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The stereochemistry of ethylene-1,2-d2 epoxidation over silver catalysts

dc.contributor.authorEgashira, Makotoen_US
dc.contributor.authorKuczkowski, Robert L.en_US
dc.contributor.authorCant, Noel W.en_US
dc.date.accessioned2006-04-07T17:21:19Z
dc.date.available2006-04-07T17:21:19Z
dc.date.issued1980-10en_US
dc.identifier.citationEgashira, Makoto, Kuczkowski, Robert L., Cant, Noel W. (1980/10)."The stereochemistry of ethylene-1,2-d2 epoxidation over silver catalysts." Journal of Catalysis 65(2): 297-310. <http://hdl.handle.net/2027.42/23136>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHJ-4CFW57J-J3/2/560822a0216e045aad0dbacfaac57f91en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23136
dc.description.abstractThe stereochemistry of the catalytic epoxidation of cis-ethylene-1,2-d2 to ethylene oxide over four unsupported and two supported silver catalysts as well as over Ag2O and AgO was studied. Variations of the stereochemistry with reaction composition including addition of C4H2Cl2 to moderate the catalyst and the use of N2O as the oxidant were also explored. Equilibration in the product ranged between 57 and 99%. A correlation in the equilibration with extent of oxidation of the surface was proposed. Several models were discussed which could rationalize the observed partial equilibration and the sensitivity of the randomization kinetics to certain reaction variables such as oxygen concentration or addition of C2H4Cl2 or N2O but not others such as temperature and catalyst selectivity.en_US
dc.format.extent1143030 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleThe stereochemistry of ethylene-1,2-d2 epoxidation over silver catalystsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationotherSchool of Chemistry, Macquarie University, North Ryde, New South Wales 2113, Australiaen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23136/1/0000060.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0021-9517(80)90307-3en_US
dc.identifier.sourceJournal of Catalysisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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