Accomplishing simple, solubility-based separations of rare earth elements with complexes bearing size-sensitive molecular apertures.
basic_science · Level V
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- Record sourced from PubMed, PMID 27956636.
- Also identified by DOI 10.1073/pnas.1612628113 and PMC identifier 5206573.
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Abstract
Rare earth (RE) metals are critical components of electronic materials and permanent magnets. Recycling of consumer materials is a promising new source of rare REs. To incentivize recycling, there is a clear need for the development of simple methods for targeted separations of mixtures of RE metal salts. Metal complexes of a tripodal hydroxylaminato ligand, TriNOx<sup>3-</sup>, featured a size-sensitive aperture formed of its three η<sup>2</sup>-(N,O) ligand arms. Exposure of cations in the aperture induced a self-associative equilibrium comprising RE(TriNOx)THF and [RE(TriNOx)]<sub>2</sub> species. Differences in the equilibrium constants K<sub>dimer</sub> for early and late metals enabled simple separations through leaching. Separations were performed on RE1/RE2 mixtures, where RE1 = La-Sm and RE2 = Gd-Lu, with emphasis on Eu/Y separations for potential applications in the recycling of phosphor waste from compact fluorescent light bulbs. Using the leaching method, separations factors approaching 2,000 were obtained for early-late RE combinations. Following solvent optimization, >95% pure samples of Eu were obtained with a 67% recovery for the technologically relevant Eu/Y separation.