The depolymerization
of dealkaline lignin in CH3OH +
H2O mixtures was investigated over various solid acid catalysts,
including commercial zeolites (H-FER, H-MOR, H-Beta, H-USY, and H-ZSM-5)
with predominantly Brønsted acid sites and zirconium-incorporated
mesoporous silicates (Zr-KIT-5 and Zr-KIT-6 with different Si/Zr ratios)
with predominantly Lewis acid sites. Gel permeation chromatography
(GPC) analyses of the product mixture, obtained from half hour batch
reactions on the various catalysts at 250 °C and under a nitrogen
pressure of 0.7 MPa, revealed a clear decrease in the molecular weight
distribution, compared to the parent lignin. The yields of aromatic
monomers (7.5 wt % of the initial lignin) and overall soluble aromatic
species (∼77%) observed over Zr-KIT-5 is higher, compared to
those observed with H-ZSM-5 (4.1% and 67%, respectively) under identical
conditions. Furthermore, the yield of catalyst deposits is lower in
Zr-KIT-5 (14%), compared to H-ZSM-5 (27%). The predominant Lewis acidity
of Zr-KIT-5 appears to reduce aldehyde condensation reactions promoted
by the Brønsted acid sites present in zeolites. However, a lack
of hydrothermal stability of the mesoporous silicates is a drawback
that must be overcome for practical viability.