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负载型Au-Pd双金属催化剂的制备及其对CO氧化的催化活性
引用本文:麻春艳,李新华,金明善,廖卫平,管仁贵,索掌怀. 负载型Au-Pd双金属催化剂的制备及其对CO氧化的催化活性[J]. 催化学报, 2007, 28(6): 535-540
作者姓名:麻春艳  李新华  金明善  廖卫平  管仁贵  索掌怀
作者单位:烟台大学应用催化研究所,山东烟台,264005
基金项目:国家自然科学基金(20473070),山东省自然科学基金(Y2004B07).
摘    要:采用改性的等体积浸渍法制备了SiO2负载的Au-Pd双金属催化剂,考察了催化剂的焙烧温度对CO氧化反应活性的影响.与623,723和773K的条件下焙烧的催化剂相比,673K焙烧的催化剂具有良好的催化CO氧化活性,CO完全转化温度低于398K.应用N2物理吸附、X射线衍射、程序升温还原、CO程序升温脱附及X射线光电子能谱等技术对催化剂进行了表征.结果表明,673K焙烧的催化剂具有最大的比表面积和最小的孔径,存在Au0,Pd0和PdO相,AuxPdy合金相很少;而773K焙烧的催化剂上除了含有Au0,Pd0和PdO相外,还存在明显的AuxPdy合金相.具有大比表面积,小孔径,Au0,Pd0和PdO多相共存的催化剂可使CO的吸附量增加,催化活性提高;而AuxPdy合金相的生成并不能提高催化剂的催化活性.

关 键 词:    二氧化硅  双金属催化剂  焙烧温度  一氧化碳  氧化
文章编号:0253-9837(2007)06-0535-06
修稿时间:2006-11-29

Preparation of Supported Au-Pd Bimetallic Catalyst and Its Catalytic Activity for CO Oxidation
MA Chunyan,LI Xinhua,JIN Mingshan,LIAO Weiping,GUAN Rengui,SUO Zhanghuai. Preparation of Supported Au-Pd Bimetallic Catalyst and Its Catalytic Activity for CO Oxidation[J]. Chinese Journal of Catalysis, 2007, 28(6): 535-540
Authors:MA Chunyan  LI Xinhua  JIN Mingshan  LIAO Weiping  GUAN Rengui  SUO Zhanghuai
Affiliation:Institute of Applied Catalysis, Yantai University, Yantai 264005, Shandong, China
Abstract:The Au-Pd/SiO2 catalyst was prepared by impregnation of SiO2 with an alkaline HAuCl4 solution by an incipient wetness method.The effect of calcination temperature on the catalytic activity for CO oxidation was evaluated.The Au-Pd/SiO2 catalyst calcined in air at 673 K shows higher catalytic activity compared with the catalysts calcined at 623,723,or 773 K.The catalyst was characterized by N2 adsorption-desorption isotherms,X-ray diffraction,temperature-programmed reduction,CO temperature-programmed desorption,and X-ray photoelectron spectroscopy.The results indicate that the catalyst calcined at 673 K has the largest surface area and the smallest pore volume,and there exist Pd0,PdO,and Au0 phases on it.The formation of AuxPdy alloy does not favor the catalyst activity.
Keywords:gold  palladium  silica  bimetallic catalyst  calcination temperature  carbon monoxide  oxidation
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