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首页> 外文期刊>International journal of hydrogen energy >Highly dispersed Pt nanoparticles confined within hierarchical pores of silicalite-1 zeolite via crystal transformation of supported Pt/S-1 catalyst for partial oxidation of methane to syngas
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Highly dispersed Pt nanoparticles confined within hierarchical pores of silicalite-1 zeolite via crystal transformation of supported Pt/S-1 catalyst for partial oxidation of methane to syngas

机译:通过负载型Pt / S-1催化剂的晶体转化,将甲烷部分氧化成合成气,将高度分散的Pt纳米颗粒限制在silicalite-1沸石的层状孔中

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Highly dispersed Pt nanoparticles confined within hierarchical pores of silicalite-1 zeolite were prepared via crystal transformation of supported Pt/S-1 catalyst. Selective dissolution and external recrystallization in tetrapropylammonium hydroxide solution enabled metal nano particles to be encapsulated in zeolites. The abundant pore structures of as-prepared Pt@S-1 catalyst were obtained by properly controlling the time of desilication and recrystallization. The properties of Pt@S-1 catalyst with hierarchical pores were characterized by XRD, ICP, SEM, TEM/HRTEM, N-2/Ar adsorption-desorption, CO adsorption, H-2-TPR and TGA techniques. Compared with the traditional supported Pt/S-1 catalyst, Pt@S-1 catalyst exhibited excellent sintering resistance, owing to the restriction of the recrystallized shell. Further, abundant pore provided access to contact with the active components, the Pt@S-1 catalyst showed excellently catalytic performance. CH4 conversion and product selectivity were significantly improved. The out-standing catalytic performance was attributed to recrystallization of silica supported Pt. The strategy afforded enriched pore structure, improved the dispersion of active metal, and reduced the size of Pt nanoparticles. In addition, hierarchical pores of silicalite-1 zeolite supports also contributed to shorten the diffusion path of reactions. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过负载型Pt / S-1催化剂的晶体转化制备了高度分散的Pt纳米颗粒,该颗粒被限制在silicalite-1沸石的分级孔中。在氢氧化四丙基铵溶液中的选择性溶解和外部重结晶使金属纳米颗粒能够包封在沸石中。通过适当控制脱硅和重结晶的时间,可以得到制备好的Pt @ S-1催化剂的大量孔结构。通过XRD,ICP,SEM,TEM / HRTEM,N-2 / Ar吸附-脱附,CO吸附,H-2-TPR和TGA技术对具有分级孔的Pt @ S-1催化剂的性能进行了表征。与传统的负载型Pt / S-1催化剂相比,由于重结晶壳的限制,Pt @ S-1催化剂具有优异的抗烧结性。此外,大量的孔提供了与活性成分接触的通道,Pt @ S-1催化剂表现出优异的催化性能。 CH4转化率和产物选择性得到显着改善。出色的催化性能归因于二氧化硅负载的Pt的重结晶。该策略提供了丰富的孔结构,改善了活性金属的分散性,并减小了Pt纳米粒子的尺寸。此外,silicalite-1沸石载体的分层孔也有助于缩短反应的扩散路径。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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