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This study investigates the hot deformation behaviour and flow stress prediction of metastable β-Ti-15Mo alloy, a promising material for biomedical applications requiring strength–modulus optimisation and thermomechanical tunability. Isothermal compression tests were performed within the temperature range of 923–1173 K and at strain rates of 0.17, 1.72, and 17.2 s−1 to assess the material’s response under industrially relevant hot working conditions. The alloy showed significant sensitivity to temperature and strain rate, with dynamic recovery (DRV) and dynamic recrystallisation (DRX) dominating the softening behaviour depending on the conditions. A strain-compensated Arrhenius-type constitutive model was developed and validated, resulting in an apparent activation energy of approximately 234 kJ/mol. Zener–Hollomon parameter analysis confirmed a transition in deformation mechanisms. Although microstructural and diffraction data suggest possible contributions from nanoscale phase transformations, including ω-phase dissolution at high temperatures, these aspects remain to be fully elucidated. The model offers reliable predictions of flow behaviour and supports optimisation of thermomechanical processing routes for biomedical β-Ti alloys.

In metallic glass-reinforced metal matrix composites, the glassy phase can serve a dual purpose: (i) it can behave as soft binder and porosity remover during consolidation; and (ii) it can act as the hard reinforcing phase after densification. The present work aimed to demonstrate the benefit of the glassy reinforcing particles for the densification of aluminum matrix composites. The consolidation behavior of Al–50 vol.% Fe-based alloy mixtures prepared using a glassy Fe66Cr10Nb5B19 alloy powder (Tg = 521 °C, Tx = 573 °C) or a crystalline Fe62Cr10Nb12B16 alloy powder was studied under spark plasma sintering (SPS) and hot pressing (HP) conditions. The powders were consolidated by heating above the glass transition temperature of the glassy alloy (up to 540 °C in SPS and 570 °C in HP). When the coarse aluminum powder was used, the reinforcing particles formed chains within the microstructure. In composites formed from the fine Al powder, the particles of the Fe-based alloy were separated from each other by the metallic matrix, and the tendency to form agglomerates was reduced. The glassy state of the alloy was shown to be beneficial for densification, as the metallic glass acted as a soft binder. The densification enhancement effect was more pronounced in the case of reinforcing particles forming chains. The hardness of the Al–50 vol.% glassy Fe66Cr10Nb5B19 composites obtained by SPS was twice the hardness of the unreinforced sintered aluminum (110 HV1 versus 45 HV1).

At present, metallic glasses are evaluated as alternative reinforcements for aluminum matrix composites. These composites are produced by powder metallurgy via consolidation of metallic glass-aluminum powder mixtures. In most studies, the goal has been to preserve the glassy state of the reinforcement during consolidation. However, it is also of interest to track the structure evolution of these composites when partial interaction between the matrix and the metallic glass is allowed during sintering of the mixtures. The present work was aimed to study the microstructure and mechanical properties of composites obtained by spark plasma sintering (SPS) of Al-20 vol.% Fe66Cr10Nb5B19 metallic glass mixtures and compare the materials, in which no significant interaction between the matrix and the Fe-based alloy occurred, with those featuring reaction product layers of different thicknesses. Composite materials were consolidated by SPS at 540 and 570 °C. The microstructure and mechanical properties of composites obtained by SPS and SPS followed by forging, composites with layers of interfacial reaction products of different thicknesses, and metallic glass-free sintered aluminum were comparatively analyzed to conclude on the influence of the microstructural features of the composites on their strength.

The present work was aimed to demonstrate the possibility of forming Fe66Cr10Nb5B19 metallic glass coatings by detonation spraying and analyze the coating formation process. A partially amorphous Fe66Cr10Nb5B19 powder with particles ranging from 45 µm to 74 µm in diameter was used to deposit coatings on stainless steel substrates. The deposition process was studied for different explosive charges (fractions of the barrel volume filled with an explosive mixture (C2H2 + 1.1O2)). As the explosive charge was increased from 35% to 55%, the content of the crystalline phase in the coatings, as determined from the X-ray diffraction patterns, decreased. Coatings formed at explosive charges of 55–70% contained as little as 1 wt.% of the crystalline phase. In these coatings, nanocrystals in a metallic glass matrix were only rarely found; their presence was confined to some inter-splat boundaries. The particle velocities and temperatures at the exit of the barrel were calculated using a previously developed model. The particle temperatures increased as the explosive charge was increased from 35% to 70%; the particle velocities passed through maxima. The coatings acquire an amorphous structure as the molten particles rapidly solidify on the substrate; cooling rates of the splats were estimated. The Fe66Cr10Nb5B19 metallic glass coatings obtained at explosive changes of 55–60% showed low porosity (0.5–2.5%), high hardness (715–1025 HV), and high bonding strength to the substrate (150 MPa).