The kinetics of anodic dissolution and corrosion of zinc are investigated b
y electrochemical impedance spectroscopy in sulfate medium for various surf
ace preparation conditions and different experimental procedures. A new ver
sion of the reaction model, which was established previously, accounts well
for the experimental results. It implies several parallel paths of dissolu
tion and three adsorbed intermediates: Zn-ad(+), Zn-ad(2+) and ZnOHad. From
the simulation of impedance data are deduced the values of quantities such
as the partial current intensities of each parallel paths or the surface c
overages by three adsorbates. It is shown that the surface preparation cond
itions may affect the balance between the competitive dissolution paths. Wh
en zinc is immersed in the electrolyte, a protective layer is formed, which
inhibits the direct dissolution of the metal, but which tends to be elimin
ated by a potential activation. These phenomena are time dependent and may
be affected by the slow formation of a corrosion product layer. (C) 2001 El
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