Oxidative Catalytic Fractionation of Lignocellulosic Biomass under Non-alkaline Conditions

• Published in: Journal of the American Chemical Society Vol. 143; no. 37; pp. 15462 - 15470
• Main Authors: Luo, Hao, Weeda, Eric P, Alherech, Manar, Anson, Colin W, Karlen, Steven D, Cui, Yanbin, Foster, Cliff E, Stahl, Shannon S
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 22.09.2021; American Chemical Society (ACS)
• Subjects: 09 BIOMASS FUELS; Biomass; Biopolymers; Catalysis; Catalysts; Cellulose - chemistry; Chemical Fractionation - methods; Hydrogen-Ion Concentration; Lignin - chemistry; Monomers; Organic polymers; Oxidation-Reduction; Populus - chemistry; Wood - chemistry
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.1c08635

Biomass pretreatment methods are commonly used to isolate carbohydrates from biomass, but they often lead to modification, degradation, and/or low yields of lignin. Catalytic fractionation approaches provide a possible solution to these challenges by separating the polymeric sugar and lignin fractions in the presence of a catalyst that promotes cleavage of the lignin into aromatic monomers. Here, we demonstrate an oxidative fractionation method conducted in the presence of a heterogeneous non-precious-metal Co-N-C catalyst and O2 in acetone as the solvent. The process affords a 15 wt% yield of phenolic products bearing aldehydes (vanillin, syring­aldehyde) and carboxylic acids (p-hydroxy­benzoic acid, vanillic acid, syringic acid), complementing the alkylated phenols obtained from existing reductive catalytic fractionation methods. The oxygenated aromatics derived from this process have appealing features for use in polymer synthesis and/or biological funneling to value-added products, and the non-alkaline conditions associated with this process support preservation of the cellulose, which remains insoluble at reaction conditions and is recovered as a solid.