4.8 Article

Two-step conversion of Kraft lignin to nylon precursors under mild conditions

Journal

GREEN CHEMISTRY
Volume 22, Issue 14, Pages 4676-4682

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0gc01220c

Keywords

-

Funding

  1. Laboratory Directed Research and Development Program (LDRD) of the Ames Laboratory
  2. U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences
  3. U.S. Department of Energy [DE-AC02-07CH11358]

Ask authors/readers for more resources

This study explores the valorization of Kraft lignin by conversion into nylon precursors in a two-step process. First, lignin was depolymerized in dilute alkaline aqueous solution under atmospheric N(2)at 200 degrees C to give guaiacol with high selectivity (>80%) with a total monomer production of 13% based on lignin input. Solution and solid state NMR analyses and reactions of model compounds indicated that depolymerization took placeviacleavage of beta-O-4 bonds in lignin. In the second step, lignin-derived guaiacol was selectively converted to the nylon precursors cyclohexanol/cyclohexanone (KA oil) using Ru/C catalyst under 1 bar H(2)and 150 degrees C. This two-step process constitutes a low-temperature and low-pressure pathway for producing value-added chemicals from lignin using water as the reaction solvent.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available