砷
铬
氧化还原
水介质
环境化学
化学
转化(遗传学)
水溶液
无机化学
有机化学
生物化学
基因
作者
Yu Fu,Lingli Wang,Wenya Peng,Qingya Fan,Qingchao Li,Yongxia Dong,Yunjiao Liu,Grzegorz Boczkaj,Zhaohui Wang
标识
DOI:10.1016/j.jhazmat.2021.126041
摘要
Simultaneous conversion of most harmful As(III) and Cr(VI) to their less toxic counterparts is environmentally desirable and cost-effective. It has been confirmed that simultaneous oxidation of As(III) to As(V) and reduction of Cr(VI) to Cr(III) can occur via free radical or mediated electron transfer processes. While Cr(VI) is reduced by reacting with H•, eaq-, photoelectron directly or undergoing ligand exchange with H2O2 and SO32-, As(III) is oxidized by HO•, SO4•-, O2•-, and holes (h+) in free radical process. The ability to concentrate Cr and As species on heterogeneous interface and conductivity determining the co-conversion efficiency in mediated electron transfer process. Acidity has positive effect on these co-conversion, while mediated electron transfer process is not much affected by dissolved oxygen (O2). Organic compounds (e.g., oxalate, citrate and phenol) commonly favor Cr(VI) reduction and inhibit As(III) oxidation. To better understand the trends in the existing data and to identify the knowledge gaps, this review elaborates the complicated mechanisms for co-conversion of As(III) and Cr(VI) by various methods. Some challenges and prospects in this active field are also briefly discussed.
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