Mechanism of efficient remediation of U(VI) using biogenic CMC-FeS complex produced by sulfate-reducing bacteria

化学 胞外聚合物 羧甲基纤维素 环境化学 吸附 硫酸盐还原菌 核化学 细菌 环境修复 硫化铁 硫酸盐 无机化学 生物膜 硫黄 有机化学 污染 地质学 古生物学 生物 生态学
作者
Siyu He,Wanrong Hu,Yali Liu,Yi Xie,Hui Zhou,Xuqian Wang,Jing Chen,Yongkui Zhang
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:420: 126645-126645 被引量:41
标识
DOI:10.1016/j.jhazmat.2021.126645
摘要

Abstract Uranium in groundwater during uranium mining activities urgently needs to be remediated through effective and environmental-friendly approaches. The reduction and immobilization of soluble U(VI) using biogenic carboxymethyl cellulose modified iron sulfide complex (biogenic CMC-FeS complex) is one of the emerging and innovative methods. However, its removal mechanism is largely unknown. Here, biogenic CMC-FeS complex with extracellular polymeric substances (EPS) and CMC was successfully synthesized by sulfate-reducing bacteria (SRB) and showed highly dispersible capacity. The tryptophan and tyrosine, which were the main components in EPS produced by SRB on CMC-FeS surface, significantly increased the U(VI) removal capacity of the biogenic CMC-FeS complex compared with chemically synthesized CMC-FeS. U(VI) removal was attributed to the adsorption of soluble U(VI) by ≡ FeO + , CMC, tryptophan, and tyrosine on the biogenic CMC-FeS complex, following its reduction by S2-, S22- and Fe2+. Moreover, biogenic CMC-FeS complex with CMC-to-FeS molar ratio of 0.0005 performed well in the presence of bicarbonate (5 mM), humic acid (10 mg/L), or co-existing cations such as Pb2+, Ni2+, Cd2+, Mn2+, and Cu2+ (200 ug/L) at pH 7.0, and displayed relatively high oxidation resistance and stability ability. This work provides an in-depth understanding of the biogenic CMC-FeS complex for the U(VI) removal and contributes to the development of cost-effective U(VI) remediation technologies.
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