We evaluated the effect of strain on the diffusion process of amorphous alloys related to the strain mode in both as-cast and plastically deformed Zr-based bulk amorphous alloy. Experimental investigations of the diffusion process and the elemental distributions in the amorphous alloy were performed by secondary ion mass spectrometry after annealing at 523 K following 30% plastic deformation by multiple cold rolling. Mathematical modeling analyses show an inhomogeneous sequence of the diffusion process by effective strain. The compressive strain near the surface of the deformed amorphous alloy retards ∼13.7% of the diffusion process compared to the as-cast amorphous alloy. The combined experimental and mathematical analyses results reveal that the diffusion process of bulk amorphous alloys can be changed by strain variation and can be adjusted by controlling the effective strain during deformation.

The specific feature of multi-component oxides synthesized by hydrothermal process under high temperature (633 K) and highly pressurized water (18.9 MPa) near critical point. Effects of hydrothermal processing duration times 24 hours and 72 hours, respectively, on the oxide formation of the Ni₅₉Zr₂₀Ti₁₆Si₂Sn₃ metallic glass synthesized by powder metallurgy process were characterized by X-ray diffractometer, differential scanning calorimeter along with the particle size, morphology and crystalline phase of the oxides. The crystallization of the needle-shape NiTiO₃, ZrTiO₄ and ZrSnO₄ ternary oxide phases observed on the surface of metallic glass at below glass transition temperature and the morphology of oxide phases changed to plate-shape around 2 μm in diameter by the increase processing time. This hydrothermal processing in subcritical water provides accelerated dense metal oxide crystals due to the reaction medium being at higher pressure than conventional oxidation processing.

The W/Cu binary system is characterized by its mutual insolubility and excellent wettability, making W/Cu composite materials ideal for managing thermal and electrical properties in electronic components. To optimize material properties, control over the microstructure is crucial, and nanocomposites with uniform dispersion offer significant advantages. In this study, W/Cu composite nanoparticles were synthesized by feeding a blended feedstock of tungsten trioxide (WO₃) micro-powder and cupric oxide (CuO) micro-powder into a reactive radio frequency (RF) argon–hydrogen thermal plasma system. Cu-coated W nanocomposite particles were obtained through the vaporization, reduction, and condensation processes. The resulting nanocomposite particles were composed of body-centered cubic (BCC) α-W, A15 β-W, and face-centered cubic (FCC) Cu phases, with a chemical composition closely matching theoretical calculations. The phase evolution and morphological changes of the synthesized particles were analyzed as a function of heat treatment temperatures up to 1000 °C in a reducing atmosphere. Up to 600 °C, the phase composition and morphology remained stable. At 800 °C, localized diffusion and coalescence of Cu led to the formation of particulate Cu, and a significant phase transformation from metastable β-W to α-W was observed. Additionally, extensive Cu segregation due to long-range diffusion resulted in distinct Cu-rich and Cu-depleted regions. In these regions, notable sintering of W particles and the complete disappearance of β-W occurred. The results showed that the temperature-dependent redistribution of Cu plays a crucial role in the phase transformation of W and the morphology of W/Cu composite particles.

We present variation of the magnetic properties of Fe_77.8Nb_0.2B₁₄P₆C₂ amorphous alloys vitrified at different temperatures by changing the atomic structures dependent on the critical cooling rate. The thermophysical properties of the amorphous state achieved after quenching the melt with cold nitrogen atomization gas are compared with those obtained using hot nitrogen gas with a temperature corresponding to the supercooled liquid of the alloy above the glass transition (T_g) but below crystallization temperature (T_x). The differently vitrified Fe_77.8Nb_0.2B₁₄P₆C₂ glasses represent different states of high pressure gas atomized amorphous powder at different temperatures obtained by adjusting the gas temperature during the atomization process. The magnetic properties of these different amorphous powders are also investigated. The saturation magnetic flux density of slowly cooled Glass2 is 1.38 T with 450 A/m coercivity corresponding to “semi-soft” magnetic materials. The fast cooled Glass1 powder shows typical soft magnetic properties with lower coercivity (174 A/m), even though the saturation magnetization flux densities are similar in both identical compositions of amorphous powder due to its entropy difference related to the formation of clusters. We can control the magnetic property of amorphous materials from soft to half-soft by adjusting freezing temperature and ordering of atoms.

This study investigated the effect of the secondary phases on multi-step phase transitions and the magnetocaloric properties depending on the Ge content in the MnFeCoPSiGe alloys. Two-step phase transitions were observed by the variations of the Fe₂P-type hexagonal structure (first-order) and secondary phases (second-order). The Curie temperature alters with non-linear behavior consistent with change of the lattice parameters. In addition, the magnetic entropy change decreased with the increase of the Ge content and, subsequently, fractions of the secondary phases. However, the morphological variation of microstructure, distributed as a circular-type shape of the Fe₂P-type hexagonal structure in the Ge-rich matrix, increased the magnetic entropy change. Therefore, the addition of Ge enables the control of the Curie temperature to be applicable for high temperature operating devices. The control of the secondary phases and morphology of the microstructure are crucial to improve the phase transition and magnetic entropy change.