This work examines bifunctional catalysts made of an acidic EMT zeolit
e into which Ni and Mo ions were introduced, and then sulfided. Their
structure and catalytic properties were compared to those of analogous
NiMo/HY. Ni and Mo were loaded onto the HEMT by wet treatment, and th
e solids were characterized in the calcined and sulfided state by mean
s of XRD, porosimetry, and TEM coupled with EDX analysis. When the oxi
dic NiMo/EMT was sulfided, the zeolite crystals fractured in a few pla
nar directions, and the fissures appeared to be filled with MoS2 parti
cles promoted with Ni. This is very different to the HY zeolite in whi
ch the sulfide slabs were scattered into the mesopores. With both supp
orts, however about half of the NiMo is present outside the zeolite as
incompletely sulfided particles. The catalytic properties of the sulf
ided NiMo/EMT were examined by measuring the conversion of an n-heptan
e and benzene mixture in a flow reactor under 8 MPa hydrogen pressure.
With the EMT as well as with the HY support, the rate of benzene hydr
ogenation varied in accordance with the amount of internal Mo. The int
rinsic activity of the internal Mo matched that of a commercial NiMo/A
l2O3. The NiMo/zeolites exhibited high activity for the conversion of
heptane, but the cracked products exceeded by far the heptane isomers.
Differences in selectivity between EMT and HY catalysts are interpret
ed on the basis of the balance between acidic and hydrogenation functi
ons. (C) 1998 Academic Press