The cyclic-oxidation behavior of (in w/o) Ti-36Al, Ti-35Al-0.1C, Ti-35
Al-1.4V-0.1C and Ti-35Al-5Nb-0.1C was studied between 800 and 1000-deg
rees-C in air. A few experiments were also performed in oxygen. Scale
spallation after oxidation in air occurs during cooling on TiAl, TiAl-
C, and TiAl-V at or close to the metal/scale interface when a critical
scale thickness has been achieved This process repeats and can lead t
o a stratified scale. These three materials form scales composed of an
inward-growing fine-grain mixture of TiO2-Al2O3 and an outward-growin
g coarse-grain TiO2 layer or TiO2 + Al2O3 mixture. The TiAl-Nb alloy h
ad a significantly different behavior. The scale on this material grew
very slowly because a protective Al2O3 layer formed at the metal/scal
e interface. This behavior resulted in much better resistance to spall
ation because the critical scale thickness was reached only after a mu
ch longer time, and is different from the behavior of the other three
alloys. Oxidation in air leads to slight nitridation of the subsurface
zone beneath the scale. In comparison to oxidation in air, oxidation
in oxygen improves the cyclic-oxidation behavior. Whereas the scale fo
rmed in air was uniformly thick over the entire surface, the scale gro
wn in oxygen varied locally in structure and thickness. A large fracti
on of the surface was covered with a thin Al2O3 layer, while the remai
ning part formed a two-layer scale similar to that formed in air. The
results are discussed briefly in the light of a recently published mod
el for scale spallation under compressive stress, however, quantitativ
e estimations are not possible due to a lack of relevant data.