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Fischer-Tropsch synthesis on bimetallic ruthenium-gold catalysts

dc.contributor.authorDatye, A. K.en_US
dc.contributor.authorSchwank, Johannes W.en_US
dc.date.accessioned2006-04-07T19:04:12Z
dc.date.available2006-04-07T19:04:12Z
dc.date.issued1985-06en_US
dc.identifier.citationDatye, A. K., Schwank, J. (1985/06)."Fischer-Tropsch synthesis on bimetallic ruthenium-gold catalysts." Journal of Catalysis 93(2): 256-269. <http://hdl.handle.net/2027.42/25650>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHJ-4CFV4YF-WV/2/50c8588b672477d2a2b2f0f9f1a27e75en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25650
dc.description.abstractThe effect of Au in the behavior of Ru as a Fischer-Tropsch catalyst was studied. Two series of catalysts were investigated, one supported on SiO2 and the other on MgO. Au did not seem to alter the product distribution on Ru at pressures up to 1 MPa and in the temperature range 490-570 K. However, the turnover frequencies for both CO hydrogenation and methanation showed a precipitous drop with the Au content in the SiO2-supported catalysts, whereas on the MgO series a maximum in activity was observed at an intermediate Au content. These activity patterns were correlated with extensive physical characterization placing major emphasis on analytical electron microscopy. The activity trends as a function of Au content were remarkably similar to those previously reported for the structure-sensitive ethane hydrogenolysis reaction. In both reactions, the effect of Au appears to be due to a dilution of the active Ru ensembles.en_US
dc.format.extent1078969 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleFischer-Tropsch synthesis on bimetallic ruthenium-gold 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, The University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemical Engineering, The University of Michigan, Ann Arbor, Michigan 48109, U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25650/1/0000202.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0021-9517(85)90173-3en_US
dc.identifier.sourceJournal of Catalysisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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