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dc.contributor.authorJUNG, KD-
dc.contributor.authorJoo, OS-
dc.contributor.authorHAN, SH-
dc.contributor.authorUhm, SJ-
dc.contributor.authorCHUNG, IJ-
dc.date.accessioned2024-01-21T21:14:26Z-
dc.date.available2024-01-21T21:14:26Z-
dc.date.created2021-09-02-
dc.date.issued1995-01-
dc.identifier.issn1011-372X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/145422-
dc.description.abstractThe deactivation of Cu/ZnO catalyst during methanol dehydrogenation to form methyl formate has been studied. The Cu/ZnO catalyst was seriously deactivated under the reaction conditions: various temperatures of 493, 523 and 553 K, atmospheric pressure and methanol GHSV of 3000 mi (STP)/g-cat h. The weight loss due to reduction of ZnO in the Cu/ZnO catalyst was monitored by a microbalance. X-ray induced Auger spectroscopy of Zn(L(3)M(4,5)M(4,5)) showed the increase in the concentration of metallic Zn on the catalyst surface after the reaction. Temperature-programmed reduction (TPR) of the Cu/ZnO catalyst with methanol demonstrated that the reduction of ZnO in Cu/ZnO was suppressed by introduction of CO2 into the stream of helium-methanol. As the concentration of CO2 in the feed gas increased, the weight loss of the Cu/ZnO catalyst due to the reduction of ZnO decreased. The deactivation of the Cu/ZnO catalyst in the methanol dehydrogenation was also retarded by the addition of CO2. In particular, oxygen injection into the reactant feed regenerated the Cu/ZnO catalyst deactivated during the reaction. Based on these observations, the cause of deactivation of the Cu/ZnO catalyst has been discussed.-
dc.languageEnglish-
dc.publisherBALTZER SCI PUBL BV-
dc.subjectCOPPER-BASED CATALYSTS-
dc.subjectMETHYL FORMATE-
dc.subjectMECHANISM-
dc.subjectZNO-
dc.subjectSURFACES-
dc.subjectOXIDE-
dc.titleDEACTIVATION OF CU/ZNO CATALYST DURING DEHYDROGENATION OF METHANOL-
dc.typeArticle-
dc.identifier.doi10.1007/BF00807187-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCATALYSIS LETTERS, v.35, no.3-4, pp.303 - 311-
dc.citation.titleCATALYSIS LETTERS-
dc.citation.volume35-
dc.citation.number3-4-
dc.citation.startPage303-
dc.citation.endPage311-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1995TH73400012-
dc.identifier.scopusid2-s2.0-33344461061-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusCOPPER-BASED CATALYSTS-
dc.subject.keywordPlusMETHYL FORMATE-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusZNO-
dc.subject.keywordPlusSURFACES-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordAuthorMETHANOL DEHYDROGENATION-
dc.subject.keywordAuthorDEACTIVATION OF CU/ZNO CATALYST-
dc.subject.keywordAuthorREDUCTION OF ZNO-
dc.subject.keywordAuthorOXIDANT EFFECT-
dc.subject.keywordAuthorREGENERATION OF DEACTIVATED CATALYST-
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