On the origin of carbon dioxide in the O + CH2O reaction
โ Scribed by Joyce Wellman; Joonbum Park; John F. Hershberger
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 503 KB
- Volume
- 178
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The reaction of oxygen atoms with formaldehyde was studied. Oxygen atoms were produced by UV-laser photolysis of NO:, and CO2 reaction products were detected by time-resolved infrared diode laser absorption. Analysis of the data combined with numerical kinetic modeling indicate that CO* is formed primarily or exclusively by a secondary reaction of oxygen atoms with HCO radicals. An upper limit of 0.05 is determined for the CO* branching channel in the title reaction.
๐ SIMILAR VOLUMES
Methylperoxy radicals were generated by the flash photolysis of azomethane-oxygen mixtures. The observed broadband spectrum of the CH302 radical is similar, but not identical to those reported previously. The CH:302 decay followed second-order kinetics a t high CH:jOz concentrations with k4, = (2.5
Mixtures of Cl:!, CH4, and 0 2 were flash photolyzed a t room temperature and pressures of -60-760 Torr to produce CH3O2. The CH3O2 radicals decay by the second-order process (6) 2CH302products with k g = (3.7 f 0.3) X cm3/sec in good agreement with other studies. This value ignores any removal by s
The rate coefficient of the reaction CHzOH + 02 -HO2 + CH20. has been measured at 300 K by the LMR flow-tube method, and found to have the unexpectedly large value k = (2J) x 1O-'2 cm3 molecule-' s-I\_ This reaction. preceded by fiomenzafion, may be an important route for the oxidation of CHJO m the
Pulse radiolysis was used to study the kinetics of the reactions of CH 3 C(O)CH 2 O 2 radicals with NO and NO 2 at By monitoring the rate of formation and decay of NO 2 295 K. using its absorption at the rate constants 400 and 450 nm k(CH C(O)CH O ฯฉ NO) ฯญ (8 ฯฎ 3 2 2 and were de-ฯช12 ฯช12 3 ฯช1 ฯช1 2) ฯซ