Synthesis and radiometric evaluation of diglycolamide functionalized mesoporous silica for the chromatographic separation of actinides Th, Pa and U

Philip D. Hopkins, Tara Mastren, Justyna Florek, Roy Copping, Mark Brugh, Kevin D. John, Meiring F. Nortier, Eva R. Birnbaum, Freddy Kleitz, Michael E. Fassbender

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

The separation of Th, Pa, and U is of high importance in many applications including nuclear power, nuclear waste, environmental and geochemistry, nuclear forensics and nuclear medicine. Diglycolamide (DGA)-based resins have shown the ability to separate many elements, however, these resins consist of non-covalent impregnation of the DGA molecules on the resin backbone resulting in co-elution of the extraction molecule during separation cycles, therefore limiting their long-term and repeated use. Covalently binding the DGA molecules onto silica is one way to overcome this issue. Herein, measured equilibrium distribution coefficients of normal extraction chromatographic DGA resin and a covalently bound form (KIT-6-N-DGA sorbent) are reported. Several differences are observed between the two systems, the most significant being observed for uranium, which demonstrated significantly lower sorption behavior on KIT-6-N-DGA. These results indicate that U can effectively be separated from Th and Pa using KIT-6-N-DGA, a task that could not be completed with the use of normal DGA alone.

Original languageEnglish
Pages (from-to)5189-5195
Number of pages7
JournalDalton Transactions
Volume47
Issue number15
DOIs
StatePublished - 2018

Funding

This material is based upon work supported by the United States Department of Energy, Office of Science, Office of Nuclear Physics, via an award (Grant FOA LAB 14-1099) from the Isotope Development and Production for Research and Applications subprogram under contract number DE-AC52-06NA253996. We also thank the technical assistance provided by LANL C-IIAC and LANSCE-AOT groups. JF and FK thank the University of Vienna for the support. Pierre Audet (Laval University, Quebec, Canada) is acknowledged for this assistance with the solid state NMR measurements.

FundersFunder number
Office of Nuclear PhysicsFOA LAB 14-1099, DE-AC52-06NA253996
United States Department of Energy
Office of Science

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