Articles | Volume 8, issue 12
Atmos. Chem. Phys., 8, 3141–3147, 2008
https://doi.org/10.5194/acp-8-3141-2008
Atmos. Chem. Phys., 8, 3141–3147, 2008
https://doi.org/10.5194/acp-8-3141-2008

  24 Jun 2008

24 Jun 2008

Atmospheric chemistry of trans-CF3CH=CHF: products and mechanisms of hydroxyl radical and chlorine atom initiated oxidation

M. S. Javadi1, R. Søndergaard1, O. J. Nielsen1, M. D. Hurley2, and T. J. Wallington2 M. S. Javadi et al.
  • 1Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark
  • 2System Analytics and Environmental Sciences Department, Ford Motor Company, Mail Drop RIC-2122, Dearborn, Michigan 48121-2053, USA

Abstract. Smog chamber/FTIR techniques were used to study the products and mechanisms of OH radical and Cl atom initiated oxidation of trans-CF3CH=CHF in 700 Torr of N2/O2 diluent at 295±1 K. Hydroxyl radical initiated oxidation leads to the formation of CF3CHO and HC(O)F in yields which were indistinguishable from 100% and were not dependent on the O2 partial pressure. Chlorine atom initiated oxidation gives HC(O)F, CF3CHO, CF3C(O)Cl, and CF3C(O)CHFCl. The yields of CF3C(O)Cl and CF3C(O)CHFCl increased at the expense of HC(O)F and CF3CHO as the O2 partial pressure was increased over the range 5–700 Torr. The results are discussed with respect to the atmospheric chemistry and environmental impact of trans-CF3CH=CHF.

Download
Altmetrics
Final-revised paper
Preprint