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Sample records for adsorption isotherm determined

  1. Determination of Differential Enthalpy and Isotherm by Adsorption Calorimetry

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    V. Garcia-Cuello

    2008-01-01

    Full Text Available An adsorption microcalorimeter for the simultaneous determination of the differential heat of adsorption and the adsorption isotherm for gas-solid systems are designed, built, and tested. For this purpose, a Calvet heat-conducting microcalorimeter is developed and is connected to a gas volumetric unit built in stainless steel to record adsorption isotherms. The microcalorimeter is electrically calibrated to establish its sensitivity and reproducibility, obtaining K=154.34±0.23 WV−1. The adsorption microcalorimeter is used to obtain adsorption isotherms and the corresponding differential heats for the adsorption of CO2 on a reference solid, such as a NaZSM-5 type zeolite. Results for the behavior of this system are compared with those obtained with commercial equipment and with other studies in the literature.

  2. The adsorption characteristics and porous structure of bentonite adsorbents as determined from the adsorption isotherms of benzene vapor

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    LEPA STOJANOVSKA

    2004-02-01

    Full Text Available The adsorption of benzene vapor on natural and acid activated bentonites was treated by the theory of volume filling of micropores. The micropore volume and characteristic values of the free energy of adsorption were determined from the adsorption isotherms. The Dubinin–Radushkevish–Stoeckli and Dubinin–Astakhov equations were used for this purpose. The results showed that natural bentonite has a more homogeneous micropore structure than the acid activated ones. The characteristic values of the free energy of adsorption for the natural bentonite were higher than those of the acid activated bentonite. This is due to differences in its structure and the pore size.

  3. A new apparatus for the determination of adsorption isotherms and adsorption enthalpies on microporous and meso-porous media

    International Nuclear Information System (INIS)

    A specific thermostated experimental device comprising a differential heat flow calorimeter coupled with a home built manometric system has been built for the simultaneous determination of adsorption isotherms and adsorption enthalpies. The differential heat flow calorimeter is a Tian Calvet Setaram C80 model which measures the heat flux of a gas and can be operated isothermally, the manometric system is a stainless steel homemade apparatus. This coupled apparatus allows measurements for pressure up to 2.5 MPa and temperature up to 423.15 K. On the one hand, the apparatus and the experimental procedures are described. On the second hand the reliability and reproducibility were established by measuring adsorption isotherms on a benchmark (Filtrasorb F400) at 318.15 K. The gravimetric method has been used at higher pressure at various temperatures. These devices allowed us to study the adsorption of supercritical fluid (nitrogen N2, methane CH4, carbon dioxide CO2) in activated carbons and microporous or meso-porous silica. The adsorption of methane on a rock of type (TGR) was also studied. These experimental results are used for the study of the interactions fluid / solid that must be taken into account in molecular simulations or DFT theory. (author)

  4. Predicting heavy metals' adsorption edges and adsorption isotherms on MnO2 with the parameters determined from Langmuir kinetics

    Institute of Scientific and Technical Information of China (English)

    Qinghai Hu; Zhongjin Xiao; Xinmei Xiong; Gongming Zhou; Xiaohong Guan

    2015-01-01

    Although surface complexation models have been widely used to describe the adsorption of heavy metals,few studies have verified the feasibility of modeling the adsorption kinetics,edge,and isotherm data with one pH-independent parameter.A close inspection of the derivation process of Langrnuir isotherm revealed that the equilibrium constant derived from the Langmuir kinetic model,Ks-kinetic,is theoretically equivalent to the adsorption constant in Langrnuir isotherm,Ks-Langmuir.The modified Langmuir kinetic model (MLK model) and modified Langmuir isotherm model (MLI model) incorporating pH factor were developed.The MLK model was employed to simulate the adsorption kinetics of Cu(Ⅱ),Co(Ⅱ),Cd(Ⅱ),Zn(Ⅱ) and Ni(Ⅱ) on MnO2 at pH 3.2 or 3.3 to get the values of Ks-kinetic.The adsorption edges of heavy metals could be modeled with the modified metal partitioning model (MMP model),and the values of Ks-Langrnuir were obtained.The values of Ks-kinetic and Ks-Langrnuir are very close to each other,validating that the constants obtained by these two methods are basically the same.The MMP model with Ks-kinetic constants could predict the adsorption edges of heavy metals on MnO2 very well at different adsorbent/adsorbate concentrations.Moreover,the adsorption isotherms of heavy metals on MnO2 at various pH levels could be predicted reasonably well by the MLI model with the Ks-kinetic constants.

  5. Modeling of Experimental Adsorption Isotherm Data

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    Xunjun Chen

    2015-01-01

    Full Text Available Adsorption is considered to be one of the most effective technologies widely used in global environmental protection areas. Modeling of experimental adsorption isotherm data is an essential way for predicting the mechanisms of adsorption, which will lead to an improvement in the area of adsorption science. In this paper, we employed three isotherm models, namely: Langmuir, Freundlich, and Dubinin-Radushkevich to correlate four sets of experimental adsorption isotherm data, which were obtained by batch tests in lab. The linearized and non-linearized isotherm models were compared and discussed. In order to determine the best fit isotherm model, the correlation coefficient (r2 and standard errors (S.E. for each parameter were used to evaluate the data. The modeling results showed that non-linear Langmuir model could fit the data better than others, with relatively higher r2 values and smaller S.E. The linear Langmuir model had the highest value of r2, however, the maximum adsorption capacities estimated from linear Langmuir model were deviated from the experimental data.

  6. Adsorption Isotherms and Surface Reaction Kinetics

    Science.gov (United States)

    Lobo, L. S.; Bernardo, C. A.

    1974-01-01

    Explains an error that occurs in calculating the conditions for a maximum value of a rate expression for a bimolecular reaction. The rate expression is derived using the Langmuir adsorption isotherm to relate gas pressures and corresponding surface coverages. (GS)

  7. Adsorption isotherm special study. Final report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    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.

  8. Adsorption isotherm special study. Final report

    International Nuclear Information System (INIS)

    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

  9. The Calculation of Adsorption Isotherms from Chromatographic Peak Shapes

    Science.gov (United States)

    Neumann, M. G.

    1976-01-01

    Discusses the relationship between adsorption isotherms and elution peak shapes in gas chromatography, and describes a laboratory experiment which involves the adsorption of hexane, cyclohexane, and benzene on alumina at different temperatures. (MLH)

  10. Kinetics and isotherms of Neutral Red adsorption on peanut husk.

    Science.gov (United States)

    Han, Runping; Han, Pan; Cai, Zhaohui; Zhao, Zhenhui; Tang, Mingsheng

    2008-01-01

    Adsorption of Neutral Red (NR) onto peanut husk in aqueous solutions was investigated at 295 K. Experiments were carried out as function of pH, adsorbent dosage, contact time, and initial concentration. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, and Toth isotherm models. The results indicated that the Toth and Langmuir models provided the best correlation of the experimental data. The adsorption capacity of peanut husk for the removal of NR was determined with the Langmuir and found to be 37.5 mg/g at 295 K. The adsorption kinetic data were modeled using the pseudo-first order, pseudo-second order, and intra-particle diffusion kinetic equations. It was seen that the pseudo-first order and pseudo-second order kinetic equations could describe the adsorption kinetics. The intraparticle diffusion model was also used to express the adsorption process at the two-step stage. It was implied that peanut husk may be suitable as adsorbent material for adsorption of NR from aqueous solutions. PMID:19143308

  11. Kinetics and isotherms of Neutral Red adsorption on peanut husk

    Institute of Scientific and Technical Information of China (English)

    HAN Runping; HAN Pan; CAI Zhaohui; ZHAO Zhenhui; TANG Mingsheng

    2008-01-01

    Adsorption of Neutral Red (NR) onto peanut husk in aqueous solutions was investigated at 295 K. Experiments were carded out as function of pH, adsorbent dosage, contact time, and initial concentration. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, and Toth isotherm models. The results indicated that the Toth and Langmuir models provided the best correlation of the experimental data. The adsorption capacity of peanut husk for the removal of NR was determined with the Langmuir and found to be 37.5 mg/g at 295 K. The adsorption kinetic data were modeled using the pseudo-first order, pseudo-second order, and intra-particle diffusion kinetic equations. It was seen that the pseudo-first order and pseudo-second order kinetic equations could describe the adsorption kinetics. The intraparticle diffusion model was also used to express the adsorption process at the two-step stage. It was implied that peanut husk may be suitable as adsorbent material for adsorption of NR from aqueous solutions.

  12. Improved Isotherm Data for Adsorption of Methane on Activated Carbons

    KAUST Repository

    Loh, Wai Soong

    2010-08-12

    This article presents the adsorption isotherms of methane onto two different types of activated carbons, namely, Maxsorb III and ACF (A-20) at temperatures from (5 to 75) °C and pressures up to 2.5 MPa. The volumetric technique has been employed to measure the adsorption isotherms. The experimental results presented herein demonstrate the improved accuracy of the uptake values compared with previous measurement techniques for similar adsorbate-adsorbent combinations. The results are analyzed with various adsorption isotherm models. The heat of adsorption, which is concentration and temperature dependent, has been calculated from the measured isotherm data. Henry\\'s law coefficients for these adsorbent-methane pairs are also evaluated at various temperatures. © 2010 American Chemical Society.

  13. Characterizing Nitrogen adsorption and desorption isotherms in soils using multifractal analysis

    Science.gov (United States)

    Paz Ferreiro, Jorge; Miranda, José G. V.; Vidal Vázquez, Eva

    2010-05-01

    The specific surface area is an attribute known to characterize the soil ability to retain and transport nutrients and water. A number of studies have shown that specific surface area correlates cation exchange capacity, organic matter content, water retention, aggregate stability and clay swelling. In the past fractal theory has been widely used to study different gas adsorption isotherms like water vapour and nitrogen adsorption isotherms. More recently we have shown that nitrogen adsorption isotherms showed multifractal nature. In this work, both N2 adsorption and desorption isotherms measured in a Mollisol were examined as a probability measure using the multifractal formalism in order to determinate its possible multifractal behaviour. Soil samples were collected in two different series of an Argiudoll located in the north of Buenos Aires and in the south of Santa Fe provinces, Argentina. Two treatments of each soil series were sampled at three depths, without replication, resulting in six samples per soil series and a total of twelve samples analyzed. Multifractal analysis was performed using the box counting method. Both, the N2 adsorption and desorption isotherms exhibited a well defined scaling behaviour indicating a fully developed multifractal structure of each isotherm branch. The singularity spectra and Rényi dimension spectra obtained for adsorption and also for desorption isotherms had shapes similar to the spectra of multifractal measures and several parameters were extracted from these spectra. The capacity dimension, D0, for both N2 adsorption and desorption data sets were not significantly different from 1.00. However, nitrogen adsorption and desorption data showed significantly different values of entropy dimension, D1, and correlation dimension, D2. For instance, entropy dimension values extracted from multifractal spectra of adsorption isotherms were on average 0.578 and varied from 0.501 to 0.666. In contrast, the corresponding figures for

  14. Derivation of the Freundlich Adsorption Isotherm from Kinetics

    Science.gov (United States)

    Skopp, Joseph

    2009-01-01

    The Freundlich adsorption isotherm is a useful description of adsorption phenomena. It is frequently presented as an empirical equation with little theoretical basis. In fact, a variety of derivations exist. Here a new derivation is presented using the concepts of fractal reaction kinetics. This derivation provides an alternative basis for…

  15. Adsorption isotherms of water on mica: redistribution and film growth.

    Science.gov (United States)

    Malani, Ateeque; Ayappa, K G

    2009-01-29

    Adsorption isotherms of water on muscovite mica are obtained using grand canonical Monte Carlo simulations over a wide range of relative vapor pressures, p/p(0) at 298 K. Three distinct stages are observed in the adsorption isotherm. A sharp rise in the water coverage occurs for 0 Clays Clay Miner. 2006 , 54 , 402 ), over the entire range of pressures investigated. Both SPC and extended simple point charge (SPC/E) water models were found to yield qualitatively similar adsorption and structural characteristics, with the SPC/E model predicting lower coverages than the SPC model for p/p(0) > 0.7. PMID:19123830

  16. Determinación de la adsorción de cadmio mediante isotermas de adsorción en suelos agrícolas venezolanos Determination of the adsorption of cadmium by adsorption isotherms in agricultural soils venezuelans

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    Nereida Sánchez

    2011-04-01

    Full Text Available El cadmio es un metal pesado que tiende a acumularse en la superficie del suelo. En los últimos años, las actividades antropogénicas han ocasionado un incremento en los niveles de este metal en suelos agrícolas generando gran preocupación ambiental debido a su movilidad y lixiviación en el perfil del suelo y a la facilidad con que es absorbido por las plantas. El objetivo de este trabajo fue determinar la capacidad de adsorción de cadmio, de cuatro suelos venezolanos de uso agrícola con diferencias texturales. Para determinar la capacidad de adsorción del metal en cada suelo, inicialmente se determinó el tiempo óptimo de agitación; el cual fue de 2 horas y la relación suelo-solución enriquecedora de Cd; la cual fue de 1:50. Con estos parámetros se elaboraron las isotermas de adsorción para los suelos y se compararon los modelos de Freundlich y Langmuir. Los resultados mostraron que el modelo matemático de Freundlich es el que mejor describe la cinética de la reacción y la capacidad de adsorción de Cd por los suelos, siendo los que poseen mayores contenidos de arcilla, MO y pH ácidos los de mayor capacidad de adsorción.Cadmium is a heavy metal which tends to accumulate in the soil surface. In recent years, anthropogenic activities have caused an increase of the levels of this metal in agricultural soils causing great environmental concern due to their mobility and leaching in the soil profile and the ease way to be absorbed by plants. The purpose of this study was to determine the adsorption capacity of cadmium in four Venezuelan agricultural soils with different texture. To determine the adsorption capacity of Cd in each soil, first of all the optimal time of stirring was determined, which was two hours and the soilenriching solution of Cd, which was (1/50. With these parameters, cadmium adsorption isotherms for all soils were developed and compared with Freundlich and Langmuir models. The data showed that the Freundlich

  17. WATER ADSORPTION AND DESORPTION ISOTHERMS ON MILK POWDER: II. WHOLE MILK

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    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.

  18. Adsorption Isotherms of CH 4 on Activated Carbon from Indonesian Low Grade Coal

    KAUST Repository

    Martin, Awaludin

    2011-03-10

    This article presents an experimental approach for the determination of the adsorption isotherms of methane on activated carbon that is essential for methane storage purposes. The experiments incorporated a constant-volume- variable-pressure (CVVP) apparatus, and two types of activated carbon have been investigated, namely, activated carbon derived from the low rank coal of the East of Kalimantan, Indonesia, and a Carbotech activated carbon. The isotherm results which cover temperatures from (300 to 318) K and pressures up to 3.5 MPa are analyzed using the Langmuir, Tóth, and Dubinin-Astakhov (D-A) isotherm models. The heat of adsorption for the single component methane-activated carbon system, which is concentration- and temperature-dependent, is determined from the measured isotherm data. © 2011 American Chemical Society.

  19. Adsorption kinetics and isotherms of zeolite coatings directly crystallized on fibrous plates for heat pump applications

    International Nuclear Information System (INIS)

    Zeolite A coatings were grown on porous fibrous metal plates by using the substrate heating synthesis method. The coatings prepared were characterized by X-ray diffraction (XRD) and laser microscopy. Kinetic measurements were performed to determine the rates of adsorption of these materials while their adsorption isotherms were obtained by thermogravimetry (TG). The overall adsorption kinetics varied with the different samples investigated. The zeolite A coating grown on a copper fibrous support generally exhibited superior overall adsorption kinetics compared to a zeolite X coating with close mass, prepared previously on a stainless steel flat plate. The coating thickness as well as the support properties affected the performances of the samples. The inclusion of an additional polymer layer exhibited adverse impact on the kinetics especially after relatively high normalized loadings. The adsorption isotherms obtained for the zeolite coatings on fibrous supports were quite typical for zeolite A while the addition of polymer changed the isotherm type. -- Highlights: • Thick zeolite A coatings were grown on fibrous metal plates. • Use of fibrous supports improved heat transfer quality. • Coating thickness influenced adsorption kinetics notably. • Inclusion of an additional polymer layer changed kinetics and isotherm type

  20. Adsorption of Reactive Black 5 on Synthesized Titanium Dioxide Nanoparticles: Equilibrium Isotherm and Kinetic Studies

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    Majeed A. Shaheed

    2014-01-01

    Full Text Available The synthesized titanium dioxide nanoparticles (TiO2-NPs were used as adsorbent to remove reactive black 5 (RB 5 in aqueous solution. Various factors affecting adsorption of RB 5 aqueous solutions such as pH, initial concentration, contact time, dose of nanoparticles, and temperature were analyzed at fixed solid/solution ratio. Langmuir and Freundlich isotherms were used as model adsorption equilibrium data. Langmuir isotherm was found to be the most adequate model. The pseudo-first-order, pseudo-second-order, and intraparticle diffusion models were used to describe the adsorption kinetics. The experimental data was fitted to pseudo-second-order kinetics. The thermodynamic parameters such as Gibbs-free energy, enthalpy, and entropy changes were determined. These parameters indicated the endothermic and spontaneity nature of the adsorption. The results demonstrated the fact that the TiO2-NPs are promising adsorbent for the removal of RB 5 from aqueous solutions.

  1. MOISTURE ADSORPTION ISOTHERMS IN YELLOW PITAHAYA (Selenicereusmegalanthus

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    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. Estimating Uranium Partition Coefficients from Laboratory Adsorption Isotherms

    International Nuclear Information System (INIS)

    An estimated 330 metric tons of uranium have been buried in the radioactive waste Subsurface Disposal Area (SDA) at the Idaho National Engineering and Environmental Laboratory (INEEL). An assessment of uranium transport parameters is being performed to decrease the uncertainty in risk and dose predictions derived from computer simulations of uranium fate and transport to the underlying Snake River Plain Aquifer. Uranium adsorption isotherms have been measured in the laboratory and fit with a Freundlich isotherm. The Freundlich n parameter was statistically identical for 14 sediment samples. The Freundlich Kf for seven samples, where material properties have been measured, is correlated to sediment surface area. Based on these empirical observations, a model has been derived for adsorption of uranium on INEEL sedimentary materials using surface complexation theory. The model was then used to predict the range of adsorption conditions to be expected at the SDA. Adsorption in the deep vadose zone is predicted to be stronger than in near-surface sediments because the total dissolved carbonate decreases with depth

  3. Adsorption isotherm of uranyl ions by fish scales of corvina

    International Nuclear Information System (INIS)

    Fish scale is by-product of fishery. The scales are mainly formed by hydroxyapatite and collagen forming a kind of natural composite with a large specific surface area that intensifies the adsorption process. In this paper the potential of adsorption of scales of Corvina fish for uranyl ions from nitric solutions was studied. The scales were washed several times with faucet water, sun-dried, triturated and sieved. Equilibrium and kinetic studies in adsorption of uranyl ions in batch systems were carried out at room temperature. Equilibrium time was reached at 5 min for 0.1 g L-1 uranyl solution with removal efficiency over 82%, and at 1 min of contact was observed about 60% of removal. The equilibrium isotherm was obtained and the Langmuir model fitted best. These preliminary results are very promising, showing great perspectives of application of the fish scales as biosorbent for uranyl ions in radioactive wastewater treatment processes with a sustainable technology. (author)

  4. Adsorption isotherm of uranyl ions by fish scales of corvina

    Energy Technology Data Exchange (ETDEWEB)

    Costa, Caroline Hastenreiter; Santos, Bruno Zolotareff dos; Yamamura, Amanda Pongeluppe Gualberto; Yamaura, Mitiko, E-mail: hc.caroline@gmail.co, E-mail: bzsantos@gmail.co, E-mail: amandaifusp@yahoo.com.b, E-mail: myamaura@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2009-07-01

    Fish scale is by-product of fishery. The scales are mainly formed by hydroxyapatite and collagen forming a kind of natural composite with a large specific surface area that intensifies the adsorption process. In this paper the potential of adsorption of scales of Corvina fish for uranyl ions from nitric solutions was studied. The scales were washed several times with faucet water, sun-dried, triturated and sieved. Equilibrium and kinetic studies in adsorption of uranyl ions in batch systems were carried out at room temperature. Equilibrium time was reached at 5 min for 0.1 g L{sup -1} uranyl solution with removal efficiency over 82%, and at 1 min of contact was observed about 60% of removal. The equilibrium isotherm was obtained and the Langmuir model fitted best. These preliminary results are very promising, showing great perspectives of application of the fish scales as biosorbent for uranyl ions in radioactive wastewater treatment processes with a sustainable technology. (author)

  5. Phosphorus isothermal adsorption characteristics of mulch of bioretention

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    Mei Ying

    2012-01-01

    Full Text Available This study aims to identify mulch of bioretention which has high phosphorus sorption capacity. The phosphorus adsorption characteristics of five types of mulch of bioretention are studied by three isothermal adsorption experiments. Results show that the Langmuir eqution is suitable for describing absorption characteristics of five types of mulch. The positive values of Gibbs free energy for phosphorus indicate that the phosphorus biosorption by five mulches is a non-spontaneous process, and the values of mean sorption free energy of mulch are less than 8 kJ/mol, which proves that the adsorption process can be dominated by physical forces. The vermiculite is the better mulch of bioretention based on high phosphorus removal capacity.

  6. Numerical estimation of adsorption energy distributions from adsorption isotherm data with the expectation-maximization method

    Energy Technology Data Exchange (ETDEWEB)

    Stanley, B.J.; Guiochon, G. [Tennessee Univ., Knoxville, TN (United States). Dept. of Chemistry]|[Oak Ridge National Lab., TN (United States)

    1993-08-01

    The expectation-maximization (EM) method of parameter estimation is used to calculate adsorption energy distributions of molecular probes from their adsorption isotherms. EM does not require prior knowledge of the distribution function or the isotherm, requires no smoothing of the isotherm data, and converges with high stability towards the maximum-likelihood estimate. The method is therefore robust and accurate at high iteration numbers. The EM algorithm is tested with simulated energy distributions corresponding to unimodal Gaussian, bimodal Gaussian, Poisson distributions, and the distributions resulting from Misra isotherms. Theoretical isotherms are generated from these distributions using the Langmuir model, and then chromatographic band profiles are computed using the ideal model of chromatography. Noise is then introduced in the theoretical band profiles comparable to those observed experimentally. The isotherm is then calculated using the elution-by-characteristic points method. The energy distribution given by the EM method is compared to the original one. Results are contrasted to those obtained with the House and Jaycock algorithm HILDA, and shown to be superior in terms of robustness, accuracy, and information theory. The effect of undersampling of the high-pressure/low-energy region of the adsorption is reported and discussed for the EM algorithm, as well as the effect of signal-to-noise ratio on the degree of heterogeneity that may be estimated experimentally.

  7. Adsorption isotherms of hog plum (Spondias mombin L. pulp powder obtained by spray dryer

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    Luís Gomes de Moura Neto

    2015-05-01

    Full Text Available Food sorption isotherms are highly important to predict drying time and storage conditions of a product. Current assay evaluates the behavior of adsorption isotherms of hog plum powder obtained by spray-dryer, through mathematical models. GAB, BET, Henderson and Oswin models were adjusted to the experimental data at 25, 30, 35 and 40ºC. The BET model best adjusted to the atomized hog plum for all temperatures tested, with an error ranging between 8.45 and 11.17%. The coefficient of determination (R2 had rates higher than 0.9900 for all the adjusted models. The behavior of hog plum powder adsorption isotherms was classified as Type III.

  8. Contribution to the study of chemical and physical properties of mineral coals and mineral active coals. New method of determination of adsorption isotherms

    International Nuclear Information System (INIS)

    For a better understanding of the influence of factors which influence the coal activation process, this research thesis aims at following, step by step, the evolution of texture and chemical properties of a mineral coal submitted to a series of treatments which allow its progressive transformation into an active coal. The first part reports sample preparation and the study of chemical properties, notably surface functions. The second part addresses physical properties of samples: study of porosity by electronic microscopy, apparatus used to study gas adsorption, helium adsorption by solid surfaces at room temperature, study of the porous texture by gas adsorption

  9. Isotherm and Kinetics of Arsenic (V Adsorption fromAqueous Solution Using Modified Wheat Straw

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    A Eslami

    2011-01-01

    Full Text Available "nBackgrounds and Objectives:Water contamination with arsenic has been recognized as a serious problem and its epidemiological problems to human health have been reported. The objective of this study was to explore the possibility modified wheat straw using sodium bicarbonate for removing arsenic from aqueous solution."nMaterials and Methods: Adsorption process was accomplished in a laboratory-scale batch with emphasis on the effect of various parameters such as pH, contact time, arsenic concentration and adsorbent dosage on adsorption efficiency. In order to understand the adsorption process, sorption kinetics and equilibrium isotherms were also determined."nResults: It was found that adsorption of the arsenic was influenced by several parameters such as arsenic initial concentration, adsorbent dosage and solution pH. Maximum absorption efficiency was achieved at pH 7. As expected the amount of arsenic adsorbed on wheat straw incresed as its concentration went up. Among the models tested, namely the Langmuir, Freundlich, and Dubinin Radushkevich isotherms, the adsorption equilibrium for arsenic was best described by the Langmuir and Freundlich models. It was also found that adsorption of arsenic by wheat straw followed pseudo second-order kinetics. Mean free energy of adsorption (15.8 kJ mol-1 indicates that adsorption of arsenic by wheat straw might follow a chemisorption mechanism. Desorption studies show that arsenic ions are strongly bounded with the adsorbent and exhibit low desorption."nConclusion: It is concluded that that adsorption by modified wheat straw is an efficient and reliable method for arsenic removal from liquid solutions.

  10. Adsorption of surfactants on sand surface in enhanced oil recovery: Isotherms, kinetics and thermodynamic studies

    Energy Technology Data Exchange (ETDEWEB)

    Bera, Achinta; Kumar, T.; Ojha, Keka; Mandal, Ajay, E-mail: mandal_ajay@hotmail.com

    2013-11-01

    Adsorption of surfactants onto reservoir rock surface may result in the loss and reduction of their concentrations in surfactant flooding, which may render them less efficient or ineffective in practical applications of enhanced oil recovery (EOR) techniques. Surfactant flooding for EOR received attraction due to its ability to increase the displacement efficiency by lowering the interfacial tension between oil and water and mobilizing the residual oil. This article highlights the adsorption of surfactants onto sand surface with variation of different influencing factors. It has been experimentally found that adsorption of cationic surfactant on sand surface is more and less for anionic surfactant, while non-ionic surfactant shows intermediate behaviour. X-ray diffraction (XRD) study of clean sand particles has been made to determine the main component present in the sand particles. The interaction between sand particles and surfactant has been studied by Fourier Transform Infrared (FTIR) Spectroscopy of the sand particles before and after aging with surfactant. Salinity plays an important role in adsorption of anionic surfactant. Batch experiments were also performed to understand the effects of pH and adsorbent dose on the sorption efficiency. The sand particles exhibited high adsorption efficiency at low pH for anionic and nonionic surfactants. But opposite trend was found for cationic surfactant. Adsorption data were analyzed by fitting with Langmuir, Freundlich, Redlich-Peterson, and Sips isotherm models. Results show that the Langmuir isotherm and pseudo-second order kinetics models suit the equilibrium and kinetics of adsorption on sand surface. Thermodynamics feasibility of the adsorption process was also studied to verify the spontaneity of the process.

  11. Adsorption of surfactants on sand surface in enhanced oil recovery: Isotherms, kinetics and thermodynamic studies

    International Nuclear Information System (INIS)

    Adsorption of surfactants onto reservoir rock surface may result in the loss and reduction of their concentrations in surfactant flooding, which may render them less efficient or ineffective in practical applications of enhanced oil recovery (EOR) techniques. Surfactant flooding for EOR received attraction due to its ability to increase the displacement efficiency by lowering the interfacial tension between oil and water and mobilizing the residual oil. This article highlights the adsorption of surfactants onto sand surface with variation of different influencing factors. It has been experimentally found that adsorption of cationic surfactant on sand surface is more and less for anionic surfactant, while non-ionic surfactant shows intermediate behaviour. X-ray diffraction (XRD) study of clean sand particles has been made to determine the main component present in the sand particles. The interaction between sand particles and surfactant has been studied by Fourier Transform Infrared (FTIR) Spectroscopy of the sand particles before and after aging with surfactant. Salinity plays an important role in adsorption of anionic surfactant. Batch experiments were also performed to understand the effects of pH and adsorbent dose on the sorption efficiency. The sand particles exhibited high adsorption efficiency at low pH for anionic and nonionic surfactants. But opposite trend was found for cationic surfactant. Adsorption data were analyzed by fitting with Langmuir, Freundlich, Redlich-Peterson, and Sips isotherm models. Results show that the Langmuir isotherm and pseudo-second order kinetics models suit the equilibrium and kinetics of adsorption on sand surface. Thermodynamics feasibility of the adsorption process was also studied to verify the spontaneity of the process.

  12. Metal adsorption by agricultural biosorbents: Adsorption isotherm, kinetic and biosorbents chemical structures.

    Science.gov (United States)

    Sadeek, Sadeek A; Negm, Nabel A; Hefni, Hassan H H; Wahab, Mostafa M Abdel

    2015-11-01

    Biosorption of Cu(II), Co(II) and Fe(III) ions from aqueous solutions by rice husk, palm leaf and water hyacinth was investigated as a function of initial pH, initial heavy metal ions concentration and treatment time. The adsorption process was examined by two adsorption isotherms: Langmuir and Freundlich isotherms. The experimental data of biosorption process were analyzed using pseudo-first order, pseudo-second order kinetic models. The equilibrium biosorption isotherms showed that the three studied biosorbents possess high affinity and sorption capacity for Cu(II), Co(II) and Fe(III) ions. Rice husk showed more efficiency than palm leaf and water hyacinth. Adsorption of Cu(II) and Co(II) was more efficient in alkaline medium (pH 9) than neutral medium due to the high solubility of metal ion complexes. The metal removal efficiency of each biosorbent was correlated to its chemical structure. DTA studies showed formation of metal complex between the biosorbents and the metal ions. The obtained results showed that the tested biosorbents are efficient and alternate low-cost biosorbent for removal of heavy metal ions from aqueous media. PMID:26282929

  13. Adsorption of metal ions onto Moroccan stevensite: kinetic and isotherm studies.

    Science.gov (United States)

    Benhammou, A; Yaacoubi, A; Nibou, L; Tanouti, B

    2005-02-15

    The aim of this paper is to study the adsorption of the heavy metals (Cd(II), Cu(II), Mn(II), Pb(II), and Zn(II)) from aqueous solutions by a natural Moroccan stevensite called locally rhassoul. We carried out, first, a mineralogical and physicochemical characterization of stevensite. The surface area is 134 m2/g and the cation exchange capacity (CEC) is 76.5 meq/100 g. The chemical formula of stevensite is Si3.78Al0.22Mg2.92Fe0.09Na0.08K0.08O10(OH)2.4H2O. Adsorption tests of Cd(II), Cu(II), Mn(II), Pb(II), and Zn(II) in batch reactors were carried out at ambient temperature and at constant pH. Two simplified models including pseudo-first-order and pseudo-second- order were used to test the adsorption kinetics. The equilibrium time and adsorption rate of adsorption were determined. The increasing order of the adsorption rates follows the sequence Mn(II) > Pb(II) > Zn(II) > Cu(II) > Cd(II). The Dubinin-Radushkevich (D-R), Langmuir, and Redlich-Peterson (R-P) models were adopted to describe the adsorption isotherms. The maximal adsorption capacities at pH 4.0 determined from the D-R and Langmuir models vary in the following order: Cu(II) > Mn(II) > Cd(II) > Zn(II) > Pb(II). The equilibrium data fitted well with the three-parameter Redlich-Peterson model. The values of mean energy of adsorption show mainly an ion-exchange mechanism. Also, the influence of solution pH on the adsorption onto stevensite was studied in the pH range 1.5-7.0. PMID:15589536

  14. Erratum to 'Comments on: The phase-shift method for determining Langmuir adsorption isotherms of over-potentially deposited hydrogen for the cathodic H{sub 2} evolution reaction at poly-Re/aqueous electrolyte interfaces [International Journal of Hydrogen Energy (2005) 485-99]'

    Energy Technology Data Exchange (ETDEWEB)

    Lasia, Andrzej [Departement de Chimie, Universite de Sherbrooke, Que. (Canada)

    2005-12-01

    Erratum to 'The phase-shift method for determining Langmuir adsorption isotherms of over-potentially deposited hydrogen for the cathodic H2 evolution reaction at poly-Re/aqueous electrolyte interfaces, International Journal of Hydrogen Energy, Volume 30, Issue 5, April 2005, Pages 485-499'. (author)

  15. Adsorptive Removal of Reactive Black 5 from Wastewater Using Bentonite Clay: Isotherms, Kinetics and Thermodynamics

    Directory of Open Access Journals (Sweden)

    Muhammad Tahir Amin

    2015-11-01

    Full Text Available The studies of the kinetics and isotherms adsorption of the Reactive Black 5 (RB5 onto bentonite clay were explored in a batch study in a laboratory. The maximum RB5 adsorption conditions of bentonite clay were optimized such as shaking speed (100 rpm, temperature (323 K, pH (10, contact time (40 min, initial dye concentration (170 mg·L−1, and particle size (177 µm. The adsorbent surface was characterized using Fourier Transform Infrared Spectroscopy spectroscopy. The mechanisms and characteristic parameters of the adsorption process were analyzed using two parameter isotherm models which revealed the following order (based on the coefficient of determination: Harkin-Jura (0.9989 > Freundlich (0.9986 and Halsey (0.9986 > Langmuir (0.9915 > Temkin (0.9818 > Dubinin–Radushkevich (0.9678. This result suggests the heterogeneous nature of bentonite clay. Moreover, the adsorption process was chemisorption in nature because it follows the pseudo-second order reaction model with R2 value of 0.9998, 0.9933 and 0.9891 at 25, 75 and 100 mg·L−1 RB5 dye in the solution, respectively. Moreover, based on the values of standard enthalpy, Gibbs free energy change, and entropy, bentonite clay showed dual nature of exothermic and endothermic, spontaneous and non-spontaneous as well as increased and decreased randomness at solid–liquid interface at 303–313 K and 313–323 K temperature, respectively.

  16. Adsorption isotherms and thermochemical data of FD&C Red n° 40 binding by Chitosan

    Directory of Open Access Journals (Sweden)

    J. S. Piccin

    2011-06-01

    Full Text Available Chitosan is a natural polymer that has been employed in dye adsorption. In this work, adsorption and thermodynamic data for the interaction of FD&C Red n° 40 food dye with chitosan in aqueous solutions were investigated. The equilibrium adsorption isotherms were determined by the batch method, from 298 to 338 K. Adsorption data were adjusted to five isotherm models: Langmuir, Freundlich, Redlich-Peterson, Temkin and Dubinin-Radushkevich, in order to determine which presented the best adjustment to the experimental data. Error analysis showed that the Langmuir isotherm model was the most appropriate for fitting the experimental data, with a maximum monolayer adsorption of 3065.8 µmol g-1 at 308 K. Negative enthalpy (-112.7 kJ mol-1, entropy (-0.338 kJ mol-1 K-1 and Gibbs free energy (-15.6 to 1.0 kJ mol-1 values demonstrated that the adsorption process is exothermic, spontaneous, favorable, and that randomness of the system decreases during the adsorption process.

  17. Study of Adsorption Isotherm Curves of Amino Acids on the Kaolinite

    Institute of Scientific and Technical Information of China (English)

    Liu Xiaolan; Zhang Zhengbin

    2002-01-01

    This paper studies the adsorption isotherm curves of four amino acids (glycine, aspartic acid, glutamic acid and lysine) and the effects of existences of different concentrations ot Cu(Ⅱ ) on them. Both the adsorption isotherm of the amino acids on the kaolinite and that when the copper ion Cu (Ⅱ) exists belong to the Langmuir type. The slopes of these adsorption isotherm increase with the increasing concentrations of Cu(Ⅱ) added. It can be explained in terms of formation of the type(Ⅰ) ternary surface complexes in these systems. The regular pattern of the effects of copper ion Cu(Ⅱ) on the adsorption isotherm of amino acids on the kaolinite is identical with that of its effects on the exchange and adsorption percentage E (%)-pH on the kaolinite in the same system.

  18. Removal of Bisphenol A from Aqueous solutions using Single walled carbon nanotubes: Investigation of adsorption isotherms

    Directory of Open Access Journals (Sweden)

    Elnaz Iravani

    2013-09-01

    Results: The maximum adsorption capacity was found to be 71.42 mg/g. The results of our experiments showed that maximum adsorption capacity at equilibrium was achieved at t = 60 min and pH = 9. Moreover, increasing the initial concentration is associated with an increase in adsorption capacity until it becomes constant. Conclusion: The BPA adsorption on SWCNT follows Freundlich-Langmuir isotherm.

  19. Use of Freundlich isotherm in the study of heavy metal adsorption in water

    International Nuclear Information System (INIS)

    It was studied the applicability of the Freundlich adsorption isotherm in cadmium, mercury, zinc, and copper extraction from water using activated carbon and cellulose as adsorbents. (author) 62 refs., 22 figs., 19 tabs

  20. Adsorption of nuclides on hydrous oxides: Sorption isotherms on natural materials

    International Nuclear Information System (INIS)

    Hydrous oxides and minerals which have adsorbing groups that behave like hydrous oxides are ubiquitous components of geological formations and may dominate the adsorptive properties of the formations at conditions of natural groundwaters. An understanding of the adsorptive behavior of hydrous oxides is therefore necessary for reliable prediction of migration of nuclides through the formations. Various isotherms are derived from equilibrium ion-exchange theory for the sorption of non-hydrolyzed ions on hydrous oxides. These isotherms are compared with experimental isotherms for sorption of Cs/sup +/, Sr/sup 2+/, Eu/sup 3+/, and TcO/sub 4//sup -/ on several hydrous oxides. General features of these isotherms are predictable from ion-exchange equilibrium theory as applied to hydrous oxides. By combining isotherms for hydrous oxides with those for layer-type clay minerals, many unusual features of isotherms found on geological materials can be explained

  1. Adsorption of Reactive Black 5 on Synthesized Titanium Dioxide Nanoparticles: Equilibrium Isotherm and Kinetic Studies

    OpenAIRE

    Majeed A. Shaheed; Falah H. Hussein

    2014-01-01

    The synthesized titanium dioxide nanoparticles (TiO2-NPs) were used as adsorbent to remove reactive black 5 (RB 5) in aqueous solution. Various factors affecting adsorption of RB 5 aqueous solutions such as pH, initial concentration, contact time, dose of nanoparticles, and temperature were analyzed at fixed solid/solution ratio. Langmuir and Freundlich isotherms were used as model adsorption equilibrium data. Langmuir isotherm was found to be the most adequate model. The pseudo-first-order, ...

  2. Isotherm and kinetic behavior of adsorption of anion polyacrylamide (APAM) from aqueous solution using two kinds of PVDF UF membranes

    International Nuclear Information System (INIS)

    To determine the isotherm parameters and kinetic parameters of adsorption of anion polyacrylamide (APAM) from aqueous solution on PVDF ultrafiltration membrane (PM) and modified PVDF ultrafiltration membrane (MPM) is important in understanding the adsorption mechanism of ultrafiltration processes. Effect of variables including adsorption time, initial solution concentration, and temperature were investigated. The Redlich-Peterson equation of the five different isotherm models we chose was the most fitted model, and the R2 was 0.9487, 0.9765 for PM and MPM, respectively; while, the pseudo-first-order model was the best choice among all the four kinetic models to describe the adsorption behavior of APAM onto membranes, suggesting that the adsorption mechanism was a chemical and physical combined adsorption on heterogeneous surface. The thermodynamic parameters were also calculated from the temperature dependence (ΔrGmθ,ΔrHmθ,ΔrSmθ), which showed that the process of adsorption is not spontaneous but endothermic process and high temperature favors the adsorption.

  3. A Sixth-Form Teaching Unit on the Langmuir Adsorption Isotherm

    Science.gov (United States)

    Walkley, G. H.

    1973-01-01

    Presents a teaching unit on the Langmuir absorption isotherm suitable for advanced secondary school chemistry classes. Describes the experimental investigation of the isothermal adsorption of sulfur dioxide on charcoal, and discusses the derivation of the Langmuir equation and some applications. (JR)

  4. The investigation of kinetic and isotherm of fluoride adsorption onto functionalize pumice stone

    Energy Technology Data Exchange (ETDEWEB)

    Asgari, Ghorban [Department of Environmental Health Engineering, School of Health, Hamadan University of Medical Sciences, Hamadan (Iran, Islamic Republic of); Roshani, Babak, E-mail: babak.roshani@gmail.com [Department of Chemical and Biological Engineering, University of Saskatchewan, 57 Campus Drive, Saskatoon, SK, S7N 5A9 (Canada); Ghanizadeh, Ghader [Health Research Center and Health School, Baqiyatallah University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2012-05-30

    Highlights: Black-Right-Pointing-Pointer Removal of fluoride from drinking water. Black-Right-Pointing-Pointer Pumice as adsorbent functionalized by the cationic surfactant. Black-Right-Pointing-Pointer Effects of HDTMA loading. Black-Right-Pointing-Pointer Best fit of equilibrium expressions. Black-Right-Pointing-Pointer Maximum amount of adsorption. - Abstract: In this research work, pumice that is functionalized by the cationic surfactant, hexadecyltrimethyl ammonium (HDTMA), is used as an adsorbent for the removal of fluoride from drinking water. This work was carried out in two parts. The effects of HDTMA loading, pH (3-10), reaction time (5-60 min) and the adsorbent dosage (0.15-2.5 g L{sup -1}) were investigated on the removal of fluoride as a target contaminate from water through the design of different experimental sets in the first part. The results from this first part revealed that surfactant-modified pumice (SMP) exhibited the best performance at dose 0.5 g L{sup -1}, pH 6, and it adsorbs over 96% of fluoride from a solution containing 10 mg L{sup -1} fluoride after 30 min of mixing time. The four linear forms of the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherms model were applied to determine the best fit of equilibrium expressions. Apart from the regression coefficient (R{sup 2}), four error functions were used to validate the isotherm and kinetics data. The experimental adsorption isotherm complies with Langmuir equation model type 1. The maximum amount of adsorption (Q{sub max}) was 41 mg g{sup -1}. The kinetic studies indicated that the adsorption of fluoride best fitted with the pseudo-second-order kinetic type 1. Thermodynamic parameters evaluation of fluoride adsorption on SMP showed that the adsorption process under the selected conditions was spontaneous and endothermic. The suitability of SMP in defluoridation at field condition was investigated with natural groundwater samples collected from a nearby fluoride endemic area

  5. Adsorption isotherm studies of chromium (VI) from aqueous solutions using sol-gel hydrotalcite-like compounds

    Energy Technology Data Exchange (ETDEWEB)

    Ramos-Ramirez, Esthela, E-mail: ramosre@quijote.ugto.mx [Centro de Investigaciones en Quimica Inorganica de la Universidad de Guanajuato, Noria Alta s/n, Col. Noria Alta, C.P. 36050, Guanajuato, Gto. (Mexico); Gutierrez Ortega, Norma L.; Conteras Soto, Cesar A. [Centro de Investigaciones en Quimica Inorganica de la Universidad de Guanajuato, Noria Alta s/n, Col. Noria Alta, C.P. 36050, Guanajuato, Gto. (Mexico); Instituto Nacional de Investigaciones Nucleares, Carretera Mexico-Toluca s/n, km 36.5, La Marquesa, Coyoacan Mexico, C.P. 52750 (Mexico); Olguin Gutierrez, Maria T. [Instituto Nacional de Investigaciones Nucleares, Carretera Mexico-Toluca s/n, km 36.5, La Marquesa, Coyoacan Mexico, C.P. 52750 (Mexico)

    2009-12-30

    In under-developed countries, industries such as paint and pigment manufacturing, leather tanning, chrome plating and textile processing, usually discharge effluents containing Cr(VI) and Cr(III) into municipal sanitary sewers. It has been reported that Cr(VI) acts as a powerful epithelial irritant and as a human carcinogen. In the present work, hydrotalcite-like compounds with a Mg/Al ratio = 2 were synthesized by the sol-gel method. The hydrotalcite-like compounds and their corresponding thermally treated products were characterized by powder X-ray diffraction, infrared spectroscopy and N{sub 2} adsorption. The hydrotalcite-like compounds and the heated solids were used as adsorbents for Cr(VI) in aqueous solutions. Adsorption isotherm studies of Cr(VI) from aqueous solution are described. The adsorbent capacity was determined using the Langmuir, Freundlich and Dubinin-Radushkevich adsorption isotherm models. The Cr(VI) adsorption isotherm data fit best to the Langmuir isotherm model. The maximum Cr(VI) uptake by hydrotalcite and the heated solids was determined using the Langmuir equation and was found to range between 26 and 29 mg Cr(VI)/g adsorbent.

  6. Adsorption isotherm studies of chromium (VI) from aqueous solutions using sol-gel hydrotalcite-like compounds

    International Nuclear Information System (INIS)

    In under-developed countries, industries such as paint and pigment manufacturing, leather tanning, chrome plating and textile processing, usually discharge effluents containing Cr(VI) and Cr(III) into municipal sanitary sewers. It has been reported that Cr(VI) acts as a powerful epithelial irritant and as a human carcinogen. In the present work, hydrotalcite-like compounds with a Mg/Al ratio = 2 were synthesized by the sol-gel method. The hydrotalcite-like compounds and their corresponding thermally treated products were characterized by powder X-ray diffraction, infrared spectroscopy and N2 adsorption. The hydrotalcite-like compounds and the heated solids were used as adsorbents for Cr(VI) in aqueous solutions. Adsorption isotherm studies of Cr(VI) from aqueous solution are described. The adsorbent capacity was determined using the Langmuir, Freundlich and Dubinin-Radushkevich adsorption isotherm models. The Cr(VI) adsorption isotherm data fit best to the Langmuir isotherm model. The maximum Cr(VI) uptake by hydrotalcite and the heated solids was determined using the Langmuir equation and was found to range between 26 and 29 mg Cr(VI)/g adsorbent.

  7. Isotherms for adsorption of cellobiohydrolase I and II from Trichoderma reesei on microcrystalline cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Medve, J.; Tjerneld, F. [Univ. of Lund (Sweden); Stahlberg, J. [Univ. of Uppsala (Sweden)

    1997-04-01

    Adsorption to microcrystalline cellulose (Avicel) of pure cellobiohydrolase I and II (CBH I and CBH II) from Trichoderma reesei has been studied. Adsorption isotherms of the enzymes were measured at 4{degree}C using CBH I and CBH II alone and in reconstituted equimolar mixtures. Several models (Langmuir, Freundlich, Temkin, Jovanovic) were tested to describe the experimental adsorption isotherms. The isotherms did not follow the basic (one site) Langmuir equation that has often been used to describe adsorption isotherms of cellulases; correlation coefficients (R{sup 2}) were only 0.926 and 0.947, for CBH I and II, respectively. The experimental isotherms were best described by a model of Langmuir type with two adsorption sites and by a combined Langmuir-Freundlich model (analogous to the Hill equation); using these models the correlation coefficients were in most cases higher than 0.995. Apparent binding parameters derived from the two sites Langmuir model indicated stronger binding of CBH II compared to CBH I; the distribution coefficients were 20.7 and 3.7 L/g for the two enzymes, respectively. The binding capacity was higher for CBH I than for CBH II. The isotherms when analyzed with the combined model indicated presence of unequal binding sites on cellulose and/or negative cooperativity in the binding of the enzyme molecules. 39 refs., 3 figs., 3 tabs.

  8. Kinetics and adsorption isotherm of C-phycocyanin from Spirulina platensis on ion-exchange resins

    OpenAIRE

    Sala, L; F. S. Figueira; G. P. Cerveira; C. C. Moraes; S. J. Kalil

    2014-01-01

    C-phycocyanin is a natural blue dye extracted from Spirulina platensis, which has many applications in the food and pharmaceutical industries. In this paper the effect of pH and temperature on the adsorption of C-phycocyanin onto two different ion exchange resins (Streamline DEAE and Streamline Q XL) for expanded bed adsorption chromatography was investigated. Moreover, the kinetics and adsorption isotherm were evaluated. The equilibrium for the Q XL matrix was reached after 60 min, while for...

  9. Biosorption of uranium (VI) and thorium (IV) onto Ulva gigantea (Kuetzing) bliding. Discussion of adsorption isotherms, kinetics and thermodynamic

    International Nuclear Information System (INIS)

    Ulva gigantea (Kuetzing) bliding (UGB) obtained from sea inlet of Izmir-Turkey has been studied as a biosorbent for removal of radioactive metals from water. In this study, unmodified UGB and modified UGB with glutaraldehyde (GUGB) characterized by FTIR spectroscopy were used as biosorbents for removal of U(VI) and Th(IV) ions from aqueous solution. Adsorption experiments performed under batch process with initial pH, contact time, adsorbent mass and temperature as variables. In order to determine the adsorption characteristics, Langmuir, Freundlich and Dubinin-Raduschkevich adsorption isotherms were applied to the adsorption data. Adsorption experiments showed that the adsorption isotherms correlated well with the Freundlich model. The sorption followed pseudo-second-order kinetics. The thermodynamic parameters such as variations of ΔH0, ΔG0 and ΔS0 were estimated as a function of temperature. The thermodynamics of the adsorption of U(VI) and Th(IV) onto UGB and GUGB indicates that the spontaneous and exothermic nature of the process. The results showed that UGB and GUGB were potential for application in removal of U(VI) and Th(IV) from aqueous solution. (author)

  10. Comparative Study of Adsorption Isotherms of Vitamin C on Multi wall and single wall Carbon Nanotube

    Directory of Open Access Journals (Sweden)

    Azin Dehmolaei

    2014-03-01

    Full Text Available We have studied the interaction of Vitamin C solution on multi-wall and single-wall carbon nanotubeAfter investigated comparative study and assigned to Vitamin C adsorption isotherm. The adsorption equilibrium isotherms were fitted by Freundlich, Langmuir, and Temkin models. It was found that the Langmuirmodel described the adsorption process better than other two isotherm models. The amount of Antioxidant drug(Vitamin C adsorbed on Multi wallcarbon nanotube surface increased with the increase of the initial Antioxidant concentration. Based on the results, under similar conditions the efficiency of adsorption of Vitamin C by Multi-wall carbon nanotube(MWCNTs was more thansingle-wall carbon nanotube.

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

    Science.gov (United States)

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

    2015-08-01

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

  12. Enhanced fluoride adsorption by nano crystalline γ-alumina: adsorption kinetics, isotherm modeling and thermodynamic studies

    Science.gov (United States)

    Chinnakoti, Prathibha; Chunduri, Avinash L. A.; Vankayala, Ranganayakulu K.; Patnaik, Sandeep; Kamisetti, Venkataramaniah

    2016-06-01

    Nano materials in particular nano oxides with enhanced surface area and an excellent catalytic surface serve as potential adsorbents for defluoridation of water. In the present study nano γ-alumina was synthesized through a simple and low cost, surfactant assisted solution combustion method. As synthesized material was characterized by XRD and FESEM for its phase, size and morphological characteristics. Surface properties have been investigated by BET method. Nano γ-alumina was further used for a detailed adsorption study to remove fluoride from water. Batches of experiments were performed at various experimental conditions such as solution pH, adsorbent dose, initial fluoride concentration and contact time to test the defluoridation ability of γ-alumina. Fluoride Adsorption by nano sized γ-alumina was rapid and reached equilibrium within two hours. The adsorption worked well at pH 4.0, where ˜96 % of fluoride was found to be adsorbed on adsorbent. It was possible to reduce fluoride levels to as low as 0.3 mg/L (within the safe limit of WHO: ≤1.5 mg/L) from an initial fluoride levels of 10 mg/L. This could be achieved using a very small quantity, 1 g/L of γ-alumina at pH 4 within 1 h of contact time. Defluoridation capacity of nano γ-alumina was further investigated by fitting the equilibrium data to various isotherm as well as kinetic models. The present study revealed that γ-alumina could be an efficient adsorbent for treating fluoride contaminated water.

  13. Adsorption of emulsified oil from metalworking fluid on activated bleaching earth-chitosan-SDS composites: Optimization, kinetics, isotherms.

    Science.gov (United States)

    Naowanat, Nitiya; Thouchprasitchai, Nutthavich; Pongstabodee, Sangobtip

    2016-03-15

    The adsorption of emulsified oil from metalworking fluid (MWF) on activated bleaching earth (BE)-chitosan-sodium dodecyl sulfate (SDS) composites (BE/MCS) was investigated under a statistical design of experiments at a 95% confidence interval to identify the critical factors and to optimize the adsorption capacity. The BE/MCS adsorbents were characterized by means of X-ray diffraction, Fourier transform infrared spectroscopy, Brunauer-Emmett-Teller adsorption/desorption isotherms, contact angle analysis (sessile drop technique) and their zeta potential. From the results of a full 2(5) factorial design with three center points, the adsorbent weight and initial pH of the MWF had a significant antagonistic effect on the adsorption capacity while the initial MWF concentration and BE:chitosan:SDS weight ratio had a synergistic influence. Temperature factor has no discernible effect on the capacity. From the FCCC-RSM design, the optimal capacity range of 2840-2922.5 mg g(-1) was achieved at sorbent weight of 1.6-1.9 g, pH of 5.5-6.5, initial MWF concentration of 52-55 g l(-1) and BE:chitosan:SDS (w/w/w) ratio of 4.7:1:1-6.2:1:1. To test the validation and sensitivity of RSM model, the results showed that the estimated adsorption capacity was close to the experimental capacity within an error range of ±3%, suggesting that the RSM model was acceptable and satisfied. From three kinetics models (pseudo-first-order, pseudo-second-order model and Avrami's equation) and two adsorption isotherms (Langmuir model and Freundlich model), assessed using an error function (Err) and the coefficient of determination (R(2)), Avrami's equation and Freundlich isotherm model provided a good fitting for the data, suggesting the presence of more than one reaction pathway in the MWF adsorption process and the heterogeneous surface adsorption of the BC/ABE-5.5 composite. PMID:26731309

  14. 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.

  15. Adsorption of di-2-pyridyl ketone salicyloylhydrazone on silica gel: characteristics and isotherms.

    Science.gov (United States)

    Antonio, P; Iha, K; Suárez-Iha, M E V

    2004-10-01

    The adsorption of DPKSH onto silica gel was investigated, at 25+/-1 degrees C and pH 1, 4.7 and 12. For the same DPKSH concentration interval, the minimum required time of contact for adsorption maximum at pH 4.7 was smaller than at pH 1 and the maximum amount of DPKSH adsorbed per gram of silica at pH 1 is smaller than at pH 4.7. At pH 12 the DPKSH adsorption onto silica gel was not significant. The adsorption data followed Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherms. The maximum amount of solute adsorbed (m(ads)(max)) and the adsorption constant, K(L), were derived from Langmuir isotherm. The Freundlich constants 1/n and K(F) related, respectively, to the energetic heterogeneity of adsorption sites and an empirical constant were evaluated. The mean sorption free energy (E) of DPKSH adsorption onto silica gel was calculated from D-R isotherm indicating a physical adsorption mode. Finally, conductimetric titrations showed the silica particle basicity and acidity as 0.002 and 0.3mmolg(-1), respectively. PMID:18969629

  16. A New Competitive Adsorption Isothermal Model of Heavy Metals in Soils

    Institute of Scientific and Technical Information of China (English)

    XUE Wen-Bo; YI Ai-Hua; ZHANG Zeng-Qiang; TANG Ci-Lai; ZHANG Xing-Chang; GAO Jin-Ming

    2009-01-01

    A new competitive adsorption isothermal model (CAIM) was developed for the coexistent and competitive binding of heavy metals to the soil surface.This model extended the earlier adsorption isothermal models by considering more than one kind of ion adsorption on the soil surface.It was compared with the Langmuir model using different conditions,and it was found that CAIM,which was suitable for competitive ion adsorption at the soil solid-liquid surface,had more advantages than the Langmuir model.The new competitive adsorption isothermal model was used to fit the data of heavy metal (Zn and Cd) competitive adsorption by a yellow soil at two temperatures.The results showed that CAIM was appropriate for the competitive adsorption of heavy metals on the soil surface at different temperatures.The fitted parameters of CAIM had explicit physical meaning.The model allowed for the calculation of the standard molar Gibbs free energy change,the standard molar enthalpy change,and the standard molar entropy change of the competitive adsorption of the heavy metals,Zn and Cd,by the yellow soil at two temperatures using the thermodynamic equilibrium constants.

  17. Eriobotrya japonica seed biocomposite efficiency for copper adsorption: Isotherms, kinetics, thermodynamic and desorption studies.

    Science.gov (United States)

    Mushtaq, Mehwish; Bhatti, Haq Nawaz; Iqbal, Munawar; Noreen, Saima

    2016-07-01

    Adsorption techniques are widely used to remove pollutants from wastewater; however, composites are gaining more importance due to their excellent adsorption properties. Bentonite composite with Eriobotrya japonica seed was prepared and used for the adsorption of copper (Cu) metal from aqueous media. The process variables such as pH, Cu(II) ions initial concentration, adsorbent dose, contact time and temperature were optimized for maximum Cu(II) adsorption. At pH 5, adsorbent dose 0.1 g, contact time 45 min, Cu(II) ions initial concentration 75 mg/L and temperature 45 °C, maximum Cu(II) adsorption was achieved. Desorption studies revealed that biocomposite is recyclable. Langmuir, Freundlich and Harkins-Jura isotherms as well as pseudo-first and pseudo-second-order kinetics models were applied to understand the adsorption mechanism. Thermodynamic parameters (ΔG(0), ΔH(0) and ΔS(0)) suggest that the adsorption process was spontaneous and endothermic in nature. The pseudo-second-order kinetic model and Langmuir isotherm fitted well to the adsorption data. Results showed that biocomposite was more efficient for Cu(II) adsorption in comparison to individuals native Eriobotrya japonica seed biomass and Na-bentonite. PMID:27039361

  18. IN-VITRO KINETICS, ADSORPTION ISOTHERM, AND EFFECT OF PH ON ANTIDOTAL EFFECT OF ACTIVATED CHARCOAL IN TRAMADOL HYDROCHLORIDE INTOXICATION

    Directory of Open Access Journals (Sweden)

    Pandeya S

    2016-02-01

    Full Text Available Tramadol overdose has been one of the most frequent causes of drug poisoning in the recent years, especially in young adult males. In the current work, the in-vitro study on adsorption kinetics and the effect of pH on antidotal effect of activated charcoal (AC in tramadol hydrochloride intoxication were carried out. For adsorption study tramadol hydrochloride solutions of various concentrations were prepared in both simulated gastric fluid (SGF and simulated intestinal fluid (SIF and analyzed by UV spectrophotometer. For kinetics study tramadol hydrochloride and charcoal in ratio 1:5 was kept in 6 different flasks and sonicated for 5, 10, 15, 20, 25 and 30 minutes and analyzed spectrophotometrically. The data were plotted among two most commonly used adsorption isotherm, Langmuir isotherm and Freundlich isotherm and their coefficient of determination (R2 was compared to get the best adsorption isotherm equation. The kinetics study was done in both SGF and SIF. The result showed that AC 50 gm can adsorb 4802.692 mg tramadol hydrochloride at gastric environment and 8064.516 mg tramadol hydrochloride at intestinal environment. The R2 value in the current study is found to be more in SIF (0.986 than in SGF (0.985. In accordance to the value of R2, the pseudo second order kinetics model fit best for this study with R2 value of 0.9997 in SGF and 0.9994 in SIF. From the current study it can be concluded that 50g AC has the capacity to adsorb sufficient amount of tramadol hydrochloride and the kinetics followed during the adsorption was pseudo-second order.

  19. Non-isothermal adsorption of radioactive methyl iodide at high temperature

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Byung Seon; Park, Geun Il; Lee, Jung Won; Yoon, Ju Hyeon [KAERI, Taejon (Korea, Republic of); Yang, Ho Yeon [KHNPC, Taejon (Korea, Republic of); Ryu, Seung Kon [Chungnam National Univ., Taejon (Korea, Republic of)

    2003-07-01

    Although activated carbon has been successfully used in nuclear power plants, it cannot be considered as a primary adsorbent in a high temperature system, because of its low ignition temperature and its adverse reaction with nitrogen oxide. Therefore, activated carbon is virtually ruled out for high temperature operating systems. The adsorption and dynamic characteristics of gaseous methyl iodide for silver ion-exchanged zeolites at high temperatures up to 400 .deg. C was evaluated. In this study a simple nonisothermal and axially dispersed plug-flow was adopted to simulate the experimental breakthrough curves. The Langmuir-Freundlich isotherm model was used to represent the equilibrium relationship, and the linear driving force (LDF) approximation was used to represent the article uptake. From the viewpoint of silver utilization for the removal of methyl iodide, both the optimal operating temperature and the effective silver ion-exchange level were also determined.

  20. 8-Hydroxyqunoline adsorption from aqueous solution using powdered orange peel: kinetic and isotherm study

    Directory of Open Access Journals (Sweden)

    Siraj Khalid

    2015-12-01

    Full Text Available Adsorption of 8-hydroxyquinoline (8HQ on powdered orange peel (POP, a locally available adsorbent, has been studied. Experiment was performed on different 8HQ concentration, particle size, and adsorbent dosage. The Langmuir and Freundlich adsorption isotherm model has been tested. The obtained results best fitted the Langmuir model, suggesting monolayer adsorption of 8HQ on POP. The kinetic studies for the adsorption process were also carried out using pseudo-first- and pseudo-second-order models, and the data obtained is best fitted to the pseudo-second-order kinetic model. Thermodynamic parameters were calculated for the adsorption process and the result showed that the values of ΔGads, ΔHads, and ΔSads are −1171.4J/mol, −140J/mol and −40.5 J/K at 303 K. Thus, it can be summarized that the adsorption of 8HQ is spontaneous, chemisorbed, monolayer, and exothermic

  1. Effect of humic acid on the adsorption/desorption behavior of glyphosate on goethite. Isotherms and kinetics.

    Science.gov (United States)

    Arroyave, Jeison Manuel; Waiman, Carolina C; Zanini, Graciela P; Avena, Marcelo J

    2016-02-01

    The effects of humic acid (HA) on the adsorption/desorption of glyphosate (Gly) on goethite were investigated under pseudo equilibrium conditions by adsorption isotherms and under kinetic conditions by ATR-FTIR spectroscopy. Isotherms reveal that the attachment of Gly is almost completely inhibited by HA molecules. The opposite effect is not observed: HA adsorption is not affected by the presence of Gly. ATR-FTIR allowed the simultaneous detection of adsorbed HA and Gly during kinetic runs, revealing that HA at the surface decreases markedly the adsorption rate of Gly likely as a result of a decreased availability of sites for Gly adsorption and because of electrostatic repulsion. In addition, HA in solution increases the desorption rate of Gly. The rate law for Gly desorption could be determined giving important insights on the desorption mechanism. The herbicide is desorbed by two parallel processes: i) a direct detachment from the surface, which is first order in adsorbed Gly; and ii) a ligand exchange with HA molecules, which is first order in adsorbed Gly and first order in dissolved HA. Rate constants for both processes were quantified, leading to half-lives of 3.7 h for the first process, and 1.4 h for the second process in a 400 mg L(-1) HA solution. These data are important for modeling the dynamics of glyphosate in environmentally relevant systems, such as soils and surface waters. PMID:26657085

  2. Freundlich and Langmuir adsorption isotherms and kinetics for the removal of Tartrazine from aqueous solutions using hen feathers

    International Nuclear Information System (INIS)

    Tartrazine, a yellow menace, is widely being used in cosmetics, foodstuffs, medicines and textile. It is carcinogenic and also catalyzes allergic problems. In the present work the ability to remove Tartrazine from aqueous solutions has been studied using waste material-hen feathers, as adsorbent. Effects of pH, concentration of the dye, temperature and adsorbent dosage have been studied. Equilibrium isotherms for the adsorption of the dye were measured experimentally. Results were analyzed by the Freundlich and Langmuir equation at different temperatures and determined the characteristic parameters for each adsorption isotherm. The adsorption process has been found endothermic in nature and thermodynamic parameters, Gibb's free energy (ΔGo), change in enthalpy (ΔHo) and change in entropy (ΔSo) have been calculated. The paper also includes results on the kinetic measurements of adsorption of the dye on hen feathers at different temperatures. By rate expression and treatment of data it has been established that the adsorption of Tartrazine over hen feathers follows a first-order kinetics and a film diffusion mechanism operates at all the temperatures

  3. The Global Approach to TPD and Isothermal Adsorption - Desorption Kinetics

    Czech Academy of Sciences Publication Activity Database

    Galíková, Anna; Galík, Aftanas

    Bratislava: Slovak University of Technology , 2003 - (Markoš, J.; Štefuca, V.), s. 108 ISBN 80-227-1889-0. [International Conference of Slovak Society of Chemical Engineering /30./. Tatranské Matliare (SK), 26.05.2003-30.05.2003] R&D Projects: GA AV ČR IAA4072107 Institutional research plan: CEZ:AV0Z4072921 Keywords : adsorption * desorption * global fitting Subject RIV: CH - Nuclear ; Quantum Chemistry

  4. Equilibrium isotherm and kinetics modeling of U(VI) adsorption by natural soil systems

    International Nuclear Information System (INIS)

    This research examined the adsorption capability of natural soils of different origin for U(VI) at soil-water interface and the mechanism involved. Adsorption kinetics study indicates that adsorption followed the pseudo-second order kinetics irrespective of soil types and was not solely controlled by the diffusion step rather surface complexation and ion-exchange plays major role. Study of adsorption isotherms indicates adsorption involves chemisorption and soil with high Fe and Mn content better fit to Langmuir model. The study provides a better insight for site selection for radioactive waste (uranium) disposal facilities as well as soil suitable for back fill or permeable reactive barrier to inhibit migration of U(VI). (author)

  5. Removal Rate of Organic Matter Using Natural Cellulose via Adsorption Isotherm and Kinetic Studies.

    Science.gov (United States)

    Din, Mohd Fadhil Md; Ponraj, Mohanadoss; Low, Wen-Pei; Fulazzaky, Mohamad Ali; Iwao, Kenzo; Songip, Ahmad Rahman; Chelliapan, Shreeshivadasan; Ismail, Zulhilmi; Jamal, Mohamad Hidayat

    2016-02-01

    In this study, the removal of natural organic matter (NOM) using coconut fiber (CF) and palm oil fiber (POF) was investigated. Preliminary analysis was performed using a jar test for the selection of optimal medium before the fabricated column model experiment. The equilibrium studies on isotherms and kinetic models for NOM adsorption were analyzed using linearized correlation coefficient. Results showed that the equilibrium data were fitted to Langmuir isotherm model for both CF and POF. The most suitable adsorption model was the pseudo-first-order kinetic model for POF and pseudo-second-order kinetic model for CF. The adsorption capacities achieved by the CF and POF were 15.67 and 30.8 mg/g respectively. Based on this investigation, it can be concluded that the POF is the most suitable material for the removal of NOM in semi polluted river water. PMID:26803100

  6. Experimental Adsorption Isotherm of Methane onto Activated Carbon at Sub- and Supercritical Temperatures

    KAUST Repository

    Rahman, Kazi Afzalur

    2010-11-11

    This paper presents the experimentally measured adsorption isotherm data for methane onto the pitch-based activated carbon type Maxsorb III for temperatures ranging from (120 to 220) K and pressures up to 1.4 MPa. These data are useful to study adsorbed natural gas (ANG) storage systems when the low temperature natural gas regasified from the liquid phase is considered to charge in the storage chamber. Adsorption parameters were evaluated from the isotherm data using the Tóth and Dubinin-Astakhov models. The isosteric heat of adsorption, which is concentration- and temperature-dependent, is extracted from the data. The Henry\\'s law coefficients for the methane/Maxsorb III pairs are evaluated at various temperatures. © 2010 American Chemical Society.

  7. Adsorption isotherms, kinetics and thermodynamic studies towards understanding the interaction between cross-linked alginate-guar gum matrix and chymotrypsin.

    Science.gov (United States)

    Woitovich Valetti, Nadia; Picó, Guillermo

    2016-02-15

    The adsorption kinetics of chymotrypsin, a pancreatic serine protease, onto an alginate-gum guar matrix cross-linked with epichlorohydrin has been performed using a batch-adsorption technique. The effect of various experimental parameters such as pH, salt presence, contact time and temperature were investigated. The pseudo-first-order and pseudo-second-order kinetic models were used to describe the kinetic data which shows that the adsorption of the enzyme followed the pseudo-second-order rate expression. The Langmuir, Freundlich and Hill adsorption isotherm models were applied to describe the equilibrium isotherms, and the isotherm constants were determined. It was found that Hill model was more suitable for our data because the isotherm data showed a sigmoidal behavior with the free enzyme concentration increasing in equilibrium. At 8°C and at pH 5.0, 1g hydrate matrix adsorbed about 7mg of chymotrypsin. In the desorption process 80% of the biological activity of chymotrypsin was recovered under the condition of 50mM phosphate buffer, pH 7.00-500mM NaCl. When successive cycles of adsorption/washing/desorption were performed, it was observed that the matrix remained functional until the fourth cycle of repeated batch enzyme adsorption. These results are important in terms of diminishing of cost and waste generation. PMID:26849187

  8. Acid Blue 25 adsorption on base treated Shorea dasyphylla sawdust: Kinetic,isotherm, thermodynamic and spectroscopic analysis

    Institute of Scientific and Technical Information of China (English)

    Megat Ahmad Kamal Megat Hanafiah; Wan Saime Wan Ngah; Shahira Hilwani Zolkafly; Lee Ching Teong; Zafri Azran Abdul Majid

    2012-01-01

    The potential of base treated Shorea dasyphylla (BTSD) sawdust for Acid Blue 25 (AB 25) adsorption was investigated in a batch adsorption process.Various physiochemical parameters such as pH,stirring rate,dosage,concentration,contact time and temperature were studied.The adsorbent was characterized with Fourier transform infrared spectrophotometer,scanning electron microscope and Brunauer,Emmett and Teller analysis.The optimum conditions for AB 25 adsorption were pH 2,stirring rate 500 r/min,adsorbent dosage 0.10 g and contact time 60 min.The pseudo second-order model showed the best conformity to the kinetic,data.The equilibrium adsorption of AB 25 was described by Freundlich and Langmuir,with the latter found to agree well with the isotherm model.The maximum monolayer adsorption capacity of BTSD was 24.39 mg/g at 300 K,estimated from the Langmuir model.Thermodynamic parameters such as Gibbs free energy,enthalpy and entropy were determined.It was found that AB 25 adsorption was spontaneous and exothermic.

  9. Kinetics and isotherm analysis of Tropaeoline 000 adsorption onto unsaturated polyester resin (UPR): a non-carbon adsorbent.

    Science.gov (United States)

    Jain, Rajeev; Sharma, Pooja; Sikarwar, Shalini

    2013-03-01

    The presence of dyes in water is undesirable due to the toxicological impact of their entrance into the food chain. Owing to the recalcitrant nature of dyes to biological oxidation, a tertiary treatment like adsorption is required. In the present study, unsaturated polyester resin (UPR) has been used as a sorbent in the treatment of dye-contaminated water. Different concentrations of Tropaeoline 000 containing water were treated with UPR. The preliminary investigations were carried out by batch adsorption to examine the effects of pH, adsorbate concentration, adsorbent dosage, contact time, and temperature. A plausible mechanism for the ongoing adsorption process and thermodynamic parameters have also been obtained from Langmuir and Freundlich adsorption isotherm models. Thermodynamic parameter showed that the sorption process of Tropaeoline 000 onto activated carbon (AC) and UPR were feasible, spontaneous, and endothermic under studied conditions. The estimated values for (ΔG) are -10.48 × 10(3) and -6.098 × 10(3) kJ mol(-1) over AC and UPR at 303 K (30 °C), indicating towards a spontaneous process. The adsorption process followed pseudo-first-order model. The mass transfer property of the sorption process was studied using Lagergren pseudo-first-order kinetic models. The values of % removal and k (ad) for dye systems were calculated at different temperatures (303-323 K). The mechanism of the adsorption process was determined from the intraparticle diffusion model. PMID:22689095

  10. Kinetics and adsorption isotherm of C-phycocyanin from Spirulina platensis on ion-exchange resins

    Directory of Open Access Journals (Sweden)

    L. Sala

    2014-12-01

    Full Text Available C-phycocyanin is a natural blue dye extracted from Spirulina platensis, which has many applications in the food and pharmaceutical industries. In this paper the effect of pH and temperature on the adsorption of C-phycocyanin onto two different ion exchange resins (Streamline DEAE and Streamline Q XL for expanded bed adsorption chromatography was investigated. Moreover, the kinetics and adsorption isotherm were evaluated. The equilibrium for the Q XL matrix was reached after 60 min, while for DEAE it was only reached after 140 min. C-phycocyanin showed the highest partition coefficient at pH 7.5 for both resins at 25 ºC. The C-phycocyanin adsorption isotherm was very well represented by the Langmuir, Freundlich and Langmuir-Freundlich models, where the estimated values for Qm and Kd obtained by the Langmuir isotherm were, respectively, 33.92 mg.mL-1 and 0.123 mg.mL-1 for DEAE, and 28.12 mg.mL-1 and 0.082 mg.mL-1 for the Q XL matrix. A negative cooperativity was observed for C-phycocyanin binding when the Q XL matrix was used, while the cooperativity was purely independent using the DEAE matrix.

  11. A review of the thermodynamics of protein association to ligands, protein adsorption, and adsorption isotherms

    DEFF Research Database (Denmark)

    Mollerup, Jørgen

    2008-01-01

    The application of thermodynamic models in the development of chromatographic separation processes is discussed. The paper analyses the thermodynamic principles of protein adsorption. It can be modeled either as a reversible association between the adsorbate and the ligands or as a steady...... adsorption is discussed. Hydrophobic and reversed phase chromatography are useful techniques for measuring solute activity coefficients at infinite dilution....

  12. Ni (II) adsorption onto Chrysanthemum indicum: Influencing factors, isotherms, kinetics, and thermodynamics.

    Science.gov (United States)

    Vilvanathan, Sowmya; Shanthakumar, S

    2016-10-01

    The study explores the adsorption potential of Chrysanthemum indicum biomass for nickel ion removal from aqueous solution. C. indicum flowers in raw (CIF-I) and biochar (CIF-II) forms were used as adsorbents in this study. Batch experiments were conducted to ascertain the optimum conditions of solution pH, adsorbent dosage, contact time, and temperature for varying initial Ni(II) ion concentrations. Surface area, surface morphology, and functionality of the adsorbents were characterized by Brunauer, Emmett, and Teller (BET) surface analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FTIR). Adsorption kinetics were modeled using pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion, Bangham's, and Boyd's plot. The equilibrium data were modeled using Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich (D-R) isotherm models. Experimental data provided the best fit to pseudo-second-order kinetic model and Langmuir isotherm model for the adsorption of Ni(II) ion on both CIF-I and CIF-II with maximum adsorption capacities of 23.97 and 44.02 mg g(-1), respectively. Thermodynamic analysis of the data proved the process to be spontaneous and endothermic in nature. Desorption studies were conducted to evaluate the possibility of reusing the adsorbents. Findings of the present study provide substantial evidence for the use of C. indicum flower as an eco-friendly and potential adsorbent for the removal of Ni(II) ions from aqueous solution. PMID:27185382

  13. Magnetic vinylphenyl boronic acid microparticles for Cr(VI) adsorption: Kinetic, isotherm and thermodynamic studies

    International Nuclear Information System (INIS)

    Highlights: • Cr(VI) can oxidize biological molecules and be one of the most harmful substance. • Magnetic seperation techniques are used on different applications in many fields. • Magnetic systems can be used for rapid and selective removal as a magnetic processor. • We investigate properties of both new material and other magnetic adsorbents reported in the literatures on the adsorption of Cr(VI) ions. • No researchments were reported on adsorption of Cr(VI) with magnetic vinylphenyl boronic acid microparticles. - Abstract: Magnetic vinylphenyl boronic acid microparticles, poly(ethylene glycol dimethacrylate(EG)–vinylphenyl boronic acid(VPBA)) [m-poly(EG–VPBA)], produced by suspension polymerization and characterized, was found to be an efficient solid polymer for Cr(VI) adsorption. The m-poly(EG–VPBA) microparticles were prepared by copolymerizing of ethylene glycol dimethylacrylate (EG) with 4-vinyl phenyl boronic acid (VPBA). The m-poly(EG–VPBA) microparticles were characterized by N2 adsorption/desorption isotherms, electron spin resonance (ESR), X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), elemental analysis, scanning electron microscope (SEM) and swelling studies. The m-poly(EG–VPBA) microparticles were used at adsorbent/Cr(VI) ion ratios. The influence of pH, Cr(VI) initial concentration, temperature of the removal process was investigated. The maximum removal of Cr(VI) was observed at pH 2. Langmuir isotherm and Dubinin–Radushkvich isotherm were found to better fit the experiment data rather than Fruendlich isotherm. The kinetics of the adsorption process of Cr(VI) on the m-poly(EG–VPBA) microparticles were investigated using the pseudo first-order, pseudo-second-order, Ritch-second-order and intraparticle diffusion models, results showed that the pseudo-second order equation model provided the best correlation with the experimental results. The thermodynamic

  14. Removal of water and iodine by solid sorbents: adsorption isotherms and kinetics

    International Nuclear Information System (INIS)

    Tritium and iodine-129 are two major radioactive elements that are present in off-gases from spent fuel reprocessing plants. Adsorption by solid sorbents is the state-of-the-art technique for removal of these species from off-gases. Modeling and simulating adsorption processes require accurate adsorption equilibrium and kinetic data to permit reasonable estimates of process parameters. We have developed a continuous flow single-pellet adsorption system to gather accurate adsorption equilibrium and kinetic data for adsorption of water by molecular sieve 3A and for adsorption of iodine by silver exchanged mordenite. In this paper, the design of the water and iodine adsorption experimental systems are briefly described and results of water adsorption experiments are presented and discussed. Water uptake curves are fitted with the linear-driving force (LDF) model and the shrinking-core model to determine kinetic parameters. It is shown that the kinetics of water adsorption on zeolite 3A under current experimental conditions is controlled by both the external film resistance and the macro-pore diffusion and can be predicted by both the LDF model and the shrinking-core model with the former one performing slightly better. Preliminary results from iodine adsorption experiments will be presented in the conference

  15. Adsorption isotherms and kinetics of methylene blue on a low-cost adsorbent recovered from a spent catalyst of vinyl acetate synthesis

    Science.gov (United States)

    Zhang, Zhengyong; Zhang, Zebiao; Fernández, Y.; Menéndez, J. A.; Niu, Hao; Peng, Jinhui; Zhang, Libo; Guo, Shenghui

    2010-02-01

    A regenerated activated carbon used as catalyst support in the synthesis of vinyl acetate has been tested as a low-cost adsorbent for the removal of dyes. After a thorough textural characterization of the regenerated activated carbon, its adsorption isotherms and kinetics were determined using methylene blue as model compound at different initial concentrations. Both Langmuir and Freundlich isotherm models were developed and then compared. It was found that the equilibrium data were best represented by the Langmuir isotherm model. The kinetic data were fitted to pseudo-first-order, pseudo-second-order and intraparticle diffusion models, and it was found that the best fitting corresponded to the pseudo-second-order kinetic model. The results showed that this novel adsorbent had a high adsorption capacity, making it suitable for use in the treatment of methylene blue enriched wastewater.

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

    International Nuclear Information System (INIS)

    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 UVI complexes on goethite or SiO2 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

  17. Optimizing Available Phosphorus in Calcareous Soils Fertilized with Diammonium Phosphate and Phosphoric Acid Using Freundlich Adsorption Isotherm

    OpenAIRE

    Asif Naeem; Muhammad Akhtar; Waqar Ahmad

    2013-01-01

    In calcareous soils, phosphorus (P) retention and immobilization take place due to precipitation and adsorption. Since soil pH is considered a major soil variable affecting the P sorption, an acidic P fertilizer could result in low P adsorption compared to alkaline one. Therefore, P adsorption from DAP and phosphoric acid (PA) required to produce desired soil solution P concentration was estimated using Freundlich sorption isotherms. Two soils from Faisalabad and T. T. Singh districts were sp...

  18. A comparative examination of the adsorption mechanism of an anionic textile dye (RBY 3GL) onto the powdered activated carbon (PAC) using various the isotherm models and kinetics equations with linear and non-linear methods

    Science.gov (United States)

    Açıkyıldız, Metin; Gürses, Ahmet; Güneş, Kübra; Yalvaç, Duygu

    2015-11-01

    The present study was designed to compare the linear and non-linear methods used to check the compliance of the experimental data corresponding to the isotherm models (Langmuir, Freundlich, and Redlich-Peterson) and kinetics equations (pseudo-first order and pseudo-second order). In this context, adsorption experiments were carried out to remove an anionic dye, Remazol Brillant Yellow 3GL (RBY), from its aqueous solutions using a commercial activated carbon as a sorbent. The effects of contact time, initial RBY concentration, and temperature onto adsorbed amount were investigated. The amount of dye adsorbed increased with increased adsorption time and the adsorption equilibrium was attained after 240 min. The amount of dye adsorbed enhanced with increased temperature, suggesting that the adsorption process is endothermic. The experimental data was analyzed using the Langmuir, Freundlich, and Redlich-Peterson isotherm equations in order to predict adsorption isotherm. It was determined that the isotherm data were fitted to the Langmuir and Redlich-Peterson isotherms. The adsorption process was also found to follow a pseudo second-order kinetic model. According to the kinetic and isotherm data, it was found that the determination coefficients obtained from linear method were higher than those obtained from non-linear method.

  19. Biosorption of the Copper and Cadmium Ions - a Study through Adsorption Isotherms Analysis

    Directory of Open Access Journals (Sweden)

    Marcia T. Veit

    2007-10-01

    Full Text Available In this work, the biosorption process of copper-cadmium ions binary mixture by using marine algae Sargassum filipendula was investigated. A set of experiments was performed to obtain equilibrium data for the given batch operational conditions - T=30°C, pH=5. The interpretation of equilibrium data was based on the binary adsorption isotherms models in the Langmuir and Freundlich forms. To evaluate the models parameters, nonlinear identification procedure was used based on the Least Square statistical method and SIMPLEX local optimizer. An analysis of the obtained results showed that the marine algae biomass has higher affinity to copper ions than to cadmium ones. The biomass maximum adsorption capacity for the binary system was about 1.16 meq/g.

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

    Science.gov (United States)

    Hameed, B H; El-Khaiary, M I

    2008-06-15

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

  1. Determination of surface-accessible acidic hydroxyls and surface area of lignin by cationic dye adsorption

    OpenAIRE

    Sipponen, Mika Henrikki; Pihlajaniemi, Ville; Littunen, Kuisma; Pastinen, Ossi; Laakso, Simo

    2014-01-01

    A new colorimetric method for determining the surface-accessible acidic lignin hydroxyl groups in lignocellulose solid fractions was developed. The method is based on selective adsorption of Azure B, a basic dye, onto acidic hydroxyl groups of lignin. Selectivity of adsorption of Azure B on lignin was demonstrated using lignin and cellulose materials as adsorbents. Adsorption isotherms of Azure B on wheat straw (WS), sugarcane bagasse (SGB), oat husk, and isolated lignin materials were determ...

  2. Kinetics and Adsorption Isotherms Studies of Acridine Orange Dye from Aqueous Solution by Activated Charcoal

    Directory of Open Access Journals (Sweden)

    *N. Qamar

    2014-12-01

    Full Text Available The goal of this research is to evaluate the efficiency of charcoal as low coast and effective adsorbent for acridine orange (a cationic dye from aqueous solution at room temperature. Effect of initial pH (2-8, shaking time (5min. - 1hour, adsorbent dose (0.1gm- 0.9gm and dye concentration (37mg/30ml-185mg/30ml were investigated. Results demonstrated that charcoal act as good adsorbent for the removal AO where 99.15% of the dye was adsorbed within 30 minutes. For the maximum dye removal efficiency (100%, optimum conditions were obtained at pH 8 (99.24%, adsorbent dose of 0.9g and dye concentration of 185 mg with charcoal. Kinetics of adsorption was investigated as well as Langmuir and Freundlich isotherms were employed to describe equilibrium studies. The Langmuir adsorption isotherms models and pseudo second order kinetics fitted the experimental data best with high regression coefficient R2. The results of the present studies points to the potential of charcoal as an effective adsorbent for the removal of dye from contaminated water sources.

  3. Adsorption isotherms, kinetics, thermodynamics and desorption studies of 2,4,6-trichlorophenol on oil palm empty fruit bunch-based activated carbon

    International Nuclear Information System (INIS)

    The adsorption characteristics of 2,4,6-trichlorophenol (TCP) on activated carbon prepared from oil palm empty fruit bunch (EFB) were evaluated. The effects of TCP initial concentration, agitation time, solution pH and temperature on TCP adsorption were investigated. TCP adsorption uptake was found to increase with increase in initial concentration, agitation time and solution temperature whereas adsorption of TCP was more favourable at acidic pH. The adsorption equilibrium data were best represented by the Freundlich and Redlich-Peterson isotherms. The adsorption kinetics was found to follow the pseudo-second-order kinetic model. The mechanism of the adsorption process was determined from the intraparticle diffusion model. Boyd plot revealed that the adsorption of TCP on the activated carbon was mainly governed by particle diffusion. Thermodynamic parameters such as standard enthalpy (ΔHo), standard entropy (ΔSo), standard free energy (ΔGo) and activation energy were determined. The regeneration efficiency of the spent activated carbon was high, with TCP desorption of 99.6%.

  4. How soil organic matter composition controls hexachlorobenzene–soil-interactions: Adsorption isotherms and quantum chemical modeling

    Energy Technology Data Exchange (ETDEWEB)

    Ahmed, Ashour A., E-mail: ashour.ahmed@uni-rostock.de [University of Rostock, Institute of Physics, D-18051 Rostock (Germany); University of Cairo, Faculty of Science, Department of Chemistry, 12613 Giza (Egypt); University of Rostock, Interdisciplinary Faculty, Department of Life, Light and Matter, D-18051 Rostock (Germany); Kühn, Oliver, E-mail: oliver.kuehn@uni-rostock.de [University of Rostock, Institute of Physics, D-18051 Rostock (Germany); University of Rostock, Interdisciplinary Faculty, Department of Life, Light and Matter, D-18051 Rostock (Germany); Aziz, Saadullah G., E-mail: saziz@kau.edu.sa [King Abdulaziz University, Faculty of Science, Chemistry Department, Jeddah 21589 (Saudi Arabia); Hilal, Rifaat H., E-mail: rhilal@kau.edu.sa [University of Cairo, Faculty of Science, Department of Chemistry, 12613 Giza (Egypt); King Abdulaziz University, Faculty of Science, Chemistry Department, Jeddah 21589 (Saudi Arabia); Leinweber, Peter, E-mail: peter.leinweber@uni-rostock.de [University of Rostock, Soil Science, D-18051 Rostock (Germany); University of Rostock, Interdisciplinary Faculty, Department of Life, Light and Matter, D-18051 Rostock (Germany)

    2014-04-01

    Hazardous persistent organic pollutants (POPs) interact in soil with the soil organic matter (SOM) but this interaction is insufficiently understood at the molecular level. We investigated the adsorption of hexachlorobenzene (HCB) on soil samples with systematically modified SOM. These samples included the original soil, the soil modified by adding a hot water extract (HWE) fraction (soil + 3 HWE and soil + 6 HWE), and the pyrolyzed soil. The SOM contents increased in the order pyrolyzed soil < original soil < soil + 3 HWE < soil + 6 HWE. For the latter three samples this order was also valid for the HCB adsorption. The pyrolyzed soil adsorbed more HCB than the other samples at low initial concentrations, but at higher concentrations the HCB adsorption became weaker than in the samples with HWE addition. This adsorption combined with the differences in the chemical composition between the soil samples suggested that alkylated aromatic, phenol, and lignin monomer compounds contributed most to the HCB adsorption. To obtain a molecular level understanding, a test set has been developed on the basis of elemental analysis which comprises 32 representative soil constituents. The calculated binding energy for HCB with each representative system shows that HCB binds to SOM stronger than to soil minerals. For SOM, HCB binds to alkylated aromatic, phenols, lignin monomers, and hydrophobic aliphatic compounds stronger than to polar aliphatic compounds confirming the above adsorption isotherms. Moreover, quantitative structure–activity relationship (QSAR) of the binding energy with independent physical properties of the test set systems for the first time indicated that the polarizability, the partial charge on the carbon atoms, and the molar volume are the most important properties controlling HCB–SOM interactions. - Highlights: • Conduction of adsorption experiment of different soil samples on HCB. • Development of a new SOM model for the study of the HCB

  5. How soil organic matter composition controls hexachlorobenzene–soil-interactions: Adsorption isotherms and quantum chemical modeling

    International Nuclear Information System (INIS)

    Hazardous persistent organic pollutants (POPs) interact in soil with the soil organic matter (SOM) but this interaction is insufficiently understood at the molecular level. We investigated the adsorption of hexachlorobenzene (HCB) on soil samples with systematically modified SOM. These samples included the original soil, the soil modified by adding a hot water extract (HWE) fraction (soil + 3 HWE and soil + 6 HWE), and the pyrolyzed soil. The SOM contents increased in the order pyrolyzed soil < original soil < soil + 3 HWE < soil + 6 HWE. For the latter three samples this order was also valid for the HCB adsorption. The pyrolyzed soil adsorbed more HCB than the other samples at low initial concentrations, but at higher concentrations the HCB adsorption became weaker than in the samples with HWE addition. This adsorption combined with the differences in the chemical composition between the soil samples suggested that alkylated aromatic, phenol, and lignin monomer compounds contributed most to the HCB adsorption. To obtain a molecular level understanding, a test set has been developed on the basis of elemental analysis which comprises 32 representative soil constituents. The calculated binding energy for HCB with each representative system shows that HCB binds to SOM stronger than to soil minerals. For SOM, HCB binds to alkylated aromatic, phenols, lignin monomers, and hydrophobic aliphatic compounds stronger than to polar aliphatic compounds confirming the above adsorption isotherms. Moreover, quantitative structure–activity relationship (QSAR) of the binding energy with independent physical properties of the test set systems for the first time indicated that the polarizability, the partial charge on the carbon atoms, and the molar volume are the most important properties controlling HCB–SOM interactions. - Highlights: • Conduction of adsorption experiment of different soil samples on HCB. • Development of a new SOM model for the study of the HCB

  6. Adsorption of fluoride to UiO-66-NH2 in water: Stability, kinetic, isotherm and thermodynamic studies.

    Science.gov (United States)

    Lin, Kun-Yi Andrew; Liu, Yu-Ting; Chen, Shen-Yi

    2016-01-01

    To provide safe drinking water, fluoride in water must be removed and adsorption processes appear to be the most widely used method. Metal organic frameworks (MOFs) represent a new class of adsorbents that have been used in various adsorption applications. To study the adsorption mechanism of fluoride to MOFs in water and obtain related adsorption parameters, we synthesized a zirconium-based MOF with a primary amine group on its ligand, named UiO-66-NH2. The kinetics, adsorption isotherm and thermodynamics of fluoride adsorption to UiO-66-NH2 were investigated. The crystalline structure of UiO-66-NH2 remained intact and the local structure of zirconium in UiO-66-NH2 did not change significantly after being exposed to fluoride. The kinetics of the fluoride adsorption in UiO-66-NH2 could be well represented by the pseudo second order rate law. The enthalpy of the adsorption indicates that the F(-) adsorption to UiO-66-NH2 was classified as a physical adsorption. However, the comparison between the adsorption capacities of UiO-66-NH2 and UiO-66 suggests that the fluoride adsorption to UiO-66-NH2 might primarily involve a strong interaction between F(-) and the metal site. The fluoride adsorption capacity of UiO-66-NH2 was found to decrease when pH>7. While the presence of chloride/bromide ions did not noticeably change the adsorption capacity of UiO-66-NH2, the ionic surfactants slightly affected the adsorption capacity of UiO-66-NH2. These findings provide insights to further optimize the adsorption process for removal of fluoride using zirconium-based MOFs. PMID:26397913

  7. Simple and Efficient Synthesis of Iron Oxide-Coated Silica Gel Adsorbents for Arsenic Removal: Adsorption Isotherms and Kinetic Study

    International Nuclear Information System (INIS)

    Iron oxide (ferrihydrite, hematite, and magnetite) coated silica gels were prepared using a low-cost, easily-scalable and straightforward method as the adsorbent material for arsenic removal application. Adsorption of the anionic form of arsenic oxyacids, arsenite (AsO2-) and arsenate (AsO4-3), onto hematite coated silica gel was fitted against non-linear 3-parameter-model Sips isotherm and 2-parameter-model Langmuir and Freundlich isotherm. Adsorption kinetics of arsenic could be well described by pseudo-second-order kinetic model and value of adsorption energy derived from non-linear Dubinin-Radushkevich isotherm suggests chemical adsorption. Although arsenic adsorption process was not affected by the presence of sulfate, chloride, and nitrate anions, as expected, bicarbonate and silicate gave moderate negative effects while the presence of phosphate anions significantly inhibited adsorption process of both arsenite and arsenate. When the actual efficiency to remove arsenic was tested against 1 L of artificial arsenic-contaminated groundwater (0.6 mg/L) in the presence competing anions, the reasonable amount (20 g) of hematite coated silica gel could reduce arsenic concentration to below the WHO permissible safety limit of drinking water of 10 μg/L without adjusting pH and temperature, which would be highly advantageous for practical field application

  8. Predicting CH4 adsorption capacity of microporous carbon using N2 isotherm and a new analytical model

    Science.gov (United States)

    Sun, Jielun; Chen, S.; Rostam-Abadi, M.; Rood, M.J.

    1998-01-01

    A new analytical pore size distribution (PSD) model was developed to predict CH4 adsorption (storage) capacity of microporous adsorbent carbon. The model is based on a 3-D adsorption isotherm equation, derived from statistical mechanical principles. Least squares error minimization is used to solve the PSD without any pre-assumed distribution function. In comparison with several well-accepted analytical methods from the literature, this 3-D model offers relatively realistic PSD description for select reference materials, including activated carbon fibers. N2 and CH4 adsorption data were correlated using the 3-D model for commercial carbons BPL and AX-21. Predicted CH4 adsorption isotherms, based on N2 adsorption at 77 K, were in reasonable agreement with the experimental CH4 isotherms. Modeling results indicate that not all the pores contribute the same percentage Vm/Vs for CH4 storage due to different adsorbed CH4 densities. Pores near 8-9 A?? shows higher Vm/Vs on the equivalent volume basis than does larger pores.

  9. Adsorption removal of Congo red from aqueous solution by polyhedral Cu2O nanoparticles: Kinetics, isotherms, thermodynamics and mechanism analysis

    International Nuclear Information System (INIS)

    Highlights: • Polyhedral Cu2O NPs with rough surfaces were prepared by a one-pot sonochemical precipitation method. • The Cu2O NPs show unprecedented adsorption capability toward Congo red. • CR adsorption onto Cu2O is a spontaneous, endothermic and chemisorption process. • The Cu2O adsorbent can be photocatalytically regenerated by visible light irradiation. - Abstract: Polyhedral cuprous oxide nanoparticles (Cu2O NPs) with rough surfaces were prepared by a one-pot sonochemical precipitation method. The products were characterized by SEM, XRD, EDS, XPS, and UV–Vis DRS, respectively. The adsorption behavior of Congo red (CR) from aqueous solution onto the as-prepared Cu2O NPs was systematically investigated. The equilibrium and kinetic studies suggested that the adsorption process followed Freundlich isotherm and pseudo-second order model, respectively. The as-prepared Cu2O NPs exhibited remarkable adsorption properties toward CR. The maximum adsorption capacity at 20 °C was 3904 mg g−1, which was the highest reported value so far in adsorption removal of CR. Together with the evaluation of the thermodynamic parameters such as Gibbs free energy, enthalpy and entropy change, our results show that the adsorption of CR onto Cu2O is a spontaneous, endothermic and chemisorption process. A putative interaction model between CR and Cu2O NPs was proposed. Moreover, the Cu2O adsorbent could be photocatalytically regenerated and reused without significant loss of its adsorption capability

  10. Kinetic Isotherm of Amoxicillin Antibiotic through Adsorption and its Removal by Electrocoagulation

    Directory of Open Access Journals (Sweden)

    Jayati Chatterjee

    2014-06-01

    Full Text Available Antibiotics are emerging contaminants in the aquatic environment because they have adverse effects on the aquatic life and humans. The use of antibiotics in human and veterinary medicine has a significant effect on the quality of surface and groundwater. The relevance of an electrocoagulation (EC process for the removal of an antibiotic was selected because of its wide application, high solubility in water, high residual toxicity and an absence of biodegradability, was examined in this study. Metal hydroxides generated during EC were used to remove Amoxicillin (AMX from aqueous solution. The knowledge regarding the removal mechanism of this substance has not yet been investigated till now. Experiments were carried out in a batch electrochemical reactor using aluminum electrodes. The removal of AMX was relatively fast and equilibrium was reached within 20 min. The effects of the main operating parameters were examined and showed that irrespective of the initial concentration and for pH ranging from 3 to 10, maximum removal efficiency remained close to 95%; while a sharp decrease was recorded at pH 2 (8 % removal. The results of this study also showed that the removal of AMX from water was strongly affected by the current intensity. The mechanism of electrocoagulation was modeled using isotherm models and showed that the Sips isotherm matched satisfactorily the experimental data, suggesting monolayer coverage of adsorbed molecules and assumed a quasi-Gaussian distribution energy owing to the high correlation also found for the Toth model. In addition, adsorption kinetic studies showed that the EC process followed a pseudo-second-order kinetic model at the various current densities, as when the pH and initial antibiotic concentrations were considered.

  11. Optimizing Available Phosphorus in Calcareous Soils Fertilized with Diammonium Phosphate and Phosphoric Acid Using Freundlich Adsorption Isotherm

    Directory of Open Access Journals (Sweden)

    Asif Naeem

    2013-01-01

    Full Text Available In calcareous soils, phosphorus (P retention and immobilization take place due to precipitation and adsorption. Since soil pH is considered a major soil variable affecting the P sorption, an acidic P fertilizer could result in low P adsorption compared to alkaline one. Therefore, P adsorption from DAP and phosphoric acid (PA required to produce desired soil solution P concentration was estimated using Freundlich sorption isotherms. Two soils from Faisalabad and T. T. Singh districts were spiked with 0, 10, and 20 % for 15 days. Freundlich adsorption isotherms ( were constructed, and theoretical doses of PA and DAP to develop a desired soil solution P level (i.e., 0.20 mg L−1 were calculated. It was observed that P adsorption in soil increased with . Moreover, at all the levels of , P adsorption from PA was lower compared to that from DAP in both the soils. Consequently, lesser quantity of PA was required to produce desired solution P, 0.2 mg L−1, compared to DAP. However, extrapolating the developed relationship between soil contents and quantity of fertilizer to other similar textured soils needs confirmation.

  12. Adsorption isotherms and kinetics for dibenzothiophene on activated carbon and carbon nanotube doped with nickel oxide nanoparticles

    Indian Academy of Sciences (India)

    MAZEN K NAZAL; GHASSAN A OWEIMREEN; MAZEN KHALED; MUATAZ A ATIEH; ISAM H ALJUNDI; ABDALLA M ABULKIBASH

    2016-04-01

    Activated carbon (AC) and multiwall carbon nanotubes (CNT) doped with 1, 5 and 10% Ni in the form of nickel oxide nanoparticles were prepared using the wetness impregnation method. These percentages were denoted by the endings NI1, NI5 and NI10 in the notations ACNI1, ACNI5, ACNI10 and CNTNI1, CNTNI5, CNTNIL10, respectively. The physicochemical properties for these adsorbents were characterized using N$_2$ adsorption–desorption surface area analyzer, thermal gravimetric analysis (TGA), scanning electron microscopy, energy-dispersive X-ray spectroscopy, field-emission transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectrometre. Adsorption isotherms were obtained and desulphurization kinetics were carried out on solutions of dibenzothiophene (DBT) and thiophene in a model fuel. The efficiencies of DBT and thiophene removal were reported. The adsorption isotherms fitted the Langmuir and Freundlich models. The highest adsorption capacity for DBT was $74\\pm 5$ mg g$^{−1}$ on ACNI5; the maximum adsorption capacities of the other adsorbents followed the trend ${\\rm ACNI1 > ACNI10 > AC > CNTNI5 > CNTNI1 > CNTNI10 > CNT}$. The adsorption rates for DBT and thiophene followed pseudo-second-order kinetics. The selective removal by these adsorbents of DBT relative to thiophene and naphthalene was evaluated. The adsorbents’ reusability and the effect of the percentage of aromaticcompounds on their adsorption capacity were also reported.

  13. Adsorption isotherms of hog plum (Spondias mombin L.) pulp powder obtained by spray dryer

    OpenAIRE

    Luís Gomes de Moura Neto; Érica Milô de Freitas Felipe Rocha; Marcos Rodrigues Amorim Afonso; José Maria Correia da Costa

    2015-01-01

    Food sorption isotherms are highly important to predict drying time and storage conditions of a product. Current assay evaluates the behavior of adsorption isotherms of hog plum powder obtained by spray-dryer, through mathematical models. GAB, BET, Henderson and Oswin models were adjusted to the experimental data at 25, 30, 35 and 40ºC. The BET model best adjusted to the atomized hog plum for all temperatures tested, with an error ranging between 8.45 and 11.17%. The coefficient of determinat...

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

    Directory of Open Access Journals (Sweden)

    Roshanak Khandanlou

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

  15. The isotherm slope. A criterion for studying the adsorption mechanism of benzotriazole on copper in sulphuric acid

    OpenAIRE

    Bastidas, D. M.; Gómez, R. R.; Cano, E.

    2005-01-01

    The adsorption of benzotriazole (BTA) on copper surfaces in 0.001, 0.005 and 0.01 M concentrations of sulphuric acid was investigated using gravimetric measurements. BTA was tested in concentrations from 1x10-5 to 1x10-1 M at temperatures from 298 to 328 K. The adsorption mechanism is discussed in terms of applicability of the conventional Frumkin, Bockris-Swinkels and Kastening-Holleck isotherms, among others. The best fit was obtained using the ...

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

    Science.gov (United States)

    Weishauptová, Zuzana; Přibyl, Oldřich

    2016-04-01

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

  17. Adsorption of Cd(II) by Mg-Al-CO3- and magnetic Fe3O4/Mg-Al-CO3-layered double hydroxides: Kinetic, isothermal, thermodynamic and mechanistic studies.

    Science.gov (United States)

    Shan, Ran-ran; Yan, Liang-guo; Yang, Kun; Hao, Yuan-feng; Du, Bin

    2015-12-15

    Understanding the adsorption mechanisms of metal cations on the surfaces of solids is important for determining the fate of these metals in water and wastewater treatment. The adsorption kinetic, isothermal, thermodynamic and mechanistic properties of cadmium (Cd(II)) in an aqueous solution containing Mg-Al-CO3- and magnetic Fe3O4/Mg-Al-CO3-layered double hydroxide (LDH) were studied. The results demonstrated that the adsorption kinetic and isotherm data followed the pseudo-second-order model and the Langmuir equation, respectively. The adsorption process of Cd(II) was feasible, spontaneous and endothermic in nature. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy were used to explain the adsorption mechanisms. The characteristic XRD peaks and FTIR bands of CdCO3 emerged in the LDH spectra after Cd(II) adsorption, which indicated that the adsorption of Cd(II) by LDHs occurred mainly via CdCO3 precipitation, surface adsorption and surface complexation. Furthermore, the magnetic Fe3O4/Mg-Al-CO3-LDH can be quickly and easily separated using a magnet before and after the adsorption process. PMID:26073520

  18. Modeling of iron adsorption on HTTA-loaded polyurethane foam using Freundlich, Langmuir and D-R isotherm expressions

    International Nuclear Information System (INIS)

    The sorption of Fe (III) at low pH range from 1 to 4.5 on open cell polyether type HTTA-loaded polyurethane foam has been carried out using batch technique. The optimum shaking time for 2.5 * 10-4M solution of Fe(III) was found to be 30 minutes. The concept of macropore and micropore nature of polyurethane foam sorbent offers unique advantages of adsorption. Freundlich and Langmuir adsorption isotherms are followed at low concentration range from 1 * 10-4 to 3 * 10 -4M solution of Fe(III). The Freundlich constant (1/n = 0.46 ± 0.013 and K = 9.16 ± 1.39 mg * g-1) and Langmuir isotherm constants (M = 21.78 mg * g-1 and b = 88.41 ± 9.731 * g-1) were established. The sorption mean free energy E = 12.22 ± 0.09 kJ * mol-1 and loading capacity Cm = 145.21 ± 6.1 mg * g-1 were evaluated using Dubinin-Radushkevich isotherm, which suggested that the adsorption mechanism was chemisorption. (author)

  19. Statistical fractal adsorption isotherms, linear energy relations, and power-law trapping-time distributions in porous media

    International Nuclear Information System (INIS)

    Drazer and Zanette [Phys. Rev. E 60, 5858 (1999)] have reported on interesting experiments which show that trapping-time distributions in porous media obey a scaling law of the negative power-law type. Unfortunately, their theoretical interpretation of the experimental data has physical and mathematical inconsistencies and errors. Drazer and Zanette assume the existence of a distribution of local adsorption isotherms for which the random parameter is not a thermodynamic function, but a kinetic parameter, the trapping time. Moreover, they mistakenly identify the reciprocal value of a rate coefficient with the instantaneous (fluctuating) value of the trapping time. Their approach leads to mathematically inconsistent probability densities for the trapping times, which they find to be non-normalizable. We suggest a different theory, which is physically and mathematically consistent. We start with the classical patch approximation, which assumes the existence of a distribution of adsorption heats, and introduce two linear energy relationships between the activation energies of the adsorption and desorption processes and the adsorption heat. If the distribution of the adsorption heat obeys the exponential law of Zeldovich and Roghinsky, then both the adsorption isotherm and the probability density of trapping times can be evaluated analytically in terms of the incomplete beta and gamma functions, respectively. Our probability density of the trapping times is mathematically consistent; that is, it is non-negative and normalized to unity. For large times it has a long tail which obeys a scaling law of the negative power-law type, which is consistent with the experimental data of Drazer and Zanette. By using their data we can evaluate the numerical values of the proportionality coefficients in the linear energy relations. The theory suggests that experimental study of the temperature dependence of the fractal exponents helps to elucidate the mechanism of the adsorption

  20. Servey Impact of Activated Alumina in Fluoride Concentration Peresent in Water and Appointment Adsorption Isotherm and Kinetics

    Directory of Open Access Journals (Sweden)

    Y Dadban Shahamat

    2009-11-01

    Full Text Available Backgrounds and Objectives: Determination of Fluoride in drinking water has received increasing interest, duo to its beneifical and detrimental effects on health. The aim of this research is investigation of Effect of  activated alumina in fluoride concentration reduction in drinking water."nMaterials and Methods: Expriment in batch system and with change effective parameters such as pH(5, 7,9, equilibration time (30, 60, 90, 120 minute, initial fluoride concentration(1.4, 2, 2.4 mg/l and activated Alumina dosage (0.1, 0.2, 0.3 gr/l was investigated. Also found data of this research were fited with Langmuir and Freundlich models, kinetic data with pseudo- first order, pseudo- second order and modifited pseudo- first order  models."nResults: The results showed that with increasing of pH of solution, removal efficiency was decreased and optimum pH was found to be in the range of 5 to 7. Also removal efficiency of fluoride was increased with increasing of adsorbent dosage and decreasing of initial concentration of fluoride. Adsorption isotherm data show that the fluoride sorption followed the Langmuir model (r2=0.98. Kinetics of sorption of fluoride onto Activated alumina was well described by pseudo- second order model."nConclusion: The concentration of Activated Alumina had significant effect on the reduction of fluoride ions concentration in water.The higher fluoride removals were observed for batch experiments at pH=5 because no free fluoride ion is present in the solutions, and it could be casued by electrostatic interactions between the surface of alumina and the dominant fluoride species in solution The kinetic model can adequately describe the removal behaviors of fluoride ion by alumina adsorption in the batch system.

  1. Investigation of adsorption kinetics and isotherm of cellulase and B-Glucosidase on lignocellulosic substrates

    Science.gov (United States)

    Clear understanding of enzyme adsorption during enzymatic hydrolysis of lignocellulosic biomass is essential to enhance the cost-efficiency of hydrolysis. However, conclusions from literatures often contradicted each other because enzyme adsorption is enzyme, biomass/pretreatment and experimental co...

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

    International Nuclear Information System (INIS)

    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. 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.

  4. Recombinant protein purification using gradient-assisted simulated moving bed hydrophobic interaction chromatography. Part I: selection of chromatographic system and estimation of adsorption isotherms.

    Science.gov (United States)

    Palani, Sivakumar; Gueorguieva, Ludmila; Rinas, Ursula; Seidel-Morgenstern, Andreas; Jayaraman, Guhan

    2011-09-16

    The design of gradient simulated moving bed (SMB) chromatographic processes requires an appropriate selection of the chromatographic system followed by the determination of adsorption isotherm parameters in the relevant range of mobile phase conditions. The determination of these parameters can be quite difficult for recombinant target proteins present in complex protein mixtures. The first part of this work includes the estimation of adsorption isotherm parameters for streptokinase and a lumped impurity fraction present in an Escherichia coli cell lysate for a hydrophobic interaction chromatography (HIC) matrix. Perturbation experiments were carried out using a Butyl Sepharose matrix with purified recombinant protein on buffer equilibrated columns as well as with crude cell lysate saturated columns. The Henry constants estimated for streptokinase were found to exhibit in a wide range a linear dependence on the salt concentration in the mobile phase. These parameters were applied in subsequent investigations to design a simulated moving bed (SMB) process capable to purify in a continuous manner recombinant streptokinase from the E. coli cell lysate. PMID:21816402

  5. Liquid phase adsorptions of Rhodamine B dye onto raw and chitosan supported mesoporous adsorbents: isotherms and kinetics studies

    Science.gov (United States)

    Inyinbor, A. A.; Adekola, F. A.; Olatunji, G. A.

    2016-04-01

    Irvingia gabonensis endocarp waste was charred (DNc) and subsequently coated with chitosan (CCDNc). Physicochemical characteristics of the two adsorbents were established, while Fourier transform infrared (FTIR), Scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) surface area methods were further employed for characterization. Efficiencies of the prepared adsorbents in the uptake of Rhodamine B (RhB) from aqueous effluent were investigated and adsorption data were tested using four isotherms and four kinetics models. The BET surface areas of the prepared adsorbent were 0.0092 and 4.99 m2/g for DNc and CCDNc, respectively, and maximum adsorption was recorded at pH between 3 and 4, respectively. While monolayer adsorption dominates the uptake of RhB onto DNc, uptake of RhB onto CCDNc was onto heterogeneous surface. The maximum monolayer adsorption capacities (q max) obtained from the Langmuir equation are 52.90 and 217.39 mg/g for DNc and CCDNc, respectively. Pseudo second order and Elovich kinetic models well described the kinetics of the two adsorption processes. The mean sorption energy (E) calculated from the D-R model and desorption efficiencies suggests that while the uptake of RhB onto DNc was physical in nature, for RhB-CCDNc system chemisorption dominates.

  6. Non-linear frequency response of non-isothermal adsorption controlled by micropore diffusion with variable diffusivity

    Directory of Open Access Journals (Sweden)

    MENKA PETKOVSKA

    2000-12-01

    Full Text Available The concept of higher order frequency response functions (FRFs is used for the analysis of non-linear adsorption kinetics on a particle scale, for the case of non-isothermal micropore diffusion with variable diffusivity. Six series of FRFs are defined for the general non-isothermal case. A non-linerar mathematical model is postulated and the first and second order FRFs derived and simulated. A variable diffusivity influences the shapes of the second order FRFs relating the sorbate concentration in the solid phase and t he gas pressure significantly, but they still keep their characteristics which can be used for discrimination of this from other kinetic mechanisms. It is also shown that first and second order particle FRFs offter sufficient information for an easy and fast estimation of all model parameters, including those defining the system non-linearity.

  7. Studies on the adsorption kinetics and isotherms for the removal and recovery of Methyl Orange from wastewaters using waste materials

    International Nuclear Information System (INIS)

    De-Oiled Soya a waste of Soya oil industries and Bottom Ash a waste of thermal power plants have been used as effective adsorbent for recovery and removal of hazardous dye Methyl Orange from wastewater. During the studies effects of amount of dye and adsorbents, pH, sieve sizes, column studies etc. have been carried out. Adsorption of the dye over both the adsorbents has been monitored through Langmuir and Freundlich adsorption isotherm models and feasibility of the process is predicted in both the cases. Different thermodynamic parameters like Gibb's free energy, enthalpy and entropy of the undergoing process are also evaluated through these adsorption models. The kinetic studies confirm the first order process for the adsorption reaction and also play an important role in finding out half-life of the adsorption process and rate constants for both the adsorbents. It is also found that over the entire concentration range the adsorption on Bottom Ash takes place via particle diffusion process, while that of De-Oiled Soya undergoes via film diffusion process. In order to establish the practical utility of the developed process, attempts have been made for the bulk removal of the dye through column operations. For the two columns saturation factors are found as 98.61 and 99.8%, respectively, for Bottom Ash and De-Oiled Soya with adsorption capacity of each adsorbent as 3.618 and 16.664 mg/g, respectively. The dye recovery has been achieved by eluting dil. NaOH through the exhausted columns

  8. Characteristics of isothermal adsorption and desorption of aluminum ion to/from humic acids

    Institute of Scientific and Technical Information of China (English)

    WANG Qiang; WEI Shiqiang; HUANG Yuming; ZHANG Jinzhong

    2008-01-01

    The adsorption and desorption characteristics of Al3+ to/from humic acids at different pH, ionic strength, and temperature were studied by the C-25 glucosan-gel chromatography method. The results showed that the maximum adsorption amount (Qmax) and adsorption constant (k) increased, whereas, the absolute value of standard thermodynamic molar free energy change (AG0. m) decreased with the increase of pH at constant ionic strength and temperature. With ionic strength increasing from 0 to 0. 15 mol/L, Qmax and k increased and the absolute value of AG0. m decreased at constant pH and temperature. High temperature was unfavorable for the adsorption reaction, as indicated by the dramatic decrease of Qmax and the absolute value of AG0. m with an increase in temperature. The standard thermodynamic molar free energy change (AG0. m) and the standard thermodynamic enthalpy change (AH0. m) of the adsorption reaction were both negative, suggesting that adsorption reaction was spontaneous and exothermic. The desorption rate of HA-AI3+ complex accelerated with the decrease of pH, and a significant linear relationship could be obtained between pH and the desorption rates of Al3+ from humic acids. These results demonstrated that the Al3+ adsorption reaction was a "biphase" reaction, and adsorption occurred at both the interior and exterior adsorption sites of humic acids.

  9. Equivalent dose determination using a quartz isothermal TL signal

    Energy Technology Data Exchange (ETDEWEB)

    Vandenberghe, D.A.G. [Laboratory of Mineralogy and Petrology (Luminescence Research Group), Department of Geology and Soil Science, Ghent University, Krijgslaan 281 (S8), B-9000 Gent (Belgium); Radiation Research Department, Riso DTU, Technical University of Denmark, DK-4000 Roskilde (Denmark); Nordic Laboratory for Luminescence Dating, Department of Earth Sciences, University of Aarhus, Riso DTU, DK-4000 Roskilde (Denmark)], E-mail: dimitri.vandenberghe@ugent.be; Jain, M. [Radiation Research Department, Riso DTU, Technical University of Denmark, DK-4000 Roskilde (Denmark); Murray, A.S. [Nordic Laboratory for Luminescence Dating, Department of Earth Sciences, University of Aarhus, Riso DTU, DK-4000 Roskilde (Denmark)

    2009-05-15

    We report on further developments in the use of an isothermal thermoluminescence (ITL) signal for determining the equivalent dose (D{sub e}) in unheated sedimentary quartz. In order to minimise sensitivity change during the first measurement, the ITL signal is measured at 270 deg. C following a preheat at 300 deg. C for 10 s. The decay curve can be represented well by the sum of two exponentially decaying functions plus a constant. The two decaying components hold the dosimetric information; they both appear to originate with the 325 deg. C region of the glow curve, and are thermally stable. This composite signal can be fully reset by sunlight, and grows with dose over at least the same range as the OSL signal. A single-aliquot regenerative-dose (SAR) protocol can be used with this ITL signal. Dose recovery experiments confirm the suitability of the measurement protocol; the D{sub e} values are in acceptable agreement with the expected burial dose in samples from a variety of depositional environments and ages. Our results suggest that measurement of the ITL signal at 270 deg. C enables the quartz 325 deg. C TL peak to be used for accurate dose measurements on a single aliquot. The signal allows dating over at least the same age range as the OSL signal, and it appears especially advantageous for application to quartz samples for which the OSL signal saturates below {approx}500 Gy.

  10. Modified Isothermal Adsorption Model of Shale Gas%修正的页岩气等温吸附模型

    Institute of Scientific and Technical Information of China (English)

    张跃磊; 李大华; 王青华; 郭东鑫

    2016-01-01

    When using Langmuir model and modified double Langmuir model on heterogeneity medium shale isotherm ad-sorption,the experimental data fitting accuracy and stability is not high. We launched a study on new isotherm adsorption equation. The study transforms the adsorption characteristics of different adsorption media within the adsorption system into the actual effect of system pressure,and corrects the pressure for double Langmuir model,getting a new P-Langmuir isotherm adsorption model,which is suitable for multi-adsorption-media system. The model is applied to fitting adsorption isotherm experimental data of 21 samples of Yuye 1 shale gas well in the Southeast of Chongqing and the result shows that average errors of Langmuir model are between-0.012 8 m3/t and 0.021 2 m3/t,D-Langmuir model between-0.003 64 m3/t and 0.021 2 m3/t, and all the values of the correlation coefficient R2 of the P-Langmuir model are between 0.992 5 and 0.999 8,and that average errors of 21 samples are between-0.003 25 m3/t and 0.003 21 m3/t. Compared to the Langmuir equation and double Lang-muir equation,P-Langmuir model is of higher fitting accuracy and better stability,has some practical significance for more accurately evaluating shale gas adsorption.%针对Langmuir等温吸附方程及修正的双朗格缪尔模型(D-Langmuir)在研究非均质吸附介质页岩等温吸附时,对实验数据拟合精度及稳定性不高的问题,展开了新的等温吸附方程研究,研究中将吸附系统内不同吸附介质的吸附特征转化为系统内压力的实际作用效果,对D-Langmuir模型进行压力修正,得到新的、适用于多吸附介质的P-Langmuir等温吸附模型。将以上模型应用于渝东南渝页1井共21个样品的等温吸附实验数据的拟合,结果表明:Langmuir模型平均误差在-0.0120∼80.0212 m3/t;D-Langmuir模型平均误差在-0.00364∼0.02120 m3/t;P-Langmuir等温吸附模型相关系数的平方0.9925≤R2≤0.9998

  11. Dependence of Elution Curve and Adsorption Isotherms of Insulin on composition of Mobile Phase of Frontal Analysis in Reversed Phase Liquid Chromatography

    Institute of Scientific and Technical Information of China (English)

    耿信笃; 弗莱德依瑞格涅尔

    2003-01-01

    With frontal analysis(FA),the dependence of adsorption isotherms of insulin on the composition of mobile phase in reversed phase liquid chromatography (RPLC) has been investigated,This is also a good example to employ the stoichiometric displacement theory (SDT) for ivestigating solute adsorption in physical chemistry.Six kinds of mobile phase in RPLC were employed to study the effects on the elution curves and adsorption isotherms of insulin.the key points of this paper are:(1) the stability of insulin due to delay time after preparing,the organic solvent concentration,the kind and the concentration of ion-pairing agent in mobile phase were found to affect both elution curve and adsorption isotherm very seriously.(2)To obtain a valid and comparable result,the composition of the mobile phase employed in FA must be as same as possible to that in usual RPLC of either analytical scale or preparative purpose.(3)Langmuir Equation and the SDT were employed to imitate these obtained adsorption isotherms.The expression for solute adsorption from solution of the SDT was found to have a better elucidation to the insulin adsorption from mobile phase in RPLC.

  12. Adsorption of methyl orange from aqueous solution by aminated pumpkin seed powder: Kinetics, isotherms, and thermodynamic studies.

    Science.gov (United States)

    Subbaiah, Munagapati Venkata; Kim, Dong-Su

    2016-06-01

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

  13. ADSORPTION OF Pb2+ IONS FROM AQUEOUS SOLUTIONS ONTO BAEL TREE LEAF POWDER: ISOTHERMS, KINETICS AND THERMODYNAMICS STUDY

    Directory of Open Access Journals (Sweden)

    P. SENTHIL KUMAR

    2009-12-01

    Full Text Available In this study, bael tree (BT leaf powder was used as an adsorbent for removal of Pb2+ ions from aqueous solutions through batch equilibrium technique. The influence of pH, equilibrium time, temperature, adsorbent dosage and initial concentration of metal ions on adsorbed amount of metals ions were investigated. Studies showed that the pH of aqueous solutions affected Pb2+ ions removal as a result of removal efficiency increased with increasing solution pH. The experimental isotherm data were analyzed using the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich equations. The monolayer adsorption capacity is 4.065 mg/g with the correlation coefficient of 0.993. The experiments showed that highest removal rate was 84.93% at solution pH 5, contact time 60 min and initial concentration of 50 mg/L. Thermodynamic parameters such as Gibbs free energy, enthalpy, and entropy have also been evaluated and it has been found that the sorption process was feasible, spontaneous and exothermic in nature. Three simplified kinetic models including a pseudo-first-order equation, pseudo-second-order equation and intraparticle diffusion equation were selected to follow the adsorption process. Kinetic parameters, rate constants, equilibrium sorption capacities and related correlation coefficients, for each kinetic model were calculated and discussed. It was shown that the adsorption of Pb2+ ions could be described by the pseudo-second order equation, suggesting that the adsorption process is presumable a chemisorption.

  14. Effect of temperature on the adsorption of short alkanes in the zeolite ssz-13-adapting adsorption isotherms to microporous materials

    NARCIS (Netherlands)

    Jiang, Tao; Göltl, Florian; Bulo, Rosa E.; Sautet, Philippe

    2014-01-01

    Understanding the diffusion and adsorption of hydrocarbons in zeolites is a highly important topic in the field of catalysis in micro-and mesoporous materials. Especially, the properties of alkanes in zeolites have been studied extensively. A theoretical description of these processes is challenging

  15. Optimization, isotherm, kinetic and thermodynamic studies of Pb(II) ions adsorption onto N-maleated chitosan-immobilized TiO2 nanoparticles from aqueous media

    Science.gov (United States)

    Shaker, Medhat A.; Yakout, Amr A.

    2016-02-01

    Chitosan, CS was chemically engineered by maleic anhydride via simple protocol to produce N-maleated chitosan, MCS which immobilized on anatase TiO2 to synthesize novel eco-friendly nanosorbent (51 ± 3.8 nm), MCS@TiO2 for cost-effective and efficient removal of Pb(II) ions from aqueous media. The chemical structure, surface properties and morphology of MCS@TiO2 were recognized by FTIR, 1H NMR, XRD, TEM, DLS and zeta-potential techniques. The relations between %removal of Pb(II) and different analytical parameters such as solution acidity (pH), MCS@TiO2 dosage, time of contact and initial Pb(II) concentration were optimized using response surface methodology (RSM) and Box-Behnken design (BBD) statistical procedures. The fitting of the experimental data to four different isotherm models at optimized conditions was carried out by various statistical treatments including the correlation coefficient (r), coefficient of determination (r2) and non-linear Chi-square (χ2) test analyses which all confirm the suitability of Langmuir model to explain the adsorption isotherm data. Also, statistics predicted that the pseudo-second-order model is the optimum kinetic model among four applied kinetic models to closely describe the rate equation of the adsorption process. Thermodynamics viewed the adsorption as endothermic and feasible physical process. EDTA could release the sorbed Pb(II) ions from MCS@TiO2 with a recovery above 92% after three sorption-desorption cycles. The novel synthesized nanosorbent is evidenced to be an excellent solid phase extractor for Pb(II) ions from wastewaters.

  16. Optimization, isotherm, kinetic and thermodynamic studies of Pb(II) ions adsorption onto N-maleated chitosan-immobilized TiO₂ nanoparticles from aqueous media.

    Science.gov (United States)

    Shaker, Medhat A; Yakout, Amr A

    2016-02-01

    Chitosan, CS was chemically engineered by maleic anhydride via simple protocol to produce N-maleated chitosan, MCS which immobilized on anatase TiO2 to synthesize novel eco-friendly nanosorbent (51±3.8 nm), MCS@TiO2 for cost-effective and efficient removal of Pb(II) ions from aqueous media. The chemical structure, surface properties and morphology of MCS@TiO2 were recognized by FTIR, (1)H NMR, XRD, TEM, DLS and zeta-potential techniques. The relations between %removal of Pb(II) and different analytical parameters such as solution acidity (pH), MCS@TiO2 dosage, time of contact and initial Pb(II) concentration were optimized using response surface methodology (RSM) and Box-Behnken design (BBD) statistical procedures. The fitting of the experimental data to four different isotherm models at optimized conditions was carried out by various statistical treatments including the correlation coefficient (r), coefficient of determination (r(2)) and non-linear Chi-square (χ(2)) test analyses which all confirm the suitability of Langmuir model to explain the adsorption isotherm data. Also, statistics predicted that the pseudo-second-order model is the optimum kinetic model among four applied kinetic models to closely describe the rate equation of the adsorption process. Thermodynamics viewed the adsorption as endothermic and feasible physical process. EDTA could release the sorbed Pb(II) ions from MCS@TiO2 with a recovery above 92% after three sorption-desorption cycles. The novel synthesized nanosorbent is evidenced to be an excellent solid phase extractor for Pb(II) ions from wastewaters. PMID:26520475

  17. How Soil Organic Matter Composition Controls Hexachlorobenzene-Soil-Interactions: Adsorption Isotherms and Quantum Chemical Modelling

    CERN Document Server

    Ahmed, Ashour; Kühn, Oliver

    2013-01-01

    Hazardous persistent organic pollutants (POPs) interact in soil with the soil organic matter (SOM) but this interaction is insufficiently understood at the molecular level. We investigated the adsorption of hexachlorobenzene (HCB) on soil samples with systematically modified SOM. These samples included the original soil, the soil modified by adding a hot water extract (HWE) fraction (soil+3 HWE and soil+6 HWE), and the pyrolyzed soil. The SOM contents increased in the order pyrolyzed soil < original soil < soil+3 HWE < soil+6 HWE. For the latter three samples this order was also valid for the HCB adsorption. The pyrolyzed soil adsorbed more HCB than the other samples at low initial concentrations, but at higher concentrations the HCB adsorption became weaker than in the samples with HWE addition. This adsorption behaviour combined with the differences in the chemical composition between the soil samples suggested that alkylated aromatic, phenol, and lignin monomer compounds contributed most to the HC...

  18. Batch adsorption of iodo-butane on silver-zeolite with henry isotherm

    International Nuclear Information System (INIS)

    Adsorption of 1-iodo-butane in n-dodecane on silver zeolite (of Ionex Research Corp., U.S.A.) was carried out in a batch tank at 50, 60 and 70degC. The adsorbate bulk concentration-time data measured at various times before the equilibrium reached gave the values of surface diffusivity, particle-fluid mass transfer coefficient and the Henry's adsorption equilibrium constant. The mass transfer coefficient was found to be in terms of Sherwood number from 2∼∞, i.e., the same theoretical curve which agreed with the measured data was predicted with any Sherwood number greater than two. This indicated that the adsorption was controlled by the mass transfer within the adsorbent particle. The adsorption equilibrium constant and surface diffusivity were, respectively, expressed by the Arrhenius type equations. (author)

  19. Adsorption of heavy metal ions using hierarchical CaCO3-maltose meso/macroporous hybrid materials: adsorption isotherms and kinetic studies.

    Science.gov (United States)

    Ma, Xiaoming; Li, Liping; Yang, Lin; Su, Caiyun; Wang, Kui; Yuan, Shibao; Zhou, Jianguo

    2012-03-30

    Highly ordered hierarchical calcium carbonate is an important phase and has technological interest in the development of functional materials. The work describes hierarchical CaCO(3)-maltose meso/macroporous hybrid materials were synthesized using a simple gas-diffusion method. The uniform hexagonal-shaped CaCO(3)-maltose hybrid materials are formed by the hierarchical assembly of nanoparticles. The pore structure analysis indicates that the sample possesses the macroporous structure of mesoporous framework. The distinguishing features of the hierarchical CaCO(3)-maltose materials in water treatment involve not only high removal capacities, but also decontamination of trace metal ions. Langmuir model fitted the equilibrium data better than the Freundlich isotherm. The maximum removal capacity of the CaCO(3)-maltose hybrid materials for Pb(2+), Cd(2+), Cu(2+), Co(2+), Mn(2+) and Ni(2+) ions was 3242.48, 487.80, 628.93, 393.70, 558.66 and 769.23 mg/g, respectively. Adsorption data were modeled using the pseudo-first-order, pseudo-second-order and intra-particle diffusion kinetics equations. The results indicate that pseudo-second-order kinetic equation and intra-particle diffusion model can better describe the adsorption kinetics. The adsorption and precipitation transformation mechanism can be considered due to hierarchical meso/macroporous structure, rich organic ligands of the CaCO(3)-maltose hybrid materials and the larger solubility product of CaCO(3). PMID:22326246

  20. Chromatographic and traditional albumin isotherms on cellulose: a model for wound protein adsorption on modified cotton

    Science.gov (United States)

    Albumin is the most abundant protein found in healing wounds. Traditional and chromatogrpahic protein isotherms of albumin binding on modified cotton fibers are useful in understanding albumin binding to cellulose wound dressings. An important consideration in the design of cellulosic wound dressin...

  1. Equilibrium Isotherm Studies of Adsorption of Pigments Extracted from Kuduk-kuduk (Melastoma malabathricum L. Pulp onto TiO2 Nanoparticles

    Directory of Open Access Journals (Sweden)

    N. T. R. N. Kumara

    2014-01-01

    Full Text Available The adsorption of natural pigments onto TiO2 nanoparticles was investigated. The pigments were extracted from the dark purple colored pulp of the berry-like capsule of Kuduk-kuduk (Melastoma malabathricum L.. The Langmuir, Freundlich, Redlich-Peterson, and Sips isotherm models were used to analyze the equilibrium experimental data. Data correlated well with the Sips isotherm model, where the heterogeneity factor (n=0.24 indicated heterogeneous adsorption characteristics, with a maximum adsorption capacity of 0.0130 mg/g. The heterogeneous adsorption character was further supported by results obtained from zeta-potential measurements. When a dye-sensitized solar cell (DSSC was sensitized with the extracted pigment, the photo-energy conversion efficiency was measured to be 0.83%, thus proving the suitability of Kuduk-kuduk fruit pulp as a sensitizer in DSSCs.

  2. Determination of surface-accessible acidic hydroxyls and surface area of lignin by cationic dye adsorption.

    Science.gov (United States)

    Sipponen, Mika Henrikki; Pihlajaniemi, Ville; Littunen, Kuisma; Pastinen, Ossi; Laakso, Simo

    2014-10-01

    A new colorimetric method for determining the surface-accessible acidic lignin hydroxyl groups in lignocellulose solid fractions was developed. The method is based on selective adsorption of Azure B, a basic dye, onto acidic hydroxyl groups of lignin. Selectivity of adsorption of Azure B on lignin was demonstrated using lignin and cellulose materials as adsorbents. Adsorption isotherms of Azure B on wheat straw (WS), sugarcane bagasse (SGB), oat husk, and isolated lignin materials were determined. The maximum adsorption capacities predicted by the Langmuir isotherms were used to calculate the amounts of surface-accessible acidic hydroxyl groups. WS contained 1.7-times more acidic hydroxyls (0.21 mmol/g) and higher surface area of lignin (84 m(2)/g) than SGB or oat husk materials. Equations for determining the amount of surface-accessible acidic hydroxyls in solid fractions of the three plant materials by a single point measurement were developed. A method for high-throughput characterization of lignocellulosic materials is now available. PMID:25033327

  3. Kinetic and isotherm studies of cadmium adsorption on manganese nodule residue

    International Nuclear Information System (INIS)

    The adsorption equilibrium and kinetics studies of cadmium (Cd) ions from aqueous solutions on manganese nodule residue were carried out by considering the influence of various parameters, such as contact time, solution pH and initial metal concentration in solution, temperature and adsorbent quantity. The adsorption of Cd increased with an increase in the concentrations of this metal in solution. Presence of manganese and iron content in manganese nodule residue (MNR) played a significant role in Cd(II) ions removal. The linear forms of the Langmuir and Freundlich equations were utilized for experiments with metal concentrations of 200 mg/L for Cd(II) as functions of solution pH (2.0-6.0). First-order rate equation and pseudo second-order rate equations were applied to study adsorption kinetics. Mass transfer study was also done to know the reaction rate. Thermodynamic parameters, such as standard Gibb's free energy (ΔGo), standard enthalpy (ΔHo) and standard entropy (ΔSo), were also evaluated by Van't Hoff equation. Thus, adsorption of Cd on this adsorbent was found to be spontaneous and exothermic thermodynamically. The adsorption capacity for Cd was found to be 19.8 mg/g of MNR. Under the optimised conditions, cadmium level was brought down from 100 mg/L to Cd less than detection limits and from 200 to 2 mg/L. Thus, the wastewater after cadmium removal could be safely disposed off on to land or sewage. Finally, the metal loaded adsorbent was subjected to desorption using different mineral acids and leaching by using toxicity characteristic leaching procedure (TCLP), synthetic precipitation leaching procedure (SPLP) tests for its further treatment or its safe disposal

  4. Combined Neutron Diffraction and Adsorption Isotherm Study of the Anomalous Wetting Properties of NH3 on Graphite

    International Nuclear Information System (INIS)

    The wetting properties of NH3 films on graphite have been examined over a temperature range of approximately 50K (centered about the bulk triple point of 195.4K) using a combination of high-resolution vapor pressure isotherms and elastic neutron diffraction. Between 172 and 215K, a single adsorption step appears at reduced pressures above 0.5. As the system is cooled, the position of this step (which is shown to be associated with the formation of a thin liquid film) increases smoothly between 0.5 and 0.95. Evidence is put forward that there is a transition from complete wetting to incomplete wetting to nonwetting. Also, the role of cluster formation and hydrogen bonding is discussed. copyright 1997 The American Physical Society

  5. Equilibrium adsorption isotherm of U(VI) at pH4 and pH5 onto synthetic magnetite nanoparticles

    International Nuclear Information System (INIS)

    The adsorption features of synthetic magnetite nanoparticles have been investigated for removal of uranyl ions from nitric solutions. These magnetic nanoparticles can be used to adsorb contaminants in wastewater and can subsequently be removed from the medium by a magnetic process because their superparamagnetic behavior. The magnetite nanoparticles were synthesized by simultaneous precipitating of Fe2+ and Fe3+ ions in a NaOH solution. Batch experiments were carried out to investigate the adsorption of UO22+ ions from nitric solution, pH 4 and 5, onto magnetic nanoparticles. The adsorption equilibrium was attained with 30 min of contact time. Two min of application of a magnetic field were sufficient for the removing of magnetite nanoparticles from the liquid medium. Equilibrium adsorption isotherm was evaluated using Freundlich and Langmuir models. The adsorption isotherm fitted well to the Langmuir equation with maximum adsorption capacity of 27 mg g-1. The adsorption was between 40% and 80% under conditions studied. The results showed that the nanoparticles of synthetic magnetite have high adsorption capacity for uranyl ions so they present good perspectives of application for the processes of uranium liquid waste treatment. (author)

  6. How Soil Organic Matter Composition Controls Hexachlorobenzene-Soil-Interactions: Adsorption Isotherms and Quantum Chemical Modelling

    OpenAIRE

    Ahmed, Ashour; Leinweber, Peter; Kühn, Oliver

    2013-01-01

    Hazardous persistent organic pollutants (POPs) interact in soil with the soil organic matter (SOM) but this interaction is insufficiently understood at the molecular level. We investigated the adsorption of hexachlorobenzene (HCB) on soil samples with systematically modified SOM. These samples included the original soil, the soil modified by adding a hot water extract (HWE) fraction (soil+3 HWE and soil+6 HWE), and the pyrolyzed soil. The SOM contents increased in the order pyrolyzed soil < o...

  7. Adsorption of Pb(II) on mesoporous activated carbons fabricated from water hyacinth using H3PO4 activation: Adsorption capacity, kinetic and isotherm studies

    International Nuclear Information System (INIS)

    Activated carbons with high mesoporosity and abundant oxygen-containing functional groups were prepared from water hyacinth using H3PO4 activation (WHAC) to eliminate Pb(II) in water. Characterizations of the WHAC were performed using Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The BET analysis showed that WHAC possesses a high mesoporosity (93.9%) with a BET surface area of 423.6 m2/g. The presence of oxygen-containing functional groups including hydroxyl, carbonyl, carboxyl and phosphate groups renders the WHAC a favorable adsorbent for Pb(II) with the maximum monolayer capacity (qm) 118.8 mg/g. The adsorption behavior follows pseudo-first order kinetic and Langmuir isotherm. The desorption study demonstrated that the WHAC could be readily regenerated using 0.1 M HCl (pH = 1.0). The desorbed WHAC could be reused at least six times without significant adsorption capacity reduction. The adsorption process was spontaneous and endothermic with ΔG (−0.27, −1.13, −3.02, −3.62, −5.54, and −9.31 kJ/mol) and ΔH (38.72 kJ/mol). Under the optimized conditions, a small amount of the adsorbent (1.0 g/L) could remove as much as 90.1% of Pb(II) (50 mg/L) in 20 min at pH 6.0 and temperature of 298 K. Therefore, the WHAC has a great potential to be an economical and efficient adsorbent in the treatment of lead-contaminated water.

  8. Adsorption of Pb(II) on mesoporous activated carbons fabricated from water hyacinth using H3PO4 activation: Adsorption capacity, kinetic and isotherm studies

    Science.gov (United States)

    Huang, Yang; Li, Shunxing; Chen, Jianhua; Zhang, Xueliang; Chen, Yiping

    2014-02-01

    Activated carbons with high mesoporosity and abundant oxygen-containing functional groups were prepared from water hyacinth using H3PO4 activation (WHAC) to eliminate Pb(II) in water. Characterizations of the WHAC were performed using Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The BET analysis showed that WHAC possesses a high mesoporosity (93.9%) with a BET surface area of 423.6 m2/g. The presence of oxygen-containing functional groups including hydroxyl, carbonyl, carboxyl and phosphate groups renders the WHAC a favorable adsorbent for Pb(II) with the maximum monolayer capacity (qm) 118.8 mg/g. The adsorption behavior follows pseudo-first order kinetic and Langmuir isotherm. The desorption study demonstrated that the WHAC could be readily regenerated using 0.1 M HCl (pH = 1.0). The desorbed WHAC could be reused at least six times without significant adsorption capacity reduction. The adsorption process was spontaneous and endothermic with ΔG (-0.27, -1.13, -3.02, -3.62, -5.54, and -9.31 kJ/mol) and ΔH (38.72 kJ/mol). Under the optimized conditions, a small amount of the adsorbent (1.0 g/L) could remove as much as 90.1% of Pb(II) (50 mg/L) in 20 min at pH 6.0 and temperature of 298 K. Therefore, the WHAC has a great potential to be an economical and efficient adsorbent in the treatment of lead-contaminated water.

  9. Isothermal Chemical Denaturation to Determine Binding Affinity of Small Molecules to G-Protein Coupled Receptors

    OpenAIRE

    Ross, Patrick; Weihofen, Wilhelm; Siu, Fai; Xie, Amy; Katakia, Hetal; Wright, S. Kirk; Hunt, Ian; Brown, Richard K; Freire, Ernesto

    2014-01-01

    The determination of accurate binding affinities is critical in drug discovery and development. Several techniques are available for characterizing the binding of small molecules to soluble proteins. The situation is different for integral membrane proteins. Isothermal chemical denaturation (ICD) has been shown to be a valuable biophysical method to determine in a direct and label-free fashion the binding of ligands to soluble proteins. In this communication, the application of isothermal che...

  10. Solvothermal synthesis of different phase N-TiO2 and their kinetics, isotherm and thermodynamic studies on the adsorption of methyl orange.

    Science.gov (United States)

    Fan, Jimin; Zhao, Zhihuan; Liu, Wenhui; Xue, Yongqiang; Yin, Shu

    2016-05-15

    The different crystal forms of nitrogen doped-titanium oxide (N-TiO2) with different particle sizes were produced by precipitation-solvothermal method and their adsorption mechanism were also investigated. The adsorption kinetics showed that rutile N-TiO2 displayed higher adsorption capacity than anatase for methyl orange (MO) and its adsorption behavior followed the pseudo-second-order kinetics. The equilibrium adsorption rate of N-TiO2 for MO was well fitted by the Langmuir isotherm model and the adsorption process was monolayer adsorption. The adsorption capacity decreased with increasing temperature. The average correlation coefficient was beyond 97%. The thermodynamic parameters (ΔaGm(ө), ΔaHm(ө), and ΔaSm(ө)) were calculated. It was found that anatase and rutile N-TiO2 had different adsorption enthalpy and entropy. The smaller the particle size, the greater the surface area and surface energy was, then ΔaGm(ө) decreased and the standard equilibrium constant increased at the same time. The adsorption process onto different crystalline phase N-TiO2 was exothermic and non-spontaneous. PMID:26945716

  11. Kinetics And Isotherm Studies On Cationic Dyes Adsorption Onto Annona Squmosa Seed Activated Carbon

    OpenAIRE

    Santhi, T.; S. Manonmani; Smitha, T

    2010-01-01

    The use of low - cost, locally available and eco-friendly adsorbents has been investigated as an ideal alternative to the current expensive methods of removing dyes from wastewater. This study investigates the potential use of activated carbon prepared from the Annona squmosa seed for the removal of methylene blue (MB) , methyl red (MR) and malachite green (MG) dyes from simulated wastewater. Adsorption of MB, MR and MG dyes on the Annona squmosa seed showed highest values at around pH 7.0, a...

  12. Determination of thermodynamic parameters of Cr(VI) adsorption from aqueous solution onto Agave lechuguilla biomass

    Energy Technology Data Exchange (ETDEWEB)

    Romero-Gonzalez, J. [Environmental Science and Engineering, University of Texas at El Paso, El Paso, TX 79968 (United States); Peralta-Videa, J.R. [Department of Chemistry, University of Texas at El Paso, El Paso, TX 79968 (United States); Rodriguez, E. [Environmental Science and Engineering, University of Texas at El Paso, El Paso, TX 79968 (United States); Ramirez, S.L. [Department of Chemistry, University of Texas at El Paso, El Paso, TX 79968 (United States); Gardea-Torresdey, J.L. [Environmental Science and Engineering, University of Texas at El Paso, El Paso, TX 79968 (United States) and Department of Chemistry, University of Texas at El Paso, El Paso, TX 79968 (United States)]. E-mail: jgardea@utep.edu

    2005-04-15

    The temperature dependence of the Cr(VI) bioadsorption and its possible reduction to Cr(III) by Agave lechuguilla biomass were studied. The experimental data obtained in batch experiments at different temperatures were fitted to the Langmuir and Freundlich isotherms to obtain the characteristic parameters of each model. The adsorption equilibrium data fitted well with the Freundlich model. The average model parameters calculated from Freundlich's isotherms (adsorption capacity K{sub F} = 4 . 10{sup -2} mol . g{sup -1} and an average adsorption intensity value n = 13.07) showed that A. lechuguilla can be considered as an effective biomaterial for Cr(VI) removal from aqueous solution. Thermodynamic parameters ({delta}G{sup .}, {delta}H{sup .}, and {delta}S{sup .}) for Cr(VI) adsorption determined in the temperature range from (283 to 313) K suggest that a portion of Cr(VI) may be bound to functional groups on the surface of the adsorbent and then reduced to Cr(III). Additionally, the parameters of the Dubinin-Radushkevick equation indicated that the sorption of chromium species onto lechuguilla biomass mainly proceeds through binding surface functional groups.

  13. Determination of thermodynamic parameters of Cr(VI) adsorption from aqueous solution onto Agave lechuguilla biomass

    International Nuclear Information System (INIS)

    The temperature dependence of the Cr(VI) bioadsorption and its possible reduction to Cr(III) by Agave lechuguilla biomass were studied. The experimental data obtained in batch experiments at different temperatures were fitted to the Langmuir and Freundlich isotherms to obtain the characteristic parameters of each model. The adsorption equilibrium data fitted well with the Freundlich model. The average model parameters calculated from Freundlich's isotherms (adsorption capacity KF = 4 . 10-2 mol . g-1 and an average adsorption intensity value n = 13.07) showed that A. lechuguilla can be considered as an effective biomaterial for Cr(VI) removal from aqueous solution. Thermodynamic parameters (ΔG., ΔH., and ΔS.) for Cr(VI) adsorption determined in the temperature range from (283 to 313) K suggest that a portion of Cr(VI) may be bound to functional groups on the surface of the adsorbent and then reduced to Cr(III). Additionally, the parameters of the Dubinin-Radushkevick equation indicated that the sorption of chromium species onto lechuguilla biomass mainly proceeds through binding surface functional groups

  14. Adsorption of methylene blue onto poly(cyclotriphosphazene-co-4,4′-sulfonyldiphenol) nanotubes: Kinetics, isotherm and thermodynamics analysis

    International Nuclear Information System (INIS)

    Highlights: • Polyphosphazene nanotube as an adsorbent could be facilely synthesized. • The adsorbent owns numerous electron-rich N and P atoms and hydroxyl groups. • The adsorbent was an efficient and specific adsorbent for the removal of MB. • The pseudo-second-order model could be better to describe the adsorption of MB. • The MB adsorption onto PZS nanotubes was endothermic and spontaneous. - Abstract: Poly(cyclotriphosphazene-co-4,4′-sulfonyldiphenol) (PZS) nanotubes, an excellent adsorbent, were successfully synthesized by an in situ template method and used for the removal of methylene blue (MB) from aqueous solution. The morphology and structures of as-synthesized PZS nanotubes were characterized by scanning electron microscopy, transmission electron microscope, Fourier transform infrared spectroscopy and N2 adsorption/desorption isotherms. The effects of temperature, concentration, pH and contact time on MB adsorption were studied. It was favorable for adsorption under the condition of basic and high temperature. The pseudo-first-order, pseudo-second-order and intraparticle diffusion models were used to fit adsorption data in the kinetic studies. And results showed that the adsorption kinetics were more accurately described by the pseudo-second-order model. The equilibrium isotherms were conducted using Freundlich and Langmuir models. It has been demonstrated that the better agreement was Langmuir isotherm with correlation coefficient of 0.9933, equilibrium absorption capacity of 69.16 mg/g and the corresponding contact time of 15 min. Thermodynamic analyses showed that MB adsorption onto the PZS nanotubes was endothermic and spontaneous and it was also a physisorption process

  15. Adsorption Geometry Determination of Single Molecules by Atomic Force Microscopy

    OpenAIRE

    Schuler, Bruno; Liu, Wei; Tkatchenko, Alexandre; Moll, Nikolaj; Meyer, Gerhard; Mistry, Anish; Fox, David; GROSS, Leo

    2013-01-01

    We measured the adsorption geometry of single molecules with intramolecular resolution using noncontact atomic force microscopy with functionalized tips. The lateral adsorption position was determined with atomic resolution, adsorption height differences with a precision of 3 pm, and tilts of the molecular plane within 0.2 degrees. The method was applied to five pi-conjugated molecules, including three molecules from the olympicene family, adsorbed on Cu(111). For the olympicenes, we found th...

  16. Thermodynamics, interfacial pressure isotherms and dilational rheology of mixed protein-surfactant adsorption layers.

    Science.gov (United States)

    Fainerman, V B; Aksenenko, E V; Krägel, J; Miller, R

    2016-07-01

    Proteins and their mixtures with surfactants are widely used in many applications. The knowledge of their solution bulk behavior and its impact on the properties of interfacial layers made great progress in the recent years. Different mechanisms apply to the formation process of protein/surfactant complexes for ionic and non-ionic surfactants, which are governed mainly by electrostatic and hydrophobic interactions. The surface activity of these complexes is often remarkably different from that of the individual protein and has to be considered in respective theoretical models. At very low protein concentration, small amounts of added surfactants can change the surface activity of proteins remarkably, even though no strongly interfacial active complexes are observed. Also small added amounts of non-ionic surfactants change the surface activity of proteins in the range of small bulk concentrations or surface coverages. The modeling of the equilibrium adsorption behavior of proteins and their mixtures with surfactants has reached a rather high level. These models are suitable also to describe the high frequency limits of the dilational viscoelasticity of the interfacial layers. Depending on the nature of the protein/surfactant interactions and the changes in the interfacial layer composition rather complex dilational viscoelasticities can be observed and described by the available models. The differences in the interfacial behavior, often observed in literature for studies using different experimental methods, are at least partially explained by a depletion of proteins, surfactants and their complexes in the range of low concentrations. A correction of these depletion effects typically provides good agreement between the data obtained with different methods, such as drop and bubble profile tensiometry. PMID:26198014

  17. The influence of carbon surface oxygen groups on Dubinin-Astakhov equation parameters calculated from CO{sub 2} adsorption isotherm

    Energy Technology Data Exchange (ETDEWEB)

    Furmaniak, Sylwester; Terzyk, Artur P; Gauden, Piotr A [N Copernicus University, Department of Chemistry, Physicochemistry of Carbon Materials Research Group, Gagarin Street 7, 87-100 Torun (Poland); Harris, Peter J F [Centre for Advanced Microscopy, University of Reading, Whiteknights, Reading RG6 6AF (United Kingdom); Kowalczyk, Piotr, E-mail: aterzyk@chem.uni.torun.p, E-mail: p.j.f.harris@rdg.ac.u [Applied Physics, RMIT University, GPO Box 2476V, Victoria 3001 (Australia)

    2010-03-03

    We present the results of a systematic study of the influence of carbon surface oxidation on Dubinin-Astakhov isotherm parameters obtained from the fitting of CO{sub 2} adsorption data. Using GCMC simulations of adsorption on realistic VPC models differing in porosity and containing the most frequently occurring carbon surface functionalities (carboxyls, hydroxyls and carbonyls) and their mixtures, it is concluded that the maximum adsorption calculated from the DA model is not strongly affected by the presence of oxygen groups. Unfortunately, the same cannot be said of the remaining two parameters of this model i.e. the heterogeneity parameter (n) and the characteristic energy of adsorption (E{sub 0}). Since from the latter the pore diameters of carbons are usually calculated, by inverse-type relationships, it is concluded that they are questionable for carbons containing surface oxides, especially carboxyls.

  18. A Simple Adsorption Experiment

    Science.gov (United States)

    Guirado, Gonzalo; Ayllon, Jose A.

    2011-01-01

    The study of adsorption phenomenon is one of the most relevant and traditional physical chemistry experiments performed by chemistry undergraduate students in laboratory courses. In this article, we describe an easy, inexpensive, and straightforward way to experimentally determine adsorption isotherms using pieces of filter paper as the adsorbent…

  19. Highly efficient ultrasonic-assisted removal of Hg(II) ions on graphene oxide modified with 2-pyridinecarboxaldehyde thiosemicarbazone: Adsorption isotherms and kinetics studies.

    Science.gov (United States)

    Tadjarodi, Azadeh; Moazen Ferdowsi, Somayeh; Zare-Dorabei, Rouholah; Barzin, Ahmad

    2016-11-01

    A novel adsorbent, based on modifying graphene oxide (GO) chemically with 2-pyridinecarboxaldehyde thiosemicarbazone (2-PTSC) as ligand, was designed by facile process for removal of Hg(II) from aqueous solution. Characterization of the adsorbent was performed using various techniques, such as FT-IR, XRD, XPS, SEM and AFM analysis. The adsorption capacity was affected by variables such as adsorbent dosage, pH solution, Hg(2+) initial concentration and sonicating time. These variables were optimized by rotatable central composite design (CCD) under response surface methodology (RSM). The predictive model for Hg(II) adsorption was constructed and applied to find the best conditions at which the responses were maximized. In this conditions, the adsorption capacity of this adsorbent for Hg(2+) ions was calculated to be 309mgg(-1) that was higher than that of GO. Appling the ultrasound power combined with adsorption method was very efficient in shortening the removal time of Hg(2+) ions by enhancing the dispersion of adsorbent and metal ions in solution and effective interactions among them. The adsorption process was well described by second-order kinetic and Langmuir isotherm model in which the maximum adsorption capacity (Qm) was found to be 555mgg(-1) for adsorption of Hg(2+) ions over the obtained adsorbent. The performance of adsorbent was examined on the real wastewaters and confirmed the applicability of adsorbent for practical applications. PMID:27245963

  20. 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.

  1. ADSORPTION OF POLYCHLORINATED BIPHENYLS BY SOILS

    OpenAIRE

    Mihaela Preda; Radu Lăcătuşu; Dumitru Marian Motelică; Nicoleta Vrînceanu; Veronica Tănase

    2010-01-01

    The behavior of polychlorinated biphenyls (PCBs) in soil is determined by several factors including adsorption, mobility and degradation. Adsorption, directly or indirectly, influences the other factors. Adsorption process is generally evaluated by using adsorption isotherms representing the relationship between the quantity of substance adsorbed per unit weight and concentration of the substance in solution at equilibrium. They allow determination of the adsorption constant, which is directl...

  2. Isotherm studies for determination of removal capacity of bi-metal (Ni and Cr) ions by aspergillus niger

    International Nuclear Information System (INIS)

    Pakistan is among the developing countries where there is a need to establish new industries to meet the demands of a growing population. This has led to industrial setup in various sectors, without proper planning and consideration for treatment of contamination, leading to disposal of untreated wastewater into nearby land and water bodies. This study was planned to investigate an indigenous Aspergillus niger for development of biosorbent for the removal of metal ions. The Aspergillus isolate's Ni and Cr removal efficiency was determined in batch mode over various pH (4.0-10.0) and temperature (25-40 deg. C) as single as well as bimetal ions. Using a single metal ion, maximum biosorption potential was obtained at pH 5.0-6.0 and 30-35 deg. C for both ions. On the other hand, Ni removal was reduced in the presence of Cr, while Ni removal influenced Cr removal with an increase showing maximum removal at an initial adsorbate concentration of 50mg/L, pH 6.0 and 35 deg. C. Effect of presence of bimetal in a solution on biosorption potential of Aspergillus niger was predicted by using equilibrium modeling. Adsorption trends for both nickel (R2 0.9916) and chromium (R2 0.8548) followed Langmuir isotherm in single metal removal system, but under bimetal condition chromium adsorption fitted better to Freundlich model and that of nickel followed Temkin isotherm, suggesting considerable change in behavior and interaction between biosorbent and metal ions. Therefore, we concluded that Aspergillus niger a viable strain for development of a biosorbent for removal of a mixture of metal ions. (author)

  3. Production of granular activated carbon from agricultural wastes and determination of their physical, chemical and adsorption properties

    Energy Technology Data Exchange (ETDEWEB)

    Ayguen, A.; Duman, I. [Istanbul Technical Univ., Inst. of Science and Technology, Dept. of Metallurgical Engineering, Istanbul (Turkey); Yenisoy-Karakas, S. [TUeBITAK Marmara Research Center (MRC), Materials and Chemical Technologies Research Inst., Gebze Kocaeli (Turkey)

    2004-07-01

    The aim of this study is to produce activated carbons with good mechanical strength and high adsorption capacities toward various organics from food wastes such as walnut, almond, hazelnut shells and apricot stones. Turkey has huge amounts of these wastes in canning industry. The chemical activation with ZnCl{sub 2} was preferred to manufacture activated carbons. The best activation temperature and time were determined. Granular activated carbons were discussed with respect to their physical, chemical, surface area and adsorption properties. For all raw materials, the specific surface areas of greater than 730 m{sup 2} g{sup -1} were reached. As a result of the adsorption studies, adsorption capacities were in order of hazelnut> apricot stones> walnut> almond. The correlation coefficients obtained from Langmuir and Freundlich isotherms are in good agreement with the experimental results. (orig.)

  4. Determination of kinetic and equilibrium parameters of the batch adsorption of Mn(II), Co(II), Ni(II) and Cu(II) from aqueous solution by black carrot (Daucus carota L.) residues

    International Nuclear Information System (INIS)

    In this study, the effect of temperature on the adsorption of Mn(II), Ni(II), Co(II) and Cu(II) from aqueous solution by modified carrot residues (MCR) was investigated. The equilibrium contact times of adsorption process for each heavy metals-MCR systems were determined. Kinetic data obtained for each heavy metal by MCR at different temperatures were applied to the Lagergren equation, and adsorption rate constants (kads) at these temperatures were determined. These rate constants related to the adsorption of heavy metal by MCR were applied to the Arrhenius equation, and activation energies (Ea) were determined. In addition, the isotherms for adsorption of each heavy metal by MCR at different temperatures were also determined. These isothermal data were applied to linear forms of isotherm equations that they fit the Langmuir adsorption isotherm, and the Langmuir constants (qm and b) were calculated. b constants determined at different temperatures were applied to thermodynamic equations, and thermodynamic parameters such as enthalpy (ΔH), free energy (ΔG), and entropy (ΔS) were calculated and these values show that adsorption of heavy metal on MCR was an endothermic process and process of adsorption was favoured at high temperatures

  5. Determination of kinetic and equilibrium parameters of the batch adsorption of Mn(II), Co(II), Ni(II) and Cu(II) from aqueous solution by black carrot (Daucus carota L.) residues

    Energy Technology Data Exchange (ETDEWEB)

    Guezel, Fuat [Department of Chemistry, Faculty of Education, Dicle University, 21280 Diyarbakir (Turkey)], E-mail: fguzel@dicle.edu.tr; Yakut, Hakan; Topal, Giray [Department of Chemistry, Faculty of Education, Dicle University, 21280 Diyarbakir (Turkey)

    2008-05-30

    In this study, the effect of temperature on the adsorption of Mn(II), Ni(II), Co(II) and Cu(II) from aqueous solution by modified carrot residues (MCR) was investigated. The equilibrium contact times of adsorption process for each heavy metals-MCR systems were determined. Kinetic data obtained for each heavy metal by MCR at different temperatures were applied to the Lagergren equation, and adsorption rate constants (k{sub ads}) at these temperatures were determined. These rate constants related to the adsorption of heavy metal by MCR were applied to the Arrhenius equation, and activation energies (E{sub a}) were determined. In addition, the isotherms for adsorption of each heavy metal by MCR at different temperatures were also determined. These isothermal data were applied to linear forms of isotherm equations that they fit the Langmuir adsorption isotherm, and the Langmuir constants (q{sub m} and b) were calculated. b constants determined at different temperatures were applied to thermodynamic equations, and thermodynamic parameters such as enthalpy ({delta}H), free energy ({delta}G), and entropy ({delta}S) were calculated and these values show that adsorption of heavy metal on MCR was an endothermic process and process of adsorption was favoured at high temperatures.

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

    Science.gov (United States)

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

    2010-08-16

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

  7. Removal of 2,4-dichlorophenol using cyclodextrin-ionic liquid polymer as a macroporous material: Characterization, adsorption isotherm, kinetic study, thermodynamics

    International Nuclear Information System (INIS)

    Highlights: • βCD-BIMOTs-TDI exhibits macropore size (77.66 nm) with 1.254 m2 g−1 surface area. • Freundlich isotherm and pseudo-second order kinetics fit well the adsorption process. • Removal was optimum at pH 6 with 83% and reached equilibrium at 80 mg L−1. • Entropy (ΔS°) and heat of adsorption (ΔH°) estimated as −55.99 J/K mol and −18.10 J/mol. • Inclusion complex and π–π interaction were found to be dominant at pH 6. -- Abstract: Cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI) was firstly synthesized using functionalized β-Cyclodextrin (CD) with 1-benzylimidazole (BIM) to form monofunctionalized CD (βCD-BIMOTs) and was further polymerized using toluene diisocyanate (TDI) linker to form insoluble βCD-BIMOTs-TDI. SEM characterization result shows that βCD-BIMOTs-TDI exhibits macropore size while the BET result shows low surface area (1.254 m2 g−1). The unique properties of the ILs allow us to produce materials with different morphologies. The adsorption isotherm and kinetics of 2,4-dichlorophenol (2,4-DCP) onto βCD-BIMOTs-TDI is studied. Freundlich isotherm and pseudo-second order kinetics are found to be the best to represent the data for 2,4-DCP adsorption on the βCD-BIMOTs-TDI. The presence of macropores decreases the mass transfer resistance and increases the adsorption process by reducing the diffusion distance. The change in entropy (ΔS°) and heat of adsorption (ΔH°) for 2,4-DCP on βCD-BIMOTs-TDI were estimated as −55.99 J/Kmol and −18.10 J/mol, respectively. The negative value of Gibbs free energy (ΔG°) indicates that the adsorption process is thermodynamically feasible, spontaneous and chemically controlled. Finally, the interactions between the cavity of βCD-BIMOTs and 2,4-DCP are investigated and the results shows that the inclusion of the complex formation and π–π interaction are the main processes involved in the adsorption process

  8. Removal of 2,4-dichlorophenol using cyclodextrin-ionic liquid polymer as a macroporous material: Characterization, adsorption isotherm, kinetic study, thermodynamics

    Energy Technology Data Exchange (ETDEWEB)

    Raoov, Muggundha [University of Malaya Centre for Ionic Liquids, Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Advanced Medical and Dental Institute, University of Science Malaysia, No. 1–8 (Lot 8), Persiaran Seksyen 4/1, Bandar Putra Bertam, Kepala Batas, Pulau Pinang 13200 (Malaysia); Mohamad, Sharifah, E-mail: sharifahm@um.edu.my [University of Malaya Centre for Ionic Liquids, Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Abas, Mohd Radzi [Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia)

    2013-12-15

    Highlights: • βCD-BIMOTs-TDI exhibits macropore size (77.66 nm) with 1.254 m{sup 2} g{sup −1} surface area. • Freundlich isotherm and pseudo-second order kinetics fit well the adsorption process. • Removal was optimum at pH 6 with 83% and reached equilibrium at 80 mg L{sup −1}. • Entropy (ΔS°) and heat of adsorption (ΔH°) estimated as −55.99 J/K mol and −18.10 J/mol. • Inclusion complex and π–π interaction were found to be dominant at pH 6. -- Abstract: Cyclodextrin-ionic liquid polymer (βCD-BIMOTs-TDI) was firstly synthesized using functionalized β-Cyclodextrin (CD) with 1-benzylimidazole (BIM) to form monofunctionalized CD (βCD-BIMOTs) and was further polymerized using toluene diisocyanate (TDI) linker to form insoluble βCD-BIMOTs-TDI. SEM characterization result shows that βCD-BIMOTs-TDI exhibits macropore size while the BET result shows low surface area (1.254 m{sup 2} g{sup −1}). The unique properties of the ILs allow us to produce materials with different morphologies. The adsorption isotherm and kinetics of 2,4-dichlorophenol (2,4-DCP) onto βCD-BIMOTs-TDI is studied. Freundlich isotherm and pseudo-second order kinetics are found to be the best to represent the data for 2,4-DCP adsorption on the βCD-BIMOTs-TDI. The presence of macropores decreases the mass transfer resistance and increases the adsorption process by reducing the diffusion distance. The change in entropy (ΔS°) and heat of adsorption (ΔH°) for 2,4-DCP on βCD-BIMOTs-TDI were estimated as −55.99 J/Kmol and −18.10 J/mol, respectively. The negative value of Gibbs free energy (ΔG°) indicates that the adsorption process is thermodynamically feasible, spontaneous and chemically controlled. Finally, the interactions between the cavity of βCD-BIMOTs and 2,4-DCP are investigated and the results shows that the inclusion of the complex formation and π–π interaction are the main processes involved in the adsorption process.

  9. Adsorption removal of Congo red from aqueous solution by polyhedral Cu{sub 2}O nanoparticles: Kinetics, isotherms, thermodynamics and mechanism analysis

    Energy Technology Data Exchange (ETDEWEB)

    Shu, Jinxia [Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002 (China); Wang, Zhonghua, E-mail: zhwangs@163.com [Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002 (China); Huang, Yijiang; Huang, Ni [Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002 (China); Ren, Chunguang [Graduate School of Materials Science, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0192 (Japan); Zhang, Wei [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China)

    2015-06-05

    Highlights: • Polyhedral Cu{sub 2}O NPs with rough surfaces were prepared by a one-pot sonochemical precipitation method. • The Cu{sub 2}O NPs show unprecedented adsorption capability toward Congo red. • CR adsorption onto Cu{sub 2}O is a spontaneous, endothermic and chemisorption process. • The Cu{sub 2}O adsorbent can be photocatalytically regenerated by visible light irradiation. - Abstract: Polyhedral cuprous oxide nanoparticles (Cu{sub 2}O NPs) with rough surfaces were prepared by a one-pot sonochemical precipitation method. The products were characterized by SEM, XRD, EDS, XPS, and UV–Vis DRS, respectively. The adsorption behavior of Congo red (CR) from aqueous solution onto the as-prepared Cu{sub 2}O NPs was systematically investigated. The equilibrium and kinetic studies suggested that the adsorption process followed Freundlich isotherm and pseudo-second order model, respectively. The as-prepared Cu{sub 2}O NPs exhibited remarkable adsorption properties toward CR. The maximum adsorption capacity at 20 °C was 3904 mg g{sup −1}, which was the highest reported value so far in adsorption removal of CR. Together with the evaluation of the thermodynamic parameters such as Gibbs free energy, enthalpy and entropy change, our results show that the adsorption of CR onto Cu{sub 2}O is a spontaneous, endothermic and chemisorption process. A putative interaction model between CR and Cu{sub 2}O NPs was proposed. Moreover, the Cu{sub 2}O adsorbent could be photocatalytically regenerated and reused without significant loss of its adsorption capability.

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

    OpenAIRE

    Dada, A. O.; J. O. Ojediran; Abiodun Paul Olalekan

    2013-01-01

    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...

  11. Adsorption of nicotine from aqueous solution onto hydrophobic zeolite type USY

    Science.gov (United States)

    Lazarevic, Natasa; Adnadjevic, Borivoj; Jovanovic, Jelena

    2011-07-01

    The isothermal adsorption of nicotine from an aqueous solution onto zeolite type USY was investigated. The adsorption isotherms of nicotine onto the zeolite at different temperatures ranging from 298 to 322 K were determined. It was found that the adsorption isotherms can be described by the model of Freundlich adsorption isotherm. Based on the adsorption isotherms the changes of adsorption heat, free energy and entropy with adsorption degree were determined. The determined decrease of adsorption heat with adsorption degree can be explained by the presence of the adsorption centers of different energy and concentration on interface of zeolite-nicotine solution. It was found that the probability function of density distribution of the heat of adsorption (DDF) has exponential form. It was concluded that the possibility of fitting the adsorption isotherms of nicotine onto the zeolite by Freundlich adsorption isotherm was a direct consequence of that. The determined increase in entropy with the increase in adsorption degree can be explained with the change of phase state of adsorbed nicotine.

  12. Equilibrium adsorption isotherm studies of Cu (II) and Co (II) in high concentration aqueous solutions on Ag-TiO2-modified kaolinite ceramic adsorbents

    Science.gov (United States)

    Ajenifuja, E.; Ajao, J. A.; Ajayi, E. O. B.

    2016-03-01

    Photocatalytic ceramic adsorbents were prepared from locally sourced kaolinite clay minerals for the removal of copper and cobalt ions from high concentration aqueous solutions. The minerals were treated with mild acid before modification using silver nanoparticles sources and titanium-oxide nanoparticles. Batch adsorption experiment was carried out on the targeted ions and the results were analyzed by Langmuir and Freundlich equation at different concentrations (100-1000 mg/l). As-received raw materials do not exhibit any adsorption capacity. However, the adsorption isotherms for modified kaolinite clay ceramic adsorbents could be fitted well by the Langmuir model for Cu2+ and Co2+ with correlation coefficient (R) of up to 0.99705. The highest and lowest monolayer coverage (q max) were 93.023 and 30.497 mg/g for Cu2+ and Co2+, respectively. The separation factor (R L ) was less than one (<1), indicating that the adsorption of metal ions on modified ceramic adsorbent is favorable. The highest adsorbent adsorption capacity (K f ) and intensity (n) constants obtained from Freundlich model are 14.401 (Cu2+ on KLN-T) and 6.057 (Co2+ on KLN-T).

  13. Adsorption isotherm and inhibition effect of a synthesized di-(m-Formylphenol)-1,2-cyclohexandiimine on corrosion of steel X52 in HCl solution

    Institute of Scientific and Technical Information of China (English)

    A karimi; I Danaee; H Eskandari; M RashvanAvei

    2016-01-01

    The potential of di-(m-Formylphenol)-1,2-cyclohexandiimine as an environmentally friendly corrosion inhibitor for steel was investigated in 1 mol/L HCl using potentiodynamic polarization, electrochemical impedance spectroscopy and chronoamperometry measurements. All electrochemical measurements suggest that this compound is an excellent corrosion inhibitor for mild steel and the inhibition efficiency increases with the increase in inhibitor concentration. The effect of temperature on the corrosion behavior of mild steel with the addition of the Schiff base was studied in the temperature range from 25 °C to 65 °C. It is found that the adsorption of this inhibitor follows the Langmuir adsorption isotherms. The value of activation energy and the thermodynamic parameters such asΔHads,ΔSads,Kads andΔGads were calculated by the corrosion currents at different temperatures using the adsorption isotherm. The morphology of mild steel surface in the absence and presence of inhibitor was examined by scanning electron microscopy (SEM) images.

  14. Determination of the aggregation number for micelles by isothermal titration calorimetry

    DEFF Research Database (Denmark)

    Olesen, Niels Erik; Holm, Rene; Westh, Peter

    2014-01-01

    Isothermal titration calorimetry (ITC) has previously been applied to estimate the aggregation number (n), Gibbs free energy (ΔG), enthalpy (ΔH) and entropy (ΔS) of micellization. However, some difficulties of micelle characterization by ITC still remain; most micelles have aggregation numbers...... insight into optimal design of titration protocols for micelle characterization. By applying the new method, the aggregation number of sodium dodecyl sulphate and glycochenodeoxycholate was determined at concentrations around their critical micelle concentration (CMC)...

  15. Protein adsorption on low temperature isotropic carbon. III. Isotherms, competitivity, desorption and exchange of human albumin and fibrinogen.

    Science.gov (United States)

    Feng, L; Andrade, J D

    1994-04-01

    In this paper we consider the adsorption of albumin and fibrinogen on low temperature isotropic carbon (LTIC). A subsequent paper considers the adsorption of other plasma proteins [Feng L, Andrade JD, Colloids and Surfaces (in press)]. Carbon fragments and silica plates were used as adsorbents. Adsorption was carried out by incubating the adsorbents in solutions of 125I-labelled and unlabelled proteins (single component system), or with buffer-diluted human plasma (multicomponent system). Adsorbed proteins then underwent displacement by buffer, by single protein solutions or by dilute plasma. Results show that the LTIC substrate adsorbs a large amount of proteins before saturation, which may be due to multilayer adsorption. LTIC also irreversibly holds adsorbed proteins against the exchange agents used; little adsorbed proteins can be displaced, even after a very short adsorption time. There is no preferential adsorption for either albumin or fibrinogen on LTIC from their binary solutions, suggesting that both proteins have high affinities for the surface. Such strong interactions between LTIC and proteins are not attributed to electrostatic interactions. On the other hand, protein adsorption on the silica surface is selective and reversible, with a much higher affinity for fibrinogen than albumin and an even higher affinity for some other plasma proteins. The paper also discusses the effect of sequential protein addition to a solution on the surface concentration and suppression of adsorption of both proteins in the presence of other plasma proteins. A very important conclusion is that the LTIC surface is very active towards proteins adsorption. PMID:8061122

  16. Structural determinants for protein adsorption/non-adsorption to silica surface

    International Nuclear Information System (INIS)

    The understanding of the mechanisms involved in the interaction of proteins with inorganic surfaces is of major interest in both fundamental research and applications such as nano-technology. However, despite intense research, the mechanisms and the structural determinants of protein/surface interactions are still unclear. We developed a strategy consisting in identifying, in a mixture of hundreds of soluble proteins, those proteins that are adsorbed on the surface and those that are not. If the two protein subsets are large enough, their statistical comparative analysis must reveal the physicochemical determinants relevant for adsorption versus non-adsorption. This methodology was tested with silica nanoparticles. We found that the adsorbed proteins contain a higher number of charged amino acids, particularly arginine, which is consistent with involvement of this basic amino acid in electrostatic interactions with silica. The analysis also identified a marked bias toward low aromatic amino acid content (phenylalanine, tryptophan, tyrosine and histidine) in adsorbed proteins. Structural analyses and molecular dynamics simulations of proteins from the two groups indicate that non-adsorbed proteins have twice as many p-p interactions and higher structural rigidity. The data are consistent with the notion that adsorption is correlated with the flexibility of the protein and with its ability to spread on the surface. Our findings led us to propose a refined model of protein adsorption. (authors)

  17. Determination of the kinetic parameters of K2YF5:Tb from isothermal decay of thermoluminescence

    International Nuclear Information System (INIS)

    Most of the existing methods for obtaining the frequency factors make use of the trap depth (activation energy) making assumptions about the order of the kinetics. This leads to inconsistencies in the reported values of trapping parameters as the values of the activation energy obtained by different methods differ appreciably among them. Then, it is necessary to employ a method independent of the trap depth as it is the case of the method that makes use of the isothermal decay of the thermoluminescence (TL). In this paper, the isothermal decay of TL was used to determine the trapping parameters of K2YF5:Tb. The results obtained by applying this method are in good agreement with those obtained using the glow curve shape method except in the value of the frequency factor

  18. Determination of the kinetic parameters of Be O using isothermal decay method

    International Nuclear Information System (INIS)

    Full text: Most of the existing methods for obtaining the frequency factors make use of the trap depth (activation energy) making some assumptions about the order of the kinetics. This causes inconsistencies in the reported values of trapping parameters due that the values of the activation energy obtained by different methods differ appreciably among them. Then, it is necessary to use a method independent of the trap depth making use of the isothermal luminescence decay method. The trapping parameters associated with the prominent glow peak of Be O (280 degrees C) are reported using isothermal luminescence decay method. As a check, the trap parameters are also calculated by glow curve shape (Chen s) method after isolating the prominent glow peak by thermal cleaning technique. Our results show a very good agreement between the trapping parameters calculated by the two methods. Isothermal luminescence decay method was used for determining the trapping parameters of Be O. Results obtained applying this method are in good agreement with those obtained using other methods, except in the value of the frequency factor. (Author)

  19. Determination of the kinetic parameters of Be O using isothermal decay method

    Energy Technology Data Exchange (ETDEWEB)

    Azorin N, J.; Torijano C, E. [Universidad Autonoma Metropolitana, Unidad Iztapalapa, Av. San Rafael Atlixco 186, Col. Vicentina, 09340 Mexico D. F. (Mexico); Azorin V, C.; Rivera M, T., E-mail: azorin@xanum.uam.mx [IPN, Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada, Av. Legaria 694, Col. Irrigacion, 11500 Mexico D. F. (Mexico)

    2015-10-15

    Full text: Most of the existing methods for obtaining the frequency factors make use of the trap depth (activation energy) making some assumptions about the order of the kinetics. This causes inconsistencies in the reported values of trapping parameters due that the values of the activation energy obtained by different methods differ appreciably among them. Then, it is necessary to use a method independent of the trap depth making use of the isothermal luminescence decay method. The trapping parameters associated with the prominent glow peak of Be O (280 degrees C) are reported using isothermal luminescence decay method. As a check, the trap parameters are also calculated by glow curve shape (Chen s) method after isolating the prominent glow peak by thermal cleaning technique. Our results show a very good agreement between the trapping parameters calculated by the two methods. Isothermal luminescence decay method was used for determining the trapping parameters of Be O. Results obtained applying this method are in good agreement with those obtained using other methods, except in the value of the frequency factor. (Author)

  20. Adsorption properties and porous structure of sulfuric acid treated bentonites determined - SHORT COMMUNICATION

    Directory of Open Access Journals (Sweden)

    SNEZANA BREZOVSKA

    2005-02-01

    Full Text Available In a previous paper adsorption isotherms of benzene vapor on natural bentonite from Ginovci, Macedonia, and forms acid activated with 10 % and 15 % solutions of hydrochloric were interpreted by means of the Dubinin–Radushkevich–Stoeckli and Dubinin–Astakhov equations; the investigation has been continued with bentonites acid activated with 10 % and 15 % solutions of sulfuric acid where X-ray analysis indicates smaller structural changes. Using the above equations, the heterogeneity of the micropores and the energetic heterogeneity of the bentonites were determined from the differential distribution of the micropore volume with respect to the structural parameter of the equations characterizing the microporous structure and to the molar free energy of adsorption. Activated bentonites obtain bigger pores but also a certain quantity of new small pores appear during acid activation with the higher concentration of acid. The micropore volumes, determined from the adsorption of benzene vapor, of bentonites activated with 10 % and 15 % solution of hydrochloric acid (144.60 cm3 kg-1 and 110.06 cm3 kg-1, respectively, decrease in comparison with that of natural bentonite (162.55 cm3 kgv.1 In contrast, the values of the micropore volume for bentonities treated with 10 % and 15 % solutions of sulfuric acids increase (169.19 cm3 kg-1 and 227.74 cm3 kg-1. That is due to the difference in the structural changes occurring during activation with hydrochloric and sulfuric acids. The values of the free energy of adsorption of benzene vapor for natural bentonite are higher than those of the acid acitivated bentonities, what is in accordance with the structural and porosity changes.

  1. Adsorption of acid and basic dyes by sludge-based activated carbon:Isotherm and kinetic studies

    Institute of Scientific and Technical Information of China (English)

    李鑫; 王广智; 李伟光; 王萍; 宿程远

    2015-01-01

    A batch experiment was conducted to investigate the adsorption of an acid dye (Acid Orange 51) and a basic dye (Safranine) from aqueous solutions by the sludge-based activated carbon (SBAC). The results show that the adsorption of Acid Orange 51 decreases at high pH values, whereas the uptake of Safranine is higher in neutral and alkaline solutions than that in acidic conditions. The adsorption time needed for Safranine to reach equilibrium is shorter than that for Acid Orange 51. The uptakes of the dyes both increase with temperature increasing, indicating that the adsorption process of the dyes onto SBAC is endothermic. The equilibrium data of the dyes are both best represented by the Redlich−Peterson model. At 25 °C, the maximum adsorption capacities of SBAC for Acid Orange 51 and Safranine are 248.70 mg/g and 525.84 mg/g, respectively. The Elovich model is found to best describe the adsorption process of both dyes, indicating that the rate-limiting step involves the chemisorption. It can be concluded that SBAC is a promising material for the removal of Acid Orange 51 and Safranine from aqueous solutions.

  2. Isotherm of fluoride ion adsorption by zeolite andγ-alumina:comparison of linear and non-linear methods%沸石与γ-氧化铝吸附氟离子等温线的线性和非线性方法比较研究

    Institute of Scientific and Technical Information of China (English)

    陈安浩; 磨季云; 郝琨妍

    2014-01-01

    采用线性和非线性方法研究沸石与γ-氧化铝对水中氟离子吸附等温线的拟合形式,并分析比较了两种数据处理方法的优劣。结果表明,非线性方法提供了一种更准确的方法来确定最佳的吸附等温线模型;沸石吸附氟离子的实验数据与Redlich-Peterson、Langmiur等温线模型拟合较好;γ-氧化铝的吸附氟离子实验数据与Redlich-Peterson等温线模型拟合较好。%Linear and non-linear methods were adopted respectively to study the fitting degree of the adsorption of fluoride ions in water by zeolite and γ-alumina ,and the advantages as well as disadvan-tages of the two methods in data processing were compared .The results show that non-linear method is more accurate in determining the optimum adsorption isotherm model ,and the experimental data of zeolite adsorption of fluoride ions fits better with Redlich Peterson and Langmiur isotherm model , while the experimental data of γ-alumina adsorption of fluoride ions fits better with Redlich Peterson isotherm model .

  3. 采用空穴阻挡层提高有机太阳电池效率的研究%Adsorption Influencing Factors and Isotherms of Squid Melanin on Pb^2+ and Cr^6+

    Institute of Scientific and Technical Information of China (English)

    鲁婷婷; 林琳; 褚梦思; 汪盼盼; 黄乾; 宋茹

    2012-01-01

    为研究BCP对有机太阳电池的影响,制备了含BCP层的体相异质结电池,器件结构为:ITO/PEDOT:PSS/P3HT+PCBM/BCP/LiF/Al。结果表明:BCP层起到了空穴阻挡和电子传输的作用,器件性能随着BCP层厚度的不同而变化,当BCP厚度为6nm时,其性能最好。%In this study, squid melanin was used as adsorbent to remove of Pb^2+ and Cr^6+ from aqueous solutions, the adsorption factors including squid melanin content, adsorption time, adsorption temperature and solution pH were investigated, as well as the adsorption isotherms were analyzed. Results showed that the added squid melanin effectively adsorbed Pb^2+ and Cr^6+ in aqueous solutions. The removal rates of Pb^2+ and Cr^6+ were above 85.00% after adsorption of 15 min by squid melain. In addition, the removal rate of Pb^2+ decreased with the increased adsorption temperatures, whereas, the maximum adsorption of Cr^6+ was found at 35℃. The low adsorption capacity of squid melanin on Pb^2+ was observed at solution pH of 5.0, and the effective solution pH for Cr^6+ removal was in the range of 4.0 to 6.0. Furthermore, results of adsorption isotherms revealed that the adsorption characteristic of squid melanin on Cr^6+ fitted well to Langmuir and Freundlich models. By comparison, the adsorption behavior of squid melanin on Pb^2+ only had a good correlation with the Langmuir isotherm.

  4. Investigation on adsorption capacity of TiO2-P25 nanoparticles in the removal of a mono-azo dye from aqueous solution: A comprehensive isotherm analysis

    Directory of Open Access Journals (Sweden)

    Behnajady Mohammad A.

    2014-01-01

    Full Text Available In this work TiO2-P25 nanoparticles with high surface area have been used as adsorbent for the removal of C.I Acid Red 27 (AR27, as an organic contaminant from aqueous solution. Characteristics of phases and crystallite size of TiO2-P25 nanoparticles were achieved from XRD and the surface area and pore size distribution were obtained from BET and BJH techniques. TiO2-P25 nanoparticles with almost 80% anatase and 20% rutile phases, the average crystallite size of 18 nm, have specific surface area of 56.82 m2 g-1. The effect of various parameters like initial AR27 concentration, pH, contact time and adsorbent dosage has been carried out in order to find desired adsorption conditions. The desired pH for adsorption of AR27 onto TiO2-P25 nanoparticles was 3. The equilibrium data were analyzed with various 2-, 3- and 4-parameter isotherm models. Equilibrium data fitted very well by the 4-parameter Fritz-Schluender model. Results of adsorption kinetics study indicated that the pseudo-second order kinetics provided the best fit with correlation coefficients close to unity.

  5. Batch kinetics, isotherm and thermodynamic studies of adsorption of strontium from aqueous solutions onto low cost rice-straw based carbons.

    Directory of Open Access Journals (Sweden)

    S. M. Yakout

    2010-09-01

    Full Text Available Present study explored the feasibility of using waste rice-straw based carbons as adsorbent for the removal of strontium under different experimental conditions. The batch sorption is studied with respect to solute concentration (2.8 - 110 mg/L, contact time, adsorbent dose (2.5 - 20 g/L and solution temperature (25 - 55oC. The Langmuir and Dubinin-Radushkevich adsorption models were applied to experimental equilibrium data and isotherm constants were calculated using linear regression analysis. A comparison of kinetic models applied to the adsorption of strontium on rice-straw carbon was evaluated for the pseudo-second-order, Elovich, intraparticle diffusion and Bangham’s kinetics models. The experimental data fitted very well the pseudosecond-order kinetic model and also followed by intra-particle diffusion model, whereas diffusion is not only the rate-controlling step. The results show that the sorption capacity increases with an increase in solution temperature from 25 to 55 oC. The thermodynamics parameters were evaluated. The positive value of ΔH (40.93 kJ indicated that the adsorption of strontium onto RS1 carbon was endothermic, which result was supported by the increasing adsorption of strontium with temperature. The positive value of ΔS (121.8 kJ/mol reflects good affinity of strontium ions towards the rice-straw based carbons. The results have establishedgood potentiality for the carbons particles to be used as a sorbent for the removal of strontium from wastewater.

  6. A new adsorption isotherm for C5 hydrocarbons on metal–organic framework Cu3(BTC)2

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Kubů, Martin

    2015-01-01

    Roč. 21, 1-2 (2015), s. 99-105. ISSN 0929-5607 R&D Projects: GA ČR GA14-07101S Institutional support: RVO:61388955 Keywords : Cu3(BTC)2 * adsorption * C5 hydrocarbons Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.771, year: 2014

  7. DETERMINATION OF EFFECTIVE MOISTURE DIFFUSIVITY AND ACTIVATION ENERGY FOR DRYING OF POWDERED PEANUT SHELL UNDER ISOTHERMAL CONDITIONS

    OpenAIRE

    Dengyu Chen,; Kai Li; Xifeng Zhu

    2012-01-01

    In this study, the effect of drying temperature, from 50 °C to 90 °C, on the drying characteristics of powdered peanut shell was investigated, and an isothermal procedure was used to determine the moisture diffusivity and the activation energy. All the experiments were performed using a thermogravimetric analyzer (TGA) for rapidly achieving the isothermal condition and accurately recording the mass loss of the sample. With increasing drying temperature, the drying rate increased and the dryin...

  8. Adsorption of Cr (III) from aqueous solution by groundnut shell

    OpenAIRE

    Tasrina Rabia Choudhury; Mustafa, A. I.

    2012-01-01

    Adsorption and de-sorption of chromium (III) ions on groundnut shell from aqueous solutions have been studied using batch adsorption techniques with respect to the influence of contact time, pH, adsorbent dose, initial chromium concentration and particle size. Appropriate adsorption isotherm and kinetic parameters of chromium (III) adsorption on groundnut shell have also been determined. The results of this study showed that adsorption of chromium (III) by groundnut shell reached to equilibr...

  9. 天鹅湖沉积物对磷的吸附动力学及等温吸附特征%Characteristics of Adsorption Kinetics and Isotherms of Phosphate on Sediments in Swan Lake

    Institute of Scientific and Technical Information of China (English)

    高丽; 侯金枝; 宋鹏鹏

    2013-01-01

    以荣成天鹅湖这一天然泻湖为研究对象,研究了6个样点沉积物对磷的吸附动力学曲线和等温吸附方程,并分析了沉积物理化性质与磷吸附参数间的关系.结果表明,天鹅湖不同区域沉积物对磷的吸附动力学均符合二级动力学方程,吸附反应主要在前10h内完成,且0~2h内反应迅速.根据Langmuir模型,6个样点沉积物对磷的理论吸附容量(Qmax)的范围为294.12~1 111.11 mg/kg,其中湖区北部和中部沉积物的吸附能力高于南部.沉积物对水体中磷的吸附解吸平衡浓度(EPC0)的变幅为0.002 ~ 0.033 mg/L,其与沉积物本底吸附态磷(NAP)呈较弱的正相关关系.本研究条件下,大部分样点的EPC0小于上覆水中磷的浓度,其中湖区西北部和东南部沉积物中磷具有向上覆水体释放的趋势.沉积物的NAP与总氮、有机质、活性铝和黏粒间均呈显著正相关,Qmax与铁铝结合态磷、有机质、活性铝和粉粒间呈显著的正相关关系.活性铝、有机质和粒度是影响沉积物磷吸附的主要因素.%Adsorption kinetics and isotherms of phosphate on six sediments collected in Rongcheng Swan Lake (a nature lagoon) were determined in laboratory, and the relationship between the physical-chemical properties and the adsorption parameters of sediments was also discussed. The results indicated that the adsorption kinetics curve of phosphate at different sites all followed the second-order adsorption kinetic model. The adsorption reaction mainly occurred within 0-10 h, and the maximum adsorption rates occurred within 0-2 h. According to the Langmuir isotherm equation, phosphate adsorption capacity (Qmax) of surface sediments from Swan Lake varied from 294.12 mg/kg to 1 111.11 mg/kg. Phosphate sorption potential on the sediments from the northern and center areas was much higher than that from the south. The zero equilibrium phosphate concentration (EPC0) changed at the range of 0.002-0.033 mg/L, which

  10. Expanded bed adsorption of bromelain (E.C. 3.4.22.33) from Ananas comosus crude extract

    OpenAIRE

    Silveira, E.; M. E. Souza-Jr; J. C. C. Santana; A. C. Chaves; L. F. Porto; E. B. Tambourgi

    2009-01-01

    This work focuses on the adsorption of Bromelain in expanded bed conditions, such as the adsorption kinetics parameters. The adsorption kinetics parameters showed that after 40 minutes equilibrium was achieved and maximum adsorption capacity was 6.11 U per resin mL. However, the maximum adsorption capacity was only determined by measuring the adsorption isotherm. Only by the Langmuir model the maximum adsorption capacity, Qm, and dissociation constant, kd, values could be estimated as 9.18 U/...

  11. A study of the adsorption of the amphiphilic penicillins cloxacillin and dicloxacillin onto human serum albumin using surface tension isotherms

    Science.gov (United States)

    Barbosa, Silvia; Leis, David; Taboada, Pablo; Attwood, David; Mosquera, Victor

    The interaction of human serum albumin (HSA) with two structurally similar anionic amphiphilic penicillins, cloxacillin and dicloxacillin, at 25°C has been examined by surface tension measurements under conditions at which the HSA molecule was positively (pH 4.5) or negatively charged (pH 7.4). Measurements were at fixed HSA concentrations (0.0125 and 0.125% w/v) and at drug concentrations over a range including, where possible, the critical micelle concentration (cmc). Interaction between anionic drugs and positively charged HSA at pH 7.4 resulted in an increase of the cmc of each drug as a consequence of its removal from solution by adsorption. Limited data for cloxacillin at pH 4.5 indicated an apparent decrease of the cmc in the presence of HSA suggesting a facilitation of the aggregation by association with the protein. Changes in the surface tension-log (drug concentration) plots in the presence of HSA have been discussed in terms of the adsorption of drug at the air-solution and protein-solution interfaces. Standard free energy changes associated with the micellization of both drugs and their adsorption at the air-solution interface have been calculated and compared.

  12. Lignite utilisation for binding of radionuclides and uranium determination by adsorptive stripping chronopotentiometry

    International Nuclear Information System (INIS)

    This work in its first part deals with non-energetic use of young brown coal - lignite. The goal of the work was to perform a complex physical and chemical characterisation of the Slovak lignite (deposit Cary) which could contribute to rts use in binding of radionuclides in the environment. The characteristics of Slovak lignite were compared to leonardite (Gascoyne, USA) and Czech lignite (the area of Mikulcice). In the samples the residual humidity was determined. as well. as the content of ashes. representation of selected inorganic (As, Ba, Cd, Co, Cr, Cu, Ni, Pb and Zn) as well as organo-elements (C, H, N, 0, S) and crystalline forms of inorganic phase in lignite. The specific surface (BET isotherm) of lignite was determined, representation of total and free humic acids and their cation exchange capacity. The samples underwent al.so gamma-spectrometric analysis (40K, 226Ra, 228Ac, 137Cs and 60Co). Using the radio-indicator method (85Sr and 137Cs) the kinetics of sorption of Cs+ and Sr+ ions in Slovak lignite was studied. The efficiency of sorption for both cations on lignite was evaluated on the basis of constructed sorption isotherms. The sorption of Cs+ ions on Slovak lignite is more suitable for the Freundlich type of isotherm, in case of Sr+ ions the sorption is better described by Langmuir isotherm. The results of sorption experiments on lignite in comparison with clinoptilolite and montmorillonite K-10 showed a more efficient sorption for Sr Ions. despite the more coarse-grained fraction of this matrix. This finding supports the possibility of lignite application for binding of a quite mobile radiostrontium, which may be applied for construction of radioactive waste repositories or for remediation of contaminated soils. The second part of the work deals with the development and validation of new fast and reliable electrochemical method of uranium determination in natural waters. It is based on physical adsorption of created complex of uranium -cupferron

  13. 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.

  14. Comparison of adsorption efficiency of Triton X-100 surfactant from industrial wastewater using synthetic and natural zeolites: isotherm and kinetic studies

    Directory of Open Access Journals (Sweden)

    A Shahbazi

    2016-01-01

    Full Text Available Background and Objectives: Rapid growing of Triton X-100 application in industries results in its appearance in effluents  and threaten the aqueous ecosystems. Triton X-100 is not biodegradable and can accumulate in food chain. Materials and Methods: In this study, sorption capacity of six synthesized zeolites with different regular porous structure was studied for triton X-100 (TX-100 surfactant and the results were compared with Clinoptilolite natural zeolite of Damavand region. Results: Within all zeolite studied, Beta(200 showed the highest sorption capacity (about 575 mg/g, which is due to its regular pore structure with large pore diameter, channel intersections, high SiO2/Al2O3 ratio and high surface area. Langmuir monolayer isotherm and pseudo-second-order kinetic equation could provide well-fitted to the experimental data in simulating adsorption behavior of TX-100 over Beta(200 zeolite. Conclusion: The adsorption feature was internal sorption and the intraparticle diffusion might be a rate-limiting control for Beta(200 zeolite. Results of experiments demonstrated that the hydrophobic zeolites with large pore diameter such as Beta(200 could be effective sorbents for industrial wastewater treatment features.

  15. Effects of 42-year long-term fertilizer management on soil phosphorus availability, fractionation, adsorption-desorption isotherm and plant uptake in flooded tropical rice

    Institute of Scientific and Technical Information of China (English)

    Pratap Bhattacharyya; Priyanka Gautam; Chinmaya Kumar Swain; Koushik Singha Roy; Pradeep Kumar Dash; Amaresh Kumar Nayak; Mohammad Shahid; Rahul Tripathi; Sangita Mohanty; Anjani Kumar; Rajagounder Raja; Bipin Bihari Panda; Banwari Lal

    2015-01-01

    Soil phosphorus (P) fractionation, adsorption, and desorption isotherm, and rice yield and P uptake were investigated in flooded tropical rice (Oryza sativa L.) following 42-year fertilizer and manure application. The treatments included low-input [unfertilized control without N, P, or K (C0N0)], farmyard manure (FYM) (C1N0), NP (C0NP), NPK (C0NPK), FYM+NP (C1NP), and high-input treatment, FYM+NPK (C1NPK). Grain yield was increased significantly by 74%over the control under the combined application of FYM+NPK. However, under low- and high-input treatments, yield as well as P uptake was maintained at constant levels for 35 years. During the same period, high yield levels and P uptake were maintained under the C0NP, C0NPK, and C1NPK treatments. These are unique characteristics of a tropical flooded ecosystem, which is a self-sustaining system for rice production. The Fe–P fraction was highest compared to the Ca–P and Al–P fractions after 42 years of fertilizer application and was significantly higher under FYM+NPK treatment. The P adsorption capacity of soil was highest under the low-input treatment and lowest under long-term balanced fertilization (FYM+NPK). In contrast, P desorption capacity was highest under NPK and lowest in the control treatment. Long-term balanced fertilization in the form of FYM+NPK for 42 years lowered the bonding energy and adsorption capacity for P in soil but increased its desorption potential, increasing P availability to the plant and leading to higher P uptake and yield maintenance.

  16. Adsorptive removal of lead and cadmium ions using Cross -linked CMC Schiff base: Isotherm, Kinetics and Catalytic Activity

    Directory of Open Access Journals (Sweden)

    P. Moganavally

    2016-03-01

    Full Text Available Water plays a vital role to human and other living organisms. Due to the effluent coming from chemical industries, the industrial activity, contamination of ground water level is goes on increasing nowadays. Therefore, there is a need to develop technologies that can remove toxic pollutants in wastewater. Hence the cross linked Carboxymethyl chitosan(CMC/ 2,3-dimethoxy Benzaldehyde Schiff base complex has been synthesized and characterized by using FT-IR and SEM analysis. All these results revealed that cross linked Schiff base has formed with high adsorption capacity. The prepared effective adsorbent used for the removal of heavy metals like lead (II and cadmium (II ions from aqueous solution and the adsorption data follow the Freundlich model, which follows pseudo first order kinetics. Effect of various parameters like solution pH, adsorbent dose and contact time for the removal of heavy metals has been studied. The synthesized sample undergoes catalytic oxidation process significantly at 24 hrs. The results showed that cross linked Schiff base is an effective, eco-friendly, low-cost adsorbent.

  17. A Poromechanical Model for Coal Seams Injected with Carbon Dioxide: From an Isotherm of Adsorption to a Swelling of the Reservoir Un modéle poromécanique pour l’injection de dioxyde de carbone dans des veines de charbon : d’une isotherme d’adsorption à un gonflement du réservoir

    Directory of Open Access Journals (Sweden)

    Nikoosokhan S.

    2012-11-01

    Full Text Available Injecting carbon dioxide into deep unminable coal seams can enhance the amount of methane recovered from the seam. This process is known as CO2-Enhanced Coal Bed Methane production (CO2-ECBM. The seam is a porous medium whose porous system is made of cleats (small natural fractures and of coal pores (whose radius can be as small as a few angström. During the injection process, the molecules of CO2 get adsorbed in the coal pores. Such an adsorption makes the coal swell, which, in the confined conditions that prevail underground, induces a closure of the cleat system of the coal bed reservoir and a loss of injectivity. In this work, we develop a poromechanical model which, starting from the knowledge of an adsorption isotherm and combined with reservoir simulations, enables to estimate the variations of injectivity of the coal bed reservoir over time during the process of injection. The model for the coal bed reservoir is based on poromechanical equations that explicitly take into account the effect of adsorption on the mechanical behavior of a microporous medium. We consider the coal bed reservoir as a dual porosity (cleats and coal porosity medium, for which we derive a set of linear constitutive equations. The model requires as an input the adsorption isotherm on coal of the fluid considered. Reversely, the model provides a way to upscale an adsorption isotherm into a meaningful swelling of the coal bed reservoir at the macroscopic scale. The parameters of the model are calibrated on data on coal samples available in the literature. Reservoir simulations of an injection of carbon dioxide in a coal seam are performed with an in-house finite volume and element code. The variations of injection rate over time during the process of injection are obtained from the simulations. The effect of the compressibility of the coal matrix on those variations is discussed. L’injection de dioxyde de carbone dans des veines de charbon profondes peut augmenter

  18. Isotermas de adsorção de Freundlich para o crômio (III em Latossolos Freundlich adsorption isotherms for chromium (III in Oxisols

    Directory of Open Access Journals (Sweden)

    Marco Aurélio Kondracki de Alcântara

    2001-09-01

    the soil adsorptive capacity is exceeded and, potentially, the metals become available for leaching. The objectives of this study were to verify if the isotherm of Freundlich describes adequately the chromium adsorption by Oxisols, to study chromium adsorption considering different soils and horizons, as well as some chemical and physical attributes, and to evaluate the influence of the pH level on chromium adsorption. Samples of the A and B horizons of two soils were collected in the São Paulo State - Brazil: a Typic Eutrorthox (LVe and b Typic Haplorthox (LVd. The pH alteration of the surface horizons was performed with the addition of calcium carbonate to reach 70% base saturation. Samples were shaken with CrCl3 solutions (prepared in Ca(NO32 5 mmol L-1 as the support electrolyte of different initial chromium concentrations Co: 0; 0.5; 1.0; 2.5; 5.0; 10.0 and 50.0 mg L-1, using two replicates for each treatment. Freundlich isotherms were adjusted to describe the chromium adsorption by the soil. This isoterm fitted well to the experimental data. Chromium adsorption was higher in the Typic Eutrorthox than in the Typic Haplorthox. The adsorption was also favored by liming in both soils. There was no difference between chromium adsorption by the two horizons of the soils.

  19. Adsorption of Pb(II) on mesoporous activated carbons fabricated from water hyacinth using H{sub 3}PO{sub 4} activation: Adsorption capacity, kinetic and isotherm studies

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Yang, E-mail: zzsfxyhy@163.com [Department of Chemistry and Environmental Science, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China); Li, Shunxing; Chen, Jianhua; Zhang, Xueliang; Chen, Yiping [Department of Chemistry and Environmental Science, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Modern Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou 363000 (China)

    2014-02-28

    Activated carbons with high mesoporosity and abundant oxygen-containing functional groups were prepared from water hyacinth using H{sub 3}PO{sub 4} activation (WHAC) to eliminate Pb(II) in water. Characterizations of the WHAC were performed using Brunauer–Emmett–Teller (BET), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The BET analysis showed that WHAC possesses a high mesoporosity (93.9%) with a BET surface area of 423.6 m{sup 2}/g. The presence of oxygen-containing functional groups including hydroxyl, carbonyl, carboxyl and phosphate groups renders the WHAC a favorable adsorbent for Pb(II) with the maximum monolayer capacity (q{sub m}) 118.8 mg/g. The adsorption behavior follows pseudo-first order kinetic and Langmuir isotherm. The desorption study demonstrated that the WHAC could be readily regenerated using 0.1 M HCl (pH = 1.0). The desorbed WHAC could be reused at least six times without significant adsorption capacity reduction. The adsorption process was spontaneous and endothermic with ΔG (−0.27, −1.13, −3.02, −3.62, −5.54, and −9.31 kJ/mol) and ΔH (38.72 kJ/mol). Under the optimized conditions, a small amount of the adsorbent (1.0 g/L) could remove as much as 90.1% of Pb(II) (50 mg/L) in 20 min at pH 6.0 and temperature of 298 K. Therefore, the WHAC has a great potential to be an economical and efficient adsorbent in the treatment of lead-contaminated water.

  20. Isotermas de adsorção de cádmio em solos ácricos Cadmium adsorption isotherms in acric oxisols

    Directory of Open Access Journals (Sweden)

    Nivea M.P. Dias

    2001-05-01

    Full Text Available O cádmio é um metal pesado que pode ser adicionado ao solo via resíduos de pneus, óleos, disposição de lixo urbano, lodo de esgoto e fertilizantes fosfatados; é facilmente absorvido e translocado nas plantas e tem potencial de entrar na cadeia alimentar humana, causando sérios problemas de saúde, razão por que se objetivou, com este trabalho, estudar a adequação dos modelos de Langmuir e de Freundlich para descrever a adsorção do cádmio em amostras superficiais (0 - 0,2 m e subsuperficiais (horizonte B de três solos do estado de São Paulo: Nitossolo Vermelho eutroférrico (NVef, Latossolo Vermelho acriférrico (LVwf e Latossolo Amarelo ácrico (LAw. Para a determinação da quantidade de cádmio adsorvido, 20 mL de solução de Ca(NO32 0,0025 mol L-1 com diferentes quantidades de cádmio (5, 10, 15, 25, 50, 75, 100, 125, 150, 175 e 200 mg dm-3 foram adicionados a 2 g de terra fina seca em estufa e agitados por 24 h. Tanto o modelo de Langmuir como o de Freundlich se adequaram bem aos valores de cádmio adsorvido pelos solos. O Nitossolo Vermelho eutroférrico apresentou maiores valores de adsorção máxima de cádmio, obtidos pela isoterma de Langmuir, e os menores foram encontrados nos horizontes subsuperficiais dos Latossolos. Ambas as equações descreveram bem a adsorção de cádmio, principalmente quando as concentrações de cádmio adicionadas foram superiores a 50 mg dm-3.Cadmium is a heavy metal that may be added to the soils through tyre residues, oils, disposal of city wastes, sewage sludge and phosphatic fertilizers. It is easily absorbed and translocated in plants and has a great potential to enter in the human food chain, with serious problems to human health. The objective of this study was to evaluate Langmuir and Freundlich isotherms applied to cadmium adsorption on soils from the State of São Paulo, Brazil. Surface (0 - 0.2 m and subsurface (B horizon samples were taken from an Rhodic Kandiudalf (RK, an

  1. Determination of thermodynamic potentials and the aggregation number for micelles with the mass-action model by isothermal titration calorimetry

    DEFF Research Database (Denmark)

    Olesen, Niels Erik; Westh, Peter; Holm, René

    2015-01-01

    The aggregation number (n), thermodynamic potentials (ΔG, ΔH, ΔS) and critical micelle concentration (CMC) for 6 natural bile salts were determined on the basis of both original and previously published isothermal titration calorimetry (ITC) data. Different procedures to estimate parameters of...

  2. FTIR spectrophotometry, kinetics and adsorption isotherms modeling, ion exchange, and EDX analysis for understanding the mechanism of Cd2+ and Pb2+ removal by mango peel waste

    International Nuclear Information System (INIS)

    Mango peel waste (MPW) was evaluated as a new sorbent for the removal of Cd2+ and Pb2+ from aqueous solution. The maximum sorption capacity of Cd2+ and Pb2+ was found to be 68.92 and 99.05 mg g-1, respectively. The kinetics of sorption of both metals was fast, reaching at equilibrium in 60 min. Sorption kinetics and equilibria followed pseudo-second order and Langmuir adsorption isotherm models. FTIR analysis revealed that carboxyl and hydroxyl functional groups were mainly responsible for the sorption of Cd2+ and Pb2+. Chemical modification of MPW for blocking of carboxyl and hydroxyl groups showed that 72.46% and 76.26% removal of Cd2+ and Pb2+, respectively, was due to the involvement of carboxylic group, whereas 26.64% and 23.74% was due to the hydroxyl group. EDX analysis of MPW before and after metal sorption and release of cations (Ca2+, Mg2+, Na+, K+) and proton H+ from MPW with the corresponding uptake of Cd2+ and Pb2+ revealed that the main mechanism of sorption was ion exchange. The regeneration experiments showed that the MPW could be reused for five cycles without significant loss in its initial sorption capacity. The study points to the potential of new use of MPW as an effective sorbent for the removal of Cd2+ and Pb2+ from aqueous solution

  3. Proton adsorption onto alumina: extension of multisite complexation (MUSIC) theory

    Energy Technology Data Exchange (ETDEWEB)

    Nagashima, K.; Blum, F.D.

    1999-09-01

    The adsorption isotherm of protons onto a commercial {gamma}-alumina sample was determined in aqueous nitric acid with sodium nitrate as a background electrolyte. Three discrete regions could be discerned in the log-log plots of the proton isotherm determined at the solution pH 5 to 2. The multisite complexation (MUSIC) model was modified to analyze the simultaneous adsorption of protons onto various kinds of surface species.

  4. Proton Adsorption onto Alumina: Extension of Multisite Complexation (MUSIC) Theory.

    Science.gov (United States)

    Nagashima; Blum

    1999-09-01

    The adsorption isotherm of protons onto a commercial gamma-alumina sample was determined in aqueous nitric acid with sodium nitrate as a background electrolyte. Three discrete regions could be discerned in the log-log plots of the proton isotherm determined at the solution pH 5 to 2. The multisite complexation (MUSIC) model was modified to analyze the simultaneous adsorption of protons onto various kinds of surface species. Copyright 1999 Academic Press. PMID:10441408

  5. Isotherms and kinetic study of dihydrogen and hydrogen phosphate ions (H{2}PO{4}- and HPO{4}2-) adsorption onto crushed plant matter of the semi-arid zones of Morocco: Asphodelus microcarpus, Asparagus albus and Senecio anthophorbium

    Science.gov (United States)

    Chiban, M.; Benhima, H.; Saadi, B.; Nounah, A.; Sinan, F.

    2005-03-01

    In the present work H{2}PO4- and HPO42- ions adsorption onto organic matter (OM) obtained from ground dried three plants growing in arid zones of Morocco has been studied. The adsorption process is affected by various parameters such as contact time, particle size and initial concentration of phosphate solution (Ci ≤ 30 mg/l). The uptake of both ions is increased by increasing the concentration of them selves. The retention of phosphate ions by Asphodelus microcarpus, Asparagus albus are well defined by several isotherms such as the Langmuir, Temkin and Freundlich.

  6. Adsorption of copper ions from aqueous solutions on natural zeolite

    OpenAIRE

    Zendelska, Afrodita; Golomeova, Mirjana; Blažev, Krsto; Krstev, Boris; Golomeov, Blagoj; Krstev, Aleksandar

    2015-01-01

    The adsorption of copper ions from synthetic aqueous solutions on natural zeolite (clinoptilolite) was examined. In order to determine the rate of adsorption and the copper uptake at equilibrium, a series of experiments were performed under batch conditions from single ion solutions. Equilibrium data were evaluated based on adsorption (Langmuir and Freundlich) isotherms. The adsorption kinetics is reasonably fast. In the first 20 min of the experiment, approximately 80% of Cu2+ io...

  7. Study of Fe(III) adsorption onto Dowex-Marathon resin, as a rate determining step of the U(IV) oxidation in 235U enrichment column

    International Nuclear Information System (INIS)

    The Fe(III) adsorption onto Dowex-Marathon resin was well described by pseudo-second order kinetics with a high correlation factor for all the experimental concentrations. The results were analyzed by Langmuir, Freundlich and Dubinin-Radushkevich isotherm models. The activation energy Ea (7.96 ± 0.2 kJ/mol) indicates a physisorption process as in the case of U(VI) adsorption onto the same resin. The thermodynamic parameters: ΔG deg = (-7.91) / (-13.68) kJ/mol, ΔH deg = 35.60 ± 0.89 kJ/mol and ΔS deg = 143.31 ± 3.58 J/mol K, were determined, the Fe(III) adsorption being spontaneous and endothermic. (author)

  8. Batch Sorption Experiments: Langmuir and Freundlich Isotherm Studies for the Adsorption of Textile Metal Ions onto Teff Straw (Eragrostis tef) Agricultural Waste

    OpenAIRE

    Mulu Berhe Desta

    2013-01-01

    Adsorption of heavy metals (Cr, Cd, Pb, Ni, and Cu) onto Activated Teff Straw (ATS) has been studied using batch-adsorption techniques. This study was carried out to examine the adsorption capacity of the low-cost adsorbent ATS for the removal of heavy metals from textile effluents. The influence of contact time, pH, Temperature, and adsorbent dose on the adsorption process was also studied. Results revealed that adsorption rate initially increased rapidly, and the optimal removal efficiency ...

  9. Determination of Kinetic and Thermodynamic Parameters that Describe Isothermal Seed Germination: A Student Research Project.

    Science.gov (United States)

    Hageseth, Gaylord T.

    1982-01-01

    Describes a project for students to collect and fit data to a theoretical mathematical model that describes the rate of isothermal seed germination, including activation energy for substrate and produce and the autocatalytic reaction, and changes in enthalpy, entropy, and the Gibb's free energy. (Author/SK)

  10. Determining the baking isotherm temperature of Söderberg electrodes and associated structural changes

    OpenAIRE

    Shoko, L.; J. P. Beukes; Strydom, C.A.

    2013-01-01

    One of the most commonly employed electrode systems in industrial metal smelting applications is continuous self-baking electrodes, i.e. the Söderberg electrode system. In this system, the temperature at which transition from a liquid/soft paste to a solid carbonaceous electrode takes place is termed the baking isotherm temperature. This temperature is extremely important within the context of electrode management. In this paper, thermo mechanical analysis (TMA) was used to measure the dimens...

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

    International Nuclear Information System (INIS)

    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

  12. 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.

  13. An improved single crystal adsorption calorimeter for determining gas adsorption and reaction energies on complex model catalysts.

    Science.gov (United States)

    Fischer-Wolfarth, Jan-Henrik; Hartmann, Jens; Farmer, Jason A; Flores-Camacho, J Manuel; Campbell, Charles T; Schauermann, Swetlana; Freund, Hans-Joachim

    2011-02-01

    A new ultrahigh vacuum microcalorimeter for measuring heats of adsorption and adsorption-induced surface reactions on complex single crystal-based model surfaces is described. It has been specifically designed to study the interaction of gaseous molecules with well-defined model catalysts consisting of metal nanoparticles supported on single crystal surfaces or epitaxial thin oxide films grown on single crystals. The detection principle is based on the previously described measurement of the temperature rise upon adsorption of gaseous molecules by use of a pyroelectric polymer ribbon, which is brought into mechanical∕thermal contact with the back side of the thin single crystal. The instrument includes (i) a preparation chamber providing the required equipment to prepare supported model catalysts involving well-defined nanoparticles on clean single crystal surfaces and to characterize them using surface analysis techniques and in situ reflectivity measurements and (ii) the adsorption∕reaction chamber containing a molecular beam, a pyroelectric heat detector, and calibration tools for determining the absolute reactant fluxes and adsorption heats. The molecular beam is produced by a differentially pumped source based on a multichannel array capable of providing variable fluxes of both high and low vapor pressure gaseous molecules in the range of 0.005-1.5 × 10(15) molecules cm(-2) s(-1) and is modulated by means of the computer-controlled chopper with the shortest pulse length of 150 ms. The calorimetric measurements of adsorption and reaction heats can be performed in a broad temperature range from 100 to 300 K. A novel vibrational isolation method for the pyroelectric detector is introduced for the reduction of acoustic noise. The detector shows a pulse-to-pulse standard deviation ≤15 nJ when heat pulses in the range of 190-3600 nJ are applied to the sample surface with a chopped laser. Particularly for CO adsorption on Pt(111), the energy input of 15 n

  14. Adsorption of Pure Nonionic Alkylethoxylated Surfactants down to Low Concentrations at a Silica/Water Interface as Determined Using a HPLC Technique

    Science.gov (United States)

    Desbene; Portet; Treiner

    1997-06-15

    The adsorption of pure nonionic alkylethoxylated surfactants of the C12 En series at silica/water interface has been determined using a very precise HPLC technique. The number of ethoxylated groups was varied from 2 to 9. The adsorption isotherms were constructed with special attention to the very low surface coverage domain. It is shown that at very low concentration, the adsorption amounts are higher as the number of ethoxylated groups increases but the reverse trend is found at higher surfactant concentration and above the critical micelle concentration. It is shown that this behavior is the consequence of the interplay of the primary and secondary adsorption mechanisms depending upon the length of the ethoxylated chain. The maximum adsorption quantities is not a linear function of the number of ethoxylated groups. This and other observations confirm the viewpoint that the behavior of nonionic surfactant aggregates adsorbed at a hydrophilic surface carries many similarities with the properties of this class of nonionic surfactant aggregates in bulk aqueous solutions. PMID:9241177

  15. Thermodynamic properties of metal amides determined by ammonia pressure-composition isotherms

    OpenAIRE

    Hino, Satoshi; Ichikawa, Takayuki; Kojima, Yoshitsugu

    2010-01-01

    Thermodynamic properties of Mg(NH2)(2) and LiNH2 were investigated by measurements of NH3 pressure-composition isotherms (PCI). Van't Hoff plot of plateau pressures of PCI for decomposition of Mg(NH2)(2) indicated the standard enthalpy and entropy change of the reactions were Delta H degrees = (120 +/- 11) kJ . mol(-1) (per unit amount of NH3) and Delta S degrees= (182 +/- 19) J . mol(-1) . K-1 for the reaction: Mg(NH2)(2) -> MgNH +NH3, and Delta H degrees= 112 kJ . mol(-1) and Delta S degree...

  16. Adsorption of phenol on wood surfaces

    Science.gov (United States)

    Mamleeva, N. A.; Lunin, V. V.

    2016-03-01

    Adsorption of phenol on aspen and pine wood is investigated. It is shown that adsorption isotherms are described by the Langmuir model. The woods' specific surface areas and adsorption interaction constants are determined. It is found that the sorption of phenol on surfaces of aspen and pine is due to Van der Waals interactions ( S sp = 45 m2/godw for aspen and 85 m2/godw for pine). The difference between the adsorption characteristics is explained by properties of the wood samples' microstructures.

  17. 几种高油脂食品等温吸湿规律的研究%Study on isotherm adsorption of several kinds of high-fat food

    Institute of Scientific and Technical Information of China (English)

    杨琴; 范柳萍

    2012-01-01

    Four kinds of fatty food including vacuum fried lotus seed ,vacuum fried carrot chips, carrot chips fried at atmospheric conditions and potato chips fried at atmospheric conditions were employed to investigate the isotherm adsorption.The data of 4 kinds of fatty food were tested,according to the commonly used 5 kinds of isothermal adsorption model. The result showed that the most suitable isothermal adsorption model was the Peleg model and the order of the suitability was vacuum fried carrot chips,carrot chips fried at atmospheric conditions ,vacuum fried lotus seed ,and potato chips fried at atmospheric conditions.%研究了真空油炸莲子、真空油炸胡萝卜脆片、常压油炸胡萝卜脆片、常压油炸土豆脆片4种高脂食品的吸湿等温曲线。根据常用的5种等温吸附模型对4种物料的吸湿实验数据进行了拟合,比较了其拟合程度(R2)。结果表明,25℃条件下,4种高脂物料最适合的等温吸附模型都是Peleg模型,且拟合程度依次为真空油炸胡萝卜脆片、常压油炸胡萝卜脆片、真空油炸莲子、常压油炸土豆脆片。

  18. Substrate binding properties of potato tuber ADP-glucose pyrophosphorylase as determined by isothermal titration calorimetry.

    Science.gov (United States)

    Cakir, Bilal; Tuncel, Aytug; Green, Abigail R; Koper, Kaan; Hwang, Seon-Kap; Okita, Thomas W; Kang, ChulHee

    2015-06-01

    Substrate binding properties of the large (LS) and small (SS) subunits of potato tuber ADP-glucose pyrophosphorylase were investigated by using isothermal titration calorimetry. Our results clearly show that the wild type heterotetramer (S(WT)L(WT)) possesses two distinct types of ATP binding sites, whereas the homotetrameric LS and SS variant forms only exhibited properties of one of the two binding sites. The wild type enzyme also exhibited significantly increased affinity to this substrate compared to the homotetrameric enzyme forms. No stable binding was evident for the second substrate, glucose-1-phosphate, in the presence or absence of ATPγS suggesting that interaction of glucose-1-phosphate is dependent on hydrolysis of ATP and supports the Theorell-Chance bi bi reaction mechanism. PMID:25953126

  19. Adsorption equilibria of butyl- and amylbenzene on monolithic silica-based columns.

    Science.gov (United States)

    Cavazzini, Alberto; Bardin, Gregory; Kaczmarski, Krzystof; Szabelski, Paweł; Al-Bokari, Majed; Guiochon, Georges

    2002-05-31

    The adsorption isotherms of butyl- and amylbenzene on silica monolithic columns were measured by frontal analysis. The external, internal and total porosities of these columns were determined by inverse size-exclusion chromatography. The adsorption isotherms are concave upward in the entire concentration range investigated. They were fitted to the anti-Langmuir model, an unusual model in liquid-solid and liquid-liquid phase equilibria. Band profiles under overloaded conditions were recorded. They were in good agreement with the profiles calculated using th,e lumped pore diffusion model of chromatography and these adsorption isotherms. PMID:12113336

  20. 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.

  1. Tailoring fibre and paper properties using physical adsorption of polyelectrolytes

    OpenAIRE

    Marais, Andrew

    2012-01-01

    The adsorption of polyelectrolytes, both as monolayers and as multilayers, was investigated as an easy and non-expensive way of producing lignocellulosic fibrous materials with enhanced mechanical properties. In the first part of the work described in this thesis, the adsorption of a polyelectrolyte monolayer onto the surface of unbleached and unbeaten kraft pulp fibres with different kappa numbers was investigated. Adsorption isotherms were obtained in order to determine the amounts of polym...

  2. Isothermal composite adsorbent. Part I: Thermal characterisation

    International Nuclear Information System (INIS)

    Adsorption and desorption are respectively exo and endothermic phenomena leading to significant temperature changes in adsorption columns. Enhanced efficiency of a sorption process could be obtained under isothermal conditions, either for gas storage, purification or separation applications. The heat transfer within the adsorbent beds can be managed in situ, using thermal energy storage material: a phase change materials (PCM) for example. The thermal behaviour of a mixture of activated carbon and PCM during CO2 adsorption has been studied. The thermal characteristics of the involved materials have been determined and experiments carried out to highlight the positive effect of the PCM to reduce the CO2 adsorption heat effects on an activated carbon bed. Calorimetry was the technique used for all the thermal characterisations. It appears that the heat effects induced by CO2 adsorption are reduced by the presence of the PCM together with the adsorbent. The endothermic effect of fusion balances the heat effect of adsorption and significantly reduces the temperature changes

  3. 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. PMID:27478226

  4. ADSORPTION OF POLYCHLORINATED BIPHENYLS BY SOILS

    Directory of Open Access Journals (Sweden)

    Mihaela Preda

    2010-01-01

    Full Text Available The behavior of polychlorinated biphenyls (PCBs in soil is determined by several factors including adsorption, mobility and degradation. Adsorption, directly or indirectly, influences the other factors. Adsorption process is generally evaluated by using adsorption isotherms representing the relationship between the quantity of substance adsorbed per unit weight and concentration of the substance in solution at equilibrium. They allow determination of the adsorption constant, which is directly proportional to the adsorption of PCBs in soil. PCBs are very insoluble in water, so they tend to accumulate in the lipids. This is the reason why polychlorinated biphenyls are more strongly adsorbed in soils with higher organic matter content. To obtain the adsorption isotherm were used standard solutions of PCB 101with initial concentrations: 0.05, 0.1, 0.5, 1 and 2 g/ml. The adsorption constants were in order: 3072 ml/g for chernozem, 2943 mg/l for chromic luvisol, 998 mg/l for aluviosol and 1443 mg/l for anthrosol. The values of adsorption constants depend on the organic matter and clay content.

  5. Adsorption dynamics and equilibrium studies of Zn (II) onto chitosan

    Indian Academy of Sciences (India)

    G Karthikeyan; K Anbalagan; N Muthulakshmi Andal

    2004-03-01

    Batch equilibration studies are conducted to determine the nature of adsorption of zinc (II) over chitosan. The factors affecting the adsorption process like particle size, contact time, dosage, pH, effects of chloride and nitrate are identified. The influence of temperature and co-ions on the adsorption process is verified. The fraction of adsorption, and the intraparticle diffusion rate constant, are calculated at different environments and the results are discussed. The nature of adsorption of the zinc (II) - chitosan system is explained using Freundlich, Langmuir isotherms and thermodynamic parameters.

  6. Adsorption of octylamine on titanium dioxide

    International Nuclear Information System (INIS)

    Processes of adsorption and desorption of a model active substance (octylamine) on the surface of unmodified titanium dioxide (E 171) have been performed. The effects of concentration of octylamine and time of the process on the character of adsorption have been studied and the efficiency of the adsorption/desorption has been determined. The samples obtained have been studied by X-ray diffraction. The nitrogen adsorption/desorption isotherms, particle size distribution and absorption capacities of water, dibutyl phthalate and paraffin oil have been determined. The efficiency of octylamine adsorption on the surface of the titanium dioxide has been found positively correlated with the concentration of octylamine in the initial solution. The desorption of octylamine has decreased with increasing concentration of this compound adsorbed. For octylamine in low concentrations the physical adsorption has been found to dominate, which is desirable when using TiO2 in the production of pharmaceuticals.

  7. Heavy metal adsorption by modified oak sawdust: Thermodynamics and kinetics

    International Nuclear Information System (INIS)

    This paper describes the adsorption of heavy metal ions from aqueous solutions by oak (Quercus coccifera) sawdust modified by means of HCl treatment. Our study tested the removal of three heavy metals: Cu, Ni, and Cr. The optimum shaking speed, adsorbent mass, contact time, and pH were determined, and adsorption isotherms were obtained using concentrations of the metal ions ranging from 0.1 to 100 mg L-1. The adsorption process follows pseudo-second-order reaction kinetics, as well as Langmuir and D-R adsorption isotherms. The paper discusses the thermodynamic parameters of the adsorption (the Gibbs free energy, entropy, and enthalpy). Our results demonstrate that the adsorption process was spontaneous and endothermic under natural conditions. The maximum removal efficiencies were 93% for Cu(II) at pH 4, 82% for Ni(II) at pH 8, and 84% for Cr(VI) at pH 3

  8. Calcium lignosulfonate adsorption and desorption on Berea sandstone.

    Science.gov (United States)

    Grigg, Reid B; Bai, Baojun

    2004-11-01

    This paper describes adsorption and desorption studies carried out with calcium lignosulfonate (CLS) on Berea sandstone. Circulation experiments were performed to determine CLS adsorption isotherms and the effects of CLS concentration, temperature, salinity, brine hardness, and injection rate on adsorption density. Flow-through experiments were performed to assess the reversibility of CLS adsorption and the influence of postflush rate, brine concentration, brine hardness, brine pH, and temperature on the desorption process. Results indicate that CLS adsorption isotherms on Berea sandstone follow the Freundlich isotherm law. The results presented in this paper on the effects of CLS adsorption and desorption on Berea sandstone show that: (1) increasing CLS concentration and salinity increases CLS adsorption density; (2) increasing temperature will decrease adsorption density; (3) increasing injection rate of CLS solution will slightly decrease CLS adsorption density; (4) postflush rate and salinity of brine have a large impact on the CLS desorption process; (5) the adsorption and desorption process are not completely reversible; and (5) temperature and pH of the postflush brine have little effect on desorption. PMID:15380409

  9. Adsorption and wetting.

    OpenAIRE

    Schlangen, L.J.M.

    1995-01-01

    Adsorption and wetting are related phenomena. In order to improve knowledge of both and their relations, experiments, thermodynamics and a theoretical interpretation have been connected, starring n-alkanes.Starting from the Gibbs adsorption equation thermodynamic relations between vapour adsorption and wetting are derived. The surface pressure of a film, formed by vapour adsorption on a solid surface, is calculated by integrating the vapour adsorption isotherm. The surface pressure at the sat...

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

    Science.gov (United States)

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

  11. Adsorption isotherms, kinetics and column operations for the removal of hazardous dye, Tartrazine from aqueous solutions using waste materials-Bottom Ash and De-Oiled Soya, as adsorbents

    International Nuclear Information System (INIS)

    Adsorbents, Bottom Ash (a power plant waste) and De-Oiled Soya (an agricultural waste) exhibit good efficacy to adsorb a highly toxic dye, Tartrazine. Through the batch technique equilibrium uptake of the dye is observed at different concentrations, pH of the solution, dosage of adsorbents and sieve size of adsorbents. Langmuir and Freundlich adsorption isotherms are successfully employed on both the adsorbents and on the basis of these models the thermodynamic parameters are evaluated. Kinetic investigations reveal that more than 50% adsorption of dye is achieved in about 1 h in both the cases, whereas, equilibrium establishment takes about 3-4 h. The linear plots obtained in rate constant and mass transfer studies further confirm the applicability of first order rate expression and mass transfer model, respectively. The kinetic data treated to identify rate controlling step of the ongoing adsorption processes indicate that for both the systems, particle diffusion process is predominant at higher concentrations, while film diffusion takes place at lower concentrations. The column studies reveal that about 96% saturation of both the columns is attained during their exhaustion, while about 88 and 84% of the dye material is recovered by eluting dilute NaOH solution through exhausted Bottom Ash and De-Oiled Soya columns, respectively

  12. Relationship between Crystal Thickness and Isothermal Crystallization Temperature for Determination of Equilibrium Melting Temperature for Syndiotatic Polypropylene

    Science.gov (United States)

    Wang, Zhi-Gang; Hsiao Hsiao, Benjamin; Srinivas, Srivatsan; Crist, Buckley

    2000-03-01

    Syndiotatic polypropylene (sPP) was used to investigate the relationship between isothermal crystallization temperature (Tc = 70-115^oC), crystal thickness and subsequent melting using simultaneous synchrotron small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD) in conjunction with DSC. The thickest lamellar crystals melt at the end of the DSC endotherm. At this temperature, the SAXS intensity (corrected formelt scattering) showed a diffuse profile, and the crystalline feature in the WAXD pattern was completely absent. This crystal thickness was estimated using an approach based on the single lamella structure factor, which will also be compared to the value determined by the interface distribution function. The equilibrium melting temperature obtained this way will be contrasted by other methods such as the Hoffman-Weeks approach. Acknowledgement: This work was supported by by a NSF grant (DMR 9732653).

  13. The use of isothermal titration calorimetry to determine the thermodynamics of metal ion binding to low-cost sorbents

    International Nuclear Information System (INIS)

    The thermodynamics of Al3+, Cr3+, and Pb2+ binding to the abundant biopolymer chitin have been determined using isothermal titration calorimetry (ITC) and compared to what is observed for binding to activated carbon. The use of ITC enables the detection of two distinct binding sites on chitin for all three metal ions. For the relative strong binding sites, free energy changes ranges from -37.6 kJ/mol to -41.8 kJ/mol while the same values are from -30.1 kJ/mol to -31.8 kJ/mol for the relative weak binding sites. All binding reactions to chitin are entropically driven. Interactions of the metal ions to activated carbon are best fitted as a single-site binding with relative weak binding with free energy changes from -26.3 kJ/mol to -26.8 kJ/mol.

  14. Determinação de isotermas de adsorção de Saccharomyces cerevisiae empregando acetato e sulfato de cádmio Cadmium adsorption isotherms by Saccharomyces cerevisiae using cadmiun acetate and sulphate

    Directory of Open Access Journals (Sweden)

    Silvana Albertini

    2007-06-01

    Full Text Available Para determinar as isotermas de adsorção de cádmio por Saccharomyces cerevisiae, foram utilizados os sais acetato e sulfato de cádmio, nas concentrações de 5; 10; 20; 40; 60; 80 e 100 mg.L-1. A biomassa foi produzida a partir de uma cultura "starter" de Saccharomyces cerevisiae IZ 1904. Após o contato de 16 horas entre o microrganismo em estudo e as soluções teste, a biomassa foi separada por centrifugação e o teor de cádmio residual foi determinado por espectrofotometria de absorção atômica diretamente no sobrenadante. Os dois sais testados demonstraram acúmulo crescente do metal nas concentrações de 5; 10; 20 e 40 mg.L-1. Porém, nas concentrações de 60; 80 e 100 mg.L-1, foi observado um acúmulo decrescente do metal, mostrando assim danos da parede celular, nem sempre evidenciados em nível de membrana citoplasmática, visualizados por microscopia eletrônica de varredura.To determine the isotherms of the adsorption of cadmium for Saccharomyces cerevisiae, acetate and sulphate salts were used at the concentrations of 5, 10, 20, 40, 60, 80, and 100 mg.L-1. The biomass was produced from a starter culture of Saccharomyces cerevisiae IZ 1904. After the contact of 16 hours among the microrganism study and the solution-test, the biomass was separated by a centrifugation and the cadmium residue content was determined directly in the supernatant by atomic absorption spectrophotometry. For the two salts which were used, a growing accumulation of cadmium was observed at concentrations of 5, 10, 20, and 40 mg.L-1. In the concentrations of 60; 80 and 100 mg.L-1 a decrease in the accumulation of the metal was observed, showing damage to the cellular wall, not always observed at the membrane citoplasmatic's level, visualized by a scanning electron microscopy.

  15. Adsorptive Stripping Voltammetry of Environmental Indicators: Determination of Zinc in Algae

    Science.gov (United States)

    Collado-Sanchez, C.; Hernandez-Brito, J. J.; Perez-Pena, J.; Torres-Padron, M. E.; Gelado-Caballero, M. D.

    2005-01-01

    A method for sample preparation and for the determination of average zinc content in algae using adsorptive stripping voltammetry are described. The students gain important didactic advantages through metal determination in environmental matrices, which include carrying out clean protocols for sampling and handling, and digesting samples using…

  16. Adsorption of gases on heterogeneous surfaces

    CERN Document Server

    Rudzinski, W

    1991-01-01

    All real solid surfaces are heterogeneous to a greater or lesser extent and this book provides a broad yet detailed survey of the present state of gas adsorption. Coverage is comprehensive and extends from basic principles to computer simulation of adsorption. Underlying concepts are clarified and the strengths and weaknesses of the various methods described are discussed.Key Features* Adsorption isotherm equations for various types of heterogeneous solid surfaces* Methods of determining the nature of surface heterogeneity and porosity from experimental data* Studies of pha

  17. Characterizations of strontium(II) and barium(II) adsorption from aqueous solutions using dolomite powder

    International Nuclear Information System (INIS)

    Highlights: → Dolomite was used for adsorption of Sr (II) and Ba (II) for the first time. → The experiments were carried out to consider the effect of adsorption parameters. → We analyzed all experimental data using isotherm, kinetic and thermodynamic models. → The maximum adsorption capacity of dolomite was compared with other adsorbents. → Thermodynamic data indicate that the adsorption process was exothermic. - Abstract: In this research, adsorption technique was applied for strontium and barium removal from aqueous solution using dolomite powder. The process has been investigated as a function of pH, contact time, temperature and adsorbate concentration. The experimental data was analyzed using equilibrium isotherm, kinetic and thermodynamic models. The isotherm data was well described by Langmuir isotherm model. The maximum adsorption capacity was found to be 1.172 and 3.958 mg/g for Sr(II) and Ba(II) from the Langmuir isotherm model at 293 K, respectively. The kinetic data was tested using first and pseudo-second order models. The results indicated that adsorption fitted well with the pseudo-second order kinetic model. The thermodynamic parameters (ΔGo, ΔHo, and ΔSo) were also determined using the equilibrium constant value obtained at different temperatures. The results showed that the adsorption for both ions was feasible and exothermic.

  18. Spectrophotometric determination of boron in complex matrices by isothermal distillation of borate ester into curcumin

    International Nuclear Information System (INIS)

    In situ distillation of borate ester into the curcumin solution has been developed for the spectrophotometric determination of boron in a variety of complex matrixes. A polypropylene vessel containing the sample solution was placed inside a vessel (PP) containing 10 ml of curcumin solution and the distillation was carried out at room temperature/on a water bath. The borate ester collected in to the curcumin solution was evaporated to dryness on the water bath, taken in acetone and the absorbance was measured at 550 nm. In situ distillation of borate ester directly into the chromogenic reagent eliminates tedious sample treatment (before and/or after borate separation), use of methanol, complicated quartz set up, possible loss of boron and reduces the analysis time significantly. In situ dehydration of sample solution by ethanolic vapour in the absence of dehydrating acid prevents the formation of fluoborate and co-distillation of potential anionic interferents (nitrate and fluoride). This developed method has been applied for the determination of traces of boric acid in boron powder by the distillation of methyl borate at room temperature. For other matrixes (water, uranium oxide, uranyl nitrate, fluoride salt, etc.) distillation of ethyl borate was carried out on the water bath. LOD (3σ) was 5 ng g-1 for water and 30 ng g-1 for solid samples

  19. Specific surface area effect on adsorption of chlorpyrifos and TCP by soils and modeling

    Science.gov (United States)

    The adsorption of chlorpyrifos and TCP (3,5,6, trichloro-2-pyridinol) was determined in four soils (Mollisol, Inceptisol, Entisol, Alfisol) having different specific surface areas (19–84 m2/g) but rather similar organic matter content (2.4–3.5%). Adsorption isotherms were derived from batch equilibr...

  20. Determination of colloidal gold nanoparticle surface areas, concentrations, and sizes through quantitative ligand adsorption.

    Science.gov (United States)

    Gadogbe, Manuel; Ansar, Siyam M; He, Guoliang; Collier, Willard E; Rodriguez, Jose; Liu, Dong; Chu, I-Wei; Zhang, Dongmao

    2013-01-01

    Determination of the true surface areas, concentrations, and particle sizes of gold nanoparticles (AuNPs) is a challenging issue due to the nanoparticle morphological irregularity, surface roughness, and size distributions. A ligand adsorption-based technique for determining AuNP surface areas in solution is reported. Using a water-soluble, stable, and highly UV-vis active organothiol, 2-mercaptobenzimidazole (MBI), as the probe ligand, we demonstrated that the amount of ligand adsorbed is proportional to the AuNP surface area. The equivalent spherical AuNP sizes and concentrations were determined by combining the MBI adsorption measurement with Au(3+) quantification of aqua regia-digested AuNPs. The experimental results from the MBI adsorption method for a series of commercial colloidal AuNPs with nominal diameters of 10, 30, 50, and 90 nm were compared with those determined using dynamic light scattering, transmission electron microscopy, and localized surface plasmonic resonance methods. The ligand adsorption-based technique is highly reproducible and simple to implement. It only requires a UV-vis spectrophotometer for characterization of in-house-prepared AuNPs. PMID:23092965

  1. 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.

  2. Radon determination by activated charcoal adsorption and liquid scintillation measurement

    International Nuclear Information System (INIS)

    A passive diffusion method for the determination of radon concentration has been optimised and calibrated. The device consists of a scintillation vial containing activated charcoal, a diffusion barrier and a desiccant agent. The response to diverse atmospheric humidity and variable exposure intervals was studied. The result is a detector, which is independent of atmospheric humidity for at least (up to) 7 days of exposure. The method was compared with electret detectors (US EPA) with very satisfactory results. The advantages of this method are its simplicity, low cost, low detection limit, the total automatization of the measurement and its total independence of humidity to measure in a wide range of radon concentrations. (author)

  3. Adsorption and thermodynamic behavior of uranium on natural zeolite

    International Nuclear Information System (INIS)

    Adsorptive behavior of natural clinoptilolite-rich zeolite from Balikesir deposites in Turkey was assessed for the removal of uranium from aqueous solutions. The uranium uptake and cation exchange capacities of zeolite were determined. The effect of initial uranium concentrations in solution was studied in detail at the optimum conditions determined before (pH 2.0, contact time: 60 minutes, temperature: 20 deg C). The uptake equilibrium is best described by Langmuir adsorption isotherm. Some thermodynamic parameters (ΔH deg, ΔS deg, ΔG deg) of the adsorption system were also determined. Application to fixation of uranium to zeolite was performed. The uptake of uranium complex on zeolite followed Langmuir adsorption isotherm for the initial concentration (25 to 100 μg/ml). Thermodynamic values of ΔG deg, ΔS deg and ΔH deg found show the spontaneous and exothermic nature of the process of uranium ions uptake by natural zeolite. (author)

  4. Equivalence of ideal, isothermal-adiabatic, and complex cycles of gas turbine power plants and determination of the maximum efficiency of their operation

    Science.gov (United States)

    Ivanov, V. A.

    2010-12-01

    The possibility of ensuring equivalence in operation and efficiency of real cycles with intermediate cooling (heating) and isothermal-adiabatic compressions (expansion) in ideal simple cycles formed on the T- S diagrams in the second stage of real cycles. The possibility of using the equivalence of cycles for determining the maximum efficiency of operation of real cycles is demonstrated.

  5. Meningococcal carriage rates in healthy individuals in Japan determined using Loop-Mediated Isothermal Amplification and oral throat wash specimens.

    Science.gov (United States)

    Takahashi, Hideyuki; Haga, Masae; Sunagawa, Tomimasa; Saitoh, Takehito; Kitahara, Takeru; Matsumoto, Sohkichi; Ohnishi, Makoto

    2016-07-01

    The detailed epidemiology of meningococcal diseases in Japan has yet to be determined and, moreover, the healthy carriage rate is also unknown. In this study, to obtain insight into the carriage rate of Neisseria meningitidis in healthy individuals in Japan, we developed a new method to detect the N. meningitidis-specific ctrB gene, one of the genes encoding enzymes for capsule synthesis, by Loop-Mediated Isothermal Amplification (LAMP) and examined the meningococcal carriage rate by using self-collected oral throat wash specimens from 836 students at a university. Examination by LAMP showed that 7 out of 836 samples were positive for N. meningitidis DNA, and the results were also verified by the nested PCR method for the meningococcus specific ggt gene. The N. meningitidis carriage rate in healthy individuals was estimated to be 0.84%. Moreover, we further confirmed by the nested-PCR-based serogroup typing method that 5 of the positive samples belonged to serogroup Y, 1 belonged to group B and 1 was unidentifiable. Considering the epidemiology for meningococcal diseases in Japan, the carriage rate and the serogroup profile seem to be consistent with low incidence of meningococcal diseases and serogroup distribution of clinical meningococcal isolates in Japan, respectively. PMID:26895673

  6. Adsorption in single-walled carbon nanotubes by experiments and molecular simulation II: Effect of morphology and temperature on organic adsorption

    Science.gov (United States)

    Agnihotri, S.; Rostam-Abadi, M.; Mota, J.P.B.; Rood, M.J.

    2005-01-01

    Hexane adsorption on single-walled carbon nanotube (SWNT) bundles was studied. Hexane adsorption capacities of two purified SWNT samples was gravimetrically determined at isothermal conditions of 25??, 37??, and 50??C for 10-4 Simulation of hexane adsorption under similar temperature and pressure conditions were performed on the external and internal sites of nanotube bundles of diameters same as those in experimental samples. The simulations could predict isotherms for a hypothetical scenario where all nanotubes in a sample would be open. This is an abstract of a paper presented at the AIChE Annual Meeting and Fall Showcase (Cincinnati, OH 10/30/2005-11/4/2005).

  7. Design, construction, and calibration of an isothermal titration calorimeter and its application in the study of the adsorption of phenolic compounds.

    Science.gov (United States)

    Moreno-Piraján, Juan Carlos; Giraldo, Liliana

    2012-01-01

    An isothermal calorimetric titration was designed and built, and some of the results obtained are presented here. For this purpose, a Calvet heat-conducting microcalorimeter was developed and connected to a titration unit built for this experiment to record titration thermograms. The microcalorimeter was electrically calibrated to establish its sensitivity and reproducibility, obtaining K = 13.56 ± 0.21 W V(-1). Additionally, the equipment was tested using the heat of neutralisation for the tris-hydroxymethyl-aminomethane-HCl (THAM-HCl) system, obtaining ΔH = -30.92 ± 0.03 kJ mol(-1). The unit was assembled to obtain titration heats and the corresponding thermodynamic variables (ΔH, ΔG, ΔS, and K(e)) with a system of phenolic derivatives-activated carbon (synthesised from potato peel). PMID:22299996

  8. Design, construction, and calibration of an isothermal titration calorimeter and its application in the study of the adsorption of phenolic compounds

    Science.gov (United States)

    Moreno-Piraján, Juan Carlos; Giraldo, Liliana

    2012-01-01

    An isothermal calorimetric titration was designed and built, and some of the results obtained are presented here. For this purpose, a Calvet heat-conducting microcalorimeter was developed and connected to a titration unit built for this experiment to record titration thermograms. The microcalorimeter was electrically calibrated to establish its sensitivity and reproducibility, obtaining K = 13.56 ± 0.21 W V-1. Additionally, the equipment was tested using the heat of neutralisation for the tris-hydroxymethyl-aminomethane-HCl (THAM-HCl) system, obtaining ΔH = -30.92 ± 0.03 kJ mol-1. The unit was assembled to obtain titration heats and the corresponding thermodynamic variables (ΔH, ΔG, ΔS, and Ke) with a system of phenolic derivatives-activated carbon (synthesised from potato peel).

  9. Simultaneous Adsorption of Cr(VI) and Phenol from Binary Mixture Using Iron Incorporated Rice Husk: Insight to Multicomponent Equilibrium Isotherm

    OpenAIRE

    Ankur Gupta; Chandrajit Balomajumder

    2016-01-01

    Fe modified rice husk was prepared as a low cost biosorbent for the removal of Cr(VI) and phenol both singly and in combination from single and binary simulated synthetic waste water. Rice husk was modified by treating with FeSO4·7H2O. The results showed that impregnation of iron onto the surface of rice husk improved the adsorption capability of both Cr(VI) and phenol. The effects of process parameters for multicomponent system such as pH, adsorbent dose, and contact time onto the percentage...

  10. Adsorption of organic compounds onto activated carbons from recycled vegetables biomass.

    Science.gov (United States)

    Mameli, Anna; Cincotti, Alberto; Lai, Nicola; Crisafulli, Carmelo; Sciré, Salvatore; Cao, Giacomo

    2004-01-01

    The removal of organic species from aqueous solution by activated carbons is investigated. The latter ones are prepared from olive husks and almond shells. A wide range of surface area values are obtained varying temperature and duration of both carbonization and activation steps. The adsorption isotherm of phenol, catechol and 2,6-dichlorophenol involving the activated carbons prepared are obtained at 25 degrees C. The corresponding behavior is quantitatively correlated using classical isotherm, whose parameters are estimated by fitting the equilibrium data. A two component isotherm (phenol/2,6-dichlorophenol) is determined in order to test activated carbon behavior during competitive adsorption. PMID:15347202

  11. Influence of geometrical structure on sorption isotherms of Jersey and yarns made of cotton at two temperatures

    OpenAIRE

    BHOURI, Neila; Ben Nasrallah, Sassi; Perre, Patrick

    2012-01-01

    This paper presents comparison between sorption isotherms of a Jersey knitted fabric and frayed yarns which constitute. An experimental device, built around a magnetic suspension balance, was conceived to determine the sorption kinetics. This device is used to measure the moisture content of bleached textile samples made of cotton at temperatures of 25 degrees C and 35 degrees C. The results show coincidence between adsorption and desorption isotherms of knitted fabric and frayed yarns at wea...

  12. The Adsorption Mechanism of Modified Activated Carbon on Phenol

    Directory of Open Access Journals (Sweden)

    Lin J. Q.

    2016-01-01

    Full Text Available Modified activated carbon was prepared by thermal treatment at high temperature under nitrogen flow. The surface properties of the activated carbon were characterized by Boehm titration, BET and point of zero charge determination. The adsorption mechanism of phenol on modified activated carbon was explained and the adsorption capacity of modified activated carbon for phenol when compared to plain activated carbon was evaluated through the analysis of adsorption isotherms, thermodynamic and kinetic properties. Results shows that after modification the surface alkaline property and pHpzc value of the activated carbon increase and the surface oxygen-containing functional groups decrease. The adsorption processes of the plain and modified carbon fit with Langmuir isotherm equation well, and the maximum adsorption capacity increase from 123.46, 111.11, 103.09mg/g to 192.31, 178.57, 163,93mg/g under 15, 25 and 35°C after modification, respectively. Thermodynamic parameters show that the adsorption of phenol on activated carbon is a spontaneously exothermic process of entropy reduction, implying that the adsorption is a physical adsorption. The adsorption of phenol on activated carbon follows the pseudo-second-order kinetics (R2>0.99. The optimum pH of adsorption is 6~8.

  13. Differential adsorption of nucleic acid bases: Relevance to the origin of life

    OpenAIRE

    Sowerby, Stephen J.; Cohn, Corey A; Heckl, Wolfgang M.; Holm, Nils G

    2001-01-01

    The adsorption of organic molecules onto the surfaces of inorganic solids has long been considered a process relevant to the origin of life. We have determined the equilibrium adsorption isotherms for the nucleic acid purine and pyrimidine bases dissolved in water on the surface of crystalline graphite. The markedly different adsorption behavior of the bases describes an elutropic series: guanine > adenine > hypoxanthine > thymine > cytosine > uracil. We propose th...

  14. Thermodynamic effects of the hydrophobic surfactant proteins on the early adsorption of pulmonary surfactant.

    OpenAIRE

    Schram, V.; Hall, S B

    2001-01-01

    We determined the influence of the two hydrophobic proteins, SP-B and SP-C, on the thermodynamic barriers that limit adsorption of pulmonary surfactant to the air-water interface. We compared the temperature and concentration dependence of adsorption, measured by monitoring surface tension, between calf lung surfactant extract (CLSE) and the complete set of neutral and phospholipids (N&PL) without the proteins. Three stages generally characterized the various adsorption isotherms: an initial ...

  15. 山西省典型土壤对重金属Cu、Zn和Pb等温吸附特征及应用%Isothermal adsorption characteristics and applications of Cu,Zn,and Pb in typical soil of Shanxi

    Institute of Scientific and Technical Information of China (English)

    秦俊梅; 刘奋武; 周俊; 卜玉山

    2013-01-01

    It was significant to find cheap and efficient adsorption materials to remove heavy metals from wastewater.In this study,the isothermal adsorption efficiencies of Cu,Zn,and Pb by calcareous clay soil,calcareous sandy soil,and alkaline bentonite were investigated through shake flask experiments.In addition,the removal efficiencies of Cu,Zn,and Pb from sewage treatment plant wastewater were studied by the above three adsorption material in the subsequent fixed bed adsorption process.Results showed that the isothermal adsorption characteristics of Cu,Zn,and Pb by calcareous clay soil,calcareous sandy soil,and alkaline bentonite was obviously correlated with Freundlich equation.The heavy metals adsorption forces of the calcareous clay soil,calcareous sandy soil,and alkaline bentonite were Zn>Cu > Pb,Cu> Zn> Pb,and Cu> Zn> Pb,respectively,while the heavy metals adsorption capacity of the calcareous clay soil,calcareous sandy soil,and alkaline bentonite were Cu>Zn>Pb,Pb>Cu>Zn,and Cu>Pb>Zn.Meanwhile,further fixed bed adsorption experiments revealed that the removal efficiency of Cu,Zn,and Pb from wastewater by calcareous clay soil adsorption were 79.9%,97.7%,and 73.4%,and the removal efficiency of Cu,Zn,and Pb by the alkaline bentonite adsorption were also reached to 70.3%,90.6%,and 90.6%,respectively.The results obtained from this study were helpful in choose of adsorbent to remove the heavy metals from wastewater.%寻求高效廉价重金属吸附材料在污水重金属去除领域具有重要意义.本研究采用摇瓶试验,研究了山西省石灰性黏壤土、石灰性砂壤土及碱性膨润土对Cu、Zn和Pb的等温吸附效果,并利用土柱吸附试验进一步研究了3类吸附材料对污水处理厂入厂污水中重金属的实际吸附去除能力.研究结果表明,石灰性黏壤土、石灰性砂壤土及碱性膨润土对污水中Cu、Zn和Pb的等温吸附行为均可用Freundlich吸附等温线显著拟合.

  16. Study on the adsorption kinetics of orthophosphate anions on layer double hydroxide

    Institute of Scientific and Technical Information of China (English)

    PENG Shuchuan; L(U) Lü; WANG Jin; HAN Lu; CHEN Tianhu; JIANG Shaotong

    2009-01-01

    A kinetic study was conducted on the adsorption of orthophosphate anions on layer double hydroxide (LDH). The adsorption has proved itself to be a spontaneous endothermic process and is large in capacity and rate. The adsorption isotherm correlates well with the Freundlich model, and a rise in temperature will lead to an increase in adsorption efficiency. Additionally, the results suggested that the adsorption is an entropy-increasing process and is in good agreement with the pseudo-second order kinetics. The free energy (ΔG) of adsorption of orthophosphate onto LDH varies within the range of -1.75- -3.34 kJ/mol, the enthalpy (ΔH) varies by 7.96 kJ/mol and the entropy (ΔS) by 33.59 kJ/mol. The adsorption activation energy is 8.3 kJ/mol, showing that the adsorption of orthophosphate onto LDH is determined to be a physical adsorption.

  17. Calculation of Thermodynamic Parameters for Freundlich and Temkin Isotherm Models

    Institute of Scientific and Technical Information of China (English)

    ZHANGZENGQIANG; ZHANGYIPING; 等

    1999-01-01

    Derivation of the Freundlich and Temkin isotherm models from the kinetic adsorption/desorption equations was carried out to calculate their thermodynamic equilibrium constants.The calculation formulase of three thermodynamic parameters,the standard molar Gibbs free energy change,the standard molar enthalpy change and the standard molar entropy change,of isothermal adsorption processes for Freundlich and Temkin isotherm models were deduced according to the relationship between the thermodynamic equilibrium constants and the temperature.

  18. 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.

  19. Adsorption of sodium alkyl aryl sulfonates on sandstone. [Berea and Benton Tar Springs sandstones

    Energy Technology Data Exchange (ETDEWEB)

    Lawson, J.B.; Dilgren, R.E.

    1976-01-01

    Equilibrium adsorption isotherms of commercial alkyl aryl sulfonates (petroleum sulfonates), and pure alkyl aryl sulfonates on disaggregated Berea and Benton Tar Springs sandstones were determined. Adsorption isotherms of commercial sulfonates were found to contain maxima, which did not necessarily correspond to the measured C.M.C. At adsorption maxima, surface coverage corresponded to about one half monomolecular layer of sulfonate, but, at high surfactant concentrations, coverage sometimes amounted to only about one-tenth of a monolayer. Pure alkyl aryl sulfonates were synthesized and adsorption on sandstone determined. These materials were found to yield conventional adsorption isotherms, with adsorption plateaus at about one half a monolayer of surface coverage. Apparently, adsorption maxima are unique to impure sulfonates. Selectivity of adsorption with respect to molecular weight and structural type was studied. Structure of petroleum sulfonate and accompanying mineral oil was determined as were structures of sulfonate and mineral oil that had been equilibrated with sandstone. Comparison showed no selectivity of adsorption based on carbon number distribution or structural type. However, aggregates relatively rich in mineral oil were found to be selectively adsorbed.

  20. Protein Adsorption Patterns and Analysis on IV Nanoemulsions—The Key Factor Determining the Organ Distribution

    Directory of Open Access Journals (Sweden)

    Mirko Jansch

    2012-12-01

    Full Text Available Intravenous nanoemulsions have been on the market for parenteral nutrition since the 1950s; meanwhile, they have also been used successfully for IV drug delivery. To be well tolerable, the emulsions should avoid uptake by the MPS cells of the body; for drug delivery, they should be target-specific. The organ distribution is determined by the proteins adsorbing them after injection from the blood (protein adsorption pattern, typically analyzed by two-dimensional polyacrylamide gel electrophoresis, 2-D PAGE. The article reviews the 2-D PAGE method, the analytical problems to be faced and the knowledge available on how the composition of emulsions affects the protein adsorption patterns, e.g., the composition of the oil phase, stabilizer layer and drug incorporation into the interface or oil core. Data were re-evaluated and compared, and the implications for the in vivo distribution are discussed. Major results are that the interfacial composition of the stabilizer layer is the main determining factor and that this composition can be modulated by simple processes. Drug incorporation affects the pattern depending on the localization of the drug (oil core versus interface. The data situation regarding in vivo effects is very limited; mainly, it has to be referred to in the in vivo data of polymeric nanoparticles. As a conclusion, determination of the protein adsorption patterns can accelerate IV nanoemulsion formulation development regarding optimized organ distribution and related pharmacokinetics.

  1. Study of application of alumina-coated carbon nanotube for removal of Hydroxy Benzene from aqueous solutions: Adsorption and determination of equilibrium and kinetics parameters

    Directory of Open Access Journals (Sweden)

    M Malakootian

    2015-08-01

    Full Text Available Background and Objective: Phenol and phenol derivatives in industrial wastewater are among the pollutants with priorities. The high cost and low efficiency of some routine treatment processes of industrial wastewater has limited their use. One of the new methods under consideration is, nowadays, adsorption using carbon nanotubes. This study was conducted in order to evaluate the application of alumina-coated multiwall carbon nanotubes in eliminating phenol from synthetic wastewater. Materials and Methods: This study was performed in laboratory at batch scale. Multi-wall carbon nanotubes were coated with Alumina. The concentration of phenol was determined by spectrophotometer through photometry. The effect of pH changes, dosage of adsorbent, contact time, the initial concentration of phenol, temperature, and the concentrations of different salts on the efficiency of absorption was evaluated. Then, the absorption results were described using the Langmuir and Freundlich isotherms and the synthetics of absorption. Results: It was found that absorption efficiency increased significantly by decreasing the initial concentration of phenol and pH and by increasing the carbon nanotube dosage, temperature, and contact time. On the other hand, the maximum elimination of phenol from the solution (98.86% occurred at 4 mg/l phenol concentration, under acidic conditions (pH=3, at adsorbent dosage of 0.05 g/l, at temperature of 45°C, and contact time of 10 min. Evaluation of the regressions isotherms showed that the process follows the Langmuir model and second-degree synthetic absorption. Conclusion: The high efficacy (98% of the adsorption process in this study showed that alumina-coated multiwall carbon nanotubes have a good capability in eliminating phenol and can be used as an appropriate and new method for eliminating phenol and its derivatives from wastewater.

  2. Adsorption isotherms and selectivity of CO/N2/CO2 on MOF-74(Ni)%CO/N2/CO2在MOF-74(Ni)上吸附相平衡和选择性

    Institute of Scientific and Technical Information of China (English)

    刘有毅; 黄艳; 何嘉杰; 肖静; 夏启斌; 李忠

    2015-01-01

    This work investigates the adsorption performance of adsorbent MOF-74(Ni) for CO/N2 and CO2/CO2 binary gas mixtures. Adsorbent MOF-74(Ni) with high density of coordinatively unsaturated sites was synthesized by a hydrothermal method, and characterized with N2 adsorption, P-XRD, and SEM. The adsorption isotherms of CO, N2 and CO2 on MOF-74(Ni) were measured, and the selectivities for CO/N2 and CO/CO2 were calculated based on ideal adsorbed solution theory (IAST). Results showed that adsorbent MOF-74(Ni) achieved superior CO adsorption capacity of 6.15 mmol·g−1 at 298 K and 0.1 MPa, and as low as 0.86 mmol·g−1 for N2. In low pressure range of 0—40 kPa, MOF-74(Ni) showed significantly higher uptake for CO than that for CO2. Moreover, IAST-predicted CO/N2 selectivity of MOF-74(Ni) is above 1000, and its CO/CO2 selectivity is in the range of 4—9. It suggests that MOF-74(Ni) is more favorable for CO adsorption than N2and CO2 adsorption.%主要研究了MOF-74(Ni)材料对CO/N2/CO2的吸附分离性能。应用水热法合成制备MOF-74(Ni),分别采用全自动表面积吸附仪、P-XRD、扫描电子显微镜对材料的孔隙结构和晶体形貌进行了表征,应用静态吸附法测定了CO、N2和CO2在MOF-74(Ni)上的吸附等温线,应用DSLF方程模拟了3种气体MOF-74(Ni)上的吸附等温线,依据IAST理论模型计算了MOF-74(Ni)对CO/N2二元混合物和CO/CO2二元混合物的吸附选择性。研究结果表明:在0.1 MPa和常温条件下,MOF-74(Ni)材料对CO吸附容量高达6.15 mmol·g−1,而相同条件下N2的吸附量只有0.86 mmol·g−1。MOF-74(Ni)在低压下(0~40 kPa)对CO的吸附量明显高于其对CO2的吸附量。应用IAST模型估算MOF-74(Ni)对二元混合物吸附选择性的结果表明:MOF-74(Ni)对CO/N2混合物的吸附选择性在1000以上;MOF-74(Ni)对 CO/CO2的吸附选择性在4~9范围,在所研究的二元气体混合物吸附体系中,MOF-74(Ni)都能优先吸附CO。

  3. Gibbs adsorption and the compressibility equation

    International Nuclear Information System (INIS)

    A new approach for deriving the equation of state is developed. It is shown that the integral in the compressibility equation is identical to the isotherm for Gibbs adsorption in radial coordinates. The Henry, Langmuir, and Frumkin adsorption isotherms are converted into equations of state. It is shown that using Henry's law gives an expression for the second virial coefficient that is identical to the result from statistical mechanics. Using the Langmuir isotherm leads to a new analytic expression for the hard-sphere equation of state which can be explicit in either pressure or density. The Frumkin isotherm results in a new equation of state for the square-well potential fluid. Conversely, new adsorption isotherms can be derived from equations of state using the compressibility equation. It is shown that the van der Waals equation gives an adsorption isotherm equation that describes both polymolecular adsorption and the unusual adsorption behavior observed for supercritical fluids. copyright 1995 American Institute of Physics

  4. Adsorption studies of Cd(II) onto Al2O3/Nb2O5 mixed oxide dispersed on silica matrix and its on-line preconcentration and determination by flame atomic absorption spectrometry

    International Nuclear Information System (INIS)

    The present study describes the adsorption characteristic of Cd(II) onto Nb2O5/Al2O3 mixed oxide dispersed on silica matrix. The characterization of the adsorbent has been carried out by infrared spectroscopy (IR), scanning electronic microscopy (SEM), energy dispersive spectroscopy (EDS), energy dispersive X-ray fluorescence analysis (EDXRF) and specific surface area (SBET). From batch experiments, adsorption kinetic of Cd(II) was described by a pseudo-second-order kinetic model. The Langmuir linear isotherm fitted to the experimental adsorption isotherm very well, and the maximum adsorption capacity was found to be 17.88 mg g-1. Using the effective material, a method for Cd(II) preconcentration at trace level was developed. The method was based on on-line adsorption of Cd(II) onto SiO2/Al2O3/Nb2O5 at pH 8.64, in which the quantitative desorption occurs with 1.0 mol L-1 hydrochloric acid towards FAAS detector. The experimental parameters related to the system were studied by means of multivariate analysis, using 24 full factorial design and Doehlert matrix. The effect of SO42-, Cu2+, Zn2+ and Ni2+ foreign ions showed no interference at 1:100 analyte:interferent proportion. Under the most favorable experimental conditions, the preconcentration system provided a preconcentration factor of 18.4 times, consumption index of 1.08 mL, sample throughput of 14 h-1, concentration efficiency of 4.35 min-1, linear range from 5.0 up to 35.0 μg L-1 and limits of detection and quantification of 0.19 and 0.65 μg L-1 respectively. The feasibility of the proposed method for Cd(II) determination was assessed by analysis of water samples, cigarette sample and certified reference materials TORT-2 (Lobster hepatopancreas) and DOLT-4 (Dogfish liver).

  5. Water vapor adsorption on activated carbon preadsorbed with naphtalene.

    Science.gov (United States)

    Zimny, T; Finqueneisel, G; Cossarutto, L; Weber, J V

    2005-05-01

    The adsorption of water vapor on a microporous activated carbon derived from the carbonization of coconut shell has been studied. Preadsorption of naphthalene was used as a tool to determine the location and the influence of the primary adsorbing centers within the porous structure of active carbon. The adsorption was studied in the pressure range p/p0=0-0.95 in a static water vapor system, allowing the investigation of both kinetic and equilibrium experimental data. Modeling of the isotherms using the modified equation of Do and Do was applied to determine the effect of preadsorption on the mechanism of adsorption. PMID:15797395

  6. The cianimetalatos as model materials for studying the adsorption of H2 and interactions that determine

    International Nuclear Information System (INIS)

    An overview of the work done in recent years in the IMRE and the Faculties of Chemistry and Physics at the University of Havana, in collaboration with the Applied Research Center for Advanced Science and Technology at the National Polytechnic Institute of Mexico is presented; on the synthesis, physico-chemical characterization, assessment and modeling of potentially usable as nanoporous materials cianometalatos model to study the adsorption of H2 at high densities, and interactions that determine it. The mechanisms of interaction of the hydrogen molecule with the crystal lattice and its consequences for the adsorption and diffusion of hydrogen in these materials are discussed. The results have been reported in dozens of articles, published in international journals, they were presented at numerous scientific events and contributed to the preparation of several thesis, master's and Ph.D. (full text)

  7. Isothermal thermoluminescence dating of K-feldspar from sediments to determine fault slip rates: development and assessment

    Science.gov (United States)

    Rhodes, E. J.; Roder, B. J.; Lawson, M. J.; Dolan, J. F.; McGill, S. F.; McAuliffe, L.

    2012-04-01

    Faults in California accommodate most of the relative motion between the Pacific and North American tectonic plates, along either one main strike-slip fault, - the San Andreas fault - or a network of sub-parallel faults (e.g., the San Jacinto, Elsinore and San Andreas faults). Slip is also accommodated along many other associated faults and folds, and the region suffers frequent damaging earthquakes. Contemporary movements of different fault-bounded blocks are relatively well established on decadal timescales using remote sensing and GPS, and on timescales of 106 to 107 years, by dating offset geologic features with radiometric methods. However, on timescales of decades to several hundred thousand years, determining total fault offset and mean slip rate is harder. Critical questions for understanding fault dynamics and improving earthquake risk assessment include the degree to which slip is clustered into episodes of more rapid movement, and how slip is accommodated by different sub-parallel faults. In many cases, streams with offset courses can be recognised, and in some cases offset terrace surfaces can be located, especially when using LiDAR data to complement field mapping. Radiocarbon and terrestrial cosmogenic nuclides have been used to date these features, but both have limitations of age range, sample suitability and availability. OSL (optically stimulated luminescence) and IRSL (infra-red stimulated luminescence) have great potential to complement these techniques, though the characteristics of quartz in some parts of southern California are suboptimal, displaying low sensitivity and other limitations. In order to overcome these limitations encountered using quartz OSL, we are developing a new geochronometer based on the isothermal thermoluminescence (ITL) signal of K feldspar measured at 250°C. Preliminary ITL age estimates from the paleoseismic site of El Paso Peaks on the Central Garlock fault in the Mojave Desert, California, agree well with a well

  8. A consideration of the correct calculation of thermodynamic parameters of adsorption

    OpenAIRE

    SLOBODAN K. MILONJIC

    2007-01-01

    The Langmuir and Freundlich isotherm equations have been widely used for interpreting various adsorption processes. There are, however, many serious mistakes in the literature in determination or calculation of thermodynamic parameters, especially in the determination of the change in the free energy of adsorption using Langmuir, Freundlich and Henry constants. Many authors used these constants for the determination of ΔG expressed instead of dimensionless in some concentration units (for exa...

  9. Evaluation of Thermodynamic Parameters of 2, 4-Dichlorophenoxyacetic Acid (2, 4-D Adsorption

    Directory of Open Access Journals (Sweden)

    A. S. Ghatbandhe

    2013-01-01

    Full Text Available Thermodynamic parameters of 2, 4-Dichlorophenoxyacetic acid (2, 4-D adsorption were evaluated by studying the adsorption equilibrium and kinetics of 2, 4-D at different temperatures. Uptake capacity of activated carbon increases with temperature. Langmuir isotherm models were applied to experimental data of 2, 4-D adsorption. Equilibrium data fitted very well to the Langmuir equilibrium model. Adsorbent monolayer capacity , Langmuir constant and adsorption rate constant were evaluated at different temperatures for activated carbon adsorption. The activation energy of adsorption ( was determined using the Arrhenius equation. Using the thermodynamic equilibrium coefficients obtained at different temperatures, the thermodynamic constants of adsorption (, , and were evaluated. The obtained values of thermodynamic parameters show that the adsorption of 2, 4-D is an endothermic process.

  10. Determination of clothing evaporative resistance on a sweating thermal manikin in an isothermal condition: heat loss method or mass loss method?

    Science.gov (United States)

    Wang, Faming; Gao, Chuansi; Kuklane, Kalev; Holmér, Ingvar

    2011-08-01

    This paper addresses selection between two calculation options, i.e heat loss option and mass loss option, for thermal manikin measurements on clothing evaporative resistance conducted in an isothermal condition (T(manikin) = T(a) = T(r)). Five vocational clothing ensembles with a thermal insulation range of 1.05-2.58 clo were selected and measured on a sweating thermal manikin 'Tore'. The reasons why the isothermal heat loss method generates a higher evaporative resistance than that of the mass loss method were thoroughly investigated. In addition, an indirect approach was applied to determine the amount of evaporative heat energy taken from the environment. It was found that clothing evaporative resistance values by the heat loss option were 11.2-37.1% greater than those based on the mass loss option. The percentage of evaporative heat loss taken from the environment (H(e,env)) for all test scenarios ranged from 10.9 to 23.8%. The real evaporative cooling efficiency ranged from 0.762 to 0.891, respectively. Furthermore, it is evident that the evaporative heat loss difference introduced by those two options was equal to the heat energy taken from the environment. In order to eliminate the combined effects of dry heat transfer, condensation, and heat pipe on clothing evaporative resistance, it is suggested that manikin measurements on the determination of clothing evaporative resistance should be performed in an isothermal condition. Moreover, the mass loss method should be applied to calculate clothing evaporative resistance. The isothermal heat loss method would appear to overestimate heat stress and thus should be corrected before use. PMID:21669906

  11. Determination of Sudan I in drinks containing Sunset yellow by adsorptive stripping voltammetry.

    Science.gov (United States)

    Gómez, Marisol; Arancibia, Verónica; Aliaga, Margarita; Núñez, Claudia; Rojas-Romo, Carlos

    2016-12-01

    An efficient, fast and sensitive method for the determination of Sudan I (SI) in drinks containing Sunset yellow (Sy) is developed and validated using an adsorptive stripping voltammetric procedure. Sy is currently added to a large number of foods; however during their synthesis SI may be produced. The determination is based on adsorption of Sy and SI onto HMDE and later reduction of the azo group at -0.71 and -0.82V, respectively. Using the best set of the experimental conditions (pH 12.3; Eads: -0.40V) for the determination of SI in Sy, a linear response for SI in the concentration range 0.5-27.2μgL(-1) was found, with a detection limit of 1.5μgL(-1) in a tads of only 30s. The method was applied to the determination of SI in commercial drinks with satisfactory results. The presence of SI was confirmed by mass spectrometry. PMID:27374598

  12. Adsorption Behaviors of Oxytetracycline onto Sediment in the Weihe River, Shaanxi, China

    Directory of Open Access Journals (Sweden)

    Dong-Hui Cheng

    2013-01-01

    Full Text Available Adsorption behaviors of oxytetracycline onto sediment in the Weihe River were described. The impact factors in the processes of adsorption, such as contact time, solution pH, temperature, and ionic strength, were determined by experiments. The experimental results were analyzed by kinetic and isotherm models. The adsorption kinetics was found to follow a pseudo-first-order model. The equilibrium adsorption data fitted well with the Langmuir and Freundlich isotherm models. However, the Langmuir isotherm was more suitable to describe the adsorption. Thermodynamics parameters such as Gibbs-free energy change (ΔG°, enthalpy change (ΔH°, and entropy change (ΔS° were calculated. Results showed that the adsorption was feasible, spontaneous, entropy increasing, and endothermic in nature, which reached equilibrium in about 24 hours. The adsorption capacity did not cause obvious change at solution pH 4.0–7.0, and both decreased in solution pH 7.0–10.0 and 4.0–2.0. The presence of electrolytes such as NaCl in aqueous solution had a significant negative effect on the adsorption. The mechanisms controlling the adsorption were supposed to be chemisorption.

  13. Determination of Lamotrigine in Pharmaceutical Preparations by Adsorptive Stripping Voltammetry Using Screen Printed Electrodes

    OpenAIRE

    M. Julia Arcos-Martínez; M. Encarnación Burgoa Calvo; Olga Domínguez-Renedo

    2008-01-01

    This paper describes a procedure that has been optimized for the determination of lamotrigine by Differential Pulse Adsorptive Stripping Voltammetry (DPAdSV) using carbon screen-printed electrodes (CSPE) and mercury coated carbon screen-printed electrodes. Selection of the experimental parameters was made using experimental design methodology. The detection limit found was 5.0 x 10-6 M and 2.0 x 10-6 M for the non modified and Hg modified CSPE, respectively. In terms of reproducibility, the p...

  14. Determination of copper in whole blood by differential pulse adsorptive stripping voltammetry

    Directory of Open Access Journals (Sweden)

    Tarik Attar

    2014-02-01

    Full Text Available A selective and sensitive method for determination of copper in blood by adsorptive differential pulse cathodic stripping voltammetry is presented. The method is based on adsorptive accumulation of the complexes of Cu (II ions with benzenesulfonyl hydrazide onto hanging mercury drop electrode (HMDE, followed by the reduction of the adsorbed species by differential pulse cathodic stripping voltammetry. The effect of various parameters such as supporting electrolyte, concentration of benzenesulfonyl hydrazide, accumulation potential, accumulation time and stirring rate on the selectivity and sensitivity were studied. The optimum conditions for determination of copper include perchloric acid 0.03 M, concentration of benzenesulfonyl hydrazide 7.5×10-5 M, the accumulation potential of -350 mV (vs. Ag/AgCl, the accumulation time of 50 s, and the scan rate of 50 mV s-1. Under optimized conditions, linear calibration curves were established for the concentration of Cu (II in the range of 0.62-275 ng mL-1, with detection limit of 0.186 ng mL-1 for Cu (II. The procedure was successfully applied to the determination of copper ion in whole blood samples.

  15. Adsorption and quantitative estimation of uranium by calcium alginate beads coated with CdS quantum dots

    International Nuclear Information System (INIS)

    A novel method has been developed for quantitative determination of uranium (VI) in the range of 5 - 70 mg/L from fluorescence quenching property of CdS quantum dots coated on calcium alginate microbeads, which revealed linear Stern Volmer plot. These CdS functionalized microbeads exhibited adsorption phenomenon where the maximum adsorption capacity (Qe) was measured to be 7.58 mg/g. The mechanism of adsorption of U (VI) favoured monolayer adsorption as reflected from Langmuir adsorption isotherm. (author)

  16. Effect of temperature on adsorption of hydrogen by catalysts of ruthenium-rhodium system in sulfuric acid solutions

    International Nuclear Information System (INIS)

    Temperature dependence has been studied of hydrogen adsorption on sceletal ruthenium-rhodium catalysts in 1 N solution of sulfuric acid in a temperature range 20-80 deg C at 20 deg C intervals. The conditions and the results of preliminary stabilization of the catalysts are described. It has been established that hydrogen adsorption on sceletal ruthenium and rhodium-ruthenium catalysts decreases with a temperature rise in the above-cited range. The temperature dependence of hydrogen adsorption has been used for plotting adsorption isotherms and for determining isosterical differential heats of hydrogen adsorption and bond energy of hydrogen with the surface

  17. Adsorption height determination of nonequivalent C and O species of PTCDA on Ag(110) using x-ray standing waves

    Science.gov (United States)

    Mercurio, G.; Bauer, O.; Willenbockel, M.; Fairley, N.; Reckien, W.; Schmitz, C. H.; Fiedler, B.; Soubatch, S.; Bredow, T.; Sokolowski, M.; Tautz, F. S.

    2013-01-01

    The normal incidence x-ray standing wave (NIXSW) technique is used to determine the adsorption geometry of submonolayer 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA) adsorbed on the Ag(110) surface. An accurate analysis of both C1s and O1s photoemission (PE) spectra allows the respective adsorption heights of carbon and oxygen atoms in different chemical environments within PTCDA to be distinguished. Due to the intricacy of the PE fitting models, a systematic error analysis of NIXSW structural parameters was developed and employed. Based on the adsorption geometry of PTCDA on Ag(110) a bonding mechanism is discussed.

  18. Adsorption of naphthalene onto sonicated talc from aqueous solutions.

    Science.gov (United States)

    Sener, Savaş; Ozyilmaz, Azat

    2010-06-01

    The adsorption behavior of naphthalene onto naturally hydrophobic talc from aqueous solution was investigated in this study. The natural talc was first pretreated by sonication to improve the surface characteristics and enhance the uptake capacity by increasing the specific surface area (SSA) of talc. The naphthalene uptake of talc was found as 276 mg g(-1) and increased to 359 mg g(-1) after the sonication. Adsorption studies also showed that the adsorption of naphthalene onto the sonicated talc was not affected by changes in pH suggesting that the main driving forces for naphthalene adsorption onto talc was hydrophobic bonding rather than electrostatic force. The pseudo-first and pseudo-second orders and intraparticle diffusion equation were used to evaluate the kinetic data and the constants were determined. Adsorption process of naphthalene onto talc followed the pseudo-second-order rate expression for different initial naphthalene concentrations. The Langmuir and Freundlich isotherm models were used to model the isotherm data for their applicability. The Freundlich isotherm best fitted for the adsorption of naphthalene onto talc. PMID:20163977

  19. Ion adsorption components in liquid/solid systems

    Institute of Scientific and Technical Information of China (English)

    WU Xiao-fu; HU Yue-li; ZHAO Fang; HUANG Zhong-zi; LEI Dian

    2006-01-01

    Experiments on Zn2+ and Cd2+ adsorptions on vermiculite in aqueous solutions were conducted to investigate the widely observed adsorbent concentration effect on the traditionally defined adsorption isotherm in the adsorbate range 25-500 mg/L and adsorbent range 10-150 g/L. The results showed that the equilibrium ion adsorption density did not correspond to a unique equilibrium ion concentration in liquid phase. Three adsorbate/adsorbent ratios, the equilibrium adsorption density, the ratio of equilibrium adsorbate concentration in liquid phase to adsorbent concentration, and the ratio of initial adsorbate concentration to adsorbent concentration, were found to be related with unique values in the tested range. Based on the assumption that the equilibrium state of a liquid/solid adsorption system is determined by four mutually related components: adsorbate in liquid phase, adsorbate in solid phase, uncovered adsorption site and covered adsorption site, and that the equilibrium chemical potentials of these components should be equalized, a new model was presented for describing ion adsorption isotherm in liquid/solid systems. The proposed model fit well the experimental data obtained from the examined samples.

  20. Adsorption of ferrous ions onto montmorillonites

    Energy Technology Data Exchange (ETDEWEB)

    Qin, Dawei, E-mail: qdw109@163.com [Qilu University of Technology, Jinan, 250353, Shandong (China); Niu, Xia [Qilu University of Technology, Jinan, 250353, Shandong (China); Qiao, Min; Liu, Gang; Li, Hongxin; Meng, Zhenxiao [Shandong SiBang pharmaceutical co., LTD, Jinan, Shandong, 250200 (China)

    2015-04-01

    Highlights: • Adsorption study of ferrous ions on montmorillonites. • Using ascorbic acid as antioxidants in adsorption process. • Fe (II)-MMT had good affinity for phosphate. - Abstract: The adsorption of Fe (II) onto montmorillonites was investigated through initial concentration, contact time, pH and temperature. During the whole adsorption process, the ascorbic acid (Vitamin C) was added as a kind of antioxidant, at the same time, deionized water (after boiling) and nitrogen protection were also used to avoid oxidation. The Fe{sup 2+}/Fe{sub total} ratio of the iron exists in the Fe-montmorillonites was found more than 95%. Two kinetic models, including pseudo-first-order and pseudo-second-order model, were used to analyze the adsorption process of Fe (II) on montmorillonites. The results of our study showed that adsorption process fitted with pseudo-second-order well. Adsorption isotherms showed that Langmuir model was better than Freundlich model. The thermodynamic parameters ΔG{sup 0} and ΔH{sup 0} were 3.696 kJ/mol and 6.689 kJ/mol (we just gave the values at 298 K), respectively. The positive values at different temperatures showed that the adsorption process was non-spontaneous and endothermic. The characteristics of materials were determined by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Surface area and porosity analyzer, Thermogravimetric analysis (TGA), Differential scanning calorimeter (DSC) and Zeta potential distribution.

  1. Adsorptive removal of Cu(II) from aqueous solutions using collagen-tannin resin

    Energy Technology Data Exchange (ETDEWEB)

    Sun Xia; Huang Xin [Department of Biomass Chemistry and Engineering, Sichuan University, Chengdu 610065 (China); Liao Xuepin, E-mail: xpliao@scu.edu.cn [Department of Biomass Chemistry and Engineering, Sichuan University, Chengdu 610065 (China); National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu 610065 (China); Shi Bi, E-mail: shibi@scu.edu.cn [National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu 610065 (China)

    2011-02-28

    The collagen-tannin resin (CTR), as a novel adsorbent, was prepared via a reaction of collagen with black wattle tannin and aldehyde, and its adsorption properties to Cu(II) were systematically investigated, including pH effect, adsorption equilibrium, adsorption kinetics, and column adsorption. The adsorption capacity of Cu(II) on CTR was pH-dependent, and it increased with the increase of solution pH. The adsorption isotherms were well described by Langmuir isotherm model with correlating constant (R{sup 2}) higher than 0.99. The adsorption capacity determined at 303 K was high up to 0.26 mmol/g, which was close to the value (0.266 mmol/g) estimated from Langmuir equation. The adsorption capacity was increased with the increase of temperature, and thermodynamic calculations suggested that the adsorption of Cu(II) on CTR is an endothermic process. The adsorption kinetics were well fitted by the pseudo-second-order rate model. Further column studies suggested that CTR was effective for the removal of Cu(II) from solutions, and more than 99% of Cu(II) was desorbed from column using 0.1 mol/L HNO{sub 3} solution. The CTR column can be reused to adsorb Cu(II) without any loss of adsorption capacity.

  2. Adsorptive removal of Cu(II) from aqueous solutions using collagen-tannin resin

    International Nuclear Information System (INIS)

    The collagen-tannin resin (CTR), as a novel adsorbent, was prepared via a reaction of collagen with black wattle tannin and aldehyde, and its adsorption properties to Cu(II) were systematically investigated, including pH effect, adsorption equilibrium, adsorption kinetics, and column adsorption. The adsorption capacity of Cu(II) on CTR was pH-dependent, and it increased with the increase of solution pH. The adsorption isotherms were well described by Langmuir isotherm model with correlating constant (R2) higher than 0.99. The adsorption capacity determined at 303 K was high up to 0.26 mmol/g, which was close to the value (0.266 mmol/g) estimated from Langmuir equation. The adsorption capacity was increased with the increase of temperature, and thermodynamic calculations suggested that the adsorption of Cu(II) on CTR is an endothermic process. The adsorption kinetics were well fitted by the pseudo-second-order rate model. Further column studies suggested that CTR was effective for the removal of Cu(II) from solutions, and more than 99% of Cu(II) was desorbed from column using 0.1 mol/L HNO3 solution. The CTR column can be reused to adsorb Cu(II) without any loss of adsorption capacity.

  3. Cathodic adsorptive stripping voltammetric determination of uranium with potassium hydrogen phthalate.

    Science.gov (United States)

    Farghaly, O A; Ghandour, M A

    1999-06-01

    The adsorption properties of dioxouranium (II)-Phathalate complexes onto hanging mercury drop electrode are exploited in developing a highly sensitive and selective stripping voltammetric procedure for the determination of uranium (VI). The reduction current of adsorbed complex ions of U(VI) was measured by both linear sweep (LSCSV) and differential pulse cathodic stripping voltammetry (DPCSV), preceded by a period of preconcentration onto the electrode surface. As low as 2x10(-9) mol dm(-3) (0.5 mug/l) and 2x10(-8) mol dm(-3) (4.8 mug/l) with accumulation time 240 and 120 s using DPCSV and LSCSV, respectively, have been determined successfully. The relative standard deviation of 2.2% at the 5 ppm level was obtained. The interferences of some metal ions and anions were studied. The application of this method was tested in the determination of uranium in superphosphate fertilizer. PMID:18967571

  4. Partitioning model of the adsorption of explosives from soils to determine its environmental fate

    Directory of Open Access Journals (Sweden)

    Rosalina González Forero

    2014-12-01

    Full Text Available The purpose of this research was to identify the principal soil characteristics that influence the adsorption of munitions constituents (MC of explosives in soils, through a partitioning model to determine the fate of the explosives. To do that, batch experiments near 1:1 (w/v soil to solution ratios reflecting field conditions were conducted using a mixture of HMX, RDX, nitroglycerine (NG, nitroguanidine (NQ, TNT and 2,4-dinitrotoluene as MC, where the mix of MC was adsorbed in twenty-five different soils that varied from 4.0 to 43.2 % clay content and 0.07 to 18.23 % total carbon, in an experiment that involved 2 days of adsorption followed by four consecutive desorption steps. The most important result was that for each MC, even if it was in a mixture, were successfully predicted the partition coefficients using the organic carbon, cation exchange capacity and extractable iron as the principal soil characteristics that determine the fate of these explosives.

  5. Effect of temperature on equilibrium and thermodynamic parameters of Cd (II) adsorption onto turmeric powder

    International Nuclear Information System (INIS)

    Summary: Batch adsorption of Cd (II) onto turmeric powder was conducted as a function of temperature. Nonlinear Langmuir, Freundlich, Dubinin-Radushkevish (D-R) and Temkin equilibrium models were employed. In addition to R 2, five different error functions were used to determine best fit equilibrium isotherm model. It was found that Freundlich isotherm model provided better fit for adsorption data at 298 and 303 K and Langmuir model was suitable for the experimental data obtained at 310 and 313 K. It was found that increase in temperature decreased maximum adsorption capacities, showing that the adsorption of Cd (II) onto turmeric powder is exothermic. Enthalpy values also confirmed the same trend. Entropy values were negative which means that randomness decreased on increasing temperature. Gibbs free energies were non spontaneous at all the temperatures studied. E values were in the range of 2.73-3.23 kJ mol/sup -1/ which indicated that adsorption mechanism is essentially physical. (author)

  6. Pore size distribution analysis of activated carbons prepared from coconut shell using methane adsorption data

    Science.gov (United States)

    Ahmadpour, A.; Okhovat, A.; Darabi Mahboub, M. J.

    2013-06-01

    The application of Stoeckli theory to determine pore size distribution (PSD) of activated carbons using high pressure methane adsorption data is explored. Coconut shell was used as a raw material for the preparation of 16 different activated carbon samples. Four samples with higher methane adsorption were selected and nitrogen adsorption on these adsorbents was also investigated. Some differences are found between the PSD obtained from the analysis of nitrogen adsorption isotherms and their PSD resulting from the same analysis using methane adsorption data. It is suggested that these differences may arise from the specific interactions between nitrogen molecules and activated carbon surfaces; therefore caution is required in the interpretation of PSD obtained from the nitrogen isotherm data.

  7. FTIR spectrophotometry, kinetics and adsorption isotherms modeling, ion exchange, and EDX analysis for understanding the mechanism of Cd{sup 2+} and Pb{sup 2+} removal by mango peel waste

    Energy Technology Data Exchange (ETDEWEB)

    Iqbal, Muhammad [Biotechnology Group, Centre for Environment Protection Studies, PCSIR Laboratories Complex, Ferozepur Road, Lahore 54600 (Pakistan)], E-mail: iqbalm@fulbrightweb.org; Saeed, Asma [Biotechnology Group, Centre for Environment Protection Studies, PCSIR Laboratories Complex, Ferozepur Road, Lahore 54600 (Pakistan); Zafar, Saeed Iqbal [School of Biological Sciences, University of Punjab, Lahore 54590 (Pakistan)

    2009-05-15

    Mango peel waste (MPW) was evaluated as a new sorbent for the removal of Cd{sup 2+} and Pb{sup 2+} from aqueous solution. The maximum sorption capacity of Cd{sup 2+} and Pb{sup 2+} was found to be 68.92 and 99.05 mg g{sup -1}, respectively. The kinetics of sorption of both metals was fast, reaching at equilibrium in 60 min. Sorption kinetics and equilibria followed pseudo-second order and Langmuir adsorption isotherm models. FTIR analysis revealed that carboxyl and hydroxyl functional groups were mainly responsible for the sorption of Cd{sup 2+} and Pb{sup 2+}. Chemical modification of MPW for blocking of carboxyl and hydroxyl groups showed that 72.46% and 76.26% removal of Cd{sup 2+} and Pb{sup 2+}, respectively, was due to the involvement of carboxylic group, whereas 26.64% and 23.74% was due to the hydroxyl group. EDX analysis of MPW before and after metal sorption and release of cations (Ca{sup 2+}, Mg{sup 2+}, Na{sup +}, K{sup +}) and proton H{sup +} from MPW with the corresponding uptake of Cd{sup 2+} and Pb{sup 2+} revealed that the main mechanism of sorption was ion exchange. The regeneration experiments showed that the MPW could be reused for five cycles without significant loss in its initial sorption capacity. The study points to the potential of new use of MPW as an effective sorbent for the removal of Cd{sup 2+} and Pb{sup 2+} from aqueous solution.

  8. Isothermal Microcalorimetry: A Review of Applications in Soil and Environmental Sciences

    Institute of Scientific and Technical Information of China (English)

    RONG Xing-Min; HUANG Qiao-Yun; JIANG Dai-Hua; CAI Peng; LIANG Wei

    2007-01-01

    Isothermal microcMorimetry provides thermodynamic and kinetic information on various reactions and processes and is thereby a powerful tool to elucidate their mechanisms.Certain improvement in isothermal microcalorimetry with regard to the studies on soil and environmental sciences is briefly described.This review mainly focuses on the use of microcalorimetry in the determination of soil microbial activity,monitoring the toxicity and biodegradation of soil organic pollutants,the risk evaluation of metals and metalloids,the heat effect of ion exchange and adsorption in soil,and environmental researches.Promising prospects for the applications of the technique in the field are also discussed.

  9. Treatment of Wastewater from a Dairy Industry Using Rice Husk as Adsorbent: Treatment Efficiency, Isotherm, Thermodynamics, and Kinetics Modelling

    Directory of Open Access Journals (Sweden)

    Uttarini Pathak

    2016-01-01

    Full Text Available Effluent from milk processing unit contains soluble organics, suspended solids, and trace organics releasing gases, causing taste and odor, and imparting colour and turbidity produced as a result of high consumption of water from the manufacturing process, utilities and service section, chemicals, and residues of technological additives used in individual operations which makes it crucial matter to be treated for preserving the aesthetics of the environment. In this experimental study after determination of the initial parameters of the raw wastewater it was subjected to batch adsorption study using rice husk. The effects of contact time, initial wastewater concentration, pH, adsorbent dosage, solution temperature and the adsorption kinetics, isotherm, and thermodynamic parameters were investigated. The phenomenon of adsorption was favoured at a lower temperature and lower pH in this case. Maximum removal as high as 92.5% could be achieved using an adsorbent dosage of 5 g/L, pH of 2, and temperature of 30°C. The adsorption kinetics and the isotherm studies showed that the pseudo-second-order model and the Langmuir isotherm were the best choices to describe the adsorption behavior. The thermodynamic parameters suggested that not only was the adsorption by rice husk spontaneous and exothermic in nature but also the negative entropy change indicated enthalpy driven process.

  10. Adsorption of ammonium dinitramide (ADN) from aqueous solutions. 1. Adsorption on powdered activated charcoal.

    Science.gov (United States)

    Santhosh, G; Venkatachalam, S; Ninan, K N; Sadhana, R; Alwan, S; Abarna, V; Joseph, M A

    2003-03-17

    Investigations on the adsorption of ammonium dinitramide (NH(4)N(NO(2))(2)) (ADN) from aqueous solutions on powdered activated charcoal (PAC) were carried out in order to find out an effective and easier method of separating ADN from aqueous solutions. The effectiveness of PAC in the selective adsorption of ADN from aqueous solutions of ADN (ADN-F) and ADN in presence of sulfate (SO(4)(2-)) and nitrate (NO(3)(-)) ions (ADN-PS) was examined and compared using batch and column methods. The adsorption process follows both Langmuir and Freundlich adsorption isotherms and the isotherm parameters for the models were determined. The observed data favor the formation of monolayer adsorption. The adsorption capacities were found to be 63.3, 119, 105.3 and 82 mg of ADN per g of PAC for ADN-F (batch), ADN-PS (batch), ADN-F (column) and ADN-PS (column), respectively. Break-through curves for ADN-F and ADN-PS were obtained for the optimization of separation of ADN from aqueous solutions. Elution curves were generated for the desorption of ADN from PAC using hot water as eluent. PMID:12628781

  11. Statistical optimization of adsorption processes for removal of 2,4-dichlorophenol by activated carbon derived from oil palm empty fruit bunches

    Institute of Scientific and Technical Information of China (English)

    Md. Zahangir ALAM; Suleyman A. MUYIBI; Juria TORAMAE

    2007-01-01

    The adsorption capacity of activated carbon produced from oil palm empty fruit bunches through removal of 2,4-dichlorophenol from aqueous solution was carried out in the laboratory. The activated carbon was produced by thermal activation at 800℃ with 30 min of activation time. The adsorption process conditions were determined with the statistical optimization followed by central composite design. A developed polynomial model for operating conditions of adsorption process indicated that the optimum conditions for maximum adsorption of phenolic compound were: agitation rate of 100 r/min, contact time of 8 h, initial adsorbate concentration of 250 mg/L and pH 4. Adsorption isotherms were conducted to evaluate biosorption process. Langmuir isotherm was more favorable (R2=0.93) for removal of 2,4-dichlorophenol by the activated carbon produced rather than the Freundlich isotherm (R2=0.88).

  12. Statistical optimization of adsorption processes for removal of 2,4-dichlorophenol by activated carbon derived from oil palm empty fruit bunches.

    Science.gov (United States)

    Alam, M Zahangir; Muyibi, Suleyman A; Toramae, Juria

    2007-01-01

    The adsorption capacity of activated carbon produced from oil palm empty fruit bunches through removal of 2,4-dichlorophenol from aqueous solution was carried out in the laboratory. The activated carbon was produced by thermal activation of activation time with 30 min at 800 degrees C. The adsorption process conditions were determined with the statistical optimization followed by central composite design. A developed polynomial model for operating conditions of adsorption process indicated that the optimum conditions for maximum adsorption of phenolic compound were: agitation rate of 100 r/min, contact time of 8 h, initial adsorbate concentration of 250 mg/L and pH 4. Adsorption isotherms were conducted to evaluate biosorption process. Langmuir isotherm was more favorable (R2 = 0.93) for removal of 2,4-dichlorophenol by the activated carbon rather than Freundlich isotherm (R2 = 0.88). PMID:17969639

  13. Determination of Lamotrigine in Pharmaceutical Preparations by Adsorptive Stripping Voltammetry Using Screen Printed Electrodes

    Directory of Open Access Journals (Sweden)

    M. Julia Arcos-Martínez

    2008-07-01

    Full Text Available This paper describes a procedure that has been optimized for the determination of lamotrigine by Differential Pulse Adsorptive Stripping Voltammetry (DPAdSV using carbon screen-printed electrodes (CSPE and mercury coated carbon screen-printed electrodes. Selection of the experimental parameters was made using experimental design methodology. The detection limit found was 5.0 x 10-6 M and 2.0 x 10-6 M for the non modified and Hg modified CSPE, respectively. In terms of reproducibility, the precision of the above mentioned methods was calculated in %RSD values at 9.83% for CSPE and 2.73% for Hg-CSPE. The Hg-coated CSPEs developed in this work were successfully applied in the determination of lamotrigine in pharmaceutical preparations.

  14. Adsorption and correlation with their thermodynamic properties of triazine herbicides on soils

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Adsorption of atrazine, prometryne and prometon was determined on six soils with different physical and chemical properties. Theadsorption isotherms of three herbicides could well fit Freundlich equation. On all of six soils, adsorption of herbicides increased in the order:atrazine ≈ prometon < prometryne. This order is quite the same to the calculation result of by means of excess thermodynamic properties oftriazine. The Freundlich adsorption constants, Kf, showed to have good correlation with organic matter(OM%) of soils for each of theseherbicides, suggesting that OM is the main factor, which dominates in the adsorption process of these triazine herbicides.

  15. Adsorption Studies of Radish Leaf Powder

    Directory of Open Access Journals (Sweden)

    Ankita

    2016-01-01

    Full Text Available Radish leaves (Raphanus sativus powder fractions was subjected to moisture adsorption isotherms at different isothermal temperature conditions from 15-45°C with an equal interval of 10°C. The sorption data obtained in gravimetric static method under 0.11–0.90 water activity conditions were subjected for sorption isotherms and found to be typical sigmoid trend. Experimental data were assessed for the applicability in the prediction through sorption models fitting and found that Polynomial and GAB equations performed well over all fitted models in describing equilibrium moisture content – equilibrium relative humidity (EMC–ERH relationships for shelf stable dehydrated radish leaf powder, over the entire range of temperatures condition under study. The net isosteric heat of sorption, differential entropy and free energy were determined at different temperatures and their dependence was seen with respect to equilibrium moisture content.

  16. Adsorptive removal of Congo red, a carcinogenic textile dye, from aqueous solutions by maghemite nanoparticles

    International Nuclear Information System (INIS)

    The adsorption of Congo red (CR) onto maghemite nanoparticles (γ-Fe2O3) and its desorption was investigated. The adsorption capacity was evaluated using both the Langmuir and Freundlich adsorption isotherm models. Maghemite nanoparticles (γ-Fe2O3) were prepared easily in a surfactant-less microemulsion by co-precipitation method. The size of the produced maghemite nanoparticles was determined by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM). Synthesized maghemite nanoparticles showed the highest adsorption capacities of CR compared to many other adsorbents and would be a good method to increase adsorption efficiency for the removal of CR in a wastewater treatment process. The maximum adsorption occurred at pH 5.9. The Langmuir adsorption capacity (qmax) was found to be 208.33 mg g-1 of the adsorbent.

  17. Preparation and adsorption properties of macroporous tannin resins

    Institute of Scientific and Technical Information of China (English)

    Zhang Li-ping; Du Jie; Liu Jian

    2006-01-01

    In this paper, a new kind of adsorption resin with multi-phenolic hydroxyl was created by immobilizing black wattle bark tannins to chloromethyl polystyrene resin. Its adsorption capacity to cation dye was tested. With an orthogonal test the optimal conditions of synthesis were determined: the concentration of sodium hydroxide solution 1.0 mol·L-1; the reaction time is one hour and the mass concentration of tannins 5%. With single factorial experiment the optimal conditions of adsorption were confirmed: a solidified pH of 5.0; an adsorption temperature of 25℃ and a cation dye concentration of 100 mg·L-1. The adsorption for cation dye can be similar to Langmuir isotherms.

  18. Adsorption calorimetry of conjugated organic molecules on metal surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Lytken, Ole; Drescher, Hans-Joerg; Bebensee, Fabian; Steinrueck, Hans-Peter; Gottfried, J. Michael [Universitaet Erlangen-Nuernberg, Lehrstuhl fuer Physikalische Chemie II (Germany)

    2011-07-01

    Traditional experimental methods for determining adsorption energies, such as temperature programmed desorption (TPD) and equilibrium adsorption isotherms, rely on desorption. However, on many metal surfaces large conjugated organic molecules, such as PTCDA and pentacene, decompose at elevated temperatures before or simultaneously with desorption. Discussions about relative bond strengths are, therefore, typically based on indirect arguments, such as the height of the adsorbed species above the surface as measured with normal incidence X-ray standing waves (NIXSW) or chemical shifts in spectroscopic techniques such as X-ray photoelectron spectroscopy (XPS). Unlike the more traditional methods, nanojoule adsorption calorimetry does not require desorption of the molecules; instead, the heat of adsorption is measured directly as an adsorption-induced temperature change of the sample. We will describe the construction of such a calorimeter at the Universitaet Erlangen-Nuernberg.

  19. Hydrogen Adsorption on Pt, Rh and Pt-Rh Electrodes

    Institute of Scientific and Technical Information of China (English)

    贾梦秋; A.M.Meretskyi

    2005-01-01

    The hydrogen adsorption on Pt-Rh alloys in sulfuric acid aqueous solutions was studied by the method of cathode pulses. Hydrogen adsorption on the electrode with all ratio of alloy components (ωRh = 0-100%) is well described by the Temkin logarithmic isotherm. The surface coverage by adsorbed hydrogen at the same potential is decreased with increasing content of rhodium in the system. A linear dependence of adsorption peak potential on the alloy compositions in the case of weakly bonded adsorbed hydrogen is established. Hydrogen adsorption heat as a function of surface coverage for Pt-Rh-electrodes was obtained. The shape of the current-potential curve and position of the weakly bonded hydrogen adsorption on the potential scale are all related to alloy compositions, thus can serve as the basis for the determination surface composition of allovs.

  20. Kinetics and thermodynamics of {beta}-carotene and chlorophyll adsorption onto acid-activated bentonite from Xinjiang in xylene solution

    Energy Technology Data Exchange (ETDEWEB)

    Wu Zhansheng [School of Life Science and Technology, Beijing Institute of Technology, Beijing 100081 (China); School of Chemistry and Chemical Engineering, Shihezi University, Shihezi, Xinjiang 832003 (China); Li Chun, E-mail: lichun@bit.edu.cn [School of Life Science and Technology, Beijing Institute of Technology, Beijing 100081 (China); School of Chemistry and Chemical Engineering, Shihezi University, Shihezi, Xinjiang 832003 (China)

    2009-11-15

    The kinetics and thermodynamics of {beta}-carotene and chlorophyll adsorption from xylene solution onto acid-activated bentonite (AAB) within the temperature range 65-95 deg. C were investigated. Adsorption of {beta}-carotene was described well with the Langmuir isotherm, whereas chlorophyll adsorption was determined well with the Freundlich isotherm, and the experimental data on chlorophyll adsorption were also fitted by the Langmuir isotherm to a certain extent, as reflected by correlation coefficients (R{sup 2}) over 0.9865. In addition, the adsorption of {beta}-carotene and chlorophyll onto AAB are favorable. The pseudo-second-order model was found to explain the kinetics of adsorption of both pigments more effectively. Increase of temperature enhanced the adsorption rate and equilibrium adsorption capacity of {beta}-carotene and chlorophyll on AAB. The activation energy for the sorption of {beta}-carotene and chlorophyll on AAB was 19.808 kJ/mol and 16.475 kJ/mol, respectively. The thermodynamic parameters {Delta}H{sup {theta}}, {Delta}S{sup {theta}} and {Delta}G{sup {theta}}, computed from K{sub F} of the adsorption isotherm constant, were 21.766 kJ/mol, 92.244 J/K mol and -9.554 kJ/mol respectively for the adsorption of {beta}-carotene on AAB at 65 deg. C, and for adsorption of chlorophyll on AAB at 65 deg. C were 31.051 kJ/mol, 93.549 J/K mol and -0.729 kJ/mol, respectively. The adsorption of {beta}-carotene and chlorophyll in xylene solution on AAB was a spontaneous and endothermic process with increasing in the randomness at the solid-solution interface.

  1. Continuous water treatment by adsorption and electrochemical regeneration.

    Science.gov (United States)

    Mohammed, F M; Roberts, E P L; Hill, A; Campen, A K; Brown, N W

    2011-05-01

    This study describes a process for water treatment by continuous adsorption and electrochemical regeneration using an air-lift reactor. The process is based on the adsorption of dissolved organic pollutants onto an adsorbent material (a graphite intercalation compound, Nyex(®)1000) and subsequent electrochemical regeneration of the adsorbent leading to oxidation of the adsorbed pollutant. Batch experiments were carried out to determine the adsorption kinetics and equilibrium isotherm for adsorption of a sample contaminant, the organic dye Acid Violet 17. The adsorbent circulation rate, the residence time distribution (RTD) of the reactor, and treatment by continuous adsorption and electrochemical regeneration were studied to investigate the process performance. The RTD behaviour could be approximated as a continuously stirred tank. It was found that greater than 98% removal could be achieved for continuous treatment by adsorption and electrochemical regeneration for feed concentrations of up to 300 mg L(-1). A steady state model has been developed for the process performance, assuming full regeneration of the adsorbent in the electrochemical cell. Experimental data and modelled predictions (using parameters for the adsorbent circulation rate, adsorption kinetics and isotherm obtained experimentally) of the dye removal achieved were found to be in good agreement. PMID:21511325

  2. Influence of organobentonite structure on toluene adsorption from water solution

    Directory of Open Access Journals (Sweden)

    Nuria Vidal

    2012-12-01

    Full Text Available Due to increase water pollution by organic compound derived from hydrocarbons such as toluene, several alternative technologies for remediation of polluted water have been originated. In this work natural bentonites were modified with cetyltrimethylammonium (CTMA+ for obtaining organophilic bentonites. The obtained CTMA-bentonites would be suitable for use as adsorbents of toluene present in water. The influence of structural characteristics of CTMA-bentonites on their adsorption capacity was studied. It was shown that adsorption of toluene depended on homogeneous interlayer space associated with arrangements of CTMA+ paraffin-monolayer and bilayer models, accompanied by a high degree ordering of the carbon chain of organic cation in both arrangements. However, packing density would not have an evident influence on the retention capacity of these materials. The solids obtained were characterized by chemical analysis, X-ray diffractions and infrared spectroscopy. Toluene adsorption was measured by UV-visible spectrophotometer. Adsorption capacity was studied by determining adsorption isotherms and adsorption coefficient calculation. The adsorption isotherms were straight-line indicating a partition phenomenon of toluene between the aqueous and organic phase present in organophilic bentonites.

  3. Simultaneous removal of binary mixture of Brilliant Green and Crystal Violet using derivative spectrophotometric determination, multivariate optimization and adsorption characterization of dyes on surfactant modified nano-γ-alumina.

    Science.gov (United States)

    Zolgharnein, Javad; Bagtash, Maryam; Shariatmanesh, Tahere

    2015-02-25

    The present study deals with the simultaneous removal of Brilliant Green (BG) and Crystal Violet (CV) by surfactant-modified alumina. The utilization of alumina nanoparticles with an anionic surfactant (sodium dodecyl sulfate (SDS)) as a novel and efficient adsorbent is successfully carried out to remove two cationic dyes from aqueous solutions in binary batch systems. A first-order derivative spectrophotometric method is developed for the simultaneous determination of BG and CV in binary solutions. The linear concentration range and limits of detection for the simultaneous determination of BG and CV were found to be: 1-20, 1-15 mg/L, 0.3 and 0.5 mg/L, respectively. The influence of various parameters, such as contact time, initial concentration of dyes and sorbent mass on the dye adsorption is investigated. A response surface methodology achieved through performing the Box-Behnken design is utilized to optimize the removal of dyes by surfactant-modified nanoparticle alumina through a batch adsorption process. The proposed quadratic model resulting from the Box-Behnken design approach fitted very well with the experimental data. The optimal conditions for dye removal were contact time t=50 min, sorbent dose=0.036 g, CBG (Initial BG concentration)=215 mg/L and CCV (Initial CV concentration)=170 mg/L. Furthermore, FT-IR analysis, the isotherms and kinetics of adsorption were also explored. PMID:25286114

  4. Equilibrium and kinetic adsorption study of Basic Yellow 28 and Basic Red 46 by a boron industry waste

    International Nuclear Information System (INIS)

    In this study, the adsorption characteristics of Basic Yellow 28 (BY 28) and Basic Red 46 (BR 46) onto boron waste (BW), a waste produced from boron processing plant were investigated. The equilibrium adsorption isotherms and kinetics were investigated. The adsorption equilibrium data were analyzed by using various adsorption isotherm models and the results have shown that adsorption behavior of two dyes could be described reasonably well by a generalized isotherm. Kinetic studies indicated that the kinetics of the adsorption of BY 28 and BR 46 onto BW follows a pseudo-second-order model. The result showed that the BW exhibited high-adsorption capacity for basic dyes and the capacity slightly decreased with increasing temperature. The maximum adsorption capacities of BY 28 and BR 46 are reported at 75.00 and 74.73 mg g-1, respectively. The dye adsorption depended on the initial pH of the solution with maximum uptake occurring at about pH 9 and electrokinetic behavior of BW. Activation energy of 15.23 kJ/mol for BY 28 and 18.15 kJ/mol for BR 46 were determined confirming the nature of the physisorption onto BW. These results indicate that BW could be employed as low-cost material for the removal of the textile dyes from effluents

  5. The adsorption of an epoxy acrylate resin on aluminium alloy conversion coatings

    OpenAIRE

    Grilli, R; Abel, ML; Baker, MA; Dunn, B.; Watts, JF

    2011-01-01

    A thermodynamic study of the adsorption of an epoxy acrylate resin used for UV-cured coatings on two different anticorrosion pretreatments on aluminium alloys relevant to aerospace industry has been undertaken. Aluminium alloy Al2219 specimens, treated with an inorganic chromate based conversion coating (Alodine 1200S) and an organic titanium based conversion coating (Nabutan STI/310), were immersed in solutions of different concentrations of the resin and adsorption isotherms were determined...

  6. Adsorptive Stripping Voltammetric Determination of Hydroquinone using an Electrochemically Pretreated Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Abdul Niaz1,

    2008-12-01

    Full Text Available A simple and efficient adsorptive stripping voltammetric (AdSV method was developed for the determination of hydroquinone at an electrochemically pretreated glassy carbon (GC electrode in waste water. Various parameters such as solvent system, accumulation potential, accumulation time and scan rate were optimized. The electrochemically pretreated GC electrode showed good response towards hydroquinone determination by using AdSV. Under the optimized conditions the peak current showed good linear relationship with the hydroquinone concentration in the range of 0.5-4.0mg L-1 and 5-30mg L-1. The 60/40 methanol/water composition was found to be the best solvent system and 0.05mol L-1 H2SO4 was found as useful supporting electrolyte concentration. The accumulation time was 60 s and the detection limit was 50µg L-1. The developed method was successfully applied for the determination of hydroquinone in polymeric industrial discharge samples waste photographic developer solution and cream sample without any significant effect of surface fouling.

  7. Theoretical and Experimental Study on the Adsorption and Desorption of Methane by Granular Activated Carbon at 25 ℃

    Institute of Scientific and Technical Information of China (English)

    E. Salehi; V. Taghikhani; C. Ghotbi; E. Nemati Lay; A. Shojaei

    2007-01-01

    A theoretical and experimental study was conducted to accurately determine the amount of adsorption and desorption of methane by various Granular Activated Carbon (GAC) under different physical conditions. To carry out the experiments, the volumetric method was used up to 500 psia at constant temperature of 25 ℃. In these experiments, adsorption as well as desorption capacities of four different GAC in the adsorption of methane, the major constituent of natural gas, at various equilibrium pressures and a constant temperature were studied. Also, various adsorption isotherm models were used to model the experimental data collected from the experiments. The accuracy of the results obtained from the adsorption isotherm models was compared and the values for the regressed parameters were reported. The results shows that the physical characteristics of activated carbons such as BET surface area, micropore volume, packing density, and pore size distribution play an important role in the amount of methane to be adsorbed and desorbed.

  8. Adsorption of malachite green and iodine on rice husk-based porous carbon

    International Nuclear Information System (INIS)

    Adsorption isotherms of I2 and malachite green (MG) by rice husk-based porous carbons (RHCs) from aqueous medium have been studied. Three samples of carbons prepared by NaOH-activation, three samples prepared by KOH-activation and two samples of commercial carbons have been studied. And the adsorption isotherms have been determined after modifying the carbon surfaces by oxidation with nitric acid and hydrogen peroxide and after degassing at 800 deg. C. The results have been found to follow the Freundlich adsorption isotherm. Three samples of N series have larger capacity for removing I2 and MG from solution compared to that of the tested commercial carbons. The adsorption capacity of I2 is similar for K series and commercial carbons. And the capacity of commercial carbons for MG is larger than K series. The adsorption capacity of I2 on oxidation carbons has increased for hydrogen peroxide treatment and decreased for nitric acid, and that of MG is decreased. But the adsorption capacities of I2 and MG increase on degassing. On the other hand, the adsorption of I2 increases after modifying the carbon surfaces by HCl without oxidation. Suitable mechanisms have been proposed

  9. Removal of Ni2+ from Aqueous Solutions by Adsorption Onto Magnetic Multiwalled Carbon Nanotube Nanocomposite

    Directory of Open Access Journals (Sweden)

    Konicki Wojciech

    2014-06-01

    Full Text Available The removal of Ni2+ from aqueous solution by magnetic multiwalled carbon nanotube nanocomposite (MMWCNTs-C was investigated. MMWCNTs-C was characterized by X-ray Diffraction method (XRD, High-Resolution Transmission Electron Microscopy (HRTEM, surface area (BET, and Fourier Transform-Infrared Spectroscopy (FTIR. The effects of initial concentration, contact time, solution pH, and temperature on the Ni2+ adsorption onto MMWCNTs-C were studied. The Langmuir and Freundlich isotherm models were applied to fit the adsorption data. The results showed that the adsorption isotherm data were fitted well to the Langmuir isotherm model with the maximum monolayer adsorption capacity of 2.11 mg g–1. The adsorption kinetics was best described by the pseudo-second-order model. The thermodynamic parameters, such as ΔHo, ΔGo and ΔSo, were also determined and evaluated. The adsorption of Ni2+ is generally spontaneous and thermodynamically favorable. The values of ΔHo and ΔGo indicate that the adsorption of Ni2+ onto MMWCNTs-C was a physisorption process.

  10. Adsorption of certain surface-active organic substances on lead, and their effect on hydrogen evolution kinetics in sulfuric acid

    Energy Technology Data Exchange (ETDEWEB)

    Sherstobitova, I.N.; Iskhakov, R.N.

    1988-02-01

    The adsorption of tetrabutylammonium sulfate, n-butyl, n-amyl, isoamyl, n-hexyl alcohol, butyric acid, butylamine, antipyrine and diantipyrylmethane was measured by differential-capacitance at a frequency of 10 kHz at smooth lead electrodes under cathodic polarization. Isotherms were determined by logarithms. Parameters in the Frumkin equation for adsorption of certain organic substances on lead were also determined and tabulated.

  11. Adsorption height determination of nonequivalent C and O species of PTCDA on Ag(110) using x-ray standing waves

    OpenAIRE

    Mercurio, Giuseppe; Bauer, O.; Tautz, Stefan; Willenbockel, Martin; Fairley, N.; Reckien, W.; Schmitz, C. H.; B. Fiedler; Subach, Sergey; Bredow, T.; Sokolowski, M.

    2013-01-01

    The normal incidence x-ray standing wave (NIXSW) technique is used to determine the adsorption geometry of submonolayer 3,4,9,10-perylene tetracarboxylic dianhydride (PTCDA) adsorbed on the Ag(110) surface. An accurate analysis of both C1s and O1s photoemission (PE) spectra allows the respective adsorption heights of carbon and oxygen atoms in different chemical environments within PTCDA to be distinguished. Due to the intricacy of the PE fitting models, a systematic error analysis of NIXSW s...

  12. Adsorption of Pb(II) present in aqueous solution on calcium, strontium and barium hydroxy apatites

    International Nuclear Information System (INIS)

    Calcium, strontium and barium hydroxy apatites were successfully synthesized by chemical precipitation method, the obtained powders were characterized by the techniques of X-ray diffraction (XRD), scanning electron microscopy (Sem), semi-quantitative elemental analysis (EDS), infrared spectroscopy (IR), and N2 physisorption studies, complementary to these analytical techniques, was determined the surface fractal dimension (Df), and the amount of surface active sites of the materials, in order to know application as ceramic for water remediation. The ability of Pb(II) ion adsorption present in aqueous solution on the hydroxy apatites synthesized by batch type experiments was studied as a function of contact time, concentration of the adsorbate and temperature. The maximum lead adsorption efficiencies obtained were 0.31, 0.32 and 0.26 mg/g for calcium, strontium and barium hydroxy apatites respectively, achieved an equilibrium time of 20 minutes in the three solid-liquid systems studied. Experimental data were adequately adjusted at the adsorption kinetic model pseudo-second order, for the three cases. Moreover, experimental data of the strontium and calcium hydroxy apatites were adjusted to the Langmuir adsorption isotherm, indicating that the adsorption was through a monolayer, whereas barium hydroxyapatite was adjusted to the Freundlich adsorption isotherm, indicating a multilayer adsorption. The thermodynamic parameters obtained during adsorption studies as a function of temperature showed physisorption, exothermic and spontaneous processes respectively. The results showed that the calcium hydroxyapatite, strontium and barium are an alternative for the Pb(II) ion adsorption present in wastewaters. (Author)

  13. Glyphosate and AMPA adsorption in soils: laboratory experiments and pedotransfer rules.

    Science.gov (United States)

    Sidoli, Pauline; Baran, Nicole; Angulo-Jaramillo, Rafael

    2016-03-01

    Adsorption of the herbicide glyphosate and its main metabolite AMPA (aminomethylphosphonic acid) was investigated on 17 different agricultural soils. Batch equilibration adsorption data are shown by Freundlich adsorption isotherms. Glyphosate adsorption is clearly affected by equilibration concentrations, but the nonlinear AMPA adsorption isotherms indicate saturation of the adsorption sites with increasing equilibrium concentrations. pHCaCl2 (i.e. experimental pH) is the major parameter governing glyphosate and AMPA adsorption in soils. However, considering pHCaCl2 values, available phosphate amount, and amorphous iron and aluminium oxide contents by using a nonlinear multiple regression equation, obtains the most accurate and powerful pedotransfer rule for predicting the adsorption constants for these two molecules. As amorphous iron and aluminium oxide contents in soil are not systematically determined, we also propose a pedotransfer rule with two variables-pHCaCl2 values and available phosphate amount-that remains acceptable for both molecules. Moreover, the use of the commonly measured pHwater or pHKCl values gives less accurate results compared to pHCaCl2 measurements. To our knowledge, this study is the first AMPA adsorption characterization for a significant number of temperate climate soils. PMID:26581693

  14. Arsenic adsorption of lateritic soil, limestone powder, lime and fly ash on arsenic-contaminated soil

    Directory of Open Access Journals (Sweden)

    Wuthiphun, L.

    2007-05-01

    Full Text Available Arsenic adsorption efficiency of soil covering materials (lateritic soil, limestone powder, lime and fly ash on arsenic-contaminated soil obtained from Ronpiboon District, Nakhon Sri Thammarat Province tosolve arsenic air pollution problem was investigated using batch experiments. The four types of the aforementioned soil covering materials were examined to determine their arsenic adsorption efficiency, equilibriumtime as well as adsorption isotherms.The results revealed that among soil covering materials mixed with arsenic-contaminated soil at 10% w/w, the efficiency of arsenic adsorption of fly ash, lateritic soil, lime and limestone powder were 84, 60,38 and 1% respectively. The equilibrium time for lateritic soil at pH 4 was achieved within 4 hrs, whereas pH 7 and 12, the equilibrium time was 6 hrs. For fly ash, 2 hrs were required to reach the equilibrium at pH 12, while the equilibrium time was attained within 6 hrs at pH 4 and 7. Furthermore, lateritic soil possessedhigh arsenic adsorption efficiency at pH 7 and 4 and best fit with the Langmuir isotherm. The fly ash showing high arsenic adsorption efficiency at pH 12 and 7 fit the Freundlich isotherm at pH 12 and Langmuirisotherm at pH 7.This indicated that lateritic soil was suitable for arsenic adsorption at low pH, whilst at high pH,arsenic was well adsorbed by fly ash. The Freundlich and Langmuir isotherm could be used to determine quantities of soil covering materials for arsenic adsorption to prevent arsenic air pollution from arseniccontaminated soils.

  15. [Determination of organic residues in macroporous adsorption resins by gas chromatography].

    Science.gov (United States)

    Jia, Cunqin; Li, Yangchun; Tu, Pengfei; Zhang, Hongquan

    2005-11-01

    A method has been developed for the simultaneous determination of benzene, toluene, xylene, styrene, decane, diethylbenzene, undecane, divinylbenzene, dodecane and naphthalene residues in macroporous adsorption resins (MARs). The organic residues were extracted from resin samples by ultrasonic extraction with dichloromethane and analyzed by gas chromatography. The chromatographic conditions were as follows: a DB-624 capillary column (30 m x 0.32 mm i.d., 1.8 microm); carrier gas, nitrogen with a flow rate of 2.5 mL/min; column temperature, programmed from 40 degrees C to 200 degrees C at a rate of 14 degrees C /min and kept at 200 degrees C for 1 min; flame ionization detector temperature, 250 degrees C; injector temperature, 220 degrees C; splitless injection, 1 microL. All the 10 organic residues were separated well in 12 min. The recoveries for spiked standards (n = 3) were 73.8% - 107.9%. The relative standard deviations were 1.3% - 4.4%. The limits of detection were 0.007 - 0.03 mg/L. This method is sensitive, accurate and quick. Nine commercial MARs and their pretreated samples were assayed, and the results show that the contents of organic residues varied greatly in two kinds of samples. And the pretreated MARs can be used safely in the production of traditional Chinese medicines. PMID:16499000

  16. solITC: A rapid method to determine solubility products and heats of solution of hydrophobic ionic liquids from in situ synthesis in isothermal titration calorimeter

    International Nuclear Information System (INIS)

    Highlights: • Novel application of ITC to determine Ksp and ΔsolH° of ILs in water is presented. • The procedure integrates IL synthesis with thermodynamic data acquisition. • Applicability of the method typically spans over five orders of Ksp magnitude. • Performance was verified on three salts of diverse physical state and behavior. • 18 Cation anion combinations potentially giving IL were examined. - Abstract: This work presents a solubility isothermal titration calorimetry (solITC), a new calorimetric method that allows the determination of solubility product (Ksp) and heat of solution (ΔsolH°) of hydrophobic ionic compound in water. Based on a single titration of dilute ionic solution into its counterionic solution the method consists of observing the abrupt change of the heat flow signal due to hydrophobic phase separation and fitting the integrated heats to exact thermodynamic model. A priori analysis shows that the applicability range spans for Ksp determination over five orders of magnitudes (typically 10-9sp-4 for |ΔsolH°|≈30kJ·mol-1) keeping at least 5% precision in both Ksp and ΔsolH° values. For Ksp-10, only ΔsolH° can be precisely determined. The method performance was validated on forming three different types of precipitate with different levels of solubility and heat of solution at T = 298.15 K. The new method is applied to explore 18 cation–anion combinations for possible ionic liquid formation

  17. Determination of the behavior and performance of commercial Li-Ion pouch cells by means of isothermal calorimeter

    DEFF Research Database (Denmark)

    Khan, Mohammad Rezwan; Swierczynski, Maciej Jozef; Kær, Søren Knudsen

    2016-01-01

    In this experiment-based research, there is an attempt to determine the evolution of surface temperature distribution, thermal behaviour and performance of a battery cell at the same time. The pouch type commercial test cell has a 13Ah capacity and Lithium Titanate Oxide (LTO) based anode...

  18. Determination of tryptamine in foods using square wave adsorptive stripping voltammetry.

    Science.gov (United States)

    Costa, Daniel J E; Martínez, Ana M; Ribeiro, Williame F; Bichinho, Kátia M; Di Nezio, María Susana; Pistonesi, Marcelo F; Araujo, Mario C U

    2016-07-01

    Tryptamine, a biogenic amine, is an indole derivative with an electrophilic substituent at the C3 position of the pyrrole ring of the indole moiety. The electrochemical oxidation of tryptamine was investigated using glassy carbon electrode (GCE), and focusing on trace level determination in food products by square wave adsorptive stripping voltammetry (SWAdSV). The electrochemical responses of tryptamine were evaluated using differing voltammetric techniques over a wide pH range, a quasi-reversible electron-transfer to redox system represented by coupled peaks P1-P3, and an irreversible reaction for peak P2 were demonstrated. The proton and electron counts associated with the oxidation reactions were estimated. The nature of the mass transfer process was predominantly diffusion-limited for the oxidation process of P1, the most selective and sensitive analytical response (acetate buffer solution pH 5.3), being used for the development of SWAdSV method, under optimum conditions. The excellent response allowed the development of an electroanalytical method with a linear response range of from 4.7-54.5)×10(-)(8)molL(-1), low detection limit (0.8×10(-)(9)molL(-)(1)), and quantification limit (2.7×10(-9)molL(-1)), and acceptable levels of repeatability (3.6%), and reproducibility (3.8%). Tryptamine content was determined in bananas, tomatoes, cheese (mozzarella and gorgonzola), and cold meats (chicken sausage and pepperoni sausage), yielding recoveries above 90%, with excellent analytical performance using simple and low cost instrumentation. PMID:27154658

  19. Room temperature isotherms for Mo and Ni

    International Nuclear Information System (INIS)

    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 (δBT/δP)T as P #-> # ∞, where BT 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 BTo, where BTo is the bulk modulus BT at P = o

  20. Removal of Pyrethrin from Aqueous Effluents by Adsorptive Micellar Flocculation

    Directory of Open Access Journals (Sweden)

    Pardon K. Kuipa

    2015-01-01

    Full Text Available The equilibrium adsorption of pyrethrin onto aggregates formed by the flocculation of micelles of the surfactant sodium dodecyl sulphate (SDS with aluminium sulphate is reported. The experimental results were analysed using different adsorption isotherms (Langmuir, Freundlich, Redlich-Peterson, Sips, Radke-Prausnitz, Temkin, linear equilibrium, and the Dubin-Radushkevich isotherms. The Freundlich and linear equilibrium isotherms best describe the adsorption of pyrethrin onto SDS micellar flocs, with the Freundlich adsorption constant, KF, and the mass distribution coefficient, KD, of 64.266 ((mg/g(L/mg1/n and 119.65 L/g, respectively. Applicability of the Freundlich adsorption model suggests that heterogeneous surface adsorption affects the adsorption. The mean free energy value estimated using the Dubinin-Radushkevich isotherm was 0.136 kJ/mol indicating that physisorption may be predominant in the adsorption process.

  1. A Study on the Pyrolysis of Peanut Shells at Different Isothermal Conditions and Determination of the Kinetic Parameters

    Directory of Open Access Journals (Sweden)

    Şeyda Taşar

    2015-12-01

    Full Text Available The pyrolysis process, which is applied for the aim of producing energy and raw materials which are implemented for the chemical industry from biomass sources, is a thermal conversion process. Determination of the pyrolysis kinetic parameters are important In order to suitable equipment and process design. In this target, in the study the pyrolysis of peanut shells was conducted in a muffle furnace at static atmosphere with temperatures ranging from 300-700 °C. The effects of various parameters on the rate of thermal decomposition rate and the solid yield were determined. The parameters of interest were temperature 300-700 °C, particle size 4-50 mesh, pelletizing, and pelletizing pressure 1.103-5.103 kgf/cm2. Regression coefficients for the total decomposition step were obtained using the thermographs were obtained as a result of the pyrolysis of the peanut shells, and 20 different theoretical model equations that represented the degradation by the Coast-Redfern method. According to regression coefficients of the theoretical model equations, we determined the kinetic model that best represented the degradation. Using this model to represent the degradation, the activation energy (Ea and Arhenius frequency factor ln(A for the total reaction were calculated to be 38.245 kJ/mol and 8.124, respectively.

  2. BINDING ISOTHERMS SURFACTANT-PROTEINS

    OpenAIRE

    Elena Irina Moater; Cristiana Radulescu; Ionica Ionita

    2011-01-01

    The interactions between surfactants and proteins shows some similarities with interactions between surfactants and polymers, but the hydrophobic amphoteric nature of proteins and their secondary and tertiary structure components make them different from conventional polymer systems. Many studies from the past about surfactant - proteins bonding used the dialysis techniques. Other techniques used to determine the binding isotherm, included ultrafiltration, ultracentrifugation, potentiometry, ...

  3. Adsorption study of copper (II) by chemically modified orange peel

    International Nuclear Information System (INIS)

    An adsorbent, the chemically modified orange peel, was prepared from hydrolysis of the grafted copolymer, which was synthesized by interaction of methyl acrylate with cross-linking orange peel. The presence of poly (acrylic acid) on the biomass surface was verified by infrared spectroscopy (IR), scanning electron microscopy (SEM) and thermogravimetry (TG). Total negative charge in the biomass surface and the zeta potentials were determined. The modified biomass was found to present high adsorption capacity and fast adsorption rate for Cu (II). From Langmuir isotherm, the adsorption capacity for Cu (II) was 289.0 mg g-1, which is about 6.5 times higher than that of the unmodified biomass. The kinetics for Cu (II) adsorption followed the pseudo-second-order kinetics. The adsorbent was used to remove Cu (II) from electroplating wastewater and was suitable for repeated use for more than four cycles.

  4. An Adsorption Equilibria Model for Steady State Analysis

    KAUST Repository

    Ismail, Azhar Bin

    2016-02-29

    The investigation of adsorption isotherms is a prime factor in the ongoing development of adsorption cycles for a spectrum of advanced, thermally-driven engineering applications, including refrigeration, natural gas storage, and desalination processes. In this work, a novel semi-empirical mathematical model has been derived that significantly enhances the prediction of the steady state uptake in adsorbent surfaces. This model, a combination of classical Langmuir and a novel modern adsorption isotherm equation, allows for a higher degree of regression of both energetically homogenous and heterogeneous adsorbent surfaces compared to several isolated classical and modern isotherm models, and has the ability to regress isotherms for all six types under the IUPAC classification. Using a unified thermodynamic framework, a single asymmetrical energy distribution function (EDF) has also been proposed that directly relates the mathematical model to the adsorption isotherm types. This fits well with the statistical rate theory approach and offers mechanistic insights into adsorption isotherms.

  5. Water adsorption in hydrophilic zeolites: experiment and simulation

    OpenAIRE

    Castillo, Juan Manuel; Silvestre Albero, Joaquín; Rodríguez Reinoso, Francisco; Vlugt, Thijs. J. H.; Calero, Sofía

    2013-01-01

    We have measured experimental adsorption isotherms of water in zeolite LTA4A, and studied the regeneration process by performing subsequent adsorption cycles after degassing at different temperatures. We observed incomplete desorption at low temperatures, and cation rearrangement at successive adsorption cycles. We also developed a new molecular simulation force field able to reproduce experimental adsorption isotherms in the range of temperatures between 273 K and 374 K. Small deviations obs...

  6. Thermodynamics of hydrogen adsorption in MOF-177 at low temperatures: measurements and modelling

    International Nuclear Information System (INIS)

    Hydrogen adsorption measurements and modelling for the Zn-based microporous metal-organic framework (MOF) Zn4O(1,3,5-benzenetribenzoate)2, MOF-177, were performed over the 50-77 K and 0-40 bar ranges. The maximum excess adsorption measured under these conditions varies over about 105-70 mg g-1. An analysis of the isotherms near saturation shows that hydrogen is ultimately adsorbed in an incompressible phase whose density is comparable to that of the bulk liquid. These liquid state properties observed under supercritical conditions reveal a remarkable effect of nanoscale confinement. The entire set of adsorption isotherms can be well described using a micropore filling model. The latter is used, in particular, to determine the absolute amounts adsorbed and the adsorption enthalpy. When expressed in terms of absolute adsorption, the isotherms show considerable hydrogen storage capacities, reaching up to 125 mg g-1 at 50 K and 25 bar. The adsorption enthalpies are calculated as a function of fractional filling and range from 3 to 5 kJ mol-1 in magnitude, in accordance with physisorption. These results are discussed with respect to a similar analysis performed on another Zn-based MOF, Zn4O(1,4-benzenedicarboxylate)3, IRMOF-1, presented recently. It is found that both materials adsorb hydrogen by similar mechanisms.

  7. Dye-adsorption capacity of bituminous fly ash and its pozzolanic property after used as dye-adsorbent

    OpenAIRE

    Penpolcharoen, M.

    2004-01-01

    Bituminous fly ash, which is an industrial waste, was used as an adsorbent to remove dyestuff from the textile-dye wastewater. The batch kinetic and isotherm experiments of the synthetic wastewater were firstly conducted to determine the adsorption behavior and optimal conditions for adsorption. The optimal conditions were then applied to the actual textile-dye wastewater. Under the original conditions of fly ash and wastewater, the results indicated that the color could be removed up to 86.6...

  8. Adsorption Mechanisms of Emerging Micro-pollutants with a clay Mineral: Case of Tramadol and Doxepine Pharmaceutical Products

    OpenAIRE

    Thiebault, Thomas; Guégan, Régis; Boussafir, Mohammed

    2015-01-01

    International audience A sodium exchanged smectite clay mineral (Mt) was used as geo-sorbent for the adsorption of tramadol and doxepin: two pharmaceutical products (PPs) defined as emerging pollutants due to their presence at significant concentration in numerous water compartments. The adsorption isotherms for both the temperatures of 20 and 40 °C and the derived data determined through the fitting procedure by using Langmuir, Freundlich and Dubinin–Radushkevich equation models explicitl...

  9. Study on the adsorption-desorption characteristics of 14C-pirimicarb in soils

    International Nuclear Information System (INIS)

    14C-pirimicarb was used to study its adsorption-desorption behavior in 8 kinds of soils. The results indicated that there were significant differences in its adsorption with different kinds of soil. The lowest adsorption percentage was only 13.16% and the highest one was 87.75%. The amount of adsorption in the same kind of soil increased with the concentration of pesticide, but concentration had little influence on the adsorption within the certain range of concentrations. Multiple linear regression equation was developed for prediction of adsorption and determination of the relative importance of the soil parameters. It was significant that the key factors, soil pH and clay content were negatively and positively correlated with the adsorption respectively. The adsorption equilibrium of pirimicarb in soils could be well described by both the Freundlich isotherm and the Langmuir isotherm. The adsorbed 14C-pirimicarb could disrobe from soil and its desorption was also influenced by soil properties described by multiple linear regression equation

  10. Adsorptive removal of heavy metals from aqueous solution by treated sawdust (Acacia arabica)

    Energy Technology Data Exchange (ETDEWEB)

    Meena, Ajay Kumar [Centre for Fire, Explosive and Environment Safety (CFEES), Defence R and D Organisation (DRDO), Brig. S.K. Mazumdar Road, Timarpur, Delhi 110054 (India); Kadirvelu, K. [Centre for Fire, Explosive and Environment Safety (CFEES), Defence R and D Organisation (DRDO), Brig. S.K. Mazumdar Road, Timarpur, Delhi 110054 (India)], E-mail: kadirvelu@lycos.com; Mishra, G.K.; Rajagopal, Chitra [Centre for Fire, Explosive and Environment Safety (CFEES), Defence R and D Organisation (DRDO), Brig. S.K. Mazumdar Road, Timarpur, Delhi 110054 (India); Nagar, P.N. [Centre for Fire, Explosive and Environment Safety (CFEES), Defence R and D Organisation (DRDO), Brig. S.K. Mazumdar Road, Timarpur, Delhi 110054 (India); Department of Chemistry, University of Rajasthan, Jaipur 302004 (India)

    2008-02-11

    The removal of Cr(VI), Pb(II), Hg(II) and Cu(II), by treated sawdust has been found to be concentration, pH, contact time, adsorbent dose and temperature dependent. The adsorption parameters were determined using both Langmuir and Freundlich isotherm models. Adsorption capacity for treated sawdust, i.e. Cr(VI) (111.61 mg/g), Pb(II) (52.38 mg/g), Hg(II) (20.62 mg/g), and Cu(II) (5.64 mg/g), respectively. Surface complexation and ion exchange are the major removal mechanisms involved. The adsorption isotherm studies clearly indicated that the adsorptive behaviour of metal ions on treated sawdust satisfies not only the Langmuir assumptions but also the Freundlich assumptions. The applicability of Lagergren kinetic model has also been investigated. The adsorption follows first-order kinetics. Thermodynamic constant (k{sub ad}), standard free energy ({delta}G{sup o}), enthalpy ({delta}H{sup o}) and entropy ({delta}S{sup o}) were calculated for predicting the nature of adsorption. The percentage adsorption increases with pH to attain a maximum at pH 6 and thereafter it decreases with further increase in pH. The results indicate the potential application of this method for effluent treatment in industries and also provide strong evidence to support the adsorption mechanism proposed.

  11. Adsorptive removal of heavy metals from aqueous solution by treated sawdust (Acacia arabica)

    International Nuclear Information System (INIS)

    The removal of Cr(VI), Pb(II), Hg(II) and Cu(II), by treated sawdust has been found to be concentration, pH, contact time, adsorbent dose and temperature dependent. The adsorption parameters were determined using both Langmuir and Freundlich isotherm models. Adsorption capacity for treated sawdust, i.e. Cr(VI) (111.61 mg/g), Pb(II) (52.38 mg/g), Hg(II) (20.62 mg/g), and Cu(II) (5.64 mg/g), respectively. Surface complexation and ion exchange are the major removal mechanisms involved. The adsorption isotherm studies clearly indicated that the adsorptive behaviour of metal ions on treated sawdust satisfies not only the Langmuir assumptions but also the Freundlich assumptions. The applicability of Lagergren kinetic model has also been investigated. The adsorption follows first-order kinetics. Thermodynamic constant (kad), standard free energy (ΔGo), enthalpy (ΔHo) and entropy (ΔSo) were calculated for predicting the nature of adsorption. The percentage adsorption increases with pH to attain a maximum at pH 6 and thereafter it decreases with further increase in pH. The results indicate the potential application of this method for effluent treatment in industries and also provide strong evidence to support the adsorption mechanism proposed

  12. Adsorption and desorption characteristics of arsenic onto ceria nanoparticles

    Science.gov (United States)

    Feng, Qinzhong; Zhang, Zhiyong; Ma, Yuhui; He, Xiao; Zhao, Yuliang; Chai, Zhifang

    2012-01-01

    The rapid increase in the use of engineered nanoparticles [ENPs] has resulted in an increasing concern over the potential impacts of ENPs on the environmental and human health. ENPs tend to adsorb a large variety of toxic chemicals when they are emitted into the environment, which may enhance the toxicity of ENPs and/or adsorbed chemicals. The study was aimed to investigate the adsorption and desorption behaviors of arsenic on ceria NPs in aqueous solution using batch technique. Results show that the adsorption behavior of arsenic on ceria NPs was strongly dependent on pH and independent of ionic strength, indicating that the electrostatic effect on the adsorption of these elements was relatively not important compared to surface chemical reactions. The adsorption isotherms fitted very well to both the Langmuir and Freundlich models. The thermodynamic parameters (Δ H 0 , Δ S 0 , and Δ G 0 ) for the adsorption of arsenic were determined at three different temperatures of 283, 303, and 323 K. The adsorption reaction was endothermic, and the process of adsorption was favored at high temperature. The desorption data showed that desorption hysteresis occurred at the initial concentration studied. High adsorption capacity of arsenic on ceria NPs suggests that the synergistic effects of ceria NPs and arsenic on the environmental systems may exist when they are released into the environment.

  13. Determination of thermodynamic potentials and the aggregation number for micelles with the mass-action model by isothermal titration calorimetry: A case study on bile salts.

    Science.gov (United States)

    Olesen, Niels Erik; Westh, Peter; Holm, René

    2015-09-01

    The aggregation number (n), thermodynamic potentials (ΔG, ΔH, ΔS) and critical micelle concentration (CMC) for 6 natural bile salts were determined on the basis of both original and previously published isothermal titration calorimetry (ITC) data. Different procedures to estimate parameters of micelles with ITC were compared to a mass-action model (MAM) of reaction type: n⋅S⇌Mn. This analysis can provide guidelines for future ITC studies of systems behaving in accordance with this model such as micelles and proteins that undergo self-association to oligomers. Micelles with small aggregation numbers, as those of bile salts, are interesting because such small aggregates cannot be characterized as a separate macroscopic phase and the widely applied pseudo-phase model (PPM) is inaccurate. In the present work it was demonstrated that the aggregation number of micelles was constant at low concentrations enabling determination of the thermodynamic potentials by the MAM. A correlation between the aggregation number and the heat capacity was found, which implies that the dehydrated surface area of bile salts increases with the aggregation number. This is in accordance with Tanford's principles of opposing forces where neighbouring molecules in the aggregate are better able to shield from the surrounding hydrophilic environment when the aggregation number increases. PMID:25978555

  14. Determination of mercury in discharge water from plastic manufactory by neutron activation analysis and copper powder adsorption

    International Nuclear Information System (INIS)

    Through copper powder adsorption, neutron activation analysis was used to determine the mercury in discharge water from a plastic manufactory where the water samples were taken from various discharge ditches. The experimental results showed that waste water from mercury cells contained 1.7x10-9 approximately 8.19x10-6 g Hg/ml while water samples taken from other areas did not show significant mercury level and were below the limit of detection. (author)

  15. Thermodynamic study of physical adsorption of oxygen on the cleavage face of lamellar crystals

    International Nuclear Information System (INIS)

    Adsorption isotherms of oxygen on the cleavage face of nine lamellar halides (NiCl2, CoBr2, CdCl2, CoI2, CdBr2, FeI2, MnI2, CaI2, PbI2) have been determined. Uniform adsorbents have been prepared by sublimation in a rapid current of inert gas. On these adsorbents, the adsorption isotherms show three steps corresponding to the formation of three successive ad-layers. At sufficiently low temperatures the ad-layers are formed during two-dimensional condensations, which are first order transitions. The analysis of the thermodynamic data derived from the adsorption isotherms, especially the entropy of the ad-layers and their critical temperature of two-dimensional condensation, suggest that the first oxygen layer is solid while the next ones are liquid. As for rare gases we observe that surface relief has an outstanding effect on the structure of the first layer. Adsorption isotherms of oxygen and argon on exfoliated graphite have also been determined. Beyond the first, the ad-layers of oxygen are liquid while these of argon are solid. (author)

  16. Modeling investigation of membrane biofouling phenomena by considering the adsorption of protein, polysaccharide and humic acid.

    Science.gov (United States)

    Demneh, Seyedeh Marzieh Ghasemi; Nasernejad, Bahram; Modarres, Hamid

    2011-11-01

    The importance of solute adsorption in the biofouling membrane has been clearly verified for the performance of membrane bioreactor (MBR). In order to quantify the mechanism of static adsorption in biofouling during of MBR process, we characterize membrane biofouling caused by model solutions containing a protein (bovine serum albumin, BSA), a humic substance (humic acid, HA) and a polysaccharide (alginic acid, Alg) on commercial hydrophilic polyethersulfone (PES) membrane. For static adsorption experiments, membranes were immersed in well-defined model solutions in three temperatures (298, 308 and 318 K) to obtain equilibrium data. To determine the characteristic parameters for this process, 7 isotherm models were applied to the experimental data. Three error analysis methods; the coefficient of nonlinear regression (R(2)), the sum of the squared errors (SSE) and standard deviation of residuals (S(yx)), were used to evaluate the data and determine the best fit isotherm for each model solutions. The error values demonstrated that the Sips isotherm model provided the best fit to the experimental data. AFM images were used for determination of changes in membrane surface after adsorption. These images confirmed the results obtained from adsorption isotherm study. Thermodynamic parameters such as standard free energy (Δ(r)G(θ)), enthalpy (Δ(r)H(θ)) and entropy (Δ(r)S(θ)) changes were determined; these adsorption processes were found to be feasible and endothermic but not spontaneous. The distribution of the substances adsorbed on PES surface were more chaotic than that in the aqueous solutions. Parameters obtained in this study can be used to determine the "fouling potential" of a given feed stream and a membrane. PMID:21798726

  17. Adsorption and magnetic removal of neutral red dye from aqueous solution using Fe3O4 hollow nanospheres

    International Nuclear Information System (INIS)

    Fe3O4 hollow nanospheres were prepared via a simple one-pot template-free hydrothermal method and were fully characterized. These magnetic spheres have been investigated for application as an adsorbant for the removal of dye contaminants from water. Because of the high specific surface area, nano-scale particle size, and hollow porous material, Fe3O4 hollow spheres showed favorable adsorption behavior for Neutral red. Factors affecting adsorption, such as, initial dye concentration, pH and contact time were evaluated. Langmuir and the Freundlich adsorption isotherms were selected to explicate the interaction of the dye and magnetic adsorbant. The characteristic parameters for each isotherm have been determined. The overall trend followed an increase of the sorption capacity with increasing dye concentration with a maximum of 90% dye removal. The monolayer adsorption capacity of magnetic hollow spheres (0.05 g) for NR in the concentration range studied, as calculated from the Langmuir isotherm model at 25 deg. C and pH 6, was found to be 105 mg g-1. Adsorption kinetic followed pseudo-second-order reaction kinetics. Thermodynamic study showed that the adsorption processes are spontaneous and endothermic. The combination of the superior adsorption and the magnetic properties of Fe3O4 nanospheres can be useful as a powerful separation tool to deal with environmental pollution.

  18. Evaluation of the potential of volatile organic compound (di-methyl benzene) removal using adsorption on natural minerals compared to commercial oxides

    International Nuclear Information System (INIS)

    Highlights: • The adsorption of dMB on natural minerals and commercial oxides was evaluated. • The adsorption capacities were discussed considering the adsorbents cost and the bed size. • The adsorption capacity of bentonite is higher than other adsorbents. • Langmuir model provide best correlation of the experimental data. • The isotherms data allow determination of isosteric heat of adsorption. -- Abstract: This study is dedicated to the investigation of the potential of volatile organic compounds (VOC) adsorption over low cost natural minerals (bentonite and diatomite). The performances of these solids, in terms of adsorption/desorption properties, were compared to commercial adsorbents, such as silica, alumina and titanium dioxide. The solids were first characterized by different physico-chemical methods and di-methyl benzene (dMB) was selected as model VOC pollutant for the investigation of adsorptive characteristics. The experiments were carried out with a fixed bed reactor under dynamic conditions using Fourier Transform InfraRed spectrometer to measure the evolution of dMB concentrations in the gaseous stream at the outlet of the reactor. The measured breakthrough curves yields to adsorbed amounts at saturation that has been used to obtain adsorption isotherms. The latters were used for determination of the heat involved in the adsorption process and estimation of its values using the isosteric method. Furthermore, the performances of the studied materials were compared considering the adsorption efficiency/cost ratio

  19. Adsorptive Transfer Stripping for Quick Electrochemical Determination of microRNAs in Total RNA Samples

    Czech Academy of Sciences Publication Activity Database

    Bartošík, M.; Hrstka, R.; Paleček, Emil; Vojtešek, B.

    2014-01-01

    Roč. 26, č. 12 (2014), s. 2558-2562. ISSN 1040-0397 R&D Projects: GA ČR(CZ) GA13-00956S Institutional support: RVO:68081707 Keywords : Adsorptive transfer stripping * Cancer * Mercury electrode Subject RIV: BO - Biophysics Impact factor: 2.138, year: 2014

  20. Adsorption studies on ground shells of hazelnut and almond.

    Science.gov (United States)

    Bulut, Yasemin; Tez, Zeki

    2007-10-01

    Adsorption behaviour of Ni(II), Cd(II) and Pb(II) from aqueous solutions by shells of hazelnut and almond were investigated. The structural properties and surface chemistry of the shells were characterized using sorption of nitrogen and Boehm titration. The equilibrium time was found to be 120 min. The equilibrium adsorption capacity of shells were obtained by using linear Langmuir and Freundlich adsorption isotherms. The equilibrium adsorption level was determined to be a function of the solution contact time, concentration and temperature. The thermodynamic parameters have been determined. The negative values of free change (DeltaG) indicated the spontaneous nature of the adsorption of Ni(II), Cd(II) and Pb(II) onto shells of hazelnut and almond and the positive values of enthalpy change (DeltaH) suggested the endothermic nature of the adsorption process. The best correlation coefficients were obtained for the pseudo second-order kinetic model. Ion exchange is probably one of the major adsorption mechanisms for binding divalent metal ions to the shells of hazelnut and almond. The selectivity order of the adsorbents is Pb(II)>Cd(II)>Ni(II). PMID:17467899

  1. Electrochemical determination of microRNAs based on isothermal strand-displacement polymerase reaction coupled with multienzyme functionalized magnetic micro-carriers.

    Science.gov (United States)

    Ma, Wen; Situ, Bo; Lv, Weifeng; Li, Bo; Yin, Xiaomao; Vadgama, Pankaj; Zheng, Lei; Wang, Wen

    2016-06-15

    MicroRNAs (miRNAs) show great potential for disease diagnostics due to their specific molecular profiles. Detection of miRNAs remains challenging and often requires sophisticated platforms. Here we report a multienzyme-functionalized magnetic microcarriers-assisted isothermal strand-displacement polymerase reaction (ISDPR) for quantitative detection of miRNAs. Magnetic micro-carriers (MMCs) were functionalized with molecular beacons to enable miRNAs recognition and magnetic separation. The target miRNAs triggered a phi29-mediated ISDPR, which can produce biotin-modified sequences on the MMCs. Streptavidin-alkaline phosphatase was then conjugated to the MMC surface through biotin-streptavidin interactions. In the presence of 2-phospho-L-ascorbic acid, miRNAs were quantitatively determined on a screen-printed carbon electrode from the anodic current of the enzymatic product. We show that this method enables detection of miRNAs as low as 9 fM and allows the discrimination of one base mismatched sequence. The proposed method was also successfully applied to analyze miRNAs in clinical tumor samples. This paper reports a new strategy for miRNAs analysis with high sensitivity, simplicity, and low cost. It would be particularly useful for rapid point-of-care testing of miRNAs in clinical laboratory. PMID:26855164

  2. The Adsorption of Reactive Blue 19 Dye onto Cucurbit[8]uril and Cucurbit[6]uril: An Experimental and Theoretical Study.

    Science.gov (United States)

    Xie, Xiaomei; Li, Xiaolei; Luo, Hanhan; Lu, Huijuan; Chen, Feifei; Li, Wei

    2016-05-01

    The adsorption behavior and mechanism of Reactive Blue 19 (RB19) on cucurbit[6]uril (CB[6]) and cucurbit[8]uril (CB[8]) were investigated. The adsorption isotherm data obtained at different temperatures were fitted well to the Langmuir isotherm, and according to this model, CB[8] and CB[6] exhibited maximum monolayer adsorption capacities of 714.29 and 100.5 mg/g, respectively, at 298.15 K. The adsorption thermodynamic functions ΔG, ΔH, and ΔS were evaluated and revealed that RB19 adsorption onto CB[8] and CB[6] is a spontaneous and enthalpy-driven process. The adsorption process was determined to follow pseudo-second-order kinetics, indicating that chemisorption dominates the adsorption process. Fourier tranform IR spectroscopy, thermogravimetric analysis, and density functional theory (DFT) calculations revealed that the formation of an inclusion complex is the main driving force of adsorption. The phenyl and sulfone moieties of RB19 reside inside the cavity of CB[8], but because of the small cavity, only the sulfone of RB19 resides inside the cavity of CB[6]. Time-dependent DFT calculations revealed that all of the absorption bands of RB19 derive from π → π* transitions, while for the adsorption product of CB[8], the bands located at 590 and 287 nm derive from π → π* transitions and the bands located at 254 and 202 nm mainly derive from intermolecular charge transfer (ICT). PMID:27064317

  3. Kinetic modeling of liquid-phase adsorption of Congo red dye using guava leaf-based activated carbon

    Science.gov (United States)

    Ojedokun, Adedamola Titi; Bello, Olugbenga Solomon

    2016-02-01

    Guava leaf, a waste material, was treated and activated to prepare adsorbent. The adsorbent was characterized using Scanning Electron Microscopy (SEM), Fourier Transform Infra Red (FTIR) and Energy-Dispersive X-ray (EDX) techniques. The carbonaceous adsorbent prepared from guava leaf had appreciable carbon content (86.84 %). The adsorption of Congo red dye onto guava leaf-based activated carbon (GLAC) was studied in this research. Experimental data were analyzed by four different model equations: Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherms and it was found to fit Freundlich equation most. Adsorption rate constants were determined using pseudo-first-order, pseudo-second-order, Elovich and intraparticle diffusion model equations. The results clearly showed that the adsorption of CR dye onto GLAC followed pseudo-second-order kinetic model. Intraparticle diffusion was involved in the adsorption process. The mean energy of adsorption calculated from D-R isotherm confirmed the involvement of physical adsorption. Thermodynamic parameters were obtained and it was found that the adsorption of CR dye onto GLAC was an exothermic and spontaneous process at the temperatures under investigation. The maximum adsorption of CR dye by GLAC was found to be 47.62 mg/g. The study shows that GLAC is an effective adsorbent for the adsorption of CR dye from aqueous solution.

  4. Porous and adsorption properties of hydrated cement paste

    Directory of Open Access Journals (Sweden)

    Marina Biljana S.

    2004-01-01

    Full Text Available Adsorption isotherms of benzene on hydrated cement pastes prepared by cement ground with and without the addition of grinding aids, triethanol amine (TEA and ethylene glycol (EG were investigated. The adsorption isotherms were interpreted by means of the Dubinin-Astakhov (DA and Dubinin-Radushkevich-Stoeckli (DRS equations. The microporous structure of cement gel (C-S-H in the cement pastes, and changes in the Gibbs free energy of adsorption were determined. The mechanical properties of the cement pastes were also measured. It was evident that pastes with additives had different parameters of the DRS and DA equations: the volume and dimensions of the gel pores, the distribution of the dimensions, the characteristic energy of adsorption, and the change in the Gibbs free energy of adsorption. The mechanical properties were also different. The dispersity of the additive-containing ground cements had a favorable effect on the hydration processes. When applying TEA, it was also necessary to analyze its influence on the chemical behavior of hydration in the starting period.

  5. Activated carbon from vetiver roots: gas and liquid adsorption studies.

    Science.gov (United States)

    Gaspard, S; Altenor, S; Dawson, E A; Barnes, P A; Ouensanga, A

    2007-06-01

    Large quantities of lignocellulosic residues result from the industrial production of essential oil from vetiver grass (Vetiveria zizanioides) roots. These residues could be used for the production of activated carbon. The yield of char obtained after vetiver roots pyrolysis follows an equation recently developed [A. Ouensanga, L. Largitte, M.A. Arsene, The dependence of char yield on the amounts of components in precursors for pyrolysed tropical fruit stones and seeds, Micropor. Mesopor. Mater. 59 (2003) 85-91]. The N(2) adsorption isotherm follows either the Freundlich law K(F)P(alpha) which is the small alpha equation limit of a Weibull shaped isotherm or the classical BET isotherm. The surface area of the activated carbons are determined using the BET method. The K(F) value is proportional to the BET surface area. The alpha value increases slightly when the burn-off increases and also when there is a clear increase in the micropore distribution width. PMID:17092643

  6. Determination of surface area of glass grains by adsorption of methylene blue and its application in the testing of relative impact strength of glasses

    International Nuclear Information System (INIS)

    Surface area of glass grains by adsorption of methylene blue has been determined. Effects of variables such as pH, glass compositions, and equilibration time on the adsorption of methylene blue on glass surfaces have been evaluated. Conditions to determine relative surface area of glass-pieces/glass-grains by adsorption of methylene blue have been found out. The method has been successfully applied to compare the impact strength of glasses by measuring the surface area of the shattered pieces generated in shattering test unit. (author)

  7. Application of zeolitic materials prepared from fly ash to water vapor adsorption for solar cooling

    International Nuclear Information System (INIS)

    Highlights: ► Water vapor isotherms of lignite ash are of type III with low adsorption capacity. ► Mild fly ash hydrothermal treatment produces a hydrophilic zeolitic material. ► The zeolitic material exhibits a type IV water vapor adsorption isotherm. ► Under irradiation, its surface temperature is reduced due to water desorption. ► Potential application of the fly ash zeolitic material for solar cooling. -- Abstract: The water vapor adsorption properties of raw and hydrothermally treated fly ashes with NaOH and their application prospect as evaporative coolers of roof surfaces were studied. Initially, samples were characterized through techniques like elemental analysis, X-ray diffraction, thermogravimetry, reflectance measurements and water vapor adsorption isotherms. Moreover, the water adsorption properties and the associated temperature variations were determined in a specific wind tunnel with controllable environmental conditions. The adsorption isotherms for fly ash were of type III indicating hydrophobic material with low water vapor adsorption. The hydrothermal treatment in an alkaline solution transformed the fly ash in hydrophilic material of type IV. Moreover, the treated samples were capable of lowering their surface temperatures due to water evaporation and the release of the latent heat. The maximum difference of temperature increase under simulated solar irradiation was observed between the treated fly ash and the concrete with values of 5.0, 5.4 and 7.5 °C for the surface, middle and bottom position, respectively. The results indicate that the zeolitic materials prepared from the fly ash samples have a significant potential for solar cooling applications.

  8. Measurement of dynamic adsorption coefficient of Xe on coconut charcoal in CO2 streams by gas-solid chromatography

    International Nuclear Information System (INIS)

    This paper presents a method for measuring the dynamic adsorption coefficients of Xe on coconut charcoal II-2 in CO2 carrier streams by SP-2305E gas chromatograph with the thermal conductivity cell. The adsorption column is made of stainless steel (diameter 4 x 240 mm) packed with 60-80 mesh coconut charcoal II-2. The CO2 content in carrier streams is about 87%. Three groups of data of Xe dynamic adsorption coefficient were obtained at temperature 15.5 deg C, 31.5 deg C and 50.5 deg C by pulse injection respectively. Another group was obtained at temperature approx. 16 deg C by continueous injection. In addition, adsorption isotherms and adsorption isometrics were determined. In this experimental system, the adsorption heat of Xe on coconut charcoal II-2 is 2820 cal/mole

  9. Adsorptive removal of heavy metals by magnetic nanoadsorbent: an equilibrium and thermodynamic study

    Science.gov (United States)

    Shirsath, D. S.; Shirivastava, V. S.

    2015-11-01

    An efficient and new magnetic nanoadsorbent photocatalyst was fabricated by co-precipitation technique. This research focuses on understanding metal removal process and developing a cost-effective technology for treatment of heavy metal-contaminated industrial wastewater. In this investigation, magnetic nanoadsorbent has been employed for the removal of Zn(II) ions from aqueous solutions by a batch adsorption technique. The adsorption equilibrium data fitted very well to Langmuir and Freundlich adsorption isotherm models. The thermodynamics of Zn(II) ions adsorption onto the magnetic nanoadsorbents indicated that the adsorption was spontaneous, endothermic and physical in nature. Surface morphology of magnetic nanoadsorbent by scanning electron microscopy (SEM) and elemental analysis by EDX technique. The structural and photocatalytic properties of magnetic nanoadsorbent were characterized using X-ray diffraction (XRD) and FTIR techniques. Also, the magnetic properties of synthesized magnetic nanoadsorbent were determined by vibrating spinning magnetometer (VSM).

  10. Adsorption characteristics of haloacetonitriles on functionalized silica-based porous materials in aqueous solution.

    Science.gov (United States)

    Prarat, Panida; Ngamcharussrivichai, Chawalit; Khaodhiar, Sutha; Punyapalakul, Patiparn

    2011-09-15

    The effect of the surface functional group on the removal and mechanism of dichloroacetonitrile (DCAN) adsorption over silica-based porous materials was evaluated in comparison with powdered activated carbon (PAC). Hexagonal mesoporous silicate (HMS) was synthesized and functionalized by three different types of organosilanes (3-aminopropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane and n-octyldimethysilane). Adsorption kinetics and isotherm models were used to determine the adsorption mechanism. The selective adsorption of five haloacetonitriles (HANs) in the single and mixed solute systems was also studied. The experiments revealed that the surface functional groups of the adsorbents largely affected the DCAN adsorption capacities. 3-Mercaptopropyl-grafted HMS had a high DCAN adsorption capacity compared to PAC. The adsorption mechanism is believed to occur via an ion-dipole electrostatic interaction in which water interference is inevitable at low concentrations of DCAN. In addition, the adsorption of DCAN strongly depended on the pH of the solution as this related to the charge density of the adsorbents. The selective adsorption of the five HANs over PAC was not observed, while the molecular structure of different HANs obviously influenced the adsorption capacity and selectivity over 3-mercaptopropyl-grafted HMS. PMID:21752539

  11. Adsorption of uranium ions by crosslinked polyester resin functionalized with acrylic acid from aqueous solutions

    International Nuclear Information System (INIS)

    In this paper, the crosslinked polyester resin containing acrylic acid functional groups was used for the adsorption of uranium ions from aqueous solutions. For this purpose, the crosslinked polyester resin of unsaturated polyester in styrene monomer (Polipol 353, Poliya) and acrylic acid as weight percentage at 80 and 20%, respectively was synthesized by using methyl ethyl ketone peroxide (MEKp, Butanox M60, Azo Nobel)-cobalt octoate initiator system. The adsorption of uranium ions on the sample (0.05 g copolymer and 5 mL of U(VI) solution were mixed) of the crosslinked polyester resin functionalized with acrylic acid was carried out in a batch reactor. The effects of adsorption parameters of the contact time, temperature, pH of solution and initial uranium(VI) concentration for U(VI) adsorption on the crosslinked polyester resin functionalized with acrylic acid were investigated. The adsorption data obtained from experimental results depending on the initial U(VI) concentration were analyzed by the Freundlich, Langmuir and Dubinin-Radushkevich (D-R) adsorption isotherms. The adsorption capacity and free energy change were determined by using D-R isotherm. The obtained experimental adsorption data depending on temperature were evaluated to calculate the thermodynamic parameters of enthalpy (ΔHo), entropy (ΔSo) and free energy change (ΔGo) for the U(VI) adsorption on the crosslinked polyester resin functionalized with acrylic acid from aqueous solutions. The obtained adsorption data depending on contact time were analyzed by using adsorption models such as the modified Freundlich, Elovich, pseudo-first order and pseudo-second-order kinetic models. (author)

  12. A consideration of the correct calculation of thermodynamic parameters of adsorption

    Directory of Open Access Journals (Sweden)

    SLOBODAN K. MILONJIC

    2007-12-01

    Full Text Available The Langmuir and Freundlich isotherm equations have been widely used for interpreting various adsorption processes. There are, however, many serious mistakes in the literature in determination or calculation of thermodynamic parameters, especially in the determination of the change in the free energy of adsorption using Langmuir, Freundlich and Henry constants. Many authors used these constants for the determination of ΔG expressed instead of dimensionless in some concentration units (for example: l mol-1, l g-1, ml mg-1, etc..

  13. Adsorption of amitraz on the clay

    Directory of Open Access Journals (Sweden)

    Jale Gülen

    2013-01-01

    Full Text Available Amitraz (AZ that is used as acaridies was tried to extract with a clay. The experimental data were modelled as using Langmuir and Freundlich isotherms. The adsorption data fit well with Langmuir isotherm that indicated the AZ adsorption is homogeneous and monolayer. The monolayer adsorption capacity was found to be 35.02 mg/g at 20 ºC temperature. Effect of the phases contact time, the initial solution pH and the initial pesticide concentration were investigated from the point of adsorption equilibrium and yield. The adsorption kinetics were investigated by applying pseudo first order, pseudo second order and intra particle diffusion laws. Adsorption of AZ was found to be best fitted by the pseudo second order model. The intra particle diffusion also plays an important role in adsorption phenomenon.

  14. Adsorption of Malachite Green dye onto activated carbon derived from Borassus aethiopum flower biomass

    International Nuclear Information System (INIS)

    In the present study, chemically prepared activated carbon derived from Borassus aethiopum flower was used as adsorbent. Batch adsorption studies were performed for the removal of Malachite Green (MG) from aqueous solutions by varying the parameters like initial solution pH, adsorbent dosage, initial MG concentration and temperature with three different particle sizes such as 100 μm, 600 μm and 1000 μm. The zero point charge was 2.5 and the maximum adsorption occurred at the pH range from 6.0 to 8.0. Experimental data were analyzed by model equations such as Langmuir, Freundlich and Temkin isotherms and it was found that the Langmuir isotherm model best fitted the adsorption data. Thermodynamic parameters such as ΔG, ΔH and ΔS were also calculated for the adsorption processes. Adsorption rate constants were determined using pseudo first-order, pseudo second-order rate equations and also Elovich model and intraparticle diffusion models. The results clearly showed that the adsorption of MG onto PFAC followed pseudo second-order model and the adsorption was both by film diffusion and by intraparticle diffusion.

  15. Preparation and adsorption behavior for metal ions and humic acid of chitosan derivatives crosslinked by irradiation

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    This article deals with the determination of the adsorption properties of metal ions and humic acid in water on crosslinked chitosan derivatives (carboxymethylchitosan) which were formed using the irradiation technique without any additives. The solubility test of these crosslinked materials were investigated in acidic, alkaline media,distilled water, and certain organic solvents. Scanning electron microscopic (SEM) images showed that the crosslinked chitosan derivatives possessed a porous morphological structure. Charged characteristic analyses demonstrated typically pH-dependent properties of the crosslinked materials. The adsorption studies were carried out by the batch method at room temperature. Adsorption of heavy metal ions (such as Cu2+, Cd2+) and humic acid onto crosslinked samples was found to be strongly pH-dependent. Adsorption kinetic studies indicated the rapid removal of metal ions, and humic acid from the aqueous solutions. Moreover, isothermal adsorption data revealed that Cu2+, Cd2+,and humic acid were removed by these crosslinked materials with high efficiency. Adsorption isothermal data were interpreted well by the Langmuir equation. These crosslinked carboxymethylated chitosan derivatives indicate favorable adsorption of metal ions and humic acid.

  16. Synthesis of thiazole silica hybrid from waste glass for adsorption of cadmium(II)

    Science.gov (United States)

    Azmiyawati, C.; TaslimahVirkyanov

    2016-02-01

    Synthesis of thiazole silica hybrid from waste glass to adsorption of cadmium (II) metal ion has been performed. The synthesis was done by attaching thiazole group through liaison compound γ- glycidoxy propyl tri-methoxy silane with silica gel obtained from waste glass. In this study, the effect of adsorption contact time and the concentration of cadmium (II) was studied to determine the reaction rate and the amount of adsorption thermodynamics. The existence of the cluster thiazole on silica gel indicated by IR spectra at wavelengths around 2576 cm-1 of mercaptan groups that previously did not appear on silica gel without modification. The synthesized TSH showed a high adsorption capacity of 9.363 mmol/g of Cd(II). The adsorption isotherm obtained with Langmuir isotherm model gives the negative values of ΔG°, i.e. -15.488 kJ/mol for Cd(II), indicating the spontaneous process of adsorption. Kinetic studies showed that the adsorption of Cd(II) ion into TSH follows the pseudo-second-order kinetics.

  17. Selective adsorption and determination of iron(III): Mn{sub 3}O{sub 4}/TiO{sub 2} composite nanosheets as marker of iron for environmental applications

    Energy Technology Data Exchange (ETDEWEB)

    Khan, Sher Bahadar, E-mail: drkhanmarwat@gmail.com [Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Rahman, Mohammed M.; Marwani, Hadi M.; Asiri, Abdullah M. [Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Alamry, Khalid A. [Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Rub, Malik Abdul [Center of Excellence for Advanced Materials Research (CEAMR), King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia); Chemistry Department, Faculty of Science, King Abdulaziz University, P.O. Box 80203, Jeddah 21589 (Saudi Arabia)

    2013-10-01

    Mn{sub 3}O{sub 4}/TiO{sub 2} composite nanosheets have been synthesized by simple and low temperature magnetic stirring method and applied for water treatment application. The synthesized Mn{sub 3}O{sub 4}/TiO{sub 2} composite nanosheets were characterized by using field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The spectroscopic techniques agreed that synthesized product is well crystalline nanosheets composed of Mn{sub 3}O{sub 4}/TiO{sub 2}. The analytical potential of synthesized Mn{sub 3}O{sub 4}/TiO{sub 2} composite nanosheets was studied for a selective separation of Fe{sup 3+} prior to its determination by inductively coupled plasma-optical emission spectrometry. The selectivity of Mn{sub 3}O{sub 4}/TiO{sub 2} composite nanosheets toward different metal ions, including Au{sup 3+}, Cd{sup 2+}, Co{sup 2+}, Cr{sup 3+}, Fe{sup 3+}, Pd{sup 2+} and Zn{sup 2+} was investigated. Results of the selectivity study demonstrated that Mn{sub 3}O{sub 4}/TiO{sub 2} composite nanosheets were the most selective toward Fe{sup 3+}. The adsorption capacity of Fe{sup 3+} was found to be 69.80 mg g{sup −1}. Moreover, adsorption isotherm data also provided that the adsorption process was mainly monolayer on a homogeneous adsorbent surface.

  18. Isothermal Titration Calorimetry of RNA

    OpenAIRE

    Salim, Nilshad N.; Feig, Andrew L.

    2008-01-01

    Isothermal titration calorimetry (ITC) is a fast and robust method to study the physical basis of molecular interactions. A single well-designed experiment can provide complete thermodynamic characterization of a binding reaction, including Ka, ΔG, ΔH, ΔS and reaction stoichiometry (n). Repeating the experiment at different temperatures allows determination of the heat capacity change (ΔCP) of the interaction. Modern calorimeters are sensitive enough to probe even weak biological interactions...

  19. Removal and recovery of hazardous triphenylmethane dye, Methyl Violet through adsorption over granulated waste materials

    International Nuclear Information System (INIS)

    Bottom Ash a power plant waste material and De-Oiled Soya, an agricultural waste product have been successfully used for the removal and recovery of a hazardous triphenylmethane dye-Methyl Violet, from wastewaters. The characterization of each adsorbent has been carried out by I.R. and D.T.A. curves. Batch adsorption studies have been made by measuring effects of pH, sieve size, amount of adsorbent, contact time, temperature, concentration of the adsorbate solution, etc. Kinetic studies have been used to determine the nature of rate controlling step of the processes and confirm the applicability of the first order rate expression in the ongoing adsorption process. Various thermodynamic parameters have also been calculated by applying the linear forms of Langmuir and Freundlich adsorption isotherms. The linear nature of adsorption isotherms obtained shows the dependence of the processes on the Freundlich and Langmuir isotherm models. Furthermore, to ascertain the adsorption processes to be particle diffusion or film diffusion mechanism, Boyd and Reichenberg's expressions have been applied. For both the adsorbents, column operations have been carried out for the bulk removal of the dye. The adsorbed dye has been recovered by eluting hydrochloric acid of pH 3 through exhausted columns

  20. Adsorption of phenol from aqueous systems onto spent oil shale

    Energy Technology Data Exchange (ETDEWEB)

    Darwish, N.A.; Halhouli, K.A.; Al-Dhoon, N.M. [Jordan Univ. of Science and Technology, Irbid (Jordan)

    1996-03-01

    To evaluate its ability to remove phenol from aqueous solution, Jordanian {open_quotes}spent{close_quotes} oil shale, an abundant natural resource, has been used in an experimental adsorption study. Equilibrium of the system has been determined at three temperatures: 30, 40, and 55{degrees}C. The resulting experimental equilibrium isotherms are well represented by Frendlich, Langmuir, and Redlich-Peterson isotherms. The relevant parameters for these isotherms, as regressed from the experimental equilibrium data, are presented. Effects of solution pH (in the range of 3-11), in addition to effects of three inorganic salts (Kl, KCl, and NaCl), on the equilibrium isotherms were also investigated. The effects of pH in the presence of KI and NaCl were also investigated for a possible interaction between salts and solution pH. The initial concentration of phenol in the aqueous system studied ranges from 10 to 200 ppm. Experimental results show that while an acidic solution has no effect on the adsorption capacity of spent oil shale to phenol, a highly basic solution reduces its adsorbability. No sound effect was observed for the inorganic salts studied on the adsorption of phenol on spent oil shale. The experimental results show that there is no interaction between the pH of solution and the presence of salts. In spite of its ability to remove phenol, spent oil shale showed a very low equilibrium capacity (of an order of magnitude of 1 mg/g). Should the adsorption capacity of the shale be improved (by different treatment processes, such as grafting, surface conditioning), results of this study will find a direct practical implication in serving as {open_quotes}raw{close_quotes} reference data for comparison purposes.

  1. Comments on "Ion adsorption components in liquid/solid systems"

    Institute of Scientific and Technical Information of China (English)

    LI Wei; PAN Gang

    2007-01-01

    @@ Recently, Wu et al. (J Environ Sci 18(2006) 1167-1175) published a paper entitled as above. In the paper, the authors proposed a plotting method for describing adsorption isotherm, where adsorption density (q e) was plotted against the ratio of equilibrium concentration/particle concentration (Ce/W0) rather than (Ce) as traditionally defined. The authors claimed that this plot can eliminate the "particle concentration effect" (i.e., adsorption isotherm declines with increasing particle concentration), which may otherwise be inevasible with traditionally defined adsorption isotherms. We think that their conclusion is conceptually flawed and the plot may cause substantial inconstancy problems in practice.

  2. Molecular simulations in microporous materials: adsorption and separation

    OpenAIRE

    J. M. Castillo

    2010-01-01

    The adsorption of water on hydrophobic zeolites such as silicalite and on hydrophilic MOF (metal-organic framework), Cu-BTC, is completely different, as described in chapters 2 and 4. While in hydrophobic materials water adsorption isotherms are very steep and difficult to measure, both experimentally and by simulation, in hydrophilic materials water adsorbs easily and its isotherms are similar to the isotherms of other molecules. The key property to understand these differences is the dipole...

  3. Isothermal Containment Module

    Science.gov (United States)

    1999-01-01

    Isothermal Containment Modules are the temperature-controlling carrier that BioServe built to carry Commercial Generic Bioprocessing Apparatus (CGBA) and in the future, Space Automated Bioproduct Lab (SABL) to the International Space Station.

  4. 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...... 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...

  5. ISOTERMAS DE ADSORCIÓN DE BIOPLÁSTICOS DE HARINA DE YUCA MOLDEADOS POR COMPRESIÓN ISOTERMAS DE ADSORÇÃO DE FARINHA DE MANDIOCA BIOPLÁSTICOS MOLDADAS POR COMPRESSÃO ADSORPTION ISOTHERMS OF CASSAVA FLOUR BIOPLASTICS COMPRESSION MOLDED

    Directory of Open Access Journals (Sweden)

    DIANA P NAVIA

    2011-06-01

    C para a variedade MBRA 383, enquanto o modelo de GAB foi a 35°C por MBRA 383. Calor isostérico de sorção diminuiu com o aumento do teor de umidade de equilíbrio foi encontrado um valor máximo de 87 kJ/mol e 78 kJ/mol, e mínima de 44,6 kJ/mol e 44,5 kJ/mol em amostras preparadas com o CM 7951-5 e MBRA 383, respectivamente.Water adsorption and isosteric heat were evaluated in biopolymers made from flour of two varieties of cassava (CM 7951-5 and MBRA 383, fique dust and glycerol by compression molding technique. The adsorption isotherms of polymeric samples were performed at 15,25, and 35°C in a water activity range of 0.12 to 0.98, using a gravimetric method. The adsorption experimental data were adjusted using the GAB, Caurie, Oswin, Smith, Henderson and Peleg models. The sorption isosteric heat (Qst was determined with Clausius-Clapeyron equation. The results showed that the Peleg model was adjusted appropriately to experimental values of adsorption at 15, 25 and 35°C in the samples prepared with the variety CM 7951-5 and 15 and 25°C for the variety MBRA 383, while the GAB model was at 35°C for MBRA 383. Isosteric heat of sorption decreased with increase in equilibrium moisture content finding the maximum in 87Kj/mol and 78 Kj/mol, and minimum in 44.6 Kj/mol and 44.5 Kj/mol in samples made with CM 7951-5y MBRA 383 respectively.

  6. Experimental determination of barium isotope fractionation during diffusion and adsorption processes at low temperatures

    Science.gov (United States)

    van Zuilen, Kirsten; Müller, Thomas; Nägler, Thomas F.; Dietzel, Martin; Küsters, Tim

    2016-08-01

    Variations in barium (Ba) stable isotope abundances measured in low and high temperature environments have recently received increasing attention. The actual processes controlling Ba isotope fractionation, however, remain mostly elusive. In this study, we present the first experimental approach to quantify the contribution of diffusion and adsorption on mass-dependent Ba isotope fractionation during transport of aqueous Ba2+ ions through a porous medium. Experiments have been carried out in which a BaCl2 solution of known isotopic composition diffused through u-shaped glass tubes filled with silica hydrogel at 10 °C and 25 °C for up to 201 days. The diffused Ba was highly fractionated by up to -2.15‰ in δ137/134Ba, despite the low relative difference in atomic mass. The time-dependent isotope fractionation can be successfully reproduced by a diffusive transport model accounting for mass-dependent differences in the effective diffusivities of the Ba isotope species (D137Ba /D134Ba =(m134 /m137) β). Values of β extracted from the transport model were in the range of 0.010-0.011. Independently conducted batch experiments revealed that adsorption of Ba onto the surface of silica hydrogel favoured the heavier Ba isotopes (α = 1.00015 ± 0.00008). The contribution of adsorption on the overall isotope fractionation in the diffusion experiments, however, was found to be small. Our results contribute to the understanding of Ba isotope fractionation processes, which is crucial for interpreting natural isotope variations and the assessment of Ba isotope ratios as geochemical proxies.

  7. Application of novel Polypyrrole/thiol-functionalized zeolite Beta/MCM-41 type mesoporous silica nanocomposite for adsorption of Hg2+ from aqueous solution and industrial wastewater: Kinetic, isotherm and thermodynamic studies

    Science.gov (United States)

    Javadian, Hamedreza; Taghavi, Mehdi

    2014-01-01

    Hierarchical zeolite consists of both microporous and unordered mesoporous structures. A composite of Polypyrrole/thiol-functionalized Beta/MCM-41 (PPy/SH-Beta/MCM-41) was prepared, characterized by FE-SEM, FT-IR, XRD, TGA and BET analysis and applied in the investigation of its adsorption characteristics for the removal of Hg2+ ions from aqueous solutions. Thiol-functionalized Beta/MCM-41 (SH-Beta/MCM-41) was prepared by 3-mercaptopropyltrimethoxysilane (MPTMS) in the presence of aerosil-200 as a silica source by two-step hydrothermal crystallization procedure. Batch mode experiments were conducted and three kinetic models were used to describe the adsorption process. The experimental data fitted very well with the Pseudo-second-order kinetic model. The calculated thermodynamic parameters (ΔH, ΔS and ΔG) revealed that the adsorption of Hg2+ onto PPy/SH-Beta/MCM-41 is an endothermic and spontaneous process. It was found that temperature has a positive effect on the removal efficiency and that PPy/SH-Beta/MCM-41 is potentially able to remove Hg2+ ions from aqueous solutions at even high concentrations (400 mg L-1). The recovery of Hg2+ from the PPy/SH-Beta/MCM-41 adsorbent was found to be more than 90% using 0.5 M H2SO4, and the ability of the absorbent to be reused for removal of Hg2+ was investigated.

  8. Application of novel Polypyrrole/thiol-functionalized zeolite Beta/MCM-41 type mesoporous silica nanocomposite for adsorption of Hg2+ from aqueous solution and industrial wastewater: Kinetic, isotherm and thermodynamic studies

    International Nuclear Information System (INIS)

    Hierarchical zeolite consists of both microporous and unordered mesoporous structures. A composite of Polypyrrole/thiol-functionalized Beta/MCM-41 (PPy/SH-Beta/MCM-41) was prepared, characterized by FE-SEM, FT-IR, XRD, TGA and BET analysis and applied in the investigation of its adsorption characteristics for the removal of Hg2+ ions from aqueous solutions. Thiol-functionalized Beta/MCM-41 (SH-Beta/MCM-41) was prepared by 3-mercaptopropyltrimethoxysilane (MPTMS) in the presence of aerosil-200 as a silica source by two-step hydrothermal crystallization procedure. Batch mode experiments were conducted and three kinetic models were used to describe the adsorption process. The experimental data fitted very well with the Pseudo-second-order kinetic model. The calculated thermodynamic parameters (ΔH, ΔS and ΔG) revealed that the adsorption of Hg2+ onto PPy/SH-Beta/MCM-41 is an endothermic and spontaneous process. It was found that temperature has a positive effect on the removal efficiency and that PPy/SH-Beta/MCM-41 is potentially able to remove Hg2+ ions from aqueous solutions at even high concentrations (400 mg L−1). The recovery of Hg2+ from the PPy/SH-Beta/MCM-41 adsorbent was found to be more than 90% using 0.5 M H2SO4, and the ability of the absorbent to be reused for removal of Hg2+ was investigated.

  9. Pb2+ adsorption from aqueous solutions on activated carbons obtained from lignocellulosic residues

    Directory of Open Access Journals (Sweden)

    L. Giraldo

    2008-03-01

    Full Text Available Activated carbons obtained from cane sugar bagasse (ACB, African palm pit (ACP and sawdust (ACS were prepared through an impregnated with HNO3 and thermal treatment in an atmosphere in N2/steam water at 1173 K. Adsorption isotherms of N2 at 77 K and of CO2 at 273 K were determined for the activated carbons for which surface area and pore volume values were from 868 to 1100 m²g-1 and from 0.27 to 0.55cm³ g-1, respectively. These results were correlated, with the ones obtained for adsorption the adsorption isotherms of Pb2+ in aqueous solutions. Impregnation of the lignocellulosic materials with nitric acid produced acid-type activated carbons with total acid site contents between 4.13 and 6.93 mmol g-1 and pH at the point of zero charge values between 2.7 and 4.1, which were within range of the adsorption, at different pH values, since they determined, the surface charge of the activated carbons. Adsorption isotherms of Pb2+ at different pH values (2-8 at 298 K were determined. The ion adsorption capacity on ACB, ACP and ACS were 13.7, 15.2 and 17.5 mg.g-1, respectively. Experimental data were fitted to the Langmuir and Freundlich models and all cases the former fit better. The highest values for the quantity adsorbed on the monolayer, qm, were at pH 4, whereas the surface, charge of activated carbons was negative and the lead species mainly present was Pb2+. For higher pHs, the quantity of Pb2+ adsorbed decreased, and this had an important effect on adsorption, the surface characteristics of the solids and the hydroxilated lead species that were formed in the system.

  10. Determinants of natural zeolite clinoptilolite adsorption capacity for removing NO2

    Directory of Open Access Journals (Sweden)

    Nabiollah Mansouri

    2010-09-01

    Full Text Available Background: NO2 is a poisonous gas that potential to cause major threat to human being health and the environment, as a result, removing this gas from environment seems to be essential. Methods: The study aimed to remove this gas from environment using Iranian natural zeolite, clinoptilolite. After crushing and preparing two sizes of 1 and 2 mm zeolite they were activated in 380 to 420 ºC for 20 minutes. NO2 was produced by reaction of copper (Cu and nitric acid (HNO3 and diluted with enough air to achieve desired concentration. A laboratory reactor set with different concentration of NO2 (20, 30, and, 45 ppm, flows through the zeolite absorbent bed was prepared. Different parameters affected No2 absorption, such as concentration, height, and diameter of zeolite bed, zeolite granulation, and activation temperature were examined.Results: In different condition, the adsorption range of the zeolite for NO2 was varied from 0.35% W for 2mm granulation and the 20 ppm concentration to 1.5% W using 1mm granulation and 45 ppm concentration of NO2. Activation temperature of 420 ºC for 20 min was the best condition removing NO2. Efficiency of 1mm granulation was higher than 2mm. Conclusion: Reducing parameters such as height and diameter of zeolite bed decreased but increasing concentration of gas flow increased adsorption capacity of zeolite. Using Iranian zeolite in gas masks still not recommended.

  11. The adsorption characteristics of osteopontin on hydroxyapatite and gold

    International Nuclear Information System (INIS)

    The adsorption of osteopontin on hydroxyapatite (HA) and reference gold (Au) surfaces was studied at different protein bulk concentrations over the temperature range 295-317 K, using quartz crystal microbalance with dissipation (QCM-D) and X-ray photoelectron spectroscopy (XPS). The QCM-D protein adsorption studies were complemented with polyclonal antibodies to examine the availability of protein sequences on the resulting protein layer. The QCM-D and XPS results show that the osteopontin surface mass uptake is larger on Au as compared to HA surfaces within the range of experimental conditions examined (protein bulk concentrations and temperature range), in accordance with the formation of a more compact protein film on Au. The specific antibody binding to the resulting adsorbed osteopontin layer as measured by QCM-D further confirms that the protein packing and conformational/orientational changes occurring during OPN adsorption on Au and HA are different, since fewer antibodies are observed to bind per OPN molecule on Au as compared to HA. The adsorption process on the respective surfaces was modeled using both the Langmuir and Hill adsorption isotherms, and from these isotherm curves, the Gibbs free energy, ΔG, of the osteopontin adsorption was determined. The estimated ΔG values indicate that the osteopontin molecules have a high affinity towards Au, while a lower affinity is observed between osteopontin and HA. By examining the changes in ΔG as a function of temperature, we additionally find that the osteopontin adsorption on HA and Au is endothermic and driven by an increase in entropy.

  12. Characterization of the Adsorption of the Lead (II by the Nonliving Biomass Spirogyra neglecta (Hasall Kutzing

    Directory of Open Access Journals (Sweden)

    Modher A. Hussain

    2009-01-01

    Full Text Available Problem statement: Conventional techniques for removing dissolved heavy metals are only practical and cost-effective when applied to high strength wastes with heavy metal ion concentrations greater than 100 ppm. The possibility of using a nonliving algal biomass to solve this problem was carried in this study. Lead (II was used in this study because it had been reported to cause several disorders in human. Approach: The nonliving algal biomass was obtained from a filamentous green alga Spirogyra neglecta. The effects of initial concentration and contact time, pH and temperature on the biosorption of lead (II by the nonliving algal biomass were studied. The equilibrium isotherms and kinetics were obtained from batch adsorption experiments. The surface characteristics of the nonliving algal biomass were examined using scanning electron microscope and Fourier Transformed Infrared. The maximum adsorption capacity of the nonliving algal biomass was also determined. Results: Maximum adsorption capacity of lead (II was affected by its initial concentration. Adsorption capacity of lead (II increased with the pH and temperature of lead (II solution. Langmuir isothermic model fitted the equilibrium data better than the Freundlich isothermic model. The adsorption kinetics followed the pseudo-second-order kinetic model. The nonliving algal biomass exhibited acaves-like, uneven surface texture along with lot of irregular surface. FTIR analysis of the alga biomass revealed the presence of carboyl, amine and carboxyl group which were responsible for adsorption of lead (II. The maximum adsorption capacity (qmax of lead (II by the nonliving biomass of Spirogyra neglecta was 132 mg g-1. Conclusion: The maximum adsorption capacity for lead (II by the nonliving biomass of Spirogyra neglecta was higher than reported for other biosorbents. Therefore, it had a great potential for removing lead (II from polluted water

  13. Facile preparation of hierarchical hollow structure gamma alumina and a study of its adsorption capacity

    Science.gov (United States)

    Lan, Shi; Guo, Na; Liu, Lu; Wu, Xiaomin; Li, Linlin; Gan, Shucai

    2013-10-01

    The hierarchical shell and hollow core structure gamma alumina (γ-Al2O3) with high adsorption affinity toward organic pollutants was fabricated via a facile homogeneous precipitation method. The microstructure, morphology, and functional groups of the as-synthesized γ-Al2O3 were characterized in detail. The N2 adsorption-desorption measurement (BET) experimental result showed the surface area of γ-Al2O3 (Al90-600) is 320.6 m2/g and the average pore size is 17.8 nm. The effects of reaction parameters on the synthesis of hierarchical hollow structure were systematically investigated. The dye removal ability of this adsorbent was determined by batch adsorption procedure. The isotherms and kinetics of adsorption process were determined and analyzed in detail, which were found to obey the Langmuir isotherm model and the pseudo-second-order for both the Congo red (CR) and Methyl orange (MO). The maximum adsorption capacity of γ-Al2O3 for CR is 835.0 mg/g, which is higher than that of many other previously reported hierarchical structured adsorbents. This facile synthetic approach is a very promising way for the design and synthesis of the typical hierarchical hollow structure materials with powerful adsorption capacity for the removal of organic contaminants from wastewater.

  14. Studies of gas adsorption in flexible Metal-Organic frameworks

    Science.gov (United States)

    Sircar, Sarmishtha

    Flexible Metal-Organic frameworks that exhibit a gate-opening (GO) adsorption mechanism have potential for gas separations and gas storage. The GO phenomenon occurs when molecular gates in the structure expand/contract in response to the activation/de-activation of a system variable e.g. temperature, pressure or gas. Sharp discontinuities in the isotherm leading to S-shapes and large adsorption-desorption hysteresis are typical of this phenomenon. This study investigates the kinetics and thermodynamics of the GO behavior by combining adsorption measurements and analytical modeling of adsorption kinetics and capacity as a function of adsorbate, GO pressure, and temperature. Basic understanding of GO mechanism will help harness GO-MOF's as adsorbents for gas separations and storage. Experiments were performed on two precharacterized MOFs with verified GO behavior. These are (1) Zn2(bpdc)2(bpee), which expands from a relative amorphous to crystalline structure and (2) Cu[(dhbc) 2(4,4f-bpy)]H2O, a mutually interdigitated 2-D structure (bpdc = biphenyldicarboxylate, bpee = 1,2]bipyridylethene; DMF = N,N-dimethyl formamide, dhbc= 2,5-dihydroxybenzoic acid, bpy=bipyridine). Both sub- and super-critical adsorption data were collected using three adsorption units: a standard low-pressure volumetric adsorption unit, a commercial high-pressure gravimetric analyzer and a custom-built high-pressure differential volumetric unit. Collected laboratory data were combined with published adsorption rate and isotherm data for analysis to broaden the range of data collection. The accuracy of the high-pressure differential unit was improved by over 300-fold by changing analytical methods of processing data to establish a reliable null correction. A pronounced effect of the allowed experimental time was found at cryogenic temperatures on (1). Tightening the stability criteria used by the adsorption equipment to determine equilibration increased the experimental time from the order of

  15. Simultaneous determination of ultra trace amounts of lead and cadmium in food samples by adsorptive stripping voltammetry.

    Science.gov (United States)

    Abbasi, Shahryar; Khodarahmiyan, Kobra; Abbasi, Freshteh

    2011-09-01

    A selective and sensitive method for simultaneous determination of lead and cadmium by adsorptive differential pulse cathodic stripping voltammetry is presented. The method is based on adsorptive accumulation of the complexes of Pb (II) and Cd (II) ions with 2-mercaptobenzothiazole onto hanging mercury drop electrode (HMDE), followed by the reduction of the adsorbed species by differential pulse cathodic stripping voltammetry. Optimal conditions were obtained at pH 8.0, 2-mercaptobenzothiazole concentration of 1.0×10(-4)M, the accumulation potential of -0.4V (vs. Ag/AgCl), the accumulation time of 160s, and the scan rate of 100mV/s. Under optimised conditions, linear calibration curves were established for the concentration of Pb (II) and Cd (II) in the range of 0.5-70 and 0.2-30ng/ml, respectively, with detection limit of 0.017ng/ml for Pb (II) and 0.01ng/ml for Cd (II). The procedure was successfully applied to the simultaneous determination of both ions in food samples (rice, soya and sugar). PMID:25214357

  16. Off-line isothermal gas chromatography of Zr and Hf compounds

    International Nuclear Information System (INIS)

    We obtained isothermal chromatographic data of Zr and Hf chlorides in a macro-scale (about 1018 molecules). The adsorption enthalpies(ΔHa) of the Zr and Hf chlorides on a quartz surface were determined to be about -78 kJ/mol and -73 kJ/mol, respectively, with analyzing these retention curves. The present ΔHa values are very different from the earlier work in micro-scale, but agree with the volatility deduced from the vapor pressure in macro-scale. (author)

  17. Adsorption characteristics and heat of adsorption measurements of R-134a on activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Saha, Bidyut B. [Mechanical Engineering Department, National University of Singapore, 10 Kent Ridge Crescent (Singapore); Habib, Khairul; Koyama, Shigeru [Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-koen, Kasuga-shi, Fukuoka 816-8580 (Japan); El-Sharkawy, Ibrahim I. [Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-koen, Kasuga-shi, Fukuoka 816-8580 (Japan); Mechanical Power Engineering Department, Faculty of Engineering, Mansoura University, El-Mansoura (Egypt)

    2009-11-15

    This paper presents adsorption isotherms of R-134a (HFC-134a) on highly porous pitch based activated carbon (Maxsorb III) in the temperature range of 5-70 C and pressures up to 12 bar, using desorption method. The experimental data have been fitted with the Dubinin-Astakhov (D-A) isotherm equation. The adsorption isotherms of R-134a on Maxsorb III obtained from the present study are compared with the adsorption isotherm results of R-134a on similar type of adsorbents obtained by other researchers and they are found to be fairly consistent. The isosteric heat of adsorption of the assorted adsorbent-refrigerant pair has also been extracted from the present experimental data. (author)

  18. The determination of adsorption capacity of anion exchange resin Dowex-Marathon for Ti(IV) and Fe(III) chlorocomplexes

    International Nuclear Information System (INIS)

    Full text: The adsorption capacity of anion exchange resin Dowex-Marathon for Ti(IV) and Fe(III) chlorocomplexes from HCl solution was determined. The measurements were performed for different HCl solution concentrations and temperatures using batch operation as contact method between solution and resin. The Fe(III) adsorption capacities increased with HCl solution concentrations and contact temperatures. In the case of Ti(IV) considerable adsorption capacities were observed only at HCl concentrations >7 M. For the same ion the adsorption capacity does not depend on temperature in the range of 30 - 70 deg C. At 50 deg C there is an important difference between adsorption capacity for Fe(III), (105.7 mg Fe/g dry resin) and for U(VI), (227 mg U/g dry resin), allowing the recovery of uranium adsorption band in the 235U enriching column, using band displacement technique. A solution of TiCl3 0.1 M in HCl >7 M can be utilized as reduction agent at the rear edge of the uranium band, according to the important adsorption capacity of Ti(IV) in those conditions. (author)

  19. Investigation of radiotracer adsorption

    International Nuclear Information System (INIS)

    Results of laboratory investigation of adsorption of radiotracers in several soil materials are presented. Compounds were chosen which are applied in hydrogeology for tracer determination of underground water flow parameters. Adsorption values were measured as functions of the following parameters: solution concentration, adsorption duration, concentration of hydrogen ions and ion strength of the solution. The most interesting results are: a linear dependence of adsorption on the solution concentration (observed in a wide range of concentrations), and an extended period (several tens of minutes) necessary for the adsorption system to achieve a state approaching dynamic equilibrium. (author)

  20. Isothermal calorimeter for reactor radiation dosimetry

    International Nuclear Information System (INIS)

    An isothermal calorimeter with thermistors for measuring absorbed dose rates from 104-5-6.105 rad/h in reactor experimental holes has been designed. A kinetics method for determining the equilibrium temperature difference has been developed, and its application in isothermal calorimetry proved. The expected accuracy in measurements within ± 2-5% has been proved by measurements carried out in the reactor. Some data obtained by measurements in the reactor RA are presented (author)

  1. Removal of Pb2+ and Cd2+ by adsorption on clay-solidified grouting curtain for waste landfills

    Institute of Scientific and Technical Information of China (English)

    CHEN Yong-gui; ZHANG Ke-neng; ZOU Yin-sheng; DENG Fei-yue

    2006-01-01

    Pb2+ and Cd2+ in leachate were adsorbed on clay-solidified grouting curtain for waste landfills with equilibrium experiment. The cation exchange capacity was determined with ammonium acetate. And the concentration of heavy metal cations in leachate was determined with atomic absorption spectrophotometer. Their equilibrium isotherms were measured, and the experimental isotherm data were analyzed by using Freundlich and Langmuir models. The results show that the adsorption capacities of the heavy metal cations are closely related to the compositions of clay-solidified grouting curtain, and the maximum adsorption appears at the ratio of cement to clay of 2: 4 in the experimental conditions. At their maximum adsorption and pH 5.0, the adsorption capacities of Pb2+ and Cd2+ are 16.19 mg/g and 1.21 mg/g. The competitive adsorption coefficients indicate that the adsorption of clay-solidified grouting curtain for Pb2+ is stronger than that for Cd2+. The adsorption process conforms to Freundlich's model with related coefficient higher than 0. 996.

  2. Polysiloxane surface modified with bipyrazolic tripodal receptor for quantitative lead adsorption

    International Nuclear Information System (INIS)

    A new silica gel compound modified N,N-bis(3,5-dimethylpyrazol-1-ylmethyl) amine (SiN2Pz) was synthesized and characterized by elemental analysis, FT-IR, 13C NMR of the solid state, nitrogen adsorption-desorption isotherm, BET surface area and BJH pore sizes. The new surface exhibits good chemical and thermal stability determined by thermogravimetry curves (TGA). The effect of pH and stirring time on the adsorption of Pb(II) were studied. The process of metal retention was followed by batch method and the optimum pH value for the quantitative adsorption of this toxic metal ion was 7. At this pH value, the new functionalized polysiloxane presents further improvements and shows higher affinity (123 mg of Pb2+/g of silica) for the effective adsorption of Pb(II) compared to others described sorbents. The extracted amounts of Pb(II) were determined by atomic absorption measurements.

  3. Application of novel Polypyrrole/thiol-functionalized zeolite Beta/MCM-41 type mesoporous silica nanocomposite for adsorption of Hg{sup 2+} from aqueous solution and industrial wastewater: Kinetic, isotherm and thermodynamic studies

    Energy Technology Data Exchange (ETDEWEB)

    Javadian, Hamedreza, E-mail: Hamedreza.Javadian@yahoo.com [Department of Chemical Engineering, Shahrood Branch, Islamic Azad University, Shahrood, Islamic Republic of Iran (Iran, Islamic Republic of); Taghavi, Mehdi [Polymer Chemistry Research Laboratory, Department of Chemistry, University of Mazandaran, Babolsar, 47416-95447, Islamic Republic of Iran (Iran, Islamic Republic of)

    2014-01-15

    Hierarchical zeolite consists of both microporous and unordered mesoporous structures. A composite of Polypyrrole/thiol-functionalized Beta/MCM-41 (PPy/SH-Beta/MCM-41) was prepared, characterized by FE-SEM, FT-IR, XRD, TGA and BET analysis and applied in the investigation of its adsorption characteristics for the removal of Hg{sup 2+} ions from aqueous solutions. Thiol-functionalized Beta/MCM-41 (SH-Beta/MCM-41) was prepared by 3-mercaptopropyltrimethoxysilane (MPTMS) in the presence of aerosil-200 as a silica source by two-step hydrothermal crystallization procedure. Batch mode experiments were conducted and three kinetic models were used to describe the adsorption process. The experimental data fitted very well with the Pseudo-second-order kinetic model. The calculated thermodynamic parameters (ΔH, ΔS and ΔG) revealed that the adsorption of Hg{sup 2+} onto PPy/SH-Beta/MCM-41 is an endothermic and spontaneous process. It was found that temperature has a positive effect on the removal efficiency and that PPy/SH-Beta/MCM-41 is potentially able to remove Hg{sup 2+} ions from aqueous solutions at even high concentrations (400 mg L{sup −1}). The recovery of Hg{sup 2+} from the PPy/SH-Beta/MCM-41 adsorbent was found to be more than 90% using 0.5 M H{sub 2}SO{sub 4}, and the ability of the absorbent to be reused for removal of Hg{sup 2+} was investigated.

  4. Adsorbent for p-phenylenediamine adsorption and removal based on graphene oxide functionalized with magnetic cyclodextrin

    Science.gov (United States)

    Wang, Dongxue; Liu, Liangliang; Jiang, Xinyu; Yu, Jingang; Chen, Xiaohong; Chen, Xiaoqing

    2015-02-01

    Recently, graphene oxide (GO) based magnetic nanocomposites have been widely used in an adsorption-based process for the removal of organic pollutants from the water system. In this study, magnetic β-cyclodextrin-graphene oxide nanocomposites (MCG) were synthesized according to covalent binding of magnetic β-cyclodextrin nanoparticles onto the GO surface and the as-made nanocomposites were successfully applied as adsorbents for the adsorption and removal of p-phenylenediamines (PPD). The composition and morphology of prepared materials were characterized by Fourier infrared spectrometry (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Effects of pH, temperature, time and reusability on the adsorption of PPD were investigated, as well as the kinetics and isotherms parameters of the adsorbents were determined. The results indicated that the maximum adsorption capacity of MCG was 1102.58 mg/g at 45 °C and pH 8. The adsorption capacity remained at 81% after five cycles. Removal rate could reach 98% after three times of adsorption. The adsorption process with PPD was found that fitted pseudo-second-order kinetics equations and the Langmuir adsorption model. The results showed the MCG had a good adsorption ability to remove organic pollutants in wastewater.

  5. Highly selective in situ metal ion determination by hybrid electrochemical 'adsorption-desorption' and colorimetric methods

    Energy Technology Data Exchange (ETDEWEB)

    Li Meng; Li Dawei; Li Yuanting [Shanghai Key Laboratory of Functional Materials Chemistry, East China University of Science and Technology, Shanghai, 200237 (China); Xu Danke [Department of Chemistry, Nanjing University, Nanjing, 210093 (China); Long Yitao, E-mail: ytlong@ecust.edu.cn [Shanghai Key Laboratory of Functional Materials Chemistry, East China University of Science and Technology, Shanghai, 200237 (China)

    2011-09-09

    Graphical abstract: A hybrid method coupling electrochemical 'adsorption-desorption' and colorimetric analyses may be used for the in situ determination of heavy metal ions in turbid water samples. Highlights: {center_dot} A novel hybrid analytical method was applied to detect Cd{sup 2+}, Pb{sup 2+} and Cu{sup 2+} in turbid, polluted water. {center_dot} Combing electrochemical 'adsorption-desorption' with colorimetric methods. {center_dot} Portable screen-printed electrodes (SPEs) used as working devices. {center_dot} Practicality was confirmed by detecting real samples and results agreed with ICP-AES. - Abstract: A novel and facile hybrid analytical method coupling electrochemical 'adsorption-desorption' and colorimetric analyses was developed to detect heavy metal ions in turbid water samples. The target metal ions were deposited onto an electrode inserted into the original sample, which was referred to as the 'adsorption' process. After changing the medium, the concentrated target metal ions were dissolved in a new, clean buffer (blank buffer), which was referred to as the 'desorption' process. The concentrations of the target metal ions were measured by colorimetric analyses after the addition of specific indicator amounts. We demonstrated the applicability of this method by detecting Cd{sup 2+}, Pb{sup 2+} and Cu{sup 2+} with co-depositing Bi{sup 3+} on portable screen-printed electrodes (SPEs). A good correlation (correlation coefficient of R = 0.997) was observed between concentrations ranging from 1 to 200 {mu}M and absorbance values. After the multiple 'desorption' process, the even better detection limits as low as 10, 10 and 100 nM were achieved for Cd{sup 2+}, Pb{sup 2+} and Cu{sup 2+}, respectively. The practicality of this hybrid method was confirmed by the detection of Cd{sup 2+}, Pb{sup 2+} and Cu{sup 2+} in wastewater samples, and these results were in agreement with inductively coupled

  6. Adsorbent for p-phenylenediamine adsorption and removal based on graphene oxide functionalized with magnetic cyclodextrin

    International Nuclear Information System (INIS)

    Highlights: • Magnetic β-cyclodextrin-graphene oxide (MCG) show high adsorption capacity. • The maximum adsorption capacity was 1102.58 mg/g at 45 °C and pH 8. • MCG can be easily and fast extracted from water by magnetic attraction. • Removal rate of MCG could reach 98% after three times of adsorption. • Adsorption capacity of MCG remained at 81% after five cycles. - Abstract: Recently, graphene oxide (GO) based magnetic nanocomposites have been widely used in an adsorption-based process for the removal of organic pollutants from the water system. In this study, magnetic β-cyclodextrin-graphene oxide nanocomposites (MCG) were synthesized according to covalent binding of magnetic β-cyclodextrin nanoparticles onto the GO surface and the as-made nanocomposites were successfully applied as adsorbents for the adsorption and removal of p-phenylenediamines (PPD). The composition and morphology of prepared materials were characterized by Fourier infrared spectrometry (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Effects of pH, temperature, time and reusability on the adsorption of PPD were investigated, as well as the kinetics and isotherms parameters of the adsorbents were determined. The results indicated that the maximum adsorption capacity of MCG was 1102.58 mg/g at 45 °C and pH 8. The adsorption capacity remained at 81% after five cycles. Removal rate could reach 98% after three times of adsorption. The adsorption process with PPD was found that fitted pseudo-second-order kinetics equations and the Langmuir adsorption model. The results showed the MCG had a good adsorption ability to remove organic pollutants in wastewater

  7. Adsorbent for p-phenylenediamine adsorption and removal based on graphene oxide functionalized with magnetic cyclodextrin

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Dongxue; Liu, Liangliang; Jiang, Xinyu; Yu, Jingang [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Chen, Xiaohong [Collaborative Innovation Center of Resource-conserving & Environment-friendly Society and Ecological Civilization, Changsha, 410083 (China); Chen, Xiaoqing, E-mail: xqchen@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Collaborative Innovation Center of Resource-conserving & Environment-friendly Society and Ecological Civilization, Changsha, 410083 (China)

    2015-02-28

    Highlights: • Magnetic β-cyclodextrin-graphene oxide (MCG) show high adsorption capacity. • The maximum adsorption capacity was 1102.58 mg/g at 45 °C and pH 8. • MCG can be easily and fast extracted from water by magnetic attraction. • Removal rate of MCG could reach 98% after three times of adsorption. • Adsorption capacity of MCG remained at 81% after five cycles. - Abstract: Recently, graphene oxide (GO) based magnetic nanocomposites have been widely used in an adsorption-based process for the removal of organic pollutants from the water system. In this study, magnetic β-cyclodextrin-graphene oxide nanocomposites (MCG) were synthesized according to covalent binding of magnetic β-cyclodextrin nanoparticles onto the GO surface and the as-made nanocomposites were successfully applied as adsorbents for the adsorption and removal of p-phenylenediamines (PPD). The composition and morphology of prepared materials were characterized by Fourier infrared spectrometry (FT-IR), transmission electron microscopy (TEM), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Effects of pH, temperature, time and reusability on the adsorption of PPD were investigated, as well as the kinetics and isotherms parameters of the adsorbents were determined. The results indicated that the maximum adsorption capacity of MCG was 1102.58 mg/g at 45 °C and pH 8. The adsorption capacity remained at 81% after five cycles. Removal rate could reach 98% after three times of adsorption. The adsorption process with PPD was found that fitted pseudo-second-order kinetics equations and the Langmuir adsorption model. The results showed the MCG had a good adsorption ability to remove organic pollutants in wastewater.

  8. Characterization and determination of the thermodynamic and kinetic properties of the adsorption of molybdenum (VI) onto microcrystalline anthracene modified with 8-hydroxyquinoline

    International Nuclear Information System (INIS)

    A reliable and effective method for the determination of trace molybdenum in effluents is proposed. Molybdenum (VI) is analyzed by Microwave Plasma Torch Optical Emission Spectrometry (MPT-OES) based on the adsorption collection onto microcrystalline anthracene modified with 8-hydroxyquinoline. The possible reaction mechanism was discussed in detail and the optimum conditions for adsorption of Mo (VI) were confirmed. The experimental data were fitted well with the pseudo-second-order kinetic model and Langmuir model at all studied temperatures. The calculated thermodynamic parameters (ΔGT, ΔHT and ΔST) showed that the adsorption of molybdenum onto microcrystalline anthracene was feasible, spontaneous and endothermic at 280-320 K. The recovery of this method is in the range of 96.5%-103.3% with preconcentration factor of 100 and the limit detection after preconcentration is 0.078 μg L-1. The proposed method has been successfully applied to the determination of trace Mo (VI) in environmental water samples with satisfactory results. Highlights: → The preparation of the sorbent, MICRO-AN-8-hydroxyquinoline, is relatively simple. → Excellent properties of the sorbent have been illustrated in detail. → Exhaustive data concerning Mo(VI) adsorption behavior are provided. → Adsorption mechanism is firstly discussed from the view of ion-exchange reaction. → Offer reference for the studies on other metal ions adsorption onto the sorbent.

  9. Characterization and determination of the thermodynamic and kinetic properties of the adsorption of molybdenum (VI) onto microcrystalline anthracene modified with 8-hydroxyquinoline

    Energy Technology Data Exchange (ETDEWEB)

    Wang Xu [College of Chemistry and Environmental Science, Henan Normal University, Henan Key Laboratory for Environmental Pollution Control, Xinxiang, Henan 453007 (China); Zhang Yan [College of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang, Henan 453003 (China); Li Quanmin, E-mail: mercury6068@hotmail.com [College of Chemistry and Environmental Science, Henan Normal University, Henan Key Laboratory for Environmental Pollution Control, Xinxiang, Henan 453007 (China)

    2011-12-01

    A reliable and effective method for the determination of trace molybdenum in effluents is proposed. Molybdenum (VI) is analyzed by Microwave Plasma Torch Optical Emission Spectrometry (MPT-OES) based on the adsorption collection onto microcrystalline anthracene modified with 8-hydroxyquinoline. The possible reaction mechanism was discussed in detail and the optimum conditions for adsorption of Mo (VI) were confirmed. The experimental data were fitted well with the pseudo-second-order kinetic model and Langmuir model at all studied temperatures. The calculated thermodynamic parameters ({Delta}G{sup T}, {Delta}H{sup T} and {Delta}S{sup T}) showed that the adsorption of molybdenum onto microcrystalline anthracene was feasible, spontaneous and endothermic at 280-320 K. The recovery of this method is in the range of 96.5%-103.3% with preconcentration factor of 100 and the limit detection after preconcentration is 0.078 {mu}g L{sup -1}. The proposed method has been successfully applied to the determination of trace Mo (VI) in environmental water samples with satisfactory results. Highlights: {yields} The preparation of the sorbent, MICRO-AN-8-hydroxyquinoline, is relatively simple. {yields} Excellent properties of the sorbent have been illustrated in detail. {yields} Exhaustive data concerning Mo(VI) adsorption behavior are provided. {yields} Adsorption mechanism is firstly discussed from the view of ion-exchange reaction. {yields} Offer reference for the studies on other metal ions adsorption onto the sorbent.

  10. Dye adsorption behavior of Luffa cylindrica fibers.

    Science.gov (United States)

    Demir, H; Top, A; Balköse, D; Ulkü, S

    2008-05-01

    Using natural Luffa cylindrica fibers as adsorbent removal of methylene blue dye from aqueous solutions at different temperatures and dye concentrations was investigated in this study. Thermodynamics and kinetics of adsorption were also investigated. The adsorption isotherms could be well defined with Langmuir model instead of Freundlich model. The thermodynamic parameters of methylene blue (MB) adsorption indicated that the adsorption is exothermic and spontaneous. The average MB adsorption capacity was found out as 49 mg/g and average BET surface area of fibers was calculated as 123 m(2)/g. PMID:17919814

  11. Dye adsorption behavior of Luffa cylindrica fibers

    International Nuclear Information System (INIS)

    Using natural Luffa cylindrica fibers as adsorbent removal of methylene blue dye from aqueous solutions at different temperatures and dye concentrations was investigated in this study. Thermodynamics and kinetics of adsorption were also investigated. The adsorption isotherms could be well defined with Langmuir model instead of Freundlich model. The thermodynamic parameters of methylene blue (MB) adsorption indicated that the adsorption is exothermic and spontaneous. The average MB adsorption capacity was found out as 49 mg/g and average BET surface area of fibers was calculated as 123 m2/g

  12. Dye adsorption behavior of Luffa cylindrica fibers

    Energy Technology Data Exchange (ETDEWEB)

    Demir, H. [Izmir Institute of Technology, Faculty of Engineering, Department of Chemical Engineering, Guelbahce Campus, 35430 Urla Izmir (Turkey)], E-mail: hasandemir@iyte.edu.tr; Top, A.; Balkoese, D.; Ulkue, S. [Izmir Institute of Technology, Faculty of Engineering, Department of Chemical Engineering, Guelbahce Campus, 35430 Urla Izmir (Turkey)

    2008-05-01

    Using natural Luffa cylindrica fibers as adsorbent removal of methylene blue dye from aqueous solutions at different temperatures and dye concentrations was investigated in this study. Thermodynamics and kinetics of adsorption were also investigated. The adsorption isotherms could be well defined with Langmuir model instead of Freundlich model. The thermodynamic parameters of methylene blue (MB) adsorption indicated that the adsorption is exothermic and spontaneous. The average MB adsorption capacity was found out as 49 mg/g and average BET surface area of fibers was calculated as 123 m{sup 2}/g.

  13. Sensitive Adsorptive Voltammetric Method for Determination of Bisphenol A by Gold Nanoparticle/Polyvinylpyrrolidone-Modified Pencil Graphite Electrode

    Directory of Open Access Journals (Sweden)

    Yesim Tugce Yaman

    2016-05-01

    Full Text Available A novel electrochemical sensor gold nanoparticle (AuNP/polyvinylpyrrolidone (PVP modified pencil graphite electrode (PGE was developed for the ultrasensitive determination of Bisphenol A (BPA. The gold nanoparticles were electrodeposited by constant potential electrolysis and PVP was attached by passive adsorption onto the electrode surface. The electrode surfaces were characterized by electrochemical impedance spectroscopy (EIS and scanning electron microscopy (SEM. The parameters that affected the experimental conditions were researched and optimized. The AuNP/PVP/PGE sensor provided high sensitivity and selectivity for BPA recognition by using square wave adsorptive stripping voltammetry (SWAdSV. Under optimized conditions, the detection limit was found to be 1.0 nM. This new sensor system offered the advantages of simple fabrication which aided the expeditious replication, low cost, fast response, high sensitivity and low background current for BPA. This new sensor system was successfully tested for the detection of the amount of BPA in bottled drinking water with high reliability.

  14. Sensitive Adsorptive Voltammetric Method for Determination of Bisphenol A by Gold Nanoparticle/Polyvinylpyrrolidone-Modified Pencil Graphite Electrode

    Science.gov (United States)

    Yaman, Yesim Tugce; Abaci, Serdar

    2016-01-01

    A novel electrochemical sensor gold nanoparticle (AuNP)/polyvinylpyrrolidone (PVP) modified pencil graphite electrode (PGE) was developed for the ultrasensitive determination of Bisphenol A (BPA). The gold nanoparticles were electrodeposited by constant potential electrolysis and PVP was attached by passive adsorption onto the electrode surface. The electrode surfaces were characterized by electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). The parameters that affected the experimental conditions were researched and optimized. The AuNP/PVP/PGE sensor provided high sensitivity and selectivity for BPA recognition by using square wave adsorptive stripping voltammetry (SWAdSV). Under optimized conditions, the detection limit was found to be 1.0 nM. This new sensor system offered the advantages of simple fabrication which aided the expeditious replication, low cost, fast response, high sensitivity and low background current for BPA. This new sensor system was successfully tested for the detection of the amount of BPA in bottled drinking water with high reliability. PMID:27231912

  15. Electrochemical behavior of folic acid at calixarene based chemically modified electrodes and its determination by adsorptive stripping voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Vishwanath D. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India); Srivastava, Ashwini K. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India)], E-mail: aksrivastava@chem.mu.ac.in

    2007-12-31

    Voltammetric behavior of folic acid at plain carbon paste electrode and electrode modified with calixarenes has been studied. Two peaks for irreversible oxidation were observed. Out of the three calixarenes chosen for modification of the electrodes, p-tert-butyl-calix[6]arene modified electrode (CME-6) was found to have better sensitivity for folic acid. Chronocoulometric and differential pulse voltammetric studies reveal that folic acid can assemble at CME-6 to form a monolayer whose electron transfer rate is 0.00273 s{sup -1} with 2-electron/2-proton transfer for the peak at +0.71 V against SCE. An adsorption equilibrium constant of 5 x 10{sup 3} l/mol for maximum surface coverage of 2.89 x 10{sup -10} mol/cm{sup 2} was obtained. The current is found to be rectilinear with concentration by differential pulse voltammetry. However, linearity in the lower range of concentration 8.79 x 10{sup -12} M to 1.93 x 10{sup -9} M with correlation coefficient of 0.9920 was achieved by adsorptive stripping voltammetry. The limit of detection obtained was found to be 1.24 x 10{sup -12} M. This method was used for the determination of folic acid in a variety of samples, viz. serum, asparagus, spinach, oranges and multivitamin preparations.

  16. Characterization and adsorption mechanism of Zn2+ removal by PVA/EDTA resin in polluted water

    International Nuclear Information System (INIS)

    Batch adsorption experiments were conducted using a PVA/EDTA resin as an adsorbent to adsorb Zn(II) ions from single component system in which experimental parameters were studied including solution pH, contact time, adsorbent dose and initial metal ions concentration. The equilibrium isotherms were determined at pH 6 under constant ionic strength and at different temperatures. The results showed that the maximum removal of Zn(II) (99.8%) with 1 g L-1 of sorbent was observed at 40 mg L-1 at an initial pH value of 6. Removals of about 60-70% occurred in 15 min, and equilibrium was attained at around 30 min. The equilibrium data for the adsorption of Zn(II) on PVA/EDTA resin was tested with various adsorption isotherm models among which three models were found to be suitable for the Zn(II) adsorption. In addition, the kinetic adsorption fitted well to the pseudo-second-order model and the corresponding rate constants were obtained. Thermodynamic aspects of the adsorption process were also investigated. Furthermore a higher desorption efficiency of Zn(II) from the PVA/EDTA resin using acid treatment was available by more than 95%.

  17. Controlled swelling and adsorption properties of polyacrylate/montmorillonite composites

    Energy Technology Data Exchange (ETDEWEB)

    Natkanski, Piotr [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Kustrowski, Piotr, E-mail: kustrows@chemia.uj.edu.pl [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Bialas, Anna; Piwowarska, Zofia [Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow (Poland); Michalik, Marek [Institute of Geological Sciences, Jagiellonian University, Oleandry 2a, 30-063 Krakow (Poland)

    2012-10-15

    A series of novel polyacrylate/montmorillonite composites was synthesized by in situ polymerization in aqueous slurry of clay. Dissociated (obtained by adding ammonium or sodium hydroxide) and undissociated forms of acrylic acid were used as monomers in the hydrogel synthesis. The structure and composition of the samples were studied by powder X-ray diffraction, diffuse reflectance infra-red Fourier transform spectroscopy, thermogravimetry and elemental analysis. It has been found that the kind of monomer influences strongly the location of a polymer chain in the formed composite. Complete intercalation of hydrogel into the interlayer space of montmorillonite was observed for sodium polyacrylate, whereas polyacrylic acid and ammonium polyacrylate mainly occupied the outer surface of the clay. The position of hydrogel determined the swelling and adsorption properties of the studied composites. The important factor influencing the kinetics of Fe(III) cation adsorption was pH. The analysis of adsorption isotherms allowed to propose the mechanism of Fe(III) cation adsorption. Highlights: Black-Right-Pointing-Pointer Polyacrylate hydrogels can be introduced into the interlayers of clay. Black-Right-Pointing-Pointer The position of hydrogel in the composite depends on the polymer type. Black-Right-Pointing-Pointer Ammonium polyacrylate places outside the clay, sodium one is intercalated into it. Black-Right-Pointing-Pointer Swelling and adsorption capacities can be controlled by the polymer position. Black-Right-Pointing-Pointer High adsorption efficiency in Fe(III) removal was observed.

  18. Visualizing Gas Adsorption on Porous Solids: Four Simple, Effective Demonstrations

    Science.gov (United States)

    Cheung, Ocean

    2014-01-01

    Gas adsorption on porous solids is a topic that is often discussed in an undergraduate chemistry or chemical engineering course. The idea of porosity and gas adsorption on a porous solid is usually discussed with adsorption isotherms recorded using commercially available equipment. This discussion can be rather abstract and can be difficult for…

  19. The adsorption mechanism of nortryptiline on C18-bonded discovery

    Energy Technology Data Exchange (ETDEWEB)

    Gritti, Fabrice [University of Tennessee, Knoxville (UTK); Guiochon, Georges A [ORNL

    2005-08-01

    The adsorption isotherms of an ionizable compound, nortriptyline, were accurately measured by frontal analysis (FA) on a C{sub 18}-Discovery column, first without buffer (in an aqueous solution of acetonitrile at 15%, v/v of ACN), then with a buffer (in 28%, v/v ACN solution). The buffers were aqueous solutions containing 20 mM of formic acid or a phosphate buffer at pH 2.70. The linear range of the isotherm could not be reached with the non-buffered mobile phase using a dynamic range larger than 40,000 (from 1.2 x 10{sup -3} g/L to 50 g/L). With a 20 mM buffer in the liquid phase, the isotherm is linear for concentrations of nortriptyline inferior to 10{sup -3} g/L (or 3 {micro} mol/L). The adsorption energy distribution (AED) was calculated to determine the heterogeneity of the adsorption process. AED and FA were consistent and lead to a trimodal distribution. A tri-Moreau and a tri-Langmuir isotherm models accounted the best for the adsorption of nortriptyline without and with buffer, respectively. The nature of the buffer affects significantly the middle-energy sites while the properties of the lowest and highest of the three types of energy sites are almost unchanged. The desorption profiles of nortriptyline show some anomalies in relation with the formation of a complex multilayer adsorbed phase of acetonitrile whose excess isotherm was measured by the minor disturbance method. The C{sub 18}-Discovery column has about the same total saturation capacity, around 200 g of nortriptyline per liter of adsorbent (or 116 mg/g), with or without buffer. About 98-99% of the available surface consists in low energy sites. The coexistence of these different types of sites on the surface solves the McCalley's enigma, that the column efficiency begins to drop rapidly when the analyte concentration reaches values that are almost one hundred times lower than those that could be predicted from the isotherm data acquired under the same experimental conditions. Due to the

  20. Study of cesium and strontium adsorption on slovak bentonite

    International Nuclear Information System (INIS)

    Bentonite is a natural clay and one of the most promising candidates for use as a buffer material in the geological disposal systems for high-level radioactive waste and spent nuclear fuel. It is intended to isolate metal canisters with highly radioactive waste products from the surrounding rocks because of its ability to retard the movement of radionuclides by adsorption. Slovak Republic avails of many significant deposits of bentonite. Adsorption of Cs and Sr on five Slovak bentonite of deposits (Jelsovy potok, Kopernica, Lieskovec, Lastovce and Dolna Ves) and montmorillonite K10 (Sigma-Aldrich) has been studied with the using batch of radiometric techniques. Natural, irradiated and natrified samples, in three different kinds of grain size: 15, 45 and 250 μm have been used in the experiments. The adsorptions of Cs and Sr on bentonite under various experimental conditions, such as contact time, adsorbent and adsorbate concentrations, pH after adsorption and effect of pH change, chemical modification, competitive ions and organic agents on the adsorption have been studied. The Kd have been determined for adsorbent-Cs/Sr solution system as a function of contact time and adsorbate and adsorbent concentration. The data have been interpreted in terms of Langmuir isotherm. The adsorption of Cs and Sr has increased with increasing metal concentrations. Adsorption of Cs and Sr has been suppressed by presence of organic agents; and of bivalent cations more than univalent cations. By adsorption on natrified samples colloidal particles and pH value increase have been formed. Adsorption experiments carried out show that the most suitable materials intended for use as barriers surrounding a canister of spent nuclear fuel are bentonite of the Jelsovy potok and Kopernica deposits. (author)

  1. Modeling the Adsorption of Hydrophobic Ethoxylated Urethane (HEUR) Thickeners onto Latex Surfaces using Self-Consistent Field Theory

    Science.gov (United States)

    Ginzburg, Valeriy; van Dyk, Antony; Chatterjee, Tirtha; Wang, Shihu; Larson, Ronald

    2015-03-01

    Hydrophobic Ethoxylated Urethane (HEUR) polymers are widely used as rheology modifiers (thickeners) in waterborne latex paints. Recently, it has been shown that the thickening effect of HEURs in paints is largely determined by their adsorption onto latex surfaces, this adsorption being a function of polymer structure, latex surface chemistry, and total available latex surface. Here, we describe the application of Self-Consistent Field Theory (SCFT) to calculate adsorption isotherms of several model HEURs onto ideal hydrophobic latex surfaces. Unlike earlier SCFT studies of adsorption, we explicitly take into account the role of HEUR micelles and competition between adsorption and micellization. The results are compared with experimental data and coarse-grained molecular dynamic (CG-MD) simulations, and good qualitative and semi-quantitative agreement is found. This work was supported by The Dow Chemical Company.

  2. Adsorption studies at ionized surface layers by means of hot atoms

    International Nuclear Information System (INIS)

    Adsorption of ions at the surface of solutions of ionic surface-active substances can directly be studied using hot atoms. Extremely small amounts of suitable radioactive ions, or ions liable to undergo induced nuclear transformations in situ, are added to such solutions, replacing some of the normal counter ions coadsorbed at the primary-adsorbed organic ions. Hot atoms with energies from about 100 keV down to a few electron volts give ranges in water from about 1000 A down to monomoleeular layers. This makes them suitable for sensitive surface layer studies. The hot atoms ejected from the surface are collected and counted. Among α-disintegration recoils, the system Bi212/Tl208 has proved to be suitable. Now, by refining the method, valuable information about adsorption conditions at sodium dodecyl sulphate surface layers could be found. The kinetics of adsorption was studied by following in time the collected recoil activity caused by Bi-ion adsorption. Adsorption isotherms of Bi-ions as a function of the bulk concentration of the surface-active substance under varying conditions of ionic strength, pH and Bi212 activity were measured. By comparing these isotherms with those obtained by measuring the surface tension of the solutions and calculating the surface excess with the aid of a suitably modified Gibbs' isotherm, the adsorption of Bi+++ and Pb++ relative to that of Na+ and H3O+, and by this the extent of ion exchange in the adsorbed layer could be determined. As the method measures the adsorption of charged species, surface reactions transforming primary-adsorbed organic anions to a non-ionic state could be followed. Conclusions could be drawn about the formation of a non-ionized acid soap in the surface and about micelle formation in the bulk under various experimental conditions. (author)

  3. Adsorption of remazol yellow FG from aqueous solution on chitosan-linked P-T-Butylcalix[4]Arene

    Science.gov (United States)

    Suci Handayani, Desi; Purnawan, Candra; Pranoto; Hastuti, Sri; Hilmiyana, Diniyah

    2016-02-01

    Chitosan-liked p-t-butylcalix[4]arene can be applied as an adsorbent of dye Remazol Yellow FG because it has an active group of hydroxy (-OH) and amine (-NH2). Adsorption had done by comparing to chitosan. Adsorption was carried out in a batch system. Several variables including pH, contact time, and initial concentration of dye Remazol Yellow FG were determined. The optimum adsorption conditions of dye Remazol Yellow FG by chitosan dan chitosan-liked p-t-butylcalix[4]arene occurred at pH 4 and a contact time of 135 minutes. The adsorption kinetics of dye Remazol Yellow FG using chitosan and chitosan-liked p-t- butylcalix[4]arene followed Ho kinetics model, pseudo-second order and the rate constant of adsorption was 2.42 x 10-4 g/mg.menit and 3.63 x 10-4 g/mg.menit. The isothermal study showed that adsorption of dye Remazol Yellow FG using chitosan and chitosan-liked p-t- butylcalix[4]arene tends to follow the Langmuir isotherm, with adsorption energy was 24.92 kJ/mol and 32.21 kJ/mol.

  4. Adsorption of cesium on cement mortar from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Volchek, Konstantin, E-mail: konstantin.volchek@ec.gc.ca [Emergencies Science and Technology Section, Environment Canada, 335 River Road, Ottawa, Ontario, Canada K1A 0H3 (Canada); Miah, Muhammed Yusuf [Emergencies Science and Technology Section, Environment Canada, 335 River Road, Ottawa, Ontario, Canada K1A 0H3 (Canada); Department of Applied Chemistry and Chemical Technology, Noakhali Science and Technology University (Bangladesh); Kuang, Wenxing; DeMaleki, Zack [Emergencies Science and Technology Section, Environment Canada, 335 River Road, Ottawa, Ontario, Canada K1A 0H3 (Canada); Tezel, F. Handan [Department of Chemical and Biological Engineering, University of Ottawa, 161 Louis-Pasteur, Ottawa, Ontario, Canada K1N 6N5 (Canada)

    2011-10-30

    Highlights: {yields} The adsorption of cesium on cement mortar was investigated in a range of temperatures and cesium concentrations. {yields} The pseudo-second order kinetic model produced a good fit with the experimental kinetic data. {yields} Equilibrium test results correlated well with the Freundlich isotherm adsorption model. {yields} The interaction between cesium ions and cement mortar was dominated by chemical adsorption. - Abstract: The adsorption of cesium on cement mortar from aqueous solutions was studied in series of bench-scale tests. The effects of cesium concentration, temperature and contact time on process kinetics and equilibrium were evaluated. Experiments were carried out in a range of initial cesium concentrations from 0.0103 to 10.88 mg L{sup -1} and temperatures from 278 to 313 K using coupons of cement mortar immersed in the solutions. Non-radioactive cesium chloride was used as a surrogate of the radioactive {sup 137}Cs. Solution samples were taken after set periods of time and analyzed by inductively coupled plasma mass spectroscopy. Depending on the initial cesium concentration, its equilibrium concentration in solution ranged from 0.0069 to 8.837 mg L{sup -1} while the respective surface concentration on coupons varied from 0.0395 to 22.34 {mu}g cm{sup -2}. Equilibrium test results correlated well with the Freundlich isotherm model for the entire test duration. Test results revealed that an increase in temperature resulted in an increase in adsorption rate and a decrease in equilibrium cesium surface concentration. Among several kinetic models considered, the pseudo-second order reaction model was found to be the best to describe the kinetic test results in the studied range of concentrations. The adsorption activation energy determined from Arrhenius equation was found to be approximately 55.9 kJ mol{sup -1} suggesting that chemisorption was the prevalent mechanism of interaction between cesium ions and cement mortar.

  5. Determination Of Adsorption And Paraffin Characterization Of Treatment To Adsorb Vegetable Oil

    International Nuclear Information System (INIS)

    Using vegetable oil repeatedly, beside affect on quality decline of food and the oil itself, it is harmful to human health. Some poisoning and carcinogenic symptom were founded with experiment using animals. According to that fact, the aim of the research is using paraffin and candle to adsorb used vegetable oil and to convert into solid sample, so it can be easily wasted. At first, 2 g of sample was poured into the heated oil, with gently stirrer until it turned cold and harden. Each sample and standard before and after treatment was characterized with Ftir, XRD, and DSc. The result shows that paraffins adsorbs 40 ml used vegetable oil with 2 g sample in proportion. That proportion is lower than the standard which can adsorb 66.67 ml vegetable oil in the same weight sample. The difference of paraffin and standard is caused by physical properties within that two materials, and it can be explained by Ftir, X-Ray Diffraction (XRD) and differential scanning calorimetry (DSc). Based on result of Ftir analysis, standard consented of saturated hydrocarbon compound (alkanes) whereas paraffin consisted of unsaturated hydrocarbon compound (alkenes). Infrared spectrum after treatment showed the changes of compound, O-H and esters group were formed and it shows characterised the adsorption process. The result of DSc analysis showed that crystalline the melting point of standard is 75,3oC and paraffin is 54,17oC. The result of analysis XRD, described that standard and paraffin before treatment are crystalline whereas after treatment are am orf

  6. High-performance liquid chromatography as a technique to determine protein adsorption onto hydrophilic/hydrophobic surfaces.

    Science.gov (United States)

    Huang, Tongtong; Anselme, Karine; Sarrailh, Segolene; Ponche, Arnaud

    2016-01-30

    The purpose of this study is to evaluate the potential of simple high performance liquid chromatography (HPLC) setup for quantification of adsorbed proteins on various type of plane substrates with limited area (Protein quantification was investigated with a liquid chromatography chain equipped with a size exclusion column or a reversed-phase column. By evaluating the validation of the method according to guidelines of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), all the results obtained by HPLC were reliable. By simple adsorption test at the contact of hydrophilic (glass) and hydrophobic (polydimethylsiloxane: PDMS) surfaces, kinetics of adsorption were determined and amounts of adsorbed bovine serum albumin, myoglobin and lysozyme were obtained: as expected for each protein, the amount adsorbed at the plateau on glass (between 0.15 μg/cm(2) and 0.4 μg/cm(2)) is lower than for hydrophobic PDMS surfaces (between 0.45 μg/cm(2) and 0.8 μg/cm(2)). These results were consistent with bicinchoninic acid protein determination. According to ICH guidelines, both Reversed Phase and Size Exclusion HPLC can be validated for quantification of adsorbed protein. However, we consider the size exclusion approach more interesting in this field because additional informations can be obtained for aggregative proteins. Indeed, monomer, dimer and oligomer of bovine serum albumin (BSA) were observed in the chromatogram. On increasing the temperature, we found a decrease of peak intensity of bovine serum albumin as well as the fraction of dimer and oligomer after contact with PDMS and glass surface. As the surface can act as a denaturation parameter, these informations can have a huge impact on the elucidation of the interfacial behavior of protein and in particular for aggregation processes in pharmaceutical applications. PMID:26621686

  7. Adsorption-transport modeling of anions through PVD membrane in the presence of the screen phenomenon

    Science.gov (United States)

    Madaeni, S. S.; Salehi, E.

    2009-01-01

    A mathematical model for transport and adsorption of chloride and sulphate ions through PVD membrane is presented at two pressures; 8 and 15 bar and 40 °C. The PVD membrane is negatively charged. Saturated brine containing NaCl with the concentration higher than 97% was challenged with the membrane as the feed. Other available ions in the solution were Fe 2+, Ca 2+, Mg 2+ and SO 42-. The screen effect of the cations on the membrane surface charge facilitates the passage of the anions through the membrane without any noticeable electrostatic repulsion. Hermia blocking laws combined with experimental results indicate that the internal pore closure of the membrane by anions and cake deposition on the membrane surface by cations are the separation mechanisms. The transmission of anions through the membrane may be predicted with a simple transport equation (convection and diffusion) combined with an adsorption isotherm. Both Langmuir and Freundlich adsorption isotherms were employed due to the simplicity and validity in liquid systems. The isotherm's parameters were determined at 10 bar during the unsteady state filtration. Under this condition, the permeate flux and concentration varied sharply due to adsorption. Finally, the model was compared with the experimental rejection data. An acceptable agreement around 95% at 8 bar and 92% at 15 bar was observed between theoretical model and experimental data.

  8. Adsorption characteristics of zinc ions on sodium dodecyl sulfate in process of micellar-enhanced ultrafiltration

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    To separate zinc ions from aqueous solution efficiently, micellar-enhanced ultrafiltration(MEUF) of hollow ultrafiltration membrane was used with sodium dodecyl sulfate(SDS) as surfactant. The formation of micellar and the adsorption mechanism were investigated, including the influence of the ratio of SDS to zinc ions on the micelle quantity, the micelle ratio, the gross adsorptive capacity, the rejection of zinc ions and the adsorption isotherm law. The results show that the rejection rate of zinc ions reaches 97% and the adsorption of zinc ions on SDS conforms to the Langmuir adsorption isotherm and the adsorption is a chemical adsorption process.

  9. Selective adsorption of tannins onto hide collagen fibres

    Institute of Scientific and Technical Information of China (English)

    廖学品; 陆忠兵; 石碧

    2003-01-01

    Hide collagen of animals is used to prepare adsorbent material and its adsorption properties to tannins are investigated. It is indicated that the collagen fibres has excellent adsorption selectivity and high adsorption capacity to tannins. The adsorption rate of tannins is more than 90% whilst less than 10% of functional components are retained by the adsorbent. The adsorption mechanism of tannins onto hide collagen fibres is hydrogen-bonding association. Freundlich model can be used to describe the adsorption isotherms, and the pseudo-second-order rate model can be used to describe adsorption kinetics.

  10. Adsorption of copper(II) on chitosan using a column in a closed hydrodynamic flow system

    International Nuclear Information System (INIS)

    The adsorption of Cu(II) ions from aqueous solution by chitosan using a column in a closed hydrodynamic flow system is described. The adsorption capacities as a function of contact time of copper(II) ions and chitosan were determined by varying the ionic strength, temperature and the flow of the metal solution. The Langmuir model reproduced the adsorption isothermal data better than the Freundlich model. The experimental kinetic data correlate properly with the second-order kinetic reaction for the whole set of experimental adsorption conditions. The rate constants exercise great influence on the time taken for equilibrium to be established by complexation or electrostatic interaction between the amino groups of chitosan and the metal. (author)

  11. Adsorptive removal of fermentation inhibitors from concentrated acid hydrolyzates of lignocellulosic biomass.

    Science.gov (United States)

    Sainio, Tuomo; Turku, Irina; Heinonen, Jari

    2011-05-01

    Adsorptive purification of concentrated acid hydrolyzate of lignocellulose was investigated. Cation exchange resin (CS16GC), neutral polymer adsorbent (XAD-16), and granulated activated carbon (GAC) were studied to remove furfural, HMF, and acetic acid from a synthetic hydrolyzate containing 20 wt.% H(2)SO(4). Adsorption isotherms were determined experimentally. Loading and regeneration were investigated in a laboratory scale column. GAC has the highest adsorption capacity, but regeneration with water was not feasible. XAD-16 and CS16GC had lower adsorption capacities but also shorter cycle times due to easier regeneration. Productivity increased when regenerating with 50 wt.% EtOH(aq) solution. To compare adsorbents, process performance was quantified by productivity and fraction of inhibitors removed. GAC yields highest performance when high purity is required and ethanol can be used in regeneration. For lower purities, XAD-16 and GAC yield approximately equal performance. When using ethanol must be avoided, CS16GC offers highest productivity. PMID:21441022

  12. Phosphate adsorption on lanthanum loaded biochar.

    Science.gov (United States)

    Wang, Zhanghong; Shen, Dekui; Shen, Fei; Li, Tianyu

    2016-05-01

    To attain a low-cost and high-efficient phosphate adsorbent, lanthanum (La) loaded biochar (La-BC) prepared by a chemical precipitation method was developed. La-BC and its pristine biochar (CK-BC) were comparatively characterized using zeta potential, BET surface area, scanning electron microscopy/energy dispersive spectrometer (SEM-EDS), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). The adsorption ability and the mechanisms during adsorption process for the La-BC samples were also investigated. La loaded on the surface of biochar can be termed as La-composites (such as LaOOH, LaONO3 and La(OH)3), leading to the decrease of negative charge and surface area of biochar. La-BC exhibited the high adsorption capacity to phosphate compared to CK-BC. Adsorption isotherm and adsorption kinetic studies showed that the Langmuir isotherm and second order model could well describe the adsorption process of La-BC, indicating that the adsorption was dominated by a homogeneous and chemical process. The calculated maximum adsorption capacity was as high as 46.37 mg g(-1) (computed in P). Thermodynamic analysis revealed that the adsorption was spontaneous and endothermic. SEM, XRD, XPS and FT-IR analysis suggested that the multi-adsorption mechanisms including precipitation, ligand exchange and complexation interactions can be evidenced during the phosphate adsorption process by La-composites in La-BC. PMID:26871732

  13. Adsorption of moble metal complexes of alumina and silica from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Knoezinger, H. [Universitaet Muenchen (Germany)

    1993-12-31

    The equilibrium of Pd and Pt complexes from aqueous solutions on alumina and silica is reported. Uptake isotherms were measured as a function of pH and added background electrolyte. Simulations based on a triple layer model permitted the determination of the mode of adsorption (electrostatic vs. ligand exchange) and of the adsorption equilibrium constants. UV/VIS and Raman spectroscopy were used to characterize the adsorbed complexes. The results provide a basis for the controlled preparation of defined concentration profiles in support pellets.

  14. Sonochemical assisted hydrothermal synthesis of ZnO: Cr nanoparticles loaded activated carbon for simultaneous ultrasound-assisted adsorption of ternary toxic organic dye: Derivative spectrophotometric, optimization, kinetic and isotherm study.

    Science.gov (United States)

    Jamshidi, M; Ghaedi, M; Dashtian, K; Hajati, S; Bazrafshan, A A

    2016-09-01

    Chromium doped zinc oxide nanoparticles (ZnO: Cr-NPs) was synthesized by ultrasonically assisted hydrothermal method and characterized by FE-SEM, XRD and TEM analysis. Subsequently, this composite ultrasonically assisted was deposited on activated carbon (ZnO: Cr-NPs-AC) and used for simultaneous ultrasound-assisted removal of three toxic organic dye namely of malachite green (MG), eosin yellow (EY) and Auramine O (AO). Dyes spectra overlap in mixture (major problem for simultaneous investigation) of this systems was extensively resolved by derivative spectrophotometric method. The magnitude of variables like initial dyes concentration, adsorbent mass and sonication time influence on dyes removal was optimized using small central composite design (CCD) combined with desirability function (DF) approach, while pH was studied by one-a-time approach. The maximized removal percentages at desirability of 0.9740 was set as follow: pH 6.0, 0.019g ZnO: Cr-NPs-AC, 3.9min sonication at 4.5, 4.8 and 4.7mgL(-1) of MG, EY and AO, respectively. Above optimized points lead to achievement of removal percentage of 98.36%, 97.24%, and 99.26% correspond to MG, EY and AO, respectively. ANOVA for each dyes based p-value less than (removal of these dyes within 95% confidence interval, while their F-value for MG, EY and AO is 935, 800.2, and 551.3, respectively, that confirm low participation of this them in signal. The value of multiple correlation coefficient R(2), adjusted and predicted R(2) for simultaneous removal of MG is 0.9982, 0.9972 and 0.9940, EY is 0.9979, 0.9967 and 0.9930 and for AO is 0.9970, 0.9952 and 0.9939. The adsorption rate well fitted by pseudo second-order and Langmuir model via high, economic and profitable adsorption capacity of 214.0, 189.7 and 211.6mgg(-1) for MG, EY and AO, respectively. PMID:27150752

  15. Adsorption of ciprofloxacin on surface-modified carbon materials.

    Science.gov (United States)

    Carabineiro, S A C; Thavorn-Amornsri, T; Pereira, M F R; Figueiredo, J L

    2011-10-01

    The adsorption capacity of ciprofloxacin (CPX) was determined on three types of carbon-based materials: activated carbon (commercial sample), carbon nanotubes (commercial multi-walled carbon nanotubes) and carbon xerogel (prepared by the resorcinol/formaldehyde approach at pH 6.0). These materials were used as received/prepared and functionalised through oxidation with nitric acid. The oxidised materials were then heat treated under inert atmosphere (N2) at different temperatures (between 350 and 900°C). The obtained samples were characterised by adsorption of N2 at -196 °C, determination of the point of zero charge and by temperature programmed desorption. High adsorption capacities ranging from approximately 60 to 300 mgCPxgC(-1) were obtained (for oxidised carbon xerogel, and oxidised thermally treated activated carbon Norit ROX 8.0, respectively). In general, it was found that the nitric acid treatment of samples has a detrimental effect in adsorption capacity, whereas thermal treatments, especially at 900 °C after oxidation, enhance adsorption performance. This is due to the positive effect of the surface basicity. The kinetic curves obtained were fitted using 1st or 2nd order models, and the Langmuir and Freundlich models were used to describe the equilibrium isotherms obtained. The 2nd order and the Langmuir models, respectively, were shown to present the best fittings. PMID:21733541

  16. Characterization and application of tourmaline and beryl from Brazilian pegmatite in adsorption process with divalent metals

    Institute of Scientific and Technical Information of China (English)

    Denis L.Guerra; Silze P.Oliveira; Ricardo A.R.Silva; Victor Leidens; Adriano C.Batista

    2012-01-01

    In this study,the original tourmaline and beryl mineral samples have been collected from a Brazilian pegmatite.The objective of this study was to examine the adsorption behavior of Brazilian ciclosilicate sampies,towards divalent metals (Pb2+,Mn2+,and Zn2+) in ethanol solution has been studies by a batch technique.The ciclosilicate samples were characterized by elemental analysis,Fourier transform infrared spectroscopy,helium picnometry,mercury porosity,and nitrogen adsorption-desorption.The Langmuir expression for adsorption isotherm was applied in order to determine the adsorption capacity to form a monolayer and the constant related to the adsorption intensity.In aqueous solution there was a significant adsorption increase with the temperature and pronounced synergistic effects were observed.The maximum number of moles adsorbed was determined to be 12.48 and 11.49 mmol/g for systems Pb2+/beryl and Pb2+/tourmaline,respectively.The energetic effects caused by metal cations adsorption were determined through calorimetric titrations.Thermodynamics indicated the existence of favorable conditions for such Pb2+-,Mn2+-,and Zn2+-OH interactions.

  17. Comparisons of kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide adsorption in aqueous solution with graphene oxide, zeolite and activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Shenteng; Lu, Chungsying, E-mail: clu@nchu.edu.tw; Lin, Kun-Yi Andrew

    2015-01-30

    Graphical abstract: A comparison of TMAH adsorption capacity with GO, NaY and GAC is conducted and the result reveals that the magnitude of qe follows the order of GO > NaY > GAC. The adsorption capacity of GO is significantly higher than those of zeolite and activated carbon in this and reported studies, showing its encouraging potential. GO also exhibits good reversibility of TMAH adsorption through 10 cycles of adsorption and desorption process. This reflects that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment. - Highlights: • Adsorption kinetics and isotherms of TMAH to GO, NaY and GAC are compared. • Thermodynamics of TMAH adsorption to GO, NaY and GAC is determined. • GO exhibits the highest TMAH adsorption capacity, followed by NaY and GAC. • Recyclabilities of NaY and GO remain above 95% but that of GAC dropped to 70%. - Abstract: Graphene oxide (GO), sodium Y-type zeolite (NaY) and granular activated carbon (GAC) are selected as adsorbents to study their kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide (TMAH) adsorption from water. The adsorption kinetics follows the pseudo-second-order rate law while the adsorption thermodynamics shows an exothermic reaction with GO and GAC but displays an endothermic reaction with NaY. The adsorbed TMAH can be readily desorbed from the surface of GO and NaY by 0.05 M NaCl solution. A comparative study on the cyclic TMAH adsorption with GO, NaY and GAC is also conducted and the results reveal that GO exhibits the greatest TMAH adsorption capacity as well as superior reversibility of TMAH adsorption over 10 cycles of adsorption and desorption process. These features indicate that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment.

  18. Comparisons of kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide adsorption in aqueous solution with graphene oxide, zeolite and activated carbon

    International Nuclear Information System (INIS)

    Graphical abstract: A comparison of TMAH adsorption capacity with GO, NaY and GAC is conducted and the result reveals that the magnitude of qe follows the order of GO > NaY > GAC. The adsorption capacity of GO is significantly higher than those of zeolite and activated carbon in this and reported studies, showing its encouraging potential. GO also exhibits good reversibility of TMAH adsorption through 10 cycles of adsorption and desorption process. This reflects that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment. - Highlights: • Adsorption kinetics and isotherms of TMAH to GO, NaY and GAC are compared. • Thermodynamics of TMAH adsorption to GO, NaY and GAC is determined. • GO exhibits the highest TMAH adsorption capacity, followed by NaY and GAC. • Recyclabilities of NaY and GO remain above 95% but that of GAC dropped to 70%. - Abstract: Graphene oxide (GO), sodium Y-type zeolite (NaY) and granular activated carbon (GAC) are selected as adsorbents to study their kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide (TMAH) adsorption from water. The adsorption kinetics follows the pseudo-second-order rate law while the adsorption thermodynamics shows an exothermic reaction with GO and GAC but displays an endothermic reaction with NaY. The adsorbed TMAH can be readily desorbed from the surface of GO and NaY by 0.05 M NaCl solution. A comparative study on the cyclic TMAH adsorption with GO, NaY and GAC is also conducted and the results reveal that GO exhibits the greatest TMAH adsorption capacity as well as superior reversibility of TMAH adsorption over 10 cycles of adsorption and desorption process. These features indicate that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment

  19. STUDY ON THE PROPERTIES OF DIFFERENT ACTIVATED CARBON FIBERS AND THEIR ADSORPTION CHARACTERISTICS FOR FORMALDEHYDE

    Institute of Scientific and Technical Information of China (English)

    H.Q. Rong; Z.Y. Ryu; J.T. Zheng

    2001-01-01

    Porous structure and surface chemistry of activated carbon fibers obtained by differ-ent precursors and activation methods were investigated. Adsorption isotherms werecharacterized by nitrogen adsorption at 77K over a relative pressure range from 10 6to 1. The regularization method according to Density Functional Theory (DFT) wasemployed to calculate the pore size distribution in the samples. Their specific surfaceareas were calculated by BET method, micropore volume and microporous specificsurface area calculated by t-plot method and MPD by Horvath-Kawazoe equation. Mi-cropore volume of rayon-based ACF was higher than that of other samples. The staticand dynamic adsorption capacity for formaldehyde on different ACFs was determined.The results show that steam activated Rayon-based A CFs had higher adsorption capac-ity than that of steam and KOH activated PAN-A CFs. Breakthrough curves illustratedthat Rayon-ACFs had longer breakthrough time, thus they possessed higher adsorp-tion capacity for formaldehyde than that of PAN-ACFs. The entire sample had smalladsorption capacity and short breakthrough time for water. Rayon-A CFs had exccl-lent adsorption selectivity for formaldehyde than PAN-ACFs. And the samples withhigh surface areas had relatively high adsorption capacity for formaldehyde. Elementaicontent of different A CFs were performed. Rayon-based A CFs contained more oxygenthan PAN-ACFs, which may be attributed to their excellent adsorption capacity forformaldehyde.

  20. A transverse isotropic model for microporous solids: Application to coal matrix adsorption and swelling

    Science.gov (United States)

    Espinoza, D. N.; Vandamme, M.; Dangla, P.; Pereira, J.-M.; Vidal-Gilbert, S.

    2013-12-01

    Understanding the adsorption-induced swelling in coal is critical for predictable and enhanced coal bed methane production. The coal matrix is a natural anisotropic disordered microporous solid. We develop an elastic transverse isotropic poromechanical model for microporous solids which couples adsorption and strain through adsorption stress functions and expresses the adsorption isotherm as a multivariate function depending on fluid pressure and solid strains. Experimental data from the literature help invert the anisotropic adsorptive-mechanical properties of Brzeszcze coal samples exposed to CO2. The main findings include the following: (1) adsorption-induced swelling can be modeled by including fluid-specific and pressure-dependent adsorption stress functions into equilibrium equations, (2) modeling results suggest that swelling anisotropy is mostly caused by anisotropy of the solid mechanical properties, and (3) the total amount of adsorbed gas measured by immersing coal in the adsorbate overestimates adsorption amount compared to in situ conditions up to ˜20%. The developed fully coupled model can be upscaled to determine the coal seam permeability through permeability-stress relationships.

  1. Equilibrium, kinetic and thermodynamic study of cesium adsorption onto nanocrystalline mordenite from high-salt solution.

    Science.gov (United States)

    Lee, Keun-Young; Park, Minsung; Kim, Jimin; Oh, Maengkyo; Lee, Eil-Hee; Kim, Kwang-Wook; Chung, Dong-Yong; Moon, Jei-Kwon

    2016-05-01

    In this study, the equilibrium, kinetics and thermodynamics of cesium adsorption by nanocrystalline mordenite were investigated under cesium contamination with high-salt solution, simulating the case of an operation and decommissioning of nuclear facilities or an accident during the processes. The adsorption rate constants were determined using a pseudo second-order kinetic model. The kinetic results strongly demonstrated that the cesium adsorption rate of nano mordenite is extremely fast, even in a high-salt solution, and much faster than that of micro mordenite. In the equilibrium study, the Langmuir isotherm model fit the cesium adsorption data of nano mordenite better than the Freundlich model, which suggests that cesium adsorption onto nano mordenite is a monolayer homogeneous adsorption process. The obtained thermodynamic parameters indicated that the adsorption involved a very stable chemical reaction. In particular, the combination of rapid particle dispersion and rapid cesium adsorption of the nano mordenite in the solution resulted in a rapid and effective process for cesium removal without stirring, which may offer great advantages for low energy consumption and simple operation. PMID:26683820

  2. Spatial modulation of the physical adsorption potential by diffusion and the theoretical consequences on multilayer adsorption

    International Nuclear Information System (INIS)

    The spatial variations of the adsorption potential parallel to the adsorbing surface were studied by measurement of the superficial diffusion coefficient. The force of attraction induced at the surface of the adsorbed film as a function of the geometry of the substrate was then examined in a non-uniform multilayer adsorption model. The superficial diffusion coefficient was determined by the use of a radioactive tracer which gives direct information without perturbing the measurement. It was shown that tritium can be physisorbed in mobile form at low temperature on monocristalline nickel without subjacent chemisorption. Similarly krypton at 40 deg K is adsorbed on graphite with a mobility strongly dependent on the degree of coverage. The potential barrier between sites, for krypton adsorbed in two-dimensional gas form, lies in the region of 250 calories per mole. With regard to multilayer adsorption the above-mentioned force of attraction, entropie in origin, must be added to the Van der Waals forces to obtain the adsorption isotherms. A theory of this pseudo-force is given for a gas adsorbed on a solid surface, based on the BET model (Brunauer, Emmett and Teller) but accounting for lateral interactions in a molecular field approximation

  3. (Amino acid + silica) adsorption thermodynamics: Effects of temperature

    International Nuclear Information System (INIS)

    Highlights: • High resolution, low concentration Gly, Lys and Glu solution adsorption isotherms. • All isotherms fitted with Langmuir–Freundlich isotherm model. • Gly, Lys and Glu show exothermic adsorption processes. • Isosteric heat analyses reveal changes in interaction strength with surface coverage. - Abstract: A thorough understanding of amino acid adsorption by mineral and oxide surfaces has a major impact on a variety of industrial and biomedical applications. Little information currently exists regarding temperature effects on most of these adsorption processes. Deeper thermodynamic analyses of their multiple temperature adsorption isotherms would aid the interpretation of the interfacial interactions. Low solution concentration adsorption isotherms for glycine, lysine and glutamic acid on a silica adsorbent were generated for T = (291, 298 and 310) K. Data analysis via the Clausius–Clapeyron method yielded the isosteric heat of adsorption as a function of fractional monolayer coverage for each adsorptive. Each amino acid showed an exothermic adsorption response. Glycine and lysine experienced a greater negative effect of increased temperature compared with glutamic acid, indicating a greater number of adsorbed molecules than glutamic acid, with the former undergoing intermolecular clustering within the adsorbed phase. Isosteric heat analyses suggest ionic interactions for lysine and hydrogen bonding for glutamic acid, both weakening with increased coverage. In contrast, initial hydrogen bonding led to ionic bonding for glycine with increasing coverage

  4. Determination of Kinetic and Equilibrium Parameters of the Batch Adsorption of Ni-63 onto Egyptian Kaolinite Clay

    International Nuclear Information System (INIS)

    This study provide the regulatory bodies and the operators that generate and manage radioactive waste with some recommendations on how to meet the IAEA safety requirements for the safe management of radioactive waste. The Sorption of Nickel from aqueous waste solutions by a natural kaolinite clay was studied. The different parameters affecting the sorption capacity of the selected elements by the investigated resins have been studied. The parameters include solution ph, metal ion concentration and presence of some competing cations. The metal sorbed percent of the investigated elements was determined for kaolinite clay. Sorption data have been interpreted in the terms of Langmuir and Freundlich isotherm equations.The metal sorbed percent of Ni-63 on the kaolinite clay sample is found to reach about 84%. The obtained data show that kaolinite clay can be considered as an efficient sorbent for the investigated metal cations of Ni-63 from their aqueous solutions. Therefore, it could be effectively used for the decontamination of waste solutions containing low concentration of radioactive nuclides of the radioisotopes under this investigation. However it is recommended that to use the kaolinite clay in decontamination purpose since it is easily to found and low cost.

  5. Determination of oleuropein using multiwalled carbon nanotube modified glassy carbon electrode by adsorptive stripping square wave voltammetry.

    Science.gov (United States)

    Cittan, Mustafa; Koçak, Süleyman; Çelik, Ali; Dost, Kenan

    2016-10-01

    A multi-walled carbon nanotube modified glassy carbon electrode was used to prepare an electrochemical sensing platform for the determination of oleuropein. Results showed that, the accumulation of oleuropein on the prepared electrode takes place with the adsorption process. Electrochemical behavior of oleuropein was studied by using cyclic voltammetry. Compared to the bare GCE, the oxidation peak current of oleuropein increased about 340 times at MWCNT/GCE. Voltammetric determination of oleuropein on the surface of prepared electrode was studied using square wave voltammetry where the oxidation peak current of oleuropein was measured as an analytical signal. A calibration curve of oleuropein was performed between 0.01 and 0.70µM and a good linearity was obtained with a correlation coefficient of 0.9984. Detection and quantification limits of the method were obtained as 2.73 and 9.09nM, respectively. In addition, intra-day and inter-day precision studies indicated that the voltammetric method was sufficiently repeatable. Finally, the proposed electrochemical sensor was successfully applied to the determination of oleuropein in an olive leaf extract. Microwave-assisted extraction of oleuropein had good recovery values between 92% and 98%. The results obtained with the proposed electrochemical sensor were compared with liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. PMID:27474292

  6. Determination of vanillin in commercial food product by adsorptive stripping voltammetry using a boron-doped diamond electrode.

    Science.gov (United States)

    Yardım, Yavuz; Gülcan, Mehmet; Şentürk, Zühre

    2013-12-01

    A method for the determination of food additive vanillin was developed by adsorptive stripping voltammetry. Its determination was carried out at the anodically pre-treated boron-doped diamond electrode in aqueous solutions. Using square-wave stripping mode, the compound yielded a well-defined voltammetric response in phosphate buffer, pH 2.5 at +1.14 V (vs. Ag/AgCl) (a pre-concentration step being carried out at open-circuit condition for 60s). A linear calibration graph was obtained in the concentration range of 0.5-15.0 μg mL(-1) (3.3×10(-6)-9.8×10(-5) mol L(-1)) with a detection limit of 0.024 μg mL(-1) (1.6×10(-7) mol L(-1)). As an example, the practical applicability of the proposed method was tested for the determination of this flavouring agent in commercial pudding powder of Keshkule (Turkish milk pudding with almond flour). PMID:23870896

  7. The adsorption of water isotopomers on carbon adsorbents

    International Nuclear Information System (INIS)

    Adsorption isotherms in the range 50-80 Deg C were measured by gas chromatography, and isosteric adsorption heats of isotopomers of water were calculated in the range of low fillings at two activated carbons (Norit and FAS) with close volume of micropores (0.38 and 0.37 cm3/g), but various surface chemistry (AC Norit with hydrophilic surface and AC FAS with hydrophobic one). Adsorption of H2O and D2O at AC Norit exceeds adsorption at AC FAS at all equilibrium pressures. Adsorption isotherms of H2O and D2O at every adsorbents are close, but some excess of isotherms and adsorption heats of D2O as compared with H2O ones observes. It is connected with the differences in adsorbate-adsorbent and adsorbate-adsorbate interactions as well as with the structure of molecules of adsorbates

  8. Isothermal Gaseous Detonation Model

    Science.gov (United States)

    Prokhorov, E. S.

    2015-05-01

    We propose an isothermal gaseous detonation model taking into account the initial pressure of the explosive mixture that permits describing in a simplified form both the self-sustaining and the supercompressed and undercompressed detonation regimes. The exactness of this model has been estimated on the basis of a comparative analysis with the results of equilibrium calculations of the gas-dynamic parameters at the front of detonation waves.

  9. Determination of adsorptive and catalytic properties of copper, silver and iron contain titanium-pillared bentonite for the removal bisphenol A from aqueous solution

    Science.gov (United States)

    Tomul, Fatma; Turgut Basoglu, Funda; Canbay, Hale

    2016-01-01

    Ti-pillared bentonite, Cu, Ag and Fe modified Ti-pillared bentonite and Cu/Ti- and Fe/Ti-mixed pillared bentonite were synthesized using different titanium sources by direct synthesis or by modification after synthesis. The effects of synthesis conditions on the surface characteristics, pore structure and acidity of the pillared bentonites were investigated by SEM-EDS, XPS, XRD, N2-adsorption/desorption and FTIR analyses before and after ammonia adsorption. The results of EDS, XPS and XRD analysis confirmed that titanium, copper, silver and iron were incorporated into the bentonite structure. In the XRD patterns, the formation of delaminated structure reflecting the non-parallel distribution of the bentonite layers by pillaring with Ti, Cu/Ti and Fe/Ti-pillars was observed. XPS spectra indicated the presence of TiO2, CuO, Ag and Ag2O and Fe2O3 species depending on the source of active metals in the synthesized samples. In the FTIR spectra, an increase in the Bronsted/Lewis peak intensity was observed with the loading of copper and iron, whereas a decrease in Lewis and Bronsted acidities was observed with incorporation of silver. Adsorption studies indicated that the adsorption capacity of the sample synthesized using titanium (IV) propoxide and incorporating iron to the structure by ion exchange (Fe-PTi-PILC) were higher than those in other samples. The adsorption of BPA (bisphenol A) by all tested samples was found to fit the Langmuir isotherm. In the catalytic wet peroxide oxidation (CWPO) over PTi-PILC (prepared by titanium (IV) propoxide), Fe-PTi-PILC and Cu-PTi-PILC (prepared by copper impregnated Ti-pillared bentonite) samples, BPA values close to complete conversion were achieved within 30 min at 25 °C, pH 4 and 5 g/L mcat. CWPO results showed that increasement of pH causes a decrease the rate of oxidation. On the other hand, by the time catalyst and BPA concentration is increased, the rate of oxidation is increased as well.

  10. Adsorption of arsenic and boron by soil

    Energy Technology Data Exchange (ETDEWEB)

    Sakata, M.

    1986-01-01

    The author reports a study of the soil adsorption of As (trivalent) and B leached from coal ash. It has been found that the amount of adsorption is greatly affected by the pH of the solution. Maximum adsorption of As occurred from solutions with pH of about 8, while pH 8-9 resulted in maximum B adsorption. Furthermore, the As adsorption is related to the quantity of iron oxides and hydrated iron oxides in the soil, while the adsorption of B is related to the quantity of hydrated aluminium oxides and allophanes. Within the range of concentrations studied, the adsorption isotherm for As obeyed the Langmuir equation, and the B isotherm, that of Freundlich. At low concentrations, both elements conform to the Henry adsorption isotherm. The author also reports that the impact on ground water of elements such as As and B leached from coal ash can be conveniently predicted or evaluated by means of a diffusive flow model. 30 references, 14 figures, 3 tables.

  11. 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...... 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 are...... chosen to investigate time dependent martensite formation. Among them, a Fe-11wt%Ni-0.6wt%C model alloy and Fe-1.6wt%Cr-1wt%C (AISI 52100), Fe-17wt%Cr-7wt%Ni (AISI 631) and Fe-16wt%Cr-5wt%Ni (AISI 630) commercial steels. The investigation was performed with in situ magnetometry, dilatometry, synchrotron...

  12. Adsorption of cationic surfactants and their effects on the interfacial properties of quartz

    Science.gov (United States)

    Jia, Renhe

    This dissertation is primarily concerned with an investigation of the interfacial behavior of natural quartz in aqueous solution where the adsorption of various cationic surfactants is involved. The broad objective of this research was to delineate the mechanisms involved in the adsorption of cationic surfactants using experimental determination of adsorption isotherms, zeta potentials, suspension turbidity, contact angles, induction times, as well as Hallimond tube flotation response. With dodecylpyridinium chloride as the model surfactant, four-region adsorption isotherms were observed and found to correlate well with zeta potential, suspension stability and contact angle measurements. Calculations of adsorption energy showed strong specific adsorption in Region I, probably resulting from H-bonding of the pyridinium headgroup to active sites on the silica. As a result of hemimicelle formation at the solid-liquid interface in Region II, pronounced increases in the adsorption density, zeta potential, and surface hydrophobicity were observed. The stability of quartz suspensions showed a significant drop in this region. In Region III, the zeta potential is reversed and the stability of the suspensions begins to increase again. In this region, the surface hydrophobicity of quartz decreases with further surfactant adsorption, suggesting reverse orientation of the adsorbed surfactant ions. In Region IV, the adsorption isotherm and zeta potential reach a plateau when the surfactant concentration reaches the CMC, and the surface becomes completely hydrophilic. The molecular structure of surfactant ions (chain length, number of hydrocarbon chains and number of headgroups) was found to significantly affect their surface activity. Increasing the hydrocarbon chain length of the surfactant lowers the concentration of surfactant required for minimum suspension stability, as well as redispersion. The adsorption is stronger for surfactants whose structure permits hydrogen bonding

  13. Surfactant loss control in chemical flooding: Spectroscopic and calorimetric study of adsorption and precipitation on reservoir minerals. Quarterly technical progress report, January 1, 1994--March 31, 1994

    Energy Technology Data Exchange (ETDEWEB)

    Somasundaran, P.

    1994-05-31

    Since surfactants are often present as mixtures, effort is being made to understand the synergetic and competitive forces involving determining adsorption of surfactants from their mixtures. Adsorption of tetradecyl trimethyl ammonium chloride (TTAC) and polyethoxylated nonyl phenol (NP-15) surfactant mixture at the alumina-water interface was studied during this reporting period. It was found that the nonionic surfactant NP-15 does not adsorb on alumina by itself, but was forced to adsorb by cationic TTAC. The adsorption density and the nature of adsorption isotherm of NP-15 were markedly dependent upon the quantity of TTAC present in the mixture and the procedure of surfactant addition. In the low concentration range the adsorption of both TTAC and NP-15 was enhanced by coadsorption, but in the high concentration range the adsorption of TTAC was depressed due to the competitive adsorption and steric hindrance. Electrokinetic behavior of alumina suspensions was also monitored along with the adsorption in order to delineate the role of electrostatic force in determining the mechanism of adsorption. Surface tension of surfactant mixtures before and after adsorption was measured to obtain information needed for developing mechanisms.

  14. Hexadecylamine adsorption at the iron oxide-oil interface.

    Science.gov (United States)

    Wood, Mary H; Welbourn, Rebecca J L; Charlton, Timothy; Zarbakhsh, Ali; Casford, M T; Clarke, Stuart M

    2013-11-12

    The adsorption behavior of a model additive, hexadecylamine, onto an iron surface from hexadecane oil has been characterized using polarized neutron reflectometry, sum-frequency generation spectroscopy, solution depletion isotherm, and X-ray photoelectron spectroscopy (XPS). The amine showed a strong affinity for the metal surface, forming a dense monolayer at relatively low concentrations; a layer thickness of 16 (±3) Å at low concentrations, increasing to 20 (±3) Å at greater amine concentrations, was determined from the neutron data. These thicknesses suggest that the molecules in the layer are tilted. Adsorption was also indicated by sum-frequency generation spectroscopy and XPS, the latter indicating that the most dominant amine-surface interaction was via electron donation from the nitrogen lone pair to the positively charged iron ions. Sum-frequency generation spectroscopy was used to determine the alkyl chain conformation order and orientation on the surface. PMID:24106786

  15. Adsorption component of the disjoining pressure in thin liquid films

    OpenAIRE

    Tsekov, R.

    2011-01-01

    The disjoining pressure isotherm in foam films is theoretically studied and an important contribution of adsorption is discovered. On the basis of the interfacial thermodynamics an adsorption disjoining pressure component is derived, which is repulsive and exponentially decaying by the film thickness. Expressions for its magnitude and decay length are derived in terms of well-known thermodynamic characteristics such as the partial Gibbs elasticity and adsorption length. Several adsorption iso...

  16. Adsorption of some laser dyes on the surface of colloidal particle

    International Nuclear Information System (INIS)

    Adsorption of crystal violet, rhodamin-B, escolin, rodhamin-6G and rohdamin-S on silica gel, zeolite, aluminium oxide and titanium oxide, were carried out in aqueous solutions. The isotherms at different temperatures have shown that the adsorption process in a multilayer one. The isotherms have the S-shape curves. Monolayer formation at the solid-liquid interface was determined according to the Polany's Theory. The uptake on the monolayer was the highest on zeolite surface relative to other substrates. The reason for that can be the energetical heterogenity and the presence of a large number of supercages in the crystalline structure of zeolite. An attempt was made to separate the dyes from either mixture through separation columns using the substrates as a solid phase, and water as a mobile phase. 6 tabs.; 15 figs.; 41 refs

  17. Expanded bed adsorption of bromelain (E.C. 3.4.22.33 from Ananas comosus crude extract

    Directory of Open Access Journals (Sweden)

    E. Silveira

    2009-03-01

    Full Text Available This work focuses on the adsorption of Bromelain in expanded bed conditions, such as the adsorption kinetics parameters. The adsorption kinetics parameters showed that after 40 minutes equilibrium was achieved and maximum adsorption capacity was 6.11 U per resin mL. However, the maximum adsorption capacity was only determined by measuring the adsorption isotherm. Only by the Langmuir model the maximum adsorption capacity, Qm, and dissociation constant, kd, values could be estimated as 9.18 U/mL and 0.591, respectively, at 25 ºC and 0.1 mol/L phosphate buffer pH 7.5. A column made of glass with an inner diameter of 1 cm was used for the expanded bed adsorption (EBA. The residence time was reduced 10 fold by increasing the expansion degree 2.5 times; nonetheless, the plate number (N value was reduced only 2 fold. After adsorption, the bromelain was eluted in packed bed mode, with a downward flow. The purification factor was about 13 fold and the total protein was reduced 4 fold. EBA showed to be feasible for purification of bromelain.

  18. Electrophotometric determination of molybdenum after separation from its pyrrolidinedithiocarbamte by adsorption of naphthalene

    Energy Technology Data Exchange (ETDEWEB)

    Shukla, R.K.; Kumar, A. [D.A. Univ., Indore (India)

    1992-05-10

    Various reagents, namely thiosemicarbazone 2,2{sup prime}-dihydroxybenzophenone, imidoylphenhydrazine, 2-thiopyrogallol, 5,7-dibro-8-hydroxyquinoline, 1,10-phenanthromine + bromopyrogallol, Alizarine Blue, benzohydroxamic acid, benzoylacetone, and 2,4-dihydroxyacetophenone oxime, are used for the determination of molybdenum. In most cases, tungsten interferes significantly, or the method requires strict monitoring of the concentration, calculation, and boiling time. In some cases, molybdenum has been determined only in alloys with high molybdenum content and with reduction of Mo(VI) to Mo(V). The authors have developed a method using solid-liquid separation extraction after liquid-liquid extraction into molten naphthalene. Although this method has a number of advantages in ordinary liquid-liquid extraction, it cannot be used for extraction of thermally unstable complexes. Recently, the authors observed that most complexes of metals in aqueous solutions can be precipitated with microcrystalline naphthalene. This method is convenient (it is carried out at room temperature), rapid (it requires no time for heating of naphthalene), and economical (only 0.4 g of naphthalene is required). The method is especially convenient for metal complexes insoluble in nonaqueous organic solvents. In this article, ammonium pyrrolidinedithiocarbamate is recommended for determination of molybdenum after coprecipitation of molybdenum pyrrolidinedithiocarbamate with microcrystalline naphthalene. The role of various parameters (pH, concentration of the reagent and naphthalene, time of separation and shaking, and volume of the aqueous phase) was established, and conditions were found for determination of molybdenum in some alloys. Because molybdenum can be adsorbed from an acid solution (pH {le} 2.5), the method is more selective than many other names described in the literature. 14 refs., 2 tabs.

  19. Relationship between carbon microstructure, adsorption energy and hydrogen adsorption capacity at different temperatures

    International Nuclear Information System (INIS)

    Various microporous materials such as activated carbons, nano-tubes, synthetic microporous carbons as well as metal organic framework materials are being considered for hydrogen storage applications by means of physical adsorption. To develop materials of practical significance for hydrogen storage it is important to understand the relationships between pore sizes, adsorption energies and adsorption capacities. The pore size distribution (PSD) characterization is traditionally obtained from the analysis of nitrogen adsorption isotherms measured at 77 K. However, a portion of the pores accessible to H2 may not be accessible to N2 at this temperature. Therefore, it was recently proposed to use the DFT analysis of H2 adsorption isotherms to characterize pore structure of materials considered for hydrogen storage applications. In present work, adsorption isotherms of H2 and N2 at cryogenic temperatures are used for the characterization of carbon materials. Adsorption measurements were performed with Autosorb 1 MP (Quantachrome Instruments, Boynton Beach, Florida, USA). As an example, Fig 1 compares PSDs calculated for the activated carbon sample (F400, Calgon Carbon) using combined H2 and N2 data, and using N2 isotherm only. The nitrogen derived PSD does not include certain amount of micropores which are accessible to H2 but not to N2 molecules. Obviously, the difference in the calculated PSDs by the two methods will depend on the actual content of small micropores in a given sample. Carbon adsorption properties can also be characterized by the isosteric heat of adsorption, Qst, related to the adsorption energy and dependent on the carbon pore/surface structure. Fig 2 shows Qst data calculated using the Clausius-Clapeyron equation from H2 isotherms measured at 77 K and 87 K for the carbon molecular sieve CMS 5A (Takeda), oxidized single wall nano-tubes (SWNT), and graphitized carbon black (Supelco). The Qst values decrease with increasing pore sizes. The highest Qst is

  20. 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. PMID:20492112

  1. Investigation of factors affecting adsorption of transition metals on oxidized carbon nanotubes

    International Nuclear Information System (INIS)

    Adsorption of nickel, copper, zinc and cadmium from aqueous solutions on carbon nanotubes oxidized with concentrated nitric acid was carried out in single, binary, ternary and quaternary systems. TEM and adsorption of nitrogen were used to determine texture and structural parameters, respectively. The surface chemistry was evaluated using the pH at the point of zero charge, FTIR spectroscopy and XPS analysis. The experimental results showed that all isotherms for Cu2+(aq) fit to Langmuir model in each system. On the other hand, the isotherms for Ni2+(aq), Cd2+(aq) and Zn2+(aq) in multi-component systems reveal the effect of competition for adsorption sites seen as a decrease in the amount adsorbed. The uptakes at the equilibrium concentration of 0-0.04 mmol L-1 in single system and 0-0.15 mmol L-1 in binary system are in the order Cu2+(aq) > Ni2+(aq) > Cd2+(aq) > Zn2+(aq) while for the ternary and quaternary, the order is Cu2+(aq) > Cd2+(aq) > Zn2+(aq) > Ni2+(aq). The results indicate that the mechanism of adsorption is governed by the surface features, ion exchange process and electrochemical potential. The latter plays a significant role in multi-component adsorption where redox reactions, not only on the adsorbent surface but also between the adsorbates, are likely to occur.

  2. Adsorption capacity of methylene blue, an organic pollutant, by montmorillonite clay

    KAUST Repository

    Feddal, I.

    2013-11-19

    The isotherms and kinetics of the adsorption of a cationic dye in aqueous solution, methylene blue, on a local Algerian montmorillonite clay mineral (raw, sodium and thermally activated at 300 and 500°C) were determined experimentally. Various parameters influencing the adsorption were optimized, mainly solid-liquid contact time, mass of adsorbent, initial concentration of dye, pH of the solution and temperature. Results showed that the adsorption kinetics were fast: 30 min for the raw clay mineral, and 20 min for sodium clay mineral (SC) and thermally activated at 300°C, whereas with the clay mineral calcined at 500°C, the equilibrium was reached after 150 min only. The maximum adsorption capacity was reached at pH 6.6. Results deducted from the adsorption isotherms also showed that the retention follows the Langmuir model. In addition, it was found that the kinetics were in the order of 2 (K = 2.457 × 106 g/mg.h) for sodium clay and were limited by an intra-particle diffusion. SC was found to be a better adsorbent to remove methylene blue from industrial wastewater. © 2013 Balaban Desalination Publications. All rights reserved.

  3. Multi-Component Adsorption of Benzene, Toluene, Ethylbenzene, and Xylene from Aqueous Solutions by Montmorillonite Modified with Tetradecyl Trimethyl Ammonium Bromide

    Directory of Open Access Journals (Sweden)

    H. Nourmoradi

    2013-01-01

    Full Text Available Multicomponent adsorption of benzene, toluene, ethylbenzene, and xylene (BTEX was assessed in aqueous solutions by montmorillonite modified with tetradecyl trimethyl ammonium bromide (TTAB-Mt. Batch experiments were conducted to determine the influences of parameters including loading rates of surfactant, contact time, pH, adsorbate concentration, and temperature on the adsorption efficiency. Scanning electron microscope (SEM and X-ray diffractometer (XRD were used to determine the adsorbent properties. Results showed that the modification of the adsorbent via the surfactant causes structural changes of the adsorbent. It was found that the optimum adsorption condition achieves with the surfactant loading rate of 200% of the cation exchange capacity (CEC of the adsorbent for a period of 24 h. The sorption of BTEX by TTAB-Mt was in the order of B< T< E< X. The experimental data were fitted by many kinetic and isotherm models. The results also showed that the pseudo-second-order kinetic model and Freundlich isotherm model could, respectively, be fitted to the experimental data better than other available kinetic and isotherm models. The thermodynamic study indicated that the sorption of BTEX with TTAB-Mt was achieved spontaneously and the adsorption process was endothermic as well as physical in nature. The regeneration results of the adsorbent also showed that the adsorption capacity of adsorbent after one use was 51% to 70% of original TTAB-Mt.

  4. Adsorption of uranyl ions in nanoparticles of magnetite

    International Nuclear Information System (INIS)

    This work studied the uranium (VI) adsorption, in the form of UO22+ ions, of the nitride solution by the syntetic magnetite. This solution was prepared by precipitation adding a solution of NaOH to the solution containing the ions Fe2+. The time of contact and the isothermal of equilibrium of ions UO22+ adsorption was verified. The isothermal of equilibrium presented more concordance with the Freundlich model, which characterized a heterogeneous adsorption surface of the magnetite. The great advantage of this technology is the combination of two separation techniques, by adsorption and magnetic, resulting in a highly efficient and reusable system

  5. Adsorption of radioactive iodide by natural zeolites

    International Nuclear Information System (INIS)

    Two natural zeolites from Iranian deposits (clinoptilolite and natrolite) were characterized and their ability for adsorption of iodide from nuclear wastewaters was evaluated. The adsorption behavior was studied on natural and modified zeolites by γ-spectrometry using 131I as radiotracer. Adsorption isotherms and distribution coefficient (Kd) were measured. The results showed that clinoptilolite is a more promising zeolite for removal of iodide compared to natrolite. Furthermore, the adsorption was higher in silver, lead and thallium forms, whereas the lowest desorption was observed in lead modified zeolite. (author)

  6. Comparison of linear and non-linear models for the adsorption of fluoride onto geo-material: limonite.

    Science.gov (United States)

    Sahin, Rubina; Tapadia, Kavita

    2015-01-01

    The three widely used isotherms Langmuir, Freundlich and Temkin were examined in an experiment using fluoride (F⁻) ion adsorption on a geo-material (limonite) at four different temperatures by linear and non-linear models. Comparison of linear and non-linear regression models were given in selecting the optimum isotherm for the experimental results. The coefficient of determination, r², was used to select the best theoretical isotherm. The four Langmuir linear equations (1, 2, 3, and 4) are discussed. Langmuir isotherm parameters obtained from the four Langmuir linear equations using the linear model differed but they were the same when using the nonlinear model. Langmuir-2 isotherm is one of the linear forms, and it had the highest coefficient of determination (r² = 0.99) compared to the other Langmuir linear equations (1, 3 and 4) in linear form, whereas, for non-linear, Langmuir-4 fitted best among all the isotherms because it had the highest coefficient of determination (r² = 0.99). The results showed that the non-linear model may be a better way to obtain the parameters. In the present work, the thermodynamic parameters show that the absorption of fluoride onto limonite is both spontaneous (ΔG 0). Scanning electron microscope and X-ray diffraction images also confirm the adsorption of F⁻ ion onto limonite. The isotherm and kinetic study reveals that limonite can be used as an adsorbent for fluoride removal. In future we can develop new technology for fluoride removal in large scale by using limonite which is cost-effective, eco-friendly and is easily available in the study area. PMID:26676015

  7. A sum-frequency generation spectroscopic study of the Gibbs analysis paradox: monolayer or sub-monolayer adsorption?

    Science.gov (United States)

    Shahir, Afshin Asadzadeh; Nguyen, Khoi Tan; Nguyen, Anh V

    2016-03-23

    The Gibbs adsorption isotherm (GAI) has been considered as the foundation of surfactant adsorption studies for over a century; however, its application in determining the limiting surface excess has recently been intensively discussed, with contradictory experimental evidence either supporting or refuting the theory. The available arguments are based on monolayer adsorption models. In this paper, we experimentally and intellectually propose and validate the contribution of sub-monolayer adsorption to the GAI paradox. We utilize a powerful intrinsically surface-sensitive technique, vibrational sum-frequency generation spectroscopy (SFG), complementing with conventional tensiometric measurements to address these controversies both quantitatively and qualitatively. Our SFG results revealed that the precipitous decrease in surface tension directly corresponds to surface occupancy by adsorbates. In addition, the Gibbs analysis was successfully applied to the soluble monolayer of a surface-active alcohol to full saturation. However, the full saturation of the topmost monolayer does not necessarily mean that the surface adsorption was completed because the adsorption was observed to continuously occur in the sub-monolayer region soon after the topmost monolayer became saturated. Nonetheless, the Gibbs isotherm failed to account for the excess of alcohol adsorbed in this sub-monolayer region. This new concept of surface excess must therefore be treated thermodynamically. PMID:26661072

  8. Ratiometric fluorescence transduction by hybridization after isothermal amplification for determination of zeptomole quantities of oligonucleotide biomarkers with a paper-based platform and camera-based detection

    Energy Technology Data Exchange (ETDEWEB)

    Noor, M. Omair; Hrovat, David [Chemical Sensors Group, Department of Chemical and Physical Sciences, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON L5L 1C6 (Canada); Moazami-Goudarzi, Maryam [Department of Cell and Systems Biology, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON L5L 1C6 (Canada); Espie, George S. [Department of Cell and Systems Biology, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON L5L 1C6 (Canada); Department of Biology, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON L5L 1C6 (Canada); Krull, Ulrich J., E-mail: ulrich.krull@utoronto.ca [Chemical Sensors Group, Department of Chemical and Physical Sciences, University of Toronto Mississauga, 3359 Mississauga Road, Mississauga, ON L5L 1C6 (Canada)

    2015-07-23

    Highlights: • Solid-phase QD-FRET transduction of isothermal tHDA amplicons on paper substrates. • Ratiometric QD-FRET transduction improves assay precision and lowers the detection limit. • Zeptomole detection limit by an iPad camera after isothermal amplification. • Tunable assay sensitivity by immobilizing different amounts of QD–probe bioconjugates. - Abstract: Paper is a promising platform for the development of decentralized diagnostic assays owing to the low cost and ease of use of paper-based analytical devices (PADs). It can be challenging to detect on PADs very low concentrations of nucleic acid biomarkers of lengths as used in clinical assays. Herein we report the use of thermophilic helicase-dependent amplification (tHDA) in combination with a paper-based platform for fluorescence detection of probe-target hybridization. Paper substrates were patterned using wax printing. The cellulosic fibers were chemically derivatized with imidazole groups for the assembly of the transduction interface that consisted of immobilized quantum dot (QD)–probe oligonucleotide conjugates. Green-emitting QDs (gQDs) served as donors with Cy3 as the acceptor dye in a fluorescence resonance energy transfer (FRET)-based transduction method. After probe-target hybridization, a further hybridization event with a reporter sequence brought the Cy3 acceptor dye in close proximity to the surface of immobilized gQDs, triggering a FRET sensitized emission that served as an analytical signal. Ratiometric detection was evaluated using both an epifluorescence microscope and a low-cost iPad camera as detectors. Addition of the tHDA method for target amplification to produce sequences of ∼100 base length allowed for the detection of zmol quantities of nucleic acid targets using the two detection platforms. The ratiometric QD-FRET transduction method not only offered improved assay precision, but also lowered the limit of detection of the assay when compared with the non

  9. Determination of (111) ordered domains on platinum electrodes by irreversible adsorption of bismuth.

    Science.gov (United States)

    Rodríguez, Paramaconi; Solla-Gullón, José; Vidal-Iglesias, Francisco J; Herrero, Enrique; Aldaz, Antonio; Feliu, Juan M

    2005-08-15

    Irreversible adsorbed bismuth can be used to determine the fraction of (111) domains on a given platinum sample. On Pt(111) electrodes, the surface redox process of adsorbed bismuth takes place at 0.63 V in a well-defined peak. The behavior of this redox process on the Pt(111) vicinal surfaces indicates that the bismuth atoms involved in the redox process are only those deposited on the (111) terrace sites and that the charge under the peak at 0.63 V is directly proportional to the number of sites on (111) ordered domains (terraces). The good linear relationship obtained between the charge for the bismuth redox process and the number of (111) terrace sites on the vicinal surfaces allows construction of a calibration curve. This calibration curve has been used to directly estimate the amount of (111) ordered domain terrace sites on polycrystalline platinum samples with different surface ordered domains. The results agree with what we would expect from our knowledge of these surfaces. PMID:16097774

  10. Solar UV-assisted sample preparation of river water for ultra-trace determination of uranium by adsorptive stripping voltammetry

    International Nuclear Information System (INIS)

    The article describes how solar ultraviolet-A radiation can be used to digest samples as needed for voltammetric ultratrace determination of uranium(VI) in river water. We applied adsorptive stripping voltammetry (AdSV) using chloranilic acid as the complexing agent. Samples from the river Warnow in Rostock (Germany) were pretreated with either soft solar UV or wit artificial hard UV from a 30-W source emitting 254-nm light. Samples were irradiated for 12 h, and both methods yielded the same results. We were able to detect around 1 μg.L-1 of uranium(VI) in a sample of river water that also contained dissolved organic carbon at a higher mg.L-1 levels. No AdSV signal was obtained for U(VI) without any UV pre-treatment. Pseudo-polarographic experiments confirmed the dramatic effect of both digestion techniques the the AdSV response. The new method is recommended for use in mobile ultratrace voltammetry of heavy metals for most kinds of natural water samples including tap, spring, ground, sea, and river waters. The direct use of solar radiation for sample pre-treatment represents a sustainable technique for sample preparation that does not consume large quantities of chemicals or energy. (author)

  11. Adsorption geometry of glycine on Cu(001) determined with low-energy electron diffraction and scanning tunnelling microscopy

    Institute of Scientific and Technical Information of China (English)

    葛四平; 赵学应; 盖峥; 赵汝光; 杨威生

    2002-01-01

    Using low-energy electron diffraction (LEED) and scanning tunnelling microscopy (STM) it has been found thatglycine molecules adsorbed on Cu(001) can form but only the (2×4) and c(2×4) superstructures. On the basis of themissing LEED spots of the surface, it has been concluded that: each (2 ×4) unit cell consists of two molecules, one beingthe mirror image of the other; the C-C axis of both molecules lies in the mirror plane of the Cu substrate without asignificant shift and twist from the plane; and the two O atoms of the carboxylate group of both molecules locate at thesame height level without significant buckling. According to these conclusions, a structural model has been proposed forthe (2×4) superstructure (a model for the c(2×4) superstructure already exists). We argue that the (2×4) and c(2×4)superstructures must have similar specific surface free energy, that their hydrogen bonds must be of N-H-OⅡ type, andthat their local adsorption geometry must be similar or even the same. The advantage of combining STM with LEEDto determine surface structures is clearly demonstrated.

  12. Adsorption geometry of glycine on Cu(001) determined with low—energy electron diffraction and scanning tunnelling microscopy

    Institute of Scientific and Technical Information of China (English)

    葛四平; 赵学应; 等

    2002-01-01

    Using low-energy electron diffraction(LEED)and scanning tunnelling microscopy (STM) it has been found that glycine molecules adsorbed on Cu(001) can form but only the (2×4) superstructures.On the basis of the missing LEED spots of the surface,it has been concluded that.each(2×4) unit cell consists of two molecules,one being the mirror image of the other,the C-C axis of both molecules lies in the mirror plane of the Cu substrate without a significant shift and twish from the plane;and the two O atoms of the carboxylate group of both molecules locate at the same height level without significant buckling.According to these conclusions,a structural model has been propsed for the (2×4) superstructure (a model for the c(2×4) supersturcture already exists).We argue that the (2×4) and c(2×4) superstructures must have similar specific surface free energy,that their hydrogen bonds must be of N-H-OII type,and that their local adsorption geometry must be similar or even the same.The advantage of combining STM with LEED to determine surface sturctures is clearly demonstrated.

  13. Determination of volatile organic compounds in workplace air by multisorbent adsorption/thermal desorption-GC/MS.

    Science.gov (United States)

    Wu, Chien-Hou; Feng, Chien-Tai; Lo, Yu-Shiu; Lin, Tsai-Yin; Lo, Jiunn-Guang

    2004-07-01

    Investigation of volatile organic compounds (VOCs) was first conducted in the air of class-100 cleanrooms at liquid crystal display (LCD) fabrication facilities. Air samples were collected on multisorbent tubes (including Carbopack B, Carbopack C, and Carbosieve S-III) and analyzed using adsorption/thermal desorption coupled with gas chromatography-mass spectrometry (GC-MS). Optimal conditions lead to average recoveries in the range of 96.2-98.2%, and method detection limits between 0.38 and 0.78 ppb, under the condition of 1-l sampling volume and 80% relative humidity. The method appears to be accurate, sensitive, simple and well-suited for determining VOC distributions from various stages of LCD manufacturing process and temporal variations of the analyte concentrations. About 15 VOCs were identified in workplace air. The major pollutants such as propylene glycol methyl ether acetate (PGMEA), butyl acetate, and acetone that are commonly used in the opto-electronics industry were detected and accurately quantified with the established method. PMID:15109881

  14. Light Hydrocarbons Adsorption Mechanisms in Two Calcium-based Microporous Metal Organic Frameworks

    KAUST Repository

    Plonka, Anna M.

    2016-01-25

    The adsorption mechanism of ethane, ethylene and acetylene (C2Hn; n=2, 4, 6) on two microporous metal organic frameworks (MOFs) is described here that is consistent with observations from single crystal and powder X-ray diffraction, calorimetric measurments and gas adsorption isotherm measurements. Two calcium-based MOFs, designated as SBMOF-1 and SBMOF-2 (SB: Stony Brook), form three-dimensional frameworks with one-dimensional open channels. As determined form single crystal diffraction experiments channel geometries of both SBMOF-1 and SBMOF-2 provide multiple adsorption sites for hydrocarbon molecules trough C-H…π and C-H…O interactions, similarly to interactions in the molecular and protein crystals. Both materials selectively adsorb C2 hydrocarbon gases over methane as determined with IAST and breakthrough calculations, with C2H6/CH4 selectivity as high as 74 in SBMOF-1.

  15. Organofunctionalized Amazon smectite for dye removal from aqueous medium-Kinetic and thermodynamic adsorption investigations

    International Nuclear Information System (INIS)

    The objective of this study is to examine the adsorption behavior of Sumifix Brilliant Orange 3R textile dye from aqueous solution on smectite sample, an abundant Amazon clay. The original smectite clay mineral has been collected from Amazon region, Brazil. The compound 2-aminomethylpyridine was anchored onto smectite surface by heterogeneous route. The ability of these materials to remove the Sumifix Brilliant Orange 3R textile dye from aqueous solution was followed by a series of adsorption isotherms, using a batchwise process. The maximum number of moles adsorbed was determined to be 1.26 and 2.07 mmol g-1 for natural and modified clay samples, respectively. The energetic effects caused by dye cations adsorption were determined through calorimetric titrations. Thermodynamics indicated the existence of favorable conditions for such dye-nitrogen interactions.

  16. Adsorption Properties of PVA/PAA/clay Composite Hydrogel Synthesized by Gamma Radiation and its Application in Removal of Crystal Violet Dye from Its Aqueous Solution

    International Nuclear Information System (INIS)

    Copolymer hydrogels composed of Poly vinyl alcohol (PVA) and Poly acrylic acid (PAA) were prepared by γ-irradiation in the presence of N,N’ methylene bis acrylamide (MBAM) as crosslinking agent or bentonite clay. The copolymers were characterized by FTIR and SEM. The dye adsorption experiments for Crystal Violet dye (CV) were carried out by using bath procedure. UV-visible absorption spectroscopy was used to determine the adsorption behavior. The effect of different copolymer composition, clay concentration, ph, contact time, adsorbent dose, initial dye concentration, and adsorption temperature were investigated to obtain the best experimental conditions. The adsorption equilibrium was attained after about 24h. of contact time. It was found that the adsorption process was correlated with Freundlich isotherm equation. Kinetic and thermodynamic studies of CV dye onto the prepared hydrogels were also evaluated

  17. Pt、Rh及Pt-Rh合金电极上氢的吸附%Hydrogen Adsorption on Pt, Rh and Pt-Rh Electrodes

    Institute of Scientific and Technical Information of China (English)

    贾梦秋; A.M.Meretskyi

    2005-01-01

    The hydrogen adsorption on Pt-Rh alloys in sulfuric acid aqueous solutions was studied by the method of cathode pulses. Hydrogen adsorption on the electrode with all ratio of alloy components (wRh = 0-100%) is well described by the Temkin logarithmic isotherm. The surface coverage by adsorbed hydrogen at the same potential is decreased with increasing content of rhodium in the system. A linear dependence of adsorption peak potential on the alloy compositions in the case of weakly bonded adsorbed hydrogen is established. Hydrogen adsorption heat as a function of surface coverage for Pt-Rh-electrodes was obtained. The shape of the current-potential curve and position of the weakly bonded hydrogen adsorption on the potential scale are all related to alloy compositions, thus can serve as the basis for the determination surface composition of alloys.

  18. Adsorption of acid dyes on Natural wool yarns

    International Nuclear Information System (INIS)

    The adsorption isotherms have been developed for two acid dyes (red and yellow azo dyes) individually on natural wool yarns. The study revealed strong interactions between the effects of solution ph, temperature and initial dye concentration. Equilibrium uptake data were fitted to the Redlich- Peterson isotherm model. The adsorption behaviour approaches Langmuir model at favourable conditions of higher temperature and lower ph for yellow dye. (authors). 9 refs., 5 tabs., 8 figs

  19. Adsorptive property of rice husk for uranium

    International Nuclear Information System (INIS)

    The adsorption experiments were researched by using the rice husk powder as the adsorbent to remove the U(VI) from aqueous solution. The affecting factors on the U(VI) removal rate such as rice husk particle size, pH, initial concentration, adsorption time, temperature and dosage of adsorbent were evaluated, kinetics and adsorption isotherm law were analyzed, and mechanisms for U(VI) removal were discussed by SEM, FT-IR and energy spectrum analysis. The results show that U(VI) removal rate increases with the decrease of the size of adsorbent, and with the increase of adsorbent dosage and temperature. The process of adsorption can be described by an equation of pseudo 2nd-order mode, and the relation coefficient is 1. The process of adsorption also fits to Freundlich isotherm (R2=0.995 4). The adsorption of uranium on rice husk changes the surface form of rice husk. Hydroxyl, carboxylic, P-O and Si-O are the main functional groups in the reaction with U(VI). The adsorption mechanism is mixture adsorption, including the physical and chemical adsorption. (authors)

  20. Modeling Cryotherapy Ice Ball Dimensions and Isotherms in a Novel Gel-based Model to Determine Optimal Cryo-needle Configurations and Settings for Potential Use in Clinical Practice

    Science.gov (United States)

    Shah, Taimur T.; Arbel, Uri; Foss, Sonja; Zachman, Andrew; Rodney, Simon; Ahmed, Hashim U.; Arya, Manit

    2016-01-01

    Objective To gain a better understanding of ice ball dimensions and temperature isotherms relevant for cell kill when using combinations of cryo-needles we set out to answer 4 questions: (1) what type of cryo-needle? (2) how many needles? (3) best spatial configuration? and (4) correct duty cycle percentage? Methods We conducted laboratory experiments to monitor ice ball dimensions and create multi-needle planar isotherm maps for 17G and 10G cryo-needles using a novel multi-needle thermocouple fixture within gel at body temperature. We tested configurations of 1-4 cryo-needles at duty cycles of 20%-100% with 1-2.5 cm spacing. Results Analysis of various combinations shows that a central core of ≤−40°C develops at a distance of ~1 cm around the cryo-needles. Temperature increases linearly from this point to the ice ball leading edge (0°C), which is a further ≈1 cm away. Thus, the −40°C isotherm is approximately 1 cm inside the leading edge of the ice ball. The optimum distance between cryo-needles was 1.5-2 cm, at duty cycle settings of 70%-100%. At distances further apart or with lower duty cycle settings, ice balls either had a central core >−40°C or had an hourglass shape. Conclusion In answer to questions 1-3, tumor length, diameter, and shape will ultimately determine the number of needles and their configuration. However, we propose a conservative distance for cryo-needle placement between 1 and 1.5 cm should be adopted for clinical practice. In answer to question 4, using low duty cycle settings runs the risk of incomplete −40°C isotherm coverage of the tumor, and thus in routine practice we suggest that settings of 70%-100% are most appropriate. PMID:26902833

  1. Investigation of adsorption performance deterioration in silica gel–water adsorption refrigeration

    International Nuclear Information System (INIS)

    Highlights: ► Adsorption deterioration of silica gel in refrigeration systems is verified. ► Possible factors to cause such deterioration are analyzed. ► Specific surface area, silanol content and adsorption capacity are tested. ► The pollution is the primary factor to decline the adsorption capacity. ► Deteriorated samples are partly restored after being processed by acid solution. - Abstract: Silica gel acts as a key role in adsorption refrigeration systems. The adsorption deterioration must greatly impact the performance of the silica gel–water adsorption refrigeration system. In order to investigate the adsorption deterioration of silica gel, many different silica gel samples were prepared according to the application surroundings of silica gel in adsorption refrigeration systems after the likely factors to cause such deterioration were analyzed. The specific surface area, silanol content, adsorption capacity and pore size distribution of those samples were tested and the corresponding adsorption isotherms were achieved. In terms of the experimental data comparisons, it could be found that there are many factors to affect the adsorption performance of silica gel, but the pollution was the primary one to decline the adsorption capacity. In addition, the adsorption performance of the deteriorated samples after being processed by acid solution was explored in order to find the possible methods to restore its adsorption performance.

  2. The adsorption of H2O and D2O on porous polystyrene adsorbents

    International Nuclear Information System (INIS)

    The adsorption of H2O and D2O on porous polymers, Chromosorb-102 (styrene-divinylbenzene copolymer) and MN-200 (super cross-linked polystyrene), was studied by gas chromatography. Test adsorbates used to study the properties of the surface of these polymers were n-alkanes (C6 C9), C6H6, and the polar compounds CHCl3, CH3NO2, CH3CN, (CH3)2CO, C2H5COOCH3, and (C2H5)2O. The experimental data on the retention of the sorbates were used to determine the contributions of dispersion and specific intermolecular interactions to the total energy of adsorption for the systems studied. The electron donor KD and electron acceptor KA characteristics of the surfaces of Chromosorb-102 and MN-200 were determined. The KD and KA values obtained allow these polymers to be classified as weakly specific adsorbents with the predominance of electron acceptor properties. The adsorption isotherms of H2O and D2O were measured at 55, 67, and 80 deg C. The dependences of the isosteric heats of adsorption Qst on adsorption values were determined. The conclusion was drawn that H2O interacted with the surface of the polymers by the adsorption mechanism, whereas absorption likely made a noticeable contribution to the retention of D2O

  3. Evaluation of vermicompost as a raw natural adsorbent for adsorption of pesticide methylparathion.

    Science.gov (United States)

    Mendes, Camila Bitencourt; Lima, Giovana de Fátima; Alves, Vanessa Nunes; Coelho, Nívia Maria Melo; Dragunski, Douglas Cardoso; Tarley, César Ricardo Teixeira

    2012-01-01

    The assessment of vermicompost (VC) as a low-cost and alternative adsorbent for the removal of the pesticide methylparathion (MP) from an aqueous medium has been investigated by batch and column experiments. Parameters related to MP adsorption, i.e. equilibrium time (61.5 min) and adsorption pH (6.8) were optimized by using Doehlert design. The initial and final MP concentrations after adsorption assays were determined by square-wave adsorptive cathodic stripping voltammetry using an electrode composed of a multiwalled carbon nanotube dispersed in mineral oil. Batch adsorption experimental data were fitted to the Langmuir and Freundlich isotherm adsorptions, and a very good fit to the Langmuir linear model, giving a maximum adsorption capacity (MAC) of 0.17 mg g(-1). This result was very similar to that obtained with the column experiments. In order to evaluate the MP desorption from column packed VC, 100.0 ml of nitric acid solution (pH 3.0) has been percolated through material. No leaching of MP was observed, thus confirming the strong interaction between MP and VC. The satisfactory MAC obtained and low cost makes the VC a reliable natural material for the removal of MP from aqueous effluents. PMID:22519100

  4. Adsorption of Chrysoidine R by using fly ash in batch process

    International Nuclear Information System (INIS)

    This investigation deals with effective utilization of fly ash as adsorbent for the removal of Chrysoidine R from the aqueous solution. The fly ash is a major byproduct generated in coal-based thermal power plants and has good potential for use as an adsorbent. A series of experiments were carried out in a batch adsorption technique to obtain the effect of process variables viz. contact time, pH (2, 4, 6 and 8) initial concentration of the dye (400, 600, 800 and 1000 mg L-1), amount of the adsorbent (125, 250, 375 and 500 mg L-1), and temperature (303, 313, 323 and 333 K) on adsorption. The concentration of dye was determined by spectrophotometer. The results showed that as the amount of the adsorbent was increased, the percentage of dye removal increased accordingly; higher adsorption percentage was observed at lower concentration of chrysoidine. The adsorption data were analyzed using Langmuir and Freundlich isotherms. The adsorption was found to obey pseudo-first order kinetics. An intra particle diffusion model was used to fit the experimental data. The thermodynamic parameters such as standard change in free energy, enthalpy and entropy of adsorption have been calculated. Adsorption of Chrysoidine R on fly ash was found to be an exothermic reaction

  5. Adsorption of methylene blue from aqueous solution on zeolitic material for color and toxicity removal

    Directory of Open Access Journals (Sweden)

    Denise Alves Fungaro

    2011-03-01

    Full Text Available The adsorption of methylene blue (MB from aqueous solution was carried out using zeolite. This adsorbent material was synthesized from fly ash as a low-cost adsorbent, allowing fly ash to become a recycled residue. Factors that affected adsorption were evaluated: initial dye concentration, contact time and temperature. The equilibrium of adsorption was modeled by Langmuir, Freundlich and Temkin models. The adsorption obtained data were well described by Temkin, the adsorption isotherm model. Thermodynamic calculations suggest that the adsorption of methylene blue on zeolite synthesized from fly ash is a spontaneous and exothermic reaction. Acute toxicity was determined for raw and adsorbed methylene blue solutions, as if it was a real liquid residue. Acute effects were substantially reduced after the adsorption treatment. The values of untreated solution of methylene blue were 16.58 ppm up to 18.64 ppm for Vibrio fischeri bacteria and from 0.16 ppm up to 0.43 ppm for Daphnia similis cladoreca exposed to the dye for 48 hours.

  6. Irreversible adsorption of phenolic compounds by activated carbons

    International Nuclear Information System (INIS)

    Studies were undertaken to determine the reasons why phenolic sorbates can be difficult to remove and recover from activated carbons. The chemical properties of the sorbate and the adsorbent surface, and the influences of changes in the adsorption and desorption conditions were investigated. Comparison of isotherms established after different contact times or at different temperatures indicated that phenolic compounds react on carbon surfaces. The reaction rate is a strong function of temperature. Regeneration of carbons by leaching with acetone recovered at least as much phenol as did regeneration with other solvents or with displacers. The physiochemical properties of adsorbents influences irreversible uptakes. Sorbates differed markedly in their tendencies to undergo irreversible adsorption. 64 refs., 47 figs., 32 tabs

  7. Sulfate adsorption and surface precipitation on a volcanic ash soil (allophanic andisol).

    Science.gov (United States)

    Ishiguro, Munehide; Makino, Tomoyuki; Hattori, Yasunobu

    2006-08-15

    Sulfate strongly adsorbs on metal oxides and soils with variable charges. However, its surface precipitation has not been clearly evaluated and its adsorption mechanism has been in dispute. In the present study, an allophanic andisol, a typical volcanic ash soil having both negative and positive variable charges, was used to identify the adsorption mechanism of sulfate. Sulfate adsorption isotherms were obtained by a batch method at pH values of 4, 5, 6, and 7 in a wide range of concentrations in an Na-H-SO(4)-OH system. Theoretical isotherms were applied to the measured values for the evaluation. The surface precipitation was detected by the measured adsorption isotherms, and the BET isotherm confirmed the presence of multilayer adsorption. Stronger and weaker adsorption sites were suggested by using the Langmuir isotherm for the monolayer adsorption. The adsorption energies obtained from the Langmuir equation and recent spectroscopic analysis suggested that the stronger adsorption corresponded to an inner-sphere surface complex and that the weaker adsorption corresponded to outer-sphere surface complexation. The BET and Langmuir equations showed three types of adsorption mechanisms for the sulfate adsorption on the soil. PMID:16750540

  8. Polydopamine-mediated surface functionalization of electrospun nanofibrous membranes: Preparation, characterization and their adsorption properties towards heavy metal ions

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • A simple and versatile approach to produce PEI-functionalized nanofibers. • Novel PEI-functionalized PVC nanofibrous membrane was prepared. • Adsorption of PVC@PDA and PVC@PDA-PEI nanofibrous membranes for Cu2+ was tested. • Isotherms, kinetic model and thermodynamic parameters were investigated. • Adsorption mechanism of Cu2+ on modified membranes was inferred. - Abstract: In this paper, a simple and versatile approach for the fabrication of a polyethyleneimine (PEI)-functionalized nanofibrous membrane utilizing polydopamine (PDA) as a mediator is proposed. The morphology and structure of the PDA-coated and PEI-grafted nanofibrous membranes were confirmed using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Due to a large specific surface area and long fibrous morphology, the synthesized membranes were used as novel adsorbents for copper ion (Cu2+) removal from aqueous solutions. The adsorption of Cu2+ was investigated on the synthesized membranes regarding the membrane dosages, initial solution pH values, initial solution concentrations, contact times and temperatures. In addition, the adsorption equilibrium data of PEI-grafted membranes were well fitted with the Langmuir adsorption isotherm, and a maximum adsorption capacity value of 33.59 mg g−1 was determined (while it was 21.94 mg g−1 for the PDA-coated membranes). The thermodynamic parameters indicated that Cu2+ absorption was a spontaneous and exothermic adsorption process. In addition, XPS peak differentiation imitating analysis permitted the proposal of a copper-amine coordination adsorption mechanism that can be used to explain changes in the adsorption properties compared to PDA coating nanofibrous membranes

  9. Polydopamine-mediated surface functionalization of electrospun nanofibrous membranes: Preparation, characterization and their adsorption properties towards heavy metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Chunlin [School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003 (China); Wang, Heyun [School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003 (China); Key Laboratory for Green Processing of Chemical Engineering of Xinjiang bingtuan, Shihezi University, Shihezi 832003 (China); Wei, Zhong, E-mail: steven_weiz@sina.com [School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003 (China); Key Laboratory for Green Processing of Chemical Engineering of Xinjiang bingtuan, Shihezi University, Shihezi 832003 (China); Li, Chuan; Luo, Zhidong [School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832003 (China)

    2015-08-15

    Graphical abstract: - Highlights: • A simple and versatile approach to produce PEI-functionalized nanofibers. • Novel PEI-functionalized PVC nanofibrous membrane was prepared. • Adsorption of PVC@PDA and PVC@PDA-PEI nanofibrous membranes for Cu{sup 2+} was tested. • Isotherms, kinetic model and thermodynamic parameters were investigated. • Adsorption mechanism of Cu{sup 2+} on modified membranes was inferred. - Abstract: In this paper, a simple and versatile approach for the fabrication of a polyethyleneimine (PEI)-functionalized nanofibrous membrane utilizing polydopamine (PDA) as a mediator is proposed. The morphology and structure of the PDA-coated and PEI-grafted nanofibrous membranes were confirmed using scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Due to a large specific surface area and long fibrous morphology, the synthesized membranes were used as novel adsorbents for copper ion (Cu{sup 2+}) removal from aqueous solutions. The adsorption of Cu{sup 2+} was investigated on the synthesized membranes regarding the membrane dosages, initial solution pH values, initial solution concentrations, contact times and temperatures. In addition, the adsorption equilibrium data of PEI-grafted membranes were well fitted with the Langmuir adsorption isotherm, and a maximum adsorption capacity value of 33.59 mg g{sup −1} was determined (while it was 21.94 mg g{sup −1} for the PDA-coated membranes). The thermodynamic parameters indicated that Cu{sup 2+} absorption was a spontaneous and exothermic adsorption process. In addition, XPS peak differentiation imitating analysis permitted the proposal of a copper-amine coordination adsorption mechanism that can be used to explain changes in the adsorption properties compared to PDA coating nanofibrous membranes.

  10. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation

    International Nuclear Information System (INIS)

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, XP (g H3PO4/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77 K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m2/g) and high pore volume (up to 1.19 cm3/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R2) and the normalized standard deviation Δq (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse. Opposite effects governing MB and phenol

  11. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation

    Energy Technology Data Exchange (ETDEWEB)

    Altenor, Sandro [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); LAQUE, Universite Quisqueya d' Haiti, Port-au-Prince (Haiti); Carene, Betty [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Emmanuel, Evens [LAQUE, Universite Quisqueya d' Haiti, Port-au-Prince (Haiti); Lambert, Jacques; Ehrhardt, Jean-Jacques [Laboratoire de Chimie Physique et Microbiologie pour l' Environnement, UMR 7564 CNRS-Nancy Universities, 405 rue de Vandoeuvre, F 54600 Villers-les-Nancy Cedex (France); Gaspard, Sarra, E-mail: sgaspard@univ-ag.fr [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France)

    2009-06-15

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, X{sub P} (g H{sub 3}PO{sub 4}/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77 K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m{sup 2}/g) and high pore volume (up to 1.19 cm{sup 3}/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R{sup 2}) and the normalized standard deviation {Delta}q (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse

  12. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation.

    Science.gov (United States)

    Altenor, Sandro; Carene, Betty; Emmanuel, Evens; Lambert, Jacques; Ehrhardt, Jean-Jacques; Gaspard, Sarra

    2009-06-15

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, X(P) (gH(3)PO(4)/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m(2)/g) and high pore volume (up to 1.19 cm(3)/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R(2)) and the normalized standard deviation Deltaq (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse. Opposite effects governing MB

  13. Adsorption of basic dye from aqueous solution onto fly ash

    Energy Technology Data Exchange (ETDEWEB)

    J.X. Lin; S.L. Zhan; M.H. Fang; X.Q. Qian; H. Yang [Zhejiang University, Hangzhou (China). College of Civil Engineering and Architecture

    2008-04-15

    The fly ash treated by H{sub 2}SO{sub 4} was used as a low-cost adsorbent for the removal of a typical dye, methylene blue, from aqueous solution. An increase in the specific surface area and dye-adsorption capacity was observed after the acid treatment. The adsorption isotherm and kinetics of the treated fly ash were studied. The experimental results were fitted using Langmuir and Freundlich isotherms. It shows that the Freundlich isotherm is better in describing the adsorption process. Two kinetic models, pseudo-first order and pseudo-second order, were employed to analyze the kinetic data. It was found that the pseudo-second-order model is the better choice to describe the adsorption behavior. The thermodynamic study reveals that the enthalpy ({Delta}H{sup 0}) value is positive (5.63 kJ/mol), suggesting an endothermic nature of the adsorption.

  14. ADSORPTION OF Mg(II) ION FROM AQUEOUS SOLUTION ON CHITOSAN BEADS AND CHITOSAN POWDER

    OpenAIRE

    Sari Edi Cahyaningrum

    2010-01-01

    A basic investigation on the removal of Mg(II) ion from aqueous solution by chitosan beads wasconducted in a batch adsorption system. The influence of different experimental parameters; pH,agitation period and different concentration of Mg(II) ion was evaluated. A pH 7.0 was found to be anoptimum pH for Mg(II) adsorption onto chitosan powder and chitosan beads. The Langmuir andFreundlich adsorption isotherm models were applied to describe the isotherms and isotherm constantsfor the adsorption...

  15. Adsorption of alkenyl succinic anhydride from solutions in carbon tetrachloride on a fine magnetite surface

    Science.gov (United States)

    Balmasova, O. V.; Ramazanova, A. G.; Korolev, V. V.

    2016-06-01

    The adsorption of alkenyl succinic anhydride from a solution in carbon tetrachloride on a fine magnetite surface at a temperature of 298.15 K is studied using fine magnetite, which forms the basis of magnetic fluids, as the adsorbent. An adsorption isotherm is recorded and interpreted in terms of the theory of the volume filling of micropores (TVFM). Adsorption process parameters are calculated on the basis of the isotherm. It is shown that at low equilibrium concentrations, the experimental adsorption isotherm is linear in the TVFM equation coordinates.

  16. Calculating henry adsorption constants of molecular hydrogen at 77 K on alumophosphate zeolites with different microchannel sizes

    Science.gov (United States)

    Grenev, I. V.; Gavrilov, V. Yu.

    2014-01-01

    Adsorption isotherms of molecular hydrogen are measured at 77 K in a series of AlPO alumophosphate zeolites with different microchannel sizes. The potential of the intermolecular interaction of H2 is calculated within the model of a cylindrical channel of variable size. Henry constants are calculated for this model for arbitrary orientations of the adsorbate molecules in microchannels. The experimental and calculated values of the Henry adsorption constant of H2 are compared at 77 K on AlPO zeolites. The constants of intermolecular interaction are determined for the H2-AlPO system.

  17. Adsorption behaviour of bulgur.

    Science.gov (United States)

    Erbaş, Mustafa; Aykın, Elif; Arslan, Sultan; Durak, Atike N

    2016-03-15

    The aim of this research was to determine the adsorption behaviour of bulgur. Three different particle sizes (2dry matter and 4.96-16.57, respectively. Constant k was between 0.85 and 0.93, and GAB equation was determined to fit very well for bulgur adsorption, because of %E values lower than 10%. Bulgur must be stored below 70% relative humidity and with less than 10 g water per 100 g of dry mater. PMID:26575716

  18. 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.

  19. Adsorption of crude oil from aqueous solution by hydrogel of chitosan based polyacrylamide prepared by radiation induced graft polymerization

    International Nuclear Information System (INIS)

    The adsorption of crude oil (initial concentration 0.5-30 g/L) from aqueous solution using hydrogel of chitosan based polyacrylamide (PAM) prepared by radiation induced graft polymerization has been investigated. The prepared hydrogel was characterized by FTIR and SEM micrographs. The experiments were carried out as a function of different initial concentrations of oil residue, acrylamide concentration, contact time and pH to determine the optimum condition for the adsorption of residue oil from aqueous solution and sea water. The results obtained showed that the hydrogel prepared at concentration of 40% acrylamide (AAm) and at a radiation dose of 5 kGy has high removal efficiency of crude oil 2.3 g/g at pH 3. Equilibrium studies have been carried out to determine the capacity of the hydrogel for adsorption of crude oil, Langmuir and Freundlich adsorption models were applied to describe the experimental isotherms and isotherms constants. Equilibrium data were found to fit very well with both Freundlich and Langmuir models. Also the adsorption of oil onto the hydrogel behaves as a pseudo-second-order kinetic models rather than the pseudo-first-order kinetic model.

  20. The adsorption of hydrogen on nano-structured carbons

    Energy Technology Data Exchange (ETDEWEB)

    Didion, A.; Gadiou, R.; Vix-Guterl, C. [Institut de Chimie des Surfaces et Interfaces, CNRS UPR 9069, 68 - Mulhouse (France); Piquero, Th.; David, P. [CEA Centre d' Etudes du Ripault, 37 - Tours (France)

    2005-07-01

    A major key point for the development of hydrogen as an energy source is the design of a safe and compact storage device. The adsorption of molecular hydrogen on various carbon structures has been widely studied during the last two decades, and the storage capacities which are obtained are of the order of a few weight percents. Nano-structured carbons can be obtained by templating from ordered meso-porous silicas, different carbon precursors have been used such as sucrose solutions, pitch, or propylene [1-3]. Compared to conventional activated carbons, these carbon materials have specific features such as an ordered network of meso-pores and a micro-porous volume which is obtained without any activation. It has been shown that the storage capacity of these carbons materials is comparable to the one of activated carbo4], and further investigation is needed to understand the influence of the pore shape and connectivity on the adsorption. The objective of this study was to obtained more insight in the determination of the pore size distribution of nano-structured carbons, and to correlate this measurement with hydrogen adsorption capacities. Five nano-structured carbons were studied and compared to three activated carbons. For all samples, the adsorption isotherms of nitrogen at 77 K, and CO{sub 2} at 273 were measured. From these isotherms, the following textural parameters were determined: BET surface area, total porous volume, the volume of micro-pores and super-micro-pores were obtained from Dubinin-Radushkevich equation on CO{sub 2} and nitrogen isotherm respectively. The pore size distribution was obtained with a DFT analysis on the N{sub 2} adsorption isotherm. DFT analysis showed that nano-structured carbon materials have a bimodal distribution with ultra-micropores and a large volume of small meso-pores. The hydrogen capacity of these carbon materials was then measured at 77 K with a manometric device. Although hydrogen is in supercritical state in the pores

  1. The adsorption of hydrogen on nano-structured carbons

    Energy Technology Data Exchange (ETDEWEB)

    Antoine Didion; Roger Gadiov; Cathie Vix Guterl [Institut de Chimie des Surfaces et Interfaces, CNRS UPR 9069, 15, rue Jean Starcky, BP 2488, 68093 Mulhouse cedex (France); Thierry Piquero; Patrick David [CEA Le Ripault, BP 16, 37260 Monts (France)

    2005-07-01

    A major key point for the development of hydrogen as an energy source is the design of a safe and compact storage device. The adsorption of molecular hydrogen on various carbon structures has been widely studied during the last two decades, and the storage capacities which are obtained are of the order of a few weight percents. Nano-structured carbons can be obtained by templating from ordered meso-porous silicas, different carbon precursors have been used such as sucrose solutions, pitch, or propylene. Compared to conventional activated carbons, these carbon materials have specific features such as an ordered network of meso-pores and a microporous volume which is obtained without activation. It has been shown that the storage capacity of these carbons materials is comparable to the one of activated carbons, and further investigation is needed to understand the influence of the pore shape and connectivity on the adsorption. The objective of this study was to obtained more insight in the determination of the pore size distribution of nano-structured carbons, and to correlate this measurement with hydrogen adsorption capacities. Five nano-structured carbons were studied and compared to three activated carbons. For all samples, the adsorption isotherms of nitrogen at 77 K, and CO{sub 2} at 273 K were measured. From these isotherms, the following textural parameters were determined: BET surface area, total porous volume, the volume of micropores and super-micropores were obtained from Dubinin-Radushkevich equation on CO{sub 2} and nitrogen isotherm respectively. The pore size distribution was obtained with a DFT analysis on the N{sub 2} adsorption isotherm. DFT analysis showed that nano-structured carbon materials have a bimodal distribution with ultra-micro-pores and a large volume of small meso-pores. The hydrogen capacity of these carbon materials was then measured at 77 K with a manometric device. Although hydrogen is in supercritical state in the pores, a first

  2. The adsorption of hydrogen on nano-structured carbons

    International Nuclear Information System (INIS)

    A major key point for the development of hydrogen as an energy source is the design of a safe and compact storage device. The adsorption of molecular hydrogen on various carbon structures has been widely studied during the last two decades, and the storage capacities which are obtained are of the order of a few weight percents. Nano-structured carbons can be obtained by templating from ordered meso-porous silicas, different carbon precursors have been used such as sucrose solutions, pitch, or propylene. Compared to conventional activated carbons, these carbon materials have specific features such as an ordered network of meso-pores and a microporous volume which is obtained without activation. It has been shown that the storage capacity of these carbons materials is comparable to the one of activated carbons, and further investigation is needed to understand the influence of the pore shape and connectivity on the adsorption. The objective of this study was to obtained more insight in the determination of the pore size distribution of nano-structured carbons, and to correlate this measurement with hydrogen adsorption capacities. Five nano-structured carbons were studied and compared to three activated carbons. For all samples, the adsorption isotherms of nitrogen at 77 K, and CO2 at 273 K were measured. From these isotherms, the following textural parameters were determined: BET surface area, total porous volume, the volume of micropores and super-micropores were obtained from Dubinin-Radushkevich equation on CO2 and nitrogen isotherm respectively. The pore size distribution was obtained with a DFT analysis on the N2 adsorption isotherm. DFT analysis showed that nano-structured carbon materials have a bimodal distribution with ultra-micro-pores and a large volume of small meso-pores. The hydrogen capacity of these carbon materials was then measured at 77 K with a manometric device. Although hydrogen is in supercritical state in the pores, a first computation of the

  3. Sorption Isotherms and Probability Theory of Complex Systems

    OpenAIRE

    Brouers, F.

    2013-01-01

    We show that most of the empirical or semi-empirical isotherms proposed to extend the Langmuir formula to sorption (adsorption, chimisorption and biosorption) on heterogeneous surfaces in the gaseous and liquid phase belong to the family and subfamily of the Burr_{XII} cumulative distribution functions. As a consequence they obey relatively simple differential equations which describe birth and death phenomena resulting from mesoscopic and microscopic physicochemical processes. Using the prob...

  4. Adsorption Desalination: A Novel Method

    KAUST Repository

    Ng, Kim Choon

    2010-11-15

    The search for potable water for quenching global thirst remains a pressing concern throughout many regions of the world. The demand for new and sustainable sources and the associated technologies for producing fresh water are intrinsically linked to the solving of potable water availability and hitherto, innovative and energy efficient desalination methods seems to be the practical solutions. Quenching global thirst by adsorption desalination is a practical and inexpensive method of desalinating the saline and brackish water to produce fresh water for agriculture irrigation, industrial, and building applications. This chapter provides a general overview of the adsorption fundamentals in terms of adsorption isotherms, kinetics, and heat of adsorption. It is then being more focused on the principles of thermally driven adsorption desalination methods. The recent developments of adsorption desalination plants and the effect of operating conditions on the system performance in terms of specific daily water production and performance ratio are presented. Design of a large commercial adsorption desalination plant is also discussed herein.

  5. Adsorption of tetracycline on soil and sediment: Effects of pH and the presence of Cu(II)

    International Nuclear Information System (INIS)

    Tetracycline (TC) is frequently detected in the environment, however, knowledge on the environmental fate and transport of TC is still limited. Batch adsorption experiments of TC by soil and sediment samples were conducted. The distribution of charge and electrostatic potential of individual atoms of various TC species in the aqueous solution were determined using MOPAC version 0.034 W program in ChemBio3D Ultra software. Most of the adsorption isotherms on the soil, river and marine sediments were well fitted with the Freundlich and Polanyi-Manes (PMM) models. The single point organic carbon (OC)-normalized adsorption distribution coefficients (KOC) and PMM saturated adsorption capacity (QOC0) values of TC were associated with the mesopore volume and clay content to a greater extent, indicating the mesopore volume of the soil and sediments and their clay content possibly influenced the fate and transport of TC in the natural environment. The adsorption of TC on soil and sediments strongly depended on the pH and presence of Cu(II). The presence of Cu(II) facilitated TC adsorption on soil and sediments at low pH (pH < 5), possibly due to the metallic complexation and surface-bridging mechanism by Cu(II) adsorption on soil and sediments. The cation exchange interaction, metallic complexation and Coulombic interaction of mechanisms for adsorption of TC to soils and sediments were further supported by quantum chemical calculation of various TC species in different pH.

  6. Determination of Sb(III) using an ex-situ bismuth screen-printed carbon electrode by adsorptive stripping voltammetry.

    Science.gov (United States)

    Rojas-Romo, Carlos; Serrano, Núria; Ariño, Cristina; Arancibia, Verónica; Díaz-Cruz, José Manuel; Esteban, Miquel

    2016-08-01

    The determination of Sb(III) on an ex-situ bismuth screen-printed carbon electrode (ex-situ BiSPCE) by means of adsorptive stripping voltammetry (AdSV) using quercetin-5'-sulfonic acid as chelating agent was optimized. The effect of different experimental parameters such pH, ligand concentration (CQSA), accumulation potential (Eacc) and accumulation time (tacc) were studied to obtain a wide linear range, the highest sensitivity and the lowest detection limit. Ex-situ BiSPCE was analytically compared with a sputtered bismuth screen-printed electrode (BispSPE) under optimal conditions. The obtained analytical parameters suggest that ex-situ BiSPCE behaves much better than BispSPE and the first was selected for this study. Optimal parameters were pH=4.6; CQSA=10.0 to 20.0×10(-6)molL(-1); Eacc=-0.5V and tacc=60s. Peak area is proportional to Sb(III) concentration up to 100.0μgL(-1) (tacc 60s) and 45.0μgL(-1) (tacc 120s) range, with detection limits of 1.2μgL(-)(1) (tacc 60s) and 0.8μgL(-1) (tacc 120s). The relative standard deviation for a Sb(III) solution (20.0μgL(-1)) was 3.9% for ten successive assays. Thus, the effect of various interfering metal ions was studied and the methodology was validated using a spiked groundwater reference material with very satisfactory results. PMID:27216652

  7. Experimental Setup for Determining Ammonia-Salt Adsorption and Desorption Behavior Under Typical Heat Pump Conditions. Experimental Results

    Energy Technology Data Exchange (ETDEWEB)

    Van der Pal, M.; De Boer, R.; Veldhuis, J.B.J. [ECN Biomass and Energy Efficiency, Petten (Netherlands)

    2013-09-15

    For the aim of obtaining a better understanding of the performance of a salt-ammonia sorption reactor/heat exchanger a new test-rig was developed. This test-rig enables the measurement of the performance in adsorption and desorption mode of different sorption reactor designs. It measures the speed of uptake and release of ammonia gas of various salt-ammonia reactions under well-controlled and well-monitored process conditions, similar to the heat pump conditions. The test-rig measures the ammonia uptake and release under controlled pressure and temperature conditions. Temperatures of the salt reactor can be varied from ambient temperature up to 200{sup o}C and the ammonia pressure can be varied between 0.02 to 2 MPa. These conditions can be set independently and repeated at regular time-intervals. Besides NH3-mass-flow meters, pressure and temperature sensors, the setup also contains an endoscope to observe any macroscopic structural changes in the material during uptake and release of ammonia. Measurements so far have shown a liquid phase of LiCl.3NH3 at pressures of 0.5 MPa and temperatures exceeding 90{sup o}C. Voilent foaming is observed at 120{sup o}C resulting in salt losses. A correlation was determined between the reaction rate of MgCl{sub 2}(2-6)NH3 and the relative pressure gradient yielding a reaction time of about 1500 seconds for a relative pressure difference of 1. Multiple sorption cycles of the CaCl{sub 2}(2-4)NH3 reaction, showed a reduced activity from 85% of the theoretical maximum sorbed mass at the first sorption cycle, to 15% after 300+ cycles.

  8. Adsorption and Desorption of Methiopyrsulfuron in Soils

    Institute of Scientific and Technical Information of China (English)

    WU Chun-Xian; WANG Jin-Jun; ZHANG Su-Zhi; ZHANG Zhong-Ming

    2011-01-01

    Methiopyrsulfuron is a new low-rate sulfonylurea herbicide for weed control in wheat; however, there is a lack of published information on its behavior in soils. In this study, methiopyrsulfuron adsorption and desorption were measured in seven soils sampled from Heilongjiang, Shandong, Jiangxi, Sichuan, Anhui, and Chongqing provinces of China using a batch equilibrium method. The Freundlich equation was used to described its adsorption and desorption. Adsorption isotherms were nonlinear with the values of Kf-ads, the Freundlich empirical constant indicative of the adsorption capacity,ranging from 0.75 to 2.46, suggesting that little of this herbicide was adsorbed by any of the seven soils. Soil pH and organic matter content (OM) were the main factors influencing adsorption; adsorption was negatively correlated with pH and positively correlated with OM. Methiopyrsulfuron desorption was hysteretic on the soils with high OM content and low pH.

  9. The effect of chemical treatment on adsorption of natural gas by multi-walled carbon nanotubes: Sorption equilibria and thermodynamic studies

    Directory of Open Access Journals (Sweden)

    Delavar M.

    2012-01-01

    Full Text Available In this study, adsorption of methane as the main constituent of natural gas was firstly studied on the pristine multi-walled carbon nanotubes (MWCNTs and then purification and chemical treatments of MWCNTs was performed to enhance the natural gas adsorption capacity. MWCNTs were chemically treated using different methods in this research. The results revealed that chemical treatment of the MWCNTs in presence of H2SO4/HNO3 acidic mixture in 3:1 volume ratio, enhanced considerably natural gas adsorption capacity (an optimal up to 45 mmol/g at temperature of 298.15 K and the pressure of 50 bar compared to the pristine MWCNTs (about 27 mmol/g at the same operating conditions. This effect can be attributed to the opening of the nanotubes caps with a major alteration in its structural properties due to chemical treatment. The experimental data of adsorption were almost equally well described by Langmuir, Freundlich and Sips equations to determine the model isotherms. The best fit was obtained by the Sips model isotherm with the r-squared value near to unity. Furthermore, using the experimental data obtained in different temperatures the isosteric heat of natural gas adsorption onto pristine MWCNTs was also calculated in the interested range of pressures and temperatures using the thermodynamic-based Clausius-Clapeyron equation from the Sips isotherm model. The results revealed an energetically heterogeneous surface of MWCNTs in natural gas adsorption. Also the natural gas adsorption process was kinetically studied through pseudo-second order and intra-particle diffusion models which indicated the intra-particular diffusion is rate limiting step in adsorption of methane on MWCNTs.

  10. Rapid determination of Cl- by light-absorption ratio variation approach using Cl——eosin Y-Ag+ adsorptive precipitation

    Institute of Scientific and Technical Information of China (English)

    Jing Bai; Hong Yan Wang; Hong Wen Gao

    2008-01-01

    The adsorptive precipitation between eosin Y (EY) and AgCl colloids at pH 3.73 caused the sensitive color change of thesolution. The reaction mechanism between EY and AgCl was analyzed and this reaction was used for determination of Cl- in tracelevel by the light-absorption radio variation approach.2008 Hong Wen Gao. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

  11. Pore and surface diffusion of liquid-phase multicomponent adsorption in fixed beds I

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jae Wye; Yoon, Se Hoon; Kim, Chul [Ajou University, Suwon (Korea, Republic of); Lee, Hwo Keun; Oh, Won Zin [Korea Atomic Energy Research Insititute, Taejon (Korea, Republic of)

    1997-12-31

    The adsorption capacity were measured through two-stage adsorption experiment with the adsorption isotherm and flow system. The 3 and more activate carbons were selected with surface area and pore size distribution, the adsorption relation of cl{sub 2} were reviewed with the characteristics of the activate carbon, 500 ppm cl{sub 2} (v/v in helium, in flow system) were selected and analyzed with G. C. The variation of adsorption rate were checked with the adsorption capacity in adsorption bed (shallow bed). Through the results, it is possible to design activate carbon adsorption of single component cl{sub 2}. (author) 2 refs., 3 figs.

  12. Pore and surface diffusion of liquid-phase multicomponent adsorption in fixed beds I

    International Nuclear Information System (INIS)

    The adsorption capacity were measured through two-stage adsorption experiment with the adsorption isotherm and flow system. The 3 and more activate carbons were selected with surface area and pore size distribution, the adsorption relation of cl2 were reviewed with the characteristics of the activate carbon, 500 ppm cl2 (v/v in helium, in flow system) were selected and analyzed with G. C. The variation of adsorption rate were checked with the adsorption capacity in adsorption bed (shallow bed). Through the results, it is possible to design activate carbon adsorption of single component cl2. (author) 2 refs., 3 figs

  13. Determinations of the Colloidal Structure of Pulp Fibres by Adsorption in Liquid Medium. The Role of Pulping Process

    OpenAIRE

    László Koltai; Miklósné Baksay; Sándor Rohrsetzer

    2008-01-01

    We used the principles of theoretical colloid chemistry and our earlier results.We developed further the measuring of the specific surface by adsorption method. The aimof the study was the change of the usability of the method in showing out the structuraldifferences of the pulping process. We found that the different pulping processes results indifferences of the specific surface of the fibres measured with iron/III/hydroxide, TiO2 andMethylene blue adsorption, and we also found that the spe...

  14. Characterization of sorption properties of selected soils from Lublin region by using water vapour adsorption method

    Science.gov (United States)

    Skic, Kamil; Boguta, Patrycja; Sokołowska, Zofia

    2016-04-01

    *The studies were carried out within the framework of a research project. The project was financed from funds of National Science Center on the base of decision number DEC-2013/11/D/NZ9/02545 Among many methods proposed to study sorption properties of soils an analysis of adsorption/ desorption isotherm is probably the easiest and most convenient one. It characterizes both quantity and quality of mineral and organic components and also their physical and physicochemical properties. The main aim of this study is comparison of sorption properties of selected Polish soils by using water vapour adsorption method. Samples were taken from the depth of 0-20 cm, from the Lublin region, eastern Poland. Soils were selected on the basis of their different physicochemical properties and were classified as: Haplic Fluvisol, Haplic Chernozem, Mollic Gleysol, Rendzic Phaeozem, Stagnic Luvisol, Haplic Cambisol (WG WRB 2006). Data taken from experimental adsorption isotherms were used to determine parameters of monolayer capacity, specific surface area and the total amount of vapour adsorbed at relative pressure of 0.974. Obtained adsorption and desorption isotherms reviled that adsorbate molecules interacted with the soil particles in different extent. Similar monolayer capacity was observed for Haplic Fluvisol, Haplic Chernozem and Stagnic Luvisol, while for Mollic Gleysol was more than 4 times higher. Mollic Gleysol was also characterized by highest values of specific surface area as well as quantity of adsorbed vapour at relative pressure of 0.974. Higher sorption was caused by presence of soil colloids which contains functional groups of a polar nature (mainly hydroxyls, phenolic and carboxyls). These groups similarly to silicates, oxides, hydratable cations as well as electric charge form adsorption centres for water vapour molecules.

  15. Adsorption of methylene blue from aqueous solution on zeolitic material for color and toxicity removal

    OpenAIRE

    Denise Alves Fungaro; Lucas Caetano Grosche; Alessandro Pinheiro; Juliana de Carvalho Izidoro; Sueli Ivone Borrely

    2011-01-01

    The adsorption of methylene blue (MB) from aqueous solution was carried out using zeolite. This adsorbent material was synthesized from fly ash as a low-cost adsorbent, allowing fly ash to become a recycled residue. Factors that affected adsorption were evaluated: initial dye concentration, contact time and temperature. The equilibrium of adsorption was modeled by Langmuir, Freundlich and Temkin models. The adsorption obtained data were well described by Temkin, the adsorption isotherm model....

  16. A Linear Diffusion Model of Adsorption Kinetics at Fluid/Fluid Interfaces

    OpenAIRE

    Staszak, Maciej

    2016-01-01

    The paper presents a new model for kinetically controlled adsorption at the fluid/fluid interface. The main purpose of the presented approach is to relate easy to estimate bulk surfactant concentration with Gibbs surface excess. Two adsorption isotherms are involved in the new model development: Frumkin and Szyszkowski isotherms. Additionally the Johannsen time profile of concentration in the adsorption layer is assumed and estimated in the model derivation. The proposed approach assumes the ...

  17. Synthesis and adsorption properties of chitosan-silica nanocomposite prepared by sol-gel method

    Science.gov (United States)

    Budnyak, Tetyana M.; Pylypchuk, Ievgen V.; Tertykh, Valentin A.; Yanovska, Elina S.; Kolodynska, Dorota

    2015-02-01

    A hybrid nanocomposite material has been obtained by in situ formation of an inorganic network in the presence of a preformed organic polymer. Chitosan biopolymer and tetraethoxysilane (TEOS), which is the most common silica precursor, were used for the sol-gel reaction. The obtained composite chitosan-silica material has been characterized by physicochemical methods such as differential thermal analyses (DTA); carbon, hydrogen, and nitrogen (CHN) elemental analysis; nitrogen adsorption/desorption isotherms, scanning electron microscopy (SEM); and Fourier transform infrared (FTIR) spectroscopy to determine possible interactions between silica and chitosan macromolecules. Adsorption of microquantities of V(V), Mo(VI), and Cr(VI) oxoanions from the aqueous solutions by the obtained composite has been studied in comparison with the chitosan beads, previously crosslinked with glutaraldehyde. The adsorption capacity and kinetic sorption characteristics of the composite material were estimated.

  18. Adsorption of Cu2+, Zn2+ and Cd2+ on Bacillus subtilis

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    A process of biosorption of Cu2+, Zn2+ and Cd2+ on Bacillus subtilis was investigated.The experiments show that the process of biosorption is quite fast. The maximum adsorption was reached after 5 min and hardly changed with time. The experimental data was analyzed using four sorption kinetic models: the pseudo-first-order, the Ritchie second-order, the modified second-order and the Elovich equations, which helped to determine the best-fit equation for the sorption of metal ions onto biomass. The results show that both the Ritchie second-order and modified secondorder equations can fit the experimental data. The Langmuir model is able to accurately describe adsorption of Cu2+ and Zn2+ on B. subtilis. The experimental data points of adsorption Cd2+ and Zn2+ on B. subtilis are described by Freundlich isotherms model.

  19. Kinetic adsorption of application of carbon nanotubes for Pb(II) removal from aqueous solution

    Institute of Scientific and Technical Information of China (English)

    Nassereldeen A Kabbashi; Muataz A Atieh; Abdullah Al-Mamun; Mohamed E S Mirghami; MD Z Alam; Noorahayu Yahya

    2009-01-01

    The capability of carbon nanotubes (CNTs) to adsorb lead (Pb) in aqueous solution was investigated. Batch mode adsorption experiment was conducted to determine the effects of pH, agitation speed, CNTs dosage and contact time. The removal of Pb(II) was reach to maximum value 85% or 83% at pH 5 or 40 mg/L of CNTs, respectively. Higher correlation coefficients from Langmuir isotherm model indicates the strong adsorptions of Pb(II) on the surface of CNTs (adsorption capacity Xm = 102.04 mg/g). From this study, the results indicates that the highest percentage removal of Pb (96.03%) can be achieved at pH 5, 40 mg/L of CNTs, contact time 80 min, and agitation speed 50 r/min.

  20. Conceptual adsorption models and open issues pertaining to performance assessment

    International Nuclear Information System (INIS)

    Recently several articles have been published that question the appropriateness of the distribution coefficient, Rd, concept to quantify radionuclide migration. Several distinct issues surrounding the modeling of nuclide retardation. The first section defines adsorption terminology and discusses various adsorption processes. The next section describes five commonly used adsorption conceptual models, specifically emphasizing what attributes that affect adsorption are explicitly accommodated in each model. I also review efforts to incorporate each adsorption model into performance assessment transport computer codes. The five adsorption conceptual models are (1) the constant Rd model, (2) the parametric Rd model, (3) isotherm adsorption models, (4) mass action adsorption models, and (5) surface-complexation with electrostatics models. The final section discusses the adequacy of the distribution ratio concept, the adequacy of transport calculations that rely on constant retardation factors and the status of incorporating sophisticated adsorption models into transport codes. 86 refs., 1 fig., 1 tab

  1. Conceptual adsorption models and open issues pertaining to performance assessment

    International Nuclear Information System (INIS)

    Recently several articles have been published that question the appropriateness of the distribution coefficient, Rd, concept to quantify radionuclide migration. Several distinct issues are raised by various critics. In this paper I provide some perspective on issues surrounding the modeling of nuclide retardation. The first section defines adsorption terminology and discusses various adsorption processes. The next section describes five commonly used adsorption conceptual models, specifically emphasizing what attributes that affect adsorption are explicitly accommodated in each model. I also review efforts to incorporate each adsorption model into performance assessment transport computer codes. The five adsorption conceptual models are (1) the constant Rd model, (2) the parametric Rd model, (3) isotherm adsorption models, (4) mass-action adsorption models, and (5) surface-complexation with electrostatics models. The final section discusses the adequacy of the distribution ratio concept, the adequacy of transport calculations that rely on constant retardation factors and the status of incorporating sophisticated adsorption models into transport codes

  2. Competitive adsorption of heavy metal ions on peat

    Institute of Scientific and Technical Information of China (English)

    LIU Zhi-rong; ZHOU Li-min; WEI Peng; ZENG Kai; WEN Chuan-xi; LAN Hui-hua

    2008-01-01

    The uptake capacities, and the adsorption kinetics, of copper, Cu(Ⅱ), nickel, Ni(Ⅱ), and cadmium, Cd(Ⅱ), on peat have been studied under static conditions. The results show that the adsorption rates are rapid: equilibrium is reached in twenty minutes. The adsorption of copper, nickel and cadmium is pH dependent over the pH range from 2 to 6. The adsorption kinetics can be excellently described by the Elovich kinetic equation. The adsorption isotherm fits a Langmuir model very well. The adsorption capacifies follow the order Cu2+>Ni2+>Cd2+ in single-component systems and the competitive adsorption capacities fall in the decreasing order Cu2+> Ni2+>Cd2+ in multi-component systems. The adsorption capacities of these three heavy metal ions on peat are consistent with their observed competitive adsorption capacities.

  3. Determination of metals in soils and sewage sludges by ion chromatography and the effect of cropping systems on metal adsorption by soils

    Energy Technology Data Exchange (ETDEWEB)

    Basta, N.T.

    1989-01-01

    An accurate and precise ion chromatographic (IC) method for determination of total Cu, Ni, and Zn in soils was developed. The metals in soil digests were extracted with dithizone in CHCl{sub 3}, and the metal-dithizonate complexes were digested with HNO{sub 3} before injection into the IC system. After separation on HPIC-CS5 column, the metals were determined by measuring the absorbance of metal complexes formed by postcolumn reaction with 4-(2-pyridylazo) resorcinol (PAR) at 520 nm. The results by this IC method agreed closely with those obtained by atomic absorption spectrophotometry (AA). Comparison of results of total Cu, Mn, Ni, Pb, and Zn with those obtained by AA showed that this method was accurate and precise for determination of metals in sewage sludges. The effect of cropping systems on adsorption of metals by soils was studied for two long-term rotation experiments, each having three crop rotations (continuous corn (CCCC), corn-soybean-corn-soybean, and corn-oats-meadow-meadow) and treatments with (+N) and without (O N) ammoniacal fertilizer. Results for soils under CCC rotations (+N) showed lower metal adsorption than those under CCCC (O N) and other crop rotations, which showed similar metal adsorption. Comparison of results obtained after adjusting the soil-solution pH with those for unadjusted solution pH showed that differences in metal adsorption by these soils were due to solution pH. Plots of the logarithm of the metal distribution coefficient (log K{sub d}) vs. pH suggested competition of protons with metal ions for exchange sites. In general, proton coefficient values (H{sup +}/M{sup 2+} ratios) followed the sequence: Pb > Cu > Cd = Ni = Zn. Calculated H{sup +}/M{sup 2+} ratios of <2 (ranging from 0.288 to 1.45) were obtained.

  4. Molecular simulations in microporous materials: adsorption and separation

    NARCIS (Netherlands)

    Castillo, J.M.

    2010-01-01

    The adsorption of water on hydrophobic zeolites such as silicalite and on hydrophilic MOF (metal-organic framework), Cu-BTC, is completely different, as described in chapters 2 and 4. While in hydrophobic materials water adsorption isotherms are very steep and difficult to measure, both experimental

  5. Development of a first-order kinetics-based model for the adsorption of nickel onto peat

    Institute of Scientific and Technical Information of China (English)

    LIU Zhi-rong; CHEN Xiao-song; ZHOU Li-min; WEI Peng

    2009-01-01

    The use of peat for the removal of nickel from aqueous solutions has been investigated at various pH values by means of static conditions. The present research shows that the ability of Ni to hind to peat increases as the pH value increases. The solutions reach adsorption equilibrium rapidly. A reasonable kinetic model, first-order in nickel concentration, has been developed and fitted to the adsorption of nickel (Ⅱ) onto peat. The first-order model provides a good correlation to the experimental data. The characteristic parameters of the Langmuir isotherm were determined at various temperatures. The relationship between kinetics and equilibrium isotherms was established through the forward- and backward-rate-constants, k and k2, and the equilibrium constant, K.

  6. 40 CFR 796.2750 - Sediment and soil adsorption isotherm.

    Science.gov (United States)

    2010-07-01

    ... Agricultural and Food Chemistry, 23:720-724 (1975). (2) Goring, C.A.I., Hamaker, J.W., (eds). Organic Chemicals... soil,” Journal of Agricultural and Food Chemistry, 23:578-581 (1973). (5) Saltzman, S.L. et al... section served as the basis for this section. The soil and colloid chemistry literature and the...

  7. PREPARATION AND CHARACTERIZATION OF NOVEL CHITOSAN DERIVATIVES:ADSORPTION EQUILIBRIUM OF IRON(Ⅲ)ION

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    The adsorption of Fe(Ⅲ)ions from aqueous solution by chitosan alpha-ketoglutaric acid(KCTS)and hydroxamated chitosan alpha-ketoglutaric acid(HKCTS)was studied in a batch adsorption system.Experiments were carried out as function of pH,temperature,agitation rate and concentration of Fe(Ⅲ)ions.The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms and isotherm constants were determined.The Langmuir model agrees very well with experimental data.The pseudo-first-order and second-order kinetic models were used to describe the kinetic data and the rate constants were evaluated.The dynamical data fit well with the second-order kinetic model.The pseudo second-order kinetic model was indicated with the activation energy of 19.61 and 7.98 KJ/mol for KCTS and HKCTS,respectively.It is suggested that the overall rate of Fe(Ⅲ)adsorption is likely to be controlled by the chemical process.Results also showed that novel chitosan derivatives(KCTS and HKCTS)were favorable adsorbents.

  8. Determination of charge carrier concentration in doped nonpolar liquids by impedance spectroscopy in the presence of charge adsorption.

    Science.gov (United States)

    Yezer, Benjamin A; Khair, Aditya S; Sides, Paul J; Prieve, Dennis C

    2016-05-01

    The impedance of dodecane doped with sorbitan trioleate (Span 85), sorbitan monooleate (Span 80) and sorbitan monolaurate (Span 20) was measured as a function of frequency using a 10mV amplitude sinusoidal voltage applied across a parallel plate cell with a 10μm spacing. The tested solutions varied in concentration from 1mM to 100mM and the frequency range was 10(-2)-10(4)Hz. Nyquist plots of all three surfactants showed the high frequency semicircle characteristic of parallel resistance and capacitance but often exhibited a second semicircle at low frequencies which was attributed to charge adsorption and desorption. The electrical conductivity of each surfactant was proportional to surfactant concentration for concentrations above 10mM. Fitting the data to models for charge migration, differential capacitance, and adsorption allowed extraction of both charge concentration and two kinetic parameters that characterize the rate of adsorption and desorption. Above 10mM the ratio of charge carriers per surfactant molecule was 22ppm for Span 20, 3ppm for Span 80, and 0.2ppm for Span 85. A higher number of charge carriers per molecule of surfactant was associated with larger micelles. The adsorption rate constants were independent of surfactant concentration while the desorption rate constants were proportional to the surfactant concentration. This dependence indicated that uncharged surfactant, whether in micelles or not, participated in the desorption of charge. Predictions of the adsorption/desorption model for large constant electric fields agreed qualitatively with data from the literature (Karvar et al., 2014). PMID:26905337

  9. Evaluating the long-term performance of low-cost adsorbents using small-scale adsorption column experiments.

    Science.gov (United States)

    Callery, O; Healy, M G; Rognard, F; Barthelemy, L; Brennan, R B

    2016-09-15

    This study investigated a novel method of predicting the long-term phosphorus removal performance of large-scale adsorption filters, using data derived from short-term, small-scale column experiments. The filter media investigated were low-cost adsorbents such as aluminum sulfate drinking water treatment residual, ferric sulfate drinking water treatment residual, and fine and coarse crushed concretes. Small-bore adsorption columns were loaded with synthetic wastewater, and treated column effluent volume was plotted against the mass of phosphorus adsorbed per unit mass of filter media. It was observed that the curve described by the data strongly resembled that of a standard adsorption isotherm created from batch adsorption data. Consequently, it was hypothesized that an equation following the form of the Freundlich isotherm would describe the relationship between filter loading and media saturation. Moreover, the relationship between filter loading and effluent concentration could also be derived from this equation. The proposed model was demonstrated to accurately predict the performance of large-scale adsorption filters over a period of up to three months with a very high degree of accuracy. Furthermore, the coefficients necessary to produce said model could be determined from just 24 h of small-scale experimental data. PMID:27295617

  10. Efficient demulsification of oil-in-water emulsions using a zeolitic imidazolate framework: Adsorptive removal of oil droplets from water.

    Science.gov (United States)

    Lin, Kun-Yi Andrew; Chen, Yu-Chien; Phattarapattamawong, Songkeart

    2016-09-15

    To demulsify oil-in-water (O/W) emulsions, a zinc-based zeolitic imidazolate framework (ZIF-8) was employed for the first time to remove oil droplets from water. ZIF-8 exhibits a high surface area and positive surface charges, making it a suitable adsorbent to adsorb negatively-charged oil droplets. Adsorption behaviors of oil droplets to ZIF-8 were studied by analyzing the adsorption kinetics and isotherm with theoretical models. The activation energy of adsorption of oil droplets to ZIF-8 was determined as 24.1kJmol(-1). The Langmuir-Freundlich (L-F) model was found to be most applicable to interpret the isotherm data and the predicated maximum adsorption capacity of ZIF-8 can reach 6633mgg(-1), revealing a promising capability of ZIF-8 for demulsification. Factors influencing the adsorption of oil droplets to ZIF-8 were investigated including temperature, pH, salt and surfactants. The adsorption capacity of ZIF-8 for oil was improved at elevated temperatures, whereas alkaline condition was unfavorable for the adsorption of oil droplets due to the electrostatic repulsion at high pH. The adsorption capacity of ZIF-8 remained similar in the presence of NaCl but it was reduced in the presence of surfactants. ZIF-8 was regenerated by a simple ethanol-washing method; the regenerated ZIF-8 exhibited more than 85% of regeneration efficiency over six cycles. Its crystalline structure also remained intact after the regeneration. These characteristics indicate that ZIF-8 can be a promising and effective adsorbent to remove oil droplets for demulsification of O/W emulsions. PMID:27288575

  11. Fósforo em solos representativos do estado da paraíba: I- isotermas de adsorção e medidas do fator capacidade de fósforo Phosphorus in representative soils of the state of paraíba: I- adsorption isotherms and indicators of the phosphorus capacity factor

    Directory of Open Access Journals (Sweden)

    Daise Ribeiro de Farias

    2009-06-01

    .Knowledge on the phosphorus capacity factor (PCF of soils of the state of Paraíba is important to improve the interpretation of the available phosphorus (P content and the recommendation of phosphate fertilization in soils of the State. The objective of this study was to evaluate the parameters of P adsorption isotherms (Langmuir and Freundlich by the techniques of non-linear regression and linearization, in soil samples of the state of Paraíba, and to correlate the values of these parameters with chemical and physical soil properties. Samples of 12 representative soils of the state of Paraíba were collected in the 0-30 cm layer (six soils with a higher and six with a lower weathering degree, with a wide variation of values of physical and chemical properties within each group of six soils. The hyperbolic model of the Langmuir isotherm was adjusted by the technique of non-linear regression (single region and of linearization (first region and second region. Correlation analyses were performed with the values of isotherm parameters and soil properties that reflect the FCP. In all soils, the model adjusted by non-linear regression fitted the data best, in comparison with the same model adjusted by linearization. In the most weathered soil group, the values of maximum adsorption capacity of phosphate (CMAP were highly correlated with the contents of remaining (equilibrium phosphorus (r = -0.95**, free Fe oxyhydroxides (r = 0.90** and water retention (r = 0.88**, but did not correlate with the clay content (r = 0.64ns. Within the group of less weathered soils, the CMAP values were correlated with the contents of equilibrium phosphorus (r = -0.99**, water retention (r = 0.93** and clay content (r = 0.97**, but did not correlate with free Fe oxyhydroxides (r = 0.10ns.

  12. Adsorption of chloroacetanilide herbicides on soil I. Structural influence of chloroacetanilide herbicide for their adsorption on soils and its components

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Adsorption of chloroacetanilide herbicide acetochlor,alachlor, metolachlor and propachlor on soils and soil components was determined, and the structural differences of these herbicides were used to explain the order of sorptivity. Adsorption isotherms for all herbicide-soil combinations conformed to the Freundlich equation, and Kf increased with increasing soil organic carbon content. Kd on soil humic acid was greater than that on clay, but association of humic acid with clay reduced the overall adsorption. On all soils and soil humic acids, herbicide adsorption decreased in the order: metolachlor > acetochlor > propachlor > alachlor. On Ca2+-montmorrilonite, the order changed to metolachlor > acetochlor > alachlor > propachlor. FT-IR spectra of herbicide-clay or herbicide-humic acid-clay mixtures showed that H-bonding and charge transfer were the primary interaction pathways between these compounds and the surface of clay or humic acids. The different moieties attached to 2-chloro-acetanilide and their unique arrangement may have influenced the binding mechanisms and thus the sorptivity of these herbicides. This study indicates that the structural difference of pesticides in the same classes may be used as a molecular probe to obtain a better understanding of sorption mechanisms of pesticides on soil.

  13. Gallium adsorption on (0001) GaN surfaces

    OpenAIRE

    Adelmann, C.; Brault, J.; G. Mula; Daudin, B.; Lymperakis, L.; Neugebauer, J.

    2003-01-01

    We study the adsorption behavior of Ga on (0001) GaN surfaces combining experimental specular reflection high-energy electron diffraction with theoretical investigations in the framework of a kinetic model for adsorption and ab initio calculations of energy parameters. The measurement of a Ga/GaN adsorption isotherm allows the quantification of the equilibrium Ga surface coverage as a function of the impinging Ga flux. The temperature dependence is discussed within an {\\em ab initio} based gr...

  14. Adsorption of Lead Ions by Linde type F(K Zeolite

    Directory of Open Access Journals (Sweden)

    Han Chenghui

    2016-01-01

    Full Text Available The Test was to examine the adsorption property of Pb(II irons by Linde type F (K zeolite. The zeolite was synthesized by fly ash. The adsorbent dosage, pH, reaction temperature and reaction time were investigated. The adsorption isotherm and adsorption kinetics equation were studied. The results showed the adsorbent dosage, pH, reaction temperature and reaction time had significant effects on the adsorption of Pb(II irons. The removal rate was improved with the increasing of zeolite dosage. The saturated adsorption capacity was decreased gradually. The adsorption of Pb(II irons tended to saturate when initial pH was 6. With the increasing of temperature, the equilibration time of adsorption was shorter. Langmuir isotherm was more applicable to explain the monolayer adsorption procedure of Pb(II on Linde type F(K zeolite. For adsorption kinetics, pseudo-second order model showed better calculation results.

  15. The Grand Ensemble of Subsystems: Applications to Fitting Single-Component Adsorption Data

    CERN Document Server

    Mosquera, Martin A

    2009-01-01

    In this work, it is reviewed the cell model of adsorption by using the small system grand ensemble method. Under the common assumption that the adsorbate phase is divided into identical and weakly-interacting subsystems, it is suggested that the general multiparametric isotherm that arise from the theory may be used to fit the experimental data of adsorption of gases and vapours on microporous adorbents (type I isotherm), even though these present heterogeneties like pore size distribution. A simplified isotherm that reduces the number of adjustable parameters with respect to the general isotherm is proposed. Both isotherms, due to their relative high accuracy, can be used to estimate thermodynamical properties like isosteric and differential heats of adsorption. Also, a simple method is presented for systems that show an apparent variation in the coverage limit as function of temperature; for several systems, this method reduces the fitting deviations. Finally, several applications to fitting data of adsorpt...

  16. Adsorption of uranium from crude phosphoric acid using activated carbon

    International Nuclear Information System (INIS)

    The adsorption of uranium from crude phosphoric acid has been investigated using conventional activated carbons. It was found that treatment with nitric acid oxidized the surface of activated carbon and significantly increased the adsorption capacity for uranium in acidic solutions. The parameters that affect the uranium(VI) adsorption, such as contact time, solution pH, initial uranium(VI) concentration, and temperature, have been investigated. Equilibrium data were fitted to a simplified Langmuir and Freundlich isotherms for the oxidized samples which indicate that the uranium adsorption onto the activated carbon fitted well with Langmuir isotherm than Freundlich isotherm. Equilibrium studies evaluate the theoretical capacity of activated carbon to be 45.24 g kg-1. (author)

  17. Analysis of Cooperativity by Isothermal Titration Calorimetry

    OpenAIRE

    Alan Brown

    2009-01-01

    Cooperative binding pervades Nature. This review discusses the use of isothermal titration calorimetry (ITC) in the identification and characterisation of cooperativity in biological interactions. ITC has broad scope in the analysis of cooperativity as it determines binding stiochiometries, affinities and thermodynamic parameters, including enthalpy and entropy in a single experiment. Examples from the literature are used to demonstrate the applicability of ITC in the characterisation of coop...

  18. Adsorption characteristics of arsenic and boron by soil

    Energy Technology Data Exchange (ETDEWEB)

    Sakata, M.

    1986-01-01

    In order to obtain baseline data concerning the surface and ground water pollution caused by coal ash disposal, adsorption characteristics of arsenic (III) and boron by soil have been studied through laboratory experiments. The main results are as follows: (1) Arsenic (III) and boron adsorption on soil was strongly dependent on pH with adsorption maxima at pH 8 and 8-9, respectively. (2) Arsenic (III) and boron adsorption on soil over the entire concentration ranges investigated could be described by the Langmuir adsorption isotherm and the Freundlich adsorption isotherm, respectively. The Henry adsorption isotherm was also applicable over the lower concentration ranges of arsenic (III) and boron (As (III): < 0.1 deltag/ml; B: < 5deltag/ml.) (3) Arsenic (III) and boron adsorption on soil is controlled mainly by the contents of extractable Fe oxide and hydroxide for arsenic (III) and by the contents of extractable Al hydroxide and allophane (amorphous aluminium silicates) for boron. (4) Adsorption and movement of arsenic (III) and boron during the infiltration of coal ash leachate in soil layer were investigated by means of the unsteady-state, one-dimensional convective-diffusive mass transport model. This model is very useful for evaluation and prediction of the contamination of ground water by trace elements such as arsenic (III) and boron leached at coal ash disposal site.

  19. Derivation of an equation of surface tension isotherm for binary mixtures

    International Nuclear Information System (INIS)

    Surface tension was determined by integration of Gibbs adsorption equation from changing composition of surface layer of binary solutions with varying composition of volume solution being in equilibrium with it. The equation, which was tested for the Cd - Pb and Pb - Bi solutions at 773 K, was obtained. The isotherms of surface tension of liquid binary solutions was noted to be calculated using relation x2(ω) = f(x2) (x2(ω) - molar fraction of the second component) with rather close approximation at known dependence of the coefficient of the second component activity from the composition of solution at T = const. Surface layer of the Cd - Pb solutions was found to enrich with lead atoms

  20. 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

    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 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 0.93 for...