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
CONICET Digital (CONICET)
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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