节点文献

以TiO2多孔微球为载体的CuO/TiO2催化剂的制备、表征及CO氧化催化性能

Preparation,Characterization and CO Oxidation Catalytic Properties of CuO/TiO2 Catalysts Supported on Porous Microspheres Composed of TiO2 Nanocrystals

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 郭先芝黄静王彦美王淑荣张保龙吴世华

【Author】 GUO Xian-Zhi,HUANG Jing,WANG Yan-Mei,WANG Shu-Rong,ZHANG Bao-Long,WU Shi-Hua(Department of Chemistry,Nankai University,Tianjin 300071,China)

【机构】 南开大学化学系南开大学化学系 天津300071天津300071

【摘要】 利用高分子反相悬浮聚合技术结合溶胶-凝胶法制备了纳米TiO2晶粒组成的多孔微球.以TiO2多孔微球为载体,利用浸渍法制备了CuO/TiO2催化剂,用示差扫描量热法、热重分析、X射线衍射和X射线光电子能谱(XPS)对TiO2多孔微球和催化剂进行了表征,并对其进行了CO催化氧化性能的评价.结果表明,于500℃焙烧的TiO2多孔微球基本为锐钛矿型结构,其粒径为19.5nm.XPS结果表明,催化剂中载体和活性组分存在相互作用,Cu除了以Cu2+的形式存在外,还以部分Cu+和Cu0的形式存在.CO催化氧化研究结果表明,催化剂的催化活性与浸渍液的浓度和催化剂的焙烧温度有关.用0.5mol/LCu(NO3)2·3H2O溶液浸渍得到的催化剂和于200℃焙烧得到的催化剂具有较好的催化活性.

【Abstract】 The porous TiO2 microspheres were prepared by the reversed-phase suspension polymerization and sol-gel method. The CuO/TiO2 catalysts with porous microspheres composed of TiO2 nanocrystals as the support were prepared by impregnation method. The properties of the porous TiO2 microspheres and CuO/TiO2 catalysts were studied by TG-DTA,X-ray diffraction,XPS and ICP. The catalytic properties of the catalysts for CO oxidation were studied via a microreactor-GC system. The results show that the porous microspheres were mainly composed of anatase TiO2 nanocrystals with a size of 19.5 nm. The XPS results indicate that there was interaction between the support and the active component,and Cu mainly existed as Cu2+ with some other form. The catalytic activity of the catalysts depends on the concentration of the impregnation solution and the calcination temperature of the CuO/TiO2 catalysts. The catalyst impregnated in 0.5 mol/L Cu ( NO3 )2 ·3H2O had a better catalytic activity. The optimum calcination temperature of the CuO/TiO2 catalysts was 200 ℃.

【基金】 国家自然科学基金(批准号:20771061)资助
  • 【文献出处】 高等学校化学学报 ,Chemical Journal of Chinese Universities , 编辑部邮箱 ,2008年06期
  • 【分类号】O643.36
  • 【被引频次】16
  • 【下载频次】623
节点文献中: 

本文链接的文献网络图示:

本文的引文网络