4.8 Article

Selective conversion of lignin in corncob residue to monophenols with high yield and selectivity

Journal

GREEN CHEMISTRY
Volume 16, Issue 9, Pages 4257-4265

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4gc00620h

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Funding

  1. National Basic Research Program of China (973 program) [2013CB228103]

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The conversion of lignin to monophenols is regarded as a promising approach to produce high-quality biofuel from renewable feedstocks, because of the higher H/C-eff of lignin than that of cellulose and hemicellulose. In this work, the selective conversion of lignin in corncob residue to monophenols was achieved via a two-step process without significant degradation of cellulose. In the first step, the lignin component in corncob residue was selectively degraded to oligomers in the H2O-tetrahydrofuran (THF) (3 : 7, v/v) co-solvent system, and the percentage of delignification reached up to 89.8%. Further reaction of the filtrate in the THF solvent led to further depolymerization of oligomers to monophenols, and the yield of total monophenols reached up to 24.3 wt% without hydrogen addition under the optimized conditions. 4-Ethylphenot (10.5 wt%), 2,6-dimethoxyphenol (6.6 wt%), and 4-ethylguaiacol (4.0 wt%) were the predominant products, which occupied 86.8% of the identified monophenols. This approach achieved high yield and selectivity to monophends directly from corncob residue, simplifying the separation process. The obtained reaction residue with high content of cellulose (83.5%) is possibly a preferable feedstock to produce biofuel such as ethanol by fermentation.

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