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At room temperature in water: efficient hydrogenation of furfural to furfuryl alcohol with a Pt/SiC–C catalyst
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-H(2) catal...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088888/ https://www.ncbi.nlm.nih.gov/pubmed/35557810 http://dx.doi.org/10.1039/c8ra08429g |
Sumario: | 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-H(2) 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-H(2) 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 Al(2)O(3). Detailed characterization using XRD, N(2)-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. |
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