The radiolytic degradation of di-ethylhexyl-isobutyramide (DEHiBA) was examined by subjecting the compound to gamma irradiation, measuring the remaining concentration of the intact compound, identifying the degradation products and measuring uranium distribution ratios. The combined effects of radiation dose, contact with aqueous solutions of HNO 3 , and aeration were also examined. The DEHiBA displayed significant stability at doses up to 1000 kGy, undergoing a slow exponential concentration decrease that was accompanied by the appearance of multiple degradation products. The most abundant compounds that were formed by radiolysis resulted from cleavage of the C carbonyl-N and C ethylhexyl-N bonds, generating di-ethylhexylamine, and mono-ethylhexyl-isobutyramide. Acid contact did alter the radiolytic pathways, with acid favoring cleavage of the C carbonyl-N bond, while a more diverse array of compounds were formed in the absence of acid. Pulsed radiolysis experiments were also conducted, in which picosecond bursts of energetic electrons were used to irradiate solutions of dodecane containing DEHiBA; formation of the dodecane radical cation was implicated, which serially reacted with DEHiBA to form radical or radical cation species intermediate in the formation of the observed products. The 2 slow degradation kinetics suggests that DEHiBA possesses good potential for selective extraction of uranium in fuel cycle extraction operations.

Gamma-radiolysis of the ligand DEHBA is accelerated under biphasic acidic conditions and yields one or more plutonium complexing degradation products.