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Preparation, characterization, and kinetic evaluation of dendrimer-derived bimetallic Pt-Ru/SiO_2 catalysts

机译:树枝状大分子双金属Pt-Ru / SiO_2催化剂的制备,表征及动力学评价

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摘要

A series of silica-supported Pt, Ru, and Pt-Ru catalysts has been synthesized using dendrimer-metal nanocomposite (DMN) precursors prepared by both co- and sequential complexation with metal salts. The catalysts have been characterized by several techniques, including electron microscopy, temperature-programmed titration of adsorbed oxygen, and X-ray diffraction. Liquid-phase selective hydrogenation of 3,4-epoxy-1-butene (EpB) was used as a probe reaction to evaluate their catalytic performance. The bimetallic catalyst prepared by the co-complexation method exhibits a superior catalytic activity compared to the sequential one, and is much more active than a conventional catalyst prepared by incipient wetness. The activity enhancement is attributed to a bifunctional performance of the PtRu alloy sites created, based on a strong correlation between turnover frequencies, and both the alloy compositions and metal surface site distributions. In addition, the co-complexation catalyst is selective toward crotonaldehyde, suggesting that this reaction pathway is favored on the PtRu sites.
机译:使用树状聚合物金属纳米复合材料(DMN)前驱体合成了一系列二氧化硅负载的Pt,Ru和Pt-Ru催化剂,该前体是通过与金属盐共配和顺序配位而制备的。催化剂已通过多种技术进行了表征,包括电子显微镜,吸附氧的程序升温滴定和X射线衍射。 3,4-环氧-1-丁烯(EpB)的液相选择性加氢用作探针反应,以评估其催化性能。通过共络合方法制备的双金属催化剂与顺序催化剂相比显示出优异的催化活性,并且比通过初期润湿制备的常规催化剂具有更高的活性。活性的提高归因于所产生的PtRu合金位点的双功能性能,这是基于周转频率与合金成分和金属表面位点分布之间的强相关性而得出的。另外,该共络合物催化剂对巴豆醛具有选择性,表明该反应途径在PtRu位点上是有利的。

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