Removal of Pb(II) from aqueous solution by adsorption using activated tea waste

A basic investigation on the removal of Pb(II) ions from aqueous solutions by using activated tea waste was conducted in batch conditions. An inexpensive and effective adsorbent was developed from waste tea leaves for the uptake of Pb(II) from aqueous solution. The influence of different experimental parameters—shaking time, particle size, adsorbent dose, initial pH, temperature, etc.—on lead uptake was evaluated. Lead is adsorbed by the developed adsorbent up to maximum of 99.7%. The initial Pb(II) concentrations were 5, 10, 15 and 20 mg/l in the experiment. The adsorption was found to be exothermic in nature. The Langmuir, Freundlich and Tempkin isotherm models were tried to represent the equilibrium data of Pb(II) adsorption. The adsorption data was fitted very well to the Langmuir isotherm model in the studied concentration range of Pb(II) adsorption. Isotherms have been used to determine thermodynamic parameters of the process: free energy change (ΔG°), enthalpy change (ΔH°) and entropy change (ΔS°). Column experiments were performed to study the practical applicability of the system. The kinetics and the factors controlling the adsorption process were also discussed. Activated tea waste is a better adsorbent compared to other adsorbents available in literature.     

Biosorption of Pb(II) and Cd(II) ions from aqueous solution using polyaniline/chitin composite

In this study, chitin (Ch) was made composite with polyaniline (PANI) and used for the removal of Pb(II) and Cd(II) ions from aqueous solution. Characterization techniques such as Fourier transform infrared spectroscopy, scanning electron microscope, energy-dispersive X-ray analyser and X-ray diffraction were employed to characterize the prepared PANI/Ch composite. Influence of various equilibrium parameters on the adsorption of Pb(II) and Cd(II) ions onto PANI/Ch composite was investigated. The adsorption process followed the Freundlich isotherm model, and the calculated maximum monolayer sorption capacity of PANI/Ch composite for Pb(II) and Cd(II) ions is 7.03 and 6.05 mg g^?1 at 303 K. The kinetic data were well described by the pseudo-second-order model.     

Effect of ZnO loading to activated carbon on Pb(II) adsorption from aqueous solution

The effect of zinc oxide loading to granular activated carbon on Pb(II) adsorption from aqueous solution was studied in comparison with zinc oxide particles and oxidized activated carbon. Cu(II), Cd(II) and nitrobenzene were used as reference adsorbates to investigate the adsorption. The BET surface area and point of zero charge (pH_PZC) in the aqueous solution were measured for the adsorbents. The adsorption isotherms were examined to characterize the adsorption of heavy metals and organic molecules. The heavy metal adsorption was improved by both the zinc oxide loading and the oxidation of activated carbon. In contrast, the adsorption of nitrobenzene was considerably reduced by the oxidation, and slightly decreased by the zinc oxide loading. The zinc oxide loading to the activated carbon was found to be effectively used for the Pb(II) adsorption whereas only a part of surface functional groups was used for the zinc oxide particles and the oxidized activated carbon. From the experimental results, the surface functional groups responsible for the Pb(II) adsorption on the zinc oxide loaded activated carbon were considered to be hydroxyl groups that formed on the oxide, while those on the oxidized activated carbon were considered to be carboxylic groups.     

Selective solid-phase extraction of trace Pb(II) from aqueous solution using Pb(II)-ion imprinted polymer

In this work, we synthesized several ions imprinted polymers based on the inclusion of 8-hydroxyquinoline, vinyl benzoic acid, and diazoaminobenzene as ligands into the polymer matrix to complex with lead ions. Besides, to optimize various parameters for the selective extraction and enrichment of lead ions using the best synthesized imprinted polymers, the selectivity of the chosen inorganic ions was investigated. These investigations indicated that the synthesized imprinted polymer particles have good potential for selective enrichment of lead ions compared with other heavy metal ions, and the selectivity of lead ion-imprinted polymers for lead ion was higher than non-imprinted polymer.     

Enhanced adsorption and recovery of Pb(II) from aqueous solution by alkali‐treated persimmon fallen leaves

Persimmon fallen leaves were employed to prepare a renewable and low‐cost biosorbent named as NPFL. Effects of initial pH, contact time, initial Pb(II) concentration, coexisting metal ions, and ionic strength on adsorption of Pb(II) from aqueous solution by NPFL were studied in detail. Enhanced removal capacity of NPFL toward Pb(II) was observed, and the maximum adsorption capacity was evaluated as 256 mg g^?1 by Langmuir modeling calculation. The fast adsorption process and the well‐fitted kinetics data with pseudo‐second‐order model indicated that chemisorption is the main rate‐limiting step for the adsorption process. NPFL had superior adsorption selectivity for Pb(II) from aqueous solution with coexisting metal ions. Characterization of NPFL and adsorption mechanism (electrostatic attraction, ion exchange, and chelation) were performed using XRD, SEM‐EDS, FT‐IR, XPS, and TGA. The results suggested that NPFL could be utilized as a potential candidate for the preconcentration of Pb(II) recovery and its removal in practice. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43656.     

Adsorption of Pb(II) from aqueous solution to Ni-doped bamboo charcoal

Bamboo charcoal (BC) obtained by pyrolysis of Makino bamboo in the absence of oxygen was used as support for the preparation of Ni-doped adsorbent (Ni-BC). The low-cost composite was characterized and used as an adsorbent for Pb(II) removal from water. The results showed that both BET surface area and total pore volume of Ni-BC increased. The adsorption of Pb(II) strongly depended on solution pH, temperature and ionic strength. The adsorption isotherms followed Langmuir isotherm model well, and the maximum adsorption capacities of Pb(II) at 298 K were 25.0 and 142.7 mg/g for BC and Ni-BC, respectively. The adsorption processes were well fitted by pseudo-second-order kinetic model. Thermodynamic parameters showed that the adsorptions of Pb(II) onto both adsorbents were feasible, spontaneous, and exothermic under the studied conditions. The spent Ni-BC could be readily regenerated for reuse.     

Adsorption of cadmium (II) and copper (II) ions from aqueous solution using chitosan composite

The binary chitosan/silk fibroin composite synthesized by reinforcement of silk fibroin fiber into the homogenous solution of chitosan in formic acid was used to investigate the adsorption of two metals of Cu(II) and Cd(II) ions in an aqueous solution. The binary composite was characterized by Fourier transform infrared and scanning electron microscopy. The optimum conditions for adsorption by using a batch method were evaluated by changing various parameters such as contact time, adsorbent dose, and pH of the solution. The experimental isotherm data were analyzed using the Freundlich and Langmuir equations, indicated to be well fitted to the Langmuir isotherm equation under the concentration range studied, by comparing the correlation co‐efficient. Adsorption kinetics data were tested using pseudo‐first‐order and pseudo‐second‐order models. Kinetics studies showed that the adsorption followed a pseudo‐second‐order reaction. Due to good performance and low cost, this binary chitosan/silk fibroin composite can be used as an adsorbent for removal of Cu(II) and Cd(II) from aqueous solutions. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Preparation and characterization of novel organo-clay minerals for Hg(II) ions adsorption from aqueous solution

Novel organo-clay minerals for adsorption of Hg(II) ions were prepared. The clay minerals were grafted with 2-(3-(2-aminoethylthio)propylthio)ethanamine (AEPE). AEPE-montmorillonite and AEPE-hectorite were characterized by X-ray diffraction (XRD), infrared spectroscopy (IR), thermogravimetric analysis (TGA), CHN element analysis (EA) and surface area analysis. The XRD patterns indicated that the chelating agents (AEPE) were mainly grafted on the external surface of montmorillonite while AEPE was grafted on both the external and interlayer surfaces of hectorite. The results from IR, TGA and EA showed a difference in chemical composition of the unmodified and modified clay minerals. The results confirmed that montmorillonite and hectorite were modified with the desired organic groups. The extent of ligand loading depended on the nature of the clay mineral. The AEPE-modified clay minerals were good chelating materials for Hg(II) ions, compared to the unmodified clay minerals. The adsorption capacity for Hg(II) of AEPE-montmorillonite and AEPE-hectorite was 46.1 and 54.7 mg g^− 1, respectively, for solution containing 140 mg L^− 1 Hg(II) ions (pH 4).     

Preparation and adsorption properties of a novel superabsorbent based on multiwalled carbon nanotubes–xylan composite and poly(methacrylic acid) for methylene blue from aqueous solution

A novel superabsorbent was prepared by the copolymerization reaction between multiwalled carbon nanotubes (MWCNTs)–xylan composite and poly(methacrylic acid) (PMAA) in the presence of N,N′‐methylenebisacrylamide as cross‐linker and the redox initiation system (NH)₄S₂O₈‐anhydrous Na₂SO₃ as initiator for adsorbing methylene blue (MB) from aqueous solution. First, covalent modification of MWCNTs with a natural polymer xylan was achieved by the nucleophilic substitution reaction. The obtained xylan modified MWCNTs–xylan composite was characterized by transmission electron microscope, Fourier transform infrared spectroscopy, X‐ray photoelectron spectrometer, and thermal gravimetric analysis. The results indicated that the hydroxyl groups of xylan participated in the formation of MWCNTs–xylan composite, and MWCNTs–xylan composite contained 32% xylan and about four molecule chains of xylan were grafted onto 5,000 carbon atoms of MWCNTs sidewalls. Subsequently, a novel superabsorbent based on MWCNTs–xylan composite and PMAA was prepared and characterized by Fourier transform infrared spectroscopy, scanning electron microscope, and swelling test. The results proved that superabsorbent was successfully prepared by copolymerization reaction and found that the superabsorbent evidently presented three‐dimensional network structure. Swelling process of superabsorbent complied with the Fick's law. Adsorption property of superabsorbent for MB was also systematically studied by investigating these parameters, such as superabsorbent dosage, initial MB concentration, contact time, ion strength, and pH. The superabsorbent presented a higher adsorption capacity and removal rate for MB. The adsorption data were fitted by Langmuir, Freundlich isotherm models, and four adsorption kinetic models. Freundlich isotherm model better fitted the equilibrium data than Langmuir, and adsorption kinetics could be well described by pseudo‐second‐order kinetic and intraparticle diffusion. These results indicated that the superabsorbent can be used as an efficient absorbent for removal of MB from aqueous solution. POLYM. COMPOS., 35:1516–1528, 2014. © 2013 Society of Plastics Engineers     

Effects of crosslinking degree of poly(vinyl alcohol) hydrogel in aqueous solution: kinetics and mechanism of copper(II) adsorption

Recently, a renewed interest in hydrogels for heavy metal removal of wastewater has been growing because of embarking opportunities in industrial applications. One of the most interesting hydrogels potentially used as absorbent is poly(vinyl alcohol) (PVA), owing to its biocompatibility. In this study, the adsorption capacity of copper(II) ion onto PVA hydrogel (PVAH) adsorbents with different crosslinking degrees of 1, 3 and 5 % from aqueous solution was investigated. The PVAH adsorbents were prepared from PVA, using glutaraldehyde as a crosslinking agent. Their properties were determined by Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), and water absorption measurement. The results showed that PVA was crosslinked with glutaraldehyde. It exhibited an equilibrium swelling ratio in the range of 195–250 %, depending on the crosslinking degree with different PVAH structures defined from SEM micrographs. The adsorption capacity of copper(II) ion onto PVAH adsorbents was investigated and found that higher crosslinking degree decreased the absorption capacity. This behavior is due to the decrease in reactive sites, resulting in the decrease of interaction between copper(II) ion and PVA. Besides, the adsorption capacity also depended on contact time, pH and temperature. The adsorption process followed pseudo-second-order kinetic, having a 0.99 correlation coefficient. Intraparticle diffusion was confirmed by the adsorption mechanism controlled by particle and film diffusions.     

Removal of Pb(II) from aqueous media using adsorption onto polyaniline coated sisal fibers

Lead is one of the toxic metals that cause detrimental health disorders. Polyaniline (PAni) coated sisal fibers were prepared via in situ polymerization and used to remove Pb(II) from wastewater. PAni/SF was investigated on batch experiment to remove Pb(II) from wastewater as a function of contact time, pH, particle size, adsorbent, and adsorbate dose. Studies on kinetics revealed adsorption of Pb(II) obeyed pseudo second order. Adsorption equilibrium was suitably fitted in Langmuir isotherm with linear coefficient 0.99. Finally, PAni/SF composites show appreciable removal efficiency with a maximum adsorption capacity of 6.53 mg/g, consistent with adsorption capacity obtained from pseudo second order. J. VINYL ADDIT. TECHNOL., 25:189–197, 2019. © 2018 Society of Plastics Engineers     

Kinetics of the exchange between battery-active manganese dioxides and manganese(II) ions in aqueous solution

The initial rate and the extent of exchange between ⁵⁶Mn-labelled dioxides and 0.1M MnSO₄ solution at 25°C and pH 5.4 were found to increase in the series: β-MoO₂ (R4), <γ-MnO₂ (R2), < ?-MnO₂. The rate of exchange between R2 and 0.1M MnSO₄ solution at pH 2.0 was higher than the corresponding results at pH 5.4 but the results were similar at the two pH values when R2 was washed with dilute acid (pH 2.0) prior to the exchange at pH 2.0. The results of the exchange for the size fraction ?120 to + 300 mesh of R2 were similar to those for the unsieved R2 under the same conditions. When either R2 or R4 were partially reduced with N₂H₄·H₂O solution prior to the exchange, the results were appreciably higher than those obtained for the unreduced solids—especially in the case of R2. When different concentrations of Mn(NO₃)₂ solution were used with R2, the percentage exchange increased to a small extent as the concentration increased ten-fold. The variation of the solid: solution ratio had a minor effect on the extent of exchange between R2 and 0.1M MnSO₄ solution.     

Kinetic and equilibrium studies of Pb(II) and Cd(II) removal from aqueous solution onto colemanite ore waste

The adsorption characteristics of Pb(II) and Cd(II) onto colemanite ore waste (CW) from aqueous solution were investigated as a function of pH, adsorbent dosage, contact time, and temperature. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) models were applied to describe the adsorption isotherms. Langmuir model fitted the equilibrium data better than the Freundlich isotherm. The adsorption capacity of CW was found to be 33.6 mg/g and 29.7 mg/g for Pb(II) and Cd(II) ions, respectively. Analyte ions were desorbed from CW using both 1 M HCl and 1 M HNO₃. The recovery for both metal ions was found to be higher than 95%. The mean adsorption energies evaluated using the D-R model indicated that the adsorption of Pb(II) and Cd(II) onto CW were taken place by chemisorption. The thermodynamic parameters (ΔG^o, ΔH^o and ΔS^o) showed that the adsorption of both metal ions was feasible, spontaneous and exothermic at 20-50 °C. Adsorption mechanisms were also investigated using the pseudo-first-order and pseudo-second-order kinetic models. The kinetic results showed that the adsorption of Pb(II) and Cd(II) onto CW followed well pseudo-second order kinetics.     

Efficient removal of Cr(VI) and Pb(II) from aqueous solution by magnetic nitrogen-doped carbon

The magnetic nitrogen-doped carbon (MNC) was prepared from polypyrrole by a simple high temperature calcination process in this paper. The structure and properties of MNC were analyzed by scanning electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction, Brunner-Emmet-Teller, vibrating sample magnetometer, and X-ray photoelectron spectroscopy. The capacity of MNC to adsorb Cr(VI) and Pb(II) was evaluated. The effects of the initial pH, dosage, concentration and temperature on the adsorption capacity of MNC were measured. MNC had a large specific surface area and a special porous structure. Its nitrogen and carbon sources were rich, and the ratio of carbon to nitrogen was fixed. The maximum Cr(VI)-adsorption capacity and maximum Pb(II) adsorption capacity of MNC could reach 456.63 and 507.13 mg∙g⁻¹ at 318 K, respectively. The pseudo-second-order model was used to describe the adsorption kinetics of MNC, and the Freundlich model was employed to discuss its isotherms. The adsorption process was affected by the electrostatic force, the reducing reaction, pores and chelation. The results of this study suggest that MNC is a material with superior performance, and is very easily regenerated, reused, and separated in the adsorption process.     

Zn(II) ion removal from aqueous solution by using a polyaniline composite

The aim of this research was to investigate the sorption characteristics of polyaniline/sawdust (PAn/SD) for the removal of Zn(II) ions from aqueous solutions. Batch sorption studies were carried out to determine the effect of initial concentration of the sorbate, agitation time, adsorbent dose, and pH on the removal of Zn(II). The sorptive removal was found to be strongly pH‐dependent. The experimental data fitted well to the Freundlich isotherm. The products were investigated in terms of morphology and chemical structure by using scanning electron microscopy and Fourier‐transform infrared spectroscopy, respectively. Also, PAn/SD was used for the removal of heavy metals from urban waste water. J. VINYL ADDIT. TECHNOL., 2011. © 2011 Society of Plastics Engineers     

Batch and fixed‐bed column adsorption of Cu(II), Pb(II) and Cd(II) from aqueous solution onto functionalised SBA‐15 mesoporous silica

Functionalised SBA‐15 mesoporous silica with polyamidoamine groups (PAMAM‐SBA‐15) was successfully prepared with the structure characterised by X‐ray diffraction, nitrogen adsorption–desorption, Fourier transform infrared spectra and thermogravimetric analysis. PAMAM‐SBA‐15 was applied as adsorbent for Cu(II), Pb(II) and Cd(II) ions removal from aqueous solution. The effects of the solution pH, adsorbent dosage and metal ion concentration were studied under the batch mode. The Langmuir model was fitted favourably to the experimental data. The maximum sorptive capacities were determined to be 1.74 mmol g^?1 for Cu(II), 1.16 mmol g^?1 for Pb(II) and 0.97 mmol g^?1 for Cd(II). The overall sorption process was fast and its kinetics was fitted well to a pseudo‐first‐order kinetic model. The mean free energy of sorption, calculated from the Dubinin–Radushkevich isotherm, indicated that the sorption of lead and copper, with E > 16 kJ mol^?1, followed the sorption mechanism by particle diffusion. The adsorbent could be regenerated three times without significant varying its sorption capacity. A series of column tests were performed to determine the breakthrough curves with varying bed heights and flow rates. The breakthrough data gave a good fit to the Thomas model. Maximum sorption capacity of 1.6, 1.3 and 1.0 mmol g^?1 were found for Cu(II), Pb(II) and Cd(II), respectively, at flow rate of 0.4 mL min^?1 and bed height of 8 cm, which corresponds to 83%, 75% and 73% of metallic ion removal, respectively, which very close to the value determined in the batch process. Bed depth service time model could describe the breakthrough data from the column experiments properly. © 2012 Canadian Society for Chemical Engineering     

Photo‐reduction and adsorption in aqueous Cr(VI) solution by titanium dioxide,carbon nanotubes and their composite

BACKGROUND: This study compared the removal of aqueous Cr(VI) by multi‐walled carbon nanotubes (CNTs) modified by sulfuric acid, titanium dioxide (TiO₂) and composite of CNTs and TiO₂. RESULTS: More than 360 h contact time was needed to completely adsorb 3 mg L^?1 of Cr(VI) by CNTs, indicating that the rate of adsorption by CNTs alone was slow. The reaction time approaching equilibrium depended on the Cr(VI) concentration. XPS analysis of CNTs after adsorbing Cr(VI) showed that the Cr(VI) on the surface of CNTs was partially reduced to Cr(III). A 3 mg L^?1 solution of Cr(VI) was fully photocatalyzed by commercial TiO₂ (Degussa P25) in less than 0.5 h under UV irradiation. Unlike P25, reduction by another commercial TiO₂ (Hombikat UV100) took 4 h and more than 2 h were necessary for reduction by the composite. Thus the efficiency of Cr(VI) photo‐reduction by the composite was lower than by TiO₂, but higher than that by CNTs. XPS analysis of TiO₂ and composite showed the existence of both Cr(VI) and Cr(III) on their surfaces. CONCLUSION: In contrast to TiO₂, the reduction rate of aqueous Cr(VI) using CNTs as adsorbent was slow. P25 had a markedly higher photocatalytic efficiency than the composite or UV100 alone. Using P25 to reduce aqueous Cr(VI) has a higher potential for practical application. The diameters of TiO₂ and CNTs and the ratio of TiO₂/CNTs are key problems in the preparation of TiO₂/CNTs composite. Copyright © 2011 Society of Chemical Industry     

Characterisation and adsorption properties of oxalate-loaded hematite composite for Cd(II) and Pb(II) adsorption: Equilibrium models,thermodynamic and kinetic studies

In this study, different reagents have been examined to improve the adsorption ability of hematite for the removal of Cd(II) and Pb(II) ions from aqueous solution. The best adsorption result has been obtained using oxalate-loaded hematite. The equilibrium isotherm studies show the best result was attained in the Langmuir model for Pb(II) and Cd(II) ions. Therefore, homogeneous adsorption is dominated, which was emphasised by three-parameter-isotherm models. The experimental data fit well with the pseudo-second-order kinetics. The Pb(II) adsorption was endothermic and spontaneous, but the Cd(II) adsorption was exothermic and unspontaneous.     

Efficient adsorption of lead (II) and copper (II) from aqueous phase using oxidized multiwalled carbon nanotubes/polypyrrole composite

Polypyrrole coated oxidized multiwalled carbon nanotubes (oMWCNT/Ppy) were applied to determine the adsorption characteristics of Pb(II) and Cu(II) from their aqueous solutions. Structural and morphological characterization studies using scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared and Raman spectroscopy showed successful preparation of the oMWCNT/Ppy composite. The influence of pH, contact time, and initial metal ion concentration on the adsorption of Pb(II) and Cu(II) was studied. The adsorption processes fitted well with Langmuir isotherm and pseudo-second-order kinetic models. The maximum adsorption capacities for Pb(II) and Cu(II) were determined as 26.32 and 24.39 mg/g, respectively. Desorption studies indicated that the oMWCNT/Ppy composite could be reused for five cycles with minimum loss of its initial adsorption capacity.