Hydroconversion of 5‐Hydroxymethylfurfural to 2, 5‐Dimethylfuran and 2, 5‐Dimethyltetrahydrofuran over Non‐promoted Ni/SBA‐15. Issue 7 (21st February 2020)

• Record Type: Journal Article
• Authors: Chen, Shuo; Ciotonea, Carmen; De Oliveira Vigier, Karine; Jérôme, François; Wojcieszak, Robert; Dumeignil, Franck; Marceau, Eric; Royer, Sebastien
• Is Part Of: ChemCatChem. Volume 12:Issue 7(2020)
• Page Start: 2050
• Page End: 2059
• Publication Date: 2020-02-21
• Subjects: HMF -- hydroconversion -- nickel -- biofuels -- incipient wetness impregnation; Catalysis -- Periodicals; 541.39505
• DOI: 10.1002/cctc.201902028
• Languages: English
• ISSNs: 1867-3880

Abstract

Abstract: The selective hydroconversion of 5‐hydroxymethylfurfural (HMF) to biofuels is currently highly sought‐for. While the literature has demonstrated that this reaction is possible on promoted Ni catalysts, we show here that a monometallic, non‐promoted Ni/SBA‐15 catalyst, prepared by incipient wetness impregnation, can convert HMF to 2, 5‐dimethylfuran (DMF) and to 2, 5‐dimethyltetrahydrofuran (DMTHF) at 180 °C, in a consecutive way. Through a control over reaction time, high yields to DMF (71 %, at conversion of 93 %) or DMTHF (97 %, at conversion of 100 %) can be achieved. Kinetic modelling suggests a preferential route to DMF via 5‐methylfurfural (MFFR) as intermediate, though the route via 2, 5‐bis(hydroxylmethyl)furan (BHMF) is also present. The favored route in the experimental conditions involves the hydrogenolysis of the hydroxyl group of HMF as first step, followed by the hydrogenation of the aldehyde function, to methylfurfuryl alcohol (MFOL). It is suggested a higher reaction rate of hydrogenation or hydrogenolysis of the side group is linked to the presence of a methyl group in the molecule. No hydrogenation of the furan ring is detected on the intermediates. Abstract : Non‐promoted monometallic Ni/SBA‐15 catalyst, prepared by Incipient Wetness Impregnation can convert HMF to 2, 5‐dimethylfuran (DMF) or to 2, 5‐dimethyltetrahydrofuran (DMTHF). Through the control over reaction time, high yields to DMF (71 %, at conversion of 93 %) and to DMTHF (97 %, at conversion of 100 %) can be achieved. The kinetic study affords the determination of a preferential reaction route from HMF to DMTHF through 5‐methylfurfural (MFFR).