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SAXS measurements of the porosity in Cu(II)-doped SnO2 xerogels during crystallization

dc.contributor.authorBrito, G. E. S. [UNESP]
dc.contributor.authorSantilli, Celso Valentim [UNESP]
dc.contributor.authorPulcinelli, Sandra Helena [UNESP]
dc.contributor.authorCraievich, A. F.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-27T11:18:15Z
dc.date.available2014-05-27T11:18:15Z
dc.date.issued1997-08-01
dc.description.abstractThe small-angle X-ray scattering (SAXS) technique was used to study the porosity which develops in Cu(II)-doped SnO2 monolithic xerogels during crystallization. The influence of the upper temperature of heat-treatment and of Cu(II) content on the structure was determined. Previous studies of the porosity in undoped SnO2 samples treated at temperatures ranging from 300 up to 600°C demonstrated the existence of a bimodal size distribution (one distribution was due to intra-aggregate and the other to inter-aggregate pores). However, the SAXS data from Cu(II)-doped samples heated to 500°C had a single mode distribution due only to inter-aggregate pores. Doped samples isothermically treated at 500°C were studied by the in situ SAXS technique. The time evolution of the scattering intensity function, or structure function of the porous material, exhibits a dynamical scaling property. The asymptotic behavior at high q (wave numbers) of the scaled function and consequently the nature and morphology of the porosity interface are a function of Cu(II) content. The kinetic exponents predicted by the statistical theory for the structure function suggest that the mechanism of porosity coarsening is controlled by surface diffusion. © 1997 Elsevier Science B.V.en
dc.description.affiliationInstitute of Chemistry UNESP, Caixa Postal 355, 14801-970 Araraquara, SP
dc.description.affiliationNatl. Synchrotron Light Laboratory CNPq, Campinas, SP
dc.description.affiliationInstitute of Physics USP, São Paulo, SP
dc.description.affiliationUnespInstitute of Chemistry UNESP, Caixa Postal 355, 14801-970 Araraquara, SP
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent41-47
dc.identifierhttp://dx.doi.org/10.1016/S0022-3093(97)00137-3
dc.identifier.citationJournal of Non-Crystalline Solids, v. 217, n. 1, p. 41-47, 1997.
dc.identifier.doi10.1016/S0022-3093(97)00137-3
dc.identifier.issn0022-3093
dc.identifier.lattes5584298681870865
dc.identifier.lattes9971202585286967
dc.identifier.orcid0000-0002-8356-8093
dc.identifier.scopus2-s2.0-0031549247
dc.identifier.urihttp://hdl.handle.net/11449/65154
dc.identifier.wosWOS:A1997XV21100005
dc.language.isoeng
dc.relation.ispartofJournal of Non-Crystalline Solids
dc.relation.ispartofjcr2.488
dc.relation.ispartofsjr0,722
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectCrystallization
dc.subjectDiffusion in solids
dc.subjectDoping (additives)
dc.subjectHeat treatment
dc.subjectInterfaces (materials)
dc.subjectMorphology
dc.subjectParticle size analysis
dc.subjectPorosity
dc.subjectPorous materials
dc.subjectReaction kinetics
dc.subjectX ray analysis
dc.subjectMonolithic xerogels
dc.subjectSmall angle X ray scattering (SAXS)
dc.subjectSol-gels
dc.titleSAXS measurements of the porosity in Cu(II)-doped SnO2 xerogels during crystallizationen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dspace.entity.typePublication
unesp.author.lattes9971202585286967
unesp.author.lattes5584298681870865[2]
unesp.author.orcid0000-0002-8356-8093[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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