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Bacterial oxidation conditions for gold extraction from Olympias refractory arsenical pyrite concentrate

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dc.contributor.author Taxiarchou, M en
dc.contributor.author Adam, K en
dc.contributor.author Kontopoulos, A en
dc.date.accessioned 2014-03-01T01:09:44Z
dc.date.available 2014-03-01T01:09:44Z
dc.date.issued 1994 en
dc.identifier.issn 0304-386X en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/11167
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-0005121475&partnerID=40&md5=c28135c140246d73f19e3e16bdb6dc12 en
dc.subject.classification Metallurgy & Metallurgical Engineering en
dc.subject.other GALVANIC INTERACTION en
dc.title Bacterial oxidation conditions for gold extraction from Olympias refractory arsenical pyrite concentrate en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1994 en
heal.abstract The arsenical pyrite concentrate produced at the Olympias mine, Macedonia, Greece, assays approximately Fe: 40%, S: 40%, As: 12% and Au: 26 g/t. Mineralogically, it consists mainly of pyrite (68-70%) and arsenopyrite (23-26%), the former includes both arsenic-free and arsenian pyrite. Gold is mainly associated with the arsenopyrite and arsenian pyrite. The concentrate is highly refractory in nature, as direct cyanidation yields gold recovery lower than 10%. An oxidative pretreatment step is, therefore, necessary before cyanidation, in order to break up the sulphide lattice and liberate gold. The present paper aims at elucidating the effect of the leaching conditions on the bacterial oxidation of the Olympias concentrate. This research subject is of particular interest because selective oxidation of the arsenopyrite and arsenical pyrite fractions may result in high gold recoveries without the need for total sulphur oxidation. Based on the above, this study is focused on the factors that enhance preferential arsenopyrite oxidation. It has shown that preferential oxidation of arsenopyrite is observed especially at short retention times and pulp densities in excess of 10% solids. Arsenopyrite oxidation is complete at EMF values of 480-550 mV, while the oxidation of pyrite is observed to commence at higher EMF values, where the oxidation of arsenopyrite is almost complete. High ferric iron concentrations in solution enhance arsenopyrite but have an adverse affect on pyrite oxidation rates. When operating at constant pH values in the range 1.0-1.2, selective oxidation of arsenopyrite is observed, while pyrite oxidation proceeds at higher pH values, around 1.5. The indirect mechanism is deduced to play a significant role in the bio-oxidation of arsenopyrite, while pyrite oxidation is mainly attributed to direct bacterial attack. en
heal.publisher ELSEVIER SCIENCE BV en
heal.journalName Hydrometallurgy en
dc.identifier.isi ISI:A1994PH11100004 en
dc.identifier.volume 36 en
dc.identifier.issue 2 en
dc.identifier.spage 169 en
dc.identifier.epage 185 en


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