Enhanced degradation of contaminants of emerging concern by electrochemically activated peroxymonosulfate: Performance, mechanism, and influencing factors

过硫酸盐 降级(电信) 电解 响应面法 羟基自由基 高级氧化法 化学 双酚A 线性扫描伏安法 化学工程 核化学 循环伏安法 电化学 色谱法 激进的 电极 有机化学 催化作用 工程类 电解质 电信 环氧树脂 物理化学 计算机科学
作者
Jie Yao,Yan Zhang,Zekun Dong
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:415: 128938-128938 被引量:52
标识
DOI:10.1016/j.cej.2021.128938
摘要

Electrochemically activated persulfate is an emerging advanced oxidation process for the removal of contaminants of emerging concern (CECs). The degradation of CECs, including carbamazepine (CBZ), bisphenol S (BPS), propranolol (PPL) and sulfamethoxazole (SMX) using electrochemically activated peroxymonosulfate (EA-PMS) was systematically investigated in this work. Over 80% of all the forementioned CECs were removed within 30 min. It exhibited a good synergistic effect between PMS and electrolysis on the degradation of CECs. The results of linear sweep voltammetry (LSV) indicated that a transition structure between BDD anode and PMS (BDD (PMS)*) was likely responsible for the synergistic effect. Hydroxyl radical (HO·) and sulfate radical (SO4·−) were proved to be the primary reactive species, of which HO· played the leading role. The increase of current density and PMS dosage accelerated the degradation of SMX, while initial pH from 3.0 to 11.0 had a limited effect on the degradation of SMX. Moreover, the influences of common ions and natural organic matter (NOM) on the degradation of SMX were comprehensively assessed using response surface methodology (RSM), and a prediction model was built via RSM. The performance of EA-PMS on the degradation of SMX in actual water was even better than that in pure water in this study. EA-PMS can serve as a novel and promising technology for the degradation of CECs and has great potential in practical application.
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