Nucleation and growth of Ti3Al \textalpha{}2 ordered domains in \textalpha{}-Ti--Al--X alloys were characterised using a combination of transmission electron microscopy, atom probe tomography and small angle X-ray scattering. Model alloys based on Ti--7Al~(wt.\%) and containing O, V and Mo were aged at \SI{550}{\celsius} for times up to \SI{120}{\day} and the resulting precipitate dispersions were observed at intermediate points. Precipitates grew to around \SI{30}{\nano\metre} in size, with a volume fraction of 6--10\% depending on tertiary solutes. Interstitial O was found to increase the equilibrium volume fraction of \textalpha{}2, while V and Mo showed relatively little influence. Addition of any of the solutes in this study, but most prominently Mo, was found to increase nucleation density and decrease precipitate size and possibly coarsening rate. Coarsening can be described by the Lifshitz-Slyozov-Wagner model, suggesting a matrix diffusion-controlled coarsening mechanism (rather than control by interfacial coherency). Solutionising temperature was found to affect nucleation number density with an activation energy of Ef=1.5±0.4~eV, supporting the hypothesis that vacancy concentration affects \textalpha{}2 nucleation. The observation that all solutes increase nucleation number density is also consistent with a vacancy-controlled nucleation mechanism.
@article{arxiv.2010.13894,
title = {Mechanisms of Ti3Al precipitation in hcp alpha-Ti},
author = {Felicity F. Dear and Paraskevas Kontis and Baptiste Gault and Jan Ilavsky and David Rugg and David Dye},
journal= {arXiv preprint arXiv:2010.13894},
year = {2021}
}