The gasification of biomass is one
of the most prominent technologies
for the conversion of the raw material feedstock to polymers, useful
chemical substances, and energy. The main engineering challenge during
the processing of wastes is the presence of tars in gaseous reaction
products, which could make this operation methodology unsuccessfully
due to the blockage of separating particle filters, fuel line flow,
and substantial transfer losses. Catalytic hydrocarbon cracking appears
to be a promising developing approach for their optimal removal. However,
it is still highly desirable to enhance the catalysts’ activity
kinetics, selectivity, stability, resistance to (ir)reversible coke
deposition, and regeneration solutions. The purpose of this Review
is to provide a comparative systematic evaluation of the various natural,
synthetic, and hybrid ways to convert the model molecular compounds
into benzene, toluene, xylene, (poly)aromatics, syngas, and others.
The recent scientific progress, including calcite, dolomite, lime,
magnesite, olivine, char, nonmetallic activated carbons, supported
alkali, noble, and transition metals, and (metal-promoted) zeolites,
is presented. A special concentrated attention is paid to effectiveness,
related to hydrogenation, peculiar pore structure, and formulations’
suitable acidity. The role of catalysis is described, recommendations
for prospective catalyzed mechanisms are provided, and future technical
feasibility is discussed as well.