Abstract
The corrosion behavior of carbon steel UNS K02600 in 50 wt. % methyldiethanolamine (MDEA) solutions was investigated, under the background of the CO2 capture process in fossil fuel-fired power plants for the carbon capture and storage (CCS) purpose. Series of experiments were conducted under regenerator conditions (120°C) with different combinations of CO2 loading, O2 and heat stable salts (HSS, including sulfate, formate, and N,N-bis(2-hydroxyethyl)glycine). The corrosion behavior of carbon steel was investigated by using electrochemical techniques (open corrosion potential, linear polarization resistance and potentiodynamic polarization), surface analytical techniques (scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction), and weight-loss method. Results showed that the corrosion rate of carbon steel initially decreased and then stabilized with time in CO2-loaded MDEA solution due to the formation of FeCO3 layer except for the case of MDEA/CO2/O2/HSS with low CO2 loading (0.05 mol/mol). It was found that the presence of HSS significantly accelerated the corrosion process at low CO2 loading, whereas the effect of oxygen on the corrosion rate was not significant at low CO2 loading. The formation mechanism of FeCO3 layer was discussed, which is a key issue to control corrosion in this environment.