4.6 Article

Chemical Transformations of Poplar Lignin during Cosolvent Enhanced Lignocellulosic Fractionation Process

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 6, Issue 7, Pages 8711-8718

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.8b01028

Keywords

Biomass recalcitrance; Cosolvent Enhanced Lignocellulosic Fractionation; Antioxidant; Lignin valorization

Funding

  1. U.S. Department of Energy (DOE) [DE-EE0007006]
  2. Center for Bioenergy Innovation (CBI)
  3. Office of Biological and Environmental Research in the DOE Office of Science
  4. DOE

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Converting lignocellulosic biomass to biofuels and bio-products is significantly hindered by the innate recalcitrance of biomass to chemical and biological breakdown, and it usually requires a pretreatment stage in order to improve conversion yields. A promising novel pretreatment named Cosolvent Enhanced Lignocellulosic Fractionation (CELF) involving dilute acid treatment of biomass in a THE-water mixture was recently developed to overcome biomass recalcitrance. Detailed elucidation of physicochemical structures of the fractionated lignin that is precipitated from CELF pretreatment of hardwood poplar, also called CELF lignin, reveals transformations in its molecular weights, monolignol composition, and hydroxyl group content. Isolated CELF lignin revealed dramatic reductions in its molecular weight by up to similar to 90% compared with untreated native lignin. Furthermore, CELF lignin's beta-O-4 interunit linkages were extensively cleaved after CELF pretreatment as indicated by a semiquantitative HSQC NMR analysis. This is further evidenced by a P-31 NMR analysis showing a significant decrease in aliphatic OH groups due to the oxidation of lignin side chains, whereas the content of total phenolic OH groups in CELF lignin significantly increased due to cleavage of interunit linkages. In conclusion, the CELF process generated a uniquely tunable and highly pure lignin feedstock of low content aryl ether linkages, low molecular weight, and high amount of phenolic hydroxyl groups, suitable for its development into fuels, chemicals, and materials.

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