Details

Autor(en) / Beteiligte

• McDuffie, Erin E.
• Fibiger, Dorothy L.
• Dubé, William P.
• Lopez‐Hilfiker, Felipe
• Lee, Ben H.
• Thornton, Joel A.
• Shah, Viral
• Jaeglé, Lyatt
• Guo, Hongyu
• Weber, Rodney J.
• Michael Reeves, J.
• Weinheimer, Andrew J.
• Schroder, Jason C.
• Campuzano‐Jost, Pedro
• Jimenez, Jose L.
• Dibb, Jack E.
• Veres, Patrick
• Ebben, Carly
• Sparks, Tamara L.
• Wooldridge, Paul J.
• Cohen, Ronald C.
• Hornbrook, Rebecca S.
• Apel, Eric C.
• Campos, Teresa
• Hall, Samuel R.
• Ullmann, Kirk
• Brown, Steven S.

Titel

Heterogeneous N2O5 Uptake During Winter: Aircraft Measurements During the 2015 WINTER Campaign and Critical Evaluation of Current Parameterizations

Ist Teil von

• Journal of geophysical research. Atmospheres, 2018-04, Vol.123 (8), p.4345-4372

Ort / Verlag

Washington: Blackwell Publishing Ltd

Erscheinungsjahr

2018

Link zum Volltext

Quelle

Wiley Online Library All Journals

Beschreibungen/Notizen

• Nocturnal dinitrogen pentoxide (N2O5) heterogeneous chemistry impacts regional air quality and the distribution and lifetime of tropospheric oxidants. Formed from the oxidation of nitrogen oxides, N2O5 is heterogeneously lost to aerosol with a highly variable reaction probability, γ(N2O5), dependent on aerosol composition and ambient conditions. Reaction products include soluble nitrate (HNO3 or NO3−) and nitryl chloride (ClNO2). We report the first‐ever derivations of γ(N2O5) from ambient wintertime aircraft measurements in the critically important nocturnal residual boundary layer. Box modeling of the 2015 Wintertime INvestigation of Transport, Emissions, and Reactivity (WINTER) campaign over the eastern United States derived 2,876 individual γ(N2O5) values with a median value of 0.0143 and range of 2 × 10−5 to 0.1751. WINTER γ(N2O5) values exhibited the strongest correlation with aerosol water content, but weak correlations with other variables, such as aerosol nitrate and organics, suggesting a complex, nonlinear dependence on multiple factors, or an additional dependence on a nonobserved factor. This factor may be related to aerosol phase, morphology (i.e., core shell), or mixing state, none of which are commonly measured during aircraft field studies. Despite general agreement with previous laboratory observations, comparison of WINTER data with 14 literature parameterizations (used to predict γ(N2O5) in chemical transport models) confirms that none of the current methods reproduce the full range of γ(N2O5) values. Nine reproduce the WINTER median within a factor of 2. Presented here is the first field‐based, empirical parameterization of γ(N2O5), fit to WINTER data, based on the functional form of previous parameterizations. Key Points Aircraft measurements over the eastern United States provide the largest number of N2O5 uptake coefficient γ(N2O5) determinations during winter Despite a large range and variability, several γ(N2O5) dependencies are statistically significant, particularly with aerosol liquid water Standard γ(N2O5) parameterizations do not capture the variability but several, including an empirical form derived here, capture the median