Uranium and U–Zr and U–Ru alloy corrosion rates in the transpassive state
Electrochemical studies of reactor-grade uranium metal and its alloys with Zr and Ru in neutral electrolyte (0.1 M NaClO 4, pH 3.0–9.0) in the potential region close to uranium's transpassivation threshold were performed. Transpassivation potentials from 320 mV/Ag/AgCl (U–1.3 at.% Zr) to 470 mV...
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Veröffentlicht in: | Journal of alloys and compounds 2007-10, Vol.444, p.345-351 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Electrochemical studies of reactor-grade uranium metal and its alloys with Zr and Ru in neutral electrolyte (0.1
M NaClO
4, pH 3.0–9.0) in the potential region close to uranium's transpassivation threshold were performed. Transpassivation potentials from 320
mV/Ag/AgCl (U–1.3
at.% Zr) to 470
mV (U–10.5
at.% Ru) were found to be weakly affected by added alloying element concentration and electrolyte pH. Comparison of
I–
t curves registered on U metal, U–1.3
at.% Zr, and –1.2
at.% Ru electrodes indicate that the electrochemical oxidation rate of alloyed uranium was lower than that of pure U metal. The difference of the electrochemical oxidation rates was dependent on electrolyte pH. The calculated corrosion rates of uranium metal and alloy increased from 0.89
mg
cm
−2
h
−1 (U–1.3
at.% Zr,
E
=
300
mV/Ag/AgCl) to 40.4
mg
cm
−2
h
−1 (U metal,
E
=
600
mV/Ag/AgCl) and were found to be independent of alloy addition and electrolyte pH. The contribution of spallation of non-oxidized uranium species from the electrode surface to the observed corrosion rates was made. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2007.06.078 |