4.8 Article

Microwave-assisted condensation of bio-based hydroxymethylfurfural and acetone over recyclable hydrotalcite-related materials

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 282, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2020.119599

关键词

Microwave-assisted organic synthesis; Biofuel production; Rehydrated hydrotalcite; Layered double hydroxide; Catalyst recycle

资金

  1. AGAUR (Generalitat de Catalunya) [2018 FI_B 01124]
  2. ESF (European Union) [2018 FI_B 01124]
  3. Ministerio de Economia y Competitividad [RTI2018-098310-B-I00]

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The study investigates the microwave-assisted neat aldol condensation of biomass-derived platform chemical HMF and acetone over hydrotalcite-based catalysts, achieving high conversions and selective product formation. Different basic properties of heterogeneous catalysts derived from the same parent hydrotalcite were tested, with successful catalyst recycling strategies explored. The most active catalyst, a meixnerite-type solid, showed low activity loss upon recycling.
The microwave-assisted neat aldol condensation of biomass-derived platform chemical 5-hydroxymethyl furfural (HMF) and acetone over hydrotalcite-based catalysts has been studied. High conversions are obtained in very short times with relatively low catalyst loadings. The condensation products, which are biofuel and functional polymer precursors, are selectively obtained. Heterogeneous catalysts with different basic properties derived from the same parent hydrotalcite have been tested. The solids were characterized by PXRD, ICP-AES, ESEM-EDX, TEM, FT-IR and Raman spectroscopy, N-2 physisorption, CO2 chemisorption and TGA-MS. The products in the final reaction mixtures were determined by GC-FID and -MS, HPLC-DAD and -TOF, and NMR. NMR was also used to determine the stereoconfiguration of the obtained products and pointed to a complete E-selectivity of our process. Different catalyst recycle strategies have been explored, and the most active catalyst, a meixnerite-type solid, can be recycled with low activity loss.

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