Time-resolved atomic absorption spectroscopy in the vacuum ultraviolet has been employed to monitor electronically excited oxygen atoms, 0(2\*D2), following their generation by the flash photolysis of ozone in the Hartley band region. We report the first values for the absolute second-order rate con
The collisional quenching of electronically excited oxygen atoms, O(21D2), by the gases NH3, H2O2, C2H6, C3H8, and C(CH3)4, using time-resolved attenuation of atomic resonance radiation
โ Scribed by Fletcher, I.S.; Husain, D.
- Book ID
- 120056892
- Publisher
- NRC Research Press
- Year
- 1976
- Tongue
- French
- Weight
- 355 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0008-4042
- DOI
- 10.1139/v76-251
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๐ SIMILAR VOLUMES
The pressure broadening and shift rates of the rubidium D2 absorption line 5 2 S 1/2 -5 2 P 3/2 (780.24 nm) with CH 4 , C 2 H 6 , C 3 H 8 , n-C 4 H 10 , and He were measured for pressures r 80 Torr using high-resolution laser spectroscopy. The broadening rates g B for CH 4 ,
Ra?e constants for the reaction of 0(3P) atoms with CaH4, CaHB and NO(M = NpO) have been measured over the temperature range 300-392ยฐK using a modulation-phase shifi technique. The Arrhenius expressions obtained are: C2H4, k2 = 3.37 X 10' exp[-(1270 -f 200)/RT] liter mole-' see-', CJH~, kz = 2.08 x