The wetting behavior and strength at aluminum/alumina interfaces has been an active subject of research. Al/alumina applications include ceramic-metal composites and several applications for electronic industries. In this paper the interface strength and microstructure of Al/alpha-alumina was investigated. We discovered that in a solid-state joining, the strength of the joint increases with increasing joining temperature. In a liquid-state joining, the strength of the joint gradually decreases due to the formation of unbonded areas. The strength, sigma sub b, is expressed by the following equation as a function of unbonded area, A: sigma sub b = 2.22 A + 143 (70% <_ A <_ 100%). The highest strength reached 400 MPa when the interface was formed at around the melting temperature of aluminum. An aluminum layer close to the interface became a single crystal when it was bonded to a sapphire. The following crystallographic orientation relationship is established: (1 bar 11) sub Al // (001) sub alpha-Al sub 2 O sub 3 , <110) sub Al // <100> sub alpha-Al sub 2 O sub 3. Amorphous alumina islands were formed at the interface. In the amorphous alumina, gamma-alumina nanocrystals grew from the sapphire, with the same orientation relationship to sapphire as above.

The spreading of liquid Ag and Ag-Mo alloys on molybdenum substrates has been studied using a drop-transfer setup. Even though initial spreading velocities as fast as ~1 m/s have been recorded in some experiments, a large variation in the spreading dynamics has been observed, and there is no unique relationship between the contact angle and the spreading velocity. This can be attributed to the formation of ridges at the triple junction, the movement of which controls spreading. The fastest spreading rates are consistent with results reported for low temperature liquids; these can be described using a molecular-kinetic model. Spreading kinetics and final contact angles were similar for pure silver and silver-molybdenum liquids.

The spreading of Sn-3Ag-xBi solders on Fe-42Ni has been studied using a drop transfer setup. Initial spreading velocities as fast as ~0.5 m/s have been recorded. The results are consistent with a liquid front moving on a metastable, flat, unreacted substrate and can be described by using a modified molecular-kinetic model for which the rate controlling step is the movement of one atom from the liquid to the surface of the solid substrate. Although the phase diagram predicts the formation of two Fe-Sn intermetallics at the solder/substrate interface in samples heated at temperatures lower than 513oC, after spreading at 250oC only a thin FeSn reaction layer could be observed. Two interfacial layers (FeSn and FeSn2) were found after spreading at 450oC.

In this work, atomic force microscopy (AFM) has been used to identify the controlling transport mechanisms at metal/oxide interfaces and measure the corresponding diffusivities. Interfacial transport rates in our experiments are two to four orders of magnitude faster than any previously reported rates for the oxide surface. The interfacial diffusivities and the degree of interfacial anisotropy depend on the oxygen activity of the system. Atomic transport at metal/oxide interfaces plays a defining role in many technological processes, and these experiments provide fundamental data for the formulation of the atomic theory needed to explain many of the observed phenomena.

Reactive spreading, in which a chemically active element is added to promote wetting of noble metals on nonmetallic materials, is evaluated mechanistically. Theories for the energetics and kinetics of the steps involved in spreading are outlined to permit comparison to the steps in the compound formation that typically accompanies reactive wetting. These include: fluid flow, active metal adsorption, including nonequilibrium effects, and triple line ridging. They can all be faster than compound nucleation under certain conditions. This analysis plus assessment of recently reported experiments on metal/ceramic systems lead to a focus on those conditions under which spreading proceeds ahead of the actual formation of a new phase at the interface. This scenario may be more typical than commonly believed, and perhaps is the most effective situation leading to enhanced spreading. A rationale for the slow spreading rates plus the pervasive variability and hysteresis observed during high temperature wetting also emerges.

Development of bioactive glass and ceramic scaffolds intended for the reconstruction of large segmental bone defects remains a challenge for materials science due to the complexities involved in clinical implantation, bone-implant reaction, implant degradation and the multiple loading modes the implants subjected to. A comprehensive evaluation of the mechanical properties of inorganic scaffolds and exploration of new ways to toughen brittle constructs are critical prior to their successful application in loaded sites. A simple and widely adopted approach involves the coating of an inorganic scaffold with a polymeric material. In this work, a systematic evaluation of the influence of a biopolymer, polycaprolactone (PCL), coating on the mechanical performance of bioactive glass scaffolds was carried out. Results from this work indicate that a biopolymer PCL coating was more effective in increasing the compressive strength and reliability of the glass scaffold under compression, but less effective in improving its flexural strength or fracture toughness. This is the first report that reveals the limited successfulness of a polymer coating in improving the toughness of strong scaffolds, suggesting that new and novel ways of toughening inorganic scaffolds should be future research directions for scaffolds applied in loaded sites. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 1209-1217, 2018.