Hydrocracking of 1-methylnaphthalene
to benzene (B), toluene (T),
and xylene (X) was performed over a series of bi-functional catalysts
(W/Beta) at 420 °C and 6 MPa. The reaction results and kinetic
study indicated that metal–acid balance (metal–acid
interaction and metal–acid ratio) and metal dispersion had
a great impact on the cracking, hydrogenation, and selective hydrogenation
activity, which directly determine the BTX yield. An inappropriate
metal–acid ratio would lead to producing plenty of intermediates
or by-products, and poor metal dispersion would result in low hydrogenation
activity. However, good metal dispersion usually accompanies the strong
metal–acid interaction, which reduces the sulfidation of metal.
In this work, a new tungsten precursor, W-complex, was used to prepare
the catalysts with good dispersion of metal oxides and high hydrogenation
activity. The external surface acidity of zeolite was modified to
regulate the metal–acid interaction by forming a layer of SiO2 on acid sites through chemical liquid deposition.