Fe2O3 enhanced high-temperature arsenic resistance of CeO2–La2O3/TiO2 catalyst for selective catalytic reduction of NOx with NH3-Reference-Cited by-同舟云学术

Fe2O3 enhanced high-temperature arsenic resistance of CeO2–La2O3/TiO2 catalyst for selective catalytic reduction of NOx with NH3

Published:2021 Issue:16 Volume:11 Page:9395-9402
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Wang Na¹²³⁴^ORCID,Ye Changfei¹²³⁴,Xie Huidong⁵⁶⁷³⁴,Yang Chang⁶⁷³⁴,Zhou Jinhong⁸⁹¹⁰⁴,Ge Chengmin¹¹¹²⁴

Affiliation:

1. College of Architecture and Civil Engineering

2. Xi'an University of Science and Technology

3. Xi'an

4. China

5. School of Chemistry and Chemical Engineering

6. Division of Laboratory and Equipment Management

7. Xi'an University of Architecture and Technology

8. College of Geography and Environment

9. Baoji University of Arts and Sciences

10. Baoji

11. Shandong Dongyuan New Material Technology Co., Ltd

12. Dongying

Abstract

The NO conversion of the CeLa_0.5Fe_0.2/Ti is obviously better than that of the commercial vanadium-based catalyst with regard to arsenic resistance and it has good N₂ selectivity, and good SO₂ resistance.

Funder

National Natural Science Foundation of China

Key Research and Development Projects of Shaanxi Province

Department of Education of Shandong Province

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA00031D

Reference41 articles.

1. Effect of MnO 2 polymorphs structure on the selective catalytic reduction of NO x with NH 3 over TiO 2 –Palygorskite

2. Selective catalytic reduction of NOx by NH3 over MoO3-promoted CeO2/TiO2 catalyst

3. Chemical and mechanistic aspects of the selective catalytic reduction of NO by ammonia over oxide catalysts: A review

4. The State of the Art in Selective Catalytic Reduction of NOxby Ammonia Using Metal‐Exchanged Zeolite Catalysts

5. Ce–Ti Amorphous Oxides for Selective Catalytic Reduction of NO with NH3: Confirmation of Ce–O–Ti Active Sites

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