The pyrolysis of vanillin (3-methoxy-4-hydroxy-benzaldehyde) was studied to
determine the reaction pathways that lead to the formation of aromatics an
d to establish an empirical kinetic model. Molecular beam mass spectrometry
and multivariate data analysis were used to follow the complicated pyrolys
is chemistry and to determine quantitative kinetic parameters of aromatic h
ydrocarbon formation. The pyrolysis of vanillin is modeled as a lumped, two
-step, sequential process. Possible identification of reaction intermediate
s is discussed utilizing known reaction mechanisms and thermochemistry for
anisole (C6H5OCH3) phenol (C6H5OH), and benzaldehyde (C6H5CHO). (C) 2001 El
sevier Science Ltd. All rights reserved.