Current Research on NO2 Removal from Flue Gas Using Adsorption Methods

Nitrogen dioxide (NO2) is a major atmospheric pollutant and also a recoverable nitrogen resource, for which adsorption offers a promising technical pathway. This review systematically summarizes the recent progress in the removal of NO2 from flue gas by adsorption methods, with a focus on material-level and process-level advancements. From the material perspective, three representative adsorbents—zeolites, activated carbons, and metal oxides—are comparatively evaluated in terms of their physicochemical properties, active sites, and adsorption mechanisms. Emphasis is placed on their adsorption capacity, selectivity, and hydrothermal stability, supported by both experimental and theoretical insights. From the process perspective, four adsorption-based technologies—Pressure Swing Adsorption (PSA), Temperature Swing Adsorption (TSA), Vacuum Pressure Swing Adsorption (VPSA), and Vacuum Temperature Swing Adsorption using multiple Gas circulations (GVTSA)—are analyzed regarding their principles, operational workflows, and engineering applications, with particular attention to the process intensification potential of GVTSA. The review identifies existing challenges in terms of material stability under complex conditions and process scalability, especially for severe environments such as nuclear reprocessing tail gases. Finally, future research directions are proposed toward developing multifunctional composite adsorbents with high capacity, strong environmental tolerance, and excellent regenerability, along with optimized and integrated adsorption processes, to achieve efficient NO2 abatement and high-value recovery.

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Publication Details

Journal
Separations
Published
2026-01-08
DOI
https://doi.org/10.3390/separations13010024
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
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article

Current Research on NO2 Removal from Flue Gas Using Adsorption Methods

S. S. Chang, GaoLiang Li, Hui He, Yulin Tong et al.
Separations
Carbon Dioxide Capture Technologies
article

Current Research on NO2 Removal from Flue Gas Using Adsorption Methods

S. S. Chang, GaoLiang Li, Hui He, Yulin Tong, Yulong Chang, Zhe Su, Bangda Wang, Xibin Ma, Hongbin Tang
article en

Abstract

Nitrogen dioxide (NO2) is a major atmospheric pollutant and also a recoverable nitrogen resource, for which adsorption offers a promising technical pathway. This review systematically summarizes the recent progress in the removal of NO2 from flue gas by adsorption methods, with a focus on material-level and process-level advancements. From the material perspective, three representative adsorbents—zeolites, activated carbons, and metal oxides—are comparatively evaluated in terms of their physicochemical properties, active sites, and adsorption mechanisms. Emphasis is placed on their adsorption capacity, selectivity, and hydrothermal stability, supported by both experimental and theoretical insights. From the process perspective, four adsorption-based technologies—Pressure Swing Adsorption (PSA), Temperature Swing Adsorption (TSA), Vacuum Pressure Swing Adsorption (VPSA), and Vacuum Temperature Swing Adsorption using multiple Gas circulations (GVTSA)—are analyzed regarding their principles, operational workflows, and engineering applications, with particular attention to the process intensification potential of GVTSA. The review identifies existing challenges in terms of material stability under complex conditions and process scalability, especially for severe environments such as nuclear reprocessing tail gases. Finally, future research directions are proposed toward developing multifunctional composite adsorbents with high capacity, strong environmental tolerance, and excellent regenerability, along with optimized and integrated adsorption processes, to achieve efficient NO2 abatement and high-value recovery.

SeparationsVol. 13(1)
Sichuan University (CN), China Institute of Atomic Energy (CN)
Responsible consumption and production
Openalex Percentile: Top 93%
Carbon Dioxide Capture Technologies
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