Explicit modeling of volatile organic compounds partitioning in the atmospheric aqueous phase

Loading...
Thumbnail Image
Date
2013
Volume
13
Issue
2
Journal
Series Titel
Book Title
Publisher
München : European Geopyhsical Union
Abstract

The gas phase oxidation of organic species is a multigenerational process involving a large number of secondary compounds. Most secondary organic species are water-soluble multifunctional oxygenated molecules. The fully explicit chemical mechanism GECKO-A (Generator of Explicit Chemistry and Kinetics of Organics in the Atmosphere) is used to describe the oxidation of organics in the gas phase and their mass transfer to the aqueous phase. The oxidation of three hydrocarbons of atmospheric interest (isoprene, octane and α-pinene) is investigated for various NOx conditions. The simulated oxidative trajectories are examined in a new two dimensional space defined by the mean oxidation state and the solubility. The amount of dissolved organic matter was found to be very low (yield less than 2% on carbon atom basis) under a water content typical of deliquescent aerosols. For cloud water content, 50% (isoprene oxidation) to 70% (octane oxidation) of the carbon atoms are found in the aqueous phase after the removal of the parent hydrocarbons for low NOx conditions. For high NOx conditions, this ratio is only 5% in the isoprene oxidation case, but remains large for α-pinene and octane oxidation cases (40% and 60%, respectively). Although the model does not yet include chemical reactions in the aqueous phase, much of this dissolved organic matter should be processed in cloud drops and modify both oxidation rates and the speciation of organic species.

Description
Keywords
atmospheric chemistry, mass transfer, modeling, nitrogen oxides, oxidation, partitioning, volatile organic compound
Citation
Mouchel-Vallon, C., Bräuer, P., Camredon, M., Valorso, R., Madronich, S., Hermann, M., & Aumont, B. (2013). Explicit modeling of volatile organic compounds partitioning in the atmospheric aqueous phase. 13(2). https://doi.org//10.5194/acp-13-1023-2013
License
CC BY 3.0 Unported