Four Turkish coals, along with two American coals for comparison, were
liquefied at various temperature-staged conditions in bench-scale mic
roautoclave reactors, 9,10-Dihydrophenanthrene was used as a strong do
nor solvent, and ammonium tetrathiomolybdate was added to some reactio
ns as a catalyst precursor for the in situ generation of a hydrogenati
on catalyst. The combination of a potent hydrogen donor and good catal
yst were sufficient to provide conversions greater-than-or-equal-to 90
% (d.a.f. basis) for all coals in this study. The most important role
of the solvent is in the initial breakdown of the coal. A catalyst is
important for upgrading of the initial products, but it is also active
in promoting hydrogen transfer from the solvent to the coal. For reac
tions of Can lignite in the absence of catalyst, most of the hydrogen
transferred to the coal derives from the solvent; when a sulfided moly
bdenum catalyst is added, most of the hydrogen consumed comes from gas
-phase H2. Oil (hexane-solubles) yield increases linearly with increas
ing hydrogen consumption. The best results in the present study were a
98.8% conversion with 72.2% oil yield, which were obtained with Seyit
Omer lignite with 2:1 solvent:coal ratio, added catalyst, and 30 minu
tes each at 275 and 425-degrees-C.