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作者:

Han, Zhuo (Han, Zhuo.) | Liu, Yuxi (Liu, Yuxi.) | Deng, Jiguang (Deng, Jiguang.) | Xie, Shaohua (Xie, Shaohua.) | Zhao, Xingtian (Zhao, Xingtian.) | Yang, Jun (Yang, Jun.) | Zhang, Kunfeng (Zhang, Kunfeng.) | Dai, Hongxing (Dai, Hongxing.) (学者:戴洪兴)

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CPCI-S EI Scopus SCIE

摘要:

The xCo(3)O(4)-MnO2 (x = 2.6, 8.8, and 13.3 wt%) catalysts were prepared using the polymethyl methacrylate microspheres-templating, incipient wetness impregnation, and acid treatment methods. Physicochemical properties of the samples were characterized by means of various techniques. Catalytic performance of the xCo(3)O(4)-MnO2 samples was evaluated for the combustion of o-xylene. It is shown that the as-prepared samples possessed a cubic crystal structure and a surface area of 51.9-63.9 m(2)/g. The 8.8Co(3)O(4)-MnO2 sample possessed the highest adsorbed oxygen species concentration and the best low-temperature reducibility, and hence performing the best: the T-10%, T-50%, and T-90% (temperatures required for achieving o-xylene conversion of 10, 50, and 90%, respectively) were 231, 251, and 273 degrees C at a space velocity of 100,000 mL/(g h). The apparent activation energies obtained over the xCo(3)O(4)-MnO2 catalysts for o-xylene combustion were 72-82 kJ/mol. The effects of space velocity, water vapor, and carbon dioxide on the catalytic activity of the 8.8Co(3)O(4)-MnO2 sample were also examined, and the partial deactivation due to water vapor and carbon dioxide introduction was reversible. It is concluded that the good catalytic performance of 8.8Co(3)O(4)-MnO2 was associated with its high adsorbed oxygen species concentration, good low-temperature reducibility, and strong interaction between Co3O4 and MnO2.

关键词:

Cobalt oxide Hard-templating preparation method Manganese oxide Mixed transition metal oxide O-Xylene combustion

作者机构:

  • [ 1 ] [Han, Zhuo]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 2 ] [Liu, Yuxi]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 3 ] [Deng, Jiguang]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 4 ] [Xie, Shaohua]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 5 ] [Zhao, Xingtian]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 6 ] [Yang, Jun]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 7 ] [Zhang, Kunfeng]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China
  • [ 8 ] [Dai, Hongxing]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China

通讯作者信息:

  • 戴洪兴

    [Liu, Yuxi]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China;;[Dai, Hongxing]Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Key Lab Beijing Reg Air Pollut Control,Coll Envir, Lab Catalysis Chem & Nanosci,Dept Chem & Chem Eng, Beijing 100124, Peoples R China

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来源 :

CATALYSIS TODAY

ISSN: 0920-5861

年份: 2019

卷: 327

页码: 246-253

5 . 3 0 0

JCR@2022

ESI学科: CHEMISTRY;

ESI高被引阀值:66

JCR分区:1

被引次数:

WoS核心集被引频次: 31

SCOPUS被引频次: 30

ESI高被引论文在榜: 0 展开所有

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