黄钾铁矾
硫酸盐
化学
溶解
动员
硫酸盐还原菌
砷
细菌
方位(导航)
环境化学
无机化学
冶金
地质学
材料科学
有机化学
政治学
法学
地理
古生物学
地图学
作者
Kun Gao,Yue Hu,Chuling Guo,Changdong Ke,Guining Lu,Zhi Dang
标识
DOI:10.1016/j.jhazmat.2020.123717
摘要
Microbial sulfidization of arsenic (As)-bearing jarosite involves complex processes and is yet to be fully elucidated. Here, we investigated the behavior of As during reductive dissolution of As(V)-bearing jarosite by a pure sulfate reducing bacterium with or without dissolved SO42− amendment. Changes of aqueous chemistry, mineralogical characteristics, and As speciation were examined in batch experiments. The results indicated that jarosite was mostly replaced by mackinawite in the system with added SO42-. In the medium without additional SO42-, mackinawite, vivianite, pyrite, and magnetite formed as secondary Fe minerals, though 24.55 % of total Fe was in form of an aqueous Fe2+ phase. The produced Fe2+ in turn catalyzed the transformation of jarosite. At the end of the incubation, 41.99 % and 48.10 % of As in the solid phase got released into the aqueous phase in the systems with and without added SO42-, respectively. The addition of dissolved SO42- mitigated the mobilization of As into the aqueous phase. In addition, all As5+ on the solid surface was reduced to As3+ during the microbial sulfidization of As-bearing jarosite. These findings are important for a better understanding of geochemical cycling of elements As, S, and Fe in acid mine drainage and acid sulfate soil environments.
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