Application of a topochemical reaction model to predict leaching behavior of high carbonate uranium ores in alkaline solutions: An experimental case study
A variant of a topochemical reaction model based on the shrinking core mechanism was developed for application to leaching of high carbonate uranium ores using sodium carbonate as leachant and oxygen as oxidant. Since the ground ore was not uniform in size, particle size distribution was incorporate...
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Veröffentlicht in: | Hydrometallurgy 2014-01, Vol.141, p.67-75 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A variant of a topochemical reaction model based on the shrinking core mechanism was developed for application to leaching of high carbonate uranium ores using sodium carbonate as leachant and oxygen as oxidant. Since the ground ore was not uniform in size, particle size distribution was incorporated in the model according to the well known Gates–Gaudin–Schumann equation which best represented the size distribution of the ground ore. The model was fitted to leaching data obtained from a uranium ore from a prospective deposit at Gogi in Karnataka, India. The ore comprised pitchblende and coffinite (0.2% as U3O8) as principal uranium minerals and a high percentage of pyrite (about 5%), calcite (62%) and quartz (13%) as main gangue minerals. Partial pressure of oxygen (0.15–3atm), temperature (70–110°C), concentration of leachant (0.47–0.94g/L) and stirring speed (573–900rpm) were tested. The activation energy for dissolution of uranium was determined to be 7kcal/mol, which implies that leaching was controlled by chemical reaction. Extraction of uranium was found to be faster at partial pressures of oxygen below 1atm and decreased significantly with increasing pressure due to the increased rate of dissolution of pyrite. Energy Dispersive X-ray spectroscopy of scanning electron micrographs of the ore and leach residue has also showed high extraction of uranium and low dissolution of pyrite at 90% and of pyrite is |
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ISSN: | 0304-386X 1879-1158 |
DOI: | 10.1016/j.hydromet.2013.10.005 |