Abstract
As a first step towards studying pitting corrosion of Zn in aerated neutral 1.0 M sodium thiosulphate solution (pH 6.6), we have reported the results of cyclic polarization measurements on the passivity and passivity breakdown of Zn in this solution. The recorded voltammograms involved two oxidation processes labeled as AI and AII, and two reduction processes labeled as CII and CI on the forward (anodic) and reverse (cathodic) scans, respectively. The cathodic peak CII was attributed to the reduction of the pitting corrosion products (process AII). On the other hand, the cathodic process CI was related to the reduction of Zn
species formed during the course of the forward scan (process AI and the subsequent formation of the passive region), and the reduction of the adsorbed S
anions to S
and SO
. The reduction products of S
, namely S
and SO
anions, were detected in solution as a function of starting potential and time of holding the electrode at a cathodic potential of −2.0 V (Ag/AgCl). These anions were found to cooperate with the aggressive S
anion itself in passivity breakdown and initiation of pitting corrosion. The effect of solution temperature (15–70 ºC) on the cyclic polarization behaviour of Zn was also studied, and metastable and stable pitting events observed at high temperatures were discussed. The morphology of pitting was also studied by
scanning electron microscopy (SEM) as a function of applied anodic potential, bulk concentration of S
and solution temperature. Cross-sectional view of pits revealed the formation of irregular deep and shallow pits. The aspect ratios (the ratio of pit width to pit depth) of the growing pits were estimated as a function of potential, electrolyte concentration and solution temperature. The aspect ratio of the growing pits was found to be potential and concentration independent, while it increased with temperature.