CF3BrH2 reaction in shock waves
β Scribed by Yoshiaki Hidaka; Takuji Nakamura; Hiroyuki Kawano; Tohru Koike
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 551 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
β¦ Synopsis
CFaBr-Hz mixtures highly diluted with Ar were studied by using a time-resolved IRemission of HBr and a gas-chromatography for reaction products. The temperature range covered was 1000-1600 K and the total pressure behind the reflected shock waves used was 1.2-2.6 atm. CF3H, C#6, and CzF4 were produced and the yields of these products were determined as a function of temperature. The main product under our experimental conditions was CF3H. The mechanism and the rate constants of CF3Br-Hz reaction at high temperatures were discussed. The experimental data was satisfactorily modeled using a 14reaction mechanism. Reaction (5) played an important role in the formation of CF3H together with reaction (4). ( 4)
The rate constant expression k5 = 2.2 X 1013 exp(-12 kcal/RT) cm3 mol-' s-l gave the best agreement between the calculated and observed results.
π SIMILAR VOLUMES
The pyrolysis of CF,H mixture, highly diluted with Ar, was studied over the temperature range 1150-I 570 K at pressures 1.5-2.6 atm behind reflected shock waves. The mechanism and the rate constant of CFXH pyrolysis at the high temperatures were discussed. The pyrolysis of CFgH was found to be inter
The UV absorption spectrum and the dissociation rate of CF$ in Ar have been measured in shock waves. For [Ar] = 1.7 X 10m5 mol cmW3, the dissociation rate constant k/[Ar] = 1.5 x 1016 exp(-168 kJ moi-'/RT) cm? mol -l s-l\_ The absorption cross section 0 = aF" [tgh(ee/ZT)] 8, = 409 K, A"o = 2370 cm-l
The possibility of proton transfer in the title complexes to form the ion pair is studied by ab initio methods at the SCF and correlated levels using a double-c basis set augmented by (I) a standard set of polanzation functions and (II) a more diffuse set. At the SCF level, the potential surface for
## Abstract The relative rate technique has been used to determine the rate constants of the reactions of OH radicals with CF~3~CClο£ΎCCl~2~ (__k__~1~), CF~3~CClο£ΎCClCF~3~ (__k__~2~) and CF~3~CFο£ΎCFCF~3~ (__k__~3~). Experiments were carried out at (298Β±2) K and atmospheric pressure using ultrapure nitr