The reaction of S(3P) atoms with nitric oxide
✍ Scribed by A. Van Roodselaar; K. Obi; O. P. Strausz
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 367 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
The flash photolysis–vacuum ultraviolet kinetic absorption spectroscopy technique has been used to measure the absolute rate constant for the reaction of ground state S(^3^P) atoms withnitric oxide,\documentclass{article}\pagestyle{empty}\begin{document}${\rm S}\left({^{\rm 3} P} \right) + {\rm NO}\mathop {\longrightarrow}\limits^{\rm M} {\rm SNO}\left({{\rm M} = {\rm CO}_2} \right)$\end{document} as a function of nitric oxide concentration and total pressure. The rateconstant was determined to be 1.9±0.1 × 10^11^ 1^2^/mol^2^.sec at 298°K, with a high‐pressure limit of 9.3 ± 2.1×10^9^ l/mol·sec^−1^. The observed kinetics are consistent with a termolecular energy transfer mechanism.
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## Abstract The reaction of O(^3^__P__) atoms with isobutane has been studied by using the discharge‐flow 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 ± 1.4)
## Abstract The kinetics of the reaction of O(^3^__P__) atoms with acetone were investigated using fast flow methods. The reaction was studied over a temperature range of 298 to 478°K. The specific rate constant obtained was (1.9 ± 0.4) × 10^12^ exp(—5040 ± 180/1.987 __T__) cm^3^/mol·sec. The obser
## Abstract The reactions of ground‐state __S__(^3^__P__~__J__~) atoms with thiirane, methylthiirane, and __trans__‐2,3‐dimethylthiirane have been studied by flash photolysis‐VUV kinetic absorption spectroscopy. From the analysis of the __S__(^3^__P__~__J__~) decay plots the following rate constant
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