Interaction of sulfur model compounds with aliphatic, aromatic and hyd
roaromatic hydrocarbons under various conditions mimicking proposed co
processing techniques are described. Results suggest that aliphatic th
ioether compounds will be much more reactive than aromatic sulfur comp
ounds unless an effective hydrogen supply is present to hydrogenate th
ese compound types. In the absence of an effective hydrogen source, ph
enyl sulfide and benzothiophene underwent retrogressive reactions prod
ucing higher molecular weight products containing new aromatic C-C and
C-S bonds.