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Partially exchanged organophilic bentonites

dc.contributor.authorDweck, Jo
dc.contributor.authorBarreto, Emerson Paes [UNESP]
dc.contributor.authorMeth, Sergio
dc.contributor.authorBuechler, Pedro Mauricio [UNESP]
dc.contributor.institutionUniversidade Federal do Rio de Janeiro (UFRJ)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniv So Calif
dc.date.accessioned2014-05-20T15:30:18Z
dc.date.available2014-05-20T15:30:18Z
dc.date.issued2011-09-01
dc.description.abstractUsing a sodium bentonite (VCNa) as substrate differently exchanged organophilic clays were obtained by reaction with hexadecyltrimethylammonium (HDTMA) chloride, at increasing reacting ratios (R) from 20 to 120 meq/100 g of clay (VC20-VC120). The sodium bentonite was previously synthesized from a Verde Claro policationic bentonite (VC) from Bravo, Paraiba State, Brazil. From the thermogravimetric (TG) and derivative thermogravimetric (DTG) analyses of these clays on calcined mass basis and from TG and DTG curves data of VCNa clay, a method was developed to estimate the mass fraction of the exchanged cation present in each organophilic clay (M (org)), as a function of R. When all sodium cations of VCNa are exchanged by HDTMA, the obtained organophilic clay presents a maximum value for M (org). From this value and TG and DTG curves data of VC and VCNa clays, the cation exchange capacity of the original VC bentonite can be estimated.en
dc.description.affiliationUniv Fed Rio de Janeiro, Sch Chem, BR-21949900 Rio de Janeiro, Brazil
dc.description.affiliationSão Paulo State Univ, Dept Chem Engn, BR-05424970 São Paulo, Brazil
dc.description.affiliationUniv So Calif, Loker Hydrocarbon Res Inst, Dept Chem, Los Angeles, CA 90089 USA
dc.description.affiliationUnespSão Paulo State Univ, Dept Chem Engn, BR-05424970 São Paulo, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipRock-Fluid Iteration Laboratory of the Petroleum Engineering and Technology Group at PUC/Rio
dc.format.extent907-913
dc.identifierhttp://dx.doi.org/10.1007/s10973-010-1254-2
dc.identifier.citationJournal of Thermal Analysis and Calorimetry. Dordrecht: Springer, v. 105, n. 3, p. 907-913, 2011.
dc.identifier.doi10.1007/s10973-010-1254-2
dc.identifier.issn1388-6150
dc.identifier.urihttp://hdl.handle.net/11449/39721
dc.identifier.wosWOS:000294014000020
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofJournal of Thermal Analysis and Calorimetry
dc.relation.ispartofjcr2.209
dc.relation.ispartofsjr0,587
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectOrganophilic bentonitesen
dc.subjectCation exchange capacityen
dc.subjectCalcined mass basisen
dc.subjectTGen
dc.titlePartially exchanged organophilic bentonitesen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication

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