Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor
Nitrogen dioxide (N<sub>2</sub>O) is a greenhouse gas that is harmful to the ozone layer and contributes to global warming. Many other nitrogen oxide emissions are controlled using the selective non-catalytic reaction (SNCR) process, but N<sub>2</sub>O reduction methods are f...
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doaj-98e190c5d9404769bc58200800476fb82021-02-23T00:01:05ZengMDPI AGEnergies1996-10732021-02-01141153115310.3390/en14041153Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal ReactorSang Ji Lee0Jae Geun Yun1Han Min Lee2Ji Yeop Kim3Jin Han Yun4Jung Goo Hong5School of Mechanical Engineering, Kyungpook National University, Buk-gu, Daegu 41566, KoreaSchool of Mechanical Engineering, Kyungpook National University, Buk-gu, Daegu 41566, KoreaSchool of Mechanical Engineering, Kyungpook National University, Buk-gu, Daegu 41566, KoreaSchool of Mechanical Engineering, Kyungpook National University, Buk-gu, Daegu 41566, KoreaDepartment of Environmental Machinery, Korea Institute of Machinery & Materials, Yuseong-gu, Daejeon 34103, KoreaSchool of Mechanical Engineering, Kyungpook National University, Buk-gu, Daegu 41566, KoreaNitrogen dioxide (N<sub>2</sub>O) is a greenhouse gas that is harmful to the ozone layer and contributes to global warming. Many other nitrogen oxide emissions are controlled using the selective non-catalytic reaction (SNCR) process, but N<sub>2</sub>O reduction methods are few. To avoid future air pollution problems, N<sub>2</sub>O reduction from industrial sources is essential. In this study, a N<sub>2</sub>O decomposition and NO formation under an argon atmospheric N<sub>2</sub>O gas mixture were observed in a lab-scale SNCR system. The reaction rate and mechanism of N<sub>2</sub>O were calculated using a reaction path analyzer (CHEMKIN-PRO). The residence time of the gas mixture and the temperature in the reactor were set as experimental variables. The results confirmed that most of the N<sub>2</sub>O was converted to N<sub>2</sub> and NO. The change in the N<sub>2</sub>O reduction rate increased with the residence time at 1013 and 1113 K, but decreased at 1213 K due to the inverse reaction. NO concentration increased with the residence time at 1013 and 1113 K, but decreased at 1213 K owing to the conversion of NO back to N<sub>2</sub>O.https://www.mdpi.com/1996-1073/14/4/1153nitrous oxide (N<sub>2</sub>O)nitric oxide (NOx)argon (Ar) ambientthermal decompositionresidence timerate of progress |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sang Ji Lee Jae Geun Yun Han Min Lee Ji Yeop Kim Jin Han Yun Jung Goo Hong |
spellingShingle |
Sang Ji Lee Jae Geun Yun Han Min Lee Ji Yeop Kim Jin Han Yun Jung Goo Hong Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor Energies nitrous oxide (N<sub>2</sub>O) nitric oxide (NOx) argon (Ar) ambient thermal decomposition residence time rate of progress |
author_facet |
Sang Ji Lee Jae Geun Yun Han Min Lee Ji Yeop Kim Jin Han Yun Jung Goo Hong |
author_sort |
Sang Ji Lee |
title |
Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor |
title_short |
Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor |
title_full |
Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor |
title_fullStr |
Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor |
title_full_unstemmed |
Dependence of N<sub>2</sub>O/NO Decomposition and Formation on Temperature and Residence Time in Thermal Reactor |
title_sort |
dependence of n<sub>2</sub>o/no decomposition and formation on temperature and residence time in thermal reactor |
publisher |
MDPI AG |
series |
Energies |
issn |
1996-1073 |
publishDate |
2021-02-01 |
description |
Nitrogen dioxide (N<sub>2</sub>O) is a greenhouse gas that is harmful to the ozone layer and contributes to global warming. Many other nitrogen oxide emissions are controlled using the selective non-catalytic reaction (SNCR) process, but N<sub>2</sub>O reduction methods are few. To avoid future air pollution problems, N<sub>2</sub>O reduction from industrial sources is essential. In this study, a N<sub>2</sub>O decomposition and NO formation under an argon atmospheric N<sub>2</sub>O gas mixture were observed in a lab-scale SNCR system. The reaction rate and mechanism of N<sub>2</sub>O were calculated using a reaction path analyzer (CHEMKIN-PRO). The residence time of the gas mixture and the temperature in the reactor were set as experimental variables. The results confirmed that most of the N<sub>2</sub>O was converted to N<sub>2</sub> and NO. The change in the N<sub>2</sub>O reduction rate increased with the residence time at 1013 and 1113 K, but decreased at 1213 K due to the inverse reaction. NO concentration increased with the residence time at 1013 and 1113 K, but decreased at 1213 K owing to the conversion of NO back to N<sub>2</sub>O. |
topic |
nitrous oxide (N<sub>2</sub>O) nitric oxide (NOx) argon (Ar) ambient thermal decomposition residence time rate of progress |
url |
https://www.mdpi.com/1996-1073/14/4/1153 |
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