Diffusion of Interstitial Solutes in the Group V Transition Metals

Publisher Website
Google Scholar
Abstract
Mechanical relaxation measurements are used extensively to obtain information on the diffusion rate of interstitial solute atoms in body‐centered cubic metals. Such studies have been stimulated by a model, developed by J. L. Snoek, which yielded a relationship between a relaxation time, an experimental parameter, and the diffusion coefficient of the solute atom. Although Snoek's model was confirmed very well for solid solutions of carbon or nitrogen in α‐iron, a number of anomalies were observed when relaxation studies were extended to the group V transition metals. An extensive experimental study has been made of the factors that influence relaxation times. The anomalous behavior of the group VA metals can be accommodated within the framework of Snoek's model by taking account of the specific nature of solid solutions based on these metals. Diffusion data obtained by a variety of relaxation techniques are presented for oxygen, nitrogen, and carbon in vanadium, niobium (columbium), and tantalum. These data are in agreement with those obtained by the more conventional concentration gradient techniques in the few instances where such information is available. The pattern of activation energies suggest that lattice strain considerations alone are insufficient to explain the activation process involved in interstitial diffusion.