4.6 Article

Ordered mesoporous TiO2/SBA-15 confined CexWy catalysts for selective catalytic reduction of NO using NH3

期刊

NEW JOURNAL OF CHEMISTRY
卷 46, 期 46, 页码 22030-22044

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2nj03801c

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资金

  1. National Natural Science Foundation of China [22206189]
  2. Major Project of Inner Mongolia Science and Technology [2019ZD018]
  3. Key Research and Development Program of Gansu Province [20YF8FA004]
  4. Major Program of the Lanzhou Institute of Chemical Physics, CAS [ZYFZFX-10]
  5. Key talent project of Gansu Province
  6. Kuancheng Wang Pioneer Talents Program of Chinese Academy of Sciences
  7. Natural Science Fund of Inner Mongolia Autonomous Region [2021MS02022]

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In this study, Ce-based catalysts with ordered mesoporous structures were prepared, and it was found that Ce10W2/TS-3 catalyst exhibited large specific surface area, excellent redox ability, surface acidity, and resistance to water and sulfur. The findings provide new insights into the design and synthesis of Ce-based catalysts with ordered mesoporous confinement for NH3-SCR applications.
Constructing Ce-based catalysts with excellent catalytic activity and toxicity resistance is an effective strategy for the selective catalytic reduction of NO by NH3. Here, ordered mesoporous structured CexWy/TiO2/SBA-15(TS) catalysts with different Ti/Si molar ratios (2 : 6, 3 : 6, 4 : 6) as well as the Ce and W contents were prepared using the vacuum impregnation method. Among them, the prepared TS-3 (Ti : Si = 3 : 6) carrier had a regular ordered mesoporous structure, which could provide a better supporting space for the attachment of active ingredients. After the active species were introduced, with the help of a series of characterization analyses, it was found that the Ce10W2/TS-3 catalyst had a large specific surface area, where the active species were stably dispersed via the pore confinement effect of the ordered mesopores' structure, and the efficient charge transfer significantly enhanced its redox ability and surface acidity. In addition, the ordered pore structure protected the active sites from the competitive adsorption of water vapor and sulfur attack. Consequentially, the ordered mesoporous confined Ce10W2/TS-3 catalyst exhibited good catalytic performance in a wide temperature window, and its water and sulfur resistance was also enhanced to some extent. This work provided new insights into the design and synthesis of ordered mesoporous confined structure Ce-based catalysts for NH3-SCR applications.

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