Fundamental Chemistry of Cesium Extraction from Acidic Media by HCCD in FS-13

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...

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Published inSolvent extraction and ion exchange Vol. 26; no. 2; pp. 163 - 174
Main Authors Scott Herbst, R., Peterman, Dean R., Tillotson, Richard D., Delmau, Lætitia H.
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis Group 01.03.2008
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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 HNO 3 and HCCD concentrations.
AbstractList 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 ~0.0005M (0.5mM). 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.
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.
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 HNO 3 and HCCD concentrations.
Author Peterman, Dean R.
Delmau, Lætitia H.
Tillotson, Richard D.
Scott Herbst, R.
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  surname: Delmau
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  organization: Oak Ridge National Laboratory (ORNL)
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10.1081/SEI-100107024
10.1016/0022-1902(76)80156-X
10.1080/01496399008050416
10.1007/s11137-005-0033-6
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References Herbst R. S. (CIT0004) 2006; 56
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  volume-title: Ion Exchange Solvent Extraction
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    fullname: Herbst R. S.
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SubjectTerms cesium
cesium extraction
chlorinated cobalt dicarbollide
Extraction
slope analysis
trifluoromethylphenyl sulfone
Title Fundamental Chemistry of Cesium Extraction from Acidic Media by HCCD in FS-13
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