4.7 Article

Ti3+ doped V2O5/TiO2 catalyst for efficient selective catalytic reduction of NOx with NH3

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 581, Issue -, Pages 76-83

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2020.07.131

Keywords

Ti3+ self-doping; Selective catalytic reaction; V2O5/TiO2; Low-temperature SCR; Oxygen vacancy

Funding

  1. National Natural Science Foundation of China [51506077]
  2. Natural Science Foundation of Jiangsu Province [BK20150488]
  3. Natural Science Foundation of Jiangsu High School [15KJB430007]
  4. Research Foundation of Jiangsu University [15JDG156]

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This study evaluates the effect of self-doping Ti3+ into catalysts on the activity of the catalysts. Various characterization methods such as XRD, XPS, and EPR confirm the presence of Ti3+ and oxygen vacancy, which significantly affect the performance of the catalysts. The results indicate potential for improving low-temperature SCR performance through strategic design of Ti3+ self-doped catalysts.
The effect of self-doping Ti3+ into V2O5/TiO2 catalysts on the activity of the catalysts was assessed by the selective catalytic reduction of NOX with NH3 (NH3-SCR). 0.2-V2O5/TiO2 (Al(acac)(3):TBOT = 0.2%) catalyst had the highest catalytic activity at low-temperature range. The as-prepared catalysts are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), H2 temperature-programmed reduction (H-2-TPR), NH3 temperature-programmed desorption (NH3-TPD), surface area and pore structure. XPS and EPR were used to confirm the existence of Ti3+ and oxygen vacancy in the catalysts. The specific surface area, surface acidity, reducibility and valence state of the active components of the catalysts are significantly affected by the self-doping of Ti3+. This work would lead to a new strategic design of Ti3+ self-doped catalysts with fine structure and that can efficiently improve low-temperature SCR performance. (C) 2020 Elsevier Inc. All rights reserved.

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