You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/132291
Full metadata record
DC FieldValueLanguage
dc.contributor.authorFrancisco, M. S. P.-
dc.contributor.authorMastelaro, V. R.-
dc.contributor.authorFlorentino, A. O.-
dc.contributor.authorBazin, D.-
dc.date.accessioned2014-05-27T11:20:23Z-
dc.date.accessioned2016-10-25T21:25:29Z-
dc.date.available2014-05-27T11:20:23Z-
dc.date.available2016-10-25T21:25:29Z-
dc.date.issued2002-01-01-
dc.identifierhttp://dx.doi.org/10.1023/A:1013845314192-
dc.identifier.citationTopics in Catalysis, v. 18, n. 1-2, p. 105-111, 2002.-
dc.identifier.issn1022-5528-
dc.identifier.urihttp://hdl.handle.net/11449/132291-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/132291-
dc.description.abstractA structural study of CuO supported on a CeO2-TiO2 system was undertaken using X-ray diffraction (XRD) and X-ray absorption spectroscopy (XAS) techniques. The results of XRD revealed the presence of only two phases, TiO2 anatase and CeO2 cerianite. A trend towards smaller TiO2 crystallites was observed when cerium content increased. When the amount of cerium increased, Ti K-edge XANES analysis showed an increasing distortion of Ti sites. The results of Ce LIII-edge EXAFS showed that Ce atoms are coordinated by eight oxygen atoms at 2.32 Å. For the sample containing a small amount of cerium, the EXAFS analysis indicated that the local structure around Ce atoms was highly distorted. The catalysts presented quite different Cu K-edge XANES spectra compared to the spectra of the CuO and Cu2O reference compounds. The Cu-O mean bond length was close to that of the CuO and the Cu atoms in the catalysts are surrounded by approximately four oxygen atoms in their first shell. Copper supported on the ceria-modified titania support catalysts displayed a better performance in the methanol dehydrogenation when compared to copper supported only on titania or on ceria. © 2002 Plenum Publishing Corporation.en
dc.format.extent105-111-
dc.language.isoeng-
dc.publisherKluwer Academic/plenum Publ-
dc.sourceScopus-
dc.subjectCatalysts-
dc.subjectCuO-CeO2-TiO2-
dc.subjectStructure-
dc.subjectXAS-
dc.subjectXRD-
dc.subjectCeO2-TiO2-
dc.subjectCerium content-
dc.subjectCu atoms-
dc.subjectCu K-edge-
dc.subjectEXAFS-
dc.subjectLocal structure-
dc.subjectMethanol dehydrogenation-
dc.subjectOxygen atom-
dc.subjectReference compounds-
dc.subjectStructural studies-
dc.subjectTiO2 anatase-
dc.subjectTitania-
dc.subjectTitania catalysts-
dc.subjectTitania supports-
dc.subjectXANES analysis-
dc.subjectXANES spectra-
dc.subjectCerium-
dc.subjectCerium compounds-
dc.subjectCopper-
dc.subjectMethanol-
dc.subjectOxygen-
dc.subjectSemiconducting bismuth compounds-
dc.subjectStructure (composition)-
dc.subjectTitanium dioxide-
dc.subjectX ray absorption spectroscopy-
dc.subjectX ray diffraction-
dc.subjectAtoms-
dc.titleStructural study of copper oxide supported on a ceria-modified titania catalyst systemen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversité Paris-Sud-
dc.description.affiliationInstituto de Física de São Carlos USP, São Carlos, S.P.-
dc.description.affiliationInstituto de Biociências, UNESP Botucatu, S.P.-
dc.description.affiliationLURE Université Paris-Sud, Orsay-
dc.description.affiliationUnespUniv Estadual Paulista Julio Mesquita Filho, Inst Biociencias, Botucatu, SP, Brazil-
dc.identifier.doi10.1023/A:1013845314192-
dc.identifier.wosWOS:000175611400018-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTopics in Catalysis-
dc.identifier.scopus2-s2.0-0242443736-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.