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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 University, Faculty of Science and Technology, Department of Chemistry.
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 (English)In: Renewable energy, ISSN 0960-1481, E-ISSN 1879-0682, Vol. 233, article id 121148Article in journal (Refereed) 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.

Place, publisher, year, edition, pages
Elsevier, 2024. Vol. 233, article id 121148
Keywords [en]
liquefaction, wood biomass, tandem catalyst, bio-aromatics, aromatic extraction, deep eutectic solvents
National Category
Organic Chemistry Analytical Chemistry Bioprocess Technology
Identifiers
URN: urn:nbn:se:umu:diva-228224DOI: 10.1016/j.renene.2024.121148Scopus ID: 2-s2.0-85201073446OAI: oai:DiVA.org:umu-228224DiVA, id: diva2:1887320
Funder
Bio4EnergyAvailable from: 2024-08-07 Created: 2024-08-07 Last updated: 2024-08-21Bibliographically approved

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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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Renewable energy
Organic ChemistryAnalytical ChemistryBioprocess Technology

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