Phosphate Removal from Aqueous Solution Using Coir-Pith Activated Carbon

The present study deals with the removal of phosphates from aqueous solution using activated carbon developed from coir pith. Batch adsorption experiments were performed to delineate the effect of initial pH, contact time, adsorbent dose and temperature on the removal of phosphates by coir-pith activated carbon (CAC) (activated by H₂SO₄). The removal was found to be maximum in the pH range of 6–10. The kinetics of adsorption showed that the phosphate adsorption onto CAC was a gradual process with a quasi-equilibrium being attained in 3 h. The adsorption equilibrium data followed the Temkin isotherm. Thermodynamic parameters such as ΔG ^o , ΔH ^o , and ΔS ^o were evaluated by applying the Arrhenius and van't Hoff equations, and it was found that the adsorption of phosphate on CAC was spontaneous and endothermic.     

Biosorption of Cd(II) From Aqueous Solution by Cocoa Pod Husk Biomass: Equilibrium,Kinetic, and Thermodynamic Studies

Cocoa pod husk biomass proved to be an effective biosorbent for the removal of Cd(II) from aqueous solution. The biosorbent was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, surface structural parameters, and proximate analysis. The effects of operational parameters were investigated. Equilibrium was reached after 120 min at 303 K and optimum biosorption capacity was obtained at pH 6. The biosorption kinetics was best predicted by the Avrami model. The results showed that the biosorption equilibrium was best described by the Freundlich isotherm model. From the thermodynamic parameters determined, the biosorption was spontaneous and endothermic.     

Removal of Zinc (II) Ions from Aqueous Solutions Using Surfactant Modified Bamboo Sawdust

The present study explores the ability of surfactant modified bamboo sawdust in removing zinc (II) ions from aqueous solutions. The modified bamboo sawdust is characterized by surface area analysis, Scanning Electron Microscope, and Fourier Transform Infrared and X-ray fluorescence analysis. Adsorption isotherm and kinetic models were used to study the adsorption characteristics of zinc (II) ions onto modified bamboo sawdust. The equilibrium adsorption isotherm data were fitted into the Langmuir and Freundlich adsorption isotherms. It was found that modified bamboo sawdust yielded maximum adsorption capacity of 111.12 mg/g at 50°C for zinc (II) ions. The kinetic data obtained at different initial concentrations were analyzed using first-order-reversible reaction, pseudo-first-order, and pseudo-second-order models. The results provide strong evidence to support the hypothesis of adsorption mechanism.     

Removal of Methyl Orange from Aqueous Solution Using Activated Papaya Leaf

The present investigation describes the potential of acid activated papaya leaf for the adsorption of methyl orange (MO) dye from aqueous solution. The FT-IR analysis indicated the presence of a wide variety of functional groups on the surface of the activated papaya leaf. Scanning electron microscopy and Electron dispersion X-ray techniques indicated the morphological behavior of adsorption onto the adsorbent, and weight percentage of chemical compositions available on the surface of adsorbent. The parameters, such as pH, contact time, and agitation rate giving the highest adsorption efficiency were obtained at 2, 120 min, and 150 rpm, respectively. The Langmuir model was found to represent the isotherm data better than other isotherms studied. Batch adsorption studies, based on the assumption of a pseudo first-order, Elovich Equation, and the pseudo second-order showed that the kinetic data followed closely a pseudo second-order mechanism. The adsorption capacity of activated papaya leaf for the removal of MO dye was found to be 333.34 mg/g. These showed that papaya leaf could be considered as a good and economical substitute of commercial activated carbon.     

交联壳聚糖磁性颗粒吸附去除水溶液中的铜

The performance of cross-linked magnetic chitosan, coated with magnetic fluids and cross-linked with epichlorohydrin, was investigated for the adsorption of copper (II) from aqueous solutions. Infrared spectra of chitosan before and after modification showed that the coating and cross-linking are effective. Experiments were performed at different pH of solution and contact time, and appropriate conditions for the adsorption of Cu(II) were determined. Experimental equilibrium data were correlated with Langmuir and Freundlich isotherms for determination of the adsorption potential. The results showed that the Langmuir isotherm was better compared with the Freundlich isotherm, and the uptake of Cu(II) was 78.13 mg•g－1. The kinetics of adsorption corresponded with the first-order Langergren rate equation, and Langergren rate constants were determined.     

Physicochemical Parameters of Cu(II) Ions Adsorption from Aqueous Solution by Magnetic-Poly(divinylbenzene-n-vinylimidazole) Microbeads

This study is aimed at the synthesis and characterization of the mesoporous magnetic-poly(divinylbenzene-1-vinylimidazole)[m-poly(DVB-VIM))microbeads(average diameter = 53–212 µm); their application as adsorbent in the removal of Cu(II) ions from aqueous solutions was investigated. The mesoporous m-poly(DVB-VIM) microbeads were prepared by copolymerizing of divinylbenzene (DVB) with 1-vinylimidazole (VIM). The mesoporous m-poly(DVB-VIM) microbeads were characterized by N₂ adsorption/desorption isotherms, ESR, elemental analysis, scanning electron microscope (SEM), and swelling studies. At fixed solid/solution ratio the various factors affecting adsorption of Cu(II) ions from aqueous solutions such as pH, initial concentration, amount of mesoporousm-poly(DVB-VIM)) microbeads, contact time, and temperature were analyzed. Langmuir, Freundlich, and Dubinin-Radushkvich isotherms were used the model adsorption equilibrium data. The Langmuir isotherm model was the most adequate. The pseudo first-order, pseudo-second-order, Ritch-second-order, and intraparticle diffusion models were used to describe the adsorption kinetics. The experimental data fitted to pseudo second-order kinetic. The study of temperature effect was quantified by calculating various thermodynamic parameters such as Gibbs free energy, enthalpy, and entropy changes. Morever, after the use in adsorption, the mesoporous m-poly(DVB-VIM) microbeads with paramagnetic property was separated via the applied magnetic force. These features make the mesoporous m-poly(DVB-VIM) microbeads a potential candidate for support of Cu(II) ions removal under magnetic field.     

Removal of Lead(II) from Aqueous Solutions using Pre-boiled and Formaldehyde-Treated Onion Skins as a New Adsorbent

The adsorption characteristics of Pb²⁺ on pre-boiled treated onion skins (PTOS) and formaldehyde-treated onion skins (FTOS) were evaluated. The effects of Pb²⁺ initial concentration, agitation rate, solution pH, and temperature on Pb²⁺ adsorption were investigated in batch systems. Pb²⁺ adsorption was found to increase with increase in initial concentration. The point of zero net charge (PZC) was 6.53. The optimum pH for the maximum removal of Pb²⁺ was 6.0. The adsorption equilibrium data was best represented by the Langmuir isotherm model for FTOS and the Freundlich isotherm model for PTOS. The maximum amounts of Pb²⁺ adsorbed (qm), as evaluated by the Langmuir isotherm, was 200 mgg^?1 for FTOS. The efficiencies of PTOS and FTOS for Pb²⁺ removal were 84,8.0% and 93.5% at 0.15 g/200 mL^?1 adsorbent dose, respectively. (C ₀ = 50 mg L^?1). Study concluded that onion skins, a waste material, have good potential as an adsorbent to remove toxic metals like Pb²⁺ from water. Boehm titration analysis was conducted to determine the surface groups. It was found that the adsorption kinetics of Pb²⁺ obeyed pseudo-first-order kinetic model as based on Δq (%) values. FTIR and SEM images before and after adsorption was recorded to explore changes in adsorbent-surface morphology. Activation energy (Ea) was obtained as 25.596 kJ/mol.     

Removal of Lead and Cadmium Ions from Aqueous Solutions Using Sulphur and Oxygen Donor Ligand Bearing Hydrogels

A new thiourea and urea functional monomers were synthesized. A series of hydrogels were prepared by photopolymerization. The hydrogels were used for the removal of Pb(II) and Cd(II) ions from aqueous solutions. The influence of the uptake conditions such as the pH, the time, and the initial feed concentration on the metal ion binding capacity of hydrogel was tested. The selectivity of the hydrogels towards the different metal ions was also tested. The adsorption isotherm models were applied. The limits of detection and quantification were calculated. The usability of the hydrogels for preconcentration studies were also investigated.     

Removal of Chromium (VI) from Aqueous Solution by Cellulose Modified with D-Glucose

Cellulose powder was grafted with the vinyl monomer glycidyl methacrylate using ceric ammonium nitrate as initiator and was further derived with D-Glucose (D-Glu) to build a adsorbent (Cell-g-GMA-D-Glu). Epoxy cellulose, which was made up of Cell-g-GMA and Cell-hydro-g-GMA, was found to contain 5.48 mmol g^?1 epoxy groups. The adsorption process of the adsorbent was described by the Langmuir model of adsorption well and the maximum adsorption capacity of chromium (VI) reached to 54.59 mg g^?1. The adsorption-desorption tests of the Cell-g-GMA-D-Glu exhibited that the reproducibility of the absorbent was well and the adsorbent could be reused six times at least.     

Removal of Cu(II), Fe(III), and Cr(III) from Aqueous Solution by Aniline Grafted Silica Gel

Abstract

The aniline moiety was covalently grafted onto silica gel surface. The modified silica gel with aniline groups (SiAn) was used for removal of Cu(II), Fe(III), and Cr(III) ions from aqueous solution and industrial effluents using a batch adsorption procedure. The maximum adsorption of the transition metal ions took place at pH 4.5. The adsorption kinetics for all the adsorbates fitted better the pseudo second‐order kinetic model, obtaining the following adsorption rate constants (k₂): 1.233 · 10^?2, 1.902 · 10^?2, and 8.320 · 10^?3 g · mg^?1 min^?1 for Cr(III), Cu(II), and Fe(III), respectively. The adsorption of these transition metal ions were fitted to Langmuir, Freundlich, Sips, and Redlich‐Peterson isotherm models; however, the best isotherm model fitting which presented a lower difference of the q (amount adsorbed per gram of adsorbent) calculated by the model from the experimentally measured, was achieved by using the Sips model for all adsorbates chosen. The SiAn adsorbent was also employed for the removal of the transition metal ions Cr(III) (95%), Cu(II) (95%), and Fe(III) (94%) from industrial effluents, using the batch adsorption procedure.     

Adsorptive Removal of Pb(II) and Cu(II) Ions from Aqueous Solutions by Cross-Linked Chitosan-Polyphosphate-Epichlorohydrin Beads

In this study, the cross-linked chitosan-polyphosphate-epichlorohydrin (CCPE) beads were prepared by cross-linking chitosan with both polyphosphate and epichlorohydrin and used as bioadsorbent for the removal of Pb(II) and Cu(II) ions from aqueous solutions. The effects of the dosage of CCPE beads, solution pH, initial metal ion concentration, contact time, and temperature were investigated. Then, three important factors were selected to optimize the removal processes by the orthogonal test. The results show that CCPE beads can effectively remove the Pb(II) and Cu(II) ions from aqueous solutions, and the maximum percentage removals for Pb(II) and Cu(II) ions are 99.7% and 91.2%, respectively. The data show also that the removal processes for both Pb(II) and Cu(II) ions fit best the pseudo-second order kinetic model. Moreover, the decrease of the adsorption ability of CCPE beads is less than 10% after reuse for 9 times, which suggests that CCPE beads have good reusability.     

Adsorption of Ce(IV) Ions from Aqueous Solution by Silica Aerogels

The adsorption process of Ce(IV) ions from aqueous solution by the silica aerogels was studied. The silica aerogels with hydrophobicity were prepared by the sol-gel process, supercritical drying, and heat treatment. The SEM image and nitrogen adsorption-desorption isotherm show that the heat-treated silica aerogel was a co-continuous porous structure with high BET surface area and narrow pore size distribution. The adsorption of Ce(IV) ions onto the silica aerogels was found to be fitted well by pseudo-second-order kinetics and Langmuir isotherm model. The activation energy for Ce(IV) adsorption onto silica aerogels could be calculated to be about 17.88 kJ/mol, which implied that the attractive forces of adsorption were weak electrostatic forces accompanying most ion-exchange reactions. The thermodynamic parameters showed that the adsorption process was spontaneous and endothermic.     

Peanut Shell Activated Carbon： Characterization,Surface Modification and Adsorption of Pb^2＋ from Aqueous Solution

Metal ion contamination of drinking water and waste water, especially with heavy metal ion such as lead, is a serious and ongoing problem. In this work, activated carbon prepared from peanut shell （PAC） was used for the removal of Pb^2＋ from aqueous solution. The impacts of the Pb25 adsorption capacities of the acid-modified carbons oxidized with HNO3 were also investigated. The surface functional groups of PAC were confirmed by Fourier transform infrared （FTIR） spectroscopy, X-ray photoelectron spectroscopy （XPS）, Boehm titration. The textural properties （surface area, total pore volume） were evaluated from the nitrogen adsorption isotherm at 77 K. The experimental results presented indicated that the adsorption data fitted better with the Langmuir adsorption model. A comparative study with a commercial granular activated carbon （GAC） showed that PAC was 10.3 times more efficient compared to GAC based on Langmuir maximum adsorption capacity. Further analysis results by the Langmuir equation showed that HNO3 [20% （by mass）] modified PAC has larger adsorption capacity of Pb^2＋ from aqueous solution （as much as 35.5 mg·g^-1）. The adsorption capacity enhancement ascribed to pore widening, increased cation-exchange capacity by oxygen groups, and the promoted hydrophilicity of the carbon surface.     

Removal Characteristics of Cd(II), Cu(II), Pb(II), and Zn(II) by Natural Mongolian Zeolite through Batch and Column Experiments

The removal characteristics of Cd(II), Cu(II), Pb(II), and Zn(II) from model aqueous solutions by 5 natural Mongolian zeolites were investigated. The adsorption of metals on zeolites reached a plateau value within 6 h. The adsorption kinetic data were fitted with adsorption kinetic models. The equilibrium adsorption capacity of the zeolites was measured and fitted using Langmuir and Freundlich isotherm models. The order of adsorption capacity of zeolite was Pb(II) > Zn(II) > Cu(II) > Cd(II). The maximum adsorption capacity of natural zeolite depends on its cation exchange capacity and pH. The leaching properties of metals were simulated using four leaching solutions. The results show that natural zeolite can be used as an adsorbent for metal ions from aqueous solutions or as a stabilizer for metal-contaminated soils.     

花生壳活性炭的表征,表面改性及吸附脱除水中Pb2+离子

Metal ion contamination of drinking water and waste water, especially with heavy metal ion such as lead, is a serious and ongoing problem. In this work, activated carbon prepared from peanut shell (PAC) was used for the removal of Pb2 from aqueous solution. The impacts of the Pb2 adsorption capacities of the acid-modified carbons oxidized with HNO3 were also investigated. The surface functional groups of PAC were confirmed by Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), Boehm titration. The textural properties (surface area, total pore volume) were evaluated from the nitrogen adsorption isotherm at 77K. The experimental results presented indicated that the adsorption data fitted better with the Langmuir adsorption model. A comparative study with a commercial granular activated carbon (GAC) showed that PAC was 10.3 times more efficient compared to GAC based on Langmuir maximum adsorption capacity. Further analysis results by the Langmuir equation showed that HNO3 [20% (by mass)] modified PAC has larger adsorption capacity of Pb2 from aqueous solution (as much as 35.5mg.g1). The adsorption capacity enhancement ascribed to pore widening, increased cation-exchange capacity by oxygen groups, and the promoted hydrophilicity of the carbon surface.     

利用钠活化膨润土去除水溶液中的Ni和Co

室温环境（22±1℃）下研究了不同实验条件下钠活化膨润土去除水溶液中Ni2＋和Co2＋的能力。所研究的参数为固液比及其溶液阳离子初始浓度,实验包括了膨润土在Ni2＋、Co2＋不同浓度溶液中分别对Ni和Co的反应。结果表明,膨润土很容易吸附2种金属,但是对Ni表现出了更高的吸附性。对溶液中2种金属离子吸附的协同或抑制作用取决于离子初始浓度,当重金属初始浓度超过膨润土对阳离子交换吸附能力（CEC）时出现过吸附。     

Removal of Mercury(II) Ions from Aqueous Solutions using Chemically Modified Banana Stem: Kinetic and Equilibrium Modeling

In this study, removal of mercury(II) ions from aqueous solutions under different experimental conditions using formaldehyde polymerized banana stem (FPBS) has been investigated. Formaldehyde treatment favored the stabilization of the organic substances of banana stem (BS). The adsorbent was characterized using IR, SEM, TG, and potentiometric titration methods. The adsorption efficiency of FPBS was compared with BS and the result showed that FPBS was found to be 1.8 times more effective than BS for mercury(II) removal. The maximum removal of 99.3 and 99.1%, respectively, for 10 and 25 mg/L in 50 mL initial concentrations was obtained at pH 7.0. Kinetic studies revealed that the adsorption occurred in two stages: external mass transport in the first stage and intra-particular diffusion in the second stage. Adsorption was found to be rapid and equilibrium was attained in 60 min. The adsorption equilibrium data fitted the Freundlich isotherm equation reasonably well. The maximum adsorption capacity of FPBS for mercury(II) was found to be 132.25 mg/g. Desorption experiments showed that the process of adsorption was reversible and the adsorbent was easily regenerated with 0.1 M HCl up to 96.0% recovery.     

Removal of lead (II) and cadmium (II) from aqueous solutions using spent Agaricus bisporus

The sorption of Pb and Cd from aqueous solutions by spent Agaricus bisporus was investigated. The effects of contact time, pH, ionic medium, initial metal concentration, other metal ions presence and ligands were studied in batch experiments at 25°C. Maximum sorption for both metals was found to occur at an initial pH of around 5.5. The equilibrium process was well described by the Langmuir isotherm model, with maximum sorption capacities of 0.2345 and 0.1273 mmol g^?1 for Pb and Cd respectively. Kinetic data followed the pseudo‐second‐order kinetic model. The presence of NaCl and NaClO₄ caused a reduction in Cd sorption, while Pb sorption was not remarkably affected. The presence of other metals did not affect Pb removal, while the Cd removal was much reduced. HCl or EDTA solutions were able to desorb Cd from the spent Agaricus bisporus (SAB) completely, while an approximately 60% and 15% desorption yield was obtained for Pb when HCl 0.01 mol L^?1 or EDTA 0.001 mol L^?1 were used, respectively. The results of FTIR, SEM and EDX analysis indicated that other mechanisms, such as surface complexation and electrostatic interactions, must be involved in the metal sorption in addition to ion exchange. © 2012 Canadian Society for Chemical Engineering