Y. Koma et al., TRIVALENT F-ELEMENT INTRAGROUP SEPARATION BY SOLVENT-EXTRACTION WITH CMPO-COMPLEXANT SYSTEM, Journal of Nuclear Science and Technology, 35(2), 1998, pp. 130-136
For trivalent actimide and lanthanide separation, the solvent extracti
on system which employs neutral bifunctional extractant tyl(phenyl)-N,
N-diisobutylcarbamoylmethylphosphine oxide (CMPO) and aminopolyacetic
acid was investigated. The system is based on CMPO-tri-n-butylphosphat
e (TBP) mixed solvent and diethylenetriaminepentaacetic acid (DTPA)-so
dium nitrate solution. The separation is achieved bq complexing trival
ent actimide preferentially with DTPA in aqueous phase and extracting
lanthanide into organic phase. Mutual separation between light lanthan
ide, Am and Cm was mainly governed by complex formation with DTPA. The
acidity is mast affecting parameter for partitioning and its increase
results in decrease of distribution ratio. For selective stripping of
trivalent actinide from 0.2 M CMPO-1.0 M TBP in n-dodecane at room te
mperature, 0.05 M DTPA and 2-4 M sodium nitrate solution (pH 2) is use
ful. From the observed distribution behavior, a basic flow sheet which
is composed of four steps was proposed. In batchwise experiments with
radioactive nuclides, separation factor of larger than 13 and 27 for
Ce/Am and Cm/Eu, respectively, were obtained and the applicability of
the system was indicated.