Abstract
Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) techniques were utilized to study the oxidation behavior of clean uranium surfaces, at very low pressures of various atmospheres (UHV, H2, O2, and CO2), at room temperature. Both for O2 and CO2, a precursor chemisorbed oxygen species has been identified at the very initial stage of the oxidation reaction. This chemisorbed oxygen transforms to the oxide form at a rate which depends on the pressure of the oxidizing atmosphere. Residual gaseous carbon compounds which are present even under UHV conditions result in the simultaneous formation of surface carbide which accompanies the initial stage of oxidation. This carbide however decomposes later as oxidation proceeds. Adventitious hydrocarbon adsorption occurs on the formed oxide layer.
Original language | English |
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Pages (from-to) | 196-200 |
Number of pages | 5 |
Journal | Journal of Nuclear Materials |
Volume | 105 |
Issue number | 2-3 |
DOIs | |
State | Published - 1 Jan 1982 |
ASJC Scopus subject areas
- Nuclear and High Energy Physics
- Materials Science (all)
- Nuclear Energy and Engineering