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Corrosion mechanisms of mild steel in chloride‐rich atmospheres
Author(s) -
de la Fuente D.,
Díaz I.,
Alcántara J.,
Chico B.,
Simancas J.,
Llorente I.,
GarcíaDelgado A.,
Jiménez J. A.,
Adeva P.,
Morcillo M.
Publication year - 2016
Publication title -
materials and corrosion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.487
H-Index - 55
eISSN - 1521-4176
pISSN - 0947-5117
DOI - 10.1002/maco.201508488
Subject(s) - corrosion , rust (programming language) , cathodic protection , chloride , materials science , carbon steel , aqueous solution , anaerobic corrosion , metallurgy , layer (electronics) , oxide , raman spectroscopy , metal , pitting corrosion , electrochemistry , inorganic chemistry , chemistry , electrode , composite material , physics , computer science , optics , programming language
This work analyses the corrosion mechanisms of carbon steel when exposed to marine atmospheres with very different chloride ion deposition rates. Two extreme situations are described, characterized by a “consolidated rust layer” (at relatively low atmospheric salinities), formed by a diffusion‐controlled corrosion mechanism in which the reduction of dissolved oxygen in the aqueous film deposited on the metal is the predominant cathodic reaction, and an “exfoliated rust layer” (at high atmospheric salinities), where the cathodic reaction of hydrogen evolution becomes important, notably accelerating the corrosion process. The research has employed a range of near‐surface and bulk sensitive analytical techniques (SEM/EDS, µXRD, and SEM/µRaman) to characterize the corrosion products and rust layers formed.

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