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1.
Leonardite, a by-product from coal mines, was applied to adsorb Cd(II) and Zn(II) from aqueous solutions. Individual and simultaneous adsorptions of the two metal ions were investigated. In a single-component adsorption system, Langmuir and Freundlich isotherms were fitted to the adsorption data. Linear and nonlinear regression methods were used for the assessment of the optimum adsorption isotherm. Error functions including root-mean-square error, sum of the squares of the errors, mean absolute percentage error, Marquardt’s percent standard deviation (MPSD), and Chi-square were applied in the nonlinear regression. The most suitable model for the adsorption of Cd(II) and Zn(II) in the single system is the Freundlich isotherm. The isotherm parameters calculated by MPSD provided the lowest sum of normalized error (SNE) value. The adsorption capacity was found to be 23.89 mg/g for Cd(II) and 16.86 mg/g for Zn(II). It was observed that the adsorption of Cd(II) on leonardite is greater than that of Zn(II). For binary component adsorption systems, Cd(II) and Zn(II) showed antagonistic behavior. The presence of the other metal ions could decrease the amount of metal adsorbed. Binary adsorption of Cd(II) and Zn(II) was tested with regard to four multi-component isotherms: Extended Langmuir, Modified Langmuir, Sheindorf–Rebuhn–Sheintuch, and Extended Freundlich. The Extended Freundlich isotherm proved to be a good fit for the experimental data.  相似文献   

2.
Hexavalent chromium has been proved to be the reason of several health hazards. This study aimed at evaluating the application of pomegranate seeds powder for chromium adsorption (VI) from aqueous solution. Chromium adsorption percentage (VI) increased with increasing the adsorbent dosage. Chromium adsorption capacity (VI), at pH = 2 and 10 mg/L initial metal concentration, decreased from 3.313 to 1.6 mg/g through increasing dosage of adsorbent from 0.2 to 0.6 g/100 ml. The adsorption rate increased through increase in chromium initial concentration (VI). However, there was a removal percentage reduction of chromium (VI). Chromium adsorption kinetics by different models (pseudo-first-order, modified pseudo-first-order, pseudo-second-order, Elovich, intraparticle diffusion, Boyd kinetic) was investigated as well. Studies on adsorption kinetic indicated that the experimental data were matched by pseudo-second-order model (R 2 = 0.999) better. Obtained results demonstrated the pomegranate seeds can be used as an effective biomaterial and biosorbent for hexavalent chromium adsorption from aqueous solutions.  相似文献   

3.
A novel biosorbent synthesized from Ficus racemosa leaves based on the treatment using NaOH was applied for removal of Acid Blue 25 from aqueous solution. The synthesized biosorbent was characterized using scanning electron microscopy, Fourier transform infrared spectroscopy and Brunauer–Emmett–Teller analysis. NaOH treatment was demonstrated to remove lignin content from the biomass and to induce the development of significant pores. Batch experiments were performed to evaluate the effect of important operating parameters such as pH (range of 2–10), biosorbent dose (range of 1–10 g/L), contact time (range of 0–5 h), initial dye concentration (range of 50–400 mg/L) and temperature (range of 293–323 K) on the extent of removal of Acid Blue 25. The established optimum conditions were pH of 2, biosorbent dose of 4 g/L, contact time of 3 h and temperature of 323 K, yielding maximum removal of dye. Pseudo-second-order model was found to best fit the kinetic data. Langmuir and Temkin isotherm models were found to best fit the equilibrium data. The obtained thermodynamic parameters confirmed endothermic and spontaneous nature of adsorption. The study established the utility of novel biosorbent for removal of Acid Blue 25 with higher adsorption capacities (83.33 mg/g) as compared to the more commonly used adsorbents. Desorption-adsorption  studies conducted for seven cycles indicated potential reusability of synthesized biosorbent for the treatment of dye effluents.  相似文献   

4.
Adsorption and desorption of uranium(VI) from dilute aqueous solutions by Eucalyptus citriodora distillation sludge was studied in a batch mode. The potential of Eucalyptus citriodora distillation sludge to remove uranium(VI) from aqueous solutions has been investigated at different conditions of solution pH, metal ion concentrations, biosorbent dosage, biosorbent particle size, contact time and temperature. The results indicated that biosorption capacity of Eucalyptus citriodora distillation sludge was strongly affected by the medium pH, the biosorbent dose, metal ion concentrations and medium temperature. Reduction in particle size increased the biosorption capacity. Langmuir and Freundlich isotherm models were applied to biosorption data to determine the biosorption characteristics. An optimum biosorption capacity (57.75 mg/g) was achieved with pH 4.0, particle size 0.255 mm, biosorbent dose 0.5 g/100 mL and initial uranium(VI) concentration of 100 mg/L. Uranium(VI) removal by Eucalyptus citriodora distillation sludge was rapid, the equilibrium was established within 60 min and pseudo-second-order model was found to fit with the experimental data. The biosorption process decreased with an increase in the temperature indicating its exothermic nature. Pretreatments of biomass with different reagents affected its biosorption capacity. A significant increase (34 %) in biosorption capacity (83.25 mg/g) was observed with benzene treatment. Fourier-transform infra-red studies showed the involvement of carbonyl, carboxyl and amide groups in the biosorption process. The results indicated that sulfuric acid had the best effects as an eluent showing 93.24 % desorption capacity.  相似文献   

5.
A novel polyurethane foam/organobentonite/iron oxide nanocomposite adsorbent was successfully prepared via in situ polymerization of toluene diisocyanate and polyol in presence of 5 wt% organobentonite/iron oxide. The obtained nanocomposite was characterized in detail, and the results revealed that the clay layers are exfoliated and/or intercalated in the polymer matrix forming a nanocomposite structure. The application of the prepared nanocomposite for adsorption of cadmium ions from aqueous solution was tested as a function of various experimental parameters using batch procedures. Adsorptive removal of Cd(II) onto the nanocomposite attained maximum at adsorbent content 1.5 g/L, pH 6, and the equilibrium was established within 60 min. Kinetic studies showed that the experimental data fit very well to pseudo-second-order model, and the adsorption process proceeds through three steps. It was found that external liquid film and intraparticle diffusion steps deeply affect the rate of Cd2+ ions adsorption onto the synthesized nanocomposite. Langmuir isotherm model fitted the adsorption data better than Freundlich with a maximum adsorption capacity (q m) for Cd(II) equal to 78 mg/g under the specified experimental conditions. The synthesized nanocomposite afforded effective extraction for Cd2+ ions from natural water samples and excellent reusability feature. This study declares the potential efficiency of a new clay/polymer nanocomposite as alternative for wastewater remediation.  相似文献   

6.
Adsorptive separation of Pb(II) and Cu(II) using modified waste Lyocell fiber adsorbent was investigated in this research. The waste Lyocell fiber was functionalized through carboxymethylation of the hydroxyl moieties using sodium chloroacetate as modifying agent and was crosslinked with epichlorohydrin to provide water stability. The maximum equilibrium batch uptake in single metal system was 353.45 mg/g for Pb(II) and 98.33 mg/g for Cu(II), according to the Langmuir isotherm model. The adsorption rates were very fast and reached equilibrium within 3 and 5?10 min for Cu(II) and Pb(II), respectively. In competitive binary metal system, the uptake of Cu(II) largely decreased to 38.40 mg/g, and Pb(II) selectivity was observed. Elemental and functional characterization suggested that the adsorption proceeded by ion exchange between the adsorbent and metal ions. In a flow-through column system, adsorption followed by desorption aided in effectively eluting ~260 mg of Pb(II) (out of ~300 mg total adsorbed) from the Pb(II)–Cu(II) binary solution. Finally, the adsorbent was very effective in four successive adsorption–desorption cycles with over 99 % uptake and 94 % desorption efficiencies. The present study may provide an alternative option for waste fiber recycling and could be useful in recovering heavy metal ions from aqueous sources to complement their depleting reserves.  相似文献   

7.
The Pb(II) and Ni(II) biosorption of a fungal biomass isolated from mine drainage of metal-processing industries in Balya (Bal?kesir province, Turkey) was optimized using a response surface methodology by altering parameters such as pH, initial metal concentration, contact time and biosorbent dosage. This strain was shown to be highly similar to Penicillium sp. Furthermore, zeta potential measurements and Fourier transform infrared spectroscopy were performed to understand the adsorption mechanism. A Box–Behnken design with 29 experiments was used to evaluate the interactions between independent variables. The results showed that the fungal biomass isolated from the metal mine drainage could have a significant environmental impact through the biosorption of Pb(II) and Ni(II) in waters polluted with heavy metals, particularly in the drainage from metal mines. The maximum removal values were 76 and 47 % at pH 4.5 for both Pb(II) and Ni(II), with 123 and 33 mg/L initial metal concentrations, 65 and 89 min contact times and 0.2 and 1.6 g/L biosorbent, respectively.  相似文献   

8.
Analysis was carried out using tangerine peel aiming its use as a potential adsorbent of eight heavy metal ions (Cd, Co, Cr, Cu, Mn, Ni, Pb and Zn) from aqueous solution. This agricultural waste was tested both in its untreated and also chemically modified form. Based on Fourier transformation infrared spectra, a comparison of biosorbent structure before and after chemical treatment was made. Batch adsorption tests were conducted at different pH and mass of sorbent to examine the influence on the effectiveness of simultaneous removal of tested ions. Kinetic studies were conducted at optimum pH 5.0 and sorbent dosage 300 mg. The pseudo-second-order kinetic model best fit the experimental data with high correlation coefficients (r2 > 0.9997). By optimizing listed parameters, high removal efficiencies (> 89%) were achieved. According to the results obtained in this study, the remediation of water polluted with heavy metals could be done using modified tangerine peel as an agricultural waste material.  相似文献   

9.
In this study, the imprinted aniline–formaldehyde was used as an adsorbent for removal of Iridium and Palladium ions from aqueous solutions through batch equilibrium. The sorbent was characterized by fourier transform infrared spectroscopy. The influence of pH, equilibrium time, temperature and initial concentration of metal ions on adsorbed amount of both ions were investigated. The maximum adsorption capacity in initial concentration of 100 mg/L was found to be 12.5 mg/g at pH 7.0 and 14.3 mg/g at pH 8.0 for Iridium and Palladium, respectively. In addition, the best desorption of the metal ions from resin was obtained by 0.5 mol/L nitric acid as eluting agent. The profile of both ions uptake on this sorbent reflects good accessibility of the chelating sites in the imprinted aniline–formaldehyde. Langmuir, Freundlich, Temkin and Redlich–Peterson isotherm models were applied to analyze the experimental data. Moreover, Langmuir linear method was used to obtain the isotherm parameters. However, Langmuir type II achieved the highest coefficient which led to the best fit for the palladium and the best fit for Iridium obtained from linear Redlich–Peterson. However, the thermodynamic parameters (ΔG°, ΔH°, and ΔS°) were also determined using the equilibrium constant values obtained at different temperatures. The results showed that the adsorption for Iridium and Palladium ions was spontaneous nature and endothermic. Moreover, the method was applied for the determination of both ions from tap water samples.  相似文献   

10.
In this study, the adsorption behavior of Ni(II) in an aqueous solution system using natural adsorbent Peganum harmala-L was measured via batch mode. The prepared sorbent was characterized by scanning electron microscope, Fourier transform infrared spectroscopy, N2 adsorption–desorption and pHzpc. Adsorption experiments were carried out by varying several conditions such as contact time, metal ion concentration and pH to assess kinetic and equilibrium parameters. The equilibrium data were analyzed based on the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherms. Kinetic data were analyzed using the pseudo-first-order, pseudo-second-order and intra-particular diffusion models. Experimental data showed that at contact time 60 min, metal ion concentration 50 mg/L and pH 6, a maximum amount of Ni(II) ions can be removed. The experimental data were best described by the Langmuir isotherm model as is evident from the high R 2 value of 0.988. The adsorption capacity (q m) obtained was 68.02 mg/g at an initial pH of 6 and a temperature of 25 °C. Kinetic studies of the adsorption showed that equilibrium was reached within 60 min of contact and the adsorption process followed the pseudo-first-order model. The obtained results show that P. harmala-L can be used as an effective and a natural low-cost adsorbent for the removal of Ni(II) from aqueous solutions.  相似文献   

11.
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   

12.
The biosorption characteristics of Cd(II) and Cu(II) ions from aqueous solutions obtained using submerged aquatic plant (Myriophyllum spicatum) biomass were investigated in terms of equilibrium, kinetics, thermodynamics, and cation competition. Langmuir and Freundlich models were applied to describe the biosorption isotherm of metal ions by M. spicatum biomass and isotherm constants considering the most important parameter, pH. The variation of sorption isotherm constants showed pH dependence. The Langmuir and Freundlich models fitted the equilibrium data well. The maximum biosorption capacity (q m) of M. spicatum biomass was determined to be 29.07 mg/g for the Cd(II) ion at pH 5.0 and 12.12 mg/g for the Cu(II) ion at pH 6.0. Chi square analysis showed that the Freundlich model fitted the equilibrium data better than the Langmuir isotherm. Competition of Cd(II) and Cu(II) in a binary solution showed that the Langmuir monolayer capacity of Cd(II) decreased from 29.07 mg/g with only Cd(II) in solution to 12.02 mg/g in the presence of Cu(II). Kinetics results showed that the biosorption processes of both metal ions followed the pseudo-second-order kinetics well. The calculated thermodynamic parameters (?G 0, ?H 0, and ?S 0) showed that biosorption of Cd(II) and Cu(II) ions onto M. spicatum biomass was feasible, spontaneous, and endothermic in nature. Fourier transform infrared spectroscopy spectrum analysis revealed that Cd(II) and Cu(II) sorption was mainly ascribed to carboxyl, hydroxyl, amine, and C–N groups in M. spicatum.  相似文献   

13.
In this study, sepiolite-nano zero valent iron composite was synthesized and applied for its potential adsorption to remove phosphates from aqueous solution. This composite was characterized by different techniques. For optimization of independent parameters (pH = 3–9; initial phosphate concentration = 5–100 mg/L; adsorbent dosage = 0.2–1 g/L; and contact time = 5–100 min), response surface methodology based on central composite design was used. Adsorption isotherms and kinetic models were done under optimum conditions. The results indicated that maximum adsorption efficiency of 99.43 and 92% for synthetic solution and real surface water sample, respectively, were achieved at optimum conditions of pH 4.5, initial phosphate concentration of 25 mg/L, adsorbent dosage of 0.8 g/L, and 46.26 min contact time. The interaction between adsorbent and adsorbate is better described with the Freundlich isotherm (R 2 = 0.9537), and the kinetic of adsorption process followed pseudo-second-order model. Electrostatic interaction was the major mechanisms of the removal of phosphates from aqueous solution. The findings of this study showed that there is an effective adsorbent for removal of phosphates from aqueous solutions.  相似文献   

14.
A zinc oxide-coated nanoporous carbon sorbent was prepared by acid modification and ZnO functionalization of mesoporous carbon. The synthesized materials, such as mesoporous carbon, oxidized mesoporous carbon and zinc oxide-coated nanoporous carbon, were characterized by nitrogen adsorption–desorption analysis, Fourier transform infrared spectra, scanning electron microscopy, and transmission electron microscopy. ZnO on oxidized mesoporous carbon gradually increased with increase in the number of cycles. Furthermore, the effects of agitation time, initial metal ions concentration, adsorbent dose, temperature and pH on the efficiency of Pb(II) ion removal were investigated as the controllable factors by Taguchi method. The value of correlation coefficients showed that the equilibrium data fitted well to the Langmuir isotherm. Among the adsorbents, zinc oxide-coated nanoporous carbon showed the largest adsorption capacity of 522.8 mg/g (2.52 mmol/g) which was almost close to that of the zinc oxide-coated (2.38 mmol/g), indicating the monolayer spreading of ZnO onto the oxidized mesoporous carbon. The results of the present study suggest that ZnO-coated nanoporous carbon can be effectively used for Pb(II) adsorption from aqueous solution, whereas a part of acidic functional groups may be contributed to binding the Pb(II) for the oxidized mesoporous carbon and mesoporous carbon. Kinetic studies indicated that the overall adsorption process of Pb(II) followed the pseudo-second-order model. The ZnO-coated nanoporous carbon was regenerated and found to be suitable of reuse of the adsorbent for successive adsorption–desorption cycles without considerable loss of adsorption capacity.  相似文献   

15.
This paper investigates the potential of alginate-immobilised Chlorella sorokiniana for removing Cu2+, Ni2+ and Cd2+ ions from drinking water solutions. The effects of initial metal concentrations, contact times and temperatures on the biosorptions and removal efficiencies of the tested metals were investigated at initial pH values of 5, and pH effects were studied within the range of 3–7. When studying the effects of initial metal concentrations, the highest experimental removal yields achieved for Cu2+, Ni2+ and Cd2+ ions were 97.10, 50.94 and 64.61 %, respectively. The maximum biosorption capacities obtained by the Langmuir isotherm model for the biosorptions of Cu2+, Ni2+ and Cd2+ ions by alginate-immobilised C. sorokiniana were found to be 179.90, 86.49 and 164.50 mg/g biosorbent, respectively. The experimental data followed pseudo-second-order kinetics. At an initial metal concentration of 25 mg/L, immobilised algae could be used in at least 5 successive biosorption–desorption cycles. SEM and EDS analyses revealed that the metals bonded to the biosorbent. Bi- and multi-metal systems of Cu2+, Ni2+ and Cd2+ were investigated at initial metal concentrations of 30, 50 and 100 mg/L. The removal of Cd2+ as well as Ni2+ in such systems was negatively affected by the presence of Cu2+. The removal efficiency for Cu2+ in multi-metal systems decreased by 5–7 %, whilst in the cases of Cd2+ and Ni2+ the efficiencies decreased by up to 30 %. Nevertheless, the results obtained show that alginate-immobilised C. sorokiniana can efficiently remove the metals tested from polluted drinking water sources.  相似文献   

16.
In recent years, the need for safe and economical methods to eliminate heavy metals from contaminated waters has necessitated research on the production of low-cost alternatives to commercially available activated carbon. In the present work, in order to enhance the removal of heavy metals from contaminated water, Zizyphus vulgaris wastes were modified chemically to produce an adsorbent rich in carboxylic groups to enhance the removal of heavy metals from contaminated water. Adsorption of Zn(II) ions on the produced adsorbent was then optimized. The optimal ratio for esterification involved the treatment of Z. vulgaris wastes (1 g) with 0.0037 mmol malic acid in the presence of a very small amount of water for 2 h at 140 °C. The maximum values for adsorption capacity, q max, were 28.7 and 164.6 mg/g on native and modified Z. vulgaris wastes, respectively, at pH 5 and 30 °C with a contact time 2 h and an initial metal ion concentration of 400 mg/L. The equilibrium data were well fitted by the Langmuir and Freundlich adsorption models and demonstrated the significant capacity for Z. vulgaris wastes in the removal of Zn(II) ions from aqueous solutions.  相似文献   

17.
The potential use of the immobilized microalgae (in Ca-alginate) of Chlamydomonas reinhardtii to remove Hg(II), Cd(II) and Pb(II) ions from aqueous solutions was evaluated using bare Ca-alginate bead as a control system. Ca-alginate beads containing immobilized microalgae were incubated for the uniform growth at 22 °C for 5 days. Effects of pH, temperature, initial concentration of metal ions and biosorbent dosages on the adsorption of Hg(II), Cd(II) and Pb(II) ions were studied. Adsorption of Hg(II), Cd(II) and Pb(II) ions on the immobilized microalgae showed highest values at around pH 5.0 to 6.0. The adsorption equilibrium was represented with Langmuir and Freundlich adsorption isotherms. The adsorption of these ions on the immobilized microalgae followed second-order kinetics and equilibrium was established in about 60 min. The temperature change in the range of 5–40 °C did not affect the adsorption capacities of the immobilized microalgae. The immobilized-algal systems can be regenerated using 2 M NaCl for Hg(II), Cd(II) and Pb(II) ions.  相似文献   

18.
A hydrophilic kapok fiber was prepared by a chemical process of the Fenton reaction and used as an adsorbent to remove Pb(II) from aqueous solution. The effects of experimental parameters including pH, contact time, Pb(II) concentration, and coexisting heavy metals were estimated as well as evaluated. The optimum concentrations of FeSO4 and H2O2 for the Fenton reaction-modified kapok fiber (FRKF) were 0.5 mol L?1 and 1 mol L?1, respectively. The adsorption kinetic models and isotherm equations of Langmuir and Freundlich were conducted to identify the most optimum adsorption rate and adsorption capacity of Pb(II) on FRKF. The FRKF displayed an excellent adsorption rate for Pb(II) in single metal solution with the maximum adsorption capacity of 94.41?±?7.56 mg g?1 at pH 6.0. Moreover, the FRKE still maintained its adsorption advantage of Pb(II) in the mixed metal solution. The FRKF exhibited a considerable potential in removal of metal content in wastewater streams.  相似文献   

19.
Unfertilizable fruiting buds of mango plant Mangifera Indica L, an agrowaste, is used as a biomass in this study. The efficacy of the biosorbent was tested for the removal of lead, copper, zinc and nickel metal ions using batch experiments in single and binary metal solution under controlled experimental conditions. It is found that metal sorption increases when the equilibrium metal concentration rises. At highest experimental solution concentration used (150 mg/L), the removal of metal ions were 82.76 % for lead, 76.60 % for copper, 63.35 % for zinc and 59.35 % for nickel while at lowest experimental solution concentration (25 mg/L), the removal of metal ions were 92.00% for lead, 86.84 % for copper, 83.96 % for zinc and 82.29 % for nickel. Biosorption equilibrium isotherms were plotted for metal uptake capacity (q) against residual metal concentrations (Cf) in solution. The q versus Cf sorption isotherm relationship was mathematically expressed by Langmuir and Freundlich models. The values of separation factor were between zero and one indicating favourable sorption for four tested metals on the biosorbent. The surface coverage values were approaching unity with increasing solution concentration indicating effectiveness of biosorbent under investigation. The non-living biomass of Mangifera indica L present comparable biosorption capacity for lead, copper, zinc and nickel metal ions with other types of biosorbent materials found in literature and is effective to remove metal ions from single metal solutions as well as in the presence of other co-ions with the main metal of solution.  相似文献   

20.
The present study attempted to identify the efficient hazardous metal-removing sorbent from specific types of soil, upper and middle layer shirasu, shell fossil, tuff, akadama and kanuma soils of Japan by physico-chemical and metal (arsenic, cadmium and lead) removal characterizations. The physico-chemical characteristics of soil were evaluated using X-ray diffraction and scanning electron microscopy with energy dispersive spectroscopy techniques, whereas metal removal properties of soil were characterized by analyzing removal capacity and sorption kinetics of potential metal-removing soils. The chemical characteristics revealed that all soils are prevalently constituted of silicon dioxide (21.83–78.58 %), aluminum oxide (4.13–38 %) and ferrous oxide (0.835–7.7 %), whereas calcium oxide showed the highest percentage (65.36 %) followed by silicon dioxide (21.83 %) in tuff soil. The results demonstrated that arsenic removal efficiency was higher in elevated aluminum oxide-containing akadama (0.00452 mg/L/g/h) and kanuma (0.00225 mg/L/g/h) soils, whereas cadmium (0.00634 mg/L/g/h) and lead (0.00693 mg/L/g/h) removal efficiencies were maximum in elevated calcium oxide-containing tuff soil. Physico-chemical sorption and ion exchange processes are the metal removal mechanisms. The critical appraisal of three metal removal data also clearly revealed cadmium > lead > arsenic order of removal efficiency in different soils, except in tuff and akadama soils followed by lead > cadmium > arsenic. It clearly signified that each type of soil had a specific metal adsorption affinity which was regulated by the specific chemical composition. It may be concluded that akadama would be potential arsenic-removing and tuff would be efficient cadmium and lead-removing soil sorbents.  相似文献   

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