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Oxidative Catalytic Fractionation of Lignocellulosic Biomass under Non-alkaline Conditions.
Luo, Hao; Weeda, Eric P; Alherech, Manar; Anson, Colin W; Karlen, Steven D; Cui, Yanbin; Foster, Cliff E; Stahl, Shannon S.
Afiliación
  • Luo H; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue Madison, Wisconsin 53706, United States.
  • Weeda EP; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue Madison, Wisconsin 53706, United States.
  • Alherech M; D.O.E. Great Lakes Bioenergy Research Center, The Wisconsin Energy Institute, University of Wisconsin-Madison, Madison, Wisconsin 53726, United States.
  • Anson CW; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue Madison, Wisconsin 53706, United States.
  • Karlen SD; D.O.E. Great Lakes Bioenergy Research Center, The Wisconsin Energy Institute, University of Wisconsin-Madison, Madison, Wisconsin 53726, United States.
  • Cui Y; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue Madison, Wisconsin 53706, United States.
  • Foster CE; D.O.E. Great Lakes Bioenergy Research Center, The Wisconsin Energy Institute, University of Wisconsin-Madison, Madison, Wisconsin 53726, United States.
  • Stahl SS; Department of Biochemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
J Am Chem Soc ; 143(37): 15462-15470, 2021 09 22.
Article en En | MEDLINE | ID: mdl-34498845
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Celulosa / Fraccionamiento Químico / Lignina Idioma: En Revista: J Am Chem Soc Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Celulosa / Fraccionamiento Químico / Lignina Idioma: En Revista: J Am Chem Soc Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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