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首页> 外文期刊>ChemCatChem >Bimetallic Au-Pd Nanoparticles Confined in Tubular Mesoporous Carbon as Highly Selective and Reusable Benzyl Alcohol Oxidation Catalysts
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Bimetallic Au-Pd Nanoparticles Confined in Tubular Mesoporous Carbon as Highly Selective and Reusable Benzyl Alcohol Oxidation Catalysts

机译:双金属Au-Pd纳米粒子限制在管状介孔碳中,作为高选择性和可重复使用的苄醇氧化催化剂

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摘要

Size-uniform and highly dispersed bimetallic AuPd nanoparticles were formed in situ and confined in tubular mesoporous carbon by successive incipient wetness impregnation and a thermal annealing method. The bimodal mesoporous carbon (CMK-5) encapsulated AuPd nanoparticles with 1 wt?% metal loading enables superior activity compared with mono-modal mesoporous carbon for benzyl alcohol oxidation. A conversion of >99?% and selectivity of >99?% can be reached within 3 h under mild conditions, for example, at 80?degrees C and at atmospheric pressure. It is found that during the catalyst preparation, the Au and Pd precursor impregnation sequence is a key factor to the formation of AuPd nanoparticles under identical conditions. A relatively high activity is realized by the first impregnation of the Au precursor, followed by the second impregnation of the Pd precursor. The crystalline structure and distribution of AuPd nanoparticles are characterized by high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX), and XRD. It is found that a larger proportion of surface-exposed Pd atoms in AuPd nanoparticles have a positive effect on catalytic activity. The AuPd nanoparticles have a narrow size distribution that is concentrated at approximately 4 nm. TEM and N2 adsorption results reveal that the catalyst has a large surface area and well-developed bimodal pore interconnectivity, which contribute to its excellent activity. The used catalyst retained a high selectivity but conversion decreased with recycling. The deactivation mechanism was attributed to the tiny amount of incompletely removed benzaldehyde adsorbed onto the active surface, which blocked access from the active sites to benzyl alcohol. Importantly, the used catalyst can be recovered by a simple heat treatment at 200?degrees C in air after the catalytic cycles have completed; the adsorbed benzaldehyde is removed from the active surface. Hence, AuPd nanoparticles confined in tubular mesoporous carbon can be used as an alternative method to develop highly dispersed nanocatalysts to improve catalytic efficiency.
机译:通过连续初始湿润浸渍和热退火方法原位形成尺寸均匀和高度分散的双金属AUPD纳米颗粒,并通过连续的初期湿度浸渍和热退火方法局限于管状介孔碳。与1wtα%金属负载的双峰介孔碳(CMK-5)包封的AUPD纳米颗粒能够与苄醇氧化的单型介孔碳相比,使优异的活性能够实现优异的活性。在温和条件下,例如,在6小时内,例如,在80℃和大气压下,可以在3小时内达到> 99〜%的转化> 99·%和选择性。结果发现,在催化剂制剂期间,Au和Pd前体浸渍序列是在相同条件下形成AUPD纳米颗粒的关键因素。通过第一次浸渍Au前体来实现相对高的活性,然后是Pd前体的第二次浸渍。通过高分辨率透射电子显微镜(HRTEM),能量分散X射线光谱(EDX)和XRD的结晶结构和分布的特征在于发现AUPD纳米颗粒中的表面暴露的PD原子比例较大比例对催化活性具有阳性作用。 AUPD纳米颗粒具有窄的尺寸分布,其浓缩在约4nm。 TEM和N 2吸附结果表明,催化剂具有大的表面积和发育良好的双峰孔隙互连,这有助于其优异的活性。使用的催化剂保留了高选择性,但随着再循环而降低转化。失活机制归因于吸附在活性表面上的微量苯甲醛的氮苯甲醛,其阻止从活性位点进入苄醇。重要的是,在催化循环完成后,可以通过200≤U的空气中的自动热处理来回收使用的催化剂;吸附的苯甲醛从活性表面中除去。因此,局限于管状介孔碳中的AUPD纳米颗粒可用作开发高度分散的纳米催化剂以改善催化效率的替代方法。

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