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  Direct measurements of NO3-reactivity in and above the boundary layer of a mountain-top site: Identification of reactive trace gases and comparison with OH-reactivity

Liebmann, J. M., Muller, J. B. A., Kubistin, D., Claude, A., Holla, R., Plaß-Dülmer, C., et al. (2018). Direct measurements of NO3-reactivity in and above the boundary layer of a mountain-top site: Identification of reactive trace gases and comparison with OH-reactivity. Atmospheric Chemistry and Physics Discussions, 18.

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 Urheber:
Liebmann, Jonathan M.1, Autor           
Muller, Jennifer B. A., Autor
Kubistin, Dagmar, Autor
Claude, Anja, Autor
Holla, Robert, Autor
Plaß-Dülmer, Christian, Autor
Crowley, John N.1, Autor           
Affiliations:
1Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826285              

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 Zusammenfassung: We present direct measurements of the summertime, total reactivity of NO3 towards organic trace gases, kOTGNO3, at a rural mountain site (988ma.s.l.) in southern Germany in 2017. The diel cycle of kOTGNO3 was strongly influenced by local meteorology with reactivity high during the day (values of up to 0.3s-1) but usually close to the detection limit (0.005s-1) at night when the measurement site was in the residual layer/free troposphere. Daytime values of kOTGNO3 were sufficiently large that the loss of NO3 due to reaction with organic trace gases competed with its photolysis and reaction with NO. Within experimental uncertainty, monoterpenes and isoprene accounted for all of the measured NO3-reactivity. Averaged over the daylight hours, more than 25% of NO3 was removed via reaction with biogenic volatile organic compounds (BVOCs), implying a significant daytime loss of NOx and formation of organic nitrates due to NO3 chemistry. Ambient NO3 concentrations were measured on one night and were comparable to those derived from a stationary state calculation using measured values of kOTGNO3. We present and compare the first simultaneous, direct-reactivity measurements for the NO3 and OH radicals. The decoupling of the measurement site from ground level emissions resulted in lower reactivity at night for both radicals, though the correlation between OH- and NO3-reactivity was weak as would be anticipated given their divergent trends in rate constants with many organic trace gases.

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Sprache(n): eng - English
 Datum: 2018
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: DOI: 10.5194/acp-2018-324
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Titel: Atmospheric Chemistry and Physics Discussions
  Kurztitel : Atmos. Chem. Phys. Discuss.
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: Katlenburg-Lindau, Germany : European Geophysical Society, Copernicus Publ.
Seiten: 30 Band / Heft: 18 Artikelnummer: - Start- / Endseite: - Identifikator: ISSN: 1680-7367
CoNE: https://pure.mpg.de/cone/journals/resource/111076360006006