Resistance of stainless steels (SS) to generalized corrosion is provid
ed by growth of a protective thin film of mixed oxides. In aqueous sol
utions, impurities can destroy this passive layer locally and increase
the intensity of localized attack. Thiosulfate ions (S2O32-) have bee
n recognized as potentially detrimental to the stability of protective
films on SS. Forms of localized corrosion with far-reaching consequen
ces have been detected in the nuclear, petroleum, and pulp and paper i
ndustries. Although S2O32- ions alone have not been found aggressive e
nough to cause damage to SS, they have been shown to act in synergy wi
th other common ions, such as chlorides or sulfates, to cause localize
d corrosion. Understanding the chronology of initial events, speculate
d to be connected to local variations in the anodic and cathodic react
ion rates, is fundamental in studying localized corrosion. During loca
lized corrosion, electrochemical noise (EN) seems to be generated by s
tochastic processes, such as passivation breakdown and repassivation e
vents, and deterministic processes caused by film formation or pit pro
pagation processes. The study of EN particularly is adapted to monitor
ing onset of events that characterize localized corrosion. Type 304 SS
(UNS S30400) specimens exposed to chloride (Cl-) and S2O32- ions were
used to generate EN signals.