The rate constants of the gas phase reaction of OH radicals with dimethyl sulfide (CH3SCH3) over the temperature range 260-393 K have been studied using the discharge flow-resonance fluorescence technique. The rate constants were fitted by the Arrhenius equation k = (11.8 2 2.2) x exp[-(236 2 150)/T
An absolute and relative rate study of the reaction of oh radicals with dimethyl sulfide
β Scribed by Ole J. Nielsen; Howard W. Sidebottom; Linda Nelson; Jack J. Treacy; Denis J. O'farrell
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 596 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The gas phase reaction of OH radicals with dimethyl sulfide (CH,SCH,, DMS) has been studied using both an absolute and a relative technique a t 295 2 2 K and a total pressure of 1 atm. The absolute rate technique of pulse radiolysis combined with kinetic spectroscopy was applied. Using this technique a rate constant of (3.5 t 0.2) x cm3 molecule-' sK1 was obtained. For the relative rate method, rate constants for the reaction of OH with DMS were found to increase with increasing concentrations of added NO. These results are compared with the large body of kinetic and mechanistic data previously reported in the literature.
π SIMILAR VOLUMES
The kinetics of the gas phase reaction of OH radicals with dimethyl sulfide (CH,SCH,) have been studied a t various temperatures and total pressures using two relative rate methods and a flash photolysis technique. For the relative rate methods, rate constants were measured at 296 L 2 K as a functio
The rate constant of the reaction of OH with DMS has been measured relative to OH + ethene in a 420 1 reaction chamber a t 760 torr total pressure and 298 t 3 K in N L + 0, buffer gas using the 254 nm photolysis of H202 as the OH source. In agreement with a recent absolute rate determination of the
Rate constants for the reaction of OH radicals in a homogeneous gas phase reaction with dhnethyl sulfide have been determined using the flash photolysis resonance fluorescence technique over the temperature range 273400 K. The data (combined with the results of another recent study) can be fit to th
## Abstract A variational transitionβstate theory calculation for the reaction of OH radical with dimethyl sulfide (DMS) in the absence of oxygen is presented. The potential energy surface was previously studied and the effects of different levels of theory were analyzed. Here we propose a kinetic
Rate constants for the gas phase reactions of hydroxyl radicals and chlorine atoms with a number of ethers have been determined at 300 2 3 K and at a total pressure of 1 atmosphere. Both OH radical and chlorine atom rate constants were determined using a relative rate technique. Values for the rate