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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75544
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dc.contributor.authorRodriguez, Larissa Santana-
dc.contributor.authorPaleari, André Gustavo-
dc.contributor.authorGiro, Gabriela-
dc.contributor.authorde Oliveira Junior, Norberto Martins-
dc.contributor.authorPero, Ana Carolina-
dc.contributor.authorCompagnoni, Marco Antonio-
dc.date.accessioned2014-05-27T11:29:35Z-
dc.date.accessioned2016-10-25T18:49:00Z-
dc.date.available2014-05-27T11:29:35Z-
dc.date.available2016-10-25T18:49:00Z-
dc.date.issued2013-06-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1532-849X.2012.00942.x-
dc.identifier.citationJournal of Prosthodontics, v. 22, n. 4, p. 292-297, 2013.-
dc.identifier.issn1059-941X-
dc.identifier.issn1532-849X-
dc.identifier.urihttp://hdl.handle.net/11449/75544-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75544-
dc.description.abstractPurpose: The objectives of this study were to investigate the flexural strength (FS) and chemical interaction between 2-tert-butylaminoethyl methacrylate (TBAEMA) and a denture base acrylic resin. Materials and Methods: Specimens were divided into five groups according to the concentration of TBAEMA incorporated in acrylic resin Onda-Cryl (0%, 1%, 2%, 3%, 4%) and were submitted to Fourier transform infrared spectroscopy (FTIR), electron spectroscopy for chemical analysis (XPS-ESCA), and differential scanning calorimetry (DSC) analyses. FS of the specimens was tested, and results were analyzed by ANOVA/Tukey's test (α < 0.05). Results: Different nitrogen ratios were observed on specimens' surfaces: 0.36%, 0.54%, 0.35%, and 0.20% for groups 1%, 2%, 3%, and 4%, respectively. FTIR indicated copolymerization of acrylic resin and TBAEMA, and DSC results demonstrated a decrease in glass transition temperature (Tg). Significant differences were found for FS (p < 0.05). The mean values were 91.1 ± 5.5,A 77.0 ± 13.1,B 67.2 ± 12.5,B 64.4 ± 13.0,B and 67.2 ± 5.9B MPa for groups 0%, 1%, 2%, 3% and 4%, respectively (same superscript letters indicate no significant difference). Conclusions: The incorporation of TBAEMA in acrylic resin resulted in copolymerization and the presence of amine groups on specimens' surfaces, and in decreases of Tg and FS. © 2012 by the American College of Prosthodontists.en
dc.format.extent292-297-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAntimicrobial agents-
dc.subjectChemical properties-
dc.subjectPoly(methyl methacrylate) resins-
dc.subjectStrength-
dc.titleChemical characterization and flexural strength of a denture base acrylic resin with monomer 2-tert-butylaminoethyl methacrylateen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Dental Materials and Prosthodontics Araraquara Dental School UNESP-São Paulo State University, Araraquara-
dc.description.affiliationUnespDepartment of Dental Materials and Prosthodontics Araraquara Dental School UNESP-São Paulo State University, Araraquara-
dc.identifier.doi10.1111/j.1532-849X.2012.00942.x-
dc.identifier.wosWOS:000320779200008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Prosthodontics-
dc.identifier.scopus2-s2.0-84879692863-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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