The hydrodeoxygenation (HDO) of three different phenolic model compounds, isoeugenol, guaiacol and vanillin was investigated using Ir/ZrO 2 and Ni/ZrO 2 as heterogeneous catalysts. The catalysts were prepared by incipient wetness impregnation and characterized by transmission electron microscopy, nitrogen adsorption, FTIR pyridine adsorption–desorption. The organic material in the spent catalysts was analyzed by organic elemental analysis and thermogravimetry. The results revealed that in guaiacol HDO at 250 °C under 30 bar total pressure the main product was cyclohexanol with 36% yield over Ni/ZrO 2 while the total deoxygenation forming cyclohexane was limited to 2%. Ir/ZrO 2 exhibited higher HDO activity compared to Ni/ZrO 2 giving 14% yield of cyclohexane. Extensive formation of methane and ethane was also observed in guaiacol HDO. Hydrodeoxygenation of isoeugenol over Ir/ZrO 2 resulted in maximally 33% yield of propylcyclohexane due to a low liquid phase mass balance. The main products in vanillin HDO at 100 °C in water was vanillyl alcohol.
CITATION STYLE
Alda-Onggar, M., Mäki-Arvela, P., Aho, A., Simakova, I. L., & Murzin, D. Y. (2019). Hydrodeoxygenation of phenolic model compounds over zirconia supported Ir and Ni-catalysts. Reaction Kinetics, Mechanisms and Catalysis, 126(2), 737–759. https://doi.org/10.1007/s11144-018-1502-1
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