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作 者:胡瑞生[1] 吴海霞[1] 马丽丽[1] 王富[1]
机构地区:[1]内蒙古大学化学化工学院稀土材料化学与物理重点实验室,内蒙古呼和浩特010021
出 处:《石油化工》2006年第4期319-323,共5页Petrochemical Technology
基 金:国家自然科学基金资助项目(20163001)内蒙古自然科学基金资助项目(200408020203)。
摘 要:以(NH4)2Ce(NO3)6为原料,选用葡萄糖为络合剂,采用研磨固相法制备了在不同温度下焙烧的氧化铈(Ce-O)和掺杂铁的氧化铈(Fe-Ce-O)催化剂。用X射线衍射法表征了催化剂的结构;用程序升温还原法测试了催化剂的还原性能;考察了经不同温度焙烧后,掺杂铁对Ce-O催化剂的CH4催化燃烧活性的影响。实验结果表明,掺杂铁后的Fe-Ce-O催化剂的粒径变小、还原性能增强、CH4催化燃烧活性提高。经400℃焙烧的Fe-Ce-O催化剂呈现单一的CeO2物相,属立方晶系;经800℃和 1 200℃焙烧的Fe-Ce-O催化剂以CeO2为主要物相,并有少量Fe2O3物相。与未掺杂铁的Ce-O催化剂相比,Fe-Ce-O催化剂具有较高的CH4催化燃烧活性。Cerium oxide (Ce-O)and Fe doped cerium oxide (Fe-Ce-O)catalysts were prepared separately by solid-phase milling of( NH4 )2Ce (NO3)6 with glucose as complex agent and by solidphase milling of ( NH4 ) 2Ce( NO3 ) 6 + Fe( NO3 ) 3 with glucose as complex agent. The milled mixtures were calcined at 400,800, and 1 200℃ for 3 h respectively. The obtained catalysts were characterized by means of XRD and TPR. Activities of catalysts were evaluated by methane combustion reaction. Doping of Fe led to particle size decreasing, improving of catalyst activities, and enhancing their reductibility. XRD spectra showed that single phase cubic CeO2 existed in Fe-Ce-O catalyst calcined at 400℃. With increasing of calcination temperature, the diffraction peaks of tetragonal Fe2O3 appeared, indicating the improvement of crystal structure of Fe-Ce-O catalyst. But CeO2 was still the main phase of Fe-Ce-O catalyst calcined at 800℃ and 1 200℃. Fe-Ce-O catalyst was higher in catalytic activity for methane combustion than Ce-O catalyst.
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