Simultaneous quantification of uranium(vi), samarium, nitric acid, and temperature with combined ensemble learning, laser fluorescence, and Raman scattering for real-time monitoring

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Abstract

Laser-induced fluorescence spectroscopy (LIFS), Raman spectroscopy, and a stacked regression ensemble was developed for near real-time quantification of uranium(vi) (1-100 μg mL−1), samarium (0-200 μg mL−1) and nitric acid (0.1-4 M) with varying temperature (20 °C-45 °C). LIFS applications range from fundamental lab-scale studies to real-time process monitoring at industrial levels, such as nuclear reprocessing applications, provided the phenomena affecting the fluorescence spectrum are accounted for (e.g., absorption, quenching, complexation). Multiple chemometric models were examined and compared to a more traditional multivariate regression approach called partial least squares (PLS). Results obtained on synthetic samples selected using D-optimal experimental design indicated that a stacked regression method, which included ridge regression, random forest, PLS, and an eXtreme gradient boost algorithm, successfully measured uranium(vi) concentrations directly in nitric acid without measuring luminescence lifetimes or standard addition. The top model resulted in percent root-mean-square error of prediction values of 5.2, 1.9, 3.0, and 2.3% for U(vi), Sm3+, HNO3, and temperature, respectively. The approach may be useful for quantifying fluorescent fission products (e.g., Sm3+) to provide information on burnup of irradiated nuclear fuel. This novel framework reinforces the applicability of LIFS for real-time applications in nuclear fuel cycle applications.

Original languageEnglish
Pages (from-to)4014-4025
Number of pages12
JournalAnalyst
Volume147
Issue number18
DOIs
StatePublished - Aug 8 2022

Funding

This manuscript has been authored by UT-Battelle LLC under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The US government retains and the publisher, by accepting the article for publication, acknowledges that the US 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 US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan ( https://energy.gov/downloads/doe-public-access-plan ). Funding for this work was provided by the National Nuclear Security Administration's (NNSA) Office of Defense Nuclear Nonproliferation Research and Development mission under contract DE-AC05-00OR22725. This work used resources at the Radiochemical Engineering Development Center operated by the US Department of Energy's Oak Ridge National Laboratory (ORNL). The authors wish to thank Alexander Braatz for helpful discussions on nuclear fuel processing. This work was supported by the NNSA and performed at ORNL.

FundersFunder number
Office of Defense Nuclear Nonproliferation Research and Development
U.S. Department of Energy
National Nuclear Security Administration
UT-BattelleDE-AC05-00OR22725

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