Pyrolysis behavior of Japanese cedar wood lignin studied with various model dimers

Abstract

Pyrolysis behavior of the milled wood lignin (MWL) isolated from Japanese cedar ( Cryptomeria Japonica) wood was studied in N 2 at 200–400 °C, as compared with the reactivities of various guaiacyl-types of lignin model dimers. The model dimer reactivity varied significantly depending on the structure including phenolic, methylated and linkage types. The C β O cleavage to cinnamyl alcohol-type structure (β-ether linkage) and C γ-elimination to stilbene-type structure (β-aryl linkage) were the major pyrolytic pathways in both dimer and MWL. With increasing the pyrolysis temperature of MWL, condensation, depolymerization and carbonization (formation of a multiple aromatic ring system) started at 250, 350 and 400 °C, respectively, in 1 min pyrolysis. Although methylation of the hydroxyl groups in MWL substantially reduced the condensation reactivity, depolymerization temperature did not change by methylation. By comparing the model dimer reactivity, roles of the linkage-types between phenylpropane-units in lignin were suggested; the phenolic end-group, which would form some conjugated C α C β structures, is important for low-temperature condensation; effective depolymerization of lignin macromolecule is related to the cleavage of the α-ether-linkage in lignin ether chain; reaction of the aromatic ring itself, which includes the O CH 3 homolysis, relates to the carbonization.