The bioleaching objective was to demonstrate that bioleaching is effective to solubilise valuable minerals. Redox potential responded similarly to laboratory results and first results indicate a ten-fold increase in copper solubilisation. “Excellent correlation between laboratory results and pilot results of the first two phases provide confidence that we can expect to confirm that objectives will be achieved.”
Hydrometallurgy objectives included election of the most economically efficient process to recover marketable metal; the definition of state-of-art technologies for iron removal and recycling from bleed streams; development of a membrane technology application specifically for solutions with compositions originating from BIOMOre technology applications; and water balance optimisation through recycling to attempt zero discharge. The pilot successfaully developed the flowsheet and the integrated mass balance for industrial scale; and was used for predicting solution compositions. The water balance was optimised through recycling for near-zero discharge; while iron removal technologies were screened and the most effective method was further developed. Final iron concentration was below ppm levels and the development of membrane technology applications (reverse osmosis, nanofiltration) saw >99% rejection of iron, copper and all other
metals; while water can be re-used.
Iron was successfully removed. The best results were obtained by Cu-solvent extraction, carbon filtration to remove residual SX reagents, pre-precipitation of Fe, As, Pb, microbial Fe(II) oxidation, precipitation of pure iron as (oxy) hydroxy-sulphate. The product is suitable as pigment for building materials Toxic elements (eg As, Pb) were removed successfully by IX, resulting in clean solutions. Laboratory tests achieved optimum conditions for leaching of fine material to ascertain upper limit of leachability. Arsenic was successfully removed by coprecipitation with iron. Opti
mum conditions were established for pure product with large grain size. Magnesium was recovered by SX, HCl strip, and precipitation as hydroxide followed by calcination to oxide to a saleable product. Optimum conditions were established. Rhenium was effectively recovered from synthetically enriched solutions (did not leach appreciably) by ion exchange and elution (IX resin already in use at KGHM plant).