A41A-0036
Experimental determination of the partitioning coefficient and volatility of important BVOC oxidation products using the Aerosol Collection Module (ACM) coupled to a PTR-ToF-MS

Thursday, 17 December 2015
Poster Hall (Moscone South)
Thorsten Hohaus1, Georgios Gkatzelis1, Ralf Tillmann2, Sebastian Schmitt3, Zhujun Yu4, Patrick Schlag5, Robert Wegener1, Martin Kaminski1 and Astrid Kiendler-Scharr3, (1)Forschungszentrum Jülich GmbH, Jülich 52428, Germany, (2)Forschungszentrum Jülich, Institute of Energy and Climate Research, IEK-8, Jülich, Germany, (3)Institute of Energy and Climate Research, IEK-8, Forschungszentrum Jülich, Jülich, Germany, (4)Organization Not Listed, Washington, DC, United States, (5)Forschungszentrum Jülich, Jülich, Germany
Abstract:
Atmospheric aerosol can alter the Earth’s radiative budget and global climate but can also affect human health. A dominant contributor to the submicrometer particulate matter (PM) is organic aerosol (OA). OA can be either directly emitted through e.g. combustion processes (primary OA) or formed through the oxidation of organic gases (secondary organic aerosol, SOA). A detailed understanding of SOA formation is of importance as it constitutes a major contribution to the total OA. The partitioning between the gas and particle phase as well as the volatility of individual components of SOA is yet poorly understood adding uncertainties and thus complicating climate modelling.

In this work, a new experimental methodology was used for compound-specific analysis of organic aerosol. The Aerosol Collection Module (ACM) is a newly developed instrument that deploys an aerodynamic lens to separate the gas and particle phase of an aerosol. The particle phase is directed to a cooled sampling surface. After collection particles are thermally desorbed and transferred to a detector for further analysis. In the present work, the ACM was coupled to a Proton Transfer Reaction-Time of Flight-Mass Spectrometer (PTR-ToF-MS) to detect and quantify organic compounds partitioning between the gas and particle phase. This experimental approach was used in a set of experiments at the atmosphere simulation chamber SAPHIR to investigate SOA formation. Ozone oxidation with subsequent photochemical aging of β-pinene, limonene and real plant emissions from Pinus sylvestris (Scots pine) were studied. Simultaneous measurement of the gas and particle phase using the ACM-PTR-ToF-MS allows to report partitioning coefficients of important BVOC oxidation products. Additionally, volatility trends and changes of the SOA with photochemical aging are investigated and compared for all systems studied.