Home / Store / Journals / Electronic Articles / Nuclear Technology / Volume 128 / Number 3 / Pages 359-371
L. R. van Loon, W. Hummel
Nuclear Technology / Volume 128 / Number 3 / Pages 359-371
Format:electronic copy (download)
The formation of water-soluble organic ligands by radiolytic and chemical degradation of several strong acidic ion-exchange resins was investigated under conditions close to those of the near field of a cementitious repository. The most important degradation products were studied and their complexing properties evaluated.Irradiation of strong acidic cation exchange resins (Powdex PCH and Lewatite S-100) resulted in the formation of mainly sulfate and dissolved organic carbon. High-performance liquid chromatography analysis indicated the presence of oxalate, contributing to 10 to 20% of the organic carbon. The identity of the remainder is unknown. The presence of oxalate as a complexant is consistent with results from earlier work. Complexation studies with Cu2+ and Ni2+ showed the presence of two ligands: oxalate and ligand X. Although ligand X could not be identified, it could be characterized by its concentration ([X]T ~ 10-5 to 10-6 M), a deprotonation constant (pKH ~ 7.4 at I = 0.1 M), and a complexation constant for the NiX complex (log KNiX ~ 7.0 at I = 0.1 M).In the absence of irradiation, no evidence for the formation of ligands was found.
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