Atmos. Chem. Phys. Discuss., 6, 5629-5670, 2006
www.atmos-chem-phys-discuss.net/6/5629/2006/
doi:10.5194/acpd-6-5629-2006
© Author(s) 2006. This work is licensed under the
Creative Commons Attribution-NonCommercial-ShareAlike 2.5 License.
Review Status
This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Formation of secondary organic aerosol and oligomers from the ozonolysis of enol ethers
A. Sadezky1,2, P. Chaimbault3, A. Mellouki2, A. Römpp1, R. Winterhalter1, G. Le Bras2, and G. K. Moortgat1
1Max-Planck-Institute for Chemistry, Atmospheric Chemistry Department, P.O. Box 3060, 55020 Mainz, Germany
2Laboratoire de Combustion et de Systèmes Réactifs, CNRS, 1C Avenue de la Recherche Scientifique, 45071 Orléans-Cedex 2, France
3Institut de Chimie Organique et Analytique, UMR 6005, BP 6759, University of Orléans, 45067 Orléans Cedex 2, France

Abstract. Formation of secondary organic aerosol has been observed in the gas phase ozonolysis of a series of enol ethers, among them several alkyl vinyl ethers (AVE, ROCH=CH2), such as ethyl, propyl, n-butyl, iso-butyl, t-butyl vinyl ether, and ethyl propenyl ether (EPE, C2H5OCH=CHCH3). The ozonolysis has been studied in a 570 l spherical glass reactor at atmospheric pressure (730 Torr) and temperature (296 K). Gas phase reaction products were investigated by in-situ FTIR spectroscopy, and secondary organic aerosol (SOA) formation was monitored by a scanning mobility particle sizer (SMPS). The chemical composition of the formed SOA was analysed by a hybrid mass spectrometer using electrospray ionization (ESI). The main stable gas phase reaction product is the respective alkyl formate ROC(O)H, formed with yields of 60 to 80%, implying that similar yields of the corresponding Criegee Intermediates (CI) CH2O2 for the AVE and CH3CHO2 for EPE are generated. Measured SOA yields are between 2 to 4% for all enol ethers. Furthermore, SOA formation is strongly reduced or suppressed by the presence of an excess of formic acid, which acts as an efficient CI scavenger.

Chemical analysis of the formed SOA by ESI(+)/MS-TOF allows to identify oligomeric compounds in the mass range 200 to 800 u as its major constituents. Repetitive chain units are identified as CH2O2 (mass 46) for the AVE and C2H4O2 (mass 60) for EPE and thus have the same chemical compositions as the respective major Criegee Intermediates formed during ozonolysis of these ethers. The oligomeric structure and chain unit identity are confirmed by HPLC/ESI(+)/MS-TOF and ESI(+)/MS/MS-TOF experiments, whereby successive and systematic loss of a fragment with mass 46 for the AVE (and mass 60 for EPE) is observed. It is proposed that the oligomer has the following basic structure of an oligoperoxide, -[CH(R)-O-O]n-, where R=H for the AVE and R=CH3 for the EPE. Oligoperoxide formation is thus suggested to be another, so far unknown reaction of stabilized Criegee Intermediates in the gas phase ozonolysis of oxygen-containing alkenes leading to SOA formation.


Citation: Sadezky, A., Chaimbault, P., Mellouki, A., Römpp, A., Winterhalter, R., Le Bras, G., and Moortgat, G. K.: Formation of secondary organic aerosol and oligomers from the ozonolysis of enol ethers, Atmos. Chem. Phys. Discuss., 6, 5629-5670, doi:10.5194/acpd-6-5629-2006, 2006.
 
Search ACPD
Discussion Paper
XML
Citation
Final Revised Paper
Share