Dependence of critical pitting temperature on the concentration of sulphate ion in chloride-containing solutions

Abstract

Effects of varying concentration of sulphate (SO 4 2−) ion on the pitting behavior of 316SS have been investigated using potentiostatic critical pitting temperature (CPT) measurements, potentiostatic current transient technique and scanning electron microscopy in NaCl solution containing 0.5% Cl − ions. The results demonstrated that when the concentration of SO 4 2− ion is less than 0.42%, the CPT is surprisingly lower than that without SO 4 2− ion, showing an accelerating effect of the SO 4 2− ion on pit initiation, which is different from the traditional concept. As the concentration of SO 4 2− ion increases beyond 0.42%, the CPT is higher than that without SO 4 2− ion, displaying an inhibiting effect of the SO 4 2− ion on pit initiation. Based on the above results, a qualitative model is proposed to explain the inhibiting and accelerating effect of SO 4 2− ion on the pit initiation using the mechanism of ions-competitive adsorption between SO 4 2− and Cl − ions. The electric charges calculated in the process of pitting corrosion indicated that the pit morphology and its dimension are dependent on the content of SO 4 2− ion in chloride-containing solutions. The higher the concentration of SO 4 2− ion, the larger the dimension of the pit, reflecting an accelerating effect on pit growth.