Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/109357
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dc.contributor.authorLebedeva, Olga E.-
dc.contributor.authorBuchelnikov, Anatoly S.-
dc.contributor.authorKalashnikova, Yulia V.-
dc.contributor.authorUstinova, Maria N.-
dc.contributor.authorSolovyeva, Anna A.-
dc.contributor.authorGudkova, Elena A.-
dc.date.accessioned2024-12-18T12:34:27Z-
dc.date.available2024-12-18T12:34:27Z-
dc.date.issued2024-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/109357-
dc.description.abstractThis study focuses on finding direct evidence of oxidative degradation of chlorophenols. The aim of the study was distinguishing major and minor degra dation products. Several chlorophenols with different numbers of chloride substituents (2-chlorophenol, 2,4-dichlorophenol, and 2,4,5-trichlorophenol) were chosen for a thorough study. UV photolysis, Fenton, and photo Fenton processes were tested as advanced oxidative processes. Photo Fenton appeared to result in higher conversions of mono and dichlorophenols. Conversions of trichlorophenol were comparable for all the processes under this study. Formic and acetic acids were shown to be the major products. Their formation was confirmed by 'H NMR spectroscopy. Other possible products are minor and are formed in negligible concentrations. The degradation methods can be considered harmless techniques of inactivating the chlorophenols, leading to the formation of products of low toxicity.vi_VN
dc.language.isoenvi_VN
dc.relation.ispartofseriesVietnam journal of Chemitry;Vol.62, Iss.04 .- P.480-485-
dc.subjectChlorophenolsvi_VN
dc.subjectFenton oxidationvi_VN
dc.subjectNMR spectroscopyvi_VN
dc.subjectPhotolysisvi_VN
dc.subjectPollutionvi_VN
dc.titleDegradation of several chlorophenols using advanced oxidative processes: Major and minor productsvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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