American Association for Aerosol Research - Abstract Submission

AAAR 36th Annual Conference
October 16 - October 20, 2017
Raleigh Convention Center
Raleigh, North Carolina, USA

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Mixing Times of Organic Molecules within Secondary Organic Aerosol Particles: A Global Planetary Boundary Layer Perspective

ADRIAN MACLEAN, Christopher Butenhoff, James Grayson, Kelley Barsanti, Jose-Luis Jimenez, Allan Bertram, University of British Columbia

     Abstract Number: 460
     Working Group: Aerosol Chemistry

Abstract
When simulating the formation and life cycle of secondary organic aerosol (SOA) with chemical transport models, it is often assumed that organic molecules are well mixed within SOA particles on the time scale of 1 h. While this assumption has been debated vigorously in the literature, the issue remains unresolved in part due to a lack of information on the mixing times within SOA particles as a function of both temperature and relative humidity. Using laboratory data, meteorological fields and a chemical transport model, we determine how often mixing times are < 1 h within biogenic SOA in the planetary boundary layer (the region of the atmosphere where SOA concentrations are on average the highest). Based on laboratory viscosity measurements, we show that the mixing times are < 1 h most of the time (> 93 % of the occurrences) when the SOA concentrations are significant. In addition, we show that a reasonable upper limit to the mixing time for most locations is 30 min. Additional measurements are needed to explore further the effect of oxidation level, oxidation type, and gas-phase precursor on the viscosity and diffusion within biogenic SOA; nevertheless, based on the available laboratory data, the assumption of well mixed SOA in chemical transport models seems reasonable for biogenic SOA in most locations in the planetary boundary layer. On the other hand, slow diffusion in biogenic SOA may still be important in the PBL for heterogeneous chemistry. Slow diffusion in biogenic SOA will also be more important in the free troposphere where both the temperature and RH are lower than in the PBL. Mixing times within anthropogenic SOA can be longer than mixing times within biogenic SOA, at least a room temperature, but additional studies of viscosities or diffusion rates of organic molecules within anthropogenic SOA as a function of both temperature and RH are needed to better constrain how often mixing times are > 1 h within anthropogenic SOA in the PBL.