Six organic and five inorganic ion exchangers were studied for the removal
of natural radionuclides from drinking water. In the first phase, distribut
ion coefficients (K-D) of uranium and radium were determined in three model
solutions: a good quality water, an Fe-Mn-rich water and a saline water si
mulant. The exchangers showing highest K-D's for U and Ra were tested in co
lumn mode experiments for the removal of U, Ra-226, Po-210 and Pb-210 from
a real ground water. Considering the total 1800 processed bed volumes, the
best decontamination factors (DF) for U, 20-120, were obtained with the str
ong base anion exchange resin. The most efficient exchangers for the remova
l of Ra-226 were the weak and strong cation resins and zeolite A. With use
of long regeneration intervals, conventional organic resins are thus most s
uitable for the removal of radionuclides. When only a few hundred bed volum
es were processed, with the corresponding regeneration interval about one w
eek, the aminophosphonate resin was most effective for the removal of both
uranium and radium. Po-210 and Pb-210 in ground water were mainly bound in
particles and adsorbed on the surface of the anion resins. The use of the a
minophosphonate resin to remove uranium and radium would therefore require
an anion resin to take up polonium and lead.