A hexavalent group actinide separation
process could streamline
used nuclear fuel recycling and waste management. The limiting factor
to such a process compatible with current fuel dissolution practices
is obtaining and maintaining hexavalent Am, AmO2
2+, in molar nitric acid because of the high reduction potential of
the Am(VI)/Am(III) couple (1.68 V vs SCE). Two strong oxidants, sodium
bismuthate and Cu3+ periodate, have demonstrated quantitative
oxidation of Am under molar acid conditions, and better than 50% recovery
by diamyl amylphosphonate (DAAP) is possible under these same conditions.
This work considers the use of Cu3+ periodate to oxidize
Np(V) to Np(VI) and Pu(IV) to Pu(VI) and to recover these elements
by extraction with DAAP. A metal:oxidant ratio of 1:1.2 and 1:3 was
necessary to quantitatively oxidize Np(V) and Pu(IV), respectively,
to the hexavalent state. Extraction of hexavalent Np, Pu, and Am by
1 M DAAP in n-dodecane was measured using ultraviolet–visible
(PuO2
2+, AmO2
2+) and near-infrared
(NpO2
2+) spectroscopy. Distribution values of
AmO2
2+ were found to match previous tracer level
studies. The organic phase spectra of Np, Pu, and Am are presented,
and molar absorptivities are calculated for characteristic peaks.
Hexavalent Pu was found to be stable in the organic phase, while NpO2
2+ showed some reduction to NpO2
+; Am was present as Am3+, AmO2
+, and AmO2
2+ species in aqueous and organic
phases during the extraction experiments. These results demonstrate,
for the first time, the ability to recover macroscopic amounts of
americium that would be present during fuel reprocessing and are the
first characterization of Am organic phase oxidation state speciation
relevant to a hexavalent group actinide separation process under acidic
conditions.