LAUSR

The corrosion mechanism and characteristics of steel in typical atmospheric environments directly affect the rationality of corrosion protection methods. This study investigates the corrosion evolution law of Q235 steel that has been exposed to the urban industrial atmosphere for seven years. The mass loss is used for corrosion dynamics analysis. The rust layers have been characterized by SEM, EDS, and XRD. Finally, the corrosion mechanism was analyzed through a combination of electrochemical methods, corrosion kinetics, and rust layer characteristics. The mass loss results indicate that a two-stage corrosion power function law can still effectively describe the corrosion rate of a seven-year exposure that complies with the power function law. The short-term corrosion results fail to fully reflect the corrosion performance of Q235 steel. The typical morphological structures of γ-FeOOH and α-FeOOH are identified, and the rust layers change from a loose and flat form to a granular and, finally, compact into a smooth surface. The crystalline phases of the rust layers include α-FeOOH, γ-FeOOH, Fe3O4/γ-Fe2O3 and α-Fe2O3. Corrosion products in the initial period are mainly γ-FeOOH, followed by α-FeOOH, and a small amount of Fe3O4/γ-Fe2O3. With the increase in exposure time, α-FeOOH and Fe3O4/γ-Fe2O3 in the rust layer increase. SO2 and Fe3O4/γ-Fe2O3 are the primary factors accelerating steel corrosion. During the first three years of atmospheric corrosion, the primary corrosion mechanism was governed by the acid cycle reaction mechanism. However, from the fifth year of atmospheric corrosion, oxygen-absorbing corrosion began to gradually dominate, specifically oxygen-absorbing corrosion.