4.7 Article

Pickering HIPEs derived hierarchical porous nitrogen-doped carbon supported bimetallic AuPd catalyst for base-free aerobic oxidation of HMF to FDCA in water

Journal

FUEL
Volume 278, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2020.118362

Keywords

5-Hydroxymethylfurfural; Base-free aerobic oxidation; 2,5-Furandicarboxylic acid; Nitrogen-doped carbon; Pickering HIPEs template; Bimetallic AuPd catalyst

Funding

  1. National Natural Science Foundation of China [21606100]
  2. Natural Science Foundation of Jiangsu Province [BK20180850]
  3. China Postdoctoral Science Foundation [2019M651740, 2019T120397]

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As an important renewable alternative to the production of petroleum-derived terephthalic acid, selective aerobic oxidation of biomass derivative 5-hydroxymethylfurfural (HMF) into high value-added 2,5-furandicarboxylic acid (FDCA) is attracting increasing attention. Herein, a novel hierarchical porous nitrogen-doped carbon (NC) supported bimetallic AuPd catalyst was synthesized by Pickering high internal phase emulsions (Pickering HIPEs) templating method, subsequent carbonization and the sol-curing technique. By varying Pickering HIPEs parameter, nitrogen-doped content and the loaded AuPd nanoparticles, AuxPdy/NC catalysts with adjustable porous structure and basicity were obtained. Benefiting from the synergistic effects of the high basicity of NC support and efficient bimetallic AuPd catalyst, tandem oxidation of HMF to FDCA reactions can be carried out under base-free condition in water, which makes the biomass transformation process environmental friendliness and economic. And the highest yield of FDCA at 96.7% was achieved under the optimal reaction conditions. Regeneration test revealed the obtained AuxPdy/NC catalyst was recovered and reused at least five times without significant loss of catalytic activity. The present work offers a versatile strategy for developing nitrogen-doped carbon supported highly efficient bimetallic catalysts with hierarchical porous structure and adjusting basicity for a wide range of base-free catalytic oxidation in water.

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