Journal
FUEL PROCESSING TECHNOLOGY
Volume 233, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.fuproc.2022.107289
Keywords
Lignin; Hydropyrolysis; Hydrodeoxygenation; Pyrolysis mechanism
Funding
- National Natural Science Foundation of China [51906215]
- Fundamental Research Funds for the Central Universities
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This study investigated the impact of atmosphere, pressure, and temperature on the product formation during lignin hydropyrolysis. The results showed that high-pressure hydrogen favored the production of condensable vapors and permanent gases while inhibiting char formation and promoting the generation of non-methoxy phenolics.
Lignin hydropyrolysis was investigated in a high-pressure micro-reactor with on-line analysis characterization of products. The influences of atmosphere, pressure, and temperature on product formation during lignin pyrolysis were quantitatively discussed. The presence of hydrogen, elevated pressure and temperature favored the production of condensable vapors and permanent gas while inhibited the formation of char. High-pressure hydrogen boosted the conversion of methoxy phenolics to non-methoxy phenolics, and facilitated the generation of hydrocarbon condensable vapors and hydrocarbon gases. Non-methoxy phenolics were major condensable vapor from lignin hydropyrolysis. Yield of non-methoxy phenolics reached 19.68C% at 3 MPa and 500 degrees C. The monocyclic and polycyclic aromatic hydrocarbons as well as condensable aliphatic hydrocarbons were observed from lignin hydropyrolysis. Methane was the most abundant gas product from lignin hydropyrolysis, yield of which was 10.27C% at 2 MPa and 600 degrees C. The formation mechanisms of typical products were proposed and verified with experiments using model compounds. The formation of non-methoxy phenolics, monocyclic aromatic hydrocarbons and aliphatic hydrocarbons is related to the substitution of methoxy (and its methyls) and phenolic hydroxyl groups on benzene rings by alkyls, alkenyls and hydrogen radicals, as well as the hydrogenation of pi bonds.
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