Abstract
In situ optical spectroscopy, spectropotentiometry, and multivariate analysis were applied to the Np(IV) nitrate system to better understand speciation and quantify HNO3 concentration. Thin-layer spectropotentiometry, or spectroelectrochemistry, was leveraged to isolate and stabilize Np(IV) without compromising the solution conditions and generate representative Vis-NIR absorption spectra from 0.5 to 10 M HNO3 and benchmark the corresponding Np(IV) molar absorptivity coefficients. Spectra were described with principal component analysis (PCA) to identify the purest Np(IV) absorbance spectra among other oxidation states [e.g., Np(V/VI)] at each acid concentration and then to identify the primary sources of variance within each Np(IV) spectrum with respect to Np(IV) nitrate complexes. Then, partial least-squares regression (PLSR) and support vector regression (SVR) models were built to predict HNO3 concentration from the Np(IV) spectral data. The nonlinear SVR model outperformed the linear PLSR model for the HNO3 concentration predictions. Finally, the inclusion of spectra collected in edge and center point HNO3 concentrations in the calibration set was determined to be crucial for producing models with strong predictive capabilities. The multivariate approach used in this study makes it possible to quantify HNO3 concentration solely based on Np(IV) absorption spectra, which is essential to quantifying processing streams in various online monitoring applications.
Original language | English |
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Pages (from-to) | 43547-43556 |
Number of pages | 10 |
Journal | ACS Omega |
Volume | 9 |
Issue number | 43 |
DOIs | |
State | Published - Oct 29 2024 |
Funding
Funding for this research was provided by the Science Mission Directorate of NASA and administered by the U.S. Department of Energy, Office of Nuclear Energy, under contract DEAC05- 00OR22725. S.E.G. would like to acknowledge the Glenn T. Seaborg Initiative for support. This work used the facilities and resources at the Radiochemical Engineering Development Center operated by the US Department of Energy\u2019s Oak Ridge National Laboratory. The authors wish to the Cannon Giglio for helpful discussions regarding chemometrics. S.E.G. wishes to thank Samantha Schrell for helpful discussions regarding actinide spectrophotometry. This work was supported by the Pu Supply Program at Oak Ridge National Laboratory.
Funders | Funder number |
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U.S. Department of Energy | |
National Aeronautics and Space Administration | |
Oak Ridge National Laboratory | |
Office of Nuclear Energy | DEAC05- 00OR22725 |
Office of Nuclear Energy |