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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Influence of ceria on physicochemical, surface and catalytic properties of alumina supported manganese catalysts
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Influence of ceria on physicochemical, surface and catalytic properties of alumina supported manganese catalysts

机译:二氧化铈对氧化铝负载锰催化剂的理化,表面和催化性能的影响

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A series of catalysts containing manganese oxides supported on alumina and ceria-promoted alumina was prepared by wet impregnation method using finely powdered support material and manganese and/or cerium nitrate. The physicochemical, surface and catalytic properties of the thermally treated solids (500, 800 and 900 degrees C) were investigated using XRD, ESR, nitrogen adsorption at -196 degrees C and hydrogen peroxide decomposition in a aqueous solution at 30-50 degrees C. Experimental results show that Mn oxidation state changes from Mn4+ to Mn2+ by increasing the calcination temperature of solids studied. However, there are two unique features associated with CeO2 as a material of interest. The first favors the dispersion of manganese oxides deposited on gamma-Al2O3 catalyst calcined at 500 degrees C. The second enhances the formation of Mn3O4 species from Mn2O3 deposited initially on the alumina support calcined at 800 and 900 degrees C. These conclusions can be discussed in terms of modifications of both the oxygen storage capacity of ceria and structural properties of manganese oxides which are found in the investigated solids. The specific surface area of Mn/Al mixed oxides system calcined at 500 degrees C was found to increase by increasing the amount of dopant added. Opposite effect was observed by increasing the clacination temperature from 500 to 900 degrees C. The doping process followed by calcination at different temperatures brought about an increase in the catalytic activity of mixed oxides system. These treatments did not modify the mechanism of the catalyzed reaction but changed the number of catalytically active sites taking place in it without changing the energetic nature of these sites.
机译:通过湿式浸渍法,使用粉末状的载体材料和锰和/或硝酸铈,制备了一系列负载在氧化铝上的氧化锰和二氧化铈促进的氧化铝的催化剂。使用XRD,ESR,-196℃下的氮吸附和30-50℃下的水溶液中的过氧化氢分解,研究了热处理后的固体(500、800和900℃)的理化,表面和催化性能。实验结果表明,通过提高所研究固体的煅烧温度,Mn的氧化态从Mn4 +变为Mn2 +。但是,与CeO2有关的材料有两个独特的特征。第一个有利于沉积在500摄氏度煅烧的γ-Al2O3催化剂上的锰氧化物的分散。第二个促进了最初沉积在800和900摄氏度煅烧的氧化铝载体上的Mn2O3形成Mn3O4物种的形成。二氧化铈的储氧能力和锰氧化物的结构性质的修饰术语,它们在所研究的固体中发现。发现通过增加添加的掺杂剂的量,在500℃下煅烧的Mn / Al混合氧化物体系的比表面积增加。通过将胶凝温度从500摄氏度提高到900摄氏度,可以观察到相反的效果。掺杂过程随后在不同温度下煅烧使混合氧化物体系的催化活性提高。这些处理没有改变催化反应的机理,但是改变了其中发生的催化活性位点的数量,而没有改变这些位点的能量性质。

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