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Effect of Milling Time and 25Ce-75Ni Addition on Hydrogen Desorption Properties of Magnesium Hydride-based Composite Produced by Mechanical Alloying
F. Z. Akbarzadeh, M. Rajabi,
Volume 36, Issue 4 (3-2018)
Abstract
In this study, the composite material with composition of MgH2-10 wt% (25Ce-75Ni) has been prepared by co-milling of magnesium hydride powder with Ce-Ni alloy produced by vacuum arc remelting method. The effect of milling time and additive on magnesium hydride structure, i.e. crystallite size, lattice strain and particle size, and also hydrogen desorption properties of obtained composite were evaluated and compared with pure milled MgH2. It has been shown that the addition of 25Ce-75Ni alloy to magnesium hydride yielded a finer particle size. As a consequence, the desorption temperature of mechanically activated MgH2 decreased from 340 °C to 280 °C for composite 1(5 h mechanical alloying) and to 290 °C for composite 2 (15 h mechanical alloying). Further improvement in the hydrogen desorption tempreture of composite 1 can be related to finer particle size and higher Mg2NiH4 phase value, which corresponded with calculated enthalpy results.

Evaluation of the Microstructure of Ni-Nb-Si Alloy During Mechanical Alloying
Gh. Akbari, M. H. Enayati, H. Minouei,
Volume 37, Issue 1 (6-2018)
Abstract

In the present study, the mechanical alloying process was used to produce the Ni-Nb-Si amorphous alloy. X-ray diffraction (XRD)analysis and high-resolution transmission electron microscopy (HRTEM) were used to approve the amorphous phase formation after 12 hours of mechanical alloying. The results obtained from the SEM morphological images of powder particles during mechanical alloying showed that increasing the milling time caused the reduction  of the powder particles size and uniformity in the shape of the particles. Enhancing the embrittlement and fracturing rate caused brittleness and the  increase in the  failure rate; these were followed by a decrease in the powder particle size to 1-5μm. Cold welding and flattening of the pure elemental powders after mechanical alloying for 2 hours formed a lamellar structure of the alternative layers of different elements lying over each other. SEM image of cross-section of powder particles showed that by increasing the milling time, the interlamellar spacing was decreased, the elements were distributed more uniformly, and finally, a uniform structure of theamorphous phase was completed.


The Effect of Boron Addition on the Microstructure, Hardness and Characteristic Temperatures of Cu-12Al-4Ni Memory Alloy Prepared by Mechanical Alloying, Pressing and Rolling
Z. Jarrahi, Sh. Raygan, M. Pourabdoli,
Volume 37, Issue 4 (3-2019)
Abstract
In this study, boron containing Cu-12wt%Al-4wt%Ni shape memory alloy was prepared by mechanical alloying, pressing and rolling. In this regard, 20 and 40 hour-milled powder was compacted and changed to the bulk alloy by cold pressing, sintering, rolling, heat treatment and quenching. Phase structure, micro-structure, micro-hardness, and transformation temperatures of the prepared samples were studied. It was found that increasing the milling time from 20 to 40 hours led to the rise of the starting temperature of martensite transformation (Ms) from 254 to 264°C. Also, the results showed that adding 0.5 wt.% B decreased the Ms temperature to 211°C and enhanced the micro-hardness from 154 (for the sample without B) to 193  vickers. These alternations were attributed to the fine structure caused by Boron rich precipitations. Moreover, two martenistic transformations with different structures were formed due to the non-homogeneity of the Al concentration in the matrix, which appeared in the form of two different transformation temperatures (Ms) in the Differential Scanning Calorimetry curves.

Effect of Amorphous Silica Addition on Martensitic Phase Transformation of Zirconia and Investigation of its Tetragonal Structure Stability Mechanisms
M. Farhadian, K. Raeissi, M. A. Golozar,
Volume 39, Issue 2 (8-2020)
Abstract
This work is focused on the effect of amorphous SiO2 addition on the phase transformation and microstructural evolution of ZrO2 particles. Considering the structural similarities between the amorphous ZrO2 and its tetragonal structure, XRD results showed initial nucleation of metastable tetragonal ZrO2 from its amorphous matrix upon heat treatment. This metastable phase is unstable in pure ZrO2 sample and transforms to a stable monoclinic phase at around 600 oC. However, addition of amorphous SiO2 to ZrO2 structure causes metastable tetragonal phase to remain stable up to around 1100 oC. The temperature range for stability of metastable tetragonal ZrO2 structure increased from about 150 oC in pure ZrO2 particles to around 500 oC in ZrO2-10 mol.% SiO2 composite powders. A further increase in SiO2 content up to 30 mol.% did not change the stabilization temperature range but the average particle size reduced around 1.6 times compared to pure ZrO2 particles. Stabilization of metastable tetragonal ZrO2 explained by constrained effect of SiO2 layer surrounding zirconia nuclei. The thickness of this SiO2 layer enhanced by increasing SiO2 content which limited the growth of ZrO2 nuclei resulting in finer particle sizes.

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