High-pressure torsion (HPT) is applied to a face-centered cubic CoCrFeMnNi high-entropy alloy at 293 and 77 K. Processing by HPT at 293 K produced a nanostructure consisted of (sub)grains of ~50 nm after a rotation for 180°. The microstructure evolution is associated with intensive deformation-induced twinning, and substructure development resulted in a gradual microstructure refinement. Deformation at 77 K produces non-uniform structure composed of twinned and fragmented areas with higher dislocation density then after deformation at room temperature. The yield strength of the alloy increases with the angle of rotation at HPT at room temperature at the cost of reduced ductility. Cryogenic deformation results in higher strength in comparison with the room temperature HPT. The contribution of Hall–Petch hardening and substructure hardening in the strength of the alloy in different conditions is discussed.

The current work presents the results of a study of the thermal stability of metastable ω‐Ti(Fe) produced by a high‐pressure torsion process and describes the phase transformations of ω‐Ti(Fe) upon heating. The titanium alloys under study contain between 1 and 7 wt% of iron, the phase transitions are investigated using a combination of in situ high‐temperature X‐ray diffraction and differential scanning calorimetry. The high‐temperature X‐ray diffraction reveals the phase sequence ω → α' → α + β → β upon heating. The differential scanning calorimetry shows that the first phase transformation is exothermal and that the temperature of this phase transition is independent of the iron concentration within the composition range under study. Subsequent phase transitions are endothermal and the respective transition temperatures depend on the iron concentration. The differences between the phase stabilities conclude from the phase diagram and the phase stabilities observe experimentally are explained by the partial coherence of the α/α′‐Ti and β‐Ti grains.

The microstructure and microhardness evolution of a Ti-15(wt.%)Mo/TiB metal-matrix composite (MMC) during high-pressure torsion (HPT) at 400 °C was studied. The composite was fabricated by spark plasma sintering of a Ti, Mo and TiB₂ powders mixture at 1200 °C. In the initial condition, the structure of the composite consisted mainly of body-centered cubic (bcc) Ti solid solution and TiB whiskers. An increase in dislocation density, a considerable decrease in a grain size in the bcc Ti matrix, and breaking/rearrangement of the TiB whiskers were observed during HPT. The (sub)grain size in the bcc Ti matrix attained after 1 revolution was ~75 nm and then gradually decreased to ~55 nm after 5 revolutions. The TiB particle sizes after 5 revolutions was found to be 130–210 nm. The microhardness increased with strain from 575 HV in the initial state to 730 HV after 5 revolutions. Various hardening mechanisms’ contributions in the Ti-15Mo/TiB were evaluated.