Waste management of nuclear fuel represents one of the major environmental
concerns of the decade. To recycle fissile valuable materials intimate know
ledge of complexation mechanisms involved in the solvent extraction process
es is indispensable. Evolution of the actinide coordination sphere of AnO(2
)(NO3)(2)TBP-type complexes (An = U, Np, Pu; TBP = tributylphosphate) with
the actinide valence state have been probed by XAS at the metal L-III edge.
Dramatic changes in the actinide coordination sphere appeared when the An(
VI) metal is reduced to An(IV). However, no significant evolution in the ac
tinide environment has been noticed across the series UO22+, NpO22+ and PUO
22+.