Recent advancements in micro-flow technologies and a drive toward more efficient, greener and safer processes have led to a renaissance in flow-chemistry for pharmaceutical production.
A poly(phenylene
sulfide) (PPS) catalytic membrane (PPSCM) was
prepared through a heterogeneous sulfonation of PPS nonwoven fabrics
with sulfur trioxide (SO3) as a sulfonation agent under
mild conditions to catalyze the reaction of oleic acid with methanol
in a flow-through mode. The results of X-ray photoelectron spectrometer
(XPS) proved that each repeated unit of PPS on the fiber surface was
attached to one sulfonic acid group. The hydrogen ion-exchange capacity
(IEC) of the PPSCM increased with SO3 concentration and
hardly changed with reaction time. As the IEC increased, the specific
surface area of the PPSCM became 2 orders of magnitude higher than
that of the fabrics before sulfonation and the pore size and mechanical
properties of the PPSCM were decreased. The PPSCM was used in the
continuous esterification reaction of oleic acid with methanol in
a flow-through mode. The conversion reached a maximum of 98.0% under
the conditions of the reaction temperature of 65 °C, the residence
time of 2104 s, and the methanol/oleic acid mass ratio of 3:1. Moreover,
the PPSCM showed good catalytic stability with a conversion of above
95% for 50 h in a flow-through mode. The results indicated that the
PPSCM was a promising solid-acid catalyst for biodiesel production.
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