With
two independent pore systems (intralayer sinusoidal channels
and interlayer supercages) and external 12 membered-ring (MR) cups, H-MCM-49 was selected as the acidic support for upgrading
palmitic acid to jet-fuel-range hydrocarbons via simultaneous hydro-deoxygenation,
hydrocracking, and hydroisomerization. Compared to other zeolites,
H-MCM-49 showed better selectivity toward cracking and isomerizing
products (C12–C14 alkanes). Postsynthesis
of H-MCM-49 could tailor acidity and catalytic performance to produce
more C12–C14 cracking and isoalkane products.
Ni/H-MCM-49 bifunctional catalysts restrained the acid-catalyzed reactions
to some extent because of enhancement in hydro-deoxygenation over
Ni particles, leading to the decrease in appropriate cracking of C12–C14 alkanes’ and isoalkanes’
selectivity. Ni/H-MCM-49 bifunctional catalysts exhibited excellent
catalytic stability on activity and selectivity of target products,
which opened a novel tailoring pathway over zeolites with independent
pore systems.