EXTRACTION BEHAVIOR OF URANIUM(VI), PLUTONIUM(IV), ZIRCONIUM(IV), RUTHENIUM(III) AND EUROPIUM(III) WITH GAMMA-PRE-IRRADIATED SOLUTIONS OF N,N'-METHYLBUTYL SUBSTITUTED AMIDES IN N-DODECANE
Pb. Ruikar et al., EXTRACTION BEHAVIOR OF URANIUM(VI), PLUTONIUM(IV), ZIRCONIUM(IV), RUTHENIUM(III) AND EUROPIUM(III) WITH GAMMA-PRE-IRRADIATED SOLUTIONS OF N,N'-METHYLBUTYL SUBSTITUTED AMIDES IN N-DODECANE, Journal of radioanalytical and nuclear chemistry, 201(2), 1995, pp. 125-134
The extraction of plutonium(IV), uranium(VI), zirconium(IV), europium(
III) and ruthenium(III) with gamma-pre-irradiated n-dodecane solutions
of methylbutyl substituted hexanamide (MBHA), octanamide (MBOA) and d
ecanamide (MBDA) from 3.5M HNO3 has been studied as a function of abso
rbed dose up to 184 x 10(4) Gray. The distribution ratios (Kd) of uran
ium(VI) decreased gradually up to a dose of 50 x 10(4) Gray and became
almost constant thereafter, while ruthenium(III) and europium(III) we
re not extracted in the entire dose range studied. The K-d values of P
u(IV) decreased gradually up to 10 x 10(4) Gray, for MBOA, and 30 x 10
(4) Gray for MBHA and MBDA and then increased up to a dose of 72 x 10(
4) Gray, indicating the synergistic effect of radiolytic products at h
igher doses. The extraction of zirconium(IV) was found to increase gra
dually up to 72 x 10(4) Gray. However, the steep fall in Kd values of
plutonium(IV), zirconium(IV) beyond a dose of 72 x 10(4) Gray was attr
ibuted to third phase formation. The radiolytic degradation of amides
was monitored by quantitative IR spectroscopy and was found to follow
the order MBOA > MBDA > MBHA at 184 x 10(4) Gray having the amines and
carboxylic acids as the main radiolytic products.