Mild hydrodeoxygenation of lignin-derived bio-oils to hydrocarbons over bifunctional ZrP2O7-Ni12P5 catalysts. (1st April 2022) - Chen, Bo
Graphical abstract: Highlights: ZrP2 O7 -Ni12 P5 catalyst is synthesized via a facile hydrothermal synthesis. The enhancement of Lewis and Brønsted acidic sites correlates the Zr species. The H2 adsorption-activation sites originate from the interaction between Zr and Ni. Cycloalkanes are produced by the hydrodeoxygenation of lignin derived bio-oils. Abstract: An imperative current challenge for the production of renewable fuels is the development of efficient catalytic hydrodeoxygenation (HDO) of phenolic-rich bio-oils into hydrocarbons. In this work, a series of bifunctional ZrP2 O7(x) -Ni12 P5 (where × represents the molar ratio of Zr/Ni in the catalysts) catalysts were prepared for HDO of lignin-derived bio-oils (LBO). The characterization results show that among these bimetallic catalysts, ZrP2 O7(0.4) -Ni12 P5 possesses the largest specific surface area, pore volume and the highest amount of acid sites (Lewis and Brønsted) due to the introduction of appropriate amount of Zr species. Meanwhile, the interaction between Ni δ+ and Zr species on its surface creates new active sites for the promotion on the hydrogen adsorption and activation, thus endowing the most excellent catalytic performance. Using the optimized catalyst of ZrP2 O7(0.4) -Ni12 P5, 95.8% cyclohexane yield could be obtained from the HDO of guaiacol as a model compound from bio-oil under mild condition (3 MPa H2 and 250 ℃). Moreover, 36.1% hydrocarbon yield is achieved from HDO of lignin-derived bio-oils (LBO) under the same hydrogen pressure and temperature. These findings not only open a novel avenue for designing a cost-effective metal–acid bifunctional catalyst, but also provide a viable approach for converting lignocellulosic biomass feedstocks into valuable hydrocarbons.