Abstract
The concept of a critical potential below which pitting of 18–8 and other passive alloys does not occur in aqueous Cl− media is affirmed. Increasing Cl− concentration shifts the critical potential to more active values. The potential is shifted to more noble values by presence of other anions, e.g., 
, 
, 
, 
, sufficient concentrations of which act as pitting inhibitors. Lowering of temperature similarly enobles the critical potential. The shift at 0°C exceeds the oxidation‐reduction potential for 
accounting for resistance of 18–8 to pitting in 
solutions at ice temperature but not at room temperature. The critical potential is not affected appreciably in the acid pH range; it moves markedly in the noble direction in the alkaline range corresponding to observed resistance to pitting in alkaline Cl− media. These results are interpreted in terms of competitive adsorption of Cl− and other anions for sites on the alloy surface. Only at a sufficiently high surface concentration of Cl− is oxygen, making up the passive film, displaced locally, and passivity thereby destroyed resulting in a pit. The special behavior of 
inhibition and factors affecting reproducibility of measurements are discussed.