E. Jakab et al., THERMAL-DECOMPOSITION OF WOOD AND CELLULOSE IN THE PRESENCE OF SOLVENT VAPORS, Industrial & engineering chemistry research, 36(6), 1997, pp. 2087-2095
The thermal decomposition of white birch wood and filter pulp was stud
ied in water and methanol vapor at 2 MPa pressure in a flow-through re
actor. The abundance of the volatile products was monitored by on-line
GC/MS using repetitive sampling in combination with fast separation o
n a short capillary column. The reactor was heated to 400 degrees C at
20 degrees C/min and the intensity profile of the product ions within
the 30-200 amu range recorded. The system was capable of separating t
he profiles of typical hemicellulose products evolved at lower tempera
ture from the characteristic cellulose and lignin products detected fr
om wood. Char yields in methanol were similar to those in an inert gas
atmosphere; however, the presence of water markedly increased the amo
unt of char produced. The product distribution of cellulose was strong
ly affected by the solvents. In methanol, pyran derivatives dominate b
esides levoglucosan and glycolaldehyde, whereas the relative abundance
of 2-furaldehyde and 5-(hydroxymethyl)-2-furaldehyde increased in the
presence of water. Water catalysis was also indicated by lowering the
decomposition temperatures of cellulose. High-pressure (6.5 MPa) ther
mogravimetric experiments in helium or hydrogen atmospheres were also
found to lower the reaction temperature of wood. This observation can
be explained by the catalytic effect of reaction water released during
the thermal decomposition of wood.