Affiliation:
1. Deconstruction Division Joint BioEnergy Institute Emeryville California United States
2. Department of Biomaterials and Biomanufacturing Sandia National Laboratories Livermore California United States
3. QB3 Institute University of California, Berkeley Berkeley California United States
4. Combustion Research Facility Sandia National Laboratories Livermore California United States
5. Biological Systems and Engineering Division Lawrence Berkeley National Laboratory Berkeley California United States
Abstract
AbstractThe efficient utilization of lignin, the direct source of renewable aromatics, into value‐added renewable chemicals is an important step towards sustainable biorefinery practices. Nevertheless, owing to the random heterogeneous structure and limited solubility, lignin utilization has been primarily limited to burning for energy. The catalytic depolymerization of lignin has been proposed and demonstrated as a viable route to sustainable biorefinery, however, low yields and poor selectivity of products, high char formation, and limited to no recycling of transition‐metal‐based catalyst involved in lignin depolymerization demands attention to enable practical‐scale lignocellulosic biorefineries. In this study, we demonstrate the catalytic depolymerization of ionic liquid‐based biorefinery poplar lignin into guaiacols over a reusable zirconium phosphate supported palladium catalyst. The essence of the study lies in the high conversion (>80 %), minimum char formation (7–16 %), high yields of guaiacols (up to 200 mg / g of lignin), and catalyst reusability. Both solid residue, liquid stream, and gaseous products were thoroughly characterized using ICP‐OES, PXRD, CHN analysis, GC‐MS, GPC, and 2D NMR to understand the hydrogenolysis pathway.
Funder
Biological and Environmental Research
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
6 articles.
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