The catalytic behavior of Al-promoted sulfated zirconia for n-butane i
somerization at low temperature in the absence of H-2 and at high temp
erature in the presence of H2 was studied. The addition of Al enhances
the activity and stability of the catalysts for reaction at 250 degre
es C and in the presence of H-2 significantly. After on stream for 120
h, the n-butane conversion of the catalyst containing 3 mol% Al2O3 ke
eps steadily at 88% of its equilibrium conversion and no observable tr
end of further deactivation has been observed. The difference in behav
ior of the promoted and unpromoted catalysts at low and high temperatu
re is associated with a change of reaction mechanism from bimolecular
to monomolecular. Experimental evidence is presented to show that the
promoting effect of Al is different from that of the transition metals
. Microcalorimetric measurements of NH3 adsorption on catalysts reveal
that the remarkable activity and stability of the Al-promoted catalys
ts are caused by an enhancement in the number of acid sites effective
for the isomerization reaction.