The corrosion behavior of zinc with a chromate conversion coating cont
aining similar to 0.02 g/m(2) Cr(VI) was investigated. X-ray photoelec
tron spectroscopy (XPS) showed Cr(VI) was Located in layers near the s
urface of the coating. Corrosion current densities and Cr(VI) content
in the coating decreased with immersion time. An electrochemical reduc
tion of Cr(VI) to Cr(III) parallel to oxygen (O-2) reduction In the fi
rst stages of immersion was reviewed. Inhibition of the corrosion rate
proceeded simultaneously with dissolution of the conversion coating.
It was concluded that the thickness of the coating wets not the most i
mportant factor to hinder O-2 reduction. Corrosion inhibition was attr
ibuted to zinc surface passivation byproducts of ionization.