Effects of Cl −, NO 3− and SO 42− anions on the anodic behavior of carbon steel in deaerated 0.50 M NaHCO 3 solutions

Abstract

The effects of Cl −, NO 3 − and SO 4 2− aggressive anions on the corrosion and passivation behavior of carbon steel electrode in deaerated 0.50 M NaHCO 3 solutions were studied using potentiodynamic anodic polarization and SEM techniques. It was found that the presence of Cl −, NO 3 − and SO 4 2− anions stimulates the anodic dissolution rate in both the active and the pre-passive potential regions. Moreover, significantly great effects were observed in both the passive and the trans-passive potential regions. Pitting corrosion was observed only in the presence of Cl − anions, while the presence of NO 3 − and SO 4 2− anions facilitate only passivation by oxygen of water without themselves participating in the cathodic process. Also, it was observed that the effect of NO 3 − anion, which is a strong oxidizing agent acting “primarily” as stimulator of the cathodic process and then its reaction product acts “indirectly” retarding the anodic process. On the other hand, the effect of SO 4 2− anion, which is a non-oxidizing agent, exerts an “indirect” effect on the cathodic reaction increasing its rate and then “directly” influence on the anodic reaction, retarding it.