碳酸盐
化学
非生物成分
地下水
铀
环境化学
缺氧水域
氧化还原
铀矿
环境修复
遗传算法
无机化学
地质学
污染
冶金
生态学
材料科学
古生物学
有机化学
生物
岩土工程
作者
Sen Yan,Maxim I. Boyanov,Bhoopesh Mishra,Kenneth Kemner,Edward J. O’Loughlin
标识
DOI:10.1021/acs.est.7b06405
摘要
Green rusts (GRs) are redox active Fe II –Fe III minerals that form in the environment via various biotic and abiotic processes. Although both biogenic (BioGR) and abiotic (ChemGR) GRs have been shown to reduce U VI, the dynamics of the transformations and the speciation and stability of the resulting U IV phases are poorly understood. We used carbonate extraction and XAFS spectroscopy to investigate the products of U VI reduction by BioGR and ChemGR. The results show that both GRs can rapidly remove U VI from synthetic groundwater via reduction to U IV . The initial products in the ChemGR system are solids-associated U IV –carbonate complexes that gradually transform to nanocrystalline uraninite over time, leading to a decrease in the proportion of carbonate-extractable U from ∼95% to ∼10%. In contrast, solid-phase U IV atoms in the BioGR system remain relatively extractable, nonuraninite U IV species over the same reaction period. The presence of calcium and carbonate in groundwater significantly increase the extractability of U IV in the BioGR system. These data provide new insights into the transformations of U under anoxic conditions in groundwater that contains calcium and carbonate, and have major implications for predicting uranium stability within redox dynamic environments and designing approaches for the remediation of uranium-contaminated groundwater.
科研通智能强力驱动
Strongly Powered by AbleSci AI