降级(电信)
药品和个人护理产品的环境影响
化学
矿化(土壤科学)
反应速率常数
可见光谱
化学工程
光化学
价(化学)
核化学
动力学
材料科学
有机化学
计算机科学
光电子学
废水
环境科学
环境工程
电信
工程类
物理
氮气
量子力学
作者
Chencheng Dong,Zexiao Zheng,Mohammad A.H. Badsha,Juhua He,Irene M.C. Lo
标识
DOI:10.1016/j.envint.2021.106572
摘要
In this study, we constructed an innovative photo-electrocatalysis-assisted peroxymonosulfate (PEC/PMS) system to degrade pharmaceuticals and personal care products (PPCPs). A hollow-structured photoanode (i.e., [email protected]2@MoS2) was specifically synthesized as a photoanode to activate PMS in the PEC system. As proof of concept, the [email protected]2@MoS2 photoanode exhibited superior degradation performance toward carbamazepine (CBZ) with PMS assistance. Specifically, the kinetic constant of PEC/PMS (k = 0.13202 min−1) could be enhanced about 87.4 times compared to that of the PEC system (0.00151 min−1) alone. The PMS activation mechanism revealed that the synergistic effect between the hollow material and the change of surface valence states (Ce3+ to Ce4+) and (Mo4+ to Mo6+) contribute to enhancing the degradation efficiency of the visible-light-driven PEC/PMS process. The scavenger testing and EPR showed that 1O2, O2•−, SO4•− and •OH play dominant roles in the SR-AOPs. Furthermore, the applicability of [email protected]2@MoS2 used in SR-AOPs was systematically investigated regarding of the reaction parameters and identification of intermediates and dominant radicals as well as the mineralization rate and stability. The outcomes of this study can provide a new platform for environmental remediation.
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