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Cited 43 time in webofscience Cited 42 time in scopus
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dc.contributor.authorPark, ED-
dc.contributor.authorHwang, YS-
dc.contributor.authorLee, CW-
dc.contributor.authorLee, JS-
dc.date.accessioned2016-03-31T12:47:51Z-
dc.date.available2016-03-31T12:47:51Z-
dc.date.created2009-02-28-
dc.date.issued2003-07-25-
dc.identifier.issn0926-860X-
dc.identifier.other2003-OAK-0000003564-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/18422-
dc.description.abstractCopper- and vanadium-catalyzed oxidation of methane into methyl trifluoroacetate and formic acid with in situ generated H2O2 from H-2 and O-2 over Pd/C was investigated in trifluoroacetic acid (TFA) and/or trifluoroacetic anhydride (TFAA) as a solvent. Metallic palladium was responsible for the in situ generation of hydrogen peroxide from dihydrogen and dioxygen. Divalent copper hydroperoxide and monoperoxomonovanadate, VO(O-2)(+), seemed to be related to C-H bond activation. The radical chain reaction did not occur in either copper- or vanadium-catalyzed methane oxidation. However, methyl radical appeared to be produced in vanadium system but not in copper system. (C) 2003 Elsevier Science B.V. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.relation.isPartOfAPPLIED CATALYSIS A-GENERAL-
dc.subjectmethane oxidation-
dc.subjectmethanol-
dc.subjectPd/C-
dc.subjectcopper-
dc.subjectvanadium-
dc.subjectXAFS-
dc.subjectACETIC-ACID SYNTHESIS-
dc.subjectC-H BONDS-
dc.subjectHYDROGEN-PEROXIDE-
dc.subject11-MOLYBDO-1-VANADOPHOSPHORIC ACID-
dc.subjectMETHYL TRIFLUOROACETATE-
dc.subjectSELECTIVE OXIDATION-
dc.subjectBIMETALLIC SYSTEM-
dc.subjectPHASE OXIDATION-
dc.subjectCARBON-MONOXIDE-
dc.subjectLOW-TEMPERATURE-
dc.titleCopper- and vanadium-catalyzed methane oxidation into oxygenates with in situ generated H2O2 over Pd/C-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1016/S0926-860X(0-
dc.author.googlePark, ED-
dc.author.googleHwang, YS-
dc.author.googleLee, CW-
dc.author.googleLee, JS-
dc.relation.volume247-
dc.relation.issue2-
dc.relation.startpage269-
dc.relation.lastpage281-
dc.contributor.id10087281-
dc.relation.journalAPPLIED CATALYSIS A-GENERAL-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS A-GENERAL, v.247, no.2, pp.269 - 281-
dc.identifier.wosid000184520300008-
dc.date.tcdate2019-01-01-
dc.citation.endPage281-
dc.citation.number2-
dc.citation.startPage269-
dc.citation.titleAPPLIED CATALYSIS A-GENERAL-
dc.citation.volume247-
dc.contributor.affiliatedAuthorLee, JS-
dc.identifier.scopusid2-s2.0-0038374169-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc29-
dc.type.docTypeArticle-
dc.subject.keywordPlusACETIC-ACID SYNTHESIS-
dc.subject.keywordPlusC-H BONDS-
dc.subject.keywordPlus11-MOLYBDO-1-VANADOPHOSPHORIC ACID-
dc.subject.keywordPlusSELECTIVE OXIDATION-
dc.subject.keywordPlusBIMETALLIC SYSTEM-
dc.subject.keywordPlusPHASE OXIDATION-
dc.subject.keywordPlusLOW-TEMPERATURE-
dc.subject.keywordPlusALKANES-
dc.subject.keywordPlusETHANE-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordAuthormethane oxidation-
dc.subject.keywordAuthormethanol-
dc.subject.keywordAuthorPd/C-
dc.subject.keywordAuthorcopper-
dc.subject.keywordAuthorvanadium-
dc.subject.keywordAuthorXAFS-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-

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