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ABSTRACT IT has been frequently suggested that the cathodic protection of iron in chloride solutions is due to the depression of its potential to or below the open-circuit potential of the
local anodes1,2. However, in neutral solutions containing dissolved oxygen the open-circuit potential of the local anodes cannot be measured directly without assuming the previous statement
to be true. Nor can it be calculated from the Nernst equation, since the ferrous ion activity in equilibrium with hydrated ferric oxide is unknown. Since the formation of hydrated ferric
oxide may be represented by an equation such as 4 Fe++ + 8 OH′ + O2 = 4 FeO.OH + 2H2O it is implicit that the open-circuit potential of the local anodes should become more electronegative
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Contact customer support SIMILAR CONTENT BEING VIEWED BY OTHERS OXIDATION AND ELECTRICAL PROPERTIES OF CHROMIUM–IRON ALLOYS IN A CORROSIVE MOLTEN ELECTROLYTE ENVIRONMENT Article Open access
09 September 2020 THE INFLUENCE OF IRON-BINDING LIGANDS IN THE CORROSION OF CARBON STEEL DRIVEN BY IRON-REDUCING BACTERIA Article Open access 03 February 2022 CATHODIC PROTECTION MECHANISM
OF IRON AND STEEL IN POROUS MEDIA Article Open access 16 February 2024 REFERENCES * Hoar, T. P., _Trans. Farad. Soc._, 30, 480 (1934). Article Google Scholar * Mears, R. B., and Brown, R.
H., _Trans. Electrochem. Soc._, 74, 519 (1938). Article Google Scholar * Pryor, M. J., and Evans, U. R., _J. Chem. Soc._, 1259 (1950). * Pryor, M. J., _J. Electrochem., Soc._, 102, 163
(1955). Article CAS Google Scholar Download references AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Metallurgical Research, Kaiser Aluminum and Chemical Corporation,
Spokane, 69, Washington M. J. PRYOR Authors * M. J. PRYOR View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions
ABOUT THIS ARTICLE CITE THIS ARTICLE PRYOR, M. Cathodic Protection of Iron. _Nature_ 178, 1245–1246 (1956). https://doi.org/10.1038/1781245a0 Download citation * Issue Date: 01 December
1956 * DOI: https://doi.org/10.1038/1781245a0 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not
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