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Co3O4/CeO2 CO氧化的原位红外光谱研究

邵建军 朱锡 张永坤 王明贵

邵建军, 朱锡, 张永坤, 王明贵. Co3O4/CeO2 CO氧化的原位红外光谱研究[J]. 燃料化学学报(中英文), 2012, 40(02): 229-234.
引用本文: 邵建军, 朱锡, 张永坤, 王明贵. Co3O4/CeO2 CO氧化的原位红外光谱研究[J]. 燃料化学学报(中英文), 2012, 40(02): 229-234.
SHAO Jian-jun, ZHU Xi, ZHANG Yong-kun, WANG Ming-gui. In situ FT-IR study on CO oxidation over Co3O4/CeO2 catalyst[J]. Journal of Fuel Chemistry and Technology, 2012, 40(02): 229-234.
Citation: SHAO Jian-jun, ZHU Xi, ZHANG Yong-kun, WANG Ming-gui. In situ FT-IR study on CO oxidation over Co3O4/CeO2 catalyst[J]. Journal of Fuel Chemistry and Technology, 2012, 40(02): 229-234.

Co3O4/CeO2 CO氧化的原位红外光谱研究

基金项目: 中国博士后科学基金(20100471808)。
详细信息
    通讯作者:

    邵建军(1967-), 男, 博士, 专业为物理化学, Tel: 0411-85888078; E-mail: sjj05@126.com。

  • 中图分类号: O643

In situ FT-IR study on CO oxidation over Co3O4/CeO2 catalyst

  • 摘要: 采用沉淀氧化法制备了Co3O4/CeO2催化剂。分别在干、湿条件下进行了一氧化碳氧化反应研究。运用FT-IR表征手段,在钴铈复合氧化物上进行了CO吸附及CO/O2共吸附研究。结果表明,与纯的Co3O4样品相比,Co3O4/CeO2具有明显的抗湿气能力。Co3O4/CeO2催化剂在进行CO氧化时,表面形成了类碳酸盐物种。当环境温度低于453 K时,催化剂上类碳酸盐的生成与形成类碳酸盐物种后受热分解存在着动态平衡。当环境温度高于493 K,催化剂上生成的类碳酸盐物全部受热分解。氧化铈的加入提高了催化剂的抗湿气性能。较小粒径的Co3O4与CeO2产生的强相互作用可使CeO2向Co3O4提供氧,因而间接提供了CO氧化需要的氧。
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出版历程
  • 收稿日期:  2011-02-11
  • 修回日期:  2011-06-03
  • 刊出日期:  2012-02-29

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