Beam-induced redox transformation of arsenic during As K-edge XAS measurements: availability of reducing or oxidizing agents and As speciation

被引:8
作者
Han, Young-Soo [1 ]
Jeong, Hoon Young [2 ]
Hyun, Sung Pil [1 ]
Hayes, Kim F. [3 ]
Chon, Chul-Min [1 ]
机构
[1] Korea Inst Geosci & Mineral Resources, Geol Environm Div, Deajeon 34132, South Korea
[2] Pusan Natinal Univ, Dept Geol Sci, Busan 46241, South Korea
[3] Univ Michigan, Dept Civil & Environm Engn, Ann Arbor, MI 48105 USA
基金
新加坡国家研究基金会;
关键词
X-ray absorption spectroscopy; photocatalytic transformation; mackinawite; arsenic; linear combination fitting; RAY-ABSORPTION SPECTROSCOPY; ADSORPTION; FES; REDUCTION; OXIDATION; SORPTION; SULFIDE; COPPER;
D O I
10.1107/S1600577518002576
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
During X-ray absorption spectroscopy (XAS) measurements of arsenic (As), beam-induced redox transformation is often observed. In this study, the As species immobilized by poorly crystallized mackinawite (FeS) was assessed for the susceptibility to beam-induced redox reactions as a function of sample properties including the redox state of FeS and the solid-phase As speciation. The beam-induced oxidation of reduced As species was found to be mediated by the atmospheric O-2 and the oxidation products of FeS [e.g. Fe(III) (oxyhydr) oxides and intermediate sulfurs]. Regardless of the redox state of FeS, both arsenic sulfide and surface-complexed As(III) readily underwent the photo-oxidation upon exposure to the atmospheric O-2 during XAS measurements. With strict O-2 exclusion, however, both As(0) and arsenic sulfide were less prone to the photo-oxidation by Fe(III) (oxyhydr) oxides than NaAsO2 and/or surface-complexed As(III). In case of unaerated As(V)-reacted FeS samples, surface-complexed As(V) was photocatalytically reduced during XAS measurements, but arsenic sulfide did not undergo the photo-reduction.
引用
收藏
页码:763 / 770
页数:8
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