化学
氯
降级(电信)
氯化物
电化学
废水
核化学
无机化学
电极
有机化学
环境工程
工程类
电信
计算机科学
物理化学
作者
Jiaqi Bu,Hongru Jiang,Tianhao Li,Chengyun Zhou,Shian Zhong
标识
DOI:10.1016/j.jclepro.2023.136914
摘要
A laboratory-scale electrochemical reaction tank was self-designed for the degradation of sulfamethoxazole (SMZ). Coupling electrocatalysis (EC) with personoxysulfate (PMS) and chloride ion (Cl−), the degradation system of EC + PMS + Cl was established. The degradation efficiency of the EC + PMS + Cl system for SMZ (10 mg/L) reached 100% within 20 min, and the degradation process of SMZ conforms to the first-order kinetics. EC + PMS + Cl system also has good degradation efficiency for other organic pollutants or polysaccharide wastewater (real wastewater) from coriolus versicolor. The electrochemical performance test shows that TiO2/RuO2–IrO2 electrode not only has a good chlorine evolution effect but also has good stability. •OH and active chlorine play a major role in the degradation system. Theoretical calculation (DFT) and XPS analyses confirm that the RuO2–IrO2 site as an active center activates PMS and Cl− into active oxygen and active chlorine, and the TiO2 site as an active center activates molecular oxygen into active oxygen. The results of liquid chromatography and mass spectrometry (LC-MS) and Toxicity Estimation Software Tool (TEST) showed that the water quality of SMZ after 20 min of degradation was almost harmless. Therefore, this research work will provide a new vision for the electrocatalytic degradation of organic wastewater.
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