The gas-phase reaction of NO 3 radicals with isoprene was investigated under flow conditions at 298 K in the pressure range 6.8 Ο½ P(mbar) Ο½ 100 using GC-MS/FID, direct MS, and long-path FT-IR spectroscopy as detection techniques. By means of a relative rate method, the rate constant for the primary
A discharge flow mass-spectrometric study of the reaction between the NO3radical and isoprene
β Scribed by U. Wille; E. Becker; R. N. Schindler; I. T. Lancar; G. Poulet; G. Bras
- Book ID
- 104626554
- Publisher
- Springer Netherlands
- Year
- 1991
- Tongue
- English
- Weight
- 583 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0167-7764
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β¦ Synopsis
The kinetics and mechanism of the reaction
were studied in two laboratories at 298 K in the pressure range 0.7-3 torr using the discharge-flow mass-spectrometric method. The rate constant obtained under pseudo-first-order conditions with excess of either NO3 or isoprene was: k~ = (7.8 + 0.6) x 10 -13 cm 3 molecule -l s -I. The product analysis indicated that the primary addition of NO 3 occurred on both n-bonds of the isprene molecule.
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Using a relative rate method, rate constants for the gas-phase reactions OF the NO, radical with methacrolein and methyl vinyl ketone were determined to be ( 4 4 2 1.7) X cm' molecule-' s-' and < 6 X cm3 molecule-' S S ' , respectively, at 296 ? 2 K. The molar formation yields of rnethacrolein and m
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