Separation of Americium and Curium in Nitric Acid Solutions via Oxidation of Am(III) by Bismuthate and Perxenate Ions

Studies have been carried out in order to develop new ways to separate Am and Cm in nitrate solutions. It was shown that Am(VI) produced by oxidation of Am(III) by sodium bismuthate in 0.1 and 3.0 M HNO3 solutions is extracted with 30% tri-n-butyl phosphate solution in Isopar M diluent. Using this extractive agent in a mixture with a synergic additive of 0.1 M of trioctylphosphine oxide with 0.1 M HClO4 makes it possible to extract into the organic phase up to 90% of the starting amount of Am with not more than 3% of Cm contained in solution. It was found that, upon introduction of Na4XeO6 center dot 8H(2)O into a 0.1 M HNO3 solution containing Am(III) and NaBiO3, the solution becomes alkaline (pH similar to 10) and Am(III) is oxidized to Am(IV) to give a stable complex of composition Am(IV)center dot XeO6. As a result, Am remains in solution. Sodium bismuthate present in solution is hydrolyzed to give the solid phase Bi2O5 by coprecipitation of hydrolyzed Cm(III). Thus, the redox separation of Am(IV) from Cm(III) in the solution formed as a result of the interaction Am(III) with a 0.1 M HNO3 solution with sodium bismuthate and perxenate it contains is a simpler and more effective way, compared with the developed extractive method.