## Abstract The reaction of O(^3^__P__) atoms with isobutane has been studied by using the dischargeβflow system described previously [1]. The rate constant was measured from determinations of the isobutane concentration in the presence of an excess of O atoms and is given by __k__~1~ = (7.9 Β± 1.4)
The reaction of atomic oxygen O(3P) with propane
β Scribed by Steven P. Jewell; Kenneth A. Holbrook; Geoffrey A. Oldershaw
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 660 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Abstract
The reaction of O(^3^P) atoms with propanehas been studied at temperatures near 300 K by using a discharge flow system. Oxygen atoms were generated in the absence of molecular oxygen by the reaction N + NO β N~2~ + O, nitrogen atoms having been generated in a microwave discharge. Rate constants for the reaction were measured in two ways, either by measurement of Oβatom decay in the presence of excess propane or by measuring the change in propane concentration after an appropriate time in the presence of an excess of oxygen atoms. The two methods were in good agreement, and the mean rate constant at 306 K is given by
A study of the products of the reaction under conditions corresponding to complete removal of oxygen atoms has shown that an important product of the reaction in the early stages is propene. This is difficult to explain interms of a mechanism involving alkoxy radicals similar to that which has been proposed for some other O(^3^P)βhydrocarbon reactions. An alternative mechanism is proposed in terms of successive hydrogen abstraction reactions.
π SIMILAR VOLUMES
## Abstract The mechanism and kinetics of the reaction of O(^3^__P__) atoms with propane were investigated using molecular modulation spectroscopy, with the O(^3^__P__) atoms being generated by the Hg photosensitized decomposition of N~2~O. The absorption spectrum of the __X__^2^II~3/2~ state of OH
the formation of higher oxides of chlorine such as Cl 2 O 4 , Cl 2 O 6 , and Cl 2 O 7 has been observed [5 -8]. The reaction mechanisms are not understood but may involve the formation of ClO 3 which has recently been observed in an inert matrix [9]. In these systems, ClO 3 can be formed via the add
The rate constant for the reaction of O(") with H202 was measured as a function of temperature and the [H202]0/[0]0 ratio. The numerical solution of the appropriate rate equations was used to arrive a t a mechanism which adequately describes our results and the rather divergent data in the literatur