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Selective catalytic oxidation over Au-Pd/titanate nanotubes and the influence of the catalyst preparation method on the activity

机译:通过AU-Pd /钛酸盐纳米管选择催化氧化及催化剂制备方法对活性的影响

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The dependence of the selective oxidation catalytic activity of Au-Pd supported on titanate nanotubes on the catalyst preparation method has been investigated. The most active Au-Pd/Ti-NT catalyst for the selective oxidation of benzyl alcohol is shown to be that prepared using colloidal synthesis and immobilization with PVA as a stabilizer, which has markedly superior catalytic activity compared to catalysts prepared by deposition-precipitation, adsorption, and dry impregnation methods. Au-Pd NPs stabilized by graphene oxide sheets and immobilized on Ti-NT has also been studied and while not optimum shows promising catalytic activity. The superior catalytic activity of the catalysts prepared by colloidal synthesis is attributed to the high metal dispersion on the external surfaces of Ti-NT, the narrow particle size distribution, and the high degree of Au-Pd alloying. This work also demonstrates that in the adsorption method of preparation using HAuCl4.3H(2)O and PdCl2 precursors, the uptake of Pd ions in solution by Ti-NT is proportional to the sodium content in Ti-NT, which implies that Na is involved in an ion-exchange reaction with Pd ions.
机译:研究了支持在催化剂制备方法上的钛酸盐纳米管上负载的AU-Pd选择性氧化催化活性的依赖性。用于选择性氧化苄醇的最活性AU-Pd / Ti-NT催化剂是使用胶体合成和用PVA固定作为稳定剂制备的,与通过沉淀沉淀制备的催化剂相比具有明显优异的催化活性,吸附和干浸渍方法。研究了通过石墨烯片稳定并固定在Ti-NT上的AU-Pd NPS,而不是最佳显示有前途的催化活性。通过胶体合成制备的催化剂的优异催化活性归因于Ti-NT的外表面上的高金属分散体,窄粒度分布和高度Au-Pd合金化。这项工作还证明,在使用HauCl4.3H(2)O和PdCl2前体的制备方法中,Ti-NT溶液中Pd离子的摄取与Ti-NT中的钠含量成比例,这意味着NA是参与与Pd离子的离子交换反应。

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