AbstractRemoval of actinides (trivalent, tetravalent and hexavalent) from nitric acid medium was studied using solid-liquid extraction technique employing polymeric encapsulated beads (PEBs) using an indigenously synthesized, unexplored novel monoamide, N,N′-bis(2-ethyl hexyl) α-hydroxy acetamide (BEHGA). The PEBs were synthesized by phase inversion technique. The structure and morphology of the synthesized PEBs were evaluated by employing various characterization techniques like FT-IR, TGA and SEM. The well characterized PEBs were studied for its Am(III), Pu(IV) and U(VI) sorption behavior from nitric acid medium. Kinetics studies showed that the sorption is fast with equilibrium being reached within 60 min of equilibration. The sorption mechanism follows pseudo-second-order mechanism with intraparticle diffusion playing an important role. Langmuir isotherm model was found to best describe the sorption isotherm. The maximum Am(III) sorption capacity of the PEBs was found to be 8.45 mg/g (experimental) and 8.43 mg/g (Langmuir). Back extraction was possible using 0.5 M HNO3. Stability of the PEBs was found to be quite good with no significant structural deformation or leaching out of the extractant in 4.0 M HNO3solution for at least up to 8 days.

An unexplored novel monoamide N,N′-bis(2-ethyl hexyl) α-hydroxy acetamide (BEHGA) was used as a carrier for transport of Am(III), Eu(III), Pu(IV/VI) and U(VI) from HNO3 medium across a supported liquid membrane (SLM). Various parameters were investigated to obtain the optimum transport conditions. Transport rates followed the trend Pu(IV)>Am(III)≥Eu(III)>U(VI)> Pu(VI). The effects of macro concentrations of U(VI) and Nd(III) on the transport rate of Am(III) were studied. The diffusion coefficient value for the Am(III)-BEHGA system in HNO3 medium was found to be ~1.8×10−6 cm2/s. The standard deviation of the results obtained from transport experiments by this extractant was found to be ±5%. The membrane was found to be highly selective for actinides and lanthanides with respect to different fission products.

Oxidative decarbonylation of the complexes (I) gives the trioxometal(VI) compounds (II), which react with transition metals to yield the complexes (IV), (VIII) and the polymeric compound (VI) (yields given in g).

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