Abstract
Electron-probe microanalysis of uranium and uranium alloys poses several problems, such as rapid oxidation, large poorly constrained correction factors, and a large number of characteristic x-ray lines. We show that U-metal can grow 10 nm of oxide within ~20 s of air exposure, increasing to 15–20 nm within a few minutes, which can produce a 30% quantification error at 5 kV. A 15 nm carbon coating on the UO2 reference material also produces an ~30% quantification error of the uncoated but surface oxidized U sample at 5 kV. Correcting for both the coating and oxide improved the analysis accuracy to better than ±1% down to 7 kV and ~2% at 5 kV, but the error increases strongly below this. The measurement of C in U identified a previously unreported U N6–O4 line interference on the C Kα peak, which can produce over 1% error in the analysis total. Oxide stoichiometry was demonstrated to have only a small impact on quantification. The measurement of the O Kα and U Mα mass absorption coefficients in U as 9,528 and 798 cm2/g, respectively, shows good agreement with recently published values and also produces small differences in a quantification error.
Original language | English |
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Pages (from-to) | 466-483 |
Number of pages | 18 |
Journal | Microscopy and Microanalysis |
Volume | 27 |
Issue number | 3 |
Early online date | 18 Mar 2021 |
DOIs | |
Publication status | Published - 18 Mar 2021 |
Bibliographical note
Funding Information:The authors thank Dr. John Spratt of the Natural History Museum, London, for providing the synthetic UO that was used as a reference material for the uranium analyses in this study. This research forms part of a doctoral study on the EPMA of Nuclear Materials funded by the AWE and carried out at the University of Bristol 2
Publisher Copyright:
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of the Microscopy Society of America.
Keywords
- carbon
- EPMA
- mass absorption coefficient
- uranium