分别采用共沉淀法、胶溶法和胶溶-共沉淀法制备了Ce0.5Zr0.5O2(12wt%)-Al2O3(CZA)储氧材料, 并通过XRD、低温N2吸附?脱附、氧脉冲吸附(OSC)、程序升温还原(H2-TPR)和O2-程序升温脱附(O2-TPD)等手段进行了表征. 材料经过1000℃焙烧后, XRD结果表明, 三种方法制备的样品均存在CeO2-ZrO2立方萤石和γ-Al2O3两种晶型. N2吸附-脱附结果表明, 胶溶-共沉淀法制备的样品, 具有最大的比表面积和孔容, 分别为146.2m2/g和0.5mL/g, 且有最佳的孔径分布; 氧脉冲吸附(OSC)和H2-TPR结果表明胶溶?共沉淀法制备的材料, 具有最佳的储氧性能和还原能力; 同时实验还比较了经1100℃焙烧对几种方法制备样品性能的影响.
Oxygen storage material of Ce0.5Zr0.5O2(12wt%)-Al2O3(CZA) was prepared by three different methods of coprecipitation, peptization and peptization-coprecipitation. The structure and physicochemical properties of materials were characterized by X-ray diffraction (XRD), N2 adsorption-desorption, oxygen pulse adsorption (OSC), H2-temperature programmed reduction (TPR) and O2-programmed desorption (O2-TPD). The XRD results demonstrate that all the samples have CeO2-ZrO2 cubic fluorite and γ-Al2O3 after calcined at 1000℃. The results according to N2 adsorption-desorption show that the sample prepared by peptization-coprecipitation has higher specific surface area (146.2 m2/g), larger pore volume (0.5 mL/g), and the best distribution of the pore size. The results from OSC and H2-TPR indicate that the sample prepared by peptization-coprecipitation has the best performance of oxygen storage and reduction capacity. At the same time, the influence of different methods on the properties of samples after calcined at 1100℃ are discussed.
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