent with the parameters obtained from the isotherm equations. Approximately, 21.49% weight loss was observed. The surface area value of sepiolite was 342 m2 g(-1) at 105 degrees C, and it increased to 357 m2 g(-1) at 200 degrees C. Further increase in temperature caused channel plugging and crystal structure deformation, as a result the surface area values showed a decrease with temperature. The data obtained from adsorption isotherms at different temperatures have been used to calculate some thermodynamic quantities such as the Gibbs energy, heat and entropy of adsorption. The thermodynamic data indicate that acid red 57 adsorption onto sepiolite is characterized by physical adsorption. The dimensionless separation factor (RL) have shown that sepiolite can be used for

  18. Sorption of a nonionic surfactant Tween 80 by minerals and soils.

    PubMed

    Kang, Soyoung; Jeong, Hoon Young

    2015-03-01

    Batch experiments were conducted to evaluate Tween 80 sorption by oxides, aluminosilicates, and soils. For oxides, the sorption by silica and alumina follow linear isotherms, and that by hematite follows a Langmuir isotherm. Considering isotherm type and surface coverage, Tween 80 may partition into the silica/alumina-water interface, whereas it may bind to hematite surface sites. Among aluminosilicates, montmorillonite shows the greatest sorption due to the absorption of Tween 80 into interlayers. For other aluminosilicates, it sorbs to surfaces, with the sorption increasing as plagioclasesorption. The greater sorption by untreated soils than H2O2-treated soils indicates that soil organic matter is a vital sorbent. The sorption hysteresis, contributed to by clay minerals and soil organic matter, is characterized by the greater sorption during the desorption than the sorption stages. This suggests the potential difficulty in removing surfactants from soils. Also, sorption of surfactants can adversely affect surfactant-enhanced remediation by decreasing the aquifer permeability and the availability of surfactants for micellar solubilization. PMID:25463228

  19. Sorption of a nonionic surfactant Tween 80 by minerals and soils.

    PubMed

    Kang, Soyoung; Jeong, Hoon Young

    2015-03-01

    Batch experiments were conducted to evaluate Tween 80 sorption by oxides, aluminosilicates, and soils. For oxides, the sorption by silica and alumina follow linear isotherms, and that by hematite follows a Langmuir isotherm. Considering isotherm type and surface coverage, Tween 80 may partition into the silica/alumina-water interface, whereas it may bind to hematite surface sites. Among aluminosilicates, montmorillonite shows the greatest sorption due to the absorption of Tween 80 into interlayers. For other aluminosilicates, it sorbs to surfaces, with the sorption increasing as plagioclasesorption. The greater sorption by untreated soils than H2O2-treated soils indicates that soil organic matter is a vital sorbent. The sorption hysteresis, contributed to by clay minerals and soil organic matter, is characterized by the greater sorption during the desorption than the sorption stages. This suggests the potential difficulty in removing surfactants from soils. Also, sorption of surfactants can adversely affect surfactant-enhanced remediation by decreasing the aquifer permeability and the availability of surfactants for micellar solubilization.

  20. Fate and transport with material response characterization of green sorption media for copper removal via desorption process.

    PubMed

    Chang, Ni-Bin; Houmann, Cameron; Lin, Kuen-Song; Wanielista, Martin

    2016-07-01

    Multiple adsorption and desorption cycles are required to achieve the reliable operation of copper removal and recovery. A green sorption media mixture composed of recycled tire chunk, expanded clay aggregate, and coconut coir was evaluated in this study for its desorptive characteristics as a companion study of the corresponding adsorption process in an earlier publication. We conducted a screening of potential desorbing agents, batch desorption equilibrium and kinetic studies, and batch tests through 3 adsorption/desorption cycles. The desorbing agent screening revealed that hydrochloric acid has good potential for copper desorption. Equilibrium data fit the Freundlich isotherm, whereas kinetic data had high correlation with the Lagergren pseudo second-order model and revealed a rapid desorption reaction. Batch equilibrium data over 3 adsorption/desorption cycles showed that the coconut coir and media mixture were the most resilient, demonstrating they could be used through 3 or more adsorption/desorption cycles. FE-SEM imaging, XRD, and EDS analyses supported the batch adsorption and desorption results showing significant surface sorption of CuO species in the media mixture and coconut coir, followed by partial desorption using 0.1 M HCl as a desorbing agent. PMID:27081796

  1. Sorption of 3,3',4,4'-tetrachlorobiphenyl by microplastics: A case study of polypropylene.

    PubMed

    Zhan, Zhiwei; Wang, Jundong; Peng, Jinping; Xie, Qilai; Huang, Ying; Gao, Yifan

    2016-09-15

    Though plastics show good chemical inertness, they could sorb polychlorinated biphenyls (PCBs) and other toxic pollutants from the surrounding environment. Thus, ingestion of microplastics by marine organisms potentially enhances the transport and bioavailability of toxic chemicals. However, there is lack of studies on the sorption capacity, mechanism and factors affecting the sorption behavior. Here, sorption of PCBs by microplastics in the simulated seawater was studied using the batch oscillation equilibration technique, in which polypropylene (PP) and 3,3',4,4'-tetrachlorobiphenyl (PCB77) acted as model plastic and PCB, respectively. Factors including particle size, temperature and solution environment were investigated. Results showed that, equilibrium sorption time is about 8h and sorption capacity increase with decreasing particle size and temperature. Different sorption capacity in three solution environments was observed. Equilibrium data in three solution environments fitted very well to the Langmuir sorption model, indicating chemical sorption is the predominant mechanism. PMID:27230985

  2. Sorption of 3,3',4,4'-tetrachlorobiphenyl by microplastics: A case study of polypropylene.

    PubMed

    Zhan, Zhiwei; Wang, Jundong; Peng, Jinping; Xie, Qilai; Huang, Ying; Gao, Yifan

    2016-09-15

    Though plastics show good chemical inertness, they could sorb polychlorinated biphenyls (PCBs) and other toxic pollutants from the surrounding environment. Thus, ingestion of microplastics by marine organisms potentially enhances the transport and bioavailability of toxic chemicals. However, there is lack of studies on the sorption capacity, mechanism and factors affecting the sorption behavior. Here, sorption of PCBs by microplastics in the simulated seawater was studied using the batch oscillation equilibration technique, in which polypropylene (PP) and 3,3',4,4'-tetrachlorobiphenyl (PCB77) acted as model plastic and PCB, respectively. Factors including particle size, temperature and solution environment were investigated. Results showed that, equilibrium sorption time is about 8h and sorption capacity increase with decreasing particle size and temperature. Different sorption capacity in three solution environments was observed. Equilibrium data in three solution environments fitted very well to the Langmuir sorption model, indicating chemical sorption is the predominant mechanism.

  3. Multifractal characteristics of Nitrogen adsorption isotherms from tropical soils

    NASA Astrophysics Data System (ADS)

    Vidal Vázquez, Eva; Paz Ferreiro, Jorge

    2010-05-01

    One of the primary methods used to characterize a wide range of porous materials, including soils, are gas adsorption isotherms. An adsorption isotherm is a function relating the amount of adsorbed gas or vapour to the respective equilibrium pressure, during pressure increase at constant temperature. Adsorption data allow easily estimates of specific surface area and also can provide a characterization of pore surface heterogeneity. Most of the properties and the reactivity of soil colloids are influenced by their specific surface area and by parameters describing the surface heterogeneity. For a restricted scale range, linearity between applied pressure and volume of adsorbate holds, which is the basis for current estimations of specific surface area. However, adsorption isotherms contain also non-linear segments of pressure versus volume so that evidence of multifractal scale has been demonstrated. The aim of this study was to analyze the multifractal behaviour of nitrogen adsorption isotherms from a set of tropical soils. Samples were collected form 54 horizons belonging to 19 soil profiles in the state of Minas Gerais, Brazil. The most frequent soil type was Oxisol, according to the Soil Survey Staff, equivalent to Latossolo in the Brazilian soil classification system. Nitrogen adsorption isotherms at standard 77 K were measured using a Thermo Finnigan Sorptomatic 1990 gas sorption analyzer (Thermo Scientific, Waltham, MA). From the raw data a distributions of mass along a support was obtained to perform multifractal analysis. The probability distribution was constructed by dividing the values of the measure in a given segment by the sum of the measure in the whole scale range. The box-counting method was employed to perform multifractal analysis. All the analyzed N2 adsorption isotherms behave like a multifractal system. The singularity spectra, f(α), showed asymmetric concave down parabolic shapes, with a greater tendency toward the left side, where moments

  4. Modeling of solute sorption by polyvinyl chloride plastic infusion bags.

    PubMed

    Jenke, D R

    1993-11-01

    Methods for estimating the equilibrium and time-dependent sorption of solutes by polymeric containers have been developed. The methods are specifically applied to the sorption of solutes by polyvinyl chloride (PVC) infusion bags. The methods correlate the partition coefficients and dissociation constant (when appropriate) of the solute, the physical dimensions of the container, and solution pH with single parameters that dictate the shape of the sorption profile. To determine the equilibrium sorption level for PVC containers, the fractional binding of a solute is correlated with its hexane-water and octanol-water partition coefficients. Calculations based on single partition coefficients are less effective in terms of mimicking the behavior of the PVC. To determine the sorption profile (fractional binding versus time), the partition coefficients are related to the fraction binding at a particular time through a single parameter referred to as the sorption number. Equilibrium fractional binding and sorption profiles for various drugs stored in PVC containers are generated with the models and agree well with reported behavior. The effect of pH on the sorption process is also examined.

  5. Gas sorption and the consequent volumetric and permeability change of coal

    NASA Astrophysics Data System (ADS)

    Lin, Wenjuan

    Experimental and numerical investigations of gas sorption on coal, and the subsequent volumetric and permeability changes of the coal were conducted. The goals of the study were to investigate the magnitude of permeability change caused by gas sorption, and develop an algorithm to simulate numerically gas sorption and sorption-induced permeability change. The amount of gas sorption and the subsequent volumetric and permeability change of coal samples as a function of pore pressure and injection gas composition were measured in the laboratory. A constant effective confining pressure (difference between the confining pressure and pore pressure) was maintained in the process of the experiments; therefore, the role of effective stress on permeability was eliminated. Several gases, including pure CO2, pure N2, and binary mixtures of CO2 and N2 of various compositions were used as the injection gas. The coal sample was first allowed to adsorb an injection gas fully at a particular pressure. The total amount (moles) of adsorption was calculated based on a volumetric method. After adsorption equilibrium was reached, gas samples were taken from the equilibrium gaseous phase and analyzed afterwards. The composition of the gaseous phase prior to and after the adsorption was used to calculate the composition of the adsorbed phase based on material balance. Permeability of the sample was then measured by flowing the injection gas through the core at varying pressure gradient or varying flow rate, and an average permeability was obtained based on Darcy's law for compressible systems. The change of the total volume of the core was monitored and recorded in the whole process of the experiment. Volumetric strain was thereby calculated. Experimental results showed that the greater the pressure the greater the amount of adsorption for all tested gases. At the same pressure, the amount of adsorption was greater for CO2 than N2. For the binary mixtures, the greater the fraction of CO 2

  6. Scale factors to quantify and predict the field scale variability of heavy metal sorption in soil

    NASA Astrophysics Data System (ADS)

    Xiao, Han; Boettcher, Juergen; Utermann, Jens

    2013-04-01

    Many studies report the close relationship between heavy metal sorption in soil and physicochemical soil properties. Since 1980s pedotransfer functions (PTF) were developed to predict the heavy metal sorption in soil, based on the Freundlich sorption isotherm with parameters K and n, and physicochemical soil properties. An important application of PTFs is to predict sorption behavior at larger scales (e.g. soil units) from easily measurable soil properties, but PTFs were also applied to predict the spatial variability of sorption at the field scale. A new method to quantify the spatial variability of heavy metal sorption in soils at the field scale is the calculation of scale factors (SF). This method reduces the broad spread of the sorption isotherms into an average relation, but saves the variation through the scale factors. For physicochemical soil properties scale factors can also be calculated. Scale factors from sorption isotherms and physicochemical soil properties are correlated. SF of isotherms are indirectly related to the Freundlich parameters K and n, but PTF directly and solely predict K. That is the reason, why SF in contrast to PTF were found in an earlier study with an acidic sandy soil under forest to increase the accuracy of model predictions. The two prediction methods, SF and PTF, were both evaluated for an agricultural field on a more or less homogeneous Luvisol developed in loess near Hannover, Germany. Samples were taken from the A and B horizon (each 50 samples) along a 250 m transect. Sorption isotherms for heavy metals (Cd, Cu, Pb and Zn) and soil properties as pH, CEC, organic carbon content, texture were measured, and scale factors were calculated. In our contribution we will present results on (1) the accuracy of PTF and SF to predict the field average sorption behavior of the soil, (2) a comparative numerical simulation of field scale heavy metal transport with spatially variable sorption behavior in unsaturated soil described by both

  7. Equilibrium and kinetic mechanisms of woody biochar on aqueous glyphosate removal.

    PubMed

    Mayakaduwa, S S; Kumarathilaka, Prasanna; Herath, Indika; Ahmad, Mahtab; Al-Wabel, Mohammed; Ok, Yong Sik; Usman, Adel; Abduljabbar, Adel; Vithanage, Meththika

    2016-02-01

    We investigated the removal of aqueous glyphosate using woody (dendro) biochar obtained as a waste by product from bioenergy industry. Equilibrium isotherms and kinetics data were obtained by adsorption experiments. Glyphosate adsorption was strongly pH dependent occurring maximum in the pH range of 5-6. The protonated amino moiety of the glyphosate molecule at this pH may interact with π electron rich biochar surface via π-π electron donor-acceptor interactions. Isotherm data were best fitted to the Freundlich and Temkin models indicating multilayer sorption of glyphosate. The maximum adsorption capacity of dendro biochar for glyphosate was determined by the isotherm modeling to be as 44 mg/g. Adsorption seemed to be quite fast, reaching the equilibrium <1 h. Pseudo-second order model was found to be the most effective in describing kinetics whereas the rate limiting step possibly be chemical adsorption involving valence forces through sharing or exchanging electrons between the adsorbent and sorbate. The FTIR spectral analysis indicated the involvement of functional groups such as phenolic, amine, carboxylic and phosphate in adsorption. Hence, a heterogeneous chemisorption process between adsorbate molecules and functional groups on biochar surface can be suggested as the mechanisms involved in glyphosate removal. PMID:26340852

  8. Equilibrium and kinetic mechanisms of woody biochar on aqueous glyphosate removal.

    PubMed

    Mayakaduwa, S S; Kumarathilaka, Prasanna; Herath, Indika; Ahmad, Mahtab; Al-Wabel, Mohammed; Ok, Yong Sik; Usman, Adel; Abduljabbar, Adel; Vithanage, Meththika

    2016-02-01

    We investigated the removal of aqueous glyphosate using woody (dendro) biochar obtained as a waste by product from bioenergy industry. Equilibrium isotherms and kinetics data were obtained by adsorption experiments. Glyphosate adsorption was strongly pH dependent occurring maximum in the pH range of 5-6. The protonated amino moiety of the glyphosate molecule at this pH may interact with π electron rich biochar surface via π-π electron donor-acceptor interactions. Isotherm data were best fitted to the Freundlich and Temkin models indicating multilayer sorption of glyphosate. The maximum adsorption capacity of dendro biochar for glyphosate was determined by the isotherm modeling to be as 44 mg/g. Adsorption seemed to be quite fast, reaching the equilibrium <1 h. Pseudo-second order model was found to be the most effective in describing kinetics whereas the rate limiting step possibly be chemical adsorption involving valence forces through sharing or exchanging electrons between the adsorbent and sorbate. The FTIR spectral analysis indicated the involvement of functional groups such as phenolic, amine, carboxylic and phosphate in adsorption. Hence, a heterogeneous chemisorption process between adsorbate molecules and functional groups on biochar surface can be suggested as the mechanisms involved in glyphosate removal.

  9. Sorption of Pseudomonas putida onto differently structured kaolinite minerals

    NASA Astrophysics Data System (ADS)

    Vasiliadou, I. A.; Papoulis, D.; Chrysikopoulos, C.; Panagiotaras, D.; Karakosta, E.; Fardis, M.; Papavassiliou, G.

    2010-12-01

    The presence of bio-colloids (e.g. bacteria and viruses) in the subsurface could be attributed to the release of particles from septic tanks, broken sewer lines or from artificial recharge with treated municipal wastewater. Bio-colloid transport in the subsurface is significantly affected by sorption onto the solid matrix. Bio-colloid attachment onto mobile or suspended in the aqueous phase soil particles (e.g. clay or other minerals) also may influence their fate and transport in the subsurface. The present study focuses on the investigation of Pseudomonas (Ps.) putida sorption onto well (KGa-1) and poorly (KGa-2) crystallized kaolinite minerals. Batch experiments were carried out to determine the sorption isotherms of Ps. putida onto both types of kaolinite particles. The sorption process of Ps. putida onto KGa-1 and KGa-2 is adequately described by a Langmuir isotherm. Attenuated Total Reflection Fourier Transform Infrared Spectroscopy as well as Nuclear Magnetic Resonance were employed to study the sorption mechanisms of Ps. putida. Experimental results indicated that KGa-2 presented higher affinity and sorption capacity than KGa-1. It was shown that electrostatic interactions and structural disorders can influence the sorption capacity of clay particles.

  10. Reliability analysis of nutrient removal from stormwater runoff with green sorption media under varying influent conditions.

    PubMed

    Jones, Jamie; Chang, Ni-Bin; Wanielista, Martin P

    2015-01-01

    To support nutrient removal, various stormwater treatment technologies have been developed via the use of green materials, such as sawdust, tire crumbs, sand, clay, sulfur, and limestone, as typical constituents of filter media mixes. These materials aid in the physiochemical sorption and precipitation of orthophosphates as well as in the biological transformation of ammonia, nitrates and nitrites. However, these processes are dependent upon influent conditions such as hydraulic residence time, influent orthophosphate concentrations, and other chemical species present in the inflow. This study aims to compare the physiochemical removal of orthophosphate by isotherm and column tests under differing influent conditions to realize the reliability of orthophosphate removal process with the aid of green sorption media. The green sorption media of interest in this study is composed of a 5:2:2:1 (by volume) mixture of cement sand, tire crumb, fine expanded clay, and limestone. Scenarios of manipulating the hydraulic residence time of the water from 18 min and 60 min, the influent dissolved phosphorus concentrations of 1.0 mg·L(-1) and 0.5 mg·L(-1), and influent water types of distilled and pond water, were all investigated in the column tests. Experimental data were compared with the outputs from the Thomas Model based on orthophosphate removal to shed light on the equilibrium condition versus kinetic situation. With ANOVA tests, significant differences were confirmed between the experimental data sets of the breakthrough curves in the column tests. SEM imaging analysis helps to deepen the understanding of pore structures and pore networks of meta-materials being used in the green sorption media. Life expectancy curves derived from the output of Thomas Model may be applicable for future system design of engineering processes. PMID:25278294

  11. Sorption-desorption of indaziflam and its three metabolites in sandy soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Indaziflam is a relatively new herbicide for which sorption-desorption information is lacking, and nothing is available on its metabolites. Information is needed on the multiple soil and pesticide characteristics known to influence these processes. Freundlich sorption isotherm slopes were < 1, there...

  12. SORPTION OF ARSENATE AND ARSENITE ON A RUTHENIUM COMPOUND: A MACROSCOPIC AND MICROSCOPIC STUDY

    EPA Science Inventory

    Sorption of arsenate and arsenite was examined on a ruthenium compound using macroscopic and microscopic techniques. Batch sorption experiments at pH 4,5,6, 7 and 8 were employed to construct constant solid solution ratio isotherms (CSI). After equilibration at the appropriate pH...

  13. SORPTION OF TOXIC ORGANIC COMPOUNDS ON WATERWATER SOLIDS: MECHANISMS AND MODELING

    EPA Science Inventory

    It is proposed that sorption is a combination of two fundamentally different processes: adsorption and partitioning. A sorption model was developed for both single-component and multicomponent systems. The model was tested using single-component experimental isotherm data of eig...

  14. SORPTION OF 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN FROM WATER BY SURFACE SOILS

    EPA Science Inventory

    The sorption of l4C-labeled 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD) from water by two uncontaminated surface soils from the Times Beach, MO, area was evalu- ated by using batch shake testing. Sorption isotherm plots for the soil with the lower fraction organic carbon (f,) wer...

  15. Lanthanide sorption on smectitic clays in presence of cement leachates

    NASA Astrophysics Data System (ADS)

    Galunin, Evgeny; Alba, María D.; Santos, Maria J.; Abrão, Taufik; Vidal, Miquel

    2010-02-01

    Due to their potential retention capacity, clay minerals have been proposed for use in the engineered barriers for the storage of high-level radioactive actinides in deep geological waste repositories. However, there is still a lack of data on the sorption of actinides in clays in conditions simulating those of the repositories. The present article examines the sorption of two lanthanides (actinide analogues) in a set of smectitic clays (FEBEX bentonite, MX80 bentonite, hectorite, saponite, Otay montmorillonite, and Texas montmorillonite). Distribution coefficients ( Kd) were determined in two media: water and 0.02 mol L -1 Ca, the latter representing the cement leachates that may modify the chemical composition of the water in contact with the clay. The Kd values of the lanthanides used in the experiments (La and Lu) varied greatly (25-50 000 L kg -1) depending on the ionic medium (higher values in water than in the Ca medium), the initial lanthanide concentration (up to three orders of magnitude decrease inversely with lanthanide concentration), and the examined clay (up to one order of magnitude for the same lanthanide and sorption medium). Freundlich and Langmuir isotherms were used to fit sorption data to allow comparison of the sorption parameters among smectites. The model based on the two-site Langmuir isotherms provided the best fit of the sorption data, confirming the existence of sorption sites with different binding energies. The sites with higher sorption affinity were about 6% of the total sorption capacity in the water medium, and up to 17% in the Ca medium, although in this latter site sorption selectivity was lower. The wide range of Kd values obtained regarding the factors examined indicated that the retention properties of the clays should also be considered when selecting a suitable clay for engineered barriers.

  16. Competitive sorption of atenolol, trimetoprim, carbamazepine and sulfamethoxazole in three soil types

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

    Transport of human and veterinary pharmaceuticals in soils and consequent ground-water contamination are influenced by many factors, including compound sorption on soil particles and dissipation. Batch sorption experiment for 9 soils (3 soil types with 3 (Greyic Phaeozem on loess), 4 (Haplic Luvisol on loess) and 2 (Haplic Cambisol on gneiss) horizons) and mixture of 4 pharmaceuticals (atenolol, trimetoprim, carbamazepine and sulfamethoxazole) was performed to study competitive sorption of compounds in each soil sample. Sorption affinities and dissipation half-lives of all compounds in topsoils were previously studied by Kodešová et al. (2015 and 2016). Ten grams of dry soil was placed directly into the plastic centrifuge tubes and 20 ml of solution of a known pharmaceutical concentration was added. The same concentrations (0.5, 1, 2.5, 5 and 10 mg/l) were used for all compounds. Three replicates of each concentration were applied for each soil. Tube was shaken for 24 h using the shaking apparatus at 20 C. After shaking, the analyzed soil suspension was centrifuged for 10 min at 6,000 rotations per minute. The actual initial and final equilibrium pharmaceutical concentrations were measured using two-dimensional liquid chromatography-tandem mass spectrometry LC/LC-MS/MS using isotope dilution and internal standard methods. The pharmaceutical concentration adsorbed on soil particles was calculated using the initial and final (i.e. after incubation) pharmaceutical concentrations. The Freundlich equations were used to fit data points of the measured adsorption isotherms. In the case of carbamazepine (neutral form) and sulfamethoxazole (partly negatively charged) sorption affinity of compounds decrease with soil depth. On the other hand in the case of atenolol and trimethoprim (both positively charged) compound sorption affinity was not depth dependent. Data obtained for top soils were compared with sorption affinities for single compounds published by (Kodešová et

  17. A breakthrough biosorbent in removing heavy metals: Equilibrium, kinetic, thermodynamic and mechanism analyses in a lab-scale study.

    PubMed

    Abdolali, Atefeh; Ngo, Huu Hao; Guo, Wenshan; Lu, Shaoyong; Chen, Shiao-Shing; Nguyen, Nguyen Cong; Zhang, Xinbo; Wang, Jie; Wu, Yun

    2016-01-15

    A breakthrough biosorbent namely multi-metal binding biosorbent (MMBB) made from a combination of tea wastes, maple leaves and mandarin peels, was prepared to evaluate their biosorptive potential for removal of Cd(II), Cu(II), Pb(II) and Zn(II) from multi-metal aqueous solutions. FTIR and SEM were conducted, before and after biosorption, to explore the intensity and position of the available functional groups and changes in adsorbent surface morphology. Carboxylic, hydroxyl and amine groups were found to be the principal functional groups for the sorption of metals. MMBB exhibited best performance at pH 5.5 with maximum sorption capacities of 31.73, 41.06, 76.25 and 26.63 mg/g for Cd(II), Cu(II), Pb(II) and Zn(II), respectively. Pseudo-first and pseudo-second-order models represented the kinetic experimental data in different initial metal concentrations very well. Among two-parameter adsorption isotherm models, the Langmuir equation gave a better fit of the equilibrium data. For Cu(II) and Zn(II), the Khan isotherm describes better biosorption conditions while for Cd(II) and Pb(II), the Sips model was found to provide the best correlation of the biosorption equilibrium data. The calculated thermodynamic parameters indicated feasible, spontaneous and exothermic biosorption process. Overall, this novel MMBB can effectively be utilized as an adsorbent to remove heavy metal ions from aqueous solutions.

  18. Isothermal Titration Calorimetry in the Student Laboratory

    ERIC Educational Resources Information Center

    Wadso, Lars; Li, Yujing; Li, Xi

    2011-01-01

    Isothermal titration calorimetry (ITC) is the measurement of the heat produced by the stepwise addition of one substance to another. It is a common experimental technique, for example, in pharmaceutical science, to measure equilibrium constants and reaction enthalpies. We describe a stirring device and an injection pump that can be used with a…

  19. Non-Equilibrium Water-Glassy Polymer Dynamics

    NASA Astrophysics Data System (ADS)

    Davis, Eric; Minelli, Matteo; Baschetti, Marco; Sarti, Giulio; Elabd, Yossef

    2012-02-01

    For many applications (e.g., medical implants, packaging), an accurate assessment and fundamental understanding of the dynamics of water-glassy polymer interactions is of great interest. In this study, sorption and diffusion of pure water in several glassy polymers films, such as poly(styrene) (PS), poly(methyl methacrylate) (PMMA), poly(lactide) (PLA), were measured over a wide range of vapor activities and temperatures using several experimental techniques, including quartz spring microbalance (QSM), quartz crystal microbalance (QCM), and time-resolved Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy. Non-Fickian behavior (diffusion-relaxation phenomena) was observed by all three techniques, while FTIR-ATR spectroscopy also provides information about the distribution of the states of water and water transport mechanisms on a molecular-level. Specifically, the states of water are significantly different in PS compared to PMMA and PLA. Additionally, a purely predictive non-equilibrium lattice fluid (NELF) model was applied to predict the sorption isotherms of water in these glassy polymers.

  20. Equilibrium and kinetics of phosphorous adsorption onto bone charcoal from aqueous solution.

    PubMed

    Ghaneian, Mohammad Taghi; Ghanizadeh, Ghader; Alizadeh, Mohammad Tahghighi Haji; Ehrampoush, Mohammad Hasan; Said, Farhan Mohd

    2014-01-01

    Pyrolysis of fresh sheep bone led to the formation of bone charcoal (BC). The structural characteristics of BC and surface area were determined by X-ray diffraction (XRD) and scanning electron microscopy (SEM). N2 gas adsorption-desorption was analysed by Brunauer-Emmett-Teller isotherm model. The prepared BC was used as an effective sorbent for the removal of phosphate from aqueous solutions. The effect of major parameters, including initial phosphorous concentration, sorbent dosage, pH and temperature, was investigated in this study. Furthermore, adsorption isotherms and kinetics were evaluated. BC was an effective sorbent in phosphate removal from aqueous solution especially in phosphate concentration between 2 and 100 mg/L. The maximum amount of sorption capacity was 30.21 mg/g, which was obtained with 100 mg/L as the initial phosphate concentration and 0.2 g as the sorbent dosage. Best reported pH in this study is 4; in higher pH, adsorption rate decreased dramatically. By increasing the temperature from 20 to 40 degrees C sorption capacity increased; this phenomenon described that adsorption is endothermic. Equilibrium data were analysed by Langmuir, Freundlich and Temkin isotherms. Pseudo first- and second-order and Elovich models were used to determine the kinetics of adsorption in this study. Collected data highly fitted with Freundlich isotherms and pseudo second-order kinetics. Achieved results have shown well the potentiality for the BC to be utilized as a natural sorbent to remove phosphorous from water and wastewater.

  1. Biosorption kinetics, thermodynamics and isosteric heat of sorption of Cu(II) onto Tamarindus indica seed powder.

    PubMed

    Chowdhury, Shamik; Saha, Papita Das

    2011-12-01

    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.

  2. Biosorption kinetics, thermodynamics and isosteric heat of sorption of Cu(II) onto Tamarindus indica seed powder.

    PubMed

    Chowdhury, Shamik; Saha, Papita Das

    2011-12-01

    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. PMID:21872453

  3. Sorption of polycyclic aromatic hydrocarbons to polystyrene nanoplastic.

    PubMed

    Liu, Lijing; Fokkink, Remco; Koelmans, Albert A

    2016-07-01

    Microplastic has become an emerging contaminant of global concern. Bulk plastic can degrade to form smaller particles down to the nanoscale (<100 nm), which are referred to as 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. Adsorption of methyl orange from aqueous solution by aminated pumpkin seed powder: Kinetics, isotherms, and thermodynamic studies.

    PubMed

    Subbaiah, Munagapati Venkata; Kim, Dong-Su

    2016-06-01

    Present research discussed the utilization of aminated pumpkin seed powder (APSP) as an adsorbent for methyl orange (MO) removal from aqueous solution. Batch sorption experiments were carried to evaluate the influence of pH, initial dye concentration, contact time, and temperature. The APSP was characterized by using Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). The experimental equilibrium adsorption data were fitted using two two-parameter models (Langmuir and Freundlich) and two three-parameter models (Sips and Toth). Langmuir and Sips isotherms provided the best model for MO adsorption data. The maximum monolayer sorption capacity was found to be 200.3mg/g based on the Langmuir isotherm model. The pseudo-first-order and pseudo-second-order model equations were used to analyze the kinetic data of the adsorption process and the data was fitted well with the pseudo-second-order kinetic model (R(2)>0.97). The calculated thermodynamic parameters such as ΔG(0), ΔH(0) and ΔS(0) from experimental data showed that the sorption of MO onto APSP was feasible, spontaneous and endothermic in the temperature range 298-318 K. The FTIR results revealed that amine and carboxyl functional groups present on the surface of APSP. The SEM results show that APSP has an irregular and porous surface which is adequate morphology for dye adsorption. Desorption experiments were carried to explore the feasibility of adsorbent regeneration and the adsorbed MO from APSP was desorbed using 0.1M NaOH with an efficiency of 93.5%. Findings of the present study indicated that APSP can be successfully used for removal of MO from aqueous solution. PMID:26921544

  5. Effect of sorption on flocculation kinetics: Experimental studies

    SciTech Connect

    Subramaniam, K.; Yiacoumi, S.; Tsouris, C.

    1997-11-01

    Sorption of copper and cadmium ions from aqueous solutions by ferric oxide particles was studied using batch equilibrium and kinetic experiments. The sorption process was found to be pH dependent, with the uptake increasing at high pH values. An increase in equilibrium pH was observed when the initial pH was in the acidic range and a decrease from initial values was observed in the basic range, in the case of both copper and cadmium sorption. The former phenomenon is due to competition between metal and proton binding and the latter is due to precipitation mechanisms at high initial pH values. A large increase in the zeta potential of the particles from baseline values was observed during equilibrium sorption. This increase occurs as a result of surface charge neutralization due to metal ion uptake. Particle destabilization appears to occur as a result of metal ion sorption. Kinetic experiments indicate that the uptake of copper by ferric oxide particles is a slow process. pH histories were similar to those obtained in the sorption equilibrium experiments. Changes in the size distribution of the ferric oxide particles due to aggregate formation during uptake of ions is observed in the kinetic studies. These findings indicate a potential role of metal ion uptake in particle flocculation kinetics through alteration of the surface electrostatic potential.

  6. “Multi-temperature” method for high-pressure sorption measurements on moist shales

    SciTech Connect

    Gasparik, Matus; Ghanizadeh, Amin; Gensterblum, Yves; Krooss, Bernhard M.

    2013-08-15

    A simple and effective experimental approach has been developed and tested to study the temperature dependence of high-pressure methane sorption in moist organic-rich shales. This method, denoted as “multi-temperature” (short “multi-T”) method, enables measuring multiple isotherms at varying temperatures in a single run. The measurement of individual sorption isotherms at different temperatures takes place in a closed system ensuring that the moisture content remains constant. The multi-T method was successfully tested for methane sorption on an organic-rich shale sample. Excess sorption isotherms for methane were measured at pressures of up to 25 MPa and at temperatures of 318.1 K, 338.1 K, and 348.1 K on dry and moisture-equilibrated samples. The measured isotherms were parameterized with a 3-parameter Langmuir-based excess sorption function, from which thermodynamic sorption parameters (enthalpy and entropy of adsorption) were obtained. Using these, we show that by taking explicitly into account water vapor as molecular species in the gas phase with temperature-dependent water vapor pressure during the experiment, more meaningful results are obtained with respect to thermodynamical considerations. The proposed method can be applied to any adsorbent system (coals, shales, industrial adsorbents) and any supercritical gas (e.g., CH{sub 4}, CO{sub 2}) and is particularly suitable for sorption measurements using the manometric (volumetric) method.

  7. ``Multi-temperature'' method for high-pressure sorption measurements on moist shales

    NASA Astrophysics Data System (ADS)

    Gasparik, Matus; Ghanizadeh, Amin; Gensterblum, Yves; Krooss, Bernhard M.

    2013-08-01

    A simple and effective experimental approach has been developed and tested to study the temperature dependence of high-pressure methane sorption in moist organic-rich shales. This method, denoted as "multi-temperature" (short "multi-T") method, enables measuring multiple isotherms at varying temperatures in a single run. The measurement of individual sorption isotherms at different temperatures takes place in a closed system ensuring that the moisture content remains constant. The multi-T method was successfully tested for methane sorption on an organic-rich shale sample. Excess sorption isotherms for methane were measured at pressures of up to 25 MPa and at temperatures of 318.1 K, 338.1 K, and 348.1 K on dry and moisture-equilibrated samples. The measured isotherms were parameterized with a 3-parameter Langmuir-based excess sorption function, from which thermodynamic sorption parameters (enthalpy and entropy of adsorption) were obtained. Using these, we show that by taking explicitly into account water vapor as molecular species in the gas phase with temperature-dependent water vapor pressure during the experiment, more meaningful results are obtained with respect to thermodynamical considerations. The proposed method can be applied to any adsorbent system (coals, shales, industrial adsorbents) and any supercritical gas (e.g., CH4, CO2) and is particularly suitable for sorption measurements using the manometric (volumetric) method.

  8. "Multi-temperature" method for high-pressure sorption measurements on moist shales.

    PubMed

    Gasparik, Matus; Ghanizadeh, Amin; Gensterblum, Yves; Krooss, Bernhard M

    2013-08-01

    A simple and effective experimental approach has been developed and tested to study the temperature dependence of high-pressure methane sorption in moist organic-rich shales. This method, denoted as "multi-temperature" (short "multi-T") method, enables measuring multiple isotherms at varying temperatures in a single run. The measurement of individual sorption isotherms at different temperatures takes place in a closed system ensuring that the moisture content remains constant. The multi-T method was successfully tested for methane sorption on an organic-rich shale sample. Excess sorption isotherms for methane were measured at pressures of up to 25 MPa and at temperatures of 318.1 K, 338.1 K, and 348.1 K on dry and moisture-equilibrated samples. The measured isotherms were parameterized with a 3-parameter Langmuir-based excess sorption function, from which thermodynamic sorption parameters (enthalpy and entropy of adsorption) were obtained. Using these, we show that by taking explicitly into account water vapor as molecular species in the gas phase with temperature-dependent water vapor pressure during the experiment, more meaningful results are obtained with respect to thermodynamical considerations. The proposed method can be applied to any adsorbent system (coals, shales, industrial adsorbents) and any supercritical gas (e.g., CH4, CO2) and is particularly suitable for sorption measurements using the manometric (volumetric) method. PMID:24007116

  9. Effects of sorption kinetics on the fate and transport of pharmaceuticals in estuaries.

    PubMed

    Liu, Dong; Lung, Wu-Seng; Colosi, Lisa M

    2013-08-01

    Many current fate and transport models based on the assumption of instantaneous sorption equilibrium of contaminants in the water column may not be valid for certain pharmaceuticals with long times to reach sorption equilibrium. In this study, a sorption kinetics model was developed and incorporated into a water quality model for the Patuxent River Estuary to evaluate the effect of sorption kinetics. Model results indicate that the assumption of instantaneous sorption equilibrium results in significant under-prediction of water column concentrations for some pharmaceuticals. The relative difference between predicted concentrations for the instantaneous versus kinetic approach is as large as 150% at upstream locations in the Patuxent Estuary. At downstream locations, where sorption processes have had sufficient time to reach equilibrium, the relative difference decreases to roughly 25%. This indicates that sorption kinetics affect a model's ability to capture accumulation of pharmaceuticals into riverbeds and the transport of pharmaceuticals in estuaries. These results offer strong evidence that chemicals are not removed from the water column as rapidly as has been assumed on the basis of equilibrium-based analyses. The findings are applicable not only for pharmaceutical compounds, but also for diverse contaminants that reach sorption equilibrium slowly.

  10. Statistical physics studies of multilayer adsorption isotherm in food materials and pore size distribution

    NASA Astrophysics Data System (ADS)

    Aouaini, F.; Knani, S.; Ben Yahia, M.; Ben Lamine, A.

    2015-08-01

    Water sorption isotherms of foodstuffs are very important in different areas of food science engineering such as for design, modeling and optimization of many processes. The equilibrium moisture content is an important parameter in models used to predict changes in the moisture content of a product during storage. A formulation of multilayer model with two energy levels was based on statistical physics and theoretical considerations. Thanks to the grand canonical ensemble in statistical physics. Some physicochemical parameters related to the adsorption process were introduced in the analytical model expression. The data tabulated in literature of water adsorption at different temperatures on: chickpea seeds, lentil seeds, potato and on green peppers were described applying the most popular models applied in food science. We also extend the study to the newest proposed model. It is concluded that among studied models the proposed model seems to be the best for description of data in the whole range of relative humidity. By using our model, we were able to determine the thermodynamic functions. The measurement of desorption isotherms, in particular a gas over a solid porous, allows access to the distribution of pore size PSD.

  11. Study of uranium(VI) and radium(II) sorption at trace level on kaolinite using a multisite ion exchange model.

    PubMed

    Reinoso-Maset, Estela; Ly, Jacques

    2016-06-01

    Uranium and the long-lived decay product radium-226 are abundantly present in mine wastes produced during uranium extraction activities. In the case of release to the surrounding environment, these radionuclides are at trace level compared to groundwater solutes, and the presence, content and properties of clay minerals in the host environment influence the extent of radionuclide sorption and, in turn, migration. Since clays are known to have the distinctive property of retaining ions, the aim of this work was to study the sorption of trace U(VI) and Ra(II) on a common phyllosilicate mineral, kaolinite, in the presence of excess K, a common groundwater cation, in order to obtain a thermodynamic database that describes the ion exchange equilibria occurring at the mineral-solution interface. Following a detailed experimental protocol using chemical and radiochemical analytical techniques, batch experiments over a wide pH range (from 2 to 11) and fixed concentration (ca. 10(-9) M), and additional adsorption isotherms at two different solution pH (6.2 and 10.4) over a concentration range (10(-10) to 10(-4) M) were carried out to measure the distribution coefficient (Kd) of U(VI) and Ra(II) sorption on kaolinite. The experimental sorption data was processed according to a general multisite sorbent/multispecies sorbate ion exchange model, which allowed deducing the charge of adsorbed species and the stoichiometry of the associated adsorption equilibria on kaolinite's surface sites. Aqueous speciation calculations predicted Ra(II) as Ra(2+) over the working pH range, and its adsorption curves and isotherms were explained using three sorption sites. Adsorption of U(VI) occurred on four sorption sites and was governed by its solution speciation, with positively charged hydroxylated (UO2(2+) and UO2(OH)(+)) and silicate (UO2(H3SiO4)(+)) species being adsorbed between pH 2 and 6, whereas its negatively charged forms (UO2(OH)3(-) and UO2(OH)4(2-)) dominated U(VI) sorption at

  12. Study of uranium(VI) and radium(II) sorption at trace level on kaolinite using a multisite ion exchange model.

    PubMed

    Reinoso-Maset, Estela; Ly, Jacques

    2016-06-01

    Uranium and the long-lived decay product radium-226 are abundantly present in mine wastes produced during uranium extraction activities. In the case of release to the surrounding environment, these radionuclides are at trace level compared to groundwater solutes, and the presence, content and properties of clay minerals in the host environment influence the extent of radionuclide sorption and, in turn, migration. Since clays are known to have the distinctive property of retaining ions, the aim of this work was to study the sorption of trace U(VI) and Ra(II) on a common phyllosilicate mineral, kaolinite, in the presence of excess K, a common groundwater cation, in order to obtain a thermodynamic database that describes the ion exchange equilibria occurring at the mineral-solution interface. Following a detailed experimental protocol using chemical and radiochemical analytical techniques, batch experiments over a wide pH range (from 2 to 11) and fixed concentration (ca. 10(-9) M), and additional adsorption isotherms at two different solution pH (6.2 and 10.4) over a concentration range (10(-10) to 10(-4) M) were carried out to measure the distribution coefficient (Kd) of U(VI) and Ra(II) sorption on kaolinite. The experimental sorption data was processed according to a general multisite sorbent/multispecies sorbate ion exchange model, which allowed deducing the charge of adsorbed species and the stoichiometry of the associated adsorption equilibria on kaolinite's surface sites. Aqueous speciation calculations predicted Ra(II) as Ra(2+) over the working pH range, and its adsorption curves and isotherms were explained using three sorption sites. Adsorption of U(VI) occurred on four sorption sites and was governed by its solution speciation, with positively charged hydroxylated (UO2(2+) and UO2(OH)(+)) and silicate (UO2(H3SiO4)(+)) species being adsorbed between pH 2 and 6, whereas its negatively charged forms (UO2(OH)3(-) and UO2(OH)4(2-)) dominated U(VI) sorption at

  13. Sorption of radionuclides by cement-based barrier materials

    SciTech Connect

    Li, Kefei Pang, Xiaoyun

    2014-11-15

    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.

  14. Analysis and modeling of moisture sorption behavior for antimicrobial composite protein films.

    PubMed

    Lei, Qiao; Pan, Jiazhen; Bao, Jianqiang; Huang, Zhiying; Zhang, Yuting

    2014-01-01

    The WPI-NaCas-GLY antimicrobial film takes full advantage of the controlled release of active or antimicrobial agents as well as demonstrates a great potential for functioning as an alternative biodegradable polymer in practical applications. The moisture sorption kinetics of the film as an important carrier of active agents was investigated at various relative humidities (RH). The results indicated that the moisture sorption characterization and procedure of this film can be described well by the empirical Peleg model with higher confidence and concordance. The model could predict the film's moisture content at any time (Mt), the time to reach any given level of R (tR), the equilibrium moisture at any RH condition (Me), and isotherm trend based upon experimental data and modeled constants k(1), k(2), a, b, c, and d without giving consideration to their physical meaning. The water vapor transmission rate of the WPI-NaCas-GLY antimicrobial film increased exponentially with increasing RH due to its hydrophilicity, which was primarily caused by the presence of glycerol in a higher content. The results also suggested that aw predominately affects the film's Me values compared with the temperature factor by fixed nonlinear multiple regression analyses.

  15. Regenerative Sorption Refrigerator

    NASA Technical Reports Server (NTRS)

    Jones, Jack A.; Wen, Liang-Chi; Bard, Steven

    1991-01-01

    Two-stage sorption refrigerator achieves increased efficiency via regenerative-heating concept in which waste heat from praseodymium/cerium oxide (PCO) chemisorption compressor runs charcoal/krypton (C/Kr) sorption compressor. Waste heat from each PCO sorption compressor used to power surrounding C/Kr sorption compressor. Flows of heat in two compressor modules controlled by gas-gap thermal switches. Has no wearing moving parts other than extremely long life, room-temperature check valves operating about twice per hour. Virtually no measurable vibration, and has potential operating life of at least ten years.

  16. Thallium(I) sorption using Prussian blue immobilized in alginate capsules.

    PubMed

    Vincent, Thierry; Taulemesse, Jean-Marie; Dauvergne, Agnès; Chanut, Thomas; Testa, Flaviano; Guibal, Eric

    2014-01-01

    Prussian blue (PB) was immobilized in alginate capsules. The composite sorbent was used for the recovery of Tl(I) ions from slightly acidic solutions: optimum pH being close to 4. The sorption isotherm can be described by the bi-site Langmuir sorption isotherm. This means that the metal ion can be bound through two different sorption sites: one having a strong affinity for Tl(I) (probably PB), the other having a lower affinity (probably the encapsulating material). The kinetics are described by either the pseudo-second order rate equation or the Crank's equation (resistance to intraparticle diffusion). The ionic strength (increased by addition of NaCl, KCl or CaCl₂) slightly decreased sorption capacity. The SEM-EDX analysis of PB-alginate capsules (before and after Tl(I) sorption) shows that the PB is homogeneously distributed in the capsules and that all reactive groups remain available for metal binding.

  17. Features of the sorption of phenylalanine by profiled ion-exchange membranes

    NASA Astrophysics Data System (ADS)

    Vasil'eva, V. I.; Goleva, E. A.; Selemenev, V. F.

    2016-10-01

    Features of the equilibrium sorption of phenylalanine from neutral media by profiled ion-exchange membranes in a wide range of concentrations is studied under static conditions. The mechanism of phenylalanine sorption by ion-exchange membranes with profiled and smooth surfaces is discussed. It is shown that phenylalanine sorption is accompanied by the formation of spatial associative structures of the aminoacid in an external equilibrium solution, and in a solution of the membrane's pore spaces or on its surface. The increased sorption capacity of the profiled membranes is explained by features of the microstructure of their surface and volume.

  18. Sorption of cesium ions by nanostructured calcium aluminosilicates

    NASA Astrophysics Data System (ADS)

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

    2016-10-01

    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.

  19. Sorption of chlorobenzenes to cape cod aquifer sediments

    USGS Publications Warehouse

    Barber, L.B.

    1994-01-01

    Sorption of tetra- and pentachlorobenzene by sediment from a glacial outwash aquifer on Cape Cod, MA, was evaluated. Particle size and mineralogical fractions (separated based on paramagnetic susceptibility) were characterized with respect to sediment organic carbon (SOC), mineralogy, surface area, metal oxide coatings, and spatial variability. SOC increases by a factor of 10 as particle size decreases from 500-1000 to ?? 25 % in the <63-??m fraction, and SOC is preferentially associated with the magnetic minerals. Sorption increases with decreasing particle size (increasing SOC, magnetic minerals, surface area, and metal oxyhydroxides), and the magnetic mineral fraction has greater sorption than the bulk or nonmagnetic fractions. Removal of SOC decreases sorption proportional to the decrease in SOC and results in a nonlinear isotherm.

  20. Studies on the sorption of praseodymium (III), holmium (III) and cobalt (II) from nitrate medium using TVEX-PHOR resin.

    PubMed

    El-Dessouky, S I; El-Sofany, E A; Daoud, J A

    2007-05-01

    The use of TVEX-PHOR resin for the sorption of praseodymium (III), holmium (III) and cobalt (II) from nitrate medium was carried out using batch and column techniques. Various parameters affecting the uptake of these metal ions such as v/m ratio, pH and the metal ion concentration were separately studied. Effect of temperature on the equilibrium distribution values has been studied to evaluate the changes in standard thermodynamic quantities. Experimental results of the investigated metal ions were found to fit to Freundlich isotherm model over the entire studied concentration range. Selectivity sequence of the resin for these metals is Ho>Pr>Co. The recovery of the investigated metals from the loaded resin is preformed with 0.1M sulphuric acid.

  1. Sorption of metals by Chlorobium spp.

    PubMed

    Garcia-Gil, J; Borrego, C

    1997-12-01

    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.

  2. Carbon Dioxide Transport and Sorption Behavior in Confined Coal Cores for Enhanced Coalbed Methane and CO2 Sequestration

    SciTech Connect

    Jikich, S.A.; McLendon, T.R.; Seshadri, K.S.; Irdi, G.A.; Smith, D.H.

    2007-11-01

    Measurements of sorption isotherms and transport properties of CO2 in coal cores are important for designing enhanced coalbed methane/CO2 sequestration field projects. Sorption isotherms measured in the lab can provide the upper limit on the amount of CO2 that might be sorbed in these projects. Because sequestration sites will most likely be in unmineable coals, many of the coals will be deep and under considerable lithostatic and hydrostatic pressures. These lithostatic pressures may significantly reduce the sorption capacities and/or transport rates. Consequently, we have studied apparent sorption and diffusion in a coal core under confining pressure. A core from the important bituminous coal Pittsburgh #8 was kept under a constant, three-dimensional external stress; the sample was scanned by X-ray computer tomography (CT) before, then while it sorbed, CO2. Increases in sample density due to sorption were calculated from the CT images. Moreover, density distributions for small volume elements inside the core were calculated and analyzed. Qualitatively, the computerized tomography showed that gas sorption advanced at different rates in different regions of the core, and that diffusion and sorption progressed slowly. The amounts of CO2 sorbed were plotted vs. position (at fixed times) and vs. time (for various locations in the sample). The resulting sorption isotherms were compared to isotherms obtained from powdered coal from the same Pittsburgh #8 extended sample. The results showed that for this single coal at specified times, the apparent sorption isotherms were dependent on position of the volume element in the core and the distance from the CO2 source. Also, the calculated isotherms showed that less CO2 was sorbed than by a powdered (and unconfined) sample of the coal. Changes in density distributions during the experiment were also observed. After desorption, the density distribution of calculated volume elements differed from the initial distribution

  3. Sorption of toxic heavy metals to soil.

    PubMed

    Alumaa, Priit; Kirso, Uuve; Petersell, Valter; Steinnes, Eiliv

    2002-02-01

    The surface soil is a major recipient of pollutants, including heavy metals, through atmospheric deposition, agricultural practices, and waste disposal. In the present work the sorption capacity of different types of soils to toxic heavy metals, i.e. chromium, copper, cadmium and lead has been studied. Experimental adsorption data for metals to the soil obtained by the batch method were fitted by linear isotherm. The various soils showed a very different behaviour in sorption of heavy metals. The distribution coefficient Kd, which is an indication of the adsorbing capacity of the substrate, varies within a wide range, from 57 to 53,000 l kg-1. Desorption of metals from the solid phase was found to be small, indicating that the soil matrix is affecting the metal mobility by modifying the bonding of pollutants to the soil system consequently affecting the potential for soil remediation processes.

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

    PubMed

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

    2016-09-01

    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. PMID:27281543

  5. Isothermal and Adiabatic Measurements.

    ERIC Educational Resources Information Center

    McNairy, William W.

    1996-01-01

    Describes the working of the Adiabatic Gas Law Apparatus, a useful tool for measuring the pressure, temperature, and volume of a variety of gases undergoing compressions and expansions. Describes the adaptation of this apparatus to perform isothermal measurements and discusses the theory behind the adiabatic and isothermal processes. (JRH)

  6. Sorption testing and generalized composite surface complexation models for determining uranium sorption parameters at a proposed in-situ recovery site

    DOE PAGESBeta

    Johnson, Raymond H.; Truax, Ryan A.; Lankford, David A.; Stone, James J.

    2016-02-03

    Solid-phase iron concentrations and generalized composite surface complexation models were used to evaluate procedures in determining uranium sorption on oxidized aquifer material at a proposed U in situ recovery (ISR) site. At the proposed Dewey Burdock ISR site in South Dakota, USA, oxidized aquifer material occurs downgradient of the U ore zones. Solid-phase Fe concentrations did not explain our batch sorption test results,though total extracted Fe appeared to be positively correlated with overall measured U sorption. Batch sorption test results were used to develop generalized composite surface complexation models that incorporated the full genericsorption potential of each sample, without detailedmore » mineralogiccharacterization. The resultant models provide U sorption parameters (site densities and equilibrium constants) for reactive transport modeling. The generalized composite surface complexation sorption models were calibrated to batch sorption data from three oxidized core samples using inverse modeling, and gave larger sorption parameters than just U sorption on the measured solidphase Fe. These larger sorption parameters can significantly influence reactive transport modeling, potentially increasing U attenuation. Because of the limited number of calibration points, inverse modeling required the reduction of estimated parameters by fixing two parameters. The best-fit models used fixed values for equilibrium constants, with the sorption site densities being estimated by the inversion process. While these inverse routines did provide best-fit sorption parameters, local minima and correlated parameters might require further evaluation. Despite our limited number of proxy samples, the procedures presented provide a valuable methodology to consider for sites where metal sorption parameters are required. Furthermore, these sorption parameters can be used in reactive transport modeling to assess downgradient metal attenuation, especially when no other

  7. Molecular Scale Assessment of Methylarsenic Sorption on Aluminum Oxide

    SciTech Connect

    Shimizu, M.; Ginder-Vogel, M; Parikh, S; Sparks, D

    2010-01-01

    Methylated forms of arsenic (As), monomethylarsenate (MMA) and dimethylarsenate (DMA), have historically been used as herbicides and pesticides. Because of their large application to agriculture fields and the toxicity of MMA and DMA, the sorption of methylated As to soil constituents requires investigation. MMA and DMA sorption on amorphous aluminum oxide (AAO) was investigated using both macroscopic batch sorption kinetics and molecular scale extended X-ray absorption fine structure (EXAFS) and Fourier transform infrared (FTIR) spectroscopic techniques. Sorption isotherm studies revealed sorption maxima of 0.183, 0.145, and 0.056 mmol As/mmol Al for arsenate (As{sup V}), MMA, and DMA, respectively. In the sorption kinetics studies, 100% of added As{sup V} was sorbed within 5 min, while 78% and 15% of added MMA and DMA were sorbed, respectively. Desorption experiments, using phosphate as a desorbing agent, resulted in 30% release of absorbed As{sup V}, while 48% and 62% of absorbed MMA and DMA, respectively, were released. FTIR and EXAFS studies revealed that MMA and DMA formed mainly bidentate binuclear complexes with AAO. On the basis of these results, it is proposed that increasing methyl group substitution results in decreased As sorption and increased As desorption on AAO.

  8. Interactions of poly(amidoamine) dendrimers with the surfactants SDS, DTAB, and C12EO6: an equilibrium and structural study using a SDS selective electrode, isothermal titration calorimetry, and small angle neutron scattering.

    PubMed

    Sidhu, J; Bloor, The Late D M; Couderc-Azouani, S; Penfold, J; Holzwarth, J F; Wyn-Jones, E

    2004-10-12

    Interactions in aqueous solutions of different generations of poly(amidoamine) (PAMAM) dendrimers containing amine, hydroxyl, or delta-glucolactone functional groups at the periphery with the anionic surfactant sodium dodecyl sulfate (SDS) were investigated. We used a SDS-specific electrode (EMF) for SDS monomer concentration monitoring, isothermal titration calorimetry (ITC) for binding information, and small angle neutron scattering (SANS) for structural studies. ITC experiments monitoring the interaction of the dendrimers with cationic dodecyltrimethylammonium bromide (DTAB) and nonionic hexaethylene glycol mono-n-dodecyl ether (C12EO6) showed no significant binding effects. In contrast, SDS binds to all of the above dendrimers. EMF and ITC data demonstrated a regular trend for both the onset of binding and binding saturation as the generation in each family of dendrimers increased. In addition, generation G6 exhibited a noncooperative binding process at very low SDS concentrations. Furthermore, the onset of cooperative binding in the EMF experiments started at lower concentrations as the weight % (w/v), the size, and the numbers of the internal or surface groups increased. On the other hand, the binding capacity of the dendrimers showed only a small dependence on the above parameters. At SDS concentrations approaching the binding limit and also at selective concentrations within the binding range, SANS measurements indicated that in all cases the bound surfactant is in the micellar form. From the electromotive force (EMF) measurements, ITC data, and SANS data, the stoichiometry of the supramolecular complexes was determined.

  9. Sorption Modeling of Strontium, Plutonium, Uranium and Neptunium Adsorption on Monosodium Titanate

    SciTech Connect

    Fondeur, F.F.

    2003-10-30

    We examined the ability of various equilibrium isotherms to replicate the available data for the adsorption of strontium (Sr), plutonium (Pu), uranium (U) and neptunium (Np) on monosodium titanate (MST) during the treatment of simulated and actual Savannah River Site high-level waste. The analysis considered 29 isotherm models from the literature. As part of this study, we developed a general method for selecting the best isotherm models. The selection criteria for rating the isotherms considered the relative error in predicting the experimental data, the complexity of the mathematical expressions, the thermodynamic validity of the expressions, and statistical significance for the expressions. The Fowler Guggenheim-Jovanovic Freundlich (FG-JF), the Fowler Guggenheim-Langmuir Freundlich (FG-LF) and the Dubinin-Astashov (DA) models each reliably predicted the actinide and strontium adsorption on MST. The first two models describe the adsorption process by single layer formation and later al interactions between adsorbed sorbates while the Dubinin-Astashov model assumes volume filling of micropores (by osmotic pressure difference). These two mechanisms include mutually exclusive assumptions. However, we can not determine which model best represents the various adsorption mechanisms on MST. Based on our analysis, the DA model predicted the data well. The DA model assumes that an initial sorption layer forms after which networking begins in the pore spaces, filling the volume by a second mechanism. If this mechanism occurs in MST, as the experimental data suggests, then we expect all the empty and closed spaces of MST to contain actinides and strontium when saturated. Prior microstructure analyses determined that the MST surface is best described as heterogeneous (i.e., a semi-crystalline outer layer on an amorphous core) or composite material for adsorption. Therefore, we expect the empty spaces (of nanometer size) between the crystalline units in the fibrous material

  10. As(V), Cr(III) and Cr(VI) sorption on biochars and soil

    NASA Astrophysics Data System (ADS)

    Diamadopoulos, Evan; Agrafioti, Evita; Kalderis, Dimitrios

    2014-05-01

    The use of biochar, as a cost effective sorbent for heavy metal removal from contaminated water and soils is becoming a very promising practice. In this study, rice husk, the organic fraction of solid wastes, as well as sewage sludge were used as precursors for biochar production. The first was chosen as one of the most abundant types of biomass worldwide and the other two in order to find alternative innovative uses of these wastes. A series of batch kinetic and equilibrium (sorption and desorption) experiments was conducted using As(V), Cr(III) and Cr(VI) as adsorbates. The specific heavy metals were chosen in order to assess biochars removal capacity towards both anionic and cationic metals. Apart from biochars, a sandy loam soil was also used as adsorbent for metal removal. Knowing the separate behavior of biochars and soil towards metal sorption, it could be the first step in explaining the fate of heavy metals in a biochar amended soil. The kinetic study showed that, for all adsorbents and metals examined, sorption can be well described by the pseudo-second order kinetic model. What is more, simulation of sorption isotherms gave a better fit for the Freundlich model, possibly due to the heterogeneous surface of the initial biomasses and the fine aggregates that soil consists of. Based on the equilibrium study, the materials examined removed more than 95% of the initial Cr(III). This is possibly related to the electrostatic interactions between adsorbents negative surface charge and Cr(III) cations. However, removal rates for As(V) and Cr(VI) anions were significantly lower. Biochar derived from sewage sludge was efficient in removing 89% of Cr(VI) and 53% of As(V). Its ash high Fe2O3 content may have enhanced metal adsorption via precipitation. Soil was the most effective material for the removal of As(V), yet it could not strongly retain metal anions compared to biochars, as a significant amount of the adsorbed metal was released during desorption

  11. Effect of Cosolutes on the Sorption of Phenanthrene onto Mineral Surface of River Sediments and Kaolinite

    PubMed Central

    2014-01-01

    Sorption of phenanthrene onto the natural sediment with low organic carbon content (OC%), organic-free sediment, and kaolinite was investigated through isotherm experiments. Effects of cosolutes (pyrene, 4-n-nonyphenol (NP), and humic acid (HA)) on phenanthrene sorption were also studied by comparing apparent solid-water distribution coefficients (Kdapp) of phenanthrene. Two addition sequences, including “cosolute added prior to phenanthrene” and “cosolute and phenanthrene added simultaneously,” were adopted. The Freundlich model fits phenanthrene sorption on all 3 sorbents well. The sorption coefficients on these sorbents were similar, suggesting that mineral surface plays an important role in the sorption of hydrophobic organic contaminants on low OC% sediments. Cosolutes could affect phenanthrene sorption on the sorbents, which depended on their properties, concentrations, and addition sequences. Pyrene inhibited phenanthrene sorption. Sorbed NP inhibited phenanthrene sorption at low levels and promoted sorption at high levels. Similar to NP, effect of HA on phenanthrene sorption onto the natural sediment depended on its concentrations, whereas, for the organic-free sediment and kaolinite, preloading of HA at high levels led to an enhancement in phenanthrene Kdapp while no obvious effect was observed at low HA levels; dissolved HA could inhibit phenanthrene sorption on the two sorbents. PMID:25147865

  12. Sorption of methane and carbon dioxide mixtures in Polish hard coals considered in terms of adsorption-absorption model

    NASA Astrophysics Data System (ADS)

    Jodłowski, G. S.; Baran, P.; Wójcik, M.; Nodzeński, A.; Porada, St.; Milewska-Duda, J.

    2007-04-01

    The measurements of gas mixture sorption of CO 2 + CH 4 (50%:50%) on hard coals were carried out using an original measurement method. The accuracy of the experimental data was controlled by using a gas chromatograph. Experimental sorption isotherms of individual gases were used for the simulation of sorption of their mixtures. A good agreement was obtained between the simulated and experimental data.

  13. Sorption Modeling and Verification for Off-Gas Treatment

    SciTech Connect

    Tavlarides, Lawrence L.; Lin, Ronghong; Nan, Yue; Yiacoumi, Sotira; Tsouris, Costas; Ladshaw, Austin; Sharma, Ketki; Gabitto, Jorge; DePaoli, David

    2015-04-29

    The project has made progress toward developing a comprehensive modeling capability for the capture of target species in off gas evolved during the reprocessing of nuclear fuel. The effort has integrated experimentation, model development, and computer code development for adsorption and absorption processes. For adsorption, a modeling library has been initiated to include (a) equilibrium models for uptake of off-gas components by adsorbents, (b) mass transfer models to describe mass transfer to a particle, diffusion through the pores of the particle and adsorption on the active sites of the particle, and (c) interconnection of these models to fixed bed adsorption modeling which includes advection through the bed. For single-component equilibria, a Generalized Statistical Thermodynamic Adsorption (GSTA) code was developed to represent experimental data from a broad range of isotherm types; this is equivalent to a Langmuir isotherm in the two-parameter case, and was demonstrated for Kr on INL-engineered sorbent HZ PAN, water sorption on molecular sieve A sorbent material (MS3A), and Kr and Xe capture on metal-organic framework (MOF) materials. The GSTA isotherm was extended to multicomponent systems through application of a modified spreading pressure surface activity model and generalized predictive adsorbed solution theory; the result is the capability to estimate multicomponent adsorption equilibria from single-component isotherms. This advance, which enhances the capability to simulate systems related to off-gas treatment, has been demonstrated for a range of real-gas systems in the literature and is ready for testing with data currently being collected for multicomponent systems of interest, including iodine and water on MS3A. A diffusion kinetic model for sorbent pellets involving pore and surface diffusion as well as external mass transfer has been established, and a methodology was developed for determining unknown diffusivity parameters from transient

  14. Sorption of non-polar organic compounds by micro-sized plastic particles in aqueous solution.

    PubMed

    Hüffer, Thorsten; Hofmann, Thilo

    2016-07-01

    The presence of microscale polymer particles (i.e., microplastics) in the environment has become a major concern in recent years. Sorption of organic compounds by microplastics may affect the phase distribution within both sediments and aqueous phases. To investigate this process, isotherms were determined for the sorption of seven aliphatic and aromatic organic probe sorbates by four polymers with different physico-chemical properties. Sorption increased in the order polyamide < polyethylene < polyvinylchloride < polystyrene. This order does not reflect the particle sizes of the investigated microplastics within the aqueous dispersions, indicating the influence of additional factors (e.g., π-π-interactions) on the sorption of aromatic compounds by polystyrene. Linear isotherms by polyethylene suggested that sorbate uptake was due to absorption into the bulk polymer. In contrast, non-linear isotherms for sorption by PS, PA, and PVC suggest a predominance of adsorption onto the polymer surface, which is supported by the best fit of these isotherms using the Polanyi-Manes model. A strong relationship between the sorption coefficients of the microplastics and the hydrophobicity of the sorbates suggests that hydrophobic interactions are of major importance. PMID:27086075

  15. Sorption of non-polar organic compounds by micro-sized plastic particles in aqueous solution.

    PubMed

    Hüffer, Thorsten; Hofmann, Thilo

    2016-07-01

    The presence of microscale polymer particles (i.e., microplastics) in the environment has become a major concern in recent years. Sorption of organic compounds by microplastics may affect the phase distribution within both sediments and aqueous phases. To investigate this process, isotherms were determined for the sorption of seven aliphatic and aromatic organic probe sorbates by four polymers with different physico-chemical properties. Sorption increased in the order polyamide < polyethylene < polyvinylchloride < polystyrene. This order does not reflect the particle sizes of the investigated microplastics within the aqueous dispersions, indicating the influence of additional factors (e.g., π-π-interactions) on the sorption of aromatic compounds by polystyrene. Linear isotherms by polyethylene suggested that sorbate uptake was due to absorption into the bulk polymer. In contrast, non-linear isotherms for sorption by PS, PA, and PVC suggest a predominance of adsorption onto the polymer surface, which is supported by the best fit of these isotherms using the Polanyi-Manes model. A strong relationship between the sorption coefficients of the microplastics and the hydrophobicity of the sorbates suggests that hydrophobic interactions are of major importance.

  16. Concurrent Co2+ and Sr2+ sorption from binary mixtures using aluminum industry waste: Kinetic study

    NASA Astrophysics Data System (ADS)

    Milenković, A.; Smičiklas, I.; Šljivić-Ivanović, M.; Vukelić, N.

    2015-12-01

    Multi-component sorption studies are essential to identify the applicability of red mud as a lowcost sorbent for the simultaneous removal of metal ions from wastewaters. Sorption kinetics of Co2+ and Sr2+ ions was investigated, at different total concentrations of mixtures and different molar ratios of two cations. Kinetics of metal sorption from binary systems was found to be well described by pseudo-second order rate model. Equilibrium sorbed amounts and equilibrium times for Co2+ sorption increased with the increase of its total concentration in the mixture, whereas pseudo-second order rate constants exhibited the opposite trend. Sr2+ sorption was strongly suppressed in the presence of Co2+ ions, and the removal efficiency decreased with increasing concentration and mole fraction of Co2+. Red mud can be used for simultaneous Co2+ and Sr2+ removal from mixtures of lower initial concentration, otherwise Co2+ sorption is dominant.

  17. RESORCINOL-FORMALDEHYDE ADSORPTION OF CESIUM (Cs+) FROM HANFORD WASTE SOLUTIONS-PART I: BATCH EQUILIBRIUM STUDY

    SciTech Connect

    HASSAN, NEGUIBM

    2004-03-30

    Batch equilibrium measurements were conducted with a granular Resorcinol-Formaldehyde (RF) resin to determine the distribution coefficients (Kds) for cesium. In the tests, Hanford Site actual waste sample containing radioactive cesium and a pretreated waste sample that was spiked with non-radioactive cesium were used. Initial concentrations of non-radioactive cesium in the waste sample were varied to generate an equilibrium isotherm for cesium. Two additional tests were conducted using a liquid to solid phase ratio of 10 and a contact time of 120 hours. The measured distribution coefficient (Kd) for radioactive cesium (137Cs) was 948 mL/g; the Kd for non-radioactive cesium (133Cs) was 1039 mL/g. The Kd for non-radioactive cesium decreased from 1039 to 691 mL/g as the initial cesium concentration increased. Very little change of the Kd was observed at initial cesium concentrations above 64 mg/mL. The maximum sorption capacity for cesium on granular RF resin was 1.17 mmole/g dry resin. T his value was calculated from the fit of the equilibrium isotherm data to the Dubinin-Radushkevich equation. Previously, a total capacity of 2.84 mmole/g was calculated by Bibler and Wallace for air-dried RF resin.

  18. Defluoridation by Bacteriogenic Iron Oxides: Sorption Studies

    NASA Astrophysics Data System (ADS)

    Evans, K.; Ferris, F.

    2009-05-01

    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

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

    PubMed

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

    2016-03-01

    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.

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

    PubMed

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

    2016-03-01

    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. PMID:27065399

  1. Sorption and transport of atrazine in an agricultural soil

    NASA Astrophysics Data System (ADS)

    Hakan Akyol, Nihat

    2014-05-01

    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.

  2. Enhanced sorption of polycyclic aromatic hydrocarbons from aqueous solution by modified pine bark.

    PubMed

    Li, Yungui; Chen, Baoliang; Zhu, Lizhong

    2010-10-01

    To enhance removal efficiency of natural sorbent with polycyclic aromatic hydrocarbons (PAHs), single-solute and bi-solute sorption of phenanthrene and pyrene onto raw and modified pine bark were investigated. Pine bark was modified using Soxhlet extraction, saponification and acid hydrolysis, yielding six bark fractions with different chemical compositions. Raw pine bark exhibited high affinities with PAHs, and sorption was dominated by partitioning. The relatively nonlinear sorption isotherms of modified bark were attributed to the specific interaction between sorbate and aromatic core of sorbent. Comparison with lipid and suberin, lignin was the most powerful sorption medium, but which was almost completely suppressed by coexisting polysaccharide. After consuming polysaccharide by acid hydrolysis, sorption of pine bark fractions was notably increased (4-17 folds); and sorption of pyrene just decreased 16-34% with phenanthrene as a competitor. These observations suggest that pine bark is of great potential for PAHs removal and can be significantly promoted by acid hydrolysis for environmental application.

  3. Competitive Sorption and Desorption of Chlorinated Organic Solvents (DNAPLs) in Engineered Natural Organic Matter

    SciTech Connect

    Tang, Jixin; Weber, Walter J., Jr.

    2004-03-31

    The effects of artificially accelerated geochemical condensation and maturation of natural organic matter on the sorption and desorption of trichloroethylene (TCE) and tetrachloroethylene (PCE) were studied. The sorption and desorption of TCE in the presence and absence of the competing PCE and 1,2-dichlorobenzene (DCB) were also examined. A sphagnum peat comprising geologically young organic matter was artificially ''aged'' using superheated water, thus increasing the aromaticity and the degree of condensation of its associated organic matter. The sorption of all solutes tested were increased remarkably and their respective desorptions reduced, by the aged peat. The sorption capacities and isotherm nonlinearities of the peat for both TCE and PCE were found to increase as treatment temperature increased. In the competitive sorption studies, both PCE and DCB were found to depress TCE sorption, with PCE having greater effects than DCB, presumably because the molecular structure o f the former is more similar to that of TCE.

  4. Antimony sorption at gibbsite-water interface.

    PubMed

    Rakshit, Sudipta; Sarkar, Dibyendu; Punamiya, Pravin; Datta, Rupali

    2011-07-01

    Antimony (Sb) is extensively used in flame retardants, lead-acid batteries, solder, cable coverings, ammunition, fireworks, ceramic and porcelain glazes and semiconductors. However, the geochemical fate of antimony (Sb) remained largely unexplored. Among the different Sb species, Sb (V) is the dominant form in the soil environment in a very wide redox range. Although earlier studies have examined the fate of Sb in the presence of iron oxides such as goethite and hematite, few studies till date reported the interaction of Sb (V) with gibbsite, a common soil Al-oxide mineral. The objective of this study was to understand the sorption behavior of Sb (V) on gibbsite as a function of various solution properties such as pH, ionic strength (I), and initial Sb concentrations, and to interpret the sorption-edge data using a surface complexation model. A batch sorption study with 20 g L(-1) gibbsite was conducted using initial Sb concentrations range of 2.03-16.43 μM, pH values between 2 and 10, and ionic strengths (I) between 0.001 and 0.1M. The results suggest that Sb (V) sorbs strongly to the gibbsite surface, possibly via inner-sphere type mechanism with the formation of a binuclear monodentate surface complex. Weak I effect was noticed in sorption-edge data or in the isotherm data at a low surface coverage. Sorption of Sb (V) on gibbsite was highest in the pH range of 2-4, and negligible at pH 10. Our results suggest that gibbsite will likely play an important role in immobilizing Sb (V) in the soil environment.

  5. Antimony sorption at gibbsite-water interface.

    PubMed

    Rakshit, Sudipta; Sarkar, Dibyendu; Punamiya, Pravin; Datta, Rupali

    2011-07-01

    Antimony (Sb) is extensively used in flame retardants, lead-acid batteries, solder, cable coverings, ammunition, fireworks, ceramic and porcelain glazes and semiconductors. However, the geochemical fate of antimony (Sb) remained largely unexplored. Among the different Sb species, Sb (V) is the dominant form in the soil environment in a very wide redox range. Although earlier studies have examined the fate of Sb in the presence of iron oxides such as goethite and hematite, few studies till date reported the interaction of Sb (V) with gibbsite, a common soil Al-oxide mineral. The objective of this study was to understand the sorption behavior of Sb (V) on gibbsite as a function of various solution properties such as pH, ionic strength (I), and initial Sb concentrations, and to interpret the sorption-edge data using a surface complexation model. A batch sorption study with 20 g L(-1) gibbsite was conducted using initial Sb concentrations range of 2.03-16.43 μM, pH values between 2 and 10, and ionic strengths (I) between 0.001 and 0.1M. The results suggest that Sb (V) sorbs strongly to the gibbsite surface, possibly via inner-sphere type mechanism with the formation of a binuclear monodentate surface complex. Weak I effect was noticed in sorption-edge data or in the isotherm data at a low surface coverage. Sorption of Sb (V) on gibbsite was highest in the pH range of 2-4, and negligible at pH 10. Our results suggest that gibbsite will likely play an important role in immobilizing Sb (V) in the soil environment. PMID:21481912

  6. Experimental study of water desorption isotherms and thin-layer convective drying kinetics of bay laurel leaves

    NASA Astrophysics Data System (ADS)

    Ghnimi, Thouraya; Hassini, Lamine; Bagane, Mohamed

    2016-02-01

    The aim of this work is to determine the desorption isotherms and the drying kinetics of bay laurel leaves (Laurus Nobilis L.). The desorption isotherms were performed at three temperature levels: 50, 60 and 70 °C and at water activity ranging from 0.057 to 0.88 using the statistic gravimetric method. Five sorption models were used to fit desorption experimental isotherm data. It was found that Kuhn model offers the best fitting of experimental moisture isotherms in the mentioned investigated ranges of temperature and water activity. The Net isosteric heat of water desorption was evaluated using The Clausius-Clapeyron equation and was then best correlated to equilibrium moisture content by the empirical Tsami's equation. Thin layer convective drying curves of bay laurel leaves were obtained for temperatures of 45, 50, 60 and 70 °C, relative humidity of 5, 15, 30 and 45 % and air velocities of 1, 1.5 and 2 m/s. A non linear regression procedure of Levenberg-Marquardt was used to fit drying curves with five semi empirical mathematical models available in the literature, The R2 and χ2 were used to evaluate the goodness of fit of models to data. Based on the experimental drying curves the drying characteristic curve (DCC) has been established and fitted with a third degree polynomial function. It was found that the Midilli Kucuk model was the best semi-empirical model describing thin layer drying kinetics of bay laurel leaves. The bay laurel leaves effective moisture diffusivity and activation energy were also identified.

  7. Bacterial sorption of heavy metals.

    PubMed Central

    Mullen, M D; Wolf, D C; Ferris, F G; Beveridge, T J; Flemming, C A; Bailey, G W

    1989-01-01

    Four bacteria, Bacillus cereus, B. subtilis, Escherichia coli, and Pseudomonas aeruginosa, were examined for the ability to remove Ag+, Cd2+, Cu2+, and La3+ from solution by batch equilibration methods. Cd and Cu sorption over the concentration range 0.001 to 1 mM was described by Freundlich isotherms. At 1 mM concentrations of both Cd2+ and Cu2+, P. aeruginosa and B. cereus were the most and least efficient at metal removal, respectively. Freundlich K constants indicated that E. coli was most efficient at Cd2+ removal and B. subtilis removed the most Cu2+. Removal of Ag+ from solution by bacteria was very efficient; an average of 89% of the total Ag+ was removed from the 1 mM solution, while only 12, 29, and 27% of the total Cd2+, Cu2+, and La3+, respectively, were sorbed from 1 mM solutions. Electron microscopy indicated that La3+ accumulated at the cell surface as needlelike, crystalline precipitates. Silver precipitated as discrete colloidal aggregates at the cell surface and occasionally in the cytoplasm. Neither Cd2+ nor Cu2+ provided enough electron scattering to identify the location of sorption. The affinity series for bacterial removal of these metals decreased in the order Ag greater than La greater than Cu greater than Cd. The results indicate that bacterial cells are capable of binding large quantities of different metals. Adsorption equations may be useful for describing bacterium-metal interactions with metals such as Cd and Cu; however, this approach may not be adequate when precipitation of metals occurs. Images PMID:2515800

  8. Removal of divalent nickel from aqueous solutions using Carissa carandas and Syzygium aromaticum: isothermal studies and kinetic modelling

    NASA Astrophysics Data System (ADS)

    Sharma, Sanjay K.; Mahiya, Suresh; Lofrano, Giusy

    2015-11-01

    Biosorptive removal of divalent nickel from aqueous solution using Carissa Carandas and Syzygium aromaticum was investigated in batch mode and the observations were correlated with the pH variation, agitation time, dose of the adsorbent and initial metal ion concentration in the solution. In the course of this study Sorption efficiency of C. carandas leaf powder found higher than that of S. aromaticum under identical experimental conditions. The maximum adsorption capacities estimated for Ni(II) through Freundlich isotherm model were 3.76 and 2.96 mg/g for C. carandas and S. aromaticum, respectively. In kinetic studies the correlation coefficient (R 2 = 0.99) for the pseudo-second order kinetics modal was higher than that of pseudo-first order kinetics model and the calculated value of q e for the pseudo-second order kinetic model resulted very close to the experimental value, which indicates that it fits well with the equilibrium data for Ni(II) sorption from aqueous solutions on biosorbents.

  9. Effects of biochar and clay amendment on nutrient sorption of an Arenosol in semi-arid NE-Brazil

    NASA Astrophysics Data System (ADS)

    Beusch, Christine; Kaupenjohann, Martin

    2014-05-01

    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

  10. Comparison of tetrachloromethane sorption to an alkylammonium-clay and an alkyldiammonium-clay

    USGS Publications Warehouse

    Smith, J.A.; Jaffe, P.R.

    1991-01-01

    The interlamellar space of Wyoming bentonite (clay) was modified by exchanging either decyltrimethyl-ammonium (DTMA) or decyltrimethyldiammonium (DTMDA) cations for inorganic ions, and tetrachloromethane sorption to the resulting two organoclays from water was studied at 10, 20, and 35??C. Only one end of the 10-carbon alkyl chain of the DTMA cation is attached to the silica surface of the clay mineral, and tetrachloromethane sorption of DTMA-clay is characterized by isotherm linearity, noncompetitive sorption, weak solute uptake, and a relatively low heat of sorption. Both ends of the 10-carbon chain of the DTMDA cation are attached to the silica surface of the clay mineral, and tetrachloromethane sorption to DTMDA-clay is characterized by nonlinear isotherms, competitive sorption, strong solute uptake, and a relatively high, exothermic heat of sorption that varies as a function of the mass of tetrachloromethane sorbed. Therefore, the attachment of both ends of the alkyl chain to the interlamellar mineral surface appears to change the sorption mechanism from a partition-dominated process to an adsorption-dominated process. ?? 1991 American Chemical Society.

  11. COSOLVENT EFFECTS ON SORPTION AND MOBILITY OF ORGANIC CONTAMINANTS IN SOILS

    EPA Science Inventory

    Batch equilibrium and column miscible displacement techniques were used to investigate the influence of an organic cosolvent (methanol) on the sorption and transport of three hydrophobic organic chemicals (HOCs) — naphthalene, phenanthrene, and diuron herbicide — in a sandy surfa...

  12. Sorption of isoflavones to river sediment and model sorbents and outcomes for larval fish exposed to contaminated sediment.

    PubMed

    Kelly, Megan M; Rearick, Daniel C; Overgaard, Camilla G; Schoenfuss, Heiko L; Arnold, William A

    2015-01-23

    Isoflavones are compounds whose presence in the aquatic environment is increasingly recognized and may be of concern due to their potential to act as endocrine disruptors. Sorption to particles may be a relevant removal mechanism for isoflavones. This work investigated the influence of pH, ionic strength, and sediment composition on sorption of genistein and daidzein, two key isoflavones, using sorption isotherms and edges. The effect of sorbed isoflavones on the survival, growth, and predator avoidance performance of larval fathead minnows (Pimephales promelas) was assessed. Sorption to goethite and kaolinite was pH-dependent, with a maximum near pH 7 for both compounds. Sorption to montmorillonite was ionic-strength dependent but largely pH-independent. Overall, sorption to sediments is likely to sequester less than 5% of isoflavones in a discharge. No statistically significant effects were observed for larvae exposed to sorbed isoflavones, suggesting that sorption to sediments reduces exposure to isoflavones. PMID:24792866

  13. Impact of coal structural heterogeneity on the nonideal sorption of organic contaminants.

    PubMed

    Shi, Xin; Fu, Heyun; Li, Yuan; Mao, Jingdong; Zheng, Shourong; Zhu, Dongqiang

    2011-06-01

    Carbonaceous geosorbents (black carbon, coal, and humin/kerogen) play a primary role in the nonideal sorption (isotherm nonlinearity, hysteresis, and multiphasic kinetics) of hydrophobic organic chemicals by soils and sediments. The present study investigated the impact of coal structural heterogeneity on sorption/desorption of two model monoaromatic compounds (1,3-dichlorobenzene and 1,3-dinitrobenzene). Due to the higher degree of aromaticity and condensation, anthracite showed stronger sorption affinity and nonlinearity and slower sorption kinetics than lignite. Removal of humic substances by alkali extraction and/or mineral fraction by acidification did not much affect organic carbon-normalized sorption coefficient to the coal, suggesting nearly complete accessibility of adsorption sites on the condensed organic carbon. However, the treatments greatly increased sorption kinetics and meanwhile alleviated hysteresis of 1,3-dinitrobenzene, as compared with the original lignite. These observations were attributed to the enhanced exposure of high-energy adsorption sites on the condensed organic carbon after exfoliating the surface coverage by humic substances and minerals. An empirical biphasic pseudo-second-order model consisting of a fast sorption phase and a slow sorption phase adequately quantified the overall sorption kinetics for the coal sorbents. The results indicated that the condensed organic carbon, in combination with other structural components, controls the nonideal sorption of unburned coal.

  14. Sorption and retardation of strontium in saturated Chinese loess: experimental results and model analysis.

    PubMed

    Huo, Lijuan; Qian, Tianwei; Hao, Junting; Zhao, Dongye

    2013-02-01

    Geological burial and landfill have been widely practiced for disposal of nuclear wastes. However, radionuclides in the waste leachate from landfill facilities can contaminate soil and groundwater. Chinese loess is widely distributed in China and has been involved in large-scale disposal of nuclear wastes. Consequently, there has been an urgent need for understanding and predicting the fate and transport of contaminants in both vadose and saturated zones in the loess. In this paper, the distribution coefficient (K(d)) values of Strontium between a Chinese loess and groundwater were determined in batch experiments. The isotherm could be described with nearly linear isotherm model, which resulted in a K(d) value of 40.0 cm(3)/g. Based on this K(d) value, the retardation factor (R(d), the ratio of pore water velocity to solute transport velocity) value was calculated to be 112.6. As an alternative approach, the R(d) value was also determined through independent column experiments and transport modeling. Bromide (Br(-)) was used as a non-reactive tracer, and reagent SrCl(2) was used as a surrogate for the radioactive isotope ((99)Sr) in the experiment because they share the same adsorption and transportation characteristics. An equilibrium-based model and a two-region non-equilibrium model were employed to interpret the column sorption data of Sr. The computer program, CXTFIT 2.1, was used to estimate the parameters by simulating the breakthrough and retention curves of Br and Sr, respectively. The resultant D (dispersion coefficient) value for Sr transport was much lower than that of Br(-), indicating the important effect of chemical non-equilibrium of Sr in the loess system. The observed Sr retention curves in the loess were best modeled by the two-site transport model. The R(d) value determined from batch equilibrium tests differed markedly from that determined from the column transport experiments, and the R(d) value decreased with increasing pore-water velocity

  15. Lead sorption-desorption from organic residues.

    PubMed

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

    2011-01-01

    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.

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

    SciTech Connect

    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.

    2013-01-02

    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.

  17. Carbon Dioxide Transport and Sorption Behavior in Confined Coal Cores for Carbon Sequestration

    SciTech Connect

    Jikich, Sinisha; McLendon, Robert; Seshadri, Kal; Irdi, Gino; Smith, Duane

    2009-01-01

    Measurements of sorption isotherms and transport properties of carbon dioxide (CO2) in coal cores are important for designing enhanced coalbed-methane/CO2-sequestration field projects. Sorption isotherms measured in the laboratory can provide the upper limit on the amount of CO2 that might be sorbed in these projects. Because sequestration sites will most likely be in unmineable coals, many of the coals will be deep and under considerable lithostatic and hydrostatic pressures. These lithostatic pressures may reduce the sorption capacities and/or transport rates significantly. Consequently, we have studied apparent sorption and diffusion in a coal core under confining pressure. A core from the important bituminous coal Pittsburgh #8 was kept under a constant, 3D effective stress; the sample was scanned by X-ray computer tomography (CT) before, then while, it sorbed CO2. Increases in sample density because of sorption were calculated from the CT images. Moreover, density distributions for small volume elements inside the core were calculated and analyzed. Qualitatively, the CT showed that gas sorption advanced at different rates in different regions of the core. and that diffusion and sorption progressed slowly. The amounts of CO2 sorbed were plotted vs. position (at fixed times) and vs. time (for various locations in the sample). The resulting sorption isotherms were compared to isotherms obtained from powdered coal from the same Pittsburgh #8 extended sample. The results showed that for this single coal at specified times, the apparent sorption isotherms were dependent on position of the volume element in the core and the distance from the CO2 source. Also, the calculated isotherms showed that less CO2 was sorbed than by a powdered (and unconfined) sample of the coal. Changes in density distributions during the experiment were also observed. After desorption, the density distribution of calculated

  18. The sorption of Zectran on bottom sediments and peat moss

    SciTech Connect

    Matthews, E.W.; Faust, S.D.

    1981-01-01

    A modified analytical method employed to determine the insecticide Zectran in natural waters frequently has resulted in erroneous data. The errors have been attributed to interferences from particulate matter in these waters. In order to evaluate analytical interferences due to sorption of Zectran on particulates, a series of experiments was performed using bottom sediments and a peat moss in contact with aqueous solutions of zectran at a pH values of 6.0 and 20 degrees C. Isotherm studies confirmed that Zectran sorption occurs in a direct relation to the amount of chemically oxidizable carbon present in the bottom sediments or peat moss. However, the extent of sorption was limited, which suggested that particulates may not be the primary interference in the modified analytical method.

  19. Evaluation of matrices for the sorption and biodegradation of phenanthrene.

    PubMed

    Leglize, Pierre; Saada, Alain; Berthelin, Jacques; Leyval, Corinne

    2006-07-01

    Permeable reactive barriers (PRBs), a new cost effective technology for the remediation of contaminated groundwater, have rarely been considered for PAH contamination. We evaluated three candidate matrices (activated carbon (AC), pouzzolana coated (PzF) or not (Pz) with heavy fuel oil) for phenanthrene (PHE) sorption capacity and the biodegradation of adsorbed PHE. Adsorption-desorption batch experiments showed higher sorption capacity of AC than PzF (60 fold) and Pz (1,500 fold). Sorption isotherms were not linear for all matrices as described by a Freundlich model. Phenanthrene desorption from AC and PzF within 48 h was limited (1-3%). Mineralization of (14)C-PHE by a PAH-degrading bacterial strain increased in the presence of AC and Pz (+16 and +12%). Among the three matrices, AC may be a good candidate for PRBs due to high adsorption, low desorption and increased PHE degradation.

  20. Sorption of heavy metals by the soil fungi 'Aspergillus niger' and Mucor rouxii

    SciTech Connect

    Mullen, M.D.; Wolf, D.C.; Beveridge, T.J.; Bailey, G.W.

    1992-01-01

    Sorption of the nitrate salts of cadmium(II), copper(II), lanthanum(III) and silver(I) by two fungi, Aspergillus niger and Mucor rouxii, was evaluated using Freundlich adsorption isotherms and energy dispersive X-ray electron microscopy. The linearized Freundlich isotherm described the metal sorption data well for metal concentrations of 5 microM-1 mM metal. Differences in metal binding were observed among metals, as well as between fungal species. Calculated Freundlich K values indicated that metal binding decreased in the order La(3+) > or = Ag(+) > Cu(2+) > Cd(2+). However, sorption of Ag(+) was greater than that of La(3+) from solutions of 0.1 and 1 mM metal and likely due to precipitation at the cell wall surface. At the 1 mM initial concentration, there were no significant differences between the two fungi in metal sorption, except for Ag(+) binding. At the 5 microM concentration, there was no difference between the fungi in their sorption capacities for the four metals. Electron microscopy-energy dispersive X-ray analysis indicated that silver precipitated onto cells as colloidal silver. The results indicate that Freundlich isotherms may be useful for describing short-term metal sorption by fungal biomass and for comparison with other soil constituents in standardized systems. (Copyright (c) 1992 Pergamon Press plc.)

  1. Experimental and Particle-Tracking Model Analysis of Anomalous Transport and Sorption of Nickel in Natural Soil Columns

    NASA Astrophysics Data System (ADS)

    Edery, Y.; Rubin, S.; Dror, I.; Berkowitz, B.

    2012-12-01

    Nickel migration measured in laboratory-scale, natural soil column experiments is shown to display anomalous (non-Fickian) transport and non-equilibrium adsorption and desorption patterns. Similar experiments using a conservative tracer also exhibit anomalous behavior. In parallel batch experiments, adsorption and desorption isotherms demonstrate hysteresis, indicating some permanent adsorption. While adsorption is described by the Langmuir isotherm, equilibrium concentrations are higher than those predicted by the same model for desorption. Furthermore, batch and flow-through column experiments show the occurrence of ion exchange of nickel with magnesium and potassium in the soil; aluminum and other ion concentrations are also affected by the presence of nickel. Strong retention of nickel during transport in soil columns leads to delayed initial breakthrough (~40 pore volumes), slow increase in concentration, and extended concentration tailing at long times. Standard models, including two-site non-equilibrium formulations, fail to capture these features quantitatively. We describe the mechanisms of transport and adsorption/desorption in terms of a continuous time random walk (CTRW) model, and use a particle tracking formulation to simulate the nickel migration in the column. This approach allows us to capture the non-Fickian transport and the subtle local effects of adsorption and desorption. The model uses transport parameters estimated from the conservative tracer and, as a starting point, adsorption/desorption parameters based on the batch experiments to account for the reactions. It is shown that the batch parameters under-estimate the actual adsorption in the column. The CTRW particle tracking model is shown to capture both the full evolution of the measured breakthrough curve and the measured spatial concentration profile. Analysis of these results provides further understanding of the interaction and dynamics between transport and sorption mechanisms in

  2. SORPTION KINETICS OF PAHS IN METHANOL-WATER SYSTEMS

    EPA Science Inventory

    The objectives of this study were to evaluate the relationships between the equilibrium sorption constant (Kp), the first-order desorption rate coefficient (k2), and the volumetric fraction of water miscible solvent (fc); and to utilize SPARC-calculated (SPARC Performs Automatic ...

  3. Characterization of nitrogen adsorption isotherms of thermally-treated organoclays using multifractal analysis

    NASA Astrophysics Data System (ADS)

    Lado, Marcos; Borisover, Mikhail; Paz-Gonzalez, Antonio

    2013-04-01

    Nitrogen adsorption isotherms of soils have been reported to exhibit multifractal behavior. In the present work, multifractal analysis is used to characterize changes in N2 adsorption isotherms of organoclays prepared with different cations and exposed to various thermal treatments. Wyoming bentonite was exchanged with benzyltrimethylammonium (BTMA-clay), tetraethylammonium (TEA-clay), and hexadecyltrimethylammonium exchanged at 41 and 90% of the cation exchange capacity of the clay (HDTMA41- and HDTMA90-clay). The resulting organoclays were exposed to temperatures ranging from 25 to 420°C during two hours, freeze-dried, and N2 adsorption isotherms were measured at 77°K. The obtained isotherms showed multifractal behavior, and parameters derived from Rényi and singularity spectra varied with changes in the organic cation and the treatment temperature. The type of cation was the dominant factor responsible for changes in spectra, and significant interactions were observed between type of cation and temperature for several parameters. Significant correlations were found between organic carbon content and multifractal parameters, indicating a relation between changes in N2 sorption sites and thermal transformations of the organic cations. Significant correlations were also found between some multifractal parameters and the heterogeneity exponent of a Freundlich model fitted to nitrobenzene isotherms measured in the organoclays, suggesting that multifractal analysis of N2 adsorption isotherms could be useful to analyze the heterogeneity of sorption sites when sorption determinations yield a limited amount of data.

  4. Sorption Properties of Iron-Magnesium and Nickel-Magnesium Mg2FeH6 and Mg2NiH4 Hydrides

    NASA Astrophysics Data System (ADS)

    Matysina, Z. A.; Zaginaichenko, S. Yu.; Shchur, D. V.; Gabdullin, M. T.

    2016-06-01

    Based on molecular-kinetic representations, theory of hydrogen absorption-desorption processes in binary Mg-Fe and Mg-Ni alloys is developed. Free energies of hydrides of these alloys are calculated. Equations of their thermodynamically equilibrium state determining the P-T-c diagrams are derived. A temperature dependence of the desorbed hydrogen concentration is established. A maximal desorption temperature is estimated. The state diagrams determining the concentration dependence of the maximal desorption temperature are constructed. Isopleths and isotherms of hydrogen solubility in the alloys are calculated. The possibility of manifestation of the hysteresis effect in hydrogen solubility isotherms is revealed and the decrease of the width and length of a hysteresis loop with increasing temperature is demonstrated together with the influence of the magnesium hydrate MgH2 in Mg2FeH6 samples and running of chemical reactions on the behavior of the isotherms and the occurrence of bends and jumps in them. All established functional dependences of the sorption properties of the examined alloys are compared with experimental data available from the literature.

  5. Ion-exchange equilibrium of N-acetyl-D-neuraminic acid on a strong anionic exchanger.

    PubMed

    Wu, Jinglan; Ke, Xu; Zhang, Xudong; Zhuang, Wei; Zhou, Jingwei; Ying, Hanjie

    2015-09-15

    N-acetyl-D-neuraminic acid (Neu5Ac) is a high value-added product widely applied in the food industry. A suitable equilibrium model is required for purification of Neu5Ac based on ion-exchange chromatography. Hence, the equilibrium uptake of Neu5Ac on a strong anion exchanger, AD-1 was investigated experimentally and theoretically. The uptake of Neu5Ac by the hydroxyl form of the resin occurred primarily by a stoichiometric exchange of Neu5Ac(-) and OH(-). The experimental data showed that the selectivity coefficient for the exchange of Neu5Ac(-) with OH(-) was a non-constant quantity. Subsequently, the Saunders' model, which took into account the dissociation reactions of Neu5Ac and the condition of electroneutrality, was used to correlate the Neu5Ac sorption isotherms at various solution pHs and Neu5Ac concentrations. The model provided an excellent fit to the binary exchange data for Cl(-)/OH(-) and Neu5Ac(-)/OH(-), and an approximate prediction of equilibrium in the ternary system Cl(-)/Neu5Ac(-)/OH(-). This basic information combined with the general mass transfer model could lay the foundation for the prediction of dynamic behavior of fixed bed separation process afterwards.

  6. Sorption of organophosphorous pesticides onto chickpea husk from aqueous solutions.

    PubMed

    Akhtar, Mubeena; Iqbal, Shahid; Bhanger, M I; Zia-Ul-Haq, Muhammad; Moazzam, Muhammad

    2009-02-15

    The sorption efficiency of chickpea husk of black gram variety (BGH), for the removal of organophosphorous pesticides (OPPs), i.e. triazophos (TAP) and methyl parathion (MP) from aqueous media has been investigated. Optimization of operating sorption parameters, i.e. particle size, sorbent dose, agitation time, pH, initial concentration of sorbates, and temperature has been studied. The sorption data fitted well to Freundlich, Langmuir and Dubinin-Radushkevich (D-R) sorption isotherms. The maximum sorption capacities of BGH for TAP and MP were calculated to be 3.5+/-0.45 and 10.6+/-0.83 mmol g(-1) by Freundlich, 0.0077+/-0.021 and 0.025+/-0.0094 mmol g(-1) by Langmuir and 0.48+/-0.037 and 0.15+/-0.077 mmol g(-1) by D-R isotherms respectively, employing 0.2g of sorbent, at pH 6, 90 min agitation time and at 303 K. Application of first order Lagergren and Morris-Weber equations to the kinetic data yielded correlation coefficients, close to unity and showed partial intra-particle diffusion. The negative values of thermodynamic parameters, i.e. DeltaH (kJ mol(-1)), DeltaS (J mol(-1) K(-1)) and DeltaG (kJ mol(-1)) indicate the exothermic and spontaneous nature of the sorption process. The sorbed pesticides were recovered by sonication with methanol, making the regeneration and reutilization of the sorbents promising. The investigated sorbent exhibited potential applications in water decontamination, treatments of industrial and agricultural waste waters and thus productively demonstrated viable use of agricultural waste material.

  7. Influence of the isomerism on the sorption of imazamethabenz-methyl by soil.

    PubMed

    Pinna, Maria Vittoria; Pusino, Alba

    2013-04-01

    The sorption of meta and para isomers of the herbicide imazamethabenz-methyl, methyl 6-[(RS)-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]-m- or p-toluate, by three soils and soil organic matter, was studied. Sorption isotherms conformed to the Freundlich equation. It was found that pH was the main factor influencing the adsorption in all of the systems. The highest level of sorption was measured on soils with low pH and high organic carbon content. Moreover, at low pH value, the soil rich in smectite clays, favoured the sorption of meta rather than para isomer. The higher affinity of clay surfaces for the meta isomer of the herbicide is due to the stabilization of the meta protonated form by resonance. At all pH values, the sorption on soil organic matter did not differ between two isomers.

  8. Effect of humic acid on the sorption of perfluorooctane sulfonate (PFOS) and perfluorobutane sulfonate (PFBS) on boehmite.

    PubMed

    Wang, Fei; Shih, Kaimin; Leckie, James O

    2015-01-01

    The sorption of PFOS and PFBS on boehmite was significantly retarded by the competitive sorption of humic acid (HA), implying that PFOS and PFBS are likely more mobile in water and groundwater systems enriched with HA. The sorption behavior of PFOS and PFBS on the HA-modified boehmite surface were also found to differ due to their different chain lengths. For a partially HA-modified boehmite surface, the isotherm study showed that PFOS had a much higher maximum sorption capacity than PFBS and that PFOS might possess additional surface interactions besides electrostatic interaction. For a HA-saturated boehmite, a linear sorption isotherm was found for PFOS while nearly no PFBS sorption was observed. This indicates that sorption behavior between PFOS and the sorbed HA on boehmite was dominated by hydrophobic interactions, instead of electrostatic interaction. In addition, a conceptual model combining hydrophobic and electrostatic interaction was established to explain the sorption behavior of PFOS and PFBS on HA-modified boehmite. Finally, the results revealed that the sorption of PFOS and PFBS on HA-modified boehmite is pH-dependent. The neutralization of negative sites on HA-modified boehmite reduced the electrostatic repulsion and enhanced the partitioning of PFBS on the sorbed HA. PMID:25268321

  9. Kinetics of sorption of lead on bed sediments of River Hindon, India.

    PubMed

    Sharma, M K; Jain, C K; Singhal, D C; Choubey, V K

    2009-10-01

    A number of low cost waste sorbent have been used for removal of heavy metals, however, few studies have been carried out on the sorption process on riverbed sediments in their natural state of occurrence. Stream sediments adsorb certain solutes from streams, thereby significantly changing the solute composition, but little is known about quantitatively describing sorption phenomena and rates of these processes. In the present investigation, sorption of lead ions on river bed sediments of river Hindon, a tributary of river Yamuna, India has been studied to demonstrate the role of bed sediments in controlling metal pollution. The effect of various operating variables, viz., initial concentration, solution pH, sediment dose, contact time and particle size has been studied. The sorption of lead ions increased with respect to pH and sorbent dose and decreased with sorbent particle size. Two important geochemical phases, iron and manganese oxide, also play important role in the sorption process. The sorption data were analysed using Langmuir and Freundlich isotherm models to determine the mechanistic parameters related to the sorption process. Further, although lead ions have more affinity for the fine fraction of the sediment, but the overall contribution of coarser fraction to sorption is more as compared to clay and silt fraction. The kinetic data suggest that the sorption of lead on bed sediments is an endothermic process, which is spontaneous at low temperature. The uptake of lead is controlled by both bulk and intraparticle diffusion mechanism. PMID:18791802

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

    PubMed

    Cui, Xiaoqiang; Hao, Hulin; Zhang, Changkuan; He, Zhenli; Yang, Xiaoe

    2016-01-01

    The objective of this study was to investigate the relationship between Cd(2+)/NH4(+) 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 NH4(+) and Cd(2+), with a maximum sorption of 13.35 and 125.8mgg(-1), respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3mgg(-1)) for Cd(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(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. PMID:26386447

  11. Kinetics of sorption of lead on bed sediments of River Hindon, India.

    PubMed

    Sharma, M K; Jain, C K; Singhal, D C; Choubey, V K

    2009-10-01

    A number of low cost waste sorbent have been used for removal of heavy metals, however, few studies have been carried out on the sorption process on riverbed sediments in their natural state of occurrence. Stream sediments adsorb certain solutes from streams, thereby significantly changing the solute composition, but little is known about quantitatively describing sorption phenomena and rates of these processes. In the present investigation, sorption of lead ions on river bed sediments of river Hindon, a tributary of river Yamuna, India has been studied to demonstrate the role of bed sediments in controlling metal pollution. The effect of various operating variables, viz., initial concentration, solution pH, sediment dose, contact time and particle size has been studied. The sorption of lead ions increased with respect to pH and sorbent dose and decreased with sorbent particle size. Two important geochemical phases, iron and manganese oxide, also play important role in the sorption process. The sorption data were analysed using Langmuir and Freundlich isotherm models to determine the mechanistic parameters related to the sorption process. Further, although lead ions have more affinity for the fine fraction of the sediment, but the overall contribution of coarser fraction to sorption is more as compared to clay and silt fraction. The kinetic data suggest that the sorption of lead on bed sediments is an endothermic process, which is spontaneous at low temperature. The uptake of lead is controlled by both bulk and intraparticle diffusion mechanism.

  12. Effect of ten quaternary ammonium cations on tetrachloromethane sorption to clay from water

    USGS Publications Warehouse

    Smith, J.A.

    1990-01-01

    The mineral surface of Wyoming bentonite (clay) was modified by replacing inorganic ions by each of 10 quaternary ammonium compounds, and tetrachloromethane sorption to the modified sorbents from water was studied. Tetrachloromethane sorption from solution to clay modified with tetramethyl-, tetraethyl-, benzyltrimethyl-, or benzyltriethylammonium cations generally is characterized by relatively high solute uptake, isotherm nonlinearity, and competitive sorption (with trichloroethene as the competing sorbate). For these sorbents, the ethyl functional groups yield reduced sorptive capacity relative to methyl groups, whereas the benzyl group appears to have a similar effect on sorbent capacity as the methyl group. Sorption of tetrachloromethane to clay modified with dodecyldimethyl(2-phenoxyethyl)-, dodecyltrimethyl-, tetradecyltrimethyl-, hexadecyltrimethyl-, or benzyldimethylhexadecylammonium bromide is characterized by relatively low solute uptake, isotherm linearity, and noncompetitive sorption. For these sorbents, an increase in the size of the nonpolar functional group(s) causes an increase in the organic carbon normalized sorption coefficient (Koc). No measurable uptake of tetrachloromethane sorption by the unmodified clay or clay modified by ammonium bromide was observed. ?? 1990 American Chemical Society.

  13. Modeling the sorption of zinc and nickel on Ca-montmorillonite

    NASA Astrophysics Data System (ADS)

    Bradbury, Michael H.; Baeyens, Bart

    1999-02-01

    In some previous work titration and Ni/Zn sorption edge/isotherm measurements carried out under a wide variety of experimental conditions on purified Na-montmorillonite were modelled in terms of cation exchange and surface complexation mass action equations. A major objective of the experimental/modelling programme is to understand and predict sorption in commercial bentonite systems. Since montmorillonite is the dominant clay mineral in bentonite and is often present in a mixed Na/Ca form, a natural extension to the previous investigations was to study Ni/Zn sorption on a conditioned Ca-montmorillonite. An important open question was whether the same basic parameters such as site types, site capacities, and acidity constants could be used for both materials and to see to what extent the Ni and Zn surface complexation constants were influenced by the form of the montmorillonite. Sorption edges for Ni and Zn at different Ca(NO 3) 2 background electrolyte concentrations, together with sorption isotherms measured over a range of pH values, are presented and modelled using the MINSORB code. The parameters characterising the sorption of Ni and Zn on Na- and Ca-montmorillonite systems are compared. Finally, examples are given that illustrate how the modelling can provide insight into the sorption processes.

  14. Sorption of methane, ethane, propane, butane, carbon dioxide, and nitrogen on kerogen

    NASA Astrophysics Data System (ADS)

    Pribylov, A. A.; Skibitskaya, N. A.; Zekel', L. A.

    2014-06-01

    Sorption isotherms of nitrogen, methane (in the pressure range of 0.1-40 MPa), ethane (0.1-3.7MPa), propane (0.01-1 MPa), butane (0.01-0.2 MPa), and carbon dioxide (0.1-6 MPa) are measured on two adsorbents with kerogen contents of 16 and 75% at temperatures of 303, 323, 343 K. Adsorption volumes are calculated for all adsorption systems using two independent methods. The BET technique is used to determine the surface area values of the two adsorbents on the basis of sorption data for ethane, propane, butane, and carbon dioxide. The initial and isosteric adheat of sorption values are calculated on the basis of sorption isotherms of ethane, propane, butane, carbon dioxide measured at three temperatures. It is found from comparing the dependences of isosteric heat of sorption on the two adsorbents that molecules of the above gases diffuse into its bulk (adsorbent 2) in addition to sorbing on the outside surface formed by kerogen molecules, while sorption of the same gases on the rock (adsorbent 1) is similar to sorption on a smooth hard adsorbent surface.

  15. Sorption of lead by settling pond soils after reclamation treatments

    NASA Astrophysics Data System (ADS)

    Asensio, Verónica; Forján, Rubén; Vega, Flora A.; Andrade, Luisa; Covelo, Emma F.

    2013-04-01

    The reclamation of degraded soils adding waste amendments can add significant concentrations of Pb. Because of this, it is important to know the sorption capacity of Pb by the soils where wastes with high concentrations of this metal are applied. To determine the sorption capacity of Pb by mine soils, before and after reclamation treatments, four different sites were selected at a settling pond mine zone: an untreated one as the control sample (B1), a vegetated one with pines for 21 years (B2v), a vegetated with eucalyptus for 6 years (B3v) and an amended with sewage sludges and paper mill residues for 5 months (B4w). All soils had one horizon except B4w, where twice were sampled (B4Aw and B4Bw). The B4Bw is considered analogous of the control soil. To evaluate the sorption capacity by the soils, sorption isotherms were constructed using single-metal solutions of Pb2+ nitrates (0.03, 0.05, 0.08, 0.1 and 0.5 mmol L-1) containing 0.01 M NaNO3 as background electrolyte (Vega et al., 2009). The overall capacity of the soil to sorb Pb was evaluated as the slope Kr (Vega et al., 2008). The obtained results show that the sorption isotherm of Pb by control soil (B1) and its analogous (B4Bw) are of L-type curve, whereas the sorption isotherms of the treated soils (B2v, B3v and B4Aw) are of H-type curve (Giles et al., 1974). The most of the obtained isotherms do not fit with the models of Langmuir or Freundlich, therefore sorption capacity was evaluated by Kr parameter. According to the obtained Kr parameter, B1 and B4Bw have the lowest Pb sorption capacity (Kr = 0.480 and 0.556, respectively), which increased two times after recently waste amending (B4Aw; Kr = 0.998). The vegetated sites (B2v and B3v) also have higher sorption capacity than B1, but lower than B4Aw (Kr = 0.692 and 0.725, respectively). The highest sorption capacity of Pb by the amended soil is due to its characteristics such as high pH and organic carbon content. This is corroborated by the significantly

  16. Status Of Sorption Cryogenic Refrigeration

    NASA Technical Reports Server (NTRS)

    Jones, Jack A.

    1988-01-01

    Report reviews sorption refrigeration. Developed for cooling infrared detectors, cryogenic research, and other advanced applications, sorption refrigerators have few moving parts, little vibration, and lifetimes of 10 years or more. Describes types of sorption stages, multistage and hybrid refrigeration systems, power requirements, cooling capacities, and advantages and disadvantages of various stages and systems.

  17. Reanalysis of experiments to quantify irreversibility of pesticide sorption-desorption in soil.

    PubMed

    Suddaby, Laura A; Beulke, Sabine; van Beinum, Wendy; Celis, Rafael; Koskinen, William C; Brown, Colin D

    2013-03-01

    Previously published research used an isotope-exchange technique to measure irreversibility of pesticide sorption-desorption in soil. Results indicated significant irreversibility (6-51%) in sorption in five pesticide-soil systems measured over 72 h. Here, we propose a three-site model to reanalyze the experimental data. The model adds a slow but reversible binding on nonequilibrium sorption sites in addition to instantaneously reversible sites and irreversible sites. The model was able to match experimental data very closely, but only if irreversible sorption was assumed to be absent. Observed asymmetry in the binding of (12)C- and (14)C-pesticide was explained on the basis of nonattainment of sorption equilibrium over the study period. Results suggest that irreversible sorption may be less significant than previously considered with important implications for understanding the fate of pesticides applied to soil.

  18. The special features of protein adsorption isotherms on silica adsorbents

    NASA Astrophysics Data System (ADS)

    Chukhrai, E. S.; Atyaksheva, L. F.; Pilipenko, O. S.

    2011-05-01

    The adsorption isotherms of hemoglobin, peroxidase, and β-galactosidase on silochrome and mesoporous and biporous silicas were comparatively studied. Adsorption developed in two stages, including fast "reversible" protein adsorption (equilibrium was reached in t ≤ 1-2 h) and a "slow stage" of irreversible binding in t ≫ 24 h (multipoint adsorption). The corresponding equilibrium constants were determined. The mechanism of unlimited linear association of peroxidase in the adsorption layer on the surface of silochrome was established.

  19. Effects of hydrodynamic conditions on the sorption behaviors of aniline on sediment with coexistence of nitrobenzene.

    PubMed

    Wang, Peng; Hua, Zulin; Cai, Yunjie; Shen, Xia; Li, Qiongqiong; Liu, Xiaoyuan

    2015-08-01

    The sorption behaviors of pollutants affected by hydrodynamic conditions were confirmed in natural water environment. The effects of hydrodynamic conditions on the sorption behaviors of aniline on sediment with coexistence of nitrobenzene were investigated. The particle entrainment simulator (PES) was used to simulate varied bottom shear stresses. The batch equilibrium method was applied to the experiments with the stress levels and the action time controlled at 0.2-0.5 N/m(2) and 24 h, respectively. The findings indicated that apparent partition coefficient of aniline on sediment increased with the shear stress significantly, while decreased with nitrobenzene concentration. On the contrary, both the sorption amount of aniline on suspended particulate matter (Q s) and the effect of nitrobenzene concentration on Q s declined as the shear stress increased. The sorption kinetic results showed that the sorption process followed the pseudo-second-order kinetics equation, and the process included two stages: fast sorption stage and slow sorption stage, among which the average sorption rate of fast stage was 7.5-9.5 times that of slow one. The effect of shear stress on the average sorption rate of aniline was enhanced with the increase of nitrobenzene concentration. And shear stress weakened the disturbance of cosolute on main solute sorption process. In addition, experiment results of sorption kinetic show that only the initial sorption rate was affected by shear stress and cosolute concentration. In the first 5 min, shear stress had positive effects on the sorption rate. After that, the sorption rate barely changed with shear stress and cosolute concentration.

  20. Sorption vacuum trap

    NASA Technical Reports Server (NTRS)

    Barrington, A. E.; Caruso, A. J.

    1970-01-01

    Modified sorption trap for use in high vacuum systems contains provisions for online regeneration of sorbent material. Trap is so constructed that it has a number of encapsulated resistance heaters and a valving and pumping device for removing gases from heated sorbing material. Excessive downtime is eliminated with this trap.

  1. Adsorption of surfactants on sand surface in enhanced oil recovery: Isotherms, kinetics and thermodynamic studies

    NASA Astrophysics Data System (ADS)

    Bera, Achinta; Kumar, T.; Ojha, Keka; Mandal, Ajay

    2013-11-01

    Adsorption of surfactants onto reservoir rock surface may result in the loss and reduction of their concentrations in surfactant flooding, which may render them less efficient or ineffective in practical applications of enhanced oil recovery (EOR) techniques. Surfactant flooding for EOR received attraction due to its ability to increase the displacement efficiency by lowering the interfacial tension between oil and water and mobilizing the residual oil. This article highlights the adsorption of surfactants onto sand surface with variation of different influencing factors. It has been experimentally found that adsorption of cationic surfactant on sand surface is more and less for anionic surfactant, while non-ionic surfactant shows intermediate behaviour. X-ray diffraction (XRD) study of clean sand particles has been made to determine the main component present in the sand particles. The interaction between sand particles and surfactant has been studied by Fourier Transform Infrared (FTIR) Spectroscopy of the sand particles before and after aging with surfactant. Salinity plays an important role in adsorption of anionic surfactant. Batch experiments were also performed to understand the effects of pH and adsorbent dose on the sorption efficiency. The sand particles exhibited high adsorption efficiency at low pH for anionic and nonionic surfactants. But opposite trend was found for cationic surfactant. Adsorption data were analyzed by fitting with Langmuir, Freundlich, Redlich-Peterson, and Sips isotherm models. Results show that the Langmuir isotherm and pseudo-second order kinetics models suit the equilibrium and kinetics of adsorption on sand surface. Thermodynamics feasibility of the adsorption process was also studied to verify the spontaneity of the process.

  2. Adsorption isotherms and kinetics of activated carbons produced from coals of different ranks.

    PubMed

    Purevsuren, B; Lin, Chin-Jung; Davaajav, Y; Ariunaa, A; Batbileg, S; Avid, B; Jargalmaa, S; Huang, Yu; Liou, Sofia Ya-Hsuan

    2015-01-01

    Activated carbons (ACs) from six coals, ranging from low-rank lignite brown coal to high-rank stone coal, were utilized as adsorbents to remove basic methylene blue (MB) from an aqueous solution. The surface properties of the obtained ACs were characterized via thermal analysis, N2 isothermal sorption, scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and Boehm titration. As coal rank decreased, an increase in the heterogeneity of the pore structures and abundance of oxygen-containing functional groups increased MB coverage on its surface. The equilibrium data fitted well with the Langmuir model, and adsorption capacity of MB ranged from 51.8 to 344.8 mg g⁻¹. Good correlation coefficients were obtained using the intra-particle diffusion model, indicating that the adsorption of MB onto ACs is diffusion controlled. The values of the effective diffusion coefficient ranged from 0.61 × 10⁻¹⁰ to 7.1 × 10⁻¹⁰ m² s⁻¹, indicating that ACs from lower-rank coals have higher effective diffusivities. Among all the ACs obtained from selected coals, the AC from low-rank lignite brown coal was the most effective in removing MB from an aqueous solution. PMID:25909729

  3. Importance of structural makeup of biopolymers for organic contaminant sorption.

    PubMed

    Wang, Xilong; Xing, Baoshan

    2007-05-15

    Sorption of pyrene, phenanthrene, naphthalene, and 1-naphthol by original (lignin, chitin, and cellulose) and coated biopolymers was examined. Organic carbon normalized distribution coefficients (Koc) of all compounds by the original biopolymers followed the order lignin > chitin > cellulose, in line with the order of their hydrophobicity. Hydrophobicity of structurally similar organic compounds is the main factor determining their ability to occupy sorption sites in biopolymers. Specific interactions (e.g., H-bonding) between 1-naphthol and chitin or cellulose increased its ability to occupy sorption sites. Lignin coating resulted in an increased Koc for phenanthrene (13.6 times for chitin and 6.9 times for cellulose) and 1-naphthol (6.0 times for chitin and 3.7 times for cellulose) relative to the acetone-treated chitin and cellulose. Also, these coated biopolymers had increased isotherm nonlinearity, due to the newly formed condensed domains. An increase in phenanthrene and 1-naphthol sorption by lignin-coated biopolymers as compared to chitin and cellulose was contributed by the newly created high-energy sites in condensed domains and coated lignin. Results of this study highlight the importance of the structural makeup of biopolymers in controlling the sorption of hydrophobic organic compounds.

  4. Chitosan sorbents for platinum sorption from dilute solutions

    SciTech Connect

    Guibal, E.; Larkin, A.; Vincent, T.; Tobin, J.M.

    1999-10-01

    Chitosan has proved efficient at removing platinum in dilute effluents. The maximum uptake capacity reaches 300 mg/g (almost 1.5 mmol/g). The optimum pH for sorption is pH 2. A glutaraldehyde cross-linking pretreatment is necessary to stabilize the biopolymer in acidic solutions. Sorption isotherms have been studied as a function of pH, sorbent particle size, and the cross-linking ratio. Surprisingly, the extent of the cross-linking (determined by the concentration of the cross-linking agent in the treatment bath) has no significant influence on uptake capacity. Competitor anions such as chloride or nitrate induce a large decrease in the sorption efficiency. Sorption kinetics show also that uptake rate is not significantly changed by increasing either the cross-linking ratio or the particle size of the sorbent. Mass transfer rates are significantly affected by the initial platinum concentration and by the conditioning of the biopolymer. Gel-bead conditioning appears to reduce the sorption rate. While for molybdate and vanadate ions, mass transfer was governed by intraparticle mass transfer, for platinum, both external and intraparticle diffusion control the uptake rate. In contrast with the former ions, platinum does not form polynuclear hydrolyzed species, which are responsible for steric hindrance of diffusion into the polymer network.

  5. Phenylurea herbicide sorption to biochars and agricultural soil

    PubMed Central

    WANG, DAOYUAN; MUKOME, FUNGAI N. D.; YAN, DENGHUA; WANG, HAO; SCOW, KATE M.; PARIKH, SANJAI J.

    2016-01-01

    Biochar is increasingly been used as a soil amendment to improve water holding capacity, reduce nutrient leaching, increase soil pH and also as a means to reduce contamination through sorption of heavy metals or organic pollutants. The sorption behavior of three phenylurea herbicides (monuron, diuron, linuron) on five biochars (Enhanced Biochar, Hog Waste, Turkey Litter, Walnut Shell and Wood Feedstock) and an agricultural soil (Yolo silt loam) was investigated using a batch equilibration method. Sorption isotherms of herbicides to biochars were well described by the Freundlich model (R2 = 0.93 -- 0.97). The adsorption KF values ranged from 6.94 to 1306.95 mg kg−1 and indicated the sorption of herbicides in the biochars and Yolo soil was in the sequence of linuron > diuron > monuron and walnut shell biochar > wood feedstock biochar > turkey litter biochar > enhanced biochar > hog waste biochar > Yolo soil. These data show that sorption of herbicides to biochar can have both positive (reduced off-site transport) and negative (reduced herbicide efficacy) implications and specific biochar properties, such as H/C ratio and surface area, should be considered together with soil type, agriculture chemical and climate condition in biochar application to agricultural soil to optimize the system for both agricultural and environmental benefits. PMID:26065514

  6. Phenylurea herbicide sorption to biochars and agricultural soil.

    PubMed

    Wang, Daoyuan; Mukome, Fungai N D; Yan, Denghua; Wang, Hao; Scow, Kate M; Parikh, Sanjai J

    2015-01-01

    Biochar is increasingly been used as a soil amendment to improve water-holding capacity, reduce nutrient leaching, increase soil pH, and also as a means to reduce contamination through sorption of heavy metals or organic pollutants. The sorption behavior of three phenylurea herbicides (monuron, diuron and linuron) on five biochars (Enhanced Biochar, Hog Waste, Turkey Litter, Walnut Shell and Wood Feedstock) and an agricultural soil (Yolo silt loam) was investigated using a batch equilibration method. Sorption isotherms of herbicides to biochars were well described by the Freundlich model (R(2) = 0.93-0.97). The adsorption KF values ranged from 6.94 to 1306.95 mg kg(-1) and indicated the sorption of herbicides in the biochars and Yolo soil was in the sequence of linuron > diuron > monuron and walnut shell biochar > wood feedstock biochar > turkey litter biochar > enhanced biochar > hog waste biochar > Yolo soil. These data show that sorption of herbicides to biochar can have both positive (reduced off-site transport) and negative (reduced herbicide efficacy) implications and specific biochar properties, such as H/C ratio and surface area, should be considered together with soil type, agriculture chemical and climate condition in biochar application to agricultural soil to optimize the system for both agricultural and environmental benefits. PMID:26065514

  7. Sorptive removal of nickel onto weathered basaltic andesite products: kinetics and isotherms.

    PubMed

    Shah, Bhavna A; Shah, Ajay V; Singh, Rajesh R; Patel, Nayan B

    2009-07-15

    The suitability of weathered basaltic andesite products (WBAP) as a potential sorbent was assessed for the removal of Ni (II) from electroplating industrial wastewater. A model study based on the batch mode of operation was carried out for Ni (II) removal from aqueous solution. The effect of various parameters such as hydronium ion concentration, shaking time, sorbent dose, initial Ni (II) concentration, and temperature on the sorption process was studied. At optimised conditions of the various parameters, the industrial wastewater loaded with Ni (II) was sorbed onto WBAP. Thermodynamic parameters for the sorption process were evaluated. Freundlich, Langmuir, Temkin, and Dubinin-Kaganer-Radushkevich isotherms were applied to the sorption pattern on the WBAP. The sorption dynamics of the process was evaluated by applying Lagergren, Bangham, and Weber & Morris equations. The sorption process follows Pseudo-second-order rate of surface diffusion which is identified as the predominating mechanism. The sorption process was found to be reversible by the recovery of sorbed Ni (II) upon extraction with 0.5 MHNO3. The sorbent before and after sorption, was characterized by Fourier transform infrared (FTIR), Powder X-Ray diffraction PXRD), and Thermogravimetric analysis (TGA) methods. The change in surface morphology and crystallanity of the mineral after sorption was analyzed by Scanning electron microscopy (SEM) and Transmission electron microscopy (TEM). Based on the previous model study, an electroplating industrial effluent was successfully treated with WBAP to minimize the pollution load caused by Ni (II).

  8. Sorptive removal of nickel onto weathered basaltic andesite products: kinetics and isotherms.

    PubMed

    Shah, Bhavna A; Shah, Ajay V; Singh, Rajesh R; Patel, Nayan B

    2009-07-15

    The suitability of weathered basaltic andesite products (WBAP) as a potential sorbent was assessed for the removal of Ni (II) from electroplating industrial wastewater. A model study based on the batch mode of operation was carried out for Ni (II) removal from aqueous solution. The effect of various parameters such as hydronium ion concentration, shaking time, sorbent dose, initial Ni (II) concentration, and temperature on the sorption process was studied. At optimised conditions of the various parameters, the industrial wastewater loaded with Ni (II) was sorbed onto WBAP. Thermodynamic parameters for the sorption process were evaluated. Freundlich, Langmuir, Temkin, and Dubinin-Kaganer-Radushkevich isotherms were applied to the sorption pattern on the WBAP. The sorption dynamics of the process was evaluated by applying Lagergren, Bangham, and Weber & Morris equations. The sorption process follows Pseudo-second-order rate of surface diffusion which is identified as the predominating mechanism. The sorption process was found to be reversible by the recovery of sorbed Ni (II) upon extraction with 0.5 MHNO3. The sorbent before and after sorption, was characterized by Fourier transform infrared (FTIR), Powder X-Ray diffraction PXRD), and Thermogravimetric analysis (TGA) methods. The change in surface morphology and crystallanity of the mineral after sorption was analyzed by Scanning electron microscopy (SEM) and Transmission electron microscopy (TEM). Based on the previous model study, an electroplating industrial effluent was successfully treated with WBAP to minimize the pollution load caused by Ni (II). PMID:19799057

  9. Sorption of inorganic and total phosphorus from dairy and swine slurries to soil.

    PubMed

    Marshall, Sarah K; Laboski, Carrie A M

    2006-01-01

    Understanding P sorption from animal manures is essential to formulate best management practices with regard to land application of manure from the standpoint of crop production and environmental quality. Little research has focused on the construction of P sorption isotherms where the P source is manure. The objectives of this study were to: (i) develop a procedure to characterize how inorganic P (P(i)) and total P (P(t)) from dairy slurry and swine slurry sorbs to soil; and (ii) compare the sorption characteristics of P(i) and P(t) where the P source was dairy slurry, swine slurry, or potassium phosphate (KH2PO4). Sorption solutions were prepared in 0.1 M KCl at pH 6 and equilibrated with soils at a 1:25 (w/v) soil/solution ratio for 24 h. Inorganic P, P(t), Al, and Fe in the equilibrated solutions were measured. For all soils, P(i) and P(t) sorption capacity of dairy slurry was greater than KH2PO4. Total P sorption capacity of swine slurry was greater than KH2PO4, while P(i) sorption capacity was less than KH2PO4. Overall, P(i) and P(t) sorption strengths of the manure slurries were less than or equal to KH2PO4. Increased P(i) sorption from dairy slurry was correlated with Fe and Al desorption. Reduction of P(i) sorption capacity from swine slurry was related to preferential sorption of organic P. Additional studies need to be conducted to determine how differences in P sorption between manures and fertilizer impact in-field P availability to a crop and potential for losses in runoff water.

  10. Measurement techniques for carbon dioxide sorption capacity on various coal samples: critical review

    NASA Astrophysics Data System (ADS)

    Abunowara, M.; Bustam, M. A.; Sufian, S.; Eldemerdash, U.

    2016-06-01

    Underground carbon sequestration is proposed as a geologic disposal technique for the long-term storage of CO2 emissions to mitigate climate change and air pollution. Coal bed seams have large CO2 adsorption capacity, long time CO2 trapping and extra enhanced coal-bed methane recovery (CBM). However, CO2 sorption capacity is one of significant steps required to be determined accurately in any feasibility evaluation of carbon sequestration. Hence, in lab scale, there are three methods for CO2 adsorption capacity measurements namely manometric/volumetric, gravimetric and new capsule techniques for gas sorption on variety of sorbents. The manometric and volumetric methods require accurate determination of cell and void volumes and suitable equation of state (EoS). The gravimetric method requires a very accurate sensitive balance and less buoyancy effect and it is the best technique for small amounts (milligrams) of sorbents and the adsorption equilibrium can be mentored. Among all gas adsorption measurement techniques, the newly developed method “capsule method” exhibits the highest CO2 adsorption capacity on Polish coal by 4.08 mmol/g because capsule method that directly measures CO2 uptake of solid coal matrix cylinders, without the application of the equation of state (EoS) for CO2 or volumetric corrections. The main advantage of capsule method is that it is independent of any Equation of State (EoS), and it has no volumetric effects or impurities distort the shape of the gas adsorption isotherm. The disadvantage of capsule method is time-consuming and it is not easy to implement.

  11. Biosorption of lead from aqueous solutions by green algae Spirogyra species: kinetics and equilibrium studies.

    PubMed

    Gupta, V K; Rastogi, A

    2008-03-21

    Biosorption is the effective method for the removal of heavy metal ions from wastewaters. Results are presented showing the sorption of Pb(II) from solutions by biomass of commonly available, filamentous green algae Spirogyra sp. Batch experiments were conducted to determine the biosorption properties of the biomass and it was observed that the maximum adsorption capacity of Pb(II) ion was around 140mgmetal/g of biomass at pH 5.0 in 100min with 200mg/L of initial concentration. Temperature change in the range 20-40 degrees C affected the adsorption capacity and the nature of the reaction was found to be endothermic in nature. Uptake kinetics follows the pseudo-second-order model and equilibrium is well described by Langmuir isotherm. Isotherms have been used to determine thermodynamic parameters of the process, viz., free energy change, enthalpy change and entropy change. Various properties of the algae, as adsorbent, explored in the characterization part were chemical composition of the adsorbent, thermal analysis by TGA, surface area calculation by BET method, surface morphology with scanning electron microscope images and surface functionality by FTIR. FTIR analysis of algal biomass revealed the presence of amino, carboxyl, hydroxyl and carbonyl groups, which are responsible for biosorption of metal ions. The results indicated that the biomass of Spirogyra sp. is an efficient biosorbent for the removal of Pb(II) from aqueous solutions.

  12. Adsorptive removal of cadmium by natural red earth: equilibrium and kinetic studies.

    PubMed

    Mahatantila, Kushani; Vithanage, Meththika; Seike, Yasushi; Okumura, Minoru

    2012-01-01

    Natural red earth (NRE), an iron-coated sand found in the north western part of Sri Lanka, was used to examine the retention behaviour of cadmium, a heavy metal postulated as a factor of chronic kidney disease in Sri Lanka. Adsorption studies were conducted as a function of pH, ionic strength, initial Cd loading and time. The Cd adsorption increased from 6% to 99% with the pH increase from 4 to 8.5. The maximum adsorption was reached at pH > 7.5. Cadmium adsorption was not changed over 100-fold variations of NaNO3, providing evidence for the dominance of an inner-sphere bonding mechanism for both 10-fold variation of initial Cd concentrations. Surface complexation modelling suggests a monodentate bonding mechanism. Isotherm data were fairly fitted to a two-site Langmuir isotherm model and sorption maximums of 9.11 x 10(-6) and 3.89 x 10(-7) mol g(-1) were obtained for two surface sites. The kinetic study reveals that Cd uptake by NRE is so fast that the equilibrium was reached within 15 min and - 1 h for 4.44 and 44.4 microM initial Cd concentrations, respectively, and the chemisorption was the dominant mechanism over intra-particle diffusion. The study indicates the potential of NRE as a material for decontaminating environmental water polluted with Cd.

  13. Isotherm ranking and selection using thirteen literature datasets involving hydrophobic organic compounds

    NASA Astrophysics Data System (ADS)

    Matott, L. Shawn; Jiang, Zhengzheng; Rabideau, Alan J.; Allen-King, Richelle M.

    2015-06-01

    Numerous isotherm expressions have been developed for describing sorption of hydrophobic organic compounds (HOCs), including "dual-mode" approaches that combine nonlinear behavior with a linear partitioning component. Choosing among these alternative expressions for describing a given dataset is an important task that can significantly influence subsequent transport modeling and/or mechanistic interpretation. In this study, a series of numerical experiments were undertaken to identify "best-in-class" isotherms by refitting 10 alternative models to a suite of 13 previously published literature datasets. The corrected Akaike Information Criterion (AICc) was used for ranking these alternative fits and distinguishing between plausible and implausible isotherms for each dataset. The occurrence of multiple plausible isotherms was inversely correlated with dataset "richness", such that datasets with fewer observations and/or a narrow range of aqueous concentrations resulted in a greater number of plausible isotherms. Overall, only the Polanyi-partition dual-mode isotherm was classified as "plausible" across all 13 of the considered datasets, indicating substantial statistical support consistent with current advances in sorption theory. However, these findings are predicated on the use of the AICc measure as an unbiased ranking metric and the adoption of a subjective, but defensible, threshold for separating plausible and implausible isotherms.

  14. Sorption of copper by vegetated copper-mine tailings

    NASA Astrophysics Data System (ADS)

    de Coninck, A.; Karam, A.; Jaouich, A.

    2009-04-01

    The lixiviation of copper (Cu) from vegetated mine tailings may present an environmental risk because of the potential adverse effects it may pose to ground and surface water around mines. However, bonding of Cu to mine tailings can limit transfer to surrounding water. The main objective of the present study is to assess Cu sorption by cultivated Cu-mine tailings containing calcite (pH 7.7) as influenced by commercial peat moss-shrimp waste compost (PSC) and chelating solution. Fresh tailing and tailing that had been used in pot experiments were tested and compared. Samples (0.50 g) of tailings were equilibrated with 20 cm3 of 0.01 M CaCl2 solution containing 100 mg Cu dm-3, as CuCl2, for 72 h at room temperature. After equilibration period, the samples were centrifuged and filtered. Concentration of Cu in the equilibrium solution was measured by atomic absorption spectrophotometry. The sorption coefficient (Ks) was used to interpret the sorption data. The sorption experiment was replicated two times. Compost was the most effective organic amendment in enhancing Cu sorption. The Ks values were positively and significantly correlated with organic matter content and Cu associated with the organic fraction of tailing samples. The mineralogy and organic matter content can influence the sorption capacity of Cu-mine tailings. Calcite-containing mine tailings amended with PSC can be used to sorb Cu from chloride solutions.

  15. Sorption-desorption of indaziflam in selected agricultural soils.

    PubMed

    Alonso, Diego G; Koskinen, William C; Oliveira, Rubem S; Constantin, Jamil; Mislankar, Suresh

    2011-12-28

    Indaziflam, a new alkylazine herbicide that inhibits cellulose biosynthesis, is under current development for soil applications in perennial crops and nonagricultural areas. Sorption and desorption of indaziflam in six soils from Brazil and three soils from the United States, with different physical chemical properties, were investigated using the batch equilibration method. Sorption kinetics demonstrated that soil-solution equilibrium was attained in <24 h. The Freundlich equation described the sorption behavior of the herbicide for all soils (R(2) > 0.99). K(f) values of the Brazilian oxisols ranged from 4.66 to 29.3, and 1/n values were ≥ 0.95. Sorption was positively correlated to %OC and clay contents. U.S. mollisol K(f) values ranged from 6.62 to 14.3; 1/n values for sorption were ≥ 0.92. K(f) values from mollisols were also positively correlated with %OC. These results suggest that indaziflam potential mobility, based solely on its sorption coefficients, would range from moderate to low in soil. Desorption was hysteretic on all soils, further decreasing its potential mobility for offsite transport.

  16. The sorption of silver by poorly crystallized manganese oxides

    USGS Publications Warehouse

    Anderson, B.J.; Jenne, E.A.; Chao, T.T.

    1973-01-01

    The sorption of silver by poorly crystallized manganese oxides was studied using synthesized samples of three members of the manganous manganite (birnessite) group, of different chemical composition and crystallinity, and a poorly organized ??-MnO2. All four oxides sorbed significant quantities of silver. The manganous manganites showed the greatest sorption (up to 0.5 moles silver/mole MnOx at pH 7) while the ??-MnO2 showed the least (0.3 moles silver/ mole MnOx at pH 7). Sorption of silver was adequately described by the Langmuir equation over a considerable concentration range. The relationship failed at low pH values and high equilibrium silver concentrations. The sorption capacity showed a direct relationship with pH. However, the rate of increase of sorption capacity decreased at the higher pH values. Silver sorption maxima. were not directly related to surface area but appeared to vary with the amount of occluded sodium and potassium present in the manganese oxide. The important processes involved in the uptake of silver by the four poorly crystallized manganese oxides ara considered to be surface exchange for manganese, potassium and sodium as well as exchange for structural manganese, potassium and sodium. ?? 1973.

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

    SciTech Connect

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

    2012-01-01

    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

  18. Adsorption Properties of Tetracycline onto Graphene Oxide: Equilibrium, Kinetic and Thermodynamic Studies

    PubMed Central

    Ghadim, Ehsan Ezzatpour; Manouchehri, Firouzeh; Soleimani, Gholamreza; Hosseini, Hadi; Kimiagar, Salimeh; Nafisi, Shohreh

    2013-01-01

    Graphene oxide (GO) nanoparticle is a high potential effective absorbent. Tetracycline (TC) is a broad-spectrum antibiotic produced, indicated for use against many bacterial infections. In the present research, a systematic study of the adsorption and release process of tetracycline on GO was performed by varying pH, sorption time and temperature. The results of our studies showed that tetracycline strongly loads on the GO surface via π–π interaction and cation–π bonding. Investigation of TC adsorption kinetics showed that the equilibrium was reached within 15 min following the pseudo-second-order model with observed rate constants of k2 = 0.2742–0.5362 g/mg min (at different temperatures). The sorption data has interpreted by the Langmuir model with the maximum adsorption of 323 mg/g (298 K). The mean energy of adsorption was determined 1.83 kJ/mol (298 K) based on the Dubinin–Radushkevich (D–R) adsorption isotherm. Moreover, the thermodynamic parameters such as ΔH°, ΔS° and ΔG° values for the adsorption were estimated which indicated the endothermic and spontaneous nature of the sorption process. The electrochemistry approved an ideal reaction for the adsorption under electrodic process. Simulation of GO and TC was done by LAMMPS. Force studies in z direction showed that tetracycline comes close to GO sheet by C8 direction. Then it goes far and turns and again comes close from amine group to the GO sheet. PMID:24302989

  19. CO2 Isotherms Measured on Moisture-Equilbrated Argonne Premium Coals at 550C and 15 Mpa

    SciTech Connect

    Goodman, A.L.

    2007-05-01

    Sorption isotherms, which describe the coal’s gas storage capacity, are important for estimating the carbon sequestration potential of coal seams. The DOE-NETL initiated a second inter-laboratory isotherm comparison of coals where CO2 sorption isotherms were collected on moisture-equilibrated coals at temperatures and pressures relevant to CO2 sequestration. Each laboratory used the same coal samples and followed the same general procedure; however, each laboratory used their own apparatus and isotherm measurement technique. This study investigated the inter-laboratory reproducibility of carbon dioxide isotherm measurements on moisture-equilibrated Argonne premium coal samples (Pocahontas #3, Illinois #6, and Beulah Zap). Six independent laboratories provided isotherm data on the three moisture-equilibrated coal samples at 55oC and pressures up to 15 MPa. Agreement among the laboratories was good up to 8 MPa. At the higher pressures, the data among the laboratories diverged significantly for two of the laboratories and coincided reasonably well for four of the laboratories. This work provides guidance for estimating the reproducibility that might be expected when comparing published sorption isotherms on moisture-equilibrated coals from different laboratories.

  20. Sorption properties of an amorphous hydroxo titanate towards Pb(2+), Ni(2+), and Cu(2+) ions in aqueous solution.

    PubMed

    Volpe, Angela; Pagano, Michele; Pastore, Carlo; Cuocci, Corrado; Milella, Antonella

    2016-11-01

    Titanates may be selectively used as inorganic adsorbents for heavy metal ions owing to their stability and fast adsorption kinetics. Nevertheless, the synthesis of such materials usually requires extreme reaction conditions. In this work, a new titanium-based material was rapidly synthesized under mild laboratory conditions. The obtained amorphous hydroxo titanate was tested for heavy metal sorption through kinetic and equilibrium batch tests, which indicated that the new material had high adsorption rates and adsorption capacities towards Cu(2+), Ni(2+) and Pb(2) ions. Adsorption kinetics were pseudo-second order, and equilibrium data fitted the Langmuir isotherm model. The calculated maximum adsorption capacities of Cu(2+), Ni(2+) and Pb(2+) in deionized water were around 1 mmol g(-1), and they decreased for Cu(2+) and Ni(2+) in the presence of Na(+), Ca(2+) and Mg(2+) ions, whereas the alkali metal ions did not influence Pb(2+) uptake. The efficiency of adsorption and recovery of lead ions were evaluated through column dynamic tests, by feeding the column with groundwater and tap water spiked with Pb(2+). The high performance of the hydroxo titanate over several cycles of retention and elution suggested that the product is potentially useful for the solid phase extraction of lead at trace levels in natural water samples, with potential use in metal pre-concentration for analytical applications. PMID:27419851

  1. Amphiphilic hollow carbonaceous microspheres for the sorption of phenol from water.

    PubMed

    Guan, Zhengrong; Liu, Li; He, Lilu; Yang, Sen

    2011-11-30

    Amphiphilic porous hollow carbonaceous spheres (PHCSs) were synthesized via mild hydrothermal treatment of yeast cells and further pyrolyzing post treatment. The morphology, chemical composition, porosity, and structure of the carbonaceous materials were investigated. It is evident that the carbonaceous materials were composed of the carbonized organic matter (COM) and the noncarbonized organic matter (NOM), and the relative COM and NOM fractions could be adjusted through changing the temperature of hydrothermal and/or pyrolyzing treatment. The phenol sorption properties of the carbonaceous materials had been investigated and the sorption isotherms fit well to the modified Freundlich equation. It was found that the sorption isotherm of phenol onto PHCSs was practically linear even at extreme high concentrations, which was fewer reported for activated carbon or other inorganic materials. This type of sorption isothermals was assigned to a partition mechanism, and the largest value of the partition coefficient (K(f)) and carbon-normalized K(f) (K(oc)) is 56.7 and 91.5 mL g(-1), respectively. Moreover, PHCSs exhibit fast sorption kinetic and facile regeneration property. The results indicate PHCSs are potential effective sorbents for removal of undesirable organic chemicals in wastewater, especially at high concentrations. PMID:21943920

  2. Thermodynamic description of the ion exchange and superequivalent sorption of phenylalanine by KU-2-8 cationite

    NASA Astrophysics Data System (ADS)

    Khokhlova, O. N.; Khokhlov, V. Yu.; Trunaeva, E. S.

    2015-02-01

    The coefficients and thermodynamic equilibrium constants, activity coefficients of the sorbent phase, and integral and differential Gibbs energies of the ion-exchange and superequivalent sorption of phenylalanine by strongly acidic KU-2-8 cationites in the H form are calculated using a new thermodynamic approach that allows us to describe the simultaneous exchange and superequivalent sorption of substances by ionites.

  3. SORPTION OF ARSENITE AND ARSENATE ON A HIGH AFFINITY OXIDE: MACROSCOPIC AND MICROSCOPIC STUDIES

    EPA Science Inventory

    Sorption of arsenate and arsenite was examined on a Ru compound using macroscopic and microscopic techniques. Isotherms were constructed from batch studies at pH 4 through 8. Solution As was measured by ICAP. Samples of the Ru compound were equilibrated with arsenite and arsenate...

  4. Characteristics of Lead Sorption by Zeolite Minerals

    NASA Astrophysics Data System (ADS)

    Al-Sewailem, M. S.

    Lead adsorption behavior was investigated using four Zeolite minerals (clinoptilolite, analcime, phillipsite and chabazite). The used Pb2+ concentrations were 0, 0.1, 0.5, 1.0, 2.0, 3.0 and 5 µmol mL-1. Results indicated that Pb2+ sorption followed the Langmuir adsorption isotherm, but over limited concentration ranges for clinoptilolite and analcime. The bindg energy (Kd) reached, 2.400 and 0.875 g L-1 for phillipsite and chabazite, respectively. The maximum adsorption capacity for such minerals reached 208.33 and 204.08 mg g-1 with correlation coefficient (R2) reached, 0.997 and 0.995, respectively. Meanwhile, two stages for Pb2+adsorption were observed with clinoptilolite and analcime in the low and high concentrations of the applied Pb2+. Data also was applicable to the Freundlich adsorption isotherm over the used entire Pb2+ concentration ranges. The binding energy (n) reached, 1.014, 1.005, 1.001 and 1.001 g L-1 for clinoptilolite, analcime, phillipsite and chabazite, respectively. However, the b values (maximum adsorption capacity) reached 202.582, 201.651, 207.062 and 206.871 mg g-1 with correlation coefficient (R2) nearly one for all studying minerals, respectively. Desorption data indicated that most of the sorbed Pb2+ was extractedin the 1st extraction following the adsorption experiment. The ability of the used zeolite minerals to retain Pb2+ was high and there were differences between the studied minerals in sorption of Pb2+. In conclusion, data eliminated that, zeolite minerals especially, philipsite and chabazite, could be successfully used as packing material in subsurface reactive barriers intercepting ground water plumes and for fixed bed reactors designed to remove Pb2+ from industrial wastewater.

  5. Time and temperature dependent sorption behaviour of dimethoate pesticide in various Indian soils

    NASA Astrophysics Data System (ADS)

    Rani, Sunita; Sud Sant, Dhiraj

    2014-10-01

    Experiments were conducted to study the sorption behaviour of dimethoate in three Indian soils at different temperatures. A kinetic study showed that adsorption equilibrium was reached within 15 h at different initial levels of pesticide concentration. Applicability of the pseudo second order kinetic model suggested that the adsorption process was complex and several mechanisms were involved. The Freundlich model explained the adsorption behaviour adequately and the isotherms were of S-type. The adsorption process was found to be strongly affected by temperature. The Gibbs free energy change, ΔGº values (from -15.81 to -16.60 kJ mol-1) indicated that the process was spontaneous and exothermic in nature. The change in enthalpy of adsorption, ΔH° values (from -17.729 to -21.539 kJ mol-1) suggested that relatively weak H-bond forces were the main driving forces for adsorption. Desorption was found to be concentration- and temperature-dependent with higher desorption occurring at higher temperature and concentration levels. The results signify the importance of temperature in controlling the mobility of dimethoate in water bodies.

  6. Moisture Sorption Behaviour and Mould Ecology of Trade Garri Sold in South Eastern Nigeria

    PubMed Central

    Samuel, Tochukwu; Ugwuanyi, J. Obeta

    2014-01-01

    Garri is a creamy white or yellow starchy grit produced by roasting to gelatinization and dryness of peeled, washed, mashed, and fermented dewatered cassava roots. It is the most important product of cassava in West and Central Africa. Mean moisture content of yellow and white garri was 11.11% and 10.81% within 24 hrs of sampling from the market, increasing to 17.27% and 16.14%, respectively, following 3 months of storage at room temperature. The water activity of samples varied from initial 0.587 to 0.934 following storage. Moisture sorption isotherms, determined by static gravimetric techniques at 20° and 30°C, showed temperature dependent BET Sigmoidal type II behaviour typical of carbohydrate rich foods but modulated very slightly by the content of palm oil. Equilibrium moisture content decreased with increase in temperature at constant water activity. A total of 10 fungal species belonging to the genera Mucor, Penicillium, Cephalosporium, Aspergillus, Scopulariopsis, Rhizopus, and Paecilomyces were identified, with range increasing with water activity of samples. PMID:26904621

  7. Hydrogen sorption characteristics of nanostructured Pd–10Rh processed by cryomilling

    SciTech Connect

    Yang, Nancy; Yee, Joshua K.; Zhang, Zhihui; Kurmanaeva, Lilia; Cappillino, Patrick; Stavila, Vitalie; Lavernia, Enrique J.; San Marchi, Chris

    2014-10-03

    Palladium and its alloys are model systems for studying solid-state storage of hydrogen. Mechanical milling is commonly used to process complex powder systems for solid-state hydrogen storage; however, milling can also be used to evolve nanostructured powder to modify hydrogen sorption characteristics. In the present study, cryomilling (mechanical attrition milling in a cryogenic liquid) is used to produce nanostructured palladium-rhodium alloy powder. Characterization of the cryomilled Pd-10Rh using electron microscopy, X-ray diffraction, and surface area analysis reveals that (i) particle morphology evolves from spherical to flattened disk-like particles; while the (ii) crystallite size decreases from several microns to less than 100 nm and (iii) dislocation density increases with increased cryomilling time. Hydrogen absorption and desorption isotherms as well as the time scales for absorption were measured for cryomilled Pd-10Rh, and correlated with observed microstructural changes induced by the cryomilling process. In short, as the microstructure of the Pd-10Rh alloy is refined by cryomilling: (i) the maximum hydrogen concentration in the α-phase increases, (ii) the pressure plateau becomes flatter, and (iii) the equilibrium hydrogen capacity at 760 Torr increases. In addition, the rate of hydrogen absorption was reduced by an order of magnitude compared to non-cryomilled (atomized) powder.

  8. Hydrogen sorption characteristics of nanostructured Pd–10Rh processed by cryomilling

    DOE PAGESBeta

    Yang, Nancy; Yee, Joshua K.; Zhang, Zhihui; Kurmanaeva, Lilia; Cappillino, Patrick; Stavila, Vitalie; Lavernia, Enrique J.; San Marchi, Chris

    2014-10-03

    Palladium and its alloys are model systems for studying solid-state storage of hydrogen. Mechanical milling is commonly used to process complex powder systems for solid-state hydrogen storage; however, milling can also be used to evolve nanostructured powder to modify hydrogen sorption characteristics. In the present study, cryomilling (mechanical attrition milling in a cryogenic liquid) is used to produce nanostructured palladium-rhodium alloy powder. Characterization of the cryomilled Pd-10Rh using electron microscopy, X-ray diffraction, and surface area analysis reveals that (i) particle morphology evolves from spherical to flattened disk-like particles; while the (ii) crystallite size decreases from several microns to less thanmore » 100 nm and (iii) dislocation density increases with increased cryomilling time. Hydrogen absorption and desorption isotherms as well as the time scales for absorption were measured for cryomilled Pd-10Rh, and correlated with observed microstructural changes induced by the cryomilling process. In short, as the microstructure of the Pd-10Rh alloy is refined by cryomilling: (i) the maximum hydrogen concentration in the α-phase increases, (ii) the pressure plateau becomes flatter, and (iii) the equilibrium hydrogen capacity at 760 Torr increases. In addition, the rate of hydrogen absorption was reduced by an order of magnitude compared to non-cryomilled (atomized) powder.« less

  9. TECHNETIUM SORPTION MEDIA REVIEW

    SciTech Connect

    DUNCAN JB; KELLY SE; ROBBINS RA; ADAMS RD; THORSON MA; HAASS CC

    2011-08-25

    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.

  10. POLANYI-BASED MODELS FOR THE COMPETITIVE SORPTION OF LOW-POLARITY ORGANIC CONTAMINANTS ON A NATURAL SORBENT. (R825406)

    EPA Science Inventory

    The development of appropriate equilibrium sorption relationships for anthropogenic organic contaminants with soils and sediments is essential to predicting the extents and rates of solid-water interactions in the environment. In this context, we previously reported results that ...

  11. Sorption of Arsenite onto Mackinawite Coated Sand

    NASA Astrophysics Data System (ADS)

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

    2004-05-01

    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

  12. Contributions of a compost-biochar mixture to the metal sorption capacity of a mine tailing.

    PubMed

    Forján, R; Asensio, V; Rodríguez-Vila, A; Covelo, E F

    2016-02-01

    One technique applied to restore degraded or contaminated soils is to use amendments made of different types of waste materials, which in turn may contain metals such as Cu, Pb and Zn. For this reason, it is important to determine the capacity of the soil to retain these materials, and to compare the sorption capacity between an amended soil and another unamended soil. The aim of this study was to determine the mobility and availability of these metals in the soil after applying the amendment, and how it affected the soil's sorption capacity. Sorption isotherms were compared with the empirical models of Langmuir and Freundlich to estimate the sorption capacity. The overall capacity of the soils to sorb Cu, Pb or Zn was evaluated as the slope Kr. The amendments used in this study were a mixture made of compost and biochar in different proportions (20, 40, 60, 100 %), which were applied to the mine tailing from a settling pond from a copper mine. The mine tailing that were amended with the mixture of compost and biochar had a higher sorption capacity than the mine tailing from the unamended pond, and their sorption isotherms had a greater affinity towards Cu, Pb and Zn than the mine tailing that was studied. Therefore, the results obtained show that adding a mixture of compost and biochar favours the retention of Cu, Pb and Zn in mine tailing.

  13. Graphical determination of metal bioavailability to soil invertebrates utilizing the Langmuir sorption model

    SciTech Connect

    Donkin, S.G.

    1997-09-01

    A new method of performing soil toxicity tests with free-living nematodes exposed to several metals and soil types has been adapted to the Langmuir sorption model in an attempt at bridging the gap between physico-chemical and biological data gathered in the complex soil matrix. Pseudo-Langmuir sorption isotherms have been developed using nematode toxic responses (lethality, in this case) in place of measured solvated metal, in order to more accurately model bioavailability. This method allows the graphical determination of Langmuir coefficients describing maximum sorption capacities and sorption affinities of various metal-soil combinations in the context of real biological responses of indigenous organisms. Results from nematode mortality tests with zinc, cadmium, copper, and lead in four soil types and water were used for isotherm construction. The level of agreement between these results and available literature data on metal sorption behavior in soils suggests that biologically relevant data may be successfully fitted to sorption models such as the Langmuir. This would allow for accurate prediction of soil contaminant concentrations which have minimal effect on indigenous invertebrates.

  14. Isothermic hemodialysis and ultrafiltration.

    PubMed

    Rosales, L M; Schneditz, D; Morris, A T; Rahmati, S; Levin, N W

    2000-08-01

    The increase in patient temperature during hemodialysis is explained by hemodynamic compensation during ultrafiltration and hypovolemia that leads to peripheral vasoconstriction and reduced heat losses. We analyzed 51 stable high-efficiency hemodialysis treatments in 27 patients during isothermic dialysis in which body temperature was maintained at a constant level (+/-0.1 degrees C) using the temperature-control option of the Blood Temperature Monitor (BTM; Fresenius Medical Care, Bad Homburg, Germany). Hemodialysis was delivered using ultrapure water (limulus amebocyte lysate test < 0. 06 endotoxin units/mL) at mean blood flows of 410 +/- 40 mL/min. During treatments lasting 178 +/- 23 minutes, 4.8% +/- 1.4% of postdialysis body weight (W%) and 9.5% +/- 2.5% of postdialysis body water were removed using mean ultrafiltration rates of 1.1 +/- 0.3 L/h. Dialysate temperatures significantly decreased from 35.9 degrees C +/- 0.3 degrees C to 35.6 degrees C +/- 0.6 degrees C during hemodialysis. During these treatments, 187 +/- 69 kJ of thermal energy were removed from the patients through the extracorporeal circulation using cool dialysate. Extracorporeal heat flow was 17 +/- 6 W. Energy expenditure (H) estimated from anthropometric data was 65 +/- 12 W. Thus, 28% +/- 10% of estimated energy expenditure (H%) was removed during isothermic dialysis. A highly significant correlation was observed between H% and W% (H% = -5.6 * W%; r(2) = 0.91; P < 0.0001). This result is in support of the volume hypothesis of intradialytic heat accumulation and provides a rule of thumb to estimate extracorporeal cooling requirements for isothermic dialysis. Approximately 6% of H must be removed through the extracorporeal circulation for each percent of ultrafiltration-induced body-weight change. The importance of body temperature control during hemodialysis increases with increased ultrafiltration requirements.

  15. Sludge-Derived Biochar for Arsenic(III) Immobilization: Effects of Solution Chemistry on Sorption Behavior.

    PubMed

    Zhang, Weihua; Zheng, Juan; Zheng, Pingping; Tsang, Daniel C W; Qiu, Rongliang

    2015-07-01

    Recycling sewage sludge by pyrolysis has attracted increasing attention for pollutant removal from wastewater and soils. This study scrutinized As(III) sorption behavior on sludge-derived biochar (SDBC) under different pyrolysis conditions and solution chemistry. The SDBC pyrolyzed at a higher temperature showed a lower As(III) sorption capacity and increasingly nonlinear isotherm due to loss of surface sites and deoxygenation-dehydrogenation. The Langmuir sorption capacity on SDBC (3.08-6.04 mg g) was comparable to other waste-derived sorbents, with the highest As(III) sorption on SDBC pyrolyzed at 400°C for 2 h. The As(III) sorption kinetics best fit with the pseudo-second-order equation, thus suggesting the significance of the availability of surface sites and initial concentration. Sorption of As(III) was faster than that of Cr(VI) but slower than that of Pb(II), which was attributed to their differences in molar volume (correlated to diffusion coefficients) and sorption mechanisms. The X-ray photoelectron spectra revealed an increase of oxide oxygen (O) with a decrease of sorbed water, indicative of ligand exchange with hydroxyl groups on SDBC surfaces. The As(III) sorption was not pH dependent in acidic-neutral range (pH < 8) due to the buffering capacity and surface characteristics of the SDBC; however, sorption was promoted by increasing pH in the alkaline range (pH > 8) because of As(III) speciation in solution. An increasing ionic strength (0.001-0.1 mol L) facilitated As(III) sorption, indicating the predominance of ligand exchange over electrostatic interactions, while high concentrations (0.1 mol L) of competing anions (fluoride, sulfate, carbonate, and phosphate) inhibited As(III) sorption. These results suggest that SDBC is applicable for As(III) immobilization in most environmentally relevant conditions. PMID:26437093

  16. Mechanisms of plutonium sorption to mineral oxide surfaces: new insights with implications for colloid-enhanced migration

    SciTech Connect

    Schwantes, J. M.; Santschi, Peter H.

    2010-11-01

    New equilibrium and kinetic models have been developed to describe rate-limited sorption and desorption of Pu onto and off of mineral oxide surfaces using a generic approach to estimate sorption constants that require minimal laboratory calibrations. Equilibrium reactions describing a total of six surface species were derived from a combination of empirical relationships previously described in the literature and generated as part of this work.

  17. Sorption and desorption of cadmium by different fractions of biosolids-amended soils.

    PubMed

    Hettiarachchi, Ganga M; Ryan, James A; Chaney, Rufus L; La Fleur, Cherie M

    2003-01-01

    To evaluate the importance of both the inorganic and organic fractions in biosolids on Cd chemistry, a series of Cd sorption and desorption batch experiments (at pH 5.5) were conducted on different fractions of soils from a long-term field experimental site. The slope of the Cd sorption isotherm increased with rate of biosolids and was different for the different biosolids. Removal of organic carbon (OC) reduced the slope of the Cd sorption isotherm but did not account for the observed differences between biosolids-amended soils and a control soil, indicating that the increased adsorption associated with biosolids application was not limited to the increased OC from the addition of biosolids. Removal of both OC and Fe/Mn further reduced the slopes of Cd sorption isotherms and the sorption isotherm of the biosolids-amended soil was the same as that of the control, indicating both OC and Fe/Mn fractions added by the biosolids were important to the increased sorption observed for the biosolids-amended soil samples. Desorption experiments failed to remove from 60 to 90% of the sorbed Cd. This "apparent hysteresis" was higher for biosolids-amended soil than the control soil. Removal of both OC and Fe/Mn fractions was more effective in removing the observed differences between the biosolids-amended soil and the control than either alone. Results show that Cd added to biosolids-amended soil behaves differently than Cd added to soils without biosolids and support the hypothesis that the addition of Fe and Mn in the biosolids increased the retention of Cd in biosolids-amended soils.

  18. Equilibrium moisture content of waste mixtures from post-consumer carton packaging.

    PubMed

    Bacelos, M S; Freire, J T

    2012-01-01

    The manufacturing of boards and roof tiles is one of the routes to reuse waste from the recycled-carton-packaging process. Such a process requires knowledge of the hygroscopic behaviour of these carton-packaging waste mixtures in order to guarantee the quality of the final product (e.g. boards and roof tiles). Thus, with four carton-packaging waste mixtures of selected compositions (A, B, C and D), the sorption isotherms were obtained at air temperature of 20, 40 and 60 degrees C by using the static method. This permits one to investigate which model can relate the equilibrium moisture content of the mixture with that of a pure component through the mass fraction of each component in the mixtures. The results show that the experimental data can be well described by the weighted harmonic mean model. This suggests that the mean equilibrium moisture content of the carton-packaging mixture presents a non-linear relationship with each single, pure compound. PMID:22720401

  19. New approach in modeling Cr(VI) sorption onto biomass from metal binary mixtures solutions.

    PubMed

    Liu, Chang; Fiol, Núria; Villaescusa, Isabel; Poch, Jordi

    2016-01-15

    In the last decades Cr(VI) sorption equilibrium and kinetic studies have been carried out using several types of biomasses. However there are few researchers that consider all the simultaneous processes that take place during Cr(VI) sorption (i.e., sorption/reduction of Cr(VI) and simultaneous formation and binding of reduced Cr(III)) when formulating a model that describes the overall sorption process. On the other hand Cr(VI) scarcely exists alone in wastewaters, it is usually found in mixtures with divalent metals. Therefore, the simultaneous removal of Cr(VI) and divalent metals in binary mixtures and the interactive mechanism governing Cr(VI) elimination have gained more and more attention. In the present work, kinetics of Cr(VI) sorption onto exhausted coffee from Cr(VI)-Cu(II) binary mixtures has been studied in a stirred batch reactor. A model including Cr(VI) sorption and reduction, Cr(III) sorption and the effect of the presence of Cu(II) in these processes has been developed and validated. This study constitutes an important advance in modeling Cr(VI) sorption kinetics especially when chromium sorption is in part based on the sorbent capacity of reducing hexavalent chromium and a metal cation is present in the binary mixture.

  20. Sorption of copper onto low molecular weight chitosan derivative from aqueous solution.

    PubMed

    Boamah, Peter Osei; Huang, Yan; Hua, Mingqing; Onumah, Jacqueline; Sam-Amoah, Livingstone K; Boamah, Paul Osei; Qian, Yaao; Zhang, Qi

    2016-07-01

    In this study, sorption of copper onto low molecular weight chitosan derivative was studied. Experimental parameters such as pH of the solution (A), temperature (B), dose of the sorbent (C), and concentration of solution (D) were considered. The statistical results indicated that the dose of sorbent (C) and Cu (II) concentration (D) influenced removal efficiency at 5% significance level. Also, some interactions such as ABCD, ACD, ABC and AC affected the removal process. The sorbent was characterized with FTIR, SEM and TG/DSC. Freundlich isotherm model was the best isotherm model. The kinetic study results correlated well with the pseudo-second-order model. The thermodynamic studies revealed that the nature of copper sorption was spontaneous and endothermic. Strong affinity of the sorbent for copper (II) was revealed by the Isothermal Titration Calorimetry (ITC) technique. PMID:27039244

  1. Can soil drying affect the sorption of pesticides in soil?

    NASA Astrophysics Data System (ADS)

    Chaplain, Véronique; Saint, Philippe; Mamy, Laure; Barriuso, Enrique

    2010-05-01

    The sorption of pesticides in soils mainly controls their further dispersion into the environment. Sorption is usually related to the physico-chemical properties of molecules but it also depends on the hydrophobic features of soils. However, the hydrophobicity of soils changes with wetting and drying cycles and this can be enhanced with climate change. The objective of this study was to measure by using controlled artificial soils the influence of the hydrophobic characteristic of soils on the retention of a model pesticide. Artificial soils consisted in silica particles covered by synthetic cationic polymers. Polymers were characterized by the molar ratio of monomers bearing an alkyl chain of 12C. Two polymers were used, with 20 and 80 % ratios, and the same degree of polymerization. In addition, porous and non-porous particles were used to study the accessibility notion and to measure the influence of diffusion on pesticide sorption kinetics. Lindane was chosen as model molecule because its adsorption is supposed mainly due to hydrophobic interactions. Results on polymers adsorption on silica showed that it was governed by electrostatic interactions, without any dependency of the hydrophobic ratio. Polymers covered the entire surface of porous particles. Kinetic measurements showed that lindane sorption was slowed in porous particles due to the molecular diffusion inside the microporosity. The adsorption of lindane on covered silica particles corresponded to a partition mechanism described by linear isotherms. The slope was determined by the hydrophobic ratio of polymers: the sorption of lindane was highest in the most hydrophobic artificial soil. As a result, modification in soil hydrophobicity, that can happen with climate change, might affect the sorption and the fate of pesticides. However additional experiments are needed to confirm these first results. Such artificial soils should be used as reference materials to compare the reactivity of pesticides, to

  2. Modeling and Uncertainty Quantification of Vapor Sorption and Diffusion in Heterogeneous Polymers

    SciTech Connect

    Sun, Yunwei; Harley, Stephen J.; Glascoe, Elizabeth A.

    2015-08-13

    A high-fidelity model of kinetic and equilibrium sorption and diffusion is developed and exercised. The gas-diffusion model is coupled with a triple-sorption mechanism: Henry’s law absorption, Langmuir adsorption, and pooling or clustering of molecules at higher partial pressures. Sorption experiments are conducted and span a range of relative humidities (0-95 %) and temperatures (30-60 °C). Kinetic and equilibrium sorption properties and effective diffusivity are determined by minimizing the absolute difference between measured and modeled uptakes. Uncertainty quantification and sensitivity analysis methods are described and exercised herein to demonstrate the capability of this modeling approach. Water uptake in silica-filled and unfilled poly(dimethylsiloxane) networks is investigated; however, the model is versatile enough to be used with a wide range of materials and vapors.

  3. Sorption of 4-ethylphenol and 4-ethylguaiacol by suberin from cork.

    PubMed

    Gallardo-Chacón, Joan-Josep; Karbowiak, Thomas

    2015-08-15

    Cork shows an active role in the sorption of volatile phenols from wine. The sorption properties of 4-ethylphenol and 4-ethylguaiacol phenols in hydro-alcoholic medium placed in contact with suberin extracted from cork were especially investigated. To that purpose, suberin was immersed in model wine solutions containing several concentrations of each phenol and the amount of the compound remaining in the liquid phase was determined by SPME-GC-MS. Sorption isotherms of 4-ethylguaiacol and 4-ethylphenol by suberin followed the Henry's model. The solid/liquid partition coefficients (KSL) between the suberin and the model wine were also determined for several other volatile phenols. Suberin displayed rather high sorption capacity, which was positively correlated to the hydrophobicity of the volatile. Finally, the capacity of suberin to decrease the concentration of 4-ethylphenol and 4-ethylguaiacol was also tested in real wines affected by a Brettanomyces character. It also lead to a significant reduction of their concentration in wine.

  4. Sorption-capacity limited retardation of radionuclides transport in water-saturated packing materials

    SciTech Connect

    Pescatore, C.; Sullivan, T.

    1984-01-01

    Radionuclides breakthrough times as calculated through constant retardation factors obtained in dilute solutions are non-conservative. The constant retardation approach regards the solid as having infinite sorption capacity throughout the solid. However, as the solid becomes locally saturated, such as in the proximity of the waste form-packing materials interface, it will exhibit no retardation properties, and transport will take place as if the radionuclides were locally non-reactive. The magnitude of the effect of finite sorption capacity of the packing materials on radionuclide transport is discussed with reference to high-level waste package performance. An example based on literature sorption data indicates that the breakthrough time may be overpredicted by orders of magnitude using a constant retardation factor as compared to using the entire sorption isotherm to obtain a concentration-dependent retardation factor. 8 references, 3 figures, 3 tables.

  5. A general computer model for predicting the performance of gas sorption refrigerators

    NASA Technical Reports Server (NTRS)

    Sigurdson, K. B.

    1983-01-01

    Projected performance requirements for cryogenic spacecraft sensor cooling systems which demand higher reliability and longer lifetimes are outlined. The gas/solid sorption refrigerator is viewed as a potential solution to cryogenic cooling needs. A software model of an entire gas sorption refrigerator system was developed. The numerical model, evaluates almost any combination and order of refrigerator components and any sorbent-sorbate pair or which the sorption isotherm data are available. Parametric curves for predicting system performance were generated for two types of refrigerators, a LaNi5-H2 absorption cooler and a Charcoal-N2 adsorption cooler. It is found that precooling temperature and heat exchanger effectiveness affect the refrigerator performance. It is indicated that gas sorption refrigerators are feasible for a number of space applications.

  6. Phosphorus sorption characteristics of a light-weight aggregate.

    PubMed

    Zhu, T; Maehlum, T; Jenssen, P D; Krogstad, T

    2003-01-01

    A light-weight aggregate (LWA) made of expanded clay used as a filter media in wastewater treatment, was tested for sorption of phosphorus (P) in laboratory experiments. The objectives were to investigate the different P retention pools and how grain size, time, temperature and changed P concentration influenced the P binding mechanisms in this type of filter. Three different grain sizes (0-2 mm, 2-4 mm and 0-4 mm) were tested in a batch experiment. The isotherm for the P sorbed by the contact medium (including retention and fixation) was obtained under laboratory conditions. Fifty percent of the P sorption occurred in the first 4-8 hours. Temperature did not substantially influence P sorption for 0-2 mm grain size LWA. In the LWA suspension system, P desorption did not occur when the P content in the loading solution decreased. Fractionation analysis indicated that Ca-bound P, loosely-bound P, and Al-bound P were the predominant P retention pools. The loosely-bound P pool was determined primarily by the equilibrated P concentration in the system. Fe-bound P was negligible in the P sorption of LWA. PMID:14621152

  7. A thermodynamically consistent explicit competitive adsorption isotherm model based on second-order single component behaviour.

    PubMed

    Ilić, Milica; Flockerzi, Dietrich; Seidel-Morgenstern, Andreas

    2010-04-01

    A competitive adsorption isotherm model is derived for binary mixtures of components characterized by single component isotherms which are second-order truncations of higher order equilibrium models suggested by multi-layer theory and statistical thermodynamics. The competitive isotherms are determined using the ideal adsorbed solution (IAS) theory which, in case of complex single component isotherms, does not generate explicit expressions to calculated equilibrium loadings and causes time consuming iterations in simulations of adsorption processes. The explicit model derived in this work is based on an analysis of the roots of a cubic polynomial resulting from the set of IAS equations. The suggested thermodynamically consistent and widely applicable competitive isotherm model can be recommended as a flexible tool for efficient simulations of fixed-bed adsorber dynamics.

  8. Modeling and predicting competitive sorption of organic compounds in soil.

    PubMed

    Faria, Isabel R; Young, Thomas M

    2010-12-01

    Binary systems consisting of 1,2-dichlorobenzene (12DCB) + competitor were investigated over a range of concentrations of competitor in three natural sorbents with distinct characteristics. Two models, the ideal adsorbed solution theory (IAST) and the potential theory (Polanyi-based multisolute model), widely used in the prediction of multisolute sorption equilibrium from single-solute data, were used to simulate competitive sorption in our systems. The goal was to determine which multisolute model best represented the experimentally obtained multisolute data in natural sorbents of varied properties. Results suggested that for the sorbents and sorbates studied, the IAST model provided much better results. On average, the IAST model provided lower errors (23%) than the potential model (45%). The effect of competitor structure on the degree of competition was also investigated to identify any relationships between competition and structure using molecular descriptors. The competitors chlorobenzene, naphthalene, 1,4-dichlorobenzene, 1,2,4-trichlorobenzene all showed very similar degrees of competition, while benzene, phenanthrene, and pyrene were the least effective competitors toward 12DCB across all sorbents. Different sorption sites or sorption mechanisms might be involved in the sorption of these molecules leading to a lack of competitive behavior. A significant relationship between competitor structure and the degree of competition was observed at environmentally relevant sorbed competitor concentrations for the soil containing the highest fraction of hard carbon (Forbes soil).

  9. Sorption and predicted mobility of herbicides in Baltic soils.

    PubMed

    Sakaliene, Ona; Papiernik, Sharon K; Koskinen, William C; Spokas, Kurt A

    2007-08-01

    This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine approximately amitrole approximately simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log K(ow)) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.

  10. Application of the new thermodynamic approach to the description of superequivalent sorption by ion exchangers

    NASA Astrophysics Data System (ADS)

    Khokhlova, O. N.

    2014-08-01

    Using the example of sorption systems with the participation of amino acids, it is shown that the novel thermodynamic approach to describing superequivalent sorption as a combination of ion exchange and nonexchangeable absorption allows us to adequately describe such equilibria. Results from calculating the activity coefficients of components of a sorbent phase and the thermodynamic constants of ion exchange equilibrium and the superequivalent absorption of phenylalanine by AV-17-8 anion exchange resin are presented.

  11. Experimental adsorption isotherms based on inverse gas chromatography.

    PubMed

    Kalogirou, E; Bassiotis, I; Artemiadi, Th; Margariti, S; Siokos, V; Roubani-Kalantzopoulou, F

    2002-09-01

    A new chromatographic perturbation method is used for studying the adsorption-desorption equilibrium in various gas-solid heterogeneous systems. It is the reversed-flow method giving accurate and precise values of many physicochemical constants including the basic and necessary adsorption isotherm values. For four inorganic oxides, namely, Cr2O3, Fe2O3, TiO2 and PbO, and two aromatic hydrocarbons (benzene, toluene) these adsorption isotherms have been determined through a non-linear model. PMID:12385379

  12. Isothermal separation processes

    NASA Technical Reports Server (NTRS)

    England, C.

    1982-01-01

    The isothermal processes of membrane separation, supercritical extraction and chromatography were examined using availability analysis. The general approach was to derive equations that identified where energy is consumed in these processes and how they compare with conventional separation methods. These separation methods are characterized by pure work inputs, chiefly in the form of a pressure drop which supplies the required energy. Equations were derived for the energy requirement in terms of regular solution theory. This approach is believed to accurately predict the work of separation in terms of the heat of solution and the entropy of mixing. It can form the basis of a convenient calculation method for optimizing membrane and solvent properties for particular applications. Calculations were made on the energy requirements for a membrane process separating air into its components.

  13. Rate of strontium sorption and the effects of variable aqueous concentrations of sodium and potassium on strontium distribution coefficients of a surficial sediment at the Idaho National Engineering Laboratory, Idaho

    USGS Publications Warehouse

    Bunde, R.L.; Rosentreter, J.J.; Liszewski, M.J.

    1998-01-01

    The rate of strontium sorption and the effects of variable aqueous concentrations of sodium and potassium on strontium sorption were measured as part of an investigation to determine strontium chemical transport properties of a surficial sediment at the Idaho National Engineering Laboratory (INEL), Idaho. Batch experimental techniques were used to determine the rate of strontium sorption and strontium distribution coefficients (K(d)s) between aqueous and solid phases. Rate experiments indicate that strontium in solution reached an apparent equilibrium with the sediment in 26 h. K(d)s were derived using the linear isotherm model at initial sodium concentrations from 100 to 5,000 mg/l and initial potassium concentrations from 2 to 150 mg/l. K(d)s ranged from 56 ?? 2 to 62 ?? 3 ml/g at initial aqueous concentrations of sodium and potassium equal to or less than 300 and 150 mg/l, respectively. K(d)s hinged from 4.7 ?? 0.2 to 19 ?? 1 ml/g with initial aqueous concentrations of sodium between 1,000 and 5,000 mg/l. These data indicate that sodium concentrations greater than 300 mg/l in wastewater increase the availability of strontium for transport beneath waste disposal ponds at the INEL by decreasing strontium sorption on the surficial sediment. Wastewater concentrations of sodium and potassium less than 300 and 150 mg/l, respectively, have little effect on the availability of strontium for transport.The rate of strontium sorption and the effects of variable aqueous concentrations of sodium and potassium on strontium sorption were measured as part of an investigation to determine strontium chemical transport properties of a surficial sediment at the Idaho National Engineering Laboratory (INEL), Idaho. Batch experimental techniques were used to determine the rate of strontium sorption and strontium distribution coefficients (Kds) between aqueous and solid phases. Rate experiments indicate that strontium in solution reached an apparent equilibrium with the sediment in 26

  14. Water vapor sorption hysteresis of ceramic bricks

    NASA Astrophysics Data System (ADS)

    Koronthalyova, Olga

    2016-07-01

    A quantification of the hysteretic effects and their thorough analysis was carried out for three types of ceramic bricks. Water vapor adsorption/desorption isotherms were measured by the standard desiccator method. The desorption measurements were carried out from capillary moisture content as well as from equilibrium moisture content corresponding to the relative humidity of 98 %. For all three tested types of bricks the hysteretic effects were present but their significance differed depending on the particular type of brick. Significant differences were noticed also in desorption curves determined from capillary moisture content and from equilibrium moisture content corresponding to the relative humidity of 98 %. Based on the measured data a possible correlation between pore structure parameters and noticed hysteretic effects as well as relevance of the open pore model are discussed. The obtained adsorption/desorption curves were approximated by an analytical relation.

  15. Characteristics and influencing factors of tetrachloroethylene sorption-desorption on soil and its components.

    PubMed

    Qiu, Zhaofu; Yang, Weiwei; He, Long; Zhao, Zhexuan; Lu, Shuguang; Sui, Qian

    2016-02-01

    To investigate the effects of soil structure, soil organic carbon (SOC), minerals, initial tetrachloroethylene (PCE) concentration (C0), and ionic strength (Ci) on PCE sorption-desorption, six types of soil were adopted as adsorbents, including two types of natural soil and four types of soil with most of the "soft carbon" pre-treated by H2O2 or with all SOC removed from the original soil by 600 °C ignition. The results showed that all of the sorption-desorption isotherms of PCE were non-linear within the experimental range, and the H2O2-treated samples exhibited higher non-linear sorption isotherms than those of the original soils. The hysteresis index of PCE sorption to original soil is less pronounced than that of the H2O2-treated and 600 °C-heated samples due to the entrapment of sorbate molecules in the "hard carbon" domain, together with the meso- and microporous structures within the 600 °C-heated samples. Both SOC and minerals have impacts on the sorption-desorption of PCE, and the sorption-desorption contribution rate of minerals increased with decreasing SOC content. C0 has almost no influence on the sorption to minerals of the soils, but the contribution rate of minerals decreased with increasing C0 in the desorption stage. As a result of the salting-out effect, PCE sorption capacity was increased by increasing Ci, especially when Ci ≥ 0.1 M. Moreover, desorption increased and hysteresis weakened with increasing Ci, except for the 600 °C-heated samples. In addition, no significant effect of Ci on desorption of PCE and no hysteresis was observed in this experimental range for the 600 °C-heated samples.

  16. Soil sorption of organic vapors and effects of humidity on sorptive mechanism and capacity

    USGS Publications Warehouse

    Chiou, C.T.; Shoup, T.D.

    1985-01-01

    Vapor sorption isotherms on dry Woodburn soil at 20-30??C were determined for benzene, chlorobenzene, p-dichlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, and water as single vapors and for benzene, m-dichlorobenzene, and 1,2,4-trichlorobenzene as functions of relative humidity (RH). Isotherms for all compounds on dry soil samples are distinctively nonlinear, with water showing the greatest capacity. Water vapor sharply reduced the sorption capacities of organic compounds with the dry soil; on water-saturated soil, the reduction was about 2 orders of magnitude. The markedly higher sorption of organic vapors at subsaturation humidities is attributed to adsorption on the mineral matter, which predominates over the simultaneous uptake by partition into the organic matter. At about 90% RH, the sorption capacities of organic compounds become comparable to those in aqueous systems. The effect of humidity is attributed to adsorptive displacement by water of organics adsorbed on the mineral matter. A small residual uptake is attributed to the partition into the soil-organic phase that has been postulated in aqueous systems. The results are essentially in keeping with the model that was previously proposed for sorption on the soil from water and from organic solvents.Vapor sorption isotherms on dry Woodburn soil at 20-30 degree C were determined for benzene, chlorobenzene, p-dichlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, and water as single vapors and for benzene, m-dichlorobenzene, and 1,2,4-trichlorobenzene as functions of relative humidity (RH). Isotherms for all compounds on dry soil samples are distinctively nonlinear, with water showing the greatest capacity. Water vapor sharply reduced the sorption capacities of organic compounds with the dry soil; on water-saturated soil, the reduction was about 2 orders of magnitude. The markedly higher sorption of organic vapors at subsaturation humidities is attributed to adsorption on the mineral matter

  17. Modeling depth-variant and domain-specific sorption and biodegradation in dual-permeability media

    NASA Astrophysics Data System (ADS)

    Ray, Chittaranjan; Vogel, Tomas; Dusek, Jaromir

    2004-05-01

    A dual-permeability model (S_1D_DUAL) was developed to simulate the transport of land-applied pesticides in macroporous media. In this model, one flow domain was represented by the bulk matrix and the other by the preferential flow domain (PFD) where water and chemicals move at faster rates. The model assumed the validity of Darcian flow and the advective-dispersive solute transport in each of the two domains with inter-domain transfer of water and solutes due to pressure and concentration gradients. It was conceptualized that sorption and biodegradation rates vary with soil depth as well as in each of the two flow domains. In addition to equilibrium sorption, kinetic sorption was simulated in the PFD. Simulations were conducted to evaluate the combined effects of preferential flow, depth- and domain-variant sorption, and degradation on leaching of two pesticides: one with strong sorption potential (trifluralin) and the other with weak sorption potential (atrazine). Simulation results for a test case showed that water flux in the PFD was three times more than in the matrix for selected storm events. When equilibrium sorption was considered, the simulated profile of trifluralin in each domain was similar; however, the atrazine profile was deeper in the PFD than in the bulk matrix under episodic storm events. With an assumption of negligible sorption in the PFD, both the atrazine and the trifluralin profiles moved twice deeper into the PFD. The simulated concentrations of the chemicals were several orders higher in the PFD than in the matrix, even at deeper depths. The volume fraction of the macropores and the sorption and biodegradation properties of the chemicals could also affect the amount of pesticides leaving the root zone. For an intense storm event, slow sorption reaction rates in the PFD produced higher breakthrough concentrations of atrazine at the bottom of the simulated soil profile, thus posing the risk for breakthrough of chemicals from the root zone.

  18. Synthesis of hydrophobic cross-linked polyzwitterionic acid for simultaneous sorption of Eriochrome black T and chromium ions from binary hazardous waters.

    PubMed

    Saleh, Tawfik A; Muhammad, Auwal M; Ali, Shaikh A

    2016-04-15

    Hydrophobic cross-linked polyzwitterionic acid (HCPZA) containing long chain (C18) hydrophobes and residues of a glutamic acid having unquenched nitrogen valency was synthesized. Exploiting the chelating ability of the amino acid residues to scavenge toxic metals and the hydrophobic surface to scoop up the organic contaminants, the resin HCPZA was evaluated for simultaneous removal of chromium and Eriochrome black T (EBT) from wastewaters. The structure and morphology of the polymer before and after sorption were characterized by using FTIR, TGA, EDX and SEM. The effect of various parameters such as contact time, pH and initial concentrations were investigated to arrive at optimum conditions. The adsorption of Eriochrome black T and Cr (III) on HCPZA reached equilibrium in 30 min. The mechanism of adsorption was investigated using kinetic, diffusion and isotherm models. The adsorption kinetic data were described well by the pseudo-second order model and by the Freundlich isotherm model. EDX analysis confirmed the adsorption of Cr (III) and EBT on the polymer. The hydrophobic resin exhibited a remarkable simultaneous adsorption capacity for EBT and Cr (III) and thus demonstrated its potential to be a promising adsorbent for removal of dyes and heavy metal ions from wastewaters.

  19. Effects of oil dispersant on solubilization, sorption and desorption of polycyclic aromatic hydrocarbons in sediment-seawater systems.

    PubMed

    Zhao, Xiao; Gong, Yanyan; O'Reilly, S E; Zhao, Dongye

    2015-03-15

    This work investigated effects of a prototype oil dispersant on solubilization, sorption and desorption of three model PAHs in sediment-seawater systems. Increasing dispersant dosage linearly enhanced solubility for all PAHs. Conversely, the dispersant enhanced the sediment uptake of the PAHs, and induced significant desorption hysteresis. Such contrasting effects (adsolubilization vs. solubilization) of dispersant were found dependent of the dispersant concentration and PAH hydrophobicity. The dual-mode models adequately simulated the sorption kinetics and isotherms, and quantified dispersant-enhanced PAH uptake. Sorption of naphthalene and 1-methylnaphthalene by sediment positively correlated with uptake of the dispersant, while sorption of pyrene dropped sharply when the dispersant exceeded its critical micelle concentration (CMC). The deepwater conditions diminished the dispersant effects on solubilization, but enhanced uptake of the PAHs, albeit sorption of the dispersant was lowered. The information may aid in understanding roles of dispersants on distribution, fate and transport of petroleum PAHs in marine systems. PMID:25616532

  20. Sorption kinetics of uranium-238 and neptunium-237 on a glacial sediment

    NASA Astrophysics Data System (ADS)

    Braithwaite, A.; Richardson, S.; Moyes, L. N.; Livens, F. R.; Bunker, D. J.; Hughes, C. R.; Smith, J. T.; Hilton, J.

    2000-02-01

    Studies of uptake of radionuclides by natural materials have shown that sorption may occur via fast equilibrium exchange and/or slow kinetic processes, which can be described using a series of box models. This paper describes the use of such models to evaluate the solid-solution partitioning of 238U and 237Np on a clay rich sediment. Experimental data are obtained using the batch sorption technique, which are then analysed using 1, 2, and 3 box kinetic models. Uptake of 238U is initially rapid, with approximately 90% sorbed within the first 30 minutes. Sorption continues, but at a slower rate. Uptake of 237Np is initially slower than U, with approximately 30% sorbed within the first 30 minutes. Sorption again continues, at a slower rate. Analysis of the experimental data indicates that sorption can be described using 2 and 3 box kinetic models. The results demonstrate that sorption of uranium and neptunium on clay rich sediments occurs via equilibrium and kinetically controlled pathways, with neptunium being controlled by kinetics to a greater extent than uranium. The 2 or 3 box model can describe sorption of neptunium, uranium requires the 3 box model.

  1. Comparison of multifractal parameters form adsorption isotherms, desorption isotherms and mercury intrusion curves

    NASA Astrophysics Data System (ADS)

    Paz-Ferreiro, Jorge; Mon, Rodolfo; Vidal Vázquez, Eva

    2013-04-01

    The soil pore space is composed of a continuum of pores extremely variable in size, which range from equivalent diameter sizes smaller than nanometers to an upper limit of the order of centimeters. So, it is quite typical for soil pore space to display a size range of more than a factor of 106 in scale. Nitrogen sorption and mercury injection provide pores size distributions in the range from about 0.1 to 0.001 μm and 150 to 0.005 μm, respectively. The aims of this study were to evaluate the scaling properties of nitrogen adsorption isotherms (NAI), nitrogen desorption isotherms (NDI) and mercury intrusion porosimetry (MIP) curves of agricultural soils from "La Pampa húmeda", in the north of Buenos Aires and south of Santa Fé provinces, Argentina. Both NAIs, NDIs and MIPs exhibited multifractal behavior but its scaling properties were different so that the multifractality index, assessed by the width of the generalized dimension and the singularity spectra ranked as follows: NAI > NDI > MIP. Also, parameterization by the Hurst exponent indicates NAIs were less persistent than NDIs and in turn, these were less persistent than MIPs. The multfractal approach was useful to characterize the heterogeneity of various domains of the soil nano- micro- and mesopore system at the scale of small aggregates.

  2. Sorption of graphites at high temperatures. Final report, February 1, 1977-June 30, 1978. [800 to 1100/sup 0/C; pseudo-isopiestic method

    SciTech Connect

    Kazi, N.I.; Pyecha, T.D.; Zumwalt, L.R.

    1980-06-30

    This report include: (1) corrected data and new data on cesium sorption by bulk graphite (H-451) with a discussion of anomalies and a comparison of the data; (2) a review of the exponential (Freundlich) isotherm theory and a derivation of the modified-exponential isotherm; (3) a report on a study by the pseudo-isopiestic method of cesium by H-451 graphite powder (size range 44 to 74 ..mu..m) of the type used in the Knudsen cell mass spectrometer method; (4) a comparison of the results on particulate graphite (powder) obtained by the Knudsen cell method and also a comparison of cesium sorption results obtained with the bulk graphite; (5) development of a theory for the kinetics of sorption of a system (cesium and graphite) which shows an exponential (Freundlich) type of sorption; (6) comparison of theoretical with observed kinetics for sorption of cesium by graphite (H-451) powder and a comparison of bulk graphite vs. particulate graphite sorption kinetics; (7) report of a study of the effects of barium on cesium sorption by H-451 graphite at 1000/sup 0/C; and (8) a thermodynamic treatment of mixed sorption and its application to mixed barium-cesium and strontium-cesium sorption by graphite.

  3. Sorption of Cu and Pb to kaolinite-fulvic acid colloids: Assessment of sorbent interactions

    NASA Astrophysics Data System (ADS)

    Heidmann, Ilona; Christl, Iso; Kretzschmar, Ruben

    2005-04-01

    The sorption of Cu(II) and Pb(II) to kaolinite-fulvic acid colloids was investigated by potentiometric titrations. To assess the possible interactions between kaolinite and fulvic acid during metal sorption, experimental sorption isotherms were compared with predictions based on a linear additivity model (LAM). Suspensions of 5 g L -1 kaolinite and 0.03 g L -1 fulvic acid in 0.01 M NaNO 3 were titrated with Cu and Pb solutions, respectively. The suspension pH was kept constant at pH 4, 6, or 8. The free ion activities of Cu 2+ and Pb 2+ were monitored in the titration vessel using ion selective electrodes. Total dissolved concentrations of metals (by ICP-MS) and fulvic acid (by UV-absorption) were determined in samples taken after each titration step. The amounts of metals sorbed to the solid phase, comprised of kaolinite plus surface-bound fulvic acid, were calculated by difference. Compared to pure kaolinite, addition of fulvic acid to the clay strongly increased metal sorption to the solid phase. This effect was more pronounced at pH 4 and 6 than at pH 8, because more fulvic acid was sorbed to the kaolinite surface under acidic conditions. Addition of Pb enhanced the sorption of fulvic acid onto kaolinite at pH 6 and 8, but not at pH 4. Addition of Cu had no effect on the sorption of fulvic acid onto kaolinite. In the LAM, metal sorption to the kaolinite surface was predicted by a two-site, 1-pK basic Stern model and metal sorption to the fulvic acid was calculated with the NICA-Donnan model, respectively. The LAM provided good predictions of Cu sorption to the kaolinite-fulvic acid colloids over the entire range in pH and free Cu 2+ ion activity (10 -12 to 10 -5). The sorption of Pb was slightly underestimated by the LAM under most conditions. A fractionation of the fulvic acid during sorption to kaolinite was observed, but this could not explain the observed deviations of the LAM predictions from the experimental Pb sorption isotherms.

  4. Sorption of perfluorooctanoic acid, perfluorooctane sulfonate and perfluoroheptanoic acid on granular activated carbon.

    PubMed

    Zhang, Di; Luo, Qi; Gao, Bin; Chiang, Sheau-Yun Dora; Woodward, David; Huang, Qingguo

    2016-02-01

    The sorption of perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), and perfluoroheptanoic acid (PFHpA) on granular activated carbon (GAC) was characterized and compared to explore the underlying mechanisms. Sorption of the three perfluoroalkyl acids (PFAAs) on GAC appeared to be a rapid intra-particle diffusion process, which were well represented by the pseudo-second-order rate model with the sorption rate following the order PFOS > PFOA > PFHpA. Sorption isotherm data were well fitted by the Freundlich model with the sorption capacity (Kf) of PFOS, PFOA and PFHpA being 4.45, 2.42 and 1.66 respectively. This suggests that the hydrophilic head group on PFAAs, i.e. sulfonate vs carboxylic, has a strong influence on their sorption. Comparison between PFOA and PFHpA revealed that hydrophobicity could also play a role in the sorption of PFAAs on GAC when the fluorocarbon chain length is different. Analyses using Attenuated Total Reflection (ATR)-Fourier Transform Infrared (FTIR) spectroscopy suggested possible formation of a negative charge-assisted H-bond between PFAAs and the functionalities on GAC surfaces, including non-aromatic ketones, sulfides, and halogenated hydrocarbons. PMID:26606188

  5. Sorption of Cu(2+) on humic acids sequentially extracted from a sediment.

    PubMed

    Yang, Kun; Miao, Gangfen; Wu, Wenhao; Lin, Daohui; Pan, Bo; Wu, Fengchang; Xing, Baoshan

    2015-11-01

    In addition to the diverse properties of humic acids (HAs) extracted from different soils or sediments, chemical compositions, functional groups and structures of HAs extracted from a single soil or sediment could also be diverse and thus significantly affect sorption of heavy metals, which is a key process controlling the transfer, transformation and fate of heavy metals in the environment. In this study, we sequentially extracted four HA fractions from a single sediment and conducted the sorption experiments of Cu(2+) on these HA fractions. Our results showed that aromaticity and acidic group content of HA fraction decreased with increasing extraction. Earlier extracted HA fraction had higher sorption capacity and affinity for Cu(2+). There were two fractions of adsorbed Cu(2+) on HAs, i.e., ion exchanged fraction and surface bonded fraction, which can be captured mechanically by the bi-Langmuir model with good isotherm fitting. The ion exchanged fraction had larger sorption capacity but lower sorption affinity, compared with the surface bonded fraction. The dissociated carboxyl groups of HAs were responsible for both fractions of Cu(2+) sorption, due to the more Cu(2+) sorption on the earlier extracted HA fraction with more carboxyl groups and at higher pH. The intensive competition between H(+) and the exchangeable Cu(2+) could result in the decrease of ion exchanged capacity and affinity for Cu(2+) on HAs. PMID:26246274

  6. Isothermal Amplification of Nucleic Acids.

    PubMed

    Zhao, Yongxi; Chen, Feng; Li, Qian; Wang, Lihua; Fan, Chunhai

    2015-11-25

    Isothermal amplification of nucleic acids is a simple process that rapidly and efficiently accumulates nucleic acid sequences at constant temperature. Since the early 1990s, various isothermal amplification techniques have been developed as alternatives to polymerase chain reaction (PCR). These isothermal amplification methods have been used for biosensing targets such as DNA, RNA, cells, proteins, small molecules, and ions. The applications of these techniques for in situ or intracellular bioimaging and sequencing have been amply demonstrated. Amplicons produced by isothermal amplification methods have also been utilized to construct versatile nucleic acid nanomaterials for promising applications in biomedicine, bioimaging, and biosensing. The integration of isothermal amplification into microsystems or portable devices improves nucleic acid-based on-site assays and confers high sensitivity. Single-cell and single-molecule analyses have also been implemented based on integrated microfluidic systems. In this review, we provide a comprehensive overview of the isothermal amplification of nucleic acids encompassing work published in the past two decades. First, different isothermal amplification techniques are classified into three types based on reaction kinetics. Then, we summarize the applications of isothermal amplification in bioanalysis, diagnostics, nanotechnology, materials science, and device integration. Finally, several challenges and perspectives in the field are discussed. PMID:26551336

  7. Isothermal Amplification of Nucleic Acids.

    PubMed

    Zhao, Yongxi; Chen, Feng; Li, Qian; Wang, Lihua; Fan, Chunhai

    2015-11-25

    Isothermal amplification of nucleic acids is a simple process that rapidly and efficiently accumulates nucleic acid sequences at constant temperature. Since the early 1990s, various isothermal amplification techniques have been developed as alternatives to polymerase chain reaction (PCR). These isothermal amplification methods have been used for biosensing targets such as DNA, RNA, cells, proteins, small molecules, and ions. The applications of these techniques for in situ or intracellular bioimaging and sequencing have been amply demonstrated. Amplicons produced by isothermal amplification methods have also been utilized to construct versatile nucleic acid nanomaterials for promising applications in biomedicine, bioimaging, and biosensing. The integration of isothermal amplification into microsystems or portable devices improves nucleic acid-based on-site assays and confers high sensitivity. Single-cell and single-molecule analyses have also been implemented based on integrated microfluidic systems. In this review, we provide a comprehensive overview of the isothermal amplification of nucleic acids encompassing work published in the past two decades. First, different isothermal amplification techniques are classified into three types based on reaction kinetics. Then, we summarize the applications of isothermal amplification in bioanalysis, diagnostics, nanotechnology, materials science, and device integration. Finally, several challenges and perspectives in the field are discussed.

  8. Biosorptive removal of mercury(II) from aqueous solution using lichen (Xanthoparmelia conspersa) biomass: kinetic and equilibrium studies.

    PubMed

    Tuzen, Mustafa; Sari, Ahmet; Mendil, Durali; Soylak, Mustafa

    2009-09-30

    The potential use of the lichen biomass (Xanthoparmelia conspersa) to remove mercury(II) ions from aqueous solution by biosorption was evaluated using the batch method. Effects of pH, contact time, biomass concentration and temperature on the removal of Hg(II) ions were studied. The Langmuir isotherm models defined the equilibrium data precisely compared to Freundlich model and the maximum biosorption capacity obtained was 82.8 mg g(-1). From the D-R isotherm model, the mean free energy was calculated as 9.5 kJ mol(-1). It shows that the biosorption of Hg(II) ions onto X. conspersa biomass was taken place by chemical ion-exchange. Experimental data were also performed to the pseudo-first-order and pseudo-second-order kinetic models. The results indicated that the biosorption of Hg(II) on the lichen biomass followed well the second-order kinetics. Thermodynamic parameters, DeltaG(o), DeltaH(o) and DeltaS(o) indicated the Hg(II) sorption to be exothermic and spontaneous with decreased randomness at the solid-solution interface. Furthermore, the lichen biomass could be regenerated using 1M HCl, with up to 85% recovery, which allowed the reuse of the biomass in ten biosorption-desorption cycles without any considerable loss of biosorptive removal capacity.

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

    PubMed

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

    2016-06-15

    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.

  10. Sorption selectivity of birnessite particle edges: a d-PDF analysis of Cd(ii) and Pb(ii) sorption by δ-MnO2 and ferrihydrite.

    PubMed

    van Genuchten, Case M; Peña, Jasquelin

    2016-08-10

    Birnessite minerals (layer-type MnO2), which bear both internal (cation vacancies) and external (particle edges) metal sorption sites, are important sinks of contaminants in soils and sediments. Although the particle edges of birnessite minerals often dominate the total reactive surface area, especially in the case of nanoscale crystallites, the metal sorption reactivity of birnessite particle edges remains elusive. In this study, we investigated the sorption selectivity of birnessite particle edges by combining Cd(ii) and Pb(ii) adsorption isotherms at pH 5.5 with surface structural characterization by differential pair distribution function (d-PDF) analysis. We compared the sorption reactivity of δ-MnO2 to that of the nanomineral, 2-line ferrihydrite, which exhibits only external surface sites. Our results show that, whereas Cd(ii) and Pb(ii) both bind to birnessite layer vacancies, only Pb(ii) binds extensively to birnessite particle edges. For ferrihydrite, significant Pb(ii) adsorption to external sites was observed (roughly 20 mol%), whereas Cd(ii) sorption was negligible. These results are supported by bond valence calculations that show comparable degrees of saturation of oxygen atoms on birnessite and ferrihydrite particle edges. Therefore, we propose that the sorption selectivity of birnessite edges follows the same order of that reported previously for ferrihydrite: Ca(ii) < Cd(ii) < Ni(ii) < Zn(ii) < Cu(ii) < Pb(ii). PMID:27183472

  11. Comparison of raw and modified activated carbon and rice industry wastes for methylene blue sorption

    NASA Astrophysics Data System (ADS)

    Befani, Maria; Manariotis, Ioannis D.; Karapanagioti, Hrissi K.; Quintero, César E.

    2015-04-01

    In Argentina the average paddy rice production was 1.3x106 tn/year in the last decade. Entre Ríos province (E.R.) accounts for 60% of national milling, resulting in a significant accumulation of waste in the local environment; husk and ashes are used as fuel in drying grain plants. The use of rice wastes, as low-cost sorbents for the removal of synthetic dyes and other contaminants may be a sustainable option. The aim of this work is the investigation of the removal capacity of methylene blue (MB) from aqueous solutions using: (a) rice husk from a rice mill located in E.R. of size between 0.15 to 1.18 mm (RH2), (b) ash from rice husk burned at 800°C in oven for the grain drying unit of the rice mill (RHA800), and (c) biochar obtained from pyrolysis of RH2 material at 850°C (RHA4). Commercial activated carbon (AC), which is a porous material of high sorption capacity, was also used to compare its sorption capacity with the rice husk products. Furthermore, the incorporation of iron in the AC was studied using two different AC/Fe weight-by-weight ratios (AC-Fe and AC-0.5 Fe). The solution pH effect was studied in a range from 2 to 6.9. The maximal MB removal was achieved at pH of 6.8 to 6.9 for all materials studied, and at pH of 6.4 for AC. Kinetic experiments were conducted for a period of 48 h at pH 7 and C0 = 50 mg MB/L. Equilibrium was reached after 24 h and the adsorption capacity was 156, 104, 90, 79, 26, and 9 mg/g for AC, AC-Fe, AC-0.5 Fe, RHA4, RH2 and RHA800, respectively. The pseudo-second-order model expressed better the sorption kinetics of MB for all adsorbent materials. The AC-based materials presented better performance. The experimental data were fitted with the Freundlich and Langmuir isotherm models. The Langmuir model fits the data better in all cases. The maximum adsorption capacity was 238, 125, 92, 91, 46 and 9 mg/g for AC, AC-Fe, AC-0.5 Fe, RHA4, RH2 and RHA800, respectively. Agricultural wastes can be considered low-cost sorbents, but

  12. Equilibrium Shaping

    NASA Astrophysics Data System (ADS)

    Izzo, Dario; Petazzi, Lorenzo

    2006-08-01

    We present a satellite path planning technique able to make identical spacecraft aquire a given configuration. The technique exploits a behaviour-based approach to achieve an autonomous and distributed control over the relative geometry making use of limited sensorial information. A desired velocity is defined for each satellite as a sum of different contributions coming from generic high level behaviours: forcing the final desired configuration the behaviours are further defined by an inverse dynamic calculation dubbed Equilibrium Shaping. We show how considering only three different kind of behaviours it is possible to acquire a number of interesting formations and we set down the theoretical framework to find the entire set. We find that allowing a limited amount of communication the technique may be used also to form complex lattice structures. Several control feedbacks able to track the desired velocities are introduced and discussed. Our results suggest that sliding mode control is particularly appropriate in connection with the developed technique.

  13. Studies of anions sorption on natural zeolites.

    PubMed

    Barczyk, K; Mozgawa, W; Król, M

    2014-12-10

    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. Picloram and napropamide sorption as affected by polymer addition and salt concentration.

    PubMed

    Lu, Jianhang; Wu, Laosheng; Letey, John; Farmer, Walter J

    2002-01-01

    Polymer application to soil is a growing practice to improve soil physical properties and reduce soil erosion. Polymer addition can potentially influence herbicide and pesticide sorption in soil. The one-point distribution coefficient Kd values of two herbicides in the absence and presence of each of 10 polymers (7 polyacrylamides and 3 polysaccharides) were determined by the batch equilibrium method. The results showed that nonionic napropamide [2-(alpha-naphthoxy)-N,N-diethyl propionamide] sorption was essentially unaffected by the presence of any of the polymers. The influence of polymers on anionic picloram (4-amino-3,5,6-trichloropicolinic acid) sorption depends on the charge characteristics of polymers and salt concentrations in the solution. Electrostatic interaction and competition for sorption sites are two primary underlying mechanisms for the polymer influence. At low salt concentration, the increased picloram sorption in the presence of both cationic and anionic polymers was attributed to different electrostatic interactions and polymer partitioning between soil and solution phases. At high salt levels, the presence of polymers had either no influence or a slightly negative influence on the picloram sorption, which was attributed to competition for sorption sites. In field conditions, it is more likely that polymers have no or a slightly negative influence on herbicide sorption due to the presence of salts. PMID:12175041

  15. Catechol and humic acid sorption onto a range of laboratory-produced black carbons (biochars).

    PubMed

    Kasozi, Gabriel N; Zimmerman, Andrew R; Nkedi-Kizza, Peter; Gao, Bin

    2010-08-15

    Although the major influence of black carbon (BC) on soil and sediment organic contaminant sorption is widely accepted, an understanding of the mechanisms and natural variation in pyrogenic carbon interaction with natural organic matter (NOM) is lacking. The sorption of a phenolic NOM monomer (catechol) and humic acids (HA) onto BC was examined using biochars made from oak, pine, and grass at 250, 400, and 650 degrees C. Catechol sorption equilibrium occurred after 14 d and was described by a diffusion kinetic model, while HA required only 1 d and followed pseudo-second-order kinetics. Catechol sorption capacity increased with increasing biochar combustion temperature, from pine < oak < grass and from coarse < fine particle size. At lower catechol concentrations, sorption affinity (Freundlich constant, K(f)) was directly related to micropore surface area (measured via CO(2) sorptometry) indicating the predominance of specific adsorption. In contrast, HA exhibited an order of magnitude less sorption (0.1% versus 1%, by weight) due to its exclusion from micropores. Greater sorption of both catechol and HA occurred on biochars with nanopores, i.e. biochars made at higher temperatures. These findings suggest that addition of BC to soil, via natural fires or biochar amendments, will sequester abundant native OM through sorption. PMID:20669904

  16. Investigation of the carbon dioxide sorption capacity and structural deformation of coal

    SciTech Connect

    Hur, Tae-Bong; Fazio, James; Romanov, Vyacheslav; Harbert, William

    2010-01-01

    Due to increasing atmospheric CO2 concentrations causing the global energy and environmental crises, geological sequestration of carbon dioxide is now being actively considered as an attractive option to mitigate greenhouse gas emissions. One of the important strategies is to use deep unminable coal seams, for those generally contain significant quantities of coal bed methane that can be recovered by CO2 injection through enhanced coal bed natural gas production, as a method to safely store CO2. It has been well known that the adsorbing CO2 molecules introduce structural deformation, such as distortion, shrinkage, or swelling, of the adsorbent of coal organic matrix. The accurate investigations of CO2 sorption capacity as well as of adsorption behavior need to be performed under the conditions that coals deform. The U.S. Department of Energy-National Energy Technology Laboratory and Regional University Alliance are conducting carbon dioxide sorption isotherm experiments by using manometric analysis method for estimation of CO2 sorption capacity of various coal samples and are constructing a gravimetric apparatus which has a visual window cell. The gravimetric apparatus improves the accuracy of carbon dioxide sorption capacity and provides feasibility for the observation of structural deformation of coal sample while carbon dioxide molecules interact with coal organic matrix. The CO2 sorption isotherm measurements have been conducted for moist and dried samples of the Central Appalachian Basin (Russell County, VA) coal seam, received from the SECARB partnership, at the temperature of 55 C.

  17. Fate and Transport of Acrylamide in Soil and Groundwater Systems: Sorption, Retardation and Numerical Simulations

    NASA Astrophysics Data System (ADS)

    Arrowood, T.; Young, M.; Yu, Z.; Labahn, S.; Moser, D.

    2007-12-01

    Acrylamide (AMD) is a known animal and suspected human carcinogen and is used to produce polyacrylamide (PAM), which has been proposed as a technology for seepage control in unlined water delivery canals. The fate and transport of AMD in groundwater systems is not well known, and previous studies have not quantified the sorption coefficient (Kd), sorption isotherms, or estimated AMD breakthrough and transport parameters in soil and water systems. In this study, batch experiments and repacked soil column tests were conducted on three soils (a control sand, and field collected sand and loam soils) to determine the Kd, retardation factor and the form of the sorption isotherm. A numerical model (HYDRUS 2D) was used to simulate a canal environment using the fate and transport parameters of AMD obtained in the laboratory. Microbial degradation rates, obtained from a companion study (Labahn et al. 2007) were used in the model. Photodegradation rates for AMD were also considered. Results from batch studies indicate a Freundlich-type sorption isotherm for AMD in the loam soil. Sorption in the sands was not significant. The preliminary results for the soil column tests show that AMD is conservative in all three types of soil tested with retardation (R) values ranging from 0.985-1.072, with most column studies showing 0.99sorption obtained from the laboratory studies.

  18. Steady-state equation of water vapor sorption for CaCl2-based chemical sorbents and its application

    NASA Astrophysics Data System (ADS)

    Zhang, Haiquan; Yuan, Yanping; Sun, Qingrong; Cao, Xiaoling; Sun, Liangliang

    2016-09-01

    Green CaCl2-based chemical sorbent has been widely used in sorption refrigeration, air purification and air desiccation. Methods to improve the sorption rate have been extensively investigated, but the corresponding theoretical formulations have not been reported. In this paper, a sorption system of solid-liquid coexistence is established based on the hypothesis of steady-state sorption. The combination of theoretical analysis and experimental results indicates that the system can be described by steady-state sorption process. The steady-state sorption equation, μ = (η ‑ γT) , was obtained in consideration of humidity, temperature and the surface area. Based on engineering applications and this equation, two methods including an increase of specific surface area and adjustment of the critical relative humidity (γ) for chemical sorbents, have been proposed to increase the sorption rate. The results indicate that the CaCl2/CNTs composite with a large specific surface area can be obtained by coating CaCl2 powder on the surface of carbon nanotubes (CNTs). The composite reached sorption equilibrium within only 4 h, and the sorption capacity was improved by 75% compared with pure CaCl2 powder. Furthermore, the addition of NaCl powder to saturated CaCl2 solution could significantly lower the solution’s γ. The sorption rate was improved by 30% under the same environment.

  19. Steady-state equation of water vapor sorption for CaCl2-based chemical sorbents and its application

    PubMed Central

    Zhang, Haiquan; Yuan, Yanping; Sun, Qingrong; Cao, Xiaoling; Sun, Liangliang

    2016-01-01

    Green CaCl2-based chemical sorbent has been widely used in sorption refrigeration, air purification and air desiccation. Methods to improve the sorption rate have been extensively investigated, but the corresponding theoretical formulations have not been reported. In this paper, a sorption system of solid-liquid coexistence is established based on the hypothesis of steady-state sorption. The combination of theoretical analysis and experimental results indicates that the system can be described by steady-state sorption process. The steady-state sorption equation, μ = (η − γT) , was obtained in consideration of humidity, temperature and the surface area. Based on engineering applications and this equation, two methods including an increase of specific surface area and adjustment of the critical relative humidity (γ) for chemical sorbents, have been proposed to increase the sorption rate. The results indicate that the CaCl2/CNTs composite with a large specific surface area can be obtained by coating CaCl2 powder on the surface of carbon nanotubes (CNTs). The composite reached sorption equilibrium within only 4 h, and the sorption capacity was improved by 75% compared with pure CaCl2 powder. Furthermore, the addition of NaCl powder to saturated CaCl2 solution could significantly lower the solution’s γ. The sorption rate was improved by 30% under the same environment. PMID:27682811

  20. Sorption of organic gases in a furnished room

    SciTech Connect

    Singer, Brett C.; Revzan, Kenneth L.; Hotchi, Toshifumi; Hodgson, Alfred T.; Brown, Nancy J.

    2003-11-30

    We present experimental data and semi-empirical models describing the sorption of organic gases in a simulated indoor residential environment. Two replicate experiments were conducted with 20 volatile organic compounds (VOCs) in a 50-m{sup 3} room finished with painted wallboard, carpet and cushion, draperies and furnishings. The VOCs span a wide volatility range and include ten Hazardous Air Pollutants. VOCs were introduced to the static chamber as a pulse and their gas-phase concentrations were measured during a net adsorption period and a subsequent net desorption period. Three sorption models were fit to the measured concentrations for each compound to determine the simplest formulation needed to adequately describe the observed behavior. Sorption parameter values were determined by fitting the models to adsorption period data then checked by comparing measured and predicted behavior during desorption. The adequacy of each model was evaluated using a goodness of fit parameter calculated for each period. Results indicate that sorption usually does not greatly affect indoor concentrations of methyl-tert-butyl ether, 2-butanone, isoprene and benzene. In contrast, sorption appears to be a relevant indoor process for many of the VOCs studied, including C{sub 8}-C{sub 10} aromatic hydrocarbons (HC), terpenes, and pyridine. These compounds sorbed at rates close to typical residential air change rates and exhibited substantial sorptive partitioning at equilibrium. Polycyclic aromatic HCs, aromatic alcohols, ethenylpyridine and nicotine initially adsorbed to surfaces at rates of 1.5 to >6 h{sup -1} and partitioned 95 to >99% in the sorbed phase at equilibrium.

  1. Adsorption isotherm special study. Final report

    SciTech Connect

    1993-05-01

    The study was designed to identify methods to determine adsorption applicable to Uranium Mill Tailings Remedial Action (UMTRA) Project sites, and to determine how changes in aquifer conditions affect metal adsorption, resulting retardation factors, and estimated contaminant migration rates. EPA and ASTM procedures were used to estimate sediment sorption of U, As, and Mo under varying groundwater geochemical conditions. Aquifer matrix materials from three distinct locations at the DOE UMTRA Project site in Rifle, CO, were used as the adsorbents under different pH conditions; these conditions stimulated geochemical environments under the tailings, near the tailings, and downgradient from the tailings. Grain size, total surface area, bulk and clay mineralogy, and petrography of the sediments were characterized. U and Mo yielded linear isotherms, while As had nonlinear ones. U and Mo were adsorbed strongly on sediments acidified to levels similar to tailings leachate. Changes in pH had much less effect on As adsorption. Mo was adsorbed very little at pH 7-7.3, U was weakly sorbed, and As was moderately sorbed. Velocities were estimated for metal transport at different pHs. Results show that the aquifer materials must be characterized to estimate metal transport velocities in aquifers and to develop groundwater restoration strategies for the UMTRA project.

  2. Sorption enhanced CO2 methanation.

    PubMed

    Borgschulte, Andreas; Gallandat, Noris; Probst, Benjamin; Suter, Riccardo; Callini, Elsa; Ferri, Davide; Arroyo, Yadira; Erni, Rolf; Geerlings, Hans; Züttel, Andreas

    2013-06-28

    The transformation from the fatuous consumption of fossil energy towards a sustainable energy circle is most easily marketable by not changing the underlying energy carrier but generating it from renewable energy. Hydrocarbons can be principally produced from renewable hydrogen and carbon dioxide collected by biomass. However, research is needed to increase the energetic and economic efficiency of the process. We demonstrate the enhancement of CO2 methanation by sorption enhanced catalysis. The preparation and catalytic activity of sorption catalysts based on Ni particles in zeolites is reported. The functioning of the sorption catalysis is discussed together with the determination of the reaction mechanism, providing implications for new ways in catalysis. PMID:23673365

  3. SORPTION BEHAVIOR OF MONOSODIUM TITANATE AND AMORPHOUS PEROXOTITANATE MATERIALS UNDER WEAKLY ACIDIC CONDITIONS

    SciTech Connect

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

    2009-11-11

    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.

  4. Sorption of selected organic compounds from water to a peat soil and its humic-acid and humin fractions: Potential sources of the sorption nonlinearity

    USGS Publications Warehouse

    Chiou, C.T.; Kile, D.E.; Rutherford, D.W.; Sheng, G.; Boyd, S.A.

    2000-01-01

    The sorption isotherms of ethylene dibromide (EDB), diuron (DUN), and 3,5-dichlorophenol (DCP) from water on the humic acid and humin fractions of a peat soil and on the humic-acid of a muck soil have been measured. The data were compared with those of the solutes with the whole peat from which the humic-acid (HA) and humin (HM) fractions were derived and on which the sorption of the solutes exhibited varying extents of nonlinear capacities at low relative concentrations (C(e)/S(w)). The HA fraction as prepared by the density-fractionated method is relatively pure and presumably free of high- surface-area carbonaceous material (HSACM) that is considered to be responsible for the observed nonlinear sorption for nonpolar solutes (e.g., EDB) on the peat; conversely, the base-insoluble HM fraction as prepared is presumed to be enriched with HSACM, as manifested by the greatly higher BET- (N2) surface area than that of the whole peat. The sorption of EDB on HA exhibits no visible nonlinear effect, whereas the sorption on HM shows an enhanced nonlinearity over that on the whole peat. The sorption of polar DUN and DCP on HA and HM display nonlinear effects comparable with those on the whole peat; the effects are much more significant than those with nonpolar EDB. These results conform to the hypothesis that adsorption onto a small amount of strongly adsorbing HSACM is largely responsible for the nonlinear sorption of nonpolar solutes on soils and that additional specific interactions with the active groups of soil organic matter are responsible for the generally higher nonlinear sorption of the polar solutes.

  5. Results of a European interlaboratory comparison on CO2 sorption on activated carbon and coals

    NASA Astrophysics Data System (ADS)

    Gensterblum, Yves; Busch, Andreas; Krooss, Bernhard; de Weireld, Guy; Billemont, Pierre; van Hemert, Patrick; Wolf, Karl-Heinz

    2013-04-01

    For the assessment of CO2 storage in coal seams or enhanced coalbed methane production (ECBM), the sorption properties of natural coals are important parameters. Since more and more laboratories worldwide are concerned with measurements of gas sorption on coal it is indispensable to establish quality standards for such experiments. The first two interlaboratory studies on CO2 sorption on coal (Goodman et al. 2004, 2007) revealed a poor agreement of sorption isotherms among the participating laboratories, particularly in the high-pressure range. During the MOVECBM (http://www.movecbm.eu/) project funded by the European Commission (6th framework), an interlaboratory comparison of CO2 sorption on selected coals and activated carbon was initiated. Measurements were performed on dry samples at 45° C using the manometric and the gravimetric method. up to a final pressure of 15 MPa. The first set of high-pressure sorption measurements was performed on a Filtrasorb 400 activated carbon sample in order to minimise heterogeneity effects and to optimize the experimental procedures for the individual (manometric or gravimetric) methods (Gensterblum et al. 2009). Since comparability for the activated carbon was excellent, the measurements were continued using natural coals of various rank (anthracite, bituminous coal and lignite) to study the influence of heterogeneities and varying starting conditions on the CO2 sorption properties (Gensterblum et al. 2010). Compared to the poor reproducibility observed in previous interlaboratory studies (Goodman et al., 2004, 2007) this European study showed excellent agreement (<5 % deviation) among the participating laboratories with good repeatability. The sorption data and technical information on the different experimental setups have been used to investigate errors and potential pitfalls in the assessment of high-pressure CO2 sorption isotherms. References Gensterblum Y., P. van Hemert, P. Billemont, A. Busch, B.M. Krooss, G. de

  6. Strong sorption of PCBs to nanoplastics, microplastics, carbon nanotubes, and fullerenes.

    PubMed

    Velzeboer, I; Kwadijk, C J A F; Koelmans, A A

    2014-05-01

    The presence of microplastic and carbon-based nanoparticles in the environment may have implications for the fate and effects of traditional hydrophobic chemicals. Here we present parameters for the sorption of 17 CB congeners to 10-180 μm sized polyethylene (micro-PE), 70 nm polystyrene (nano-PS), multiwalled carbon nanotubes (MWCNT), fullerene (C60), and a natural sediment in the environmentally relevant 10(-5)-10(-1) μg L(-1) concentration range. Effects of salinity and sediment organic matter fouling were assessed by measuring the isotherms in fresh- and seawater, with and without sediment present. Sorption to the "bulk" sorbents sediment organic matter (OM) and micro-PE occurred through linear hydrophobic partitioning with OM and micro-PE having similar sorption affinity. Sorption to MWCNT and nano-PS was nonlinear. PCB sorption to MWCNT and C60 was 3-4 orders of magnitude stronger than to OM and micro-PE. Sorption to nano-PS was 1-2 orders of magnitude stronger than to micro-PE, which was attributed to the higher aromaticity and surface-volume ratio of nano-PS. Organic matter effects varied among sorbents, with the largest OM fouling effect observed for the high surface sorbents MWCNT and nano-PS. Salinity decreased sorption for sediment and MWCNT but increased sorption for the polymers nano-PS and micro-PE. The exceptionally strong sorption of (planar) PCBs to C60, MWCNT, and nano-PS may imply increased hazards upon membrane transfer of these particles.

  7. Sorption and degradation of selected pharmaceuticals in representative soils of the Czech Republic

    NASA Astrophysics Data System (ADS)

    Kodesova, Radka; Kocarek, Martin; Klement, Ales; Golovko, Oksana; Grabic, Roman; Fer, Miroslav; Nikodem, Antonin; Jaksik, Ondrej

    2015-04-01

    Knowledge of contaminant behavior (e.g. its sorption onto soil particle, degradation etc.) is essential when assessing contaminant migration in soil and groundwater environment. This study was focused on evaluating sorption isotherms and half-lives for 7 pharmaceuticals (clarithromycin, trimethoprim, metoprolol, atenolol, clindamycin, carbamazepine, sulfamethoxazole) on 13 soils of different soil properties. Sorption of ionizable compounds was 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. Sorption coefficients for the remaining pharmaceuticals (trimethoprim, metoprolol, atenolol, and carbamazepine) were also positively correlated with the base cation saturation and cation exchange capacity. Degradation rates in some degree reflected sorption of studied pharmaceuticals on soil particles and increased with decreasing sorption. The highest mobility in studied soils was observed for sulfamethoxazole, but this pharmaceutical was relatively quickly degraded. The second highest mobility was found for carbamazepine, which mostly did not noticeably degrade during our experiments. Thus this pharmaceutical has the highest potential to migrate in water environment. The lowest mobility was observed for clarithromycin. However, this pharmaceutical due to its stability may be retained in an environment for a long time. Acknowledgement: The authors acknowledge the financial support of the Czech Science Foundation (Project No. 13-12477S, Transport of pharmaceuticals in soils). References: Kodesova, R., Grabic, R., Kocarek, M., Klement, A., Golovko, O., Fer, M., Nikodem, A., Jaksik, O., Pharmaceuticals' sorptions relative to

  8. Phosphorus sorption capacities and physicochemical properties of nine substrate materials for constructed wetland

    SciTech Connect

    Cui, L.H.; Zhu, X.Z.; Ma, M.; Ouyang, Y.; Dong, M.; Zhu, W.L.; Luo, S.M.

    2008-08-15

    Constructed wetland (CW) is a promising technique for removal of pollutants from wastewater and agricultural runoff. The performance of a CW to remove pollutants, however, hinges on the use of suitable substrate materials. This study examined the physicochemical properties and phosphorus (P) sorption capacities of nine different CW substrate materials using both batch experiments and the Freundlich as well as the Langmuir isotherm. The nine substrate materials used in this study were turf, topsoil, gravel, midsized sand (MSS), blast furnace slag (BFS), coal burn slag (CBS), blast furnace artificial slag (BFAS), coal burn artificial slag (CBAS), and midsized artificial sand (MSAS). Experimental data showed that sorption of P increased with initial solution P concentrations for all nine substrate materials. The maximum P sorption capacity of the substrate materials estimated by Langmuir isotherm was in the following order: turf (4243 mg/kg substrate) > BFAS (2116 mg/kg substrate) > BFS (1598 mg/kg substrate) > CBS (1449 mg/kg substrate) > top soil (1396 mg/kg substrate) > CBAS (1194 mg/kg substrate) > MSAS (519 mg/kg substrate) > gravel (494 mg/kg substrate) > MSS (403 mg/kg substrate). The specific gravity of eight substrate materials (except gravel) had very significant negative correlations with the P sorption, whereas the particle diameter of D-60 and uniformity coefficient (K-60) had positive correlations with the P sorption. The cation exchange capacity, organic matter, available ferrous, and exchangeable aluminum of the eight substrate materials also had very significant positive correlations with the P sorption, while the pH of the substrate materials showed a very significant negative correlation with the P sorption. Our study further suggests that turf and CBAS are the two relatively ideal substrate materials suitable for removal of P from a CW system.

  9. Phosphorus sorption capacities and physicochemical properties of nine substrate materials for constructed wetland.

    PubMed

    Cui, Lihua; Zhu, Xizhen; Ma, Mei; Ouyang, Ying; Dong, Mei; Zhu, Wenling; Luo, Shiming

    2008-08-01

    Constructed wetland (CW) is a promising technique for removal of pollutants from wastewater and agricultural runoff. The performance of a CW to remove pollutants, however, hinges on the use of suitable substrate materials. This study examined the physicochemical properties and phosphorus (P) sorption capacities of nine different CW substrate materials using both batch experiments and the Freundlich as well as the Langmuir isotherm. The nine substrate materials used in this study were turf, topsoil, gravel, midsized sand (MSS), blast furnace slag (BFS), coal burn slag (CBS), blast furnace artificial slag (BFAS), coal burn artificial slag (CBAS), and midsized artificial sand (MSAS). Experimental data showed that sorption of P increased with initial solution P concentrations for all nine substrate materials. The maximum P sorption capacity of the substrate materials estimated by Langmuir isotherm was in the following order: turf (4243 mg/kg substrate) > BFAS (2116 mg/kg substrate) > BFS (1598 mg/kg substrate) > CBS (1449 mg/kg substrate) > top soil (1396 mg/kg substrate) > CBAS (1194 mg/kg substrate) > MSAS (519 mg/kg substrate) > gravel (494 mg/kg substrate) > MSS (403 mg/kg substrate). The specific gravity of eight substrate materials (except gravel) had very significant negative correlations with the P sorption, whereas the particle diameter of D(60) and uniformity coefficient (K(60)) had positive correlations with the P sorption. The cation exchange capacity, organic matter, available ferrous, and exchangeable aluminum of the eight substrate materials also had very significant positive correlations with the P sorption, while the pH of the substrate materials showed a very significant negative correlation with the P sorption. Our study further suggests that turf and CBAS are the two relatively ideal substrate materials suitable for removal of P from a CW system.

  10. The Langmuir isotherm: a commonly applied but misleading approach for the analysis of protein adsorption behavior.

    PubMed

    Latour, Robert A

    2015-03-01

    The Langmuir adsorption isotherm provides one of the simplest and most direct methods to quantify an adsorption process. Because isotherm data from protein adsorption studies often appear to be fit well by the Langmuir isotherm model, estimates of protein binding affinity have often been made from its use despite that fact that none of the conditions required for a Langmuir adsorption process may be satisfied for this type of application. The physical events that cause protein adsorption isotherms to often provide a Langmuir-shaped isotherm can be explained as being due to changes in adsorption-induced spreading, reorientation, clustering, and aggregation of the protein on a surface as a function of solution concentration in contrast to being due to a dynamic equilibrium adsorption process, which is required for Langmuir adsorption. Unless the requirements of the Langmuir adsorption process can be confirmed, fitting of the Langmuir model to protein adsorption isotherm data to obtain thermodynamic properties, such as the equilibrium constant for adsorption and adsorption free energy, may provide erroneous values that have little to do with the actual protein adsorption process, and should be avoided. In this article, a detailed analysis of the Langmuir isotherm model is presented along with a quantitative analysis of the level of error that can arise in derived parameters when the Langmuir isotherm is inappropriately applied to characterize a protein adsorption process.

  11. Silica Precipitation and Lithium Sorption

    SciTech Connect

    Jay Renew

    2015-09-20

    This file contains silica precipitation and lithium sorption data from the project. The silica removal data is corrected from the previous submission. The previous submission did not take into account the limit of detection of the ICP-MS procedure.

  12. Binding Isotherms and Time Courses Readily from Magnetic Resonance

    PubMed Central

    2016-01-01

    Evidence is presented that binding isotherms, simple or biphasic, can be extracted directly from noninterpreted, complex 2D NMR spectra using principal component analysis (PCA) to reveal the largest trend(s) across the series. This approach renders peak picking unnecessary for tracking population changes. In 1:1 binding, the first principal component captures the binding isotherm from NMR-detected titrations in fast, slow, and even intermediate and mixed exchange regimes, as illustrated for phospholigand associations with proteins. Although the sigmoidal shifts and line broadening of intermediate exchange distorts binding isotherms constructed conventionally, applying PCA directly to these spectra along with Pareto scaling overcomes the distortion. Applying PCA to time-domain NMR data also yields binding isotherms from titrations in fast or slow exchange. The algorithm readily extracts from magnetic resonance imaging movie time courses such as breathing and heart rate in chest imaging. Similarly, two-step binding processes detected by NMR are easily captured by principal components 1 and 2. PCA obviates the customary focus on specific peaks or regions of images. Applying it directly to a series of complex data will easily delineate binding isotherms, equilibrium shifts, and time courses of reactions or fluctuations. PMID:27458657

  13. Binding Isotherms and Time Courses Readily from Magnetic Resonance.

    PubMed

    Xu, Jia; Van Doren, Steven R

    2016-08-16

    Evidence is presented that binding isotherms, simple or biphasic, can be extracted directly from noninterpreted, complex 2D NMR spectra using principal component analysis (PCA) to reveal the largest trend(s) across the series. This approach renders peak picking unnecessary for tracking population changes. In 1:1 binding, the first principal component captures the binding isotherm from NMR-detected titrations in fast, slow, and even intermediate and mixed exchange regimes, as illustrated for phospholigand associations with proteins. Although the sigmoidal shifts and line broadening of intermediate exchange distorts binding isotherms constructed conventionally, applying PCA directly to these spectra along with Pareto scaling overcomes the distortion. Applying PCA to time-domain NMR data also yields binding isotherms from titrations in fast or slow exchange. The algorithm readily extracts from magnetic resonance imaging movie time courses such as breathing and heart rate in chest imaging. Similarly, two-step binding processes detected by NMR are easily captured by principal components 1 and 2. PCA obviates the customary focus on specific peaks or regions of images. Applying it directly to a series of complex data will easily delineate binding isotherms, equilibrium shifts, and time courses of reactions or fluctuations. PMID:27458657

  14. Sorption of organic cations to phyllosilicate clay minerals: CEC-normalization, salt dependency, and the role of electrostatic and hydrophobic effects.

    PubMed

    Droge, Steven T J; Goss, Kai-Uwe

    2013-12-17

    Sorption to the phyllosilicate clay minerals Illite, kaolinite, and bentonite has been studied for a wide variety of organic cations using a flow-through method with fully aqueous medium as the eluent. Linear isotherms were observed at concentrations below 10% of the cation-exchange capacity (CEC) for Illite and kaolinite and below 1 mmol/kg (<1% CEC) for bentonite. Sorption to clays was strongly influenced by the electrolyte composition of the eluent but with a consistent trend for a diverse set of compounds on all clays, thus allowing for empirical correction factors. When sorption affinities for a given compound to a given clay are normalized to the CEC of the clay, the differences in sorption affinities between clays are reduced to less than 0.5 log units for most compounds. Although CEC-normalized sorption of quaternary ammonium compounds to clay was up to 10-fold higher than CEC-normalized sorption to soil organic matter, CEC-normalized sorption for most compounds was comparable between clays and soil organic matter. The clay fraction is thus a potentially relevant sorption phase for organic cations in many soils. The sorption data for organic cations to clay showed several regular trends with molecular structure but also showed quite a few systematic effects that we cannot explain. A model on the basis of the molecular size and charge density at the ionized nitrogen is used here as a tool to obtain benchmark values that elucidate the effect of specific polar moieties on the sorption affinity.

  15. Effect of electrochemical oxidation of activated carbon fiber on competitive and noncompetitive sorption of trace toxic metal ions from aqueous solution.

    PubMed

    Harry, I D; Saha, B; Cumming, I W

    2006-12-01

    A viscose-rayon-based activated carbon cloth (ACC) was electrochemically oxidized to enhance its cation sorption capacity for comparison with as-received ACC. The ACCs were characterized by sodium capacity measurement, pH titration, zeta potential measurement, elemental analysis, Brunauer-Emmet-Teller surface area, and pore size distribution. Batch sorption experiments showed that electrochemically oxidized ACC (EO) is more effective for the removal of lead and copper ions compared to unoxidized ACC (UO) for both competitive and noncompetitive sorption. For electrochemically oxidized fibers the copper and lead sorption capacities of ACC increased 17 and 4 times, respectively, for noncompetitive sorption and 8.8 and 8.6 times, respectively, for competitive sorption. However, reduction in the sorption capacities for both metals was observed for the competitive sorption. The sorption of lead and copper onto EO was by ion exchange, while that onto UO was likely to be due to surface complex formation. The affinity order of the two metal ions sorbed by UO and EO is Pb(2+)>Cu(2+). The effect of pH on sorption isotherms indicated that metal uptake increased with an increase in solution pH.

  16. Ground rubber: Sorption media for ground water containing benzene and O-xylene

    SciTech Connect

    Kershaw, D.S.; Pamukcu, S.; Kulik, B.C.

    1997-04-01

    The purpose of the current study is to examine the ability of ground rubber to sorb benzene and O-xylene from water contained with aromatic hydrocarbons. The study consisted of running both batch and packed bed column tests to determine the sorption capacity, the required sorption equilibration time, and the flow through utilization efficiency of ground rubber under various contact times when exposed to water contaminated with various amounts of benzene or O-xylene. Initial batch test results indicate that ground rubber can attain equilibrium sorption capacities up to 1.3 or 8.2 mg of benzene or O-xylene, respectively, per gram of tire rubber at solution equilibrium concentrations of 10 mg/L. Packed bed column tests indicate that ground tire rubber has on the average a 40% utilization rate when a hydraulic residence time of 15 min is used. Possible future uses of round rubber as a sorption media could include, but are not limited to, the use of ground rubber as an aggregate in slurry cutoff walls that are in contact with petroleum products. Ground rubber could also be used as a sorption media in pump-and-treat methodologies or as a sorption media in in-situ reactive permeable barriers.

  17. Kinetics of selenate sorption in soil as influenced by biotic and abiotic conditions: a stirred flow-through reactor study.

    PubMed

    Garcia-Sanchez, L; Loffredo, N; Mounier, S; Martin-Garin, A; Coppin, F

    2014-12-01

    This study (i) quantified the kinetics of selenate sorption and (ii) measured the influence of biotic processes in soil selenate stabilisation. Stirred flow-through reactor experiments were conducted on samples of a silty clay soil (pH = 8, Eh = 240-300 mV) from Bure (France) in both non-sterile and sterile conditions. Parameters of the proposed two-site sorption model (EK), adapted from van Genuchten and Wagenet (1989), were estimated by nonlinear regression. Fast selenate sorption on type-1 sites was moderate, with an equilibrium constant of 25.5 and 39.1 L/kg for non-sterile and sterile conditions. Rate-limited sorption on type-2 sites increased with time, and was predominant for longer periods of time in non-sterile conditions. At equilibrium, it would represent over 96% of the sorbed inventory, with mean sorption times of 17 h and 191 h for non-sterile and sterile conditions. Our results showed for Bure soil that (i) selenate sorption in flowing and mildly-oxidising conditions was strongly kinetically controlled, especially in non-sterile conditions, (ii) selenate desorption was much slower than sorption, which suggests its pseudo-irreversible stabilisation, and (iii) microbial activity increased the contribution of rate-limited sorption on type-2 sites, for which it increased sorption rate by a factor 7 but also facilitated its reversibility. This work stresses the limits of the Kd approach to represent selenate sorption in flowing conditions and supports an alternative formulation like the EK model, but also points out that biotic conditions are significant sources of variability for sorption parameters. PMID:25151638

  18. Kinetics of selenate sorption in soil as influenced by biotic and abiotic conditions: a stirred flow-through reactor study.

    PubMed

    Garcia-Sanchez, L; Loffredo, N; Mounier, S; Martin-Garin, A; Coppin, F

    2014-12-01

    This study (i) quantified the kinetics of selenate sorption and (ii) measured the influence of biotic processes in soil selenate stabilisation. Stirred flow-through reactor experiments were conducted on samples of a silty clay soil (pH = 8, Eh = 240-300 mV) from Bure (France) in both non-sterile and sterile conditions. Parameters of the proposed two-site sorption model (EK), adapted from van Genuchten and Wagenet (1989), were estimated by nonlinear regression. Fast selenate sorption on type-1 sites was moderate, with an equilibrium constant of 25.5 and 39.1 L/kg for non-sterile and sterile conditions. Rate-limited sorption on type-2 sites increased with time, and was predominant for longer periods of time in non-sterile conditions. At equilibrium, it would represent over 96% of the sorbed inventory, with mean sorption times of 17 h and 191 h for non-sterile and sterile conditions. Our results showed for Bure soil that (i) selenate sorption in flowing and mildly-oxidising conditions was strongly kinetically controlled, especially in non-sterile conditions, (ii) selenate desorption was much slower than sorption, which suggests its pseudo-irreversible stabilisation, and (iii) microbial activity increased the contribution of rate-limited sorption on type-2 sites, for which it increased sorption rate by a factor 7 but also facilitated its reversibility. This work stresses the limits of the Kd approach to represent selenate sorption in flowing conditions and supports an alternative formulation like the EK model, but also points out that biotic conditions are significant sources of variability for sorption parameters.

  19. Kinetics of neptunium(V) sorption and desorption on goethite: An experimental and modeling study

    NASA Astrophysics Data System (ADS)

    Tinnacher, Ruth M.; Zavarin, Mavrik; Powell, Brian A.; Kersting, Annie B.

    2011-11-01

    Various sorption phenomena, such as aging, hysteresis and irreversible sorption, can cause differences between contaminant (ad)sorption and desorption behavior and lead to apparent sorption 'asymmetry'. We evaluate the relevance of these characteristics for neptunium(V) (Np(V)) sorption/desorption on goethite using a 34-day flow-cell experiment and kinetic modeling. Based on experimental results, the Np(V) desorption rate is much slower than the (ad)sorption rate, and appears to decrease over the course of the experiment. The best model fit with a minimum number of fitting parameters was achieved with a multi-reaction model including (1) an equilibrium Freundlich site (site 1), (2) a kinetically-controlled, consecutive, first-order site (site 2), and (3) a parameter ψ, which characterizes the desorption rate on site 2 based on a concept related to transition state theory (TST). This approach allows us to link differences in adsorption and desorption kinetics to changes in overall reaction pathways, without assuming different adsorption and desorption affinities (hysteresis) or irreversible sorption behavior a priori. Using modeling as a heuristic tool, we determined that aging processes are relevant. However, hysteresis and irreversible sorption behavior can be neglected within the time-frame (desorption over 32 days) and chemical solution conditions evaluated in the flow-cell experiment. In this system, desorption reactions are very slow, but they are not irreversible. Hence, our data do not justify an assumption of irreversible Np(V) sorption to goethite in transport models, which effectively limits the relevance of colloid-facilitated Np(V) transport to near-field environments. However, slow Np(V) desorption behavior may also lead to a continuous contaminant source term when metals are sorbed to bulk mineral phases. Additional long-term experiments are recommended to definitely rule out irreversible Np(V) sorption behavior at very low surface loadings and

  20. Effects of oil dispersant and oil on sorption and desorption of phenanthrene with Gulf Coast marine sediments.

    PubMed

    Gong, Yanyan; Zhao, Xiao; O'Reilly, S E; Qian, Tianwei; Zhao, Dongye

    2014-02-01

    Effects of a model oil dispersant (Corexit EC9500A) on sorption/desorption of phenanthrene were investigated with two marine sediments. Kinetic data revealed that the presence of the dispersant at 18 mg/L enhanced phenanthrene uptake by up to 7%, whereas the same dispersant during desorption reduced phenanthrene desorption by up to 5%. Sorption isotherms confirmed that at dispersant concentrations of 18 and 180 mg/L, phenanthrene uptake progressively increased for both sediments. Furthermore, the presence of the dispersant during desorption induced remarkable sorption hysteresis. The effects were attributed to added phenanthrene affinity and capacity due to sorption of the dispersant on the sediments. Dual-mode models adequately simulated sorption isotherms and kinetic data in the presence of the dispersant. Water accommodated oil (WAO) and dispersant-enhanced WAO increased phenanthrene sorption by up to 22%. This information is important for understanding roles of oil dispersants on the distribution and transport of petroleum PAHs in seawater-sediments. PMID:24291613

  1. Sorption of cadmium and lead by clays from municipal incinerator ash- water suspensions

    USGS Publications Warehouse

    Roy, W.R.; Krapac, I.G.; Steele, J.D.

    1993-01-01

    The effect of Cl complexation in extracts of a flue gas-scrubber incinerator fly ash sample on the sorption of Cd and Pb by kaolinite and illite was investigated using batch-sorption methods. In the pH range of 5 to 9, Cl complexation may reduce sorption and thus increase the mobility of these metals. When an ash-water suspension was acidified to pH 6.85, the dissolution of Cl and Ca essentially eliminated Cd sorption because of complexation and cationic competition. Cadmium would be considered as either mobile or very mobile under these conditions. Lead was not soluble in the pH- 6.85 suspension. At pH 12, the approximate pH of water in contact with flue gas-scrubber fly ash, Cd was essentially insoluble and Pb occurred as anionic Pb hydroxide. Anionic Pb was sorbed by the two clays, and the extent of sorption was not influenced by Cl or carbonate complexation. Sorption constants, derived from isotherms, suggested that Pb would be relatively immobile in saturated soil-water systems. The recent concern that highly alkaline, flue gas-scrubber fly ash may release environmentally significant concentrations of mobile Pb when placed in an ash-disposal site with a soil liner should be reevaluated in light of this study.

  2. Uranium sorption onto natural sands as a function of sediment characteristics and solution pH

    SciTech Connect

    Rosentreter, J.J.; Quarder, S.H.; Smith, R.W.; McLing, T.

    1996-10-01

    Uranium sorption studies were conducted on twenty-five sandy sediments obtained from Virginia`s Easter Shore Peninsula using batch contact methods. Distribution coefficient (Kd) and sorption isotherms have been determined as function of solution pH. All sediment samples strongly sorbed dissolved uranium species at pH values above 5. Sediments characterized by high iron, aluminum, and surface area, possessed the highest sorption characteristics. Both, Freundlich and Dubinin Radushkevich equations were able to describe the sorption behavior. From the Dubinin-Radushkevich equation, the solution-component-solid surface bounding energy and the sorption capacities, were estimated. Least square regression utilizing sediment characteristics provided an effective statistical method for Kd prediction. Predictions with relative errors of about 30% were obtained using only two sediment variables, such as, iron or aluminum content and surface area. In conclusion, the results support that ion exchange and surface complexation reactions with the ferric and aluminum oxide/oxyhydroxides groups are the predominant sorption mechanisms.

  3. Sorption characteristics of N-nitrosodimethylamine onto biochar from aqueous solution.

    PubMed

    Chen, Cuiping; Zhou, Wenjun; Lin, Daohui

    2015-03-01

    N-nitrosodimethylamine (NDMA) is an emerging carcinogenic disinfection by-product in water environment. Biochars utilized as sorbents for the removal of NDMA from aqueous solution, and the sorption characteristics and mechanism were investigate. Biochars were prepared from bamboo, rice straw and wood sawdust at 300-700°C. The pseudo-second-order model provided the best fit for the sorption kinetics of NDMA onto biochar and the sorption isotherms were described best with the Slips model. Biochar produced at 500°C removed NDMA from aqueous solution relatively efficiently, and the bamboo char demonstrated the best sorption potential among the three types of biochars. Solution chemistry such as pH and metal ions did not show obvious effect on NDMA removal. Three sorption mechanisms are suggested for NDMA sorption onto biochars, H-bond attraction between -N=O and the O-containing moieties, hydrophobic force between -CH3 and the ordered graphitic structure, and partition process of NDMA into the non-carbonization part of biochar. PMID:25553566

  4. Influence of molecular structure and adsorbent properties on sorption of organic compounds to a temperature series of wood chars.

    PubMed

    Lattao, Charisma; Cao, Xiaoyan; Mao, Jingdong; Schmidt-Rohr, Klaus; Pignatello, Joseph J

    2014-05-01

    Chars from wildfires and soil amendments (biochars) are strong adsorbents that can impact the fate of organic compounds in soil, yet the effects of solute and adsorbent properties on sorption are poorly understood. We studied sorption of benzene, naphthalene, and 1,4-dinitrobenzene from water to a series of wood chars made anaerobically at different heat treatment temperatures (HTT) from 300 to 700 °C, and to graphite as a nonporous, unfunctionalized reference adsorbent. Peak suppression in the NMR spectrum by sorption of the paramagnetic relaxation probe TEMPO indicated that only a small fraction of char C atoms lie near sorption sites. Sorption intensity for all solutes maximized with the 500 °C char, but failed to trend regularly with N2 or CO2 surface area, micropore volume, mesopore volume, H/C ratio, O/C ratio, aromatic fused ring size, or HTT. A model relating sorption intensity to a weighted sum of microporosity and mesoporosity was more successful. Sorption isotherm linearity declined progressively with carbonization of the char. Application of a thermodynamic model incorporating solvent-water and char-graphite partition coefficients permitted for the first time quantification of steric (size exclusion in pores) and π-π electron donor-acceptor (EDA) free energy contributions, relative to benzene. Steric hindrance for naphthalene increases exponentially from 9 to 16 kJ/mol (∼ 1.6-2.9 log units of sorption coefficient) with the fraction of porosity in small micropores. π-π EDA interactions of dinitrobenzene contribute -17 to -19 kJ/mol (3-3.4 log units of sorption coefficient) to sorption on graphite, but less on chars. π-π EDA interaction of naphthalene on graphite is small (-2 to 2 kJ/mol). The results show that sorption is a complex function of char properties and solute molecular structure, and not very predictable on the basis of readily determined char properties.

  5. Influence of molecular structure and adsorbent properties on sorption of organic compounds to a temperature series of wood chars.

    PubMed

    Lattao, Charisma; Cao, Xiaoyan; Mao, Jingdong; Schmidt-Rohr, Klaus; Pignatello, Joseph J

    2014-05-01

    Chars from wildfires and soil amendments (biochars) are strong adsorbents that can impact the fate of organic compounds in soil, yet the effects of solute and adsorbent properties on sorption are poorly understood. We studied sorption of benzene, naphthalene, and 1,4-dinitrobenzene from water to a series of wood chars made anaerobically at different heat treatment temperatures (HTT) from 300 to 700 °C, and to graphite as a nonporous, unfunctionalized reference adsorbent. Peak suppression in the NMR spectrum by sorption of the paramagnetic relaxation probe TEMPO indicated that only a small fraction of char C atoms lie near sorption sites. Sorption intensity for all solutes maximized with the 500 °C char, but failed to trend regularly with N2 or CO2 surface area, micropore volume, mesopore volume, H/C ratio, O/C ratio, aromatic fused ring size, or HTT. A model relating sorption intensity to a weighted sum of microporosity and mesoporosity was more successful. Sorption isotherm linearity declined progressively with carbonization of the char. Application of a thermodynamic model incorporating solvent-water and char-graphite partition coefficients permitted for the first time quantification of steric (size exclusion in pores) and π-π electron donor-acceptor (EDA) free energy contributions, relative to benzene. Steric hindrance for naphthalene increases exponentially from 9 to 16 kJ/mol (∼ 1.6-2.9 log units of sorption coefficient) with the fraction of porosity in small micropores. π-π EDA interactions of dinitrobenzene contribute -17 to -19 kJ/mol (3-3.4 log units of sorption coefficient) to sorption on graphite, but less on chars. π-π EDA interaction of naphthalene on graphite is small (-2 to 2 kJ/mol). The results show that sorption is a complex function of char properties and solute molecular structure, and not very predictable on the basis of readily determined char properties. PMID:24758543

  6. Using QSAR to evaluate phenomenological models for sorption of organic compounds by soil

    SciTech Connect

    Brusseau, M.L. . Soil and Water Science Dept. and Hydrology and Water Resources Dept.)

    1993-10-01

    The functional dependencies of equilibrium and nonequilibrium sorption parameters on solute molecular descriptors were analyzed for 29 organic compounds and two soils. Similar correlation patterns were obtained with all three evaluated size/shape descriptors (molecular surface area, van der Waals volume, molecular connectivity). The functional dependencies of equilibrium distribution of coefficients on the solute molecular descriptors were analyzed for three systems used as phenomenological models of sorption by soil. The correlation patterns exhibited by the three models were compared to those reported for the soil systems. The correlation patterns exhibited by the soil data were similar to the patterns exhibited by the polymer systems and dissimilar to those exhibited by the octanol and RPLC systems. In addition, the correlation pattern between the sorption rate coefficient and molecular connectivity was similar to that between polymer-diffusion coefficients and molecular connectivity. Hence, it appears that the polymer analog may be the most appropriate of the three models for representing both equilibrium and nonequilibrium sorption by soil. Based on these results, the polymer analog is suggested as the phenomenological model of choice for investigating and evaluating the sorption dynamics of low-polarity organic compounds in soil systems.

  7. Effect of the adsorbate (Bromacil) equilibrium concentration in water on its adsorption on powdered activated carbon. Part 2: Kinetic parameters.

    PubMed

    Al Mardini, Fadi; Legube, Bernard

    2009-10-30

    The application of several monosolute equilibrium models has previously shown that Bromacil adsorption on SA-UF (Norit) powdered activated carbon (PAC) is probably effective on two types of sites. High reactivity sites were found to be 10-20 less present in a carbon surface than lower reactivity sites, according to the q(m) values calculated by isotherm models. The aims of this work were trying, primarily, to identify the kinetic-determinant stage of the sorption of Bromacil at a wide range of initial pesticide concentrations (approximately 5 to approximately 500 microg L(-1) at pH 7.8), and secondly, to specify the rate constants and other useful design parameters for the application in water treatment. It was therefore not possible to specify a priori whether the diffusion or surface reaction is the key step. It shows that many of the tested models which describe the stage of distribution or the surface reaction are correctly applied. However, the diffusivity values (D and D(0)) were found to be constant only constants for some specific experimental concentrations. The HSDM model of surface diffusion in pores was also applied but the values of the diffusion coefficient of surface (D(s)) were widely scattered and reduce significantly with the initial concentration or the equilibrium concentration in Bromacil. The model of surface reaction of pseudo-second order fitted particularly well and led to constant values which are independent of the equilibrium concentration, except for the low concentrations where the constants become significantly more important. This last observation confirms perfectly the hypothesis based on two types of sites as concluded by the equilibrium data (part 1).

  8. Sorption behavior of U(VI) on phyllite: experiments and modeling.

    PubMed

    Arnold, T; Zorn, T; Zänker, H; Bernhard, G; Nitsche, H

    2001-02-01

    The sorption of U(VI) onto low-grade metamorphic rock phyllite was modeled with the diffuse double layer model (DDLM) using the primary mineralogical constituents of phyllite, i.e. quartz, chlorite, muscovite, and albite, as input components, and as additional component, the poorly ordered Fe oxide hydroxide mineral, ferrihydrite. Ferrihydrite forms during the batch sorption experiment as a weathering product of chlorite. In this process, Fe(II), leached from the chlorite, oxidizes to Fe(III), hydrolyses and precipitates as ferrihydrite. The formation of ferrihydrite during the batch sorption experiment was identified by Mössbauer spectroscopy, showing a 2.8% increase of Fe(III) in the phyllite powder. The ferrihydrite was present as Fe nanoparticles or agglomerates with diameters ranging from 6 to 25 nm, with indications for even smaller particles. These Fe colloids were detected in centrifugation experiments of a ground phyllite suspension using various centrifugal forces. The basis for the successful interpretation of the experimental sorption data of uranyl(VI) on phyllite were: (1) the determination of surface complex formation constants of uranyl with quartz, chlorite, muscovite, albite, and ferrihydrite in individual batch sorption experiments, (2) the determination of surface acidity constants of quartz, chlorite, muscovite, and albite obtained from separate acid-base titration, (3) the determination of surface site densities of quartz, chlorite, muscovite, and albite evaluated independently of each other with adsorption isotherms, and (4) the quantification of the secondary phase ferrihydrite, which formed during the batch sorption experiments with phyllite. The surface complex formation constants and the protolysis constants were optimized by using the experimentally obtained data sets and the computer code FITEQL. Surface site densities were evaluated from adsorption isotherms at pH 6.5. The uranyl(VI) sorption onto phyllite was accurately modeled with

  9. Sorption behavior of U(VI) on phyllite: experiments and modeling.

    PubMed

    Arnold, T; Zorn, T; Zänker, H; Bernhard, G; Nitsche, H

    2001-02-01

    The sorption of U(VI) onto low-grade metamorphic rock phyllite was modeled with the diffuse double layer model (DDLM) using the primary mineralogical constituents of phyllite, i.e. quartz, chlorite, muscovite, and albite, as input components, and as additional component, the poorly ordered Fe oxide hydroxide mineral, ferrihydrite. Ferrihydrite forms during the batch sorption experiment as a weathering product of chlorite. In this process, Fe(II), leached from the chlorite, oxidizes to Fe(III), hydrolyses and precipitates as ferrihydrite. The formation of ferrihydrite during the batch sorption experiment was identified by Mössbauer spectroscopy, showing a 2.8% increase of Fe(III) in the phyllite powder. The ferrihydrite was present as Fe nanoparticles or agglomerates with diameters ranging from 6 to 25 nm, with indications for even smaller particles. These Fe colloids were detected in centrifugation experiments of a ground phyllite suspension using various centrifugal forces. The basis for the successful interpretation of the experimental sorption data of uranyl(VI) on phyllite were: (1) the determination of surface complex formation constants of uranyl with quartz, chlorite, muscovite, albite, and ferrihydrite in individual batch sorption experiments, (2) the determination of surface acidity constants of quartz, chlorite, muscovite, and albite obtained from separate acid-base titration, (3) the determination of surface site densities of quartz, chlorite, muscovite, and albite evaluated independently of each other with adsorption isotherms, and (4) the quantification of the secondary phase ferrihydrite, which formed during the batch sorption experiments with phyllite. The surface complex formation constants and the protolysis constants were optimized by using the experimentally obtained data sets and the computer code FITEQL. Surface site densities were evaluated from adsorption isotherms at pH 6.5. The uranyl(VI) sorption onto phyllite was accurately modeled with

  10. Polycyclic aromatic hydrocarbon (PAH) sorption process to the "black carbon" (BC) component in river sediments

    NASA Astrophysics Data System (ADS)

    Zhang, Jing; Séquaris, Jean-Marie; Narres, Hans-Dieter; Vereecken, Harry; Klumpp, Erwin

    2010-05-01

    The importance of BC for the long term sequestration of organic carbon is actually discussed for mitigating climate change. In this context, the role of BC as a filter or source of nutrients or toxic chemicals is questioned. The fate of polycyclic aromatic hydrocarbons (PAHs) is especially concerned. In this study, we have investigated the binding of PAH compounds, pyrene and phenanthrene, to Yangtze River sediments. For this purpose, the PAHs sorption to pristine and preheated sediments at 375°C was studied, which allow discriminating the contributions of amorphous organic carbon (AOC) and black carbon (BC) fractions to the PAH sorption extent. An analytical procedure for the determination of PAHs in the solution phase of the batch experiments has been developed with fluorescence spectroscopy. The PAHs sorption isotherms to pristine sediments were fitted by Freundlich and composite models as linear Langmuir model (LLM) and linear Polanyi-Dubinin-Manes model (LPDMM). The sequential application of composite models LLM and LPDMM to the sorption isotherms allows assessing the partition of PAHs into AOC and its nonlinear adsorption in the porous structure of BC. The modelling results indicate that the PAHs sorption to minor BC component of sediments (< 0.2 % TOC) is more effective than that to the major AOC component (< 1.3 % TOC). A similar sorption capacity of BC in pristine and preheated sediments is also calculated at high PAHs concentrations, which indicates that the AOC fraction does not block the micropore filling of BC. The microporous structure and the hydrophobic nature of BC component in sediments are thus factors, which create favourable energetic sites for the sorption of PAHs in the river sediments. It can also be shown that a BC molecular sieving plays an important role in the competitive PAHs sorption in a multi-solute system. J. Zhang, Ph.D. Dissertation, RWTH Aachen, Germany, 2010 J. Zhang et al., Effects of organic carbon and clay fractions on the

  11. Sorption of radionuclides on Yucca Mountain tuffs

    SciTech Connect

    Meijer, A.; Triay, I.; Knight, S.; Cisneros, M.

    1989-11-01

    A substantial database of sorption coefficients for important radionuclides on Yucca Mountain tuffs has been obtained by Los Alamos National Laboratory over the past ten years. Current sorption studies are focussed on validation questions and augmentation of the existing database. Validation questions concern the effects of the use of crushed instead of solid rock samples in the batch experiments, the use of oversaturated stock solutions, and variations in water/rock ratios. Sorption mechanisms are also being investigated. Database augmentation activities include determination of sorption coefficients for elements with low sorption potential, sorption on psuedocolloids, sorption on fracture lining minerals, and sorption kinetics. Sorption can provide an important barrier to the potential migration of radionuclides from the proposed repository within Yucca Mountain to the accessible environment. In order to quantify this barrier, sorption coefficients appropriate for the Yucca Mountain groundwater system must be obtained for each of the important radionuclides in nuclear waste. Los Alamos National Laboratories has conducted numerous batch (crushed-rock) sorption experiments over the past ten years to develop a sorption coefficient database for the Yucca Mountain site. In the present site characterization phase, the main goals of the sorption test program will be to validate critical sorption coefficients and to augment the existing database where important data are lacking. 11 refs., 1 fig., 3 tabs.

  12. Isotherm study of reactive Blue 19 adsorption by an alum sludge

    NASA Astrophysics Data System (ADS)

    Khim, Ong Keat; Nor, Mohd Asri Md; Mohamad, Syuriya; Nasaruddin, Nas Aulia Ahmad; Jamari, Nor Laili-Azua; Yunus, Wan Md Zin Wan

    2015-05-01

    This study investigates the adsorption of Reactive Blue 19 using dewatered alum sludge. The dewatered alum sludge was a sludge produced from drinking water treatment plant. Batch adsorption experiments were performed to investigate the mechanism of the dye adsorption. The adsorption was rapid at its initial stage but the rate decreased as it approached equilibrium. The adsorption data were evaluated by Langmuir and Freundlich isotherm models but was best described by the Langmuir isotherm model as it gave the highest correlation.

  13. Single-pellet dynamics for the soil organic matter effect on dichloromethane sorption

    SciTech Connect

    Cabbar, C.; Dogu, G.; Dogu, T.; McCoy, B.J.

    1996-07-01

    The migration of volatile organic compounds (VOCs) in soil is strongly influenced by soil composition, for example, amount and type of clay, organic matter, and moisture. Halogenated hydrocarbons are frequently detected in the soil gas, and thus the sorption of these VOCs in soils has become an active area of research. Recent studies reported sorption rates and equilibrium data for some chlorinated hydrocarbons and for benzene by means of a single-pellet moment technique. In low-moisture soils, sorption occurs mainly on mineral surfaces, but the influence of soil organic matter (SOM) can also be significant. In the current study the authors use the single-pellet moment method to determine the effect of SOM on dichloromethane sorption in a dry simulated soil.

  14. Geochemical heterogeneity in a sand and gravel aquifer: Effect of sediment mineralogy and particle size on the sorption of chlorobenzenes

    USGS Publications Warehouse

    Barber, L.B.; Thurman, E.M.; Runnells, D.R.; ,

    1992-01-01

    The effect of particle size, mineralogy and sediment organic carbon (SOC) on solution of tetrachlorobenzene and pentachlorobenzene was evaluated using batch-isotherm experiments on sediment particle-size and mineralogical fractions from a sand and gravel aquifer, Cape Cod, Massachusetts. Concentration of SOC and sorption of chlorobenzenes increase with decreasing particle size. For a given particle size, the magnetic fraction has a higher SOC content and sorption capacity than the bulk or non-magnetic fractions. Sorption appears to be controlled by the magnetic minerals, which comprise only 5-25% of the bulk sediment. Although SOC content of the bulk sediment is < 0.1%, the observed sorption of chlorobenzenes is consistent with a partition mechanism and is adequately predicted by models relating sorption to the octanol/water partition coefficient of the solute and SOC content. A conceptual model based on preferential association of dissolved organic matter with positively-charged mineral surfaces is proposed to describe micro-scale, intergranular variability in sorption properties of the aquifer sediments.The effect of particle size, mineralogy and sediment organic carbon (SOC) on sorption of tetrachlorobenzene and pentachlorobenzene was evaluated using batch-isotherm experiments on sediment particle-size and mineralogical fractions from a sand and gravel aquifer, Cape Cod, Massachusetts. Concentration of SOC and sorption of chlorobenzenes increase with decreasing particle size. For a given particle size, the magnetic fraction has a higher SOC content and sorption capacity than the bulk or non-magnetic fractions. Sorption appears to be controlled by the magnetic minerals, which comprise only 5-25% of the bulk sediment. Although SOC content of the bulk sediment is <0.1%, the observed sorption of chlorobenzenes is consistent with a partition mechanism and is adequately predicted by models relating sorption to the octanol/water partition coefficient of the solute and

  15. Effects of radiation and temperature on iodide sorption by surfactant-modified bentonite.

    PubMed

    Choung, Sungwook; Kim, Minkyung; Yang, Jung-Seok; Kim, Min-Gyu; Um, Wooyong

    2014-08-19

    Bentonite, which is used as an engineered barrier in geological repositories, is ineffective for sorbing anionic radionuclides because of its negatively charged surface. This study modified raw bentonite using a cationic surfactant (i.e., hexadecyltrimethylammonium [HDTMA]-Br) to improve its sorption capability for radioactive iodide. The effects of temperature and radiation on the iodide sorption of surfactant-modified bentonite (SMB) were also evaluated under alkaline pH condition similar to that found in repository environments. Different amounts of surfactant, equivalent to the 50, 100, and 200% cation-exchange capacity of the bentonite, were used to produce the HDTMA-SMB for iodide sorption. The sorption reaction of the SMB with iodide reached equilibrium rapidly within 10 min regardless of temperature and radiation conditions. The rate of iodide sorption increased as the amount of the added surfactant was increased and nonlinear sorption behavior was exhibited. However, high temperature and γ-irradiation ((60)Co) resulted in significantly (∼2-10 times) lower iodide Kd values for the SMB. The results of FTIR, NMR, and XANES spectroscopy analysis suggested that the decrease in iodide sorption may be caused by weakened physical electrostatic force between the HDTMA and iodide, and by the surfactant becoming detached from the SMB during the heating and irradiation processes.

  16. Effects of Radiation and Temperature on Iodide Sorption by Surfactant-Modified Bentonite

    SciTech Connect

    Choung, Sungwook; Kim, Min Kyung; Yang, Jungseok; Kim, Min-Gyu; Um, Wooyong

    2014-08-04

    Bentonite, which is used as an engineered barrier in geological repositories, is ineffective for sorbing anionic radionuclides because of its negatively charged surface. This study modified raw bentonite using a cationic surfactant (i.e., hexadecyltrimethylammonium [HDTMA]-Br) to improve its sorption capability for radioactive iodide. The effects of temperature and radiation on the iodide sorption of surfactant-modified bentonite (SMB) were evaluated under alkaline pH condition similar to that found in repository environments. Different amounts of surfactant, equivalent to the 50, 100, and 200% cation-exchange capacity of the bentonite, were used to produce the HDTMA-SMB for iodide sorption. The sorption reaction of the SMB with iodide reached equilibrium rapidly within 10 min regardless of temperature and radiation conditions. The rate of iodide sorption increased as the amount of the added surfactant was increased and nonlinear sorption behavior was exhibited. However, high temperature and γ-irradiation (60Co) resulted in significantly (~2–10 times) lower iodide Kd values for the SMB. The results of Fourier transform infrared spectroscopy analysis suggested that the decrease in iodide sorption may be caused by weakened physical electrostatic force between the HDTMA and iodide, and by the surfactant becoming detached from the SMB during the heating and irradiation processes.

  17. Effect of dissolved organic matter from treated effluents on sorption of atrazine and prometryn by soils

    SciTech Connect

    Seol, Y.; Lee, L.S.

    2000-01-02

    The apparent enhanced transport of soil-applied atrazine following irrigation of treated effluents has been hypothesized to be from complexation of atrazine with effluent-borne dissolved organic matter (DOM). Under long-term effluent irrigation, even small DOM-induced decreases in pesticide sorption can result in significant enhanced pesticide movement due to cumulative effects. The effect of atrazine and prometryn association with DOM extracted from municipal wastewater (MW), swine-derived lagoon wastewater (SW), and dissolved Aldrich humic acid (HA) on sorption by two soils was measured in batch equilibration studies. Individual association of pesticides to DOM, sorption of DOM to soil, and pesticide sorption by soil were also quantified. Pesticide association to DOM normalized to organic carbon (OC) ranged from 30 to 1000 L/kg OC. DOM sorption by soil ranged from 1.5 to 10 L/kg with a silt loam having a higher affinity for the DOM than the sandy loam. DOM up to 150 mg OC/L did not significantly suppress sorption by soils of either atrazine or prometryne in agreement with predictions using the independently measured binary distribution coefficients in a model that assumed linear equilibrium behavior among pesticide, soil, and DOM. A sensitivity analysis was performed using the same model to identify what combination of soil, pesticide, and DOC variables may suppress sorption, resulting in facilitated transport. Results from the sensitivity analysis are presented and the potential for effluent properties other than DOM to facilitate pesticide transport is discussed.

  18. Determination of Chlorinated Solvent Sorption by Porous Material—Application to Trichloroethene Vapor on Cement Mortar

    PubMed Central

    Musielak, Marion; Brusseau, Mark L.; Marcoux, Manuel; Morrison, Candice; Quintard, Michel

    2014-01-01

    Experiments have been performed to investigate the sorption of trichloroethene (TCE) vapor by concrete material or, more specifically, the cement mortar component. Gas-flow experiments were conducted using columns packed with small pieces of cement mortar obtained from the grinding of typical concrete material. Transport and retardation of TCE at high vapor concentrations (500 mg L−1) was compared to that of a non-reactive gas tracer (Sulfur Hexafluoride, SF6). The results show a large magnitude of retardation (retardation factor = 23) and sorption (sorption coefficient = 10.6 cm3 g−1) for TCE, compared to negligible sorption for SF6. This magnitude of sorption obtained with pollutant vapor is much bigger than the one obtained for aqueous-flow experiments conducted for water-saturated systems. The considerable sorption exhibited for TCE under vapor-flow conditions is attributed to some combination of accumulation at the air-water interface and vapor-phase adsorption, both of which are anticipated to be significant for this system given the large surface area associated with the cement mortar. Transport of both SF6 and TCE was simulated successfully with a two-region physical non-equilibrium model, consistent with the dual-medium structure of the crushed cement mortar. This work emphasizes the importance of taking into account sorption phenomena when modeling transport of volatile organic compounds through concrete material, especially in regard to assessing vapor intrusion. PMID:25530647

  19. Sorption-desorption of 1,2,4-trichlorobenzene on soil: Anionic surfactant and cationic polyelectrolyte effects

    SciTech Connect

    DiVincenzo, J.P.; Dentel, S.K.

    1996-11-01

    Anionic surfactants and cationic polymers are two classes of anthropogenic chemicals that are released to the environment in significant amounts. In particular, this occurs in the land disposal of sludges, potentially altering the terrestrial mobility of other contaminants such as hydrophobic organics. Thus, we examined the 1,2,4-trichlorobenzene (TCB) sorption-desorption on soil with sodium dodecyl sulfate (SDS) and/or a cationic polyelectrolyte (Percol 757) present. Initial experiments varying sorbent mass resulted in nonconstant partitioning and a nonlinear isotherm; a model of incomplete colloidal separation by centrifugation could not explain the nonlinearity. A proposed model quantifies this isotherm behavior with a BET isotherm equation related to the limiting sorption capacity of the organic matter phase, Q{sub om}{degrees}. Additions of SDS and/or polyelectrolyte led to significant changes in TCB sorption. The SDS decreased TCB sorption significantly, but only with SDS exceeding the critical micelle concentration (CMC). The CMC value itself varied with electrolyte and soil presence. Increasing the SDS concentration above the CMC caused TCB desorption from soil. The SDS also increased residual colloidal solids, but primarily below the CMC. Percol 757 slightly increased TCP sorption. With polymer added to soil containing SDS, TCB sorption was unaffected until charge equivalence was approached, whereupon sorption increased severalfold. This trend reversed when the SDS exceeded the sum of the polymer equivalence and the CMC. These results are explained in terms of polymer-surfactant interactions. Environmental implications include effects on transport of hydrophobic organics resulting form sludge disposal on land. 27 refs., 10 figs.

  20. Transport and sorption behavior of individual phthalate esters in sandy aquifer: column experiments.

    PubMed

    Zakari, Sissou; Liu, Hui; Li, Yan-Xi; He, Xi; Tong, Lei

    2016-08-01

    This work aimed to quantify the transport and sorption behavior of four individual phthalate esters (PAEs) in sandy aquifer using column experiments so as to provide important parameters for the prediction and control of PAEs pollution plume in groundwater system. The transport curves of four individual PAEs were simulated with HYDRUS-1D through fitting linear and nonlinear equilibrium (LE/NO), linear and nonlinear, first-order, one-site non-equilibrium (LO/NO), linear and nonlinear, first-order, two-site non-equilibrium (LFO/NFO) sorption models. Simulation results showed that two-site models (LFO and NFO) displayed similar best fittings. The results from LFO model simulation showed that when water flowed 1000 m in sandy aquifer, PAEs with shorter carbon chains (DMP and DEP) transport 31.6 and 22.2 m, respectively. Unexpectedly for the same water transport distance, PAEs with longer carbon chains (DBP and DiBP) transported 40.2 and 60.7 m, respectively, which were faster than DMP and DEP, mainly due to the limited accessibility of type-2 sorption sites. The retardations were mainly caused by the sorption of PAEs on the time-dependent type-2 sites. DBP and DiBP exhibited higher mass transfer speed to and fro type-2 sites but showed lower total sorption coefficient (K) due to the limited accessibility of sorption sites. Coexistence of PAEs and smaller sorbent particles increased total K values of DBP and DiBP due to synergic development of more sorption sites with DMP and DEP. PMID:27146532

  1. Sorption/desorption behavior of iodine on graphite. [HTGR

    SciTech Connect

    Lorenz, R.A.; Dyer, F.F.; Towns, R.L.

    1982-11-01

    An experimental program was undertaken to extend the data on the sorption and desorption of iodine on graphite to more realistic high-temperature gas-cooled reactor (HTGR) operating conditions. This was accomplished by heating compacts of H-451 or S-2020 graphite at 250 to 1000/sup 0/C in continuously flowing helium (at atmospheric pressure) that contained iodine at pressures of 10/sup -6/ Pa (10/sup -11/ to 10/sup -1/ to 10/sup -6/ bar). Equilibrium adsorption data were generally well-behaved and reproducible with the H-451 graphite. Type S-2020 graphite sorbed more iodine, especially in the temperature range 700 to 800/sup 0/C. Although desorption appeared to initiate as reversible sorption, the rate of loss of iodine decreased with time. During desorption from the S-2020 graphite at 700 and 800/sup 0/C, a temporary plateau was reached that was sensitive to helium flow and pressure.

  2. Analysis of the sorption and migration of substances in soil with the use of mathematical models

    NASA Astrophysics Data System (ADS)

    Frid, A. S.

    2012-09-01

    Little-discussed aspects of mathematical models of migration, which contribute to better understanding of soil processes, were considered. These are the effect of the sorption isotherm parameters and sorption kinetics on the complexity of the migration models, the potentially great contribution of the diffusion of adsorbed ions to the general migration in the soil, the probability of an anomalously high diffusion flux through the soil under high sorption conditions, and the possibility for the nontrivial assessment of the exchangeable and mobile forms of substances in the soil from the migration parameters. The migration analysis features under field conditions and related additional uncertainties compared to the laboratory experiments were discussed, as well as new opportunities for the control of the technogenic contamination of the environment.

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

    PubMed

    Zhang, Yulong; Ma, Xiaoxuan; Ran, Yong

    2014-02-01

    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.

  4. Sorption of wastewater containing reactive red X-3B on inorgano-organo pillared bentonite.

    PubMed

    Zeng, Xiu-qiong

    2006-04-01

    Bentonite is a kind of natural clay with good exchanging ability. By exchanging its interlamellar cations with various soluble cations, such as quaternary ammonium cations and inorganic metal ions, the properties of natural bentonite can be greatly improved. In this study, hexadecyltrimethylammonium bromide (HDTMA), CaCl(2), MgCl(2), FeCl(3), AlCl(3) were used as organic and inorganic pillared materials respectively to produce several kinds of Ca-, Mg-, Fe-, Al-organo pillared bentonites. Sorption of reactive red X-3B on them was studied to determine their potential application as sorbents in wastewater treatment. The results showed that these pillared bentonites had much improved sorption properties, and that the dye solutions' pH value had some effect on the performance of these inorgano-organo pillared bentonites. Isotherms of reactive X-3B on these pillared bentonites suggested a Langmuir-type sorption mechanism. PMID:16532535

  5. Sorption of cesium and strontium on Savannah River soils impregnated with colloidal silica

    SciTech Connect

    Hakem, N.; Al Mahamid, I.; Apps, J.; Moridis, G.

    1997-01-01

    Colloidal silica (CS) is being considered as an injectable low viscosity fluid for creation of impermeable barrier containment of low level radioactive waste at the Savannah River Site (SRS), South Carolina. The sorption behavior of cesium and strontium on Savannah River Site Soils impregnated with Colloidal Silica was studied using a batch experimental method. The samples were prepared by addition of CS and an aqueous solution of CaCl{sub 2} to the soil materials. Sorption studies were conducted after the gelation of the CS samples had occurred. The variation of the sorption ratio, R, as a function of cesium or strontium concentration was examined. The Freundlich isotherm was used to fit the data and very good results were obtained.

  6. Sorption mechanism and predictive models for removal of cationic organic contaminants by cation exchange resins.

    PubMed

    Jadbabaei, Nastaran; Zhang, Huichun

    2014-12-16

    Understanding the sorption mechanism of organic contaminants on cation exchange resins (CXRs) will enable application of these resins for the removal of cationic organic compounds from contaminated water. In this study, sorption of a diverse set of 12 organic cations and 8 neutral aromatic solutes on two polystyrene CXRs, MN500 and Amberlite 200, was examined. MN500 showed higher sorbed concentrations due to its microporous structure. The sorbed concentrations followed the same trend of aromatic cations > aliphatic cations > neutral solutes for both resins. Generally, solute-solvent interactions, nonpolar moiety of the solutes, and resin matrix can affect selectivity of the cations. Sorbed concentrations of the neutral compounds were significantly less than those of the cations, indicating a combined effect of electrostatic and nonelectrostatic interactions. By conducting multiple linear regression between Gibbs free energy of sorption and Abraham descriptors for all 20 compounds, polarity/polarizability (S), H-bond acidity (A), induced dipole (E), and electrostatic (J(+)) interactions were found to be involved in the sorption of the cations by the resins. After converting the aqueous sorption isotherms to sorption from the ideal gas-phase by water-wet resins, a more significant effect of J(+) was observed. Predictive models were then developed based on the linear regressions and validated by accurately estimating the sorption of different test set compounds with a root-mean-square error range of 0.91-1.1 and 0.76-0.85 for MN500 and Amberlite 200, respectively. The models also accurately predicted sorption behavior of aniline and imidazole between pH 3 and 10. PMID:25409479

  7. Sorption and Transport of Sildenafil in Natural Soils

    NASA Astrophysics Data System (ADS)

    Boudinot, F. G.; Vulava, V. M.

    2013-12-01

    Pharmaceutical Chemicals (PCs) mainly enter our ecosystems from discharges of treated wastewater and have direct effects on the ecological health of that area. Sildenafil citrate (Viagra) is one such PC, whose presence has been reported in stream waters. Although one study has shown that sildenafil is not harmful in bacterial and fungal environments, there remains much unknown about its fate elsewhere in ecosystems. Sildenafil is a complex organic molecule with two amino functional groups that result in pKa's of 7.27 and 5.97. It also has a high solubility of 3.5 g/L. Given that sildenafil consumption (and concurrently disposal) is on the rise, it is essential that its behavior in the natural environment be better understood. The goal of this study was to quantify the sorption and transport behavior of sildenafil in differing natural soils with varying compositions. Pristine A- and B- horizon soil samples from several soil series were collected in a managed forest near Charleston, SC and used for these studies. The soils were characterized for physical and chemical properties: soil organic matter content ranged between 0.6-7.6%, clay content between 6-20%, and soil pH between 4-5. These soils were then used to perform kinetic reaction, sorption, and column transport experiments. Batch kinetic experiments showed a fast reaction rate in both clay-rich and organic-rich soils and an equilibration time of less than 24 hours. Batch reactor sorption experiments provided data for sorption isotherms (plot of sildenafil in solution, C vs. sildenafil sorbed in soil, q) which were nonlinear. The isotherms were fit using Freundlich model (q=KfCn, where Kf and n are fitting parameters). Sildenafil sorbed more strongly to clay-rich soils compared with organic-rich soils with less clay. It is hypothesized that permanent negative charge on clay mineral surfaces form ionic bonds with positively charged amines in sildenafil in acidic pHs. Transport experiments were conducted using

  8. Arsenic Sorption in Dried Leaves

    NASA Astrophysics Data System (ADS)

    Silva, Gabriela C.; de Carvalho, Regina P.; Duarte, Grazielle; Santos, Mércia H.

    2005-10-01

    Biosorption is the retention of metal ions from aqueous solutions by biomasses. This phenomenon can be helpful in the design of alternative filters for the depollution of industrial and mining waste waters. The recovery of filtered metal ions can also be commercially interesting. Although many studies about the sorptive capacity of biomasses have been done for different metals, few have investigated sorption sites and mechanisms in these systems. We studied the retention of arsenic ions from aqueous solutions using dried lettuce leaves (L. sativa) as biomass. The toxic arsenic forms As(III) and As(V) are commonly found in mining waste waters. Early studies have shown that lettuce leaves have a good sorptive capacity for copper and iron ions, comparable to other sorbents such as activated carbon or ionic-exchange resins. Arsenic sorption by lettuce dried leaves was not found to be effective when in natura biomass was used. Sorptive capacity was improved and became comparable to the sorption of the other ions studied when the biomass was charged with Fe(III). The sorption mechanism of arsenic in Fe-charged biomass must be similar to the one proposed for As sorption by mineral clays, where As ions bind to Fe(III) atoms in the clay structure.

  9. Solving chemical equilibrium problems using nonlinear optimization. [NEWT

    SciTech Connect

    Parkinson, W.J.; Sanderson, J.G.

    1984-06-01

    This report describes a program that will solve general chemical equilibrium problems of the type found in synthetic fossil-fuel plants. The program described here will also solve chemical equilibrium problems that are associated with unit operations that are found in refineries and ammonia plants. The most common problem encountered involves finding the equilibrium composition of a mixture, given feed composition, and the desired equilibrium temperature and pressure. Another less common problem requires the computation of the equilibrium temperature as well as the equilibrium composition for an adiabatic or other nonisothermal reaction. A constrained multidimensional Newton's method is used to solve the common isothermal equilibrium problem. The nonisothermal problem is solved by nesting the same multidimensional Newton's method inside a one-dimensiona