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- Ikumapayi, Fatai, et al.
(författare)
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Recycling of process water in sulphide flotation : Effect of calcium and sulphate ions on flotation of galena
- 2011
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Ingår i: 5th International Flotation Conference 2011. - Red Hook : Curran Associates, Inc.. - 9781618393951 ; , s. 222-249
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Konferensbidrag (refereegranskat)abstract
- The effects of major components of calcium and sulphate species present in recycled process water on galena flotation has been investigated through Hallimond flotation, zeta-potential, diffuse reflectance FTIR spectroscopy and XPS measurements using pure galena mineral as well as bench scale flotation tests using complex sulphide ore. The significance of process water species in flotation has been assessed using deionised water, process water and simulated water containing calcium and sulphate ions in experiments. In addition, the effect of temperature in bench scale flotation tests has also been examined.Hallimond flotation indicated lower recoveries of galena in the presence of calcium and sulphate ions using potassium amyl xanthate as collector. Calcium ions increase zeta-potential of galena while sulphate ions have no effect. FTIR and XPS studies revealed the presence of surface oxidised sulfoxy, hydroxyl and carbonate species on galena at pH 10.5 in deionised and process water, which surface species affected xanthate adsorption. Bench scale flotation using two different complex sulphide ores showed that galena recovery is better in process water than tap water at room temperature. Flotation results also indicated decrease of galenarecovery at temperatures lower than 22oC in either tap water or process water.
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- Ikumapayi, Fatai, et al.
(författare)
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Recycling of process water in sulphide flotation : effect of calcium and sulphate ions on flotation of galena
- 2012
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Ingår i: Minerals Engineering. - : Elsevier BV. - 0892-6875 .- 1872-9444. ; 39, s. 77-88
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Tidskriftsartikel (refereegranskat)abstract
- The effects of major components of calcium and sulphate species present in recycled process water on galena flotation has been investigated through Hallimond flotation, zeta-potential, diffuse reflectance FTIR spectroscopy and XPS measurements using pure galena mineral. The significance of process water species in flotation has been understood using deionised water, process water and simulated tap water containing equivalent calcium and sulphate ions concentration as in process water.Hallimond flotation indicated marginally lower recoveries of galena in the presence of calcium and sulphate ions using potassium amyl xanthate as collector. Zeta-potential shows the adsorption of calcium ions whereby the potential are seen to increase while sulphate ions have no significant effect. FTIR and XPS studies revealed surface calcium carbonate and/or calcium sulphate species in process water which affected xanthate adsorption. Presence of surface oxidised species such as sulfoxy, hydroxyl species on galena at pH 10.5 in deionised and process water was also revealed.
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- Ikumapayi, Fatai, et al.
(författare)
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Recycling process water in complex sulphide ore flotation
- 2012
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Ingår i: XXVI International Mineral Processing Congress (IMPC) 2012. - New Dehli : The Indian Institute of Metals. - 9788190171434 ; , s. 4411-4425
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Konferensbidrag (refereegranskat)abstract
- An approach to environmental sustainability and improved process economy, in sulphide minerals production is recycling of process water in flotation of complex sulphide ores, although the chemistry of process water may be a critical issue to flotation efficiency. The influence of major components of calcium and sulphate ions in process water on xanthate collector adsorption and flotation response using pure chalcopyrite, galena and sphalerite minerals were investigated by Hallimond flotation, zeta-potential measurement, FTIR and XPS spectroscopy studies, while bench scale flotation tests were also carried out using complex sulphide ores. The impact of the species in flotation was comprehended using deionised water, tap water, process water and simulated water containing equivalent amount of calcium and sulphate species in process water. Hallimond flotation results showed a decrease of chalcopyrite and galena recovery in process water and also in the presence of calcium and sulphate ions in both deionised and process waters, whereas sphalerite does not respond to flotation. The adsorption of calcium and metal ions but not sulphate ions on the minerals is evidenced by zeta-potential data. FTIR and XPS studies revealed the presence of surface oxidized sulfoxy species and surface calcium carbonates on chalcopyrite in the presence of process water and water containing calcium ions, surface oxidized sulfoxy and carbonate species on galena in the presence of deionised water, process water and water containing calcium and sulphate ions, all at flotation pH 10.5, and these surface species influenced xanthate adsorption. The presence of surface oxidized sulfoxy and carbonate species at the sphalerite flotation pH 11.5 were seen in the presence of deionised water, process water and water containing calcium and sulphate ions, but the surface species does not influence xanthate adsorption. Bench scale flotation using two different complex sulphide ores showed that chalcopyrite, galena and sphalerite recoveries are better in process water than tap water. The studies showed that the process water can be recycled in flotation with no detrimental effect on grade and recovery of sulphide minerals.
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- Javadi Nooshabadi, Alireza, et al.
(författare)
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Formation of hydrogen peroxide by pyrite and its influence on flotation
- 2013
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Ingår i: Minerals Engineering. - : Elsevier BV. - 0892-6875 .- 1872-9444. ; 49, s. 128-134
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Tidskriftsartikel (refereegranskat)abstract
- Formation of hydrogen peroxide (H2O2), an oxidizing agent stronger than oxygen, by pyrite (FeS2), the most abundant metal sulphide on Earth, during grinding was investigated. It was found that pyrite generated H2O2 in pulp liquid during wet grinding and also the solids when placed in water immediately after dry grinding. Type of grinding medium on formation of hydrogen peroxide revealed that the mild steel produced more H2O2 than stainless steel grinding medium, where Fe2+ and/or Fe3+ ions played a key role in producing higher amounts of H2O2. The effect of grinding atmosphere of air and N2 gas showed that nitrogen environment free from oxygen generated more H2O2 than air atmosphere suggesting that the oxygen in hydrogen peroxide is derived from water molecules. In addition, the solids after dry grinding producing more H2O2 than wet grinding indicate the role of pyrite surface or its catalytic activity in producing H2O2 from water. This study highlights the necessity of relooking into the electrochemical and/or galvanic interaction mechanisms between the grinding medium and pyrite in terms of its flotation behaviour.
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