SCI和EI收录∣中国化工学会会刊

中国化学工程学报 ›› 2023, Vol. 62 ›› Issue (10): 1-10.DOI: 10.1016/j.cjche.2023.08.004

• Full Length Article •    下一篇

High catalytic performance of CuCe/Ti for CO oxidation and the role of TiO2

Tingting Chang1, Ziyan Wang2, Zhimiao Wang1,3, Hualiang An1,3, Fang Li1,3, Wei Xue1,3, Yanji Wang1,3,4   

  1. 1. Hebei Provincial Key Laboratory of Green Chemical Technology and High Efficient Energy Saving, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China;
    2. Purification Equipment Research Institute of CSIC, Handan 056027, China;
    3. Tianjin Key Laboratory of Chemical Process Safety, Tianjin 300130, China;
    4. Hebei Industrial Technology Research Institute of Green Chemical Industry, Huanghua 061100, China
  • 收稿日期:2023-02-20 修回日期:2023-08-20 出版日期:2023-10-28 发布日期:2023-12-23
  • 通讯作者: Fang Li,E-mail:lifang@hebut.edu.cn;Wei Xue,E-mail:weixue@hebut.edu.cn
  • 基金资助:
    This work was supported by the National Natural Science Foundation of China (U21A20306, U20A20152) and Natural Science Foundation of Hebei Province (B2022202077). We thank Ian McNaught, Ph.D., from Liwen Bianji, (Edanz) China (www.liwenbianji.cn/), for editing the English text of a draft of this manuscript.

High catalytic performance of CuCe/Ti for CO oxidation and the role of TiO2

Tingting Chang1, Ziyan Wang2, Zhimiao Wang1,3, Hualiang An1,3, Fang Li1,3, Wei Xue1,3, Yanji Wang1,3,4   

  1. 1. Hebei Provincial Key Laboratory of Green Chemical Technology and High Efficient Energy Saving, School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China;
    2. Purification Equipment Research Institute of CSIC, Handan 056027, China;
    3. Tianjin Key Laboratory of Chemical Process Safety, Tianjin 300130, China;
    4. Hebei Industrial Technology Research Institute of Green Chemical Industry, Huanghua 061100, China
  • Received:2023-02-20 Revised:2023-08-20 Online:2023-10-28 Published:2023-12-23
  • Contact: Fang Li,E-mail:lifang@hebut.edu.cn;Wei Xue,E-mail:weixue@hebut.edu.cn
  • Supported by:
    This work was supported by the National Natural Science Foundation of China (U21A20306, U20A20152) and Natural Science Foundation of Hebei Province (B2022202077). We thank Ian McNaught, Ph.D., from Liwen Bianji, (Edanz) China (www.liwenbianji.cn/), for editing the English text of a draft of this manuscript.

摘要: CuCe/Ti-A and CuCe/Ti-R catalysts were prepared using anatase TiO2 (TiO2-A) and rutile TiO2 (TiO2-R) as supports using the incipient wetness impregnation method for the carbon monoxide (CO) oxidation reaction and were compared with a CuCe-C catalyst prepared using the co-precipitation method. The CuCe/Ti-A catalyst exhibited the highest activity, with complete CO conversion at 90 ℃, when the gas hourly space velocity was 24000 ml·g-1·h-1 and the CO concentration was approximately 1% (vol). A series of characterizations of the catalysts revealed that the CuCe/Ti-A catalyst has a larger specific surface area, more Cu+ species and oxygen vacancies, and the Cu species of CuCe/Ti-A catalyst is more readily reduced. In situ FT-IR results indicate that the bicarbonate species generated on the CuCe/Ti-A catalyst have lower thermal stability than the carbonate species on CuCe/Ti-R, and will decompose more readily to form CO2. Therefore, CuCe/Ti-A has excellent catalytic activity for CO oxidation.

关键词: CO oxidation, TiO2 crystal phase, CuCe/Ti, Reaction mechanism

Abstract: CuCe/Ti-A and CuCe/Ti-R catalysts were prepared using anatase TiO2 (TiO2-A) and rutile TiO2 (TiO2-R) as supports using the incipient wetness impregnation method for the carbon monoxide (CO) oxidation reaction and were compared with a CuCe-C catalyst prepared using the co-precipitation method. The CuCe/Ti-A catalyst exhibited the highest activity, with complete CO conversion at 90 ℃, when the gas hourly space velocity was 24000 ml·g-1·h-1 and the CO concentration was approximately 1% (vol). A series of characterizations of the catalysts revealed that the CuCe/Ti-A catalyst has a larger specific surface area, more Cu+ species and oxygen vacancies, and the Cu species of CuCe/Ti-A catalyst is more readily reduced. In situ FT-IR results indicate that the bicarbonate species generated on the CuCe/Ti-A catalyst have lower thermal stability than the carbonate species on CuCe/Ti-R, and will decompose more readily to form CO2. Therefore, CuCe/Ti-A has excellent catalytic activity for CO oxidation.

Key words: CO oxidation, TiO2 crystal phase, CuCe/Ti, Reaction mechanism