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Selective production of arenes via direct lignin upgrading over a niobium-based catalyst

Lignin is the only large-volume renewable source of aromatic chemicals. Efficient depolymerization and deoxygenation of lignin while retaining the aromatic functionality are attractive but extremely challenging. Here we report the selective production of arenes via direct hydrodeoxygenation of organ...

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Detalles Bibliográficos
Autores principales: Shao, Yi, Xia, Qineng, Dong, Lin, Liu, Xiaohui, Han, Xue, Parker, Stewart F., Cheng, Yongqiang, Daemen, Luke L., Ramirez-Cuesta, Anibal J., Yang, Sihai, Wang, Yanqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527281/
https://www.ncbi.nlm.nih.gov/pubmed/28737172
http://dx.doi.org/10.1038/ncomms16104
Descripción
Sumario:Lignin is the only large-volume renewable source of aromatic chemicals. Efficient depolymerization and deoxygenation of lignin while retaining the aromatic functionality are attractive but extremely challenging. Here we report the selective production of arenes via direct hydrodeoxygenation of organosolv lignin over a porous Ru/Nb(2)O(5) catalyst that enabled the complete removal of the oxygen content from lignin. The conversion of birch lignin to monomer C(7)–C(9) hydrocarbons is nearly quantitative based on its monomer content, with a total mass yield of 35.5 wt% and an exceptional arene selectivity of 71 wt%. Inelastic neutron scattering and DFT calculations confirm that the Nb(2)O(5) support is catalytically unique compared with other traditional oxide supports, and the disassociation energy of C(aromatic)–OH bonds in phenolics is significantly reduced upon adsorption on Nb(2)O(5), resulting in its distinct selectivity to arenes. This one-pot process provides a promising approach for improved lignin valorization with general applicability.