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

出版社

MDPI
DOI: 10.3390/ijerph18073344

关键词

singlet oxygen; peroxydisulfate; peroxymonosulfate; activation; organic contaminants; degradation

资金

  1. Natural Science Foundation of China [41907153]
  2. Hubei Provincial Engineering Research Center of Systematic Water Pollution Control [20190729]
  3. Natural Science Foundation of Hubei Province [2018CFB262]
  4. Fundamental Research Funds for the Central Universities of the China University of Geosciences (Wuhan) [CUG170646]

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In recent years, advanced oxidation processes based on PDS/PMS activation have attracted significant research attention for the degradation of recalcitrant organic contaminants, mainly focusing on the generation of sulfate and hydroxyl radicals along with the involvement of singlet oxygen. Studies have primarily explored the generation mechanisms and reaction pathways of singlet oxygen in the process.
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 (SO4 center dot-) and hydroxyl ((OH)-O-center dot) 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-1(2)) during PDS/PMS-based AOPs. Typically, O-1(2) can be produced either along with SO4 center dot- and (OH)-O-center dot or discovered as the dominant reactive oxygen species (ROSs) for pollutants degradation. This paper reviews recent advances in O-1(2) generation during PDS/PMS activation. First, it introduces the basic chemistry of O-1(2), 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-1(2) production by activating PDS/PMS. Moreover, although O-1(2) 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.

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