Spherical particles of ferrite (intermediate between Fe3O4 and γ-Fe2O3) were grown on seed crystals (∼9 nm) via the green rust route in an aqueous solution added with sucrose, which promotes spherical growth. By highly dispersing the seed crystals in an HNO3 solution, we could control the diameter of the particles over a wide range of 20–200 nm (geometric standard deviation: 1.1–1.4) by changing the amount of the seed crystals. At the beginning of the seed growth, clusters of the seed crystals were resolved into smaller clusters, each composed of a few seed crystals.

Fully dense HfC and TaC-based composites containing 15 vol% TaSi2 or MoSi2 were produced by hot pressing at 1750–1900 °C. TaSi2 enhanced the sinterability of the composites and nearly fully dense materials were obtained at lower temperatures than in the case of MoSi2-containing ones. The TaC-based composites performed better than HfC composites at room temperature, showing values of mechanical strength up to 900 MPa and a fracture toughness of 4.7 MPa·m1/2. However, preliminary oxidation tests carried out in air at 1600 °C revealed that HfC-based composites have a superior high temperature stability compared to TaC-based materials.

Effects of Fe incorporation into Al–Ti–B4C reactants on the combustion behaviors, reaction mechanism, synthesized products, and possible natural convection of fluids were investigated. The incorporation of Fe significantly promotes the self-propagating reaction and decreases the reaction dependence on the B4C particle size. The prior reaction of Fe with B4C leads to the decomposition of B4C and formation of Fe2B and free carbon. On the other hand, the reaction of Fe with Ti and Al gives rise to the emergence of Fe–Ti and Fe–Ti–Al eutectic liquids. As a result, the diffusivity and reactivity of the dissociated carbon and boron atoms are greatly facilitated and the reaction is substantially promoted, yielding a desirable product of TiC, TiB2, and FeAl phases. Moreover, the incorporation of Fe may enhance free convection of the molten phase in the reaction zone and thus contribute to the combustion synthesis process.

This investigation analyzed the effect of reactant particle size on the stress development characteristics of NiAl synthesized through self-propagating high temperature synthesis. Four sample combinations of NiAl were synthesized based on initial particle diameters of the reactants: (i) 10 μm Al and 10 μm Ni (S1), (ii) 10 μm Al and 100 nm Ni (S2), (iii) 50 nm Al and 10 μm Ni (S3), and (iv) 50 nm Al and 100 nm Ni (S4). Characterization of NiAl was performed by parallel comparison of the distribution of residual stresses of the samples prior to and after the reaction. Residual stresses were quantified using x-ray diffraction. Upon characterization it was found that combinations S1, S2, and S3 exhibited tensile residual stresses, while combination S4 exhibited compressive residual stresses. Statistical analysis confirmed that self-propagating high temperature synthesis products derived from nanoparticle reactant sizes exhibited compressive residual stresses offering improved fatigue resistance in composite production.

Nanostructured bulk NiAl materials were prepared at high pressure and temperature (0–5.0 GPa and 600–1500 °C, respectively). The sintered samples were characterized by x-ray diffraction, scanning electron microscope, density, and indentation hardness measurements. The results show that NiAl nanoparticles may have a compressed surface shell, which may be the reason why NiAl nanomaterials were difficult to densify sintering using conventional methods and why high-pressure sintering was an effective approach. We also observed that B2-structured NiAl could undergo a temperature-dependent phase transition and could be transformed into Al0.9Ni4.22 below 1000 °C for the first time. It is interesting to note that Vickers hardness decreased as grain size decreased below ∼30 nm, indicating that the inverse Hall-Petch effect may be observed in nano-polycrystalline NiAl (n-NiAl) samples. Moreover, a tentative interpretation was developed for high-pressure nanosintering, based on the shell-core model of nanoparticles.

To clarify the texture evolution mechanism of Fe-Mn-Si-based shape memory alloys, the rolling texture of an Fe-14Mn-5Si-9Cr-5Ni shape memory alloy is investigated during rolling to a final reduction of 82% at 873 K. A new rolling texture caused by single slip plane slipping is observed from such alloy, which is different from the conventional copper-type and brass-type textures. By means of the {111} pole figure scattering analysis of the local deformation structure, we conclude that such single slip plane slipping results in the weakness of brass orientation in the α fiber and the great enhancement of β fiber connecting S′ {331}<213> and B′ orientations {110}<114>.

A new powder metallurgy technique for creating porous NiTi is demonstrated, combining liquid phase sintering of prealloyed NiTi powders by Nb additions and pore creation by NaCl space-holders. The resulting foams exhibit well-densified NiTi–Nb walls surrounding interconnected pores created by the space-holder, with controlled fraction, size, and shape. Only small amounts of Nb (3 at.%) are needed to produce a eutectic liquid that considerably improves the otherwise poor densification of NiTi powders. NiTi–Nb foams with 34–44% porosity exhibit high compressive failure stress (>1,500 MPa), ductile behavior (>50% compressive strain), low stiffness (10–20 GPa), and large shape-memory recovery strains. These thermomechanical properties, together with the known biocompatibility of the alloy, make these open-cell foams attractive for bone implant applications.

We report on the formation of ultrafine-grained Ti66Nb13Cu8Ni6.8Al6.2 composites with in situ precipitated micrometer-sized β-Ti(Nb) phase by spark plasma sintering with crystallization. Microstructure analysis indicated that all alloys consisted of soft (Cu, Ni)Ti2 regions surrounded by hard β-Ti(Nb) regions but displayed different microstructures. The alloys exhibited high fracture strength of more than 2200 MPa and remarkable plasticity of ∼25%. The results provided a promising method for fabricating large-sized bulk composites with excellent mechanical properties by powder metallurgy.

A high-conductivity and super-high-strength alloy, Cu-8.0Ni-1.8Si-0.6Sn-0.15Mg, has been developed. The processing conditions of the alloy have been investigated. The evolution of microstructure of the alloy on aging has been examined by transmission electron microscopy. The processing condition giving the highest hardness and good electrical conductivity is as follows: solution treatment at 970 °C for 4 h, cold rolling to 60% reduction, and aging at 500 °C for 30 min. The processed alloy has an average tensile strength of 1180 MPa, 0.2% proof strength of 795 MPa, elongation of 2.75%, and average electrical conductivity of 26.5% IACS. Orthorhombic Ni2Si precipitates are responsible for the age-hardening effect. The orientation relationship between the precipitates and the matrix is (110)m(211)p and. DO22 ordering together with spinodal decomposition also contributed to the hardening.

In this work, we report a new Mg-based glass-forming system of Mg–Ni–(Gd,Nd), which can be produced into glassy rods with maximum diameters of 2–5 mm by copper mold casting. The Mg75Ni15Gd10–xNdx(x = 0–10) BMGs simultaneously possess a high level of glass transition temperatures, high specific strength up to 2.75 × 105 Nm/kg, and enhanced malleability with plastic strains over 1%. In particular, the Mg75Ni15Gd5Nd5 BMG with the glass-forming ability (GFA) up to 5 mm, exhibited compressive yield strength over 900 MPa and plastic strain up to 50% without failure for the specimen with an aspect ratio of 0.5. The improved GFA and malleability for the Mg75Ni15Gd10–x Ndx(x = 0–10) BMGs were discussed, which exhibited their promising potentials for the application as lightweight engineering materials.

The current study shows that there is a preferred orientation relationship between Ag3Sn and Ag in reaction between molten Sn and Ag. Due to the preferred orientation relationship, the morphology of Ag3Sn grains formed on (001) Ag single crystal is different from those formed on (011), (358) single crystal Ag, and polycrystalline Ag Facet scallop-type Ag3Sn grains formed irregularly on (011), (358) single crystal Ag, and polycrystalline Ag; whereas the regular Ag3Sn grains with parallel edges grew on (001) Ag single crystal, and they were elongated along two perpendicular directions. The orientation relationship between Ag3Sn grains and (001) Ag single crystal was determined using electron backscattered diffraction. The preferential growth of regular Ag3Sn grains with parallel edges formed on (001) Ag single crystal can be attributed to their minimum misfit.

Commercial-grade dense Ti-6Al-4V alloy substrate was mechanically roughened, cleaned, and treated with a globular protein [bovine serum albumin (BSA)] for 4 h. Biomimetic calcium phosphate (Ca-P) coating was applied onto the above-treated substrate by immersion into simulated body fluid (SBF) at 25 °C for a period of 4 days, with periodic replacement by freshly prepared SBF at 48-h intervals. After 4 days, branched micron-sized fibers of hydroxyapatite (HAp), resembling the structure of bone, were obtained, connecting the clusters of HAp crystal plates in the coating (thickness ∼200 μm) on the substrate surface. Structural and compositional characterization of the coating was carried out using field emission scanning electron microscopy (FE-SEM) with energy-dispersive x-ray analysis unit (EDX) facility, x-ray diffraction (XRD), and Fourier transform infrared (FTIR) data. In vitro cytotoxicity (ISO 10993-5, 1999), cell adhesion assays, and phase contrast microscopy were performed using NIH 3T3 fibroblast cell lines to ascertain the bioactivity of the coated substrates, with and without protein treatment. Based on our study, we propose a correlation between a specific physical structure of the HAp coating and its biological properties.

Calcium phosphate crystals were synthesized by diffusing calcium ions into silica hydrogels containing phosphate ions. Hydroxyapatite [HAp, Ca10(PO4)6(OH)2] and octacalcium phosphate [OCP, Ca8(HPO4)2(PO4)4.5H2O] with different types of crystal morphology were formed in the gel. The HAp had an irregular or rod shape, a few micrometers in length, while the OCP had an irregular, spherulite, rod- or ribbonlike shape, ranging in size from a few micrometers to several tens of micrometers, depending on the amount of phosphoric acid added and the reaction temperature. The morphology of the OCP changed from an irregular shape to a ribbonlike or rod shape, via a spherulite shape, depending on the amount of phosphoric acid added and the reaction temperature. The degree of supersaturation of the reaction environment and the rate-determining step in the HAp and OCP crystal growth mechanism have been ascribed to the changes in crystal morphology of the HAp and OCP.

A study was made to investigate cavity growth behavior during the superplastic deformation of submicrometer-grained titanium alloy and to compare that to cavity growth in a coarse-grained counterpart. A series of tension tests were performed at a temperature of 973 K and a strain rate of 10−4 s−1. Microstructures revealed that both the size and the volume fraction of the cavities obviously decreased as the grain size decreased. Working within the framework provided by creep models for understanding cavity growth behavior, we found the dominant growth mechanism to be superplastic diffusion, which leads to high-tensile ductility in submicrometer-grained titanium alloy.