Abstract

Electrochemical kinetics of steel bar corrosion in concrete is of complex nature, especially when it is subjected to alternate wet and dry environments with changes in conditions of steel-concrete interface and rust properties. In this paper, a quantitative electrochemical mechanism was proposed based on thermodynamics and anodic polarisation kinetics to account for variations of microcell and macrocell current densities in reinforced concrete (RC) slabs subjected to periodic wetting and drying cycles. Effects of environmental conditions on corrosion process were incorporated into anodic Tafel slope through three quantifiable parameters, namely, corrosion potential, linear polarisation resistance and ferrous ion concentration at the steel bar surface. A numerical model was established based on the proposed mechanism to quantify microcell and macrocell current densities. An experimental programme of two RC slabs with multiple steel bars arranged at different layers was conducted to verify the numerical model. It shows that the model could reasonably predict variations of both microcell and macrocell corrosion under different wet and dry environments. When concrete was moistened, current density was substantially increased compared to that in dry concrete. Macrocell contribution from uncorroded steel bars at different layers was more significant than microcell corrosion on the corroded bar itself, especially in wet environments.

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