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Cited 42 time in webofscience Cited 40 time in scopus
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dc.contributor.authorChoi, SH-
dc.contributor.authorLee, JS-
dc.date.accessioned2016-03-31T13:28:33Z-
dc.date.available2016-03-31T13:28:33Z-
dc.date.created2009-02-28-
dc.date.issued2000-07-25-
dc.identifier.issn0021-9517-
dc.identifier.other2000-OAK-0000001470-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19909-
dc.description.abstractAlumina-supported palladium catalyst, which is active for the hydrogenation of 1,3-butadiene, was modified by tin using various tin precursors. The structure of modified catalysts was studied by XAFS and TPR. Before modification, palladium on alumina existed in an electron-deficient hydride state, which was revealed by a shift to a higher Pd K-edge energy in XANES and by an increased Pd-Pd distance in EXAFS fitting. However, tin modification caused the palladium edge energy to decrease to the value of zero valent palladium metal and destroyed the Pd ensembles by making Pd-Sn bonds, irrespective of the nature of tin precursor. This was responsible for the increased 1-butene selectivity in the hydrogenation of 1,3-butadiene in the presence of 1-butene. A carbonaceous species was formed in the catalyst modified with an organic tin precursor, while the inorganic tin modification produced a tin oxide-like species in addition to the formation of Sn-Pd bonds. (C) 2000 Academic Press.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC-
dc.relation.isPartOfJOURNAL OF CATALYSIS-
dc.subjectXAFS-
dc.subject1,3-butadiene hydrogenation-
dc.subjectPd catalyst-
dc.subjecttin modification-
dc.subjectSURFACE ORGANOMETALLIC CHEMISTRY-
dc.subjectX-RAY-ABSORPTION-
dc.subjectCONTROLLED HYDROGENOLYSIS-
dc.subjectBIMETALLIC CATALYSTS-
dc.subjectFINE-STRUCTURE-
dc.subjectMETALS-
dc.subjectSN(N-C4H9)(4)-
dc.titleXAFS study of tin modification of supported palladium catalyst for 1,3-butadiene hydrogenation in the presence of 1-butene-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1006/jcat.2000.2893-
dc.author.googleChoi, SH-
dc.author.googleLee, JS-
dc.relation.volume193-
dc.relation.issue2-
dc.relation.startpage176-
dc.relation.lastpage185-
dc.contributor.id10087281-
dc.relation.journalJOURNAL OF CATALYSIS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF CATALYSIS, v.193, no.2, pp.176 - 185-
dc.identifier.wosid000088488700002-
dc.date.tcdate2019-01-01-
dc.citation.endPage185-
dc.citation.number2-
dc.citation.startPage176-
dc.citation.titleJOURNAL OF CATALYSIS-
dc.citation.volume193-
dc.contributor.affiliatedAuthorLee, JS-
dc.identifier.scopusid2-s2.0-0000078866-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc37-
dc.type.docTypeArticle-
dc.subject.keywordPlusSURFACE ORGANOMETALLIC CHEMISTRY-
dc.subject.keywordPlusX-RAY-ABSORPTION-
dc.subject.keywordPlusCONTROLLED HYDROGENOLYSIS-
dc.subject.keywordPlusBIMETALLIC CATALYSTS-
dc.subject.keywordPlusFINE-STRUCTURE-
dc.subject.keywordPlusMETALS-
dc.subject.keywordPlusSN(N-C4H9)(4)-
dc.subject.keywordAuthorXAFS-
dc.subject.keywordAuthor1,3-butadiene hydrogenation-
dc.subject.keywordAuthorPd catalyst-
dc.subject.keywordAuthortin modification-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-

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