{"title":"Deep oxidation of NO via catalytic ozonation.","authors":"Li Si Ko, Kuan Lun Pan, Moo Been Chang","doi":"10.1080/10962247.2024.2416047","DOIUrl":null,"url":null,"abstract":"<p><p>In addition to selective catalytic reduction (SCR) and selective non-catalytic reduction (SNCR) which are available to remove NO<sub>x</sub> from flue gas, oxidation method is receiving more and more attention because this method makes it possible to remove NO<sub>x</sub> and SO<sub>2</sub> from flue gas simultaneously by wet scrubbing. O<sub>3</sub> as a strong oxidant has a high oxidation capacity and it can oxide NO to N<sub>2</sub>O<sub>5</sub> which has a higher water solubility compared with NO<sub>2</sub>. However, it needs a long reaction time and the escape of unreacted ozone may cause secondary pollution. In this study, FeMnCo/Al<sub>2</sub>O<sub>3</sub> catalyst and FeMnCe/Al<sub>2</sub>O<sub>3</sub> catalyst were prepared and applied to enhance the deep oxidation of NO<sub>x</sub> with ozone and reduce O<sub>3</sub> slip. Effects of various operating parameters such as O<sub>3</sub>/NO ratio, gas residence time, and operating temperature were evaluated, and the results demonstrate that N<sub>2</sub>O<sub>5</sub> began to generate when O<sub>3</sub>/NO ratio was higher than 1.0 and increased with increasing O<sub>3</sub>/NO ratio. Little residual O<sub>3</sub> was formed in the presence of catalyst, while 350 ppm O<sub>3</sub> was measured at the outlet gas when O<sub>3</sub>/NO ratio was controlled at 2.0. The N<sub>2</sub>O<sub>5</sub> conversion efficiency increased with increasing gas residence time and operating temperature, and the highest N<sub>2</sub>O<sub>5</sub> conversion efficiency was achieved at 100°C. Furthermore, the conversion efficiency remained around 90% during 20 h operation over FeMnCe/Al<sub>2</sub>O<sub>3</sub> catalyst with an O<sub>3</sub>/NO ratio of 1.73, a gas residence time of 1.2 s, and a temperature of 100°C. On the other hand, the N<sub>2</sub>O<sub>5</sub> conversion efficiency remained around 80% during 3 h operation over FeMnCo/Al<sub>2</sub>O<sub>3</sub> catalyst. Overall, FeMnCe/Al<sub>2</sub>O<sub>3</sub> catalyst reveals good potential for deep oxidation of NO by O<sub>3</sub> and can be further developed as a viable catalyst for reducing NO emission from industries.<i>Implications</i>: In this study, FeMnCo/Al<sub>2</sub>O<sub>3</sub> catalyst and FeMnCe/Al<sub>2</sub>O<sub>3</sub> catalyst were applied to enhance the deep oxidation of NO into N<sub>2</sub>O<sub>5</sub> with O<sub>3</sub>. The catalysts can improve the conversion of NO into N<sub>2</sub>O<sub>5</sub>, shorten the reaction time and reduce the unreacted O<sub>3</sub> 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 NO<sub>x</sub> and SO<sub>2</sub> from flue gas by wet scrubbing for reducing NO emissions from industries, especially small and medium scaled industries, to meet increasingly stringent emission standards.</p>","PeriodicalId":49171,"journal":{"name":"Journal of the Air & Waste Management Association","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Air & Waste Management Association","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1080/10962247.2024.2416047","RegionNum":4,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
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.
期刊介绍:
The Journal of the Air & Waste Management Association (J&AWMA) is one of the oldest continuously published, peer-reviewed, technical environmental journals in the world. First published in 1951 under the name Air Repair, J&AWMA is intended to serve those occupationally involved in air pollution control and waste management through the publication of timely and reliable information.