Kinetics and mechanism of selenate and selenite removal in solution by green rust-sulfate

被引:30
作者
Onoguchi, Aina [1 ]
Granata, Giuseppe [1 ]
Haraguchi, Daisuke [2 ]
Hayashi, Hiroshi [2 ]
Tokoro, Chiharu [1 ]
机构
[1] Waseda Univ, Dept Resources & Environm Engn, Shinju Ku, Okubo 3-4-1, Tokyo 1698555, Japan
[2] Mitsubishi Mat Corp, Cent Res Inst, 15-2 Fukimatsu, Iwaki, Fukushima, Japan
来源
ROYAL SOCIETY OPEN SCIENCE | 2019年 / 6卷 / 04期
关键词
green rust; selenium; immobilization; kinetics; mechanism; ZERO-VALENT IRON; NITRATE REDUCTION; AQUEOUS-SOLUTION; WATER; IMMOBILIZATION; CHROMATE; ADSORPTION; HYDROXIDE; SORPTION; IONS;
D O I
10.1098/rsos.182147
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This work investigated the removal of selenite and selenate from water by green rust (GR) sulfate. Selenite was immobilized by simple adsorption onto GR at pH 8, and by adsorption-reduction at pH 9. Selenate was immobilized by adsorption-reduction to selenite and zero valent selenium (Se-0) at both pH 8 and 9. In the process, GR oxidized to a mixture of goethite (FeOOH) and magnetite (Fe3O4). The kinetics of selenite and selenate sorption at the GR-water interface was described through a pseudo-second-order model. X-ray absorption spectroscopy data enabled to elucidate the concentration profiles of Se and Fe species in the solid phase and allowed to distinguish two removal mechanisms, namely adsorption and reduction. Selenite and selenate were reduced by GR through homogeneous solidphase reaction upon adsorption and by heterogeneous reaction at the solid-liquid interface. The selenite reduced through heterogeneous reduction with GR was adsorbed onto GR but not reduced further. The redox reaction between GR and selenite/selenate was kinetically described through an irreversible second-order bimolecular reaction model based on XAFS concentration profiles. Although the redox reaction became faster at pH 9, simple adsorption was always the fastest removal mechanism.
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页数:13
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