ABSTRACT
The effects of severe plastic deformation (SPD) with a forward-backward rotating die (KOBO extrusion) on pure magnesium, in the form of cold-compacted powder, sintered powder, or cast ingots as reference, were examined. This method is known to reinforce metals, but the role of the initial form of magnesium applied in the fabrication of metal-based rods, as well as related phenomena, has not been characterized until now. The problem is important in the potential processing of commercial metal powders, the recycling of metal shavings, and the fabrication of metal matrix composites with discontinuous reinforcing phases. In the presented experiments, rods of 8 mm in diameter and 400 mm in length were obtained, and the structural effects induced by KOBO that occurred on a macro- and microscale on the surface and cross sections were characterized. Changes in the size and orientation of α-Mg crystallites were determined by XRD. The porosity, hardness, tensile strength, and compressive strength were measured, and the mechanisms of decohesion dependent on starting metal form were analyzed. After KOBO extrusion, significant differences were observed in the microstructure and properties between the materials derived from cold-compacted powder, sintered powder, and reference cast magnesium. Due to the application of KOBO, apart from α-Mg grain refinement, the MgO derived from the initial powder's surface was refined to fine regular particles surrounded by magnesium. Their bands curved in the perpendicular plane and were oriented with the extrusion direction of the formed network, which augmented some mechanical properties and changed the decohesion mechanism. The conducted experiments revealed that before extrusion by KOBO, the magnesium powder required sintering under pressure.
ABSTRACT
This article presents the influence of the applied extrusion method on the microstructure and mechanical properties of the WE43 magnesium alloy. The materials for tests were ingots made from magnesium alloy, with dimensions of 40 × 90 mm, marked with the symbol WE43. Two extrusion methods were used: the classic one-concurrent extrusion, and the complex one-concurrent extrusion with a reversible die (KoBo). As a result of the application of deformation processes, rods were obtained. The implemented deformation methods made it possible to determine the influence of the deformation process parameters on changes in the structure and properties of the WE43 alloy. In addition, compression tests were performed to determine the values of the yield stress and to analyze changes in the microstructure after plastic deformation. The hot plastic deformation activation energy and the process parameters, for which the course of plastic flow is affected by the presence of twins in the microstructure, were determined for the WE43 alloy. The effects of superplastic flow at 350 °C (250% elongation) and microstructure refinement (d = 1 µm) were demonstrated after applying the KoBo method. The results will be useful in the development of forming technology of selected construction elements, which serve as light substitutes for currently used materials.
ABSTRACT
The binary as-cast Al-Cu alloys Al-5%Cu, Al-25%Cu, and Al-33%Cu (in wt %), composed of the intermetallic θ-Al2Cu and α-Al phases, were prepared from pure components and were subsequently severely plastically deformed by extrusion combined with reversible torsion (KoBo) to refinement of α-Al and Al2Cu phases. The extrusion combined with reversible torsion was carried out using extrusion coefficients of λ = 30 and λ = 98. KoBo applied to the Al-Cu alloys with different initial structures (differences in fraction and phase size) allowed us to obtain for alloys (Al-25%Cu and Al-33%Cu), with higher value of intermetallic phase, large elongations in the range of 830-1100% after tensile tests at the temperature of 400 °C with the strain rate of 10-4 s-1. The value of elongation depended on extrusion coefficient and increase, with λ increasing as a result of α-Al and Al2Cu phase refinement to about 200-400 nm. Deformation at the temperature of 300 °C, independently of the extrusion coefficient (λ), did not ensure superplastic properties of the analyzed alloys. A microstructural study showed that the mechanism of grain boundary sliding was responsible for superplastic deformation.
ABSTRACT
The problem of preparing a ternary powder mixture, which was meant to fabricate sintered heterophase composite, and consisted of micro- and two nanosized powders, was analyzed. The microsized powder was a pure magnesium, and as nanocomponents, a silicon powder (nSi) and carbon nanotubes (CNTs) with 2% and 1% volume fractions, respectively, were applied. The powder mixtures were prepared using ultrasonic and mechanical mixing in technological fluid, and four mixing variants were applied. The morphology of the powder mixtures was characterized with scanning electron microscopy (SEM), and then, composite sinters were fabricated in a vacuum with hot temperature pressing at 580 °C under 15 MPa pressure, using a Degussa press. The reaction between the nSi and the Mg matrix, which caused the creation of the Mg2Si phase in the fabricated Mg-Mg2Si-CNT composite, was confirmed with X-ray diffraction (XRD). The porosity and hardness of the composite sinters were examined, and optical microscopy (OM) and quantitative image analyses were carried out to characterize the microstructure of the composites. In the manufacturing process of the Mg-nSi-CNT mixtures, the best results were the following: first separate de-agglomeration of nanocomponents, then their common mixing, and finally, the deposition of nanocomponents at the surface of the microsized magnesium powder. The applied procedure ensured the uniform layer formation of de-agglomerated nanocomponents on the Mg powder, without re-agglomerated nSi and CNTs. Moreover, this type of powder mixture morphology allows to obtain sinters with lower porosity and higher hardness, which is accompanied by precipitation of a finer Mg2Si phase. In the Mg-Mg2Si-CNT composite, the carbon phase was present, and it was located in the magnesium matrix and in silicide.
