The mechanism by which high concentrations
(1.5 M in n-dodecane) of N,N-di-2-ethylhexyl-isobutyramide
(DEHiBA) extracts HNO3 and UO2(NO3)2 is under examination. Most prior studies have examined
the extractant and the mechanism at a concentration of 1.0 M in n-dodecane; however, under the higher loading conditions
that can be achieved by a higher concentration of extractant, this
mechanism could change. Increased extraction of both nitric acid and
uranium is observed with an increased concentration of DEHiBA. The
mechanisms are examined by thermodynamic modeling of distribution
ratios, 15N nuclear magnetic resonance (NMR) spectroscopy,
and Fourier transform infrared (FTIR) spectroscopy coupled with principal
component analysis (PCA). Speciation diagrams produced through thermodynamic
modeling have been qualitatively reproduced through PCA of the FTIR
spectra. The predominant extracted species of HNO3(DEHiBA),
HNO3(DEHiBA)2, and UO2(NO3)2(DEHiBA)2 are in good agreement with prior
literature reports for 1.0 M DEHiBA systems. Evidence for an additional
species of either UO2(NO3)2(DEHiBA)
or UO2(NO3)2(DEHiBA)2(HNO3) also contributing to the extraction of uranium species is
given.