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CO oxidation over Co-catalysts supported on silica-titania – The effects of the catalyst preparation method and the amount of incorporated Ti on the formation of more active Co3+ species

dc.contributor.authorLima, Thiago M.
dc.contributor.authorCastelblanco, William N.
dc.contributor.authorRodrigues, Ariano D.
dc.contributor.authorRoncolatto, Rodolfo E.
dc.contributor.authorMartins, Leandro [UNESP]
dc.contributor.authorUrquieta-González, Ernesto A.
dc.contributor.institutionSão Carlos Federal University
dc.contributor.institutionIlha do Fundão
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal Fluminense (UFF)
dc.date.accessioned2018-12-11T16:54:56Z
dc.date.available2018-12-11T16:54:56Z
dc.date.issued2018-09-05
dc.description.abstractHerein, a sol-gel one-pot methodology to tune the activity of Co-catalysts supported on silica-titania to CO oxidation is described. SEM, TEM, EDS, XPS and H2-TPR evidenced a higher Co dispersion from that method when compared to catalysts prepared by impregnation. Furthermore, the simultaneous addition of cobalt oxalate during the incorporation by sol-gel of a controlled low Ti amount into the silica (Si/Ti = 5.7) was determinant to improve the Co dispersion and to avoid the formation of Co-species with strong support interaction. Moreover, XPS analyses evidenced that the mentioned low Ti amount favoured a higher formation of superficial Co3+ and lattice O2− species, which promoted a higher CO oxidation specific activity and, more importantly, strongly decreasing the light-off temperature. On the other hand, Rietveld analyses, Raman spectroscopy, H2-TPR and XPS data showed that the incorporation of higher amounts of Ti into the silica (Si/Ti = 0.2) led to the formation of cobalt titanate, decreasing the concentration of superficial Co3+ and lattice O2− species and, consequently, decreasing the specific activity toCO oxidation.en
dc.description.affiliationResearch Center on Advanced Materials and Energy São Carlos Federal University, C. Postal 676
dc.description.affiliationDepartment of Physics São Carlos Federal University, C. Postal 676
dc.description.affiliationCenpes/Petrobras Ilha do Fundão, Av. Horácio Macedo 950
dc.description.affiliationInstituto de Química UNESP - Univ. Estadual Paulista, Rua Prof. Francisco Degni 55
dc.description.affiliationDepartamento de Química Inorgânica Universidade Federal Fluminense Campus do Valonguinho, Outeiro São João Batista s/n, Centro
dc.description.affiliationUnespInstituto de Química UNESP - Univ. Estadual Paulista, Rua Prof. Francisco Degni 55
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent152-162
dc.identifierhttp://dx.doi.org/10.1016/j.apcata.2018.08.006
dc.identifier.citationApplied Catalysis A: General, v. 565, p. 152-162.
dc.identifier.doi10.1016/j.apcata.2018.08.006
dc.identifier.file2-s2.0-85051636458.pdf
dc.identifier.issn0926-860X
dc.identifier.lattes5782696565602340
dc.identifier.scopus2-s2.0-85051636458
dc.identifier.urihttp://hdl.handle.net/11449/171339
dc.language.isoeng
dc.relation.ispartofApplied Catalysis A: General
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectCO oxidation
dc.subjectCobalt oxide
dc.subjectOne-pot methodology
dc.subjectSilica
dc.subjectSilica-titania
dc.subjectTitania
dc.titleCO oxidation over Co-catalysts supported on silica-titania – The effects of the catalyst preparation method and the amount of incorporated Ti on the formation of more active Co3+ speciesen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes5782696565602340
unesp.author.orcid0000-0001-8750-4057 0000-0001-8750-4057[1]
unesp.author.orcid0000-0002-4965-4350[2]

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