Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/91466
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dc.titleElectrochemical impedance and X-ray photoelectron spectroscopic studies of the inhibition of mild steel corrosion in acids by cyclohexylamine
dc.contributor.authorLi, P.
dc.contributor.authorLin, J.Y.
dc.contributor.authorTan, K.L.
dc.contributor.authorLee, J.Y.
dc.date.accessioned2014-10-09T08:18:24Z
dc.date.available2014-10-09T08:18:24Z
dc.date.issued1997
dc.identifier.citationLi, P.,Lin, J.Y.,Tan, K.L.,Lee, J.Y. (1997). Electrochemical impedance and X-ray photoelectron spectroscopic studies of the inhibition of mild steel corrosion in acids by cyclohexylamine. Electrochimica Acta 42 (4) : 605-615. ScholarBank@NUS Repository.
dc.identifier.issn00134686
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91466
dc.description.abstractThe inhibition of mild steel corrosion in 0.5 M H2SO4 by simple amines (cyclohexylamine, pyridine, triethylamine) was investigated by dc polarization, electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS). The results indicate a strong dependence of the inhibition performance on the nature of the metal surface, in addition to the structural effects of amines. Inhibition is accomplished by amine adsorption on the metal surface without detectable changes in the chemistry of corrosion. Adsorption is predominantly chemisorptive in the active region and by hydrogen bond formation in the passive region. Amine molecules with delocalized π electrons or high electron densities at their nitrogen atoms are effective inhibitors in the active region. The effectiveness for corrosion control in the passive region, however, is proportional to the number of NH linkages in the amine molecules. Copyright © 1996 Elsevier Science Ltd.
dc.sourceScopus
dc.subjectAdsorption
dc.subjectCorrosion
dc.subjectElectrochemical impedance spectroscopy (EIS)
dc.subjectInhibitor
dc.subjectPassivation
dc.subjectX-ray photoelectron spectroscopy (XPS)
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.contributor.departmentPHYSICS
dc.description.sourcetitleElectrochimica Acta
dc.description.volume42
dc.description.issue4
dc.description.page605-615
dc.description.codenELCAA
dc.identifier.isiutNOT_IN_WOS
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