The kinetics of the reactions O( 3 P) ϩ CF 2 "CCl 2 and O( 3 P) ϩ CF 3 CF "CF 2 were studied at room temperature in a discharge flow tube system. The overall rate constants based on the measured afterglow reactions were (3.10 Ϯ 0.40) ϫ 10 Ϫ13 and (3.00 Ϯ 0.60) ϫ 10 Ϫ14 cm 3 molecule Ϫ1 s Ϫ1 , respec
Rate coefficients and ClO radical yields in the reaction of O(1D) with CClF2CCl2F, CCl3CF3, CClF2CClF2, and CCl2FCF3
✍ Scribed by Munkhbayar Baasandorj; Karl J. Feierabend; James B. Burkholder
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 145 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
Rate coefficients, k, and ClO radical product yields, Y, for the gas‐phase reaction of O(^1^D) with CClF~2~CCl~2~F (CFC‐113) (k~2~), CCl~3~CF~3~ (CFC‐113a) (k~3~), CClF~2~CClF~2~ (CFC‐114) (k~4~), and CCl~2~FCF~3~ (CFC‐114a) (k~5~) at 296 K are reported. Rate coefficients for the loss of O(^1^D) were measured using a competitive reaction technique, with n‐butane (n‐C~4~H~10~) as the reference reactant, employing pulsed laser photolysis production of O(^1^D) combined with laser‐induced fluorescence detection of the OH radical temporal profile. Rate coefficients were measured to be k~2~ = (2.33 ± 0.40) × 10^−10^ cm^3^ molecule^−1^ s^−1^, k~3~ = (2.61 ± 0.40) × 10^−10^ cm^3^ molecule^−1^ s^−1^, k~4~ = (1.42 ± 0.25) × 10^−10^ cm^3^ molecule^−1^ s^−1^, and k~5~ = (1.62 ± 0.30) × 10^−10^ cm^3^ molecule^−1^ s^−1^. ClO radical product yields for reactions (2)–(5) were measured using pulsed laser photolysis combined with cavity ring‐down spectroscopy to be 0.80 ± 0.10, 0.79 ± 0.10, 0.85 ± 0.12, and 0.79 ± 0.10, respectively. The quoted errors in k and Y are at the 2σ (95% confidence) level and include estimated systematic errors. © 2011 Wiley Periodicals, Inc.*This article is a U.S. Government work and, as such, is in the public domain of the United States of America
Int J Chem Kinet 43: 393–401, 2011
📜 SIMILAR VOLUMES
## Abstract Relative rate techniques were used to study the title reactions in 930–1200 mbar of N~2~ diluent. The reaction rate coefficients measured in the present work are summarized by the expressions __k__(Cl + CH~2~F~2~) = 1.19 × 10^−17^ __T__^2^ exp(−1023/T) cm^3^ molecule^−1^ s^−1^ (253–553
or from the thermal decomposition of larger radicals formed in the degradation of oxygenated hydrocarbons, e.g., the OH-initiated oxidation of methylglyoxal [2]: (2)