Effect of the extrapolation of the experimental molecular electron-scattering intensity to low angles on the radial-distribution curve

1968 ◽  
Vol 9 (4) ◽  
pp. 513-516
Author(s):  
L. V. Vilkov ◽  
V. S. Mastryukov
1954 ◽  
Vol 32 (12) ◽  
pp. 759-763 ◽  
Author(s):  
C. F. A. Beaumont

A new potential function for liquid helium is obtained by modifying the Margenau potential function and summing over a suggested structure for the liquid. The new potential function leads to fair agreement with the first peak of the radial distribution curve for liquid helium, with the isothermal compressibility, and with second virial coefficient data at high temperatures.


1977 ◽  
Vol 38 (22) ◽  
pp. 1259-1262 ◽  
Author(s):  
I. Sick ◽  
J. B. Bellicard ◽  
J. M. Cavedon ◽  
B. Frois ◽  
M. Huet ◽  
...  

1940 ◽  
Vol 60 (2) ◽  
pp. 182-191 ◽  
Author(s):  
G. S. Rushbrooke

The radial distribution of the atoms (or molecules) of liquids, as of solids, can be found from X-ray scattering photographs (Zernike and Prins, 1927; Warren and Gingrich, 1934), and in this way many such distributions have been determined experimentally (Harvey, 1938, 1939; Gingrich, 1940; references in Coulson and Rushbrooke, 1939). The results are generally given as distribution curves showing p(r) or r2p(r) as a function of r, where 4πr2p(r)dr measures the probability that two arbitrarily selected atoms (or molecules) of the liquid are distant r to r + dr apart. Such distribution curves show a sequence of peaks—for ρ(r) these are usually of diminishing amplitude—and for atomic liquids successive peaks may conveniently be ascribed to successive co-ordination shells (of atoms) about any (arbitrarily selected) central atom. The position and precise shape of the peaks depends, of course, upon the temperature as well as the substance of the liquid.


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