Time-dependent electrochemical behavior of carbon steel in MEA-based CO₂ capture process
By Xiang, Yong; Yan, Maocheng; Choi, Yoon-Seok; Young, David & Nesic, Srdjan
Published in International Journal of Greenhouse Gas Control
NULL
2014
Abstract
Time-dependent electrochemical behavior of carbon steel was evaluated in CO₂-loaded monoethanolamine (MEA) solutions in simulated carbon capture environments. Tests were conducted in 30 wt.% MEA solution with different combinations of controlling factors (oxygen [O₂], heat stable salts [HSS], flow and temperature) for 7 days. Corrosion behavior of carbon steel was evaluated by using electrochemical techniques (linear polarization resistance [LPR] and potentiodynamic polarization measurements), weight loss method and surface analytical techniques. Solution pH and ferrous/ferric ion concentration were also measured to monitor the change of water chemistry with time. The results showed that the corrosion rate of carbon steel decreased with time and then stabilized to very low values in the MEA/CO₂ condition. XPS characterization revealed formation of a very thin protective FeCO₃ layer on the surface, as well as adsorption of MEA. However, when O₂ was present in the system, the corrosion rates remained at relatively high values, further increasing with flow. The presence of HSS resulted in a higher corrosion rate at the initial stage, but had a minimal effect on the corrosion rate for longer time exposure. Temperature had a slight effect on the corrosion rate because the solubility of CO₂ and O₂ decreases with increasing temperature.
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