Multi-Phase Field Model of Localized Corrosion Kinetics with Corrosion Products Formation

Abstract

Localized corrosion is one of the complex forms of corrosion which makes it difficult to detect and design-against. During metal corrosion in the corrosive environment, corrosion products are also formed as a result of electrochemical reactions inside the electrolyte. These products can precipitate on the corroding surface and stop/ slowdown the overall corrosion process. In order to understand this complex phenomenon, a multi-phase field model is proposed to simulate metal corrosion with corrosion products formation. Both anodic (metal oxidation) and cathodic (oxygen reduction) reactions along with other electrochemical reactions in the electrolyte are considered. The free energy of the system is described in terms of its metal ion concentration and the order parameters. Rather than considering linear kinetics (Allen-Cahn equation), inspired from classical rate theory, non-linear (Butler-Volmer) kinetics is considered to describe the temporal evolution of order parameters. The time dependent evolution of ionic species is governed by Nernst-Plank equations while electrostatic potential is governed by Poisson equation. The model results are compared with experimental findings and several examples are presented to show the practical applications of this model. One interesting example, which can be studied in detail with this methodology, is the formation of metal oxide nanowires (zinc/ aluminum oxide).