Mechanisms of arsenic-containing pyrite oxidation by aqueous arsenate under anoxic conditions

被引:56
|
作者
Qiu, Guohong [1 ]
Gao, Tianyu [1 ]
Hong, Jun [1 ]
Tan, Wenfeng [1 ]
Liu, Fan [1 ]
Zheng, Lirong [2 ]
机构
[1] Huazhong Agr Univ, Coll Resources & Environm, Minist Agr, Key Lab Arable Land Conservat Middle & Lower Reac, Wuhan 430070, Hubei, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Arsenic-containing pyrite; Arsenate; Adsorption; Redox; Goethite; X-RAY PHOTOELECTRON; SYNTHETIC PYRITE; ELECTRICAL-PROPERTIES; ABIOTIC OXIDATION; NI IMPURITIES; SOLID-PHASES; FES2; SPECIATION; MACKINAWITE; REDUCTION;
D O I
10.1016/j.gca.2017.08.030
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
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.
引用
收藏
页码:306 / 319
页数:14
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