Infrared spectroscopic and X-ray diffraction characterization of the nature of adsorbed arsenate on ferrihydrite

被引:322
作者
Jia, Yongfeng [1 ]
Xu, Liying
Wang, Xin
Demopoulos, George P.
机构
[1] Chinese Acad Sci, Key Lab Terrestrial Proc, Inst Appl Ecol, Shenyang 110016, Peoples R China
[2] McGill Univ, Dept Mining Met & Mat Engn, Montreal, PQ H3A 2B2, Canada
基金
中国国家自然科学基金; 加拿大自然科学与工程研究理事会;
关键词
SURFACE-CHARGE REDUCTION; IRON-OXIDES; ADSORPTION; ARSENITE; MECHANISMS; SULFATE; EXAFS; PRECIPITATION; COMPLEXATION; SPECIATION;
D O I
10.1016/j.gca.2006.12.021
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Fourier transformed infrared (FTIR) spectroscopy was used to characterize arsenate-ferrihydrite sorption solids synthesized at pH 3-8. The speciation of sorbed arsenate was determined based on the As-O stretching vibration bands located at 650-950 cm(-1) and O-H stretching vibration bands at 3000-3500 cm(-1). The positions of the As-O and O-H stretching vibration bands changed with pH indicating that the nature of surface arsenate species on ferrihydrite was strongly pH dependent. Sorption density and synthesis media (sulfate vs. nitrate) had no appreciable effect. At acidic pH (3, 4), ferric arsenate surface precipitate formed on ferrihydrite and constituted the predominant surface arsenate species. X-ray diffraction (XRD) analyses of he sorption solids synthesized at elevated temperature (75 degrees C), pH 3 clearly showed the development of crystalline ferric arsenate (i.e. scorodite). In neutral and alkaline media (pH 7, 8), arsenate sorbed as a bidentate surface complex (in both protonated FeO2As(O)(OH)(-) and unprotonated FeO2As(O)(2)(2-) forms). For the sorption systems in slightly acidic media (pH 5, 6), both ferric arsenate and surface complex were probably present on ferrihydrite. It was further determined that the incorporated sulfate in ferrihydrite during synthesis was substituted by arsenate and was more easily exchangeable with increasing pH. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1643 / 1654
页数:12
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