Abstract
Internal localized corrosion of carbon steel pipelines severely threatens the service safety of oil and gas transportation facilities in CO2-containing aqueous environments. In this work, the corrosion evolution and localized corrosion initiation mechanisms of carbon steel in CO2–Cl−–HCO3− coexisting environments were systematically investigated under varying temperatures and HCO3− concentrations. The results demonstrate that the initiation of localized corrosion is primarily attributed to the formation of loose and porous FeCO3 films, which fail to block the permeation of aggressive Cl− and expose the steel substrate to continuous corrosion. In contrast, the synergistic effect of elevated temperature and appropriate HCO3− concentration significantly improves FeCO3 supersaturation and promotes the formation of dense, uniform, and protective FeCO3 films, which effectively isolate the substrate from corrosive media and inhibit localized corrosion. Furthermore, this study quantitatively clarifies the optimal matching relationship between temperature and HCO3− concentration for the growth of high-quality protective FeCO3 films. The findings provide fundamental mechanistic insights and practical guidance for the targeted regulation of HCO3− to mitigate localized corrosion of carbon steel in CO2-saturated oil and gas production systems.
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