TY - JOUR
T1 - Atmospheric chemistry of CF3CH2OCH2CF3
T2 - UV spectra and kinetic data for CF3CH(·)OCH2CF3 and CF3CH(OO·)OCH2CF3 radicals and atmospheric fate of CF3CH(O·)OCH2CF3 radicals
AU - Wallington, T. J.
AU - Guschin, A.
AU - Stein, T. N.N.
AU - Platz, J.
AU - Sehested, J.
AU - Christensen, L. K.
AU - Nielsen, O. J.
PY - 1998/2/12
Y1 - 1998/2/12
N2 - Pulse radiolysis transient UV absorption spectroscopy was used to study the ultraviolet absorption spectra (220-320 nm) and kinetics of CF3CH(·)OCH2CF3 and CF3CH(OO·)OCH2CF3 radicals at 296 K. At 230 nm σ(CF3CH(·)OCH2CF3) = (1.95 ± 0.24) × 10-18 and σ(CF3CH(OO·)OCH2CF3) = (4.40 ± 0.51) × 10-18 cm2 molecule-1. Rate constants for the reaction of F atoms with CF3CH2OCH2CF3, the self-reactions of CF3CH(·)OCH2CF3 and CF3CH(OO·)OCH2CF3 radicals, the association reaction of CF3CH(·)OCH2CF3 radicals with O2, and the reactions of CF3CH(OO·)OCH2CF3 radicals with NO and NO2 were (1.5 ± 0.7) × 10-11, (2.6 ± 0.4) × 10-11, (5.4 ± 0.7) × 10-12 (uncorrected for possible secondary chemistry), (2.3 ± 0.3) × 10-12, (1.45 ± 0.4) × 10-11, and (8.4 ± 0.8) × 10-12 cm3 molecule-1 s-1, respectively. Using an FTIR technique, rate constants for the reaction of Cl atoms with CF3CH2OCH2CF3 and CF3C(O)OCH2CF3 were determined to be (7.1 ± 0.9) × 10-13 and (9.4 ± 1.3) × 10-16 cm3 molecule-1 s-1. Finally, it was determined that the atmospheric fate of CF3CH(O·)OCH2CF3 radicals is decomposition via C-C bond scission to give CF3 radicals and 2,2,2-trifluoroethyl formate (CF3CH2OCHO) which occurs at a rate of approximately 7 × 105 s-1. The results are discussed with respect to the atmospheric chemistry of CF3CH2OCH2CF3 and analogous compounds.
AB - Pulse radiolysis transient UV absorption spectroscopy was used to study the ultraviolet absorption spectra (220-320 nm) and kinetics of CF3CH(·)OCH2CF3 and CF3CH(OO·)OCH2CF3 radicals at 296 K. At 230 nm σ(CF3CH(·)OCH2CF3) = (1.95 ± 0.24) × 10-18 and σ(CF3CH(OO·)OCH2CF3) = (4.40 ± 0.51) × 10-18 cm2 molecule-1. Rate constants for the reaction of F atoms with CF3CH2OCH2CF3, the self-reactions of CF3CH(·)OCH2CF3 and CF3CH(OO·)OCH2CF3 radicals, the association reaction of CF3CH(·)OCH2CF3 radicals with O2, and the reactions of CF3CH(OO·)OCH2CF3 radicals with NO and NO2 were (1.5 ± 0.7) × 10-11, (2.6 ± 0.4) × 10-11, (5.4 ± 0.7) × 10-12 (uncorrected for possible secondary chemistry), (2.3 ± 0.3) × 10-12, (1.45 ± 0.4) × 10-11, and (8.4 ± 0.8) × 10-12 cm3 molecule-1 s-1, respectively. Using an FTIR technique, rate constants for the reaction of Cl atoms with CF3CH2OCH2CF3 and CF3C(O)OCH2CF3 were determined to be (7.1 ± 0.9) × 10-13 and (9.4 ± 1.3) × 10-16 cm3 molecule-1 s-1. Finally, it was determined that the atmospheric fate of CF3CH(O·)OCH2CF3 radicals is decomposition via C-C bond scission to give CF3 radicals and 2,2,2-trifluoroethyl formate (CF3CH2OCHO) which occurs at a rate of approximately 7 × 105 s-1. The results are discussed with respect to the atmospheric chemistry of CF3CH2OCH2CF3 and analogous compounds.
UR - http://www.scopus.com/inward/record.url?scp=0032002364&partnerID=8YFLogxK
M3 - Journal article
AN - SCOPUS:0032002364
SN - 1089-5639
VL - 102
SP - 1152
EP - 1161
JO - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
JF - Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment and General Theory
IS - 7
ER -