EIectronicalJy excited oxygen atoms, O(2lD23, generated by the pulsed irradiatkn of ozone in the Hartley continuum, have been observed by bsorption spectroscopy using time-resolved attenuation of resonance radiation in the vacuum ultra-violet (O(31D2$41(21D ) 2 , h 115.2 nm). The concentration profi
Electronically excited oxygen atoms, O(21D2). A time-resolved study of the collisional quenching by the gases H2, D2, CH4, NO, NO2, N2O, and C3O2 using atomic absorption spectroscopy in the vacuum ultraviolet
✍ Scribed by R. F. Heidner III; D. Husain
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 597 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
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 constants describing the removal of the excited atom on collision with the molecules Hz, D?, CH,, NO, NO,, N20, and ( 2 3 0 2 . Where possible, these data are considered within the context of restrictions arising from spin and orbital symmetry and are further discussed in tems of previously reported relative rate data derived from indirect measurements. Consideration is given to the importance of these rate constants in discussing processes taking place in the earth's atmosphere and in systems giving rise to chemical laser action.
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## Abstract Electronically excited oxygen atoms O(2^1^__D__~2~) have been generated by the pulsed irradiation of ozone in the Hartley‐band continuum and monitored photoelectrically in absorption by time‐resolved attenuation of atomic resonance radiation at λ = 115.2 nm [O(3^1^__D__~2~°) → O(2^1^__D