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Aqueous Phase Conversion of Hexoses into 5-Hydroxymethylfurfural and Levulinic Acid in the Presence of Hydrochloric Acid: Mechanism and Kinetics
Author(s) -
Diego Garcés,
Eva Dı́az,
Salvador Ordóñez
Publication year - 2017
Publication title -
industrial and engineering chemistry research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.878
H-Index - 221
eISSN - 1520-5045
pISSN - 0888-5885
DOI - 10.1021/acs.iecr.7b00952
Subject(s) - levulinic acid , chemistry , furfural , monosaccharide , catalysis , fructose , aqueous solution , hydroxymethylfurfural , organic chemistry , kinetics , dehydration , batch reactor , acid catalysis , hydroxymethyl , selectivity , biochemistry , physics , quantum mechanics
The kinetics of the acid-catalyzed dehydration of two common monosaccharides (glucose and fructose) to 5-hydroxymethyl-furfural (HMF) and levulinic acid is studied in this work. Reaction studies were performed in a stirred batch reactor using aqueous sugar solutions (150 g/L). The influence of reaction temperature (363–403 K) and catalyst concentration (0.05–0.25 mol/L) was also studied. The formation of the main products, as well as other minor products such as humins (in both cases) or glucose dimers and anhydroglucose (in glucose processing), is modeled considering a serial-parallel scheme reaction. The proposed model allows predicting the formation of both main and side products. Obtained results suggest that it is possible to work at total conversions of both monosaccharides, and to tune the selectivity to HMF-LA by changing the operation temperature and/or catalyst concentration. As a general trend, higher selectivities are obtained (to HMF or to LA, depending on reaction conditions) when fructose i...

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