G. De La Puente et al., Effects of support surface chemistry in hydrodeoxygenation reactions over CoMo/activated carbon sulfided catalysts, LANGMUIR, 15(18), 1999, pp. 5800-5806
The influence of the nature of the surface of activated carbon supports on
the activity of CoMo/activated carbon sulfided catalysts for hydrodeoxygena
tion of model compounds representative of the composition of pyrolysis oils
has been studied. For this purpose, an activated carbon support was subjec
ted to oxidative treatments with HNO3 at various temperatures to modify its
surface chemistry. Supported sulfided CoMo catalysts on the resulting acti
vated carbons were prepared. These catalysts were tested for hydrodeoxygena
tion of model compounds, 4-methylacetophenone (4MA), ethyl decanoate (ED) a
nd 2-methoxyphenol (GUA), representative of the oxygenated functions that s
hould be eliminated for improving oil stability. The activities of the vari
ous CoMo catalysts for the hydrogenation of the carbonyl group of 4MA were
very similar, and the conversion reached 100% in less than 120 min at 280 d
egrees C and 7 MPa. Introduction of oxygen-containing functional groups to
the carbon supports led to higher decarboxylation in the conversion of the
carboxyl group of ED and higher phenol/catechol selectivity from 2-methoxyp
henol. The surface chemistry of the support determined the precursor/suppor
t interaction and, hence, the nature of the sulfided phases present in the
catalyst after activation. The different natures of the metal sulfides form
ed from the oxide precursors that were bound or not to the oxygen groups on
the carbon supports could be responsible for the differences in selectivit
y displayed by these catalysts. Almost no coking reactions were observed. T
he results suggest that catalytic conversion of oils obtained from biomass
pyrolysis can be controlled and modified by appropriate modifications of th
e surface chemistry of the activated carbon supports.