4.6 Article

Hydrogenolysis of 5-Hydroxymethylfurfural to 2,5-Dimethylfuran Over a Modified CoAl-Hydrotalcite Catalyst

Journal

FRONTIERS IN CHEMISTRY
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fchem.2022.907649

Keywords

5-hydroxymethylfurfural; 2; 5-dimethylfuran; hydrogenolysis; hydrotalcite; metal oxide

Funding

  1. Shandong Provincial Natural Science Foundation of China [ZR2017MB035]
  2. Fluorosilicone Materials Joint Funds of Shandong Provincial Natural Science Foundation [ZR2019LFG009]

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A novel mixed metal oxide catalyst was prepared and applied for the hydrogenolysis of 5-hydroxymethylfurfural to 2,5-dimethylfuran. The CuCoNiAl-MMO catalyst exhibited high initial activity and selectivity under relatively mild reaction conditions. Characterization studies revealed the structural features of the catalyst surface have important implications for selective DMF synthesis.
The catalytic hydrogenolysis of 5-hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) is a promising route towards sustainable liquid fuels with a high energy density. Herein, a novel CuCoNiAl-containing mixed metal oxide catalyst (CuCoNiAl-MMO) was prepared by calcination a layered double hydroxide (LDH) precursor in N-2 at 500 degrees C, then applied for the catalytic hydrogenolysis of HMF to DMF. The effects of reaction time, reaction temperature and hydrogen pressure on DMF selectivity were investigated. Under relatively mild reaction conditions (180 degrees C, 1.0 MPa H-2, 6.0 h), CuCoNiAl-MMO showed both a high initial activity and selectivity for hydrogenolysis of HMF to DMF, with HMF conversion rate of 99.8% and DMF selectivity of 95.3%. Catalysts characterization studies using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) revealed the presence of various metal oxides and metallic copper on the surface of the CuCoNiAl-MMO catalyst, with the presence of mixed metal-oxide-supported metallic Cu nanoparticles being responsible good hydrogenolysis activity of the catalyst for selective DMF synthesis.

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