Sm. Richardson et al., INITIAL COKE DEPOSITION ON A NIMO GAMMA-AL2O3 BITUMEN HYDROPROCESSINGCATALYST/, Industrial & engineering chemistry research, 35(11), 1996, pp. 3940-3950
Athabasca bitumen was hydrocracked over a commercial NiMo/gamma-Al2O3
catalyst in two reactors, a microbatch reactor and a 1-L continuous st
irred tank reactor (CSTR). Coke deposition on catalyst was measured as
a function of hydrogen pressure, time on stream, and liquid compositi
on by measuring the carbon content of the cleaned spent catalyst. The
carbon content ranged from 11.3% to 17.6% over the pressure range 6.9-
15.2 MPa in CSTR experiments. Batch and CSTR experiments showed a rapi
d approach to a constant coke content with increasing oil/catalyst rat
io. Coke deposition was independent of product composition for residue
concentrations ranging from 8% to 32% by weight. Removal of the coke
by tetralin at reaction conditions suggested reversible adsorption of
residue components on the catalyst surface. A physical model based on
clearance of coke by hydrogen in the vicinity of metal crystallites is
presented for the coke deposition behavior during the first several h
ours of hydrocracking use. This model gives good agreement with experi
mental data, including the effect of reaction time, the ratio of total
feed weight to catalyst weight, hydrogen pressure, and feed compositi
on, and it agrees with general observations from industrial usage. The
model implies that except at the highest coke levels the active surfa
ces of the metal crystallites remain exposed. Severe mass-transfer lim
itations are caused by the overall narrowing of the pore structure, wh
ich in gamma-Al2O3 would give very low effective diffusivity for resid
uum molecules in micropores.