4.7 Article

Self-support semi-hollow carbon nanosphere supported palladium catalyst for biomass upgrading

Journal

RENEWABLE ENERGY
Volume 191, Issue -, Pages 101-109

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.renene.2022.03.012

Keywords

Self-support semi-hollow carbon; nanosphere; Hydrodeoxygenation; Vanillin; Pd nanoparticles; Shell-void-core structure; Carbon defect

Funding

  1. National Natural Science Foundation of China [22108056]
  2. Scientific Research Projects of Hebei Education Department [QN2019050]
  3. National Natural Science Foundation of Hebei Province [B2020202004]

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This study reports a self-supported semi-hollow carbon nanospheres supported palladium catalyst for the hydrodeoxygenation of vanillin under mild conditions. The catalyst exhibits excellent catalytic performance and stability.
Catalytic removal of oxygen from biomass by hydrodeoxygenation (HDO) as a promising process has been pursued for efficient utilization of biomass resources. Here we report a self-support semi-hollow carbon nanospheres (SHCN) supported palladium (Pd) catalyst for vanillin HDO under mild conditions. The shell-void-core structure of carbon nanospheres originates from the modulation of growth kinetics of resorcinol/formaldehyde resin precursors by a given volume of acetone. Notably, 0.5%Pd/SHCN-60 (acetone of 60 mL) catalyst exhibits > 99.9% of vanillin conversion and creosol selectivity under 25 ? and 0.1 MPa of H-2. The good catalytic results can derive from the self-support hollow carbon support and active metallic Pd. Raman results show that 0.5%Pd/SHCN-60 possesses the most abundant defect carbon (AD1/Ac 1/4 2.02), which leads to the small particle size (mean size of 2.9 nm) and well dispersion (29.5%) of Pd. Higher H2-desorption temperature (similar to 440 ?) of 0.5%Pd/SHCN-60 by H-2-TPD demonstrates the strong interaction of Pd-defect carbon. The strong interaction favors the hydrogen storage and activation of substrates under low pressure of H2 and reaction temperature, which improves the hydrogenation and hydrogenolysis. Additionally, the contribution of unique core structure to support the shell to enhance mechanical stability leads to intact morphology of catalyst and stable catalytic performance after reused six times. This investigation can provide a design idea of carbon-based catalysts for mild HDO. (c) 2022 Elsevier Ltd. All rights reserved.

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