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• W3080787368 startingPage "128067" @default.
• W3080787368 abstract "The greatest constraint in the advanced oxidation processes involved Fe(II)/PMS was the low utilization of Fe(II) and PMS. In the present study, the co-catalytic effect of WS2 on the Fe(II)/PMS system for the degradation of organics was investigated. In the presence of WS2, Fe(III) was reduced to Fe(II) during the reaction and resulted in improved decomposition of PMS as well as the degradation of 4-chloriphenol (4-CP). The decomposition rate of PMS and degradation efficiency of 4-CP were 10% and 25% in the Fe(II)/PMS process, while the efficiencies respectively increased to 99% and 100% in the WS2 assisted Fe(II)/PMS system. The degradation of 4-CP was completed via the free radical pathway and SO4•- played a more important role than other active species. Low concentration of inorganic ions such as Cl− and HCO3− exhibited irrelevant effect while humic acid showed significant suppression on the WS2/Fe(II)/PMS system. Additionally, characterization and recycle results implied that WS2 maintained a good stability during the co-catalytic processes." @default.
• W3080787368 created "2020-09-01" @default.
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• W3080787368 date "2021-01-01" @default.
• W3080787368 modified "2023-10-17" @default.
• W3080787368 title "WS2 as highly active co-catalyst for the regeneration of Fe(II) in the advanced oxidation processes" @default.
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• W3080787368 doi "https://doi.org/10.1016/j.chemosphere.2020.128067" @default.
• W3080787368 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33182131" @default.
• W3080787368 hasPublicationYear "2021" @default.
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