Non-equiatomic W10Mo27Cr21Ti22Al20 high-entropy alloy produced by mechanical alloying and spark plasma sintering: Phase evolution and mechanical properties

In this work, non-equiatomic W10Mo27Cr21Ti22Al20 refractory high-entropy alloy (RHEA) was produced using mechanical alloying followed by spark plasma sintering. The phase formation, microstructure, and compressive mechanical properties of the alloy were studied. During mechanical alloying, a Body-centered cubic (BCC) solid solution phase with a particle size of less than 1 µm was obtained after 18 h ball milling. The microstructure of the sintered sample exhibits three distinct phases consisting of two solid solution phases BCC1 and BCC2 as well as fine TiCxOy precipitates distributed in them. The volume fractions of each phase were about 79%, 8%, and 13%, respectively. The sintered W10Mo27Cr21Ti22Al20 showed yield strengths of 2465, 1506, 405, and 290 MPa at room temperature 600, 1000, and 1200°C, respectively, which are about twice that of the same refractory high-entropy alloy produced by vacuum arc melting. At 1000 and 1200°C, the strength after yielding gradually increased to 970 and 718 MPa at a compressive strain of 60%. The studied refractory high-entropy alloy can have good potential in high-temperature applications due to its high specific strength at elevated temperatures compared to conventional Ni-based superalloys and most as-reported refractory high-entropy alloys.

Mechanical Alloying Process Applied for Obtaining a New Biodegradable Mg-xZn-Zr-Ca Alloy

The aim of the present paper is to apply the mechanical alloying process to obtain from powder components a new biodegradable Mg-based alloy powder from the system Mg-xZn-Zr-Ca, with high biomechanical and biochemical performance. Various processing parameters for mechanical alloying have been experimented with the ultimate goal to establish an efficient processing route for the production of small biodegradable parts for the medical domain. It has been observed that for the same milling parameters, the composition of the powders has influenced the powder size and shape. On the other hand, for the same composition, the highest experimented milling speed and time conduct to finer powder particles, almost round-shaped, without pores or various inclusions. The most uniform size has been obtained for the powder sample with 10 wt.%Zn. These powders were finally processed by selective laser melting, an additive manufacturing technology, to obtain a homogeneous experimental sample, without cracking, for future more systematical trials.

The effect of milling time on the alumina phase transformation in the AMCs powder metallurgy reinforced by silica-sand-tailings

This study aims to determine the effect of milling time and sintering temperature parameters on the alumina transformation phase in the manufacture of Aluminium Matrix Composites (AMCs) reinforced by 20 % silica sand tailings using powder metallurgy technology. The matrix and fillers use waste to make the composites more efficient, clean the environment, and increase waste utilization. The milling time applied to the Mechanical Alloying (MA) process was 0.5, 6, 24, 48, and 96 hours, with a ball parameter ratio of 15:1 and a rotation of 93 rpm. Furthermore, hot compaction was carried out using a 100 MPa two-way hydraulic compression machine at a temperature of 300 °C for 20 minutes. The temperature variables of the sintering parameter process were 550, 600 to 650 °C, with a holding time of 10 minutes. Characterization of materials carried out included testing particle size, porosity, X-Ray Diffraction (XRD), SEM-Image, and SEM-EDX. The particle measurement of mechanical alloying processed, using Particle Size Analyzer (PSA) instrument and based on XRD data using the Scherrer equation, showed a relatively similar trend, decreasing particle size occurs when milling time was increased 0.5 to 24 hours. However, when the milling time increases to 48 and 96 hours, the particle size tends to increase slightly, due to cold-weld and agglomeration when the Mechanical Alloying is processed. The impact is the occurrence of the matrix and filler particle pairs in the cold-weld state. So, the results of XRD and SEM-EDX characterization showed a second phase transformation to form alumina compounds at a relatively low sintering temperature of 600 °C after the mechanical alloying process was carried out with a milling time on least 24 hours

Pulse Plasma Sintering of NiAl-Al2O3 Composite Powder Produced by Mechanical Alloying with Contribution of Nanometric Al2O3 Powder

NiAl-Al2O3 composites, fabricated from the prepared composite powders by mechanical alloying and then consolidated by pulse plasma sintering, were presented. The use of nanometric alumina powder for reinforcement of a synthetized intermetallic matrix was the innovative concept of this work. Moreover, this is the first reported attempt to use the Pulse Plasma Sintering (PPS) method to consolidate composite powder with the contribution of nanometric alumina powder. The composite powders consisting of the intermetallic phase NiAl and Al2O3 were prepared by mechanical alloying from powder mixtures containing Ni-50at.%Al with the contribution of 10 wt.% or 20 wt.% nanometric aluminum oxide. A nanocrystalline NiAl matrix was formed, with uniformly distributed Al2O3 inclusions as reinforcement. The PPS method successfully consolidated NiAl-Al2O3 composite powders with limited grain growth in the NiAl matrix. The appropriate sintering temperature for composite powder was selected based on analysis of the grain growth and hardness of Al2O3 subjected to PPS consolidation at various temperatures. As a result of these tests, sintering of the NiAl-Al2O3 powders was carried out at temperatures of 1200 °C, 1300 °C, and 1400 °C. The microstructure and properties of the initial powders, composite powders, and consolidated bulk composite materials were characterized by SEM, EDS, XRD, density, and hardness measurements. The hardness of the ultrafine-grained NiAl-Al2O3 composites obtained via PPS depends on the Al2O3 content in the composite, as well as the sintering temperature applied. The highest values of the hardness of the composites were obtained after sintering at the lowest temperature (1200 °C), reaching 7.2 ± 0.29 GPa and 8.4 ± 0.07 GPa for 10 wt.% Al2O3 and 20 wt.% Al2O3, respectively, and exceeding the hardness values reported in the literature. From a technological point of view, the possibility to use sintering temperatures as low as 1200 °C is crucial for the production of fully dense, ultrafine-grained composites with high hardness.