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Toxicity identification of gamma-ray treated phenol and chlorophenols

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dc.contributor.authorShim, S. B.-
dc.contributor.authorJo, H. J.-
dc.contributor.authorJung, J.-
dc.date.accessioned2021-09-08T18:34:37Z-
dc.date.available2021-09-08T18:34:37Z-
dc.date.created2021-06-10-
dc.date.issued2009-04-
dc.identifier.issn0236-5731-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120362-
dc.description.abstractIonizing radiation, such as gamma-rays and electron-beams, has been applied to modify toxicity of refractory pollutants and industrial wastewaters, however, very few studies reported the cause of toxicity changes by radiation treatment. In this work, degradation of phenol and chlorophenols (5 center dot 10(-4)M) by gamma-ray treatment and consequent toxicity changes were evaluated. Toxicity of 2,4-dichlorophenol (2,4-DCP) and 2,4,6-trichlorophenol (2,4,6-TCP) was gradually decreased with increasing absorbed dose of gamma-radiation. However, in the case of phenol and monochlorophenols (2-, 3-, and 4-CPs), toxicity was dramatically increased particularly, for a dose of as low as 1 kGy. Hydroquinone, benzoquinone, catechol, chlorohydroquinone, and 4-chlorocatechol were identified to be main by-products of gamma-ray treatment. From the solid phase extraction (SPE) fractionation study, toxicity-causing by-products were found to be hydroquinone, benzoquinone, chlorohydroquinone, and/or 4-chlorocatechol.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER-
dc.subjectAQUEOUS-SOLUTION-
dc.subjectDEGRADATION-
dc.subjectDETOXIFICATION-
dc.subjectEFFLUENT-
dc.titleToxicity identification of gamma-ray treated phenol and chlorophenols-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, J.-
dc.identifier.doi10.1007/s10967-008-7388-z-
dc.identifier.scopusid2-s2.0-62949085757-
dc.identifier.wosid000264325900006-
dc.identifier.bibliographicCitationJOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, v.280, no.1, pp.41 - 46-
dc.relation.isPartOfJOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-
dc.citation.titleJOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-
dc.citation.volume280-
dc.citation.number1-
dc.citation.startPage41-
dc.citation.endPage46-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaNuclear Science & Technology-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.relation.journalWebOfScienceCategoryNuclear Science & Technology-
dc.subject.keywordPlusAQUEOUS-SOLUTION-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusDETOXIFICATION-
dc.subject.keywordPlusEFFLUENT-
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