Aerosol and trace gas vehicle emission factors measured in a tunnel using an Aerosol Mass Spectrometer and other on-line instrumentation
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Authors
Chirico, Roberto
Prevot, Andre S.H.
DeCarlo, Peter F.
Heringa, Maarten F.
Richter, Rene
Baltensperger, Urs
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Publication date
04/2011
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01A - Journal article
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Atmospheric Environment
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Volume
45
Issue / Number
13
Pages / Duration
2182-2192
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Elsevier
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Abstract
In this study we present measurements of gas and aerosol phase composition for a mixed vehicle fleet in the Gubrist tunnel (Switzerland) in June 2008. PM1 composition measurements were made with a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (AMS) and a Multi Angle Absorption Photometer (MAAP). Gas-phase measurements of CO, CO2, NOx and total hydrocarbons (THC) were performed with standard instrumentation. Weekdays had a characteristic diurnal pattern with 2 peaks in concentrations for all traffic related species corresponding to high vehicle density (∼300 ± 30 vehicles per 5 min) in the morning rush hour between 06:00 and 09:00 and in the afternoon rush hours from approximately 15:30 to 18:30.
The emission factors (EF) of OA were heavily influenced by the OA mass loading. To exclude this partitioning effect, only organic aerosol mass concentrations from 60 μg m−3 to 90 μg m−3 were considered and for these conditions the EF(OA) value for HDV was 33.7 ± 2.3 mg km−1 for a temperature inside the tunnel of 20–25 °C. This value is not directly applicable to ambient conditions because it is derived from OA mass concentrations that are roughly a factor of 10 higher than typical ambient concentrations. An even higher EF(OA)HDV value of 47.4 ± 1.6 mg km−1 was obtained when the linear fit was applied to all data points including OA concentrations up to 120 μg m−3.
Similar to the increasing EF, the OA/BC ratio in the tunnel was also affected by the organic loading and it increased by a factor of ∼3 over the OA range 10–120 μg m−3. This means that also the OA emission factors at ambient concentrations of around 5–10 μg m−3 would be 2–3 times lower than the emission factor given above. For OA concentrations lower than 40 μg m−3 the OA/BC mass ratio was below 1, while at an OA concentration of 100–120 μg m−3 the OA/BC ratio was ∼1.5. The AMS mass spectra (MS) acquired in the tunnel were highly correlated with the primary organic aerosol (POA) MS from a EURO 3 diesel vehicle with a speed similar to the average tunnel speed.
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Subject (DDC)
500 - Naturwissenschaften und Mathematik
530 - Physik
530 - Physik
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1352-2310
0004-6981
0004-6981
Language
English
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No
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Published
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Closed
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Citation
CHIRICO, Roberto, Andre S.H. PREVOT, Peter F. DECARLO, Maarten F. HERINGA, Rene RICHTER, Ernest WEINGARTNER und Urs BALTENSPERGER, 2011. Aerosol and trace gas vehicle emission factors measured in a tunnel using an Aerosol Mass Spectrometer and other on-line instrumentation. Atmospheric Environment. April 2011. Bd. 45, Nr. 13, S. 2182–2192. DOI 10.1016/j.atmosenv.2011.01.069. Verfügbar unter: https://irf.fhnw.ch/handle/11654/46254