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首页> 外文期刊>Advances in Materials Physics and Chemistry >La_2O_3/Fe_2O_3-CeO_2 Composite Oxide Catalyst and Its Performance
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La_2O_3/Fe_2O_3-CeO_2 Composite Oxide Catalyst and Its Performance

机译:LA_2O_3 / FE_2O_3-CEO_2复合氧化物催化剂及其性能

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The La_2O_3/Fe_2O_3-CeO_2 composite oxide catalysts were prepared by coprecipitation method, sol-gel method and hydrothermal method. The effect of preparation methods on structure morphology and photocatalytic properties of La_2O_3/Fe_2O_3-CeO_2 samples was investigated. The results show that the cubic CeO_2 structure can be obtained at 600. The rod-shaped sample prepared by coprecipitation method, displays the highest crystalline and the strongest diffraction peak intensity. The spherical sample is acquired from sol-gel method, while the small granular sample prepared by hydrothermal method tends to aggregate. The maximum specific surface area of the sample prepared by coprecipitation method is 76.21 m~2/g, the minimum specific area of the sample from sol-gel method is 32.66 m~2/g and the maximum pore size is 13.84 nm, while the minimum pore volume and pore size of the sample by hydrothermal method are 0.038 cm~3/g and 3.95 nm respectively. The band gap energy of catalyst samples is in the following order: sample-CP sample-SG sample-HT. The sample obtained by coprecipitation method has the best catalytic degradation performance for methylene blue. Under the excitation of visible light, the degradation rate was 99.58% at 50 minutes, which was higher than those of sol-gel method and hydrothermal method by 5.58% and 9.54% respectively. The catalytic degradation reaction is a first-order kinetic model: ln (c_0/ct) = kt + q_e. The maximum k-value of the sample degradation process obtained by coprecipitation method is 0.074 min~(-1).
机译:通过共沉淀法,溶胶 - 凝胶法和水热法制料制备LA_2O_3 / FE_2O_3-CEO_2复合氧化物催化剂。研究了制备方法对La_2O_3 / Fe_2O_3-CeO_2样品的结构形态和光催化性能的影响。结果表明,立方CEO_2结构可以在600中获得。通过共沉淀法制备制备的棒状样品,显示出最高的结晶和最强的衍射峰强度。从溶胶 - 凝胶法中获得球形样品,而通过水热法制备的小粒状样品倾向于聚集。通过共沉淀法制备制备的样品的最大比表面积为76.21m〜2 / g,来自溶胶 - 凝胶法的样品的最小特定面积为32.66m〜2 / g,最大孔径为13.84nm,而且通过水热法的最小孔体积和样品的孔径分别为0.038cm〜3 / g和3.95nm。催化剂样品的带间隙能量是以下顺序:样品-CP <样品-Sg <样品-HT。通过共沉淀方法获得的样品具有最佳的亚甲基催化降解性能。在可见光的激发下,50分钟的降解速率为99.58%,分别高于溶胶 - 凝胶法和水热法的5.58%和9.54%。催化降解反应是一阶动力学模型:LN(C_0 / CT)= KT + Q_E。通过共沉淀法获得的样品降解过程的最大K值为0.074分钟〜(-1)。

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