UiO-66及其功能材料负载的超低Pd高效降解甲苯:反应机理、耐水性及SO2的影响

Fukun Bi , Zhenyuan Zhao , Yang Yang , Qiang Liu , Wenyuan Huang , Yuandong Huang , Xiaodong Zhang
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引用次数: 49

摘要

在此,负载在UiO-66上的Pd及其具有超低Pd负载量的NH2-和NO2功能材料(0.05​wt%)用于甲苯氧化。以UiO-66为载体的Pd–U表现出优异的催化性能、耐水性和抗SO2性能。一系列实验和表征表明,小Pd团簇的高分散性、高Pd0/Pd总比例、对甲苯的更好吸附以及对气态氧的最佳吸附和活化能力增强了甲苯对Pd–U的降解。此外,还揭示和讨论了钯基催化剂的催化机理。此外,还测试和分析了耐水性和SO2浓度的影响。引入H2O抑制了甲苯和气态氧的吸附和活化,降低了三种催化剂的催化性能。研究并阐明了SO2对三种催化剂不同影响的机理。该研究为合理设计现场操作条件下的脱甲苯催化剂提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Efficient degradation of toluene over ultra-low Pd supported on UiO-66 and its functional materials: Reaction mechanism, water-resistance, and influence of SO2

Herein, Pd supported on UiO-66 as well as its NH2- and NO2-functional materials with ultra-low Pd loadings (0.05 ​wt%) were synthesized for toluene oxidation. Pd–U, using UiO-66 as the support, exhibited superb catalytic performance, water resistance, and resistance to SO2. A series of experiments and characterizations revealed that a high dispersion of small Pd clusters, high Pd0/Pdtotal proportion, better adsorption for toluene, and the best adsorption and activation capacities of gaseous oxygen species enhanced toluene degradation over Pd–U. Additionally, the catalytic mechanism over the Pd-based catalysts was revealed and discussed. Furthermore, the water-resistance and the SO2 concentration influence were tested and analyzed. Introducing H2O suppressed the adsorption and activation of toluene as well as gaseous oxygen species, and decreased catalytic performance over the three catalysts. The mechanism of the different impacts of SO2 on the three catalysts was investigated and elucidated. This study provides guidance for rationally designing catalysts for removing toluene under in-field operating conditions.

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