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Isotopic oxygen exchange on supported Ru and Au catalysts

dc.contributor.authorSchwank, Johannes W.en_US
dc.contributor.authorGalvagno, S.en_US
dc.contributor.authorParravano, Guiseppeen_US
dc.date.accessioned2006-04-07T17:24:24Z
dc.date.available2006-04-07T17:24:24Z
dc.date.issued1980-06en_US
dc.identifier.citationSchwank, J., Galvagno, S., Parravano, G. (1980/06)."Isotopic oxygen exchange on supported Ru and Au catalysts." Journal of Catalysis 63(2): 415-424. <http://hdl.handle.net/2027.42/23234>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHJ-4CFV3VW-HT/2/9035accaecdfa88c2985eb6763b13c7cen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23234
dc.description.abstractThe isotopic exchange reaction of molecular oxygen is applied to supported ruthenium and gold catalysts. The results on supported ruthenium are similar to those on RuO2. The exchange reaction seems to be unaffected by differences in particle size or nature of the support (MgO or SiO2, respectively). The heterogeneous exchange kinetics deviate from an exponential law. This indicates the presence of nonuniformities on the catalyst surface and/or a contribution of oxygen diffusion. On supported gold, high exchange activity and massive uptake of labeled oxygen by the solid phase are observed. Au/MgO is one order of magnitude more active than Au/SiO2. The activation of support oxygen for the isotopic exchange reaction is related to an interaction between gold and support.en_US
dc.format.extent846622 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleIsotopic oxygen exchange on supported Ru and Au 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 Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.; Istituto Donegani, Novara, Italy.en_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23234/1/0000167.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0021-9517(80)90095-0en_US
dc.identifier.sourceJournal of Catalysisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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