Adsorption of monothioarsenate on amorphous aluminum hydroxide under anaerobic conditions
Adsorption of monothioarsenate on amorphous aluminum hydroxide under anaerobic conditions
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厌氧条件下无定形氢氧化铝对硫代砷酸盐的吸附
DOI:
10.1016/j.chemgeo.2015.04.018
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发表时间:
2015-06
期刊:
影响因子:
3.9
通讯作者:
Yongfeng Jia
中科院分区:
文献类型:
--
作者:
Fan Xiao;Shaofeng Wang;Liying Xu;Ying Wang;Zidan Yuan;Yongfeng Jia
Thioarsenates have been found to be major arsenic species in some sulfidic waters and their interactions with minerals play an important role in the geochemical cycling of arsenic. This work investigated the sorption behavior of monothioarsenate (mtAsV) on amorphous aluminum hydroxide (am-Al(OH)3) at various pHs and characterized the adsorbed arsenic by using X-ray absorption spectroscopy (XAS) and Fourier transform infrared spectroscopy (FTIR). The uptake of arsenic by am-Al(OH)3from mtAsVsolution (86–16 mg·g− 1) was found to be much less than that from arsenate (AsV) solution (112–50.5 mg·g− 1) at all pHs applied (4–10). MtAsVwas partly reduced to arsenite with concurrent production of elemental sulfur, and the interaction with am-Al(OH)3at acidic pH enhanced the reduction, which is attributed to acid-catalysis at the am-Al(OH)3surface. Transformation of mtAsVto arsenate also occurred during the adsorption process. The linear combination fitting (LCF) of As K-edge X-ray absorption near edge structure (XANES) spectra indicated that the arsenic adsorbed on am-Al(OH)3was present dominantly as mtAsV, with minor amounts as arsenite and arsenate. The As K-edge extended X-ray absorption fine structure (EXAFS) and FTIR results suggested that bidentate binuclear complexation was involved in the adsorption of mtAsVon am-Al(OH)3. This study is the first documentation of mtAsVsorption on aluminum hydroxides and is necessary to assess geochemical cycling of arsenic in sulfidic natural or mining-impacted environments.
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影响因子:
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