The influence of the acid sites in the hydrodeoxygenation
of anisole
performed over Ni catalysts supported on SBA-15 modified with metal
oxides (Ni/M-SBA-15, M = Ti, Zr, Al, or Nb) was demonstrated. Catalysts
were characterized by SEM–EDX, nitrogen physisorption, XRD,
UV–visible DRS, TPR, TPD of ammonia, IR-Py, O2 chemisorption,
and high-resolution transmission electron microscopy. The mesoporous
structure and the hexagonal arrangement of the supports were maintained
in the catalysts. Ni catalysts supported on modified M-SBA-15 exhibited
a higher metal-support interaction, an increase in the acidity and,
as a consequence, improved selectivity to cyclohexane. The deoxygenation
reaction rate constants increased as Ni/SBA-15 < Ni/Ti-SBA-15 <
Ni/Nb-SBA-15 < Ni/Zr-SBA-15 < Ni/Al-SBA-15, which is attributed
to the increase in the amount and strength of acid sites, especially
of the Brønsted ones, which promotes the cleavage of the C–O
bond. It is also important to keep the metal/acid sites together to
obtain high activity and selectivity to hydrodeoxygenated products.