We present 1 study of the collisional behaviour of chlorine atoms in the 2P t12 spin orbit state, 881 cm-l above the 3pxz level in the 3ps ground state configuration. Cl(32P,,2) was generated by the repetitive, pulsed irradiation of CC& and monitored photoeIectricalIy in absorption by time-resolved
A study of the collisional quenching of O(21D2) by the noble gases employing time-resolved attenuation of atomic resonance radiation in the vacuum ultraviolet
β Scribed by R. F. Heidner III; D. Husain
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 524 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Abstract
Electronically excited oxygen atoms O(2^1^D~2~) have been generated by the pulsed irradiation of ozone in the Hartleyβband continuum and monitored photoelectrically in absorption by timeβresolved attenuation of atomic resonance radiation at Ξ» = 115.2 nm [O(3^1^D~2~Β°) β O(2^1^D~2~)]. Collisional quenching of the excited atom has been investigated for all the noble gases, and the first absolute values for the secondβorder deactivation rate constants are reported. The resulting rate data are discussed in terms of a curveβcrossing mechanism based on existing spectroscopic data for the noble gas oxides. The absolute rate constants are compared with previous relative rate data for the deactivation of O(2^1^D~2~) by the noble gases.
π SIMILAR VOLUMES
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
A kinetic investigation of electronically excited arsenic atoms in the low-lying states, As(4ps ' 0 5 ) and As(4p3 2P~), ca. 1.33 and 2.28 eV, respectively, above the 44S312 ground state, has been carried out by atomic absorption spectroscopy. Atoms in these optically metastable states were generate
A kinetic study of lead atoms in the spin orbit states, Pb(63P1) and Pb Pb(63Pz), 0.969 and 1.320 eV, respectively, above the 6 3 P ~ ground state, has been carried out by atomic absorption spectroscopy. The electronically excited lead atoms were generated by the pulsed irradiation of lead tetraethy
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
A kinetic investigation is described of the reaction of ground state atomic carbon, c(2p2(3PJ)), monitored by time-resolved atomic resonance absorption spectroscopy, with a wide range of halogenated olefins and aromatic compounds. Atomic carbon was generated by the repetitive pulsed irradiation (A >