The sulfidation behavior of two Fe-Ce alloys containing approximately
15 and 30 wt% cerium has been studied at 600-800 degrees C in H-2-H2S
mixtures providing a sulfur pressure of 10(-8) atm. The alloys corrode
more slowly than pure iron, but more rapidly than pure cerium. The su
lfidation rates generally decrease with time and tend to become parabo
lic after an initial stage intermediate between linear and parabolic,
except for Fe-15Ce which corrodes linearly after an initial quasi-para
bolic behavior. Both alloys produce complex scales, containing an oute
rmost layer of practically pure iron sulfide and an inner complex laye
r where the sulfides of both alloy components are simultaneously prese
nt. Finally, a thin region of internal sulfidation of cerium is also g
enerally present in contact with the alloy which is not depleted in ce
rium. Cerium is not able to diffuse out of the alloy consumption regio
n, where it forms a cerium sulfide mixed with iron sulfide. The iron s
ulfide forms a continuous network which allows the growth of the exter
nal FeS layer, even though at rates reduced with respect to pure iron.
Thus, a cerium/content up to 30 wt% is not sufficient to prevent the
sulfidation of pure iron. These results as well as the details of the
microstructure of the scales grown on the two alloys are interpreted b
y taking into account the limited solubility of cerium in the base met
al and the presence of intermetallic compounds in the alloys. (C) 1997
Elsevier Science Ltd.