Aqueous Zr/HfIV-Oxo Cluster Speciation and Separation

Abstract

Many industrial separations of chemically-similar elements are achieved by solvent extraction, exploiting differences in speciation and solubility across aqueous-organic interfaces. We recently identified [OM₄(OH)₆(SCN)₁₂]⁴⁻ (OM₄, M=Zr/Hf^IV) tetrahedral oxoclusters as the main species in industrial processes that produce nuclear-grade Zr and Hf from crude ore. However, isostructural/isoelectronic OM₄-oxoclusters do not explain selective extraction of Hf into the organic phase. Here we have characterized heterometal Hf−Zr clusters in solution and the solid-state yielding key information about their fundamentally different chemistry that engenders separation. Clusters prepared with both ammonium (industrial process) and tetramethylammonium counter cations revealed that 1) heterometal clusters (instead of a mixture of homometal clusters) assemble, and 2) Hf-rich OM₄ selectively precipitates over Zr-rich OM₄, providing a separation process that does not require an organic extractant. Mass spectrometry, small-angle X-ray scattering, solution-state ¹H nuclear magnetic resonance (NMR) spectroscopy, and solid-state ¹⁷O NMR evidence both mixed-metal speciation and selective Hf-precipitation. Raman spectroscopy suggests greater Zr-ligand lability than Hf-ligand lability, consistent with higher aqueous solubility of Zr-rich clusters, enabling both extraction and precipitation-based separation. Fundamentally, we also identify a key difference between these chemically similar elements that has enabled diversification of Zr-polyoxocation chemistry over the last decade, while Hf-polyoxocation chemistry lags.