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A highly reactive and enhanced thermal stability nanocomposite catalyst based on Pt nanoparticles assembled in the inner surface of mesoporous SiO2 spherical shell

机译:一种基于Pt纳米颗粒的高反应性和增强的热稳定性纳米复合催化剂,该催化剂组装在介孔SiO2球形壳的内表面中

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摘要

A synthetic strategy has been developed to encapsulate Pt nanoparticles in heterogeneous catalysts to prevent their sintering. This method involves the preparation of Ptanocarbon spheres composites, the formation of mesoporous silica layers, and finally the removal of CTAB surfactant and NCSs by refluxing and calcination, respectively. TEM images were used to confirm the success of each step, and the catalytic evaluation was tested on the reduction of p-NPh to p-APh monitored by a UV-vis spectra. Besides, the prepared samples were characterized by X-ray diffraction (XRD), N-2 adsorption-desorption isotherms, energy dispersion X-ray analysis (EDX), scanning electron microscope (SEM), and thermogravimetric analysis (TGA) as well. It was found that the encapsulated Pt nanopartides could resist sintering up to 750 degrees C, whereas the catalysts without silica layer protection were shown to sinter by 350 degrees C. When the calcination temperature is 550 degrees C, the obtained materials exhibited the highest catalytic activity. Thus, the hollow sphere structure and the mesoporous silica played a key role in the high catalytic performance. Besides, the sample has an excellent reusability without obvious decrease of the catalytic activities even after five cycles. Finally, a possible mechanism was proposed to explain the well catalytic performance. (C) 2015 Elsevier B.V. All rights reserved.
机译:已经开发出一种合成策略来将Pt纳米颗粒封装在非均相催化剂中,以防止其烧结。该方法涉及制备Pt /纳米碳球复合材料,形成介孔二氧化硅层,最后分别通过回流和煅烧除去CTAB表面活性剂和NCS。使用TEM图像确认每个步骤的成功,并通过UV-vis光谱监测对p-NPh还原为p-APh的反应进行了催化评估。此外,制备的样品还通过X射线衍射(XRD),N-2吸附-解吸等温线,能量色散X射线分析(EDX),扫描电子显微镜(SEM)和热重分析(TGA)进行了表征。发现所包封的Pt纳米粒子在高达750℃的温度下仍能抵抗烧结,而没有二氧化硅层保护的催化剂显示出在350℃下烧结。当煅烧温度为550℃时,所获得的材料表现出最高的催化活性。 。因此,空心球结构和中孔二氧化硅在高催化性能中起关键作用。此外,该样品即使在五个循环后仍具有优异的可重复使用性,而没有明显降低催化活性。最后,提出了一种可能的机理来解释良好的催化性能。 (C)2015 Elsevier B.V.保留所有权利。

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