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Liquefaction of lignocellulosic biomass into phenolic monomers and dimers over multifunctional Pd/NbOPO4 catalyst
Laboratory of Industrial Chemistry and Reaction Engineering, Johan Gadolin Process Chemistry Centre, Åbo Akademi University, Henrikinkatu 2, 20500 Turku, Finland;Bioeconomy Institute, Biorenewables Research Laboratory, Iowa State University, Ames, IA 50011 .ORCID-id: 0000-0003-2269-1191
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Laboratory of Industrial Chemistry and Reaction Engineering, Johan Gadolin Process Chemistry Centre, Åbo Akademi University, Henrikinkatu 2, 20500 Turku, Finland.ORCID-id: 0000-0002-7055-9358
Laboratory of Industrial Chemistry and Reaction Engineering, Johan Gadolin Process Chemistry Centre, Åbo Akademi University, Henrikinkatu 2, 20500 Turku, Finland.ORCID-id: 0000-0002-4588-6832
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2024 (Engelska)Ingår i: Renewable energy, ISSN 0960-1481, E-ISSN 1879-0682, Vol. 233, artikel-id 121148Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

For the first time, a tandem catalytic material, 5 wt. % Pd/NbOPO4, was utilized in the depolymerization of wood in supercritical ethanol under hydrogen atmosphere. The experiments were conducted under various conditions, with fresh, and acetone extracted birch. A comprehensive analysis was performed to elucidate the dissolution efficiency and achieved product distribution. The results indicated that with fresh birch, 34 wt. % of lignin monomer yield with 84 wt. % delignification efficiency were obtained while with extracted wood, 35 wt. % of lignin monomer yield with 78 wt. % delignification efficiency were achieved. The total lignin monomer content extracted from the fresh birch is composed of 76.9 wt. % of dimethoxyphenols and 16.5 wt. % with the guaiacol structure. Major lignin monomer product was homosyringaldehyde (61.9 wt. %). With extracted wood, 93.2 wt. % of dimethoxyphenols (63.6 wt. % homosyringaldehyde) and 6.8 wt. % of guaiacol-monomers were achieved. It was concluded that the depolymerization occurred via breaking of the ether bonds in lignin, including ether hydrolysis by Lewis acid sites over the solid acid catalyst and with subsequent deoxygenation of monophenols over Pd. In addition, an extraction process was proposed to extract the aromatic fraction from the obtained biocrude.

Ort, förlag, år, upplaga, sidor
Elsevier, 2024. Vol. 233, artikel-id 121148
Nyckelord [en]
liquefaction, wood biomass, tandem catalyst, bio-aromatics, aromatic extraction, deep eutectic solvents
Nationell ämneskategori
Organisk kemi Analytisk kemi Bioprocessteknik
Identifikatorer
URN: urn:nbn:se:umu:diva-228224DOI: 10.1016/j.renene.2024.121148ISI: 001295524400001Scopus ID: 2-s2.0-85201073446OAI: oai:DiVA.org:umu-228224DiVA, id: diva2:1887320
Forskningsfinansiär
Bio4EnergyTillgänglig från: 2024-08-07 Skapad: 2024-08-07 Senast uppdaterad: 2025-04-24Bibliografiskt granskad

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Samikannu, AjaikumarMukesh, ChandrakantMikkola, Jyri-Pekka

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Jogi, RamakrishnaSamikannu, AjaikumarMäki-Arvela, PäiviVirtanen, PasiMukesh, ChandrakantMikkola, Jyri-Pekka
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