Detailed characterization of the thermal transformation of a decant oi
l, obtained from a fluid catalytic cracking (FCC), in a closed system
makes it possible to determine the mode and timing of coke production.
A fast dismutation process into light and heavy liquid products is ob
served, followed by slow production of coke with an activation energy
of only 150 kJ mol-1. From elemental analysis, nuclear magnetic resona
nce (n.m.r.) and mass spectra, dehydrogenation and condensation reacti
ons are detected. These results are well modelled by the pyrolysis of
a set of 1-aryl,2-phenylethylene compounds (aryl = two to four aromati
c rings) under the same conditions. The phenanthrenic derivative prese
nts a similar thermal profile towards coke production. The first steps
are mainly dominated by non-radical processes such as electrocyclic r
eactions.