TY - JOUR
T1 - UV absorption spectrum, and kinetics and mechanism of the self reaction of CF3CF2O2 radicals in the gas phase at 295 K
AU - Sehested, Jens
AU - Ellermann, Thomas
AU - Nielsen, Ole John
AU - Wallington, Timothy J.
AU - Hurley, Michael D.
PY - 1993/1/1
Y1 - 1993/1/1
N2 - The ultraviolet absorption spectrum, kinetics, and mechanism of the self reaction of CF3CF2O2 radicals have been studied in the gas phase at 295 K. Two techniques were used; pulse radiolysis UV absorption to measure the spectrum and kinetics, and long‐path length FTIR spectroscopy to identify and quantify the reaction products. Absorption cross sections were quantified over the wavelength range 220–270 nm. At 230 nm, σ CF 3CF 2O 2 = (2.74 ± 0.46) ×10−18 cm2 molecule−1. This absorption cross section was used to derive the observed self reaction rate constant for reaction (1), defined as, −d[CF3CF2O2]/dt = 2k1obs[CF3CF2O2]2: (Formula Presented.) k1obs = (2.10 ± 0.38) ×10−12 cm3 molecule−1 s−1 (2σ). The observed products following the self reaction of CF3CF2O2 radicals were COF2, CF3O3CF3, CF3O3C2F5, and CF3OH. CF3O2CF3 was tentatively identified as a product. The carbon balance was 90–100%. The self reaction of CF3CF2O2 radicals was found to proceed via one channel to produce CF3CF2O radicals which then decompose to give CF3 radicals and COF2. In the presence of O2, CF3 radicals are converted into CF3O radicals. CF3O radicals have several fates; self reaction to give CF3O2CF3; reaction with CF3O2 radicals to give CF3O3CF3; reaction with C2F5O2 radicals to give CF3O3C2F5; or reaction with CF3CF2H to give CF3OH. As part of this work a rate constant of (2.5 ± 0.6) ×10−16 cm3 molecule−s−1 was measured for the reaction of Cl atoms with CF3CHF2 using a relative rate technique. Results are discussed with respect to the atmospheric chemistry of CF3CF2H (HFC‐125). © 1993 John Wiley & Sons, Inc.
AB - The ultraviolet absorption spectrum, kinetics, and mechanism of the self reaction of CF3CF2O2 radicals have been studied in the gas phase at 295 K. Two techniques were used; pulse radiolysis UV absorption to measure the spectrum and kinetics, and long‐path length FTIR spectroscopy to identify and quantify the reaction products. Absorption cross sections were quantified over the wavelength range 220–270 nm. At 230 nm, σ CF 3CF 2O 2 = (2.74 ± 0.46) ×10−18 cm2 molecule−1. This absorption cross section was used to derive the observed self reaction rate constant for reaction (1), defined as, −d[CF3CF2O2]/dt = 2k1obs[CF3CF2O2]2: (Formula Presented.) k1obs = (2.10 ± 0.38) ×10−12 cm3 molecule−1 s−1 (2σ). The observed products following the self reaction of CF3CF2O2 radicals were COF2, CF3O3CF3, CF3O3C2F5, and CF3OH. CF3O2CF3 was tentatively identified as a product. The carbon balance was 90–100%. The self reaction of CF3CF2O2 radicals was found to proceed via one channel to produce CF3CF2O radicals which then decompose to give CF3 radicals and COF2. In the presence of O2, CF3 radicals are converted into CF3O radicals. CF3O radicals have several fates; self reaction to give CF3O2CF3; reaction with CF3O2 radicals to give CF3O3CF3; reaction with C2F5O2 radicals to give CF3O3C2F5; or reaction with CF3CF2H to give CF3OH. As part of this work a rate constant of (2.5 ± 0.6) ×10−16 cm3 molecule−s−1 was measured for the reaction of Cl atoms with CF3CHF2 using a relative rate technique. Results are discussed with respect to the atmospheric chemistry of CF3CF2H (HFC‐125). © 1993 John Wiley & Sons, Inc.
UR - http://www.scopus.com/inward/record.url?scp=0027659232&partnerID=8YFLogxK
U2 - 10.1002/kin.550250903
DO - 10.1002/kin.550250903
M3 - Journal article
AN - SCOPUS:0027659232
SN - 0538-8066
VL - 25
SP - 701
EP - 717
JO - International Journal of Chemical Kinetics
JF - International Journal of Chemical Kinetics
IS - 9
ER -