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Noble-Metal-Based Catalysts Supported on Zeolites and Macro-Mesoporous Metal Oxide Supports for the Total Oxidation of Volatile Organic Compounds

机译:支持在沸石和宏观介孔金属氧化物的基于贵金属的催化剂用于总氧化挥发性有机化合物

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The use of porous materials to eliminate volatile organic compounds (VOCs) has proven very effective towards achieving sustainability and environmental protection goals. The activity of zeolites and macro-mesoporous metal-oxide supports in the total oxidation of VOCs has been investigated, with and without noble-metal deposition, to develop highly active catalyst systems where the formation of by-products was minimal. The first catalysts employed were zeolites, which offered a good activity in the oxidation of VOCs, but were rapidly deactivated by coke deposition. The effects of the acido-basicity and ionic exchange of these zeolites showed that a higher basicity was related to exchanged ions with lower electronegativities, resulting in better catalytic performances in the elimination of VOCs. Following on from this work, noble metals were deposited onto macro-mesoporous metal-oxide supports to form mono and bimetallic catalysts. These were then tested in the oxidation of toluene to study their catalytic performance and their deactivation process. PdAu/TiO(2) and PdAu/TiO(2)-ZrO(2)80/20 catalysts demonstrated the best activity and life span in the oxidation of toluene and propene and offered the lowest temperatures for a 50% conversion of VOCs and the lowest coke content after catalytic testing. Different characterization techniques were employed to explain the changes occurring in catalyst structure during the oxidation of toluene and propene.
机译:多孔材料消除挥发性有机化合物(VOC)已经证明非常有效地实现可持续性和环境保护目标。已经研究了沸石和宏观介孔金属氧化物载体的总氧化物的活性,并且已经研究了并且没有贵金属沉积,以开发高活性催化剂体系,其中副产物的形成最小。使用的第一催化剂是沸石,其在VOC的氧化中提供了良好的活性,但是通过焦沉积迅速去激活。这些沸石的酸碱性和离子交换的影响表明,更高的碱性与具有较低电气的交换离子有关,导致在消除VOC中的催化性能更好。在此工作之后,将贵金属沉积在宏观 - 中孔金属氧化物载体上以形成单体和双金属催化剂。然后在甲苯的氧化中进行测试以研究其催化性能及其失活过程。 PDAU / TiO(2)和PDAU / TiO(2)-Zro(2)80/20催化剂证明了甲苯和丙烯氧化的最佳活性和寿命,并提供了50%转换的最低温度催化测试后的最低焦炭含量。使用不同的表征技术来解释甲苯和丙烯氧化过程中催化剂结构中发生的变化。

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