The corrosion behavior of a Co-Ce alloy containing approximately 15 wt% Ce
has been studied at 600-800 degrees C in several H-2-H2S-CO2 mixtures, prov
iding sulfur pressures of 10(-8) atm at 600, 700 and 800 degrees C and of 1
0(-7) atm at 800 degrees C, and oxygen pressures of 10(-24) atm at 600 degr
ees C and 10(-20) atm at 700 and 800 degrees C. At 600 degrees C, the alloy
corrodes more slowly than pure cobalt but more rapidly than pure cerium wh
ile, at 700 degrees C, it corrodes at about the same rate as pure cerium, b
ut much faster than pure cobalt. At 800 degrees C under 10(-8) atm S-2, i.e
. a value below the stability of the cobalt sulfides, the alloy corrodes ra
ther slowly but, under 10-7 atm St, the rate is very high, although slightl
y lower than that of pure cobalt. The scaring kinetics are generally interm
ediate between linear and parabolic but are sometimes irregular. The corros
ion of this alloy produces multilayered scales, containing an outermost lay
er of almost pure cobalt sulfide, an intermediate complex layer composed of
a mixture of compounds of the two metals and, finally, an innermost region
of internal attack of cerium by both oxygen and sulfur. Cerium is not able
to diffuse outwards and remains in the alloy consumption region. In the in
termediate region cobalt sulfide forms a continuous network which allows th
e growth of the external CoSy layer, although at rates that are reduced wit
h respect to those of pure cobalt. Thus, a cerium content of 15 wt% is not
sufficient to prevent or even to significantly reduce the sulfidation of th
e base metal. These results, as well as the details of the microstructure o
f the scales, are interpreted by taking into account the limited solubility
of cerium in the base metal and the presence of an intermetallic compound,
rich in cerium, in the alloy. (C) 1999 Elsevier Science Ltd. All rights re
served.