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Sample records for moisture sorption isotherm

  1. Moisture sorption isotherms of dehydrated whey proteins

    OpenAIRE

    Suzana Rimac Brnčić; Vesna Lelas; Zoran Herceg; Marija Badanjak

    2010-01-01

    Moisture sorption isotherms describe the relation between the moisture content of the dry material (food) and relative humidity of the surrounding environment. The data obtained are important in modelling of drying process conditions, packaging and shelf-life stability of food that will provide maximum retaining of aroma, colour and texture as well as nutritive and biological value. The objective of this research was to establish the equilibrium moisture content and water activity, as well as...

  2. Moisture sorption isotherms of dehydrated whey proteins

    Directory of Open Access Journals (Sweden)

    Suzana Rimac Brnčić

    2010-03-01

    Full Text Available Moisture sorption isotherms describe the relation between the moisture content of the dry material (food and relative humidity of the surrounding environment. The data obtained are important in modelling of drying process conditions, packaging and shelf-life stability of food that will provide maximum retaining of aroma, colour and texture as well as nutritive and biological value. The objective of this research was to establish the equilibrium moisture content and water activity, as well as monolayer value of two commercial powdered whey protein isolates before and after tribomechanical micronisation and enzymatic hydrolysis, respectively. At the same time it was necessary to evaluate the best moisture sorption isotherm equation to fit the experimental data. The equilibrium moisture contents in investigated samples were determined using standard gravimetric method at 20 °C. The range of water activities was 0.11 to 0.75. The monolayer moisture content was estimated from sorption data using Brunauer-Emmett-Teller (BET and Guggenheim-Anderson-de Boer (GAB models. The results have shown that tribomechanically treated whey protein isolates as well as protein hydrolizates had lower monolayer moisture content values as well as higher corresponding water activity. Therefore, in spite of the fact that they have lower moisture content, they can be storage at higher relative humidity compared to untreated samples. BET model gave better fit to experimental sorption data for a water activity range from 0.11-0.54, while GAB model gave the closest fit for a water activity to 0.75.

  3. Moisture sorption isotherms and thermodynamic properties of bovine leather

    Science.gov (United States)

    Fakhfakh, Rihab; Mihoubi, Daoued; Kechaou, Nabil

    2018-04-01

    This study was aimed at the determination of bovine leather moisture sorption characteristics using a static gravimetric method at 30, 40, 50, 60 and 70 °C. The curves exhibit type II behaviour according to the BET classification. The sorption isotherms fitting by seven equations shows that GAB model is able to reproduce the equilibrium moisture content evolution with water activity for moisture range varying from 0.02 to 0.83 kg/kg d.b (0.9898 thermodynamic properties such as isosteric heat of sorption, sorption entropy, spreading pressure, net integral enthalpy and entropy. Net isosteric heat of sorption and differential entropy were evaluated through direct use of moisture isotherms by applying the Clausius-Clapeyron equation and used to investigate the enthalpy-entropy compensation theory. Both sorption enthalpy and entropy for desorption increase to a maximum with increasing moisture content, and then decrease sharply with rising moisture content. Adsorption enthalpy decreases with increasing moisture content. Whereas, adsorption entropy increases smoothly with increasing moisture content to a maximum of 6.29 J/K.mol. Spreading pressure increases with rising water activity. The net integral enthalpy seemed to decrease and then increase to become asymptotic. The net integral entropy decreased with moisture content increase.

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

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    Amel Saad

    2014-01-01

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

  5. Moisture Sorption Isotherms and Properties of Sorbed Water of Neem ( Azadirichta indica A. Juss) Kernels

    Science.gov (United States)

    Ngono Mbarga, M. C.; Bup Nde, D.; Mohagir, A.; Kapseu, C.; Elambo Nkeng, G.

    2017-01-01

    A neem tree growing abundantly in India as well as in some regions of Asia and Africa gives fruits whose kernels have about 40-50% oil. This oil has high therapeutic and cosmetic qualities and is recently projected to be an important raw material for the production of biodiesel. Its seed is harvested at high moisture contents, which leads tohigh post-harvest losses. In the paper, the sorption isotherms are determined by the static gravimetric method at 40, 50, and 60°C to establish a database useful in defining drying and storage conditions of neem kernels. Five different equations are validated for modeling the sorption isotherms of neem kernels. The properties of sorbed water, such as the monolayer moisture content, surface area of adsorbent, number of adsorbed monolayers, and the percent of bound water are also defined. The critical moisture content necessary for the safe storage of dried neem kernels is shown to range from 5 to 10% dry basis, which can be obtained at a relative humidity less than 65%. The isosteric heats of sorption at 5% moisture content are 7.40 and 22.5 kJ/kg for the adsorption and desorption processes, respectively. This work is the first, to the best of our knowledge, to give the important parameters necessary for drying and storage of neem kernels, a potential raw material for the production of oil to be used in pharmaceutics, cosmetics, and biodiesel manufacturing.

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

    Science.gov (United States)

    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.

  7. PENGARUH ISOTERM SORPSI AIR TERHADAP STABILITAS BERAS UBI [Effect of Moisture Sorption Isotherm to Stability of “Sweet Potato Rice”

    Directory of Open Access Journals (Sweden)

    Sri Widowati1*

    2010-12-01

    Full Text Available “Sweet Potato Rice” stability as a dry food product was determined by water activity (aw and equilibrium moisture content (Me. This relationship is known as moisture sorption isotherm. This research were aimed 1 to study moisture sorption isotherm of “Sweet Potato Rice” from sweet potato flour (Cangkuang variety and native/heat moisture treatment (HMT starch which was stored at the range of aw:0.06 - 0.96 and 28oC; 2 to determine an appropriate model for describing product moisture sorption isotherm and 3 to predict “Sweet Potato Rice” shelf of life. Experimental design used was a random complete design with two factor, namely: 1 sweet potato starch: native and HMT, and 2 packaging material: polyethylene (PE and polypropylene (PP.The result showed that the moisture sorption isotherm profiles were sigmoid. Smith equation was the best model which described moisture sorption isotherm with R2= 0,991-0,993 for adsorption and R2= 0,964-0,971 for desorption. Shelf life test showed that “Sweet Potato Rice” from Cangkuang flour and modified starch had longer shelf life (5.67 months when packed in PP bag and 2.3 months when packed in PE bag; while shelf life artificial sweet potato made from Cangkuang flour and native starch was 4.24 months when packed in PP bag and 1.72 months when packed in PE bag.

  8. Modeling and Prediction of Soil Water Vapor Sorption Isotherms

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per

    2015-01-01

    Soil water vapor sorption isotherms describe the relationship between water activity (aw) and moisture content along adsorption and desorption paths. The isotherms are important for modeling numerous soil processes and are also used to estimate several soil (specific surface area, clay content.......93) for a wide range of soils; and (ii) develop and test regression models for estimating the isotherms from clay content. Preliminary results show reasonable fits of the majority of the investigated empirical and theoretical models to the measured data although some models were not capable to fit both sorption...... directions accurately. Evaluation of the developed prediction equations showed good estimation of the sorption/desorption isotherms for tested soils....

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

    Science.gov (United States)

    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.

  10. Moisture sorption of Thai red curry powder

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    Sudathip Inchuen

    2009-12-01

    Full Text Available Moisture sorption study was conducted on Thai red curry powder prepared by two different drying methods, viz. microwave and hot-air drying. Moisture sorption isotherms of the red curry powder at 30 C and water activity in the range of 0.113-0.970 were determined by a static gravimetric method. The isotherms exhibited Type III behaviour. The moisture sorption data were fitted to several sorption models and a non-linear regression analysis method was used to evaluate the constants of the sorption equations. The fit was evaluated using the coefficient of determination (R2, the reduced chi-square (2 and the root mean square error (RMSE. The GAB model followed by the Lewiski-3 model gave the best fit to the experimental data. The monolayer moisture content, taken as the safe minimum moisture level in the red curry powder, was determined using the BET equation and was found to range between 0.080 - 0.085 gram water per gram dry matter.

  11. ISOTERMI SORPSI AIR DAN ANALISIS UMUR SIMPAN IKAN KAYU TONGKOL (Euthynnus affinis DARI ACEH [Moisture Sorption Isotherm and Shelf Life Analysis of Dried Tongkol (Euthynnus affinis from Aceh

    Directory of Open Access Journals (Sweden)

    Rita Hayati1

    2004-12-01

    Full Text Available Tongkol dried fish (Ikan Kayu Tongkol is lumps of less salted dried fish usually used as popular ingredient for some traditional fish dishes in Aceh as well as in Malaysia. In Japan it is further processed into Katsou-bushi for preparation of special soup. The objective of this research was to find out water relation parameters in the less salted dried fish as related to shelf life, characteristic changes during storage and estimate analysis of its expired date. Dried fish samples were equilibrated in 15 levels of RH at 28oC and their equilibrium moisture contents were determined.Moisture sorption isotherm derived from the correlation of equilibrium moisture content data indicated a typical sigmoidal curve implying 3 regions of water adsorption. The water sorption regions accounted for three fractions of bound water as analyzed using three different mathematical models. The first water fraction ranged 0 - 5.95 %, the second 5.95 - 17.52 % and the third fraction ranged 17.52 - 91.12 % dry basis, equivalent to 0 - 5.6 %, 5.6 - 14.9 % and 14.9 - 47.4 % wet basis respectively. Storage simulation experiment in two packaging materials as carried out at 30oC and 90 % RH resulted shelf life of 2749 days (91 months in the packaging of plastic impregnated allumunium and 1204 days (40 months in plastic packaging. These very long shelf life was due to the added salt in the produt which increased Mc as high as 46.9 % to cause mold growth. This estimate analysis of shelf life using the mathematical model of Labuza (1984 is one of the appropriate methods to determining expired date of dry food products.

  12. Mathematical modelling of the sorption isotherms of quince

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    Mitrevski Vangelce

    2017-01-01

    Full Text Available The moisture adsorption isotherms of quince were determined at four temperatures 15, 30, 45, and 60°C over a range of water activity from 0.110 to 0.920 using the standard static gravimetric method. The experimental data were fitted with generated three parameter sorption isotherm models on Mitrevski et al., and the referent Anderson model known in the scientific and engineering literature as Guggenheim- Anderson-de Boer model. In order to find which models give the best results, large number of numerical experiments was performed. After that, several statistical criteria for estimation and selection of the best sorption isotherm model was used. The performed statistical analysis shows that the generated three parameter model M11 gave the best fit to the sorption data of quince than the referent three parameter Anderson model.

  13. ANALISIS FRAKSI-FRAKSI KURVA ISOTERMI SORPSI AIR DARI TEPUNG ROSELA DAN PENGARUHNYA TERHADAP SIFAT-SIFAT MUTU PRODUK [Analysis of Moisture Sorption Isotherm Fraction of Roselle Powder and Its Effect on Products the Quality Characteristics

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    Rita Hayati

    2013-06-01

    Full Text Available The purpose of this study was to determine the fractions of moisture sorption isotherm curve and the critical water content of roselle powder and its effect on the product quality during storage. Roselle flowers were harvested at 25 days after flowering and sun dried (30ºC for 3 days. The result showed that the moisture sorption isotherm curve of the roselle powder was sigmoid. The critical transition points among the three fractions of the bound water in the roselle flour were first at moisture content (Mp and water activity (ap of 7.97% dry basis (db and 0.23 respectively, and second at Ms 21.1% db water content and water activity (as of 0.65%. Roselle powder samples were stored for 20 days at three relative humidity (RH fractions represented by RH 22% (moisture content at 7.2% db, RH 57 % (20.5% db and 84 % (54.2% db. The samples stored in the first fraction was stable in texture, colour and appearance, while the sample in the secondary bound water fraction (21.1% db, changed in colour into darker red. The sample stored in the tertiary bound water fraction (54.2% db changed into brown colour with musty smell and mouldy after 15 days.

  14. Sorption isotherms, GAB parameters and isosteric heat of sorption

    NARCIS (Netherlands)

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

    2005-01-01

    The diffusion-sorption drying model has been developed as a physics-based way to model the decreasing drying rate at low moisture contents. This new model is founded on the existence of different classes of water: free and bound water. The transition between these classes and the corresponding

  15. Determination of storage conditions for new biscuits using their sorption isotherms

    OpenAIRE

    G. Diukareva; A. Pak; A. Gasanova

    2015-01-01

    Introduction For the formation of biscuits quality natural carrier of iodine and sweetener from stevia leaves were used. Desorption of moisture is the dominant process, which will determine the guaranteed shelf life of biscuits. The conditions for the developed biscuits storage was determined by investigating of sorption isotherms and kinetics of reaching the equilibrium moisture content. Materials and Methods. The objects of stud...

  16. Study of thermodynamic water properties and moisture sorption hysteresis of mango skin

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    Silvio José Ferreira de Souza

    2015-03-01

    Full Text Available The equilibrium moisture content for adsorption and desorption isotherms of mango skin was determined using the static gravimetric method at temperatures of 20, 26, 33, 38 and 44 oC in the 0.056 to 0.873 water activity range. Both sorption curves show a decrease in equilibrium moisture content as the temperature increasing. The hysteresis effect was observed at constant water activity. The Guggenheim, Anderson, and de Boer (GAB model presented the best fitting accuracy among a group of models and was used to determine the thermodynamic properties of water sorption. Integral enthalpy and integral entropy areas showed inverted values for the adsorption and desorption isotherms over the wide range of water activity studied. These values confirm, in energetic terms, the difference between adsorption and desorption isotherms observed in the hysteresis phenomenon. Finally, the Gibbs free energy revealed that the sorption process was spontaneous for both sorption isotherms.

  17. Column Chromatography To Obtain Organic Cation Sorption Isotherms.

    Science.gov (United States)

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

    2016-08-02

    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.

  18. Experience of Implementing Moisture Sorption Control in Historical Archives

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    P. Zítek

    2006-01-01

    Full Text Available This paper deals with a novel approach to inhibiting the harmful impact of moisture sorption in old art works and historical exhibits preserved in remote historic buildings that are in use as depositories or exhibition rooms for cultural heritage collections. It is a sequel to the previous work presented in [2], where the principle of moisture sorption stabilization was explained. Sorption isotherm investigations and EMC control implementation in historical buildings not provided with heating are the main concern in this paper. The proposed microclimate adjustment consists in leaving the interior temperature to run almost its spontaneous yearly cycle, while the air humidity is maintained in a specific relationship to the current interior temperature. The interior air humidity is modestly adjusted to protect historical exhibits and art works from harmful variations in the content of absorbed moisture, which would otherwise arise owing to the interior temperature drifts. Since direct measurements of moisture content are not feasible, the air humidity is controlled via a model-based principle. Two long-term implementations of the proposed microclimate control have already proved that it can permanently maintain a constant moisture content in the preserved exhibits. 

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

    Science.gov (United States)

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

    2017-04-01

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

  20. Sorption isotherms for oat flakes (Avena sativa L.

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    José Edgar Zapata M.

    2014-04-01

    Full Text Available Moisture sorption isotherms of oat flakes were determined at temperatures of 5, 25 and 37°C, using a gravimetric technique in an a w range of between 0.107 and 0.855. These curves were modeled using six equations commonly applied in food. The quality of the fit was assessed with the regression coefficient (r² and the mean relative percentage error (MRPE. The best fit were obtained with the Caurie model with r² of 0.996, 0.901 and 0.870, and MRPE of 7.190, 17.878 and 16.206, at 5, 25 and 37°C, respectively. The equilibrium moisture presented a dependence on temperature in the studied a w range, as did the security moisture (X S. These results suggest that the recommended storage conditions of oat flakes include: a relative air humidity of 50% between 5 and 25°C and of 38% up to 37°C.

  1. Isothermal, kinetic and thermodynamic studies on basic dye sorption ...

    African Journals Online (AJOL)

    Isothermal, kinetic and thermodynamic studies on basic dye sorption onto tartaric acid esterified wheat straw. ... African Journal of Biotechnology ... esterified wheat straw (EWS), was originally prepared by solid phase thermochemistry method.

  2. Isothermal, kinetic and thermodynamic studies on basic dye sorption ...

    African Journals Online (AJOL)

    PRECIOUS

    2009-12-15

    Dec 15, 2009 ... The isothermal data correlated with the Langmuir model better than the. Freundlich model. ... there were two intra-particle diffusion steps in the dye sorption processes. .... rated monolayer of sorbate molecule on the sorbent.

  3. Sorption isotherms modeling approach of rice-based instant soup mix stored under controlled temperature and humidity

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    Yogender Singh

    2015-12-01

    Full Text Available Moisture sorption isotherms of rice-based instant soup mix at temperature range 15–45°C and relative humidity from 0.11 to 0.86 were determined using the standard gravimetric static method. The experimental sorption curves were fitted by five equations: Chung-Pfost, GAB, Henderson, Kuhn, and Oswin. The sorption isotherms of soup mix decreased with increasing temperature, exhibited type II behavior according to BET classification. The GAB, Henderson, Kuhn, and Oswin models were found to be the most suitable for describing the sorption curves. The isosteric heat of sorption of water was determined from the equilibrium data at different temperatures. It decreased as moisture content increased and was found to be a polynomial function of moisture content. The study has provided information and data useful in large-scale commercial production of soup and have great importance to combat the problem of protein-energy malnutrition in underdeveloped and developing countries.

  4. Moisture Sorption in Porous Materials

    DEFF Research Database (Denmark)

    Nielsen, Lauge Fuglsang

    2007-01-01

    pressure and weight data can be "translated" to pore geometry by known physical relationships. In this context, analytical descriptions are important which can relate moisture condensation in pore structures to ambient vapor pressure. Such a description, the extended BET-relation, is presented...... physical parameters, the so-called BET-parameters: The heat property factor, C, and the pore surface, SBET (derived from the so-called uni-molecular moisture content uBET). A software ‘SORP07’ has been developed to handle any calculations made in the paper. For readers who have a special interest...... in the subject considered this software is available on request to the author. Keywords: Porous materials, moisture, adsorption, desorption, BET-parameters....

  5. Prediction of water vapour sorption isotherms and microstructure of hardened Portland cement pastes

    International Nuclear Information System (INIS)

    Burgh, James M. de; Foster, Stephen J.; Valipour, Hamid R.

    2016-01-01

    Water vapour sorption isotherms of cementitious materials reflect the multi-scale physical microstructure through its interaction with moisture. Our ability to understand and predict adsorption and desorption behaviour is essential in the application of modern performance-based approaches to durability analysis, along with many other areas of hygro-mechanical and hygro-chemo-mechanical behaviour. In this paper, a new physically based model for predicting water vapour sorption isotherms of arbitrary hardened Portland cement pastes is presented. Established thermodynamic principles, applied to a microstructure model that develops with hydration, provide a rational basis for predictions. Closed-form differentiable equations, along with a rational consideration of hysteresis and scanning phenomena, makes the model suitable for use in numerical moisture simulations. The microstructure model is reconciled with recently published 1 H NMR and mercury intrusion porosimetry results.

  6. Sorption isotherms: A review on physical bases, modeling and measurement

    Energy Technology Data Exchange (ETDEWEB)

    Limousin, G. [Atomic Energy Commission, Tracers Technology Laboratory, 38054 Grenoble Cedex (France) and Laboratoire d' etude des Transferts en Hydrologie et Environnement (CNRS-INPG-IRD-UJF), BP 53, 38041 Grenoble Cedex (France)]. E-mail: guillaumelimousin@yahoo.fr; Gaudet, J.-P. [Laboratoire d' etude des Transferts en Hydrologie et Environnement (CNRS-INPG-IRD-UJF), BP 53, 38041 Grenoble Cedex (France); Charlet, L. [Laboratoire de Geophysique Interne et Techtonophysique - CNRS-IRD-LCPC-UJF-Universite de Savoie, BP 53, 38041 Grenoble Cedex (France); Szenknect, S. [Atomic Energy Commission, Tracers Technology Laboratory, 38054 Grenoble Cedex (France); Barthes, V. [Atomic Energy Commission, Tracers Technology Laboratory, 38054 Grenoble Cedex (France); Krimissa, M. [Electricite de France, Division Recherche et Developpement, Laboratoire National d' Hydraulique et d' Environnement - P78, 6 quai Watier, 78401 Chatou (France)

    2007-02-15

    The retention (or release) of a liquid compound on a solid controls the mobility of many substances in the environment and has been quantified in terms of the 'sorption isotherm'. This paper does not review the different sorption mechanisms. It presents the physical bases underlying the definition of a sorption isotherm, different empirical or mechanistic models, and details several experimental methods to acquire a sorption isotherm. For appropriate measurements and interpretations of isotherm data, this review emphasizes 4 main points: (i) the adsorption (or desorption) isotherm does not provide automatically any information about the reactions involved in the sorption phenomenon. So, mechanistic interpretations must be carefully verified. (ii) Among studies, the range of reaction times is extremely wide and this can lead to misinterpretations regarding the irreversibility of the reaction: a pseudo-hysteresis of the release compared with the retention is often observed. The comparison between the mean characteristic time of the reaction and the mean residence time of the mobile phase in the natural system allows knowing if the studied retention/release phenomenon should be considered as an instantaneous reversible, almost irreversible phenomenon, or if reaction kinetics must be taken into account. (iii) When the concentration of the retained substance is low enough, the composition of the bulk solution remains constant and a single-species isotherm is often sufficient, although it remains strongly dependent on the background medium. At higher concentrations, sorption may be driven by the competition between several species that affect the composition of the bulk solution. (iv) The measurement method has a great influence. Particularly, the background ionic medium, the solid/solution ratio and the use of flow-through or closed reactor are of major importance. The chosen method should balance easy-to-use features and representativity of the studied

  7. Sorption Isotherm of Southern Yellow Pine—High Density Polyethylene Composites

    Directory of Open Access Journals (Sweden)

    Feihong Liu

    2015-01-01

    Full Text Available Temperature and relative humidity (RH are two major external factors, which affect equilibrium moisture content (EMC of wood-plastic composites (WPCs. In this study, the effect of different durability treatments on sorption and desorption isotherms of southern yellow pine (SYP-high density polyethylene (HDPE composites was investigated. All samples were equilibriumed at 20 °C and various RHs including 16%, 33%, 45%, 66%, 75%, 85%, 93%, and100%. EMCs obtained from desorption and absorption for different WPC samples were compared with Nelson’s sorption isotherm model predictions using the same temperature and humidity conditions. The results indicated that the amount of moisture absorbed increased with the increases in RH at 20 °C. All samples showed sorption hysteresis at a fixed RH. Small difference between EMC data of WPC samples containing different amount of ultraviolet (UV stabilizers were observed. Similar results were observed among the samples containing different amount of zinc borate (ZB. The experimental data of EMCs at various RHs fit to the Nelson’s sorption isotherm model well. The Nelson’s model can be used to predicate EMCs of WPCs under different RH environmental conditions.

  8. Determination of storage conditions for new biscuits using their sorption isotherms

    Directory of Open Access Journals (Sweden)

    G. Diukareva

    2015-05-01

    Full Text Available Introduction For the formation of biscuits quality natural carrier of iodine and sweetener from stevia leaves were used. Desorption of moisture is the dominant process, which will determine the guaranteed shelf life of biscuits. The conditions for the developed biscuits storage was determined by investigating of sorption isotherms and kinetics of reaching the equilibrium moisture content. Materials and Methods. The objects of study arenewly developed biscuits: "Health" (rich in iodine and with the replacement of 50 % sugar by stevioside, "Light" (with the replacement of 75% of sugar by stevioside and enriched with wheat bran, "Fortified" (containselamine, which is a natural source of iodine. Control – the biscuit prepared according to traditional recipes. Tenzometric method was used to study the sorption equilibrium moisture content. Differential function of pore radius distribution was determined using sorption isotherms and then have been subjected to approximation. Results. New biscuits samples are in the area of polymolecular and monomolecular sorption in the range of the relative air humidity (RAH from 10 to 75 ... 80%. The control sample has less distinct plot of monomolecular sorption (10 to 20% and short- moisture range wich is corresponding with polymolecularsorption (from 20 to 65 ... 70%. There is a moisture absorbtion ofmicrocapillary and swelling of samples when RAHincreases to 75 ... 80% for all the samples. The ratio of average pore radius tothe most likely of the test samples are differentthat wasshown by the investigation of differential function of pore distribution. So this ratio for biscuit "Health" is 5.73, for biscuit "Light" − 2.98,forbiscuit "Fortified"− 4.91 and for the control − 3.88. Conclusions. There’s the sense to store developed biscuits in a cardboard packaging with polymeric covering, if RAH is not more than 75%, and vapor-proof if RAH is above that.

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

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Svensson, Staffan

    2007-01-01

    In the cellular structure of wood, bound-water diffusion and water-vapor diffusion interact via sorption in a complex moisture-transportation system. At low relative humidities, moisture transport may be modeled by a Fickian diffusion equation with a good approximation. At higher relative......-35% in moisture content. Hence, for a precise moisture content computation, sorption hysteresis must be taken into account. The present paper explains the relation between sorption hysteresis and multi-Fickian moisture transport, and clarifies how models for the two phenomena are coupled. To illustrate...

  10. Thermodynamic Properties, Sorption Isotherms and Glass Transition Temperature of Cape Gooseberry (Physalis peruviana L.

    Directory of Open Access Journals (Sweden)

    Jessica López

    2014-01-01

    Full Text Available Adsorption and desorption isotherms of fresh and dried Cape gooseberry (Physalis peruviana L. were determined at three temperatures (20, 40 and 60 °C using a gravimetric technique. The data obtained were fitted to several models including Guggenheim-Anderson- De Boer (GAB, Brunauer-Emmett-Teller (BET, Henderson, Caurie, Smith, Oswin, Halsey and Iglesias-Chirife. A non-linear least square regression analysis was used to evaluate the models. The Iglesias-Chirife model fitted best the experimental data. Isosteric heat of sorption was also determined from the equilibrium sorption data using the Clausius-Clapeyron equation and was found to decrease exponentially with increasing moisture content. The enthalpy-entropy compensation theory was applied to the sorption isotherms and indicated an enthalpy-controlled sorption process. Glass transition temperature (Tg of Cape gooseberry was also determined by differential scanning calorimetry and modelled as a function of moisture content with the Gordon-Taylor, the Roos and the Khalloufi models, which proved to be excellent tools for predicting glass transition of Cape gooseberry.

  11. Determination of field-based sorption isotherms for Cd, Cu, Pb and Zn in Dutch soils

    NARCIS (Netherlands)

    Otte JG; Grinsven JJM van; Peijnenburg WJGM; Tiktak A; LBG; ECO

    1999-01-01

    Sorption isotherms for metals in soil obtained in the laboratory generally underpredict the observed metal content in the solid phase in the field. Isotherms based on in-situ data are therefore required. The aim of this study is to obtain field-based sorption isotherms for Cd, Cu, Pb and Zn as input

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

    DEFF Research Database (Denmark)

    Rode, Carsten; Hansen, Kurt Kielsgaard

    2011-01-01

    measurements of hysteresis and temperature dependency of the moisture sorption characteristics of three different porous building materials: aerated concrete, cement paste and spruce. Scanning curves are measured for all three materials where periods with adsorption and desorption interrupt each other...... intermittently. For one of the materials, aerated concrete, the sorption curves are determined at three different temperatures....

  13. Moisture Sorption in Artificially aged wood-plastic composites

    Science.gov (United States)

    B. Kristoffer Segerholm; Rebecca E. Ibach; Magnus E.P. Wålinder

    2012-01-01

    Moisture sorption in wood-plastic composites (WPCs) affects their durability and dimensional stability. In certain outdoor exposures, the moisture properties of WPCs are altered due to e.g. cracks induced by swelling and shrinkage of the components, as well as UV degradation or biological attack. The aim of this work was to study the effect of different artificial...

  14. Acquisition of sorption isotherms for modified woods by the use of dynamic vapour sorption instrumentation. Principles and Practice

    DEFF Research Database (Denmark)

    Engelund, Emil Tang; Klamer, Morten; Venås, Thomas Mark

    2010-01-01

    The complex wood-water relationship has been the topic of numerous studies. Sorption isotherms – in particular – have been derived for hundreds of wood species, their sap- and heartwood sections as well as for decayed, engineered and modified wood materials. However, the traditional methods...... for obtaining sorption isotherms are very time consuming. With new dynamic vapour sorption (DVS) instrumentation, the acquisition of data for constructing sorption isotherms is suddenly dramatically lowered. Where the traditional methods often required months, data can now be obtained in a matter of days...... depending on the number of data points required. The fast data acquisition makes DVS a useful tool in studying the sorption properties of wood, and especially in studying the effect of different modification treatments on these properties. This study includes an investigation of the sorption properties...

  15. Nonlinear chemical sorption isotherms in the assessment of nuclear fuel waste disposal

    International Nuclear Information System (INIS)

    Walker, J.R.; LeNeveu, D.M.

    1987-01-01

    Radionuclides emplaced in an underground disposal vault can possibly migrate from the vault, and through the geosphere, to enter Man's environment. Chemical sorption is a primary mechanism for retarding this migration. The effects of nonlinear chemical sorption isotherms on radionuclide transport are discussed. A method is given by which nonlinear isotherms can be approximated by the linear sorption isotherm used in the vault submodel. The relevance of nonlinear isotherms to transport in the geosphere is discussed, and it is shown that the linear isotherm model is conservative for deep geologic disposal. 22 refs

  16. Determination of drying kinetics and sorption isotherm of black pepper (Piper Nigrum)

    Science.gov (United States)

    De Vera, Flordeliza C.; Atienza, Vanessa Bernadette B.; Capili, Jomicah B.; Sauli, Zaliman

    2017-11-01

    In the present study of food products, determination of the drying characteristics of black pepper using an oven is not yet completely established. This study aimed to determine the drying kinetics and sorption isotherm of black pepper using a convective oven at 30°C, 40°C and 50°C. The data gathered in this study were used to fit in selected mathematical models for drying kinetics and sorption isotherm. Among these models, the Midilli model (MR=0.5338exp(0.7273t-0.0551)+-0.0005t for 30°C, MR=0.5814exp(0.6293t-0.0764)+ -0.0008t for 40°C and MR=0.3187exp(1.1777t-0.0466)+ -0.0011t for 50°C) was the best fit to explain the moisture transfer in black pepper, while the GAB Model (m/0.1302=((0.1906)(0.7811)aw)/(1-(0.7811)aw)[1-(0.7811)aw+(0.1906)(0.7811)aw])) was for the equilibrium moisture content and water activity relationship. After evaluating the data, the drying characteristics of black pepper at 40°C yielded better results than 30°C and 50°C. XLSTAT and ANOVA Add-in of Microsoft Excel was the software used to compute for the necessary values in the assessment of the mathematical models for this study.

  17. Limitations of sorption isotherms on modeling groundwater contaminant transport

    International Nuclear Information System (INIS)

    Silva, Eduardo Figueira da

    2007-01-01

    Design and safety assessment of radioactive waste repositories, as well as remediation of radionuclide contaminated groundwater require the development of models capable of accurately predicting trace element fate and transport. Adsorption of trace radionuclides onto soils and groundwater is an important mechanism controlling near- and far- field transport. Although surface complexation models (SCMs) can better describe the adsorption mechanisms of most radionuclides onto mineral surfaces by directly accounting for variability of system properties and mineral surface properties, isotherms are still used to model contaminant transport in groundwater, despite the much higher system dependence. The present work investigates differences between transport model results based on these two approaches for adsorption modeling. A finite element transport model is used for the isotherm model, whereas the computer program PHREEQC is used for the SCM approach. Both models are calibrated for a batch experiment, and one-dimensional transport is simulated using the calibrated parameters. At the lower injected concentrations there are large discrepancies between SCM and isotherm transport predictions, with the SCM presenting much longer tails on the breakthrough curves. Isotherms may also provide non-conservative results for time to breakthrough and for maximum concentration in a contamination plume. Isotherm models are shown not to be robust enough to predict transport behavior of some trace elements, thus discouraging their use. The results also illustrate the promise of the SCM modeling approach in safety assessment and environmental remediation applications, also suggesting that independent batch sorption measurements can be used, within the framework of the SCM, to produce a more versatile and realistic groundwater transport model for radionuclides which is capable of accounting more accurately for temporal and spatial variations in geochemical conditions. (author)

  18. Moisture ingress into electronics enclosures under isothermal conditions

    DEFF Research Database (Denmark)

    Staliulionis, Zygimantas; Jabbaribehnam, Mirmasoud; Hattel, Jesper Henri

    2016-01-01

    loads are still not understood well by design engineers, therefore this field has become one of the bottlenecks in the electronics system design. The objective of this paper is to model moisture ingress into an electronics enclosure under isothermal conditions. The moisture diffusion model is based......The number of electronics used in outdoor environment is constantly growing. The humidity causes about 19 % of all electronics failures and, especially, moisture increases these problems due to the ongoing process of miniaturization and lower power consumption of electronic components. Moisture...

  19. Non-isothermal Moisture Transport Through Insulation Materials

    DEFF Research Database (Denmark)

    Peuhkuri, Ruut Hannele; Rode, Carsten; Hansen, Kurt Kielsgaard

    2008-01-01

    An experimental investigation was conducted in order to draw some conclusions on the magnitude of moisture transport due to temperature gradient on a range of porous light-weight building materials. A special constructed non-isothermal set-up allowed the creation of a temperature gradient of 10K...... and given humidity gradient over the sample. The resulting moisture ux as well as the hygrothermal states around and within the material were monitored. The hypothesis of relative humidity being a driving force for non-isothermal moisture transport already in the hygroscopic range could not be confirmed....... On the contrary, indications exist that the temperature gradient itself is driving the moisture from the warm side towards the cold side. An attempt to identify and quantify the single contributions of the different transport forms involved is also presented. The diferent results gave, however, diverging...

  20. Moisture ingress into electronics enclosures under isothermal conditions

    International Nuclear Information System (INIS)

    Staliulionis, Ž.; Jabbari, M.; Hattel, J. H.

    2016-01-01

    The number of electronics used in outdoor environment is constantly growing. The humidity causes about 19 % of all electronics failures and, especially, moisture increases these problems due to the ongoing process of miniaturization and lower power consumption of electronic components. Moisture loads are still not understood well by design engineers, therefore this field has become one of the bottlenecks in the electronics system design. The objective of this paper is to model moisture ingress into an electronics enclosure under isothermal conditions. The moisture diffusion model is based on a 1D quasi-steady state (QSS) approximation for Fick’s second law. This QSS approach is also described with an electrical analogy which gives a fast tool in modelling of the moisture response. The same QSS method is applied to ambient water vapour variations. The obtained results are compared to an analytical solution and very good agreement is found.

  1. Sorption Isotherm Modelling Of Fermented Cassava Flour by Red Yeast Rice

    Science.gov (United States)

    Cahyanti, M. N.; Alfiah, M. N.; Hartini, S.

    2018-04-01

    The objective of the study is to determine the characteristic of moisture sorption isotherm from fermented cassava flour by red yeast rice using various modeling. This research used seven salt solutions and storage temperature of 298K, 303K, and 308K. The models used were Brunauer-Emmet-Teller (BET), Guggenheim-Anderson-de Boer (GAB) and Caurie model. The monolayer moisture content was around 4.51 – 5.99% db. Constant related to absorption heat in the multilayer area of [GAB model was around 0.86-0,91. Constant related to absorption heat in the monolayer area of GAB model was around 4.67-5.97. Constant related to absorption heat in the monolayer area of BET model was around 4.83-7.04. Caurie constant was around 1.25-1.59. The equilibrium and monolayer moisture content on fermented cassava flour by red yeast rice was decreasing as increasing temperature. GAB constant value indicated that the process of moisture absorption on the fermented cassava flour by red yeast rice categorized in type II.

  2. Moisture Sorption Characteristics of Dambu-nama – A Nigerian ...

    African Journals Online (AJOL)

    Moisture sorption characteristics of traditional Dambu-nama (control) (TDBN) and laboratory Dambu-nama (LDBN), a cooked, pounded, shredded and dried Nigerian meat product, were determined at four different temperatures (10oC, 20oC, 30oC and 40oC) and relative humidities of 10 – 96% using the standard static, ...

  3. Moisture sorption in mixtures of biopolymer, disaccharides and water

    NARCIS (Netherlands)

    Sman, van der R.G.M.

    2013-01-01

    The moisture sorption of ternary mixtures of biopolymer, sugar and water is investigated by means of the Free-Volume-Flory-Huggins (FVFH) theory. The earlier FVFH theory developed for binary mixtures of biopolymer/water and sugar/water has to be modified to account for two effects: 1) the change in

  4. Thermodynamic analysis of water vapor sorption isotherms and mechanical properties of selected paper-based food packaging materials.

    Science.gov (United States)

    Rhim, Jong-Whan; Lee, Jun Ho

    2009-01-01

    Adsorption isotherms of 3 selected paper-based packaging materials, that is, vegetable parchment (VP) paper, Kraft paper, and solid-bleached-sulfate (SBS) paperboard, were determined at 3 different temperatures (25, 40, and 50 degrees C). The GAB isotherm model was found to fit adequately for describing experimental adsorption isotherm data for the paper samples. The monolayer moisture content of the paper samples decreased with increase in temperature, which is in the range of 0.0345 to 0.0246, 0.0301 to 0.0238, and 0.0318 to 0.0243 g water/g solid for the MG paper, the Kraft paper, and the SBS paperboard, respectively. The net isosteric heats of sorption (q(st)) for the paper samples decreased exponentially with increase in moisture content after reaching the maximum values of 18.51, 27.39, and 26.80 kJ/mol for the VP paper, the Kraft paper, and the SBS paperboard, respectively, at low-moisture content. The differential enthalpy and entropy of 3 paper samples showed compensation phenomenon with the isokinetic temperature of 399.7 K indicating that water vapor had been adsorbed onto the paper samples with the same mechanism. Depending on the paper material, tensile strength of paper samples was affected by moisture content.

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

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per

    2016-01-01

    sorption isotherms of building materials, food, and other industrial products, knowledge about the 24 applicability of these functions for soils is noticeably lacking. We present validation of nine models for characterizing adsorption/desorption isotherms for a water activity range from 0.03 to 0...

  6. Thermodynamic properties of water sorption of jackfruit (Artocarpus heterophyllus Lam. as a function of moisture content

    Directory of Open Access Journals (Sweden)

    Ana Paula Prette

    2013-03-01

    Full Text Available The Jackfruit tree is one of the most significant trees in tropical home gardens and perhaps the most widespread and useful tree in the important genus Artocarpus. The fruit is susceptible to mechanical and biological damage in the mature state, and some people find the aroma of the fruit objectionable, particularly in confined spaces. The dehydration process could be an alternative for the exploitation of this product, and the relationship between moisture content and water activity provides useful information for its processing and storage. The aim of this study was to determine the thermodynamic properties of the water sorption of jackfruit (Artocarpus heterophyllus Lam. as a function of moisture content. Desorption isotherms of the different parts of the jackfruit (pulp, peduncle, mesocarp, peel, and seed were determined at four different temperatures (313.15, 323.15, 333.15, and 343.15 K in a water activity range of 0.02-0.753 using the static gravimetric method. Theoretical and empirical models were used to model the desorption isotherms. An analytical solution of the Clausius-Clapeyron equation was proposed to calculate the isosteric heat of sorption, the differential entropy, and Gibbs' free energy using the Guggenhein-Anderson-de Boer and Oswin models considering the effect of temperature on the hygroscopic equilibrium.

  7. Experiences of fitting isotherms to data from batch sorption experiments for radionuclides on tuffs

    International Nuclear Information System (INIS)

    Polzer, W.L.; Fuentes, H.R.

    1989-11-01

    Laboratory experiments have been performed on the sorption of radionuclides on tuff as site characterization information for the Yucca Mountain Project. This paper presents general observations on the results of curve-fitting of sorption data by isotherm equations and the effects of experimental variables on their regressional analysis. Observations are specific to the effectiveness and problems associated with fitting isotherms, the calculation and value of isotherm parameters, and the significance of experimental variables such as replication, particle size, mode of sorption, and mineralogy. These observations are important in the design of laboratory experiments to ensure that collected data are adequate for effectively characterizing sorption of radionuclides on tuffs or other materials. 13 refs., 2 figs., 4 tabs

  8. Model Based Control of Moisture Sorption in a Historical Interior

    Directory of Open Access Journals (Sweden)

    P. Zítek

    2005-01-01

    Full Text Available This paper deals with a novel scheme for microclimate control in historical exhibition rooms, inhibiting moisture sorption phenomena that are inadmissible from the preventive conservation point of view. The impact of air humidity is the most significant harmful exposure for a great deal of the cultural heritage deposited in remote historical buildings. Leaving the interior temperature to run almost its spontaneous yearly cycle, the proposed non-linear model-based control protects exhibits from harmful variations in moisture content by compensating the temperature drifts with an adequate adjustment of the air humidity. Already implemented in a medieval interior since 1999, the proposed microclimate control has proved capable of permanently maintaining constant a desirable moisture content in organic or porous materials in the interior of a building. 

  9. Nitrate sorption on activated carbon modified with CaCl2: Equilibrium, isotherms and kinetics

    Directory of Open Access Journals (Sweden)

    Zanella Odivan

    2015-01-01

    Full Text Available In this study, nitrate (NO3- removal from aqueous solutions was investigated using granular activated carbon (GAC modified with CaCl2. Batch sorption studies were performed as a function of sorbent dose, initial nitrate concentration and pH. Sorption was maximized between pH 3 and 9. Studies on the effect of pH showed that the ion exchange mechanism might be involved in the sorption process. The percentage of nitrate removed increased with increasing sorbent concentration, and the ideal sorbent dose was found to be 20 g•L-1. Four isotherm models-Langmuir, Freundlich, Redlich-Peterson and Sips-were used to fit the experimental data. The Redlich-Peterson isotherm model explained the sorption process well and showed the best coefficient of determination (0.9979 and Chi-square test statistic (0.0079. Using the Sips isotherm model, the sorption capacity (qe was found to be 1.93 mg nitrate per g of sorbent. Kinetic experiments indicated that sorption was a fast process, reaching equilibrium within 120 min. The nitrate sorption kinetic data were successfully fitted to a pseudo-second-order kinetic model. The overall results demonstrated potential applications of modified GAC for nitrate removal from aqueous solutions.

  10. Considerations about the correct evaluation of sorption thermodynamic parameters from equilibrium isotherms

    International Nuclear Information System (INIS)

    Salvestrini, Stefano; Leone, Vincenzo; Iovino, Pasquale; Canzano, Silvana; Capasso, Sante

    2014-01-01

    Highlights: • Different methods to derive sorption thermodynamic parameters have been discussed. • ΔG° and, ΔS° values depend on the selected standard states. • Isosteric heat values help in evaluating the applicability of the sorption models. -- Abstract: This is a comparative analysis of popular methods currently in use to derive sorption thermodynamic parameters from temperature dependence of sorption isotherms. It is emphasized that the standard and isosteric thermodynamic parameters have sharply different meanings. Moreover, it is shown with examples how the sorption model adopted conditions the standard state and consequently the value of ΔG° and ΔS°. These trivial but often neglected aspects should carefully be considered when comparing thermodynamic parameters from different literature sources. An effort by the scientific community is needed to define criteria for the choice of the standard state in sorption processes

  11. A Study of Moisture Sorption and Dielectric Processes of Starch and Sodium Starch Glycolate : Theme: Formulation and Manufacturing of Solid Dosage Forms Guest Editors: Tony Zhou and Tonglei Li.

    Science.gov (United States)

    Hiew, Tze Ning; Huang, Rongying; Popov, Ivan; Feldman, Yuri; Heng, Paul Wan Sia

    2017-12-01

    This study explored the potential of combining the use of moisture sorption isotherms and dielectric relaxation profiles of starch and sodium starch glycolate (SSG) to probe the location of moisture in dried and hydrated samples. Starch and SSG samples, dried and hydrated, were prepared. For hydrated samples, their moisture contents were determined. The samples were probed by dielectric spectroscopy using a frequency band of 0.1 Hz to 1 MHz to investigate their moisture-related relaxation profiles. The moisture sorption and desorption isotherms of starch and SSG were generated using a vapor sorption analyzer, and modeled using the Guggenheim-Anderson-de Boer equation. A clear high frequency relaxation process was detected in both dried and hydrated starches, while for dried starch, an additional slower low frequency process was also detected. The high frequency relaxation processes in hydrated and dried starches were assigned to the coupled starch-hydrated water relaxation. The low frequency relaxation in dried starch was attributed to the local chain motions of the starch backbone. No relaxation process associated with water was detected in both hydrated and dried SSG within the frequency and temperature range used in this study. The moisture sorption isotherms of SSG suggest the presence of high energy free water, which could have masked the relaxation process of the bound water during dielectric measurements. The combined study of moisture sorption isotherms and dielectric spectroscopy was shown to be beneficial and complementary in probing the effects of moisture on the relaxation processes of starch and SSG.

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

    Science.gov (United States)

    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.

  13. Water sorption isotherms of skimmed milk powder within the temperature range of 5–20 °C

    Directory of Open Access Journals (Sweden)

    Jitka Langová

    2012-01-01

    Full Text Available Moisture sorption isotherms (MSI’s of skimmed milk powder in the temperature range of 5–20 °C were determined using manometric method. MSI’s, which show the water content versus water activity (Aw at a constant temperature, are used to describe relationships between water content and equilibrium state relative vapour pressure (RVP. The equilibrium moisture content (EMC of skimmed milk powder samples is growing with an increase of Aw at a constant temperature both for water adsorption and desorption. Isotherms were found to be type II of Brunauer-Emmett-Teller classification. It is the type most common for foods. The shape of created isotherms was sigmoid. Structural modifications of crystals were observed during adsorption in the microscope, too. Critical value of EMC of tested samples corresponding to the Aw equal to 0.6 for adsorption was 6.50% MC (w.b. at temperature 5 °C, 9.15% MC (w.b. at temperature 10 °C, and 7.71% MC (w.b. at temperature 20 °C. These values determine optimal conditions for storage from the point of view microorganisms grow, Aw<0.6.

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

    Directory of Open Access Journals (Sweden)

    A. O. Dada

    2013-01-01

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

  15. Moisture sorption and thermal characteristics of polyaramide blend fabrics

    OpenAIRE

    Genç, Gözde; Alp, Burcu; Balköse, Devrim; Ülkü, Semra; Cireli, Aysun

    2006-01-01

    Four types of fabrics woven from various polyaramid fibers of Nomex and Kevlar blends were characterized by morphology, XRD, elemental analysis, thermal analysis, and moisture adsorption isotherms. The blends consisted of Polybenzimidazole/ Kevlar blend (40% FBI and 60% Kevlar®), Nomex Delta A (blend of 60% Kevlar and 40% Nomex®), Nomex Delta T (blend of 75% Nomex, 23% Kevlar, and 2% P140 antistatic fiber), and Nomex III (fabric with a 95/5 blend of Nomex and Kevlar) containing 1% steel fiber...

  16. Gas Permeation Related to the Moisture Sorption in Films of Glassy Hydrophilic Polymers

    NARCIS (Netherlands)

    Laksmana, F. L.; Kok, P. J. A. Hartman; Frijlink, H. W.; Vromans, H.; Maarschalk, K. Van Der Voort

    2010-01-01

    The purpose of this article is to elucidate the effect of integral sorption of moisture on gas permeation in glassy hydrophilic polymers. The oxygen and the simultaneous moisture sorption into various hydroxypropyl methylcellulose (HPMC) films were measured under a wide range of relative humidities

  17. Studies of Dye Sensitisation Kinetics and Sorption Isotherms of Direct Red 23 on Titania

    Directory of Open Access Journals (Sweden)

    Peter J. Holliman

    2008-01-01

    Full Text Available Sorption kinetics and isotherms have been measured for a commercial dye (Direct Red 23 on different samples of powdered Titania, and the data were analysed to better understand the dye sensitization process for dye sensitised solar cells (DSSCs. For the sorption kinetics, the data show rapid initial sorption (<1 hour followed by slower rate of increasing uptake between 1 and 24 hours. While higher initial concentrations of dye correspond to higher sorption overall, less dye is absorbed from higher initial dye concentrations when considered as percentage uptake. The correlation between the sorption data and model isotherms has been considered with time. The Langmuir model shows better correlations compared to the Freundlich isotherm. The dye uptake data has also been correlated with Titania characterization data (X-ray diffraction, scanning electron microscopy, BET and zero point charge analysis. Kinetic data show significantly better fits to second-order models compared to first order. This suggests that chemisorption is taking place and that the interaction between the dye sorbate and the Titania sorbent involves electron sharing to form an ester bond.

  18. Isothermal titration calorimetry of sorption processes. A promising approach

    Energy Technology Data Exchange (ETDEWEB)

    Jordan, Norbert; Foerstendorf, Harald [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes; Drobot, B. [Technische Univ. Dresden (Germany); Fahmy, Karim [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Biophysics; Reder, Christian

    2017-06-01

    As a consequence of nuclear waste disintegration heat, elevated temperatures in the near field may influence radionuclide retention significantly. However, there is a nearly complete lack of spectroscopic investigations of sorption processes at elevated temperatures. In addition, experimental data on free Gibbs energy (Δ{sub R}G), enthalpy (Δ{sub R}H) and entropy (Δ{sub R}S) of reactions of most radionuclides including fission products such as {sup 79}Se are sparse. Using the Se(IV)/hematite system, we show that microcalorimetry can provide these thermodynamic parameters with high accuracy and in a manner that allows studying various radionuclides.

  19. Moisture Sorption Behaviour and Mould Ecology of Trade Garri Sold in South Eastern Nigeria

    Directory of Open Access Journals (Sweden)

    Tochukwu Samuel

    2014-01-01

    Full Text Available 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.

  20. A study of sorption mechanism onto cement hydrates by isotherm measurements

    International Nuclear Information System (INIS)

    Sugiyama, Daisuke; Fujita, Tomonari

    2003-01-01

    In the concept for TRU waste disposal in Japan, cement is a potential waste packaging and backfilling material and is expected to provide chemical containment. In particular, the sorption of radionuclides onto cement material, which controls the aqueous concentrations of elements in the porewater, is a very important parameter when considering the release of radionuclides from the near field of a repository. Many safety assessment calculations currently assume radionuclide retardation as linear sorption equilibrium and describe it with a distribution ratio (R d value). In this study, the sorption mechanism is discussed by measuring the sorption isotherm of caesium, strontium and thorium onto Ordinary Portland Cement (OPC) and Calcium Silicate Hydrate (C-S-H gel), to justify and support this assumption. In addition, the effect of competitive sorption between thorium and uranium and other groundwater ions is studied by examining sorption using a range of sodium chloride concentrations to simulate different groundwater ionic strengths. Based on the experimental results, we have showed that: Caesium and strontium sorb by substitution for Ca in C-S-H phases and the presence of some calcium sites with different ion-exchange log K values is suggested; Thorium would be fixed in a surface co-precipitation to form a solubility-limiting phase. The results of sorption experiments are reasonably well modelled by the ion-exchange model for caesium and strontium and the surface co-precipitation model for thorium, respectively. (author)

  1. Adsorption-desorption isotherms and heat of sorption of prickly pear fruit (Opuntia ficus indica)

    International Nuclear Information System (INIS)

    Lahsasni, S.; Kouhila, M.; Mahrouz, M.

    2004-01-01

    The equilibrium moisture contents were determined for prickly pear fruit using the gravimetric static method at t=30, 40 and 50 deg. C over a range of relative humidities from 0.05 to 0.9. The sorption curves of prickly pear fruit decreased with increase in temperature at constant relative humidity. The hysteresis effect was observed. The GAB, modified Halsey, modified Chung-Pfost, modified Oswin and modified Henderson models were tested to fit the experimental data. The GAB model was found to be the most suitable for describing the sorption curves. The monolayer moisture content values for the sorption at different temperatures are calculated using a modified BET equation. The isosteric heats of desorption and adsorption of water were determined from the equilibrium data at different temperatures

  2. Adsorption-desorption isotherms and heat of sorption of prickly pear fruit (Opuntia ficus indica)

    Energy Technology Data Exchange (ETDEWEB)

    Lahsasni, S.; Kouhila, M. E-mail: kouhila@hotmail.com; Mahrouz, M

    2004-01-01

    The equilibrium moisture contents were determined for prickly pear fruit using the gravimetric static method at t=30, 40 and 50 deg. C over a range of relative humidities from 0.05 to 0.9. The sorption curves of prickly pear fruit decreased with increase in temperature at constant relative humidity. The hysteresis effect was observed. The GAB, modified Halsey, modified Chung-Pfost, modified Oswin and modified Henderson models were tested to fit the experimental data. The GAB model was found to be the most suitable for describing the sorption curves. The monolayer moisture content values for the sorption at different temperatures are calculated using a modified BET equation. The isosteric heats of desorption and adsorption of water were determined from the equilibrium data at different temperatures.

  3. A study of the water vapor sorption isotherms of hardened cement pastes: Possible pore structure changes at low relative humidity and the impact of temperature on isotherms

    DEFF Research Database (Denmark)

    Wu, Min; Johannesson, Björn; Geiker, Mette Rica

    2014-01-01

    cement paste samples and a model material MCM-41. The pronounced impact of temperature on desorption isotherms of cement based materials as reported in literature was not found in this investigation. The results suggest that the differences between the sorption isotherms measured at different...

  4. Summary report on the evaluation of a 1977--1985 edited sorption data base for isotherm modeling

    International Nuclear Information System (INIS)

    Polzer, W.L.; Beckman, R.J.; Fuentes, H.R.; Yong, C.; Chan, P.; Rao, M.G.

    1993-01-01

    Sorption data bases collected by Los Alamos National Laboratory (LANL) from 1977 to 1985 for the Yucca Mountain Project.(YMP) have been inventoried and fitted with isotherm expressions. Effects of variables (e.g., particle size) on the isotherm were also evaluated. The sorption data are from laboratory batch measurements which were not designed specifically for isotherm modeling. However a limited number of data sets permitted such modeling. The analysis of those isotherm data can aid in the design of future sorption experiments and can provide expressions to be used in radionuclide transport modeling. Over 1200 experimental observations were inventoried for their adequacy to be modeled b isotherms and to evaluate the effects of variables on isotherms. About 15% of the observations provided suitable data sets for modeling. The data sets were obtained under conditions that include ambient temperature and two atmospheres, air and CO 2

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

    Energy Technology Data Exchange (ETDEWEB)

    Bonner, Ian J. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Thompson, David N. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Teymouri, Farzaneh [Michigan Biotechnology Inst., Lansing, MI (United States); Campbell, Timothy [Michigan Biotechnology Inst., Lansing, MI (United States); Bals, Bryan [Michigan Biotechnology Inst., Lansing, MI (United States); Tumuluru, Jaya Shankar [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    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.

  6. Effective moisture diffusivity, moisture sorption, thermo-physical properties and infrared drying kinetics of germinated paddy

    Directory of Open Access Journals (Sweden)

    Supawan Tirawanichakul

    2014-02-01

    Full Text Available Temperature and relative humidity (RH dependence of moisture sorption phenomena for agricultural products provide valuable information related to the thermodynamics of the system. So the equilibrium moisture contents (EMC, effective moisture diffusivity (Deff and thermo-physical properties in terms of void fraction, specific heat capacity, and the apparent density of germinated non-waxy Suphanburi 1 paddy were evaluated. Five commonly cited EMC equations were fitted to the experimental data among temperatures of 40-60°C correlating with RH of 0-90%. The results showed that the modified GAB equation was the best function for describing experimental results while those evaluated thermo-physical properties depended on moisture content. To determine drying kinetics model, the simulated values using Midilli et al. (2002 model and Page’s model was the best fitting to exact drying kinetics values for infrared (IR and hot air (HA drying, respectively. Finally, the Deff value of paddy dried with IR and HA sources were also evaluated and the calculated Deff value of both HA and IR drying was in order of 10-9 m2/s.

  7. A new method to determine the water activity and the net isosteric heats of sorption for low moisture foods at elevated temperatures.

    Science.gov (United States)

    Tadapaneni, Ravi Kiran; Yang, Ren; Carter, Brady; Tang, Juming

    2017-12-01

    In recent years, research studies have shown that the thermal resistance of foodborne pathogens in the low moisture foods is greatly influenced by the water activity (a w ) at temperatures relevant to thermal treatments for pathogen control. Yet, there has been a lack of an effective method for accurate measurement of a w at those temperatures. Thus, the main aim of this study was to evaluate a new method for measuring a w of food samples at elevated temperatures. An improved thermal cell with a relative humidity and temperature sensor was used to measure the a w of the three different food samples, namely, organic wheat flour, almond flour, and non-fat milk powder, over the temperature range between 20 and 80°C. For a constant moisture content, the a w data was used to estimate the net isosteric heat of sorption (q st ). The q st values were then used in the Clausius Clapeyron equation (CCE) equation to estimate the moisture sorption isotherm for all test food samples at different temperatures. For all the tested samples of any fixed moisture content, a w value generally increased with the temperature. The energy for sorption decreased with increasing moisture content. With the experimentally determined q st value, CCE describes well about the changes in a w of the food samples between 20 and 80°C. This study presents a method to obtain a w of a food sample for a specific moisture content at different temperatures which could be extended to obtain q st values for different moisture contents and hence, the moisture sorption isotherm of a food sample at different temperatures. Copyright © 2017 Elsevier Ltd. All rights reserved.

  8. Dynamic Moisture Sorption and Desorption in Fumed Silica-filled Silicone Foam

    Energy Technology Data Exchange (ETDEWEB)

    Trautschold, Olivia Carol [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-09-02

    Characterizing dynamic moisture sorption and desorption in fumed silica-filled silicone foam is necessary for determining material compatibilities and life predictions, particularly in sealed environments that may be exposed to a range of environmental conditions. Thermogravimetric analysis (TGA) and near infrared spectroscopy (NIR) were performed on S5470 fumed silica-filled silicone foam to determine the weight percent of moisture at saturation. Additionally, TGA was used to determine the time, temperature, and relative humidity levels required for sorption and desorption of physisorbed moisture in S5470.

  9. Isotherms and isosteric heat of sorption of two varieties of Peruvian quinoa

    Directory of Open Access Journals (Sweden)

    Augusto Pumacahua-Ramos

    2016-01-01

    Full Text Available The isosteric heats of sorption of two varieties of quinoa (Chenopodium quinoaWilld. grain were determined by the static gravimetric method at four temperatures (40, 50, 60 and 70 °C andin relative humidity environments provided by six saturated salt solutions. Six mathematical equations were used to model the experimental data: GAB, Oswin, Henderson, Peleg, Smith and Halsey. The isosteric heat of sorption was determined using the parameters of the GAB model. All the equations were shown to be appropriate by the coefficients of determination (R2 and the mean absolute error (MA%E. The influence of temperature was observed because the adsorption of water by the grains was lower at highertemperatures. The equilibrium moisture contents for security of storage, for long periods of time at water activity lower than 0.65, were 12 -13%. The effect of temperature on the parameters of the GAB model was analysed using the exponential Arrhenius equation. The isosteric heats of sorption were determined by applying the Clausius-Clapeyron equation as a function of humidity. The isosteric heat at 5% moisture for grains of the Blanca de Juli variety was 3663 kJ/kg and for the Pasankalla variety it was 3393 kJ/kg. The experimental data for isosteric heat as a function of humidity were satisfactorily modelled using three mathematical equations.

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

    Science.gov (United States)

    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. Copyright © 2014 Elsevier Ltd. All rights reserved.

  11. Effectiveness of Protective Action of Coatings from Moisture Sorption into Surface Layer of Sand Moulds

    Directory of Open Access Journals (Sweden)

    Kaźnica N.

    2016-12-01

    Full Text Available The results of investigations of the sorption process of surface layers of sand moulds covered by zirconium and zirconium - graphite alcohol coatings are presented in the paper. Investigations comprised two kinds of sand grains (silica sand and reclaimed sand of moulding sand with furan resin. Tests were performed under conditions of a high relative air humidity 75 - 85% and a constant temperature within the range 28 – 33°C. To evaluate the effectiveness of coatings protective action from moisture penetration into surface layers of sand moulds gravimetric method of quantitavie moisture sorption and ultrasonic method were applied in measurements.

  12. Sorption of Lead (Pb from Aqueous Solutions by Sepiolite and Bentonite Modified with Chitosan Biopolymers: Isotherms and Kinetics

    Directory of Open Access Journals (Sweden)

    Hamid Reza Rafiei

    2016-07-01

    Full Text Available In this study, sepiolite and bentonite clay minerals were modified with a natural chitosan biopolymer and the modified-clays were characterized using XRF, XRD, FTIR, SEM, and TOC analyses. The isothermal and kinetic parameters of lead (Pb sorption by both the minerals and the modified-minerals were determined in a batch mode under various conditions such as different contact times and initial concentrations of Pb. It was found that the Freundlich model described well the isotherm experimental data of Pb sorption by the sorbents. Modification with chitosan, however, decreased the Pb adsorption capacity of sepiolite from 83 to 27 mg g-1 and that of bentonite from 56 to 29 mg g-1. Kinetic results showed that more than 24 hours was required for Pb sorption by the natural clays to reach equilibrium, while the equilibrium time reduced to 16 and 4 hours for Pb sorption on chitosan-sepiolite and chitosan–bentonite, respectively. The pseudo-second-order model well described the time-dependent Pb sorption data by sepiolite, chitosan-sepiolite, and chitosan-bentonite, suggesting that chemical sorption is the rate-limiting step of Pb adsorption mechanism. The Pb sorption data by bentonite showed the best fit with Elovich model.

  13. Incorporating classic adsorption isotherms into modern surface complexation models: implications for sorption of radionuclides

    International Nuclear Information System (INIS)

    Kulik, D.A.

    2005-01-01

    Full text of publication follows: Computer-aided surface complexation models (SCM) tend to replace the classic adsorption isotherm (AI) analysis in describing mineral-water interface reactions such as radionuclide sorption onto (hydr) oxides and clays. Any site-binding SCM based on the mole balance of surface sites, in fact, reproduces the (competitive) Langmuir isotherm, optionally amended with electrostatic Coulomb's non-ideal term. In most SCM implementations, it is difficult to incorporate real-surface phenomena (site heterogeneity, lateral interactions, surface condensation) described in classic AI approaches other than Langmuir's. Thermodynamic relations between SCMs and AIs that remained obscure in the past have been recently clarified using new definitions of standard and reference states of surface species [1,2]. On this basis, a method for separating the Langmuir AI into ideal (linear) and non-ideal parts [2] was applied to multi-dentate Langmuir, Frumkin, and BET isotherms. The aim of this work was to obtain the surface activity coefficient terms that make the SCM site mole balance constraints obsolete and, in this way, extend thermodynamic SCMs to cover sorption phenomena described by the respective AIs. The multi-dentate Langmuir term accounts for the site saturation with n-dentate surface species, as illustrated on modeling bi-dentate U VI complexes on goethite or SiO 2 surfaces. The Frumkin term corrects for the lateral interactions of the mono-dentate surface species; in particular, it has the same form as the Coulombic term of the constant-capacitance EDL combined with the Langmuir term. The BET term (three parameters) accounts for more than a monolayer adsorption up to the surface condensation; it can potentially describe the surface precipitation of nickel and other cations on hydroxides and clay minerals. All three non-ideal terms (in GEM SCMs implementation [1,2]) by now are used for non-competing surface species only. Upon 'surface dilution

  14. The impact of non-isothermal soil moisture transport on evaporation fluxes in a maize cropland

    Science.gov (United States)

    Shao, Wei; Coenders-Gerrits, Miriam; Judge, Jasmeet; Zeng, Yijian; Su, Ye

    2018-06-01

    The process of evaporation interacts with the soil, which has various comprehensive mechanisms. Multiphase flow models solve air, vapour, water, and heat transport equations to simulate non-isothermal soil moisture transport of both liquid water and vapor flow, but are only applied in non-vegetated soils. For (sparsely) vegetated soils often energy balance models are used, however these lack the detailed information on non-isothermal soil moisture transport. In this study we coupled a multiphase flow model with a two-layer energy balance model to study the impact of non-isothermal soil moisture transport on evaporation fluxes (i.e., interception, transpiration, and soil evaporation) for vegetated soils. The proposed model was implemented at an experimental agricultural site in Florida, US, covering an entire maize-growing season (67 days). As the crops grew, transpiration and interception became gradually dominated, while the fraction of soil evaporation dropped from 100% to less than 20%. The mechanisms of soil evaporation vary depending on the soil moisture content. After precipitation the soil moisture content increased, exfiltration of the liquid water flow could transport sufficient water to sustain evaporation from soil, and the soil vapor transport was not significant. However, after a sufficient dry-down period, the soil moisture content significantly reduced, and the soil vapour flow significantly contributed to the upward moisture transport in topmost soil. A sensitivity analysis found that the simulations of moisture content and temperature at the soil surface varied substantially when including the advective (i.e., advection and mechanical dispersion) vapour transport in simulation, including the mechanism of advective vapour transport decreased soil evaporation rate under wet condition, while vice versa under dry condition. The results showed that the formulation of advective soil vapor transport in a soil-vegetation-atmosphere transfer continuum can

  15. An investigation of the moisture sorption and permeability properties of mill-fabricated oriented strandboard

    Science.gov (United States)

    Timusk, Paul Christopher

    This thesis brings the disciplines of Building Science and Wood Science together in the study of the moisture-related properties of oriented strand board (OSB). Using controlled mill-manufactured panels specifically made for this project, this research reveals how the sorption and permeance properties of OSB are affected by several variables including production parameters and physical panel properties, moisture-history, and relative humidity exposure. Since OSB varies in composition through its thickness, this study isolated and tested various core and surface components. Permeability and sorption properties of individual OSB layers, intact panel sections, and panel sections that had undergone cyclic wetting and drying or relative humidity cycling prior to testing, were evaluated. After laboratory testing and analysis, a set of OSB permeance and sorption values were entered into the material database of a finite-element hygrothermal computer modeling program. Relying on this data, a series of hygrothermal wall simulations were carried out using standard wall sections exposed to various climate conditions found throughout North America. These simulations revealed that the results vary widely depending upon the permeance and sorption values used. Thus the common practice of characterizing a range of OSB products with various moisture histories by using a single permeance or sorption value may not be wise.

  16. [Study on moisture sorption process model and application traditional Chinese medicine extract powder].

    Science.gov (United States)

    Lin, Tingting; He, Yan; Xiao, Xiong; Yuan, Liang; Rao, Xiaoyong; Luo, Xiaojian

    2010-04-01

    Study on the moisture sorption process characteristics of traditional Chinese medicine extract powder, to establish a mathematical model, provide a new method for in-depth study for moisture sorption behavior of traditional Chinese medicine extract powder and a reference for determine the production cycle, and predict product stability. Analyzed moisture absorption process of traditional Chinese medicine extract powder by utilized the law of conservation of mass and Fick's first law to establish the double exponential absorption model, fitted the moisture absorption data and compared with other commonly used five kinds of model to estimate the double-exponential absorption model. The statistical analysis showed that the coefficient of determination (R2) of double exponential model, Weibull distribution model and first order kinetics model were large, but the residues sum of squares (RSS) and AIC values were small. Synthesized the practical application meaning, we consided that the double exponential model was more suitable for simulating the process of Chinese medicine extract powder moisture absorption. The double exponential is suitable for characterization the process of traditional Chinese medicine extract moisture absorption.

  17. Dynamic moisture sorption characteristics of enzyme-resistant recrystallized cassava starch.

    Science.gov (United States)

    Mutungi, Christopher; Schuldt, Stefan; Onyango, Calvin; Schneider, Yvonne; Jaros, Doris; Rohm, Harald

    2011-03-14

    The interaction of moisture with enzyme-resistant recrystallized starch, prepared by heat-moisture treatment of debranched acid-modified or debranched non-acid-modified cassava starch, was investigated in comparison with the native granules. Crystallinities of the powdered products were estimated by X-ray diffraction. Moisture sorption was determined using dynamic vapor sorption analyzer and data fitted to various models. Percent crystallinities of native starch (NS), non-acid-modified recrystallized starch (NAMRS), and acid-modified recrystallized starch (AMRS) were 39.7, 51.9, and 56.1%, respectively. In a(w) below 0.8, sorption decreased in the order NS > NAMRS > AMRS in line with increasing sample crystallinities but did not follow this crystallinity dependence at higher a(w) because of condensation and polymer dissolution effects. Adsorbed moisture became internally absorbed in NS but not in NAMRS and AMRS, which might explain the high resistance of the recrystallized starches to digestion because enzyme and starch cannot approach each other over fairly sufficient surface at the molecular level.

  18. Sorption of alkylphenols on Ebro River sediments: Comparing isotherms with field observations in river water and sediments

    Energy Technology Data Exchange (ETDEWEB)

    Navarro, Alicia [Center of Applied Geoscience, University of Tuebingen, Sigwartstrasse 10, 72076 Tuebingen (Germany); Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18-26, 08034 Barcelona (Spain)], E-mail: anoqam@iiqab.csic.es; Endo, Satoshi; Gocht, Tilman [Center of Applied Geoscience, University of Tuebingen, Sigwartstrasse 10, 72076 Tuebingen (Germany); Barth, Johannes A.C. [Center of Applied Geoscience, University of Tuebingen, Sigwartstrasse 10, 72076 Tuebingen (Germany); Lehrstuhl fuer Angewandte Geologie, GeoZentrum Nordbayern, Universitaet Erlangen-Nuernberg, Schlossgarten 5, 91054 Erlangen (Germany); Lacorte, Silvia [Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18-26, 08034 Barcelona (Spain); Barcelo, Damia [Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18-26, 08034 Barcelona (Spain); Institut Catala de Recerca de l' Aigua (ICRA), Parc Cientific i Tecnologic de la Universitat de Girona, Pic de Peguera, 15, 17003 Girona (Spain); Grathwohl, Peter [Center of Applied Geoscience, University of Tuebingen, Sigwartstrasse 10, 72076 Tuebingen (Germany)

    2009-02-15

    This study reports sorption isotherms of the endocrine disruptors nonylphenol (NP) and octylphenol (OP) in three sediment samples from the Ebro River basin (NE Spain), with organic carbon fractions (f{sub OC}) ranging from 0.0035 to 0.082 g{sub OC} g{sup -1}. All isotherms were fitted to the Freundlich model with slightly nonlinear exponents ranging from 0.80 to 0.94. The solubility of the compounds as well as the organic carbon (OC) content had the strongest influences on the sorption behavior of these compounds. Comparison of the laboratory-spiked samples with the native contamination of NP of 45 water and concurrent sediment samples resulted in reasonable matches between both data sets, even though the lowest concentrations in the field were not completely reached in laboratory tests. This good agreement indicates that sorption laboratory data can be extrapolated to environmental levels and therefore the distribution of nonylphenol between sediments and water can be predicted with a precision of one order of magnitude. Furthermore, laboratory experiments with simultaneous loading of NP and OP revealed negligible competition for sorption sites at low concentrations. - Laboratory sorption of nonylphenol compared to field concentrations showed good agreements.

  19. Sorption of alkylphenols on Ebro River sediments: Comparing isotherms with field observations in river water and sediments

    International Nuclear Information System (INIS)

    Navarro, Alicia; Endo, Satoshi; Gocht, Tilman; Barth, Johannes A.C.; Lacorte, Silvia; Barcelo, Damia; Grathwohl, Peter

    2009-01-01

    This study reports sorption isotherms of the endocrine disruptors nonylphenol (NP) and octylphenol (OP) in three sediment samples from the Ebro River basin (NE Spain), with organic carbon fractions (f OC ) ranging from 0.0035 to 0.082 g OC g -1 . All isotherms were fitted to the Freundlich model with slightly nonlinear exponents ranging from 0.80 to 0.94. The solubility of the compounds as well as the organic carbon (OC) content had the strongest influences on the sorption behavior of these compounds. Comparison of the laboratory-spiked samples with the native contamination of NP of 45 water and concurrent sediment samples resulted in reasonable matches between both data sets, even though the lowest concentrations in the field were not completely reached in laboratory tests. This good agreement indicates that sorption laboratory data can be extrapolated to environmental levels and therefore the distribution of nonylphenol between sediments and water can be predicted with a precision of one order of magnitude. Furthermore, laboratory experiments with simultaneous loading of NP and OP revealed negligible competition for sorption sites at low concentrations. - Laboratory sorption of nonylphenol compared to field concentrations showed good agreements

  20. Fluoride Sorption Efficiency of Vermiculite Functionalised with Cationic Surfactant: Isotherm and Kinetics

    Directory of Open Access Journals (Sweden)

    Tayo Oladipo Ologundudu

    2016-09-01

    Full Text Available Groundwater is a major source of water, especially in rural communities. The presence of excess fluoride in groundwater has been a health concern for many decades because it causes fluorosis. The persistence of this problem led to the development of several approaches for reducing fluoride in groundwater to ≤1.5 mg/L, which is the World Health Organization’s (WHO permissible limit. Despite recorded success in fluoride reduction, drawbacks such as cost and efficiency have remained apparent, thus necessitating further research on defluoridation. This paper aims at assessing the defluoridation capacity of a clay mineral, vermiculite, when modified with the cationic surfactant hexadecyltrimethylammonium bromide. The effects of experimental parameters such as pH, agitation time, mass of adsorbent, and temperature were examined to determine the most favourable adsorption conditions. Using batch technique, the results showed a fluoride sorption of 51% from an 8 mg/L fluoride solution. The adsorption conformed more to Freundlich than Langmuir isotherm with an adsorption capacity of 2.36 mg/g, while the kinetics conformed to a pseudo-second-order reaction. pH emerged as the most influential factor in optimisation. The findings of this study indicated that modified vermiculite could be efficient in reducing fluoride in groundwater to more tolerable limits, but requires adequate pH control.

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

    Energy Technology Data Exchange (ETDEWEB)

    Björklund, Sebastian, E-mail: sebastianbjorklund@gmail.com; Kocherbitov, Vitaly [Department of Biomedical Science, Faculty of Health and Society, Malmö University, Malmö (Sweden); Biofilms—Research Center for Biointerfaces, Malmö University, Malmö (Sweden)

    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.

  2. A hygroscopic method to measure the adsorption isotherm of porous construction materials

    NARCIS (Netherlands)

    Taher, A.; Zanden, van der A.J.J.; Brouwers, H.J.H.; Stephan, D.; Daake, von H.; Markl, V.; Land, G.

    2013-01-01

    A sorption isotherm is the relationship between the moisture content in a material and the relative humidity of the surrounding atmosphere in an equilibrium situation. Most often, the sorption isotherm is measured with a gravitational method. This work presents a method to measure the adsorption

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

    Science.gov (United States)

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

    2016-07-15

    The correlation between octanol-water partition coefficient (KOW) and the transport of aqueous samples containing single organic compound is well documented. The concept of the KOW of river water containing the mixture of organics was evolved by Pradhan et al. (2015). The present study aims at determining the KOW and sorption parameters of synthetic aqueous samples and river water to finding out the correlation, if any. The laboratory scale columns packed with aquifer materials were fed with synthetic and river water samples. Under the operating conditions, the compounds in the samples did not separate, and all the samples that contain more than one organic compound yielded a single breakthrough curve. Breakthrough curves simulated from sorption isotherms were compared with those from the column runs. The sorption parameters such as retardation factor (Rf), height of mass transfer zone (HMTZ), rate of mass transfer zone (RMTZ), breakpoint column capacity (qb) and maximum column capacity (qx) estimated from column runs, sorption isotherms and models developed by Yoon-Nelson, Bohart-Adam and Thomas were in agreement. The empirical correlations were found between the KOW and sorption parameters. The transport of the organics measured as dissolved organic carbon (DOC) through the aquifer can be predicted from the KOW of the river water and other water samples. The novelty of the study is to measure KOW and to envisage the fate of the DOC of the river water, particularly during riverbank filtration. Statistical analysis of the results revealed a fair agreement between the observed and computed values. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. Moisture sorption characteristics of extrusion-cooked starch protective loose-fill cushioning foams

    Science.gov (United States)

    Combrzyński, Maciej; Mościcki, Leszek; Kwaśniewska, Anita; Oniszczuk, Tomasz; Wójtowicz, Agnieszka; Sołowiej, Bartosz; Gładyszewska, Bożena; Muszyński, Siemowit

    2017-10-01

    The aim of this work was to determine the water vapour sorption properties of thermoplastic starch filling foams processed by extrusion-cooking technique from various combinations of potato starch and two foaming agents: poly(vinyl) alcohol and Plastronfoam, in amount of 1, 2 and 3% each. Foams were processed with the single screw extruder-cooker at two different screw rotational speeds 100 and 130 r.p.m. The sorption isotherms of samples were determined and described using the Guggenheim-Anderson-de Boer model. Also, the kinetics of water vapour adsorption by foams, as a function of time, was measured and fitted with Peleg model. On the basis of the analysis the influence of the applied foaming agents, as well as the technological parameters of extrusion-cooking process in relation to water vapour adsorption by thermoplastic starch foams was demonstrated. There was no difference between the shapes of the isotherms for poly(vinyl) alcohol foams while for Plastronfoam foams a notable difference among foams extruded at 100 r.p.m. was observed in the regions of low and high humidity content. The analysis of the Guggenheim-Anderson-de Boer model parameters showed that the water molecules were less strongly bound with the foam surface when extruded at a lower screw speed.

  5. Moisture Adsorption Isotherm and Storability of Hazelnut Inshells and Kernels Produced in Oregon, USA.

    Science.gov (United States)

    Jung, Jooyeoun; Wang, Wenjie; McGorrin, Robert J; Zhao, Yanyun

    2018-02-01

    Moisture adsorption isotherms and storability of dried hazelnut inshells and kernels produced in Oregon were evaluated and compared among cultivars, including Barcelona, Yamhill, and Jefferson. Experimental moisture adsorption data fitted to Guggenheim-Anderson-de Boer (GAB) model, showing less hygroscopic properties in Yamhill than other cultivars of inshells and kernels due to lower content of carbohydrate and protein, but higher content of fat. The safe levels of moisture content (MC, dry basis) of dried inshells and kernels for reaching kernel water activity (a w ) ≤0.65 were estimated using the GAB model as 11.3% and 5.0% for Barcelona, 9.4% and 4.2% for Yamhill, and 10.7% and 4.9% for Jefferson, respectively. Storage conditions (2 °C at 85% to 95% relative humidity [RH], 10 °C at 65% to 75% RH, and 27 °C at 35% to 45% RH), times (0, 4, 8, or 12 mo), and packaging methods (atmosphere vs. vacuum) affected MC, a w , bioactive compounds, lipid oxidation, and enzyme activity of dried hazelnut inshells or kernels. For inshells packaged at woven polypropylene bag, MC and a w of inshells and kernels (inside shells) increased at 2 and 10 °C, but decreased at 27 °C during storage. For kernels, lipid oxidation and polyphenol oxidase activity also increased with extended storage time (P adsorption and physicochemical and enzymatic stability during storage. Moisture adsorption isotherm of hazelnut inshells and kernels is useful for predicting the storability of nuts. This study found that water adsorption and storability varied among the different cultivars of nuts, in which Yamhill was less hygroscopic than Barcelona and Jefferson, thus more stable during storage. For ensuring food safety and quality of nuts during storage, each cultivar of kernels should be dried to a certain level of MC. Lipid oxidation and enzyme activity of kernel could be increased with extended storage time. Vacuum packaging was recommended to kernels for reducing moisture adsorption

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

    NARCIS (Netherlands)

    Pikaar, I.; Koelmans, A.A.; Noort, van P.C.M.

    2006-01-01

    Sorption to 'hard carbon' (black carbon, coal, kerogen) in soils and sediments is of major importance for risk assessment of organic pollutants. We argue that activated carbon (AC) may be considered a model sorbent for hard carbon. Here, we evaluate six sorption models on a literature dataset for

  7. Isotherms and isosteric heat of sorption of two varieties of Peruvian quinoa

    OpenAIRE

    Augusto Pumacahua-Ramos; José Antonio Gomez Vieira; Javier Telis-Romero; Harvey Alexander Villa-Vélez; Jose Francisco Lopes Filho

    2016-01-01

    The isosteric heats of sorption of two varieties of quinoa (Chenopodium quinoaWilld.) grain were determined by the static gravimetric method at four temperatures (40, 50, 60 and 70 °C) andin relative humidity environments provided by six saturated salt solutions. Six mathematical equations were used to model the experimental data: GAB, Oswin, Henderson, Peleg, Smith and Halsey. The isosteric heat of sorption was determined using the parameters ...

  8. Isotherms and isosteric heat of sorption of two varieties of Peruvian quinoa

    OpenAIRE

    Pumacahua-Ramos, Augusto; Gomez Vieira, José Antonio; Telis- Romero, Javier; Villa-Vélez, Harvey Alexander; Lopes Filho, Jose Francisco

    2016-01-01

    The isosteric heats of sorption of two varieties of quinoa (Chenopodium quinoa Willd.) grain were determined by the static gravimetric method at four temperatures (40, 50, 60 and 70 °C) and in relative humidity environments provided by six saturated salt solutions. Six mathematical equations were used to model the experimental data:  GAB, Oswin, Henderson, Peleg, Smith and Halsey. The isosteric heat of sorption was determined using the parameters of the GAB model. All the equations were shown...

  9. Isotherms and thermodynamics by linear and non-linear regression analysis for the sorption of methylene blue onto activated carbon: Comparison of various error functions

    International Nuclear Information System (INIS)

    Kumar, K. Vasanth; Porkodi, K.; Rocha, F.

    2008-01-01

    A comparison of linear and non-linear regression method in selecting the optimum isotherm was made to the experimental equilibrium data of methylene blue sorption by activated carbon. The r 2 was used to select the best fit linear theoretical isotherm. In the case of non-linear regression method, six error functions, namely coefficient of determination (r 2 ), hybrid fractional error function (HYBRID), Marquardt's percent standard deviation (MPSD), average relative error (ARE), sum of the errors squared (ERRSQ) and sum of the absolute errors (EABS) were used to predict the parameters involved in the two and three parameter isotherms and also to predict the optimum isotherm. For two parameter isotherm, MPSD was found to be the best error function in minimizing the error distribution between the experimental equilibrium data and predicted isotherms. In the case of three parameter isotherm, r 2 was found to be the best error function to minimize the error distribution structure between experimental equilibrium data and theoretical isotherms. The present study showed that the size of the error function alone is not a deciding factor to choose the optimum isotherm. In addition to the size of error function, the theory behind the predicted isotherm should be verified with the help of experimental data while selecting the optimum isotherm. A coefficient of non-determination, K 2 was explained and was found to be very useful in identifying the best error function while selecting the optimum isotherm

  10. Sorption of cobalt and nickel on anaerobic granular sludges: isotherms and sequential extraction

    NARCIS (Netherlands)

    Hullebusch, van E.D.; Peerbolte, A.; Zandvoort, M.H.; Lens, P.N.L.

    2005-01-01

    The objective of this study was to investigate the sorption capacity and the fractionation of sorbed nickel and cobalt onto anaerobic granular sludges. Two different anaerobic granular sludges (non-fed, pH = 7) were loaded with nickel and cobalt in. adsorption experiments (monometal and competitive

  11. TWO-PARAMETER ISOTHERMS OF METHYL ORANGE SORPTION BY PINECONE DERIVED ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    M. R. Samarghandi ، M. Hadi ، S. Moayedi ، F. Barjasteh Askari

    2009-10-01

    Full Text Available The adsorption of a mono azo dye methyl-orange (MeO onto granular pinecone derived activated carbon (GPAC, from aqueous solutions, was studied in a batch system. Seven two-parameter isotherm models Langmuir, Freundlich, Dubinin-Radushkevic, Temkin, Halsey, Jovanovic and Hurkins-Jura were used to fit the experimental data. The results revealed that the adsorption isotherm models fitted the data in the order of Jovanovic (X2=1.374 > Langmuir > Dubinin-Radushkevic > Temkin > Freundlich > Halsey > Hurkins-Jura isotherms. Adsorption isotherms modeling showed that the interaction of dye with activated carbon surface is localized monolayer adsorption. A comparison of kinetic models was evaluated for the pseudo-second order, Elovich and Lagergren kinetic models. Lagergren first order model was found to agree well with the experimental data (X2=9.231. In order to determine the best-fit isotherm and kinetic models, two error analysis methods of Residual Mean Square Error and Chi-square statistic (X2 were used to evaluate the data.

  12. Drum drying of banana pulp on the sorption isotherm and flexible ...

    African Journals Online (AJOL)

    The dried product had moisture content of approximately 2.0% which was equivalent to (aw)of 5.11 of 38.5 oC. The storage condition should be such that does not go beyond 0.15 which is equivalent to about 2.5% moisture. In this range of (aw), Polyethylene (density 0.954) of thickness more than 5 mil or saran 517 of 1 mil ...

  13. Monolayer and multilayer adsorption isotherm models for sorption from aqueous media

    Energy Technology Data Exchange (ETDEWEB)

    Saadi, Reyhaneh; Saadi, Zahra; Fazaeli, Reza; Fard, Narges Elmi [Islamic Azad University, Tehran (Iran, Islamic Republic of)

    2015-05-15

    Industrial wastewater polluted with various contaminants, including heavy metals, dyes, etc., endangers human health and the environment. Various separation techniques have been developed for the removal of pollutants from aqueous solutions. Adsorption process has drawn considerable attention due to its simplicity of design, high removal efficiency, even at dilute concentration, and economical aspect. We reviewed the most common two, three, four, and five parameter adsorption isotherm models corresponding to monolayer and multilayer adsorption on the basis of parameters that can be used for exploring novel adsorbents. Thermodynamic assumptions of the models give information about the surface properties, capacity of the adsorbent and adsorption mechanism. Seven error functions were investigated to evaluate the fitness quality of isotherm models with the experimental equilibrium data.

  14. Applicability of the Linear Sorption Isotherm Model to Represent Contaminant Transport Processes in Site Wide Performance Assessments

    International Nuclear Information System (INIS)

    FOGWELL, T.W.; LAST, G.V.

    2003-01-01

    The estimation of flux of contaminants through the vadose zone to the groundwater under varying geologic, hydrologic, and chemical conditions is key to making technically credible and sound decisions regarding soil site characterization and remediation, single-shell tank retrieval, and waste site closures (DOE 2000). One of the principal needs identified in the science and technology roadmap (DOE 2000) is the need to improve the conceptual and numerical models that describe the location of contaminants today, and to provide the basis for forecasting future movement of contaminants on both site-specific and site-wide scales. The State of Knowledge (DOE 1999) and Preliminary Concepts documents describe the importance of geochemical processes on the transport of contaminants through the Vadose Zone. These processes have been identified in the international list of Features, Events, and Processes (FEPs) (NEA 2000) and included in the list of FEPS currently being developed for Hanford Site assessments (Soler et al. 2001). The current vision for Hanford site-wide cumulative risk assessments as performed using the System Assessment Capability (SAC) is to represent contaminant adsorption using the linear isotherm (empirical distribution coefficient, K d ) sorption model. Integration Project Expert Panel (PEP) comments indicate that work is required to adequately justify the applicability of the linear sorption model, and to identify and defend the range of K d values that are adopted for assessments. The work plans developed for the Science and Technology (S and T) efforts, SAC, and the Core Projects must answer directly the question of ''Is there a scientific basis for the application of the linear sorption isotherm model to the complex wastes of the Hanford Site?'' This paper is intended to address these issues. The reason that well documented justification is required for using the linear sorption (K d ) model is that this approach is strictly empirical and is often

  15. Histerese das isotermas de sorção da polpa de manga (Mangifera indica L. variedade manteiga Hysteresis of the sorption isotherms of mango pulp (Mangifera indica L. manteiga variety

    Directory of Open Access Journals (Sweden)

    Camila de S. Paglarini

    2013-03-01

    Full Text Available As isotermas de sorção são de grande importância para predizer processos de secagem e armazenamento de um produto. A histerese é um fenômeno que ocorre devido à diferença entre as curvas de adsorção e dessorção. O presente trabalho teve o objetivo de analisar a influência da temperatura nas isotermas de sorção e na histerese da polpa de manga variedade manteiga. As isotermas foram determinadas pelo método gravimétrico estático, com a utilização de diferentes concentrações ácidas, nas temperaturas de 20, 30, 40 e 50 °C e atividade de água variando de 4,3 a 88,8% até atingir a umidade de equilíbrio. Foram analisados seis modelos matemáticos para isotermas de sorção (GAB, BET, Halsey, Henderson-Thompson, Oswin e Luikov ajustados aos dados experimentais, através de regressão não-linear. A histerese foi calculada pela área compreendida entre as curvas de dessorção e adsorção. De acordo com os resultados obtidos o modelo de GAB foi o que melhor se ajustou às isotermas de equilíbrio da manga. A área da histerese reduziu 51% entre as temperaturas de 20 e 50 °C.The sorption isotherms are of great importance for predicting drying and storage of a product. Hysteresis is a phenomenon that occurs due to the difference between the curves of adsorption and desorption. This study aimed to analyse the influence of temperature on sorption isotherms and hysteresis of mango pulp manteiga variety. The isotherms were determined by the static method with the use of different acid concentrations. The samples were submitted to temperatures of 20, 30, 40 and 50 °C and water activity ranging from 4.3 to 88.8% until the equilibrium moisture content. Six mathematical models for the sorption isotherms (GAB, BET, Halsey, Henderson-Thompson, Oswin and Luikov were analysed and adjusted to the experimental data using nonlinear regression. The hysteresis was calculated as the area between the curves of adsorption and desorption

  16. PENENTUAN WAKTU KADALUARSA DAN MODEL SORPSI ISOTERMIS BIJI DAN BUBUK LADA HITAM (Piper ningrum L. [Shelf Life Prediction and Isotherm Sorption Model of Dried Grain and Powdered Black Pepper (Piper ningrum L.

    Directory of Open Access Journals (Sweden)

    Erika Diah2

    2005-04-01

    Full Text Available Black pepper is one of the most popular spice traded around the globe, either in dried grain form or in bulky powder. However, for retailing purpose both are usually packaged in plastic film. This research was conducted to predict the shelf life of packaged black pepper (both dried grain and powder by applying isotherm sorption and Labuza models. Initial moisture content of dried grain was 12.17 % d.b and for the powder was 10.27 % d.b. The shelf life of black pepper calculated for the dried grain was longer than the powder. When stored at 90 % RH, the dried grain black pepper packaged in HDPE demonstrated the longest shelf life which was equal to 2187 days and for the powder equal to 2037 days. The volatile oil loss for dried grain black pepper after 30 days of preservation was 1.36 % and for the powder was 40.82%.

  17. Sorption studies of heavy metal ions by salicylic acid–formaldehyde–catechol terpolymeric resin: Isotherm, kinetic and thermodynamics

    Directory of Open Access Journals (Sweden)

    Riddhish R. Bhatt

    2015-05-01

    Full Text Available Terpolymeric resin has been synthesized by condensing salicylic acid with catechol employing formaldehyde as a cross linking agent at 80 ± 5 °C using DMF as a solvent. The resin was characterized by elemental analysis, FTIR, XRD and thermal analysis (TGA, DTA and DTG. The morphology of the resin was studied by optical photographs and scanning electron micrographs (SEM at different magnifications. The physico-chemical properties have been studied. The uptake behavior of various metal ions viz. Ni(II, Cu(II, Zn(II, Cd(II and Pb(II towards synthesized resin has been studied depending on contact time, pH and temperature. The selectivity order found is: Cu(II > Zn(II > Pb(II > Ni(II > Cd(II. The sorption data obtained at optimized conditions were analyzed by six two parameter isotherm models like Langmuir, Freundlich, Temkin, Dubinin–Radushkevich (D–R, Halsey and Harkins–Jura. The Langmuir, Freundlich and Dubinin–Radushkevich (D–R isotherms were found better to describe the sorption data with high correlation for the adsorption with a low SSE value for all the metals under study. The adsorption capacities of the SFC resin for removal of Ni(II, Cu(II, Zn(II, Cd(II and Pb(II were determined with the Langmuir equation and found to be 0.815, 1.104, 1.215, 0.498, and 0.931 mmol/g respectively. The adsorption process follows first order kinetics and specific rate constant Kr was obtained by the application of Lagergren equation. Thermodynamic parameters viz. ΔGads, ΔSads and ΔHads have also been calculated for the metal-resin systems. The external diffusion rate constant (Ks and intra-particle diffusion rate constant (Kid were calculated by Spahn–Schlunder and Weber–Morris models respectively. Desorption studies were done using various desorbing agents viz. de-ionized water, boiled water, various concentrations of HCl, ammonia, thiourea, citric acid and tartaric acid.

  18. Sorption performance of activated nkaliki clay in removing chromium (vi) ion from aqueous solution: kinetics, isotherm, and thermodynamic studies

    International Nuclear Information System (INIS)

    Ajemba, R.O.; Ugonabo, V.I.; Okafor, V.N.

    2017-01-01

    Bentonite from Nkaliki was modified by acid activation using different concentrations of sulphuric acid. The physicochemical properties of the raw and modified samples were analyzed. The sorption performance of the modified and raw bentonite was studied in the removal of chromium (VI) ion from aqueous solution. Effect of key process parameters on the adsorption process was studied. Results of the physicochemical analyses showed that the acid activation altered the structural arrangements of the bentonite. The surface area and adsorption capacity increased from 37.6m/sup 2//g to 74m/sup 2//g and 45 to 98%, respectively, after activating with 6mol/l of H/sub 2/SO/sub 4/. The chromium (VI) ion adsorption increased with increase in process parameters studied. The kinetics analysis of the adsorption data follows the pseudo second-order kinetics, while equilibrium analysis conformed to the Langmuir isotherm. The thermodynamic parameters revealed that adsorption process is spontaneous and endothermic. This study shows that modified Nkaliki bentonite could be used for wastewater treatment. (author)

  19. Natural composites: Strength, packing ability and moisture sorption of cellulose fibres, and the related performance of composites

    DEFF Research Database (Denmark)

    Lilholt, Hans; Madsen, Bo

    2012-01-01

    Biobased materials are becoming of increasing interest as potential structural materials for the future. A useful concept in this context is the fibre reinforcement of materials by stiff and strong fibres. The bio-resources can contribute with cellulose fibres and (bio) polymers from hemicelluloses...... in stiffness, on the packing ability of cellulose fibres and the related maximum fibre volume fraction in composites, on the moisture sorption of cellulose fibres and the related mass increase and (large) hygral strains induced, and on the mechanical performance of composites....

  20. Analysis of water sorption isotherms of amorphous food materials by solution thermodynamics with relevance to glass transition: evaluation of plasticizing effect of water by the thermodynamic parameters.

    Science.gov (United States)

    Shimazaki, Eriko; Tashiro, Akiko; Kumagai, Hitomi; Kumagai, Hitoshi

    2017-04-01

    Relation between the thermodynamic parameters obtained from water sorption isotherms and the degree of reduction in the glass transition temperature (T g ), accompanied by water sorption, was quantitatively studied. Two well-known glassy food materials namely, wheat gluten and maltodextrin were used as samples. The difference between the chemical potential of water in a solution and that of pure water ([Formula: see text]), the difference between the chemical potential of solid in a solution and that of a pure solid ([Formula: see text]), and the change in the integral Gibbs free energy ([Formula: see text]) were obtained by analyzing the water sorption isotherms using solution thermodynamics. The parameter [Formula: see text] correlated well with ΔT g (≡T g  - T g0 ; where T g0 is the glass transition temperature of dry material), which had been taken to be an index of plasticizing effect. This indicates that plasticizing effect of water on foods can be evaluated through the parameter [Formula: see text].

  1. Determination of effective moisture diffusivity and drying kinetics for poplar sawdust by thermogravimetric analysis under isothermal condition.

    Science.gov (United States)

    Chen, Dengyu; Zheng, Yan; Zhu, Xifeng

    2012-03-01

    The current study presents a thermogravimetric method to determine the effective moisture diffusivity and drying kinetics of biomass. Drying experiments on poplar sawdust were performed at four temperatures (60, 70, 80, and 90°C) by a thermogravimetric analyzer (TGA). The major assumption in experimentally determining effective diffusivity by Fick's diffusion equation is that drying is mass transfer limited and temperature remains isothermal during drying. The results indicated that TGA could well achieve these determining conditions. The drying process of sawdust mostly took place in the falling rate period. Midilli-Kucuk model showed the best fit for all experimental data. The effective diffusivity values changed from 9.38 × 10(-10)m(2)/s to 1.38 × 10(-9)m(2)/s within the given temperature range, and the activation energy was calculated to be 12.3 kJ/mol. Copyright © 2011 Elsevier Ltd. All rights reserved.

  2. Swelling, stiffness, and stress in gel material - as related to moisture sorption

    DEFF Research Database (Denmark)

    Nielsen, Lauge Fuglsang

    1996-01-01

    A method is presented by which estimates can be made on swelling, bulk modulus, and internal stresses in gel materials as related to water sorption. Porous gel materials are considered as gel materials made porous by capillary pores large enough not to create capillary condensation and capillary...

  3. Water sorption and water permeability properties of edible film made from potato peel waste

    Directory of Open Access Journals (Sweden)

    Siti Hajar OTHMAN

    Full Text Available Abstract The water sorption and permeability properties of edible film produced from potato peel waste was investigated under different levels of relative humidity (23, 33, 43, 57, 75% RH and temperatures (5, 30, 50 °C. The water sorption behaviour and isotherms of the film were investigated by fitting water sorption data to the Peleg model and the Guggenheim, Anderson de Boer model (GAB model. The amount of moisture content, time required for the moisture content of the film to reach equilibrium, water sorption rate, and water sorption capacity increased when the relative humidity increased. The effect of temperature on moisture content, water sorption rate, water sorption capacity, and monolayer moisture content is complex and related to the water activity as well as the moisture content. Based on R2 and RMSE values, the Peleg and GAB models were respectively determined as excellent models to predict the water sorption properties of the films, thus supporting the reliability of water sorption behaviour prediction. The water vapour transmission rate and water vapour permeability increased with an increase in relative humidity and temperature. The sorption and permeability properties of the film are worth investigation since the final application of the film as food packaging is ultimately dependent on these behaviours.

  4. Physical stability and moisture sorption of aqueous chitosan-amylose starch films plasticized with polyols

    DEFF Research Database (Denmark)

    Cervera, Mirna Fernández; Karjalainen, Milja; Airaksinen, Sari

    2004-01-01

    The short-term stability and the water sorption of films prepared from binary mixtures of chitosan and native amylose maize starch (Hylon VII) were evaluated using free films. The aqueous polymer solutions of the free films contained 2% (w/w) film formers, glycerol, or erythritol as a plasticizer...... in the crystallinity of the films are evident within a 3-month period of storage, and the changes in the solid state are dependent on the plasticizer and storage conditions. When stored at ambient conditions for 3 months, the aqueous chitosan-amylose starch films plasticized with erythritol exhibited a partly...

  5. The vibrational properties of Chinese fir wood during moisture sorption process

    Science.gov (United States)

    Jiali Jiang; Jianxiong Lu; Zhiyong Cai

    2012-01-01

    The vibrational properties of Chinese fir (Cunninghamia lanceolata) wood were investigated in this study as a function of changes in moisture content (MC) and grain direction. The dynamic modulus of elasticity (DMOE) and logarithmic decrement σ were examined using a cantilever beam vibration testing apparatus. It was observed that DMOE and 6 of wood vaned...

  6. A two-phase moisture transport model accounting for sorption hysteresis in layered porous building constructions

    DEFF Research Database (Denmark)

    Johannesson, Björn; Janz, Mårten

    2009-01-01

    Building constructions most commonly consists of layered porous materials such as masonry on bricks. The moisture distribution and its variations due to change in surrounding environment is of special interest in such layered construction since materials adsorb different amounts of water and exhi......Building constructions most commonly consists of layered porous materials such as masonry on bricks. The moisture distribution and its variations due to change in surrounding environment is of special interest in such layered construction since materials adsorb different amounts of water....... The model is developed by carefully examining the mass balance postulates for the two considered constituents together with appropriate and suitable constitutive assumptions. A test example is solved by using an implemented implicit finite element code which uses a modified Newton-Raphson scheme to tackle...

  7. Sorption Properties of Some Romanian Gingerbread

    Directory of Open Access Journals (Sweden)

    Tulbure Anca

    2014-06-01

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

  8. Isosteric Vapor Pressure – Temperature Data for Water Sorption in Hardened Cement Paste: Enthalpy, Entropy and Sorption Isotherms at Different Temperatures

    DEFF Research Database (Denmark)

    Radjy, Fariborz; Sellevold, Erik J.; Hansen, Kurt Kielsgaard

    . The accuracies for pressure, enthalpy and entropy are found to be 0.5% or less. PART II: The TPA-system has been used to generate water vapor pressure – temperature data for room temperature – and steam cured hardened cement pastes as well as porous vycor glass. The moisture contents range from saturated to dry...... and the temperatures range from 2 to 95 °C, differing for the specimen types. The data has been analyzed to yield differential enthalpy and entropy of adsorption, as well as the dependence of the relative vapor pressure on temperature at various constant moisture contents. The implications for the coefficient......PART I: In order to generate isosteric (constant mass) vapor pressure – temperature data (P-T data) for adsorbed pore water in hydrated cement paste, the Thermo Piestic Analysis system (the TPA system) described herein was developed. The TPA system generates high precision equilibrium isosteric P...

  9. Assessment of the possibility of using data mining methods to predict sorption isotherms of selected organic compounds on activated carbon

    Directory of Open Access Journals (Sweden)

    Dąbek Lidia

    2017-01-01

    Full Text Available The paper analyses the use of four data mining methods (Support Vector Machines. Cascade Neural Networks. Random Forests and Boosted Trees to predict sorption on activated carbons. The input data for statistical models included the activated carbon parameters, organic substances and equilibrium concentrations in the solution. The assessment of the predictive abilities of the developed models was made with the use of mean absolute error (MAE, mean absolute percentage error (MAPE, and root mean squared error (RMSE. The computations proved that methods of data mining considered in the study can be applied to predict sorption of selected organic compounds 011 activated carbon. The lowest values of sorption prediction errors were obtained with the Cascade Neural Networks method (MAE = 1.23 g/g; MAPE = 7.90% and RMSE = 1.81 g/g, while the highest error values were produced by the Boosted Trees method (MAE=14.31 g/g; MAPE = 39.43% and RMSE = 27.76 g/g.

  10. Water adsorption isotherms and thermodynamic properties of cassava bagasse

    International Nuclear Information System (INIS)

    Polachini, Tiago Carregari; Betiol, Lilian Fachin Leonardo; Lopes-Filho, José Francisco; Telis-Romero, Javier

    2016-01-01

    Highlights: • Adsorption isotherms and composition of cassava bagasse were determined. • GAB equation was the best-fitted model to sorption data of type II isotherm. • Isosteric heat of sorption was calculated in a range of equilibrium moisture content. • Differential enthalpy and entropy confirmed the isokinetic compensation theory. • Water adsorption by cassava bagasse is considered an enthalpy driven process. - Abstract: Losses of food industry are generally wet products that must be dried to posterior use and storage. In order to optimize drying processes, the study of isotherms and thermodynamic properties become essential to understand the water sorption mechanisms of cassava bagasse. For this, cassava bagasse was chemically analyzed and had its adsorption isotherms determined in the range of 293.15–353.15 K through the static gravimetric method. The models of GAB, Halsey, Henderson, Oswin and Peleg were fitted, and best adjustments were found for GAB model with R"2 > 0.998 and no pattern distribution of residual plots. Isosteric heat of adsorption and thermodynamic parameters could be determined as a function of moisture content. Compensation theory was confirmed, with linear relationship between enthalpy and entropy and higher values of isokinetic temperature (T_B = 395.62 K) than harmonic temperature. Water adsorption was considered driven by enthalpy, clarifying the mechanisms of water vapor sorption in cassava bagasse.

  11. Sorption Characteristics of Mixed Molecules of Glutaraldehyde from Water on Mesoporous Acid-Amine Modified Low-Cost Activated Carbon: Mechanism, Isotherm, and Kinetics

    Directory of Open Access Journals (Sweden)

    Mukosha Lloyd

    2015-01-01

    Full Text Available The environmental discharge of inefficiently treated waste solutions of the strong biocide glutaraldehyde (GA from hospitals has potential toxic impact on aquatic organisms. The adsorption characteristics of mixed polarized monomeric and polymeric molecules of GA from water on mesoporous acid-amine modified low-cost activated carbon (AC were investigated. It was found that the adsorption strongly depended on pH and surface chemistry. In acidic pH, the adsorption mechanism was elaborated to involve chemical sorption of mainly hydroxyl GA monomeric molecules on acidic surface groups, while in alkaline pH, the adsorption was elaborated to involve both chemical and physical sorption of GA polymeric forms having mixed functional groups (aldehyde, carboxyl, and hydroxyl on acidic and amine surface groups. The optimum pH of adsorption was about 12 with significant contribution by cooperative adsorption, elucidated in terms of hydrogen bonding and aldol condensation. Freundlich and Dubinin-Radushkevich models were fitted to isotherm data. The adsorption kinetics was dependent on initial concentration and temperature and described by the Elovich model. The adsorption was endothermic, while the intraparticle diffusion model suggested significant contribution by film diffusion. The developed low-cost AC could be used to supplement the GA alkaline deactivation process for efficient removal of residual GA aquatic toxicity.

  12. Effect of molecular weight, temperature, and additives on the moisture sorption properties of polyethylene glycol.

    Science.gov (United States)

    Baird, Jared A; Olayo-Valles, Roberto; Rinaldi, Carlos; Taylor, Lynne S

    2010-01-01

    Polyethylene glycol (PEG) is a hygroscopic polymer that undergoes the phenomenon of deliquescence once a critical relative humidity (RH(0)) is reached. The purpose of this study was to test the hypothesis that the deliquescence behavior of PEG will be affected by the polymer molecular weight, temperature, and the presence of additives. The deliquescence relative humidity for single component (RH(0)) and binary mixtures (RH(0,mix)) were measured using an automated gravimetric moisture analyzer at 25 and 40 degrees C. Changes in PEG crystallinity after exposure to moisture were qualitatively assessed using powder X-ray diffraction (PXRD). Optical microscopy was used to visually observe the deliquescence phenomenon. For single component systems, decreasing PEG MW and elevating the temperature resulted in a decrease in the observed RH(0). Physical mixtures of acetaminophen and anhydrous citric acid with both PEG 3350 and PEG 100,000 exhibited deliquescence (RH(0,mix)) at a relative humidity below that of either individual component. Qualitative changes in crystallinity were observed from the X-ray diffractograms for each PEG MW grade at high relative humidities, indicating that phase transformation (deliquescence) of the samples had occurred. In conclusion, it was found that the deliquescence behavior of PEG was affected by the polymer MW, temperature, and the presence of additives. This phenomenon may have important implications for the stability of PEG containing formulations.

  13. A fully coupled diffusion-reaction scheme for moisture sorption-desorption in an anhydride-cured epoxy resin

    KAUST Repository

    El Yagoubi, Jalal; Lubineau, Gilles; Roger, Frederic; Verdu, Jacques

    2012-01-01

    Thermoset materials frequently display non-classical moisture sorption behaviors. In this paper, we investigated this issue from an experimental point of view as well as in terms of modeling the water transport. We used the gravimetric technique to monitor water uptake by epoxy samples, with several thicknesses exposed to different levels of humidity during absorption and desorption tests. Our results revealed that the polymer displays a two-stage behavior with a residual amount of water that is desorbed progressively. We proposed a phenomenological reaction-diffusion scheme to describe this behavior. The model describes water transport as a competition between diffusion and the reaction, during which the local diffusivity and solubility depend on the local advancement of the reaction. We then implemented our model using COMSOL Multiphysics and identified it using a MATLAB-COMSOL optimization tool and the experimental data. We discussed the relation between the hydrophilicity of the product of the reaction and the diffusion behavior. We examined the reaction-induced modification of the water concentration field. It is worth noting that part of the phenomenology can be explained by the presence of hydrolyzable groups. © 2012 Elsevier Ltd. All rights reserved.

  14. A fully coupled diffusion-reaction scheme for moisture sorption-desorption in an anhydride-cured epoxy resin

    KAUST Repository

    El Yagoubi, Jalal

    2012-11-01

    Thermoset materials frequently display non-classical moisture sorption behaviors. In this paper, we investigated this issue from an experimental point of view as well as in terms of modeling the water transport. We used the gravimetric technique to monitor water uptake by epoxy samples, with several thicknesses exposed to different levels of humidity during absorption and desorption tests. Our results revealed that the polymer displays a two-stage behavior with a residual amount of water that is desorbed progressively. We proposed a phenomenological reaction-diffusion scheme to describe this behavior. The model describes water transport as a competition between diffusion and the reaction, during which the local diffusivity and solubility depend on the local advancement of the reaction. We then implemented our model using COMSOL Multiphysics and identified it using a MATLAB-COMSOL optimization tool and the experimental data. We discussed the relation between the hydrophilicity of the product of the reaction and the diffusion behavior. We examined the reaction-induced modification of the water concentration field. It is worth noting that part of the phenomenology can be explained by the presence of hydrolyzable groups. © 2012 Elsevier Ltd. All rights reserved.

  15. Evaluation of a Fully Automated Analyzer for Rapid Measurement of Water Vapor Sorption Isotherms for Applications in Soil Science

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per

    2014-01-01

    The characterization and description of important soil processes such as water vapor transport, volatilization of pesticides, and hysteresis require accurate means for measuring the soil water characteristic (SWC) at low water potentials. Until recently, measurement of the SWC at low water...... potentials was constrained by hydraulic decoupling and long equilibration times when pressure plates or single-point, chilled-mirror instruments were used. A new, fully automated Vapor Sorption Analyzer (VSA) helps to overcome these challenges and allows faster measurement of highly detailed water vapor...

  16. MODELADO DE LAS ISOTERMAS DE SORCIÓN Y DEL CALOR ISOSTÉRICO DE SORCIÓN EN PULPA DE MANGO cv. TOMMY ATKINS MODELAGEM DE ISOTERMAS DE SORÇÃO E CALOR ISOSTÉRICO DE SORÇÃO DE POLPA DE MANGA cv. TOMMY ATKINS MODELING SORPTION ISOTHERMS AND ISOSTERIC HEAT OF SORPTION OF MANGO PULP cv. TOMMY ATKINS

    Directory of Open Access Journals (Sweden)

    JOSÉ BON

    2012-12-01

    polpa de manga (Mangifera indica L. cv. Tommy Atkins foi analisada para determinar as isotermas de sorção. A atividade de água foi medida empregando um higrômetro elétrico a cinco diferentes temperaturas (10, 20, 30, 40 e 50 °C e amplas faixas de conteúdo de umidade (2.829 - 0.031 kg kg-1 b.s. e atividade de água (0.977 - 0.215. O modelo de teórico de GAB e os modelos empíricos de (Oswin, Henderson, Halsey e Ratti foram empregados para modelar as isotermas de sorção. Depois de considerar diferentes critérios, o modelo de GAB apresentou a melhor opção para representar o equilíbrio higroscópico da polpa de manga (RMSE = 0.057, VAR = 0.996.As isotermas mostraram um comportamento acorde aos materiais agroalimentícios e similar ao reportado para polpa de manga de outras variedades. O calor isostérico de sorção foi calculado utilizando a equação de Clausius-Clapeyron a partir do modelo de GAB. Observou-se uma diminuição no calor isostérico de sorção quando aumentou o conteúdo de umidade de equilíbrio, com um grande efeito da umidade em valores abaixo de 0.8 kg kg-1 (b.s..Mango is an agricultural product of great economic importance for various developing countries, which has increased demand for its nutritional properties and exotic characteristics. The relationship between moisture content and water activity provides useful information for mango processing, especially for drying and storage operations. Water activity and moisture content of mango pulp (Mangiferaindica L. cv. Tommy Atkins were analyzed to determine the sorption isotherms. The water activity was measured using an electric hygrometer at five different temperatures (10, 20, 30, 40 and 50 °C and wide ranges of moisture content (2.829-0.031 kg kg-1 d.b. and water activity (0.977-0.215. One theoretical (GAB and four empirical equations (Oswin, Henderson, Halsey and Ratti were used for modeling the sorption isotherms. After following several criteria to evaluate the models, the GAB

  17. Effect of Mechanical Impact Energy on the Sorption and Diffusion of Moisture in Reinforced Polymer Composite Samples on Variation of Their Sizes

    Science.gov (United States)

    Startsev, V. O.; Il'ichev, A. V.

    2018-05-01

    The effect of mechanical impact energy on the sorption and diffusion of moisture in polymer composite samples on variation of their sizes was investigated. Square samples, with sides of 40, 60, 80, and 100 mm, made of a KMKU-2m-120.E0,1 carbon-fiber and KMKS-2m.120.T10 glass-fiber plastics with different resistances to calibrated impacts, were compared. Impact loading diagrams of the samples in relation to their sizes and impact energy were analyzed. It is shown that the moisture saturation and moisture diffusion coefficient of the impact-damaged materials can be modeled by Fick's second law with account of impact energy and sample sizes.

  18. Uranium (VI) Sorption and Transport in Unsaturated, Subsurface Hanford Site Sediments - Effect of Moisture Content and Sediment Texture: Final Report for Subtask 2b

    International Nuclear Information System (INIS)

    Gamerdinger, A.P.; Resch, C.T.; Kaplan, D.I.

    1998-01-01

    A series of experiments were conducted in fiscal year 1998 at the Pacific Northwest National Laboratory as part of the Immobilized Low-Activity Waste-Performance Assessment. These experiments evaluated the sorption and transport of uranium, U(VI), under conditions of partial moisture saturation that are relevant to arid region burial sites and vadose-zone far-field conditions at the Hanford Site. The focus was on measuring breakthrough curves (from which distribution coefficient [K d ] values can be calculated) for U(W) in three Hanford Site sediments that represent different texture classes in two unsaturated moisture conditions. Previous research showed that K d values measured during transport in unsaturated sediments varied with moisture saturation

  19. A Numerical Approach for Non-Linear Moisture Flow in Porous Materials with Account to Sorption Hysteresis

    DEFF Research Database (Denmark)

    Johannesson, Björn; Nyman, U.

    2010-01-01

    . History-dependent sorption behaviour is introduced by considering scanning curves between the bounding desorption and absorption curves. The method, therefore, makes it possible to calculate equilibrium water contents for arbitrary relative humidity variations at every material point considered...

  20. Isotermas de sorção de tâmaras: determinação experimental e avaliação de modelos matemáticos Dates sorption isotherms: experimental determination and mathematics models evaluation

    Directory of Open Access Journals (Sweden)

    Mônica E.T. PRADO

    1999-01-01

    Full Text Available As isotermas de sorção de tâmaras (Phoenix dactylifera L., da variedade Zahidi, foram determinadas para três temperaturas, 60, 70 e 80° C pelo método estático gravimétrico. As curvas experimentais foram ajustadas pelas equações de BET, BET linearizada, GAB, HALSEY, OSWIN e PELEG. O desvio relativo entre os valores experimentais e os valores estimados foi calculado para cada curva, a fim de se avaliar qual equação melhor se ajustou aos dados experimentais.Dates sorption isotherms were determined by gravimetric at three differents temperatures (60, 70 and 80° C. Experimental data was adjusted to six sorption models de BET, linear BET, GAB, HALSEY, OSWIN and PELEG. The average relative deviations between calculated and experimental data were calculated do select best fit model.

  1. PHOSPHORUS SORPTION ISOTHERMS AND EXTERNAL ...

    African Journals Online (AJOL)

    ACSS

    Zhang et al., 2005). For instance, in strongly acidic soils with pH<5.5 and high P sorbing soils, application of rock phosphate is more effective and cheaper than using TSP (Bationo et al., 2011). Moreover, it enables determination of the external P.

  2. PHOSPHORUS SORPTION ISOTHERMS AND EXTERNAL ...

    African Journals Online (AJOL)

    ACSS

    les capacités d'adsorption ont été obtenues en équilibrant 3.0 g de chaque échantillon avec 30 ml de CaCl2 à 0.01. Molaire, ces ... kg-1 ; ils étaient alors classés sols à haut potentiel d'adsorption de P. les ions échangeables Al3+ et Fe2+ etaient positivement .... involves 3.0 g of air-dried sample of each soil, transferred in to ...

  3. Moisture sorption–desorption characteristics and the corresponding thermodynamic properties of carvedilol phosphate

    Directory of Open Access Journals (Sweden)

    Ravikiran Allada

    2017-01-01

    Full Text Available Aims: Carvedilol phosphate (CDP is a nonselective beta-blocker used for the treatment of heart failures and hypertension. In this work, moisture sorption–desorption characteristics and thermodynamic properties of CDP have been investigated. Materials and Methods: The isotherms were determined using dynamic vapor sorption analyzer at different humidity conditions (0%–90% relative humidity and three pharmaceutically relevant temperatures (20°C, 30°C, and 40°C. The experimental sorption data determined were fitted to various models, namely, Brunauer–Emmett–Teller; Guggenheim-Anderson-De Boer (GAB; Peleg; and modified GAB. Isosteric heats of sorption were evaluated through the direct use of sorption isotherms by means of the Clausius-Clapeyron equation. Statistical Analysis Used: The sorption model parameters were determined from the experimental sorption data using nonlinear regression analysis, and mean relative percentage deviation (P, correlation (Correl, root mean square error, and model efficiency were considered as the criteria to select the best fit model. Results: The sorption–desorption isotherms have sigmoidal shape – confirming to Type II isotherms. Based on the statistical data analysis, modified GAB model was found to be more adequate to explain sorption characteristics of CDP. It is noted that the rate of adsorption and desorption is specific to the temperature at which it was being studied. It is observed that isosteric heat of sorption decreased with increasing equilibrium moisture content. Conclusions: The calculation of the thermodynamic properties was further used to draw an understanding of the properties of water and energy requirements associated with the sorption behavior. The sorption–desorption data and the set of equations are useful in the simulation of processing, handling, and storage of CDP and further behavior during manufacture and storage of CDP formulations.

  4. Using the internal stress concept to assess the importance of moisture sorption-induced swelling on the moisture transport through the glassy HPMC films

    NARCIS (Netherlands)

    Laksmana, Fesia L.; Kok, Paul J.A. Hartman; Frijlink, Henderik W.; Vromans, Herman; Van der Voort Maarschalk, Kees

    2008-01-01

    The purpose of this research was to elucidate the significance of the changes in the mechanical and the volumetric properties on the moisture diffusivity through the polymer films. The internal stress concept was adapted and applied to estimate the relative impact of these property changes on the

  5. Effect of drying method on the adsorption isotherms and isosteric heat of passion fruit pulp powder

    Directory of Open Access Journals (Sweden)

    Maria Angélica Marques Pedro

    2010-12-01

    Full Text Available The sorption behavior of dry products is generally affected by the drying method. The sorption isotherms are useful to determine and compare thermodynamic properties of passion fruit pulp powder processed by different drying methods. The objective of this study is to analyze the effects of different drying methods on the sorption properties of passion fruit pulp powder. Passion fruit pulp powder was dehydrated using different dryers: vacuum, spray dryer, vibro-fluidized, and freeze dryer. The moisture equilibrium data of Passion Fruit Pulp (PFP powders with 55% of maltodextrin (MD were determined at 20, 30, 40 and 50 ºC. The behavior of the curves was type III, according to Brunauer's classification, and the GAB model was fitted to the experimental equilibrium data. The equilibrium moisture contents of the samples were little affected by temperature variation. The spray dryer provides a dry product with higher adsorption capacity than that of the other methods. The vibro-fluidized bed drying showed higher adsorption capacity than that of vacuum and freeze drying. The vacuum and freeze drying presented the same adsorption capacity. The isosteric heats of sorption were found to decrease with increasing moisture content. Considering the effect of drying methods, the highest isosteric heat of sorption was observed for powders produced by spray drying, whereas powders obtained by vacuum and freeze drying showed the lowest isosteric heats of sorption.

  6. Humidity sorption on natural building stone

    Science.gov (United States)

    Franzen, C.; Mirwald, P.

    2003-04-01

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

  7. A new model for predicting moisture uptake by packaged solid pharmaceuticals.

    Science.gov (United States)

    Chen, Y; Li, Y

    2003-04-14

    A novel mathematical model has been developed for predicting moisture uptake by packaged solid pharmaceutical products during storage. High density polyethylene (HDPE) bottles containing the tablet products of two new chemical entities and desiccants are investigated. Permeability of the bottles is determined at different temperatures using steady-state data. Moisture sorption isotherms of the two model drug products and desiccants at the same temperatures are determined and expressed in polynomial equations. The isotherms are used for modeling the time-humidity profile in the container, which enables the prediction of the moisture content of individual component during storage. Predicted moisture contents agree well with real time stability data. The current model could serve as a guide during packaging selection for moisture protection, so as to reduce the cost and cycle time of screening study.

  8. Isotermas de sorção de metais pesados em solos do cerrado de Goiás Sorption isotherm of heavy metals in soils of 'Cerrado' of Goiás

    Directory of Open Access Journals (Sweden)

    Luiz F. C. Oliveira

    2010-07-01

    Full Text Available A contaminação do solo e das águas subterrâneas por metais pesados é, extremamente perniciosa por serem basntante persistentes no ambiente. Objetivou-se, com este trabalho, a análise da sorção do Cu, Cr, Zn, Cd, Pb e Ni em Latossolo Vermelho Acriférrico (LVwf, Argissolo Vermelho Eutrófico (PVe, Nitossolo Vermelho Eutroférrico (NVef e Neossolo Quartzarênico (RQ pelos modelos potencial e linear da isoterma Freundlich. Para o estabelecimento de isotermas de sorção adicionaram-se a 5,0 mL de solo e 50,0 mL de solução contendo o metal pesado a ser avaliado com diferentes concentrações, respeitando-se os limites aceitáveis. As isotermas de sorção potencial e linear apresentaram bom ajuste para descrever o comportamento de adsorção dos metais pesados nas diferentes classes de solo estudadas. A sequência da retenção dos metais pesados em ordem decrescente, foi, para: o PVe: Cr+3 > Cr+6 > Ni+2 > Zn+2 > Cu+2 > Pb+2 > Cd+2; o LVwf: Cr+3 > Cr+6 > Ni+2 > Cu+2 > Cd+2 > Zn+2 > Pb+2; o RQ: Cr+6 > Cr+3 >Cu+2 > Pb+2 > Ni+2 > Zn+2 > Cd+2 e, para, o NVef: Cr+3 > Cr+6 > Pb+2 > Cu+2 > Zn+2 > Ni+2 >Cd+2. O RQ foi a classe de solo que apresentou menor retenção de metais em comparação com as demais classes de solo sendo, portanto, mais vulnerável à contaminação de águas subterrâneas.The contamination of soil and groundwater by heavy metals is extremely damaging due to high persistence of heavy metals in the environment. This work targeted the analysis of the sorption in Oxisol Typic Acrustox(LVwf, Ultisol (PVe, Kandic Oxisol (NVef and Quartzipsamment (RQ of heavy metals Cu, Cr, Zn, Cd, Pb and Ni. The sorption of the heavy metals in the soil was evaluated by batch method and described by potential and linear models of the Freundlich isotherm. For the establishment the of sorption isotherm, 50.0 mL of solution containing the heavy metal were added in 5.0 mL of soil, assessing with different concentrations within the acceptable soil

  9. Phosphorus Sorption Characteristics in Aluminum-based Water Treatment Residuals Reacted with Dairy Wastewater: 1. Isotherms, XRD, and SEM-EDS Analysis.

    Science.gov (United States)

    Zohar, Iris; Massey, Michael S; Ippolito, James A; Litaor, M Iggy

    2018-05-01

    We examined P sorption characteristics in Al-based water treatment residuals (Al-WTR) generated from slightly alkaline surface water and in an organic residual composite (WW-Al/O-WTR), produced by using the Al-WTR to treat organic-rich and high P concentration dairy wastewater. Solids from both residuals were examined using scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) and X-ray diffraction (XRD), and exposed to P additions of 0 to 4000 mg L in a sorption experiment. The Al-WTR removed ∼97% of the added P, whereas WW-Al/O-WTR removed only 78% of the added P in the addition range of 0 to 100 mg P L. With P additions of ≥100 mg L, the removal rate declined to XRD indicated that the major mineral was calcite, with some silica and poorly crystalline Al hydroxides. Analysis by SEM-EDS, which used three-element overlay maps of the residual surfaces, indicated that P was sparsely sorbed on both calcic and Al (hydr)oxide surfaces, along with a few clusters, even at low P concentrations of the treated waters. Ternary clusters of P, Al, and Ca were more abundant on the WW-Al/O-WTR. Carbon distribution suggested that organic substances covered Al surfaces. Sorption of P onto WW-Al/O-WTR may be reversible due to relatively weak Ca-P and Al-P bonds induced by the slight alkaline nature and in the presence of organic moieties, enhancing the WW-Al/O-WTR potential to act as a P source, rather than a P sink, in agricultural applications. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  10. Comparison of salt solution and air drying methods for moisture fixation in highly porous building materials

    DEFF Research Database (Denmark)

    Antonov, Yovko Ivanov; Jensen, Rasmus Lund; Møldrup, Per

    2017-01-01

    In recent years, research has identified some bio-based, porous building materials as good or excellent regulators of moisture in buildings. The ability of a material to absorb, release and store moisture is described by vapour sorption isotherms. It is necessary input to simulations of indoor...... building materials by a standardized testing method, using saturated salt solutions. Furthermore, results from the standard method are compared to values of moisture content for the same materials, obtained by air-drying at different relative humidity. This is done with the aim to compare the findings from...... the two methods with respect to time and repeatability of the results. Derived isotherms are further used as direct input in the building simulation software BSim, which is capable of predicting indoor environment parameters by solving coupled, transient heat and moisture transport equations using finite...

  11. Adsorption isotherms of pear at several temperatures

    Directory of Open Access Journals (Sweden)

    Mitrevski Vangelče

    2015-01-01

    Full Text Available The moisture adsorption isotherms of pear were determined at 15ºC, 30ºC and 45ºC using the standard static gravimetric method over a range of water activity from 0.112 to 0.920. The experimental data were fitted with isotherm equations recommended in ASAE Standard D245.5. In order to find which equation gives the best results, large number of numerical experiments were performed. After that, several statistical criteria proposed in scientific literature for estimation and selection of the best sorption isotherm equations were used. For each equation and experimental data set, the average performance index was calculated and models were ranked afterwards. After that, some statistical rejection criteria were checked (D’Agostino-Pearson test of normality, single-sample run test and significance and precision of the model parameters. The performed statistical analysis shows that the Guggenheim-Anderson-de Boer (GAB equation has the highest value of average performance index, but higher correlation between pair of parameters leads to lower precision of estimated parameters.[Projekat Ministarstva nauke Republike Srbije, br. TR 31058

  12. Moisture diffusion and permeability characteristics of hydroxypropylmethylcellulose and hard gelatin capsules.

    Science.gov (United States)

    Barham, Ahmad S; Tewes, Frederic; Healy, Anne Marie

    2015-01-30

    The primary objective of this paper is to compare the sorption characteristics of hydroxypropylmethylcellulose (HPMC) and hard gelatin (HG) capsules and their ability to protect capsule contents. Moisture sorption and desorption isotherms for empty HPMC and HG capsules have been investigated using dynamic vapour sorption (DVS) at 25°C. All sorption studies were analysed using the Young-Nelson model equations which distinguishes three moisture sorption types: monolayer adsorption moisture, condensation and absorption. Water vapour diffusion coefficients (D), solubility (S) and permeability (P) parameters of the capsule shells were calculated. ANOVA was performed with the Tukey comparison test to analyse the effect of %RH and capsule type on S, P, and D parameters. The moisture uptake of HG capsules were higher than HPMC capsules at all %RH conditions studied. It was found that values of D and P across HPMC capsules were greater than for HG capsules at 0-40 %RH; whereas over the same %RH range S values were higher for HG than for HPMC capsules. S values decreased gradually as the %RH was increased up to 60% RH. To probe the effect of moisture ingress, spray dried lactose was loaded into capsules. Phase evolution was characterised by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), and differential scanning calorimetry (DSC). The capsules under investigation are not capable of protecting spray dried lactose from induced solid state changes as a result of moisture uptake. For somewhat less moisture sensitive formulations, HPMC would appear to be a better choice than HG in terms of protection of moisture induced deterioration. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Ellipsometry-based combination of isothermal sorption-desorption measurement and temperature programmed desorption technique: A probe for interaction of thin polymer films with solvent vapor

    Science.gov (United States)

    Efremov, Mikhail Yu.; Nealey, Paul F.

    2018-05-01

    An environmental chamber equipped with an in situ spectroscopic ellipsometer, programmatic vapor pressure control, and variable temperature substrate holder has been designed for studying polymer coating behavior during an exposure to a solvent vapor and also for probing the residual solvent in the film afterwards. Both sorption-desorption cycle at a constant temperature and temperature programmed desorption (TPD) of the residual solvent manifest themselves as a change of the film thickness. Monitoring of ellipsometric angles of the coating allows us to determine the thickness as a function of the vapor pressure or sample temperature. The solvent vapor pressure is precisely regulated by a computer-controlled pneumatics. TPD spectra are recorded during heating of the film in an oil-free vacuum. The vapor pressure control system is described in detail. The system has been tested on 6-170 nm thick polystyrene, poly(methyl methacrylate), and poly(2-vinyl pyridine) films deposited on silicon substrates. Liquid toluene, water, ethanol, isopropanol, cyclohexane, 1,2-dichloroethane, and chlorobenzene were used to create a vapor atmosphere. Typical sorption-desorption and TPD curves are shown. The instrument achieves sub-monolayer sensitivity for adsorption studies on flat surfaces. Polymer-solvent vapor systems with strong interaction demonstrate characteristic absorption-desorption hysteresis spanning from vacuum to the glass transition pressure. Features on the TPD curves can be classified as either glass transition related film contraction or low temperature broad contraction peak. Typical absorption-desorption and TPD dependencies recorded for the 6 nm thick polystyrene film demonstrate the possibility to apply the presented technique for probing size effects in extremely thin coatings.

  14. Isotherm Studies of Equilibrium Sorption of Cu2+ and Cd2+ from Aqueous Solutions by Modified and Unmodified Breadfruit Seed Hull

    Directory of Open Access Journals (Sweden)

    Christopher Uchechukwu Sonde

    2015-09-01

    Full Text Available The ability of an economically cheap adsorbent material of natural origin, African breadfruit seed hull, was assessed for Cu(II and Cd(II ions’ adsorption from aqueous solutions. The effects of adsorbent dose, particle size and initial metal ion concentrations were investigated in a batch adsorption process. The experimental data were analyzed using five two-parameter isotherm equations (i.e., Langmuir, Freundlich, Temkin, Harkins-Jura and Halsey isotherm models. Freundlich and Halsey models provided the best description for the adsorption data while the other three models gave fairly good interpretation to the experimental adsorption data. The maximum adsorption capacity corresponding to saturation of sites (qmax, obtained from the Langmuir plots, were 7.76 and 8.06 mg g-1 for Cu(II and Cd(II onto the unmodified breadfruit seed hull (UBSH and 12.67 and 13.97 mg g-1, respectively for Cu(II and Cd(II adsorption onto the modified breadfruit seed hull (MBSH. The experimental results showed that there was an enhancement in the removal of the metal ions by the mercaptoacetic acid-modified breadfruit seed hull. DOI: http://dx.doi.org/10.17807/orbital.v7i3.625 

  15. Water sorption and transport in dry crispy bread crust

    NARCIS (Netherlands)

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

    2010-01-01

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

  16. Water sorption kinetics of damaged beans: GAB model

    Directory of Open Access Journals (Sweden)

    Fernanda M. Baptestini

    Full Text Available ABSTRACT The objective of this study was to model the water sorption kinetics of damaged beans. Grains with initial moisture content of 53.85%, dry basis (d.b., were used. One portion of the grains was used to obtain desorption isotherms, while the other was subjected to drying until the moisture content of 5.26% (d.b., so that it was subjected to the adsorption. For the induction of damage, a Stein Breakage Tester was used. To obtain the equilibrium moisture content, grains were placed in a climatic chamber at 20, 30, 40 and 50 ± 1 °C combined with relative humidity of 30, 40, 50, 70 and 90 ± 3%. The GAB model fitted well to the equilibrium moisture experimental data of damaged grains and control. With increasing temperature, the monolayer moisture contents decreased in adsorption and desorption processes, ranging from 9.84 to 5.10% d.b. The lower moisture content in the monolayer in damaged grains indicates that lower moisture content is necessary to ensure their conservation.

  17. Moisture transport in coated wood

    NARCIS (Netherlands)

    Meel, P.A. van; Erich, S.J.F.; Huinink, H.P.; Kopinga, K.; Jong, J. DE; Adan, O.C.G.

    2011-01-01

    Moisture accumulation inside wood causes favorable conditions for decay. Application of a coating alters the moisture sorption of wood and prevents accumulation of moisture. This paper presents the results of a nuclear magnetic resonance (NMR) study on the influence of a coating on the moisture

  18. Experimental study of Pb (II) solution sorption behavior onto Coffee Husk Bioactivated Carbon

    Science.gov (United States)

    Fona, Z.; Habibah, U.

    2018-04-01

    Coffee husk which is abundantly produced in the coffee plantations is potential to be a challenging adsorbent. The fate of Pb (II) solution in the sorption mechanism onto the adsorbent has been investigated. This paper aimed to study the efficiency of Pb (II) aqueous solution removal using activated carbon from coffee husk (CAC). The sorption characteristics were using two isotherm models, Langmuir and Freundlich, were also reported. The coffee husk from local plantations in Middle Aceh was carbonized and sieved to 120/140 mesh. The charcoal was activated using hydrochloric acid before contacted with the different initial concentrations of Pb (II) solution. The remaining concentrations of the metal in the specified contact times were determined using Atomic Adsorption Spectrophotometer at 283.3 wavelength. The result showed that the equilibrium concentrations were obtained in about 30 minutes which depended on the initial concentration. The sorption mechanism followed Freundlich isotherm model where the adsorption constant and capacity were accordingly 1.353 and 1.195 mgg‑1. The iodine sorption was up to 1,053 mgg‑1. Based on the ash and moisture content, as well as iodine sorption, the activated carbon met the national standard.

  19. Experimental study of a laboratory concrete material representative of containment buildings: desorption isotherms and permeability determination

    International Nuclear Information System (INIS)

    Semete, P.; Fevrier, B.; Delorme, J.; Sanahuja, J.; Desgree, P.; Le Pape, Y.

    2015-01-01

    The isotherm sorption curve is a first order parameter for the calculations of concrete drying and/or creep using Finite Element Analysis. An experimental campaign was undertaken by EDF MMC in order to characterize the first desorption isotherm at room temperature of a laboratory material representative of concrete containment buildings. Long term drying tests were carried out on cement paste and on three samples geometries on concrete (with radial and axial one-dimensional drying on thin disks and multi-dimensional drying on Representative Elementary Volumes). The measurements results (porosity, densities and mass loss curves) are provided and the isotherms obtained for the four different configurations are compared. Several analyses of the results are proposed including the assessment of a criterion for the determination of the moisture content final balance (estimation of the asymptotic mass loss) and the back-analysis of equivalent permeability. (authors)

  20. Kinetic and isotherm studies of bisphenol A adsorption onto orange albedo(Citrus sinensis): Sorption mechanisms based on the main albedo components vitamin C, flavones glycosides and carotenoids.

    Science.gov (United States)

    Kamgaing, Theophile; Doungmo, Giscard; Melataguia Tchieno, Francis Merlin; Gouoko Kouonang, Jimmy Julio; Mbadcam, Ketcha Joseph

    2017-07-03

    Orange albedo and its adsorption capacity towards bisphenol A (BPA) were studied. Adsorption experiments were conducted in batch mode at 25-55°C. Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) and Fourier transform infrared (FTIR) spectroscopy were used to characterise the biosorbent. The effects of various parameters including adsorption time, equilibrium pH, adsorbent dosage and initial adsorbate concentration were investigated. The optimum contact time and pH for the removal of BPA were 60 min and 2, respectively. It was found that the adsorption isotherms best matched the Freundlich model, the adsorption of BPA being multilayer and that of the albedo surface heterogeneous. From the kinetic studies, it was found that the removal of BPA best matched the pseudo-second order kinetic model. An adsorption mechanism based on the albedo surface molecules is proposed and gives a good account of π-π interactions and hydrogen bonding. Orange albedo, with a maximum BPA loading capacity of 82.36 mg g -1 (significantly higher than that of most agricultural residues), is a good candidate for BPA adsorption in aqueous media.

  1. Sorption isotherms, kinetic and optimization process of amino acid proline based polymer nanocomposite for the removal of selected textile dyes from industrial wastewater.

    Science.gov (United States)

    Raghunath, Sharista; Anand, K; Gengan, R M; Nayunigari, Mithil Kumar; Maity, Arjun

    2016-12-01

    In this article, adsorption and kinetic studies were carried out on three textile dyes, namely Reactive Blue 222 (RB 222), Reactive Red 195 (RR 195) and Reactive Yellow 145 (RY 145). The dyes studied in a mixture were adsorbed under various conditions onto PRO-BEN, a bentonite modified with a new cationic proline polymer (l-proline-epichlorohydrin polymer). The proline polymer was characterized by 1 H NMR, Fourier transform infrared spectroscopy (FT-IR), dynamic light scattering (DLS) and TEM. The PRO-BEN composite was characterized by FT-IR, dynamic light scattering (DLS) (zeta potential), TEM imaging, SEM/EDX and X-ray photoelectron spectroscopy (characterize the binding energy). During adsorption studies, factors involving pH, temperature, the initial concentrations of the dyes and the quantity of PRO-BEN used during adsorption were established. The results revealed that the adsorption mechanism was categorized by the Langmuir type 1 isotherm. The adsorption data followed the pseudo-second order kinetic model. The intraparticle diffusion model indicated that adsorption did not only depend on the intraparticle diffusion of the dyes. The thermodynamic parameters verified that the adsorption process was spontaneous and exothermic. The Gibbs free energy values indicated that physisorption had occurred. Successful adsorption of dyes from an industrial effluent was achieved. Desorption studies concluded that PRO-BEN desorbed the dyes better than alumina. This can thereby be viewed as a recyclable remediation material. The PRO-BEN composite could be a cost efficient alternative towards the removal of organic dyes in wastewater treatment. Copyright © 2016 Elsevier B.V. All rights reserved.

  2. A Literature Review on the Study of Moisture in Polymers

    Energy Technology Data Exchange (ETDEWEB)

    Trautschold, Olivia Carol [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-05-25

    This literature review covers the main chemical and physical interactions between moisture and the polymer matrix. Fickian versus Non-Fickian diffusion behaviors are discussed in approximating the characteristics of moisture sorption. Also, bound water and free water sorbed in polymers are distinguished. Methods to distinguish between bound and free water include differential scanning calorimetry, infrared spectroscopy, and time-domain nuclear magnetic resonance spectroscopy. The difference between moisture sorption and water sorption is considered, as well as the difficulties associated with preventing moisture sorption. Furthermore, specific examples of how moisture sorption influences polymers include natural fiber-polymer composites, starch-based biodegradable thermoplastics, and thermoset polyurethane and epoxies.

  3. ISOTERMAS DE SORCION DE AGUA EN RESIDUOS DE EXTRACCIÓN DE JUGO DE NARANJA ISOTERMAS DE SORCAO DA AGUA EM RESIDUOS DE EXTRACAO DE SUCO DE LARANJA SORPTION ISOTHERMS OF WATER IN ORANGE JUICE EXTRACTION RESIDUES

    Directory of Open Access Journals (Sweden)

    MÓNICA OMAÑA

    2010-06-01

    não varié ou alcance o equilibrio. Além demais, realizouse um ajuste com o modelo proposto pelo Smith obtendose erros medios de 8.56% e 7.57% para Túnez e Pomelo, respectivamente.Waste from orange juice extraction, such as skins, shells and seeds, are known as citrus pulp, they may cause two major impacts, be a potential source ofraw material in the food industry concentrates for animals, and reduce problem posed to the environment with unnecessary use of landfills. The purpose of this paper is to obtain experimental sorption isotherms of this waste, at a temperature of 20° in a wide range of water activity (0.33 -0.97 from the two producers of orange juice, called Túnez and Pomelo. The process used to determine isothermal sorption curves, is the method recommended by the COST Project 90, which consisted of placing a known amount of sample in an airtight container with a given relative humidity until the weight does not vary orreaches balance. In addition, an adjustment to the model proposed by Smith obtained average errors of 8.56% and 7.57% for Túnez and Pomelo, respectively.

  4. Sorption characteristics of pectin isolated from Jerusalem Artichoke tubers (Helianthus tuberosus L.

    Directory of Open Access Journals (Sweden)

    N. Toshkov

    2015-05-01

    Full Text Available Introduction. The aim of the present study is the isolation of pectin from Jerusalem artichoke tubers (Helianthus tuberosus L. and the analysis of its sorption characteristics Materials and methods. Research was carried out on the pectin content of the tubers of Jerusalem artichoke plants cultivated in Bulgaria. The polyuronide content (PUC was determined via the МсCready method. The static gravimetric method was used for analysis of the sorption characteristics of pectins. Results and discussion. The polysaccharide was extracted. The isolated pectins were analyzed in physical terms: the equilibrium sorption isotherms, belonging to type II in Brunauer’s classification, were obtained experimentally. The entire isotherm length demonstrated statistically significant hysteresis. The Henderson and Chung-Pfost models provided adequate isotherm description. The pectin content of the three Jerusalem artichoke samples is 14.8, 9.2 and 11.9 % a.d.m., respectively. The monomolecular moisture content of pectin was within the 7.42 – 7.92% dry basis range, its corresponding water activity value –within the 0.14 –0.16 range. Conclusion. The resultsof research are advisablefor use indevelop of functional food ingredient which is used pectin as a gelling agent and a stabilizer.

  5. Investigation of metal ions sorption of brown peat moss powder

    Science.gov (United States)

    Kelus, Nadezhda; Blokhina, Elena; Novikov, Dmitry; Novikova, Yaroslavna; Chuchalin, Vladimir

    2017-11-01

    For regularities research of sorptive extraction of heavy metal ions by cellulose and its derivates from aquatic solution of electrolytes it is necessary to find possible mechanism of sorption process and to choice a model describing this process. The present article investigates the regularities of aliovalent metals sorption on brown peat moss powder. The results show that sorption isotherm of Al3+ ions is described by Freundlich isotherm and sorption isotherms of Na+ i Ni2+ are described by Langmuir isotherm. To identify the mechanisms of brown peat moss powder sorption the IR-spectra of the initial brown peat moss powder samples and brown peat moss powder samples after Ni (II) sorption were studied. Metal ion binding mechanisms by brown peat moss powder points to ion exchange, physical adsorption, and complex formation with hydroxyl and carboxyl groups.

  6. Package selection for moisture protection for solid, oral drug products.

    Science.gov (United States)

    Waterman, Kenneth C; MacDonald, Bruce C

    2010-11-01

    This review describes how best to select the appropriate packaging options for solid, oral drug products based on both chemical and physical stability, with respect to moisture protection. This process combines an accounting for the initial moisture content of dosage form components, moisture transfer into (out of) packaging based on a moisture vapor transfer rate (MVTR), and equilibration between drug products and desiccants based on their moisture sorption isotherms to provide an estimate of the instantaneous relative humidity (RH) within the packaging. This time-based RH is calculationally combined with a moisture-sensitive Arrhenius equation (determined using the accelerated stability assessment program, ASAP) to predict the drug product's chemical stability over time as a function of storage conditions and packaging options. While physical stability of dosage forms with respect to moisture has been less well documented, a process is recommended based on the threshold RH at which changes (e.g., dosage form dissolution, tablet hardness, drug form) become problematic. The overall process described allows packaging to be determined for a drug product scientifically, with the effect of any changes to storage conditions or packaging to be explicitly accounted for. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association

  7. The sorption behaviour of 99Tc on activated carbon

    International Nuclear Information System (INIS)

    Xia Deying; Zeng Jishu

    2004-01-01

    The sorption behaviour of 99 Tc on apricot-pit activated carbon with batch experiment is studied. The influence of such factors as sorbent particle size, temperature, pH value on sorption ratio, and the Freundlich sorption isotherms are reported in this paper. (author)

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

    Science.gov (United States)

    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. Copyright © 2012 Elsevier Ltd. All rights reserved.

  9. Thermodynamic properties of water sorption of jackfruit (Artocarpus heterophyllus Lam. as a function of moisture content Propriedades termodinâmicas de sorção de água da jaca (Artocarpus heterophyllus Lam. em função do teor de umidade

    Directory of Open Access Journals (Sweden)

    Ana Paula Prette

    2013-03-01

    Full Text Available The Jackfruit tree is one of the most significant trees in tropical home gardens and perhaps the most widespread and useful tree in the important genus Artocarpus. The fruit is susceptible to mechanical and biological damage in the mature state, and some people find the aroma of the fruit objectionable, particularly in confined spaces. The dehydration process could be an alternative for the exploitation of this product, and the relationship between moisture content and water activity provides useful information for its processing and storage. The aim of this study was to determine the thermodynamic properties of the water sorption of jackfruit (Artocarpus heterophyllus Lam. as a function of moisture content. Desorption isotherms of the different parts of the jackfruit (pulp, peduncle, mesocarp, peel, and seed were determined at four different temperatures (313.15, 323.15, 333.15, and 343.15 K in a water activity range of 0.02-0.753 using the static gravimetric method. Theoretical and empirical models were used to model the desorption isotherms. An analytical solution of the Clausius-Clapeyron equation was proposed to calculate the isosteric heat of sorption, the differential entropy, and Gibbs' free energy using the Guggenhein-Anderson-de Boer and Oswin models considering the effect of temperature on the hygroscopic equilibrium.A jaqueira é uma das árvores mais significativas nos quintais tropicais e, talvez, a árvore mais importante e útil do gênero Artocarpus. O fruto é suscetível a danos mecânicos e biológicos no estado maduro, e seu aroma é desagradável para algumas pessoas, quando em espaços fechados. O processo de desidratação pode ser uma alternativa para a exploração deste produto, e a relação entre a umidade e a atividade de água fornece informações úteis para seu processamento e armazenamento. O objetivo do trabalho foi determinar as propriedades termodinâmicas de sorção da água em frutos de jaca (Artocarpus

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

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

  12. Modeling temperature and moisture fields in conditioned spaces using zonal approach, including sorption phenomena in buildings materials; Modelisation thermo-hydro-aeraulique des locaux climatises selon l'approche zonale (prise en compte des phenomenes de sorption d'humidite)

    Energy Technology Data Exchange (ETDEWEB)

    Cordeiro Mendoca, K.

    2004-05-15

    Building simulation models represent in our days an important tool for building conception and performance analysis. Although moisture interacts in many ways with the whole building affecting therefore its behavior, frequently these models neglects the interactions between them. In addition, in most of them, indoor air conditions are considered uniform, which is a non-realistic assumption in conditioned spaces. In this work, a model to predict temperature and moisture fields in conditioned spaces, using zonal approach, is proposed. This method is based in dividing spatially a room in a relative small number of zones, typically on the order of tens to hundreds, where the state variables of air are considered uniform, with the exception of pressure that varies hydrostatically. While not as fine-grained as CFD simulation, zonal models do give useful information about temperature and moisture distributions that is important in comfort analysis. The proposed model was structured in three groups of sub-models representing the three building domains: indoor air, envelope and HVAC system. The indoor air sub-model is related to the indoor air space, where airflow speed can be considered weak. The envelope sub-model is related to the radiation exchanges between envelope and its neighborhood, and to the simultaneous heat and mass transfers across the envelope material. This latest can be represented by four sub-models of different complexity levels, with two of them taking into account moisture adsorption and desorption by building materials. Concerning to the HVAC system model, it refers to the whole system that means equipment, control and specific airflow from equipment. All sub-models were coupled into a modular simulation environment, SPARK, well-adapted to compare different models. The applicability of the proposed model is shown by two examples. The first one shows the importance of considering moisture sorption phenomena in the prediction of indoor air conditions

  13. THERMODYNAMICS AND ADSORPTION ISOTHERMS FOR THE ...

    African Journals Online (AJOL)

    BAFFA

    The use of maize (Zea mays) cob for the biosorption of Cr(VI), Ni(II) and Cd(II) is ... Variations in the concentration of the different adsorbates during the adsorption process .... Langmuir isotherm is the dimensionless separation .... The use of Sago waste for the sorption of lead and copper. Water S. Afr., 24 (3), p251-256.

  14. Effects of sorption behaviour on contaminant migration

    International Nuclear Information System (INIS)

    Melnyk, T.W.

    1985-11-01

    The effects of sorption behaviour on contaminant migration in groundwater systems are varied. Retardation of migration and dispersive effects can vary widely and contaminant concentration profiles can take a number of different shapes. This report examines the nature of some of these effects, especially those due to sorption behaviours that are dependent on the concentration of the contaminant in the groundwater. The effects are calculated using, in most cases, analytical solutions to the chemical equations imbedded in a simple reaction-cell or box-model transport algorithm. The hydrogeological parameters are held constant, and radioactive decay and hydrodynamic dispersion are excluded. A general discussion of the role of sorption equations in transport modelling is followed by presentation of migration results for a number of models of sorption behaviour varying from linear isotherms, Langmuir, Freundlich and ion-exchange isotherms, to precipitation reactions and multiple-site sorption reactions. The results are compared and general conclusions are drawn about the various migration behaviours calculated. The conclusions are that equilibrium sorption of trace contaminants can be modelled with linear isotherms (constant distribution coefficients or constant retardation factors) but the evaluation and extrapolation of the distribution coefficient are not easy. Nonlinear isotherms lead to unsymmetrical migration fronts. A comparison of Freundlich and linear isotherms is made. Sorption/desorption kinetic factors can be significant on the time scale of laboratory experiments and can cause large dispersive effects. Slow but important reactions can be missed altogether. Precipitation or mineralization behaviour cannot be modelled with constant distribution coefficients. Also, mineralization reactions can be kinetically slow even on the geological time scale. 89 refs

  15. Sorption mechanisms and sorption models

    International Nuclear Information System (INIS)

    Fedoroff, M.; Lefevre, G.; Duc, M.; Neskovic, C.; Milonjic, S.

    2004-01-01

    Sorption at the solid-liquid interfaces play a major role in many phenomena and technologies: chemical separations, catalysis, biological processes, transport of toxic and radioactive species in surface and underground waters. The long term safety of radioactive waste repositories is based on artificial and natural barriers, intended to sorb radionuclides after the moment when the storage matrixes and containers will be corroded. Predictions on the efficiency of sorption for more than 10 6 years have to be done in order to demonstrate the safety of such depositories, what is a goal never encountered in the history of sciences and technology. For all these purposes, and, especially for the long term prediction, acquiring of sorption data constitutes only a first step of studies. Modeling based on a very good knowledge of sorption mechanisms is needed. In this review, we shall examine the main approaches and models used to quantify sorption processes, including results taken from the literature and from our own studies. We shall compare sorption models and examine their adequacy with sorption mechanisms. The cited references are only a few examples of the numerous articles published in that field. (orig.)

  16. Sorption of uranium and cesium by Hanford basalts and associated secondary smectite

    International Nuclear Information System (INIS)

    Ames, L.L.; McGarrah, J.E.; Walker, B.A.; Salter, P.F.

    1982-01-01

    Three characterized basalts and an associated secondary smectite were used in comparative uranium and cesium sorption studies. Experiments utilizing two synthetic characteristic basalt groundwaters at 23 and 60 0 C allowed comparison of increased temperature and carbonate concentration effects on Cs and U sorption. The sorption data were fitted to the Dubinin-Radushkevich (D-R) isotherm, and loading maxima and energetics derived. An increase in temperature caused a decrease in Cs sorption maxima on all solids from all groundwaters studied and an increase in U sorption maxima, especially from the higher-carbonate-content groundwater. Sorption energies were characteristic of ion exchange for both Cs and U sorption processes. Basalt U sorption maxima were relatively insignificant, but smectite U sorption maxima surpassed Cs sorption maxima in both groundwaters at 60 0 C. The uranyl carbonate complexes thus may be relatively temperature-sensitive. Upon removal of excess Fe-oxides from the secondary smectite, U sorption decreased and the D-R isotherm reverted to a normal Freundlich sorption isotherm. Removal of excess Fe-oxides from the basalts and secondary smectite would probably result in Freundlich sorption isotherms for both Cs and U. (Auth.)

  17. ISOTERMAS DE DESORCION DE HUMEDAD EN PITAHAYA AMARILLA (Selenicereus megalanthus ISOTERMAS DE DESSORÇÃO DE UMIDADE EM PITAIAIÁS AMARELO (Selenicereus megalanthus MOISTURE DESORPTION ISOTHERMS IN YELLOW PITAHAYA (Selenicereus megalanthus

    Directory of Open Access Journals (Sweden)

    ALFREDO A. AYALA-APONTE

    2012-12-01

    Full Text Available Se determinaron las isotermas de desorción de humedad en pitahaya amarilla a 15, 25 y 35°C mediante el método gravimétrico en el intervalo de actividad de agua entre 0.111 y 0.901. Los valores experimentales de desorción se ajustaron mediante los modelos de GAB, Henderson, Smith, Oswin y Chung y Fost, usualmente usados en alimentos. El calor isostérico de desorción (Qst se determinó mediante la ecuación de Clausius-Clapeyron. Los resultados mostraron que las isotermas fueron de tipo III. El contenido de humedad de equilibrio (CHE presentó dependencia con la temperatura, esta disminuyó con el aumento de la temperatura para un valor constante de actividad de agua. El modelo GAB fue el de mejor ajuste de los valores experimentales. El Qst disminuyó con el aumento del CHE, desde 61.43 hasta 45.11 kJ/mol para humedades de 0.08 hasta 0.56 (g agua/g ms respectivamente.Se determinaram as isotermas de dessorção de humidade da pitaiaiás amarela, 15, 25 y 35°C utilizando-se o método estático gravimétrico numafaixa de atividade de água entre 0.111 e 0.90, Os valores experimentais de adsorçãoforam ajustados pelos modelos de GAB, Henderson, Smith, Oswin y Chung y Fost, O calor isostérico de adsorção (Qst foi determinado pela ecuação de Clausius-Clapeyron. Os resultados mostraram que as isotermas obtidasforam do tipo III. O teor de humidade de equilíbrio (CHE apresentoudependênciacom a temperatura, diminuindocom o aumento desta a um valor constante de atividade de água. O modelo de GAB foi o que apresentou o melhor ajuste dos valores experimentais. O Qstdiminuíocom o aumento de CHE, obténdo-se um máximo e um mínimo entre 61.43 a 45.11 kJ / mol de humidade entre 0.08 e 0.56 (g de água / g bs, respectivamente.Moisture desorption isotherms for yellow pitahaya fruits were studied at 15, 25, and 35°C using the gravimetric method for a 0.111-0.901 water activity range. Experimental values were adjusted by using the GAB, Henderson

  18. Results of a European interlaboratory comparison on CO2 sorption on activated carbon and coals

    Science.gov (United States)

    Gensterblum, Yves; Busch, Andreas; Krooss, Bernhard; de Weireld, Guy; Billemont, Pierre; van Hemert, Patrick; Wolf, Karl-Heinz

    2013-04-01

    -laboratory comparison of high pressure CO2 sorption isotherms. I: Activated carbon" Carbon 47 ( 2009 ) 2958 -2969 Goodman, A.L., Busch, A., Duffy, G., Fitzgerald, J.E., Gasem, K.A.M., Gensterblum, Y., Krooss, B.M., Levy, J., Ozdemir, E., Pan, Z., Robinson, Jr., R.L., Schroeder, K., Sudibandriyo, M., White, C. (2004). An Inter-laboratory Comparison of CO2 Isotherms Measured on Argonne Premium Coal Samples. Energy and Fuels 18, 1175-1182. Goodman, A.L., Busch, A., Day, S., Duffy, G.J., Fitzgerald, J.E., Gasem, K.A.M., Gensterblum, Y., Hartman, C., Krooss, B.M., Pan, Z., Pratt, T., Robinson, Jr., R.L., Romanov, V., Sakurovs, R., Schroeder, K., Sudibandriyo, M., White, C.M. (2007) "Inter-laboratory Comparison II: CO2 Isotherms Measured on Moisture-Equilibrated Argonne Premium Coals at 55oC and 15 MPa", International Journal of Coal Geology 72, 153-164.

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

    Science.gov (United States)

    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. Sorption equilibria of ethanol on cork.

    Science.gov (United States)

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

    2013-06-05

    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.

  1. MOISTURE ADSORPTION ISOTHERMS IN YELLOW PITAHAYA (Selenicereusmegalanthus

    Directory of Open Access Journals (Sweden)

    ALFREDO AYALA APONTE

    2011-01-01

    Full Text Available Se determinaron las isotermas de adsorción de humedad en pitahaya amarrilla a 15, 25, y 35ºC mediante el método gravímetro en el intervalo de actividad de agua (aw entre 0.111 y 0.901. Los valores experimentales de adsorción se ajustaron mediante los modelos de GAB, BET, Henderson, Smith, Caurie, y Peleg. El calor isostérico de adsorción (Qst se determinó mediante la ecuación de Clausius- Clapeyron. Los resultados mostraron que las isotermas fueron de tipo III. El contenido de humedad de equilibrio (CHE presentó dependencia con la temperatura, disminuyendo con el aumento de esta para un valor constante de aw. El modelo GAB fue el que presentó mejor ajuste de los valores experimentales. El Qst disminuyó con el aumento del CHE, variando de 57.154 a 45.79 kJ/mol para humedades de 0.05 y 0.4 (g agua/g ms, respectivamente. Estos resultados son de interés para establecer las mejores condiciones de almacenamiento de la pitahaya deshidratada, así como la predicción de la vida útil, y el diseño de empaque.

  2. suitability of murram for phosphorus sorption in constructed wetlands

    African Journals Online (AJOL)

    Mimi

    sorption isotherms, determination of Phosphorus sorption capacity of the substrates, determination of. Phosphorus sorption as the function of time and determination of effect of temperature on the ... (Na2O + K2O) % SiO2. %. P2O5. %. TiO2. %. LOI. %. 19.2. 1.3. 0.69. 5.13. 0.05. 6.7. 61.9. 0.04. 0.51. 4.4. As presented in ...

  3. Thermal denaturation of sunflower globulins in low moisture conditions

    International Nuclear Information System (INIS)

    Rouilly, A.; Orliac, O.; Silvestre, F.; Rigal, L.

    2003-01-01

    DSC analysis in pressure resisting pans of sunflower oil cake makes appear the endothermic peak of sunflower globulins denaturation. Its temperature decreases from 189.5 to 119.9 deg. C while the corresponding enthalpy increases from 2.6 to 3.3 J/g of sample, or from 6.7 to 12.2 J/g of dry protein, when the samples moisture content varies from 0 to 30.0% of the total weight. The plot of the denaturation temperature versus the moisture content is not linear but has a rounded global shape and seems to follow the hydration behavior of the proteins, modeled with the sorption isotherm. As it can be seen on scanning electron microscopy (SEM) micrographs, protein corpuscles 'melt' after such a thermal treatment and large aggregates form by coagulation. Moisture dependence of the 'fusion' temperature of native proteic organization, in low moisture conditions, offers so a new characterization method for the use of vegetable proteins in agro-materials

  4. Thermal denaturation of sunflower globulins in low moisture conditions

    Energy Technology Data Exchange (ETDEWEB)

    Rouilly, A.; Orliac, O.; Silvestre, F.; Rigal, L

    2003-03-05

    DSC analysis in pressure resisting pans of sunflower oil cake makes appear the endothermic peak of sunflower globulins denaturation. Its temperature decreases from 189.5 to 119.9 deg. C while the corresponding enthalpy increases from 2.6 to 3.3 J/g of sample, or from 6.7 to 12.2 J/g of dry protein, when the samples moisture content varies from 0 to 30.0% of the total weight. The plot of the denaturation temperature versus the moisture content is not linear but has a rounded global shape and seems to follow the hydration behavior of the proteins, modeled with the sorption isotherm. As it can be seen on scanning electron microscopy (SEM) micrographs, protein corpuscles 'melt' after such a thermal treatment and large aggregates form by coagulation. Moisture dependence of the 'fusion' temperature of native proteic organization, in low moisture conditions, offers so a new characterization method for the use of vegetable proteins in agro-materials.

  5. Analysis of sorption into single ODS-silica gel microparticles in acetonitrile-water.

    Science.gov (United States)

    Nakatani, Kiyoharu; Kakizaki, Hiroshi

    2003-08-01

    Intraparticle mass transfer processes of Phenol Blue (PB) in single octadecylsilyl (ODS)-silica gel microparticles in acetonitrile-water were analyzed by microcapillary manipulation and microabsorption methods. An absorption maximum of PB, the sorption isotherm parameters, and the sorption rate in the microparticle system were highly dependent on the percentage of acetonitrile in solution. The results are discussed in terms of the microscopic polarity surrounding PB in the ODS phase and the relationship between the isotherm parameters and the sorption rate.

  6. Influence of the temperature in the uranium (Vi) sorption in zirconium diphosphate

    International Nuclear Information System (INIS)

    Garcia G, N.; Solis, D.; Ordonez R, E.

    2012-10-01

    In the present work was evaluated the uranium (Vi) sorption at 10, 20, 30, 40 and 60 C on the zirconium diphosphate (ZrP 2 O 7 ). They were carried out kinetic and isotherms using the method by lots, these will allow to fix the sorption time (kinetic) and to explain the behavior of this sorption in different ph conditions and temperature (isotherm). The quantity of retained uranium in the surface was quantified by means of the fluorescence technique. (Author)

  7. Moisture-induced caking of beverage powders.

    Science.gov (United States)

    Chávez Montes, Edgar; Santamaría, Nadia Ardila; Gumy, Jean-Claude; Marchal, Philippe

    2011-11-01

    Beverage powders can exhibit caking during storage due to high temperature and moisture conditions, leading to consumer dissatisfaction. Caking problems can be aggravated by the presence of sensitive ingredients. The caking behaviour of cocoa beverage powders, with varying amounts of a carbohydrate sensitive ingredient, as affected by climate conditions was studied in this work. Sorption isotherms of beverage powders were determined at water activities (a(w) ) ranging from 0.1 to 0.6 in a moisture sorption analyser by gravimetry and fitted to the Brunauer-Emmett-Teller (BET) or the Guggenheim-Anderson-de Boer (GAB) equation. Glass transition temperatures (T(g) ) at several a(w) were analysed by differential scanning calorimetry and fitted to the Gordon-Taylor equation. Deduced T(g) = f(a(w) ) functions helped to identify stability or caking zones. Specific experimental methods, based on the analysis of mechanical properties of powder cakes formed under compression, were used to quantify the degree of caking. Pantry tests complemented this study to put in evidence the visual perception of powder caking with increasing a(w) . The glass transition approach was useful to predict the risks of caking but was limited to products where T(g) can be measured. On the other hand, quantification of the caking degree by analysis of mechanical properties allowed estimation of the extent of degradation for each product. This work demonstrated that increasing amounts of a carbohydrate sensitive ingredient in cocoa beverages negatively affected their storage stability. Copyright © 2011 Society of Chemical Industry.

  8. Moisture transport and equilibrium in organic coatings

    NARCIS (Netherlands)

    Wel, van der G.K.; Adan, O.C.G.

    2000-01-01

    Improving coating performance in regard of protection of substrates and structures against moisturerelated degradation requires detailed knowledge of underlying transport mechanisms. In this paper a review is given on transport and equilibrium sorption of moisture in polymer films and organic

  9. Gas Sorption, Diffusion, and Permeation in Nafion

    KAUST Repository

    Mukaddam, Mohsin Ahmed; Litwiller, Eric; Pinnau, Ingo

    2015-01-01

    The gas permeability of dry Nafion films was determined at 2 atm and 35 °C for He, H2, N2, O2, CO2, CH4, C2H6, and C3H8. In addition, gas sorption isotherms were determined by gravimetric and barometric techniques as a function of pressure up to 20

  10. Preparation and Properties of Moisture-absorbing Film Impregnated with Polyacrylic Acid Partial Sodium Salt Material

    International Nuclear Information System (INIS)

    Lee, Youn Suk; Park, Insik; Choi, Hong Yeol

    2014-01-01

    Moisture is a major factor causing the deteriorative physical change, microbial growth, and chemical reaction of the products. In this study, the moisture absorbing composite films have been prepared with moisture absorbing material of polyacrylic acid partial sodium salt (PAPSS) impregnated on LLDPE polymer for the functional packaging applications. The results showed that PAPSS impregnated film illustrated uniformly dispersed PAPSS particles in the LLDPE polymer matrix. The transparency of the PAPSS impregnated film decreased slightly at higher PAPSS concentrations. An increase in the PAPSS content for moisture-absorbing films showed a similar decrease in tensile strength, percent elongation at break, and tear strength. Their values of films impregnated with PAPSS of 0.5, 1, and 2% showed no significant difference. Meanwhile, 4% PAPSS films significantly decreased the values of mechanical properties compared to the films impregnated with different PAPSS levels. Values of the oxygen permeability and water vapor permeability for PAPSS impregnated films decreased significantly with greater PAPSS. The results indicate that 4% PAPSS impregnated in LLDPE films had high affinity of moisture absorbencies compared to the other films. The mathematical equation that best described the moisture sorption isotherm of each film sample was the GAB equation at 25 .deg. C. The crystallization and melting temperatures of PAPSS films were influenced by the addition of PAPSS material, but showed good thermal stability

  11. Preparation and Properties of Moisture-absorbing Film Impregnated with Polyacrylic Acid Partial Sodium Salt Material

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Youn Suk; Park, Insik [Yonsei University, Wonju (Korea, Republic of); Choi, Hong Yeol [CJ Cheiljedang, Seoul (Korea, Republic of)

    2014-08-15

    Moisture is a major factor causing the deteriorative physical change, microbial growth, and chemical reaction of the products. In this study, the moisture absorbing composite films have been prepared with moisture absorbing material of polyacrylic acid partial sodium salt (PAPSS) impregnated on LLDPE polymer for the functional packaging applications. The results showed that PAPSS impregnated film illustrated uniformly dispersed PAPSS particles in the LLDPE polymer matrix. The transparency of the PAPSS impregnated film decreased slightly at higher PAPSS concentrations. An increase in the PAPSS content for moisture-absorbing films showed a similar decrease in tensile strength, percent elongation at break, and tear strength. Their values of films impregnated with PAPSS of 0.5, 1, and 2% showed no significant difference. Meanwhile, 4% PAPSS films significantly decreased the values of mechanical properties compared to the films impregnated with different PAPSS levels. Values of the oxygen permeability and water vapor permeability for PAPSS impregnated films decreased significantly with greater PAPSS. The results indicate that 4% PAPSS impregnated in LLDPE films had high affinity of moisture absorbencies compared to the other films. The mathematical equation that best described the moisture sorption isotherm of each film sample was the GAB equation at 25 .deg. C. The crystallization and melting temperatures of PAPSS films were influenced by the addition of PAPSS material, but showed good thermal stability.

  12. Modelling of a diffusion-sorption experiment on sandstone

    International Nuclear Information System (INIS)

    Smith, P.A.

    1989-11-01

    The results of a diffusion-sorption experiment on a sample of Darley Dale sandstone, using simulated groundwater spiked with a mixture of 125 I, 85 Sr and 137 Cs, are modelled by a one-dimensional porous medium approach in which sorption is described by Freundlich isotherms. The governing equations are solved analytically for the special case of a linear isotherm, and numerically using the computer code RANCHDIFF for non-linear isotherms. A set of time-dependent, ordinary differential equations is obtained using the Lagrange interpolation technique and integrated by Gear's variable order predictor-corrector method. It is shown that the sorption behaviour of 85 Sr can be modelled successfully by a linear isotherm, using a sorption parameter consistent with batch-sorption tests. The behaviour of 137 Cs may be modelled by a non-linear isotherm, but the amount of 137 Cs sorbed is less than that anticipated from batch-sorption tests. 125 I is assumed to be non-sorbing and is used to determine the porosity of the sandstone. (author) 10 figs., 4 tabs., 6 refs

  13. Nitrate Sorption in an Agricultural Soil Profile

    Directory of Open Access Journals (Sweden)

    Wissem Hamdi

    2013-01-01

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

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

    Science.gov (United States)

    Ghnimi, Thouraya; Hassini, Lamine; Bagane, Mohamed

    2016-12-01

    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.

  15. Environmental Conditions Influencing Sorption of Inorganic Anions to Multiwalled Carbon Nanotubes Studied by Column Chromatography.

    Science.gov (United States)

    Metzelder, Florian; Schmidt, Torsten C

    2017-05-02

    Sorption to carbon-based nanomaterials is typically studied in batch experiments. An alternative method offering advantages to study sorption is column chromatography. Sorbent packed columns are used and sorption data are determined by relating sorbate retention to that of a nonretarded tracer. We have now for the first time applied this technique to study the influence of environmental conditions on sorption of inorganic anions (bromide, nitrite, nitrate, and iodide) to multiwalled carbon nanotubes. Deuterium oxide was used as nonretarded tracer. Sorption isotherms were best described by the Freundlich model. Sorption increased in the order bromide 4.5 the surface charge was negative, but sorption was still detectable at pH 6 and 9. Consequently, other forces than electrostatic attraction contributed to sorption. These forces may include H-bonding as indicated by sorption enthalpy determined by variation of column temperature. Overall, column chromatography represents a promising alternative in sorption studies to reveal sorbent properties.

  16. 137Cs sorption onto Fullers' Earth (calcium montmorillonite) -the influence of sulphate reducing bacteria

    International Nuclear Information System (INIS)

    West, J.M.; Haigh, D.G.; Hooker, P.J.; Rowe, E.J.

    1987-12-01

    The influences of Desulfovibrio desulfuricans on the sorption of 137 Cs onto Fullers' Earth (Calcium montmorillonite) has been studied using batch sorption methods. Results were expressed as distributions ratios (Rd) and as Freundlich and Dubinin-Radushkevich isotherms. They show that microbes present naturally in the Fullers' Earth did not influence sorption data, however the addition of microbes in the aqueous phase alters the sorption properties in a complex manner. (author)

  17. Sorption of Heterocyclic Organic Compounds to Multiwalled Carbon Nanotubes.

    Science.gov (United States)

    Metzelder, Florian; Funck, Matin; Schmidt, Torsten C

    2018-01-16

    Sorption is an important natural and technical process. Sorption coefficients are typically determined in batch experiments, but this may be challenging for weakly sorbing compounds. An alternative method enabling analysis of those compounds is column chromatography. A column packed with the sorbent is used and sorption data are determined by relating sorbate retention to that of a nonretarded tracer. In this study, column chromatography was applied for the first time to study sorption of previously hardly investigated heterocyclic organic compounds to multiwalled carbon nanotubes (MWCNTs). Sorption data for these compounds are very limited in literature, and weak sorption is expected from predictions. Deuterium oxide was used as nonretarded tracer. Sorption isotherms were well described by the Freundlich model and data showed reasonable agreement with predicted values. Sorption was exothermic and physisorption was observed. H-bonding may contribute to overall sorption, which is supported by reduced sorption with increasing ionic strength due to blocking of functional groups. Lowering pH reduced sorption of ionizable compounds, due to electrostatic repulsion at pH 3 where sorbent as well as sorbates were positively charged. Overall, column chromatography was successfully used to study sorption of heterocyclic compounds to MWCNTs and could be applied for other carbon-based sorbents.

  18. Sorption of polycyclic aromatic hydrocarbons on particulate organic matters

    International Nuclear Information System (INIS)

    Guo Xueyan; Luo Lei; Ma Yibing; Zhang Shuzhen

    2010-01-01

    Particulate organic matter (POM) is a key organic matter fraction which can influence soil fertility. Its interactions with hydrophobic organic pollutants (HOCs) have not been characterized and the mechanisms of retention of HOCs by POM remain unclear. In the present study, sorption behaviors of polycyclic aromatic hydrocarbons (PAHs) naphthalene (NAP), phenanthrene (PHE), and pyrene (PYR) by POMs separated from different soils were examined and the POMs were characterized by elemental analysis, solid state 13 C NMR, and Fourier transform infrared spectroscopy (FT-IR). The results indicated that POMs were mainly composed of aliphatic components with high polarity. The different original POMs showed similar chemical composition and configuration. Sorption behaviors of PAHs indicated that there was no significant difference in sorption capacity among the POMs. Sorption of NAP and PHE by POMs displayed a nonlinear isotherm, while sorption of PYR yielded a linear isotherm. No significant hysteresis and ionic strength effect were observed for PAH desorption from the POMs.

  19. Experimental study of strontium sorption on fissure filling material

    Energy Technology Data Exchange (ETDEWEB)

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

    1994-12-01

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

  20. Experimental study of strontium sorption on fissure filling material

    International Nuclear Information System (INIS)

    Eriksen, T.E.; Cui, Daqing

    1994-12-01

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

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

    Directory of Open Access Journals (Sweden)

    Ahmadreza Sheikhhosseini

    2017-03-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Tsair-Fuh [Univ. of California, Berkeley, CA (United States)

    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.

  3. Sorption of metaldehyde using granular activated carbon

    Directory of Open Access Journals (Sweden)

    S. Salvestrini

    2017-09-01

    Full Text Available In this work, the ability of granular activated carbon (GAC to sorb metaldehyde was evaluated. The kinetic data could be described by an intra-particle diffusion model, which indicated that the porosity of the sorbent strongly influenced the rate of sorption. The analysis of the equilibrium sorption data revealed that ionic strength and temperature did not play any significant role in the metaldehyde uptake. The sorption isotherms were successfully predicted by the Freundlich model. The GAC used in this paper exhibited a higher affinity and sorption capacity for metaldehyde with respect to other GACs studied in previous works, probably as a result of its higher specific surface area and high point of zero charge.

  4. Effects of carbohydrate/protein ratio on the microstructure and the barrier and sorption properties of wheat starch-whey protein blend edible films.

    Science.gov (United States)

    Basiak, Ewelina; Lenart, Andrzej; Debeaufort, Frédéric

    2017-02-01

    Starch and whey protein isolate and their mixtures were used for making edible films. Moisture sorption isotherms, water vapour permeability, sorption of aroma compounds, microstructure, water contact angle and surface properties were investigated. With increasing protein content, the microstructure changes became more homogeneous. The water vapour permeability increases with both the humidity gradient and the starch content. For all films, the hygroscopicity increases with starch content. Surface properties change according to the starch/whey protein ratio and are mainly related to the polar component of the surface tension. Films composed of 80% starch and 20% whey proteins have more hydrophobic surfaces than the other films due to specific interactions. The effect of carbohydrate/protein ratio significantly influences the microstructure, the surface wettability and the barrier properties of wheat starch-whey protein blend films. © 2016 Society of Chemical Industry. © 2016 Society of Chemical Industry.

  5. KAJIAN FORMULASI BUMBU INSTAN BINTHE BILUHUTA, KARAKTERISTIK HIDRATASI DAN PENDUGAAN UMUR SIMPANNYA DENGAN MENGGUNAKAN METODE PENDEKATAN KADAR AIR KRITIS [Study of Binthe Biluhuta Seasoning Formulation, Hydratation of Characteristic and Prediction of the Shelf Life Using Moisture Critical Method

    Directory of Open Access Journals (Sweden)

    Dorkas Sianipar1

    2008-06-01

    Full Text Available Binthe biluhuta is a native food of Gorontalo, made from mixture of corn, onion, leek, basil, desicated coconut, chili and fish. The objective of this research was to find the best formulation for binthe biluhuta seasoning andprediction of it’s shelf life. Moisture sorption isotherm derived from the correlation of moisture content data indicated a typical sigmoidal curve implying 3 regions of water adsorption. The water sorption region accounted for three fractions of bound water analyzed using three different mathematical models. The first water fraction ranged 0-3.148 (%db, the second ranged 3.148-13.438 (% db and the third fraction ranged 13.438-52.970 (%db. The binthe biluhuta seasoning packaged in alumina and stored at 80 and 90% RH, demonstrated the longest shelf life which were equal to 748 and 423 days, respectively.

  6. A model to predict moisture conditions in concrete reactor containments

    International Nuclear Information System (INIS)

    Ahs, M.; Nilsson, L.O.; Poyet, S.; L'Hostis, V.

    2015-01-01

    Moisture has an impact in many of the degradation mechanisms that appear in the structures of a nuclear power plant. Moisture conditions in a reactor containment wall have been simulated by using a hygro-thermal model of drying concrete. Methods to estimate the temperature dependency of the sorption isotherms and moisture transport properties is suggested and applied in the model. This temperature dependency is included as there is a temperature gradient present through the containment wall. The hygro-thermal model was applied on a full scale 3D model of a real reactor containment building and the concrete relative humidity has been computed at 4 different moments: 1, 10, 20 and 30 years. The results show that the major part of the concrete is not dried at all even after 30 years of operation. It is also clear that the temperature distribution inside the whole concrete volume is affected by the variable boundary conditions. It was concluded that the suggested hygro-thermal model was appropriate to use as a method to estimate the existing conditions in a PWR reactor containment wall

  7. Sorption of uranyl ions on hydrous oxides

    International Nuclear Information System (INIS)

    Gupta, A.R.; Venkataramani, B.

    1988-01-01

    Sorption of uranyl ions on hydrous titanium oxide (HTiO), magnetite (MAG), and hydrous thorium oxide (HThO) has been studied as a function of pH. Hydrous oxides have been characterized by their pH-titration curves, intrinsic dissociation constants (pK ai * ) and point of zero charge (pH pzc ). The fraction of protonated surface hydroxyl groups as well as the surface pH (pH surf ) as a function of solution pH have been computed. The distribution of various hydrolyzed species of uranyl ions with solution pH have been compared with uranyl sorption isotherm on these oxides. Sorption edge in all the cases occurs when free hydroxyl groups are available on the surface and pH surf is sufficiently high to favor the formation of dimer-like species on the surface. A new model for the sorption process, called surface hydrolysis model, which explains these and other features of uranyl sorption on hydrous oxides has been proposed. The model visualizes the sorption process as linking of uranyl ions with two adjacent free surface hydroxyl groups without deprotonation (provided the surface pH is high for the hydrolysis of uranyl ions) and formation of dimer-like structures on the surface. The new model has been successfully applied to the present and other available data on uranyl ion sorption on hydrous oxides. (author)

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

    Science.gov (United States)

    Wadsö, Lars; Jannasch, Patric

    2013-07-18

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

  9. Study of the enthalpy-entropy mechanism from water sorption of orange seeds (C. sinensis cv. Brazilian for the use of agro-industrial residues as a possible source of vegetable oil production

    Directory of Open Access Journals (Sweden)

    Daniele Penteado Rosa

    2013-02-01

    Full Text Available Orange seeds are a promising agroindustry-waste which can be implemented in the extraction and production of vegetable oil. The relationship between moisture content and water activity provides useful information for the processing and storage of this waste item. The aim of this study was to determine the mechanism of water sorption enthalpy-entropy of orange seeds (C. sinensis cv. Brazilians according to the moisture content. Therefore, desorption isotherms were determined at five different temperature (30, 40, 50, 60, and 70 ºC under a wide range of moisture content (0.005-0.057 kg kg-1 d.b. and water activity (0.02-0.756. Theoretical and empirical models were used for modeling the desorption isotherms. An analytical solution of the Clausius-Clapeyron equation was proposed to compute the isosteric heat of sorption, the differential entropy, and Gibbs free energy using the Oswin model when the effect of temperature on the hygroscopic equilibrium was considered.

  10. Sorption of natural uranium by algerian bentonite

    International Nuclear Information System (INIS)

    Megouda, N.; Kadi, H.; Hamla, M.S.; Brahimi, H.

    2004-01-01

    Full text.Batch sorption experiments have been used to assess the sorption behaviour of uranium onto natural and drilling bentonites. The operating parameters (pH, aolis-liquid ratio, particle size, time and initial uranium concentration) influenced the rate of adsorption. The distribution coefficient (Kd) range values at equilibrium time are 45.95-1079.26 ml/g and 32.81-463053 ml/g for the drilling and natural bentonites respectively. The equilibrium isotherms show that the data correlate with both Freundlich and Langmuir models

  11. Numerical analysis of coupled water transport in wood with a focus on the coupling parameter sorption

    DEFF Research Database (Denmark)

    Hozjan, T.; Turk, G.; Rodman, U.

    2011-01-01

    This paper presents a study of sorption rate function in a so-called multi-Fickian or multi-phase model. This model describes the complex moisture transport system in wood, which consists of separate water-vapour and bound-water diffusion interacting through sorption. In the numerical example inf...... influence of the sorption rate function on water transport is presented. It can be seen that the sorption rate function has a noticeable influence on coupled water transport in wood....

  12. Computer simulation of molecular sorption in zeolites

    International Nuclear Information System (INIS)

    Calmiano, Mark Daniel

    2001-01-01

    The work presented in this thesis encompasses the computer simulation of molecular sorption. In Chapter 1 we outline the aims and objectives of this work. Chapter 2 follows in which an introduction to sorption in zeolites is presented, with discussion of structure and properties of the main zeolites studied. Chapter 2 concludes with a description of the principles and theories of adsorption. In Chapter 3 we describe the methodology behind the work carried out in this thesis. In Chapter 4 we present our first computational study, that of the sorption of krypton in silicalite. We describe work carried out to investigate low energy sorption sites of krypton in silicalite where we observe krypton to preferentially sorb into straight and sinusoidal channels over channel intersections. We simulate single step type I adsorption isotherms and use molecular dynamics to study the diffusion of krypton and obtain division coefficients and the activation energy. We compare our results to previous experimental and computational studies where we show our work to be in good agreement. In Chapter 5 we present a systematic study of the sorption of oxygen and nitrogen in five lithium substituted zeolites using a transferable interatomic potential that we have developed from ab initio calculations. We show increased loading of nitrogen compared to oxygen in all five zeolites studied as expected and simulate adsorption isotherms, which we compare to experimental and simulated data in the literature. In Chapter 6 we present work on the sorption of ferrocene in the zeolite NaY. We show that a simulated, low energy sorption site for ferrocene is correctly located by comparing to X-ray powder diffraction results for this same system. The thesis concludes with some overall conclusions and discussion of opportunities for future work. (author)

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

    International Nuclear Information System (INIS)

    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 0 C and equilibrium was defined at 48 hours. The solute concentrations ranged from 0 to 500 mg/L. The radioactive isotopes 60 Co, 137 Cs, and 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

  14. Effects of sorption hysteresis on radionuclide releases from waste packages

    International Nuclear Information System (INIS)

    Barney, G.S.; Reed, D.T.

    1985-01-01

    A one-dimensional, numerical transport model was used to calculate radionuclide releases from waste packages emplaced in a nuclear waste repository in basalt. The model incorporates both sorption and desorption isotherm parameters measured previously for sorption of key radionuclides on the packing material component of the waste package. Sorption hysteresis as described by these isotherms lowered releases of some radionuclides by as much as two orders of magnitude. Radionuclides that have low molar inventories (relative to uranium), high solubility, and strongly sorbed, are most affected by sorption hysteresis. In these cases, almost the entire radionuclide inventory is sorbed on the packing material. The model can be used to help optimize the thickness of the packing material layer by comparing release rate versus packing material thickness curves with Nuclear Regulatory Commission (NRC) and Environmental Protection Agency (EPA) release limits

  15. Sorption and pertechnetate by salts of molybdophosphoric acid

    International Nuclear Information System (INIS)

    Suess, M.; Pfrepper, G.

    1983-01-01

    The sorption of pertechnetate on salts of molybdophosphoric acid from nitric acid and in the presence of electrolytes was investigated. Distribution coefficients from 10 to 100 ml/g were found. The sorption of pertechnetate can be increased by the addition of K + , NH 4 + , Rb + and Cs + salts. A saturation capacity of proportional 0,19 mmol/g ammonium phosphomolybdate was found from the adsorption isotherms. The formation of alkali metal pertechnetate associates in the sorbent phase is supposed. (orig.)

  16. Modeling Fission Product Sorption in Graphite Structures

    International Nuclear Information System (INIS)

    Szlufarska, Izabela; Morgan, Dane; Allen, Todd

    2013-01-01

    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 products

  17. Sorption behaviour of herbicides in soils

    International Nuclear Information System (INIS)

    Luchini, L.C.; Wiendl, F.M.; Ruegg, E.F.; Instituto Biologico, Sao Paulo

    1988-01-01

    Environmental contamination by herbicides is related with the sorption phenomenon of these compounds in the soils. The behaviour of paraquat, 2,4-D and diuron was studied in soils with different physico-chemical properties, through the Freundlich adsorption and desorption isotherms, using 14 C-radiolabeled herbicides. Results of the range of the adsorption-desorption of each herbicide was related mainly with the chemical characteristics of these compounds. (author) [pt

  18. Sorption equilibrium of mercury onto ground-up tree fern.

    Science.gov (United States)

    Ho, Yuh-Shan; Wang, Chung-Chi

    2008-08-15

    The sorption behavior of mercury at different temperatures onto ground-up tree fern was investigated. The experimental results were fitted to two two-parameter isotherms, the Freundlich and Langmuir isotherms, as well as to two three-parameter isotherms, the Redlich-Peterson and Sips isotherms to obtain the characteristic parameters of each model. A comparison of best-fitting was performed using the coefficient of determination and Chi-square test. Both the Langmuir and Redlich-Peterson isotherms were found to well represent the measured sorption data. According to the evaluation using the Langmuir equation, the saturated monolayer sorption capacity of mercury ions onto ground-up tree fern was 26.5 mg/g at 298 K. It was noted that an increase in temperature resulted in a higher mercury ion loading per unit weight of the tree fern. In addition, various thermodynamic parameters, such as DeltaG degrees, DeltaH degrees, and DeltaS degrees, were calculated and compared with the sorption of mercury by other sorbents.

  19. Sorption equilibrium of mercury onto ground-up tree fern

    Energy Technology Data Exchange (ETDEWEB)

    Ho, Y.-S. [Department of Chemical Engineering, I-Shou University, No. 1, Section 1, Hsueh-Cheng Road, Ta-Hsu Hsiang, Kaohsiung County 840, Taiwan (China)], E-mail: ysho@isu.edu.tw; Wang, C.-C. [Department of Chemical Engineering, I-Shou University, No. 1, Section 1, Hsueh-Cheng Road, Ta-Hsu Hsiang, Kaohsiung County 840, Taiwan (China)

    2008-08-15

    The sorption behavior of mercury at different temperatures onto ground-up tree fern was investigated. The experimental results were fitted to two two-parameter isotherms, the Freundlich and Langmuir isotherms, as well as to two three-parameter isotherms, the Redlich-Peterson and Sips isotherms to obtain the characteristic parameters of each model. A comparison of best-fitting was performed using the coefficient of determination and Chi-square test. Both the Langmuir and Redlich-Peterson isotherms were found to well represent the measured sorption data. According to the evaluation using the Langmuir equation, the saturated monolayer sorption capacity of mercury ions onto ground-up tree fern was 26.5 mg/g at 298 K. It was noted that an increase in temperature resulted in a higher mercury ion loading per unit weight of the tree fern. In addition, various thermodynamic parameters, such as {delta}G{sup o}, {delta}H{sup o}, and {delta}S{sup o}, were calculated and compared with the sorption of mercury by other sorbents.

  20. Sorption equilibrium of mercury onto ground-up tree fern

    International Nuclear Information System (INIS)

    Ho, Y.-S.; Wang, C.-C.

    2008-01-01

    The sorption behavior of mercury at different temperatures onto ground-up tree fern was investigated. The experimental results were fitted to two two-parameter isotherms, the Freundlich and Langmuir isotherms, as well as to two three-parameter isotherms, the Redlich-Peterson and Sips isotherms to obtain the characteristic parameters of each model. A comparison of best-fitting was performed using the coefficient of determination and Chi-square test. Both the Langmuir and Redlich-Peterson isotherms were found to well represent the measured sorption data. According to the evaluation using the Langmuir equation, the saturated monolayer sorption capacity of mercury ions onto ground-up tree fern was 26.5 mg/g at 298 K. It was noted that an increase in temperature resulted in a higher mercury ion loading per unit weight of the tree fern. In addition, various thermodynamic parameters, such as ΔG o , ΔH o , and ΔS o , were calculated and compared with the sorption of mercury by other sorbents

  1. Modeling of the process of moisture loss during the storage of dried apricots.

    Science.gov (United States)

    Miranda, G; Berna, A; Bon, J; Mulet, A

    2011-10-01

    Moisture content is a reference parameter for dried food because the growth of most microorganisms is inhibited below certain water activity levels. In addition, it has a determining influence on the evolution of important parameters, such as color and flavor, and on other properties and deterioration reactions, such as texture, oxidation processes and nutritional value. During the storage of some dried fruits, moisture is produced due to Maillard reactions and exchanged with the surrounding environment through the packaging. The evolution of dried foods during their shelf life depends on the storage conditions. The aim of this study is to analyze the evolution of the moisture content in dried apricots packaged in different types of containers, namely glass and thermosealed polypropylene trays. The samples were stored at constant temperatures: 5, 15, 25 and 35 °C and were analyzed periodically over a period of 12 months. The sorption isotherms of apricots used in this study were also determined. In order to model how the moisture evolved, an empirical kinetic model was tested. This model considers both water transfer from the fruit and also water production as a result of the Maillard processes. The explained variance was higher than 95% in the samples stored in trays, which were thermosealed with film.

  2. Sorption of organophosphate esters by carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-05-01

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

  3. Effect of natural organic materials on cadmium and neptunium sorption

    International Nuclear Information System (INIS)

    Kung, K.S.; Triay, I.R.

    1994-01-01

    In a batch sorption study of the effect of naturally occurring organic materials on the sorption of cadmium and neptunium on oxides and tuff surfaces, the model sorbents were synthetic goethite, boehmite, amorphous silicon oxides, and a crushed tuff material from Yucca Mountain, Nevada. An amino acid, 3-(3,4-dihydroxypheny)-DL-alanine (DOPA), and an aquatic-originated fulvic material, Nordic aquatic fulvic acid (NAFA), were used as model organic chemicals. Sorption isotherm results showed that DOPA sorption followed the order aluminum oxide > iron oxide > silicon oxide and that the amount of DOAP sorption for a given sorbent increased as the solution pH was raised. The sorption of cadmium and neptunium on the iron oxide was about ten times higher than that on the aluminum oxide. The sorption of cadmium and neptunium on natural tuff material was much lower than that on aluminum and iron oxides. The sorption of cadmium on iron and aluminum oxides was found to be influenced by the presence of DOPA, and increasing the amount of DOPA coating resulted in higher cadmium sorption on aluminum oxide. However, for iron oxide, cadmium sorption decreased with increasing DOPA concentration. The presence of the model organic materials DOPA and NAFA did not affect the sorption of neptunium on tuff material or on the iron and aluminum oxides. Spectroscopic results indicate that cadmium complexes strongly with DOPA. Therefore, the effect of the organic material, DOPA, on the cadmium sorption is readily observed. However, neptunium is possibly complexed weakly with organic material. Thus, DOPA and NAFA have little effect on neptunium sorption on all sorbents selected for study

  4. Adsorption isotherms of pear at several temperatures

    OpenAIRE

    Mitrevski Vangelče; Lutovska Monika; Mijakovski Vladimir; Pavkov Ivan S.; Babić Mirko M.; Radojčin Milivoje T.

    2015-01-01

    The moisture adsorption isotherms of pear were determined at 15ºC, 30ºC and 45ºC using the standard static gravimetric method over a range of water activity from 0.112 to 0.920. The experimental data were fitted with isotherm equations recommended in ASAE Standard D245.5. In order to find which equation gives the best results, large number of numerical experiments were performed. After that, several statistical criteria proposed in scientific literature for...

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

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Soyoung, E-mail: soyoung@pusan.ac.kr; Jeong, Hoon Young, E-mail: hjeong@pusan.ac.kr

    2015-03-02

    Highlights: • Tween 80 sorption varies significantly among soil minerals. • Sorption mechanisms and atomic compositions explain to mineral-specific sorption. • Clay minerals and SOM in soils are the key contributors to Tween 80 sorption. • Hysteresis suggests the potential difficulty in removing residual surfactants. - Abstract: 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 plagioclase < vermiculite < kaolinite. This results from the relative reactivity among surface sites: ≡NaOH, ≡CaOH << ≡SiOH < ≡AlOH. Experiments using dry- and wet-sieved soils reveal that fine-grained clay minerals, difficult to separate by dry-sieving, contribute significantly to Tween 80 sorption. The greater sorption by untreated soils than H{sub 2}O{sub 2}-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.

  6. Interim report on modeling sorption with EQ3/6

    International Nuclear Information System (INIS)

    Viani, B.

    1988-01-01

    Reversible, equilibrium models of sorption to be incorporated into the EQ3/6 geochemical modeling package are summarized. Empirical sorption models as formulated in linear, Langmuir, and Freundlich isotherms will be developed as options to EQ3/6. This work will be done at LLNL. Options for modeling sorption using surface- complexation constructs (diffuse, constant capacitance, and triple-layer models) will also be developed. Development of the surface-complexation options will require part of the work be done under contract. 27 refs., 1 fig

  7. Sorption behaviour of cobalt-60 on Suez Canal bottom sediments

    International Nuclear Information System (INIS)

    Abdel Gawad, S.A.; El-Shinawy, R.M.K.; Abdel Malik, W.E.Y.

    1981-01-01

    Mineralogical, elemental analysis and sorption behaviour of the Suez Canal bottom sediments in the Port Said area were investigated. It was found that the bottom sediment consist mainly of quartz, feldspars and traces of calcite mineral. The cation-exchange capacity was found to increase as the particle size of the sediment decreased. Sorption of 60 Co by the bottom sediment increased with contact time up to 6 h. Variation of the solution pH from 4 to 9 showed limited increase in the sorption of 60 Co. As carrier concentrations increase from 10 -7 N to 10 -3 N, sorption of Co was found to increase linearly following Freundlich isotherm. The presence of Mg 2+ and Fe 3+ in solution depressed the sorption of 60 Co by the sediments. The desorption of 60 Co from bottom sediment with distilled and Suez Canal water was found to increase with contact time. (author)

  8. Sorption of phosphates and thiocyanates on isomorphic substituted Mg/Zn–Al-type hydrotalcites

    Directory of Open Access Journals (Sweden)

    RODICA PODE

    2008-08-01

    Full Text Available The sorption equilibriums of phosphate and thiocyanate anions on isomorphic substituted Mg/Zn–Al-type hydrotalcites were investigated in this study. Langmuir and Freundlich isotherms were used to interpret the equilibrium data for phosphate. The sorption equilibriums of phosphate on Mg3Al, Mg2ZnAl and Mg1.5Zn1.5Al hydrotalcites were well described by the Langmuir isotherm. The highest maximum sorption capacities for these adsorbents were as follows: 111, 101 and 95 mg g-1. The equilibrium constant and standard Gibbs energy changes were also calculated from the sorption data. Standard Gibbs energy changes of about –20 kJ mol-1 indicated that the process might be considered as physical adsorption. The sorption equilibriums of phosphate on isomorphic substituted samples of MgZn2Al and Zn3Al were well described by the Freundlich isotherm. Thiocyanate showed a relative low affinity for the studied materials, as indicated by both the “S”-shaped isotherms and low sorption capacities. The sorption of phosphate and thiocyanate on the investigated hydrotalcites showed a continuous decrease of the sorption capacity in the following order: Mg3Al > Mg2ZnAl > Mg1.5Zn1.5Al > MgZn2Al > Zn3Al.

  9. Kinetic and equilibrium characteristics of sorption of saponin of Quillaja Saponaria Molina on chitosan

    Science.gov (United States)

    Mironenko, N. V.; Smuseva, S. O.; Brezhneva, T. A.; Selemenev, V. F.

    2016-12-01

    The equilibrium and kinetic curves of the sorption of saponin of Quillaja saponaria molina on chitosan were analyzed. The inner diffusion was found to be limiting, and its coefficients were calculated. It was found that the form of the curves of the sorption isotherms of saponin is determined by the competing processes of association in solution and absorption by chitosan.

  10. Sorption/desorption reversibility of polycyclic aromatic hydrocarbons (PAHs) in soils and carbonaceous materials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guohui

    2008-07-01

    Understanding sorption/desorption is an important prerequisite for the prediction of fate and transport of pollutants in the environment. During the last two decades, numerous studies have reported hysteresis phenomenon for the interaction of hydrophobic organic contaminants (HOCs) with natural organic matter (NOM). It manifests as nonsingular sorption/desorption isotherms or different rates for sorption and desorption, where during desorption a higher affinity of a compound on a given sorbent and a longer time scale for release than for sorption is observed. Other studies showed that some of the reported sorption/desorption hysteresis phenomena are due to experimental artifacts, mainly resulting from non-attainment of sorption equilibrium before desorption experiments, which result in 'pseudo-hysteresis'. Except for the hypothesis of sorbent reconfiguration, clear experimental evidence for the physical or chemical mechanisms proposed to lead to hysteresis is still lacking. In this study, sorption/desorption equilibrium and kinetics of phenanthrene sorption/desorption from two soils and three carbonaceous samples were investigated using both batch and column techniques. The main objective of this work was to monitor hysteresis phenomenon by carefully recovering the solute mass in the system and to compare sorption/desorption equilibria and kinetics thermodynamically. Nonsingular isotherms and higher desorption enthalpies as well as increased activation energies with proceeding desorption are expected if significant hysteresis exists. Sorption-desorption cycles were carried out to compare equilibrium isotherms and associated sorption/desorption enthalpies (AeH, isosteric heats). Instead of the traditional decant-and-refill batch method, the experiments were conducted using a newly designed batch protocol, which enables the determination of sorption/desorption isotherms at different temperatures using a closed batch system. This method additionally allows

  11. Sorption/desorption reversibility of polycyclic aromatic hydrocarbons (PAHs) in soils and carbonaceous materials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guohui

    2008-07-01

    Understanding sorption/desorption is an important prerequisite for the prediction of fate and transport of pollutants in the environment. During the last two decades, numerous studies have reported hysteresis phenomenon for the interaction of hydrophobic organic contaminants (HOCs) with natural organic matter (NOM). It manifests as nonsingular sorption/desorption isotherms or different rates for sorption and desorption, where during desorption a higher affinity of a compound on a given sorbent and a longer time scale for release than for sorption is observed. Other studies showed that some of the reported sorption/desorption hysteresis phenomena are due to experimental artifacts, mainly resulting from non-attainment of sorption equilibrium before desorption experiments, which result in 'pseudo-hysteresis'. Except for the hypothesis of sorbent reconfiguration, clear experimental evidence for the physical or chemical mechanisms proposed to lead to hysteresis is still lacking. In this study, sorption/desorption equilibrium and kinetics of phenanthrene sorption/desorption from two soils and three carbonaceous samples were investigated using both batch and column techniques. The main objective of this work was to monitor hysteresis phenomenon by carefully recovering the solute mass in the system and to compare sorption/desorption equilibria and kinetics thermodynamically. Nonsingular isotherms and higher desorption enthalpies as well as increased activation energies with proceeding desorption are expected if significant hysteresis exists. Sorption-desorption cycles were carried out to compare equilibrium isotherms and associated sorption/desorption enthalpies (AeH, isosteric heats). Instead of the traditional decant-and-refill batch method, the experiments were conducted using a newly designed batch protocol, which enables the determination of sorption/desorption isotherms at different temperatures using a closed batch system. This method additionally allows the

  12. Preparation, characterization of electrospun meso-hydroxylapatite nanofibers and their sorptions on Co(II)

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hualin, E-mail: hlwang@hfut.edu.cn [School of Chemical Technology, Hefei University of Technology, Hefei, Anhui 230009 (China); Zhang, Peng; Ma, Xingkong; Jiang, Suwei; Huang, Yan; Zhai, Linfeng [School of Chemical Technology, Hefei University of Technology, Hefei, Anhui 230009 (China); Jiang, Shaotong [School of Biotechnology and Food Engineering, Hefei University of Technology, Hefei, Anhui 230009 (China)

    2014-01-30

    Highlights: • PVA/HA nanofibers could change into meso-HA nanofibers by calcination process. • Sorption of Co(II) on meso-HA was strongly dependent on pH and ionic strength. • Sorption kinetic data were well fitted by the pseudo-second-order rate equation. • Sorption isotherms could be well described by the Langmuir model. • Sorption process of Co(II) on meso-HA nanofibers was spontaneous and endothermic. -- Abstract: In this work, mesoporous hydroxylapatite (meso-HA) nanofibers were prepared via calcination process with polyvinyl alcohol/HA (PVA/HA) hybrid nanofibers fabricated by electrospinning technique as precursors, and the removal efficiency of meso-HA nanofibers toward Co(II) was evaluated via sorption kinetics and sorption isotherms. Furthermore, the sorption behaviors of Co(II) on meso-HA nanofibers were explored as a function of pH, ionic strength, and thermodynamic parameters. There existed hydrogen bonds between HA and PVA matrix in precursor nanofibers which could change into meso-HA nanofibers with main pore diameter at 27 nm and specific surface area at 114.26 m{sup 2}/g by calcination process. The sorption of Co(II) on meso-HA was strongly dependent on pH and ionic strength. Outer-sphere surface complexation or ion exchange was the main mechanisms of Co(II) adsorption on meso-HA at low pH, whereas inner-sphere surface complexation was the main adsorption mechanism at high pH. The sorption kinetic data were well fitted by the pseudo-second-order rate equation. The sorption isotherms could be well described by the Langmuir model. The thermodynamic parameters (ΔH°, ΔS° and ΔG°) calculated from the temperature-dependent sorption isotherms suggested that the sorption process of Co(II) on meso-HA nanofibers was spontaneous and endothermic.

  13. Review of sorption models, and their suitability for use in performance assessments

    International Nuclear Information System (INIS)

    Harvey, K.B.

    1997-02-01

    The sorption of radionuclides on mineral surfaces is an important mechanism for retarding the movement of radionuclides from a geological nuclear fuel disposal vault, through the geosphere, to the biosphere. Sorption processes are known to increase the travel times for some radionuclides by 103 to 106 times relative to the groundwater flow, and this delay can provide the opportunity for radioactive decay before the radionuclide enters the biosphere. Sorption models are, or can be, used as a means of including the effects of sorption in the transport equations which describe the movement of radionuclides through the geosphere. Sorption models are, or could be, based on sorption isotherms, such as the Langmuir and Freundlich isotherms, ion-exchange models, surface-complexation models, or parametric models that are, essentially, interpolated databases. All national nuclear fuel waste disposal programs currently assume the linear adsorption isotherm, which states that the degree of sorption on a surface is a linear function of the concentration of sorbing ion in solution. The sorption models that are, or could be, applied to the movement of radionuclides in the geosphere are reviewed. It is concluded that, at the present state of knowledge, no single model has been demonstrated to provide an adequate description of radionuclide sorption. Reasons for this inadequacy vary, ranging from lack of data, through restricted ability to describe sorption under a variety of conditions, to current levels of development of the models. It is concluded that a parametric model, associated with a linear sorption isotherm, is currently the most practical choice that can be made. Following the completion of an earlier draft of this report, a new approach to surface complexation modelling, the 'discrete-log-K-spectrum' model, was published. This model appears to have the potential to achieve a synthesis of many of the concepts used in sorption modelling. For this reason, a description of

  14. Sorption of fluoride using chemically modified Moringa oleifera leaves

    Science.gov (United States)

    Dan, Shabnam; Chattree, Amit

    2018-05-01

    Contamination of drinking water due to fluoride is a severe health hazard problem. Excess of fluoride (> 1.5 mg/L) in drinking water is harmful to human health. Various treatment technologies for removing fluoride from groundwater have been investigated. The present study showed that the leaves of Moringa oleifera, a herbal plant is an effective adsorbent for the removal of fluoride from aqueous solution. Acid treated Moringa oleifera leaves powder showed good adsorption capacity than alkali treated Moringa oleifera leaves powder. Batch sorptive defluoridation was conducted under the variable experimental condition such as pH, contact time, adsorbent dose and initial fluoride ion concentration. Maximum defluoridation was achieved at pH 1. The percentage of fluoride removal increases with adsorbent dose. The equilibrium sorption data were fitted into Langmuir, Freundlich and Temkin isotherms. Of the three adsorption isotherms, the R 2 value of Langmuir isotherm model was the highest. The maximum monolayer coverage ( Q max) from Langmuir isotherm model was determined to be 1.1441 mg/g, the separation factor indicating a favorable sorption experiment is 0.035. It was also discovered that the adsorption did not conform to the Freundlich adsorption isotherm. The heat of sorption process was estimated from Temkin Isotherm model to be - 0.042 J/mol which vividly proved that the adsorption experiment followed a physical process.

  15. Migration and sorption phenomena in packaged foods.

    Science.gov (United States)

    Gnanasekharan, V; Floros, J D

    1997-10-01

    Rapidly developing analytical capabilities and continuously evolving stringent regulations have made food/package interactions a subject of intense research. This article focuses on: (1) the migration of package components such as oligomers and monomers, processing aids, additives, and residual reactants in to packaged foods, and (2) sorption of food components such as flavors, lipids, and moisture into packages. Principles of diffusion and thermodynamics are utilized to describe the mathematics of migration and sorption. Mathematical models are developed from first principles, and their applicability is illustrated using numerical simulations and published data. Simulations indicate that available models are system (polymer-penetrant) specific. Furthermore, some models best describe the early stages of migration/sorption, whereas others should be used for the late stages of these phenomena. Migration- and/or sorption-related problems with respect to glass, metal, paper-based and polymeric packaging materials are discussed, and their importance is illustrated using published examples. The effects of migrating and absorbed components on food safety, quality, and the environment are presented for various foods and packaging materials. The impact of currently popular packaging techniques such as microwavable, ovenable, and retortable packaging on migration and sorption are discussed with examples. Analytical techniques for investigating migration and sorption phenomena in food packaging are critically reviewed, with special emphasis on the use and characteristics of food-simulating liquids (FSLs). Finally, domestic and international regulations concerning migration in packaged foods, and their impact on food packaging is briefly presented.

  16. Influence of sorption competition on sorption data for MX-80 bentonite used in performance assessment

    International Nuclear Information System (INIS)

    Bradbury, M.H.; Baeyens, B.; Marques Fernandes, M.

    2012-01-01

    Document available in extended abstract form only. In order to obtain a (quasi) mechanistic understanding of radionuclide uptake on clay minerals and argillaceous rocks, the majority of sorption experiments have been carried out on purified clay minerals such as montmorillonite and illite at trace concentrations (sorption edges), or as a function of concentration (sorption isotherms), with a single radionuclide under well-defined conditions in simple background electrolytes. As a result of such studies the 2 site proto-lysis non electrostatic surface complexation cation exchange (2SPNE SC/CE) sorption model, was developed and has been successfully applied to quantitatively describe the uptake of numerous radionuclides of differing valences as a function of pH and concentration on montmorillonite. In a deep geological repository for high level waste, stable impurities arise from many sources: they are present in the pore waters, in the tunnel back fill materials and host rock formations, they arise from the corrosion of the carbon steel canister and finally they are dissolved from the spent fuel and vitrified high level waste simultaneously with the radionuclides. These impurities, which are an integral part of a realistic repository system, can potentially compete with radionuclides for the sorption sites on the backfill materials and host rock and thus reduce their uptake on them. The influence of competitive sorption is not intrinsically included (or only partly so) in the sorption model. It is clearly an inherently important issue to quantify the influence of sorption competition on the transport of released radionuclides through the multi-barrier system in a deep repository. In this study an extreme case of a competitive sorption scenario in the near field of a HLW repository is presented. Two factors are considered: one associated with the high concentrations and the other with competitive sorption effects. The tendency in both cases is to cause a reduction in

  17. Sorption of radionuclides by tertiary clays

    International Nuclear Information System (INIS)

    Wagner, J.F.; Czurda, K.A.

    1990-01-01

    The sorption capacity of different clay types for some metals (Co, Cs, Sr and Zn), occurring as common radionuclides in radioactive waste deposits, had been analysed by a static (batch technique) and a dynamic method (percolation tests, in which the driving force is a hydraulic gradient). Sorption capacity generally increased with an increasing pH of solution. A decrease of sorption capacity had been observed in the order Zn > Cs ≥ Co > Sr for the batch and Cs > Zn > Sr > Co for the percolation tests. Clay marls showed a distinctly higher sorption respectively retention capacity as pure clays. Sorption capacity depends on solution parameters like type and concentration of radionuclide, pH, salt concentration, etc., and on rock parameters like mineral content (e.g. swelling clay minerals and carbonates), organic material, rock pH, micro fabric, etc. A third parameter of great influence is the contact time between clay and solution. The adsorption isotherms reflect two different adsorption mechanisms: a very rapid adsorption (a few minutes) on the external surfaces of clay minerals and a slow adsorption process (weeks and longer), due to the diffusion of metal ions into the interlayer space of clay minerals. 12 refs., 9 figs., 1 tab

  18. Sorption of organophosphate and triazine agrochemicals on biochars and soils

    Science.gov (United States)

    Biochars are known to strongly sorb polar and nonpolar organic compounds, and biochar soil amendment can have counteracting impacts on the efficacy of, and runoff contamination by agrochemicals. This study investigated the sorption-desorption isotherms and kinetics of triazine (deisopropylatrazine)...

  19. Sorption characteristics of methylene blue onto Nypa fruiticans lignin ...

    African Journals Online (AJOL)

    The sorption characteristics of soda lignin extracted from Nypa fruiticans for the removal of methylene blue dye from aqueous solution was investigated in this study, as an ethically sound way of utilizing this unexploited abundant natural resource. Equilibrium data were fitted to the Langmuir and Freundlich isotherm ...

  20. Neptunium(V) sorption on kaolinite

    Energy Technology Data Exchange (ETDEWEB)

    Amayri, S.; Jermolajev, A.; Reich, T. [Mainz Univ. (Germany). Inst. of Nuclear Chemistry

    2011-07-01

    The sorption behavior of neptunium(V) onto the clay mineral kaolinite was studied in batch experiments under different experimental conditions: [Np(V)] = 7 x 10{sup -12}-8 x 10{sup -6} M, solid-to-liquid ratio 2-20 g L{sup -1}, I = 0.1 and 0.01 M NaClO{sub 4}, pH = 6-10, ambient air and Ar atmosphere. The short-lived isotope {sup 239}Np (T{sub 1/2} = 2.36 d) was used instead of {sup 237}Np (T{sub 1/2} = 2.14 x 10{sup 6} a) to study the sorption behavior of Np(V) at environmentally-relevant concentrations, i.e., 7 x 10{sup -12} M Np. In addition, {sup 239}Np(V) served as tracer to measure sorption isotherms over six orders of magnitude in Np concentration (4.8 x 10{sup -12}-1.0 x 10{sup -4} M). The results show that Np(V) sorption on kaolinite is strongly influenced by pH, CO{sub 2}, and ionic strength. The sorption of 8 x 10{sup -6} M Np(V) at pH 9.0, and ionic strength of 0.1 M NaClO{sub 4} was proportional to the solid-to-liquid ratio of kaolinite in the range of 2-10 g L{sup -1}. In the absence of CO{sub 2}, the Np(V) uptake increased continuously with increasing pH value up to 97% at pH 10. Under ambient CO{sub 2}, the sorption of Np decreased above pH 8 up to zero at pH 10. An increase of Np(V) concentration from 7 x 10{sup -12} to 8 x 10{sup -6} M resulted in a shift of the sorption pH edge by up to one pH unit to higher pH values. The ionic strength influenced the Np(V) sorption onto kaolinite only in the presence of ambient CO{sub 2}. Under Ar atmosphere the sorption of Np(V) was independent from ionic strength, indicating the formation of inner-sphere complexes of Np(V) with kaolinite. Time-dependent batch experiments at pH 9.0 under ambient CO{sub 2} showed that the sorption of Np(V) on kaolinite is fast and fully reversible over six orders in Np(V) concentration. (orig.)

  1. Competitive sorption between glyphosphate and inorganic phosphate on clay minerals and low organic matter soils

    International Nuclear Information System (INIS)

    Dion, H.M.; Hill, H.H.Jr.; Washington State Univ., Pullmann, WA; Harsh, J.B.; Washington State Univ., Pullmann, WA

    2001-01-01

    Inorganic phosphate may influence the adsorption of glyphosate to soil surface sites. It has been postulated that glyphosphate sorption is dominated by the phosphoric acid moiety, therefore, inorganic phosphate could compete with glyphosate for surface sorption sites. Sorption of glyphosate is examined in low organic carbon systems where clay minerals dominate the available adsorption sites using 32 P-labeled phosphate and 14 C-labeled glyphosate to track sorption. Glyphosate sorption was found to be strongly dependent on phosphate additions. Isotherms were generally of the L type, which is consistent with a limited number of surface sites. Most sorption on whole soils could be accounted for by sorption observed on model clays of the same mineral type as found in the soils. (author)

  2. Sorption Energies for Atrazine onto Devolatalized Vitellaria paradoxa

    International Nuclear Information System (INIS)

    Itodo, A. U.; Abdulrahman, F. W.; Hassan, L. G.; Happiness, U. I.

    2012-01-01

    We utilize isotherm models in contributing to scholarly knowledge in simple terms, to measure the forces or energy defining certain adsorption phenomenon. Gas Chromatography coupled with Mass Spectrophotometer detector was utilized to measure equilibrium phase atrazine after adsorption onto Shea nut Shells acid derived activated carbon. Data were fitted into the D-R and Temkin isotherm relationships for energy data estimation of Sorption energy value (B D ), mean free energy (E D ) and heat of sorption (B). They were estimated as 0.7600mol 2 KJ -2 , 0.8111 kjmor -1 and 0.790Jmol -1 respectively. The parameter predicting the type of adsorption was evaluated B D , B D 2 = 0.979 proves a better choice in explaining sorption energies. Generally, shea nut shells can be used as alternative precursors for activated carbon production via the two steps and acid treatment method.

  3. Sorption and desorption of diuron in Oxisol under biochar application

    Directory of Open Access Journals (Sweden)

    Fabiano André Petter

    Full Text Available ABSTRACT The objective of this study was to verify the kinetics of sorption and desorption of diuron in an Oxisol under application of biochar. The samples were collected in a field experiment conducted in randomized design blocks consisted of 2 base fertilization levels (0 and 400 kg∙ha−1 NPK 00-20-20 fertilizer formula and 3 doses of biochar (0, 8 and 16 Mg∙ha−1. In the evaluation of sorption and desorption, Batch Equilibrium method was used. The kinetics of sorption and desorption of diuron, total organic carbon, fulvic acid, humic acid and humin, pH and partition coefficient to organic carbon were evaluated. The Freundlich isotherm was adjusted appropriately to describe diuron sorption kinetics in all the studied treatments. The application of biochar provided increment in the sorption (Kf and reduction in the desorption of diuron in 64 and 44%, respectively. This effect is attributed to the biochar contribution to the total organic carbon and C-humin and of these to diuron through hydrophobic interactions and hydrogen bonds. The positive correlation between the partition coefficient to organic carbon and Kf confirms the importance of soil organic compartment in the sorption of diuron. There was no competition of NPK fertilizer for the same sorption site of diuron. The increase and reduction in sorption and desorption, respectively, show that the application of biochar is an important alternative for the remediation of soil leaching of diuron, especially in sandy soils.

  4. Rapid and fully automated Measurement of Water Vapor Sorption Isotherms

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Møldrup, Per

    2014-01-01

    Eminent environmental challenges such as remediation of contaminated sites, the establishment and maintenance of nuclear waste repositories, or the design of surface landfill covers all require accurate quantification of the soil water characteristic at low water contents. Furthermore, several...

  5. Application of Humidity-Controlled Dynamic Mechanical Analysis (DMA-RH to Moisture-Sensitive Edible Casein Films for Use in Food Packaging

    Directory of Open Access Journals (Sweden)

    Laetitia M. Bonnaillie

    2015-01-01

    Full Text Available Protein-based and other hydrophilic thin films are promising materials for the manufacture of edible food packaging and other food and non-food applications. Calcium caseinate (CaCas films are highly hygroscopic and physical characterization under broad environmental conditions is critical to application development and film optimization. A new technology, humidity-controlled dynamic mechanical analysis (DMA-RH was explored to characterize CaCas/glycerol films (3:1 ratio during isohume temperature (T ramps and steps, and isothermal RH ramps and steps, to determine their mechanical and moisture-sorption properties during extensive T and RH variations. When RH and/or T increased, CaCas/Gly films became strongly plasticized and underwent several primary and secondary humidity-dependent transition temperatures (or transition humidities; the CaCas/Gly network hypothetically rearranged itself to adapt to the increased water-content and heat-induced molecular mobility. Between 5–40 °C and 20%–61% RH, moisture-sorption was rapid and proportional to humidity between transition points and accelerated greatly during transitions. CaCas/Gly films seemed unsuitable for storage or utilization in warm/humid conditions as they lost their mechanical integrity around Tm ~ 40 °C at 50% RH and Tm decreased greatly with increased RH. However, below Tm, both moisture- and heat-induced structural changes in the films were fully reversible and casein films may withstand a variety of moderate abuse conditions.

  6. WATER SORPTION PROPERTIES AND ANTIMICROBIAL ACTION OF ZINC OXIDE NANO PARTICLES LOADED SAGO STARCH FILM

    Directory of Open Access Journals (Sweden)

    Sunil Bajpai

    2013-02-01

    Full Text Available In this work, sago starch based films have been loaded with ZnO nanoparticles prepared insitu via using an unique equilibration-cum-hydrothermal approach. The films have been characterized by XRD, DSC,SPR ,FTIR and SEM analysis. The moisture absorption behavior of plain and ZnO nanoparticles loaded films have been studied at 23, 31 and 37o C.The equilibrium moisture uptake data was found to fit well on GAB isotherm model and the monolayer sorption capacity Mo for the plain and ZnO nanoparticles loaded films was 0.089, 0.039 ,0.021 g/g and 0.042, 0.012, 0.007 g/g at 23,31 and 37 oC respectively. Moreover, the water vapor transmission rates (WVTR for plain and ZnO nanoparticles loaded films at 23,31,37 oC were 11.19x10-4, 48.9x10-4, 62.1x10-4 and 3.73 x10-4, 6.21x10-4, 24.8x10-4 respectively. These films have shown excellent antibacterial action against model bacteria E.coli when investigated qualitatively by zone inhibition method. Films exhibit great potential to be used as packaging films to protect food stuff against microbial contaminents.

  7. Simulations of hydrogen sorption in rht-MOF-1: identifying the binding sites through explicit polarization and quantum rotation calculations

    KAUST Repository

    Pham, Tony; Forrest, Katherine A.; Hogan, Adam; McLaughlin, Keith; Belof, Jonathan L.; Eckert, Juergen; Space, Brian

    2014-01-01

    . This is a charged rht-MOF that contains extra-framework nitrate counterions within the material. For the simulations performed herein, excellent agreement with experiment was achieved for the simulated hydrogen sorption isotherms and calculated isosteric

  8. Edible moisture barriers: how to assess of their potential and limits in food products shelf-life extension?

    Science.gov (United States)

    Bourlieu, C; Guillard, V; Vallès-Pamiès, B; Guilbert, S; Gontard, N

    2009-05-01

    Control of moisture transfer inside composite food products or between food and its environment remains today a major challenge in food preservation. A wide rage of film-forming compounds is now available and facilitates tailoring moisture barriers with optimized functional properties. Despite these huge potentials, a realistic assessment of the film or coating efficacy is still critical. Due to nonlinear water sorption isotherms, water-dependent diffusivities, and variations of physical state, modelling transport phenomena through edible barriers is complex. Water vapor permeability can hardly be considered as an inherent property of films and only gives a relative indication of the barrier efficacy. The formal or mechanistic models reported in literature that describe the influence of testing conditions on the barrier properties of edible films are reviewed and discussed. Most of these models have been validated on a narrow range of conditions. Conversely, few original predictive models based on Fick's Second Law have been developed to assess shelf-life extension of food products including barriers. These models, assuming complex and realistic hypothesis, have been validated in various model foods. The development of nondestructive methods of moisture content measurement should speed up model validation and allow a better comprehension of moisture transfer through edible films.

  9. Possible use of tannin resins belonging to the luztan family in the Cd (II) sorption of watery sources

    International Nuclear Information System (INIS)

    Melchor, K.; Lima, L.; Luzardo, F. M.; Vargas, L. M.; Santana, J. L.; E.mail: keniamr@ctn.isctn.edu.cu

    2003-01-01

    There are studied the optimum sorption conditions of the Cd (II) in five different natural sorbent variants obtained from the tannin immobilization and re-immobilization in the vegetal bark of the species Ecualiptus saligna and Pinus caribea for being used to remove this metal from waste water. It was determined the sorption balance time of the Cd (II) in every sorbent, as well as, the corresponding sorption isotherms. The breakdown curves were obtained under dynamic conditions for the absorbents, that experienced a higher sorption for the Cd (II), from these curves, it was obtained the dynamic sorption capacity of them for the Cd (II)

  10. Sorption behaviour of uranium and thorium on cryptomelane-type hydrous manganese dioxide from aqueous solution

    International Nuclear Information System (INIS)

    El-Naggar, I.M.; El-Absy, M.A.; Abdel-Hamid, M.M.; Aly, H.F.

    1993-01-01

    The kinetics of sorption of uranium and thorium from aqueous nitrate solutions on cryptomelane-type hydrous manganese dioxide (CRYMO) was studied. The exchange of uranium is particle diffusion controlled while that of thorium is chemical reaction at the exchange sites. Sorption of uranium and thorium by CRYMO has been also studied as a function of metal concentrations and temperature. The sorption of both cations is found to be an endothermic process and increases markedly with temperature between 30 and 60 degree C. The sorption results have been analysed by the langmuir adsorption isotherm over the entire range of uranium and thorium concentrations investigated. 35 refs., 8 figs., 5 tabs

  11. Moisture buffer capacity of different insulation materials

    DEFF Research Database (Denmark)

    Peuhkuri, Ruut Hannele; Rode, Carsten; Hansen, Kurt Kielsgaard

    2004-01-01

    . In the isothermal tests the material samples were exposed to the same change in the relative humidity of the ambient air on both sides, while the samples were exposed to variations in relative humidity only on the cold side in the non-isothermal tests. The results of these rather different measurement principles...... lead to more durable constructions. In this paper, a large range of very different thermal insulation materials have been tested in specially constructed laboratory facilities to determine their moisture buffer capacity. Both isothermal and nonisothermal experimental set-ups have been used...... are discussed, and different ways are presented how to determine the moisture buffer capacity of the materials using partly standard material parameters and partly parameters determined from the actual measurements. The results so far show that the determination of moisture buffer capacity is very sensitive...

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

    Energy Technology Data Exchange (ETDEWEB)

    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

  13. Recent progress in sorption mechanisms and models

    International Nuclear Information System (INIS)

    Fedoroff, M.; Lefevre, G.

    2005-01-01

    Full text of publication follows: Sorption-desorption phenomena play an important role in the migration of radioactive species in surface and underground waters. In order to predict the transport of these species, we need a good knowledge of sorption processes and data, together with reliable models able to be included in transport calculation. Traditional approaches based on experimentally determined distribution coefficients (Kd) and sorption isotherms have a limited predictive capability, since they are very sensitive to the numerous parameters characterizing the solution and the solid. Models based on thermodynamic equilibria were developed to account for the influence these parameters: the ion exchange model and the surface complexation models (2-pK mono-site, 1-pK multi-site, with several different electrostatic models: CCM, DLM, BSM, TLM,...). Although these models are very useful, studies performed in recent years showed that they have important theoretical and experimental limitations, which result in the fact that we must be very careful when we use them for extrapolating sorption data to long term and to large natural systems. Among all problems which can be found are: the possibility to fit a set of experimental data with different models, sometimes bad adequacy with the real sorption processes, some theoretical limitations such as a rigorous definition of reference and standard states in surface equilibria, slow kinetics which prevent from equilibrium achievement, irreversibility, solubility and evolution of solid phases... Through the increase of the number of sensitive spectroscopic methods, we are now able to know more about sorption processes at the atomic scale. Models such as the 1-pK CD-MUSIC model can account for the influence of orientation of the faces of the solid. More and more examples of the influence of this orientation on the sorption properties are known. Calculations performed by 'ab initio' modeling is also useful to predict the

  14. Determination and modeling of desorption isotherms of Maria biscuits from different brands

    OpenAIRE

    Pereira, DFC; Correia, PMR; Guiné, Raquel

    2012-01-01

    Biscuits (sweet, strongly sweet, semi-sweet biscuits, crackers, wafers) are characterized by a low moisture content in the final product and high levels of fat and sugar [1]. Dehydrated foods, such as biscuits, are very sensitive to gain moisture from the surrounding atmosphere, resulting in a consequent deterioration. When, at constant temperature, the product's moisture increases from the atmosphere, is obtained the adsorption isotherm and when it loses moisture is obtained the desorption i...

  15. Radionuclide sorption database for Swiss safety assessment

    International Nuclear Information System (INIS)

    McKinley, I.G.; Hadermann, J.

    1984-10-01

    Recommended sorption data for use in transport models for a Swiss High-Level Waste repository are presented. The models used in 'Project Gewaehr 1985' assume linear sorption isotherms and require elemental partition coefficient (Kd) data. On the basis of a literature search 'realistic' Kd data for 22 elements have been selected for weathered crystalline rock and sediments in contact with a reducing groundwater and also sediments with a less reducing groundwater. In an appendix sorption data for 28 elements on bentonite backfill are given. These data are supplemented with 'conservative' estimates taken to represent minimum reasonable values. Available data are discussed for each element clearly exhibiting (i) the large gaps in knowledge, (ii) their unbalanced distribution between different elements and, hence, (iii) the need for further experiments in the laboratory, the field and analogue studies. An overview of the theoretical concepts of sorption, experimental methodology and data interpretation is given in order to put the values into context. General problem areas are identified. (Auth.)

  16. Investigation of solution chemistry effects on sorption behavior of radionuclide 64Cu(II) on illite

    International Nuclear Information System (INIS)

    Shitong Yang; Guodong Sheng; Zhiqiang Guo; Yubing Sun; Donglin Zhao

    2011-01-01

    In this work, a series of batch experiments were carried out to investigate the effect of various environmental factors such as contact time, pH, ionic strength, coexisting electrolyte ions, humic substances and temperature on the sorption behavior of illite towards 64 Cu(II). The results indicated that 64 Cu(II) sorption on illite achieved equilibrium quickly. The pH- and ionic strength-dependent sorption suggested that 64 Cu(II) sorption on illite was dominated by ion exchange or outer-sphere surface complexation at pH 7. A positive effect of humic substances on 64 Cu(II) sorption was found at pH 6.5. The Langmuir and Freundlich models were used to simulate the sorption isotherms of 64 Cu(II) at three different temperatures of 293, 313, and 333 K. The thermodynamic parameters (ΔH 0 , ΔS 0 , and ΔG 0 ) of 64 Cu(II) sorption on illite were calculated from the temperature dependent sorption isotherms, and the results indicated that the sorption of 64 Cu(II) on illite was endothermic and spontaneous. From the experimental results, it is possible to conclude that illite has good potentialities for cost-effective treatments of 64 Cu(II)-contaminated wastewaters. (author)

  17. Evaluation of sorption affinity of cadmium(II) on Haro river sand from aqueous solutions

    International Nuclear Information System (INIS)

    Hasany, S.M.; Chaudhary, M.H.

    2001-01-01

    The sorption of Cd(II) on Haro river sand from deionized water is reported. The sorption system obeyed according to the Freundlich and Dubinin-Radushkevich (D-R) isotherms. The Freundlich parameters 1/n = 0.67±0.05 and of A = 1.38±1.14 mmole x g -1 have been ascertained. D-R isotherm yields the values of β = -0.003741±0.000321 kJ 2 x mole -2 , X m = 0.23±0.21 μmole x g -1 and of E = 11.6±0.5 kJ x mole -1 . The influence of common anions and cations on the sorption was examined. Trivalent Bi enhances the sorption whereas Fe, Cr, Al and chromate ions reduce the sorption significantly. Hf(IV) and Ag(I) indicate substantial sorption (61-98%) whereas Gd(III), Re(VII) and Sc(III) show low sorption (<5%). The elements having low sorption can be separated from elements indicating higher sorption using Haro river sand column. (author)

  18. Sorption behavior of Sn(II) onto Haro river sand from aqueous acidic solutions

    International Nuclear Information System (INIS)

    Hasany, S.M.; Khurshid, S.J.

    1999-01-01

    The sorption behavior of Sn(II) onto Haro river sand has been examined with respect to nature of electrolyte, agitation time, dosage of sorbent and concentration of sorbate. Maximum sorption (95.5%) has been achieved from 0.034M hydrochloric acid solution after equilibrating sorbate (2 x 10 -5 M) and sorbent (50 mg) for 120 minutes at a V/W ratio of 90 cm 3 x g -1 . The kinetic data have been subjected to Morris-Weber and Lagergren equations. The kinetics of sorption proceeds a two stage process consisting of a relatively slow initial uptake followed by a much rapid increase in the sorption. The rate constant of intraparticle transport, K d , comes out to be 8.75 x 10 -8 mol x g -1 x min -1/2 and the first order rate constant for sorption is 0.0416 min -1 . The sorption data of Sn(II) onto Haro river sand followed Langmuir, Freundlich and Dubinin-Radushkevich (D-R) type isotherms. The Langmuir constant, Q, related to sorption capacity and, b, related to sorption energy are computed to be 10.6±1.1 μmol x g -1 and 1123±137 dm 3 x mol -1 , respectively. The D-R isotherm yields the values of C m = 348±151 μmol x g -1 and β = -0.01044±0.0008 mol 2 x kJ -2 and of E = 6.9±0.3 kJ x mol -1 . In all three isotherms correlation factor (γ) is ≥ 0.99. The influence of common anions and cations on the sorption has been investigated. Zn(II), Mg(II), oxalate, Pb(II), Mn(II) and tartrate reduce the sorption significantly whereas Fe(II) causes substantial increase in the sorption. (author)

  19. Generalized isothermic lattices

    International Nuclear Information System (INIS)

    Doliwa, Adam

    2007-01-01

    We study multi-dimensional quadrilateral lattices satisfying simultaneously two integrable constraints: a quadratic constraint and the projective Moutard constraint. When the lattice is two dimensional and the quadric under consideration is the Moebius sphere one obtains, after the stereographic projection, the discrete isothermic surfaces defined by Bobenko and Pinkall by an algebraic constraint imposed on the (complex) cross-ratio of the circular lattice. We derive the analogous condition for our generalized isothermic lattices using Steiner's projective structure of conics, and we present basic geometric constructions which encode integrability of the lattice. In particular, we introduce the Darboux transformation of the generalized isothermic lattice and we derive the corresponding Bianchi permutability principle. Finally, we study two-dimensional generalized isothermic lattices, in particular geometry of their initial boundary value problem

  20. Kinetics and equilibrium studies for sorption of Cu (II) and Cr (VI) ions onto polymeric composite resins

    International Nuclear Information System (INIS)

    El-Zahhhar, A.A.; Abdel-Aziz, H.M.; Siyam, T.

    2005-01-01

    The sorption behavior of Cu (II) and Cr (VI) ions from aqueous solutions was studied using polymeric composite resins. Batch sorption experiments were performed as a function of hydrogen ion concentration, complexing agent concentration, resin weight and ionic strength. Kinetic parameters as a function of initial ion concentration were determined to predict the sorption behavior of Cu (II) and Cr (VI) onto polymeric composite resins. The equilibrium data could be fitted by the frendlich adsorption isotherm equation

  1. Study of sorption processes of copper on synthetic hydroxyapatite

    International Nuclear Information System (INIS)

    Rosskopfova, O.; Galambos, M.; Ometakova, J.; Rajec, P.; Caplovicova, M.

    2012-01-01

    The sorption of copper on synthetic hydroxyapatite was investigated using a batch method and radiotracer technique. The hydroxyapatite sample prepared by a wet precipitation process was of high crystallinity with Ca/P ratio of 1.688. The sorption of copper on hydroxyapatite was pH independent ranging from 4 to 6 as a result of buffering properties of hydroxyapatite. The adsorption of copper was rapid and the percentage of Cu sorption was >98% during the first 15-30 min of the contact time. The experimental data for sorption of copper have been interpreted in the term of Langmuir isotherm. The sorption of Cu 2+ ions was performed by ion-exchange with Ca 2+ cations on the crystal surface of hydroxyapatite under experimental conditions. The competition effect of Zn 2+ , Fe 2+ and Pb 2+ towards Cu 2+ sorption was stronger than that of Co 2+ , Ni 2+ and Ca 2+ ions. The ability of the bivalent cations to depress the sorption of copper on hydroxyapatite was in the following order Pb 2+ > Fe 2+ > Zn 2+ > Co 2+ ∼ Ni 2+ . (author)

  2. Sorption of U(VI) species on hydroxyapatite

    International Nuclear Information System (INIS)

    Thakur, P.; Moore, R.C.; Choppin, G.R.

    2005-01-01

    The sorption of uranyl (UO 2 2+ ) cations to hydroxyapatite was studied as a function of the amount of sorbent, ionic strength, U(VI) concentration, pH and temperature. The rate of uranyl sorption on hydroxyapatite decreased with increased uranyl concentrations. The amount sorbed decreased with increased ionic strength and increased with pH to a maximum at 7-8. The sorption data for UO 2 2+ were fitted well by the Freundlich and Dubinin-Radushkevich (D-R) isotherms. The anions Cl - , NO 3 - , SO 4 2- and CH 3 COO - decreased the sorption of uranium on hydroxyapatite while S 2 O 3 2- slightly increased it. The sorbed uranium was desorbed by 0.10 M and 1.00 M solutions of HCl and HNO 3 . The thermodynamic parameters for the sorption of UO 2 2+ were measured at temperatures of 298, 313, 323 and 333 K. The temperature dependence confirmed an endothermic heat of sorption. The activation energy for the sorption process was calculated to be +2.75±0.02 kJ/mol. (orig.)

  3. A mechanistic approach to the generation of sorption databases

    International Nuclear Information System (INIS)

    Bradbury, M.H.; Baeyens, B.

    1992-01-01

    Sorption of radionuclides in the near and far fields of an underground nuclear waste repository is one of the most important processes retarding their release to the environment. In the vast majority of cases sorption data have been presented in terms of empirical parameters such as distribution coefficients and isotherm equations. A consequence of this empirical methodology is that the sorption data are only strictly valid under the experimental conditions at which they were measured. Implicit in this approach is the need to generate large amounts of data and fitting parameters necessary for an empirical description of sorption under all realistically conceivable conditions which may arise in space and time along the migration pathway to Man. An alternative approach to the problem is to try to understand, and develop model descriptions of, underlying retention mechanisms and to identify those systems parameters which essentially determine the extent of sorption. The aim of this work is to see to what extent currently existing mechanistic models, together with their associated data, can be applied to predict sorption data from laboratory experiments on natural systems. This paper describes the current status of this work which is very much in an early stage of development. An example is given whereby model predictions are compared with laboratory results for the sorption of Np at trace concentrations under oxidizing conditions on a series of minerals relevant to granite formations. 31 refs., 11 figs., 5 tabs

  4. Isotherms of ion exchange on titanates of alkaline metals

    International Nuclear Information System (INIS)

    Fillina, L.P.; Belinskaya, F.A.

    1986-01-01

    Present article is devoted to isotherms of ion exchange on titanates of alkaline metals. Therefore, finely dispersed hydrated titanates of alkaline metals (lithium, sodium, potassium) with ion exchange properties are obtained by means of alkaline hydrolysis of titanium chloride at high ph rates. Sorption of cations from salts solution of Li 2 SO 4 , NaNO 3 , Ca(NO 3 ) 2 , AgNO 3 by titanates is studied.

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

    Directory of Open Access Journals (Sweden)

    Yinghong Wu

    2014-01-01

    Full Text Available 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.

  6. Study of sorption properties of nickel on chitosan; Studium sorpcnych vlastnosti niklu na chitosan

    Energy Technology Data Exchange (ETDEWEB)

    Pivarciova, L; Rosskopfova, O; Galambos, M [Univerzita Komenskeho v Bratislave, Prirodovedecka fakulta, Katedra jadrovej chemie, 84215 Bratislava (Slovakia)

    2012-04-25

    Sorption of nickel on the selected sorbent was studied by a batch method. The effect of contact time and pH to reach sorption equilibrium was studied. During sorption of Ni{sup 2+} ions there proceed predominantly ion-exchange reactions on its surface. Time to reach sorption equilibrium of nickel on chitosan was 14 hours. Sorption percentage after 14 hours reached a value of 84 %. Solutions with starting pH value between 3.9 and 8.1 were used for sorption of nickel. A sorption of nickel on chitosan was > 97% in monitored interval of pH after 24 hours of contact . At an initial pH from 3.9 to 6.4 was the final pH 6.6 due to protonisation of amino groups. A pH value was 6.4 after sorption of 7.1. Sorption of nickel is reduced by increasing of concentrations of Ni{sup 2+} ions in the solution. Langmuir isotherm was used for interpretation of nickel sorption on chitosan. A maximum sorption capacity for chitosan was 2,67 {center_dot} 10{sup -3} mol/g{sup -}1. (authors)

  7. Sorption Hysteresis of Light Hydrocarbons and Carbon Dioxide in Shale and Kerogen

    KAUST Repository

    Zhao, Huangjing

    2017-11-20

    We present adsorption and desorption isotherms of methane, ethane, propane, n-butane and iso-butane as well as carbon dioxide for two shales and isolated kerogens determined by a gravimetric method. The sorption measurements of two shales were performed at three different temperatures, 308.15, 323.15, and 338.15 K. For the isolated kerogens, the measurements were conducted at 338.15 K. Methane and ethane sorption isotherms were measured to 35 bar. Carbon dioxide sorption isotherms were studied to 30 bar. Due to the low vapor pressure at room temperature, the sorption isotherms of propane, n-butane and iso-butane were measured to 8, 2, and 2 bar, respectively. The adsorptions of propane, n-butane, and iso-butane were much higher than methane at the highest pressures where the measurements were conducted. The adsorption of n-butane was 10 times higher than methane by mole at 2 bar, followed by iso-butane and propane. Our data show significant adsorption hysteresis in ethane, propane, n-butane and iso-butane. The most pronounced hysteresis was found in n-butane and iso-butane. Significant hysteresis is attributed to the reversible structural changes of kerogens. Dissolution of adsorbates into organic matter may also affect the hysteresis. This is the first report of propane and butane sorption isotherms in shales.

  8. Sorption Hysteresis of Light Hydrocarbons and Carbon Dioxide in Shale and Kerogen

    KAUST Repository

    Zhao, Huangjing; Lai, Zhiping; Firoozabadi, Abbas

    2017-01-01

    We present adsorption and desorption isotherms of methane, ethane, propane, n-butane and iso-butane as well as carbon dioxide for two shales and isolated kerogens determined by a gravimetric method. The sorption measurements of two shales were performed at three different temperatures, 308.15, 323.15, and 338.15 K. For the isolated kerogens, the measurements were conducted at 338.15 K. Methane and ethane sorption isotherms were measured to 35 bar. Carbon dioxide sorption isotherms were studied to 30 bar. Due to the low vapor pressure at room temperature, the sorption isotherms of propane, n-butane and iso-butane were measured to 8, 2, and 2 bar, respectively. The adsorptions of propane, n-butane, and iso-butane were much higher than methane at the highest pressures where the measurements were conducted. The adsorption of n-butane was 10 times higher than methane by mole at 2 bar, followed by iso-butane and propane. Our data show significant adsorption hysteresis in ethane, propane, n-butane and iso-butane. The most pronounced hysteresis was found in n-butane and iso-butane. Significant hysteresis is attributed to the reversible structural changes of kerogens. Dissolution of adsorbates into organic matter may also affect the hysteresis. This is the first report of propane and butane sorption isotherms in shales.

  9. A revised multi-Fickian moisture transport model to describe non-Fickian effects in wood

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Damkilde, Lars; Svensson, Staffan

    2007-01-01

    This paper presents a study and a refinement of the sorption rate model in a so-called multi-Fickian or multi-phase model. This type of model describes the complex moisture transport system in wood, which consists of separate water vapor and bound-water diffusion interacting through sorption...... sorption allow a simplification of the system to be modeled by a single Fickian diffusion equation. To determine the response of the system, the sorption rate model is essential. Here the function modeling the moisture-dependent adsorption rate is investigated based on existing experiments on thin wood...

  10. The Effect of Temperature on Moisture Transport in Concrete.

    Science.gov (United States)

    Wang, Yao; Xi, Yunping

    2017-08-09

    Most concrete structures and buildings are under temperature and moisture variations simultaneously. Thus, the moisture transport in concrete is driven by the moisture gradient as well as the temperature gradient. This paper presents an experimental approach for determining the effect of different temperature gradients on moisture distribution profiles in concrete. The effect of elevated temperatures under isothermal conditions on the moisture transport was also evaluated, and found not to be significant. The non-isothermal tests show that the temperature gradient accelerates the moisture transport in concrete. The part of increased moisture transfer due to the temperature gradient can be quantified by a coupling parameter D HT , which can be determined by the present test data. The test results indicated that D HT is not a constant but increases linearly with the temperature variation. A material model was developed for D HT based on the experimental results obtained in this study.

  11. Enthalpy-entropy compensation based on isotherms of mango Compensação entalpia-entropia baseada nas isotermas de mango

    Directory of Open Access Journals (Sweden)

    Javier Telis-Romero

    2005-06-01

    Full Text Available Moisture equilibrium data of mango pulp were determined using the static gravimetric method. Adsorption and desorption isotherms were obtained in the range of 30-70 ºC, to water activities (a w from 0.02 to 0.97. The application of the GAB model to the experimental results, using direct nonlinear regression analysis, provided agreement between experimental and calculated values. The net isosteric heat of sorption was estimated from equilibrium sorption data, using the Clausius-Clapeyron equation. Isosteric heats of sorption were found to increase with increasing temperature and could be well adjusted by an exponential relationship. The enthalpy-entropy compensation theory was applied to sorption isotherms and plots of deltaH versus deltaS provided the isokinetic temperatures, indicating an enthalpy controlled sorption process.Dados de equilíbrio da umidade da polpa de manga foram determinados utilizando-se o método estático gravimétrico. As isotermas de adsorção e dessorção foram obtidas na faixa de 30-70 ºC e as atividades de água (a w de 0,02 a 0,97. A utilização do modelo de GAB nos resultados experimentais, através da análise de regressão não linear, proporcionou um bom ajuste entre os dados experimentais e os valores calculados. O calor isostérico de sorção foi estimado a partir dos dados de equilíbrio de sorção, utilizando-se a equação de Clausius-Clayperon. Notou-se que os calores isostéricos de sorção crescem com o aumento da temperatura e pode ser bem ajustado através de uma relação exponencial. A teoria da compensação entalpia-entropia foi aplicada às isotermas de sorção e gráficos deltaH versus deltaS forneceram as temperaturas isocinéticas, indicando um processo de sorção entalpicamente controlado.

  12. Moisture adsorption properties and shelf-life estimation of dried and pulverised edible house cricket Acheta domesticus (L.) and black soldier fly larvae Hermetia illucens (L.).

    Science.gov (United States)

    Kamau, E; Mutungi, C; Kinyuru, J; Imathiu, S; Tanga, C; Affognon, H; Ekesi, S; Nakimbugwe, D; Fiaboe, K K M

    2018-04-01

    Edible insects are part of the diets of a significant proportion of rural populations in the tropics especially Africa and Asia, and their use as source of key nutrients for better nutrition is re-emerging. Indigenously, elemental methods are used to process the insects before they are consumed or sold in retail outlets. In recent years, better knowledge of processing, packaging and storage has become necessary because of commercialisation needs. A common processing approach involves drying after a brief heat-treatment step, and then milling into a powdered product which is sold to manufacturers or consumers as ingredient for processing final products. The hydration properties of dried powders of edible house cricket and black soldier fly larvae (BSFL) were studied with the aim of predicting shelf-life stability under typical packaging and storage temperatures experienced in the tropics. Moisture adsorption isotherms were determined gravimetrically at 25, 30 and 35 °C, over 0.11-0.97 water activity (a W ) range, and the data fitted to various models. Sorption isotherms were of type II according to Brunauer classification indicating monolayer-multilayer sorption behaviour. Cricket powder exhibited higher hydration capacity, and a W of this product was less sensitive to temperature variation as compared to BSFL powder. In the two products, water exhibited transitions from bound- to free- state at ~5 g/100 g moisture content. Based on Heiss-Eichner model, a shelf-life of 7 months at 25 °C can be achieved if the cricket and BSFL powders are dried to ca. 5 g/100 g moisture content and packaged in 80 μm thick polyethylene films. At 35 °C the shelf-life of the cricket product is shortened three- to four-fold whereas the BSFL powder is unable to store. Copyright © 2018 Elsevier Ltd. All rights reserved.

  13. Sorption by cation exchange

    International Nuclear Information System (INIS)

    Bradbury, M.H.; Baeyens, B.

    1994-04-01

    A procedure for introducing exchange into geochemical/surface complexation codes is described. Beginning with selectivity coefficients, K c , defined in terms of equivalent fractional ion occupancies, a general expression for the molar based exchange code input parameters, K ex , is derived. In natural systems the uptake of nuclides onto complex sorbents often occurs by more than one mechanism. The incorporation of cation exchange and surface complexation into a geochemical code therefore enables sorption by both mechanisms to be calculated simultaneously. The code and model concepts are tested against sets of experimental data from widely different sorption studies. A proposal is made to set up a data base of selectivity coefficients. Such a data base would form part of a more general one consisting of sorption mechanism specific parameters to be used in conjunction with geochemical/sorption codes to model and predict sorption. (author) 6 figs., 6 tabs., 26 refs

  14. Defluoridation by Bacteriogenic Iron Oxides: Sorption Studies

    Science.gov (United States)

    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

  15. Surface complexation modeling of zinc sorption onto ferrihydrite.

    Science.gov (United States)

    Dyer, James A; Trivedi, Paras; Scrivner, Noel C; Sparks, Donald L

    2004-02-01

    A previous study involving lead(II) [Pb(II)] sorption onto ferrihydrite over a wide range of conditions highlighted the advantages of combining molecular- and macroscopic-scale investigations with surface complexation modeling to predict Pb(II) speciation and partitioning in aqueous systems. In this work, an extensive collection of new macroscopic and spectroscopic data was used to assess the ability of the modified triple-layer model (TLM) to predict single-solute zinc(II) [Zn(II)] sorption onto 2-line ferrihydrite in NaNO(3) solutions as a function of pH, ionic strength, and concentration. Regression of constant-pH isotherm data, together with potentiometric titration and pH edge data, was a much more rigorous test of the modified TLM than fitting pH edge data alone. When coupled with valuable input from spectroscopic analyses, good fits of the isotherm data were obtained with a one-species, one-Zn-sorption-site model using the bidentate-mononuclear surface complex, (triple bond FeO)(2)Zn; however, surprisingly, both the density of Zn(II) sorption sites and the value of the best-fit equilibrium "constant" for the bidentate-mononuclear complex had to be adjusted with pH to adequately fit the isotherm data. Although spectroscopy provided some evidence for multinuclear surface complex formation at surface loadings approaching site saturation at pH >/=6.5, the assumption of a bidentate-mononuclear surface complex provided acceptable fits of the sorption data over the entire range of conditions studied. Regressing edge data in the absence of isotherm and spectroscopic data resulted in a fair number of surface-species/site-type combinations that provided acceptable fits of the edge data, but unacceptable fits of the isotherm data. A linear relationship between logK((triple bond FeO)2Zn) and pH was found, given by logK((triple bond FeO)2Znat1g/l)=2.058 (pH)-6.131. In addition, a surface activity coefficient term was introduced to the model to reduce the ionic strength

  16. Sorption behaviour of perfluoroalkyl substances in soils.

    Science.gov (United States)

    Milinovic, Jelena; Lacorte, Silvia; Vidal, Miquel; Rigol, Anna

    2015-04-01

    The sorption behaviour of three perfluoroalkyl substances (PFASs), perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA) and perfluorobutane sulfonic acid (PFBS), was studied in six soils with contrasting characteristics, especially in the organic carbon content. Sorption isotherms were obtained by equilibrating the soil samples with 0.01 mol L(-1) CaCl2 solutions spiked with increasing concentrations of the target PFAS. The sorption reversibility of PFASs was also tested for some of the samples. Liquid chromatography coupled to tandem mass spectrometry was used to quantify the target PFASs in the solutions. Both the Freundlich and linear models were appropriate to describe the sorption behaviour of PFASs in soils, and enabled us to derive solid-liquid distribution coefficients (Kd) for each compound in each soil. Kd values increased from 19 to 295 mL g(-1) for PFOS, from 2.2 to 38 mL g(-1) for PFOA and from 0.4 to 6.8 mL g(-1) for PFBS, and were positively correlated with the organic carbon content of the soil. KOC values obtained from the correlations were 710, 96 and 17 mL g(-1) for PFOS, PFOA and PFBS, respectively. Whereas Kd values decreased in the sequence PFOS>PFOA>PFBS, desorption yields were lower than 13% for PFOS, from 24 to 58% for PFOA, and from 32 to 60% for PFBS. This shows that the physicochemical characteristics of PFASs, basically their hydrophobicity, controlled their sorption behaviour in soils, with PFOS being the most irreversibly sorbed PFAS. Copyright © 2014 Elsevier B.V. All rights reserved.

  17. Sorption data bases and mechanistic sorption studies

    International Nuclear Information System (INIS)

    Bradbury, M.H.

    2000-01-01

    In common with many other countries with a nuclear programme, the Swiss concept for the disposal of radioactive waste is focused on deep burial in specially constructed repositories in geologically stable host rocks. Under such conditions, the most likely means whereby radionuclides might return to the biosphere involves their transport in slowly moving groundwater. The sorption of radionuclides by solid phases in the engineered barriers within the repository, and in the surrounding geological media, limits their release and retards their movement. Performance assessment studies for disposal concepts are carried out by Nagra, the National Cooperative for the Disposal of Radioactive Waste, in which various release scenarios are examined, and 'doses to man' calculated. The uptake of radionuclides by immobile phases is one of the pillars upon which the safety case rests. Hence, sorption databases are very important data sets for performance assessments. The methodology lying behind the construction of sorption databases, and some aspects of the supporting experimental work, are briefly described in this report. Flexible, long-term, focused research programmes are required to properly understand the radionuclide/rock/groundwater system, and this is an essential pre-requisite for producing robust state-of-the-art sorption databases. (author)

  18. Sorption data bases and mechanistic sorption studies

    Energy Technology Data Exchange (ETDEWEB)

    Bradbury, M.H

    2000-07-01

    In common with many other countries with a nuclear programme, the Swiss concept for the disposal of radioactive waste is focused on deep burial in specially constructed repositories in geologically stable host rocks. Under such conditions, the most likely means whereby radionuclides might return to the biosphere involves their transport in slowly moving groundwater. The sorption of radionuclides by solid phases in the engineered barriers within the repository, and in the surrounding geological media, limits their release and retards their movement. Performance assessment studies for disposal concepts are carried out by Nagra, the National Cooperative for the Disposal of Radioactive Waste, in which various release scenarios are examined, and 'doses to man' calculated. The uptake of radionuclides by immobile phases is one of the pillars upon which the safety case rests. Hence, sorption databases are very important data sets for performance assessments. The methodology lying behind the construction of sorption databases, and some aspects of the supporting experimental work, are briefly described in this report. Flexible, long-term, focused research programmes are required to properly understand the radionuclide/rock/groundwater system, and this is an essential pre-requisite for producing robust state-of-the-art sorption databases. (author)

  19. Isothermal Martensite Formation

    DEFF Research Database (Denmark)

    Villa, Matteo

    Isothermal (i.e. time dependent) martensite formation in steel was first observed in the 40ies of the XXth century and is still treated as an anomaly in the description of martensite formation which is considered as a-thermal (i.e. independent of time). Recently, the clarification of the mechanism...... of lattice strains provided fundamental information on the state of stress in the material and clarified the role of the strain energy on martensite formation. Electron backscatter diffraction revealed that the microstructure of the material and the morphology of martensite were independent on the cooling...... leading to isothermal kinetics acquired new practical relevance because of the identification of isothermal martensite formation as the most likely process responsible for enhanced performances of sub-zero Celsius treated high carbon steel products. In the present work, different iron based alloys...

  20. Adiabatic and isothermal resistivities

    International Nuclear Information System (INIS)

    Fishman, R.S.

    1989-01-01

    The force-balance method is used to calculate the isothermal resistivity to first order in the electric field. To lowest order in the impurity potential, the isothermal resistivity disagrees with the adiabatic results of the Kubo formula and the Boltzmann equation. However, an expansion of the isothermal resistivity in powers of the impurity potential is divergent, with two sets of divergent terms. The first set arises from the density matrix of the relative electron-phonon system. The second set arises from the explicit dependence of the density matrix on the electric field, which was ignored by force-balance calculations. These divergent contributions are calculated inductively, by applying a recursion relation for the Green's functions. Using the λ 2 t→∞ limit of van Hove, I show that the resummation of these divergent terms yields the same result for the resistivity as the adiabatic calculations, in direct analogy with the work of Argyres and Sigel, and Huberman and Chester

  1. Sorption of citalopram, irbesartan and fexofenadine in soils: Estimation of sorption coefficients from soil properties.

    Science.gov (United States)

    Klement, Aleš; Kodešová, Radka; Bauerová, Martina; Golovko, Oksana; Kočárek, Martin; Fér, Miroslav; Koba, Olga; Nikodem, Antonín; Grabic, Roman

    2018-03-01

    The sorption of 3 pharmaceuticals, which may exist in 4 different forms depending on the solution pH (irbesartan in cationic, neutral and anionic, fexofenadine in cationic, zwitter-ionic and anionic, and citalopram cationic and neutral), in seven different soils was studied. The measured sorption isotherms were described by Freundlich equations, and the sorption coefficients, K F (for the fixed n exponent for each compound), were related to the soil properties to derive relationships for estimating the sorption coefficients from the soil properties (i.e., pedotransfer rules). The largest sorption was obtained for citalopram (average K F value for n = 1 was 1838 cm 3  g -1 ) followed by fexofenadine (K F  = 35.1 cm 3/n μg 1-1/n g -1 , n = 1.19) and irbesartan (K F  = 3.96 cm 3/n μg 1-1/n g -1 , n = 1.10). The behavior of citalopram (CIT) in soils was different than the behaviors of irbesartan (IRB) and fexofenadine (FEX). Different trends were documented according to the correlation coefficients between the K F values for different compounds (R IRB,FEX  = 0.895, p-valuesoil properties in the pedotransfer functions. While the K F value for citalopram was positively related to base cation saturation (BCS) or sorption complex saturation (SCS) and negatively correlated to the organic carbon content (Cox), the K F values of irbesartan and fexofenadine were negatively related to BCS, SCS or the clay content and positively related to Cox. The best estimates were obtained by combining BCS and Cox for citalopram (R 2  = 93.4), SCS and Cox for irbesartan (R 2  = 96.3), and clay content and Cox for fexofenadine (R 2  = 82.9). Copyright © 2017 Elsevier Ltd. All rights reserved.

  2. Impact of water quality parameters on the sorption of U(VI) onto hematite

    International Nuclear Information System (INIS)

    Zhao Donglin; Wang Xianbiao; Yang Shitong; Guo Zhiqiang; Sheng Guodong

    2012-01-01

    In this study, the sorption of U(VI) from aqueous solution on hematite was studied as a function of various water quality parameters such as contact time, pH, ionic strength, soil humic acid (HA) or fulvic acid (FA), solid content and temperature by using a batch technique. The results demonstrated that the sorption of U(VI) was strongly dependent on ionic strength at pH 6.0 and the sorption was mainly dominated by inner-sphere surface complexation. The presence of HA/FA increases U(VI) sorption at low pH, whereas decreases U(VI) sorption at high pH. The thermodynamic parameters (ΔH 0 , ΔS 0 , and ΔG 0 ) were calculated from the temperature dependent sorption isotherms, and the results suggested that U(VI) sorption was a spontaneous and endothermic process. The results might be important for the application of hematite in U(VI) pollution management. Highlights: ► The sorption of U(VI) was strongly dependent on ionic strength at pH 6.0. ► A positive effect of HA/FA on U(VI) sorption was found at low pH, whereas a negative effect was observed at high pH. ► U(VI) sorption was a spontaneous and endothermic process. ► The results are quite important for the application of hematite in U(VI) pollution management.

  3. Determination of the moisture capacity of porous building materials

    NARCIS (Netherlands)

    Carmeliet, J.

    2002-01-01

    The moisture capacity, which is required to solve the isothermal moisture transport equation, is generally expressed by parametric functions covering both the hygroscopic and over-hygroscopic regime. The modality or number of analytical functions needed to describe the corresponding pore volume

  4. Determining the critical relative humidity at which the glassy to rubbery transition occurs in polydextrose using an automatic water vapor sorption instrument.

    Science.gov (United States)

    Yuan, Xiaoda; Carter, Brady P; Schmidt, Shelly J

    2011-01-01

    Similar to an increase in temperature at constant moisture content, water vapor sorption by an amorphous glassy material at constant temperature causes the material to transition into the rubbery state. However, comparatively little research has investigated the measurement of the critical relative humidity (RHc) at which the glass transition occurs at constant temperature. Thus, the central objective of this study was to investigate the relationship between the glass transition temperature (Tg), determined using thermal methods, and the RHc obtained using an automatic water vapor sorption instrument. Dynamic dewpoint isotherms were obtained for amorphous polydextrose from 15 to 40 °C. RHc was determined using an optimized 2nd-derivative method; however, 2 simpler RHc determination methods were also tested as a secondary objective. No statistical difference was found between the 3 RHc methods. Differential scanning calorimetry (DSC) Tg values were determined using polydextrose equilibrated from 11.3% to 57.6% RH. Both standard DSC and modulated DSC (MDSC) methods were employed, since some of the polydextrose thermograms exhibited a physical aging peak. Thus, a tertiary objective was to compare Tg values obtained using 3 different methods (DSC first scan, DSC rescan, and MDSC), to determine which method(s) yielded the most accurate Tg values. In general, onset and midpoint DSC first scan and MDSC Tg values were similar, whereas onset and midpoint DSC rescan values were different. State diagrams of RHc and experimental temperature and Tg and %RH were compared. These state diagrams, though obtained via very different methods, showed relatively good agreement, confirming our hypothesis that water vapor sorption isotherms can be used to directly detect the glassy to rubbery transition. Practical Application: The food polymer science (FPS) approach, pioneered by Slade and Levine, is being successfully applied in the food industry for understanding, improving, and

  5. Thermodynamic parameters and sorption of U(VI) on ACSD

    International Nuclear Information System (INIS)

    Donat, R.; Cilgi, G.K.; Cetisli, H.; Aytas, S.

    2009-01-01

    This paper discusses the sorption properties for U(VI) by alginate coated CaSO 4 x 2H 2 O sepiolite and calcined diatomite earth (Kieselguhr) (ACSD). The removal of U(VI) from aqueous solution by sorption onto ACSF in a single component system with various contact times, pH, temperatures, and initial concentrations of U(VI) was investigated. The sorption patterns of uranium on the composite adsorbent followed the Langmuir, Freundlich and Dubinin-Radushkhevic (D-R) isotherms. The Freundlich, Langmuir, and D-R models have been applied and the data correlated well with Freundlich model and that the sorption was physical in nature (sorption energy, E a = 17.05 kJ/mol). The thermodynamic parameters such as variation of enthalpy ΔH, variation of entropy ΔS and variation of Gibbs free energy ΔG were calculated from the slope and intercept of lnK 0 vs. 1/T plots. Thermodynamic parameters (ΔH ads = 31.83 kJ/mol, ΔS ads = 167 J/mol x K, ΔGdeg ads (293.15 K) = -17.94 kJ/mol) showed the endothermic heat of sorption and the feasibility of the process. The thermodynamics of U(VI) ion/ACSD system indicates the spontaneous and endothermic nature of the process. It was noted that an increase in temperature resulted in a higher uranium loading per unit weight of the adsorbent. (author)

  6. Sorption Coefficients for Iodine, Silver, and Cesium on Dust Particles

    International Nuclear Information System (INIS)

    Stempniewicz, M.M.; Goede, P.

    2014-01-01

    This paper describes the work performed to find relevant experimental data and find the sorption coefficients that represent well the available data for cesium, iodine, and silver on dust particles. The purpose of this work is to generate a set of coefficients that may be recommended for the computer code users. The work was performed using the computer code SPECTRA. Calculations were performed for the following data: • I-131 on AVR dust; • Ag-110m on AVR dust; • Cs-13 and Cs-137 on AVR dust. Available data was matched using the SPECTRA Sorption Model. S = A(T) · C_V-B(T) · C_d. The results are summarized as follows: • The available data can be correlated. The data scatter is about 4 orders of magnitude. Therefore the coefficients of the Langmuir isotherms vary by 4 orders of magnitude. • Sorption rates are higher at low temperatures and lower at high temperatures. This tendency has been observed in the data compiled at Oak Ridge. It is therefore surmised that the highest value of the sorption coefficients are appropriate for the low temperatures and the lowest value of the sorption coefficients are appropriate for the high temperatures. The recommended sorption coefficients are presented in this paper. • The present set of coefficients is very rough and should be a subject for future verification against experimental data. (author)

  7. Sorption properties of wool

    Directory of Open Access Journals (Sweden)

    Radetić Maja M.

    2004-01-01

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

  8. Thermodynamic characteristics of sorption of metal-ions by ion exchangers

    OpenAIRE

    ABBASOV ALIADDIN DAYYAN; JAFARLI MAHNUR MOYSUN; MEMMEDOVA FIZZA SADIKH; HEYDEROVA FARAH FARMAN

    2016-01-01

    Conditions of sorption equilibrium of copper, zinc, cadmium and lead-ions by chelatforming resins Diaion CR 11, Dowex M 4195 and Duolite C 467 depending on the degree of neutralization of their ionogenic groups, the acidity of the medium and concentration of solutions are studied; corresponding equations expressing the isotherms of sorption are offered. Kinetics of these processes is studied; on the basis of equilibrium and kinetic parameters are calculated thermodynamic quantities. It is sho...

  9. Effects of biochar and manure amendments on water vapor sorption in a sandy loam soil

    DEFF Research Database (Denmark)

    Arthur, Emmanuel; Tuller, Markus; Moldrup, Per

    2015-01-01

    Over the last few years, the application of biochar (BC) as a soil amendment to sequester carbon and mitigate global climate change has received considerable attention. While positive effects of biochar on plant nutrition are well documented, little is known about potential impacts on the physical....... Hysteresis of the water vapor sorption isotherms increased with increasing BC application rates. Biochar age did not significantly affect vapor sorption and SSA....

  10. Data for the sorption of actinides on candidate materials for use in repositories

    International Nuclear Information System (INIS)

    Morgan, R.D.; Pryke, D.C.; Rees, J.H.

    1988-02-01

    The sorptive behaviour of the actinides uranium, neptunium, plutonium and americium has been investigated under air-saturated conditions on a number of candidate near-field materials by batch sorption experiments. Distribution ratios were measured with respect to initial actinide concentration, the solid:liquid ratio and contact time. Desorption experiments were carried out to help elucidate the mechanism of sorption. The fit of the data to the Freundlich isotherm was assessed. This work contains the data obtained in the investigation. (author)

  11. Gas sorption properties of microporous metal organic frameworks

    International Nuclear Information System (INIS)

    Lee, JeongYong; Li Jing; Jagiello, Jacek

    2005-01-01

    A low-temperature gas sorption study has been carried out on four three-dimensional microporous metal organic framework (MMOF) structures and two two-dimensional layered structures. The pore characteristics are analyzed based on the argon adsorption-desorption isotherms at 87 K. The results from hydrogen sorption experiments conducted at 77 and 87 K show that all MMOFs have a relatively high hydrogen uptake, with adsorbed hydrogen densities falling in the range of liquid hydrogen. Isosteric heats of hydrogen adsorption data calculated based on the Clausius-Clapeyron equation are consistent with these observations, indicating strong sorbent-sorbate interactions. - Graphical abstract: Hydrogen adsorption isotherms measured at 77 and 87 K

  12. Amide mediated enhancement of sorption efficiency of trivalent f-elements on functionalized carbon nanotube: evidence of physiosorption

    International Nuclear Information System (INIS)

    Gupta, Nishesh K.; Sengupta, Arijit; Rane, Vinayak G.; Kadam, R.M.

    2017-01-01

    Amide Functionalized multi-walled carbon nanotube (CNT-DHA) was found to enhance the sorption efficiency of trivalent lanthanides and actinides from aqueous acidic solution. Langmuir, Freundlich, Dubinin-Radushkevich (D-R) and Temkin isotherm models were employed to understand the sorption mechanism revealing the predominance of Fruendlich isotherm. The sorption energy evaluated from D-R isotherm revealed the sorption process is physisorption, which was confirmed by the no shift in the IR frequency of amide functionality of carbon nanotube on sorption. The EPR spectra of the Gd"3"+ sorbed on carbon nanotube also showed no perturbation on the local environment of Gd"3"+ on sorption again revealing the physisorption. Analysis of the sorption kinetics through Lagergren's first order kinetics, intra particle diffusion model and pseudo second order kinetics revealed that the sorption kinetics followed pseudo second order kinetics for Am"3"+ and Eu"3"+ with rate constants 4.04E-05mg g"-"1 min"-"1 and 8.27E-05 mg g"-"1 min"-"1 respectively. The radiolytic stability of CNT-DHA was evaluated and found to be satisfactory. EDTA was found to strip the trivalent lanthanides and actinides almost quantitatively. (author)

  13. Equilibrium moisture content of waste mixtures from post-consumer carton packaging.

    Science.gov (United States)

    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.

  14. Lead sorption-desorption from organic residues.

    Science.gov (United States)

    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.

  15. Determination of Sorption Coefficient of Phosphorus Applied for Sugarcane Production in Southwestern Florida.

    Science.gov (United States)

    Muwamba, A; Nkedi-Kizza, P; Morgan, K T

    2016-09-01

    Phosphorus is among the essential nutrients applied to sugarcane ( L.) fields in the form of a fertilizer mixture (N, P, and K) in southwestern Florida. Sorption coefficient is used for modeling P movement, and in this study, we hypothesized that the sorption coefficient determined using fertilizer mixture (N, P, and K) will be significantly different from values determined using KCl and CaCl, the electrolytes most commonly used for conducting sorption experiments. Supporting electrolytes, 0.01 mol L KCl, 0.005 mol L CaCl, deionized (DI) water, simulated Florida rain, and fertilizer mixture prepared in Florida rain were used to characterize P sorption. Immokalee (Sandy, siliceous, hyperthermic Arenic Alaquods) and Margate (Sandy, siliceous hyperthermic Mollic Psammaquents) are the dominant mineral soils used for sugarcane production in southwestern Florida; we used the A and B horizons of Margate soil and the A and B horizons of the Immokalee soil for sorption experiments in this study. Freundlich sorption isotherms described P sorption data. The Freundlich sorption isotherm coefficients followed the trend 0.005 mol L CaCl > 0.01 mol L KCl ≈ fertilizer mixture > simulated Florida rain ≈ DI water. Sorption coefficients were used for modeling P movement with HYDRUS 1D; similar P results were obtained with the 0.01 mol L KCl and fertilizer mixture electrolyte treatments. The sorption coefficient for DI water and simulated Florida rain overpredicted P movement. The P sorption data showed the importance of choosing the appropriate electrolyte for conducting experiments based on the composition of fertilizer. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.

  16. Sorption of neptunium(V) on opalinus clay under aerobic/anaerobic conditions

    International Nuclear Information System (INIS)

    Froehlich, D.R.; Amayri, S.; Drebert, J.; Reich, T.

    2011-01-01

    The interaction between neptunium(V) and a natural argillaceous rock (Opalinus Clay (OPA), Mont Terri, Switzerland) has been investigated in batch sorption experiments by varying pH (6-10), Np(V) concentration (10 -12 -10 -4 M), solid-to-liquid ratio (2-20 g/L), and partial pressure of CO 2 (10 -3.5 and 10 -2.3 atm) under aerobic/anaerobic conditions in saturated calcite solution. All batch experiments were carried out using well characterized aerobic and anaerobic dry powders of OPA. The results show a great influence of pH on Np(V) sorption. Under aerobic conditions sorption increases with increasing pH until maximum sorption is reached between pH 8-9. At pH > 9 sorption decreases due to the formation of negatively charged Np(V)-carbonate complexes. By increasing p CO 2 from 10 -3.5 to 10 -2.3 atm, the sorption edge is shifted ∼ 0.5 units to lower pH values. Under anaerobic conditions stronger sorption of 8 x 10 -6 M Np(V) was found, possibly due to partial reduction of Np(V) to Np(IV). The sorption of 8 x 10 -6 M Np(V) under aerobic conditions at pH 8.2 in saturated calcite solution increases continuously with increasing solid-to-liquid ratio of OPA in the range of 2-20 g/L with a constant K d value of 126 ± 13 L/kg. The sorption isotherm was measured over seven orders of magnitude in Np(V) concentration using 239 Np as tracer. The sorption isotherm could be divided in a part of linear sorption behaviour between 10 -13 -10 -9 M Np(V) and non-linear behaviour in the range of 10 -9 -10 -4 M Np(V). (orig.)

  17. Comparison of sorption measurements on argillaceous rocks and bentonite with predictions using the SGT-E2 approach to derive sorption data bases

    Energy Technology Data Exchange (ETDEWEB)

    Bradbury, M. H.; Baeyens, B; Marques Fernandes, M.

    2014-11-15

    In Stage 1 of the Sectoral Plan for Deep Geological Repositories, four rock types have been identified as being suitable host rocks for a radioactive waste repository, namely, Opalinus Clay for a high-level (HLW) and a low- and intermediate-level (L/ILW) repository, and 'Brauner Dogger', Effingen Member and Helvetic Marls for a L/ILW repository. Sorption data bases (SDBs) for all of these host rocks are required for the provisional safety analyses, including all of the bounding porewater and mineralogical composition combinations. In addition, SDBs are needed for the rock formations lying below Opalinus Clay (lower confining units) and for the bentonite backfill in the HLW repository. A detailed procedure was developed for deriving SDBs for argillaceous rocks (and bentonite) based on sorption edge measurements on illite (and montmorillonite), the hypothesis that 2:1 clay minerals are the dominant sorbents and a series of so called conversion factors which take into account the different radionuclide speciations in the different porewaters. Since this methodology for generating SDBs is relatively new, a validation and demonstration of the robustness and reliability of the sorption values derived was required. This report describes an extensive piece of work in which blind predictions of sorption values were compared with measured ones. Sorption isotherms were measured for the following metal ions Cs(I), Co(II), Ni(II), Eu(III), Th(IV) and U(VI) in a range of realistic porewater chemistries for a range of host rock mineralogies. In the end 53 isotherm data sets were measured. For each of these isotherms a prediction was made of the sorption at trace concentrations using the SDB derivation methodology. A comparison between measured and predicted values for each case was then made. This validation study shows that the methodology used for the derivation of the sorption data bases for argillaceous rocks and bentonite produces reliable sorption values. (authors)

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

    DEFF Research Database (Denmark)

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

    2010-01-01

    of 36 to 93% of the dithionite-extractable FeIII (FeBD). Langmuir fitted Pi sorption isotherms showed a Pi release of up to 1.1 mmol kg-1 in six soils when Pi concentrations in the matrix (Psol) were lower than 10 µM. Phosphate desorption was attributed to dissolution of amorphous iron oxides......, and higher pH under anoxic conditions. The point of zero net sorption (EPC0) increased 2- to 10-fold on reduction. Five soils showed higher Pi sorption capacities in the anoxic than in the oxic state at higher Psol concentrations. Solubility calculations indicated that precipitation of vivianite or similar...

  19. An inverse moisture diffusion algorithm for the determination of diffusion coefficient

    Science.gov (United States)

    Jen Y. Liu; William T. Simpson; Steve P. Verrill

    2000-01-01

    The finite difference approximation is applied to estimate the moisture-dependent diffusion coefficient by utilizing test data of isothermal moisture desorption in northern red oak (Quercus rubra). The test data contain moisture distributions at discrete locations across the thickness of specimens, which coincides with the radial direction of northern red oak, and at...

  20. Properties comparison of biochars from corn straw with different pretreatment and sorption behaviour of atrazine.

    Science.gov (United States)

    Zhao, Xuchen; Ouyang, Wei; Hao, Fanghua; Lin, Chunye; Wang, Fangli; Han, Sheng; Geng, Xiaojun

    2013-11-01

    Biochar has been recognised as an efficient pollution control material. In this study, biochars (CS450 and ADPCS450) were produced using corn straw with different pretreatment techniques (without and with ammonium dihydrogen phosphate (ADP)). The character of the two biochars was compared using elemental analysis, specific surface area (SSA) and Fourier transform infrared spectra (FTIR). ADPCS450 had a higher residue yield and a much larger specific surface area than CS450. The Freundlich, Langmuir and Redlich-Peterson models were used to interpret the sorption behaviour of atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine), and the results fit the Redlich-Peterson equation best. The isothermal sorption parameters indicated that the sorption capacity of atrazine on ADPCS450 was much larger than the sorption capacity of atrazine on CS450. Atrazine sorption was also favoured in acidic solution and under higher temperature conditions. Copyright © 2013 Elsevier Ltd. All rights reserved.

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

    Science.gov (United States)

    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. Copyright © 2012 Elsevier Ltd. All rights reserved.

  2. Effect of biosurfactant[0] on the sorption of phenanthrene onto original and H2O2-treated soils

    Institute of Scientific and Technical Information of China (English)

    PEI Xiaohong; ZHAN Xinhua; ZHOU Lixiang

    2009-01-01

    The objective of this study was to examine the effect of biosurfactant on sorption of phenanthrene (PHE) onto the original or H2O2-treated black loamy soil (typic isohumisols) and red sandy soil (typic ferralisols). The sorption isotherms were performed with the original and "soft" carbon-removed soils in the presence and absence of biosurfactant (200 mg/L). The sorption and degradation of biosurfactant were investigated. The result showed that organic matter played an important role in PHE sorption onto the black loamy and red sandy soils, and the PHE sorption isotherms on the "soft" carbon-removed soils exhibited more nonlinearity than those on the original soils. The values of partition coefficient (Kd) on the original black loamy soil with or without 200 mg/L biosurfactant were 181.6 and 494.5 mL/g, respectively. Correspondingly, in the red sandy soil, Kd was 246.4 and 212.8 mL/g in the presence or absence of biosurfactant, respectively. The changes of Kd suggested that biosurfactant inhibited PHE sorption onto the black loamy soil, but facilitated PHE sorption onto the red sandy soil. The nonlinearity of PHE sorption isotherm was decreased in the presence of biosurfactant. Site specific sorption might occur during PHE sorption onto both the original and the "soft" carbon-removed soils in the presence of biosurfactant. It was noted that biosurfactant could also be sorbed onto soils. The maximal sorption capacity of the red sandy soil for biosurfactant was (76.9 ± 0.007) μg/g, which was 1.31 times that of black loamy soil. Biosurfactant was degraded quickly in the two selected soils, and 92% of biosurfactant were mineralized throughout the incubation experiment for 7 d. It implied that biosurfactant should be added frequently when the remediation of polycyclic aromatic hydrocarbon (PAH)-contaminated soils was conducted through PAH desorption approach facilitated by biosurfactant.

  3. Sorption of Cs onto γ-Al2O3 using batch technique

    International Nuclear Information System (INIS)

    Wang Xiangke

    2004-01-01

    The sorption of Cs onto γ-Al 2 O 3 is studied by using batch technique, ultra-filtration method and UV vis spectrophotometer at room temperature, pH 4.0, 6.0 and 8.0, the ionic strength of NaClO 4 is from 0.001 mol/L to 0.1 mol/L. The concentration of humic acid in the solution is determined at wavelength of 254 nm. The sorption of humic acid on the γ-Al 2 O 3 is strong (≅98% HA is sorbed on the surface of alumina at pH zpc =9.2)) and strongly dependent on pH values. At pH>9.2, the sorption of HA is decreased markedly with the increasing of pH. Humic acid has a little negative effect on the sorption of Cs onto alumina, this may be attributed to the formation of HA-Cs complexation in the solution. The sorption of Cs onto γ-Al 2 O 3 is weakly dependent on the pH and independent on the ionic strength. Freundlich isotherm can fit the sorption isotherms very well. The sorption of Cs onto γ-Al 2 O 3 may be contributed to cation exchange and surface complexation mechanisms. (authors)

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

    Science.gov (United States)

    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.

  5. Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride.

    Science.gov (United States)

    Krajišnik, Danina; Daković, Aleksandra; Milojević, Maja; Malenović, Anđelija; Kragović, Milan; Bogdanović, Danica Bajuk; Dondur, Vera; Milić, Jela

    2011-03-01

    In this study an investigation of a model drug sorption onto cationic surfactant-modified natural zeolites as a drug formulation excipient was performed. Natural zeolite was modified with cetylpyridinium chloride in amounts equivalent to 100, 200 and 300% of its external cation-exchange capacity. The starting material and obtained organozeolites were characterized by Fourier transform infrared spectroscopy, zeta potential measurements and thermal analysis. In vitro sorption of diclofenac sodium as a model drug was studied for all surfactant/zeolite composites by means of sorption isotherm measurements in aqueous solutions (pH 7.4). The modified zeolites with three levels of surfactant coverage within the short activation time were prepared. Zeta potential measurements and thermal analysis showed that when the surfactant loading level was equal to external cation-exchange value, almost monolayer of organic phase were present at the zeolitic surface while higher amounts of surfactant produced less extended bilayers, ordered bilayers or admicelles at the zeolitic surface. Modified zeolites, obtained in this manner, were effective in diclofenac sodium sorption and the organic phase derived from adsorbed cetylpyridinium chloride was the primary sorption phase for the model drug. The Langmuir isotherm was found to describe the equilibrium sorption data well over the entire concentration range. The separate contributions of the adsorption and partition to the total sorption of DS were analyzed mathematically. Results revealed that that adsorption and partitioning of the model drug take place simultaneously. 2010 Elsevier B.V. All rights reserved.

  6. Ammonia-nitrogen and phosphates sorption from simulated reclaimed waters by modified clinoptilolite

    International Nuclear Information System (INIS)

    Huo, Hanxin; Lin, Hai; Dong, Yingbo; Cheng, Huang; Wang, Han; Cao, Lixia

    2012-01-01

    Highlights: ► The salt and thermally modified clinoptilolite can effectively sorb NH 3 -N and phosphates. ► The phosphorus and nitrogen removal was consistent with Langmuir isotherm model. ► The modified clinoptilolite possesses rapid adsorption and slow balance characteristics. ► The adsorption is more in line with the Elovich adsorption dynamics equation. ► The entropy effect plays the role of the main driving force in the adsorption. - Abstract: This paper presents the investigation of the ammonia-nitrogen and phosphates sorption from simulated reclaimed wastewater by modified clinoptilolite. The results showed that the modified clinoptilolite has a high sorption efficiency and removal performance. The ammonia-nitrogen and phosphates removal rate of the modified clinoptilolite reached to 98.46% and 99.80%, respectively. The surface of modified clinoptilolite became loose and some pores appeared, which enlarged the specific surface area; the contents of Na and Fe increased, and the contents of Ca and Mg decreased. The modified clinoptilolite possesses rapid sorption and slow balance characteristics and ammonia-nitrogen and phosphates sorption is more consistent with the Langmuir isotherm model. The adsorption kinetics of ammonia-nitrogen and phosphates follows the Elovich adsorption dynamics equation, which describes the sorption of ammonia-nitrogen and phosphates in aqueous solution as mainly a chemical sorption. Results from the thermodynamics experiment involving ammonia-nitrogen and phosphates sorption reveal that the process is a spontaneous and endothermic process, and is mainly driven by entropy effect.

  7. Metal sorption on kaolinite

    International Nuclear Information System (INIS)

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

    1997-01-01

    A key issue in performance assessment of low-level radioactive waste sites is predicting the transport and retardation of radionuclides through local soils under a variety of hydrologic and geochemical conditions. Improved transport codes should include a mechanistic model of radionuclide retardation. The authors have been investigating metal sorption (Cs + , Sr 2+ , and Ba 2+ ) on a simple clay mineral (kaolinite) to better understand the geochemical interactions of common soil minerals with contaminated groundwaters. These studies include detailed characterizations of kaolinite surfaces, experimental adsorption measurements, surface complexation modeling, and theoretical simulations of cation sorption. The aluminol edge (010) site has been identified as the most likely site for metal sorption on kaolinite in natural solutions. Relative metal binding strengths decrease from Ba 2+ to Sr 2+ to Cs + , with some portion sorbed on both kaolinite edges and basal surfaces. Some Cs + also appears to be irreversibly sorbed on both sites. Molecular dynamics simulations suggest that Cs + is sorbed at aluminol (010) edge sites as an inner-sphere complex and weakly sorbed as an outer-sphere complex on (001) basal surfaces. These results provide the basis to understand and predict metal sorption onto kaolinite, and a framework to characterize sorption processes on more complex clay minerals

  8. The effect of particle size on sorption of estrogens, androgens and progestagens in aquatic sediment

    International Nuclear Information System (INIS)

    Sangster, Jodi L.; Oke, Hugues; Zhang, Yun; Bartelt-Hunt, Shannon L.

    2015-01-01

    Highlights: • Two sediments were used to evaluate the effects of particle size on steroid sorption. • Sorption capacity did not increase with decreasing particle size for all steroids. • Particle interactions affect the distribution of steroids within the whole sediments. • Preferential sorption to fine particles was observed. - Abstract: There is growing concern about the biologic effects of steroid hormones in impacted waterways. There is increasing evidence of enhanced transport and biological effects stemming from steroid hormones associated with soils or sediments; however, there are limited studies evaluating how steroid hormone distribution between various particle sizes within whole sediments affects steroid fate. In this study, sorption of 17β-estradiol, estrone, progesterone, and testosterone was evaluated to different size fractions of two natural sediments, a silty loam and a sandy sediment, to determine the steroid sorption capacity to each fraction and distribution within the whole sediment. Sorption isotherms for all steroid hormones fit linear sorption models. Sorption capacity was influenced more by organic carbon content than particle size. Interactions between size fractions were found to affect the distribution of steroids within the whole sediments. All four steroids preferentially sorbed to the clay and colloids in the silty loam sediment at the lowest aqueous concentration (1 ng/L) and as aqueous concentration increased, the distribution of sorbed steroid was similar to the distribution by weight of each size fraction within the whole sediment. In the sandy sediment, preferential sorption to fine particles was observed.

  9. Comparative evaluation for the sorption capacity of four carbonaceous sorbents to phenol

    Directory of Open Access Journals (Sweden)

    Ding Feng Jin

    2016-10-01

    Full Text Available Sorption kinetics and isotherms of phenol by four carbonaceous sorbents (activated carbon (AC, mesoporous carbon (MPC, bamboo biochar (BBC and oak wood biochar (OBC were compared in this study. MPC has the fastest sorption rate and initial sorption potential, which were indicated by sorption rate constants and initial sorption rate “h” in a pseudo-second-order kinetic model. The ordered and straight pore structure of MPC facilitated the accessibility of phenol. The AC showed the greatest sorption capacity towards phenol with maximum sorption of 123 mg/g as calculated by the Langmuir model. High surface area, complexity of pore structure, and the strong binding force of the π–π electron-donor-acceptor interaction between phenol molecules and AC were the main mechanisms. The BBC and OBC had much slower sorption and lower sorption capacity (33.04 and 29.86 mg/g, respectively, compared to MPC (73.00 mg/g and AC, indicating an ineffective potential for phenol removal from water.

  10. Sorption of Arsenic from Desalination Concentrate onto Drinking Water Treatment Solids: Operating Conditions and Kinetics

    Directory of Open Access Journals (Sweden)

    Xuesong Xu

    2018-01-01

    Full Text Available Selective removal of arsenic from aqueous solutions with high salinity is required for safe disposal of the concentrate and protection of the environment. The use of drinking water treatment solids (DWTS to remove arsenic from reverse osmosis (RO concentrate was studied by batch sorption experiments. The impacts of solution chemistry, contact time, sorbent dosage, and arsenic concentration on sorption were investigated, and arsenic sorption kinetics and isotherms were modeled. The results indicated that DWTS were effective in removing arsenic from RO concentrate. The arsenic sorption process followed a pseudo-second-order kinetic model. Multilayer adsorption was simulated by Freundlich equation. The maximum sorption capacities were calculated to be 170 mg arsenic per gram of DWTS. Arsenic sorption was enhanced by surface precipitation onto the DWTS due to the high amount of calcium in the RO concentrate and the formation of ternary complexes between arsenic and natural organic matter (NOM bound by the polyvalent cations in DWTS. The interactions between arsenic and NOM in the solid phase and aqueous phase exhibited two-sided effects on arsenic sorption onto DWTS. NOM in aqueous solution hindered the arsenic sorption onto DWTS, while the high organic matter content in solid DWTS phase enhanced arsenic sorption.

  11. The effect of particle size on sorption of estrogens, androgens and progestagens in aquatic sediment

    Energy Technology Data Exchange (ETDEWEB)

    Sangster, Jodi L.; Oke, Hugues; Zhang, Yun; Bartelt-Hunt, Shannon L., E-mail: sbartelt2@unl.edu

    2015-12-15

    Highlights: • Two sediments were used to evaluate the effects of particle size on steroid sorption. • Sorption capacity did not increase with decreasing particle size for all steroids. • Particle interactions affect the distribution of steroids within the whole sediments. • Preferential sorption to fine particles was observed. - Abstract: There is growing concern about the biologic effects of steroid hormones in impacted waterways. There is increasing evidence of enhanced transport and biological effects stemming from steroid hormones associated with soils or sediments; however, there are limited studies evaluating how steroid hormone distribution between various particle sizes within whole sediments affects steroid fate. In this study, sorption of 17β-estradiol, estrone, progesterone, and testosterone was evaluated to different size fractions of two natural sediments, a silty loam and a sandy sediment, to determine the steroid sorption capacity to each fraction and distribution within the whole sediment. Sorption isotherms for all steroid hormones fit linear sorption models. Sorption capacity was influenced more by organic carbon content than particle size. Interactions between size fractions were found to affect the distribution of steroids within the whole sediments. All four steroids preferentially sorbed to the clay and colloids in the silty loam sediment at the lowest aqueous concentration (1 ng/L) and as aqueous concentration increased, the distribution of sorbed steroid was similar to the distribution by weight of each size fraction within the whole sediment. In the sandy sediment, preferential sorption to fine particles was observed.

  12. Comparative sorption and desorption behaviors of PFHxS and PFOS on sequentially extracted humic substances

    Institute of Scientific and Technical Information of China (English)

    Lixia Zhao; Yifeng Zhang; Shuhong Fang; Lingyan Zhu; Zhengtao Liu

    2014-01-01

    The sorption and desorption behaviors of two perfluoroalkane sulfonates (PFSAs),including perfluorohexane sulfonate (PFHxS) and perfluorooctane sulfonate (PFOS) on two humic acids (HAs) and humin (HM),which were extracted from a peat soil,were investigated.The sorption kinetics and isotherms showed that the sorption of PFOS on the humic substances (HSs) was much higher than PFHxS.For the same PFSA compound,the sorption on HSs followed the order of HM > HA2 > HA1.These suggest that hydrophobic interaction plays a key role in the sorption of PFSAs on HSs.The sorption capacities of PFSAs on HSs were significantly related to their aliphaticity,but negatively correlated to aromatic carbons,indicating the importance of aliphatic groups in the sorption of PFSAs.Compared to PFOS,PFHxS displayed distinct desorption hysteresis,probably due to irreversible pore deformation after sorption of PFHxS.The sorption of the two PFSAs on HSs decreased with an increase in pH in the solution.This is ascribed to the electrostatic interaction and hydrogen bonding at lower pH.Hydrophobic interaction might also be stronger at lower pH due to the aggregation of HSs.

  13. Sorption of radionickel to goethite: Effect of water quality parameters and temperature

    International Nuclear Information System (INIS)

    Baowei Hu; ShaoXing University, ShaoXing; Wen Cheng; Hui Zhang; Guodong Sheng; Chinese Academy of Sciences, Hefei

    2010-01-01

    In this work, sorption of Ni(II) from aqueous solution to goethite as a function of various water quality parameters and temperature was investigated. The results indicated that the pseudo-second-order rate equation fitted the kinetic sorption well. The sorption of Ni(II) to goethite was strongly dependent on pH and ionic strength. A positive effect of HA/FA on Ni(II) sorption was found at pH 8.0. The Langmuir, Freundlich, and D-R models were applied to simulate the sorption isotherms at three different temperatures of 293.15 K, 313.15 K and 333.15 K. The thermodynamic parameters (ΔH 0 , ΔS 0 and ΔG 0 ) were calculated from the temperature dependent sorption, and the results indicated that the sorption was endothermic and spontaneous. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation or ion exchange with Na + /H + on goethite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. (author)

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

    International Nuclear Information System (INIS)

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

    2012-01-01

    Highlights: ► Organic pollutants are present as complex mixtures in the marine environment. ► The competitive sorption of phenanthrene and DDT in a bi-solute system was investigated onto PVC and PE. ► DDT outcompeted phenanthrene for sorption onto plastic. ► DDT also appeared to have a negative effect on the sorption of phenanthrene onto plastic when added at high concentration. - Abstract: 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.

  15. KINETIC MODELING AND ISOTHERM STUDIES ON A BATCH REMOVAL OF ACID RED 114 BY AN ACTIVATED PLANT BIOMASS

    Directory of Open Access Journals (Sweden)

    N. RAJAMOHAN

    2013-12-01

    Full Text Available In this paper, the dye Acid Red 114(AR 114 was removed from aqueous solutions using Acid-Activated Eichornia Crassipes (AAEC under batch conditions. The optimum conditions for AR 114 removal were found to be pH 1.5, adsorbent dosage = 1.25 g/L of solution and equilibrium time = 3 h. The equilibrium data were evaluated for compliance with Langmuir, Freundlich and Temkin isotherms and Langmuir isotherm was found to fit well. The maximum sorption capacity was estimated as 112.34 mg/g of adsorbent. Also, adsorption kinetics of the dye was studied and the rates of sorption were found to follow pseudo-second order kinetics with good correlation (R2 ≥ 0.997.The kinetic study at different temperatures revealed that the sorption was an endothermic process. The activation energy of the sorption process was estimated as 9.722 kJ/mol.

  16. Sorption mechanisms of phenanthrene, lindane, and atrazine with various humic acid fractions from a single soil sample.

    Science.gov (United States)

    Wang, Xilong; Guo, Xiaoying; Yang, Yu; Tao, Shu; Xing, Baoshan

    2011-03-15

    The sorption behavior of organic compounds (phenanthrene, lindane, and atrazine) to sequentially extracted humic acids and humin from a peat soil was examined. The elemental composition, XPS and (13)C NMR data of sorbents combined with sorption isotherm data of the tested compounds show that nonspecific interactions govern sorption of phenanthrene and lindane by humic substances. Their sorption is dependent on surface and bulk alkyl carbon contents of the sorbents, rather than aromatic carbon. Sorption of atrazine by these sorbents, however, is regulated by polar interactions (e.g., hydrogen bonding). Carboxylic and phenolic moieties are key components for H-bonding formation. Thermal analysis reveals that sorption of apolar (i.e., phenanthrene and lindane) and polar (i.e., atrazine) compounds by humic substances exhibit dissimilar relationships with condensation and thermal stability of sorption domains, emphasizing the major influence of domain spatial arrangement on sorption of organic compounds with distinct polarity. Results of pH-dependent sorption indicate that reduction in sorption of atrazine by the tested sorbents is more evident than phenanthrene with increasing pH, supporting the dependence of organic compound sorption on its polarity and structure. This study highlights the different interaction mechanisms of apolar and polar organic compounds with humic substances.

  17. Sorption of malachite green from aqueous solution by potato peel: Kinetics and equilibrium modeling using non-linear analysis method

    Directory of Open Access Journals (Sweden)

    El-Khamsa Guechi

    2016-09-01

    Full Text Available Potato peel (PP was used as a biosorbent to remove malachite green (MG from aqueous solution under various operating conditions. The effect of the experimental parameters such as initial dye concentration, biosorbent dose, initial pH, stirring speed, temperature, ionic strength and biosorbent particle size was investigated through a number of batch sorption experiments. The sorption kinetic uptake for MG by PP at various initial dye concentrations was analyzed by non-linear method using pseudo-first, pseudo-second and pseudo-nth order models. It was found that the pseudo-nth order kinetic model was the best applicable model to describe the sorption kinetic data and the order n of sorption reaction was calculated in the range from 0.71 to 2.71. Three sorption isotherms namely the Langmuir, Freundlich and Redlich–Peterson isotherms in their non-linear forms were applied to the biosorption equilibrium data. Both the Langmuir and Redlich–Peterson models were found to fit the sorption isotherm data well, but the Redlich–Peterson model was better. Thermodynamic parameters show that the sorption process of MG is endothermic and more effective process at high temperatures. The results revealed that PP is very effective for the biosorption of MG from aqueous solutions.

  18. Thermodynamics of imidacloprid sorption in Croatian soils

    Science.gov (United States)

    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

  19. Study of sorption processes of strontium on the synthetic hydroxyapatite

    International Nuclear Information System (INIS)

    Rosskopfova, O.; Galambos, M.; Rajec, P.

    2011-01-01

    The sorption of strontium on synthetic hydroxyapatite was investigated using batch method and radiotracer technique. The hydroxyapatite samples were prepared by a wet precipitation process followed by calcination of calcium phosphate that precipitated from aqueous solution. Also, commercial hydroxyapatites were used. The sorption of strontium on hydroxyapatite depended on the method of preparation and it was pH independent ranging from 4 to 9 as a result of buffering properties of hydroxyapatite. The distribution coefficient K d was significantly decreased with increasing concentration of Sr 2+ and Ca 2+ ions in solution with concentration above 1 x 10 -3 mol dm -3 . The percentage strontium sorption for commercial and by wet method prepared hydroxyapatite was in the range of 83-96%, while calcined hydroxyapatite was ranging from 10 to 30%. The experimental data for sorption of strontium have been interpreted in the term of Langmuir isotherm. The sorption of Sr 2+ ions was performed by ion-exchange with Ca 2+ cations on the crystal surface of hydroxyapatite. Although calcined hydroxyapatite is successfully used as biomaterial for hard tissues repair, it is not used for the treatment of liquid wastes. (author)

  20. Sorption of Emerging Organic Wastewater Contaminants to Four Soils

    Directory of Open Access Journals (Sweden)

    Sarah Roberts

    2014-04-01

    Full Text Available Conventional onsite wastewater treatment system design relies on a septic tank and soil treatment unit (STU for treatment of wastewater and integration of the final effluent into the environment. Organic water contaminants (OWCs, chemicals found in pharmaceutical drugs, detergents, surfactants, and other personal care and cleaning products, have been observed in septic tank effluent and the environment. Sorption of OWC mass to soil is a key mechanism in the removal and retardation of many of these chemicals in effluent as it travels through an STU. The primary purpose of this study was to investigate the relationship between the fraction of organic carbon of soil and the equilibrium sorption partitioning coefficient of a selected group of relevant and diverse OWCs. A secondary goal is to evaluate current methods of modeling the sorption of selected OWCs in soil. Five point Freundlich isotherms were constructed from equilibrium sorption batch tests for target OWCs with four different soils. For soils with organic carbon fraction between 0.021 and 0.054, Kd values were calculated between 60 and 185 for 4-nonylphenol, 75 to 260 for triclosan, 115 to 270 for bisphenol-A, 3 to 255 for 17β-estradiol, 40 to 55 for 17α-ethynylestradiol, and 28 to 70 for estrone. An empirically derived, direct relationship between foc and Kd may be a useful approach to estimating sorption for a soil based on organic carbon content.

  1. Sorption and desorption kinetics of diuron, fluometuron, prometryn and pyrithiobac sodium in soils.

    Science.gov (United States)

    Baskaran, S; Kennedy, I R

    1999-11-01

    The sorption and desorption characteristics of four herbicides (diuron, fluometuron, prometryn and pyrithiobac-sodium) in three different cotton growing soils of Australia was investigated. Kinetics and equilibrium sorption and desorption isotherms were determined using the batch equilibrium technique. Sorption was rapid (> 80% in 2 h) and sorption equilibrium was achieved within a short period of time (ca 4 h) for all herbicides. Sorption isotherms of the four herbicides were described by Freundlich equation with an r2 value > 0.98. The herbicide sorption as measured by the distribution coefficient (Kd) values ranged from 3.24 to 5.71 L/kg for diuron, 0.44 to 1.13 L/kg for fluometuron, 1.78 to 6.04 L/kg for prometryn and 0.22 to 0.59 L/kg for pyrithiobac-sodium. Sorption of herbicides was higher in the Moree soil than in Narrabri and Wee Waa soils. When the Kd values were normalised to organic carbon content of the soils (Koc), it suggested that the affinity of the herbicides to the organic carbon increased in the order: pyrithiobac-sodium diuron. The desorption isotherms were also adequately described by the Freundlich equation. For desorption, all herbicides exhibited hysteresis and the hysteresis was stronger for highly sorbed herbicides (diuron and prometryn) than the weakly sorbed herbicides (fluometuron and pyrithiobac-sodium). Hysteresis was also quantified as the percentage of sorbed herbicides which is not released during the desorption step (omega = [nad/nde - 1] x 100). Soil type and initial concentration had significant effect on omega. The effect of sorption and desorption properties of these four herbicides on the off-site transport to contaminate surface and groundwater are also discussed in this paper.

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

    International Nuclear Information System (INIS)

    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+ /NH 4 + sorption and physicochemical properties of biochars produced from different wetland plants. Biochars from six species of wetland plants (i.e., Canna indica, Pennisetum purpureum Schum, Thalia dealbata, Zizania caduciflora, Phragmites australis and Vetiveria zizanioides) were obtained at 500 °C and characterized, and their sorption for ammonium and cadmium was determined. There were significant differences in elemental composition, functional groups and specific surface area among the biochars derived from different wetland plant species. Sorption of ammonium and cadmium on the biochars could be described by a pseudo second order kinetic model, and the simple Langmuir model fits the isotherm data better than the Freundlich or Temkin model. The C. indica derived biochar had the largest sorption capacity for NH 4 + and Cd 2+ , with a maximum sorption of 13.35 and 125.8 mg g −1 , respectively. P. purpureum Schum derived biochar had a similar maximum sorption (119.3 mg g −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. - Highlights: • Biochars varied in physicochemical properties and adsorption capacity. • Canna indica derived biochar has a high sorption capacity for Cd 2+ . • NH 4 + and Cd 2+ sorption on biochars fits a pseudo second order and Langmuir model. • Sorption mechanism is related to complexation, cation exchange and precipitation.

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

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Xiaoqiang [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); Hao, Hulin [Ningbo Raw Water Resource Research Academy, Ningbo (China); Zhang, Changkuan [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China); He, Zhenli [Indian River Research and Education Center, Institute of Food and Agricultural Sciences, University of Florida, Fort Pierce, FL 34945 (United States); Yang, Xiaoe, E-mail: xyang571@yahoo.com [Ministry of Education Key Laboratory of Environmental Remediation and Ecological Health, College of Environmental and Resource Sciences, Zhejiang University, Hangzhou 310058 (China)

    2016-01-01

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

  4. Effects of nitrate, fulvate, phosphate, phthalate, salicylate and catechol on the sorption of uranyl onto SiO2. A comparative study

    International Nuclear Information System (INIS)

    Zhang Hongxia; Wen Chuanxi; Tao Zuyi; Wu Wangsuo

    2011-01-01

    We have performed a large number of batch sorption experiments of uranyl onto SiO 2 and examined the effects of nitrate or ionic strength, phosphate, fulvic acid(FA), phthalic acid (PH), salicylic acid (SA), and catechol (CA) on the uranyl sorption onto SiO 2 . Three sorption edges and three sorption isotherms at ionic strengths 0.05, 0.1, and 0.5 mol/L KNO 3 were used to investigate the effect of ionic strength or nitrate on the sorption and the Langmuir, Freundlich, and Dubinin-Radushkevich models are used to simulate the sorption isotherms, respectively. Five sorption edges in the presence of phosphate, FA, PH, SA, and CA were compared with that in the absence of complexing ligand. The results suggest that the effect of complexation of uranyl with nitrate on the uranyl sorption can be negligible and the sorption can be described Freundlich and D-R model very well. The positive effect of phosphate on the uranyl sorption was found, though the extent of effect was decreased with increasing pH. The positive effect and the negative effect of FA on the uranyl sorption were found at low pH and high pH ranges, respectively. The sorption edge of uranyl sorption remained unaffected in the presence of PH in the pH 2-10. In the presence of SA, the no effect and the negative effect on the uranyl sorption were, respectively, found at low pH and high pH ranges. The negative effect of CA on the uranyl sorption was found in the pH 2-10. (author)

  5. EVALUTION OF MONOLAYER MOISTURE CAPACITY AND THE ENERGY CONSTANT OF SOME POEDERED SPICES BY USING BET AND GAB MODELS

    Directory of Open Access Journals (Sweden)

    E.Nurlela2

    2004-08-01

    Full Text Available BET equation (IUPAC standard and GAB equation (European Project Group on physical properties of food recommendation standard for monolayer capacity value evaluations were used for testing the moisture adsorption experimental data of powdered white and black papper, cloves, nutmeg and cinnamon. The BET equation fits only up to aw = 0.44, while the GAB isotherm fits and covers a much wider range (0.06sorption isotherm curve on the regression range as well as its typical upswing that began at water activity value equals to 0.6. It was also found that the values for water content adsorbed in the monolayer, expressed as the mass of water adsorbed on 100 gram dry-matter of sample, obtained by the GAB equation were higher than those obtained by the BET model but the energy constant value of BET that were higher than the GAB vakue was observed only for black pepper sample.

  6. Saturated salt method determination of hysteresis of Pinus sylvestris L. wood for 35 ºC isotherms

    Directory of Open Access Journals (Sweden)

    García Esteban, L.

    2004-12-01

    Full Text Available The saturated salts method was used in this study to quantify hysteresis in Pinus sylvestris L. wood, in an exercise that involved plotting the 35 ºC desorption and sorption isotherms. Nine salts were used, all of which establish stable and known relative humidity values when saturated in water The wood was kept at the relative humidity generated by each of these salts until the equilibrium moisture content (EMC was reached, both in the water loss or desorption, and the water uptake or sorption processes. The Guggenheim method was used to fit the values obtained to the respective curves. Hysteresis was evaluated in terms of the hysteresis coefficient, for which a mean value of 0.87 was found.

    Con este trabajo se ha cuantificado la histéresis de la madera de Pinus sylvestris L. Para ello, se han construido las isotermas de 35 ºC de adsorción y sorción, mediante el método de las sales saturadas. Se han utilizado nueve sales que cuando se saturan en agua dan lugar a unas humedades relativas estables y conocidas. La madera fue colocada bajo las distintas humedades relativas que confieren cada una de las sales hasta que alcanzaron las distintas humedades de equilibrio higroscópico, tanto en el proceso de pérdida de agua o desorción, como en el de adquisición de agua o de sorción. Los valores obtenidos fueron ajustados a las respectivas sigmoides, haciendo uso del método de Guggenheim. La valoración de la histéresis se determinó mediante el coeficiente de histéresis, obteniendo un valor medio de 0,87.

  7. Influence of the temperature in the uranium (Vi) sorption in zirconium diphosphate; Influencia de la temperatura en la sorcion de uranio (VI) en difosfato de circonio

    Energy Technology Data Exchange (ETDEWEB)

    Garcia G, N.; Solis, D. [Universidad Autonoma del Estado de Mexico, Facultad de Quimica, Paseo Colon y Paseo Tollocan, 50120 Toluca, Estado de Mexico (Mexico); Ordonez R, E., E-mail: nidgg@yahoo.com.mx [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2012-10-15

    In the present work was evaluated the uranium (Vi) sorption at 10, 20, 30, 40 and 60 C on the zirconium diphosphate (ZrP{sub 2}O{sub 7}). They were carried out kinetic and isotherms using the method by lots, these will allow to fix the sorption time (kinetic) and to explain the behavior of this sorption in different ph conditions and temperature (isotherm). The quantity of retained uranium in the surface was quantified by means of the fluorescence technique. (Author)

  8. Characterization of phosphorus sorption on the sediments of Yangtze River Estuary and its adjacent areas

    International Nuclear Information System (INIS)

    Cao, Xiaoyan; Liu, Xiaoyue; Zhu, Jiamei; Wang, Lisha; Liu, Sumei; Yang, Guipeng

    2017-01-01

    This paper studied the kinetics, isotherm and thermodynamics of phosphorus sorption onto the sediments of the Yangtze River estuary and its adjacent waters, as well as the sediments' compositions and physicochemical properties. The process could be described well by a two-compartment first order equation. The sorbed phosphorus mainly consisted of Ex-P and Fe-P, with Ex-P being the dominant. The equilibrium isotherms could be fitted well with a modified Langmuir equation. The calculations of the thermodynamic parameters indicated that the process was spontaneous and exothermic. The CEC and the fractions of clay, calcite and organic matter were correlated with the sorption parameters, while the surface proton charge of the sediments was significantly negatively correlated with them. Considering the kinetics and phosphorus forms changes during the process, the sorption in our study could be considered that the physical process plays an important role. - Highlights: • The kinetic curves and phosphorus fractions changes during sorption were studied. • The sorbed phosphorus mainly consisted of Ex − P and Fe-P, with Ex − P being dominant. • The equilibrium isotherms and thermodynamic parameters were investigated. • Sediment composition and surface characteristics influenced phosphorus sorption parameters.

  9. Equilibrium and kinetic studies for the sorption of 3-methoxybenzaldehyde on activated kaolinites

    Energy Technology Data Exchange (ETDEWEB)

    Koyuncu, Huelya [Forensic Medicine Foundation, Nasuhpasa Bath Street, No. 12, 16010 Heykel, Bursa (Turkey)]. E-mail: hkoyuncu@yyu.edu.tr; Kul, Ali Riza [Yuzuncu Yil University, Faculty of Art and Science, Department of Chemistry, 65080 Van (Turkey)]. E-mail: alirizakul@yyu.edu.tr; Yildiz, Nuray [Ankara University, Faculty of Engineering, Department of Chemical Engineering, 06100 Tandogan, Ankara (Turkey)]. E-mail: nyildiz@eng.ankara.edu.tr; Calimli, Ayla [Ankara University, Faculty of Engineering, Department of Chemical Engineering, 06100 Tandogan, Ankara (Turkey)]. E-mail: calimli@eng.ankara.edu.tr; Ceylan, Hasan [Yuzuncu Yil University, Faculty of Art and Science, Department of Chemistry, 65080 Van (Turkey)]. E-mail: hceylan@yyu.edu.tr

    2007-03-06

    The sorption of 3-methoxybenzaldehyde on activated kaolinites has been investigated at different temperatures. Two types of activation tests were performed. The sorption equilibrium was studied by sorption isotherms in the temperature range 303-333 K for natural (untreated), thermally and acid activated kaolinites. It was shown that the isotherm shapes were not affected by temperature and activation types of kaolinite. The absorbance data at 312 nm were fitted reasonably well with the Langmuir and Freundlich isotherm models and the model parameters were determined for different temperatures. Thermodynamic quantities such as Gibbs free energy ({delta}G), the enthalpy ({delta}H) and the entropy change of sorption ({delta}S) were determined for natural, thermally and acid activated kaolinites. It was shown that the sorption processes were an endothermic reactions, controlled by physical mechanisms and spontaneously. Adsorption capacity of acid activated kaolinite for 3-methoxybenzaldehyde was higher compared to that of natural and thermally activated kaolinites at various temperatures. The adsorption and desorption rate constants (k {sub a} and k {sub d}) were obtained separately by applying a geometric approach to the first order Langmuir model. This method provided good conformity between the K from Langmuir parameters and K {sub geo} (k {sub a}/k {sub d}) from geometric approach.

  10. Equilibrium and kinetic studies for the sorption of 3-methoxybenzaldehyde on activated kaolinites

    International Nuclear Information System (INIS)

    Koyuncu, Huelya; Kul, Ali Riza; Yildiz, Nuray; Calimli, Ayla; Ceylan, Hasan

    2007-01-01

    The sorption of 3-methoxybenzaldehyde on activated kaolinites has been investigated at different temperatures. Two types of activation tests were performed. The sorption equilibrium was studied by sorption isotherms in the temperature range 303-333 K for natural (untreated), thermally and acid activated kaolinites. It was shown that the isotherm shapes were not affected by temperature and activation types of kaolinite. The absorbance data at 312 nm were fitted reasonably well with the Langmuir and Freundlich isotherm models and the model parameters were determined for different temperatures. Thermodynamic quantities such as Gibbs free energy (ΔG), the enthalpy (ΔH) and the entropy change of sorption (ΔS) were determined for natural, thermally and acid activated kaolinites. It was shown that the sorption processes were an endothermic reactions, controlled by physical mechanisms and spontaneously. Adsorption capacity of acid activated kaolinite for 3-methoxybenzaldehyde was higher compared to that of natural and thermally activated kaolinites at various temperatures. The adsorption and desorption rate constants (k a and k d ) were obtained separately by applying a geometric approach to the first order Langmuir model. This method provided good conformity between the K from Langmuir parameters and K geo (k a /k d ) from geometric approach

  11. Computational Studies of CO 2 Sorption and Separation in an Ultramicroporous Metal–Organic Material

    KAUST Repository

    Forrest, Katherine A.; Pham, Tony; Hogan, Adam; McLaughlin, Keith; Tudor, Brant; Nugent, Patrick; Burd, Stephen D.; Mullen, Ashley; Cioce, Christian R.; Wojtas, Lukasz; Zaworotko, Michael J.; Space, Brian

    2013-01-01

    . This MOM was recently shown to have an unprecedented selectivity for CO2 over N2, CH4, and H 2 under industrially relevant conditions. The simulated CO 2 sorption isotherms and calculated isosteric heat of adsorption, Qst, values were in excellent agreement

  12. A Universal Isotherm Model to Capture Adsorption Uptake and Energy Distribution of Porous Heterogeneous Surface

    KAUST Repository

    Ng, Kim Choon; Burhan, Muhammad; Shahzad, Muhammad Wakil; Ismail, Azahar Bin

    2017-01-01

    The adsorbate-adsorbent thermodynamics are complex as it is influenced by the pore size distributions, surface heterogeneity and site energy distribution, as well as the adsorbate properties. Together, these parameters defined the adsorbate uptake forming the state diagrams, known as the adsorption isotherms, when the sorption site energy on the pore surfaces are favorable. The available adsorption models for describing the vapor uptake or isotherms, hitherto, are individually defined to correlate to a certain type of isotherm patterns. There is yet a universal approach in developing these isotherm models. In this paper, we demonstrate that the characteristics of all sorption isotherm types can be succinctly unified by a revised Langmuir model when merged with the concepts of Homotattic Patch Approximation (HPA) and the availability of multiple sets of site energy accompanied by their respective fractional probability factors. The total uptake (q/q*) at assorted pressure ratios (P/P s ) are inextricably traced to the manner the site energies are spread, either naturally or engineered by scientists, over and across the heterogeneous surfaces. An insight to the porous heterogeneous surface characteristics, in terms of adsorption site availability has been presented, describing the unique behavior of each isotherm type.

  13. A Universal Isotherm Model to Capture Adsorption Uptake and Energy Distribution of Porous Heterogeneous Surface

    KAUST Repository

    Ng, Kim Choon

    2017-08-31

    The adsorbate-adsorbent thermodynamics are complex as it is influenced by the pore size distributions, surface heterogeneity and site energy distribution, as well as the adsorbate properties. Together, these parameters defined the adsorbate uptake forming the state diagrams, known as the adsorption isotherms, when the sorption site energy on the pore surfaces are favorable. The available adsorption models for describing the vapor uptake or isotherms, hitherto, are individually defined to correlate to a certain type of isotherm patterns. There is yet a universal approach in developing these isotherm models. In this paper, we demonstrate that the characteristics of all sorption isotherm types can be succinctly unified by a revised Langmuir model when merged with the concepts of Homotattic Patch Approximation (HPA) and the availability of multiple sets of site energy accompanied by their respective fractional probability factors. The total uptake (q/q*) at assorted pressure ratios (P/P s ) are inextricably traced to the manner the site energies are spread, either naturally or engineered by scientists, over and across the heterogeneous surfaces. An insight to the porous heterogeneous surface characteristics, in terms of adsorption site availability has been presented, describing the unique behavior of each isotherm type.

  14. THE SORPTION OF OFLOXACIN BY HYDRATED ALUMINA AND SILICON

    Directory of Open Access Journals (Sweden)

    A. N. Chebotarev

    2016-11-01

    Full Text Available The sorption of ofloxacin (OFL – the antibiotic from class of fluoroquinolones has been studied on alumina (γ-Al2O3 different acid-base modifications – acidic Al2O3(acidic, neutral Al2O3 (Neutral and the basic Al2O3 (core and amorphous silica – silica gel (SG L 5/40 and aerosil A-300. Determination of ofloxacin in solutions has been carried out by spectrophotometry on spectrophotometer SF-46 at λ = 291 nm and acidity 7. To clarify the nature of the sorption surfaces of OFL hydrated on aluminum and silicon oxides were studied according to the degree of extraction (S% from pH, contact time of the phases (min. sample from the sorbent mass (g; sorption isotherms were built and antibiotic desorption was studied. The OFL significant recovery (~ 60% is observed at the pH range of 4 ÷ 8, and reaches its maximum (80-85% at pH 7. The maximum degree of extraction of the antibiotic on aerosil A-300 and L 5/40 silica realized at pH 6 and it was ~ 80%. Comparative analysis of the forms constructed isotherms (L – type indicates a significant affinity investigated hydrated oxides to sorbate. The value of the static exchange capacity and concentration ratios can proof that. Differences in the quantitative characteristics of sorption of aluminum and silicon oxides are associated with nature and the acid-base properties of adsorption sites. In the study of the OFL concentrates desorption in static mode dilute NaOH and HNO3 solutions it was found that growth desorption degree occured with increasing concentration. Desorption was 2-3 times better in the case of aluminum oxide than silicon oxide when there were the same concentrations of acid and alkali. This is another confirmation of the participation in various sorption interactions forces of physical and chemical nature.

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

    Directory of Open Access Journals (Sweden)

    Bambang Rusdiarso

    2016-12-01

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

  16. The sorption behavior of DDT onto sediment in the presence of surfactant cetyltrimethylammonium bromide

    International Nuclear Information System (INIS)

    Cao Xiaoyan; Han Huayu; Yang Guipeng; Gong Xiaofei; Jing Jianning

    2011-01-01

    Highlights: → The sorption behavior of a complex system consists of DDT and CTAB onto marine sediment was studied. → Batch experiments were carried out to investigate the kinetics and thermodynamics. → The presence of CTAB could remarkably accelerate and enhance the sorption of DDT. → The sorption of DDT had relatively more negative ΔG 0 and ΔH 0 in the presence of CTAB. - Abstract: The sorption behavior of p,p'- and o,p'-dichlorodiphenyltrichloroethane (DDT) in the presence of a cationic surfactant cetyltrimethylammonium bromide (CTAB) on sediment was studied. Batch experiments were carried out to investigate the kinetics and thermodynamics of the process. The kinetic behavior of these three chemicals on sediment was described by pseudo-second-order kinetic equations, and the isotherms followed the Freundlich model well. The presence of CTAB was able to remarkably accelerate and enhance the sorption of DDT, whereas DDT showed no effect on the sorption of CTAB in our considered concentration ranges. The thermodynamic parameters, such as standard enthalpy change (ΔH 0 ), standard entropy change (ΔS 0 ) and standard Gibbs free energy change (ΔG 0 ) showed that the sorption process of p,p'- and o,p'-DDT was physical, spontaneous and exothermic, and the randomness at the solid-liquid interface increased during the process. In the presence of CTAB, the sorption of DDT showed significantly negative ΔG 0 and ΔH 0 values.

  17. Sorption of benzothiazoles onto sandy aquifer material under equilibrium and nonequlibrium conditions

    Directory of Open Access Journals (Sweden)

    Kragulj Marijana M.

    2014-01-01

    Full Text Available In this study, the sorption behaviour of 1,3-benzothiazole (BT and 2-(methylthiobenzothiazole (MTBT was investigated on Danube geosorbent under equilibrium and nonequilibrium conditions. All sorption isotherms fitted well with the Freundlich model (R2=0.932-0.993. The results showed that organic matter of the Danube geosorbent has a higher sorption affinity for the more hydrophobic MTBT compared to BT. However, sorption-desorption experiments showed that MTBT was more easily desorbed than BT molecules, which indicates the importance of absorption relative to adsorption in the overall sorption mechanism of MTBT. In general, molecules of BT and MTBT were more easily desorbed in the lower concentration range, which resulted in an increase in the hysteresis indices with increasing concentrations. Column experiments revealed that retention of the investigated compounds on the aquifer material followed the compound’s hydrophobicity. BT showed a lower retention, in accordance with its lower sorption affinity obtained in the static experiments, while MTBT showed a greater sorption affinity, and thus had a longer retention time on the column. Thus during transport BT represent greater risk for groundwaters than MTBT. These results have increased our understanding of benzothiazoles sorption and desorption process which represent one of the most important factors which influence the behaviour of organic compounds in the environment.

  18. β-Zeolite modified by ethylenediamine for sorption of Th(IV)

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Peng; Wu, Hanyu; Yuan, Ni; Yin, Zhuoxin; Pan, Duoqiang; Wu, Wangsuo [Lanzhou Univ. (China). Radiochemistry Lab.; Ministry of Education, Lanzhou (China). Key Lab. of Special Function Materials and Structure Design

    2017-08-01

    β-Zeolite-EDA was modified with ethylenediamine (EDA) after synthesized. The synthesized material was characterized and used for removal of Th(IV) from aqueous solutions. The influences of pH, ionic strength, contact time, temperature and humic acid (HA) on Th(IV) sorption onto synthesized β-zeolite-EDA was studied by batch technique. The dynamic process showed that the sorption of Th(IV) onto β-zeolite-EDA matched the pseudo-second-order kinetics model. The sorption of Th(IV) on β-zeolite-EDA was significantly dependent on pH values, the sorption percentage increased markedly at pH 3.5-4.5, and then maintained a steady state as pH values increased. Through simulating the sorption isotherms by Langmuir, Freundlich and Dubini-Radushkevich (D-R) models, it could be seen respectively that the sorption pattern of Th(IV) on β-zeolite-EDA was mainly controlled by surface complexation, and that the sorption processes was endothermic and spontaneous. The presence of HA increased Th(IV) sorption on β-zeolite-EDA.

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

    Science.gov (United States)

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

    2017-12-01

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

  20. A new Model Applicable for Finite Element Simulations of Moisture Transport in Wood

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Svensson, Staffan; Damkilde, Lars

    2006-01-01

    The moisture content in wood near the surface depends not only on the current relative humidity in the ambient air but also on preceeding variations. This hysteresis phenomenon of sorption implies in worst case that the moisture content for a given relative humidity may deviate 30-35%. Current...

  1. Effects of processing method and moisture history on laboratory fungal resistance of wood-HDPE composites.

    Science.gov (United States)

    Craig M. Clemons; Rebecca E. Ibach

    2004-01-01

    The purpose of this study was to clarify the effects of composite processing and moisture sorption on laboratory fungal resistance of wood-plastic composites. A 2-week water soaking or cyclic boiling-drying procedure was used to infuse moisture into composites made from high-density polyethylene filled with 50 percent wood flour and processed by extrusion, compression...

  2. Hemp yarn reinforced composites – III. Moisture content and dimensional changes

    DEFF Research Database (Denmark)

    Madsen, Bo; Hoffmeyer, Preben; Lilholt, Hans

    2012-01-01

    Based on a comprehensive set of experimental data it is demonstrated that the moisture properties of aligned hemp fibre yarn/thermoplastic matrix composites are showing low moisture sorption capacity and low dimensional changes. Using a reference humidity of 65% RH, and a common span of ambient...

  3. Unfired clay bricks – moisture properties and compressive strength

    DEFF Research Database (Denmark)

    Hansen, E.J. de Place; Hansen, Kurt Kielsgaard

    2002-01-01

    Apparatus, methods and test results from an experimental investigation of (1) the properties for moisture performance of the materials, including water vapour sorption and water vapour transmission, (2) humidity buffering of the indoor climate by an absorbent material, and (3) the compressive...... strength are presented....

  4. Sorption and desorption of glyphosate in Mollisols and Ultisols soils of Argentina.

    Science.gov (United States)

    Gómez Ortiz, Ana Maria; Okada, Elena; Bedmar, Francisco; Costa, José Luis

    2017-10-01

    In Argentina, glyphosate use has increased exponentially in recent years as a result of the widespread adoption of no-till management combined with genetically modified glyphosate-resistant crops. This massive use of glyphosate has created concern about its potential environmental impact. Sorption-desorption of glyphosate was studied in 3 Argentinean soils with contrasting characteristics. Glyphosate sorption isotherms were modeled using the Freundlich equation to estimate the sorption coefficient (K f ). Glyphosate sorption was high, and the K f varied from 115.6 to 1612 mg 1-1/n L 1/n /kg. Cerro Azul soil had the highest glyphosate sorption capacity as a result of a combination of factors such as higher clay content, cation exchange capacity, total iron, and aluminum oxides, and lower available phosphorus and pH. Desorption isotherms were also modeled using the Freundlich equation. In general, desorption was very low (glyphosate strongly sorbs to the soils and that it is almost an irreversible process. Anguil soil had a significantly higher desorption coefficient (K fd ) than the other soils, associated with its lower clay content and higher pH and phosphorus. Glyphosate high sorption and low desorption to the studied soils may prevent groundwater contamination. However, it may also affect its bioavailability, increasing its persistence and favoring its accumulation in the environment. The results of the present study contribute to the knowledge and characterization of glyphosate retention in different soils. Environ Toxicol Chem 2017;36:2587-2592. © 2017 SETAC. © 2017 SETAC.

  5. Sorption of cobalt in zeolites and natural clays of the clinoptilolite and kaolinite type

    International Nuclear Information System (INIS)

    Davila R, J.I.; Solache R, M.

    2006-01-01

    In this work the sorption of cobalt of aqueous solutions in two natural zeolites (clinoptilolite) and a clay (kaolinite) of origin in the center-north region of Mexico is evaluated. The effect of the pH and the time of contact in the process of sorption were evaluated. The cobalt retained in the aluminosilicates was determined by neutron activation analysis. The cobalt sorption in the materials in a range of pH from 4 to 7 does not present significant variations. The studies of reaction kinetics show a very fast sorption in the first 5 hours of contact, reaching the equilibrium in approximately 24 hours. The kinetics of sorption of the cobalt ions was represented better by the Ritchie reaction model modified of second order. The experimental data for the zeolites obtained at ambient temperature and varying the concentration were adjusted to the models of Freundlich, Langmuir and Freundlich-Langmuir isotherms and it was observed that the cobalt sorption it behaves according to the Freundlich isotherm model. (Author)

  6. Microplastics play a minor role in tetracycline sorption in the presence of dissolved organic matter.

    Science.gov (United States)

    Xu, Baile; Liu, Fei; Brookes, Philip C; Xu, Jianming

    2018-05-02

    Microplastics have a great potential to sorb organic pollutants from the adjacent environment. In this study, the sorption of tetracycline, a polar and ionizable antibiotic, on three types of microplastics (polyethylene (PE), polypropylene (PP) and polystyrene (PS)) were investigated in batch sorption experiments. The sorption isotherms were well fitted by the Langmuir model, indicating that not only hydrophobic interactions but also other interactions (e.g. electrostatic interactions) played important roles in the sorption process. PS had the maximum sorption capacity, following the order PS > PP > PE, which can be attributed to polar interactions and π-π interactions. The sorption of tetracycline on microplastics was significantly influenced by pH, with sorption capacity increasing gradually, peaking at pH 6.0 and then decreasing, likely due to the influence of tetracycline speciation with the change of pH. Fulvic acid was selected as representative dissolved organic matter (DOM) to examine the effect on sorption. The increasing concentration of fulvic acid inhibited the sorption of tetracycline on three microplastics, decreasing them by more than 90% at the fulvic acid concentration of 20 mg/L, which implied a greater affinity of tetracycline to fulvic acid than to microplastics. Increasing salinity from 0.05 to 3.5% had negligible effects on the sorption of tetracycline on the three microplastics. Our results highlight the importance of pH and DOM on the sorption of tetracycline on microplastics, and suggest the relatively minor role of microplastics in the fate and transport of tetracycline in the aquatic environment in the presence of DOM. Copyright © 2018 Elsevier Ltd. All rights reserved.

  7. Gas Sorption, Diffusion, and Permeation in Nafion

    KAUST Repository

    Mukaddam, Mohsin Ahmed

    2015-12-22

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

  8. Detailed sorption characteristics of the anti-diabetic drug metformin and its transformation product guanylurea in agricultural soils.

    Science.gov (United States)

    Briones, Rowena M; Sarmah, Ajit K

    2018-07-15

    Detection of metformin, an antidiabetic drug and its transformation product guanylurea in various environmental matrices such as surface water and groundwater, coupled with their effects on aquatic organisms warrant an understanding of the compounds fate and behaviour in the environment. Batch studies were conducted with the aim of evaluating the sorption of these two emerging contaminants in six New Zealand agricultural soils of contrasting physico-chemical properties. Kinetic studies revealed that metformin and guanylurea sorption in Te Kowhai soil was very rapid initially achieving 90% sorption within the first 4 and 13h, respectively. Fit of several isotherm models to the measured batch sorption data showed that the hybrid models Langmuir-Freundlich and Redlich-Peterson best described the isotherms. Freundlich isotherm showed higher linearity for guanylurea (n F =0.58-0.93) in all soils compared to metformin (n F =0.25-0.71). A linear isotherm was fitted at environmentally relevant low concentrations (< 3mg/L) of target compounds and calculated values of sorption distribution coefficient (K d ) were in the range of 8.97 to 53.49L/kg for metformin and between 10.6 and 37.51L/kg for guanylurea. Sorption of both metformin and guanylurea was dependent on the soil characteristics, however, no generalisation could be made as to which had higher affinity to soils studied. Pearson's correlation and multiple regression analyses indicate that Si/Al (p=0.042) and clay (p=0.015) significantly influenced metformin K d values, whereas the soil's cation exchange capacity (p=0.024) is the single most significant factor determining guanylurea sorption in soils. It is likely that the type of minerals present in soils and its ion-exchange capacity could play an important role in metformin and guanylurea sorption, respectively. Copyright © 2018. Published by Elsevier B.V.

  9. SORPTION OF Ga (III ON FLEXIBLE OPEN CELL POLYURETHANE FOAM OF POLYETHER TYPE IMPREGNATED WITH TRI-N-BUTHYL PHOSPATE

    Directory of Open Access Journals (Sweden)

    Lavinia Tofan

    2007-06-01

    Full Text Available The obtained results concerning the Ga (III ion retention on flexible open cell polyurethane foam of polyether type pretreated with tri-n-butyl phosphate are presented. The influence of solution acidity, phases contact time, Ga (III concentration and solution temperature have been investigated. The parameters of Ga (III batch sorption have been optimized. On the basis of Langmuir isotherms, the sorption constants and the thermodynamic parameters, ∆G, ∆Η and ∆S have been calculated.

  10. Internal and external moisture transport resistance during non-stationary adsorption of moisture into wood

    OpenAIRE

    Bučar, Bojan

    2007-01-01

    The assumption that non-stationary sorption processes associated with wood canbe evaluated by analysis of their transient system response to the disturbance developed is undoubtedly correct. In general it is, in fact, possible to obtain by time analysis of the transient phenomenon - involving the transition into an arbitrary new state of equilibrium - all data required for a credible evaluation of the observed system. Evaluation of moisture movement during drying or moistening requires determ...

  11. Technetium Sorption Media Review

    International Nuclear Information System (INIS)

    Duncan, J.B.; Kelly, S.E.; Robbins, R.A.; Adams, R.D.; Thorson, M.A.; Haass, C.C.

    2011-01-01

    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.

  12. TECHNETIUM SORPTION MEDIA REVIEW

    Energy Technology Data Exchange (ETDEWEB)

    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.

  13. Investigation of sorption of Hg(II) ions onto coconut husk from aqueous solution using radiotracer technique

    Energy Technology Data Exchange (ETDEWEB)

    Hasany, S.M.; Ahmad, R.; Chaudhary, M.H. [Nuclear Chemistry Div., Pakistan Inst. of Nuclear Science and Technology, Islamabad (Pakistan)

    2003-07-01

    The sorption of Hg(II) ions onto coconut (Cocos nucifera) husk has been studied using radiotracer technique. Maximum sorption (96%) of Hg(II) ions (7.39 x 10{sup -6} M) onto sorbent surface is achieved from 10{sup -3} M HNO{sub 3} solution in 30 min agitation time using 100 mg of coconut husk. The sorption data follow the Freundlich and Dubinin-Radushkevich (D-R) isotherms. Sorption capacity (6.84{+-}0.45 mmol g{sup -1}) and sorption energy (10.6{+-}0.13 kJ mol{sup -1}) have been evaluated using these isotherms. Among the ions tested to monitor their influence on the sorption, Ba(II), fluoride and tartarate increased the sorption, while thiosulfate, bromide and thiocyanate reduced (< 63 > 26%) the sorption. The cations K(I), Ce(III), Cr(III), Fe(III) and Zr(IV) partially suppressed the sorption. The variation of sorption with temperature yields thermodynamic parameters {delta}H = -37.4{+-}2 kJ mol{sup -1} {delta}S = -105{+-}7 J mol{sup -1} K{sup -1} and {delta}G = -2.58{+-}0.05 kJ mol{sup -1} at 298 K. The negative values of enthalpy and free energy reflect the spontaneous and exothermic nature of sorption, respectively. The selectivity studies of sorbent show that the coconut husk column can be used to separate Hg(II) ions from Se(IV), Zn(II), I(I) and Tc (VII). The sorbent has a potential in radiochemistry to separate gamma energies of {sup 203}Hg (279 keV) from {sup 75}Se (265 and 280 keV). (orig.)

  14. Influence of organic matter type and medium composition on the sorption affinity of C12-benzalkonium cation

    International Nuclear Information System (INIS)

    Chen, Yi; Hermens, Joop L.M.; Droge, Steven T.J.

    2013-01-01

    We used the 7-μm polyacrylate ion-exchange SPME fibers to investigate C12-benzalkonium sorption to 10 mg/L natural organic matter at concentrations well below the cation-exchange capacity. C12-BAC sorption at constant medium conditions differed within 0.4 log units for two humic acids (Aldrich, Leonardite) and peat (Sphagnum, Pahokee), with similar nonlinear sorption isotherms (K F ∼ 0.8). Sorption to the SPME fibers and Aldrich humic acid (AHA) was reduced at both low pH and high electrolyte concentration, and reduced more strongly by Ca 2+ compared with Na + at similar concentrations. Sorption isotherms for AHA (5–50–500 mM Na + , pH 6) was modeled successfully by the NICA-Donnan approach, resulting in an intrinsic sorption coefficient of 5.35 (C aq = 1 nM). The NICA-Donnan model further explained the stronger specific binding of Ca 2+ compared to Na + by differences in Boltzmann factors. This study provides relevant information to interpret bioavailability of quaternary ammonium compounds, and possibly for other organic cations. -- Highlights: •The ion-exchange SPME was used to investigate C12-benzalkonium sorption behavior. •Sorption to different organic matter differed within 0.4 log units (5 mM Ca 2+ , pH6). •Sorption to AHA was reduced at both low pH and high electrolyte concentration. •The NICA-Donnan approach lead to an intrinsic log D OC,IE of 5.35 (C aq = 1 nM). •The Boltzmann factors in NICA-Donnan model explained the specific binding of Ca 2+ . -- C12-BAC sorption to the four organic matter samples were investigated by the ion-exchange SPME and the NICA-Donnan model explained the different sorption affinities caused by Na + and Ca 2+

  15. Investigation of sorption of Hg(II) ions onto coconut husk from aqueous solution using radiotracer technique

    International Nuclear Information System (INIS)

    Hasany, S.M.; Ahmad, R.; Chaudhary, M.H.

    2003-01-01

    The sorption of Hg(II) ions onto coconut (Cocos nucifera) husk has been studied using radiotracer technique. Maximum sorption (96%) of Hg(II) ions (7.39 x 10 -6 M) onto sorbent surface is achieved from 10 -3 M HNO 3 solution in 30 min agitation time using 100 mg of coconut husk. The sorption data follow the Freundlich and Dubinin-Radushkevich (D-R) isotherms. Sorption capacity (6.84±0.45 mmol g -1 ) and sorption energy (10.6±0.13 kJ mol -1 ) have been evaluated using these isotherms. Among the ions tested to monitor their influence on the sorption, Ba(II), fluoride and tartarate increased the sorption, while thiosulfate, bromide and thiocyanate reduced ( 26%) the sorption. The cations K(I), Ce(III), Cr(III), Fe(III) and Zr(IV) partially suppressed the sorption. The variation of sorption with temperature yields thermodynamic parameters ΔH = -37.4±2 kJ mol -1 ΔS = -105±7 J mol -1 K -1 and ΔG = -2.58±0.05 kJ mol -1 at 298 K. The negative values of enthalpy and free energy reflect the spontaneous and exothermic nature of sorption, respectively. The selectivity studies of sorbent show that the coconut husk column can be used to separate Hg(II) ions from Se(IV), Zn(II), I(I) and Tc (VII). The sorbent has a potential in radiochemistry to separate gamma energies of 203 Hg (279 keV) from 75 Se (265 and 280 keV). (orig.)

  16. Understanding the sorption behavior of Pu{sup 4+} on poly(amidoamine) dendrimer functionalized carbon nanotube. Sorption equilibrium, mechanism, kinetics, radiolytic stability, and back-extraction studies

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Parveen [Indian Institute of Technology, Himachal Pradesh (India); Sengupta, Arijit [Bahbha Atomic Research Centre, Mumbai (India). Radiochemistry Div.; Deb, Ashish Kumar Singha; Ali, S. Musharaf [Bahbha Atomic Research Centre, Mumbai (India). Chemical Engineering Div.; Homi Bhabha National Institute, Mumbai (India); Dasgupta, Kinshuk [Bhabha National Institute, Mumbai (India). Mechanical Metallurgy Div.

    2017-07-01

    Poly(amidoamine) dendrimer functionalized carbon nanotube was demonstrated as highly efficient sorbent of the Pu{sup 4+} from radioactive waste solution. The second generation dendrimer was found to have more efficiency as compared to the 1{sup st} generation might be due to the availability of more functionality for coordinating to the Pu{sup 4+} ion. Analysis of different isotherm models revealed that, Langmuir isotherm was predominantly operating through chemi-sorption (with the sorption energy 10.07 and 16.95 kJ mol{sup -1} for 1{sup st} and 2{sup nd} generation dendrimer) with the sorption capacity 89.22 mg g{sup -1} and 92.48 mg g{sup -1} for 1{sup st} and 2{sup nd} generation dendrimer, respectively. Analysis of different sorption kinetics model revealed that the sorption proceeded via pseudo 2{sup nd} order reaction. The 2{sup nd} generation dendrimer was found to be radiolytically more stable while oxalic acid was found to be suitable for quantitative back extraction of Pu{sup 4+}.

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

    Energy Technology Data Exchange (ETDEWEB)

    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.)

  18. Sorption of cesium in young till soils

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-10-01

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

  19. Sorption of actinides onto nanodiamonds

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-06-01

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

  20. Sorption of actinides onto nanodiamonds

    International Nuclear Information System (INIS)

    Buchatskaya, Yulia; Romanchuk, Anna; Yakovlev, Ruslan; Kulakova, Inna; Shiryaev, Andrei; Russian Academy of Sciences, Moscow; Kalmykov, Stepan; Russian Academy of Sciences, Moscow; Russian Academy of Sciences, Moscow

    2015-01-01

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

  1. Sorption-capacity limited retardation of radionuclides transport in water-saturated packing materials

    International Nuclear Information System (INIS)

    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 become 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 indicated 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 refs., 3 figs., 3 tabs

  2. Sorption-capacity limited retardation of radionuclides transport in water-saturated packing materials

    International Nuclear Information System (INIS)

    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

  3. Agro-waste biosorbents: Effect of physico-chemical properties on atrazine and imidacloprid sorption.

    Science.gov (United States)

    Mandal, Abhishek; Singh, Neera; Nain, Lata

    2017-09-02

    Low cost agro-waste biosorbents namely eucalyptus bark (EB), corn cob (CC), bamboo chips (BC), rice straw (RS) and rice husk (RH) were characterized and used to study atrazine and imidacloprid sorption. Adsorption studies suggested that biosorbents greatly varied in their pesticide sorption behaviour. The EB was the best biosorbent to sorb both atrazine and imidacloprid with K F values of 169.9 and 85.71, respectively. The adsorption isotherm were nonlinear in nature with slope (1/n) values imidacloprid sorption parameter [K F .(1/n)] with the physicochemical properties of the biosorbents suggested that atrazine adsorption correlated significantly to the aromaticity, polarity, surface area, fractal dimension, lacunarity and relative C-O band intensity parameters of biosorbents. Probably, both physisorption and electrostatic interactions were responsible for the pesticide sorption. The eucalyptus bark can be exploited as low cost adsorbent for the removal of these pesticides as well as a component of on-farm biopurification systems.

  4. Modification of zirconium diphosphate with salicylic acid and its effect on the uranium (Vi) sorption

    International Nuclear Information System (INIS)

    Almazan T, M. G.; Garcia G, N.; Simoni, E.

    2014-10-01

    The surface of zirconium diphosphate (ZrP 2 O 7 ) was modified with salicylic acid and its effect was evaluated on the uranium (Vi) sorption. The modified surface of the material was analyzed with different analytical techniques among which are included the atomic force microscopy, scanning electron microscopy and X-ray photoelectron spectroscopy. This analysis allowed showing that the salicylic acid is being held on the surface of the zirconium diphosphate. The reactivity of modified zirconium diphosphate compared with uranium (Vi) was investigated using the classical method of batch sorption. The analysis of sorption isotherms shows that the salicylic acid has an important effect in the uranium (Vi) sorption. According to the study conducted, the interaction among the uranium (Vi) and the surface of zirconium diphosphate modified with the salicylic acid most likely leads to the complexes formation of binary (U(Vi)/ZrP 2 O 7 ) and ternary (U(Vi)/salicylate/ZrP 2 O 7 ) surface. (Author)

  5. Sorption/desorption of Cs on clay and soil fractions from various regions of Turkey

    International Nuclear Information System (INIS)

    Erten, H.N.

    1988-01-01

    The sorption/desorption behaviour of Cs ion in the concentration region of 10 -8 to 10 -4 meqml -1 have been studied using clay and soil fractions from various regions of Turkey. The sorption curves for all the material studied show similar behaviour indicating at least two different sorption processes. One with high and the other with low distribution coefficients. The results of desorption studies indicate that Cs cation is to a large extent attached to the solid material in a reversible manner. The adsorption isotherms were found to be nonlinear in all cases. The increase of R D values with decreasing particle size in most cases, suggests that sorption and/or exchange is primarily a surface phenomenon in the clay and soil fractions studied. 14 figs.; 4 tabs

  6. Moisture conditions in buildings

    DEFF Research Database (Denmark)

    Rode, Carsten

    2012-01-01

    Growth of mould requires the presence of moisture at a certain high level. In a heated indoor environment such moisture levels occur only if there is a reason for the moisture supply. Such moisture can come from the use of the building, because of malfunctioning constructions, or it can be the re......Growth of mould requires the presence of moisture at a certain high level. In a heated indoor environment such moisture levels occur only if there is a reason for the moisture supply. Such moisture can come from the use of the building, because of malfunctioning constructions, or it can...

  7. Sorption of fission nuclides on model milk components. I. Sorption of radiostrontium on hydroxyapatite in aqueous solutions

    International Nuclear Information System (INIS)

    Rosskopfova, O.; Kopunec, R.; Matel, L.; Macasek, F.; Kristin, J.

    1999-01-01

    Hydroxyapatite, Ca 10 (PO 4 ) 6 (OH) 2 is a mineral widely spread in nature as a main constituent of phosphate rocks, and also as the major inorganic component of bones and teeth. It was found that sorption process occurs by an ion exchange reaction mechanism between strontium ions in solution and calcium ions in apatite. Ca 2+ → Sr 2+ substitution in hydroxyapatite is important since it explains the mechanism of incorporation of beta-active Sr-90 of atomic debris into the human skeletal system. The strontium uptake at 100 grad C is done by adsorption and diffusion while at 25 grad C it is done by the process of adsorption only. The hydroxyapatite was prepared from aqueous solutions and characterized by standard analytical methods. Some samples of hydroxyapatite were modified by heating after its precipitation from aqueous solution. The sample obtained had characteristics of well crystallized stoichiometric hydroxyapatite. Also, commercial hydroxy-apatites were used. Sorption of strontium ions on synthetic hydroxyapatite was examined using batch method and sorption depends on the method of preparation of hydroxyapatite. In generally, sorption of strontium decreases with the increase in the particle size of hydroxyapatite and decreases with the increase in the pH ( hydroxyapatite surface is amphoteric and acts as a buffer in a wide pH range). The sorption of strontium increases with the increase in [Sr 2+ ] or [Ca 2+ ] in solution to ∼ 10 -5 mol · dm -3 for the hydroxyapatite prepared by heating. The experimental data for sorption of strontium has been fitted with Langmuir-adsorption isotherm. (authors)

  8. Effect of hydrolyzed whey protein on surface morphology, water sorption, and glass transition temperature of a model infant formula.

    Science.gov (United States)

    Kelly, Grace M; O'Mahony, James A; Kelly, Alan L; O'Callaghan, Donal J

    2016-09-01

    Physical properties of spray-dried dairy powders depend on their composition and physical characteristics. This study investigated the effect of hydrolyzed whey protein on the microstructure and physical stability of dried model infant formula. Model infant formulas were produced containing either intact (DH 0) or hydrolyzed (DH 12) whey protein, where DH=degree of hydrolysis (%). Before spray drying, apparent viscosities of liquid feeds (at 55°C) at a shear rate of 500 s(-1) were 3.02 and 3.85 mPa·s for intact and hydrolyzed infant formulas, respectively. On reconstitution, powders with hydrolyzed whey protein had a significantly higher fat globule size and lower emulsion stability than intact whey protein powder. Lactose crystallization in powders occurred at higher relative humidity for hydrolyzed formula. The Guggenheim-Anderson-de Boer equation, fitted to sorption isotherms, showed increased monolayer moisture when intact protein was present. As expected, glass transition decreased significantly with increasing water content. Partial hydrolysis of whey protein in model infant formula resulted in altered powder particle surface morphology, lactose crystallization properties, and storage stability. Copyright © 2016 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

  9. Sorption of simazine to corn straw biochars prepared at different pyrolytic temperatures

    International Nuclear Information System (INIS)

    Zhang Guixiang; Zhang Qing; Sun Ke; Liu Xitao; Zheng Wenjuan; Zhao Ye

    2011-01-01

    Simazine sorption to corn straw biochars prepared at various temperatures (100-600 deg. C) was examined to understand its sorption behavior as influenced by characteristics of biochars. Biochars were characterized via elemental analysis, BET-N 2 surface area (SA), FTIR and 13 C NMR. Freundlich and dual-mode models described sorption isotherms well. Positive correlation between log K oc values and aromatic C contents and negative correlation between log K oc values and (O + N)/C ratios indicate aromatic-rich biochars have high binding affinity to simazine (charge transfer (π-π*) interactions) and hydrophobic binding may overwhelm H-bonding, respectively. Dual-mode model results suggest adsorption contribution to total sorption increases with carbonization degree. Positive correlation between amounts of adsorption (Q ad ) and SA indicates pore-filling mechanism. Comparison between our results and those obtained with other sorbents indicates corn straw biochars produced at higher temperature can effectively retain simazine. These observations will be helpful for designing biochars as engineered sorbents to remove triazine herbicides. - Highlights: → Biochars were characterized via elemental analysis, BET-N 2 , FTIR and 13 C NMR. → Freundlich and dual-mode models described sorption isotherms well. → Biochar produced at higher temperature had larger sorption capacity for simazine. → Aromatic-rich biochars have high binding affinity to simazine. → Dual-mode model results suggest adsorption contribution to total sorption. - The corn straw biochar prepared at higher temperature with stronger hydrophobicity, more aromatic C and larger surface area had higher sorption capacity for simazine.

  10. Effect made by the colloids to the sorption behavior of strontium on granite fracture-fillings

    Science.gov (United States)

    Wang, L.; Zuo, R.

    2017-12-01

    The objective of this study was to investigate the effects made by the colloid to the sorption capacity of colloids in granite fracture-fillings in aqueous solutions. The granite fracture-fillings were collected from three different depth of the research mine in Gansu province. According to the composition of the local soil and groundwater, two colloids were chosen to investigate this sorption process. Batch tests had been investigated at 27° under the air atmosphere as a function of pH(3 11), initial uranium concentration(5 400 mg/L) and water-rock ratio on the sorption of Sr on granite fracture-fillings. The batch experimental results showed that the sorption capacity presented a positive relationship with pH value, which may be caused by the hydrolytic adsorption raised by the reaction between Sr(OH)+ and OH- groups on the surface on the adsorbent. Initial strontium concentration also showed a positive relationship with sorption capacity when the concentration was lower than 200mg/mL, when the concentration was higher than 200mg/ml sorption reached the equilibrium. Sorption percentage showed a positive relationship with water/solid ratios, when the ratio was lower than 1:100 the system got equilibrium. When other experiment parameters were fixed and only the solid-liquid ratio changed, the adsorption capacity increased with the increasing solid-water ratio. The reason was that the total amount of Sr in the adsorption system remained unchanged, the adsorption sites increased with the solid-liquid ratio, and the adsorption capacity increased gradually with the increasing adsorption sites. The experiments data were interpreted in terms of Freundlich and Langmuir isotherms and the data fitted the former better. Equilibrium isotherm studies were used to evaluate the maximum sorption capacity of colloid.

  11. Adsorption isotherm special study. Final report

    International Nuclear Information System (INIS)

    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

  12. Kinetics and equilibrium modeling of uranium(VI) sorption by bituminous shale from aqueous solution

    International Nuclear Information System (INIS)

    Ortaboy, Sinem; Atun, Gülten

    2014-01-01

    Highlights: • Oil shales are sedimentary rocks containing a polymeric matter in a mineral matrix. • Sorption potential of bituminous shale (BS) for uranium recovery was investigated. • U(VI) sorption increased with decreasing pH and increasing temperature. • Kinetic data were analyzed based on single and two resistance diffusion models. • The results fit well to the McKay equation assuming film and intraparticle diffusion. - Abstract: Sorption of U(VI) onto a bituminous shale (BS) from a nuclear power plant project site in Black Sea region was investigated for potential risk assessment when it releases into the environment with contaminated ground and surface water. The sorption characteristics of the BS for U(VI) recovery were evaluated as a function of contact time, adsorbent dosage, initial concentration, pH and temperature. Kinetic results fit better with pseudo-second-order model rather than pseudo-first-order. The possibility of diffusion process was analyzed based on Weber–Morris intra-particle diffusion model. The McKay equation assuming film- and intraparticle diffusion better predicted the data than the Vermeulen approximation presuming surface diffusion. Equilibrium sorption data were modeled according to the Langmuir, Dubinin–Radushkevich (D–R) and Freundlich isotherm equations. Sorption capacity increased from 0.10 to 0.15 mmol g −1 in 298–318 K temperature range. FT-IR analysis and pH dependent sorption studies conducted in hydroxide and carbonate media revealed that U(VI) species were sorbed in uranyl and its hydroxo forms on the BS. Desorption studies showed that U(VI) leaching with Black Sea water was negligible from the loaded BS. The activation parameters (E a , ΔH ∗ and ΔG ∗ ) estimated from diffusion coefficients indicated the presence of an energy barrier in the sorption system. However, thermodynamic functions derived from sorption equilibrium constants showed that overall sorption process was spontaneous in nature

  13. Sorption of uranyl ions on silica. Effects of contact time, pH, ionic strength, concentration and phosphate

    International Nuclear Information System (INIS)

    Zhang Hongxia; Tao Zuyi

    2002-01-01

    The sorption of UO 2 2+ and phosphate on silica were simultaneously studied. The effect of contact time between the solid phase and aqueous solution, pH and ionic strength on the UO 2 2+ sorption in the absence and the presence of phosphate was investigated. The effect of contact time between the solid phase and aqueous solution, pH and ionic strength on the phosphate sorption was investigated too. The isotherms of UO 2 2+ and phosphate sorption at different pH values were determined. It was found that as compared with the sorption in the absence of phosphate, the sorption of UO 2 2+ on silica in the presence of phosphate is increased at low pH and decreased at high pH; the abruptly increased with increasing pH in the pH range 3-6; the sorption is gradually decreased with increasing pH in the pH range 2-12; the sorption insensitive and the sorption of phosphate is sensitive to ionic strength. (author)

  14. Tritium sorption by cement and subsequent release

    International Nuclear Information System (INIS)

    Ono, F.; Yamawaki, M.

    1995-01-01

    In a fusion reactor or tritium-handling facilities, contamination of concrete by tritium and subsequent release from it to the reator or experimental room is a matter of problem for safe control of tritium and management of operational environment. In order to evaluate this tritium behavior, interaction of tritiated water with concrete or cement should be clarified. In the present study, HTO sorption and subsequent release from cement were experimentally studied.(1)Sorption experiments were conducted using columns packed with cement particles of different sizes. From the analysis of the breakthrough curve, tritium diffusivity in macropores and microparticles were evaluated.(2)From the short-term tritium release experiments, effective desorption rate constants were evaluated and the effects of temperature and moisture were studied.(3)In the long-term tritium release experiments to 6000h, the tritium release mechanism was found to be composed of three kinds of water: initially from capillary water, and in the second stage from gel water and from the water in the cement crystal.(4)Tritium release behavior by heat treatment to 800 C was studied. A high temperature above 600 C was required for the tritium trapped in the crystal water to be released. (orig.)

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

    Science.gov (United States)

    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.

  16. Sorption of lambda-cyhalothrin, cypermethrin, deltamethrin and fenvalerate to quartz, corundum, kaolinite and montmorillonite.

    Science.gov (United States)

    Oudou, H Chaaieri; Hansen, H C Bruun

    2002-12-01

    Sorption to mineral surfaces may be important for retention and degradation of hydrophobic pesticides in subsoils and aquifers poor in organic matter. In this work the title pyrethroids have been used to investigate selective interactions with the surfaces of four minerals. Sorption of the four pyrethroids was quantified in batch experiments with initial pyrethroid concentrations of 1-100 microg/l. Sorption to centrifuge tubes used in the batch experiments accounted for 25-60% of total sorption. Net sorption was obtained from total sorption after subtracting the amounts of pyrethroids sorbed to centrifuge tubes used. All isotherms could be fitted by the Freundlich equation with n ranging between 0.9 and 1.1. Bonding affinities per unit surface area decreased in the order: corundum > quartz > montmorillonite approximately equal kaolinite. A similar sequence as found for the total surface tension of the minerals. All minerals showed the same selectivity order with respect to sorption affinity of the four pyrethroids: lambda-cyhalothrin > deltamethrin > cypermethrin > fenvalerate, which shows that the most hydrophobic compound is sorbed most strongly. Stereochemical properties of the four pyrethroid formulations may also contribute to the selectivity pattern.

  17. Sorption of perfluorooctanoic acid, perfluorooctane sulfonate and perfluoroheptanoic acid on granular activated carbon.

    Science.gov (United States)

    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. Copyright © 2015 Elsevier Ltd. All rights reserved.

  18. Sorption of graphites at high temperatures. Progress report, February 1, 1976--January 31, 1977

    International Nuclear Information System (INIS)

    Pyecha, T.D.; Zumwalt, L.R.

    1977-01-01

    Preliminary to mixed isotherm studies, one additional cesium isotherm was obtained with a finned-rod H-451 graphite sample at 1100 0 C. The results indicated that not only are long times required to reach saturation, but also there is a hysteresis effect at low vapor pressures and concentrations and that under these conditions sorption of cesium in graphite is not readily reversible. Several cesium isotherms (at 1000 0 C) were obtained of H-451 graphite which had been pre-impregnated with selected concentrations of Sr-85-tagged strontium. The runs were of long duration to attain equilibrium. The data obtained showed a substantial effect of the presence (concentration) of strontium on cesium sorption. End-of-run cesium and strontium concentration profiles were obtained. As yet the data on the mixed-sorption behavior, relative to possible models, has not been analyzed in depth. As a preliminary to the mixed-sorption studies, strontium impregnation in the absence of cesium was studied and a few experiments on the effect of concentration on strontium diffusion were carried out with interesting results. Finally a few experiments on sample characterization and on the microdistribution of cesium and strontium were conducted. It was found difficult to obtain distributions at the concentration levels characteristic of our experiments

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

    Science.gov (United States)

    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 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.

  20. Effect of the cationic composition of sorption solution on the quantification of sorption-desorption parameters of heavy metals in soils

    International Nuclear Information System (INIS)

    Sastre, J.; Rauret, G.; Vidal, M.

    2006-01-01

    We obtained the sorption isotherms of Cd, Cu, Pb and Zn in clay, clay saline and organic soils. The distribution coefficients (K d ) were determined in 0.02 eq l -1 CaCl 2 and in a solution that simulated the soil solution cationic composition. The K d values greatly varied with the composition of the sorption solution and the initial metal concentration. The sorption experiments were complemented with the quantification of the extractable metal, to estimate the reversibility of metal sorption. The extraction yields depended on the metal-soil combination, and the initial metal concentration, showing no correlation with previous K d values. The effect of the solution composition in mobility predictions was estimated through a Retention Factor, defined as the ratio of the K d versus the extraction yield. Results showed that risk was over- or underestimated using the CaCl 2 medium in soils with a markedly different soil solution composition. - Sorption solution composition modifies metal sorption-desorption pattern in soils

  1. Influence of sodium, calcium, magnesium, and ammonium in the sorption of cadmium in a zeolite rock

    International Nuclear Information System (INIS)

    Teutli S, E.A.

    2007-01-01

    The cadmium is one of the more toxic heavy metals and the water pollution by this metal, is originated by industries whose turn is the production of batteries, electroplating processes, the production of pigments and in the refinement process of others metals. The objective of this work was to evaluate the ion exchange of cadmium using natural zeolite, obtained from the Arroyo zone, La Haciendita Municipality, in the State of Chihuahua. The parameters considered in this investigation were: the sorption time, the pH, the initial concentration of cadmium and the influence of sodium, calcium, magnesium and ammonium on the sorption of cadmium in the natural zeolite. Also, the theoretical pattern for kinetics and isotherm that better it is adjusted to those experimental results it was determined. The experimentation results allowed to establish the following conclusions: the sorption of the cadmium doesn't depend on the pH in an interval between 4 and 6; the pattern that better it describes the kinetics it is that of Pseudo-second order of Ho and Mc Kay; the Langmuir-Freundlich pattern is the one that better it describes the sorption isotherm and the calcium is the component that interferes in an important manner in the sorption of cadmium. The carried out investigation contributes to the definition of some of the parameters that should be considered in the development of ion exchangers for the cadmium removal. (Author)

  2. Sorption and desorption reactions of radionuclides with a crushed basalt-bentonite packing material

    International Nuclear Information System (INIS)

    Barney, G.S.; Lane, D.L.; Allen, C.C.; Jones, T.E.

    1985-04-01

    Current design of waste packages for disposal of high-level radioactive wastes in underground basalt formations includes a layer of packing material that surrounds the waste container. One of the functions of this material is to limit the release of radionuclides from a breached container into groundwater by providing a low hydraulic conductivity zone and by sorbing dissolved radionuclides. The objective of this study was to assess the radionuclide sorption capability of a proposed packing material composed of 25% sodium bentonite and 75% crushed basalt (by weight). Sorption and desorption reactions of several important waste radioelements (neptunium, uranium, plutonium, technetium, selenium, and radium) were investigated in the absence of air at 90 0 C. Uranium and neptunium were sorbed by slow reactions that follow first-order kinetics. The reaction rates are probably controlled by reduction of weakly sorbed uranium(VI) and neptunium(V) by ferrous iron in the crushed basalt component. Technetium(VII) was not reduced or sorbed under these conditions. Freundlich sorption and desorption isotherms for a given radionuclide were non-singular and show a strong tendency for sorption hysteresis. Applying the isotherm data to a one-dimensional transport model indicated that hysteretic sorption on the packing material provides an important safety factor in controlling releases of some radionuclides

  3. Surface modification to improve the sorption property of U(VI) on mesoporous silica

    International Nuclear Information System (INIS)

    Lijuan Song; Yulong Wang; Lu Zhu; Bolong Guo; Suwen Chen; Wangsuo Wu

    2014-01-01

    Polyoxometalates K 7 [α-PW 11 O 39 ]·14H 2 O (PW11) modified mesoporous silica (MCM-48) with cubic structure, was prepared by impregnation and calcination methods. The modified mesoporous silica sorbent (PW11/MCM-48) was studied as a potential adsorbent for U(VI) from aqueous solutions. MCM-48 and PW11/MCM-48 were confirmed by X-ray diffraction and nitrogen physisorption techniques. The results indicate the original keggin structure of PW11 and mesoporous structure of MCM-48 are maintained after supporting PW11 on mesoporous silica MCM-48. The effects of contact time, solid-to-liquid ratio (m/V), solution pH and ionic strength on U(VI) sorption behaviors of the pure and modified mesoporous silicas were also studied. Typical sorption isotherms such as Langmuir and Freundlich isotherms were determined for sorption process. The results suggest that the sorption of U(VI) on MCM-48 or PW11/MCM-48 are strongly dependent on pH values but independent of ionic strength. The sorption capacity of PW11/MCM-48 for U(VI) is about ten times more than that of MCM-48. (author)

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

    Science.gov (United States)

    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. Copyright © 2013 Elsevier Ltd. All rights reserved.

  5. FORMULASI TEPUNG PENYALUT BERBASIS TEPUNG JAGUNG DAN PENENTUAN UMUR SIMPANNYA DENGAN PENDEKATAN KADAR AIR KRITIS [Formulation of Corn Flour-Based Batter and Prediction of Its Shelf Life using Critical Moisture Approach

    Directory of Open Access Journals (Sweden)

    Sugiyono1*

    2010-12-01

    Full Text Available The objectives of this study were to obtain the best formula for corn flour-based batter and to predict its shelf life using critical moisture approach. According to a hedonic test, the best batter formula was composed of 60% corn flour, 12.5% rice flour, 12.5% tapioca starch, and 15% glutinous rice flour. Addition of glutinous rice flour in the formula changed the proportion of amylose and amylopectin in the batter. As a result, the retrogradation of the batter decreased and the texture of its fried product was preferred. A critical moisture approach was used to predict the shelf life of the batter. The critical moisture content of the batter was 0.16 g H2O/g solid.The isotherm sorption phenomenon of the batter was best described using Hasley model. The shelf life of the product was 7 months when packaged in polypropylene (0,07 g/m2day.mmHg at 85% RH.

  6. Isotherms of Capillary Condensation Influenced by Formation of Adsorption Films.

    Science.gov (United States)

    Churaev; Starke; Adolphs

    2000-01-15

    Isotherms of capillary condensation are often used to determine the vapor sorption capacity of porous adsorbents as well as the pore size distribution by radii. In this paper, for calculating the volume of capillary condensate and of adsorption films in a porous body, an approach based on the theory of surface forces is used. Adsorption isotherms and disjoining pressure isotherms of wetting films are presented here in an exponential form discussed earlier. The calculations were made for straight cylindrical capillaries of different radii and slit pores of different width. The mechanisms of capillary condensation differ in cylindrical and slit pores. In cylindrical pores capillary condensation occurs due to capillary instability of curved wetting films on a capillary surface, when film thickness grows. In the case of slit pores, coalescence of wetting films formed on opposite slit surfaces proceeds under the action of attractive dispersion forces. Partial volumes of liquid in the state of both capillary condensate and adsorbed films are calculated dependent on the relative vapor pressure in a surrounding media. Copyright 2000 Academic Press.

  7. Isotermas de adsorção do pedúnculo seco do caju Adsorption isotherms of the dry cashew apple

    Directory of Open Access Journals (Sweden)

    Siumara R. Alcântara

    2009-02-01

    Full Text Available A atividade de água constitui um fator importante no processo de fermentação semi-sólida, haja vista sua relação com a quantidade de água disponível ao microrganismo responsável pelo metabolismo do produto, sendo necessário à obtenção de isotermas de sorção para caracterização do substrato. Ante o exposto, objetivou-se a construção das isotermas de adsorção do pedúnculo seco do caju (Anacardium occidentale L. nas temperaturas usuais de fermentação (25, 30, 35 e 40 ºC. Ajustaram-se as isotermas com os modelos de BET, GAB, Oswin, Henderson e Smith. Observou-se que o modelo de GAB apresentou melhor ajuste, de vez que, na faixa de atividade de água que maximiza a biossíntese do microrganismo, para produção de pectinases por Aspergillus niger, a umidade do substrato deve estar acima de 35% b.s.Water activity is a very important factor in a solid state fermentation process due to its relation with the water quantity available to the microorganism that will synthesize the product. Therefore, it is necessary to obtain the sorption isotherms for the characterization of the substrate. The objective of this study is to obtain adsorption isotherms of the dry cashew apple (Anacardium occidentale L. at normal temperatures of fermentation process (25, 30, 35 e 40 ºC. Five mathematical models were fitted to the experimental data: BET, GAB, Oswin, Henderson e Smith. The GAB model was better fitted to the product. The isotherms allowed the determination of the appropriate moisture content to obtain the water activities that maximize the biosynthesis of the microorganism for the pectin production by solid state fermentation process. The moisture content of the substrate should be above 35% d.b.

  8. Isothermal and hygrothermal agings of hybrid glass fiber/carbon fiber composite

    Science.gov (United States)

    Barjasteh, Ehsan

    in the oxygen-transport properties (diffusivity and solubility of oxygen). The effect of thermal aging on mechanical properties of the aged composites was investigated. A relationship was derived relating TOL to tensile strength of the hybrid composite. The tensile strength remained essentially unchanged by thermal oxidation after 52 weeks of exposure. On the contrary, the oxidation resulted in a decrease in short-beam-shear (SBS) strength (a matrix-dominated property) due to degradation of matrix and fiber/matrix interface strength. However, the filled composites showed a lower reduction in SBS strength than that of the unfilled one for an identical duration of exposure. In addition, the effect of thermal aging on glass transition temperature (T g) was determined for isothermal exposures at 180ºC and 200ºC. The simultaneous effects of post-curing and thermal degradation resulted in the change in Tg during exposure. Another study on the composite rod was performed to investigate the sorption kinetics and the effects of moisture on mechanical and physical properties. Sorption curves were obtained for both hybrid and non-hybrid composite rods to determine characteristic parameters, including the diffusion coefficient (D) and the maximum moisture uptake (Minfinity ). The moisture uptake for the hybrid composites generally exhibited Fickian behavior (no hybridization effects), behaving much like non-hybrid composites. A two-dimensional diffusion model was employed to calculate moisture diffusivities in the longitudinal direction. Interfaces and thermally-induced residual stresses affected the moisture diffusion. In addition, the effect of hygrothermal aging on glass transition temperature (Tg), short beam shear strength (SBS), and tensile strength was determined for hygrothermal exposure at 60°C and 85% relative humidity (RH). Property retention and reversibility of property degradation was also measured. Microscopic inspection revealed no evidence of damage

  9. Experimental studies of Cs, Sr, Ni, and Eu sorption on Na-illite and the modelling of Cs sorption

    International Nuclear Information System (INIS)

    Poinssot, C.; Baeyens, B.; Bradbury, M.H.

    1999-08-01

    A natural illite (illite du Puy) was purified and converted to the homo-ionic Na-form. The conditioned Na-illite was characterised in terms of its mineralogy, chemical inventory and physico-chemical properties. The structural formula was determined from energy dispersive spectroscopic analyses (SEM/TEM-EDS) and bulk chemistry measurements. A cation exchange capacity of 127 meq kg -1 was determined by the 22 Na isotope dilution method at neutral pH. The Na-CEC was also measured as a function of pH. The stability of Na-illite as a function of pH in the range between 3 and 6 was investigated. At low pH values partial dissolution of the illite occurs releasing the structural elements Al, Si, Mg, and K into solution. The presence of Ca and Sr in solution was interpreted as being due to desorption from cation exchange sites. All of these elements are also present at neutral pH but at considerably lower levels. Such effects cannot be avoided and must be considered in the interpretation of the sorption measurements. The main focus of the experimental work presented here is on the sorption behaviour of Cs, Sr, Ni and Eu on conditioned Na-illite as a function of NaClO 4 background electrolyte concentration (0.1 and 0.01 M), nuclide concentration and pH in the range between 3 and 11. Sorption edge data (R d versus pH) and sorption isotherms (quantity of nuclide sorbed versus equilibrium nuclide concentration) are presented for these four elements. Prior to beginning these experiments, sorption kinetics were measured. The broad based pool of sorption measurements generated from this work will provide the source data sets for subsequent modelling. So far only the Cs sorption measurements have been modelled. A two site cation exchange model was developed to describe the sorption of Cs over the whole range of experimental conditions. The two site types were termed 'frayed edge sites' (FES, high affinity/low capacity) and 'type II sites' (low affinity/high capacity). Selectivity

  10. Investigations of the sorption of pertechnetate on salts of molybdophosphoric acid

    International Nuclear Information System (INIS)

    Suess, M.; Pfrepper, G.

    1983-01-01

    Studies were made to investigate the sorption of pertechnetate on neutral and acid salts of molybdophosphoric acid from nitric acid and in the presence of electrolytes and non-electrolytes. Particular, distribution coefficients from 10 to 100 were found. The sorption of pertechnetate can be increased by the addition of K + , NH 4 + , Rb + and Cs + salts, by the addition of non-electrolytes the distribution coefficients decrease. A saturation capacity of about 0.19 mmol Tc/g ammonium phosphomolybdate was determined from the adsorption isotherms. The formation of alkali metal pertechnetate associates in the sorbent phase can be supposed. (author)

  11. Sorption and desorption of remazol yellow by a Fe-zeolitic tuff

    International Nuclear Information System (INIS)

    Solache R, M. J.; Villalva C, R.; Diaz N, M. C.

    2010-01-01

    The adsorption of remazol yellow from aqueous solution was evaluated using a Fe-zeolitic tuff. The adsorbent was characterized by scanning electron microscopy, IR spectroscopy and X-ray diffraction. Sorption kinetic and isotherms were determined and the adsorption behavior was analyzed. Kinetic pseudo-second order and Langmuir-Freundlich models were successfully applied to the experimental results, indicating chemisorption on a heterogeneous material. The regeneration of the material was best accomplished by using a H 2 O 2 solution. The sorption capacity of the Fe-zeolitic tuff increased when the saturated samples were treated with a H 2O2 or FeCl 3 solution. (Author)

  12. Effect of the gamma irradiation on the bio-sorption of Cr (Vi) by orange peel

    International Nuclear Information System (INIS)

    Lugo L, V.; Barrera D, C. E.; Sanchez M, V.; Urena N, F.

    2009-01-01

    The orange peel (Citrus sp.) is a bioadsorbent that contains functional groups able to remove Cr (Vi). To study the effect of gamma irradiation in the sorption capacity, the Nn materials were irradiated with gamma rays using a Co 60 source to dose from 10 to 3500 KGy (Nlγ). The biomass irradiation with gamma rays was successful since it increased the hexavalent chromium removal obtaining a maximum removal percentage of 100%. Sorption isotherms were realized to determine the concentration effect of initial Cr (Vi), the ph effect of the solution and the relationship m/v. (Author)

  13. Sorption study of U+6 in Brazilian soils

    International Nuclear Information System (INIS)

    Junior, Antonio P.; Wasserman, Maria A.V.; Mantovano, Jose L.; Carvalho, Leonel M.; Perez, Daniel V.

    2015-01-01

    The uranium mining is one of the main activities of the nuclear fuel cycle that can contribute to the increased exposure to radioactive materials and is one of the main routes of contamination of soil by natural radionuclides. This study investigated the sorption of uranium in brazilian soils, through sorption isotherms performed in batch. In this study, two types of soils were selected: Ferralsols Red and Nitosol. The adjustment of the experimental data to the kinetic models were evaluated by two approaches: the traditional, based on the coefficient of determination (R 2 ); and the theoretical and informative, based on Corrected Akaike Information Criteria (AIC C ). The coefficient of determination (R 2 ), revealed that, although empirical, both the kinetic model, Freundlich and Langmuir, describes satisfactorily the experimental data, showing R 2 values higher than 0.9, while the partition constant model was not suitable for describe these sorption data. The AICC model analysis showed that the Langmuir model fit the U sorption curve well for Ferralsols Red, while the Freundlich model fits better to Nitosol. This study has highlighted the role of organic matter on the sorption of uranium in highly weathered soils, rich in oxyhydroxides and low activity clays. The Kd values reported in this study differ from those recommended by the United States Environmental Protection Agency, therefore must be considered as reference values for highly weathered soils, since it refers to Brazilian pedoenvironmental conditions. The low Kd values obtained in this study allowed to evaluate the high vulnerability of highly weathered soils to uranium contamination. (author)

  14. Sorption study of U{sup +6} in Brazilian soils

    Energy Technology Data Exchange (ETDEWEB)

    Junior, Antonio P.; Wasserman, Maria A.V.; Mantovano, Jose L.; Carvalho, Leonel M., E-mail: apjunior@ien.gov.br, E-mail: mwasserman@ien.gov.br, E-mail: mantovan@ien.gov.br, E-mail: leonel@ien.gov.br [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Perez, Daniel V., E-mail: daniel@cnps.embrapa.br [Empresa Brasileira de Pesquisas Agropecuarias (Embrapa Solos-CNPS), Rio de Janeiro, RJ (Brazil)

    2015-07-01

    The uranium mining is one of the main activities of the nuclear fuel cycle that can contribute to the increased exposure to radioactive materials and is one of the main routes of contamination of soil by natural radionuclides. This study investigated the sorption of uranium in brazilian soils, through sorption isotherms performed in batch. In this study, two types of soils were selected: Ferralsols Red and Nitosol. The adjustment of the experimental data to the kinetic models were evaluated by two approaches: the traditional, based on the coefficient of determination (R{sup 2}); and the theoretical and informative, based on Corrected Akaike Information Criteria (AIC{sub C}). The coefficient of determination (R{sup 2}), revealed that, although empirical, both the kinetic model, Freundlich and Langmuir, describes satisfactorily the experimental data, showing R{sup 2} values higher than 0.9, while the partition constant model was not suitable for describe these sorption data. The AICC model analysis showed that the Langmuir model fit the U sorption curve well for Ferralsols Red, while the Freundlich model fits better to Nitosol. This study has highlighted the role of organic matter on the sorption of uranium in highly weathered soils, rich in oxyhydroxides and low activity clays. The Kd values reported in this study differ from those recommended by the United States Environmental Protection Agency, therefore must be considered as reference values for highly weathered soils, since it refers to Brazilian pedoenvironmental conditions. The low Kd values obtained in this study allowed to evaluate the high vulnerability of highly weathered soils to uranium contamination. (author)

  15. Sorption of selected organic compounds from water to a peat soil and its humic-acid and humin fractions: Potential sources of the sorption nonlinearity

    Science.gov (United States)

    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.

  16. How the sorption of benzene in soils contaminated with aromatic hydrocarbons is affected by the presence of biofuels

    Directory of Open Access Journals (Sweden)

    Maria Manuela Carvalho

    2015-04-01

    Full Text Available The increasing use of biofuels as additives to gasoline may have potential indirect effects on the efficiency of soil remediation technologies used to remediate fuel spills. This problem has not yet been studied. Sorption is one of the controlling processes in soil remediation. The effect of biofuels on sorption and phase distribution of contaminants by different natural soils has not been reported on the literature. The present work examines how two different biofuels, n-butanol and soybean biodiesel, affect benzene sorption in two naturally occurring subsoils (granite and limestone. Sorption isotherms were made with soils deliberately contaminated with benzene, benzene and n-butanol and benzene plus biodiesel, using lab-scale reactors operated at constant temperature, each one loaded with 700 grams of wet sterilized soil. For each type of soil, five isotherms were determined corresponding to different contamination profiles. It was concluded that sorption was strongly affected by the nature of the soil. The partition of benzene into the different phases of the soil was significantly affected by the presence of biofuels. The experimental data was fitted to conventional sorption models, Freundlich, Langmuir and a second order polynomial. Model parameters were determined using a non-linear least squares (NLLS optimization algorithm and showed a good agreement between experimental and fitted data.

  17. Lead sorption by waste biomass of hazelnut and almond shell.

    Science.gov (United States)

    Pehlivan, Erol; Altun, Türkan; Cetin, Serpil; Iqbal Bhanger, M

    2009-08-15

    The potential to remove Pb(2+) ion from aqueous solutions using the shells of hazelnut (HNS) (Corylus avellana) and almond (AS) (Prunus dulcis) through biosorption was investigated in batch experiments. The main parameters influencing Pb(2+) ion sorption on HNS and AS were: initial metal ion concentration, amount of adsorbent, contact time and pH value of solution. The influences of initial Pb(2+) ion concentration (0.1-1.0mM), pH (2-9), contact time (10-240 min) and adsorbent amount (0.1-1.0 g) have been investigated. Equilibrium isotherms have been measured and modelled. Adsorption of Pb(2+) ions was in all cases pH-dependent showing a maximum at equilibrium pH values between 6.0 and 7.0, depending on the biomaterial, that corresponded to equilibrium pH values of 6.0 for HNS and 7.0 for AS. The equilibrium sorption capacities of HNS and AS were 28.18 and 8.08 mg/g for lead, respectively after equilibrium time of 2h. The adsorption data fit well with the Langmuir isotherm model and the experimental result inferred that adsorption, chelation and ion exchange are major adsorption mechanisms for binding Pb(2+) ion to the sorbents.

  18. Sorption of cesium on montmorillonite and effect of salt concentration

    International Nuclear Information System (INIS)

    Atun, G.; Bilgin, B.; Mardinli, A.

    1996-01-01

    The sorption behavior of cesium on montmorillonite type[e clay was studied by using radioactivity measurements. Concentrations of Cs + ions ranged from 10 -6 to 10 -2 M. Cesium retention reduced with increasing salt concentration which was varied between 10 -4 and 10 -1 M. Selectivity coefficients K CsNa for the exchange between Cs and Na were calculated for different equivalent fractions of Cs on the solid phase. Using the K CsNa values, free energy change was found to be 7.8 kJ/mol. The data could be fitted to a Freundlich isotherm, and empirical Freundlich parameters enabled the generation of a site distribution function. By fitting the data to the Dubinin-Radushkevich (D-R) isotherm, a mean energy of sorption of 8.6kJ/mole was calculated which corresponds to the energy of ion exchange reactions. The values of energy changes calculated by using two different methods were in good agreement. (author)

  19. Kinetic and isotherm studies of Cu(II) biosorption onto valonia tannin resin

    Energy Technology Data Exchange (ETDEWEB)

    Sengil, I. Ayhan [Department of Environmental Engineering, Engineering Faculty, Sakarya University, 54100 Sakarya (Turkey)], E-mail: asengil@sakarya.edu.tr; Ozacar, Mahmut [Department of Chemistry, Science and Arts Faculty, Sakarya University, 54100 Sakarya (Turkey); Tuerkmenler, Harun [Institute of Sciences and Technology, Sakarya University, 54040 Sakarya (Turkey)

    2009-03-15

    The biosorption of Cu(II) from aqueous solutions by valonia tannin resin was investigated as a function of particle size, initial pH, contact time and initial metal ion concentration. The aim of this study was to understand the mechanisms that govern copper removal and find a suitable equilibrium isotherm and kinetic model for the copper removal in a batch reactor. The experimental isotherm data were analysed using the Langmuir, Freundlich and Temkin equations. The equilibrium data fit well in the Langmuir isotherm. The experimental data were analysed using four sorption kinetic models - the pseudo-first- and second-order equations, the Elovich and the intraparticle diffusion model equation - to determine the best fit equation for the biosorption of copper ions onto valonia tannin resin. Results show that the pseudo-second-order equation provides the best correlation for the biosorption process, whereas the Elovich equation also fits the experimental data well.

  20. Sorption of phenanthrene and benzene on differently structural kerogen: Important role of micropore-filling

    International Nuclear Information System (INIS)

    Zhang, Yulong; Ma, Xiaoxuan; Ran, Yong

    2014-01-01

    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 (V o,d ) initially increase and then decrease. The V o,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 V o,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. -- Highlights: • The microporosity estimated by benzene vapor differs greatly from that by N 2 . • The micropore volume changes with kerogen maturation. • The phenanthrene or benzene sorption is related to the microporosity of kerogen. • Higher adsorption volume for benzene than for phenanthrene suggests molecular sieve effect. • The pore-filling plays an important role in the sorption of phenanthrene and benzene. -- The sorption behaviors of benzene and phenanthrene are related to the microporosity of the differently matured kerogen, indicating the importance of pore-filling

  1. Phosphate Sorption Characteristics and External P Requirements of Selected South African Soils

    Directory of Open Access Journals (Sweden)

    E. M. Gichangi

    2008-10-01

    Full Text Available The Transkei is the largest consolidated area in South Africa where land is held by smallholder farmers but little is known about the extent of phosphate fixation in the region. This study was conducted to determine the phosphate sorption properties and external P requirements (EPR of selected soils from the Transkei region, South Africa and to relate derived sorption values to selected soil parameters. The P sorption maxima and EPR values varied widely ranging from 192.3 to 909.1 mg P kg−1 and from 2 to 123 mg P kg−1−1 soil, respectively. Citrate dithionite bicarbonate-extractable aluminum explained most of the observed variations in P sorption. About 43% of the soils were found to be moderate P fixers and may need management interventions to ensure adequate P availability to crops. The single point sorption index accurately predicted the EPR of the soils obviating the need to use multiple point sorption isotherms. The results suggested that the use of blanket phosphate fertilizer recommendations may not be a good strategy for the region as it may lead to under-application or over-application of P in some areas.

  2. Sorption studies of radioiodine on soils with special references to soil microbial biomass

    Energy Technology Data Exchange (ETDEWEB)

    Bors, J. (Niedersaechsisches Inst. fuer Radiooekologie, Hannover (Germany, F.R.)); Erten, H. (Bilkent Univ., Ankara (Turkey). Dept. of Chemistry); Martens, R. (Bundesforschungsanstalt fuer Landwirtschaft, Braunschweig (Germany, F.R.). Inst. fuer Bodenbiologie)

    1991-01-01

    In batch experiments with two types of soils, chernozem and podzol, radioiodine ({sup 125}I) showed an initial rapid sorption, followed by a long and slow further increase. Very little sorption (R{sub d} < 1) was detected in clay minerals. Generally, higher R{sub d}-values were observed for the chernozem soil, characterized by a higher amount of organic substance and of soil biomass. The sorption process was predominantly irreversible, the isotherms were linear at low ion concentrations and deviated from linearity starting at 10{sup -5} mmol.ml{sup -1}. Sorption ratio was found to increase with increasing volume to mass ratio. The composition of liquid phases (bidistilled water, synthetic soil water, rain water) highly affected iodine sorption. In experiments with KBr solution, the sorption of I{sup -} was found to be strongly preferred to Br{sup -}. Incubation of soil samples under varied conditions (decreased or increased soil biomass, O{sub 2}-concentration, incubation temperature, soil water content and storage conditions) delivered indications for the participation of soil microflora in iodine immobilization. Test with isolated soil bacteria and fungi showed that radioiodine can be incorporated by soil microorganisms under certain conditions only: Considerable uptake of radioiodine was found in washed (NaCl, CaCl{sub 2}) cells with both bacteria and fungi, but no incorporation was detected into cells incubated with radioiodine in the culture medium. (orig.).

  3. Sorption studies of radioiodine on soils with special references to soil microbial biomass

    International Nuclear Information System (INIS)

    Bors, J.; Erten, H.; Martens, R.

    1991-01-01

    In batch experiments with two types of soils, chernozem and podzol, radioiodine ( 125 I) showed an initial rapid sorption, followed by a long and slow further increase. Very little sorption (R d d -values were observed for the chernozem soil, characterized by a higher amount of organic substance and of soil biomass. The sorption process was predominantly irreversible, the isotherms were linear at low ion concentrations and deviated from linearity starting at 10 -5 mmol.ml -1 . Sorption ratio was found to increase with increasing volume to mass ratio. The composition of liquid phases (bidistilled water, synthetic soil water, rain water) highly affected iodine sorption. In experiments with KBr solution, the sorption of I - was found to be strongly preferred to Br - . Incubation of soil samples under varied conditions (decreased or increased soil biomass, O 2 -concentration, incubation temperature, soil water content and storage conditions) delivered indications for the participation of soil microflora in iodine immobilization. Test with isolated soil bacteria and fungi showed that radioiodine can be incorporated by soil microorganisms under certain conditions only: Considerable uptake of radioiodine was found in washed (NaCl, CaCl 2 ) cells with both bacteria and fungi, but no incorporation was detected into cells incubated with radioiodine in the culture medium. (orig.)

  4. Sorption of cadmium and lead by clays from municipal incinerator ash- water suspensions

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

  6. Sorption to soil, biochar and compost: is prediction to multicomponent mixtures possible based on single sorbent measurements?

    Directory of Open Access Journals (Sweden)

    Melanie Kah

    2018-06-01

    Full Text Available Amendment with biochar and/or compost has been proposed as a strategy to remediate soil contaminated with low levels of polycyclic aromatic hydrocarbons. The strong sorption potential of biochar can help sequestering contaminants while the compost may promote their degradation. An improved understanding of how sorption evolves upon soil amendment is an essential step towards the implementation of the approach. The present study reports on the sorption of pyrene to two soils, four biochars and one compost. Detailed isotherm analyzes across a wide range of concentration confirmed that soil amendments can significantly increase the sorption of pyrene. Comparisons of data obtained by a classical batch and a passive sampling method suggest that dissolved organic matter did not play a significant role on the sorption of pyrene. The addition of 10% compost to soil led to a moderate increase in sorption (<2-fold, which could be well predicted based on measurements of sorption to the individual components. Hence, our result suggest that the sorption of pyrene to soil and compost can be relatively well approximated by an additive process. The addition of 5% biochar to soil (with or without compost led to a major increase in the sorption of pyrene (2.5–4.7-fold, which was, however, much smaller than that suggested based on the sorption measured on the three individual components. Results suggest that the strong sorption to the biochar was attenuated by up to 80% in the presence of soil and compost, much likely due to surface and pore blockage. Results were very similar in the two soils considered, and collectively suggest that combined amendments with compost and biochar may be a useful approach to remediate soils with low levels of contamination. Further studies carried out in more realistic settings and over longer periods of time are the next step to evaluate the long term viability of remediation approaches based on biochar amendments.

  7. Sorption properties of carbon nanostructures

    International Nuclear Information System (INIS)

    Eletskii, Aleksandr V

    2004-01-01

    The current status of research in sorption properties of carbon nanotubes (CNTs) is reviewed. The structural peculiarities of CNTs, determining their sorption characteristics, are considered. The mechanisms of sorption of gaseous and condensed substances by such structures are analyzed. Special attention is paid to the problem of using CNTs for storing hydrogen and other gaseous substances. Methods for filling CNTs with liquid materials, based on capillary phenomena and wetting the graphite surface of the CNT with liquids of various nature, are considered. Properties of 'peapods' formed as a result of filling single-walled CNTs with fullerene molecules are reviewed. Also considered are perspectives on the applied usage of the sorption properties of CNTs in electrochemical and fuel cells, and material storage devices, as well as for producing superminiature metallic conductors. (reviews of topical problems)

  8. Research on the phenomenon of graphitization. Crystallographic study - Study of bromine sorption

    International Nuclear Information System (INIS)

    Maire, Jacques

    1967-01-01

    This research thesis reports the study of the mechanism of graphitization of carbon by using X-ray diffraction analysis and the physical and chemical study of lamellar reactions between carbon and bromine. The author first presents generalities and results of preliminary studies (meaning of graphitization, presentation of the various carbon groups and classes), and then reports the study of the graphitization of compact carbons (soft carbons). More precisely, he reports the crystallographic study of partially graphitized carbons: methods and principles, experimental results and their analysis, discussion of the graphitization mechanism. In the next part, the author reports the study of bromine sorption on carbons: experimental method, isotherms of a natural graphite and of a graphitized carbon, structure of carbon-bromine complexes, isotherms of graphitizable carbons and of all other carbons, distribution of bromine layers in partially graphitized carbons, bromine sorption and Fermi level

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

    International Nuclear Information System (INIS)

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

    2006-01-01

    U(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

  10. Investigating the gas sorption mechanism in an rht -metal-organic framework through computational studies

    KAUST Repository

    Pham, Tony T.

    2014-01-09

    Grand canonical Monte Carlo (GCMC) simulations were performed to investigate CO2 and H2 sorption in an rht-metal-organic framework (MOF) that was synthesized with a ligand having a nitrogen-rich trigonal core through trisubstituted triazine groups and amine functional groups. This MOF was synthesized by two different groups, each reporting their own distinct gas sorption measurements and crystal structure. Electronic structure calculations demonstrated that the small differences in the atomic positions between each group\\'s crystal structure resulted in different electrostatic parameters about the Cu2+ ions for the respective unit cells. Simulations of CO2 sorption were performed with and without many-body polarization effects and using our recently developed CO2 potentials, in addition to a well-known bulk CO2 model, in both crystallographic unit cells. Simulated CO2 sorption isotherms and calculated isosteric heats of adsorption, Qst, values were in excellent agreement with the results reported previously by Eddaoudi et al. for both structures using the polarizable CO2 potential. For both crystal structures, the initial site for CO2 sorption were the Cu 2+ ions that had the higher positive charge in the unit cell, although the identity of this electropositive Cu2+ ion was different in each case. Simulations of H2 sorption were performed with three different hydrogen potentials of increasing anisotropy in both crystal structures and the results, especially with the highest fidelity model, agreed well with Eddaoudi et al.\\'s experimental data. The preferred site of H 2 sorption at low loading was between two Cu2+ ions of neighboring paddlewheels. The calculation of the normalized hydrogen dipole distribution for the polarizable model in both crystal structures aided in the identification of four distinct sorption sites in the MOF, which is consistent to what was observed in the experimental inelastic neutron scattering (INS) spectra. Lastly, while the

  11. Sorption of Np(V) by synthetic hydroxyapatite

    International Nuclear Information System (INIS)

    Moore, R.C.; Holt, K.; Zhao, H.; Hasan, A.; Awwad, N.; Gasser, M.; Sanchez, C.

    2003-01-01

    The sorption of Np(V) to synthetic hydroxyapatite was determined in batch experiments in a 0.1 M NaClO 4 solution. The hydroxyapatite used was of high purity as determined by SEM, EDS, XRD, FT-IR and ICP-MS analysis. Results from kinetic experiments with an initial Np(V) concentration of 1 x 10 -7 to 1 x 10 -6 M indicate the sorption process is relatively fast with more than 90% of the Np(V) being sorbed in approximately 3 hours. Equilibrium experiments performed over the pH range of 6 to 11 indicated sorption is strongly pH dependent with distribution coefficients, K d values (mL/g), increasing from 123 L/mole at pH 6 to 69 200 L/mole at pH 8.5. K d values are observed to decrease as pH further increases. Data points over a range of Np(V) concentrations were collected at pH 8 and fitted to the Langmuir isotherm model for simple adsorption. The Langmuir equation gave an excellent representation of the data. Langmuir parameters were determined to be C a = 0.032 mole/mole and K = 1.22 x 10 6 L/mole, indicating the high affinity of hydroxyapatite for Np(V) adsorption. (orig.)

  12. Enriched fluoride sorption using alumina/chitosan composite

    Energy Technology Data Exchange (ETDEWEB)

    Viswanathan, Natrayasamy, E-mail: natrayasamy_viswanathan@rediffmail.com [Department of Chemistry, Anna University Tiruchirappalli - Dindigul Campus, Dindigul 624 622, Tamil Nadu (India); Meenakshi, S., E-mail: drs_meena@rediffmail.com [Department of Chemistry, Gandhigram Rural University, Gandhigram 624 302, Tamil Nadu (India)

    2010-06-15

    Alumina possesses an appreciable defluoridation capacity (DC) of 1566 mg F{sup -}/kg. In order to improve its DC, it is aimed to prepare alumina polymeric composites using the chitosan. Alumina/chitosan (AlCs) composite was prepared by incorporating alumina particles in the chitosan polymeric matrix, which can be made into any desired form viz., beads, candles and membranes. AlCs composite displayed a maximum DC of 3809 mg F{sup -}/kg than the alumina and chitosan (52 mg F{sup -}/kg). The fluoride removal studies were carried out in batch mode to optimize the equilibrium parameters viz., contact time, pH, co-anions and temperature. The equilibrium data was fitted with Freundlich and Langmuir isotherms to find the best fit for the sorption process. The calculated values of thermodynamic parameters indicate the nature of sorption. The surface characterisation of the sorbent was performed by FTIR, AFM and SEM with EDAX analysis. A possible mechanism of fluoride sorption by AlCs composite has been proposed. Suitability of AlCs composite at field conditions was tested with a field sample taken from a nearby fluoride-endemic village. This work provides a potential platform for the development of defluoridation technology.

  13. The effect of carbonate on neptunium sorption by hydroxyapatite

    International Nuclear Information System (INIS)

    Moore, R.C.; Holt, K.

    2005-01-01

    Full text of publication follows: Hydroxyapatite, Ca 10 (PO 4 ) 6 (OH) 2 , is a common mineral, the main inorganic compound in bone and exhibits strong sorptive properties for many radionuclides. It has been widely studied and proposed as a backfill material for nuclear waste repositories. Neptunium is one the radionuclides sorbed by hydroxyapatite. Neptunium is of particular importance to nuclear waste repository performance because of its relatively high aqueous solubility, high mobility in the environment and long half-life. In this work, we report on the effects of carbonate on sorption of neptunium by hydroxyapatite. Batch sorption and desorption studies for neptunium were performed as a function of carbonate concentration in water using a synthetic hydroxyapatite. The results indicate even low concentrations of carbonate significantly reduce neptunium sorption and enhance desorption. The data were fit to several simple isotherm equations with the Langmuir equation giving the best results. The results of the work are discussed with respect to nuclear waste repository performance. (authors)

  14. Hollow fiber adsorbents for CO2 capture: Kinetic sorption performance

    KAUST Repository

    Lively, Ryan P.

    2011-07-01

    We describe a CO 2 capture platform based on hollow polymeric fibers with sorbent particles embedded in the porous fiber wall for post-combustion CO 2 capture. These fibers are intended for use in a rapid temperature swing adsorption (RTSA) process. The RTSA system utilizes the hollow fiber morphology by flowing cooling water on the bore-side of the fibers during sorption to prevent temperature rise associated with the sorption enthalpy. Steam or hot water is flowed through the bores during desorption to desorb CO 2 rapidly. To minimize material transfer between the bore and the fiber wall, a dense Neoprene ® lumen layer is cast on the bore-side of the fiber wall. In this paper, the key sorption step and associated kinetic resistances for the uncooled fibers are examined and evaluated for this portion of the RTSA process. Chopped fibers in a packed bed, as well as fibers assembled into a parallel flow module, have been tested in a simulated flue gas stream. Kinetic limitations in the hollow fiber modules are largely overcome by increasing the superficial gas velocity and the fiber packing in the module-indicating that film diffusion is the controlling mass transfer limitation in the fiber system. The un-cooled fiber modules lose apparent capacity as superficial velocities are increased, likely indicating non-isothermal operation, whereas the actively-cooled fibers in the packed bed maintain apparent capacity at all flowrates studied. © 2011 Elsevier B.V.

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

    International Nuclear Information System (INIS)

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

    2015-01-01

    Highlights: • The objective of the study is to investigate the potential application of a selective EIR for sorption of U(VI) and Th(IV) ions. • The effects of several physiochemical parameters were investigated. • The sorption kinetics and sorption isotherms were used to explain the sorption mechanism. • The thermodynamic studies showed the feasibility of sorption process. • The EIR beads showed a great potential for effective removal of U(VI) and Th(IV) ions. - Abstract: 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

  16. Settlement determination of operating moisture of autoclaved aerated concrete in different climatic zones

    Directory of Open Access Journals (Sweden)

    Pastushkov Pavel Pavlovich

    Full Text Available In the process of operation of buildings the moisture state of enveloping structures materials is changing depending on their construction features, properties of the material, temperature and moisture conditions in the premises, climatic conditions of the construction area. Moisture mode determines the operational properties of the enveloping structures of a building. It directly influences the thermal characteristics of enveloping structure and energy efficiency of the applied materials. The analysis of the methods for calculation of moisture behavior of enclosing structures is carried out. The research relevance of operational moisture of AAC is substantiated. Experimental studies and results of the sorption moisturizing and water vapor permeability of leading marks of aerated concrete are carried out. The authors offer the results of numerical calculations of the moisture behavior of aerated concrete in the walls with mark D400 with facade thermal insulation composite systems - with external plaster layers for different climatic zones of construction.

  17. Moisture in Crawl Spaces

    Science.gov (United States)

    Anton TenWolde; Samuel V. Glass

    2013-01-01

    Crawl space foundations can be designed and built to avoid moisture problems. In this article we provide a brief overview of crawl spaces with emphasis on the physics of moisture. We review trends that have been observed in the research literature and summarize cur-rent recommendations for moisture control in crawl spaces.

  18. A study of sorption of cadmium by goethite in aqueous solution

    Directory of Open Access Journals (Sweden)

    N. Salami

    2002-06-01

    Full Text Available Investigation has been carried out on the potential of a locally sourced goethite for the removal of cadmium ion from aqueous solutions using batch equilibration technique. The maximum uptake of cadmium is 6.4  10-2 mg/g-goethite. The sorption kinetics appears to be rapid as equilibrium was attained within a period of 1 hour. The highest sorption capacity was obtained for particle size with diameter (Φ 0.09 mm. Both infrared spectrophotometric and X-ray diffraction (XRD techniques have also provided evidence for cadmium fixation on to the surface of the goethite. The sorption mechanism appears to follow Langmuir adsorption isotherm model. The Langmuir constants K and Xm (mass of Cd2+ required to form monolayer on the entire surface of the goethite were 0.096 mg/g-goethite and 0.075 mg/g-goethite, respectively.

  19. Effects of sorption and temperature on solute transport in unsaturated steady flow

    International Nuclear Information System (INIS)

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

    1986-01-01

    It is known that temperature affects physical and chemical processes and that these processes may alter the transport of solutes in the environment. Laboratory column studies were performed in unsaturated flow conditions with a composite pulse containing iodide, cobalt, cesium and strontium each at 10 -3 M. The experiments were performed with Bandelier Tuff and produced breakthrough curves that indicate significant changes in transport due to a temperature change from 25 0 C to 5 0 C for nonconservative solutes. Also, the interpretation of the temperature and sorption data suggest that the differences in transport between 5 0 C and 25 0 C for nonconservative solutes may be predicted in a qualitative manner from batch equilibrium and nonequilibrium sorption data and the theory of sorption used in deriving the modified Freundlich isotherm equation. These effects should be of concern in modeling and management of spills and waste disposal within this range of environmental temperatures

  20. Enhanced sorption of radiocobalt from water by Bi(III) modified montmorillonite: A novel adsorbent

    International Nuclear Information System (INIS)

    Guo Zhiqiang; Li Yuan; Zhang Shouwei; Niu Haihong; Chen Zhesheng; Xu Jinzhang

    2011-01-01

    Highlights: → Bi-Mt has higher surface area than Ca-Mt. → The sorption of Co(II) on Bi-Mt is dependent on ionic strength and pH. → The sorption of Co(II) on Bi-Mt is an spontaneous and endothermic process. → Bi-Mt has good practical application potential in wastewater disposal. - Abstract: In this study, Ca-montmorillonite (Ca-Mt) modified with Bi 3+ was used as a novel adsorbent for the sorption of Co(II) from aqueous solutions. The sorption of Co(II) on Bi-montmorillonite (Bi-Mt) was investigated as a function of contact time, pH, ionic strength, adsorbent content, Co(II) concentrations, fulvic acid (FA) and temperature. Compared to Ca-Mt, Bi-Mt showed a higher affinity to bind Co(II) ions. The sorption percentage of Co(II) on Bi-Mt increased with increasing pH at pH 3.0-8.5, and then maintained the high level at pH 8.5-12. The sorption of Co(II) on Bi-Mt was dependent on ionic strength at low pH, and independent of ionic strength at high pH. The presence of FA enhanced Co(II) sorption at low pH, but suppressed Co(II) sorption at high pH. The thermodynamic data derived from temperature dependent sorption isotherms suggested that the sorption of Co(II) on Bi-Mt was spontaneous and endothermic process. Outer-sphere surface complexation and/or ion exchange were the main mechanisms of Co(II) sorption on Bi-Mt at low pH, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. From the experimental results, it is possible to conclude that Bi-Mt is suitable for application of Co(II) removal from aqueous solutions.

  1. Neptunium redox behavior and sorption onto goethite and hematite in the presence of humic acids with different hydroquinone content

    International Nuclear Information System (INIS)

    Khasanova, A.B.; Kalmykov, St.N.; Perminova, I.V.; Clark, S.B.

    2007-01-01

    The effect of humic acids (HA) on neptunium redox behavior and sorption onto hematite, α-Fe 2 O 3 , and goethite, α-FeOOH, colloids was established in batch sorption experiments that were carried out in broad pH interval. The sorption isotherms were provided for two samples of HA: commercial sample of leonardite humic acid and its hydroquinone-enriched derivative obtained using formaldehyde copolycondensation. The distribution of Np fitted the distribution of hydroquinone-enriched HA at low pH values in case of both solids while the influence of parent HA on Np sorption was negligible. This is due to Np(V) reduction upon interaction with hydroquinone-enriched derivative having higher reducing capacity compared to the parent HA. The order of components addition was found to be significant for Np retention

  2. Potential sources for nonlinear sorption of organic compounds to soils and natural solids

    Science.gov (United States)

    Chiou, C. T.

    2003-04-01

    The sorption isotherms of ethylene dibromide (EDB), diuron (DUN), and 3,5-dichlorophenol (DCP) from water to the humic acid and humin fractions of a peat soil have been measured. The data were compared with those of the same solutes on whole peat from which the humic acid (HA) and humin (HM) fractions were derived and on which the sorption of solutes exhibited varying extents of nonlinear capacities at low relative concentrations (Ce/Sw). The HA fraction as prepared by a 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 presumably 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.

  3. Sorption of vanillin on highly basic anion exchanger under static conditions

    Science.gov (United States)

    Sholokhova, A. Yu.; Eliseeva, T. V.; Voronyuk, I. V.

    2017-11-01

    The kinetics of the sorption of vanillin by a granulated anion exchanger is studied under static conditions. A comparison of the kinetic curves of the uptake of hydroxybenzaldehyde by gel and macroporous anion exchanger shows that macroporous sorbent has better kinetic characteristics. The effect temperature has on the capacity of an anion exchanger and the time needed to establish sorption equilibrium is found, and the activation energy of vanillin uptake is determined. Studying the effect experimental factors have on the rate of sorption and using the formal kinetics approach, it is established that in the investigated range of concentrations, the limiting stage of the uptake of vanillin by an anion exchanger with the functional groups of a quaternary ammonium base is that of external diffusion. Vanillin sorption by a highly basic anion exchanger in hydroxyl form is characterized by polymolecular uptake best described by a BET isotherm; at the same time, the uptake of sorbate by a chloride form is of a monomolecular character and can be described by a Freindlich isotherm. Structural changes in the anion exchanger sorbed hydroxybenzaldehyde are identified via FTIR spectroscopy.

  4. Sorption – desorption of imidacloprid insecticide on Indian soils of five different locations

    Directory of Open Access Journals (Sweden)

    Shailendra Singh Chauhan

    2013-07-01

    Full Text Available Sorption-desorption processes govern the movement of all chemicals including pesticides in soils. The present investigation was undertaken to study the sorption-desorption of imidacloprid, using a batch method, on soils of five different location of India. Sorption data were fitted to Freundlich isotherm. The log K value was the highest for loam type soil (1.830 and the lowest for clay type soil (1.661. The value of 1/n was the maximum for silt loam soil (0.909 but minimum for loam soil (0.723. Simple correlation analysis indicated that among soil properties only electrical conductivity showed a higher but marginally non-significant negative correlation with log K (r = -0.826 indicating that higher concentration of solutes solutes are conducive to low sorption capacity of soil. The desorption data conformed to two surfaces Freundlich desorption isotherm. The values of 1/n1' corresponding to easily desorbed fraction of imidacloprid showed significant negative correlation with soil pH (r = -0.886, significant at p ≤0.05 but significant positive correlation with clay content (r = 0.980, significant at p ≤0.01. The desorption index for easily desorbed fraction of imidacloprid (n1’/n also had significant negative correlation with soil pH (r = 0.953, significant at p ≤0.05. From cumulative desorption data, it appeared that bioavailability of imidacloprid would be lower in neutral soil than acidic or alkaline soils.

  5. Atrazine sorption by biochar, tire chips, and steel slag as media for blind inlets: A kinetic and isotherm sorption approach

    Science.gov (United States)

    Surface inlets are installed in subsurface drainage systems to reduce ponding duration and surface runoff, but can contribute to water quality concerns by allowing water to directly enter buried drains. Blind inlets, consist of perforated pipes covered with gravel and are separated from an overlying...

  6. Sorption and Transport of Sildenafil in Natural Soils

    Science.gov (United States)

    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

  7. Europium sorption on zirconia at elevated temperatures: experimental study and modeling

    International Nuclear Information System (INIS)

    Eglizaud, N.; Catalette, H.

    2005-01-01

    Full text of publication follows: Direct disposal of spent nuclear fuel in deep underground repository is being considered by several countries. The waste package maintains an elevated temperature for thousands of years. As sorption is one of the main phenomenon limiting the dispersion of radionuclides in the environment, it has to be studied at elevated temperatures. Zirconia is an oxide produced by cladding oxidation which is suspected in the near field of a nuclear repository. It then could possibly be in contact with waste elements as Europium (III), the sorption of which is therefore studied on zirconia. Experiments were performed by the batch method at a solid/liquid ratio of 10 g.L-1. The sorption edges were recorded in the pH-range from 2 to 10 at 2.10 -5 mol.L -1 Eu(NO 3 ) 3 (I = 0.1 mol.L -1 KNO 3 ). An over-pressure device in an autoclave with an incorporated filtering system allowed the experiments, carbonate free, at 25 deg. C, 50 deg. C, 80 deg. C, 120 deg. C and 150 deg. C and in situ pH measurements. Filtrates were analyzed by the ICP-AES method. Sorption isotherms show an increase in the sorption phenomenon when the temperature raises. The half sorption pH decreases from 7 at 25 deg. C to 3,6 at 150 deg. C. The distribution coefficients that were obtained at elevated temperatures enriched the databases of integrated performance assessment codes. Raw data were modeled with the surface complexation theory using the double layer model (DLM). Several possible surface complexes were examined and discussed, taking into account aqueous hydrolyzed and precipitated species of Europium. A good agreement between experimental values and modeled isotherms was found at all studied temperatures. Results were consistent with a bidentate complex formed by Europium (III) on the zirconia surface. Associated formation constants were then determined with the geochemical computer code CHESS. (authors)

  8. Sorption of Atrazine in Tropical Soil by Biochar Prepared from Cassava Waste

    Directory of Open Access Journals (Sweden)

    Hui Deng

    2014-09-01

    Full Text Available Biochar (BC is a carbonaceous and porous product generated from the incomplete combustion of biomass and has been recognized as an efficient adsorbent. This study evaluated the ability of BC to sorb atrazine pesticide in tropical soil, and explored potential environmental values of BC on mitigating organic micro-pollutants. BC was produced from cassava waste via pyrolyzation under oxygen-limiting conditions at 350, 550, and 750 °C (MS350, MS550, and MS750, respectively. Three biochars were characterized and investigated as sorbents for the removal atrazine from tropical soil. BC pyrolyzed at higher temperatures more quickly reached equilibrium. The pseudo-second-order model perfectly simulated the sorption kinetics for atrazine with the coefficients R2 above 0.996, and the sorption amount at equilibrium (qe was 0.016 mg/g for MS350, 0.025 mg/g for MS550 and 0.050 mg/g for MS750. The isotherms of MS350 displayed relatively linear behavior, whereas the sorption of atrazine on MS550 and MS750 followed a nonlinear isotherm. The sorption data were well described by the Freundlich model with logKF of 0.476 for MS350, 0.771 for MS550, 1.865 for MS750. A thermodynamic study indicated that the sorption of atrazine in BC-added soil was a spontaneous and endothermic process and was primarily controlled by physisorption. In addition, lower pH was conducive to the sorption of atrazine in BC-added soil.

  9. Effect of competing cations on strontium sorption to surficial sediments

    International Nuclear Information System (INIS)

    Bunde, R.L.; Rosentreter, J.J.

    1995-01-01

    The following study was conducted to determine strontium distribution coefficients (K d 'S) of a surficial sediment at the Idaho National Engineering Laboratory (INEL), Idaho. Batch experimental techniques were used to determine K d 's which describe the partitioning of a solute between the solution and solid phase. A surficial sediment was mixed with synthesized aqueous solutions designed to chemically simulate wastewater disposed to infiltrations ponds near the Idaho Chemical Processing Plant at the INEL with respect to major ionic character and pH. The effects of variable concentrations of competing cations (sodium, potassium, calcium and magnesium) on strontium sorption were investigated at a fixed pH of 8.00. The pH of the natural system shows no appreciable variation, whereas a marked variability in cation concentration has been noted. Strontium sorption was impacted to a greater degree by the concentration of calcium and magnesium in solution than by the presence of sodium or potassium. However, extreme sodium solution concentrations of 1.0 to 5.0 g/L dramatically reduced strontium sorption. In all cases, strontium K d 's decreased as the concentration of calcium and magnesium in solution increased. Linear isotherm model K d 's ranged from 12.0 to 84.7 mL/g. Analysis of data from these experiments indicated that moderate concentrations of calcium and magnesium (less than 40 mg/L) and high concentrations of sodium (1.0 to 5.0 g/L) in wastewater increase strontium mobility by decreasing the sorption of strontium on surficial sediments beneath infiltration ponds at the INEL

  10. Sorption behavior of congo red on different plant leaves (abstract)

    International Nuclear Information System (INIS)

    Khan, M.I.; Mirza, M.L.; Zafar, S.; Khalid, N.

    2011-01-01

    Batch adsorption studies were carried out to evaluate the potential of different plant leaves (Bougainvillaea Glabra and Citrus Sinensis) for the removal of Congo red dye from aqueous solution by optimizing different parameters such as effect of shaking time, adsorbent dose, initial adsorbate concentration, temperature etc. The experimental data was subjected to different types of isotherm models such as Freundlich, Langmuir and Dubinin-Radushkevich. The maximum adsorption capacity was calculated and was comparable for both the leaves through Freundlich isotherm by using the optimized parameters of weight and time at room temperature. The sorption mean free energy from Dubinin-Radushkevich isotherm was also determined and compared. Pseudo-first and Pseudo-second order kinetics models were tested for the adsorption of Congo red on plant leaves powder. The experimental data fitted well for Pseudo-second order model. The uptake of Congo red was also studied with the variation of temperature. Thermodynamic parameters have been calculated. The results indicate that the plant leaves of Bougainvilia Glabra and Citrus Sinensis are efficient adsorbents for Congo red dye from aqueous solutions and can be used for wastewater management. (author)

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

    Directory of Open Access Journals (Sweden)

    Shengye Wang

    2016-09-01

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

  12. Effects of oil dispersant on solubilization, sorption and desorption of polycyclic aromatic hydrocarbons in sediment–seawater systems

    International Nuclear Information System (INIS)

    Zhao, Xiao; Gong, Yanyan; O’Reilly, S.E.; Zhao, Dongye

    2015-01-01

    Highlights: • Oil dispersant enhances solubilization of PAHs more effectively than surfactants. • Dispersant and dispersed oil enhance sediment sorption of PAHs and induce hysteresis. • Partitioning to sediment-sorbed dispersant is the mechanism for enhanced PAH uptake. • Dual-mode models well simulate dispersant-facilitated sorption of PAHs on sediment. • Deepwater conditions reduce solubilization of PAHs and lessen dispersant effects. - Abstract: 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

  13. Sorption of carbamazepine by commercial graphene oxides: a comparative study with granular activated carbon and multiwalled carbon nanotubes.

    Science.gov (United States)

    Cai, Nan; Larese-Casanova, Philip

    2014-07-15

    Graphene nanosheet materials represent a potentially new high surface area sorbent for the treatment of endocrine disrupting compounds (EDCs) in water. However, sorption behavior has been reported only for laboratory graphene prepared by a laborious and hazardous graphite exfoliation process. A careful examination of commercially available, clean, high-volume produced graphene materials should reveal whether they are appropriate for sorbent technologies and which physicochemical properties most influence sorption performance. In this study, three commercially available graphene oxide powders of various particle sizes, specific surface areas, and surface chemistries were evaluated for their sorption performance using carbamazepine and nine other EDCs and were compared to that of conventional granular activated carbon (GAC) and multi-walled carbon nanotubes (MWCNTs). Sorption kinetics of carbamazepine on graphene oxide powders was rapid and reversible with alcohol washing, consistent with π-π interactions. The various sorption extents as described by Freundlich isotherms were best explained by available surface area, and only the highest surface area graphene oxide (771 m(2)/g) out-performed GAC and MWCNTs. Increasing pH caused more negative surface charge, a twofold decrease in sorption of anionic ibuprofen, a onefold increase in sorption of cationic atenolol, and no change for neutral carbamazepine, highlighting the role of electrostatic interactions. Copyright © 2014 Elsevier Inc. All rights reserved.

  14. Studies on sorption of cadmium (II) ions onto Haro river sand from aqueous media using radiotracer and voltammetric techniques

    International Nuclear Information System (INIS)

    Ahmed, R.; Hasany, S.M.; Yamin, T.; Ansari, M.S.

    2006-01-01

    Sorption of Cd(II) ions on Haro river sand has been studied using radiotracer technique. The effects of pH and acid concentrations on the sorption were studied. The sorption increases with pH. reaches a maximum at pH 7 and decreases at higher pH values. With acids, it was found that sorption decreases with increasing acid concentration, and for more oxidizing acids sorption was less. Kinetic studies indicate that mostly intra particle diffusion occurs with first order rate constant of 18.45 x 10 -2 min -1 . The sorption data follow the Freundlich and Dubinin-Radushkevich (D-R) isotherms. In addition to the radiotracer method, voltammetric technique was applied and the results by the two techniques are in good agreement. The sorption free energy value indicates that adsorption process is chemisorption. The effect of temperature was studied and values of ΔH, ΔS and ΔG for Cd(II) have been calculated which are 20.15 kJ mol -1 , 74.04 J mol -1 K -1 and -1.754 kJ mol -1 . Adsorption of Cd(II) on Haro river sand is endothermic, spontaneous and entropy driven. The effect of different anions and cations at different concentrations was studied. Levels of cadmium have been monitored in water and sediments. (orig.)

  15. Understand rotating isothermal collapses yet

    International Nuclear Information System (INIS)

    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

  16. Sorption of Ni(II) on GMZ bentonite: effects of pH, ionic strength, foreign ions, humic acid and temperature.

    Science.gov (United States)

    Yang, Shitong; Li, Jiaxing; Lu, Yi; Chen, Yixue; Wang, Xiangke

    2009-09-01

    Bentonite has been widely studied in nuclear waste management because of its special physicochemical properties. In this work, the sorption of Ni(II) from aqueous solution onto GMZ bentonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and temperature was investigated under ambient conditions. The results indicated that the pseudo-second-order rate equation simulated the kinetic sorption process well. The sorption of Ni(II) on GMZ bentonite was strongly dependent on pH and on ionic strength. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na(+)/H(+) on GMZ bentonite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. A positive effect of HA on Ni(II) sorption was found at pH8. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of Ni(II) at three different temperatures: 303.15, 318.15 and 333.15K. The thermodynamic parameters (DeltaH(0), DeltaS(0) and DeltaG(0)) of Ni(II) sorption on GMZ bentonite at the three different temperatures were calculated from the temperature-dependent sorption isotherms. The results indicated that the sorption process of Ni(II) on GMZ bentonite was endothermic and spontaneous. Experimental results indicate that GMZ bentonite is a suitable sorbent for pre-concentration and solidification of Ni(II) from large volume solutions.

  17. Sorption of Ni(II) on GMZ bentonite: Effects of pH, ionic strength, foreign ions, humic acid and temperature

    International Nuclear Information System (INIS)

    Yang Shitong; Li Jiaxing; Lu Yi; Chen Yixue; Wang Xiangke

    2009-01-01

    Bentonite has been widely studied in nuclear waste management because of its special physicochemical properties. In this work, the sorption of Ni(II) from aqueous solution onto GMZ bentonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and temperature was investigated under ambient conditions. The results indicated that the pseudo-second-order rate equation simulated the kinetic sorption process well. The sorption of Ni(II) on GMZ bentonite was strongly dependent on pH and on ionic strength. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na + /H + on GMZ bentonite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. A positive effect of HA on Ni(II) sorption was found at pH 8. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of Ni(II) at three different temperatures: 303.15, 318.15 and 333.15 K. The thermodynamic parameters (ΔH 0 , ΔS 0 and ΔG 0 ) of Ni(II) sorption on GMZ bentonite at the three different temperatures were calculated from the temperature-dependent sorption isotherms. The results indicated that the sorption process of Ni(II) on GMZ bentonite was endothermic and spontaneous. Experimental results indicate that GMZ bentonite is a suitable sorbent for pre-concentration and solidification of Ni(II) from large volume solutions.

  18. Evaluation of sorption distribution coefficient of Cs onto granite using sorption data collected in sorption database and sorption model

    International Nuclear Information System (INIS)

    Nagasaki, S.

    2013-01-01

    Based on the sorption distribution coefficients (K d ) of Cs onto granite collected from the JAERI Sorption Database (SDB), the parameters for a two-site model without the triple-layer structure were optimized. Comparing the experimentally measured K d values of Cs onto Mizunami granite carried out by JAEA with the K d values predicted by the model, the effect of the ionic strength on the K d values of Cs onto granite was evaluated. It was found that K d values could be determined using the content of biotite in granite at a sodium concentration ([Na]) of 1 x 10 -2 to 5 x 10 -1 mol/dm 3 . It was suggested that in high ionic strength solutions, the sorption of Cs onto other minerals such as microcline should also be taken into account. (author)

  19. Evaluation of sorption distribution coefficient of Cs onto granite using sorption data collected in sorption database and sorption model

    Energy Technology Data Exchange (ETDEWEB)

    Nagasaki, S., E-mail: nagasas@mcmaster.ca [McMaster Univ., Hamilton, Ontario (Canada)

    2013-07-01

    Based on the sorption distribution coefficients (K{sub d}) of Cs onto granite collected from the JAERI Sorption Database (SDB), the parameters for a two-site model without the triple-layer structure were optimized. Comparing the experimentally measured K{sub d} values of Cs onto Mizunami granite carried out by JAEA with the K{sub d} values predicted by the model, the effect of the ionic strength on the K{sub d} values of Cs onto granite was evaluated. It was found that K{sub d} values could be determined using the content of biotite in granite at a sodium concentration ([Na]) of 1 x 10{sup -2} to 5 x 10{sup -1} mol/dm{sup 3} . It was suggested that in high ionic strength solutions, the sorption of Cs onto other minerals such as microcline should also be taken into account. (author)

  20. Sorption of the organic cation metoprolol on silica gel from its aqueous solution considering the competition of inorganic cations.

    Science.gov (United States)

    Kutzner, Susann; Schaffer, Mario; Börnick, Hilmar; Licha, Tobias; Worch, Eckhard

    2014-05-01

    Systematic batch experiments with the organic monovalent cation metoprolol as sorbate and the synthetic material silica gel as sorbent were conducted with the aim of characterizing the sorption of organic cations onto charged surfaces. Sorption isotherms for metoprolol (>99% protonated in the tested pH of around 6) in competition with mono- and divalent inorganic cations (Na(+), NH4(+), Ca(2+), and Mg(2+)) were determined in order to assess their influence on cation exchange processes and to identify the role of further sorptive interactions. The obtained sorption isotherms could be described well by an exponential function (Freundlich isotherm model) with consistent exponents (about 0.8). In general, a decreasing sorption of metoprolol with increasing concentrations in inorganic cations was observed. Competing ions of the same valence showed similar effects. A significant sorption affinity of metoprolol with ion type dependent Freundlich coefficients KF,0.77 between 234.42 and 426.58 (L/kg)(0.77) could still be observed even at very high concentrations of competing inorganic cations. Additional column experiments confirm this behavior, which suggests the existence of further relevant interactions beside cation exchange. In subsequent batch experiments, the influence of mixtures with more than one competing ion and the effect of a reduced negative surface charge at a pH below the point of zero charge (pHPZC ≈ 2.5) were also investigated. Finally, the study demonstrates that cation exchange is the most relevant but not the sole mechanism for the sorption of metoprolol on silica gel. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Microcomputerized neutron moisture gauge

    International Nuclear Information System (INIS)

    Liu Shengkang; Mei Yu

    1987-01-01

    A microcomputerized neutron moisture gauge is introduced. This gauge consists of a neutron moisture sensor and instruments. It is developed from the neutron moisture gauge for concrete mixer. A TECH-81 single card microcomputer is used for count, computation and display. It has the function of computing compensated quantity of sand. It can acquire the data from several neutron sensors by the multichanneling sampling, therefore it can measure moisture values of sand in several hoppers simultaneously. The precision of the static state calibration curve is 0.24% wt. The error limits of the dynamic state check is < 0.50% wt

  2. Moisture Transport in Wood

    DEFF Research Database (Denmark)

    Astrup, Thomas; Hansen, Kurt Kielsgaard; Hoffmeyer, Preben

    2005-01-01

    Modelling of moisture transport in wood is of great importance as most mechanical and physical properties of wood depend on moisture content. Moisture transport in porous materials is often described by Ficks second law, but several observations indicate that this does not apply very well to wood....... Recently at the Technical University of Denmark, Department of Civil Engineering, a new model for moisture transport in wood has been developed. The model divides the transport into two phases, namely water vapour in the cell lumens and bound water in the cell walls....

  3. Plutonium-239 sorption and transport on/in unsaturated sediments. Comparison of batch and column experiments for determining sorption coefficients

    International Nuclear Information System (INIS)

    Jinchuan Xie; Jiachun Lu; Xiaohua Zhou; Xuhui Wang; Mei Li; Lili Du; Yueheng Liu; Guoqing Zhou

    2013-01-01

    Sorption (distribution) coefficients of plutonium were most often derived by static batch experiments. However, it is not clear how unsaturated flow conditions including moisture content and pore water velocity change the sorption coefficients. Transport experiments of plutonium through the unsaturated sediments packed into the columns were then performed in order to determine the sorption coefficients (column-K ds ). Static batch experiments were also conducted to obtain batch-K ds and then compare the differences between batch-K ds and column-K ds . The results show that unsaturated flow conditions had no significant effect on column-K ds , and the average column-K d value was 1.74 ± 0.02 m 3 /kg. By comparison, batch-K d values spanned several orders of magnitude, regardless of the specified liquid-solid conditions. Moreover, the batch-K d (22.7 m 3 /kg) at the standard L/S (4 mL/g) recommended by ASTM D 4319 was over an order of magnitude larger than the average column-K d . (author)

  4. Sorption of uranyl species on zircon and zirconia

    International Nuclear Information System (INIS)

    Lomenech, C.; Drot, R.; Simoni, E.; Ehrhardt, J.J.; Mielczarski, J.

    2002-01-01

    The safety of a long-term storage of radioactive waste in deep geological repositories would be strongly affected by the migration properties of radionuclides through the different barriers to the surface of the earth. Since the main process involved in the retention of radioactive ions is their sorption at the water/ mineral interface, a quantitative description of the sorption reactions is needed. Macroscopic data have for a long time been the only source of information used to propose a modelling of sorption equilibria, although they bring no direct information on the nature of the sorbed species; a microscopic structural investigation of the surface complexes is difficult indeed, because of the small amount of matter sorbed. Thus, in this study, parallel to the macroscopic measurements, different complementary spectroscopic techniques have been used in order to determine the nature of the surface species. As the final purpose of such a study is the simulation of the experimental retention data, the precise structural identification of the sorption equilibria will then be very useful to constrain the data simulation code. In this work, we present the results of both macroscopic and microscopic studies of the sorption of uranyl species on zircon and zirconia. The first part of our macroscopic approach was the surface characterisation of the non-sorbed materials by the determination of the specific areas, of the pH of the isoelectric points, and of the sorption site numbers, while the second part aimed at obtaining the sorption isotherms (percentage of sorption versus pH), which was performed using alpha spectrometry, for different uranyl concentrations, media (NaClO 4 or KNO 3 ) and ionic strengths. The spectroscopic identification of the different surface complexes and sorption sites has been carried out using four different spectroscopies. Whereas tune-resolved laser spectro-fluorimetry gave a direct answer concerning the number of surface species (only for a

  5. Behaviors and mechanism of acid dyes sorption onto diethylenetriamine-modified native and enzymatic hydrolysis starch

    International Nuclear Information System (INIS)

    Wang Zuohua; Xiang Bo; Cheng Rumei; Li Yijiu

    2010-01-01

    In this paper, different starches were modified by diethylenetriamine. The native starch reacted with diethylenetriamine giving CAS, whereas the enzymatic hydrolysis starch was modified by diethylenetriamine producing CAES. Adsorption capacities of CAES for four acid dyes, namely, Acid orange 7 (AO7), Acid orange 10 (AO10), Acid green 25 (AG25) and Acid red 18 (AR18) have been determined to be 2.521, 1.242, 1.798 and 1.570 mmol g -1 , respectively. In all cases, CAES has exhibited higher sorption ability than CAS, and the increment for these dyes took the sequence of AO7 (0.944 mmol g -1 ) > AO10 (0.592 mmol g -1 ) > AR18 (0.411 mmol g -1 ) > AG25 (0.047 mmol g -1 ). Sorption kinetics and isotherms analysis showed that these sorption processes were better fitted to pseudo-second-order equation and Langmuir equation. Chemical sorption mechanisms were confirmed by studying the effects of pH, ionic strength and hydrogen bonding. Thermodynamic parameters of these dyes onto CAES and CAS were also observed and it indicated that these sorption processes were exothermic and spontaneous in nature.

  6. Examination of competitive lanthanide sorption onto smectites and its significance in the management of radioactive waste

    Energy Technology Data Exchange (ETDEWEB)

    Galunin, Evgeny [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Alba, Maria D. [Instituto de Ciencia de Materiales de Sevilla, Consejo Superior de Investigaciones Cientificas - Universidad de Sevilla, Av. Americo Vespucio 49, 41092 Sevilla (Spain); Santos, Maria J. [Departamento de Quimica, Universidade Estadual de Londrina, Londrina, PR 86051-990 (Brazil); Abrao, Taufik [Instituto de Ciencia de Materiales de Sevilla, Consejo Superior de Investigaciones Cientificas - Universidad de Sevilla, Av. Americo Vespucio 49, 41092 Sevilla (Spain); Vidal, Miquel, E-mail: miquel.vidal@ub.edu [Departament de Quimica Analitica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2011-02-28

    The competitive effect of La and Lu (analogues of radionuclides appearing in radioactive waste) in the sorption in four smectites was examined. Sorption and desorption distribution coefficients (K{sub d}; K{sub d,des}), and desorption rates (R{sub des}) were determined from batch tests in two media: deionized water and, to consider the influence of cement leachates, 0.02 mol L{sup -1} Ca. The competitive effect was lower when high-affinity sites were available, as in the water medium at the lowest range of initial lanthanide concentration, with high K{sub d} for La and for Lu (5-63 x 10{sup 4} L kg{sup -1}). Lower K{sub d} was measured at higher initial concentrations and in the Ca medium, where Lu showed a stronger competitive effect. This was confirmed by fitting the sorption data to a two-solute Langmuir isotherm. The desorption data indicated that sorption was virtually irreversible for the scenarios with high sorption, with an excellent correlation between K{sub d} and K{sub d,des} (R{sup 2} around 0.9 for the two lanthanides). Assuming that radioactive waste is a mixture of radionuclides, and that Ca ions will be provided by the cement leachates, this would reduce the retention capacity of clay engineered barriers.

  7. Kinetic studies on phosphorus sorption by selected soil amendments for septic tank effluent renovation.

    Science.gov (United States)

    Cheung, K C; Venkitachalam, T H

    2006-01-01

    A systematic kinetic study of phosphorus (P) sorption by various materials in the soil infiltration system of septic tanks was undertaken by following the time course of P sorption by sorbents in contact with various P solutions over periods up to 360 days. Uptake of P seemed to consist of two distinct stages. Initial uptake was very rapid and this phase was completed in 4 days or less. A slower removal stage followed for some materials over many months. Phosphorus sorption during the fast reaction stage appeared to be associated with the soluble Ca content of the materials. The fast reaction of calcareous materials accounted for the bulk (>70%) of the total P removed. Merribrook loamy sand exhibited the highest proportion of P sorption during the slow phase. It should be noted, however, that for solution P concentrations in the range found in typical effluents (approximately 20 mg L(-1)) the fast reaction phase seemed to be responsible for virtually all P removed. None of the six kinetic formulae examined possessed the sophistication and detail needed to portray accurately the time course of P sorption for all the sorbents investigated. The Elovich equation and the kinetic modification of the Freundlich isotherm expression appeared to provide a reasonable fit of the experimental data.

  8. Moisture Absorption of Epoxy Matrix Composites Immersed in Liquids and in Humid Air.

    Science.gov (United States)

    1979-10-01

    Eq. 4). -34- TEMPERATURE, T (K) 165 40 350 300 Neat ResinA / Fit to Data 0\\ 0 o Composite Calculated 0- Data Delasi and Whiteside (1977) 168 AS/3501...moisture ab - sorption characteristics of T300/1034, AS/3501-5 and T300/5208 graphite-epoxy composites. 1) Material immersed in liquid at temperatures 300 to

  9. Water Sorption and Gamma Radiolysis Studies for Uranium Oxides

    Energy Technology Data Exchange (ETDEWEB)

    Icenhour, A.S.

    2002-02-27

    During the development of a standard for the safe, long-term storage of {sup 233}U-containing materials, several areas were identified that needed additional experimental studies. These studies were related to the perceived potential for the radiolytic generation of large pressures or explosive concentrations of gases in storage containers. This report documents the results of studies on the sorption of water by various uranium oxides and on the gamma radiolysis of uranium oxides containing various amounts of sorbed moisture. In all of the experiments, {sup 238}U was used as a surrogate for the {sup 233}U. For the water sorption experiments, uranium oxide samples were prepared and exposed to known levels of humidity to establish the water uptake rate. Subsequently, the amount of water removed was studied by heating samples in a oven at fixed temperatures and by thermogravimetric analysis (TGA)/differential thermal analysis (DTA). It was demonstrated that heating at 650 C adequately removes all moisture from the samples. Uranium-238 oxides were irradiated in a {sup 60}Co source and in the high-gamma-radiation fields provided by spent nuclear fuel elements of the High Flux Isotope Reactor. For hydrated samples of UO{sub 3}, H{sub 2} was the primary gas produced; but the total gas pressure increase reached steady value of about 10 psi. This production appears to be a function of the dose and the amount of water present. Oxygen in the hydrated UO{sub 3} sample atmosphere was typically depleted, and no significant pressure rise was observed. Heat treatment of the UO{sub 3} {center_dot} xH{sub 2}O at 650 C would result in conversion to U{sub 3}O{sub 8} and eliminate the H{sub 2} production. For all of the U{sub 3}O{sub 8} samples loaded in air and irradiated with gamma radiation, a pressure decrease was seen and little, if any, H{sub 2} was produced--even for samples with up to 9 wt % moisture content. Hence, these results demonstrated that the efforts to remove trace

  10. Equilíbrio higroscópico da palma forrageira: relação com a umidade ótima para fermentação sólida Hygroscopic equilibrium of the cactus pear: relation with the optimum moisture for the solid fermentation

    Directory of Open Access Journals (Sweden)

    Lúcia de F. Araújo

    2005-09-01

    Full Text Available No estudo do processo de enriquecimento protéico da palma forrageira (Opuntia ficus-indica Mill através da levedura Saccharomyces cerevisiae em meio semi-sólido, a atividade de água é uma das variáveis que mais afetam não apenas o processo fermentativo mas, também, o armazenamento desse enriquecido; desta forma, o presente trabalho foi realizado com o objetivo de se obter isotermas de dessorção da cactácea palma forrageira, nas temperaturas usuais dos processos das fermentações, 30, 35 e 40 oC, de modo a correlacionar atividade de água e umidade. As isotermas obtidas foram analisadas mediante os modelos de GAB e BET sendo que, em geral, o modelo de GAB foi o que melhor se ajustou aos dados experimentais. A partir das isotermas obtidas, encontraram-se as faixas de umidades adequadas para obtenção das atividades de água recomendadas para o processo fermentativo e durante o armazenamento do enriquecido.In the study of the protein enrichment process of the cactus pear (Opuntia ficus-indica Mill through the yeast Saccharomyces cerevisiae in semi-solid state fermentation, the water activity is one of the variables that most affects the fermentation process as well as the storage. The present work had the objective of obtaining isotherms of sorption of the cactus pear, in the usual temperatures of the fermentations processes, 30, 35 and 40 oC, in order to correlate water activity and moisture content. The obtained isotherms were analyzed by the GAB and BET models, the GAB model being, in general, the one that adjusted better to the experimental data. The isotherms allowed to find appropriate moisture content to obtain the water activities recommended for the fermentation process as well as during the storage of this enriched product.

  11. Improved understanding of tributyltin sorption on natural and biochar-amended sediments.

    Science.gov (United States)

    Xiao, Xiaoyu; Sheng, G Daniel; Qiu, Yuping

    2011-12-01

    A poor understanding of tributyltin (TBT) sorption on sediments has hindered an accurate evaluation of its environmental fate. The present study determined TBT sorption by a freshwater sediment (BH) and a coastal marine sediment (TZ) as influenced by pH, salinity, and biochar (BC) amendment into TZ. The isotherms were essentially linear, with K(OC) values in the range of 10(4) to 10(5) L/kg. Tributyltin sorption at pH 3.56 and 8.00 occurred mainly via partitioning. It reached maxima at pH equal to its pK(a) (=6.25) because of added ion exchange. A salinity increase from 5 to 35 practical salinity units enhanced TBT sorption at pH 3.56 and 8.00 on TZ by approximately 30% and on BH by approximately 80%, ascribed to the salting-out effect that reduced the solubilities of tributyltin hydroxide (TBTOH) and tributyltin chloride (TBTCl). At pH 6.25, the same salinity increase reduced TBT sorption on TZ by approximately 20% but enhanced TBT sorption on BH by approximately 35%. This was attributed to the enhancing role of salting out and the reducing role of metal competition for ion exchange. Tributyltin was two orders of magnitude more effectively sorbed by BC than by total organic carbon of TZ, mainly because of the high level of surface area of the BC. Although BC affinity for TBT may be significantly diminished when present in TZ, it was considered to be the primary contributor to TBT sorption from water. Biochar may thus be used to immobilize TBT in sediment for potential remediation. Copyright © 2011 SETAC.

  12. Behavior of Cs in Grimsel granodiorite. Sorption on main minerals and crushed rock

    Energy Technology Data Exchange (ETDEWEB)

    Muuri, Eveliina; Ikonen, Jussi; Matara-aho, Minja; Voutilainen, Mikko; Siitari-Kauppi, Marja [Helsinki Univ. (Finland). Dept. of Chemistry; Lindberg, Antero [Geological Survey of Finland, Espoo (Finland); Holgersson, Stellan [Chalmers University of Technology, Goeteborg (Sweden). Dept. of Chemical and Biological Engineering, Nuclear Chemistry; Martin, Andrew [Nagra (National Cooperative for the Disposal of Radioactive Waste), Wettingen (Switzerland)

    2016-11-01

    In this study the sorption of cesium was investigated on four different minerals; quartz, plagioclase, potassium feldspar and biotite as well as granodiorite obtained from the Grimsel test site in Switzerland. The experiments were conducted in the presence of the weakly saline Grimsel groundwater simulant by determining the distribution coefficients using batch sorption experiments and PHREEQC-modelling across a large concentration range. In addition, the purity of the minerals was measured by XRD and the specific surface areas by BET method using krypton. The distribution coefficients of cesium were largest on biotite (0.304±0.005 m{sup 3}/kg in 10{sup -8} M). Furthermore, the sorption of cesium on quartz was found to be negligibly small in all investigated concentrations and the sorption of cesium on potassium feldspar and plagioclase showed similar behavior against a concentration isotherm with distribution coefficients of 0.0368±0.0004 m{sup 3}/kg and 0.18±0.04 m{sup 3}/kg in 10{sup -8} M. Finally, cesium sorption behavior on crushed granodiorite followed the trend of one of its most abundant mineral, plagioclase with distribution coefficient values of 0.107±0.003 m{sup 3}/kg in 10{sup -8} M. At low concentrations (<1.0.10{sup -6} M) cesium was sorbed on the frayed edge sites of biotite and once these sites are fully occupied cesium sorbs additionally to the Type II and Planar sites. As a consequence, the sorption of cesium on biotite is decreased at concentrations >1.0.10{sup -6} M. Secondly cesium sorption on potassium feldspar and plagioclase showed similar non-linear behavior with varying concentration. The results were used to assist the interpretation of cesium diffusion process in the 2.5 year in-situ experiment carried out in the underground laboratory at Grimsel test site in Switzerland (2007-2009).

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

    Science.gov (United States)

    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.

  14. p-Nitrophenol, phenol and aniline sorption by organo-clays

    International Nuclear Information System (INIS)

    Ko, C.H.; Fan Chihhao; Chiang, P.N.; Wang, M.K.; Lin, K.C.

    2007-01-01

    The aims of this study were to make use of organo-clays (i.e., Cloisite-10A, Cloisite-15A, Cloisite-30B and Cloisite-93A), to remove p-nitrophenol, phenol and aniline of organic pollutants. The organo-clays were characterized by X-ray diffraction (XRD). Sorption isotherm, kinetic and pH effect of p-nitrophenol, phenol and aniline sorbed by four organo-clays were evaluated. The d-spacings (0 0 1) of the XRD peak of Cloisite-10A, Cloisite-15A, Cloisite-30B and Cloisite-93A are 1.98, 2.76, 1.93 and 2.64 nm, respectively. The d(0 0 1)-spacings of XRD indicated that these p-nitropheno, phenol and aniline could penetrate into the interlayer of clays and expand the d(0 0 1)-spacings. The linear sorption isotherm of constant partition was employed to describe the sorption isotherms of phenols sorbed by organo-clays through hydrophobic-hydrophobic chemical reactions. The parabolic diffusion and power-function of kinetic models were employed to describe properly the kinetic experiments. The rate limiting step of the p-nitrophenol sorption reactions on organo-clays were diffusion-controlled processes (i.e., 15A, 30B, 93A) and chemical-controlled process for 10A organo-clays. The pre-exponential factor of the p-nitrophenol sorbed by four organo-clays showed the trend as follows: 10A > 30B > 93A > 15A. The efficiency of these organo-clays in removing phenol compounds in water treatments merit further study

  15. Predicting the uptake of Cs, Co, Ni, Eu, Th and U on argillaceous rocks using sorption models for illite

    International Nuclear Information System (INIS)

    Marques Fernandes, Maria; Vér, Nóra; Baeyens, Bart

    2015-01-01

    Highlights: • Contaminant retention in argillaceous rocks controlled by sorption on clay minerals. • Cs, Ni, Co, Eu, Th and UO 2 sorption isotherm measurements on Boda and Opalinus Clay. • Boda and Opalinus Clay exhibit different mineralogies and porewater compositions. • Blind predictions using quasi-mechanistic sorption models developed for illite. • Good agreement between measurements and blind predictions. - Abstract: Reliable predictions of radiocontaminant migration are a requirement for the establishment of radioactive waste repositories. Parametrization of the necessary sorption models seems to be, however, extremely challenging given the multi-mineralic composition of the lithosphere. In this study it is shown for two argillaceous rocks – Boda and Opalinus Clay relevant for the Hungarian and Swiss repository concepts, respectively – that this task can be substantially simplified by taking into account only the most sorptive mineral fraction, namely the 2:1 clay minerals illite and illite/smectite mixed layers. Two different models were required to blind predict the sorption isotherms of Cs, Co, Ni, Eu, Th and UO 2 measured on the two clay rock samples in a synthetic porewater. Cs sorption was modelled with the generalised Cs (GCs) sorption model and the sorption of the other cations with the 2site protolysis non electrostatic surface complexation and cation exchange (2SPNE SC/CE) model. The 2SPNE SC/CE model for illite was extended with surface complexation reactions on weak sites for Co, Ni, Eu, UO 2 and on strong sites for Eu-carbonato complexes. Complementary to the sorption measurements and modelling, extended X-ray absorption fine structure (EXAFS) spectroscopy was used to probe the retention mechanism of Ni on illite, Boda and Opalinus Clay at higher loadings. The reliable blind predictions of the selected metal cations, which are representative for monovalent alkaline metals, divalent transition metals, lanthanides, and trivalent

  16. Sorption on inactive repository components

    International Nuclear Information System (INIS)

    Gardiner, M.P.; Smith, A.J.; Williams, S.J.

    1990-11-01

    The near-field of an intermediate level/low level radioactive waste repository will contain significant quantities of iron and steel, Magnox and Zircaloy. Their corrosion products may possess significant sorption capacity for radioelements. The sorption of americium and plutonium onto magnesium hydroxide, zirconium hydroxide, colloidal magnetite and colloidal haematite has been studied under conditions typical of the porewater of a cementitious near-field. R D values ≥ 10 5 m g -1 were measured for both actinides on the oxides and hydroxides. These values are at least as great as those measured on crushed 3:1 Blast Furnace Slag/Ordinary Portland cement. Competitive sorption experiments have shown that sorption onto the corrosion products does not take place in preference to that on the cement or the converse. Magnetite and haematite colloids are positively charged in cement-equilibrated water whilst zirconium hydroxide is negatively charged. Crushed cement was found to be positively charged. Simple experiments show that only a small proportion of haematite colloids is potentially mobile through a column of crushed cement. (author)

  17. Sorption on inactive repository components

    International Nuclear Information System (INIS)

    Gardiner, M.P.; Smith, A.J.; Williams, S.J.

    1990-07-01

    The near-field of an intermediate level/low level radioactive waste repository will contain significant quantities of iron and steel, Magnox and Zircaloy. Their corrosion products may possess significant sorption capacity for radioelements. The sorption of americium and plutonium onto magnesium hydroxide, zirconium hydroxide, colloidal magnetite and colloidal haematite has been studied under conditions typical of the porewater of a cementitious near-field. R D values ≥ 10 5 ml g -1 were measured for both actinides on the oxides and hydroxides. These values are at least as great at those measured on crushed 3:1 Blast Furnace Slag/Ordinary Portland Cement. Competitive sorption experiments have shown that sorption onto the corrosion products does not take place in preference to that on the cement or the converse. Magnetite and haematite colloids are positively charged in cement-equilibrated water whilst zirconium hydroxide is negatively charged. Crushed cement was found to be positively charged. Simple experiments show that only a small proportion of haematite colloids is potentially mobile through a column of crushed cement. (author)

  18. Sorption-desorption of samarium in Febex bentonite

    International Nuclear Information System (INIS)

    Ramirez-Guinart, O.; Rigol, A.; Vidal, M.; Fernandez-Poyatos, P.; Alba, M. D.

    2012-01-01

    Document available in extended abstract form only. The chemical and physical nature of the clay is a key issue in the design of engineered barriers. The FEBEX bentonite is one of the clays candidates to be used in engineered barriers in deep geology repositories (DGR). Here, its performance was tested with respect to the sorption-desorption of samarium, which is a lanthanide that, besides being considered as a natural analogue of actinides, may also be present in high level radioactive waste in the form of the radioactive isotope 151 Sm. FEBEX bentonite was used in this study. This is a di-octahedral smectite, with isomorphic substitutions in tetrahedral and octahedral sheets. Its theoretical cation exchange capacity value is 1500 meq kg -1 . Sorption isotherms were obtained for Sm in the range of initial concentrations of 0.01 and 9 meq l -1 . Tests were carried out in deionized water and in a medium simulating the composition of interstitial water. Sorption tests were performed equilibrating 30 ml of the Sm solution with 0.2 g of clay. After a contact time of 24 hours, supernatants were decanted off after centrifugation. The quantification of the concentration of Sm in the initial and final solutions allowed us to quantify the Sm equilibrium concentration (C eq ), the fraction sorbed in the FEBEX bentonite (C sorb ) and to derive the sorption K d data. Desorption tests were applied to determine the desorption K d and the percentage of Sm reversibly sorbed. Desorption tests were performed with the bentonite residue from the sorption step, under the same experimental conditions, but without Sm. Powder X-ray diffractograms were obtained from 3 to 70 deg. 2θ with a step of 0.05 deg. and a counting time of 3 s. The crystalline phases were identified using the computer program X'Pert HighScore. The morphology of the samples was analyzed by SEM at 20 kV. An EDX system was fitted to the SEM equipment to perform chemical analyses of the samples using a Si/Li detector

  19. Sorption and Transport of Ranitidine in Natural Soils

    Science.gov (United States)

    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

  20. Predicting moisture state of timber members in a continuously varying climate

    DEFF Research Database (Denmark)

    Svensson, Staffan; Turk, Goran; Hozjan, Tomaz

    2011-01-01

    A prerequisite for a sensible estimate of moisture induced stresses in timber members is an accurate prediction of the members’ moisture states during their service life. There are, however, an infinite number of possible moisture states for an arbitrary timber member in a natural varying climate...... the realizations were made, are based on a fully coupled transport model including a model for the influential sorption hysteresis of wood. A format containing required information suitable for assessing the “moisture” action on timber members is proposed. In addition it is illustrated how a model of high...

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

    Science.gov (United States)

    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

  2. Sorption Enhanced Reaction Process (SERP) for production of hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Anand, M.; Hufton, J.; Mayorga, S. [Air Products and Chemicals, Inc., Allentown, PA (United States)] [and others

    1996-10-01

    Sorption Enhanced Reaction Process (SERP) is a novel process that is being developed for the production of lower cost hydrogen by steam-methane reforming (SMR). In this process the reaction of methane with steam is carried out in the presence of an admixture of a catalyst and a selective adsorbent for carbon dioxide. The key consequences of SERP are: (i) reformation reaction is carried out at a significantly lower temperature (300-500{degrees}C) than that in a conventional SMR reactor (800-1100{degrees}C), while achieving the same conversion of methane to hydrogen, (ii) the product hydrogen is obtained at reactor pressure (200-400 psig) and at 98+% purity directly from the reactor (compared to only 70-75% H{sub 2} from conventional SMR reactor), (iii) downstream hydrogen purification step is either eliminated or significantly reduced in size. The first phase of the program has focused on the development of a sorbent for CO{sub 2} which has (a) reversible CO{sub 2} capacity >0.3 mmol/g at low partial pressures of CO{sub 2} (0.1 - 1.0 atm) in the presence of excess steam (pH{sub 2}O/pCO{sub 2}>20) at 400-500{degrees}C and (b) fast sorption-desorption kinetics for CO{sub 2}, at 400-500{degrees}C. Several families of supported sorbents have been identified that meet the target CO{sub 2} capacity. A few of these sorbents have been tested under repeated sorption/desorption cycles and extended exposure to high pressure steam at 400-500{degrees}C. One sorbent has been scaled up to larger quantities (2-3 kg) and tested in the laboratory process equipment for sorption and desorption kinetics of CO{sub 2}. The CO{sub 2}, sorption and desorption kinetics are desirably fast. This was a critical path item for the first phase of the program and now has been successfully demonstrated. A reactor has been designed that will allow nearly isothermal operation for SERP-SMR. This reactor was integrated into an overall process flow diagram for the SERP-SMR process.

  3. Effect of pyrolysis temperature on polycyclic aromatic hydrocarbons toxicity and sorption behaviour of biochars prepared by pyrolysis of paper mill effluent treatment plant sludge.

    Science.gov (United States)

    Devi, Parmila; Saroha, Anil K

    2015-09-01

    The polycyclic aromatic hydrocarbons (PAHs) toxicity and sorption behaviour of biochars prepared from pyrolysis of paper mill effluent treatment plant (ETP) sludge in temperature range 200-700 °C was studied. The sorption behaviour was found to depend on the degree of carbonization where the fractions of carbonized and uncarbonized organic content in the biochar act as an adsorption media and partition media, respectively. The sorption and partition fractions were quantified by isotherm separation method and isotherm parameters were correlated with biochar properties (aromaticity, polarity, surface area, pore volume and ash content). The risk assessment for the 16 priority EPA PAHs present in the biochar matrix was performed and it was found that the concentrations of the PAHs in the biochar were within the permissible limits prescribed by US EPA (except BC400 and BC500 for high molecular weight PAHs). Copyright © 2015 Elsevier Ltd. All rights reserved.

  4. Sorption of tetracycline on organo-montmorillonites

    International Nuclear Information System (INIS)

    Liu, Niu; Wang, Ming-xia; Liu, Ming-ming; Liu, Fan; Weng, Liping; Koopal, Luuk K.; Tan, Wen-feng

    2012-01-01

    Highlights: ► The sorption capacity of tetracycline on Mont. modified with QACs was highly promoted. ► Tetracycline adsorbed on organoclay was affected by the amount and the length of QACs. ► Tetracycline adsorption on organoclay exhibited high pH-dependence below 5. - Abstract: Tetracycline (TC) is a veterinary antibiotic that is frequently detected as pollutant in the environment. Powerful adsorbents are required for removing TC. The present paper compares the TC adsorption capacity of Na-montmorillonite (Na-mont) with six organo-montmorillonites (organo-monts). Three quaternary ammonium cations (QACs) with different alkyl-chain lengths were used as modifiers. Powder X-ray diffraction indicated that the d 001 values of organo-monts increased with increasing the QACs loading and alkyl-chain length. The CECs of the organo-monts were substantially lower than that of Na-mont and decreased with QACs chain length and increased loading. The modeling of the adsorption kinetics revealed that the processes of TC adsorption on the tested samples could be well fitted by the pseudo-second-order equation. The maximum adsorption capacities of TC on the organo-monts (1000–2000 mmol/kg) were considerably higher than that on Na-mont (769 mmol/kg). Both the Langmuir and Freundlich model could fit the adsorption isotherms. The TC adsorption to the organo-monts increase significantly with decreasing the pH below 5.5 because of the electrostatic interaction, and a high QACs loading performed better than a low loading at around pH 3.

  5. Sorption of different phenol derivatives on functionalized macroporous nanocomposite of poly (glycidyl methacrylate-co-ethylene glycol dimethacrylate and acid modified bentonite

    Directory of Open Access Journals (Sweden)

    Marinović Sanja R.

    2014-01-01

    Full Text Available Macroporous nanocomposite of poly (glycidyl methacrylate-co-ethylene glycol dimethacrylate and acid modified bentonite was prepared by radical suspension copolymerization. Nanocomposite was functionalized with diethylene triamine (deta, by ring-opening reaction of the pendant epoxy groups. Functionalization was performed in order to enable phenol derivatives sorption. This new, not sufficiently investigated material, with developed porous structure was denoted CP-SA-deta. In this study, the influence of temperature on 4-nitrophenol (4NP sorption on CP-SA-deta was investigated. The chemisorption was estimated as dominant process since activation energy of sorption of 4NP of 54.8 kJ mol-1 was obtained. After determining the optimal sorption conditions for 4NP, the sorption of 2-nitrophenol (2NP and 2-chloro 4-nitrophenol (2Cl4NP on CP-SA-deta was investigated with respect to pH, initial concentration and contact time. The 2NP sorption was seldom tested, while according to our knowledge, the 2Cl4NP sorption was not investigated. The isotherm data were best fitted with Langmuir model, while the sorption dynamics obeyed the pseudo-second-order kinetic model for all derivatives. [Projekat Ministarstva nauke Republike Srbije, br. III 45001 i br. III 43009

  6. Room temperature isotherms for Mo and Ni

    International Nuclear Information System (INIS)

    Masse, J.L.

    1986-11-01

    Isotherms at room temperature for Mo and Ni are proposed. They are of three types: BIRCH, KEANE and BORN-MIE. The adjustable constants appearing in these isotherms have been determined from experimental quantities at zero pressure. An evaluation of the limit of (δB T /δP) T as P #-> # ∞, where B T is the isothermal bulk modulus, has been also used. These three isotherms obtained for Mo and Ni are compared with isotherms derived from shock-wave data according to the PRIETO's model. There is a good agreement between these and these derived from shock-wave data. The three isotherms proposed for Mo and Ni can be considered as valid until pressures of several B To , where B To is the bulk modulus B T at P = o [fr

  7. Sorption of cobalt in zeolites and natural clays of the clinoptilolite and kaolinite type; Sorcion de cobalto en zeolitas y arcillas naturales del tipo clinoptilolita y caolinita

    Energy Technology Data Exchange (ETDEWEB)

    Davila R, J.I.; Solache R, M. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)

    2006-07-01

    In this work the sorption of cobalt of aqueous solutions in two natural zeolites (clinoptilolite) and a clay (kaolinite) of origin in the center-north region of Mexico is evaluated. The effect of the pH and the time of contact in the process of sorption were evaluated. The cobalt retained in the aluminosilicates was determined by neutron activation analysis. The cobalt sorption in the materials in a range of pH from 4 to 7 does not present significant variations. The studies of reaction kinetics show a very fast sorption in the first 5 hours of contact, reaching the equilibrium in approximately 24 hours. The kinetics of sorption of the cobalt ions was represented better by the Ritchie reaction model modified of second order. The experimental data for the zeolites obtained at ambient temperature and varying the concentration were adjusted to the models of Freundlich, Langmuir and Freundlich-Langmuir isotherms and it was observed that the cobalt sorption it behaves according to the Freundlich isotherm model. (Author)

  8. Moisture buffering capacity of highly absorbing materials

    Energy Technology Data Exchange (ETDEWEB)

    Cerolini, S.; D' Orazio, M.; Stazi, A. [Department of Architecture, Construction and Structures (DACS), Faculty of Engineering, Polytechnic University of Marche, Via Brecce Bianche, 60100 Ancona (Italy); Di Perna, C. [Department of Energetics, Faculty of Engineering, Polytechnic University of Marche, Via Brecce Bianche, 60100 Ancona (Italy)

    2009-02-15

    This research investigates the possibility to use highly absorbing materials to dampen indoor RH% variations. The practical MBV of sodium polyacrylate, cellulose-based material, perlite and gypsum is evaluated for a daily cyclic exposure that alternates high (75%) and low (33%) RH% levels for 8 h and 16 h, respectively. The adjustment velocity to RH% variations and the presence of hysteretic phenomena are also presented. The cellulose-based material proves to be the most suitable for moisture buffering applications. Starting from this material's properties, the effect of thickness, vapour resistance factor ({mu}) and mass surface exchange coefficient (Z{sub v}) on sorption capacity is evaluated by the use of a numerical model. (author)

  9. WATER ADSORPTION AND DESORPTION ISOTHERMS ON MILK POWDER: II. WHOLE MILK

    OpenAIRE

    Edgar M. Soteras; Julio Gil; Paola Yacanto; Silvana Muratona; Clidia Abaca; María G. Sustersic

    2014-01-01

    The aim of this research was the determination of adsorption and desorption isotherms of cow whole milk powder. The experiments have been carried out at 15, 25 and 40 ºC, in ranges of moisture and water activity characteristic of normal conditions in which the processes of drying, packaging and storage are developed. By studying the influence of the temperature on the experimental plots, the isosteric adsorption heat was determined. Experimental data were correlated to the referential model ...

  10. WATER ADSORPTION AND DESORPTION ISOTHERMS ON MILK POWDER: II. WHOLE MILK

    Directory of Open Access Journals (Sweden)

    Edgar M. Soteras

    2014-03-01

    Full Text Available The aim of this research was the determination of adsorption and desorption isotherms of cow whole milk powder. The experiments have been carried out at 15, 25 and 40 ºC, in ranges of moisture and water activity characteristic of normal conditions in which the processes of drying, packaging and storage are developed. By studying the influence of the temperature on the experimental plots, the isosteric adsorption heat was determined. Experimental data were correlated to the referential model of Guggenheim, Anderson and Boer (GAB. For both, adsorption and desorption, a good model fit was observed. The isotherms showed very similar shapes between them and, by comparing adsorption and desorption isotherms, the phenomenon of hysteresis was confirmed.

  11. Inverse method to estimate kinetic degradation parameters of grape anthocyanins in wheat flour under simultaneously changing temperature and moisture.

    Science.gov (United States)

    Lai, K P K; Dolan, K D; Ng, P K W

    2009-06-01

    Thermal and moisture effects on grape anthocyanin degradation were investigated using solid media to simulate processing at temperatures above 100 degrees C. Grape pomace (anthocyanin source) mixed with wheat pastry flour (1: 3, w/w dry basis) was used in both isothermal and nonisothermal experiments by heating the same mixture at 43% (db) initial moisture in steel cells in an oil bath at 80, 105, and 145 degrees C. To determine the effect of moisture on anthocyanin degradation, the grape pomace-wheat flour mixture was heated isothermally at 80 degrees C at constant moisture contents of 10%, 20%, and 43% (db). Anthocyanin degradation followed a pseudo first-order reaction with moisture. Anthocyanins degraded more rapidly with increasing temperature and moisture. The effects of temperature and moisture on the rate constant were modeled according to the Arrhenius and an exponential relationship, respectively. The nonisothermal reaction rate constant and activation energy (mean +/- standard error) were k(80 degrees C, 43% (db) moisture) = 2.81 x 10(-4)+/- 1.1 x 10(-6) s(-1) and DeltaE = 75273 +/- 197 J/g mol, respectively. The moisture parameter for the exponential model was 4.28 (dry basis moisture content)(-1). One possible application of this study is as a tool to predict the loss of anthocyanins in nutraceutical products containing grape pomace. For example, if the process temperature history and moisture history in an extruded snack fortified with grape pomace is known, the percentage anthocyanin loss can be predicted.

  12. Physicochemical characteristics and sorption capacities of heavy metal ions of activated carbons derived by activation with different alkyl phosphate triesters

    Science.gov (United States)

    Wang, Jing; Liu, Hai; Yang, Shaokun; Zhang, Jian; Zhang, Chenglu; Wu, Haiming

    2014-10-01

    Five alkyl phosphate triesters (APTEs), including trimethyl phosphate (TMP), triethyl phosphate (TEP), triisopropyl phosphate (TPP), tributyl phosphate (TBP) and trioctyl phosphate (TOP), were used as activating agents for preparing activated carbons (AC-APTEs) with high surface acidity and metal ion sorption capacity. N2 adsorption/desorption isotherms, surface morphologies, elemental compositions, results of Boehm's titration and sorption capacities of heavy metal ions of the carbons were investigated. AC-APTEs contained much more acidic groups and exhibited much less surface area (phosphoric acid activation. For the AC-APTEs, AC-TOP had the highest surface area (488 m2/g), AC-TMP showed the highest yield (41.1%), and AC-TBP possessed the highest acidic groups (2.695 mmol/g), oxygen content (47.0%) and metal ion sorption capacities (40.1 mg/g for Ni(II) and 53.5 mg/g for Cd(II)). For the carbons, AC-APTEs showed much larger Ni(II) and Cd(II) sorption capacities than AC-PPA, except AC-TPP. The differences of the carbons in the physicochemical and sorption properties suggested surface chemistry of the carbons was the main factor influencing their sorption capacities whereas the pore structure played a secondary role.

  13. Investigating H₂ Sorption in a Fluorinated Metal-Organic Framework with Small Pores Through Molecular Simulation and Inelastic Neutron Scattering.

    Science.gov (United States)

    Forrest, Katherine A; Pham, Tony; Georgiev, Peter A; Pinzan, Florian; Cioce, Christian R; Unruh, Tobias; Eckert, Juergen; Space, Brian

    2015-07-07

    Simulations of H2 sorption were performed in a metal-organic framework (MOF) consisting of Zn(2+) ions coordinated to 1,2,4-triazole and tetrafluoroterephthalate ligands (denoted [Zn(trz)(tftph)] in this work). The simulated H2 sorption isotherms reported in this work are consistent with the experimental data for the state points considered. The experimental H2 isosteric heat of adsorption (Qst) values for this MOF are approximately 8.0 kJ mol(-1) for the considered loading range, which is in the proximity of those determined from simulation. The experimental inelastic neutron scattering (INS) spectra for H2 in [Zn(trz)(tftph)] reveal at least two peaks that occur at low energies, which corresponds to high barriers to rotation for the respective sites. The most favorable sorption site in the MOF was identified from the simulations as sorption in the vicinity of a metal-coordinated H2O molecule, an exposed fluorine atom, and a carboxylate oxygen atom in a confined region in the framework. Secondary sorption was observed between the fluorine atoms of adjacent tetrafluoroterephthalate ligands. The H2 molecule at the primary sorption site in [Zn(trz)(tftph)] exhibits a rotational barrier that exceeds that for most neutral MOFs with open-metal sites according to an empirical phenomenological model, and this was further validated by calculating the rotational potential energy surface for H2 at this site.

  14. Characteristics, kinetics and thermodynamics of Congo Red bio sorption by activated sulfidogenic sludge from an aqueous solution

    International Nuclear Information System (INIS)

    Rasool, K.; Lee, D. S.

    2015-01-01

    The kinetics and thermodynamics of the bio sorption of textile dye Congo Red on anaerobic activated sulfidogenic sludge were examined. The influence of different adsorption parameters such as p H, temperature, contact time and initial dye concentrations on the bio sorption capacity was also investigated. The sulfidogenic sludge showed a maximum bio sorption density of 238.90 mg dye/g cell for Congo Red at an initial dye concentration of 1,000 mg/L, p H 3.5 and 22 C, which is higher than that of many other adsorbents reported in the literature. The bio sorption processes obeyed the Langmuir isotherm and exhibited pseudo-second-order rate kinetics. The thermodynamic parameters indicated the spontaneous and exothermic nature of Congo Red bio sorption. The Fourier transform infrared spectra revealed the dye interaction with the biomass. Scanning electron microscopy showed significant changes in the surface morphology of the sludge after dye bio sorption. These results showed that sulfidogenic sludge biomass is an attractive alternative low-cost bio sorbent for the removal of the dye from aqueous media.

  15. MEASUREMENT AND MODELLING OF SORPTION EQUILIBRIUM CURVE OF WATER ON PA6, PP, HDPE AND PVC BY USING FLORY-HUGGINS MODEL

    Directory of Open Access Journals (Sweden)

    Suherman Suherman

    2012-02-01

    Full Text Available The sorption of water on granular polyamide-6 (PA6, granular polypropylene (PP, and powdery high density polyethylene (HDPE and powdery polyvinyl chloride (PVC were measured using a gravimetric method in a magnetic suspension balance (MSB. The Flory-Huggins model was successfully applied on the sorption equilibrium curve of all investigated polymers. The influence of temperature is low. The value of Flory-Huggins parameters(c of PA6, PVC, PP and HDPE were 1.8, 5.8, 6.3, and 8.1, respectively. The water in PA6 is mainly bound moisture, while in PP, HDPE and PVC it is mainly surface moisture.

  16. Sorption of zinc on synthetic hydroxyapatite from aqueous solution

    International Nuclear Information System (INIS)

    Pivarciova, L.; Rosskopfova, O.; Galambos, M.; Rajec, P.

    2014-01-01

    The sorption of Zn 2+ on synthetic hydroxyapatite was investigated using a batch method and radiotracer technique. This work was aimed to study influence of the contact time, effect of pH and different concentration of Zn 2+ ions in the solution. The percentage of zinc adsorption on HA1 and HA2 was more than 96 % during 1 h for initial Zn 2+ concentration of 1·10 -4 .5·10 -4 and 1·10 -3 mol·dm -3 . The equilibrium time of 2 h was chosen for further experiments. The sorption of zinc on hydroxyapatite was pH independent ranging from 4.5 to 6.5 as a result of buffering properties of hydroxyapatite. The experimental data for adsorption of zinc have been interpreted in the term of Langmuir isotherm and the value of maximum adsorption capacity of zinc on a commercial hydroxyapatite and hydroxyapatite prepared by wet precipitation process was calculated to be 0.437 mmol·g -1 and 0.605 mmol·g -1 , respectively. (authors)

  17. Factors affecting sorption of radiocobalt by river sediments

    International Nuclear Information System (INIS)

    El-Din, M.R.E.; Ramadan, A.B.; Atta, E.R.

    2001-01-01

    Analysis of the principal factors affecting the interaction of radio cobalt with fresh water sediments and their importance for migration of radio cobalt in surface water streams. The uptake percent (U%) of radio cobalt by Ismailia Cannal bottom sediments (ICUBS) have been studied as a function of contact time, ph, competing ion, carrier concentration and natural ligands such as humic acid using batch technique. Mineralogical analyses of the sediment samples were carried out. The amount sorbed per gram sediment, (X/m), increased as the carrier concentration increased from 10 -8 mol. Following a Freundlich type isotherm. The uptake of radio cobalt was found to be affected by changing in the ph of the aqueous phase. Presence of Mg 24 ions as competing cation decreases the sorption of 60 Co. Presence of humic acid shows a slight effect on the sorption of 60 Co. Desorption of the investigated metal ion from the loaded sediment samples was also studied. A mathematical model for the migration of the investigated radioisotope in Ismailia canal water stream was developed to predict the concentrations of cobalt ion at different distances in X-direction

  18. Behavior of Samarium III during the sorption process

    International Nuclear Information System (INIS)

    Ordonez R, E.; Garcia G, N.; Garcia R, G.

    2004-01-01

    In this work the results of the behavior of samarium in solution are presented, in front of a fine powder of zirconium silicate (zircon). For that which is necessary to characterize the zircon, studying the crystallinity, the morphology, the surface area and the isoelectric point. The behavior of samarium in solution is studied by means of the elaboration of isotherm of sorption, using the technique by lots. One observes that to pH values of nearer to the isoelectric point (pH = 7.23) the process of sorption of the samarium begins, reaching a maximum to near pH at 9. The technique of luminescence is used to determine the concentration of the sipped samarium (phosphorescence) and also to make the speciation of the species formed in the surface of the zircon (phosphorescence). The results can be extrapolated with the plutonium when making the modeling of the migration of alpha emitting coming from the repositories of radioactive waste since both they have similar chemical properties (they are homologous). (Author)

  19. Effect of humic substances on P sorption capacity of three different soils

    Science.gov (United States)

    Delgado, Antonio

    2010-05-01

    Organic matter decreases P sorption by soils. It has been demonstrated the effect of low molecular weight compounds decreasing P adsorption on active surfaces and the effect of humic and fulvic acids inhibiting the precipitation of hydroxyapatite and favouring the formation of more soluble phosphates. This contributes to increase the recovery of applied P fertilizer. The objective of this work was to study the effect of 4 different humic substances (commercially available and provided by Tradecorp Internacional S.A.) on the sorption capacity of three soils differing widely in chemical properties (two calcareous from south Spain, pH 8 and 8.5, and other acidic from Brazil, pH 5.9 and 50 % of exchangeable basic cations). To this end, sorption isotherms were performed at a soil:0.01 M CaCl2 ratio of 1:10 at 6, 30 and 90 days. 2.5 mg of humic substances per g of soil were added to the solution. Data were fitted to the best model and linearized sorption curves for each humic substance were compared with the linearized sorption curve for the control without humic substances application (intersection point and slopes). Soil from Brazil showed a much higher sorption capacity (400 mg P kg-1 soil sorbed at 1 mg L-1 of P in the solution at 1 day) than the other two soils (50 and 100 mg P kg-1). Slow reactions significantly contributed to P sorption in the three soils, amounts sorbed at 90 days being twice than those sorbed at 1 day. Two of the products increased P sorption in the soil from Brazil at 1 day. At 90 days all the products increased P sorption significantly. This increased P sorption can be only explained by metal complexation by the substances applied, which may result in organo-metallic compounds with a high P sorption capacity. This effect was independent of the proportion of humic and fulvic acids in the applied products because the amounts of metal complexed by these compouds depend on the amount of functional groups to coordinate with metals. In the Spanish

  20. Cesium and strontium sorption by selected tropical and subtropical soils around nuclear facilities

    International Nuclear Information System (INIS)

    Chiang, P.N.; Wang, M. K.; Huang, P.M.; Wang, J.J.; Chiu, C.Y.

    2010-01-01

    The dynamics of Cs and Sr sorption by soils, especially in the subtropics and tropics, as influenced by soil components are not fully understood. The rates and capacities of Cs and Sr sorption by selected subtropical and tropical soils in Taiwan were investigated to facilitate our understanding of the transformation and dynamics of Cs and Sr in soils developed under highly weathering intensity. The Langmuir isotherms and kinetic rates of Cs and Sr sorption on the Ap1 and Bt1 horizons of the Long-Tan (Lt) and the A and Bt1 horizons of the Kuan-Shan (Kt), Mao-Lin (Tml) and Chi-Lo (Cl) soils were selected for this study. Air-dried soil ( -5 to 1.88 x 10 -3 M of CsCl (pH 4.0) or 1.14 x 10 -4 to 2.85 x 10 -3 M of SrCl 2 (pH 4.0) solutions at 25 deg. C. The sorption maximum capacity (q m ) of Cs by the Ap1 and Bt1 horizons of the Lt soil (62.24 and 70.70 mmol Cs kg -1 soil) were significantly (p -1 soil in Kt soil and 34.83 and 29.96 mmol Cs kg -1 soil in Cl soil, respectively), however, the sorption maximum capacity values of the Lt and Tml soils did not show significant differences. The amounts of pyrophosphate extractable Fe (Fe p ) were correlated significantly with the Cs and Sr sorption capacities (for Cs sorption, r 2 = 0.97, p -4 ; for Sr sorption, r 2 = 0.82, p -3 ). The partition coefficient of radiocesium sorbed on soil showed the following order: Cl soil >> Kt soil > Tml soil > Lt soil. It was due to clay minerals. The second-order kinetic model was applied to the Cs and Sr sorption data. The rate constant of Cs or Sr sorption on the four soils was substantiality increased with increasing temperature. This is attributable to the availability of more energy for bond breaking and bond formation brought about by the higher temperatures. The rate constant of Cs sorption at 308 K was 1.39-2.09 times higher than that at 278 K in the four soils. The activation energy of Cs and Sr sorbed by the four soils ranged from 7.2 to 16.7 kJ mol -1 and from 15.2 to 22.4 kJ mol

  1. Sorption of Pb(II) from aqueous solution by konjac glucomannan beads

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Konjac glucomannan beads have been investigated as metal biosorbent for Pb(II) from aqueous solu-tions. The effect of contact time, solution pH, initial metal concentration, and desorption were studied in batch experiments at 20℃±2℃. Maximum mental sorption was found to occur at initial pH 4.0―5.5. Kinetic studies revealed that the initial uptake was rapid and equilibrium was established in 3 h and that the data followed the prseudo-second order reaction. The equilibrium sorption data at initial pH 4.0 were described by the Langmuir and Freundlich isotherm models; however, Langmuir isotherm model has been found to provide the best correlation. The highest value of Langmuir maximum uptake (qmax) was found to be 105.71 mg·g-1. Similar Freundlich empirical constant (KF) was obtained to be 1.98 for lead. Adsorption-complexation may be involved in the sorption process of lead. Desorption experi- ments showed evidence that after two contacts neither HCl nor EDTA solutions were able to desorb lead from the konjac glucomannan beads, but the desorbtion efficacy of HCl solution was higher than EDTA solution. The results obtained show that konjac glucomannan beads may be used for the treat-ment of wastewater contaminated with lead.

  2. Sorption of uranium anionic species from aqueous solutions on HDTMA-bentonite Jelsovy potok

    International Nuclear Information System (INIS)

    Krajnak, A.; Viglasova, E.; Galambos, M.; Rosskopfova, O.

    2014-01-01

    Bentonite deposit Jelsovy potok in Slovakia has great potential for use as a engineering barrier in the multi-barrier system of deep geological repository. In this paper, HDTMA-modified bentonite J15m from Slovak bentonite Jelsovy potok was prepared and its sorption properties (sorption isotherms, kinetics) towards anionic uranium species was investigated. The removal of uranium anionic species from aqueous solutions (initial concentration: 10-1,000 mg/L) by J15m was studied in the absence of background electrolytes at initial pH range (pH init ) 8.5; 9.5; 10.5. The amount of the sorbed U was determined spectrophotometrically using the Arsenazo III method. The maximum uptake capacity observed was 31.35 (mg/g) at 298 K. Experimental results were analysed by the Langmuir, Freundlich Dubinin-Redushkevich and Tempkin isotherm. The kinetics of adsorption of U(VI) ions was also discussed using the pseudo-first-order and the pseudo-second-order at three different temperatures. The activation energy of the sorption for J15m was calculated as 23.534 kJ·mol -1 . (authors)

  3. Sorption study of methylene blue on activated carbon prepared from Jatropha curcas and Terminalia catappa seed coats

    Directory of Open Access Journals (Sweden)

    Ismaila Olalekan Saheed

    2016-12-01

    Full Text Available This research work targets the effectiveness of the prepared activated carbon from Jatropha curcas and Terminalia catappa seed coats for the sorption of methylene blue (MB from aqueous solution. The prepared Jatropha activated carbon (JAC and Terminalia activated carbon (TAC were characterised using Fourier transform infrared spectroscopy (FTIR, Scanning electron microscopy (SEM and Branauer- Emmett-Teller (BET surface area analysis. Effect of initial concentration, pH, contact time, adsorbent dose and temperature on the sorption experiments were studied and the adsorption capacity of these adsorbents were found to be 37.84 mg/g and 17.44 mg/g for methylene blue uptake by JAC and TAC respectively. The experimental data were analysed using Langmuir, Fruendlich, and Dubinin-Radushkevich isotherms. The data fitted best into Langmuir isotherm for Methylene blue-JAC and Methylene blue-TAC systems. The kinetic studies fitted into pseudo second order kinetics model. The process chemistry was exothermic.

  4. DETERMINATION OF THE ISOSTERIC HEAT TO PLANTAIN PULP (musa paradisiaca BY SORPTION ISOTHERMS

    Directory of Open Access Journals (Sweden)

    HÉCTOR CIRO

    2008-01-01

    Full Text Available Las isotermas de sorción para ser usadas en la simulación y diseño de procesos de secado y almacenamiento de alimentos deben ser representadas por modelos válidos dentro de las condiciones encontradas en la práctica industrial. Usando el modelo de Chung-Pfost y ajustado por desorción el calor isostérico neto y totalpara pulpa de plátano fueron determinados. El calor neto isotérico neto decreció con el contenido de humedad del producto variando desde 1670 kJ/kg (5%.d.b a 215 kJ/kg (26%.d.b donde esta variación fue representada por el modelo potencial y polinomial.

  5. Prediction of clay content from water vapour sorption isotherms considering hysteresis and soil organic matter content

    DEFF Research Database (Denmark)

    Arthur, E.; Tuller, M.; Møldrup, Per

    2015-01-01

    Soil texture, in particular the clay fraction, governs numerous environmental, agricultural and engineering soil processes. Traditional measurement methods for clay content are laborious and impractical for large-scale soil surveys. Consequently, clay prediction models that are based on water...... within a RH range from 3 to 93%. The clay contents, which ranged between 1 and 56%, were measured with a combination of sieving and sedimentation methods. Two regression models were developed for both adsorption and desorption at 10 RH levels (5, 10, 20, 30, 40, 50, 60, 70, 80 and 90%). While the first...

  6. Lunar ash flows - Isothermal approximation.

    Science.gov (United States)

    Pai, S. I.; Hsieh, T.; O'Keefe, J. A.

    1972-01-01

    Suggestion of the ash flow mechanism as one of the major processes required to account for some features of lunar soil. First the observational background and the gardening hypothesis are reviewed, and the shortcomings of the gardening hypothesis are shown. Then a general description of the lunar ash flow is given, and a simple mathematical model of the isothermal lunar ash flow is worked out with numerical examples to show the differences between the lunar and the terrestrial ash flow. The important parameters of the ash flow process are isolated and analyzed. It appears that the lunar surface layer in the maria is not a residual mantle rock (regolith) but a series of ash flows due, at least in part, to great meteorite impacts. The possibility of a volcanic contribution is not excluded. Some further analytic research on lunar ash flows is recommended.

  7. Instabilities of isothermal liquid films

    International Nuclear Information System (INIS)

    Solesio, J.N.

    1977-04-01

    The integral forms of the mass and linear momentum balances are given for a two-phase flow system with surface tension and without material surface properties. The instantaneous local laws for each phase and the jump conditions for the interface are derived from these balance laws. Then, these laws are systematically simplified by means of dimensional analysis for an isothermal liquid film flowing down a plane. The stability studies of films are critically reviewed. The different methods are divided into two groups: the first one deals with the global approach, the second one with the perturbation theory. This group includes a new technique based upon the method of quadrature by differentiation. Finally, the different methods are compared [fr

  8. an intermediate moisture meat

    African Journals Online (AJOL)

    STORAGESEVER

    2008-07-04

    Jul 4, 2008 ... traditional SM muscle without compromising quality. ... technique is intermediate moisture food processing. ... Traditionally, most tsire suya producers use ..... quality of Chinese purebred and European X Chinese crossbred ...

  9. CPC Soil Moisture

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The monthly data set consists of a file containing 1/2 degree monthly averaged soil moisture water height equivalents for the globe from 1948 onwards. Values are...

  10. Response to the comments of Y. S. Ho to the paper 'Sorption of radionickel to goethite. Effect of water quality parameters and temperature'

    International Nuclear Information System (INIS)

    Baowei Hu; ShaoXing University, ShaoXing, Zhejiang; Wen Cheng; Hui Zhang; Guodong Sheng; Chinese Academy of Sciences, Hefei

    2011-01-01

    In our published paper entitled 'Sorption of radionickel to goethite: effect of water quality parameters and temperature' published in JRNC 285 (2010) 389-398 [1], the sorption of radionickel to goethite as affected by various environmental conditions such as pH, humic substances, ionic strength and temperature on radionickel sorption has been investigated by using batch technique. The sorption mechanism of radionickel on goethite was discussed according to the experimental data and the fitting results of sorption isotherms by Langmuir, Freundlich and D-R models. Kinetic sorption data was fitted by a pseudo-second-order rate equation. Ho et al. firstly reported the pseudo-second-order rate equation [2, 3], and then further developed this frame work in their following works [4, 5]. In our previous research, we had ever cited the original paper about the sorption isotherms such as Langmuir or Freundlich models. However, the reviewers gave the comments that the models had been widely used and it was not necessary for us to cite the original paper about the sorption isotherm. Similar condition can be also observed for carbon nanotubes that there are a lot of papers about carbon nanotubes not citing the original paper reported by Iijima [6]. In our published paper [1], we think that the pseudo-second-order rate equation has been widely applied and the equation is now a famous model to fit the sorption kinetic data. However, it is essential for us to cite all the relative references accurately so as to transmit scientific knowledge more effectively. We are so sorry to the fact that the original papers [2, 3] were not cited in our published paper [1], but it is not meant to show the disrespect to the author Ho [2]. In our future work, we wish to cite the papers published by Ho whose work are interesting and useful to simulate the sorption kinetic data of metal ions at solid-water interfaces. The physicochemical behavior of radionickel in environment is quite important to

  11. Buffer moisture protection system

    International Nuclear Information System (INIS)

    Ritola, J.; Peura, J.

    2013-11-01

    With the present knowledge, bentonite blocks have to be protected from the air relative humidity and from any moisture leakages in the environment that might cause swelling of the bentonite blocks during the 'open' installation phase before backfilling. The purpose of this work was to design the structural reference solution both for the bottom of the deposition hole and for the buffer moisture protection and dewatering system with their integrated equipment needed in the deposition hole. This report describes the Posiva's reference solution for the buffer moisture protection system and the bottom plate on basis of the demands and functional requirements set by long-term safety. The reference solution with structural details has been developed in research work made 2010-2011. The structural solution of the moisture protection system has not yet been tested in practice. On the bottom of the deposition hole a copper plate which protects the lowest bentonite block from the gathered water is installed straight to machined and even rock surface. The moisture protection sheet made of EPDM rubber is attached to the copper plate with an inflatable seal. The upper part of the moisture protection sheet is fixed to the collar structures of the lid which protects the deposition hole in the disposal tunnel. The main function of the moisture protection sheet is to protect bentonite blocks from the leaking water and from the influence of the air humidity at their installation stage. The leaking water is controlled by the dewatering and alarm system which has been integrated into the moisture protection liner. (orig.)

  12. FLUORIDE SORPTION USING MORRINGA INDICA-BASED ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    G. Karthikeyan, S. Siva Ilango

    2007-01-01

    Full Text Available Batch adsorption experiments using activated carbon prepared from Morringa Indica bark were conducted to remove fluoride from aqueous solution. A minimum contact time of 25 min was required for optimum fluoride removal. The influence of adsorbent, dose, pH, co-ions (cations and anions on fluoride removal by the activated carbon has been experimentally verified. The adsorption of fluoride was studied at 30 C, 40 C and 50 C. The kinetics of adsorption and adsorption isotherms at different temperatures were studied. The fluoride adsorption obeyed both Langmuir and Freundlich isotherms and followed a pseudo first order kinetic model. The thermodynamic studies revealed that the fluoride adsorption by Morringa Indica is an endothermic process indicating an increase in sorption rate at higher temperatures. The negative values of G indicate the spontaneity of adsorption. SEM and XRD studies confirmed the surface morphological characteristics of the adsorbent and the deposition of fluoride on the surface of the material.

  13. Theoretical analysis of moisture transport in wood as an open porous hygroscopic material

    DEFF Research Database (Denmark)

    Hozjan, Tomaz; Svensson, Staffan

    2010-01-01

    Moisture transport in an open porous hygroscopic material such as wood is a complex system of coupled processes. For seasoned wood in natural climate three fully coupled processes active in the moisture transport are readily identified: (1) diffusion of vapor in pores; (2) phase change from one...... state to another, also called moisture sorption; and (3) diffusion of bound water in wood tissue (in the cell wall). A mathematical model for predicting moisture transport in wood for a given condition must at least consider the dominating active processes simultaneously to be considered accurate...... of the three processes on the outcome of the coupled model. Least significant is the bound water diffusion. Based on the results from the sensitivity analyses, a simplified model for moisture transport in wood is proposed....

  14. Sorption studies of Sn(II) and Zr(IV) on pistachio shell from different aqueous media

    International Nuclear Information System (INIS)

    Abdel-Fattah, A.A.; EI-Khouly, S.H.

    2007-01-01

    Sorption of Sn(lI) and Zr(IV) on pistachio shell as a solid sorbent material of particle sizes (0.5-1 mm) has been investigated from HNO 3 , H CI, HBr, NaNO 3 , Na CI, KBr and KI aqueous solutions. Before use, this substance was subjected to characterization tools including surface area, thermogravimetric analysis, infrared spectroscopy and X-R diffraction. The effect of contact time, weight of the resin, acid and salt concentrations and equilibrium ph on K d values have been studied. Sorption of both elements was found to verify Freundlich adsorption isotherm. The effect of temperature on thc sorption processes have been investigated and the thermodynamic functions δG, δH and δS have been determined. Adsorption processes have been discussed in the light of the obtained results

  15. Sorption studies of Sn(II) and Zr(IV) on pistachio shell from different aqueous media

    Energy Technology Data Exchange (ETDEWEB)

    Abdel-Fattah, A A [Nuclear Chemistry Dept., Atomic Energy Authority, Cairo (Egypt); EI-Khouly, S H [Radioisotopes and Generators Dept., Radioisotopes Prod. Division, Hot Lahoratories Center, Atomic Energy Authority, Cairo (Egypt)

    2007-07-01

    Sorption of Sn(lI) and Zr(IV) on pistachio shell as a solid sorbent material of particle sizes (0.5-1 mm) has been investigated from HNO{sub 3}, H CI, HBr, NaNO{sub 3}, Na CI, KBr and KI aqueous solutions. Before use, this substance was subjected to characterization tools including surface area, thermogravimetric analysis, infrared spectroscopy and X-R diffraction. The effect of contact time, weight of the resin, acid and salt concentrations and equilibrium ph on K{sub d} values have been studied. Sorption of both elements was found to verify Freundlich adsorption isotherm. The effect of temperature on thc sorption processes have been investigated and the thermodynamic functions {delta}G, {delta}H and {delta}S have been determined. Adsorption processes have been discussed in the light of the obtained results.

  16. Sorption Energy Maps of Clay Mineral Surfaces

    International Nuclear Information System (INIS)

    Cygan, Randall T.; Kirkpatrick, R. James

    1999-01-01

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

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

    Directory of Open Access Journals (Sweden)

    Fawwaz I. Khalili

    2013-01-01

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

  18. Sorption of cesium and strontium from concentrated brines by backfill barrier materials

    International Nuclear Information System (INIS)

    Winslow, C.D.

    1981-03-01

    The sorption of radionuclides from potentially intruding groundwater at a nuclear waste repository is a major chemical function of backfill barriers. In this study, various materials (including clays, zeolites and an inorganic ion exchanger) were screened for the sorption of the fission products cesium and strontium in concentrated brines. Representative brines A and B for the Waste Isolation Pilot Plant (WIPP), a proposed radioactive waste repository and test facility in bedded salt were used. Sorption properties were quantified using empirical distribution coefficients, k/sub d/. Of the materials examined, sodium titanate had the highest k/sub d/ for the sorption of Sr(II) in both brine A (k/sub d/ = 125 ml/g) and brine B(k/sub d/ = 500 to 600 ml/g). A mordenite-type zeolite was the most effective getter for Cs(I) in brine A (k/sub d = 27 ml/g), while illite yielded the highest k/sub d/ for Cs(I) in brine B (k/sub d/ = 115 ml/g). The relative merit of these k/sub d/ values is evaluated in terms of calculated estimates of breakthrough times for a backfill barrier containing the getter. Results show that a backfill mixture containing these getters is potentially an effective barrier to the migration of Sr(II) and Cs(I), although further study (especially for the sorption of cesium from brine A) is recommended. Initial mechanistic studies revealed competing ion effects which would support an ion exchange mechanism. K/sub d/'s were constant over a Sr(II) concentration range of 10 -11 to 10 -5 M and a Cs(I) concentration range of 10 -8 to 10 -5 M, supporting the choice of a linear sorption isotherm as a model for the results. Constant batch composition was shown to be attained within one week

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

    International Nuclear Information System (INIS)

    Stephens, J.A.

    1997-07-01

    Laboratory measurements of the sorption and desorption of 134 Cs and 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 134 Cs and 85 Sr were used to trace the sorption properties of the main contaminants found in the reservoir which are 137 Cs and 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 3 for 134 Cs after 60 d and (1 ± 0.2) x 10 3 for 85 Sr after 7 d at pH ∼ 6 and slurry ratio of 1:1000 g/ml. The K d for 134 Cs ranged from 2 x 10 2 to 3 x 10 4 depending on pH and conductivity. The 85 Sr reached equilibrium in a few days, while 134 Cs reached an apparent equilibrium in 1--2 months. The K d for 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 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 134 Cs to Par Pond sediments under homogeneous laboratory conditions

  20. Cadmium removal by bioclastic granules (Lithothamnium calcareum): batch and fixed-bed column systems sorption studies.

    Science.gov (United States)

    Veneu, Diego Macedo; Schneider, Claudio Luiz; de Mello Monte, Marisa Bezerra; Cunha, Osvaldo Galvão Caldas; Yokoyama, Lídia

    2017-06-19

    The potential of Bioclastic Granules - BG (calcium-carbonate-based material) using the algae Lithothamnium calcareum as sorbent for the removal of Cd(II) from aqueous solutions by sorption was evaluated through batch and continuous systems tests using a fixed-bed column. Sorption process variables, in particular pH (2-7), particle size (<38-300 μm), initial BG concentration (0.1-1.0 g L -1 ), initial Cd(II) concentrations (5-400 mg L -1 ) and contact time (5-240 min), were evaluated. Adsorption isotherm profiles of Cd(II) per BG were similar to an L-type, or Langmuir type, with the adsorption forming a monolayer of approximately 0.61 μm, with a q max of 188.74 mg g -1 and k L of 0.710 L mg -1 . Thomas's model considers that sorption is not limited to a chemical reaction but is controlled by mass transfer at the interface. In the present study, the obtained value of k Th was 0.895 mL h -1  mg -1 , reaching a sorption capacity q o of 124.4 mg g -1 . For the Yoon-Nelson model, it was possible to obtain two important parameters to describe the behavior of the column, the rate constant (k YN ), obtaining a value of 0.09 h -1 and an τ of 82.12 h corresponding to the time required for sorption to occur of 50% of the solute in the rupture curve. X-ray diffraction and scanning electron microscopy analyses coupled to the X-ray dispersive energy system (SEM/EDS) of the BG after the Cd(II) ion sorption tests evidenced the formation of crystals with the prevalence of a new mineral phase (otavite).

  1. Sorption and reduction of selenite on chlorite surfaces in the presence of Fe(II) ions.

    Science.gov (United States)

    Baik, Min Hoon; Lee, Seung Yeop; Jeong, Jongtae

    2013-12-01

    The sorption and reduction of selenite on chlorite surfaces in the presence of Fe(II) ions were investigated as a function of pH, Se(IV) concentration, and Fe(II) concentration under an anoxic condition. The sorption of Se(IV) onto chlorite surfaces followed the Langmuir isotherm regardless of the presence of Fe(II) ions in the solution. The Se(IV) sorption was observed to be very low at all pH values when the solution was Fe(II)-free or the concentration of Fe(II) ions was as low as 0.5 mg/L. However, the Se(IV) sorption was enhanced at a pH > 6.5 when the Fe(II) concentration was higher than 5 mg/L because of the increased sorption of Fe(II) onto the chlorite surfaces. XANES (X-ray absorption near edge structure) spectra of the Se K-edge showed that most of the sorbed Se(IV) was reduced to Se(0) by Fe(II) sorbed onto the chlorite surfaces, especially at pH > 9. The combined results of field-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) also showed that elemental selenium and goethite were formed and precipitated on the chlorite surfaces during the sorption of selenite. Consequently it can be concluded that Se(IV) can be reduced to Se(0) in the presence of Fe(II) ions by the surface catalytic oxidation of Fe(II) into Fe(III) and the formation of goethite at neutral and particularly alkaline conditions. Thus the mobility of selenite in groundwater is expected to be reduced by the presence of a relatively higher concentration of Fe(II) in subsurface environments. Copyright © 2013 Elsevier Ltd. All rights reserved.

  2. Sorption of caesium and strontium onto calcium silicate hydrate in saline groundwater

    International Nuclear Information System (INIS)

    Sugiyama, D.; Fujita, T.

    2005-01-01

    Full text of publication follows: In the concept for radioactive waste disposal in Japan, cement is a potential waste packaging and backfilling material and is expected to provide chemical containment. The sorption of radionuclides onto cement materials, which controls the aqueous concentrations of elements in the pore-water, is a very important parameter when considering the release of radionuclides from the near field of a cementitious radioactive waste repository. Many safety assessment calculations currently assume radionuclide retardation as linear sorption equilibrium and describe it with a distribution ratio (R d value). In this study, the sorption mechanism is discussed by measuring the sorption isotherm of caesium, strontium (10 -5 ∼ 10 -2 mol dm -3 ) and sodium (10 -4 ∼ 10 -1 mol dm -3 ) onto Calcium Silicate Hydrate (C-S-H gel, Ca/Si 0.65 ∼ 1.2) at a liquid:solid ratio of 100:1, to support the assumption. In addition, the competitive sorption between caesium or strontium, and sodium is studied by sorption measurements using a range of sodium chloride concentration to simulate different ionic strengths in saline groundwater. The initial and equilibrated aqueous compositions were measured in the sorption experiments and it was found that caesium, strontium and sodium were sorbed by substitution for Ca in C-S-H phases by examining the mass balance. Based on the experimental results, we propose a modelling approach in which the ion-exchange model is employed and the presence of some calcium sites with different ion-exchange log K values in C-S-H is assumed by considering the composition and the structure of C-S-H. The modelling calculation results predict the measured Rd values well and also describe the competition of sorption of caesium or strontium, and sodium in the experiments. The log K values for sorption of each cation element decreased as Ca/Si ratio of C-S-H gel increased. This agrees with the trend that C-S-H gel is negatively charged at low

  3. Sorption Behavior of Dye Compounds onto Natural Sediment of Qinghe River.

    Science.gov (United States)

    Liu, Ruixia; Liu, Xingmin; Tang, Hongxiao; Su, Yongbo

    2001-07-15

    The objective of this study is to assess the adsorption behavior of C.I. Basic Yellow X-5GL, C.I. Basic Red 13, C.I. Direct Blue 86, C.I. Vat Yellow 2, and C.I. Mordant Black 11 on natural sediment and to identify sediment characteristics that play a predominant role in the adsorption of the dyes. The potentiometric titration experiment is used to investigate acid-base properties of the sediment surface with a constant capacitance surface complexation model. The parameters controlling the sorption such as solution pH and ion strength, as well as the influence of organic carbon and Ca(2+) ion on the adsorption, are evaluated. It is shown that the titration data can be successfully described by the surface protonation and deprotonation model with the least-squares FITEQL program 2.0. The sorption isotherm data are fitted to the Freundlich equation in a nonlinear form (1/n=0.3-0.9) for all tested dyes. With increasing pH value, the sorption of C.I. Mordant Black 11 and C.I. Direct Blue 86 on the sediment decreases, while for C.I. Basic Yellow X-5GL and C.I. Basic Red 13, the extent of sorption slightly increases. In addition, ion strength also exhibits a considerably different effect on the sorption behavior of these dye compounds. The addition of Ca(2+) can greatly reduce the sorption of C.I. Basic Red 13 on the sediment surface, while it enhances the sorption of C.I. Direct Blue 6. The removal of organic carbon decreases the sorption of C.I. Mordant Black 11 and C.I. Direct Blue 86. In contrast, the sorption of C.I. Basic Red 13 and C.I. Basic Yellow X-5GL is obviously enhanced after the removal of organic carbon. The differences in adsorption behavior are mainly attributed to the physicochemical properties of these dye compounds. Copyright 2001 Academic Press.

  4. Fluoride ions sorption of the water using natural and modified hematite with aluminium hydroxide

    International Nuclear Information System (INIS)

    Teutli S, E. A.

    2011-01-01

    sorbent, increased when using from 0.02 to 0.14 g of hematite. The results showed that the Elovich model described the process of sorption kinetics, and Langmuir, Freundlich and Langmuir-Freundlich models the sorption isotherm. These results indicated that the mechanism of sorption was the chemisorption. Also, desorption studies were carried out, and it was observed that the fluoride ions can be removed from the modified hematite using NaCl or NaOH solutions, desorption was more efficient using NaOH solution. (Author)

  5. Sorption of a branched nonylphenol isomer and perfluorooctanoic acid on geosorbents and carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Li, Chengliang

    2011-10-13

    As metabolites of organic surfactants, both nonylphenol (NP) and perfluorooctanoic acid (PFOA) are toxic and ubiquitous in the environment. Their sorption on soils and sediments is of importance for their fate and transport in the environment. Especially in China, there is still a lack of consolidated knowledge on the sorption behavior of NP and PFOA on geosorbents such as Yangtze River sediments. Thus, the present thesis investigates the sorption of a branched NP isomer [4-(1-ethyl-1, 3-dimethylpentyl) phenol] (NP111) and PFOA on Yangtze River sediments and their model components, i.e. a clay mineral (illite), metal oxides (goethite and {delta}-Al{sub 2}O{sub 3}) and organic matter (isolated from Yangtze River sediments and commercial organic matter) by both batch and dialysis techniques. NP111 is the most environmentally relevant NP isomer and its fate in the environment is unknown. Because PFOA is weakly adsorbed on geosorbents, multi-walled carbon nanotubes (MWCNTs) were studied as promising adsorbents. One of the MWCNTs studied contained traces of metal catalyst on the outer surface. Sorption isotherms of NP111 and PFOA on the sediments and their model components were fitted well by the Freundlich model. Sorption of NP111 on the sediments depended largely on their organic carbon content, resulting in organic carbon-normalized sorption coefficient (K{sub OC}) values between 6.3 x 10{sup 3} and 1.1 x 10{sup 4} L kg{sup -1}. The sorption of NP111 on {delta}-Al{sub 2}O{sub 3} and illite was comparable to that on sediments, but significantly lower than that on goethite. In contrast, the sorption of PFOA on the sediments was significantly lower. The affinity of PFOA to goethite and {delta}-Al{sub 2}O{sub 3} was slightly higher than to the sediments, but it was negligible to natural organic matter and illite. The results suggest that the organic carbon content of the sediments plays a dominant role in the sorption of NP111, whereas goethite acts as a potential sink

  6. Applicability of microautoradiography to sorption studies

    International Nuclear Information System (INIS)

    Thompson, J.L.; Wolfsberg, K.

    1979-01-01

    The technique of microautoradiography was applied to the study of the sorption of uranium and americium on five rock types which exist at the Nevada Test Site. It was found that autoradiograms could be prepared in a few days which would allow the specific minerals responsible for sorption to be identified. Furthermore, the state of aggregation of the sorbed species was clearly indicated. It was concluded that microautoradiography was a useful adjunct to currently used methods for studying sorption of certain radionuclides

  7. THERMODYNAMICS AND ADSORPTION ISOTHERMS FOR THE ...

    African Journals Online (AJOL)

    BAFFA

    data were tested using Freundlich and Langmuir adsorption isotherms. The values of the numeric constants ... Keywords: Adsorbate, Adsorbent, Adsorption isotherms, Maize cob, Thermodynamics. INTRODUCTION. Maize (Zea mays) ... several times with water, air – dried and ground to. 850μm particle size and finally kept ...

  8. Sorption Behavior of CO2 and CH4 of Glassy Polymeric Membranes and Analytical Discussion of Partial Immobilization Model

    Directory of Open Access Journals (Sweden)

    M. Mahdavian

    2007-06-01

    Full Text Available Among various reported membrane-based gas separation processes, the best explanation is generally achieved by the solution-diffusion model. The main factors in this model are the solubility and diffusivity of permeationcomponents through the membrane. The prediction of permeability and diffusivity in multicomponent gas permeation as well as the separation evaluation equilibrium and kinetic interactions requires a proper explanation of sorption and diffusion phenomena in the polymer matrix. Investigation made by various researchers in this area shows that the equilibrium interaction (sorption step plays the key role in determining diffusion and permeation in multicomponent system. Therefore, the proper description of sorption behaviour of gas mixture in the polymer is an essential task. The dual-mode sorption (Langmuir-Henry is usually used for the description of equilibrium isotherm of gases in glassy polymers based on this model; the diffusive behaviour of the system is subsequently analyzed by the partial immobilization model. In this study, the equilibrium sorption of CO2/CH4 mixture in various polymers was modelled using the experimental data available in the literature. The differences in the mechanism of adsorption for CO2 and CH4 were analyzed by considering variations in mode of sorption for each adsorbed component at different pressures. By introducing a new adsorption parameter, P50/50, (the pressure at which the portion of two modes in sorption are equal the contribution of each adsorbed component in occupying Langmuir sites was evaluated. The results indicate that the relative significance of sorption mode for each component is a function of pressure and it is different for various polymers.

  9. Preparation of pure TiO2 sorption material

    International Nuclear Information System (INIS)

    Špendlíková, Irena; Raindl, Jakub; Němec, Mojmír

    2013-01-01

    procedure with respect to the sorption properties of the resulting material towards uranium. Therefore, an organic compound, tetrabutylorthotitanate, was used for the preparation of a series of titanium dioxide samples. The conditions of the preparation procedure slightly varied (e.g. different washing solutions - ethanol, acetone or both) but the important steps like sample drying remain unchanged. One of the aspects which should be considered in the preparation of TiO 2 -based absorbers is the fact that the sorption properties of titanium dioxide strongly depend on the crystal structure and their capacities increase in order: rutile 2 : 1 N 2 at the temperature of 77 K. Sorption capacities for uranium were deduced from their sorption isotherms determined with fixed uranium concentration (20 mmol.L -1 ) and variable values of V/m (10 - 1400 mL.g -1 ). Based on this characterization, the most promising material has been chosen. In the future study, this material will be prepared in larger quantity using 'uranium free' water and used for the uranium concentration from environmental samples and for the consecutive determination of 236 u/ 238 U ratios using Accelerator Mass Spectrometry which will outline the contamination with anthropogenic 236 U and/or its natural abundance. (author)

  10. Water activity reduction of intermediate moisture yellowstrip trevally (Selaroides leptolepis

    Directory of Open Access Journals (Sweden)

    Phomajun, P.

    2005-05-01

    Full Text Available Water activity reduction of intermediate moisture yellowstrip trevally was studied. The optimal time (8, 12, 16, 20 hrs. for curing marinade was investigated. The effects of different humectants (glycerol, sorbitol, lactitol, glucose syrup at 50% w/w of curing ingredients were compared. Results showed that moisture content and water activity of cured yellowstrip trevally decreased as curing time increased (p0.05. However, the hardness of intermediate moisture Yellowstrip trevally, determined by texture analyzer, decreased. Hardness, shear force, L a b value of sample added with various humectants were lower than those of the control (p0.05. The glycerol-added samples had the highest overall acceptability score and were higher than control, whereas the glucose syrup-added samples had the lowest score. Moisture content of the samples with the addition of various humectants was higher than that of the control (18.28 %. The samples added with glycerol retained the highest moisture (24.94%. The adsorption isotherm studies showed that the equilibrium moisture of sample added with glycerol was higher than that added with lactitol.

  11. A simplified model of saltcake moisture distribution. Letter report

    International Nuclear Information System (INIS)