## Abstract Rate constants for the gas‐phase reactions of CH~3~OCH~2~CF~3~ (__k__~1~), CH~3~OCH~3~ (__k__~2~), CH~3~OCH~2~CH~3~ (__k__~3~), and CH~3~CH~2~OCH~2~CH~3~ (__k__~4~) with NO~3~ radicals were determined by means of a relative rate method at 298 K. NO~3~ radicals were prepared by thermal d
UV absorption spectrum of CH3OCH2 radicals and kinetics of the reaction of CH3OCH2O2 radicals with NO and NO2 in the gas phase
✍ Scribed by Sarka Langer; Evert Ljungström; Thomas Ellermann; Ole J. Nielsen; Jens Sehested
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 252 KB
- Volume
- 240
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Alkyl and alkylperoxy radicals originating from dimethyl ether have been studied in the gas phase at 296 K. A pulse radiolysis-UV absorption technique was used. Absorption cross-sections were quantified over the wavelength range 220-350 nm. At 230 nm, O'cH3oclJ2 = (4.2 + 0.5)× 10 -18 cm 2 molecule-l has been obtained. Rate constants for the reaction of the alkylperoxy radical with NO and NO 2 were determined to be (9.1 ± 1.0) × 10 -12 cm 3 molecule-1 s-1 and (7.9 ± 0.4) × 10-12 cm 3 molecule-1 s-1, respectively.
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The rate constant for the reaction CH302 + NO2 -(products) has been measured directly by flash photolysis and kinetic spectroscopy. At room temperature and a t total pressures between 53 and 580 Torr, k:, = (9.2 f 0.4) X lo8 liter/mole sec so that the rate of formation of the probable primary produc
Rate constants for the reactions of OH radicals and Cl atoms with CH,CH,NO>, CH,CH,CH,NO,, CH3CH2CH2CHzN02, and CH,CH2CH2CH,CH2N02 have been determined at 295+3 K and a total pressure of approximately 1 atm. The OH rate data were obtained using both the absolute rate technique of pulse radiolysis co
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The reaction of NO with the peroxy radical CFC12CH202, and with CH3CFClO2 was investigated at 8-20 torr and 263-321 K by UV flash photolysis of CFCI2CH3/O2/NO gas mixtures The kinetics were determined from observations of the growth rate of the CFC12CH20 radical and the decay rate of NO by time-reso