Abstract
We previously published a model for cesium extraction from acidic media by the protonated form of the hexachlorinated derivative of the chloro-protected cobalt bis(dicarbollide), HCCD, dissolved in trifluoromethylphenyl sulfone, FS-13. The model indicated that Cs extraction proceeds through a series of ion-paired and/or dissociated extraction equilibria. Additional Cs distribution ratio data has been obtained and the model refined and simplified. It is demonstrated that the equilibrium exclusively involving the exchange of proton for cesium by formation of ion-paired CsCCD models the Cs distribution data very well, particularly for the concentrations of HCCD greater than ∼0.0005 M (0.5 mM). Finally, activity corrections for the aqueous phase to the Cs distribution data results in good agreement to the theoretical value of -1 for slope (log-log) analysis of the data over a wide range of HNO3 and HCCD concentrations.
Original language | English |
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Pages (from-to) | 163-174 |
Number of pages | 12 |
Journal | Solvent Extraction and Ion Exchange |
Volume | 26 |
Issue number | 2 |
DOIs | |
State | Published - Mar 2008 |
Funding
This research was sponsored by the Laboratory Directed Research and Development Program, U.S. Department of Energy under DOE Idaho Operations Office contract DE-AC07-05ID14517 with the Idaho National Laboratory, managed by Battelle Energy Alliance, LLC.
Funders | Funder number |
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Battelle Energy Alliance | |
U.S. Department of Energy | DE-AC07-05ID14517 |
Laboratory Directed Research and Development | |
Idaho National Laboratory |
Keywords
- Cesium
- Cesium extraction
- Chlorinated cobalt dicarbollide
- Extraction
- Slope analysis
- Trifluoromethylphenyl sulfone