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Selective electrochemical capture and release of uranyl from aqueous alkali, lanthanide, and actinide mixtures using redox-switchable carboranes
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https://doi.org/10.1039/d1sc07070cAbstract
We report the selective electrochemical biphasic capture of the uranyl cation (UO2 2+) from mixed-metal alkali (Cs+), lanthanide (Nd3+, Sm3+), and actinide (Th4+, UO2 2+) aqueous solutions to an organic, 1,2-dichloroethane (DCE), phase using the ortho-substituted nido-carborane anion, [1,2-(Ph2PO)2-1,2-C2B10H10]2- (POCb2-). The reduced POCb2- is generated by electrochemical reduction of the closo-carborane, POCb, prior to mixing with the aqueous mixed-metal solution. Subsequent UO2 2+ release from the captured product, [UO2(POCb)2]2-, was performed by galvanostatic bulk electrolysis of the DCE phase and back-extraction of UO2 2+ to a fresh aqueous phase. The selective capture and release of UO2 2+ was confirmed by combined ICP-OES and NMR spectral analyses of the aqueous and organic phases, respectively, against the newly synthesized nido-carborane complexes, [[CoCp*2][Cs(POCb)]]2, [CoCp*2]3[Nd(POCb)3], [CoCp*2]3[Sm(POCb)3], and [CoCp*2]2[Th(POCb)3].
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