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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/18996
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dc.contributor.authorFrancisco, MSP-
dc.contributor.authorMastelaro, V. R.-
dc.contributor.authorNascente, PAP-
dc.contributor.authorFlorentino, A. O.-
dc.date.accessioned2014-05-20T13:53:16Z-
dc.date.accessioned2016-10-25T17:03:54Z-
dc.date.available2014-05-20T13:53:16Z-
dc.date.available2016-10-25T17:03:54Z-
dc.date.issued2001-11-01-
dc.identifierhttp://dx.doi.org/10.1021/jp0109675-
dc.identifier.citationJournal of Physical Chemistry B. Washington: Amer Chemical Soc, v. 105, n. 43, p. 10515-10522, 2001.-
dc.identifier.issn1089-5647-
dc.identifier.urihttp://hdl.handle.net/11449/18996-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/18996-
dc.description.abstractStructural and textural studies of a CuO/TiO2 System modified by cerium oxide were conducted using Raman spectroscopy, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and N-2 absorption (BET specific surface area). The introduction of a minor amount of CeO2 (Ce0.09Ti0.82O1.91CU0.09 sample) resulted in a material with the maximum surface area value. The results of Raman spectroscopy revealed the presence of only two crystalline phases, TiO2 anatase and CeO2 cerianite, with well-dispersed copper species. TEM micrographs showed a trend toward smaller TiO2 crystallites when the cerium oxide content was increased. The XPS analysis indicated the rise of a second peak in Ti 2p spectra with the increasing amount of CeO2 located at higher binding energies than that due to the Till in a tetragonal symmetry. The CuO/TiO2 system modified by CeO2 displayed a superior performance for methanol dehydrogenation than the copper catalyst supported only on TiO2 or CeO2.en
dc.format.extent10515-10522-
dc.language.isoeng-
dc.publisherAmer Chemical Soc-
dc.sourceWeb of Science-
dc.titleActivity and characterization by XPS, HR-TEM, Raman spectroscopy, and BET surface area of CuO/CeO2-TiO2 catalystsen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv São Paulo, Dept Fis & Ciência Mat, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil-
dc.description.affiliationUniv Fed Sao Carlos, Dept Mat Engn, Ctr Caracterizacao & Desenvolvimento Mat, BR-13565905 Sao Carlos, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Inst Biociencias, Dept Quim, BR-18618000 Botucatu, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biociencias, Dept Quim, BR-18618000 Botucatu, SP, Brazil-
dc.identifier.doi10.1021/jp0109675-
dc.identifier.wosWOS:000172020200011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Physical Chemistry B-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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