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Titel |
Characterisation of the photolytic HONO-source in the atmosphere simulation chamber SAPHIR |
VerfasserIn |
F. Rohrer, B. Bohn, T. Brauers, D. Brüning, F.-J. Johnen, A. Wahner, J. Kleffmann |
Medientyp |
Artikel
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Sprache |
Englisch
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ISSN |
1680-7316
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Digitales Dokument |
URL |
Erschienen |
In: Atmospheric Chemistry and Physics ; 5, no. 8 ; Nr. 5, no. 8 (2005-08-12), S.2189-2201 |
Datensatznummer |
250003036
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Publikation (Nr.) |
copernicus.org/acp-5-2189-2005.pdf |
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Zusammenfassung |
HONO formation has been proposed as an important OH radical source in
simulation chambers for more than two decades. Besides the heterogeneous
HONO formation by the dark reaction of NO2 and adsorbed water, a
photolytic source has been proposed to explain the elevated reactivity in
simulation chamber experiments. However, the mechanism of the photolytic
process is not well understood so far.
As expected, production of HONO and NOx was also observed inside the
new atmospheric simulation chamber SAPHIR under solar irradiation. This
photolytic HONO and NOx formation was studied with a sensitive HONO
instrument under reproducible controlled conditions at atmospheric
concentrations of other trace gases. It is shown that the photolytic HONO
source in the SAPHIR chamber is not caused by NO2 reactions and that it
is the only direct NOy source under illuminated conditions. In
addition, the photolysis of nitrate which was recently postulated for the
observed photolytic HONO formation on snow, ground, and glass surfaces, can
be excluded in the chamber. A photolytic HONO source at the surface of the
chamber is proposed which is strongly dependent on humidity, on light
intensity, and on temperature. An empirical function describes these
dependencies and reproduces the observed HONO formation rates to within 10%. It is shown that the photolysis of HONO represents the dominant
radical source in the SAPHIR chamber for typical tropospheric
O3/H2O concentrations. For these conditions, the HONO
concentrations inside SAPHIR are similar to recent observations in ambient
air. |
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