Ordered mesoporous MCo2O4 (M = Cu, Zn and Ni) spinel catalysts with high catalytic performance for methane combustion

Tae Hwan Lim , Su Bin Park , Ji Man Kim , Do Heui Kim
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引用次数: 42

Abstract

Ordered mesoporous MCo2O4 (M = Cu, Zn and Ni) spinel catalysts were synthesized via nano-replication method using mesoporous silica KIT-6 as the hard template. They were applied to methane combustion, in comparison with bulk MCo2O4 spinel catalysts prepared by co-precipitation method. A combined N2 adsorption-desorption, XRD and TEM results clearly confirm that mesoporous MCo2O4 (m-MCo2O4) spinel catalysts contain ordered mesostructure, resulting in the higher BET surface area and pore volume than bulk ones (b-MCo2O4). Moreover, the former catalysts demonstrate the better thermal stability as indicated by larger amount of MCo2O4 phase and smaller size of crystallite domain after calcination at 550 °C. Therefore, such excellent properties rationalize that the m-MCo2O4 spinel catalysts reveal higher catalytic activity for methane combustion than bulk counterparts. When it comes to the catalytic performance of the meso catalysts for methane combustion, the m-CuCo2O4 spinel catalyst has superior performance, which is related to the high normalized amount of Co3+ cations on the surface, as evidenced by XPS.

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有序介孔MCo2O4 (M = Cu, Zn和Ni)尖晶石催化剂具有较高的甲烷燃烧催化性能
以介孔二氧化硅KIT-6为硬模板,采用纳米复制法制备了有序介孔MCo2O4 (M = Cu, Zn和Ni)尖晶石催化剂。将其应用于甲烷燃烧,并与共沉淀法制备的大块MCo2O4尖晶石催化剂进行了比较。N2吸附-脱附、XRD和TEM的综合分析结果清楚地证实了介孔MCo2O4 (m-MCo2O4)尖晶石催化剂具有有序的介孔结构,使得其BET比表面积和孔体积均高于块体MCo2O4 (b-MCo2O4)。在550℃下煅烧后,前者的MCo2O4相数量较多,晶域尺寸较小,表现出较好的热稳定性。因此,这些优异的性能证明m-MCo2O4尖晶石催化剂对甲烷燃烧的催化活性比块状催化剂更高。在甲烷燃烧介观催化剂的催化性能方面,m-CuCo2O4尖晶石催化剂表现出更优异的性能,这与XPS证明其表面Co3+阳离子的规范化量高有关。
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2.8 months
期刊介绍: The Journal of Molecular Catalysis A: Chemical publishes original, rigorous, and scholarly full papers that examine the molecular and atomic aspects of catalytic activation and reaction mechanisms in homogeneous catalysis, heterogeneous catalysis (including supported organometallic catalysis), and computational catalysis.
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