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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74124
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dc.contributor.authorTrivinho-Strixino, Francisco-
dc.contributor.authorDa Silva, Donizete X.-
dc.contributor.authorPaiva-Santos, Carlos O.-
dc.contributor.authorPereira, Ernesto C.-
dc.date.accessioned2014-05-27T11:27:27Z-
dc.date.accessioned2016-10-25T18:40:47Z-
dc.date.available2014-05-27T11:27:27Z-
dc.date.available2016-10-25T18:40:47Z-
dc.date.issued2013-01-01-
dc.identifierhttp://dx.doi.org/10.1007/s10008-012-1883-4-
dc.identifier.citationJournal of Solid State Electrochemistry, v. 17, n. 1, p. 191-199, 2013.-
dc.identifier.issn1432-8488-
dc.identifier.urihttp://hdl.handle.net/11449/74124-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74124-
dc.description.abstractPlasma electrolytic oxidation (PEO) is a coating procedure that utilises anodic oxidation in aqueous electrolytes above the dielectric breakdown voltage to produce oxide coatings that have specific properties. These conditions facilitate oxide formation under localised high temperatures and pressures that originate from short-lived microdischarges at sites over the metal surface and have fast oxide volume expansion. Anodic ZrO2 films were prepared by subjecting metallic zirconium to PEO in acid solutions (H2C 2O4 and H3PO4) using a galvanostatic DC regime. The ZrO2 microstructure was investigated in films that were prepared at different charge densities. During the anodic breakdown, an important change in the amplitude of the voltage oscillations at a specific charge density was observed (i.e., the transition charge density (Q T)). We verified that this transition charge is a monotonic function of both the current density and temperature applied during the anodisation, which indicated that Q T is an intrinsic response of this system. The oxide morphology and microstructure were characterised using SEM and X-ray diffraction experiments (XRD) techniques. X-ray diffraction analysis revealed that the change in voltage oscillation was correlated with oxide microstructure changes during the breakdown process. © 2012 Springer-Verlag Berlin Heidelberg.en
dc.format.extent191-199-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectAnodic breakdown-
dc.subjectAnodic films-
dc.subjectMicrostructure-
dc.subjectPhase transformation-
dc.subjectPlasma electrolytic oxidation (PEO)-
dc.subjectValve metals-
dc.subjectZrO2-
dc.subjectPlasma electrolytic oxidation-
dc.subjectValve metal-
dc.subjectAnodic oxidation-
dc.subjectCharge density-
dc.subjectElectric breakdown-
dc.subjectElectrolysis-
dc.subjectPhase transitions-
dc.subjectProtective coatings-
dc.subjectX ray diffraction analysis-
dc.subjectZirconium-
dc.subjectZirconium alloys-
dc.subjectFilm preparation-
dc.titleTetragonal to monoclinic phase transition observed during Zr anodisationen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de Tocantins-
dc.description.affiliationDepartamento de Física, Química e Matemática Universidade Federal de São Carlos, São Carlos SP-
dc.description.affiliationLaboratório Computacional de Análises Cristalográ ficas e Cristalinas Depto de Físico-Química Universidade Estadual Paulista, Araraquara SP-
dc.description.affiliationDepartamento de Química Universidade Federal de São Carlos, Rod. Washington Luis Km 235, Cx 676, São Carlos SP-
dc.description.affiliationUniversidade Federal de Tocantins, Palmas, TO-
dc.description.affiliationUnespLaboratório Computacional de Análises Cristalográ ficas e Cristalinas Depto de Físico-Química Universidade Estadual Paulista, Araraquara SP-
dc.identifier.doi10.1007/s10008-012-1883-4-
dc.identifier.wosWOS:000313046100021-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Solid State Electrochemistry-
dc.identifier.scopus2-s2.0-84872299505-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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