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Innovative Route to Prepare of Au/C Catalysts by Replication of Gold-containing Mesoporous Silicas

机译:通过复制含金的介孔二氧化硅制备Au / C催化剂的创新途径

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摘要

Gold-catalyzed aerobic epoxidations in the liquid phase are generally performed in low-polarity solvents, in which conventional oxide-supported catalysts are poorly dispersed. To improve the wettability of the catalytic powder and, thus, the efficiency of the catalyst, gold nanoparticles (NPs) have been dispersed on meso-structured carbons. Gold is first introduced in functionalized mesostructured silica and particles are formed inside the porosity. Silica pores are then impregnated with a carbon precursor and the composite material is heated at 900 °C under vacuum or nitrogen. Silica is then removed by acid leaching, leading to partially encapsulated gold particles in mesoporous carbon. Carbon prevents aggregation of gold particles at high temperature, both the mean size and distribution being similar to those observed in silica. However, while Au@SiO2 exhibit significant catalytic activity in the aerobic oxidation of trans-stilbene in the liquid phase, its Au@C mesostructured replica is quite inactive.
机译:液相中金催化的好氧环氧化反应通常在低极性溶剂中进行,其中传统的氧化物负载型催化剂分散较差。为了提高催化粉末的润湿性,从而提高催化剂的效率,金纳米颗粒(NPs)已分散在介观结构的碳上。首先将金引入功能化的介孔结构二氧化硅中,并在孔隙内部形成颗粒。然后用碳前驱物浸渍二氧化硅孔,并将复合材料在真空或氮气中于900°C加热。然后通过酸浸除去二氧化硅,从而在中孔碳中产生部分包封的金颗粒。碳可防止金颗粒在高​​温下聚集,其平均大小和分布均与二氧化硅相似。然而,尽管Au @ SiO2在液相的反式二苯乙烯的好氧氧化中显示出显着的催化活性,但其Au @ C介观结构的复制品却非常无活性。

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