Impact of aftertreatment devices on primary emissions and secondary organic aerosol formation potential from in-use diesel vehicles: results from smog chamber experiments
Open Access
- 6 December 2010
- journal article
- research article
- Published by Copernicus GmbH in Atmospheric Chemistry and Physics
- Vol. 10 (23) , 11545-11563
- https://doi.org/10.5194/acp-10-11545-2010
Abstract
Diesel particulate matter (DPM) is a significant source of aerosol in urban areas and has been linked to adverse health effects. Although newer European directives have introduced increasingly stringent standards for primary PM emissions, gaseous organics emitted from diesel cars can still lead to large amounts of secondary organic aerosol (SOA) in the atmosphere. Here we present results from smog chamber investigations characterizing the primary organic aerosol (POA) and the corresponding SOA formation at atmospherically relevant concentrations for three in-use diesel vehicles with different exhaust aftertreatment systems. One vehicle lacked exhaust aftertreatment devices, one vehicle was equipped with a diesel oxidation catalyst (DOC) and the third vehicle used both a DOC and diesel particulate filter (DPF). The experiments presented here were obtained from the vehicles at conditions representative of idle mode, and for one car in addition at a speed of 60 km/h. An Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was used to measure the organic aerosol (OA) concentration and to obtain information on the chemical composition. For the conditions explored in this paper, primary aerosols from vehicles without a particulate filter consisted mainly of black carbon (BC) with a low fraction of organic matter (OM, OM/BC < 0.5), while the subsequent aging by photooxidation resulted in a consistent production of SOA only for the vehicles without a DOC and with a deactivated DOC. After 5 h of aging ~80% of the total organic aerosol was on average secondary and the estimated "emission factor" for SOA was 0.23–0.56 g/kg fuel burned. In presence of both a DOC and a DPF, only 0.01 g SOA per kg fuel burned was produced within 5 h after lights on. The mass spectra indicate that POA was mostly a non-oxidized OA with an oxygen to carbon atomic ratio (O/C) ranging from 0.10 to 0.19. Five hours of oxidation led to a more oxidized OA with an O/C range of 0.21 to 0.37.Keywords
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This publication has 51 references indexed in Scilit:
- Aged organic aerosol in the Eastern Mediterranean: the Finokalia Aerosol Measurement Experiment – 2008Atmospheric Chemistry and Physics, 2010
- Influence of aging effects on the conversion efficiency of automotive exhaust gas catalystsCatalysis Today, 2009
- Collection Efficiencies in an Aerodyne Aerosol Mass Spectrometer as a Function of Particle Phase for Laboratory Generated AerosolsAerosol Science and Technology, 2008
- Evolving mass spectra of the oxidized component of organic aerosol: results from aerosol mass spectrometer analyses of aged diesel emissionsAtmospheric Chemistry and Physics, 2008
- Impact of Propene on Secondary Organic Aerosol Formation fromm-XyleneEnvironmental Science & Technology, 2007
- Transformation of diesel engine exhaust in an environmental chamberAtmospheric Environment, 2007
- Transmission Efficiency of an Aerodynamic Focusing Lens System: Comparison of Model Calculations and Laboratory Measurements for the Aerodyne Aerosol Mass SpectrometerAerosol Science and Technology, 2007
- Deactivation of diesel oxidation catalysts: Vehicle- and synthetic aging correlationsApplied Catalysis B: Environment and Energy, 2007
- Diesel emission control: Catalytic filters for particulate removalScience and Technology of Advanced Materials, 2007
- Secondary Organic Aerosol Formation by Irradiation of 1,3,5-Trimethylbenzene−NOx−H2O in a New Reaction Chamber for Atmospheric Chemistry and PhysicsEnvironmental Science & Technology, 2005