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Environmental Chemistry Environmental Chemistry Society
Environmental problems - Chemical approaches
RESEARCH ARTICLE

Gaseous and Particulate Products from the Atmospheric Ozonolysis of a Biogenic Hydrocarbon, Sabinene

Laura Chiappini A E , Nathalie Carrasco B , Brice Temine C , Benedicte Picquet-Varrault A , Régine Durand-Jolibois A , John C. Wenger D and Jean-François Doussin A
+ Author Affiliations
- Author Affiliations

A Laboratoire Interuniversitaire des Systèmes Atmosphériques, Universités de Paris 12 et 7, Créteil Cedex 94010, France.

B Laboratoire de Chimie Physique, Université Paris Sud, Orsay Cedex 91405, France.

C Laboratoire de Chimie et Environnement, Université de Provence, Marseille Cedex 13331, France.

D Department of Chemistry and Environmental Research Institute, University College, Cork, Ireland.

E Corresponding author. Email: chiappini@lisa.univ-paris12.fr

Environmental Chemistry 3(4) 286-296 https://doi.org/10.1071/EN06037
Submitted: 23 June 2006  Accepted: 10 August 2006   Published: 5 September 2006

Environmental Context. Volatile organic compounds (VOCs) are a source of ozone and secondary organic aerosols, which have significant effects in the lower troposphere and on human health. The emission rate of VOCs from plants exceeds anthropogenic emissions by a factor of ten. In order to understand how these plant-derived compounds influence global ozone budgets, studies into the atmospheric reactions of these compounds are needed. This study investigates the ozonolysis of sabinene, a VOC abundantly emitted by trees in Europe.

Abstract. This work investigates both the gaseous and particulate phase products from the ozonolysis of sabinene in smog chamber experiments. The gaseous phase was analyzed in situ by FTIR. The particulate phase was analyzed after sampling with a supercritical fluid extraction technique directly coupled to gas chromatography and mass spectrometry (SFE-GC-MS) and to an in situ derivatization method. Sabinaketone, formaldehyde, and formic acid have been detected in the gaseous phase. More than 30 products have been observed in the secondary organic aerosol formed from sabinene oxidation and among them 10 have been identified as compounds containing carbonyl, hydroxyl and carboxyl groups. Hypotheses concerning reaction formation pathways have been proposed for each identified product in gaseous and particulate phases.

Keywords. : atmospheric chemistry — ozonolysis — plant emissions — secondary organic aerosols — volatile organic compounds


Acknowledgements

The authors would like to thank INERIS (Institut National de l’Environnement et des RISques), EGIDE, a French leading agency for international mobility and EUROCHAMP, an Integrated Infrastructure Initiative of the 6th framework European program, for financial support.


References


[1]   J. Williams, Environ. Chem. 2004, 1,  125.
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |   (In press).
          (In press).
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
         
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  
        | Crossref |  GoogleScholarGoogle Scholar |  open url image1