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Schumann-Runge band

Ackermann M and Biaume F 1970 Structure of the Schumann-Runge bands from the 0-0 to the 13-0 band J. Mol. Spectrosc. 35 73-82... [Pg.2150]

High-temperature sulfur vapor at low pressure is said to be pale-violet due to the presence of S2 [22]. The S2 molecule in its triplet ground state has also been produced by photolysis of H2S2 [23], S2CI2 [20, 24], and Me2S2 [25], for example. The S2 vapor spectrum is characterized by the Schumann-Runge bands transition Voo=316 nm [26]) which at high temper-... [Pg.36]

The setup used for crossed beam experiments is basically the same apparatus used in the H2O photodissociation studies but slightly modified. In the crossed beam study of the 0(1D) + H2 — OH + H reaction and the H + HD(D2) — H2(HD) + D reaction, two parallel molecular beams (H2 and O2) were generated with similar pulsed valves. The 0(1D) atom beam was produced by the 157 photodissociation of the O2 molecule through the Schumann-Runge band. The 0(1D) beam was then crossed at 90° with the... [Pg.94]

Yoshino, K., J. R. Esmond, A. S.-C. Cheung, D. E. Freeman, and W. H. Parkinson, High Resolution Absorption Cross Sections in the Transmission Window Region of the Schumann-Runge Bands and Herzberg Continuum of 02, Planet. Space Sci.., 40, 185-192... [Pg.129]

B. Atomspheric photochemistry. The photodissociation of oxygen in sunlight is the major photochemical process occurring in earth s atmosphere. The first intense allowed transition in O., is B - X 32 which occurs at 202.6 nm and is called the Schumann-Runge band system (Section 2.8). It merges intoa continuum beyond 175.9 nm and correlates with one oxygen atom 0(23P) in the ground state and one in the excited state O (2 D)... [Pg.223]

Fig. V-12. Absorption coefficients of O, in the region 1100 to 2000 A. k is in units of atm em 0°C, base e. 1300 to 1700 A, Schumann-Runge continuum. 1750 to 1950 A, Schumann-Runge bands. From Watanabe c al. (1014), reprinted by permission. Copyright 1953 by the American Institute of Physics. Fig. V-12. Absorption coefficients of O, in the region 1100 to 2000 A. k is in units of atm em 0°C, base e. 1300 to 1700 A, Schumann-Runge continuum. 1750 to 1950 A, Schumann-Runge bands. From Watanabe c al. (1014), reprinted by permission. Copyright 1953 by the American Institute of Physics.
Fig. V-13. The absorption cross sections of the 02 continuum in the 1814 to 2350 A region, a is in units of 10"22 cm2 molec base e, at room temperature. The absorption cross sections are measured at minima between the well-separated rotational lines of the Schumann-Runge bands for X < 2025 A. a increases with pressure probably as a result of the formation of 04. The data are values at the low pressure limit. From Ogawa (755), reprinted by permission. Copyright 1971 by the American Institude of Physics. Fig. V-13. The absorption cross sections of the 02 continuum in the 1814 to 2350 A region, a is in units of 10"22 cm2 molec base e, at room temperature. The absorption cross sections are measured at minima between the well-separated rotational lines of the Schumann-Runge bands for X < 2025 A. a increases with pressure probably as a result of the formation of 04. The data are values at the low pressure limit. From Ogawa (755), reprinted by permission. Copyright 1971 by the American Institude of Physics.
The Schumann-Runge bands converge to the limit at 1750 A corresponding to the production of Of3/3) + Of1/)). The integrated absorption coefficients of the Schumann-Runge system from (0,0) to (20,0) have been... [Pg.172]

Fig. V-14. Potential energy curves of Oj. S-R, Schumann-Runge bands H, Herzberg bands A-A, atmospheric bands. The line-broadening was observed at r = 4 of the fl3 state at which point the repulsive 3n. state crosses the B5I state. See Murrell and Taylor (726). From Dissociation Energies and the Spectra of Diatomic Molecules" by Caydon, 3rd Ed. 1968, p. 74, reprinted by permission of Associated Book Publishers Ltd. Fig. V-14. Potential energy curves of Oj. S-R, Schumann-Runge bands H, Herzberg bands A-A, atmospheric bands. The line-broadening was observed at r = 4 of the fl3 state at which point the repulsive 3n. state crosses the B5I state. See Murrell and Taylor (726). From Dissociation Energies and the Spectra of Diatomic Molecules" by Caydon, 3rd Ed. 1968, p. 74, reprinted by permission of Associated Book Publishers Ltd.
Plwtodissociatiqn of 02 in the Upper Atmosphere. The source of O atoms above an altitude of 50 km is mainly from the photolysis of 02 in the Herzberg I and Schumann-Runge continua (488). The predissociation of 02 in the Schumann Runge bands (r > 3) [Wray and Fried (1054)] is the additional source of O atoms between 65 and 95 km. Supporting evidence of the predissoeiation is that no fluorescence of the Schumann-Runge bands above v > 1 has been observed in the upper atmosphere. [Pg.174]

Another important spectral range, between 200 and 175 nm, is related to the 02 Schumann-Runge band system which includes 18 bands, (2-0) to (19-0) subject to the predissociation processes, particularly in the mesosphere. [Pg.64]

Fig. 2. Absorption spectrum of oxygen in the Schumann-Runge band system. The absorption coefficient, k, is defined by the equation I = la exp ( — kx), where h and I are the incident and transmitted light intensities and x is the layer thickness of the absorbing gas reduced to STP. This figure is taken from ref. (101) with the permission of The Journal of Chemical Physics. Fig. 2. Absorption spectrum of oxygen in the Schumann-Runge band system. The absorption coefficient, k, is defined by the equation I = la exp ( — kx), where h and I are the incident and transmitted light intensities and x is the layer thickness of the absorbing gas reduced to STP. This figure is taken from ref. (101) with the permission of The Journal of Chemical Physics.
The most recent measurements of the absorption coefficients of oxygen have been made by Watanabe et al. (101). For the transition 32u- -32 absorption intensities in the Schumann-Runge bands are shown in Figure 2 and in the Schumann-Runge continuum in Figure 3. [Pg.47]

The most recent studies have been carried out below the convergence limit of the Schumann-Runge band system at 1720 A. (76) and above the convergence limit at 1849 A. (95). Earlier studies in both regions (75) have been critically evaluated, (76) and it was concluded that the analytical procedures used were incorrect. The results obtained by Vol-man above the convergence limit are not substantially different from those reported by Smith and Napravnik below the convergence limit. [Pg.73]

Schumann-Runge bands. From Watanabe et al. (1014), reprinted by permission. Copyright 1953 by the American Institute of Physics. [Pg.28]

Spectra with Special Reference to the Schumann—Runge Bands of O2. [Pg.204]

From Ossenbriiggen s work, we know very well the structure of the Schumann-Runge band system of O2, a S —> transition, according to... [Pg.7]


See other pages where Schumann-Runge band is mentioned: [Pg.2140]    [Pg.3]    [Pg.3]    [Pg.230]    [Pg.47]    [Pg.49]    [Pg.60]    [Pg.28]    [Pg.305]    [Pg.166]    [Pg.411]    [Pg.166]    [Pg.148]    [Pg.157]    [Pg.33]    [Pg.49]    [Pg.41]    [Pg.43]   
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See also in sourсe #XX -- [ Pg.2 , Pg.59 ]

See also in sourсe #XX -- [ Pg.130 ]




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Oxygen Schumann-Runge bands

Runge

Rungs

Schumann

Schumann-Runge

Schumann-Runge band system

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