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Changes in the composition of the passive layer and pitting corrosion of stainless steel in phosphate—borate buffer containing chloride ions

✍ Scribed by M. Urretabizkaya; C.D. Pallotta; N. De Cristofaro; R.C. Salvarezza; A.J. Arvia


Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
709 KB
Volume
33
Category
Article
ISSN
0013-4686

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✦ Synopsis


The influence of the passive layer properties on the pitting corrosion of 316SS was studied in phosphate-borate buffer containing chloride ions by using potential step and potentiodynamic techniques complemented with scanning electron microscopy. The increase of the anodization time in the passive region decreases the nucleation rate and the mean number of corrosion pits formed on the 316% surface. Results are explained through changes in the structure and composition of the passive layer during anodization. Two different Cr(II1) species can be voltammetrically detected at short anodization times, an outer weakly bound Cr(II1) species which is electrooxidized to soluble CrO: -andan inner Cr(III)species which is electrooxidixed to Cr(VI) but retained in the film at potentials lying in the transpassive region. As the anodization time in the passive region increases, the weakly bound Cr(II1) species is transformed into another more stable ohe, probably an iron chromite, which exhibits an electrooxidation potential more positive than that of Cr(II1) species. The aged passive layer becomes more resistant to pit initiation, due to either a decrease in the density of active sites or a decrease in the nucleation rate constant for pit initiation.


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