4.8 Article

CaCl2 molten salt hydrate-promoted conversion of carbohydrates to 5-hydroxymethylfurfural: an experimental and theoretical study

Journal

GREEN CHEMISTRY
Volume 23, Issue 5, Pages 2058-2068

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0gc04356g

Keywords

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Funding

  1. National Key Research and Development Program of China [2019YFC1906603]
  2. Jiangsu Synergetic Innovation Center for Advanced Bio-Manufacture [XTC1806]
  3. National Natural Science Foundation of China [22078152, 21703099, 21973044]
  4. Six Talent Peaks Project in Jiangsu Province [SWYY-030, SWYY-118]
  5. Nanjing Tech University [39837123, 39837132]

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Alkaline earth metal salts are environmentally friendly and economical catalysts that have shown great potential in biomass conversion processes. Experimental and theoretical studies on the CaCl2-catalyzed glucose-to-fructose isomerization and fructose-to-HMF dehydration demonstrated high efficiency and the possibility of catalyst recycling. Coordination between specific sites of sugar molecules and CaCl2 plays a crucial role in promoting the conversion of glucose to fructose and fructose to HMF.
Alkaline earth metal salts are environmentally friendly and economical. They have attracted much attention in the process of biomass conversion, especially for isomerization and dehydration. However, the lack of understanding of the alkaline earth metal-mediated catalytic mechanism prevents the achievement of high HMF yields from glucose or fructose. Herein, we performed experimental and theoretical studies on CaCl2-catalyzed glucose-to-fructose isomerization and fructose-to-HMF dehydration. In CaCl2 solution, the highest fructose yield (33.6%) from glucose can be achieved at 80 degrees C. Meanwhile, the presence of CaCl2 in fructose-to-HMF dehydration notably improved fructose conversion. A one-pot isomerization-dehydration of glucose to prepare HMF was designed and 100% conversion and 52.1% HMF yield were obtained. The CaCl2 solution can be reused for five runs while maintaining catalytic activity without regeneration. Through H-1 NMR, C-13 NMR, DOSY-NMR and DFT calculations, we concluded that the coordination between the C1/C2 sites of the beta-glucopyranose tautomer and CaCl2 promoted the 1,2-intramolecular hydride shift of glucose, thus rapidly converting glucose into fructose. Similarly, Ca2+ can complex with the C2/C6-OH of beta-d-fructofuranose and stabilize this tautomer, which easily forms HMF. This is the main reason that CaCl2 can promote the preparation of HMF from fructose.

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