Ozone–isoprene reactions: Product formation and aerosol potential
✍ Scribed by R. M. Kamens; M. W. Gery; H. E. Jeffries; M. Jackson; E. I. Cole
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 890 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
Dark-phase experiments between isoprene and 0 3 are discussed. UNC outdoor chamber experiments have shown that in high-concentration systems of isoprene and 0 3 (5 ppm C and 1 ppm) approximately 75% of the reacted carbon can be observed in the product formation of HCHO, CO, methacrolein, methylvinylketone, methylglyoxal, acetaldehyde, and propylene.
Mechanisms were developed which gave reasonable fits to dark-phase chamber experiments of MACR, MVK, isoprene, and 03. Experimental data and modeling results were used to generate 0 3 rates of attack on MVK and MACR. An isoprene-03 rate of 1.67 X ppm-l-rnin-l was used and is consistent with other rates reported in the literature. Dark isoprene-03 systems appear to form homogeneously nucleated aerosol. Most of these particles appear and remain a t diameters well below the optical cutoff region (0.3-0.5 Fm), as opposed to the particles from similar a-pinene-03 systems, which also form at smaller sizes hut then grow into the optical size range (>0.5 Fm). Lower concentrations of a-pinene and O3 (0.2 ppm C and 0.12 ppm) still generated substantial aerosol, hut by comparison, rapid CN nucleation was not observed during a similar side-by-side system of isoprene and 03.
📜 SIMILAR VOLUMES
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
## Abstract In this paper, a real‐time laboratory study of the heterogeneous oxidation reaction of gas‐phase ozone with anthracene on surface substrates by using infrared spectroscopy in two distinctly different experimental configurations is reported. One set of kinetic measurements was made by at
## Abstract In the investigation of the redox potential changes of the oxidative fermentation of L‐sorbose to 2‐keto‐L‐gulonic acid, it was found that the 2‐keto‐L‐gulonic acid formation proceeded favourably at low negative redox potential values. Low redox potentials were maintained in a continuou