Fh. Stott et N. Hiramatsu, Breakdown of protective scales during the oxidation of thin foils of Fe-20Cr-5Al alloys at high temperatures, MATER HIGH, 17(1), 2000, pp. 93-99
The oxidation behaviour of alumina-forming Fe-20Cr-5Al and similar alloys c
ontaining small concentrations of lanthanum or lanthanum plus molybdenum in
air at 1,150 degrees C has been studied, with emphasis on thin (0.05 mm) s
pecimens, where the aluminium reservoir in the substrate is soon depleted t
o a very low value. Oxidation of these alloys involves establishment and gr
owth of protective alumina scales. However, once the residual aluminium con
centration in the alloy drops below a critical level, a layer of chromia is
able to develop and grow at the alumina-alloy substrate interface. Eventua
lly, breakaway oxidation occurs and iron-rich oxides form and engulf the sp
ecimen.
This paper presents some kinetics of oxidation of these alloys and discusse
s the growth and breakdown of the protective scales, drawing on the results
of detailed examinations of the oxidized specimens using analytical scanni
ng and transmission electron microscopy in cross section. It has been shown
that lanthanum increases the time to the onset of breakaway oxidation, pro
bably due to beneficial effects on the mechanical integrity of the scale. M
olybdenum additions have been found to decrease significantly the rate at w
hich breakaway oxides are able to penetrate and engulf the alloy substrate.
Such additions stabilize the ferrite phase in the substrate at the alloy-s
cale interface, thereby maintaining a high rate of diffusion of chromium to
the interface and facilitating establishment of a healing and partially pr
otective chromium-rich oxide layer at the base of the breakaway oxide scale
. In the absence of such additions, depletions of chromium in the substrate
adjacent to the alloy/scale interface, arising from oxidation of chromium,
enable the austenite phase to be stabilized. The relatively low rate of di
ffusion of chromium in this phase allows chromium-rich oxide to form as int
ernal precipitates in the alloy rather than as a continuous, healing layer;
hence, the breakaway oxide scale is able to penetrate and consume the subs
trate more rapidly than in the presence of molybdenum additions.