Natural gas may be used instead of hydrogen as fuel for the molten car
bonate fuel cell (MCFC) by steam reforming the natural gas inside the
MCFC, using a nickel catalyst (internal reforming). The severe conditi
ons inside the MCFC, however, require that the catalyst has a very hig
h stability. In order to find suitable types of nickel catalysts and t
o obtain more knowledge about the deactivation mechanism(s) occurring
during internal reforming, a series of nickel catalysts was prepared a
nd subjected to stability tests at 973 K in an atmosphere containing s
team and lithium and potassium hydroxide vapours. All the catalysts pr
epared showed a significant growth of the nickel crystallites during t
he test, especially one based on alpha-Al2O3 and a coprecipitated Ni/A
l2O3 sample having a very high nickel content. However, this growth of
nickel crystallites only partially explained the very strong deactiva
tion observed in most cases. Only a coprecipitated nickel/alumina cata
lyst with high alumina content and a deposition-precipitation catalyst
showed satisfactory residual activities. Addition of magnesium or lan
thanum oxide to a coprecipitated nickel/alumina catalyst decreased the
stability. Adsorption and retention of the alkali was the most import
ant factor determining the stability of a catalyst in an atmosphere co
ntaining alkali hydroxides. This is because the catalyst bed may remai
n active if a small part of the catalyst bed retains all the alkali.