Selective Hydrodeoxygenation of Lignin-Derived Phenols to Aromatics Catalyzed by Nb2O5-Supported Iridium

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Abstract

The dominating catalytic approach to aromatic hydrocarbons from renewables, deoxygenation of phenol-rich depolymerized lignin bio-oils, is hard to achieve: Hydrodeoxygenation (HDO) of phenols typically leads to the loss of aromaticity and to non-negligible fractions of cyclohexanones and cyclohexanols. Here, we report a catalyst, niobia-supported iridium nanoparticles (Ir@Nb2O5), which combines full conversion in the HDO of lignin-derived phenols with appreciable and tunable selectivity for aromatics (25-95%) under mild conditions (200-300 °C, 2.5-10 bar of H2). A simple approach to the removal of Brønsted-acidic sites via Hünig's base prevents coking and allows reaction conditions (T > 225 °C, 2.5 bar of H2), promoting high yields of aromatic hydrocarbons.

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Jeantelot, G., Følkner, S. P., Manegold, J. I. S., Ingebrigtsen, M. G., Jensen, V. R., & Le Roux, E. (2022). Selective Hydrodeoxygenation of Lignin-Derived Phenols to Aromatics Catalyzed by Nb2O5-Supported Iridium. ACS Omega, 7(35), 31561–31566. https://doi.org/10.1021/acsomega.2c04314

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