International audienceSpark Plasma Sintering (SPS) is a process which allows powder densification, applying simultaneously a uniaxial external load and pulsed direct current of very high intensity through tools. This process is attracting significant attention, with a tremendous increase of studies in the metal powder densification field. Its growing popularity lies in the very fast heating rate and short cycle time driven by the Joule effect, which limits grain growth. However, this process implements different coupled electrical, thermal and mechanical phenomena. All this makes the process difficult to develop and to apply for routine industrial production, which has motivated the development of numerical simulation tools in order to understand and optimize the process. Up to now, very few models integrating the coupling between heat generation, electric transfer and mechanics have been proposed. In particular, a numerical predictive model for powder densification requires a good understanding of the mechanical behavior, in our case a viscoplastic compressive law (Abouaf mechanical model). In this article, we will discuss the characterization of the material during densification, focusing on the creep behaviors of dense and porous state materials used to simulate sintering in the Abouaf framework. Validations of the creep law parameters and also of the densification parameters will be presented and subsequently discussed
Ti3AlC2 and Ti3Al0.8Sn0.2C2 MAX phase powders are densified using Spark Plasma Sintering (SPS) technique to obtain dense bulk materials. Oxidation tests are then performed over the temperature range 800°C‐1000°C under synthetic air on the two different materials in order to compare their oxidation resistance. It is demonstrated that, in the case of the Ti3Al0.8Sn0.2C2 solid solution, the oxide layers consist in TiO2, Al2O3, and SnO2. The presence of Sn atoms in the A planes of the solid solution leads to an easy diffusion of Sn out of the MAX phase which promote the formation of the nonprotective and fast growing SnO2 oxide. Moreover, the small Al/Ti atom's ratio promotes the growth of a nonprotective rutile‐TiO2 scale as well. In the case of the Ti3AlC2 MAX phase, the oxide layer consists in a protective alumina scale; a few TiO2 grains being observed on the top of the Al2O3 layer. The parabolic oxidation rate constants are about 3 orders of magnitude smaller for Ti3AlC2 compared to Ti3Al0.8Sn0.2C2.
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