The rate constants for the reaction of OH radicals with a series of 1 chloroalkanes were measured at 295 K and at a total pressure of 1 atm. The rate constants were obtained by using the absolute technique of pulse radiolysis combined with kinetic UV-spectroscopy. The results are discussed in terms
Absolute rate constants for the gas-phase reaction of OH radicals with cyclohexane and ethane at 295 K
β Scribed by Ole J. Nielsen; Jette Munk; Palle Pagsberg; Alfred Sillesen
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 289 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The absolute rate constants for the gas-phase H-atom abstraction by hydroxyl radicals from cyclohexane and ethane have been determined at room temperature.
OH radicals were produced by pulse radiolysis of an H,O-Ar mixture, and the decay of OH was followed by monitoring the transient light absorption around 309 nm. The rate constants were found to be k = (5.24*0.36)x10-I2 and (2.98&0.21)X10-'3 cm3 molecule-' s-' for cyclohexane and ethane, respectively. These results are compared with literature data.
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Using a pulse radiolysis UV absorption technique and subsequent simulations of experimental NO1 and FNO absorption transients, rate constants for reaction between CF90 and CFsO2 radicals with NO were determined, CFp02+NO+CF,O+N02 (3 ), CF,OtNO~CF,OtFNO(5).k~wasderivedtobe(1.68~0.26)X10~~'cm3molecuIe
We present absolute measurements of the rate constant for the reactions of OH with cyclohexane: k, = (8.6 rtO.8) x lo-" cm3 molecule-' s-l and with ethane: k3= (2.74f0.3) x lo-l3 cm3 molecule-\* s-l, both measured at room temperature by discharge flow resonance fluorescence. Our result fork, is abov