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dc.contributor.authorLee, EK-
dc.contributor.authorJung, KD-
dc.contributor.authorJoo, OS-
dc.contributor.authorShul, YG-
dc.date.accessioned2024-01-21T06:39:20Z-
dc.date.available2024-01-21T06:39:20Z-
dc.date.created2021-09-02-
dc.date.issued2004-08-
dc.identifier.issn0133-1736-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/137381-
dc.description.abstractThe room temperature wet catalytic oxidation was conducted in a batch reactor with V/MgO catalyst. The XRD study of the catalyst used indicated that V/MgO could not only oxidize H2S to sulfur selectively, but also prevent the sulfidation of metal oxide effectively at room temperature. The XPS study indicated that the H2S oxidation with V/MgO could proceed by a redox mechanism (V5+ <----> V4+) and that V3+ formation (V4+--> V3+), was responsible for the deactivation of V/MgO.-
dc.languageEnglish-
dc.publisherSPRINGER-
dc.subjectSELECTIVE OXIDATION-
dc.subjectHYDROGEN-SULFIDE-
dc.subjectOXIDE CATALYSTS-
dc.subjectSULFUR-
dc.titleRedox behavior of V/MgO catalyst in H2S wet oxidation at room temperature-
dc.typeArticle-
dc.identifier.doi10.1023/B:REAC.0000037372.59994.f7-
dc.description.journalClass1-
dc.identifier.bibliographicCitationREACTION KINETICS AND CATALYSIS LETTERS, v.83, no.1, pp.25 - 30-
dc.citation.titleREACTION KINETICS AND CATALYSIS LETTERS-
dc.citation.volume83-
dc.citation.number1-
dc.citation.startPage25-
dc.citation.endPage30-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000224049400004-
dc.identifier.scopusid2-s2.0-4143136709-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusSELECTIVE OXIDATION-
dc.subject.keywordPlusHYDROGEN-SULFIDE-
dc.subject.keywordPlusOXIDE CATALYSTS-
dc.subject.keywordPlusSULFUR-
dc.subject.keywordAuthorwet catalytic oxidation-
dc.subject.keywordAuthorV/MgO catalyst-
dc.subject.keywordAuthorH2S-
dc.subject.keywordAuthorredox mechanism-
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