Inelastic Collisions Between Excited Alkali Atoms and Molecules X. Temperature Dependence of Cross Sections for 2P1/2↔2P3/2 Mixing in Cesium, Induced in Collisions with Deuterated Hydrogens, Ethanes, and Propanes

1974 ◽  
Vol 52 (7) ◽  
pp. 589-591 ◽  
Author(s):  
E. Walentynowicz ◽  
R. A. Phaneuf ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Temperature Dependence ◽  
Isotope Effect ◽  
Cross Sections ◽  
Rotational Energy ◽  
Inelastic Collisions ◽  
Atoms And Molecules ◽  
Rotational Energy Transfer ◽  
Alkali Atoms ◽  
The Cross

The dependence on temperature of the cross sections for 2P1/2 ↔ 2P3/2 mixing in cesium, induced in collisions with various deuterated hydrogen, ethane and propane molecules, has been studied in the range 290–650 K. In the cases of hydrogen and ethane, the behavior of the cross sections was found to depend on the degree of deuteration of the molecules. The very large sizes of the mixing cross sections and the isotope effect observed in their variation with temperature, are ascribed to the phenomenon of electronic to rotational energy transfer.

Inelastic Collisions Between Excited Alkali Atoms and Molecules IX. An Isotope Effect in the Cross Sections for 62P1/2↔62P3/2 Mixing in Cesium, Induced in Collisions with Deuterated Methanes

1974 ◽  
Vol 52 (7) ◽  
pp. 584-588 ◽  
Author(s):  
E. Walentynowicz ◽  
R. A. Phaneuf ◽  
W. E. Baylis ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Isotope Effect ◽  
Cross Sections ◽  
Noble Gas ◽  
Inelastic Collisions ◽  
Semiclassical Theory ◽  
Vibrational States ◽  
Rotational Energy Transfer ◽  
Alkali Atoms ◽  
The Cross

The temperature dependence of cross sections for 62P1/2 ↔ 62P3/2 mixing in cesium, induced in collisions with CH4, CH3D, CH2D2, CHD3, and CD4 molecules, has been investigated in a series of sensitized fluorescence experiments over a temperature range 290–650 K. The various cross sections which are of the order of 10−15 cm2, and which exceed similar cross sections for cesium–noble gas collisions by 4 – 6 orders of magnitude, exhibit differences in their variation with temperature. This isotope effect in the collision cross sections is interpreted on the basis of a novel semiclassical theory of electronic to rotational energy transfer. The cross section for mixing induced by collisions with CF4, which was determined in a subsidiary experiment, and which is 2–3 times larger than the methane cross sections, does not show comparable behavior with temperature, probably because the energy transfer takes place to closely lying molecular vibrational states.

52P1/2 ↔ 52P3/2 excitation transfer in rubidium induced in collisions with CH4, CH2D2, and CD4 molecules

1980 ◽  
Vol 58 (7) ◽  
pp. 1047-1048 ◽  
Author(s):  
R. A. Phaneuf ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Temperature Dependence ◽  
Isotope Effect ◽  
Cross Sections ◽  
Noble Gas ◽  
Rotational Energy ◽  
Excitation Transfer ◽  
Sensitized Fluorescence ◽  
Temperature Range ◽  
Rotational Energy Transfer

The temperature dependence of cross sections for 52P1/2 ↔ 52P3/2 excitation transfer in rubidium, induced in collisions with CH4, CH2D2, and CD4 molecules, has been investigated using methods of sensitized fluorescence over a temperature range 300–650 K. The cross sections, which are of the order of 30 Å2 and which exceed similar cross sections for collisions with noble gas atoms by at least two orders of magnitude, exhibit an isotope effect which is ascribed to the phenomenon of electronic-to-rotational energy transfer.

Temperature dependence of cross sections for 72P1/2 ↔ 72P3/2 excitation transfer and for quenching in cesium, induced in collisions with H2, N2, CH4, and CD4

1982 ◽  
Vol 60 (2) ◽  
pp. 239-244 ◽  
Author(s):  
I. N. Siara ◽  
R. U. Dubois ◽  
L. Krause
Keyword(s):  
Energy Transfer ◽  
Temperature Dependence ◽  
Cross Sections ◽  
Rotational Energy ◽  
Excitation Transfer ◽  
Sensitized Fluorescence ◽  
Temperature Range ◽  
Rotational Energy Transfer ◽  
Order Of Magnitude

The temperature dependence of cross sections for 72P1/2 ↔ 72P3/2 excitation transfer in cesium, as well as the effective quenching of these states, induced in collisions with H2, N2, CH4, and CD4 molecules have been investigated in a series of sensitized fluorescence experiments over a temperature range 390–640 K. The 72P mixing cross sections are of the order of 10−15 cm2 and exceed by at least one order of magnitude similar cross sections for mixing by collisions with Ne, Ar, Kr, and Xe. The large sizes of the mixing cross sections and their variation with temperature are ascribed to a phenomenon of electronic-to-rotational energy transfer.

Correlations in rotational energy transfer for NO–D2 inelastic collisions

2020 ◽  
Vol 153 (6) ◽  
pp. 064301
Author(s):  
Guoqiang Tang ◽  
Matthieu Besemer ◽  
Tim de Jongh ◽  
Quan Shuai ◽  
Ad van der Avoird ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Rotational Energy ◽  
Inelastic Collisions ◽  
Rotational Energy Transfer

Inelastic collisions between excited alkali atoms and molecules. V. Sensitized fluorescence in mixtures of sodium with N2, H2, HD, and D2

1968 ◽  
Vol 46 (19) ◽  
pp. 2127-2131 ◽  
Author(s):  
M. Stupavsky ◽  
L. Krause
Keyword(s):  
Cross Sections ◽  
Ground State ◽  
Resonance Effect ◽  
Excitation Transfer ◽  
Inelastic Collisions ◽  
Sodium Vapor ◽  
Sensitized Fluorescence ◽  
Atoms And Molecules ◽  
Alkali Atoms ◽  
Exciting Beam

3 2P1/2 ↔ 3 2P3/2 excitation transfer in sodium, induced in inelastic collisions with ground-state N2, H2, HD, and D2 molecules, has been investigated in a series of sensitized fluorescence experiments. Mixtures of sodium vapor at a pressure of 5 × 10−7 Torr, and the gases, were irradiated with each NaD component in turn, and the fluorescence which contained both D components was monitored at right angles to the direction of the exciting beam. Measurements of the relative intensities of the NaD fluorescent components yielded the following collision cross sections for excitation transfer. For Na–N2 collisions: Q12(2P1/2 → P3/2) = 144 Å2, Q21(2P1,2 ← 2P3/2) = 76 Å2 for Na–H2 collisions: Q12 = 80 Å2, Q21 = 42 Å2. For Na–HD collisions: Q12 = 84 Å2, Q21 = 44 Å2. For Na–D2 collisions: Q12 = 98 Å2, Q21 = 52 Å2. The cross sections Q21 exhibit a slight resonance effect between the atomic and molecular rotational transitions.

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