Abstract

The photo-oxidation of two potential extractants, the N, N′-dimethyl, N, N′-dibutyl, tetradecyl malonamide (DMDBTDMA) and the N, N′-dimethyl, N, N′-dibutyl, dodecylethoxy malonamide (DMDBDDEMA) for minor actinides in nuclear fuel reprocessing was followed. The main photoproducts, identified by coupled techniques (GC/FTIR and GC/MS) are malonamides, monoamides and carbonylate derivatives. An irradiation, for 1 h, with a low mercury pressure lamp can destroy initial diamides diluted at 0.075 mol l −1 in n-dodecane. With pure solutions of diamides (2.05 mol l −1), destruction needs several hours to be complete. Both diamides only differ by an ether bond, their reactivity under different conditions of photo-oxidation is discussed.

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