Removal of U-234,U-238, Ra-226, Po-210 and Pb-210 from drinking water by ion exchange

Citation
K. Vaaramaa et al., Removal of U-234,U-238, Ra-226, Po-210 and Pb-210 from drinking water by ion exchange, RADIOCH ACT, 88(6), 2000, pp. 361-367
Citations number
19
Categorie Soggetti
Inorganic & Nuclear Chemistry
Journal title
RADIOCHIMICA ACTA
ISSN journal
00338230 → ACNP
Volume
88
Issue
6
Year of publication
2000
Pages
361 - 367
Database
ISI
SICI code
0033-8230(2000)88:6<361:ROURPA>2.0.ZU;2-O
Abstract
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.