Eight substituted cyclic amides have been synthesized and the extraction of
U(VI) and Pu(IV) by the amides was investigated under various conditions.
From the results of distribution ratio measurement for U(VI) and Pu(IV) (D-
U and D-Pu), as functions of nitric acid and cyclic amide concentrations, t
he effects of the cyclic amide ring size and the structure of substituents
attached to different positions in the cyclic ring on the extraction were d
iscussed. N-(2-ethylhexyl)-buty rolactam (EHBLA), N-(2-ethylhexyl-valerolac
tam (EHVLA) and N-(2-ethylhexyl)-caprolactam (EHCLA) at a concentration of
1 kmol/m(3) in dodecane have produced a third phase at relatively high HNO3
concentration in the aqueous phase. By introducing an octyl group to the r
ing, the third phase disappeared. EHVLA extracted U(VI) and Pu(IV) more str
onger than EHBLA and EHCLA. DU and D-Pu values for 2-octyl-N-(2-ethylhexyl)
-caprolactam (2OEHCLA) were lower than for the mixture of 3-octyl-N-(2-ethy
lhexyl)-caprolactam (3OEHCLA) and 5-octyl-N-(2-ethylhexyl)-caprolactam (5OE
HCLA). Steric hindrance by an n-octyl group next to the C=O group was great
er in the extraction of Pu(IV) than U(VI).