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Variability in nocturnal nitrogen oxide processing and its role in regional air quality.
Brown, S S; Ryerson, T B; Wollny, A G; Brock, C A; Peltier, R; Sullivan, A P; Weber, R J; Dubé, W P; Trainer, M; Meagher, J F; Fehsenfeld, F C; Ravishankara, A R.
Afiliação
  • Brown SS; National Oceanic and Atmospheric Administration (NOAA) Earth System Research Laboratory, R/CSD2, 325 Broadway, Boulder, CO 80305, USA. steven.s.brown@noaa.gov
Science ; 311(5757): 67-70, 2006 Jan 06.
Article em En | MEDLINE | ID: mdl-16400145
ABSTRACT
Nitrogen oxides in the lower troposphere catalyze the photochemical production of ozone (O3) pollution during the day but react to form nitric acid, oxidize hydrocarbons, and remove O3 at night. A key nocturnal reaction is the heterogeneous hydrolysis of dinitrogen pentoxide, N2O5. We report aircraft measurements of NO3 and N2O5, which show that the N2O5 uptake coefficient, g(N2O5), on aerosol particles is highly variable and depends strongly on aerosol composition, particularly sulfate content. The results have implications for the quantification of regional-scale O3 production and suggest a stronger interaction between anthropogenic sulfur and nitrogen oxide emissions than previously recognized.
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Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2006 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2006 Tipo de documento: Article