4.2 Article

Enhanced NOx removal performance of amorphous Ce-Ti catalyst by hydrogen pretreatment

Journal

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume 423, Issue -, Pages 371-378

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcata.2016.07.040

Keywords

Ce-Ti; Hydrogen; Pretreatment; NH3-SCR; Amorphous

Funding

  1. Assembly Foundation of The Industry and Information Ministry of the People's Republic of China
  2. National Natural Science Foundation of China [51408309, 51578288]
  3. Science and Technology Support Program of Jiangsu Province [BE2014713]
  4. Natural Science Foundation of Jiangsu Province [BK20140777]
  5. Industry-Academia Cooperation Innovation Fund Projects of Jiangsu Province [BY2014004-10]
  6. Science and technology project of Nanjing [201306012]
  7. Jiangsu Province Scientific and Technological Achievements into a Special Fund Project [BA2015062]
  8. Priority Academic Program Development of Jiangsu Higher Education of Jiangsu Higher Education Institutions

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Hydrogen pretreatment was processed on the amorphous Ce-Ti catalyst which notably enhanced its NH3-SCR performance. We concluded that 3-h and 400 degrees C were the most suitable and efficient pretreatment conditions, whereas the NOx conversion rate was above 95% from 210 degrees C to 360 degrees C for such pretreated catalyst. XRD, PL, H-2-TPR, XPS and Raman analyses found that the enhancement was attributed to the effects generated by the pretreatment: Ce4+ reduced to active Ce3+, the incerase of the oxygen vacancies, the chemisorbed oxygen, and the formation of superoxide ions. The NO adsorption oxidation capability, and the acid sites were also promoted by the pretreatment, which were favorable for the SCR reaction. The reaction among NO, O-2 and NH3 on catalysts were studied by in-situ DRIFT. The adsorption of NH3 was dominant under the SCR reaction conditions The enhancement demonstrated good durability. The stability of catalyst under water vapor and sulfur dioxide were also tested. (C) 2016 Elsevier B.V. All rights reserved.

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