The kinetics of OH reactions with furan (kl), thiophene (k2), and tetrahydrothiophene ( k 3 ) , have been investigated over the temperature range 254-425 K. OH radicals were produced by flash photolysis of water vapor at h > 165 nm and detected by timeresolved resonance fluorescence spectroscopy. Th
Kinetic study for the reactions of OH radicals with dimethylsulfide, diethylsulfide, tetrahydrothiophene, and thiophene
โ Scribed by D. Martin; J. L. Jourdain; G. LeBras
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 732 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0538-8066
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โฆ Synopsis
The reactions of OH radicals with dimethylsulfide (DMS) diethylsulfide (DES), tetrahydrothiophene (THT), and thiophene have been studied at room temperature for DES and THT, a t 273,293, and 318 K for DMS, and at 293 and 318 K for thiophene by the discharge flow EPR technique in a halocarbon wax coated reactor. The following rate constants were obtained a t room temperature. (1) OH + DMS: k, = (3.22 2 0.16) x OH + DES: k, = (1.2 2 0.14) x lo-" OH + THT: k3 = (2.12 2 0.16) x lo-" OH + thiophene: k, = (1.2 ? 0.1) x lo-' ' (units are cm3 molecule-' s-l)
For the reaction OH + DMS (l), a very low temperature dependence was noticed. are also reported. Some additional results concerning the mass spectrometric analysis of the products
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Rate constants for the reactions of 0 3 and OH radicals with furan and thiophene have been determined at 298 f 2 K. The rate constants obtained for the 0 3 reactions were (2.42 f 0.28) X 1O-lS cm3/molec.s for furan and <6 X cm3/molec-s for thiophene. The rate constants for the OH radical reactions,