Investigating Np(VI) Nitrate Speciation Control through Temperature and Optical Spectroscopy

Numerous areas of nuclear processing, such as radioisotope production, nuclear waste remediation, and separations, depend upon the speciation of f-elements in the solution state. However, fundamental knowledge of the actinidesparticularly Nplags behind most of the elements on the periodic table. Despite the importance of Np-(VI) chemistry in separations and nuclear processing, its speciation in HNO(3) remains uncertain. This work addresses some of these gaps by investigating the effect of HNO(3) concentration and temperature on the spectra and speciation of the Np-(VI) nitrate system. Six samples of Np in 1 to 10 M HNO(3) were prepared and treated with (NH(4))(2)[Ce-(NO(3))(6)] to stabilize the hexavalent oxidation state. The absorbance spectrum of the 10 M HNO(3) is drastically different from the spectra of the other samples; the 10 M spectrum indicates coordination of nitrate ligands to the Np-(VI)-O(2) (2+) ion to form a complex with high symmetry. Additionally, absorbance spectra were recorded over the temperature range of 15 to 40 °C, and systematic increases and decreases in certain spectral features of the ultraviolet-visible (UV-vis)-near-infrared (NIR) spectra are present in the spectra. The difference in spectral features suggests that Np-(VI) nitrate speciation depends on temperature. Dilution studies of this sample were monitored with UV-vis-NIR and Raman spectroscopies. Spectral data indicate the presence of multiple complexes with different symmetries, including a high-symmetry complex with an inversion center. As samples are diluted and aquo ligands replace nitrate ligands bound to the Np-(VI) neptunyl cation, changes in spectroscopic signals indicate a decrease in the high-symmetry nitrate complex and an increase in the lower-symmetry aquo complex. Additionally, the Raman band associated with the Np-(VI)-O(2) (2+) symmetric stretch broadens with dilution and is fitted with two peaks. These peaks are assigned to Np-(VI) aquo and nitrato complexes, indicating that this vibrational mode is sensitive to the coordination environment of the Np-(VI) neptunyl cation and that contributions from these two Np-(VI) complexes can be distinguished. This unique experimental data could be used to advance computational models describing the electronic transitions of complex actinyl ions.