3. Electronic Theses and Dissertations (ETDs) - All submissions
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Item An electrochemical investigation into the floatability of pyrrhotite(1998) Buswell, Andrew MarkImpala's Minerals Processing Plant in the Rustenburg Area, South Africa, uses flotation to beneficiate precious metal bearing ores from the Bushveld Complex. Pyrrhotite is one of the sulphide minerals that is targeted but it is the least amenable to current flotation conditions having the lowest recovery. Electrochemical techniques (mixed potential measurements, cyclic voltammetry and current transient techniques) were used to study the relevant reactions on the surface of pyrrhotite mineral electrodes. Aspects investigated included the oxidation of the mineral in aqueous alkaline solutions, activation by copper sulphate, kinetics of oxygen reduction and the adsorption of isobutyl xanthate. Mixed potential measurements of mineral electrodes were taken in batch flotation test work. In addition a novel qualitative measure of hydrophobicity was investigated. The oxidised surface of pyrrhotite is likely to be covered with iron hydroxides and a sulphur rich sub-lattice. No direct evidence was found for the activation of pyrrhotite by copper sulphate in alkaline solutions. It was shown however that activation could be achieved in mildly acidic media and that the surface remained activated if subsequently exposed to alkaline conditions. When achieved under acidic conditions activation was observed to enhance the degree of interaction between the mineral and the xanthate collector. Also copper sulphate appeared to aid the formation of a more hydrophobic surface (as indicated by the hydrophobicity tests). Copper activation conducted in acidic media did not significantly enhance the kinetics of oxygen reduction, a reaction seen as crucial to the adsorption of xanthate. No evidence was found for the initial chemisorption of xanthate onto the mineral surface. However evidence was found for the oxidation of xanthate to dixanthogen at sufficiently anodic potentials. It Was concluded that the relatively poor flotation performance of pyrrhotite could be combated by minimising the extent of the oxidation, adding reagents as soon as possible before the mineral becomes extensively oxidised and by removing surface hydroxides through lowering the pH during conditioning.