Separation of Am3+ from Eu3+ was
demonstrated
by extraction column chromatography using a tripodal diglycolamide
ligand (T-DGA). A clean separation was achieved by selective complexation
of Am3+ in the feed with 2,6-bis(5,6-di(sulfophenyl)-1,2,4-triazin-3-yl)pyridine
(SO3Ph-BTP) with a separation factor of about 2000. The
extraction chromatography resin material with particle size in the
range of 175–250 μm contained only 7.4% T-DGA ligand
(53 μmol/g) and is one of the most efficient materials used
for this purpose until date. Parameters such as feed acidity and SO3Ph-BTP concentration were varied, while keeping the other
parameters constant for getting the best optimized condition for the
separation of Am3+ from Eu3+ ions. The optimized
feed condition was 0.1 M HNO3 containing 10 mM SO3Ph-BTP for the clean separation of Am3+ from the Eu3+ fraction. In the feed solution containing Eu3+ and Am3+, the latter was complexed with SO3Ph-BTP and, therefore, was not retained on the column, whereas the
uncomplexed Eu3+ could be efficiently held onto the column.
Finally, the loaded Eu3+ from the column was eluted with
0.1 M HEDTA (N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic
acid), giving a sharp and narrow elution curve. The radiation stability
of the resin was excellent up to 1000 KGy gamma dose, and an identical
separation efficiency of the resin was noted with the irradiated resin
column, as was obtained with the pristine resin.