TY - JOUR
T1 - Evaluation of Zn-Al-SO4 layered double hydroxide for the removal of arsenite and arsenate from a simulated soil solution
T2 - Isotherms and kinetics
AU - Bagherifam, Saeed
AU - Komarneni, Sridhar
AU - Lakzian, Amir
AU - Fotovat, Amir
AU - Khorasani, Reza
AU - Huang, Wenyan
AU - Ma, Jianfeng
AU - Wang, Yujue
N1 - Funding Information:
This research was supported by the College of Agricultural Sciences under Station Research Project No. PEN04319 . The senior author Saeed Bagherifam gratefully acknowledges the financial support provided by Ferdowsi University of Mashhad and Ministry of Science, Research and Technology of Iran to conduct some parts of his PhD thesis as visiting scholar at the Materials Research Laboratory, The Pennsylvania State University, U.S.A. Ms. Huang Wenyan gratefully acknowledges the financial sponsorship of Changzhou University Overseas Research & Training Program through an award. Dr. Ma Jianfeng gratefully acknowledges the financial sponsorship of Jiangsu Overseas Research & Training Program for University Prominent Young & Middle-aged Teachers and Presidents through an award.
PY - 2014/6
Y1 - 2014/6
N2 - The main objective of the present study was to evaluate the effectiveness of synthetic Zn-Al-SO4 layered double hydroxide (LDH) for the removal of arsenite and arsenate from a simulated soil solution. The Zn-Al-SO4 was synthesized using a hydrothermal method and the adsorption of arsenic was studied using Langmuir and Freundlich models. Moreover, the kinetics of adsorption was tested using pseudo-first, pseudo-second, intraparticle diffusion and Elovich models. The results of the experiments revealed that the adsorption isotherms of arsenite and arsenate on the Zn-Al-SO4 LDHs can be described well with Langmuir isotherm and maximum adsorption capacities were calculated to be 34.24 and 47.39mgg-1 for arsenite and arsenate, respectively. The adsorption kinetics of arsenate followed pseudo-second order while arsenite uptake showed better correlation with intra-particle diffusion model. Furthermore, the effects of two major coexisting and competing divalent anions such as SO42- and CO32- on the uptakes of arsenite and arsenate were studied and the results showed that CO32- had greater adverse effect on the uptakes of arsenite and arsenate by Zn-Al-SO4 than SO42-. Based on X-ray diffraction results, the main underplaying adsorption mechanism of arsenite and arsenate might be the exchange on the external surfaces and edges of Zn-Al-SO4 LDHs, but possibly some topotactic exchange may occur through the substitution of arsenic anions with sulfate in the interlayer region.
AB - The main objective of the present study was to evaluate the effectiveness of synthetic Zn-Al-SO4 layered double hydroxide (LDH) for the removal of arsenite and arsenate from a simulated soil solution. The Zn-Al-SO4 was synthesized using a hydrothermal method and the adsorption of arsenic was studied using Langmuir and Freundlich models. Moreover, the kinetics of adsorption was tested using pseudo-first, pseudo-second, intraparticle diffusion and Elovich models. The results of the experiments revealed that the adsorption isotherms of arsenite and arsenate on the Zn-Al-SO4 LDHs can be described well with Langmuir isotherm and maximum adsorption capacities were calculated to be 34.24 and 47.39mgg-1 for arsenite and arsenate, respectively. The adsorption kinetics of arsenate followed pseudo-second order while arsenite uptake showed better correlation with intra-particle diffusion model. Furthermore, the effects of two major coexisting and competing divalent anions such as SO42- and CO32- on the uptakes of arsenite and arsenate were studied and the results showed that CO32- had greater adverse effect on the uptakes of arsenite and arsenate by Zn-Al-SO4 than SO42-. Based on X-ray diffraction results, the main underplaying adsorption mechanism of arsenite and arsenate might be the exchange on the external surfaces and edges of Zn-Al-SO4 LDHs, but possibly some topotactic exchange may occur through the substitution of arsenic anions with sulfate in the interlayer region.
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U2 - 10.1016/j.clay.2014.02.028
DO - 10.1016/j.clay.2014.02.028
M3 - Article
AN - SCOPUS:84902121115
SN - 0169-1317
VL - 95
SP - 119
EP - 125
JO - Applied Clay Science
JF - Applied Clay Science
ER -