Please use this identifier to cite or link to this item: https://doi.org/10.1149/2.0651610jes
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dc.titleEffect of molybdate on the passivation of carbon steel in alkaline solutions under open-circuit conditions
dc.contributor.authorTan, Y.T
dc.contributor.authorWijesinghe, S.L
dc.contributor.authorBlackwood, D.J
dc.date.accessioned2020-10-23T08:03:34Z
dc.date.available2020-10-23T08:03:34Z
dc.date.issued2016
dc.identifier.citationTan, Y.T, Wijesinghe, S.L, Blackwood, D.J (2016). Effect of molybdate on the passivation of carbon steel in alkaline solutions under open-circuit conditions. Journal of the Electrochemical Society 163 (10) : C649-C658. ScholarBank@NUS Repository. https://doi.org/10.1149/2.0651610jes
dc.identifier.issn0013-4651
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/179614
dc.description.abstractThe effect of molybdate on the passivation of AISI 1020 carbon steel under open-circuit conditions in pH 12.5 calcium hydroxide solutions containing chloride was investigated via electrochemical tests and surface characterization techniques. In the early stage, molybdate increased the rate of passivation, with inhibition efficiency being positive. During the later stage, after the carbon steel has passivated, precipitation of calcium molybdate over parts of the sample surface resulted in slight negative inhibition efficiency and the passive film was found to have a higher proportion of ferrous cations and a smaller thickness. However, the precipitation of a thick calcium molybdate film over the entire surface can reverse this situation, increasing the polarization resistance through a cathodic inhibition mechanism. The electrochemical and XPS results showed that regardless of its effect on the final polarization resistance, the presence of calcium molybdate precipitates led to a decrease in the total extent of carbon steel oxidation, indicating an overall beneficial effect. Molybdate was also shown to be effective against localized corrosion, with 14.6 mM molybdate sufficient in preventing passivity breakdown in pH 12.5 solution containing 564 mM chloride. © The Author(s) 2016.
dc.publisherElectrochemical Society Inc.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectAlkalinity
dc.subjectCalcium
dc.subjectCarbon steel
dc.subjectChlorine compounds
dc.subjectEfficiency
dc.subjectPassivation
dc.subjectPolarization
dc.subjectPulse analyzing circuits
dc.subjectReconfigurable hardware
dc.subjectCalcium hydroxide solution
dc.subjectElectrochemical test
dc.subjectInhibition efficiency
dc.subjectInhibition mechanisms
dc.subjectLocalized corrosion
dc.subjectOpen circuit conditions
dc.subjectPolarization resistances
dc.subjectSurface characterization
dc.subjectCorrosion
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1149/2.0651610jes
dc.description.sourcetitleJournal of the Electrochemical Society
dc.description.volume163
dc.description.issue10
dc.description.pageC649-C658
dc.published.statePublished
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