Journal of Siberian Federal University. Chemistry / Catalytic Hydrogenation of Furfural in Alcoholic Media

Full text (.pdf)
Issue
Journal of Siberian Federal University. Chemistry. 2015 8 (4)
Authors
Simakova, Irina L.; Tarabanko, Valery E.; Chernyak, Mikhail Yu.; Kondrasenko, Alexander A.; Simonov, Mikhail N.
Contact information
Simakova, Irina L.:Boreskov Institute of Catalysis 5 pr. Lavrentieva, Novosibirsk, 630090, Russia; Tarabanko, Valery E.:Institute of Chemistry and Chemical Technology SB RAS 50/24 Akademgorodok, Krasnoyarsk, 660036, Russia; Siberian Federal University 79 Svobodny, Krasnoyarsk, 660041, Russia; E-mail: ; Chernyak, Mikhail Yu.:Institute of Chemistry and Chemical Technology SB RAS 50/24 Akademgorodok, Krasnoyarsk, 660036, Russia; Kondrasenko, Alexander A.:Institute of Chemistry and Chemical Technology SB RAS 50/24 Akademgorodok, Krasnoyarsk, 660036, Russia; Simonov, Mikhail N.:Boreskov Institute of Catalysis 5 pr. Lavrentieva, Novosibirsk, 630090, Russia
Keywords
furfural; propanol; butanol; furfural acetals; propylfurfuryl ether; 2-butoxymethylfuran; hydrogenation; catalysis; copper-ruthenium catalysts; platinum catalysts; biofuels
Abstract

The processes of furfural hydrogenation in the alcohol solutions over copper-ruthenium and platinum catalysts were studied. The equilibrium of acetals formation is shown to establish in the solutions. Both substances, furfural and the acetals of furfural are hydrogenated in the system. The acetals hydrogenation produces alkylfurfuryl ethers, and selectivity of their formation attains 30 and 60 % over platinum and copper-ruthenium catalysts, correspondingly. Furfuryl alcohol and 2-methylfuran are formed among other products. Tetrahydrofuran analogues of the furfural acetals, furfuryl alcohol, and 2-methylfuran are also formed over the platinum catalysts

Pages
482-490
Paper at repository of SibFU
https://elib.sfu-kras.ru/handle/2311/20112