Cell for Measurements of the Far Ultraviolet Reflectivity of Rare Gas Liquids at Low Temperatures

1968 ◽  
Vol 39 (6) ◽  
pp. 921-922
Author(s):  
D. Beaglehole
1984 ◽  
Vol 62 (12) ◽  
pp. 1665-1672 ◽  
Author(s):  
A. R. W. McKellar ◽  
N. H. Rich

The absorption spectrum of the fundamental band of HD (λ ≈ 2.7 μm) has been studied at high resolution in mixtures with the rare gases He, Ne, and Ar at low temperatures (77 and 145 K) and moderate densities (<205 amagat). Interference effects that occur between the collision-induced transitions and the dipole-allowed transitions of free HD were analyzed as a function of density and collision-partner. The R(0) and R(1)dipole transitions exhibited large changes in shape and intensity at high densities, but their behaviours were quite different from each other. Like the pure HD samples, the line shapes were well represented by series of Fano profiles, and the density dependences of the lines were well explained by the theory of Herman, Tipping, and Poll. These results should greatly improve the understanding of the physical processes underlying the interference effects.


1985 ◽  
Vol 83 (9) ◽  
pp. 4504-4510 ◽  
Author(s):  
K. Nakamura ◽  
N. Masaki ◽  
S. Sato ◽  
K. Shimokoshi

1976 ◽  
Vol 54 (13) ◽  
pp. 2154-2161 ◽  
Author(s):  
Koji Kobashi ◽  
Yosuke Kataoka ◽  
Tsunenobu Yamamoto

Theoretical study has been carried out on the Raman spectra of the ν3 and ν4 vibration bands of methane in Ar, Kr, and Xe matrices at low temperatures. The present study is a continuation of a theoretical work by Nishiyama and Yamamoto on the infrared spectra of the same Systems. We consider the symmetry of the System under the group [Formula: see text] introducing the inversion functions to generalize Wigner's rotational functions. As a result, dual assignments are given to each vibration–rotation state. The allowed transitions of the Raman scattering are compared with those of the infrared absorption, and it is found that a kind of 'rule of mutual exclusion' holds. The relative intensities and spacings of the Raman spectra are calculated and successfully compared with experiment.


1987 ◽  
Vol 17 (1) ◽  
pp. 106-107 ◽  
Author(s):  
N G Basov ◽  
M G Voĭtik ◽  
V S Zuev ◽  
A D Klementov ◽  
V P Kutakhov ◽  
...  

1975 ◽  
Vol 53 (19) ◽  
pp. 2060-2067 ◽  
Author(s):  
A. R. W. McKellar ◽  
J. W. Mactaggart ◽  
H. L. Welsh

The collision induced fundamental band of H2 has been studied in H2–He mixtures with absorption paths of 110 and 165 m in a low temperature multiple traversal cell. Spectra were obtained at 18 and 61.5 K with densities in the range of 9 to 60 amagat. Under these conditions the structure of the band is particularly simple and amenable to analysis; the results of a profile analysis of the present spectra are compared with the higher temperature and density results in paper I (Mactaggart and Welsh) of this series. The long observed splitting of the Q branch of the H2 fundamental is manifested here as very sharp dips in the absorption profile at the Q1(0) and Q1(1) molecular frequencies and these provide a striking confirmation of Van Kranendonk's explanation of the 'splitting' as due to an intercollisional interference effect.


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