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1.
Nanosilica particles modified by Schiff base ligands 3-methoxy salicylaldimine propyl triethoxysilane (MNS1), 5-bromo salicylaldimine propyl triethoxysilane (MNS2) and 3-hydroxy salicylaldimine propyl triethoxysilane (MNS3) were prepared, and their potential for separation of copper, lead, zinc, cadmium, cobalt and nickel ions from aqueous solutions was examined. The effect of parameters influencing adsorption efficiency including aqueous-phase pH, amount of adsorbent, stirring time and initial concentration of the metal ions was assessed and discussed. Although MNS1 and MNS3 removed lead ions efficiently, all adsorbents showed strong selectivity toward copper ions. It was shown that, under some circumstances, MNS3 decreased the amount of other ions, particularly cobalt, in the aqueous phase. The adsorbents were also applied for removal of copper and lead ions from real samples. Possible quantitative desorption of the metal ions loaded onto the adsorbents suggests their multiple uses in adsorption–desorption process. Investigation of temperature dependency of the process led to determination of the ΔH°, ΔS° and ΔG° values. This investigation indicates that the adsorption of copper ions onto the all studied adsorbents and lead ions onto MNS1 and MNS3 is endothermic. The Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherms were tested to describe the equilibrium data. Pseudo-first-order, pseudo-second-order, Elovich and intra-particle diffusion equations were applied to study the kinetics of copper and lead adsorption onto the modified nanoparticles. This investigation indicates that the process for all adsorbents follows pseudo-second-order kinetics and suggests a chemisorption mechanism for the adsorption processes by the studied adsorbents.  相似文献   

2.
Graphene oxide nanosheets were synthesized by electrochemical exfoliation. X-ray diffraction, scanning electron microscopy, atomic force microscopy, Raman spectrometry and Fourier transform infrared spectrometry were used to characterize crystal structure, particle size, thickness and function groups of the nanosheets. The nanosheets were examined for adsorption of methyl orange, an anionic dye, in aqueous solution at different pHs and temperatures. The maximum adsorption capacity of methyl orange on graphene oxide nanosheets obtained from the Langmuir isotherm was 138.69 mg/g at pH 2.0, which is larger than that of other carbonaceous adsorbents. The large adsorption affinity of graphene oxide nanosheets to methyl orange might be due to the presence of hydrogen bonding and π–π interaction between methyl orange and graphene oxide nanosheets. Adsorption kinetics followed a pseudo-second-order kinetic model, and the isotherm adsorption results were fitted with Langmuir isotherm model in a monolayer adsorption manner. The thermodynamic studies indicated that the adsorption reaction was a spontaneous physisorption process.  相似文献   

3.
Homogenized samples of raw clays resulting from two (2) different lots of natural clays from Maghnia (Algeria) have been assessed for their potential use in the removal of Pb2+ and Zn2+ ions from industrial liquid wastes (LW). Raw and acid-activated samples have been characterized by powder X-ray diffraction, FT-IR spectroscopy, electron microscopy (SEM), and X-ray fluorescence (XRF) and used as adsorbents for the removal of Pb2+ and Zn2+ ions from aqueous system using adsorption method under different conditions. The effect of factors including contact time, pH, and dosage on the adsorption properties of Pb2+ and Zn2+ ions onto clays was investigated at 25 °C. The obtained results revealed that the removal percentages of Pb2+ and Zn2+ ions, from both aqueous solution (AS) and LW, were varying between 90 and 98% for 40 min and optimal pH values ranged from 5 to 6 for Pb2+ and Zn2+ ions, respectively. The kinetics of both Pb2+ and Zn2+ ion adsorption fitted well with the pseudo-second-order model. Langmuir, Freundlich, and Temkin adsorption isotherms were used, and their constants were evaluated. The values of thermodynamic parameters, ΔH°, ΔS°, and ΔG° indicated that the adsorption of Pb2+ and Zn2+ ions was spontaneous and exothermic process in nature. The adsorption and desorption isotherms indicated that Pb2+ and Zn2+ adsorption to raw clays was reversible. The experimental results obtained showed that the raw clays from Maghnia (Algeria) had a great potential for removing Pb2+ and Zn2+ ions from industrial liquid wastes using adsorption method.  相似文献   

4.
Acacia nilotica was used for the adsorption of Reactive Black 5 (RB5) dye from an aqueous solution. Both the raw and activated (with H3PO4) carbon forms of Acacia nilotica (RAN and ANAC, respectively) were used for comparison. Various parameters (including dye concentration, contact time, temperature, and pH) were optimized to obtain the maximum adsorption capacity. RAN and ANAC were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The maximum experimental adsorption capacities for RAN and ANAC were 34.79 and 41.01 mg g?1, respectively, which agreed with the maximum adsorption capacities predicted by the Langmuir, Freundlich, and Dubinin–Radushkevich equilibrium isotherm models. The adsorption data of ANAC showed a good fit to the isotherm models based on the coefficient of determination (R 2): Langmuir type II (R 2 = 0.99) > Freundlich (R 2 = 0.9853) > Dubinin–Radushkevich (R 2 = 0.9659). This result suggested monolayer adsorption of RB5 dye. The adsorption of RB5 dye followed pseudo-second-order kinetics. The RAN adsorbent reflected an exothermic reaction (enthalpy change, ΔH = ?0.006 kJ mol?1) and increased randomness (standard entropy change, ΔS = 0.038 kJ mol?1) at the solid–solution interface. In contrast, ANAC reflected both exothermic [?0.011 kJ mol?1 (303–313 K)] and endothermic [0.003 kJ mol?1 (313–323 K)] reactions. However, the ΔS value of ANAC was lower when the RB5 adsorption increased from 313 to 323 K. The negative values for the Gibbs free energy change at all temperatures indicated that the adsorption of RB5 dye onto RAN and ANAC was spontaneous in the forward direction.  相似文献   

5.
This paper presents the first attempt to investigate the potential of Tunisian palygorskite-rich clay (Pal-clay) on the effectiveness of a textile dye “Direct orange 34” (DO34) removal. Important parameters which affect adsorption, such as initial solution pH, contact time, adsorbent mass, initial dye concentration, and temperature, were investigated. The raw Pal-clay was characterized using X-ray diffractometer (XRD), X-ray fluorescence (XRF), Fourier transform infrared spectroscopy (FTIR), cation exchange capacity (CEC), specific surface area (SSA) analysis, and point of zero charge (PZC) determination. The results showed that the Pal-clay has a high selectivity for DO34 and had maximum removal efficiency reaching up to about 91 %. The highest adsorption capacity was obtained at 25 °C and pH of 2. The dye uptake process fitted well to the pseudo-second-order kinetic expression and was best described by the Langmuir and Freundlich isotherms. Intra-particle diffusion studies showed that the adsorption mechanism was not exclusively controlled by the diffusion step and was more likely to be governed by external mass transfer. Thermodynamic parameters such as change in free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) were also calculated. The parameters revealed that the adsorption of dye by the raw clay is spontaneous and exothermic. The results indicate that the Pal-clay has a moderate adsorption capacity towards anionic dye.  相似文献   

6.
Vitis vinifera (grape) leaf litter, an abundant agricultural waste in South Africa was chemically modified with H3PO4 and carbonized for use as biosorbent. Characterization and the potential application of the adsorbent in simultaneous removal of 4-nitrophenol and 2-nitrophenol from aqueous solutions were investigated. The adsorbent was characterized using FTIR, SEM and EDX elemental microanalysis. The EDX and FTIR analysis revealed the presence of surface oxygen moieties capable of binding to adsorbate molecules while the SEM micrographs showed the development of pores and cavities in the adsorbent. Batch adsorption experiments were conducted at a varying contact time, adsorbent dosage, pH and initial adsorbate concentration to investigate optimal conditions. The maximum adsorption capacity of the adsorbent was 103.09 and 103.10 mg/g for 4-nitrophenol and 2-nitrophenol, respectively. The adsorption process was best fitted into Freundlich isotherm while the adsorption kinetics followed a pseudo-second-order model. Liquid film and intra-particle diffusion contributed to the adsorption process. Thermodynamic parameters of ΔG°, ΔH° and ΔS° were evaluated. The adsorption was exothermic, feasible and spontaneous. The results suggest a possible application of grape leaf litter as a precursor for activated carbon and for cheaper wastewater treatment technologies.  相似文献   

7.
Novel composite adsorbents PPTA-AOx were synthesized by grafting polyacrylonitrile onto poly(p-phenylene terephthalamide) (PPTA) followed by converting the acrylonitrile into the amidoxime (AO) groups. Their structures were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, elemental analysis, transmission electron microscopy, etc. Scanning electron microscopy analysis and pore structure analysis manifested that PPTA-AOx adsorbents are all composed of nanoparticles aggregation. The as-synthesized PPTA-AOx adsorbents showed good adsorption capacity for Hg2+ with a maximum adsorption capacity of 2.50 mmol g?1. The pseudo-second-order model can reasonably describe the adsorption kinetics of the three adsorbents for Hg2+. Langmuir model provided better fit for the isothermal adsorption of Hg2+ on PPTA-AO1 and PPTA-AO2, while the Freundlich model was better for PPTA-AO3. The adsorption process might involve both chemisorption and physisorption. According to the calculated thermodynamic parameters, it can be concluded that the adsorption is an endothermic, spontaneous and entropy-driven process.  相似文献   

8.
Evans blue (EB) dye has been successfully removed from aqueous solution through chemisorption process with synthetic layered double hydroxides (LDH) [Zn1?x Al x (OH)2NO3·nH2O, x = 0.2–0.33]. Detailed evaluation of dye adsorption characteristics in aqueous medium has been studied for different layer charged hydroxides. The objective of the study was efficient removal of a dye by LDH and understanding the structure–property relationship of the LDH on its adsorption behaviour. Highest Langmuir monolayer adsorption capacity (Qt) of 113.64 mg g?1 was observed for highest layer charge x = 0.33, and it is higher than previously reported values for the LDH-EB dye system. Under optimized condition, 99% of EB dye is removed from aqueous solution within 60 min at 313 K. The monotonous increase in Qt value with increasing layer charge is correlated with layer charge density (LCD) and lower particle size of the synthetic LDH. The variation in Qt among different layer charged materials is marginal (3.46–4.17%) with respect to the respective anion exchange capacity (AEC) of LDH NO3. The limited contribution of AEC surmises the occurrence of surface-only adsorption and absence of intercalation as validated by the XRD analysis. The spontaneity of the EB dye removal increases with increasing temperature and LCD. The chemisorption nature of the adsorption reaction is well supported by the thermodynamics values.  相似文献   

9.
Low-cost adsorbents, e.g., cow manure-based carbon, provide alternatives to remove veterinary antibiotic sulfamethazine (SMT) from contaminated water bodies. In this study, the chemical structures and compositions of cow manure (CM) carbonized at 400, 600, and 800 °C (CM400, CM600, and CM800) were examined using elemental analyzer (EA), Brunauer–Emmett–Teller, and spectroscopic techniques. Adsorptions of SMT on CM samples were conducted as functions of pH, hydrophobicity, and ionic strengths. Results of EA and spectroscopic analyses suggested that the raw CM and CM400 samples contained the highest amounts of O-containing groups and aliphatic domains. Amounts of such two chemical groups decreased as carbonization temperatures increased. The specific surface areas and total pore volumes of CM samples increased significantly when the carbonization temperatures exceeded 600 °C. SMT adsorption on CM samples could be described essentially by the pseudo-second-order kinetic, intra-particle diffusion, and Freundlich isotherm models. Low pH and ionic strength were favorable for SMT adsorption in CM samples, particularly for the CM800, because a strong π +–π electron donor–acceptor interaction (π +–π EDA) was formed between SMT and CM surfaces enriched with hydrophobic domains. Further, the high adsorption affinity of SMT to the CM600 and CM800 samples was attributed in part to their larger surface areas and total pore volumes. Generally, CM-based materials carbonized >600 °C showed relatively stable structures and exhibited strong aromatic properties. Moreover, maximum adsorption capacities of SMT on the CM800 sample (37–39 mM/kg) were significantly higher than those of other common adsorbents (0.02–35.93 mM/kg).  相似文献   

10.
Moringa oleifera seed was used as a biosorbent for the removal of water treatment disinfection by-products, haloethers, trihalomethanes and haloketones from water samples. M. oleifera seed has polar functional groups such as O–H, C=O, C–N and others which facilitate the extraction of these disinfection by-products. Experiments were conducted in batch and fixed bed column modes. Using batch mode, different parameters were optimized such as M. oleifera seed dosage, sample pH, contact time and agitation speed. The effect of the thickness layer and flow rate were also studied using the fixed bed mode. Maximum adsorption occurs using the batch mode with removal efficiencies of 120.5, 114 and 111.5 mg/g for haloethers, trihalomethanes and haloketones, respectively. Adsorption equilibrium followed Langmuir model, and the kinetic data obeyed the pseudo-second-order model, revealing that the M. oleifera seed had higher adsorption capacity than other reported sorbents. Shorter removal time with higher adsorption capacity of disinfection by-products by M. oleifera seed suggests that this material was effective for water treatment, in dealing with the removal of the disinfection by-products considered.  相似文献   

11.
In the present experimental study, solid waste was used as an adsorbent and the effectiveness of the adsorbent was increased by novel treatment methods. Red mud, acid-treated activated red mud and iron oxide-coated acid-treated activated red mud were used for the removal of lead (II). The structural and functional groups were identified to confirm the removal of lead (II) by powder X-ray diffraction and Fourier transform infrared spectroscopy analyses. The enhancement of surface area was confirmed by Brunauer–Emmett–Teller analysis. Batch adsorption experiment was also conducted, and various parameters such as the effect of adsorbent dosage, pH, contact time and initial ion concentration were analyzed and reported. Adsorption equilibrium data were investigated using Langmuir, Freundlich and Dubinin–Radushkevich isotherm models with three parameters, and the rate of reaction was examined through kinetic models. The results indicate that in particular a novel modified form of red mud, namely iron oxide-coated acid-treated activated red mud was well fitted in lead (II) removal compared with reported adsorbents. The Langmuir isotherm shows that the maximum adsorption of adsorbate per gram was greater than other adsorbents (27.02 mg/g). In Freundlich isotherm, the Freundlich constant n values lie between 1 and 10 indicate the favorable adsorption. The calculated n values for normal red mud, acid-treated activated red mud and iron oxide-coated acid-treated activated red mud were found to be 1.9, 2.1 and 2.0 respectively. The correlation coefficient value was higher and the rate of reaction follows the pseudo-second-order kinetic model.  相似文献   

12.
This study assesses the ability of two low-cost adsorbents made from waste of Rapanea ferruginea treated with ethanol (WRf) and its H2SO4-treated analog (WRf/H2SO4) for the removal of two cationic dyes methylene blue (MB) and crystal violet (CV) from aqueous solutions. The adsorbent was characterized by scanning electron microscopy, Fourier transform infrared spectrometry, thermogravimetric analysis, point of zero charge (pHpzc), specific surface, and functional groups. The adsorption of dye onto the adsorbents was studied as a function of pH solution (2–12), contact time (up to 120 min) and initial concentration (20–120 mg/L), and temperature (25, 35, and 55 °C). The influence of these parameters on adsorption capacity was studied using the batch process. The response surface methodology (RSM) was used in the experimental design, modeling of the process, and optimizing of the variables and was optimized by the response involving Box–Behnken factorial design (15 runs). The results show that the data correlated well with the Sips isotherm. The maximum adsorption capacities of MB and CV onto WRf were found to be 69 and 106 mg/g, and onto WRf/H2SO4, the adsorption capacities were 33 and 125 mg/g, respectively. The kinetic data revealed that adsorption of cationic dyes onto the adsorbents closely follows the pseudo-second-order kinetic model. Regression analysis showed good fit of the experimental data to the second-order polynomial model, with coefficient of determination (R2) values for MB (R2?=?0.9685) and MB (R2?=?0.9832) for WRf and CV (R2?=?0.9685) and CV (R2?=?0.9832) for WRf/H2SO4 indicated that regression analysis is able to give a good prediction of response for the adsorption process in the range studied. The results revealed that waste from R. ferruginea is potentially an efficient and low-cost adsorbent for adsorption of MB and CV.  相似文献   

13.
In this study, teff (Eragrostis tef) straw has been chemically treated and tested as an adsorbent for Cr(VI) removal. Chemically treatment of teff straw was done by NaOH, H3PO4 and ZnCl2 solutions. Scanning electron micrograph and X-ray diffraction were used for anatomical characterization, whereas Fourier transform infrared spectroscopy was used for surface change characterization of adsorbents. Effects of different experimental parameters like pH (2–12), initial Cr(VI) concentration (100–900 mg/L), adsorbent dose (2.5–20 g/L), contact time (15–360 min) and temperature (288–318 K) were studied. Temperature increment was found to stimulate the adsorption process. Langmuir isotherm was found to give better representation over wide range of temperature for untreated, H3PO4- as well as ZnCl2-treated teff straw, and Freundlich isotherm best represented the isotherm data for NaOH-treated teff straw. Maximum Cr(VI) adsorption capacity of untreated, NaOH-, H3PO4- and ZnCl2-treated teff straw was found to be 86.1, 73.8, 89.3 and 88.9 mg/g, respectively. Respective values of average effective diffusion coefficient (D e) were found to be 2.8 × 10?13, 2.59 × 10?14, 1.32 × 10?13 and 1.14 × 10?13 m2/s, respectively. The negative value of ΔG o for all the adsorbents indicates Cr(VI) spontaneous adsorption. Isosteric heat of adsorption (ΔH st,a) was found to vary with surface coverage (θ). ΔH st,a increased for untreated, H3PO4- and ZnCl2-treated teff straw, and decreased steadily with θ for NaOH-treated teff straw.  相似文献   

14.
Bimetallic Fe/Ni nanoparticles were synthesized and used for the removal of profenofos organophosphorus pesticide from aqueous solution. These novel bimetallic nanoparticles (Fe/Ni) were characterized by scanning electron microscopy, energy-dispersive X-ray analysis spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The effect of the parameters of initial pesticide concentration, pH of the solution, adsorbent dosage, temperature, and contact time on adsorption was investigated. The adsorbent exhibited high efficiency for profenofos adsorption, and equilibrium was achieved in 8 min. The Langmuir, Freundlich, and Temkin isotherm models were used to determine equilibrium. The Langmuir model showed the best fit with the experimental data (R 2 = 0.9988). Pseudo-first-order, pseudo-second-order, and intra-particle diffusion models were tested to determine absorption kinetics. The pseudo-second-order model provided the best correlation with the results (R 2 = 0.99936). The changes in the thermodynamic parameters of Gibb’s free energy, enthalpy, and entropy of the adsorption process were also evaluated. Thermodynamic parameters indicate that profenofos adsorption using Fe/Ni nanoparticles is a spontaneous and endothermic process. The value of the activation energy (E a = 109.57 kJ/mol) confirms the nature of the chemisorption of profenofos onto Fe/Ni adsorbent.  相似文献   

15.
Here, a novel one-dimensional composite of poly(m-phenylenediamine)s coating on filamentous Streptomyces was successfully constructed via a controllable polymerization reaction. The synthesized composites were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. Their adsorption isotherm and kinetics for aqueous hexavalent chromium were also systematically examined. The results of scanning electron microscopy analysis indicated that the obtained composites based on Streptomyces were showed a uniform and stable one-dimensional morphology with distinct core–shell configuration. Moreover, the Langmuir isotherm model (R 2 > 0.96) and pseudo-second-order equation (R 2 = 0.9996) described well the equilibrium adsorption behavior and kinetics of hexavalent chromium adsorption by the composites. In addition, bath adsorption experiments demonstrated the highest adsorption capacity of hexavalent chromium by the composites reached 320.03 mg g?1 in an acid solution, which was 5.6 times as that of the pure Streptomyces filaments. The results of Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses suggested that the adsorption of hexavalent chromium by the composites possibly involved the protonation, redox, and chelation reactions. Therefore, a promising application of these composites in treating acid hexavalent chromium-contaminated wastewater is expectable.  相似文献   

16.
Surface modification of two algal biomasses, Nizimuddinia zanardini and Stoechospermum marginatum, using 4-phenyl-3-thiosemicarbazide ligand was performed to investigate the consequences on the adsorption of heavy metals from aqueous solution. Stabilization of amino group of 4-phenyl-3-thiosemicarbazide on the surface of biomasses was confirmed using Fourier transform infrared spectroscopy. Chemical modification was found to exert significant positive effects on biosorption. Adsorption capacities for Pb(II), Cd(II) and Cr(VI) using modified N. zanardini were observed to be 19.3, 16.75 and 15.75 mg/g, respectively, compared to 17.48, 14.18 and 11.85 mg/g for raw N. zanardini biomass. Also, adsorption of Pb(II), Cd(II) and Cr(VI) by the modified S. Marginatum was found to be 17.54, 15.62 and 14.77 mg/g, respectively, in comparison with that of the raw biomass which were 16.86, 12.9 and 11.2 mg/g. The obtained results of the equilibrium adsorption were studied through different isotherm models of Langmuir, Freundlich and Temkin, where the Langmuir model was observed to agree well with the results. Prevalent kinetic models including pseudo-second order and intra-particle diffusion were applied, and the pseudo-second order was found to describe the adsorption kinetics data adequately. Intra-particle model was also utilized in order to show penetration of metal ions, where it was realized that the biosorption took place in two or three steps including film diffusion, molecular diffusion and chemical reaction.  相似文献   

17.
Novel bionanocomposites, S. cerevisiae–AgNPs, were synthesized by in situ formation of AgNPs on S. cerevisiae surface using fulvic acids as reductants under simulated sunlight. S. cerevisiae–AgNPs were characterized using UV–Vis spectroscopy, scanning electron microscope, transmission electron microscope and Fourier transform infrared spectroscopy. These analyses showed that AgNPs were distributed on the surface of S. cerevisiae. The application of S. cerevisiae–AgNPs in bacteria killing and heavy metal removal was studied. S. cerevisiae–AgNPs effectively inhibited the growth of E. coli with increasing concentrations of S. cerevisiae–AgNPs. E. coli was killed completely at high concentration S. cerevisiae–AgNPs (e.g., 100 or 200 µg mL?1). S. cerevisiae–AgNPs as excellent heavy metal absorbents also have been studied. Using Cd2+ as model heavy metal, batch experiments confirmed that the adsorption behavior fitted the Langmuir adsorption isotherms and the Cd2+ adsorption capacity of S. cerevisiae–AgNPs was 15.01 mg g?1. According to adsorption data, the kinetics of Cd2+ uptake by S. cerevisiae–AgNPs followed pseudo second-order kinetic model. Moreover, S. cerevisiae–AgNPs possessed ability of different heavy metals’ removal (e.g., Cr5+, As5+, Pb2+, Cu2+, Mn2+, Zn2+, Hg2+, Ni2+). The simulated contaminated water containing E. coli, Cd2+ and Pb2+ was treated using S. cerevisiae–AgNPs. The results indicated that the bionanocomposites can be used to develop antibacterial agents and bioremediation agents for water treatment.  相似文献   

18.
In this study, nickel ions adsorption from zinc ingot factory wastewater by brown algae (Sargassum glaucescens) and chitosan/polyvinyl alcohol nano-fiber membrane at continuous system was studied. The continuous process included a biosorption reactor and fixed-bed reactor that were optimized by predicting two batch steps with response surface modeling, based on the Box–Behnken in the novel approach. Nano-biosorbent characterized by scanning electron microscopy, Brunauer–Emmett–Teller and Fourier transform infrared spectrometer analysis. Maximum biosorption in this continuous system was at pH 6, biosorbent doses 8 g L?1 S. glaucescens and 0.48 g L?1 nano-fiber. The study of the reaction rate showed kinetic data best fitted by pseudo-first-order model with R 2 > 0.95 than pseudo-second-order and intraparticle diffusion models. Biosorption equilibrium data were performed using Langmuir isotherm and Freundlich isotherm, Langmuir isotherm fit better with equilibrium data.  相似文献   

19.
The most appropriate method in designing the adsorption systems and assessing the performance of the adsorption systems is to have an idea on adsorption isotherms. Comparison analysis of linear least square method and nonlinear method for estimating the isotherm parameters was made using the experimental equilibrium data of Zn(II) and Cu(II) onto kaolinite. Equilibrium data were fitted to Freundlich, Langmuir, and Redlich–Peterson isotherm equations. In order to confirm the best-fit isotherms for the adsorption system, the data set using the chi-square (χ 2), combined with the values of the determined coefficient (r 2) was analyzed. Nonlinear method was found to be a more appropriate method for estimating the isotherm parameters. The best fitting isotherm was the Langmuir and Redlich–Peterson isotherm. The Redlich–Peterson is a special case of Langmuir when the Redlich–Peterson isotherm constant g was unity. The sorption capacity of kaolinite to uptake metal ions in the increasing order was given by Cu (4.2721 mg/g)?<?Zn (4.6710 mg/g).  相似文献   

20.
Adsorption of Cr(VI) using native and chemically modified marine green macroalgae Codium tomentosum biomass and its adsorption kinetics were studied under specific conditions. Maximum Cr(VI) removal occurred at pH 2 for both untreated and acid-treated biomass. However, base-treated biomass exhibited maximum adsorption at pH 6 due to the hydrolysis of methyl esters present in the cellulose, hemicellulose and lignin molecules resulting in carboxyl groups (COO?) on the surface. The effect of adsorbent dose revealed that untreated and acid-treated biomass follows Henry’s linear isotherm, while base-treated biomass exhibited sigmoidal curve indicating energetic heterogeneity on the adsorbing surface. The monolayer adsorption capacity of untreated, acid-treated and base-treated biomasses was 5.032 ± 0.644, 5.445 ± 0.947, 3.814 ± 0.559 mg g?1, respectively. Adsorption was found to follow Ho and McKay’s pseudo-second-order kinetic model with decreasing pseudo-second-order rate constant (K 2, g mg?1 min?1) of 0.088 ± 0.037 (acid-treated), 0.019 ± 0.003 (untreated) and 0.012 ± 0.003 (base-treated).  相似文献   

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