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PMID: 40414030 Published · ppublish English Journal Article

Substrate engineering-enhanced low-temperature NOx and CO removal by Co1Mn2Ox@CuO/copper mesh monolithic catalyst.

Journal of colloid and interface science ·Vol. 697 ·2025-11-00 ·页码 137936

Ma J, Gao Y, Gui R, Ren P, Su L, Wei J, Wang Q

Abstract

This paper addresses the challenges of simultaneously removing nitrogen oxides (NOx) and carbon monoxide (CO) from industrial flue gas at low temperatures. A highly efficient Co1Mn2Ox@CuO/copper mesh (CM) monolithic catalyst with higher oxygen vacancies was developed by growing Cu(OH)2 nanorods in-situ on a copper mesh and subsequently synthesizing via a hydrothermal method. Experimental results show that the Co1Mn2Ox@CuO/CM catalyst can achieve 99.7 % NOx conversion and 99.4 % CO conversion at 160 °C, with strong resistance to H2O and SO2 and outstanding long-term stability. Characterization results demonstrated that the excellent catalytic performance can be ascribed to the presence of abundant high-valent Co3+, Mn4+, and Cu2+ species, an increased number of reducible species, more acidic sites, and a higher concentration of oxygen vacancies. The interaction between ammonia-based selective catalytic reduction (NH3-SCR) and CO oxidation reactions revealed that NH3 primarily inhibited CO oxidation, whereas CO had no significant inhibitory effect on NH3-SCR. Additionally, this study explored the factors contributing to the enhanced water resistance and the underlying mechanisms of both NH3-SCR and CO oxidation reactions using in-situ diffuse reflectance infrared transform spectroscopy (in-situ DRIFTS). In terms of application, computational fluid dynamics (CFD) simulations demonstrated that the copper mesh-based monolithic catalyst provided better heat distribution, preventing partial deactivation and contributed to the improvement of catalytic activity. This research provides an efficient solution for industrial flue gas treatment and highlights its potential for environmental applications.

Keywords
CO oxidation Computational fluid dynamics simulation Copper substrate Monolithic bifunctional catalysts NH(3)-SCR Simultaneous removal
作者与单位
共 7 位作者,点击展开单位 / ORCID
Ma Jianing
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China.
Gao Yanshan
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China. Electronic address: [email protected].
Gui Rongrong
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China.
Ren Penghui
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China.
Su Liyao
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China.
Wei Jiaqi
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China.
Wang Qiang
College of Environmental Science and Engineering, Beijing Forestry University, Beijing 100083, China; State Key Laboratory of Efficient Production of Forest Resources, Beijing Forestry University, Beijing 100083, China. Electronic address: [email protected].
Article Info
Journal
Journal of colloid and interface science
Abbr.
J Colloid Interface Sci
ISSN
1095-7103
Published
2025-11-00
电子出版
2025-00-19
页码
137936
Language
English
Country/Region
United States
NLM ID
0043125
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