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Distribution of fission products in the homogeneous liquid-liquid extraction of uranium

Thesis/Dissertation ·
OSTI ID:6795463

Separation of uranium from fission products by homogeneous liquid-liquid extraction of uranium from one molar nitric acid solution with addition of ferric nitrate as salting-out reagent, into propylene carbonate has been performed. Uranium(VI) was quantitatively extracted into propylene carbonate from an aqueous medium of 0.5 g/l Fe(NO{sub 3}){sub 3} 9H{sub 2}O and 1 M HNO{sub 3} at 99 C, then quantitatively stripped from the organic phase with 0.1 M sodium carbonate at pH 9. Final separation of uranium(VI) was obtained by extracting uranium(VI) into 0.1 M dibenzoyl methane in propylene carbonate using the homogeneous technique at pH 7. Precipitation of ferric hydroxide affords efficient decontamination from significant fission products. The representative fission product elements, molybdenum, strontium, ruthenium, zirconium, and cerium, remained in the aqueous solution after after extracting uranium(VI) into propylene carbonate to an extent grater than 97%; i.e., less than three percent of the respective elements were found in the carbonate stripping solution. After the final separation step, the extraction of uranyl ion into propylene carbonate containing dibenzoly methane, these fission product elements were not longer detectable. Ten percent of the original concentration of iodide was found in the carbonate stripping solution. However, it was removed in the final separation step. This uranium extraction method can be applied as a practical method for separating uranium from fission products to recover the uranium from spent fuel elements. The capacity of ferric hydroxide for adsorption of fission products and the ability to convert to the somewhat refractory ferric oxide also promises convenience for long term storage.

Research Organization:
City Univ. of New York, NY (USA)
OSTI ID:
6795463
Country of Publication:
United States
Language:
English