In this paper we demonstrate the use of variable temperature deuterium
line shape and relaxation time studies to characterise the modificati
on to adsorption sites and thermally activated inter-site jump process
es occurring within zeolite HY at various stages during coke depositio
n. In the examples presented here the adsorption and transport propert
ies of probe benzene molecules are studied. Coke was produced using tw
o different feed molecules; ethanol and n-hexane. The data presented s
how that the extent to which the sites for benzene adsorption are modi
fied during coking depends both on the time-on-stream and the nature o
f the feed molecule producing the coke. The results suggest that coke
produced by ethanol deactivates the zeolite by selective coverage of o
ne of the two types of site initially available for benzene adsorption
. After 15 h on stream there is evidence that the effective co-ordinat
ion of the pore network has been reduced from 4 to 3.4. In contrast, d
eactivation by n-hexane cracking causes deposition of coke within the
pore structure which blocks adsorption of probe molecules onto the nat
ive adsorption sites of the zeolite.