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Molybdenum carbide catalysts for water–gas shift
dc.contributor.authorPhillips, Coryen_US
dc.contributor.authorPatt, Jeremyen_US
dc.contributor.authorMoon, Dong Juen_US
dc.contributor.authorThompson, Levi T.en_US
dc.date.accessioned2006-09-11T14:30:44Z
dc.date.available2006-09-11T14:30:44Z
dc.date.issued2000-12en_US
dc.identifier.citationPatt, Jeremy; Moon, Dong Ju; Phillips, Cory; Thompson, Levi; (2000). "Molybdenum carbide catalysts for water–gas shift." Catalysis Letters 65(4): 193-195. <http://hdl.handle.net/2027.42/44257>en_US
dc.identifier.issn1011-372Xen_US
dc.identifier.issn1572-879Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44257
dc.description.abstractMolybdenum carbide (Mo 2 C) was demonstrated to be highly active for the water–gas shift of a synthetic steam reformer exhaust stream. This catalyst was more active than a commercial Cu–Zn–Al shift catalyst under the conditions employed (220–295°C and atmospheric pressure). In addition, Mo 2 C did not catalyze the methanation reaction. There was no apparent deactivation or modification of the structure during 48 h on‐stream. The results suggest that high surface area carbides are promising candidates for development as commercial water–gas shift catalysts.en_US
dc.format.extent52156 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Kluwer Academic Publishers ; Springer Science+Business Mediaen_US
dc.subject.otherIndustrial Chemistry/Chemical Engineeringen_US
dc.subject.otherNovel Catalystsen_US
dc.subject.otherChemistryen_US
dc.subject.otherPhysical Chemistryen_US
dc.subject.otherPharmacyen_US
dc.subject.otherWater–Gas Shiften_US
dc.subject.otherMolybdenum Carbideen_US
dc.subject.otherPEM Fuel Cellsen_US
dc.titleMolybdenum carbide catalysts for water–gas shiften_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, 3026 H.H. Dow Building, 2300 Hayward Ave., Ann Arbor, MI, 48109‐2136, USAen_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, 3026 H.H. Dow Building, 2300 Hayward Ave., Ann Arbor, MI, 48109‐2136, USAen_US
dc.contributor.affiliationumDepartment of Chemical Engineering, University of Michigan, 3026 H.H. Dow Building, 2300 Hayward Ave., Ann Arbor, MI, 48109‐2136, USAen_US
dc.contributor.affiliationotherCFC Alternative Research Center, Korea Institute of Science and Technology, PO Box 131, Cheongryang, Seoul, 130‐650, Koreaen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44257/1/10562_2004_Article_327161.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1019098112056en_US
dc.identifier.sourceCatalysis Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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