Cathodic corrosion of titanium aluminide (TiAl) during hydrogen chargi
ng in various acidic aqueous solutions and in molten salt at 160 degre
es C was studied. At constant potential, the rate of cathodic corrosio
n (V) was much higher than during anodic dissolution, and V increased
linearly with increasing current. V was 10 times higher in the acid so
lution than in the salt solution under the same current. Disruption of
the surface film by local hydride formation during cathodic polarizat
ion was shown to be the key step.