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作者:

Li, Qinglei (Li, Qinglei.) | Fang, De (Fang, De.) | Hou, Sensheng (Hou, Sensheng.) | Sheng, Fenghe (Sheng, Fenghe.) | He, Feng (He, Feng.) | Xie, Junlin (Xie, Junlin.)

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摘要:

By controlling preparation conditions, a series of catalysts were synthesized. Among them, ST-400 presented primary CuMn2O4 spinel phase and expectant denitration efficiency at low temperature. Then, various concentrations Hexadecyl trimethyl ammonium Bromide (hereinafter referred to as CTAB) were added into ST-400. Among them, 0.3C-ST-400 showed higher NO removal rate, more acid sites and greater redox performance. What's more, due to the strong interaction and electron transfer of metal ions, there was equilibrium: 2Mn(3+) -><- Mn2+ + Mn4+ and Cu2+ + Mn3+ -><- Cu+ + Mn4+, and the addition of CTAB could promote the equilibrium to the right. More concentration of Mn4+ and chemisorbed oxygen would be the facilitation for catalytic activity at low temperatures. In situ DRIFT experiments indicated that Langmuir-Hinshelwood mechanism plays a major role over both ST-400 and 0.3C-ST-400. However, compared with ST-400, the addition of CTAB results in the present of Eley-Rideal mechanism over 0.3C-ST-400. Besides, the CTAB promotes the adsorption intensity of NH3 and nitrate species as well as the conversion to active nitrate species, which will markedly stimulate the effect of Langmuir-Hinshelwood mechanism. In consequence, the propre addition of CTAB is a novel strategy in favor of NH3-SCR activity-enhancement research.

关键词:

Calcination temperature NH3-SCR CTAB Reaction mechanism CuMn2O4

作者机构:

  • [ 1 ] [Li, Qinglei]Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
  • [ 2 ] [Fang, De]Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
  • [ 3 ] [Hou, Sensheng]Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
  • [ 4 ] [Sheng, Fenghe]Wuhan Univ Technol, State Key Lab Silicate Mat Architectures, Wuhan 430070, Peoples R China
  • [ 5 ] [Li, Qinglei]Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
  • [ 6 ] [Hou, Sensheng]Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
  • [ 7 ] [Sheng, Fenghe]Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
  • [ 8 ] [Fang, De]Wuhan Univ Technol, Ctr Mat Res & Anal, Wuhan 430070, Peoples R China
  • [ 9 ] [He, Feng]Beijing Univ Technol, Coll Mat Sci & Engn, Beijing 100124, Peoples R China
  • [ 10 ] [Xie, Junlin]Beijing Univ Technol, Coll Mat Sci & Engn, Beijing 100124, Peoples R China

通讯作者信息:

  • [He, Feng]Beijing Univ Technol, Coll Mat Sci & Engn, Beijing 100124, Peoples R China

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来源 :

REACTION KINETICS MECHANISMS AND CATALYSIS

ISSN: 1878-5190

年份: 2024

期: 3

卷: 137

页码: 1401-1418

1 . 8 0 0

JCR@2022

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SCOPUS被引频次: 3

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