Surveying Phase Modifier Functional Groups for Applications to Ln(III) Separations

The application of <i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-tetraoctyl diglycolamide (TODGA) in solvent extraction systems for lanthanide (Ln) separations is well understood. In these systems, the formation of a third phase has motivated the use of phase modifiers to enable higher concentrations of H<sup>+</sup> and Ln common to industrial processes. Several different phase modifiers with applications to diglycolamide (DGA) systems have previously been reported, with a focus on tri-<i>n</i>-butyl phosphate (TBP), <i>N</i>,<i>N</i>'-dihexylactanamide (DHOA), <i>N,N</i>-dioctyl-2-hydroxyacetamide (DOHyA), <i>N</i>,<i>N</i>'-dimethyl-<i>N</i>,<i>N</i>'-dioctylhexylethoxy malonamide (DMDOHEMA), and octanol. While the primary utility of phase modifiers is the increased metal loading, they can have significant effects on the metal distribution ratios, which are well described by the energetics of the extraction process itself. However, the mechanisms by which phase modifiers impact distribution ratios are not generally understood. This work considers the ability of phase modifiers to affect Ln distribution ratios by using phase modifiers with two different functional groups (-Cl and -C≡N) and an octyl alkyl chain in a TODGA and <i>n</i>-dodecane system. Determining the effect of chlorooctane and octane nitrile is important for understanding how phase modifier functional groups and their hydrogen bonding interactions affect Ln extraction. Through combining distribution ratio measurements with organic phase spectroscopic investigations, the impact of chlorooctane and octane nitrile on Ln extraction and their inner-sphere complexes is reported. The addition of either chlorooctane or octane nitrile to TODGA in <i>n</i>-dodecane decreases Ln extraction while maintaining the same inner-sphere Ln complex. The lack of change in inner-sphere Ln-TODGA coordination upon incorporation of phase modifiers and the significant impact of these phase modifiers on distribution ratios suggest the importance of a supramolecular structure. Understanding the role of chlorooctane and octane nitrile on the organic phase structure at longer length scales has been identified as an avenue for future investigations.

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Publication Details

Journal
ACS Omega
Published
2024-11-07
DOI
https://doi.org/10.1021/acsomega.4c06084
Citations
3
Primary Topic
Radioactive element chemistry and processing
Type
article
Field-Weighted Citation Impact
0.48

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article

Surveying Phase Modifier Functional Groups for Applications to Ln(III) Separations

Allison A. Peroutka, Jenifer C. Shafer, Michael J. Servis
3 citations
ACS Omega
Radioactive element chemistry and processing
0.48
article

Surveying Phase Modifier Functional Groups for Applications to Ln(III) Separations

Allison A. Peroutka, Jenifer C. Shafer, Michael J. Servis
article en
3 citations

Abstract

The application of <i>N</i>,<i>N</i>,<i>N</i>',<i>N</i>'-tetraoctyl diglycolamide (TODGA) in solvent extraction systems for lanthanide (Ln) separations is well understood. In these systems, the formation of a third phase has motivated the use of phase modifiers to enable higher concentrations of H<sup>+</sup> and Ln common to industrial processes. Several different phase modifiers with applications to diglycolamide (DGA) systems have previously been reported, with a focus on tri-<i>n</i>-butyl phosphate (TBP), <i>N</i>,<i>N</i>'-dihexylactanamide (DHOA), <i>N,N</i>-dioctyl-2-hydroxyacetamide (DOHyA), <i>N</i>,<i>N</i>'-dimethyl-<i>N</i>,<i>N</i>'-dioctylhexylethoxy malonamide (DMDOHEMA), and octanol. While the primary utility of phase modifiers is the increased metal loading, they can have significant effects on the metal distribution ratios, which are well described by the energetics of the extraction process itself. However, the mechanisms by which phase modifiers impact distribution ratios are not generally understood. This work considers the ability of phase modifiers to affect Ln distribution ratios by using phase modifiers with two different functional groups (-Cl and -C≡N) and an octyl alkyl chain in a TODGA and <i>n</i>-dodecane system. Determining the effect of chlorooctane and octane nitrile is important for understanding how phase modifier functional groups and their hydrogen bonding interactions affect Ln extraction. Through combining distribution ratio measurements with organic phase spectroscopic investigations, the impact of chlorooctane and octane nitrile on Ln extraction and their inner-sphere complexes is reported. The addition of either chlorooctane or octane nitrile to TODGA in <i>n</i>-dodecane decreases Ln extraction while maintaining the same inner-sphere Ln complex. The lack of change in inner-sphere Ln-TODGA coordination upon incorporation of phase modifiers and the significant impact of these phase modifiers on distribution ratios suggest the importance of a supramolecular structure. Understanding the role of chlorooctane and octane nitrile on the organic phase structure at longer length scales has been identified as an avenue for future investigations.

ACS OmegaVol. 9(46)
Argonne National Laboratory (US), Colorado School of Mines (US)
Oak Ridge Institute for Science and Education, Basic Energy Sciences, Workforce Development for Teachers and Scientists, Argonne National Laboratory
Openalex Percentile: Top 42%
Radioactive element chemistry and processing
0.48
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