Related Experiment Video
Updated: Jun 10, 2025

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for CuII Through Microwave Pre-Pyrolysis
Published on: February 12, 2019
Deep oxidation of NO via catalytic ozonation
Li Si Ko1, Kuan Lun Pan2, Moo Been Chang1
1Graduate Institute of Environmental Engineering, National Central University, Taoyuan City, Taiwan.
Abstract:
In addition to selective catalytic reduction (SCR) and selective non-catalytic reduction (SNCR) which are available to remove NOx from flue gas, oxidation method is receiving more and more attention because this method makes it possible to remove NOx and SO2 from flue gas simultaneously by wet scrubbing. O3 as a strong oxidant has a high oxidation capacity and it can oxide NO to N2O5 which has a higher water solubility compared with NO2. However, it needs a long reaction time and the escape of unreacted ozone may cause secondary pollution. In this study, FeMnCo/Al2O3 catalyst and FeMnCe/Al2O3 catalyst were prepared and applied to enhance the deep oxidation of NOx with ozone and reduce O3 slip. Effects of various operating parameters such as O3/NO ratio, gas residence time, and operating temperature were evaluated, and the results demonstrate that N2O5 began to generate when O3/NO ratio was higher than 1.0 and increased with increasing O3/NO ratio. Little residual O3 was formed in the presence of catalyst, while 350 ppm O3 was measured at the outlet gas when O3/NO ratio was controlled at 2.0. The N2O5 conversion efficiency increased with increasing gas residence time and operating temperature, and the highest N2O5 conversion efficiency was achieved at 100°C. Furthermore, the conversion efficiency remained around 90% during 20 h operation over FeMnCe/Al2O3 catalyst with an O3/NO ratio of 1.73, a gas residence time of 1.2 s, and a temperature of 100°C. On the other hand, the N2O5 conversion efficiency remained around 80% during 3 h operation over FeMnCo/Al2O3 catalyst. Overall, FeMnCe/Al2O3 catalyst reveals good potential for deep oxidation of NO by O3 and can be further developed as a viable catalyst for reducing NO emission from industries.Implications: In this study, FeMnCo/Al2O3 catalyst and FeMnCe/Al2O3 catalyst were applied to enhance the deep oxidation of NO into N2O5 with O3. The catalysts can improve the conversion of NO into N2O5, shorten the reaction time and reduce the unreacted O3 slip, which are beneficial to reduce the size of the reactor required and cost of APCDs (air pollution control devices) in practical application. This method can make it possible to simultaneously remove NOx and SO2 from flue gas by wet scrubbing for reducing NO emissions from industries, especially small and medium scaled industries, to meet increasingly stringent emission standards.
Related Concept Videos
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Catalysis
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Radical Autoxidation
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Radical Oxidation of Allylic and Benzylic Alcohols

