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Abraitis, P. K., D. Pattrick, R. A., Kelsall, G. H., Vaughan, D. J. (2004) Acid leaching and dissolution of major sulphide ore minerals: processes and galvanic effects in complex systems. Mineralogical Magazine, 68 (2) 343-351 doi:10.1180/0026461046820191

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Reference TypeJournal (article/letter/editorial)
TitleAcid leaching and dissolution of major sulphide ore minerals: processes and galvanic effects in complex systems
JournalMineralogical Magazine
AuthorsAbraitis, P. K.Author
D. Pattrick, R. A.Author
Kelsall, G. H.Author
Vaughan, D. J.Author
Year2004 (April)Volume68
Issue2
PublisherMineralogical Society
DOIdoi:10.1180/0026461046820191Search in ResearchGate
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Mindat Ref. ID243541Long-form Identifiermindat:1:5:243541:5
GUID0
Full ReferenceAbraitis, P. K., D. Pattrick, R. A., Kelsall, G. H., Vaughan, D. J. (2004) Acid leaching and dissolution of major sulphide ore minerals: processes and galvanic effects in complex systems. Mineralogical Magazine, 68 (2) 343-351 doi:10.1180/0026461046820191
Plain TextAbraitis, P. K., D. Pattrick, R. A., Kelsall, G. H., Vaughan, D. J. (2004) Acid leaching and dissolution of major sulphide ore minerals: processes and galvanic effects in complex systems. Mineralogical Magazine, 68 (2) 343-351 doi:10.1180/0026461046820191
Abstract/NotesAbstractThe kinetics and mechanisms of dissolution of the major base metal sulphide minerals, pyrite, chalcopyrite, galena and sphalerite in acidic (chloride) media have been investigated. Minerals were ground in air, then dissolved in air-equilibrated solutions at pH 2.5, while monitoring the redox potential. Solution samples were analysed by ICP-AES and HPLC, and surfaces of residual sulphides analysed using XPS. Dissolution of aerial oxidation products on pyrite particles in the first 15 min apparently led to a sulphur-rich surface, and was followed by slower dissolution of pyrite itself, driven by oxygen reduction, and resulting in net production of protons. Chalcopyrite dissolution resulted in a Cu, S-rich (near) surface layer, accompanied by net consumption of protons. Apparently incongruent dissolution of galena and sphalerite may reflect the formation of elemental S at the surface. The rates of dissolution of chalcopyrite, galena and sphalerite in the presence of pyrite were determined, respectively, as 18, 31 and 1.5 times more rapid than in single-mineral experiments. These data were consistent with galvanically-promoted mineral oxidation of the other sulphides in the presence of pyrite. In the case of galena, the experimental data suggested extensive release of Pb ions and development of a sulphur-rich surface during galvanically-promoted dissolution.


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