At room temperature in water: efficient hydrogenation of furfural to furfuryl alcohol with a Pt/SiC-C catalyst
Guimei Wang1, Ruihua Yao1, Huiyue Xin1
1Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University 3663 North Zhongshan Rd. Shanghai 200062 China xhli@chem.ecnu.edu.cn +86-21-62238590 +86-21-62238590.
Abstract:
Selective hydrogenation of furfural (FAL) to furfuryl alcohol (FOL) is challenging because of many side reactions. The highly selective hydrogenation of FAL to FOL can be achieved over a Pt catalyst supported on nanoporous SiC-C composites even at room temperature in water. A Pt/SiC-C-200-H2 catalyst, which had a Pt loading of 3 wt% and was reduced in flowing hydrogen at 500 °C after calcination in air at 200 °C for 2 h, furnished complete FAL conversion and over 99% selectivity to FOL at 25 °C under 1 MPa of hydrogen in water. The kinetic behaviour of the selective hydrogenation of FAL to FOL with the 3 wt% Pt/SiC-C-200-H2 catalyst was also investigated and the turnover frequency (TOF) reached 1148 h-1. Moreover, the Pt/SiC-C catalyst is more active than other Pt catalysts supported on ordered mesoporous carbon CMK-3, activated carbon, periodic mesoporous silica SBA-15 or Al2O3. Detailed characterization using XRD, N2-sorption, SEM, TEM and XPS techniques reveals that the striking performance of the Pt/SiC-C catalyst can be attributed to the optimal metal-support interaction and the interfacial effect.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide


