Outer-Sphere Water Clusters Tune the Lanthanide Selectivity of Diglycolamides

Anna G. Baldwin, Alexander S. Ivanov, Neil J. Williams, Ross J. Ellis, Bruce A. Moyer, Vyacheslav S. Bryantsev, Jenifer C. Shafer

Research output: Contribution to journalArticlepeer-review

81 Scopus citations

Abstract

Fundamental understanding of the selective recognition and separation of f-block metal ions by chelating agents is of crucial importance for advancing sustainable energy systems. Current investigations in this area are mostly focused on the study of inner-sphere interactions between metal ions and donor groups of ligands, while the effects on the selectivity resulting from molecular interactions in the outer-sphere region have been largely overlooked. Herein, we explore the fundamental origins of the selectivity of the solvating extractant N,N,N′,N′-tetraoctyl diglycolamide (TODGA) for adjacent lanthanides in a liquid-liquid extraction system, which is of relevance to nuclear fuel reprocessing and rare-earth refining technologies. Complementary investigations integrating distribution studies, quantum mechanical calculations, and classical molecular dynamics simulations establish a relationship between coextracted water and lanthanide extraction by TODGA across the series, pointing to the importance of the hydrogen-bonding interactions between outer-sphere nitrate ions and water clusters in a nonpolar environment. Our findings have significant implications for the design of novel efficient separation systems and processes, emphasizing the importance of tuning both inner- and outer-sphere interactions to obtain total control over selectivity in the biphasic extraction of lanthanides.

Original languageEnglish
Pages (from-to)739-747
Number of pages9
JournalACS Central Science
Volume4
Issue number6
DOIs
StatePublished - Jun 27 2018

Funding

A portion of this research is based upon work supported by the U.S. Department of Homeland Security under Grant Award 2012-DN-130-NF0001. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the official policies, either expressed or implied, of the U.S. Department of Homeland Security (A.G.B. and J.C.S.). A.S.I., B.A.M, and V.S.B. were supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. This research used resources of the National Energy Research Scientific Computing Center, a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract DE-AC02-05CH11231. This material is based upon work supported by the U.S. Department of Energy, Office of Science, Office of Workforce Development for Teachers and Scientists, Office of Science Graduate Student Research (SCGSR) program. The SCGSR program is administered by the Oak Ridge Institute for Science and Education for the DOE under Contract DESC0014664. The United States Government retains and the publisher, by accepting the article for publication, acknowledges that the United States Government retains, a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript, or allow others to do so, for United States Government purposes. The Department of Energy will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).

FundersFunder number
Office of Science Graduate Student Research
SCGSR
U.S. Department of EnergyDESC0014664
U.S. Department of Homeland Security2012-DN-130-NF0001
Office of ScienceDE-AC02-05CH11231
Basic Energy Sciences
Workforce Development for Teachers and Scientists
Oak Ridge Institute for Science and Education
Chemical Sciences, Geosciences, and Biosciences Division

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