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Road tunnel, roadside, and urban background measurements of aliphatic compounds in size-segregated particulate matter

MPG-Autoren
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Caseiro,  Alexandre
Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society;

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Zitation

Alves, C. A., Oliveira, C., Martins, N., Mirante, F., Caseiro, A., Pio, C., et al. (2016). Road tunnel, roadside, and urban background measurements of aliphatic compounds in size-segregated particulate matter. Atmospheric Research, 168, 139-148. doi:10.1016/j.atmosres.2015.09.007.


Zitierlink: https://hdl.handle.net/11858/00-001M-0000-002A-205E-F
Zusammenfassung
Particulate matter samples were collected in a road tunnel in Lisbon PM0.5, PM0.5-1, PM1-2.5, and PM2.5-10) and at two urban locations representing roadside and background stations (PM2.5 and PM2.5-10). Samples were analysed for organic and elemental carbon (OC and EC), n-alkanes, n-alkenes, hopanes, some isoprenoid compounds, and steranes. Particulate matter concentrations in the tunnel were 17-31 times higher than at roadside in the vicinity, evidencing an aerosol origin almost exclusively in fresh vehicle emissions. PM0.5 in the tunnel comprised more than 60% and 80% of the total OC and EC mass in PM10, respectively. Concentrations of the different aliphatic groups of compounds in the tunnel were up to 89 times higher than at roadside and 143 times higher than at urban background. Based on the application of hopane-to-OC or hopanes-to-EC ratios obtained in the tunnel, it was found that vehicle emissions are the dominant contributor to carbonaceous particles in the city but do not represent the only source of these triterpenic compounds. Contrary to what has been observed in other studies, the Sigma hopane-to-EC ratios were higher in summer than in winter, suggesting that other factors (e.g. biomass burning, dust resuspension, and different fuels/engine technologies) prevail in relation to the photochemical decay of triterpenoid hydrocarbons from vehicle exhaust (C) 2015 Elsevier B.V. All rights reserved.