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Highly active Pd-based catalysts with hierarchical pore structure for toluene oxidation: Catalyst property and reaction determining factor

机译:具有分级孔隙结构的高活性钯基催化剂,用于甲苯氧化:催化剂性质和反应决定因素

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A series of micro/mesoporous hybridized materials with coke-resistant ZSM-5 and three-dimensional large pore KIT-6 as their micro- and mesoporous components were synthesized and investigated for toluene deep oxidation. The characterization results show that most of Al atoms are tetrahedrally coordinated in the framework of the samples, and the ratio of ZSM-5 to KIT-6 can be systematically controlled by varying the Si/Al molar ratio in the synthesis mixture. The acid sites over the supports are favorable for Pd nanoparticle dispersion and metallic Pd oxidation due to their electrophilic characters. All Pd supported composite materials are found to be powerful catalysts for the total oxidation of toluene. Particularly, Pd/ZK-50 possesses the highest catalytic activity with 90% toluene decomposition at 197℃, this temperature is much lower than that of Pd/KIT-6 (T_(90) = 234℃). CO2 desorption capability has positive effects on catalytic activity, while the influence of toluene adsorption property is negligible. The superior activity of the composite catalysts can be ascribed to the cumulative of specific surface area, support acidity, Pd particles dispersion and CO2 desorption capability.
机译:合成了一系列以耐焦炭ZSM-5和三维大孔KIT-6为微孔和中孔组分的微孔/介孔杂化材料,并研究了甲苯的深度氧化作用。表征结果表明,大多数Al原子在样品框架内呈四面体配位,并且可以通过改变合成混合物中的Si / Al摩尔比来系统控制ZSM-5与KIT-6的比例。载体上的酸位点由于其亲电特性而有利于Pd纳米颗粒分散和金属Pd氧化。发现所有Pd负载的复合材料都是甲苯全部氧化的有力催化剂。特别是,Pd / ZK-50在197℃具有最高的催化活性,甲苯分解率为90%,该温度远低于Pd / KIT-6(T_(90)= 234℃)。 CO 2的解吸能力对催化活性有积极影响,而甲苯吸附性能的影响可以忽略不计。复合催化剂的优异活性可以归因于比表面积,载体酸度,Pd颗粒分散和CO 2解吸能力的累积。

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