A. Takasaki et al., HIGH-TEMPERATURE OXIDATION OF CATHODICALLY HYDROGEN-CHARGED 2-PHASE (TI3AL, TIAL) TITANIUM ALUMINIDES, Metallurgical and materials transactions. A, Physical metallurgy andmaterials science, 25(11), 1994, pp. 2491-2496
Ti-42Al, Ti-45Al, and Ti-50Al (at. pct) titanium aluminides, which wer
e cathodically hydrogen charged in a 5 pet H2SO4 solution for charging
times between 1.8 ks (0.5 hours) and 14.4 ks (4 hours), were oxidized
in a static air under atmospheric pressure at temperatures between 11
70 K (897 degrees C) and 1350 K (1077 degrees C). All the hydrogen-cha
rged alloys, as well as alloys without hydrogen charging, followed par
abolic oxidation kinetics. The weight gains of the alloys after hydrog
en charging for normally less than 3.6 ks (1 hour) were 20 to 30 pct l
ess than those without hydrogen charging. In the alloys charged with h
ydrogen for more than 7.2 ks (2 hours), the weight gains increased wit
h increasing the charging time. The activation energies of oxidation i
ndicated that the oxidation-controlling factor would change after a ch
arging time of 7.2 ks (2 hours) in all the alloys. The decrease in the
activation energies with charging time was more drastic in the Ti-50A
l alloy, which suggested that hydrogen damage, such as cracking, was m
ore severe in the Ti-50Al alloy than in the Ti-42Al or Ti-45Al alloys.
The formation of cracks during hydrogen charging provides titanium-di
ffusion paths and accelerates formation of rutile (TiO2) scale on the
surface of the alloys. The TiO2 on the alloys after hydrogen charging
formed at a comparatively lower temperature than that on the alloys wi
thout charging.