Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms
- Autores
- Cejas, Ezequiel; Mancinelli, Beatriz Rosa; Prevosto, Leandro
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A model of a stationary glow-type discharge in atmospheric-pressure air operated in high-gas-temperature regimes (1000 K < Tg < 6000 K), with a focus on the role of associative ionization reactions involving N(2D,2P)-excited atoms, is developed. Thermal dissociation of vibrationally excited nitrogen molecules, as well as electronic excitation from all the vibrational levels of the nitrogen molecules, is also accounted for. The calculations show that the near-threshold associative ionization reaction, N(2D) + O(3P) NO+ + e, is the major ionization mechanism in air at 2500 K < Tg < 4500 K while the ionization of NO molecules by electron impact is the dominant mechanism at lower gas temperatures and the high-threshold associative ionization reaction involving ground-state atoms dominates at higher temperatures. The exoergic associative ionization reaction, N(2P) + O(3P) NO+ + e, also speeds up the ionization at the highest temperature values. The vibrational excitation of the gas significantly accelerates the production of N2(A3∑u+) molecules, which in turn increases the densities of excited N(2D,2P) atoms. Because the electron energy required for the excitation of the N2(A3∑u+) state from N2(X1∑g+, v) molecules (e.g., 6.2 eV for v = 0) is considerably lower than the ionization energy (9.27 eV) of the NO molecules, the reduced electric field begins to noticeably fall at Tg > 2500 K. The calculated plasma parameters agree with the available experimental data.
Fil: Cejas, Ezequiel. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina
Fil: Mancinelli, Beatriz Rosa. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina
Fil: Prevosto, Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina - Materia
-
glow discharge
air
ionization kinetics - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/170268
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spelling |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited AtomsCejas, EzequielMancinelli, Beatriz RosaPrevosto, Leandroglow dischargeairionization kineticshttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1A model of a stationary glow-type discharge in atmospheric-pressure air operated in high-gas-temperature regimes (1000 K < Tg < 6000 K), with a focus on the role of associative ionization reactions involving N(2D,2P)-excited atoms, is developed. Thermal dissociation of vibrationally excited nitrogen molecules, as well as electronic excitation from all the vibrational levels of the nitrogen molecules, is also accounted for. The calculations show that the near-threshold associative ionization reaction, N(2D) + O(3P) NO+ + e, is the major ionization mechanism in air at 2500 K < Tg < 4500 K while the ionization of NO molecules by electron impact is the dominant mechanism at lower gas temperatures and the high-threshold associative ionization reaction involving ground-state atoms dominates at higher temperatures. The exoergic associative ionization reaction, N(2P) + O(3P) NO+ + e, also speeds up the ionization at the highest temperature values. The vibrational excitation of the gas significantly accelerates the production of N2(A3∑u+) molecules, which in turn increases the densities of excited N(2D,2P) atoms. Because the electron energy required for the excitation of the N2(A3∑u+) state from N2(X1∑g+, v) molecules (e.g., 6.2 eV for v = 0) is considerably lower than the ionization energy (9.27 eV) of the NO molecules, the reduced electric field begins to noticeably fall at Tg > 2500 K. The calculated plasma parameters agree with the available experimental data.Fil: Cejas, Ezequiel. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; ArgentinaFil: Mancinelli, Beatriz Rosa. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; ArgentinaFil: Prevosto, Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; ArgentinaMDPI AG2020-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/170268Cejas, Ezequiel; Mancinelli, Beatriz Rosa; Prevosto, Leandro; Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms; MDPI AG; Plasma; 3; 1; 2-2020; 12-262571-6182CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2571-6182/3/1/3info:eu-repo/semantics/altIdentifier/doi/10.3390/plasma3010003info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:53:04Zoai:ri.conicet.gov.ar:11336/170268instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:53:04.841CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
title |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
spellingShingle |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms Cejas, Ezequiel glow discharge air ionization kinetics |
title_short |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
title_full |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
title_fullStr |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
title_full_unstemmed |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
title_sort |
Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms |
dc.creator.none.fl_str_mv |
Cejas, Ezequiel Mancinelli, Beatriz Rosa Prevosto, Leandro |
author |
Cejas, Ezequiel |
author_facet |
Cejas, Ezequiel Mancinelli, Beatriz Rosa Prevosto, Leandro |
author_role |
author |
author2 |
Mancinelli, Beatriz Rosa Prevosto, Leandro |
author2_role |
author author |
dc.subject.none.fl_str_mv |
glow discharge air ionization kinetics |
topic |
glow discharge air ionization kinetics |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
A model of a stationary glow-type discharge in atmospheric-pressure air operated in high-gas-temperature regimes (1000 K < Tg < 6000 K), with a focus on the role of associative ionization reactions involving N(2D,2P)-excited atoms, is developed. Thermal dissociation of vibrationally excited nitrogen molecules, as well as electronic excitation from all the vibrational levels of the nitrogen molecules, is also accounted for. The calculations show that the near-threshold associative ionization reaction, N(2D) + O(3P) NO+ + e, is the major ionization mechanism in air at 2500 K < Tg < 4500 K while the ionization of NO molecules by electron impact is the dominant mechanism at lower gas temperatures and the high-threshold associative ionization reaction involving ground-state atoms dominates at higher temperatures. The exoergic associative ionization reaction, N(2P) + O(3P) NO+ + e, also speeds up the ionization at the highest temperature values. The vibrational excitation of the gas significantly accelerates the production of N2(A3∑u+) molecules, which in turn increases the densities of excited N(2D,2P) atoms. Because the electron energy required for the excitation of the N2(A3∑u+) state from N2(X1∑g+, v) molecules (e.g., 6.2 eV for v = 0) is considerably lower than the ionization energy (9.27 eV) of the NO molecules, the reduced electric field begins to noticeably fall at Tg > 2500 K. The calculated plasma parameters agree with the available experimental data. Fil: Cejas, Ezequiel. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina Fil: Mancinelli, Beatriz Rosa. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina Fil: Prevosto, Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe; Argentina. Universidad Tecnológica Nacional. Facultad Reg.venado Tuerto. Departamento de Ing.electromecanica. Laboratorio de Descargas Eléctricas; Argentina |
description |
A model of a stationary glow-type discharge in atmospheric-pressure air operated in high-gas-temperature regimes (1000 K < Tg < 6000 K), with a focus on the role of associative ionization reactions involving N(2D,2P)-excited atoms, is developed. Thermal dissociation of vibrationally excited nitrogen molecules, as well as electronic excitation from all the vibrational levels of the nitrogen molecules, is also accounted for. The calculations show that the near-threshold associative ionization reaction, N(2D) + O(3P) NO+ + e, is the major ionization mechanism in air at 2500 K < Tg < 4500 K while the ionization of NO molecules by electron impact is the dominant mechanism at lower gas temperatures and the high-threshold associative ionization reaction involving ground-state atoms dominates at higher temperatures. The exoergic associative ionization reaction, N(2P) + O(3P) NO+ + e, also speeds up the ionization at the highest temperature values. The vibrational excitation of the gas significantly accelerates the production of N2(A3∑u+) molecules, which in turn increases the densities of excited N(2D,2P) atoms. Because the electron energy required for the excitation of the N2(A3∑u+) state from N2(X1∑g+, v) molecules (e.g., 6.2 eV for v = 0) is considerably lower than the ionization energy (9.27 eV) of the NO molecules, the reduced electric field begins to noticeably fall at Tg > 2500 K. The calculated plasma parameters agree with the available experimental data. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-02 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/170268 Cejas, Ezequiel; Mancinelli, Beatriz Rosa; Prevosto, Leandro; Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms; MDPI AG; Plasma; 3; 1; 2-2020; 12-26 2571-6182 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/170268 |
identifier_str_mv |
Cejas, Ezequiel; Mancinelli, Beatriz Rosa; Prevosto, Leandro; Modelling of an Atmospheric–Pressure Air Glow Discharge Operating in High–Gas Temperature Regimes: The Role of the Associative Ionization Reactions Involving Excited Atoms; MDPI AG; Plasma; 3; 1; 2-2020; 12-26 2571-6182 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://www.mdpi.com/2571-6182/3/1/3 info:eu-repo/semantics/altIdentifier/doi/10.3390/plasma3010003 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
MDPI AG |
publisher.none.fl_str_mv |
MDPI AG |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844613625256345600 |
score |
13.069144 |