Dec 3, 2024
2:00pm - 2:15pm
Hynes, Level 2, Room 203
Petra Spörk-Erdely1,2,Gloria Graf3,2,Christoph Gammer4,Simon Fellner4,Peter Presoly2,Johanna Byloff5,2,Helmut Clemens2,Andreas Stark6,Peter Staron6
Graz University of Technology1,Montanuniversität Leoben2,KTH Royal Institute of Technology3,Austrian Academy of Sciences4,Empa-Swiss Federal Laboratories for Materials Science and Technology5,Helmholtz-Zentrum Hereon6
Petra Spörk-Erdely1,2,Gloria Graf3,2,Christoph Gammer4,Simon Fellner4,Peter Presoly2,Johanna Byloff5,2,Helmut Clemens2,Andreas Stark6,Peter Staron6
Graz University of Technology1,Montanuniversität Leoben2,KTH Royal Institute of Technology3,Austrian Academy of Sciences4,Empa-Swiss Federal Laboratories for Materials Science and Technology5,Helmholtz-Zentrum Hereon6
Intermetallic γ-TiAl based alloys are innovative structural materials for lightweight high-temperature applications. While previous generations of these alloys were notoriously difficult to deform, some of the latest generation β-stabilized γ-TiAl based alloys have demonstrated significantly improved hot workability, which nowadays even enables conventional forging. In this work, ternary Ti-Al-Mo model alloys are investigated with regard to the influence of β-stabilizing elements, such as Mo, on the phase transformation behavior of this group of γ-TiAl based alloys. Here, in particular, the transformation of a strongly supersaturated, ordered body-centered cubic β
o phase into the ordered tetragonal γ phase is addressed.
Previous studies on the β
o → γ phase transformation in a Ti-44Al-7Mo (at.%) alloy have combined in-situ high-energy X-ray diffraction (HEXRD), high-energy small-angle X-ray scattering (SAXS), and atom probe tomography as a direct imaging technique to study early stages of the γ growth sequence. Specimens were homogenized in the β single phase region at 1450 °C, water-quenched, and subsequently continuously re-heated in a dilatometer setup at beamline P07 at the Deutsches Elektronen-Synchrotron (DESY) in Hamburg, Germany. Tracing the diffusional processes and growth kinetics of the γ particles within the supersaturated β
o matrix during these in-situ HEXRD/SAXS experiments, it was found that the growth sequence is controlled by elemental redistribution. Based on the diffraction data, it was suggested that coherent γ precipitates are formed initially, which may lose coherency upon further heating.
Here, we provide first experimental proof of this previous assumption as to the coherency of the precipitates formed. Transmission electron microscopy (TEM) was used to characterize γ precipitates in selected heat-treated conditions in terms of their relationship with the β
o matrix. Combining the TEM results with those gained by means of differential scanning calorimetry, it is shown that, in fact, two competing populations of γ precipitates are involved in the phase transformation. Finally, all experimental results are summarized in a consistent and comprehensive description of the β
o → γ phase transformation.