Temperature dependence of the rate constants of the reactions of oxygen atoms with trans-2-butene, cis-2-butene, 2-methylpropene, 2-methyl-2-butene, and 2,3-dimethyl-2-butene
✍ Scribed by H. Biehl; J. Bittner; B. Bohn; R. Geers-Müller; F. Stuhl
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 559 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The kinetics of the reactions of ground state oxygen atoms with trans‐2‐butene, cis‐2‐butene, 2‐methylpropene, 2‐methyl‐2‐butene, and 2,3‐dimethyl‐2‐butene was investigated in the temperature range 200 to 370K. In this range, the rate constants are (in units 10^−11^ cm^3^ s^−1^): (1.1 ± 0.1) exp[+(180 ± 24)K/T]; (0.98 ± 0.09) exp[+(149 ± 23)K/T]; (1.14 ± 0.13) exp[+(128 ± 33)K/T]; (2.34 ± 0.16) exp[+(250 ± 16)K/T]; and (3.31 ± 0.50) exp[+(257 ± 36)K/T], respectively. The atoms were generated by the H~2~ laser photolysis of NO and detected by the time resolved chemiluminescence in the presence of NO. The concentrations of the O(^3^P) atoms were kept so low that secondary reactions with products are unimportant. © 1995 John Wiley & Sons, Inc.
📜 SIMILAR VOLUMES
## Etheriücation of reactive oleüns available in light ýuidized catalytic cracking (FCC) gas-C 5 oline is an attractive way to decrease the oleüns and to increase the octane number. The reactivities of 2-methyl-1-butene (2M1B) and 2-methyl-2-butene (2M2B) in the etheriücation reaction with ethanol
## Abstract An analytical and kinetic study of the thermal reaction of __cis__‐ or __trans__‐2‐butene has been performed in a static system over the temperature range of 480–550°C and at a low extent of reaction and initial pressures of 10–100 torr. The rate constant of the unimolecular __cis–tran
## Abstract The kinetics of the gas‐phase reactions of O~3~ with a series of selected terpenes has been investigated under flow‐tube conditions at a pressure of 100 mbar synthetic air at 295 ± 0.5 K. In the presence of a large excess of __m__‐xylene as an OH radical scavenger, rate coefficients __k