中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Mechanisms of arsenic-containing pyrite oxidation by aqueous arsenate under anoxic conditions

文献类型:期刊论文

作者Hong, J; Zheng LR(郑黎荣); Gao, TY; Zheng, LR; Qiu, GH; Liu, F; Tan, WF
刊名GEOCHIMICA ET COSMOCHIMICA ACTA
出版日期2017
卷号217页码:306-319
关键词Arsenic-containing pyrite Arsenate Adsorption Redox Goethite
ISSN号0016-7037
DOI10.1016/j.gca.2017.08.030
文献子类Article
英文摘要Adsorption and redox reactions occur between arsenic-containing pyrite and arsenate, which affect the migration and conversion of arsenic in soils and waters. However, the influence of arsenic incorporated in pyrite on the interaction processes is still enigmatic. In this work, arsenic-containing pyrites were hydrothermally synthesized with composition similar to naturally surface-oxidized pyrites in supergene environments. The effects of arsenic incorporation on the chemical composition and physicochemical properties were analyzed, and the interaction mechanism between arsenic-containing pyrites and aqueous arsenate was also studied within pH 3.0-11.0. Arsenic-containing pyrites with the arsenic contents of 0 (Apy0), 4.4 (Apy5) and 9.9 wt.% (Apy10) were produced in hydrothermal systems. As(III) and As(-I) respectively substituted Fe(II) and S-2(-II) in the pyrite, and their relative contents respectively reached 76.6% and 17.2% in Apy5, and 91.0% and 8.0% in Apy10. Arsenic substitution resulted in a high content of Fe(III) in the form of Fe(III) AS and a decrease in pyrite crystallinity. During the redox processes of arsenic-containing pyrites and arsenate, elemental S-0, SO42- and goethite were formed as the main products with the adsorption of As(III, V), and As(III) was released due to the collapse of the crystal structure of pyrite and the oxidation of As(-I). Different redox mechanisms were achieved with pH increasing from 3.0 to 11.0 in the reaction system. At pH 3.0-6.0, Fe(III) contributed much to the oxidation of arsenic-containing pyrites, and arsenate and released As (III) were adsorbed on the surface of solid products. At pH 7.0-11.0, aqueous arsenate worked as the major oxidant, and its oxidation capacity increased with increasing pH. When the pH was increased from 3.0 to 7.0 and 11.0, the release ratio of incorporated arsenic from Apy10 particles increased from 34.1% to 45.0% and 56.8%, respectively. The present study facilitates a better understanding about the interaction mechanisms between arsenic-containing pyrite and arsenate in supergene environments. (C) 2017 Elsevier Ltd. All rights reserved.
电子版国际标准刊号1872-9533
WOS关键词X-RAY PHOTOELECTRON ; SYNTHETIC PYRITE ; ELECTRICAL-PROPERTIES ; ABIOTIC OXIDATION ; NI IMPURITIES ; SOLID-PHASES ; FES2 ; SPECIATION ; MACKINAWITE ; REDUCTION
WOS研究方向Geochemistry & Geophysics
语种英语
WOS记录号WOS:000411362000018
源URL[http://ir.ihep.ac.cn/handle/311005/284778]  
专题高能物理研究所_多学科研究中心
作者单位中国科学院高能物理研究所
推荐引用方式
GB/T 7714
Hong, J,Zheng LR,Gao, TY,et al. Mechanisms of arsenic-containing pyrite oxidation by aqueous arsenate under anoxic conditions[J]. GEOCHIMICA ET COSMOCHIMICA ACTA,2017,217:306-319.
APA Hong, J.,郑黎荣.,Gao, TY.,Zheng, LR.,Qiu, GH.,...&Tan, WF.(2017).Mechanisms of arsenic-containing pyrite oxidation by aqueous arsenate under anoxic conditions.GEOCHIMICA ET COSMOCHIMICA ACTA,217,306-319.
MLA Hong, J,et al."Mechanisms of arsenic-containing pyrite oxidation by aqueous arsenate under anoxic conditions".GEOCHIMICA ET COSMOCHIMICA ACTA 217(2017):306-319.

入库方式: OAI收割

来源:高能物理研究所

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