Preparation of AlRu intermetallic compounds by mechanical alloying

2006 ◽  
Vol 352 (32-35) ◽  
pp. 3718-3720 ◽  
Author(s):  
S.N. de Medeiros ◽  
F.L.A. Machado ◽  
R.B. Zampiere ◽  
I.A. Santos ◽  
A. Paesano
1993 ◽  
Vol 8 (11) ◽  
pp. 2819-2829 ◽  
Author(s):  
M. Oehring ◽  
T. Klassen ◽  
R. Bormann

Elemental Ti–Al powder blends were mechanically alloyed in order to study phase formation during the alloying process. In addition, the stability of intermetallic phases upon milling was investigated separately in order to determine the origins of phase selection during the milling process. It was found that by mechanical alloying of powder blends, as well as by ball milling of Ti-aluminides for long milling times, the same metastable phases were formed for corresponding compositions, i.e., the hep solid solution for Al concentrations up to 60 at. % and the fcc solid solution for 75 at. % Al. X-ray diffraction (XRD) analyses indicated that the process of mechanical alloying occurred via the diffusion of Al into Ti. By lowering the milling intensity, a two-phase mixture of the hcp solid solution and the amorphous phase was observed for Ti50Al50 and confirmed by transmission electron microscopy (TEM). The results show that phase selection in the final state during mechanical alloying of Ti–Al powder blends and milling of intermetallic compounds is mainly determined by the energetic destabilization of the competing phases caused by the milling process. The destabilization is most pronounced in the case of intermetallic compounds due to the decrease in long-range order upon milling. For the final milling stage, phase formation can be predicted by considering the relative stabilities of the respective phases calculated by the CALPHAD method using the available thermodynamic data for the Ti–Al system.


2009 ◽  
Vol 469 (1-2) ◽  
pp. 483-487 ◽  
Author(s):  
Hung-Hua Sheu ◽  
Le-Chun Hsiung ◽  
Jiun-Rung Sheu

Energies ◽  
2021 ◽  
Vol 14 (18) ◽  
pp. 5758
Author(s):  
Yuchen Liu ◽  
Djafar Chabane ◽  
Omar Elkedim

Hydrogen energy is a very attractive option in dealing with the existing energy crisis. For the development of a hydrogen energy economy, hydrogen storage technology must be improved to over the storage limitations. Compared with traditional hydrogen storage technology, the prospect of hydrogen storage materials is broader. Among all types of hydrogen storage materials, solid hydrogen storage materials are most promising and have the most safety security. Solid hydrogen storage materials include high surface area physical adsorption materials and interstitial and non-interstitial hydrides. Among them, interstitial hydrides, also called intermetallic hydrides, are hydrides formed by transition metals or their alloys. The main alloy types are A2B, AB, AB2, AB3, A2B7, AB5, and BCC. A is a hydride that easily forms metal (such as Ti, V, Zr, and Y), while B is a non-hydride forming metal (such as Cr, Mn, and Fe). The development of intermetallic compounds as hydrogen storage materials is very attractive because their volumetric capacity is much higher (80–160 kgH2m−3) than the gaseous storage method and the liquid storage method in a cryogenic tank (40 and 71 kgH2m−3). Additionally, for hydrogen absorption and desorption reactions, the environmental requirements are lower than that of physical adsorption materials (ultra-low temperature) and the simplicity of the procedure is higher than that of non-interstitial hydrogen storage materials (multiple steps and a complex catalyst). In addition, there are abundant raw materials and diverse ingredients. For the synthesis and optimization of intermetallic compounds, in addition to traditional melting methods, mechanical alloying is a very important synthesis method, which has a unique synthesis mechanism and advantages. This review focuses on the application of mechanical alloying methods in the field of solid hydrogen storage materials.


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