Abstract
In situ Synchrotron Radiation X-ray Diffraction (SR-XRD) is employed to follow the evolution of corrosion products on X65 carbon steel in a CO2-containing aqueous environment (80 °C, pH 6.3–7.3). A custom-designed flow cell is used to follow the real-time concomitant changes in electrochemical behaviour and corrosion product growth during stages of both natural and potentiodynamically driven ‘pseudo-passivation’. We show that no detectable crystalline magnetite (Fe3O4) phase forms during ‘pseudo-passivation’ across all conditions studied. Furthermore, the results suggest the significant ennoblement observed during ‘pseudo-passivation’ in these experiments can be strongly related to the accumulation of iron carbonate (FeCO3) on the steel surface.
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