含铁、含铜氧化物催化剂制备方法对其一氧化碳氧化制二氧化碳反应活性的影响

S. Zulfugarova, G. Azimova, Z. Aleskerova, R.J. Qasimov, M. Bayramov, E. H. Ismailov, D. Tagiyev
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引用次数: 1

摘要

以有机试剂柠檬酸、甘氨酸、尿素为络合剂和“燃料”,采用自燃烧溶胶-凝胶技术合成了含铁、含铜氧化物催化剂;研究了它们在一氧化碳氧化成二氧化碳中的活性。采用x射线粉末衍射、红外光谱和电子顺磁共振等方法对所得样品进行了表征,并通过测量样品的比表面积来确定样品的织构特征。结果表明,无论采用何种制备方法,所有合成的样品都是铁氧化物fe2o3、铜CuO和铁氧体铜CuFe2O4的混合物。研究发现,有机试剂的性质对合成催化剂的催化活性有一定的影响。采用溶胶-凝胶法制备Cu:Fe=1:1的催化剂,用尿素自燃烧,在130℃下可实现CO的完全转化。用柠檬酸合成的相同催化剂在250°C时具有活性,而在用甘氨酸制备的催化剂上,CO在350°C的更高温度下完全转化。假设不同性质的燃烧导致不同表面形貌和织构的形成,最终决定了催化活性。因此,使用尿素作为“燃料”获得的催化活性最高的样品比其他两种样品具有更高的比表面积(25 m2 / g)(对于使用柠檬酸和甘氨酸获得的样品,比表面积分别为9 m2 / g和5.8 m2 / g)。
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EFFECT OF PREPARATION METHOD OF IRON-, COPPER- CONTAINING OXIDE CATALYSTS ON THEIR ACTIVITY IN THE REACTION OF OXIDATION OF CARBON MONOXIDE TO CARBON DIOXIDE
Iron- and copper-containing oxide catalysts have been synthesized by sol-gel technology with autocombustion using organic reagents - citric acid, glycine, urea as a complexing agent and "fuel"; studied their activity in the oxidation of carbon monoxide to dioxide. The obtained samples were characterized by the methods of X-ray powder diffraction, infrared spectroscopy and electronic paramagnetic resonance, the texture characteristics of these samples was determined by measuring the specific surface area. It is shown that, regardless of the preparation method, all synthesized samples are mixtures of iron oxides Fe 2O3, copper CuO, and copper ferrite CuFe2O4. It was found that the nature of the organic reagent affects the catalytic activity of the synthesized catalysts. On a catalyst with a Cu:Fe=1:1 ratio, prepared by the sol-gel method with autocombustion using urea, the complete conversion of CO is achieved at 130°C. The same catalyst, synthesized with citric acid, is active at 250°C and on a catalyst prepared using glycine, complete conversion of CO occurs at a higher temperature of 350°C. It is assumed that the different nature of combustion leads to the formation of different surface morphology and texture, which ultimately determines the catalytic activity. Thus, the most catalytically active sample was obtained using urea as a "fuel" has a higher specific surface area (25 m2 / g) than the other two samples (for the samples obtained with citric acid and glycine, the specific surface area is 9 m2 / g and 5.8 m2 / g, respectively).
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