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Upgrading of furfural to biofuel precursors via aldol condensation with acetone over magnesium hydroxide fluorides MgF 2−x (OH)x
Minrui Xu, Stéphane Célérier, Jean-Dominique Comparot, Julie Rousseau, Matthieu Corbet, Frederic Richard, Jean-Marc Clacens

Upgrading of furfural to biofuel precursors via aldol condensation with acetone over magnesium hydroxide fluorides MgF 2−x (OH)x

Science & Mathematics Published 2019 Verification Pending

Overview & Synopsis

Wastes from ligno-cellulosic material, especially hemicellulose, are extremely promising resources to produce fuels from renewable raw materials. Furfural, resulting from the depolymerization of hemicellulose, is often considered as an extremely interesting platform molecule. Particularly, new biofuels containing molecules with 8 and 13 carbon atoms can be produced from aldol condensation of furfural and acetone followed by a deoxygenation reaction. In this work, several magnesium hydroxide fluorides MgF2-x(OH)x were prepared by a sol-gel method with various F/Mg ratios (0 to 2) at 100 °C. All solid samples were fully characterized by several technics (nitrogen adsortion-desorption, TEM, IR, XRD and ICP). MgF2-x(OH)x were mainly composed of an intimate mixture of MgF2 and Mg(OH)2-x(OCH3)x and exhibited both acid-base properties and high surface area. From CO2 adsorption experiments, a basicity scale corresponding to basic sites with moderate strength was established: MgF1.5(OH)0.5 > MgF(OH) ~ MgF1.75(OH)0.25 > MgF0.5(OH)1.5 > Mg(OH)2 >> MgF2. It was proposed that the presence of fluorine allowed to stabilize the basic sites with moderate strength at ambient atmosphere. The aldol condensation of furfural and acetone was carried out under mild reaction conditions (50 °C, Patm) over MgF2-x(OH)x. These catalysts were involved in this reaction without using classical activation step for basic solid catalysts, which constitutes a major advantage for energy saving and thus, economical efficiency. The solid with the F/Mg ratio equal to 1.5 (MgF1.5(OH)0.5) exhibited the highest activity, the furanic dimer (1,5-di(furan-2-yl)penta-1,4-dien-3-one) being the main product. A good correlation between the catalytic activity and the basicity scale was highlighted. Based on these results, the nature of active sites was proposed: a combination of a Lewis acid site (coordinatively unsaturated metal site) in the vicinity of a basic site (hydroxyl groups of Mg(OH)2-x(OCH3)x). The effect of the furfural/acetone ratio on the catalytic properties of MgF1.5(OH)0.5 was also investigated.

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Document Information

Document Title Upgrading of furfural to biofuel precursors via aldol condensation with acetone over magnesium hydroxide fluorides MgF 2−x (OH)x
Author / Organization Minrui Xu, Stéphane Célérier, Jean-Dominique Comparot, Julie Rousseau, Matthieu Corbet, Frederic Richard, Jean-Marc Clacens
Subject & Discipline Multidisciplinary Academic Open Research
Categories Science & Mathematics
Publication Year 2019
License / Rights Open Access / Creative Commons
Resource Verification Listed PDF (Verification Pending)
Original Host Website HAL Open Science (hal.science)
File Format application/pdf (Portable Document Format)
Language EN
Catalog ID DOC-22712
Original Source Link Visit Source Page on hal.science »