陆安慧

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教授

博士生导师

硕士生导师

主要任职:校长助理

其他任职:精细化工国家重点实验室副主任,辽宁省低碳资源高值化利用重点实验室主任

性别:男

毕业院校:中科院山西煤化所

学位:博士

所在单位:化工学院

学科:工业催化. 化学工艺. 能源化工

办公地点:大连市凌工路2号大连理工大学西部校区化工楼,邮编:116024

联系方式:0411-84986112

电子邮箱:anhuilu@dlut.edu.cn

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Bimetallic Au-Pd Nanoparticles Confined in Tubular Mesoporous Carbon as Highly Selective and Reusable Benzyl Alcohol Oxidation Catalysts

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论文类型:期刊论文

发表时间:2021-01-12

发表刊物:CHEMCATCHEM

卷号:4

期号:10,SI

页面范围:1595-1602

ISSN号:1867-3880

关键字:carbon; mesoporous materials; nanoparticles; oxidation; transition metals

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.