4.7 Article

A mechanistic insight into glucose conversion in subcritical water: Complex reaction network and the effects of acid-base catalysis

Journal

FUEL
Volume 289, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2020.119969

Keywords

Glucose; Reaction mechanism; Subcritical water; Dispersion-corrected density functional theory; Acid-base bifunctional catalysis

Funding

  1. National Natural Science Foundation of China [51703153, 21908156]
  2. Key Research and Development Program of Shanxi province [201903D121032]
  3. Shanxi Province Science Foundation for Youths [201801D221365]

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Based on density functional theory, a systematic investigation of glucose conversion in subcritical water showed differences in reaction pathways between fructose and glucose, with fructose favoring dehydration through a cyclic pathway. The conversion of 5-HMF to 1,2,4-Benzenetriol exhibited a high activation energy, and retro-aldol condensation of C4 compounds preferred the formation of C2 compounds. The study provides fundamental insights into the glucose conversion mechanism in subcritical water.
Based on the concept of system thinking and system design, a systematically mechanistic network of glucose conversion toward fructose, 5-hydroxymethyl furfural, 1,6-anhydroglucose, 1,2,4-Benzenetriol, levulinic acid, furfural, erythrose, glyceraldehyde, dihydroxyacetone, pyruvaldehyde, lactic acid, glycolaldehyde in subcritical water were performed by employing dispersion-corrected density functional theory. Fukui functions results predict the most highest reactivity of O(5) of glucose to suffer protonation in subcritical water, which may readily lead to the formation of 1,6-anhydroglucose or fructose with the comparable apparent activation energies (29.441 vs 29.305 kcal/mol). Further dehydration of monosaccharide to 5-HMF is more favorable via cyclic pathway for fructose in comparison to the acyclic pathway for glucose. The formation of levulinic acid has an apparent activation energy of 33.321 kcal/mol but the rate is limited by the numerous steps. The consumption of 5-HMF to 1,2,4-Benzenetriol exhibits a high activation energy of 76.682 kcal/mol. Retro-aldol condensation of C4 compounds prefer to give C2 rather than C3 compounds. The thermodynamic results involving the generation of C2, C3 and C4 compounds by retro-aldol condensation of open-chain C6 intermediates agree with the experimental product distribution and reactivity over temperature at the initial stage of glucose or fructose subcritical hydrolysis. Furthermore, the assistance of H+ may be responsible for the isomerization and retro-aldol condensation in glucose conversion. This comprehensive reaction network provides a fundamental understanding and deeper insight into glucose conversion, which reasonably explains experimental activity and selectivity reported for glucose and fructose conversion in subcritical water.

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