Pitting corrosion
Form of insidious localized corrosion in which a pit develops at the anode site

Pitting corrosion, or pitting, is a form of extremely localized corrosion that leads to the random creation of small holes in metal. The driving power for pitting corrosion is the depassivation of a small area, which becomes anodic (oxidation reaction) while an unknown but potentially vast area becomes cathodic (reduction reaction), leading to very localized galvanic corrosion. The corrosion penetrates the mass of the metal, with a limited diffusion of ions.
Another term arises, pitting factor, which is defined as the ratio of the depth of the deepest pit (from localized corrosion) to the average penetration depth (mean thickness of the corrosion layer produced by the general uniform corrosion), which can be calculated based on the weight loss and corrosion products density.
Development and kinetics of pitting
According to Frankel (1998) who performed a review on pitting corrosion, it develops in three successive steps: (1) initiation (or nucleation) by breakdown of the passive film protecting the metal surface from oxidation, (2) growth of metastable pits (growing up to the micron scale and then repassivating), and (3) the growth of larger and stable pits.
The evolution of the pit density (number of pits per surface area) as a function of time follows a sigmoid curve with the characteristic shape of a logistic function curve, or a hyperbolic tangent. Guo et al. (2018), after a statistical analysis of hundreds of individual pits observed on carbon steel surfaces at the nano-to-micro- scales, distinguish three stages of pitting corrosion: induction, propagation, and saturation.
Mechanism
The pit formation can be essentially regarded as a two step process: nucleation followed by a growth.
Depassivation of the protective layer
The process of pit nucleation is initiated by the depassivation of the protective oxide layer isolating the metal substrate from a corrosive solution.
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