The present work is focused on the investigation of the time, potentia
l and pH dependence of SO42- and HSO3- accumulations on surface oxide
layers of low carbon steel. From the experimental results it can be co
ncluded that 1. Surface excess values of SO42- and HSO3- ions on steel
surface undergoing structural transformation are very high and the Ga
mma values corresponding to the quasi-stationary state cannot be attai
ned even after 4 hours. The high surface coverages measured (between 4
and 10 monolayers) give a strong indication that significant incorpor
ation of both aggressive anions into the surface oxide layer occurs. T
he presence of sulfite ions in the solution phase accelerates the corr
osion of low carbon steel. 2. Changes in the solution pH have no signi
ficant effect on the time and potential dependence of sorption process
es in the pH region studied (between 3.5 and 6.5). 3. During anodic po
larization of low carbon steel at more positive potentials than 0.40 V
the surface excess concentration of anions increases. On the other ha
nd, in the course of potential shirts in the negative direction at: pH
= 3.5 below E = 0.40 V (or at pH = 6.5 below E = 0.20 V) a significan
t decrease in the Gamma values can be observed. The latter effect, in
accordance with literature data (1-2), reveals that dissolution of low
carbon steel taking place in the above mentioned potential regions le
ads to a decomposition of the surface layer and, therefore, to a decre
ase in the surface excess concentration of incorporated anions. 4. The
surface intensity versus time curves measured in studies of the mobil
ity of labeled sorbed species can be considered to be superpositions o
f - at least - two processes (exchange and increased accumulation of l
abeled aggressive anions). The strong embedding of anions detected is
probably the result of some selective chemical interactions (chemisorp
tion) between SO42-/HSO3- ions and the active sites of tile steel surf
ace undergoing structural transformation.