## Abstract Rate constants for the gas‐phase reactions of CH~3~OCH~2~CF~3~ (__k__~1~), CH~3~OCH~3~ (__k__~2~), CH~3~OCH~2~CH~3~ (__k__~3~), and CH~3~CH~2~OCH~2~CH~3~ (__k__~4~) with NO~3~ radicals were determined by means of a relative rate method at 298 K. NO~3~ radicals were prepared by thermal d
A kinetic study of the reaction of fluorine atoms with CH3F, CH3Cl, CH3Br, CF2H2, CO, CF3H, CF3CHCl2, CF3CH2F, CHF2CHF2, CF2ClCH3, CHF2CH3, and CF3CF2H at 295 ± 2 K
✍ Scribed by Timothy J. Wallington; Michael D. Hurley; Jichun Shi; M. Matti Maricq; Jens Sehested; Ole J. Nielsen; Thomas Ellermann
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 807 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
A variety of relative and absolute techniques have been used to measure the reactivity of fluorine atoms with a series of halogenated organic compounds and CO. The following rate constants were derived, in units of cm3 molecule-' s-l: CH3F, (3.7 2 0.8) X CH3C1, (3.3 2 0.71 X 10 -'I; CH3Br, (3.0 2 0.7) X lo-"; CF2H2, (4.3 2 0.9) x 10-l2; CO, (5.5 5 1.0) X CF3CC12H (HCFC-1231, (1.2 2 0.4) X lo-''; CF3CFH2 (HFC-l34a), (1.3 2 0.3) X 10-l2, CHF2CHF2 (HFC-1341, (1.0 2 0.3) X lo-''; CF2ClCH3 (HCFC-l42b), (3.9 2 0.9) x CF2HCH3 (HFC-l52a), (1.7 2 0.4) X lo-''; and CF3CF2H (HFC-1251, (3.5 5 0.8) x
Quoted errors are statistical uncertainties ( 2 ~) .
For rate constants derived using relative rate techniques, an additional uncertainty has been added to account for potential systematic errors in the reference rate constants used. Experiments were performed at 295 2 2 K. Results are discussed with respect to the previous literature data and to the interpretation of laboratory studies of the atmospheric chemistry of HCFCs and HFCs.
📜 SIMILAR VOLUMES
The rate constants for the reactions of OH radicals with CH 3 OCF 2 CF 3 , CH 3 OCF 2 CF 2 CF 3 , and CH 3 OCF(CF 3 ) 2 have been measured over the temperature range 250-430 K. Kinetic measurements have been carried out using the flash photolysis, laser photolysis, and discharge flow methods combine
## Abstract Rate constants were determined for the reactions of OH radicals with the hydrofluoroethers (HFEs) CH~2~FCF~2~OCHF~2~(__k__~1~), CHF~2~CF~2~OCH~2~CF~3~ (__k__~2~), CF~3~CHFCF~2~OCH~2~CF~3~(__k__~3~), and CF~3~CHFCF~2~OCH~2~CF~2~CHF~2~(__k__~4~) by using a relative rate method. OH radical
## Abstract The intermolecular interaction energy curves of CH~3~OCH~3~CH~2~F~2~, CF~3~OCH~3~CH~2~F~2~, CF~3~OCF~3~CH~2~F~2~, CH~3~OCH~3~CHF~3~, CF~3~OCH~3~CHF~3~, and CF~3~OCF~3~CHF~3~ complexes were calculated by the MP2 level __ab initio__ molecular orbital method using the 6‐311G\*\* basi
Rate constant ratios, k d /k c , for the disproportionation/combination reaction at a temperature of 295 Ϯ 2 K, have been measured as 0.034 Ϯ 0.009 for the collision between CF 3 CH 2 CF 2 ϩ CF 3 radicals and as 0.075 Ϯ 0.019 for CF 3 CH 2 CF 2 ϩ CF 3 CH 2 CF 2 radicals. The effect of the two fluori
The rate coefficients for the removal of C1 atoms by reaction with three HCFCs, CF3CHC12 (HCFC-123), CF3CHFCl (HCFC-124), and CH3CFC12 (HCFC 141b), were measured as a function of temperature between 276 and 397 K. CH3CF2C1 (HCFC-142b) was studied only a t 298 K. The Arrhenius expressions obtained ar