Reactor development for a one‐step hybrid catalytic conversion of D‐glucose to HMF
- 25 January 2024
- journal article
- research article
- Published by Wiley in ChemCatChem
- Vol. 16 (4)
Abstract
The design of an “H”‐shaped reactor has been studied to satisfy the possibility of using a triphasic medium to transform d‐glucose into 5‐hydroxymethylfurfural (HMF) by a hybrid catalytic process using an immobilized glucose isomerase, allowing the isomerization of D‐glucose to d‐fructose, and a heterogeneous chemical catalyst to catalyze the dehydration of d‐fructose to HMF. The various parameters influencing the transport of d‐fructose within the reactor were studied, namely the difference in pH between the two aqueous phases, the agitation and the quantity of 3,4‐DCPBA/Aliquat336® used to extract and transport continuously the d‐fructose. The pH discrepancy, which must be between 5.0 and 5.5, turns out to be the real driving force behind the extraction of D‐fructose. The D‐Fru/3,4‐DCPBA molar ratio of 1/0.25 allowed the transport of more than 80 % of the D‐fructose initially present and shows that the same molecule of 3,4‐DCPBA is involved at least twice in the transport of D‐fructose and that the 3,4‐DCPBA/Aliquat336® couple performs a turnover within the organic phase. Finally, a HMF production yield of 30.9 % and an isomerization yield of 79.1 % were obtained, illustrating the shift in the isomerization equilibrium made possible by a D‐fructose extraction yield of 96.8 %.Keywords
This publication has 22 references indexed in Scilit:
- Integrated catalysis opens new arylation pathways via regiodivergent enzymatic C–H activationNature Communications, 2016
- High yield 5-(hydroxymethyl)furfural production from biomass sugars under facile reaction conditions: a hybrid enzyme- and chemo-catalytic technologyGreen Chemistry, 2016
- Cooperative Catalysis of Noncompatible Catalysts through Compartmentalization: Wacker Oxidation and Enzymatic Reduction in a One‐Pot Process in Aqueous MediaAngewandte Chemie International Edition, 2015
- Tandem Catalytic Conversion of Glucose to 5-Hydroxymethylfurfural with an Immobilized Enzyme and a Solid AcidACS Catalysis, 2014
- Combining the ‘two worlds’ of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous mediaCurrent Opinion in Chemical Biology, 2014
- Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable ResourcesChemical Reviews, 2013
- Chemo‐Enzymatic Conversion of Glucose into 5‐Hydroxymethylfurfural in SeawaterChemSusChem, 2012
- Engineering a Biometallic Whole Cell Catalyst for Enantioselective Deracemization ReactionsACS Catalysis, 2011
- Green Chemistry: Principles and PracticeChemical Society Reviews, 2009
- Competitive transport of reducing sugars through a lipophilic membrane facilitated by aryl boron acidsTetrahedron, 1997