Summary
In Electrochemical Ion-exchange (EIX), the absorption and elution behaviour of ion-exchangers incorporated into an electrode is controlled by an external potential. A negative potential applied to a weak acid cation exchanger electrode causes cations to be absorbed progressively to low concentrations as the feed passes up through the cell — thus giving large decontamination factors, even at high cation loadings. On polarity reversal, the absorbed ions can be eluted into a limited volume to give a concentrated product for subsequent immobilization. By making multiple and complete use of ion-exchange capacity in this way, large volume reduction factors can be achieved for minimal energy expenditure. Both anion and cation systems are available — based on either organic or Inorganic absorbers, although the latter have a higher radiation tolerance.
A number of genuine waste streams have been treated successfully in bench-top trials — including the Harwell site LLW, MTR pond water and PWR wastes — reducing residual activity to low levels at relatively high throughputs. The system has also been scaled-up successfully on a number of these streams, initially by a factor of 11 to a single cell of 0.1 m3/h nominal throughput, and more recently in a multi-modular unit by a further factors of 5.
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References
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© 1991 ECSC, EEC, EAEC, Brussels and Luxembourg
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Turner, A.D., Bridger, N.J., Jones, C.P., Neville, M.D., Junkison, A.R. (1991). The EIX Process for Radioactive Waste Treatment. In: Cecille, M.L., Casarci, M., Pietrelli, L. (eds) New Separation Chemistry Techniques for Radioactive Waste and Other Specific Applications. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3654-9_36
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DOI: https://doi.org/10.1007/978-94-011-3654-9_36
Publisher Name: Springer, Dordrecht
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