A combined steady-state
and transient approach is employed to investigate
the corrosion behavior of X80 pipeline steel in carbon dioxide-saturated
brines. Continuous bubbling of carbon dioxide into a test vessel with
1 liter capacity is performed to simulate the flowing condition. The
measurement of time-dependent open-circuit potential, polarization
resistance, and electrochemical impedance spectroscopy (EIS) is conducted
to interpret the evolution of dissolution processes at the corroding
interface. Three distinguishing stages are observed at a temperature
of 60 °C during a whole exposure of 144 h. Analyses mainly based
on the consecutive mechanism show that after the first stage of the
active-adsorption state, the anodic reaction is significantly retarded
by the accumulation of (FeOH)ads on the iron surface, causing
a sharp increase in the polarization resistance and the open-circuit
potential, as well as the disappearance of the inductive loop in EIS.
At the third stage, the formation of the corrosion product layer similarly
reduces both the anodic and cathodic reactions, which arouses a linear
increase in the polarization resistance with time and a capacitive
loop in EIS but changes the open-circuit potential slightly. An increase
in salinity in this study reduces the polarization resistance and
enhances iron dissolution by promoting the formation and relaxation
of (FeOH)ads; however, it brings little change to the developing
time of the three stages obviously. At a low temperature of 20 °C,
a protective product layer is not observed in carbon dioxide-saturated
brine, and the dissolution of iron is mainly under activation control
during the whole exposure. A notable enlarged polarization resistance
and different interfacial processes are observed in an alkaline solution
compared with those in acidic environments, which is deduced to be
resulted from an impedance in the relaxation of (FeOH)ads by increasing pH. The observations in this study support well that
the iron dissolution reaction at the initial stage exposed in carbon
dioxide aqueous environments is dominant by water adsorption on the
iron surface, and further investigation should be performed on the
role that carbon dioxide plays in the evolution of corrosion products
and the formation of a protective film on the steel surface by taking
into account local water chemistry.