Pure titanium and Ti-6Al-4V were exposed at 750 degrees C in an H-2/H2
O/H2S (P(O2)similar to 10(-18) Pa and P(S2)similar to 10(-1) Pa), H-2/
H2O (P(O2)similar to 10(-18) Pa) and air environments for up to 240 hr
. The corrosion kinetics, obtained by the discontinuous gravimetric me
thod, showed that the sulfidation/oxidation kinetics were linear for T
i and linear-parabolic for Ti-6Al-4V in the H-2/H2O/H2S environment. B
oth materials obeyed parabolic rate laws in the H-2/H2O atmosphere aft
er a transient period, and linear-parabolic rate laws in air. After ex
posure to the H-2/H2O/H2S atmosphere, the titanium specimen displayed
a double scale of TiO2 with an intervening TiS2 film between the doubl
e-layered scale of TiO2 and the substrate. Ti-6Al-4V also contained,a
double layer of TiO2 together with a stratum consisting of Al2S3, TiS2
and vanadium sulfide at the junction of the inner TiO2 layer and subs
trate. Some Al2O3 precipitated in the external portion of the outer Ti
O2 layer. Following oxidation in the low-P-O2 atmosphere a double-laye
red oxide of TiO2 scale formed on both Ti and Ti-6Al-4V. The scale on
Ti-6Al-4V also contained an alpha-Al2O3 film situated between the oute
r and inner (TiO2) layers. For both materials, multilayered scale form
ation characterized air oxidation. In detail a multilayered oxide scal
e of TiO2 formed on the air-oxidized Ti, while a multilayered oxide sc
ale with alternating layers of Al2O3/TiO2 developed on Ti-6Al-4V oxidi
zed in air.