自催化
化学
尾矿
污染物
环境化学
转化(遗传学)
镉
光化学
金属
化学转化
光催化
氧气
硫化物
光伏系统
二甲基硫醚
硫化镉
光解
氧化还原
析氧
降级(电信)
化学工程
食腐动物
电化学
动力学
动能
太阳能燃料
载流子
电子受体
工作(物理)
反应机理
扩散
作者
Jiacheng Sun,Shuchen Tu,Zemin Li,Ke Li,Yang Zhang,Qinzi Huang,Tao Chen,Hongxing Chen,Lingtian Xie,Bo Yan
标识
DOI:10.1021/acs.est.5c09059
摘要
Heavy metal-xanthate complexes (HMXs), formed during processing in nonferrous metal mines, have attracted increasing attention due to their complex transformation pathways and ecological risks. Solar radiation plays a key role in driving the transformation of HMXs in tailings ponds. This study revealed an overlooked transformation pathway and environmental impact of mining pollutants─the photochemical ROS-Driven autocatalytic transformation of typical HMXs such as cadmium-xanthate (CdX). CdX conversion pathways and their kinetic characteristics were investigated by the comprehensive material characterization and substance analysis. Charge transferring and radical formation-attacking were demonstrated through the joint survey of electrochemical measurements, oxygen activation monitoring, and quantum chemical calculations. Results shows that 94.93% of CdX transformed after 28 days of solar exposure. The autocatalytic kinetic matches the accelerated characteristics described by the logistic model, with its half-lives varied significantly among different types of HMX: zinc-xanthate (ZnX) (4.3 days) < CdX (19.2 days) < plumbum-xanthate (PbX) (23.6 days). Light-induced charge carriers in CdX initiated the ROS production and its conversion to cadmium sulfide (CdS). CdS accumulation enhanced the photochemical activity and the ROS generation, resulting in the autocatalytic conversion. This work provides molecular-level insights into the transformation mechanisms of HMXs, and offers theoretical foundations for controlling mine-related pollutants.
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