Binary magnesium–silver (Mg–Ag) alloys were designed as antibacterial material to treat infections in an implant site. The mechanical and electrochemical measurements were performed on three casting Mg–Ag alloys under cell culture conditions. The composition and distribution of the corrosion layer was analyzed by microscopy and X‐ray photoelectron spectroscopy. In cell culture media, Mg–Ag alloys show higher, but still acceptable general corrosion rates while less susceptibility to pitting corrosion than pure Mg with increasing content of silver. This study indicates that Mg–Ag alloys have satisfactory corrosion properties and much better mechanical properties than pure magnesium as a functional biodegradable material.

Magnesium‐based biomaterials are gaining increasing interest, while in vitro corrosion tests are not standardized yet. Moreover, the effects of different corrosion media on the corrosion products are still not fully understood. To compare and evaluate the three main corrosion media applied in most in vitro studies, an XPS investigation of magnesium surfaces was carried out after exposure of the specimens to Dulbecco's modified eagle medium (DMEM), Hank's buffered salt solution (HBSS), and simulated body fluid (SBF). The effects of rinsing the specimens after immersion were also determined. XPS investigations especially on the Mg 2p state showed that MgO, Mg(OH)2, and MgCO3 species were the dominant corrosion products presenting in all specimens despite of the different corrosion media. However, the ratio of corrosion products depends on the medium composition. It was also shown that rinsing specimens after immersion experiments is a necessary procedure when surface analysis is employed afterward.

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Up to now, the role of particle sizes on the impact behavior of ceramic particles in aerosol deposition not yet fully understood. Hence, with the aim to supply a more general understanding, modeling series of low strain rate compression and high-speed impact were performed by molecular dynamics on single-crystalline particles in sizes of 10-300 nm that are tuned to match mechanical properties of TiO2-anatase. The modeling results reveal that particles with original diameter of 25-75 nm exhibit three different impact behaviors that could be distinguished as (i) rebounding, (ii) bonding and (iii) fragmentation, depending on their initial impact velocity. In contrast, particles larger than 75 nm do not exhibit the bonding behavior. Detailed stress and strain field distributions reveal that combination of “localized inelastic deformation” along the slip systems and “shear localization” cause bonding of the small and large particles to the substrate. The analyses of associated temperature rise by the inelastic deformation revealed that heat diffusion at these small scales depend on size. Whereas small particles could reach a rather homogeneous temperature distribution, the evolved heat in the larger ones keeps rather localized to areas of highest deformation and may support deformation and the formation of dense layers in aerosol deposition.

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