dc.contributorUniversidade Federal do Ceará (UFC)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniv Barcelona
dc.date.accessioned2014-05-20T14:18:03Z
dc.date.accessioned2022-10-05T15:15:15Z
dc.date.available2014-05-20T14:18:03Z
dc.date.available2022-10-05T15:15:15Z
dc.date.created2014-05-20T14:18:03Z
dc.date.issued2002-07-05
dc.identifierElectrochimica Acta. Oxford: Pergamon-Elsevier B.V., v. 47, n. 17, p. 2823-2831, 2002.
dc.identifier0013-4686
dc.identifierhttp://hdl.handle.net/11449/25436
dc.identifier10.1016/S0013-4686(02)00169-X
dc.identifierWOS:000176919600019
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3898539
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.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationElectrochimica Acta
dc.relation5.116
dc.relation1,439
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectAl-Zn-Mg alloys
dc.subjectpitting corrosion
dc.subjectelectrochemical impedance spectroscopy
dc.subjectchloride plus sulphate solutions
dc.titleElectrochemical behaviour of heat-treated Al-Zn-Mg alloys in chloride solutions containing sulphate
dc.typeArtigo


Este ítem pertenece a la siguiente institución