1Department of Civil and Environmental Engineering, University of California, Davis, CA, 95616, USA
2Division of Engineering and Applied Science, California Institute of Technology, Pasadena, CA, 91125, USA
3Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125, USA
Received: 14 Sep 2012 – Published in Atmos. Chem. Phys. Discuss.: 15 Oct 2012
Abstract. Laboratory chamber experiments are the main source of data on the mechanism of oxidation and the secondary organic aerosol (SOA) forming potential of volatile organic compounds. Traditional methods of representing the SOA formation potential of an organic do not fully capture the dynamic, multi-generational nature of the SOA formation process. We apply the Statistical Oxidation Model (SOM) of Cappa and Wilson (2012) to model the formation of SOA from the formation of the four C12 alkanes, dodecane, 2-methyl undecane, cyclododecane and hexylcyclohexane, under both high- and low-NOx conditions, based upon data from the Caltech chambers. In the SOM, the evolution of reaction products is defined by the number of carbon (NC) and oxygen (NO) atoms, and the model parameters are (1) the number of oxygen atoms added per reaction, (2) the decrease in volatility upon addition of an oxygen atom and (3) the probability that a given reaction leads to fragmentation of the molecules. Optimal fitting of the model to chamber data is carried out using the measured SOA mass concentration and the aerosol O:C atomic ratio. The use of the kinetic, multi-generational SOM is shown to provide insights into the SOA formation process and to offer promise for application to the extensive library of existing SOA chamber experiments that is available.
Revised: 23 Jan 2013 – Accepted: 25 Jan 2013 – Published: 08 Feb 2013
Citation: Cappa, C. D., Zhang, X., Loza, C. L., Craven, J. S., Yee, L. D., and Seinfeld, J. H.: Application of the Statistical Oxidation Model (SOM) to Secondary Organic Aerosol formation from photooxidation of C12 alkanes, Atmos. Chem. Phys., 13, 1591-1606, doi:10.5194/acp-13-1591-2013, 2013.