RESUMO
Cobalt-Rhenium (Co-Re)-based alloys are currently investigated as potential high-temperature materials with melting temperatures beyond those of nickel-based superalloys. Their attraction stems from the binary Co-Re phase diagram, exhibiting complete miscibility between Co and Re, whereby the melting temperature steadily increases with the Re-content. Thus, depending on the Re-content, one can tune the melting temperature between that of pure Co (1495 °C) and that of pure Re (3186 °C). Current investigations focus on Re-contents of about 15 at.%, which makes melting with standard equipment still feasible. In addition to solid solution strengthening due to the mixture of Co- and Re-atoms, particle strengthening by tantalum carbide (TaC) and titanium carbide (TiC) precipitates turned out to be promising in recent studies. Yet, it is currently unclear which of the two particle types is the best choice for high temperature applications nor has the strengthening mechanism associated with the monocarbide (MC)-precipitates been elucidated. To address these issues, we perform compression tests at ambient and elevated temperatures on the particle-free base material containing 15 at.% of rhenium (Re), 5 at.% of chromium (Cr) and cobalt (Co) as balance (Co-15Re-5Cr), as well as on TaC- and TiC-containing variants. Additionally, transmission electron microscopy is used to analyze the shape of the precipitates and their orientation relationship to the matrix. Based on these investigations, we show that TiC and TaC are equally suited for precipitation strengthening of Co-Re-based alloys and identify climb over the elongated particles as a rate controlling particle strengthening mechanism at elevated temperatures. Furthermore, we show that the Re-atoms are remarkably strong obstacles to dislocation motion, which are overcome by thermal activation at elevated temperatures.
RESUMO
This study reassesses the optimum matrix composition of Co-Re-Cr-based alloys for strengthening by MC-type carbides. It is found that the composition of Co-15Re-5Cr is ideally suited for this purpose as it allows the solution of the carbide-forming elements such as Ta, Ti, Hf, and C within a matrix consisting entirely of fcc-phase (typically at 1450 °C), having a high solubility for these elements, while precipitation heat treatment (typically at 900-1100 °C) occurs in a hcp-Co matrix, displaying a much lower solubility. In the case of the monocarbides TiC and HfC, this was investigated and achieved for the first time in Co-Re-based alloys. TaC and TiC emerged as suitable particles in Co-Re-Cr alloys for creep applications due to a large population of nano-sized particle precipitation, which is not the case for the mainly coarse HfC. Both Co-15Re-5Cr-xTa-xC and Co-15Re-5Cr-xTi-xC exhibit a formerly unknown maximum solubility close to x = 1.8 at.%. Therefore, further research on the particle-strengthening effect and the governing creep mechanisms of carbide-strengthened Co-Re-Cr alloys should focus on alloys with the following compositions: Co-15Re-5Cr-1.8Ta-1.8C and Co-15Re-5Cr-1.8Ti-1.8C.