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在室温下于水中:使用Pt/SiC-C催化剂将糠醛高效加氢制得糠醇。

At room temperature in water: efficient hydrogenation of furfural to furfuryl alcohol with a Pt/SiC-C catalyst.

作者信息

Wang Guimei, Yao Ruihua, Xin Huiyue, Guan Yejun, Wu Peng, Li Xiaohong

机构信息

Shanghai 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

出版信息

RSC Adv. 2018 Nov 6;8(65):37243-37253. doi: 10.1039/c8ra08429g. eCollection 2018 Nov 1.

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-H 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 catalyst was also investigated and the turnover frequency (TOF) reached 1148 h. 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 AlO. Detailed characterization using XRD, N-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.

摘要

由于存在许多副反应,糠醛(FAL)选择性加氢制糠醇(FOL)具有挑战性。即使在室温下于水中,负载在纳米多孔SiC-C复合材料上的Pt催化剂也能实现FAL到FOL的高选择性加氢。一种Pt/SiC-C-200-H催化剂,其Pt负载量为3 wt%,在200 °C空气中煅烧2 h后于500 °C的流动氢气中还原,在25 °C、1 MPa氢气压力下于水中可实现FAL的完全转化以及对FOL超过99%的选择性。还研究了3 wt% Pt/SiC-C-200-H催化剂上FAL选择性加氢制FOL的动力学行为,其周转频率(TOF)达到1148 h⁻¹。此外,Pt/SiC-C催化剂比负载在有序介孔碳CMK-3、活性炭、周期性介孔二氧化硅SBA-15或Al₂O₃上的其他Pt催化剂更具活性。使用XRD、N吸附、SEM、TEM和XPS技术进行的详细表征表明,Pt/SiC-C催化剂的显著性能可归因于最佳的金属-载体相互作用和界面效应。

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