Extraction of uranium (VI) with neutral organic phosphorus extractants: A calorimetric and spectroscopic comparison of di(1-methylheptyl) methylphosphonate vs. tri-n-butylphosphate

Both tri-n-butyl phosphate and di(1-methylheptyl) methylphosphonate demonstrate exceptional extraction capabilities for 233 U from irradiated thorium. While extensive literature exists regarding tri-n-butyl phosphate-based extraction systems, comparative studies on di(1-methylheptyl) methylphosphonate remain notably limited. This systematic investigation provides a parallel comparison of the chemical behaviors between these two extractants under identical experimental conditions. Results reveal that the di(1-methylheptyl) methylphosphonate system exhibits enhanced hydrophobicity relative to tri-n-butyl phosphate, correlating with reduced water co-extraction during the uranium recovery process. Raman spectroscopic analysis demonstrated about ∼30 cm –1 shifts in the uranyl symmetric stretching vibration for di(1-methylheptyl) methylphosphonate complexes compared to ∼15 cm –1 shifts of tri-n-butyl phosphate complexes. This significant spectral displacement indicates stronger coordination bonding between phosphoryl oxygen of di(1-methylheptyl) methylphosphonate and uranyl ions. Isothermal titration calorimetry measurements quantified the extraction thermodynamics, yielding enthalpy changes of -12.83 kJ·mol –1 and -11.32 kJ·mol –1 for tri-n-butyl phosphate and di(1-methylheptyl) methylphosphonate systems, respectively. Di(1-methylheptyl) methylphosphonate exhibits marginally less exothermic enthalpy despite its superior extraction efficiency. The counterintuitive observation suggests distinct thermodynamic compensation mechanisms. This likely involves more favorable entropy contributions in the di(1-methylheptyl) methylphosphonate extraction system and greater energy consumption during desolvation. This comprehensive comparison clarifies fundamental differences in extraction mechanisms between tri-n-butyl phosphate and di(1-methylheptyl) methylphosphonate extractants, providing critical thermodynamic parameters for optimizing 233 U recovery processes.

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Publication Details

Journal
Chinese Journal of Analytical Chemistry
Published
2025-06-27
DOI
https://doi.org/10.1016/j.cjac.2025.100583
Citations
1
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.54
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article

Extraction of uranium (VI) with neutral organic phosphorus extractants: A calorimetric and spectroscopic comparison of di(1-methylheptyl) methylphosphonate vs. tri-n-butylphosphate

Shufeng Zhao, Xiang Li, Jun Tu, Xingliang Li et al.
1 citations
Chinese Journal of Analytical Chemistry
Radioactive element chemistry and processing
0.54
article

Extraction of uranium (VI) with neutral organic phosphorus extractants: A calorimetric and spectroscopic comparison of di(1-methylheptyl) methylphosphonate vs. tri-n-butylphosphate

Shufeng Zhao, Xiang Li, Jun Tu, Xingliang Li, Xiang Xie, Qianxi Zhou, Zeng Huang, Yuyu Liang
article en
1 citations

Abstract

Both tri-n-butyl phosphate and di(1-methylheptyl) methylphosphonate demonstrate exceptional extraction capabilities for 233 U from irradiated thorium. While extensive literature exists regarding tri-n-butyl phosphate-based extraction systems, comparative studies on di(1-methylheptyl) methylphosphonate remain notably limited. This systematic investigation provides a parallel comparison of the chemical behaviors between these two extractants under identical experimental conditions. Results reveal that the di(1-methylheptyl) methylphosphonate system exhibits enhanced hydrophobicity relative to tri-n-butyl phosphate, correlating with reduced water co-extraction during the uranium recovery process. Raman spectroscopic analysis demonstrated about ∼30 cm –1 shifts in the uranyl symmetric stretching vibration for di(1-methylheptyl) methylphosphonate complexes compared to ∼15 cm –1 shifts of tri-n-butyl phosphate complexes. This significant spectral displacement indicates stronger coordination bonding between phosphoryl oxygen of di(1-methylheptyl) methylphosphonate and uranyl ions. Isothermal titration calorimetry measurements quantified the extraction thermodynamics, yielding enthalpy changes of -12.83 kJ·mol –1 and -11.32 kJ·mol –1 for tri-n-butyl phosphate and di(1-methylheptyl) methylphosphonate systems, respectively. Di(1-methylheptyl) methylphosphonate exhibits marginally less exothermic enthalpy despite its superior extraction efficiency. The counterintuitive observation suggests distinct thermodynamic compensation mechanisms. This likely involves more favorable entropy contributions in the di(1-methylheptyl) methylphosphonate extraction system and greater energy consumption during desolvation. This comprehensive comparison clarifies fundamental differences in extraction mechanisms between tri-n-butyl phosphate and di(1-methylheptyl) methylphosphonate extractants, providing critical thermodynamic parameters for optimizing 233 U recovery processes.

Chinese Journal of Analytical ChemistryVol. 53(10)
China Academy of Engineering Physics (CN)
Clean water and sanitation
Openalex Percentile: Top 35%
Radioactive element chemistry and processing
0.54
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