4.6 Article

Organosolv Fractionation of Walnut Shell Biomass to Isolate Lignocellulosic Components for Chemical Upgrading of Lignin to Aromatics

Journal

ACS OMEGA
Volume 6, Issue 12, Pages 8142-8150

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.0c05936

Keywords

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Funding

  1. University of California, Santa Barbara (UCSB)
  2. Edison International
  3. UCSB McNair for an Undergraduate Summer Research Fellowship
  4. Mellichamp Initiative for Sustainable Manufacturing graduate fellowship

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Research on utilizing lignocellulosic biomass, such as walnut shell, for renewable carbon sources is rapidly growing. By isolating protected walnut shell lignin using methanol and dilute sulfuric acid with formaldehyde as a protecting group at 170 degrees C, a 64% yield was achieved, showing potential for high value product production.
Renewable carbon sources are a rapidly growing field of research because of the finite supply of fossil carbon. The lignocellulosic biomass walnut shell (WS) is an attractive renewable feedstock because it has a high lignin content (38-44 wt %) and is an agricultural waste stream. Lignin, a major component of lignocellulosic biomass that is currently a waste stream in pulping processes, has unique potential for chemical upgrading because its subunits are aromatic. In the interest of improving the sustainability and reducing the environmental impact of biomass processing, valorization of agricultural waste streams is important. Herein, three lab-scale, batch organosolv procedures are explored in the interest of optimal isolation of protected WS lignin (WSL). One system uses acetic acid, one MeOH, and the final EtOH as the primary solvent. The optimal condition for protected WSL isolation, which resulted in a 64% yield, was methanol and dilute sulfuric acid with formaldehyde to act as a protecting group at 170 degrees C. Select samples were upgraded by hydrogenolysis over a nickel catalyst. Protected lignin recovered from the optimal condition showed 77% by weight conversion to monomeric phenols, demonstrating that the protected WSL can selectively afford high value products. One key finding from this study was that MeOH is a superior solvent for isolating WSL versus EtOH because the latter exhibited lignin recondensation. The second was that the Ni/C-catalyzed reductive catalytic fractionation (RCF) directly of WS biomass was not selective relative to RCF of isolated WSL; conversion of raw WS to monomers produced significantly more side products.

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