Throughout human history, any society’s capacity to fabricate and refine new materials to satisfy its demands has resulted in advances to its performance and worldwide standing. Life in the twenty-first century cannot be predicated on tiny groupings of materials; rather, it must be predicated on huge families of novel elements dubbed “advanced materials”. While there are several approaches and strategies for fabricating advanced materials, mechanical milling (MM) and mechanochemistry have garnered much interest and consideration as novel ways for synthesizing a diverse range of new materials that cannot be synthesized by conventional means. Equilibrium, nonequilibrium, and nanocomposite materials can be easily obtained by MM. This review article has been addressed in part to present a brief history of ball milling’s application in the manufacture of a diverse variety of complex and innovative materials during the last 50 years. Furthermore, the mechanism of the MM process will be discussed, as well as the factors affecting the milling process. Typical examples of some systems developed at the Nanotechnology and Applications Program of the Kuwait Institute for Scientific Research during the last five years will be presented in this articles. Nanodiamonds, nanocrystalline hard materials (e.g., WC), metal-matrix and ceramic matrix nanocomposites, and nanocrystalline titanium nitride will be presented and discussed. The authors hope that the article will benefit readers and act as a primer for engineers and researchers beginning on material production projects using mechanical milling.
The global interest in MgH2 is due to the natural availability of Mg and its capacity to retain hydrogen at a concentration of up to 7.60 wt.%. Despite its appealing characteristics and ease of production on an industrial scale at ambient temperature using the reactive ball milling (RBM) technique, MgH2 is a highly stable chemical with sluggish hydrogenation and dehydrogenation rates below 300 °C. Among the different methods used to improve the hydrogenation/dehydrogenation kinetic behavior of MgH2, mechanical treatment and/or catalysis are regarded to be the most effective methods. The purpose of this research was to explore the effectiveness of several cold rolling (CR) stages on the hydrogenation properties of recycled magnesium rods, as well as the effect of the resulting RBM on the final product. For this process, the as-received waste Mg-rods were firstly cold-rolled 200 times and then remilled under H2 atmosphere for 100 h. The as-RBM powders were then cold-rolled for 100 passes and then ball-milled with 10 and 15 wt.% Nb2O5 powders for 50 h. The results showed that when the materials were subjected to different types of defects (dislocations, stacking faults, and twining) generated by CR and RBM, their gas absorption/desorption kinetics were improved. This was indexed by their ability to achieve a long cycle lifetime at lower temperatures when compared with the as-received materials. The powders were further improved in terms of kinetics and decomposition temperature upon RBM with Nb2O5 for 50 h. The nanocomposite MgH2/10 wt.% and 15 wt.% Nb2O5 exhibit good hydrogen storage capabilities at a comparatively low temperature (225 °C) with a long cycle life that extended from 110 h to 170 h, without serious degradation in storage capacity and kinetics.
A simple and inexpensive thermal oxidation process is used to grow β-Ga2O3 oxide (β-Ga2O3) thin films/nanorods on a c-plane (0001) sapphire substrate using Ag/Au catalysts. The effect of these catalysts on the growth mechanism of Ga2O3 was studied by different characterization techniques, including X-ray diffraction analysis (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive X-ray analysis (EDX). The XRD results of the grown Ga2O3 on a sapphire substrate show three sharp diffraction peaks located at 19.31°, 38.70° and 59.38° corresponding to the and planes of β-Ga2O3. Field Emission Scanning Electron Microscope (FESEM) analysis showed the formation of longer and denser Ga2O3 nanowires at higher temperatures, especially in the presence of silver nanoparticles as catalysts.