The geologic sequestration of CO2 is a proposed method to reduce greenhouse gas emissions and has
been the subject of many studies in the last decade. Wellbore systems achieve isolation of the
sequestration reservoir through a combination of steel (generally carbon steel) and Portland cement.
CO2 and brine leakage along the steel-cement interface has the potential to accelerate corrosion. We
conducted experiments to assess the corrosion risk at the cement-steel interface under in situ wellbore
conditions. In this study, we focus on the mass-transfer limits of corrosion by simulating wellbore
interfaces with assemblies constructed of J55 mild steel and epoxy. Corrosion was investigated in
supercritical CO2 saturated brines (NaCl=1 wt%) at T = 50 °C, pCO2=1 MPa with an interface gap
between steel and epoxy of 20 and100 µm as well as an open steel surface. The corrosion kinetics
were measured by electrochemical techniques including linear polarization resistance and
electrochemical impedance spectroscopy. The corrosion scales were analyzed using scanning
electron microscopy, energy dispersive spectroscopy and x-ray diffraction. Corrosion rates decreased
with time with or without an interface gap. The initial corrosion rates were controlled by mass transfer
barrier through the interface gap while the final steady corrosion rates were limited by the mass transfer
barrier of scale formation. Corrosion rates of steel with scale were two orders of magnitude less than
fresh steel. The corrosion scale was composed of iron carbonates and was pseudo-crystalline at the
open steel surface. Well-crystallized scale was observed with epoxy-steel interface gaps of 20-100 µm.
Key words: Carbon dioxide, cement, corrosion, interface, surface analysis