Journal
ACS CATALYSIS
Volume 6, Issue 2, Pages 1316-1328Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b02062
Keywords
lignin valorization; lignin nitration; layered double hydroxide; catalyst recycle; catalyst regeneration
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Funding
- NREL CRADA [13-513]
- Shell Global Solutions, Inc.
- U.S. Department of Energy Bioenergy Technologies Office
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Hydrotalcites (HTCs) exhibit multiple adjustable parameters to tune catalytic activity, including interlayer anion composition, metal hydroxide layer composition, and catalyst preparation methods. Here, we report the influence of several of these parameters on beta-O-4 bond scission in a lignin model dimer, 2-phenoxy-l-phenethanol (PE), to yield phenol and acetophenone. We find that the presence of both basic and NO3- anions in the interlayer increases the catalyst activity by 2-3-fold. In contrast, other anions or transition metals do not enhance catalytic activity in comparison to blank HTC. The catalyst is not active for C-C bond cleavage on lignin model dimers and has no effect on dimers without an alpha-OH group. Most importantly, the catalyst is highly active in the depolymerization of two process-relevant lignin substrates, producing a significant amount of low-molecular-weight aromatic species. The catalyst can be recycled until the NO3- anions are depleted, after which the activity can be restored by replenishing the NO3- reservoir and regenerating the hydrated HTC structure. These results demonstrate a route to selective lignin depolymerization in a heterogeneous system with an inexpensive, earth-abundant, commercially relevant, and easily regenerated catalyst.
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