摘要
采用柠檬酸络合法合成了La1-xBaxCoO3(x=0,0.1,0.2,0.3)系列钙钛矿型氧化物催化剂。考察了催化剂分解NO的催化活性。结果表明,掺杂量为0.2时分解NO活性最佳,850℃时,催化分解NO为N2的转化率达到69.6%。O2-TPD和H2-TPR测试结果表明:掺入少量的Ba有利于氧空位的还原和迁移,增强了钴离子的氧化还原性能,可使催化剂分解NO的催化活性明显提高。
The perovskite La1-xBaxCoO3 (x = 0. 1,0.2,0.3 ) catalysts were prepared by citric acid sol- gel method. The activity of NO direct decomposition over these catalysts have been investigated, the results show that Lao.s Ba0.2CoO3 is the most active. NO conversion increases with reaction temperature, and at 1 123 K, NO conversion to N2 attained values of 69.6%. O2 - TPD and H2 - TPR results show that doping small Ba at La site of LaCoO3 is favorable in reducing and moving of oxygen vacancy, which enhancing the redox ability of cobalt ion and increasing the NO decomposition activity.
出处
《黑龙江大学自然科学学报》
CAS
北大核心
2008年第5期667-670,共4页
Journal of Natural Science of Heilongjiang University
基金
国家自然科学基金资助项目(20271019)
黑龙江省博士后科研启动基金资助项目(LBH-Q07111)
关键词
氮氧化物
直接分解
钙钛矿氧化物
氧空位
氧迁移
nitric oxide
direct decomposition
perovskite - type catalysts
oxygen vacancy
oxygen mobility