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Mg 77+ x Ni 20- x La 3 ( x = 0, 5, 10, 15) alloys were successfully prepared by the vacuum induction melting method. The structural characterizations of the alloys were performed by using X-ray diffraction and scanning electron microscope. The effects of nickel content on the microstructure and hydrogen storage kinetic of the as-cast alloys were investigated. The results showed that the alloys are composed of a primary phase of Mg 2 Ni, lamella eutectic composites of Mg + Mg 2 Ni, and some amount of LaMg 12 and La 2 Mg 17 . Nickel addition significantly improved the hydrogen-absorption kinetic performance of the alloy. At 683 K, Mg 77 Ni 20 La 3 alloy and Mg 82 Ni 15 La 3 alloy underwent hydrogen absorption and desorption reactions for 2 h, respectively, and their hydrogen absorption and desorption capacities were 4.16 wt.% and 4.1 wt.%, and 4.92 wt.% and 4.69 wt.%, respectively. Using the Kissinger equation, it was calculated that the activation energy values of Mg 77 Ni 20 La 3 , Mg 82 Ni 15 La 3 , Mg 87 Ni 10 La 3 and Mg 92 Ni 5 La 3 alloys were in the range of 68.5~75.2 kJ/mol, much lower than 150~160 kJ/mol of MgH 2 .

Magnesium-based alloys are widely used in the construction of automotive, aviation, and medical applications. The solutions presently used for the production of biodegradable materials are characterized by considerable energy consumption and limitations resulting from the use of different devices and technologies. The proposed material is easier to manufacture due to mechanical alloying (MA). Thanks to the MA process, it is possible to carefully tailor the desired chemical composition and microstructure. There are many parameters that can be modified during synthesis in order to obtain an alloy with the desired microstructure and specific expected alloy properties. The duration of grinding of the alloy, the size and number of balls, and the protective atmosphere have a great influence on the process of mechanical alloying and the properties of the obtained products. So, the aim of this work was to determine the influence of milling time on the phase composition and structure of Mg-based alloy synthesis products. The tested samples were milled for 5, 8, 13, 20, 30, 50, and 70 h. X-ray diffraction analysis (XRD) and scanning electron microscopy studies (SEM) with energy-dispersive spectroscopy (EDS) were performed to obtain the powder morphology and chemical composition of Mg 66-x Zn 30 Ca 4 Ag x (where x = 1, 2) powders. Structure characterization based on the Rietveld refinement and crystallite size determination based on the Williamson-Hall theory of milling products were also carried out.

Magnesium-based materials are interesting alternatives for medical implants, as they have promising mechanical and biological properties. Thanks to them, it is possible to create biodegradable materials for medical application, which would reduce both costs and time of treatment. Magnesium as the sole material, however, it is not enough to support this function. It is important to determine proper alloying elements and methods. A viable method for creating such alloys is mechanical alloying, which can be used to design the structure and properties for proper roles. Mechanical alloying is highly influenced by the milling time of the alloy, as the time of the process affects many properties of the milled powders. X-ray diffraction (XRD) and scanning electron microscopy (SEM) with energy-dispersive spectroscopy (EDS) were carried out to study the powder morphology and chemical composition of Mg 65 Zn 30 Ca 4 Gd 1 powders. Moreover, the powder size was assessed by granulometric method and the Vickers hardness test was used for microhardness testing. The samples were milled for 6 min, 13, 20, 30, 40, and 70 h. The hardness correlated with the particle size of the samples. After 30 h of milling time, the average value of hardness was equal to 168 HV and it was lower after 13 (333 HV), 20 (273 HV), 40 (329 HV), and 70 (314 HV) h. The powder particles average size increased after 13 (31 μm) h of milling time, up to 30 (45-49 μm) hours, and then sharply decreased after 40 (28 μm) and 70 (12 μm) h.