Deep oxidation of NO via catalytic ozonation.

IF 2.1 4区 环境科学与生态学 Q3 ENGINEERING, ENVIRONMENTAL Journal of the Air & Waste Management Association Pub Date : 2024-11-04 DOI:10.1080/10962247.2024.2416047
Li Si Ko, Kuan Lun Pan, Moo Been Chang
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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.

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通过催化臭氧深度氧化 NO。
除了选择性催化还原法(SCR)和选择性非催化还原法(SNCR)可以去除烟气中的氮氧化物外,氧化法也受到越来越多的关注,因为这种方法可以通过湿法洗涤同时去除烟气中的氮氧化物和二氧化硫。O3 作为一种强氧化剂,具有很强的氧化能力,它能将 NO 氧化成 N2O5,而 N2O5 的水溶性比 NO2 高。然而,它需要较长的反应时间,未反应的臭氧逸出可能会造成二次污染。本研究制备并应用了 FeMnCo/Al2O3 催化剂和 FeMnCe/Al2O3 催化剂,以增强 NOx 与臭氧的深度氧化并减少 O3 的滑移。评估了 O3/NO 比、气体停留时间和操作温度等各种操作参数的影响,结果表明,当 O3/NO 比大于 1.0 时,开始生成 N2O5,并随着 O3/NO 比的增加而增加。在催化剂存在的情况下,几乎不会产生残余 O3,而当 O3/NO 比控制在 2.0 时,出口气体中测得的 O3 为 350 ppm。随着气体停留时间和操作温度的增加,N2O5 的转化效率也随之增加,在 100°C 时,N2O5 的转化效率最高。此外,在 O3/NO 比为 1.73、气体停留时间为 1.2 秒、温度为 100°C 的条件下,FeMnCe/Al2O3 催化剂运行 20 小时后,转化效率仍保持在 90% 左右。另一方面,在 FeMnCo/Al2O3 催化剂上运行 3 小时期间,N2O5 的转化效率保持在 80% 左右。总之,FeMnCe/Al2O3 催化剂显示出利用 O3 深度氧化 NO 的良好潜力,可进一步开发为减少工业 NO 排放的可行催化剂。
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来源期刊
Journal of the Air & Waste Management Association
Journal of the Air & Waste Management Association ENGINEERING, ENVIRONMENTAL-ENVIRONMENTAL SCIENCES
CiteScore
5.00
自引率
3.70%
发文量
95
审稿时长
3 months
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.
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