Catalytic persulfate activation for oxidation of organic pollutants: A critical review on mechanisms and controversies

被引:74
作者
Chen, Na [1 ,2 ]
Lee, Donghyun [1 ,2 ]
Kang, Hyeonseok [1 ,2 ]
Cha, Dongwon [1 ,2 ]
Lee, Jaesang [3 ]
Lee, Changha [1 ,2 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, Inst Chem Proc ICP, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Inst Engn Res, 1 Gwanak Ro, Seoul 08826, South Korea
[3] Korea Univ, Sch Civil Environm & Architectural Engn, 145 Anam Ro, Seoul 02841, South Korea
来源
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING | 2022年 / 10卷 / 03期
基金
新加坡国家研究基金会;
关键词
Persulfate; Catalytic oxidation; Radical; Nonradical; Mechanistic controversy; N-DOPED GRAPHENE; EFFICIENT PEROXYDISULFATE ACTIVATION; ELECTRON-SPIN-RESONANCE; ZERO-VALENT IRON; SINGLET OXYGEN; PEROXYMONOSULFATE ACTIVATION; RATE CONSTANTS; HYDROXYL RADICALS; BISPHENOL-A; NONRADICAL ACTIVATION;
D O I
10.1016/j.jece.2022.107654
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Persulfate-based advanced oxidation processes (PS-AOPs) have received increasing attention as new approaches to oxidize refractory organic pollutants in contaminated water and soil. In particular, PS-AOPs using catalysts have been the most intensively studied because a broad spectrum of materials can catalyze the reaction without requiring external input of energy. Despite recent advances in catalytic PS-AOPs, their activation mechanisms are still challenged by uncertainties. Persulfate can be activated via a radical mechanism to generate sulfate radical and hydroxyl radical, as well as via a nonradical mechanism to mediate electron transfer or generate other nonradical reactive oxidants (e.g., single oxygen or high valent metal species). The mechanisms of catalytic persulfate activation and the identities of dominant reactive oxidants remain controversial for many reported catalysts. Herein, we endeavor to address radical and nonradical mechanisms and their identification methods in catalytic persulfate activation, focusing on controversies over widely investigated catalysts. This article will improve the mechanistic understanding of catalytic PS-AOPs and offer a theoretical foundation for exploring novel PS-AOPs with better specificity and performance.
引用
收藏
页数:18
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