Frequency Factor and Activation Energy for the Volume Diffusion of Metals
Open Access
- 1 November 1950
- journal article
- Published by AIP Publishing in Journal of Applied Physics
- Vol. 21 (11) , 1189-1192
- https://doi.org/10.1063/1.1699563
Abstract
The theoretical equations proposed for calculating D0 of the diffusion-constant-temperature relation D=D0e−E/RT are critically discussed in the light of presently available data. It is concluded that none of the relations gives satisfactory agreement with experiment. Empirical analysis of experimental data covering a wide range of D0 and E values showed that the quantity E/Tm, where Tm is the melting point in °K, is the main factor in determining the value of D0, and that D0 depends approximately exponentially on E/Tm. In addition to many other diffusion constants, it is shown that the anisotropic diffusion of zinc and the widely differing diffusion constants for self-diffusion in α- and γ-iron are included in the proposed empirical correlation. A possible theoretical basis for the empirical correlation is described based on the idea of local melting or disordering. The quantity E/Tm is identified with the entropy of activation.This publication has 3 references indexed in Scilit:
- Slip at Grain Boundaries and Grain Growth in MetalsProceedings of the Physical Society, 1948
- Self-Diffusion in IronJournal of Applied Physics, 1948
- The rate of unimolecular and bimolecular reactions in solution as deduced from a kinetic theory of liquidsTransactions of the Faraday Society, 1937