To clarify the mechanism of pitting corrosion of Al, the effect of a large amount of Zn (up to 2%) on Al pitting was studied in terms of pitting potential (Epit), repassivation potential (Erep), and pit nucleation transients. Epit in 0.5 M sodium chloride (NaCl) decreased with increased Zn content, and Erep was 50 mV to 60 mV below Epit, independent of Zn content. The shift of the anodic polarization curve in 6 M hydrochloric acid ([HCl] pit-like solution) was consistent with the change of Epit with Zn content. Analysis of passive current noise at the pA level in buffered solutions, with or without chloride (Cl), showed noise caused by Cl started at roughly the lowest potential where pitting occurred and had a similar potential dependence, irrespective of Zn content. Therefore, it was considered that pit nucleation had the same potential dependence, and possibly the same frequency, in Al-Zn alloys and pure Al and that the effect of Zn simply was to enhance dissolution kinetics in the local environment, facilitating the transition to stable pitting. A previously proposed model for the atomistics of activation was detailed.

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