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  4. Arsenate Sorption on Lithium/Aluminum Layered Double Hydroxide Intercalated by Chloride and on Gibbsite:  Sorption Isotherms, Envelopes, and Spectroscopic Studies
 
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Arsenate Sorption on Lithium/Aluminum Layered Double Hydroxide Intercalated by Chloride and on Gibbsite:  Sorption Isotherms, Envelopes, and Spectroscopic Studies

Journal
Environ. Sci. Technol.
Series/Report No.
Environmental Science and Technology
Journal Volume
40
Journal Issue
24
Start Page
7784
End Page
7789
ISSN
0013-936X
1520-5851
Date Issued
2006-12-15
Author(s)
Yu Ting Liu
Ming Kuang Wang
Tsan Yao Chen
Po Neng Chiang  
Pan Ming Huang
Jhy Fu Lee
DOI
10.1021/es061530j
DOI
10.1021/es061530j
URI
https://www.scopus.com/record/display.uri?eid=2-s2.0-33845873607&origin=resultslist
https://scholars.lib.ntu.edu.tw/handle/123456789/724402
Abstract
The objective of this study was to provide fundamental knowledge of arsenate sorption on lithium/aluminum layered double hydroxide intercalated by chloride (Li/Al LDH-Cl) and further to reveal the contribution of exposed positive charge surface of Li/Al LDH-Cl created by intercalating LiCl into Al(OH)3 layers to arsenate sorption. Therefore, sorption isotherms, envelopes and extended X-ray absorption fine structure (EXAFS) technique were employed to examine the reaction of arsenate on Li/Al LDH-Cl and on gibbsite. Based on an isotherm study, the sorption maximum of Li/Al LDH-Cl for arsenate was approximately six times higher than that of gibbsite. Sorption envelopes of arsenate on Li/Al LDH-Cl displayed a pH-sensitive behavior from pH 4.0 to 7.0, but it was insensitive to pH above pH 7.0, approaching to the pHpzc of Li/Al LDH-Cl (7.22). This transformation with shifted pHs illustrated that there were two types of reaction sites within Li/Al LDH-Cl that participate in arsenate sorption; one is pH-sensitive and the other is not. From EXAFS analysis, arsenate sorbed on Li/Al LDH, reacted not only with Al in the edges of Al-(OH)3 layers, but also with Li located in the vacant octahedral sites within Al(OH)3 layers; however, the decreasing intensity of As(V)-Al shells with increasing pH represented there were fewer As(V)-Al complex existed at higher pH, i.e., the complex between arsenate and Al is pH-sensitive. The superior sorption capability of Li/Al LDH-Cl to that of gibbsite could be attributed to the intercalated Li cations which served as the permanent sorption sites and made the surface of Al(OH)3 have high affinity to arsenate.
SDGs

[SDGs]SDG6

Publisher
American Chemical Society (ACS)
Type
journal article

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