Alkaline Leaching of Uranium
Uranium is soluble in alkaline solutions of carbonate or ammonium and forms the complex UO2(CO3)34- that is very stable.
The main reactions are listed below.
Hexavalent uranium.
UO3 + 3CO32- + H2O = [UO2(CO3)3]4 - + 2(OH)-
Tetravalent uranium requires oxidant conditions.
UO2 + 3CO32- + H2O + ½ O2 = [UO2(CO3)3]4- + 2(OH)-
OH- ions increase pH. Uranium precipitation can occur if pH values are higher than his precipitation pH.
2[UO2(CO3)3]4 - + 6(OH)- + 2Na+ = U2O7Na2 + 6(CO3)2- + 3H2O
In order to avoid uranium precipitation must be added bicarbonate so that OH- ion can be neutralized.
UO3 + CO32- + 2HCO3- = [UO2(CO3)3]4 - + H2O
Bicarbonate is added considering the type of uranium mineral and gangue present in the ore. Sulphide, silicates and aluminates consume carbonate, and calcium hydroxide can be employed.
2FeS2 + 7O2 + 8CO32- + 6H2O = 2Fe(OH)2 + 4SO42- + 8HCO3
SiO2 + H2O + CO32- = SiO32- + 2HCO32-
Al2O3 + 3H2O + CO32- = 2AlO22- + 2HCO3- + 2H2O
Ca(OH)2 + 2HCO3- = CaCO3 + CO32- + 2H2O
Normal parameters during leaching are 40-50 g/l Na2CO3 and 10-20 g/l NaHCO3. Alkaline leaching is appropriate for ores with high content of limestone due to the high consumption of acid. Limestone is not attacked by carbonates.
According to reaction (b) tetravalent uranium needs oxygen in alkaline leaching. Oxygen can be obtained directly or introduced in the ore.
Oxidation is possible employing oxidant reagents or catalyzers that act like intermediaries between the oxidant agent and the ore.
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