This paper is focussed on anodic dissolution processes controlled by m
ass transport. After the recall of the results obtained for a classic
redox system, four examples are discussed: (i) iron dissolution in sul
phuric acid for which a liquid layer of high visosity is formed at the
interface; (ii) copper dissolution in hydrochloric acid and (iii) in
phosphate acid, where in both solutions a solid salt layer is existing
at the electrode surface; and (iv) nickel dissolution in sulphate aci
d media, where a very high Schmidt number is involved in the mass tran
sport. On the basis of the analysis of steady-state results and electr
ohydrodynamic impedance, it is evidenced that each system needs a part
icular description.