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Sol phase and sol-gel transition in SnO2 colloidal suspensions

dc.contributor.authordos Santos, LRB
dc.contributor.authorCraievich, A. F.
dc.contributor.authorSantilli, Celso Valentim [UNESP]
dc.contributor.authorPulcinelli, Sandra Helena [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:19:48Z
dc.date.available2014-05-20T15:19:48Z
dc.date.issued2000-06-01
dc.description.abstractThe effect of concentration on the structure of SnO2 colloids in aqueous suspension, on their spatial correlation and on the gelation process was studied by small angle x-ray scattering (SAXS). The shape of the experimental SAXS curves varies with suspension concentration. For diluted suspensions ([SnO2] less than or equal to 0.13 mol L-1), SAXS results indicate the presence of colloidal fractal aggregates with an internal correlation length xi congruent to 20 Angstrom, without any noticeable spatial correlation between them. This suggests that the aggregates are spatially arranged without any significant interaction like in ideal gas structures. For higher concentrations ([SnO2] = 0.16, 0.32, and 0.64 mol L-1), the colloidal aggregates are larger (xi = 24 Angstrom) and exhibit a certain degree of spatial correlation between them. The pair correlation function corresponding to the sol with the highest concentration (0.92 mol L-1) reveals a rather strong short range order between aggregates, characteristic of a fluid-like structure, with an average nearest-neighbor distance between aggregates d(1) = 125 Angstrom and an average second-neighbor distance d(2) = 283 Angstrom. The pair distribution function remains essentially invariant during the sol-gel transition, suggesting that gelation involves the formation of a few points of connection between the aggregates resulting in a gel network constituted by essentially linear chains of clusters..en
dc.description.affiliationUNESP, Inst Chem, BR-14800970 Araraquara, SP, Brazil
dc.description.affiliationUSP, Inst Phys, BR-05315970 São Paulo, Brazil
dc.description.affiliationUnespUNESP, Inst Chem, BR-14800970 Araraquara, SP, Brazil
dc.format.extent609-613
dc.identifierhttp://dx.doi.org/10.1107/S0021889899012686
dc.identifier.citationJournal of Applied Crystallography. Copenhagen: Munksgaard Int Publ Ltd, v. 33, n. 1, p. 609-613, 2000.
dc.identifier.doi10.1107/S0021889899012686
dc.identifier.fileWOS000087248600046.pdf
dc.identifier.issn0021-8898
dc.identifier.lattes5584298681870865
dc.identifier.lattes9971202585286967
dc.identifier.orcid0000-0002-8356-8093
dc.identifier.urihttp://hdl.handle.net/11449/31184
dc.identifier.wosWOS:000087248600046
dc.language.isoeng
dc.publisherMunksgaard Int Publ Ltd
dc.relation.ispartofJournal of Applied Crystallography
dc.relation.ispartofsjr1,635
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.titleSol phase and sol-gel transition in SnO2 colloidal suspensionsen
dc.typeArtigo
dcterms.licensehttp://journals.iucr.org/services/copyrightpolicy.html
dcterms.rightsHolderMunksgaard Int Publ Ltd
dspace.entity.typePublication
unesp.author.lattes9971202585286967
unesp.author.lattes5584298681870865[3]
unesp.author.orcid0000-0002-8356-8093[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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