(695a) Gas Phase Catalytic Oxidation of Lignin to Produce Phenolic Compounds over Vanadia Catalysts
AIChE Annual Meeting
2018
2018 AIChE Annual Meeting
Catalysis and Reaction Engineering Division
Catalytic Processing of Fossil and Biorenewable Feedstocks II: Upgrading Bio-Oils & Lignin
Thursday, November 1, 2018 - 3:30pm to 3:48pm
The pretreatment of lignocellulosic biomass to create fermentable sugar streams en route to fuel/chemical production may also produce streams of insoluble lignin. These lignin stream can be burned to produce process heat and power. An alternative use of the lignin streams could be the production of valuable products such as phenolic compounds. This work explores the pyrolysis of lignin residue to produce gas phase products which can be passed of vanadia-based catalysts to oxidatively remove methoxy side chains to produce phenolic compounds, which could be used in the production of polymers and resins. Because lignin contains a complex mixture of linkages with methoxy groups, as well as both C-C and C-O bonds linking phenyl groups, there are number of bonds that must be broken in order to funnel lignin into the desired slate of phenolic compounds without methoxy groups (simple phenols). The subject of this presentation uses pyrolysis of lignin to create a mixture of gas phase species that can be passed over a catalyst to oxidatively cleave the methoxy groups to produce simple phenols. Because the goal is to partially oxidize the lignin pyrolysis vapors to produce phenols, as opposed to over-oxidation which would result in CO and CO2 production, the oxidation activity of the catalysts must be controlled. Catalysts with varying vanadium-oxygen bond strength, which affects the oxidation activity, were designed by altering the catalytic support and synthesized using incipient wetness impregnation. Reaction experiments were conducted by passing lignin pyrolysis vapors over the catalysts at 500 °C and were shown to produce simple phenols from methoxy phenols. The effect of catalyst composition will be discussed along with relevant characterization techniques, coupled with computational modeling, to help understand the role of metal-oxygen bond strength in the catalytic activity.