4.8 Article

Three-Phase Catalytic System of H2O, Ionic Liquid, and VOPO4-SiO2 Solid Acid for Conversion of Fructose to 5-Hydroxymethylfurfural

期刊

CHEMSUSCHEM
卷 7, 期 6, 页码 1703-1709

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201400119

关键词

5-hydroxymethylfurfural; biomass; fructose; ionic liquids; solid acid catalysts; vanadium phosphate

资金

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, US Department of Energy [De-AC05-00OR22725]
  2. Oak Ridge National Laboratory
  3. Oak Ridge National Laboratory by the Scientific User Facilities Division, Office of Basic Energy Science, US Department of Energy
  4. National Basic Research Program of China [2010CB732300, 2013CB933201]
  5. Program for New Century Excellent Talents in University [NCET-09-0343]
  6. Shu Guang Project [10SG30]
  7. 111 Project [B08021]

向作者/读者索取更多资源

Efficient transformation of biomass-derived feedstocks to chemicals and fuels remains a daunting challenge in utilizing biomass as alternatives to fossil resources. A three-phase catalytic system, consisting of an aqueous phase, a hydrophobic ionic-liquid phase, and a solid-acid catalyst phase of nanostructured vanadium phosphate and mesostructured cellular foam (VPO-MCF), is developed for efficient conversion of biomass-derived fructose to 5-hydroxymethylfurfural (HMF). HMF is a promising, versatile building block for production of value-added chemicals and transportation fuels. The essence of this three-phase system lies in enabling the isolation of the solid-acid catalyst from the aqueous phase and regulation of its local environment by using a hydrophobic ionic liquid, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIM][Tf2N]). This system significantly inhibits the side reactions of HMF with H2O and leads to 91mol% selectivity to HMF at 89% of fructose conversion. The unique three-phase catalytic system opens up an alternative avenue for making solid-acid catalyst systems with controlled and locally regulated microenvironment near catalytically active sites by using a hydrophobic ionic liquid

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