Low temperature catalytic conversion of oligomers derived from lignin in pubescens on Pd/NbOPO4

[Display omitted] •lignin-derived oligomers (LDO) obtained from solvothermal conversion of pubescens.•LDO could be converted mainly to monomers, dimers and trimmers on Pd/NbOPO4.•Pd/NbOPO4 catalyzed the selective hydrogenation of side chain and furans.•Low temperature hydrogenolysis avoided repolyme...

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Bibliographic Details
Published in:Applied catalysis. B, Environmental Vol. 263; p. 118325
Main Authors: Fang, Qianying, Jiang, Zhicheng, Guo, Kai, Liu, Xudong, Li, Zheng, Li, Guiying, Hu, Changwei
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 01-04-2020
Elsevier BV
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Summary:[Display omitted] •lignin-derived oligomers (LDO) obtained from solvothermal conversion of pubescens.•LDO could be converted mainly to monomers, dimers and trimmers on Pd/NbOPO4.•Pd/NbOPO4 catalyzed the selective hydrogenation of side chain and furans.•Low temperature hydrogenolysis avoided repolymerization of the intermediates. Two-step conversion of pubescens to aromatic monomers and small molecular weight oligomers (mainly dimers and trimers) was studied. Lignin-derived oligomers (LDO) were obtained by formic acid assisted solvo-thermal conversion of pubescens in the H2O-ethanol system at 160 ℃. In the second step, hydrogenolysis of LDO on Pd/NbOPO4 catalyst was carried out over the temperature range of 60–120 ℃. Pd/NbOPO4 showed acceptable catalytic performance for efficient degradation of oligomers at low temperature. The NbOx species on the catalyst facilitated the breakage of COC bonds to depolymerize the oligomers toward small molecules, while Pd species accelerated the selective hydrogenation of side chain and furans. The esterification of S (Syringol) unit phenols took place simultaneously with the depolymerization of LDO. The hydrogenated mixture at 100 ℃ and reaction time of 20 h had an average molecular weight of 908 g/mol, and the yield of aromatic monomers was 22.4 wt.% based on lignin contained.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2019.118325