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In recent years, near-nano (submicron) and nanostructured materials have attracted increasingly more attention from the materials community. Nanocrystalline materials are characterized by a microstructural length or grain size of up to about 100 nm. Materials having grain size of $0.1 to 0.3 mm are classified as submicron materials. Nanocrystalline materials exhibit various shapes or forms, and possess unique chemical, physical or mechanical properties. When the grain size is below a critical value ($10-20 nm), more than 50 vol.% of atoms is associated with grain boundaries or interfacial boundaries. In this respect, dislocation pile-ups cannot form, and the Hall-Petch relationship for conventional coarse-grained materials is no longer valid. Therefore, grain boundaries play a major role in the deformation of nanocrystalline materials. Nanocrystalline materials exhibit creep and super plasticity at lower temperatures than conventional micro-grained counterparts. Similarly, plastic deformation of nanocrystalline coatings is considered to be associated with grain boundary sliding assisted by grain boundary diffusion or rotation. In this review paper, current developments in fabrication, microstructure, physical and mechanical properties of nanocrystalline materials and coatings will be addressed. Particular attention is paid to the properties of transition metal nitride nanocrystalline films formed by ion beam assisted deposition process. #

This paper summarizes and reviews the state‐of‐the‐art processing methods, structures and mechanical properties of the metal matrix composites reinforced with ceramic nanoparticles. The metal matrices of nanocomposites involved include aluminum and magnesium. The processing approaches for nanocomposites can be classified into ex‐situ and in‐situ synthesis routes. The ex‐situ ceramic nanoparticles are prone to cluster during composite processing and the properties of materials are lower than the theoretical values. Despite the fact of clustering, ex‐situ nanocomposites reinforced with very low loading levels of nanoparticles exhibit higher yield strength and creep resistance than their microcomposite counterparts filled with much higher particulate content. Better dispersion of ceramic nanoparticles in metal matrix can be achieved by using appropriate processing techniques. Consequently, improvements in both the mechanical strength and ductility can be obtained readily in aluminum or magnesium by adding ceramic nanoparticles. Similar beneficial enhancements in mechanical properties are observed for the nanocomposites reinforced with in‐situ nanoparticles.

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A novel approach to the preparation of polymer nanocomposites utilizing a low-molecular-weight reactive modifying reagent has been developed in this study. This is the first report on the fabrication of in situ nanocomposites using maleic anhydride as a reactive reagent that acts both as a modifying additive for the polymeric matrix and as a swelling agent for the silicate. Accordingly, polypropylene−vermiculite nanocomposites with an intercalated or exfoliated structure can be achieved by simple melt mixing of maleic anhydride-modified vermiculite with polypropylene. The nanocomposite structure is evidenced by the absence of vermiculite reflections in the X-ray powder diffraction patterns. Tensile tests show that the tensile modulus and strength of the nanocomposites tend to increase dramatically with vermiculite addition. Such enhancement in mechanical properties results from the formation of intercalated and exfoliated vermiculite reinforcement in the composites. Finally, the thermal properties of the nanocomposites were investigated by means of dynamic mechanical analysis (DMA), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The effects of maleic anhydride addition on the formation of nanometric reinforcement and on the mechanical properties of nanocomposites are discussed.

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