February 28, 2013
Journal Article

Experimental Determination of Chemical Diffusion within Secondary Organic Aerosol Particles

Abstract

Formation, properties, transformations, and temporal evolution of secondary organic aerosols (SOA) particles strongly depend on particle phase. Recent experimental evidence from a number of groups indicates that SOA is in a semi-solid phase, the viscosity of which remained unknown. We find that when SOA is made in the presence of vapors of volatile hydrophobic molecules the SOA particles absorb and trap them. Here, we illustrate that it is possible to measure the evaporation rate of these molecules that is determined by their diffusion in SOA, which is then used to calculate a reasonably accurate value for the SOA viscosity. We use pyrene as a tracer molecule and a-pinene SOA as an illustrative case. It takes ~24 hours for half the pyrene to evaporate to yield a viscosity of 10^8 Pa s for a-pinene. This viscosity is consistent with measurements of particle bounce and evaporation rates. We show that viscosity of 10^8 Pa s implies coalescence times of minutes, consistent with the findings that SOA particles are spherical. Similar measurements on aged SOA particles doped with pyrene yield a viscosity of 10^9 Pa s, indicating that hardening occurs with time, which is consistent with observed decrease in water uptake and evaporation rate with aging.

Revised: March 6, 2013 | Published: February 28, 2013

Citation

Abramson E.H., D. Imre, J. Beranek, J. Wilson, and A. Zelenyuk. 2013. Experimental Determination of Chemical Diffusion within Secondary Organic Aerosol Particles. Physical Chemistry Chemical Physics. PCCP 15, no. 8:2983-2991. PNNL-SA-87296. doi:10.1039/C2CP44013J