Abstract
AbstractPassivity of iron in acidic solutions is ascribed to a thin film of iron‐deficient magnetite with the limiting compositions Fe3O4 and Fe2.67O4. If the composition at the oxide/solution interface is close to the formula Fe2.67O4, it follows theoretically that the stationary corrosion current density ic is virtually independent of the voltage U with respect to a standard hydrogen electrode. This is in accord with available experimental data. The Flade potential UF of iron is interpreted as the potential at which the composition of the oxide approaches the formula Fe2.83O4 halfway between the limiting compositions Fe3O4 and Fe2.67O4.For the oxide layer on passivated nickel, another model is suggested, which yields a quasi‐exponential increase of ic with U in accord with available experimental data.
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Dates
Type | When |
---|---|
Created | 1 year, 10 months ago (Oct. 19, 2023, 2 a.m.) |
Deposited | 1 year, 10 months ago (Oct. 19, 2023, 2 a.m.) |
Indexed | 1 month, 3 weeks ago (July 8, 2025, 3:26 p.m.) |
Issued | 51 years, 9 months ago (Dec. 1, 1973) |
Published | 51 years, 9 months ago (Dec. 1, 1973) |
Published Online | 15 years, 3 months ago (May 5, 2010) |
Published Print | 51 years, 9 months ago (Dec. 1, 1973) |
@article{Wagner_1973, title={Models for Lattice Defects in Oxide Layers on Passivated Iron and Nickel}, volume={77}, ISSN={0005-9021}, url={http://dx.doi.org/10.1002/bbpc.19730771211}, DOI={10.1002/bbpc.19730771211}, number={12}, journal={Berichte der Bunsengesellschaft für physikalische Chemie}, publisher={Wiley}, author={Wagner, Carl}, year={1973}, month=dec, pages={1090–1097} }