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

Smog chamber/FTIR techniques were used to study the products and mechanisms of OH radical and Cl atom initiated oxidation of trans-CF<sub>3</sub>CH=CHF in 700 Torr of N<sub>2</sub>/O<sub>2</sub> diluent at 295&plusmn;1 K. Hydroxyl radical initiated oxidation l...

Full description

Bibliographic Details
Main Authors: T. J. Wallington, M. D. Hurley, O. J. Nielsen, M. S. Javadi, R. Søndergaard
Format: Article
Language:English
Published: Copernicus Publications 2008-06-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/8/3141/2008/acp-8-3141-2008.pdf
Description
Summary:Smog chamber/FTIR techniques were used to study the products and mechanisms of OH radical and Cl atom initiated oxidation of trans-CF<sub>3</sub>CH=CHF in 700 Torr of N<sub>2</sub>/O<sub>2</sub> diluent at 295&plusmn;1 K. Hydroxyl radical initiated oxidation leads to the formation of CF<sub>3</sub>CHO and HC(O)F in yields which were indistinguishable from 100% and were not dependent on the O<sub>2</sub> partial pressure. Chlorine atom initiated oxidation gives HC(O)F, CF<sub>3</sub>CHO, CF<sub>3</sub>C(O)Cl, and CF<sub>3</sub>C(O)CHFCl. The yields of CF<sub>3</sub>C(O)Cl and CF<sub>3</sub>C(O)CHFCl increased at the expense of HC(O)F and CF<sub>3</sub>CHO as the O<sub>2</sub> 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-CF<sub>3</sub>CH=CHF.
ISSN:1680-7316
1680-7324