期刊
APPLIED CLAY SCIENCE
卷 48, 期 3, 页码 485-491出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.clay.2010.02.011
关键词
Arsenate adsorption kinetics; X-ray absorption spectroscopy; Diffusion
资金
- National Science Council, Taiwan [NSC 912313-B-002-361, 92-2313-B-002-090, 93-2313-B-002-008]
Lithium/aluminum layered double hydroxide intercalated by chloride (Li/AI LDH-CI) was considered as a superior adsorbent for anionic compounds. This study aimed to establish the adsorption behavior of arsenate on Li/AI LDH-Cl by employing X-ray absorption spectroscopy (XAS) and adsorption kinetics. The XAS analysis demonstrated that inner-sphere complexes were the dominant arsenate adsorption configurations on the planar surfaces and edges of Li/AI LDH-Cl. Based on a kinetic study, arsenate adsorption on Li/AI LDH-CI could be separated into fast and slow reactions. This biphasic arsenate adsorption behavior was partially attributable to: (i) two different adsorption sites associated with Li, exposing on planar surfaces, and Al, existing on the edges of double hydroxyl layers, and (ii) micropore adsorption sites within the Li/AI LDH-CI surfaces. Activation energies derived by the Arrhenius equation indicated that the diffusion process was the rate-limiting step of arsenate adsorption on Li/AI LDH-Cl. (C) 2010 Elsevier B.rate-limiting step of arsenate adsorption on Li/AI LDH-Cl. 2010 Elsevier B.V. All rights reserved. All rights reserved.
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