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dc.contributor.authorMoreira, A. H.-
dc.contributor.authorBenedetti, Assis Vicente-
dc.contributor.authorSumodjo, PTA-
dc.contributor.authorGarrido, J. A.-
dc.contributor.authorCabot, P. L.-
dc.date.accessioned2014-05-20T14:18:03Z-
dc.date.accessioned2016-10-25T17:40:20Z-
dc.date.available2014-05-20T14:18:03Z-
dc.date.available2016-10-25T17:40:20Z-
dc.date.issued2002-07-05-
dc.identifierhttp://dx.doi.org/10.1016/S0013-4686(02)00169-X-
dc.identifier.citationElectrochimica Acta. Oxford: Pergamon-Elsevier B.V., v. 47, n. 17, p. 2823-2831, 2002.-
dc.identifier.issn0013-4686-
dc.identifier.urihttp://hdl.handle.net/11449/25436-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/25436-
dc.description.abstractThe electrochemical corrosion and passivation of Al-5Zn-1.7Mg-0.23Cu-0.053Nb alloys, submitted to different heat treatments (cold-rolled, annealed, quenched and aged, and quenched in two steps and aged), in sulphate-containing chloride solutions, has been studied by means of cyclic polarization, electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and X-ray photoelectron spectroscopy (XPS). The cyclic polarization curves showed that sulphate addition to the chloride solution produced a poor reproducible shift of the breakdown potential to more positive potentials. The repassivation potentials, much more reproducible, and practically separating the passive from the pitting potential region, were slightly displaced in the negative direction with that addition. When the alloys were potentiodynamically polarized in the passive potential region, sulphate was incorporated in the oxide film, thus precluding chloride ingress. In addition, Zn depletion was favoured, whereas Mg losses were avoided. Different equivalent circuits corresponding to different alloys and potentials in the passive and pitting regions were employed to account for the electrochemical processes taking place in each condition. This work shows that sulphate makes these alloys more sensitive to corrosion, increasing the fracture properties of the surface layer and favouring the pitting attack over greater areas than chloride alone. (C) 2002 Elsevier B.V. Ltd. All rights reserved.en
dc.format.extent2823-2831-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectAl-Zn-Mg alloyspt
dc.subjectpitting corrosionpt
dc.subjectelectrochemical impedance spectroscopypt
dc.subjectchloride plus sulphate solutionspt
dc.titleElectrochemical behaviour of heat-treated Al-Zn-Mg alloys in chloride solutions containing sulphateen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal do Ceará (UFC)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniv Barcelona-
dc.description.affiliationUniv Fed Ceara, Dept Quim Anal & Fis Quim, BR-451970 Fortaleza, Ceara, Brazil-
dc.description.affiliationUNESP, Inst Quim, Dept Fis Quim, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUniv São Paulo, Inst Quim, Cidade Univ, BR-01498 São Paulo, Brazil-
dc.description.affiliationUniv Barcelona, Fac Quim, Dept Quim Fis, LCTEM, Barcelona 08028, Spain-
dc.description.affiliationUnespUNESP, Inst Quim, Dept Fis Quim, BR-14801970 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/S0013-4686(02)00169-X-
dc.identifier.wosWOS:000176919600019-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofElectrochimica Acta-
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