𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Kinetics of the reaction OH + CO under atmospheric conditions

✍ Scribed by McCabe, David C.; Gierczak, Tomasz; Talukdar, Ranajit K.; Ravishankara, A. R.

Book ID
118661655
Publisher
American Geophysical Union
Year
2001
Tongue
English
Weight
587 KB
Volume
28
Category
Article
ISSN
1944-8007

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Kinetics of the reactions of OH radicals
Kinetics of the reactions of OH radicals with selected acetates and other esters under simulated atmospheric conditions
✍ Dale C. Williams; Lawrence N. O'Rji; Daniel A. Stone πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 554 KB

The relative hydroxyl radical reaction rate constants from the simulated atmospheric oxidation of selected acetates and other esters have been measured. Reactions were carried out at 297 2 2 K in 100-liter FEP Teflon@-film bags. The OH radicals were generated from the photolysis of methyl nitrite in

Kinetics of the reactions of OH radicals
Kinetics of the reactions of OH radicals with some oxygenated volatile organic compounds under simulated atmospheric conditions
✍ BΓ©nΓ©dicte Picquet; SΓ©bastien Heroux; Abderraouf Chebbi; Jean-FranΓ§ois Doussin; R πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 169 KB πŸ‘ 2 views

Some relative rate experiments have been carried out at room temperature and at atmospheric pressure. This concerns the OH-oxidation of some oxygenated volatile organic compounds including methanol (k 1 ), ethanol (k 2 ), MTBE (k 3 ), ethyl acetate (k 4 ), n-propyl acetate (k 5 ), isopropyl acetate

Kinetics of the reaction of OH radicals
Kinetics of the reaction of OH radicals with a series of ethers under simulated atmospheric conditions at 295 K
✍ Timothy J. Wallington; Jean M. Andino; Loretta M. Skewes; Walter O. Siegl; Steve πŸ“‚ Article πŸ“… 1989 πŸ› John Wiley and Sons 🌐 English βš– 453 KB

Ethers are being increasingly used as motor fuel additives to increase the octane number and to reduce CO emissions. Since their reaction with hydroxyl radicals (OH) is a major loss process for these oxygenated species in the atmosphere, we have conducted a relative rate study of the kinetics of the