Key parameters controlling OH‐initiated formation of secondary organic aerosol in the aqueous phase (aqSOA)
Open Access
- 5 March 2014
- journal article
- research article
- Published by American Geophysical Union (AGU) in Journal of Geophysical Research: Atmospheres
- Vol. 119 (7) , 3997-4016
Abstract
Secondary organic aerosol formation in the aqueous phase of cloud droplets and aerosol particles (aqSOA) might contribute substantially to the total SOA burden and help to explain discrepancies between observed and predicted SOA properties. In order to implement aqSOA formation in models, key processes controlling formation within the multiphase system have to be identified. We explore parameters affecting phase transfer and OH(aq)‐initiated aqSOA formation as a function of OH(aq) availability. Box model results suggest OH(aq)‐limited photochemical aqSOA formation in cloud water even if aqueous OH(aq) sources are present. This limitation manifests itself as an apparent surface dependence of aqSOA formation. We estimate chemical OH(aq) production fluxes, necessary to establish thermodynamic equilibrium between the phases (based on Henry's law constants) for both cloud and aqueous particles. Estimates show that no (currently known) OH(aq) source in cloud water can remove this limitation, whereas in aerosol water, it might be feasible. Ambient organic mass (oxalate) measurements in stratocumulus clouds as a function of cloud drop surface area and liquid water content exhibit trends similar to model results. These findings support the use of parameterizations of cloud‐aqSOA using effective droplet radius rather than liquid water volume or drop surface area. Sensitivity studies suggest that future laboratory studies should explore aqSOA yields in multiphase systems as a function of these parameters and at atmospherically relevant OH(aq) levels. Since aerosol‐aqSOA formation significantly depends on OH(aq) availability, parameterizations might be less straightforward, and oxidant (OH) sources within aerosol water emerge as one of the major uncertainties in aerosol‐aqSOA formation.Keywords
Funding Information
- Office of Naval Research (N00014-10-1-0811, N00014-04-1-0118)
- National Science Foundation (1052611)
This publication has 88 references indexed in Scilit:
- Particle partitioning potential of organic compounds is highest in the Eastern US and driven by anthropogenic waterAtmospheric Chemistry and Physics, 2013
- A General Scavenging Rate Constant for Reaction of Hydroxyl Radical with Organic Carbon in Atmospheric WatersEnvironmental Science & Technology, 2013
- Cloud water composition over the southeastern Pacific Ocean during the VOCALS regional experimentAtmospheric Environment, 2012
- A two-dimensional volatility basis set: 1. organic-aerosol mixing thermodynamicsAtmospheric Chemistry and Physics, 2011
- Model Representation of Secondary Organic Aerosol in CMAQv4.7Environmental Science & Technology, 2010
- Sources and sinks of hydroxyl radical in sea‐salt particlesJournal of Geophysical Research: Atmospheres, 2007
- Chemical composition and photochemical formation of hydroxyl radicals in aqueous extracts of aerosol particles collected in Okinawa, JapanAtmospheric Environment, 2006
- Photoformation of hydroxyl radical and hydrogen peroxide in aerosol particles from Alert, Nunavut: implications for aerosol and snowpack chemistry in the ArcticAtmospheric Environment, 2004
- Chemistry of fog waters in California's Central Valley: 1. In situ photoformation of hydroxyl radical and singlet molecular oxygenAtmospheric Environment, 2001
- Measurements of atmospheric hydrogen peroxide in the gas phase and in cloud water at Mt. Mitchell, North CarolinaJournal of Geophysical Research: Atmospheres, 1991