Abstract
CO2 corrosion experiments of X65 steel with and without trace amount of H2S under three flow velocities were performed using high temperature and high pressure autoclaves. Corrosion morphology and corrosion scale were investigated by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS) and X-ray diffraction (XRD), respectively. Linear polarization electrochemical method was also used to investigate the corrosion behaviors of X65 steel in the two kinds of environment. The results indicated that CO2-H2S corrosion rates were remarkably smaller than those of CO2 corrosion. CO2 corrosion scale was loose and prone to localized destruction which in turn presented uniform corrosion, pitting corrosion and mesa corrosion with the increase of flow velocities; CO2-H2S corrosion scale was compact and had high protective property to the metal matrix as well as high resistance to the flow impact which resulted in uniform corrosion at various flow velocities. Mackinawite (FeS1-x), the main corrosion product in the CO2-H2S environments, had higher protective property to the metal matrix than FeCO3. Mackinawite with smaller solubility product in comparison with FeCO3 was more prone to precipitate on the metal surface to form compact corrosion scale with high protective property, which was the fundamental reason for the difference of corrosion rates and morphologies between CO2 and CO2-H2S corrosion.