Thorium metal-organic framework crystallization for efficient recovery from rare earth element mixtures

Madeleine A. Gaidimas, Courtney S. Smoljan, Zi Ming Ye, Charlotte L. Stern, Christos D. Malliakas, Kent O. Kirlikovali, Omar K. Farha*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Rare earth (RE) elements are critical materials that underpin many modern technologies, particularly in the clean energy industry. Despite their importance, these vital resources are difficult to obtain due to the presence of numerous metals and radioactive contaminants, such as thorium, that are present in RE ores. Current processing methods, which are dominated by homogeneous solvent extraction, are inefficient and produce substantial hazardous waste. In this work, we describe an alternative strategy to separate thorium from REs through metal-organic framework (MOF) crystallization. Starting from a mixture of thorium and rare earth ions in solution, we utilize the simple carboxylate ligand trimesic acid to selectively crystallize a novel thorium MOF, NU-2500, leaving the remaining rare earth ions in solution. By leveraging the increased oxophilicity of Th(iv) compared to RE(iii) ions, we observe the exclusive formation of the thermodynamically preferred Th-MOF product. This valence-selective crystallization strategy occurs rapidly (within 30 minutes) at mild temperatures (80 °C) with an environmentally-friendly ethanol/water solvent system to produce phase-pure NU-2500 containing >98% molar fraction of thorium. Sequestering the radioactive Th(iv) ions within a solid framework enables facile separation of REs through simple filtration. We demonstrate that our selective crystallization platform retains its high selectivity for Th crystallization even at low initial Th concentrations and in complex mixtures with multiple different REs. We anticipate that further insights into the kinetics and thermodynamics of MOF crystallization can be applied to additional challenging industrial separations.

Original languageEnglish (US)
Pages (from-to)3895-3903
Number of pages9
JournalChemical Science
Volume16
Issue number9
DOIs
StatePublished - Jan 31 2025

Funding

The authors gratefully acknowledge financial support from the Army Research Office (award number W911NF2020136) and the Defense Threat Reduction Agency (HDTRA1-19-1-0007). M. A. G. and C. S. S. gratefully acknowledge support from the Ryan Fellowship and the International Institute for Nanotechnology (IIN) at Northwestern University. This work made use of the IMSERC Crystallography facility at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-2025633), and Northwestern University. Metal analysis was performed at the Northwestern University Quantitative Bio-element Imaging Center (QBIC). M. A. G. would like to thank Rebecca Sponenburg from QBIC for her guidance with ICP-OES measurements. This work also made use of the EPIC facility of Northwestern University's NUANCE Center, which has received support from the SHyNE Resource (NSF ECCS-2025633), the IIN, and Northwestern's MRSEC program (NSF DMR-2308691).

ASJC Scopus subject areas

  • General Chemistry

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