4.5 Article

One-pot synthesis of 5-hydroxymethylfurfural from cellobiose and sucrose using niobium-modified montmorillonite catalysts

期刊

MOLECULAR CATALYSIS
卷 532, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.mcat.2022.112720

关键词

Sucrose; Cellobiose; Niobium -modified montmorillonite; 5-hydroxymethylfurfural; Catalysis

资金

  1. R & D Program of Beijing Municipal Education Commission
  2. Research Foundation for Youth Scholars of Beijing Technology and Business University
  3. [KM202210011010]
  4. [QNJJ2021-10]
  5. [2022 BTBU]
  6. [19008022056]

向作者/读者索取更多资源

The synthesis of highly active niobium-modified montmorillonite catalysts and their application in the conversion of cellobiose and sucrose to 5-hydroxymethylfurfural (5-HMF) is reported. The presence of Lewis and Bronsted acid sites on the Nb-Mont catalyst facilitates the hydrolysis of substrates and plays a crucial role in the isomerization and dehydration processes. The catalytic approach provides a promising strategy for the efficient synthesis of 5-HMF from carbohydrates.
The synthesis of platform chemical 5-hydroxymethylfurfural (5-HMF) provides favorable and efficient paths for the utilization of renewable biomass resources. In this work, highly active niobium-modified montmorillonite (Nb-Mont) catalysts were synthesized by a facile and ion-exchange method and were used for the one-pot conversion of cellobiose and sucrose to 5-HMF with optimal results. 5-HMF yield of 68.6% was obtained from cellobiose in a methyl isobutyl ketone (MIBK)/saturated salt water (SSW) biphasic solvent at 170 degrees C after 3 h. With sucrose as substrate in DMSO at 140 degrees C after 2 h, 5-HMF yield was 65.4%. The presence of Lewis and Bronsted acid sites on Nb-Mont facilitate the hydrolysis of cellobiose and sucrose and play essential roles in the subsequent isomerization of glucose monomer and the dehydration of fructose monomer. A possible reaction mechanism was proposed for the transformation of cellobiose and sucrose into 5-HMF, and the isomerization process of glucose monomer was the most critical step, confirmed by density functional theory (DFT) calcula-tions. [NbO(OH)2]+ species as active sites could effectively reduce the activation energy of the isomerization process, which accelerated the synergetic proton transfer process. Nb-Mont was recycled at least four times without a prominent loss in the catalytic activity. In this study, a promising catalytic strategy was provided for heterogeneous Nb containing catalysts used in the effective synthesis of 5-HMF from carbohydrates.

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