4.5 Article

Volatile organic compounds sources in Paris in spring 2007. Part I: qualitative analysis

Journal

ENVIRONMENTAL CHEMISTRY
Volume 8, Issue 1, Pages 74-90

Publisher

CSIRO PUBLISHING
DOI: 10.1071/EN10068

Keywords

diurnal variation; emission; Ile de France; oxygenated compounds; VOC

Funding

  1. Agence Nationale de la Recherche
  2. CNRS
  3. CEA
  4. Centre francais pour l'accueil et les echanges internationaux (EGIDE)-Deutscher Akademischer Austauschdienst (DAAD)
  5. Region Ile de France
  6. Agence De l'Environnement et de la Maitrise de l'Energie (ADEME)

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High-time-resolution measurements of volatile organic compounds (VOCs) were performed in the Paris city centre in spring 2007. The studied region was influenced mainly by air masses of two origins: (1) from the Atlantic Ocean, and (2) from north-eastern Europe. Although the baseline levels (i.e. those not influenced by local emissions) of non-methane hydrocarbons (NMHC) and CO were only slightly impacted by changes in the air-mass origin, oxygenated compounds such as acetone and methanol showed much higher baseline levels in continentally influenced air masses. This suggests that NMHC and CO mixing ratios were mainly influenced by local-to-regional-scale sources whereas oxygenated compounds had a more significant continental-scale contribution. This highlights the importance of measuring VOCs instead of NMHC alone in source classification studies. The period of Atlantic air influence was used to characterise local pollution, which was dominated by traffic-related emissions, although traffic represents the source of only one third of total VOCs emissions in the local inventory. In addition to traffic-related sources, additional sources were identified; in particular, emissions from dry-cleaning activities were identified by the use of a specific tracer (i.e. tetrachloroethylene).

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