Extraction of Ytterbium from Nitric Acid Solutions with Solutions of 2-Ethylhexyl Hydrogen 2-Ethylhexylphosphonate in Hexane

The extraction of ytterbium from nitric acid solutions with solutions of 2-ethylhexyl hydrogen 2-ethylhexylphosphonate (HEH[EHP]) in hexane was studied. The HEH[EHP] concentration was varied from 0.5 to 2.0 M; acidity, from 0.1 to 2.0 M; and lanthanide concentration, from 0.1 to 5 g/L. The dependences of the ytterbium distribution ratio on the solution acidity are described by equations of the type log D = a log[H+] + b, where the coefficient a depends on the extractant and lanthanide concentrations and varies from –1.26 to –3.0. Its variation is probably caused by the occurrence of the extraction by both cation-exchange and solvation mechanism. The model describing the dependence of the ytterbium distribution ratio on its concentration in the aqueous phase at different concentrations of the extractant and acid was suggested. The data predicted by the model reasonably agree with the experimental data.

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Publication Details

Journal
Radiochemistry
Published
2024-12-01
DOI
https://doi.org/10.1134/s1066362224060079
Citations
3
Primary Topic
Chemical Synthesis and Characterization
Type
article
Field-Weighted Citation Impact
0.88
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article

Extraction of Ytterbium from Nitric Acid Solutions with Solutions of 2-Ethylhexyl Hydrogen 2-Ethylhexylphosphonate in Hexane

R. A. Kuznetsov, K. S. Bobrovskaya
3 citations
Radiochemistry
Chemical Synthesis and Characterization
0.88
article

Extraction of Ytterbium from Nitric Acid Solutions with Solutions of 2-Ethylhexyl Hydrogen 2-Ethylhexylphosphonate in Hexane

R. A. Kuznetsov, K. S. Bobrovskaya
article en
3 citations

Abstract

The extraction of ytterbium from nitric acid solutions with solutions of 2-ethylhexyl hydrogen 2-ethylhexylphosphonate (HEH[EHP]) in hexane was studied. The HEH[EHP] concentration was varied from 0.5 to 2.0 M; acidity, from 0.1 to 2.0 M; and lanthanide concentration, from 0.1 to 5 g/L. The dependences of the ytterbium distribution ratio on the solution acidity are described by equations of the type log D = a log[H+] + b, where the coefficient a depends on the extractant and lanthanide concentrations and varies from –1.26 to –3.0. Its variation is probably caused by the occurrence of the extraction by both cation-exchange and solvation mechanism. The model describing the dependence of the ytterbium distribution ratio on its concentration in the aqueous phase at different concentrations of the extractant and acid was suggested. The data predicted by the model reasonably agree with the experimental data.

RadiochemistryVol. 66(6)
Ulyanovsk State University (RU), Research Institute of Technology (Russia) (RU)
Openalex Percentile: Top 24%
Chemical Synthesis and Characterization
0.88
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