The reaction CH(X \*II) +NZ was studied as a function of temperature in the range 301-894 K at 20 Torr total pressure. CH radicals were generated by excimer laser photolysis of CHClBr\*/Ar mixtures and were detected by laser-induced fluorescence. The reaction proceeds along two pathways, below 673 K
Pressure and temperature dependence of the reactions of CH with N2
โ Scribed by Alan S. Rodgers; Gregory P. Smith
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 581 KB
- Volume
- 253
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
Canonical RRKM theory has been applied to the two channels of the reaction CH + N 2. The transition state parameters used to describe the system were formulated from theoretical potential energy surface parameters and experimental rate constants. Rate constant expressions are presented for the pressure dependent low temperature channel of HCNN adduct formation, and the high temperature prompt NO reaction in which HCN + N are produced by a spin-forbidden surface crossing from a different complex. The expressions fit existing data well and provide a basis for extrapolation to combustion conditions.
๐ SIMILAR VOLUMES
The reaction of NO with the peroxy radical CFC12CH202, and with CH3CFClO2 was investigated at 8-20 torr and 263-321 K by UV flash photolysis of CFCI2CH3/O2/NO gas mixtures The kinetics were determined from observations of the growth rate of the CFC12CH20 radical and the decay rate of NO by time-reso
Absolulc KIIC constants for the rcac11on ofOH WIII acctylcnc wcrc dctcrmmcd at 297 and 419 K for thu 101.d pru~rc\ ol'20-403 Torr usmg a flash photolysa-rcsonancc lluorcsccnre tcchmquc The rate coclTic~cnt k was found to bc pwrurc dcpcndcnt below 200 Torr at both 297 and 429 K, but \\a m the high-pr
Mixtures of N20, Hz, 0 2 , and trace amounts of NO and NO2 were photolyzed at 213.9 nm, at 245'-328'K, and at about 1 atm total pressure (mostly H2). HO2 radicals are produced from the photolysis and they react as follows: (la) Reaction (lb) is unimportant under all of our reaction conditions. Rea