Abstract
AbstractTri‐n‐butyl phosphate (TBP), a universally recognized solvent, has got lesser organic phase splitting or third phase formation tendency during the extraction of U(VI) as compared to tetravalent metal ions. Thus, the lighter members of trialkyl phosphates (TalP) (i. e.) tri‐n‐propyl phosphate (TPP) and triethyl phosphate (TEP) having higher third phase formation tendency would provide an opportunity to comprehend the aggregation of U(VI) loaded TalP solvents. As the above lighter TalPs exhibit higher aqueous solubility, the conventional measurement of third phase limit or Limiting Organic Concentration (LOC) by mixing organic and aqueous phases cannot be employed for the investigation of U(VI) third phase in TalPs. This has led to the development of a novel method to examine U(VI) third phase in aqueous soluble TalP solvent systems without aqueous feed solution. After validation, the newly developed method has then been utilized to determine the LOC for 1.1 M TPP in n‐alkane. The variation of extractant structure, diluent chain length, nature of metal ion and temperature on the third phase of 1.1 M TalP systems has been evaluated along with their molecular level understanding using Dynamic Light Scattering.
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