article·1964-01-01

The Kinetics of Anodic Oxidation of Iron in Neutral Solution

Norio Sato, Morris Cohen

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Abstract

Iron was anodically oxidized under both potentiostatic and galvanostatic conditions. It was found that the rate of film growth could be expressed by the over‐all equation where Q T is the film thickness, E the potential, and κ', β, and B are constants. A model is proposed based on a "place‐ exchange" mechanism in which all the M‐O exchanges in a given row take place simultaneously. β is then related to the transfer of oxygen from the OH − in the solution to the oxide and B is related to the activation energy for an equivalent ion‐pair exchange. The activation energy for a single place exchange was calculated to be 3.5 kcal. This mechanism would lead to an increase of activation energy with thickness and a probable change of mechanism at some finite thickness.
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Research context

OpenAlex topics: Corrosion Behavior and Inhibition · Hydrogen embrittlement and corrosion behaviors in metals · Concrete Corrosion and Durability

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