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dc.contributor.authorGolding, R. M.
dc.contributor.authorHarris, B.
dc.contributor.authorRalph, B. J.
dc.contributor.authorRickard, P. A. D.
dc.contributor.authorVanselow, D. G.
dc.date.accessioned2020-06-30T14:00:38Z
dc.date.available2020-06-30T14:00:38Z
dc.date.issued1977
dc.date.submitted2020-06
dc.identifier.urihttp://hdl.handle.net/10033/622327
dc.description.abstractEvidence has been presented by Corrans et al. [1] that in the synthetic leaching of synthetic covellite, a direct mechanism operates by preventing the accumulation of a protective layer of sulphur and by the depolarisation of a cathodic reaction. The process of covellite passivation has been further studied, using sensitive methods for measurement of the consumption of oxygen and acid, and for the production of cupric and sulphate ions. The results indicate that passivation arises from the accumulation of approximately 30 micromole of elemental sulphur per square metre of covellite surface. The oxygen consumed during depassivation by various strains of Thiobacillus ferrooxidans supported this conclusion. Assuming an even distribution of sulphur over the surface, the passivation film has been calculated to be one or two atoms thick.en_US
dc.language.isoenen_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.titleTHE NATURE OF THE PASSIVATION FILM ON COVELLITE EXPOSED TO OXYGENen_US
dc.typeBook chapteren_US
dc.typeconference paperen_US
dc.contributor.departmentSchool of Chemistry, School of Metallurgy, School of Biological Technology, University of New South Wales, Kensington, N.S.W., Australiaen_US
dc.identifier.journalConference Bacterial Leaching 1977, 191-200en_US
refterms.dateFOA2020-06-30T14:00:39Z


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