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作 者:Li Shunqing Zou Guojun Wang Xiaolai
机构地区:[1]State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China [2]Graduate University of Chinese Academy of Sciences, Beijing 100049, China
出 处:《Journal of Rare Earths》2006年第5期523-523,共1页稀土学报(英文版)
摘 要:Different metal substituted hexaaluminate catalysts (Ba0.8 La0.2 MAl11 O19-α) were the M = Mn, Fe, Co, Cu were prepared using alumina sol as the (NH4)2CO3 coprecipitation precursor and supercritical drying (SCD) method. Meanwhile the catalysts were characterized using BET, XRD, TEM, UV-Vis-DR and O2-TPD techniques. The rod-like hexaaluminate nanoparticles with high surface area ranging from 42 to 73 m^2·g^-1 were obtained after calcinations at 1200℃. The XRD results reveal that the main crystal phase of the catalyst is hexaaluminate and small amount of α-Al2O3 existed except for Ba0.8La0.2MnAl11O19-α catalyst. Moreover, the UV-Vis-DR results verify that Fe^3+ , Mn^3+ occupy the Oh sites in the hexaaluminate structure while Co^3+ , Cu^2+ locate at the Oh and Td sites.Different metal substituted hexaaluminate catalysts (Ba0.8 La0.2 MAl11 O19-α) were the M = Mn, Fe, Co, Cu were prepared using alumina sol as the (NH4)2CO3 coprecipitation precursor and supercritical drying (SCD) method. Meanwhile the catalysts were characterized using BET, XRD, TEM, UV-Vis-DR and O2-TPD techniques. The rod-like hexaaluminate nanoparticles with high surface area ranging from 42 to 73 m^2·g^-1 were obtained after calcinations at 1200℃. The XRD results reveal that the main crystal phase of the catalyst is hexaaluminate and small amount of α-Al2O3 existed except for Ba0.8La0.2MnAl11O19-α catalyst. Moreover, the UV-Vis-DR results verify that Fe^3+ , Mn^3+ occupy the Oh sites in the hexaaluminate structure while Co^3+ , Cu^2+ locate at the Oh and Td sites.
关 键 词:METHANE catalytic combustion HEXAALUMINATE supercritical drying rare earths
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