Non-catalytic
hydrogenation with a hydrogen donor is a beneficial
way for effective conversion of asphaltene to distillate with minimal
coke formation. In this work, detailed product distribution, which
includes gas, light oil [initial boiling point (IBP)–350 °C],
middle oil (350–540 °C), heavy oil (>540 °C),
asphaltene,
and coke, obtained from non-catalytic hydrogenation of asphaltene
with tetralin as a hydrogen donor, was investigated in an autoclave.
The effects of reaction conditions, including reaction time, reaction
temperature, and hydrogen donor/asphaltene weight ratio, on asphaltene
conversion, detailed product distribution, liquid product yield, and
liquid product selectivity were studied. Results showed that through
controlling the reaction condition, asphaltene conversion and total
liquid yield reached 72.72 and 70.34 wt %, respectively, and produced
only 2 wt % coke and 0.34 wt % gas. We then developed a seven-lump
kinetic model, including an active hydrogen lump to describe the reaction
behaviors of asphaltene hydroliquefaction. Activation energies ranged
from 106.07 to 237.50 kJ mol–1. The activation energies
of the main reaction that asphaltene decomposed and hydrogenated by
active hydrogen to produce heavy oil and middle oil were 106.07 and
109.06 kJ mol–1, respectively, which were lower
than those of thermal cracking. The activation energy of distillate
formation from active hydrogen combined with macromolecule radicals
was 143.78 kJ mol–1. The detailed product yield
predicted by the developed seven-lump kinetic model exhibited good
consistency with the experimental data.