The rate constants for the reaction of OH radicals with a series of 1 chloroalkanes were measured at 295 K and at a total pressure of 1 atm. The rate constants were obtained by using the absolute technique of pulse radiolysis combined with kinetic UV-spectroscopy. The results are discussed in terms
Rate constants for the reaction of OH radicals with a series of alkenes and dialkenes at 295 ± 1 K
✍ Scribed by Roger Atkinson; Sara M. Aschmann
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 570 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Using a relative rate technique, rate constants for the gas phase reactions of the OH radical with n-butane, n-hexane, and a series of alkenes and dialkenes, relative to that for propene, have been determined in one atmosphere of air at 295 f 1 K. The rate constant ratios obtained were (propene = 1.00): ethene, 0.323 2 0.014; 1-butene, 1.19 i 0.06; 1-pentene, 1.19 2 0.05; 1-hexene, 1.40 0.04; 1-heptene, 1.51 2 0.06; 3-methyl-1-butene, 1.21 2 0.04; isobutene, 1.95 2 0.09; cis-2-butene, 2.13 2 0.05; trans-2-butene, 2.43 2 0.05; 2-methyl-2-butene, 3.30 2 0.13; 2,3-dimethyl-2-butene, 4.17 i 0.18; propadiene, 0.367 0.036; 1,3-butadiene, 2.53 2 0.08; 2-methyl-1,3butadiene, 3.81 2 0.15; n-butane, 0.101 2 0.012; and n-hexane, 0.198 ? 0.017. From a least-squares fit of these relative rate data to the most reliable literature absolute flash photolysis rate constants, these relative rate constants can be placed on an absolute basis using a rate constant for the reaction of OH radicals with propene of 2.63 x lo-" cm3 molecule-' s-'. The resulting rate constant data, together with previous relative rate data from these and other laboratories, lead to a self-consistent data set for the reactions of OH radicals with a large number of organics at room temperature.
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## Abstract Using methyl nitrite photolysis in air as a source of hydroxyl radicals, relative rate constants for the reaction of OH radicals with a series of alkanes and alkenes have been determined at 299 ± 2 K. The rate constant ratios obtained are: relative to __n__‐hexane = 1.00, neopentane 0.1
The absolute rate constants for the gas-phase H-atom abstraction by hydroxyl radicals from cyclohexane and ethane have been determined at room temperature. OH radicals were produced by pulse radiolysis of an H,O-Ar mixture, and the decay of OH was followed by monitoring the transient light absorpti
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## Abstract Relative rate constants for the reaction of OH radicals with a series of ketones have been determined at 299 ± 2 K, using methyl nitrite photolysis in air as a source of hydroxyl radicals. Using a rate constant for the reaction of OH radicals with cyclohexane of 7.57 × 10^−12^ cm^3^ mol
Using a relative rate technique, rate constants for the gas-phase reactions of the OH radical with a series of monoterpenes have been determined in one atmosphere of air at 294 5 1 K. Relative to a rate constant for the reaction of OH radicals with 2,3-dimethyl-2-butene of 1.12 lo-'' cm3 molecule-'