Several new types of bifunctional anion-exchange resin have been desig
ned, synthesized, and tested for their ability to remove Pu(TV) from n
itric acid. The functional group present in all of these resins is a p
yridinium unit derived from the host poly(4-vinylpyridine) resin. Bifu
nctionality was achieved by adding a second anion-exchange site to the
pyridine nitrogen via an alkylene spacer that encompassed ethylene th
rough hexylene. The attached anion-exchange sites include trimethylamm
onium, pyridinium, and trimethylphosphonium. The sorption kinetics and
distribution coefficients of Pu(IV) from 5 to 9 M nitric acid general
ly were best when the two anion-exchange sites were separated by a fiv
e-carbon spacer. The order of affinity for Pu(TV) from 7 M nitric acid
was pyridinium>phosphonium>trimethylammonium. Replacing the central m
ethylene unit in a five-carbon spacer with an ether-oxygen further enh
anced the sorption of Pu(IV) onto the trimethylammonium-containing res
in. Because these bifunctional resins are modifications of existing co
mmercial Reillex(TM) resins, they are much easier to prepare than resi
ns that require complete synthesis. We plan to evaluate these and rela
ted bifunctional resin structures for their ability to selectively rem
ove other targeted anions from groundwater and industrial waste stream
s.