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
Kinetics of the reactions of the IO radical with dimethyl sulfide, methanethiol, ethylene, and propylene
β Scribed by F. Maguin; A. Mellouki; G. Laverdet; G. Poulet; G. Le Bras
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 504 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Abstract
The reactions of IO radicals with CH~3~SCH~3~, CH~3~SH, C~2~H~4~, and C~3~H~6~ have been studied using the discharge flow method with direct detection of IO radicals by mass spectrometry. The absolute rate constants obtained at 298 K are the following: IO + CH~3~SCH~3~ β products (1): k~1~ = (1.5 Β± 0.2) Γ 10^β14^; IO + CH~3~SH β products (2): k~2~ = (6.6 Β± 1.3) Γ 10^β16^; IO + C~2~H~4~ βproducts (3): k~3~ < 2 Γ 10^β16^; IO + C~3~H~6~ β products (4): k~4~ < 2 Γ 10^β16^ (units are cm^3^ molecule^β1^ s^β1^). CH~3~S(O)CH~3~ and HOI were found as products of reactions (1) and (2), respectively. The present lower value of k~1~ compared to our previous determination is discussed.
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
## 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
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
Absolute rate coeficients for the reactions of the hydroxyl radical with dimethyl ether i k , ) and diethyl ether ( k 2 ) were measured over the temperature range 295-442 K. The rate coefficient data, in the units cm3 molecule s-l, were fitted to the Arrhenius equationsk,(T) = (1.04 2 0.10) x 10-"ex
The molecular-modulation-UV/visibleabsorption+ectroscopy technique has been used to investigate the simultaneous time. resolved behaviour of10 and HO2 produced by the pbotolysis of O3 in the presence of CH30H, Iz, O2 and Ar. This has enabled a direct measurement of the rate coefficient for the react