Cyclic voltammetry of iron in phosphate solutions of varying pH show mostly active dissolution in acid solutions of 0.1 M H,PO, and NaH,PO,; complete passivity is observed in alkaline 0.1 M Na,HPO, and Na,PO,. The composition of the corrosion film formed in the latter solutions was determined by las
Surface enhanced Raman spectroelectrochemical studies of the corrosion films on iron and chromium in aqueous solution environments
β Scribed by C.A. Melendres; M. Pankuch; Y.S. Li; R.L. Knight
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 739 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
In
situ" laser Raman spectra of the corrosion films on iron have been observed in aerated 5 M KOH and 0.15 M NaCl solutions via surface enhancement by the electrodeposition of a silver overlayer. Essentially the same spectra are observed in the two solutions as a function of applied potential in spite of a breakdown of passivity on iron in the chloride solution. FeJOH), and Fe,O, are found in the prepassive potential region while FeOOH is present in the passive region. A film which is very diilicult to reduce appears to be always present on the electrode surface even at hydrogen evolution potentials; this film is believed to be a-FeOOH. Surface enhanced Raman spectra of the corrosion films on chromium have also been obtained in NaCl solution for the first time. The passive film has a composition that corresponds most closely to an amorphous form of Cr,O, , with some Cr(OH), also present. The film is converted in the transpassive region to a higher oxide form, presumably CrO:-. Reversible reduction of this species to Cr,O, is indicated.
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