| Literature DB >> 33012881 |
J D Haskins1, F D Lopez-Hilfiker1, B H Lee1, V Shah1, G M Wolfe2,3, J DiGangi4, D Fibiger5,6, E E McDuffie5,7,6, P Veres5, J C Schroder5,7, P Campuzano-Jost5,7, D A Day5,7, J L Jimenez5,7, A Weinheimer8, T Sparks9, R C Cohen9, T Campos8, A Sullivan10, H Guo11, R Weber11, J Dibb12, J Greene13, M Fiddler13, S Bililign13, L Jaeglé1, S S Brown7,6, J A Thornton1.
Abstract
During winter in the mid-latitudes, photochemical oxidation is significantly slower than in summer and the main radical oxidants driving formation of secondary pollutants, such as fine particulate matter and ozone, remain uncertain, owing to a lack of observations in this season. Using airborne observations, we quantify the contribution of various oxidants on a regional basis during winter, enabling improved chemical descriptions of wintertime air pollution transformations. We show that 25-60% of NOx is converted to N2O5 via multiphase reactions between gas-phase nitrogen oxide reservoirs and aerosol particles, with ~93% reacting in the marine boundary layer to form >2.5 ppbv ClNO2. This results in >70% of the oxidizing capacity of polluted air during winter being controlled, not by typical photochemical reactions, but from these multiphase reactions and emissions of volatile organic compounds, such as HCHO, highlighting the control local anthropogenic emissions have on the oxidizing capacity of the polluted wintertime atmosphere.Entities:
Year: 2019 PMID： 33012881 PMCID： PMC7526063 DOI： 10.1029/2019GL085498
Source DB: PubMed Journal: Geophys Res Lett ISSN： 0094-8276 Impact factor: 4.720