Intra-lanthanide separation performance of DOTP: Solid-phase extraction and selective precipitation studies

Abstract

The applicability of 1,4,7,10-Tetraazacyclododecane-1,4,7,10-tetra(methylene phosphonic acid) (DOTP) for intra-lanthanide (Ln) separation was investigated through two approaches: the synthesis of inorganic–organic hybrid sorbents and selective precipitation in an aqueous solution. Hybrid sorbents combining zirconium oxide and DOTP were fabricated through post-synthetic grafting and hydrothermal synthesis. The successful syntheses were verified by FTIR and 31P magic-angle spinning (MAS) NMR spectroscopies. All the hybrid sorbents showed a lanthanide uptake of approximately 10–20 μmol/g at pH 3 and displayed only moderate selectivity, with the highest separation factor (SF) of about 10 for Lu3+ over La3+. In contrast, the selective precipitation of lanthanides by DOTP in an aqueous solution was successful in the presence of Cu2+. When a Cu-DOTP complex was introduced into a La/Lu equimolar solution, lanthanide ions were selectively precipitated with an SF of approximately 30–190. When the initial stoichiometry was set to Ln:Cu-DOTP = 8:1, roughly 95 % of the lanthanides in the precipitate were Lu3+, regardless of the pH ranging from 3 to 5. This precipitation process demonstrated selectivity even for adjacent lanthanide pairs. The selectivity is assumed to be a result of structural variations in the precipitates of Ln-Cu-DOTP, which is supported by the characterization results obtained from X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and UV–Vis spectroscopy. The findings presented in this study indicate that DOTP has the potential for use in the selective extraction of lanthanides, which may offer promising advancements in intra-lanthanide separation.