Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH

Detalhes bibliográficos
Autor(a) principal: Zhang, Lei
Data de Publicação: 2008
Outros Autores: Luo, Pingya, Huang, Zhiyu, Chen, Hong, Varandas, António J. C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10254
https://doi.org/10.1021/jp803686j
Resumo: We report a theoretical study of highly excited O3 in collisions with vibrationally cold OH. Special emphasis is placed on initial vibrational energies of O3 between 9 and 21 kcal mol−1. All calculations have employed the quasiclassical trajectory method and the realistic double many-body expansion potential energy surface for HO4(2A). Many aspects of the title relaxation process are presented. The results indicate that it may not be ignorable in studying the stratospheric ozone budget.
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spelling Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OHWe report a theoretical study of highly excited O3 in collisions with vibrationally cold OH. Special emphasis is placed on initial vibrational energies of O3 between 9 and 21 kcal mol−1. All calculations have employed the quasiclassical trajectory method and the realistic double many-body expansion potential energy surface for HO4(2A). Many aspects of the title relaxation process are presented. The results indicate that it may not be ignorable in studying the stratospheric ozone budget.American Chemical Society2008info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10254http://hdl.handle.net/10316/10254https://doi.org/10.1021/jp803686jengThe Journal of Physical Chemistry A. 112:31 (2008) 7238-7243.1089-5639Zhang, LeiLuo, PingyaHuang, ZhiyuChen, HongVarandas, António J. C.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-05-25T13:13:05Zoai:estudogeral.uc.pt:10316/10254Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:10.739370Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
title Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
spellingShingle Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
Zhang, Lei
title_short Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
title_full Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
title_fullStr Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
title_full_unstemmed Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
title_sort Vibrational Relaxation of Highly Vibrationally Excited O3 in Collisions with OH
author Zhang, Lei
author_facet Zhang, Lei
Luo, Pingya
Huang, Zhiyu
Chen, Hong
Varandas, António J. C.
author_role author
author2 Luo, Pingya
Huang, Zhiyu
Chen, Hong
Varandas, António J. C.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Zhang, Lei
Luo, Pingya
Huang, Zhiyu
Chen, Hong
Varandas, António J. C.
description We report a theoretical study of highly excited O3 in collisions with vibrationally cold OH. Special emphasis is placed on initial vibrational energies of O3 between 9 and 21 kcal mol−1. All calculations have employed the quasiclassical trajectory method and the realistic double many-body expansion potential energy surface for HO4(2A). Many aspects of the title relaxation process are presented. The results indicate that it may not be ignorable in studying the stratospheric ozone budget.
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10254
http://hdl.handle.net/10316/10254
https://doi.org/10.1021/jp803686j
url http://hdl.handle.net/10316/10254
https://doi.org/10.1021/jp803686j
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv The Journal of Physical Chemistry A. 112:31 (2008) 7238-7243.
1089-5639
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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