Catalytic Exhaust Aftertreatment, General Concepts*

2021 ◽  
pp. 475-481
Author(s):  
Martin Votsmeier ◽  
Thomas Kreuzer ◽  
Jürgen Gieshoff ◽  
Gerhard Lepperhoff ◽  
Barbara Elvers
2021 ◽  
Vol 156 ◽  
pp. 105781
Author(s):  
Louise Gren ◽  
Vilhelm B. Malmborg ◽  
John Falk ◽  
Lassi Markula ◽  
Maja Novakovic ◽  
...  

2004 ◽  
Vol 59 (22-23) ◽  
pp. 5301-5309 ◽  
Author(s):  
Cristian Ciardelli ◽  
Isabella Nova ◽  
Enrico Tronconi ◽  
Brigitte Konrad ◽  
Daniel Chatterjee ◽  
...  

2017 ◽  
Vol 10 (4) ◽  
pp. 44-49
Author(s):  
Klaus Schrewe ◽  
Dominik Lamotte ◽  
Thomas Kästner ◽  
Ingo Zirkwa

2010 ◽  
Vol 10 (6) ◽  
pp. 16055-16109 ◽  
Author(s):  
R. Chirico ◽  
P. F. DeCarlo ◽  
M. F. Heringa ◽  
T. Tritscher ◽  
R. Richter ◽  
...  

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 final 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, primary particles with a mobility diameter above 5 nm were 300±19 cm−3, and 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 0.097 to 0.190. Five hours of oxidation led to a more oxidized OA with an O/C range of 0.208 to 0.369.


Author(s):  
Robert Szolak ◽  
Bernd Danckert ◽  
Alexander Susdorf ◽  
Paul Beutel ◽  
Katharina Pautsch ◽  
...  

2020 ◽  
Vol 222 ◽  
pp. 117021
Author(s):  
Soheil Zeraati-Rezaei ◽  
Mohammed S. Alam ◽  
Hongming Xu ◽  
David C. Beddows ◽  
Roy M. Harrison

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