Purpose
– This paper aims to clarify the semi-conductive behavior of the passive layer formed in concrete environment without and with presence of chloride ions under different loading conditions. Passivation and depassivation of steel play an essential role in the subsequent stages of the corrosion process. Due to the nature of passive films on metals, they show electrochemical properties of a semi-conductor.
Design/methodology/approach
– A C-ring model was proposed in this experiment to induce stress on the specimens. Specimens under different levels of compressive and tensile loadings were exposed to chloride-free and chloride-contaminated solutions and their semi-conductive behavior was investigated using Mott–Schottky technique.
Findings
– Irrespective of the type and magnitude of the applied load, the passive film on rebars in simulated concrete pore solution is a highly disordered n-type semi-conductor. In all specimens, the presence of chloride ions decreases the slope of the Mott-Schottky plots, the donor density and the space charge layer thickness, which leads to a thinner passive film. Results indicate that steel specimens immersed in chloride-free pore solution under tensile loadings passivate more rapidly compared to those under compressive loadings. However, the situation in chloride-contaminated solution is different, and steel under tensile stress exhibits more corrosion than steel under compressive stress or under no load.
Originality/value
– Reinforced concrete structures inevitably experience variable mechanical loads, and continuous degradation from aggressive environments. Therefore, it is imperative to study the synergic impact of different types of mechanical loadings and exposure to chloride ions on this process. This paper fulfils this need.
Electrochemical Analysis of Carbon Steel Corrosion Induced by Chloride and Sulfate Ions in Simulated Concrete Pore Solution