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Corrosion mechanisms for nickel exposed to the atmosphere

Journal Article · · Journal of the Electrochemical Society
DOI:https://doi.org/10.1149/1.1393305· OSTI ID:20030658
Physical and chemical information on nickel corrosion layer formation, evolution, morphology, and chemical makeup is organized and presented, together with information on nickel-containing minerals and other crystalline structures that might be expected to be present. The chemical reactions involved in the formation of these constituents during the corrosion process are then surveyed. By far the most abundant of the typical corrosion products are various forms of nickel sulfates, including hydroxysulfates and the mineral retgersite ({alpha}-NiSo{sub 4}{sm_bullet}6H{sub 2}O). The presence of these species is shown to be a natural consequence of the thin aqueous layer chemistry involving atmospheric SO{sub 2} and SO{sub 4}{sup {minus}2} that occurs on nickel in humid environments. Formation pathways for retgersite and gaspetite are shown in schematic diagrams. Comprehensive kinetic simulations of the corrosion processes have begun to provide insight into the corrosion chemistry but are limited by a shortage of laboratory determinations of the rates of dissolution, precipitation, and transformation of nickel-containing chemical species.
Research Organization:
Yale Univ., New Haven, CT (US)
OSTI ID:
20030658
Journal Information:
Journal of the Electrochemical Society, Journal Name: Journal of the Electrochemical Society Journal Issue: 3 Vol. 147; ISSN JESOAN; ISSN 0013-4651
Country of Publication:
United States
Language:
English

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