4.7 Article Proceedings Paper

Novel TiO2 catalyst carriers with high thermostability for selective catalytic reduction of NO by NH3

Journal

CATALYSIS TODAY
Volume 327, Issue -, Pages 279-287

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.cattod.2018.04.038

Keywords

TiO2; Catalyst carrier; Thermostability; Nitrogen oxide; Selective catalytic reduction; Cerium oxide

Funding

  1. National Natural Science Foundation of China [51772149]
  2. National Key Research and Development Program of China [2016YFC0205500]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  4. U.S. NSF-PREM program [DMR 1205302]
  5. National Institute of Allergy and Infectious Disease of the NIH [R21AI107415]
  6. Emily Koenig Meningitis Fund of Philadelphia Foundation
  7. Postgraduate Research & Practice Innovation Program of Jiangsu Province
  8. Medical Center of the Americas Foundation
  9. 1000 Talents program from Tianjin, China

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A series of TiO2 catalyst carriers with ceria additives were prepared by a precipitation method and tested for selective catalytic reduction (SCR) of NO by NH3. These samples were characterized by XRD, N-2-BET, NH3-TPD, H-2-TPR, TEM, XPS and in situ DRIFTS, respectively. Results showed that the appropriate addition of ceria can enhance the catalytic activity and thermostability of TiO2 catalyst carriers significantly. The maximum catalytic activity of Ti-Ce-O-x-500 is 98.5% at 400 degrees C with a GHSV of 100 000 h(-1) and the high catalytic activity still remains even after the treatment at high temperature for 24 h. The high catalytic performance of Ti-Ce-O-x-500 can be attributed to a series of superior properties, such as larger specific surface area, more Bronsted acid sites, more hydrogen consumption, and the higher proportion of chemisorbed oxygen. Ceria atoms can inhibit the crystalline grain growth and the collapse of small channels caused by high temperatures. Furthermore, in situ DRIFTS in different feed gases show that the SCR reaction over Ti-Ce-O-x-500 follows both E-R and L-H mechanisms.

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