Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0169-4332(99)00593-0
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dc.titleXPS investigation of the oxidation/corrosion of melt-spun Mg
dc.contributor.authorYao, H.B.
dc.contributor.authorLi, Y.
dc.contributor.authorWee, A.T.S.
dc.date.accessioned2014-10-16T09:48:58Z
dc.date.available2014-10-16T09:48:58Z
dc.date.issued2000-05-01
dc.identifier.citationYao, H.B., Li, Y., Wee, A.T.S. (2000-05-01). XPS investigation of the oxidation/corrosion of melt-spun Mg. Applied Surface Science 158 (1) : 112-119. ScholarBank@NUS Repository. https://doi.org/10.1016/S0169-4332(99)00593-0
dc.identifier.issn01694332
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/98598
dc.description.abstractThe oxide films formed on the surfaces of melt-spun Mg exposed to air, immersed in distilled water or 3% NaCl solution saturated with Mg(OH)2 have been investigated by X-ray photoelectron spectroscopy (XPS). High resolution XPS spectra revealed two distinct oxygen species on the surface films: one assigned to O2- in MgO, the other to OH- in Mg(OH)2. Depth profiling revealed that the two species had different depth distributions in the films. The oxide film formed in air comprised a contamination outer layer and a relatively thick (5-6 nm) predominantly MgO inner layer. The film formed in distilled water or 3% NaCl solution saturated with Mg(OH)2 was mainly a mixture of Mg(OH)2 and MgO. Mg(OH)2 was predominant at the top layer and decreased gradually with depth while MgO exhibited the opposite behavior. The corrosion product formed in 3% NaCl solution was more hydrated and much thicker that the films formed in the other two conditions. Cl- ion was incorporated in the oxide film formed in 3% NaCl solution. There exists both partial and complete dissociation of adsorbed water when melt-spun pure Mg ribbons are immersed in distilled water or 3% NaCl solution saturated with Mg(OH)2.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0169-4332(99)00593-0
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE
dc.contributor.departmentPHYSICS
dc.description.doi10.1016/S0169-4332(99)00593-0
dc.description.sourcetitleApplied Surface Science
dc.description.volume158
dc.description.issue1
dc.description.page112-119
dc.description.codenASUSE
dc.identifier.isiut000087605300016
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