Absolute rate constants for the gas phase reaction of OH radicals with pyrrole tk,) and thiophene ( k , ) have been measured over the temperature ranges 298-440 and 274-382 K, respectively, using the flash photolysis-resonance fluorescence technique. The rate constants obtained were independent of t
Kinetics of the gas-phase reactions of OH radicals with a series of trimethylphenols
✍ Scribed by Iustinian Bejan; Anna Schürmann; Ian Barnes; Thorsten Benter
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 399 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The kinetics of the reactions of hydroxyl (OH) radicals with 2,3,5‐trimethylphenol (235TMP), 2,3,6‐trimethylphenol (236TMP), 2,4,5‐trimethylphenol (245TMP), 2,4,6‐trimethylphenol (246TMP), and 3,4,5‐trimethylphenol (345TMP) have been investigated at 298 ± 2 K and atmospheric pressure of air using a relative rate method. The experiments were performed in a 1080 L volume photoreactor using in situ FTIR analysis to monitor the decay of the trimethylphenols and the reference compounds. The following rate coefficients (in cm^3^ molecule^−1^ s^−1^) were obtained at 298 ± 2 K and 1 atm of air: k(235TMP) = (1.48 ± 0.42) × 10^−10^; k(236TMP) = (1.35 ± 0.39) × 10^−10^; k(245TMP) = (1.23 ± 0.48) × 10^−10^; k(246TMP) = (1.67 ± 0.48) × 10^−10^; k(345TMP) = (1.55 ± 0.43) × 10^−10^. The present kinetic data are discussed in terms of OH addition reactivity trends, and comparisons are made with the reactivity trends observed for successive methylation of benzene and phenol and successive hydroxylation of benzene. © 2011 Wiley Periodicals, Inc. Int J Chem Kinet 44: 117–124, 2012
📜 SIMILAR VOLUMES
## Abstract Sabinaketone is one major photooxidation product of sabinene, an important biogenic volatile organic compound. This article provides the first product study and the second rate constant determination of its reaction with OH radicals. Experiments were investigated under controlled condit
Relative rate constants for the reaction of OH radicals with a seqies of cY,P-unsaturated carbonyls have been determined at 299 & 2 K, using methyl nitrite photolysis in air as a source of OH radicals. Using a rate constant for the reaction of OH radicals with propene of 2.52 X 10-l' cm3/molec.s, th
## Abstract Relative rate constants for the gas‐phase reactions of OH radicals with a series of alkyl nitrates have been determined at 299 ± 2 K, using methyl nitrite photolysis in air as a source of OH radicals. Using a rate constant for the reaction of OH radicals with cyclohexane of 7.57 × 10^−1
Rate constants for three dimethylbenzaldehydes and two trimethylphenols have been determined for the OH reactions at and atmospheric pressure using a relative rate method. The OH reaction rate constants were placed on an absolute basis using the literature rate constant for 1,2,4-trimethylbenzene of