A novel method for online analysis of gas and particle composition: description and evaluation of a Filter Inlet for Gases and AEROsols (FIGAERO)
- 1Department of Atmospheric Sciences, University of Washington, Seattle, WA 98195, USA
- 2Department of Physics, P.O. Box 64, 00014, University of Helsinki, Helsinki, Finland
- 3Institute for Energy and Climate Research (IEK-8), Forschungszentrum Jülich, 52425 Jülich, Germany
- 4Institute of Bio- and Geosciences (IBG-2), Forschungszentrum Jülich, 52425 Jülich, Germany
- 5Atmospheric Science, Department of Chemistry and Molecular Biology, University of Gothenburg, 412 96 Gothenburg, Sweden
- 6Center for Aerosol and Cloud Chemistry, Aerodyne Research, Inc., Billerica, MA, USA
Abstract. We describe a novel inlet that allows measurement of both gas and particle molecular composition when coupled to mass spectrometric, chromatographic, or optical sensors: the Filter Inlet for Gases and AEROsols (FIGAERO). The design goals for the FIGAERO are to allow unperturbed observation of ambient air while simultaneously analyzing gases and collecting particulate matter on a Teflon® (hereafter Teflon) filter via an entirely separate sampling port. The filter is analyzed periodically by the same sensor on hourly or faster timescales using temperature-programmed thermal desorption. We assess the performance of the FIGAERO by coupling it to a high-resolution time-of-flight chemical-ionization mass spectrometer (HRToF-CIMS) in laboratory chamber studies of α-pinene oxidation and field measurements at a boreal forest location. Low instrument backgrounds give detection limits of ppt or lower for compounds in the gas-phase and in the picogram m−3 range for particle phase compounds. The FIGAERO-HRToF-CIMS provides molecular information about both gases and particle composition on the 1 Hz and hourly timescales, respectively for hundreds of compounds. The FIGAERO thermal desorptions are highly reproducible (better than 10%), allowing a calibrated assessment of the effective volatility of desorbing compounds and the role of thermal decomposition during the desorption process. We show that the often multi-modal desorption thermograms arising from secondary organic aerosol (SOA) provide additional insights into molecular composition and/or particle morphology, and exhibit changes with changes in SOA formation or aging pathways.