The hydrocracking properties of Ni, Mo and NiMo sulphides supported on
an ultrastable HY zeolite were examined by studying the hydroconversi
on of n-decane at moderate pressure (3 MPa). All catalysts were found
to deactivate during the first hours on-stream, then reaching almost c
onstant conversion values. Their cracking conversions are significantl
y higher than that of the HY support. A strong imbalance between the h
ydrogenation and the acidic function of catalysts was observed. The pr
oduct selectivities did not depend on the conversion and the secondary
cracking occurred. In the binary NiMo samples no synergetic effect be
tween the individual Ni and Mo phases was observed. A reasonable corre
lation between the n-decane steady-state conversions at 598 K, the sul
phidation degree of the metals and Bronsted acidities of catalysts wer
e found. (C) 1998 Elsevier Science B.V.