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首页> 外文期刊>Fuel Processing Technology >Understanding catalytic hydrogenolysis of 5-hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) using carbon supported Ru catalysts
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Understanding catalytic hydrogenolysis of 5-hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) using carbon supported Ru catalysts

机译:了解使用碳负载的Ru催化剂的5-羟甲基糠醛(HMF)至2,5-二甲基呋喃(DMF)的催化氢解

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摘要

Herein, our study has demonstrated that microporous carbon supported Ru catalysts can selectively convert 5-hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) in isopropanol through hydrogenolysis in a catalytic ratio of 2.47mol% under 5 bar of hydrogen at 125 degrees C for 1 h. DMF yield can reach 69.52% with complete HMF conversion. The effects of reaction temperature, hydrogen pressure, metal loading and reaction solvent for hydrogenolysis have been carefully investigated. In addition, to better understand the influence of the intrinsic nature of carbonaceous material, carbon materials possessing different surface texture including microporosity, mesoporosity and nonporous carbon black were used as catalyst supports, and structural properties have been comprehensively characterized by powder X-ray diffraction spectrometer (PXRD), transmission electron microscopy (TEM), nitrogen and CO2 sorption, thermogravimetric analysis (TGA), and X-ray absorption spectroscopy (XAS). We have concluded that the nature of the carbonaceous material affects the Ru nanoparticle formation upon thermal reduction. The atomic configuration of Ru nanoparticles on carbon support (i.e., metallic Ru or RuOx) would direct the catalytic pathway differently and could be attributed to the interaction between ruthenium and carbon surface.
机译:在此,我们的研究表明,微孔碳负载的Ru催化剂可以通过在125度下催化比为2.47mol%的催化比为247mol%的催化比在异丙醇中选择性地转化5-羟甲基糠醛(HMF)至2,5-二甲基呋喃(DMF)。 c为1小时。 DMF产量可以达到69.52%,完整的HMF转换。已经仔细研究了反应温度,氢气压力,金属加载和反应溶剂的影响。此外,为了更好地了解碳质材料的内在性质的影响,使用具有不同表面纹理的碳材料,包括微孔,中孔隙度和无孔炭黑作为催化剂载体,并通过粉末X射线衍射光谱仪全面地表征结构性能(PXRD),透射电子显微镜(TEM),氮气和CO2吸附,热重分析(TGA)和X射线吸收光谱(XAs)。我们已经得出结论,碳质材料的性质在热还原时影响Ru纳米粒子形成。 Ru纳米颗粒对碳载体(即金属Ru或Ruox)的原子构型将不同地引导催化途径,并且可归因于钌和碳表面之间的相互作用。

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