Classically 13% Cr is required for stable passivity of steel in acidic and neutral solutions not containing inhibitors. Some authors (Mansfeld, Fujimoto) have published potential cycling procedures that generate thick Cr-rich films. Fujimoto cycles right to the transpassivity potential and back in sulphuric acid solution. Our idea is to work very close to the reactivation potential where the passive film (Fe 2 O 3 ) is reductively dissolved to Fe 2+ . We have used an equimolar sodium acetate/acetic acid buffer, at pH 4.7. In exploring this possibility we have obtained new insights into the reactivation process itself. It is under a kind of thermodynamic control, in that the film cannot be reduced, and the metal cannot be dissolved, faster than would exceed the equilibrium concentration of Fe 2+ at the electrode surface. Reductive dissolution leads to a gel-like Cr-rich film, but this is not protective if formed in a single step -Fe dissolution just occurs through it. However alternating formation and reductive dissolution of a Fe-rich film assist the formation of a more robust Cr-rich film.iii