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Chemical reactivity of supported gold : III. Atomic binding and coordination of gold from X-ray absorption fine structure spectroscopy

dc.contributor.authorBassi, I. W.en_US
dc.contributor.authorLytle, F. W.en_US
dc.contributor.authorParravano, Guiseppeen_US
dc.date.accessioned2006-04-07T16:29:35Z
dc.date.available2006-04-07T16:29:35Z
dc.date.issued1976-04en_US
dc.identifier.citationBassi, I. W., Lytle, F. W., Parravano, G. (1976/04)."Chemical reactivity of supported gold : III. Atomic binding and coordination of gold from X-ray absorption fine structure spectroscopy." Journal of Catalysis 42(1): 139-147. <http://hdl.handle.net/2027.42/21796>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHJ-4CFVFWY-8K/2/dc3c431bde946cda53f89ebb555d6617en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/21796
dc.description.abstractPreparations of Au and Pt supported on Al2O3, MgO, and SiO2 were subjected to analysis by extended X-ray absorption fine structure spectroscopy (EXAFS). The samples contained 0.20, 5.00, and 8.00 wt% Au, and 5.00 wt% Pt. Metal dispersion ranged between 0.3 to 45%. Anisotropic growth was detected in the larger particles. The liii X-ray absorption coefficient was normalized to the same atom basis and Fourier transformed to yield the radial structure function for each preparation. From bond distance comparison with reference materials, assignments were made to specific peaks of the radial structure function. The analysis of the results showed that the metals were present in two distinct phases: metallic with coordination and metal-to-metal distance characteristic of bulk Au, and Pt (particulate phase), and a highly disperse one (dissolved phase). It was concluded that the latter consisted of metal atomically dispersed, or condensed in small, flat clusters of a few atoms. It was further estimated that the majority of Au and Pt was present in the highly disperse form, i.e., 60% for Au and 86% for Pt. Au atoms did not simply substitute Mg in the MgO matrix to form the dissolved Au-MgO phase and they carried an average charge +1.en_US
dc.format.extent723680 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleChemical reactivity of supported gold : III. Atomic binding and coordination of gold from X-ray absorption fine structure spectroscopyen_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 48104, USAen_US
dc.contributor.affiliationotherIstituto Donegani, Novara, Italyen_US
dc.contributor.affiliationotherBoeing Aerospace Company, Seattle, Washington, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/21796/1/0000195.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0021-9517(76)90101-9en_US
dc.identifier.sourceJournal of Catalysisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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