An N.M.R. study of the pressure dependence of molecular self-diffusion and reorientation in organic plastic crystals

1973 ◽  
Vol 26 (1) ◽  
pp. 27-40 ◽  
Author(s):  
R. Folland ◽  
S.M. Ross ◽  
J.H. Strange
1976 ◽  
Vol 32 (1) ◽  
pp. 45-48 ◽  
Author(s):  
M. Y. Al-shaker ◽  
A. H. Brooks ◽  
A. V. Chadwick

2009 ◽  
Vol 289-292 ◽  
pp. 775-782 ◽  
Author(s):  
Zbigniew Jurasz ◽  
Krzysztof Adamaszek ◽  
Romuald Janik ◽  
Zbigniew Grzesik ◽  
Stanisław Mrowec

Detailed investigations of nonstoichiometry as well as chemical and self-diffusion in nickel oxide have shown that doubly ionised cation vacancies and electron holes are the predominant defects in this material. The present work is an attempt to demonstrate that aliovalent impurities (Cr, Al, Na and Li) may considerably influence the concentration of these defects and, consequently, the oxidation rate of nickel at high temperatures. It has been shown that small amounts of tri-valent impurities (Cr, Al) bring about an increase of the oxidation rate, while mono-valent ones (Li, Na) decrease the rate of oxidation. These phenomena may satisfactorily be explained in terms of a doping effect. All experiments have been carried out as a function of temperature (1373-1673 K) and oxygen pressure (1-105 Pa) and consequently, it was possible to determine the influence of impurities not only on the oxidation rate but also on the activation energy of reaction and its pressure dependence. The results of these investigations could again be elucidated in terms of doping effect.


1990 ◽  
Vol 94 (3) ◽  
pp. 336-342 ◽  
Author(s):  
T. Vardag ◽  
F. Bachl ◽  
S. Wappmann ◽  
H.-D. Lüdemann

1998 ◽  
Vol 77 (3) ◽  
pp. 653-660
Author(s):  
P. Knorr ◽  
Chr. Herzig

2020 ◽  
Vol 132 (27) ◽  
pp. 11064-11073 ◽  
Author(s):  
Amit Mondal ◽  
Biswajit Bhattacharya ◽  
Susobhan Das ◽  
Surojit Bhunia ◽  
Rituparno Chowdhury ◽  
...  

1976 ◽  
Vol 54 (5) ◽  
pp. 783-789 ◽  
Author(s):  
C. A. Fyfe ◽  
D. Harold-Smith

A simple but physically well–defined model for self-diffusion in molecular solids is described. This is combined with semi-empirical atom–atom pair potentials for nonbonded atoms to test various possible diffusion mechanisms in the two phases of adamantane. For adamantane it is found that (1) diffusion occurs by jumps to single-vacancy holes at nearest-neighbor lattice sites, (2) the four molecules closest to the midpoint of the jumps are cooperatively distributed among their equilibrium orientations, and (3) the jump trajectory is curved. The computed enthalpy of activation is in good agreement with the experimental value obtained from T1ρ and vapor pressure measurements. The rate of self-diffusion in β-adamantane has not been reported, but the enthalpy of activation has been calculated for various mechanisms and indicates the critical role of lattice disorder in the self-diffusion of plastic crystals.


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