V. Gopalakrishnan et al., EXTRACTION AND EXTRACTION CHROMATOGRAPHIC-SEPARATION OF MINOR ACTINIDES FROM SULFATE BEARING HIGH-LEVEL WASTE SOLUTIONS USING CMPO, Journal of radioanalytical and nuclear chemistry, 191(2), 1995, pp. 279-289
Bench-Scale studies on the partitioning and recovery of minor actinide
s from the actual and synthetic sulphate-bearing high level waste (SBH
LW) solutions have been carried out by giving two contacts with 30% TB
P to deplete uranium content followed by four contacts with 0.2M CMPO
+ 1.2M TBP in dodecane. The acidity of the SBHLW solutions was about 0
.3M. In the case of actual SSHLW, the final raffinate contained about
0.4% alpha-activity originally present in the HLW whereas with synthet
ic SBHLW the or-activity was reduced to the background level, Ce-144 i
s extracted almost quantitative in the CMPO phase, Ru-106 about 12% an
d Cs-137 is practically not extracted at all. The extraction chromatog
raphic column studies with synthetic SBHLW (after two TBP contacts) ha
s shown that large volume of waste solutions could be passed through t
he column without break-through of actinide metal ions. Using 0.04M HN
O3 > 99% Am(III) and rare earths could be eluted/stripped. Similarly >
99% Pu(IV) and U(VI) could be eluted/stripped using 0.01M oxalic acid
and 0.25M sodium carbonate, respectively, In the presence of 0.16M SO
42- (in the SBHLW) the complex ions AmSO4+. UO2SO4, PuSO42+ and Pu(SO4
)(2) were formed in the aqueous phase but the species extracted into t
he organic phase (CMPO+TBP) were only the nitrate complexes Am(NO3)(3)
. 3CMPO, UO2(NO3)(2) . 2CMPO and Pu(NO3)(4) . 2CMPO. A scheme for the
recovery of minor actinides from SBHLW solution with two contacts of
30% TBP followed by either solvent extraction or extraction chromatogr
aphic techniques has been proposed.