Cobalt and cobalt-iron spinel oxides as bulk and silica supported catalysts in the ethanol combustion reaction

Yasmina Hammiche-Bellal , Nabila Zouaoui-Mahzoul , Ibtissem Lounas , Amel Benadda , Rafik Benrabaa , Aline Auroux , Laaldja Meddour-Boukhobza , Amar Djadoun
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引用次数: 15

Abstract

Cobalt and mixed iron-cobalt spinel oxides CoxFe(3-x)O4 supported on SiO2 ‘IMP-Cox-500′ and their bulk analogues ‘CP-Cox-500′ were prepared via impregnation and co-precipitation methods respectively and calcined at 500 °C. Thermogravimetric analysis ‘ATG/DTG’, X-ray Diffraction method ‘XRD’, Texture measurements ‘BET/BJH’ and Temperature Programmed Reduction technique ‘TPR’ were used for their characterization. Their catalytic behavior in ethanol combustion was investigated. Results showed that nanostructured oxide materials with spinel structure were obtained with a good dispersion of the active phase at the surface of silica in the case of IMP-Cox-500 compounds. The reduction behavior of the prepared samples is highly dependent on the oxide composition and interaction with the support; which is directly related to the catalytic behavior. The use of supported catalysts improves the catalytic performance and leads the reaction towards a total oxidation by decreasing greatly the formation of partial oxidation products. The obtained values of activation energies are relatively low in comparison with the literature data. A compensation effect was found by carrying out ethanol combustion through the spinel systems considered in this work.

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钴和钴铁尖晶石氧化物作为乙醇燃烧反应的体积和二氧化硅负载催化剂
采用浸渍法和共沉淀法分别制备了负载在SiO2 ' IMP-Cox-500 '及其大块类似物' CP-Cox-500 '上的钴和铁钴混合尖晶石氧化物CoxFe(3-x)O4,并在500℃下煅烧。采用热重分析ATG/DTG、x射线衍射法XRD、织构测量BET/BJH和程序升温还原技术TPR对其进行表征。研究了它们在乙醇燃烧中的催化行为。结果表明,在IMP-Cox-500化合物的情况下,获得了具有尖晶石结构的纳米氧化材料,其活性相在二氧化硅表面具有良好的分散性。所制备样品的还原行为高度依赖于氧化物组成和与载体的相互作用;这直接关系到催化行为。负载型催化剂的使用提高了催化性能,并通过大大减少部分氧化产物的形成,使反应向全氧化方向发展。所得的活化能值与文献数据相比相对较低。通过本文所考虑的尖晶石体系进行乙醇燃烧,发现了补偿效应。
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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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