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Selective Hydrodeoxygenation of Lignin‐Derived Phenolic Monomers and Dimers to Cycloalkanes on Pd/C and HZSM‐5 Catalysts

Chen Zhao, Johannes A. Lercher

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Abstract

Suffocating phenols: A catalyst system consisting of Pd/C and HZSM-5 shows an extremely high selectivity in removing oxygen-containing groups (hydroxyl, methoxy, ketone, alkylOaryl, and arylOaryl) in lignin-derived substituted phenolic monomers and dimers through a metal-acid catalyzed cascade cleavage of CO bonds in phenolic dimers and the integrated hydrogenation and dehydration reactions in water at 473 K.

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Suffocating phenols: A catalyst system consisting of Pd/C and HZSM-5 shows an extremely high selectivity in removing oxygen-containing groups (hydroxyl, methoxy, ketone, alkylOaryl, and arylOaryl) in lignin-derived substituted phenolic monomers and dimers through a metal-acid catalyzed cascade cleavage of CO bonds in phenolic dimers and the integrated hydrogenation and dehydration reactions in water at 473 K.

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Available abstract

Suffocating phenols: A catalyst system consisting of Pd/C and HZSM-5 shows an extremely high selectivity in removing oxygen-containing groups (hydroxyl, methoxy, ketone, alkylOaryl, and arylOaryl) in lignin-derived substituted phenolic monomers and dimers through a metal-acid catalyzed cascade cleavage of CO bonds in phenolic dimers and the integrated hydrogenation and dehydration reactions in water at 473 K.

Key concepts: Hydrodeoxygenation, Chemistry, Aryl, Catalysis, Monomer, Phenols, Organic chemistry, Ketone

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Selective Hydrodeoxygenation of Lignin‐Derived Phenolic Monomers and Dimers to Cycloalkanes on Pd/C and HZSM‐5 Catalysts — Research Paper | ScholarLens