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Efficient Furfuryl Alcohol Synthesis from Furfural over Magnetically Recoverable Catalysts: Does the Catalyst Stabilizing Medium Matter?

机译:从富含磁性回收的催化剂上产生的有效的呋喃醇合成:催化剂稳定培养基吗?

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摘要

We report hydrogenation of furfural (FF) to furfuryl alcohol (FA) with novel Pt-and Pd-containing magnetite nanoparticles (NPs) stabilized by polyphenylquinoxaline (PPQ) and hyperbranched pyridylphenylene polymer (PPP). FF is one of the major ingredients of biooil produced by biomass pyrolysis, while FA is a source of value-added chemicals, thus, creating a sustainable path from biomass to important compounds. We demonstrate that catalytic NPs (Pt~0 or Pd~0) of approximately 3 nm in diameter form in the polymer shells of magnetite NPs and the catalysts are magnetically recoverable. The search for optimal reaction conditions of the FF hydrogenation revealed that the highest selectivity is obtained at 120℃ and 6 MPa hydrogen pressure in i-propanol as solvent. The solvent effect is due to combination of good FF solubility and accessibility of catalytic NPs for the FF adsorption. A comparison of the catalytic activities of the Pd-containing magnetite NPs stabilized by PPQ and PPP validates the advantages of the open and rigid structure of the hyperbranched PPP vs. linear PPQ. For Pdcontaining magnetite NPs stabilized by PPP, the high selectivity to FA of 99.3% at nearly 100% FF conversion was achieved at a remarkable activity of 871 min1 and high catalyst stability.
机译:我们报告用新型的PT和PD磁铁矿纳米颗粒(NPS)和多苯基喹啉(PPQ)和超支的吡idylenyleneylenephenylene Polymer(PPP)稳定的新型PT和PD的磁铁矿纳米颗粒(NPS)将呋喃(FF)氢化为呋喃醇(FA)。 FF是生物质热解产生的生物油的主要成分之一,而FA是增值化学物质的来源,因此,从生物量到重要化合物创造了可持续的路径。我们证明,在磁铁矿NP的聚合物壳和催化剂的催化NP(PT〜0或Pd〜0)中,直径约为3 nm。对FF氢化的最佳反应条件的搜索表明,在I-propanol作为溶剂中,在120℃和6 MPa氢压力下获得最高的选择性。溶剂效应是由于良好的FF溶解度和催化NP在FF吸附中的可及性的组合。通过PPQ和PPP稳定的含Pd的磁铁矿NP的催化活性的比较验证了超支PPP与线性PPQ的开放和刚性结构的优势。对于通过PPP稳定的PDCONTAINT磁铁矿NP,在871 min1的显着活性和高催化剂稳定性下,实现了在接近100%FF转换时FA的高选择性99.3%。

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