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过硫酸盐和过一硫酸盐激活产生单线态氧的研究进展:综述

Evolution of Singlet Oxygen by Activating Peroxydisulfate and Peroxymonosulfate: A Review.

机构信息

School of Environmental Studies, China University of Geosciences, Wuhan 430074, China.

出版信息

Int J Environ Res Public Health. 2021 Mar 24;18(7):3344. doi: 10.3390/ijerph18073344.

DOI:10.3390/ijerph18073344
PMID:33804931
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8036714/
Abstract

Advanced oxidation processes (AOPs) based on peroxydisulfate (PDS) or peroxymonosulfate (PMS) activation have attracted much research attention in the last decade for the degradation of recalcitrant organic contaminants. Sulfate (SO) and hydroxyl (OH) radicals are most frequently generated from catalytic PDS/PMS decomposition by thermal, base, irradiation, transition metals and carbon materials. In addition, increasingly more recent studies have reported the involvement of singlet oxygen (O) during PDS/PMS-based AOPs. Typically, O can be produced either along with SO and OH or discovered as the dominant reactive oxygen species (ROSs) for pollutants degradation. This paper reviews recent advances in O generation during PDS/PMS activation. First, it introduces the basic chemistry of O, its oxidation properties and detection methodologies. Furthermore, it elaborates different activation strategies/techniques, including homogeneous and heterogeneous systems, and discusses the possible reaction mechanisms to give an overview of the principle of O production by activating PDS/PMS. Moreover, although O has shown promising features such as high degradation selectivity and anti-interference capability, its production pathways and mechanisms remain controversial in the present literatures. Therefore, this study identifies the research gaps and proposes future perspectives in the aspects of novel catalysts and related mechanisms.

摘要

基于过一硫酸盐(PDS)或过氧单硫酸盐(PMS)活化的高级氧化工艺(AOPs)在过去十年中引起了广泛的研究关注,用于降解难降解的有机污染物。硫酸根(SO)和羟基(OH)自由基通常是通过热、碱、辐照、过渡金属和碳材料催化 PDS/PMS 分解产生的。此外,越来越多的最新研究报告表明,在基于 PDS/PMS 的 AOPs 中会涉及单线态氧(O)。通常,O 可以与 SO 和 OH 一起产生,或者被发现是污染物降解的主要活性氧物质(ROSs)。本文综述了 PDS/PMS 活化过程中 O 生成的最新进展。首先,它介绍了 O 的基础化学、氧化特性和检测方法。此外,它阐述了不同的活化策略/技术,包括均相和多相体系,并讨论了可能的反应机制,以概述通过激活 PDS/PMS 产生 O 的原理。此外,尽管 O 表现出高降解选择性和抗干扰能力等有前景的特性,但在目前的文献中,其生成途径和机制仍存在争议。因此,本研究确定了研究空白,并提出了在新型催化剂和相关机制方面的未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/60eb0d99e881/ijerph-18-03344-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/7236a2c72099/ijerph-18-03344-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/b25e4b639864/ijerph-18-03344-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/488696f6086c/ijerph-18-03344-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/75d261aec83f/ijerph-18-03344-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/60eb0d99e881/ijerph-18-03344-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/7236a2c72099/ijerph-18-03344-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/b25e4b639864/ijerph-18-03344-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/488696f6086c/ijerph-18-03344-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/75d261aec83f/ijerph-18-03344-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f11/8036714/60eb0d99e881/ijerph-18-03344-g005.jpg

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