The processing of plastics, particularly reinforced composites, necessitates the use of corrosion-and wear-resistant materials for tools that come into contact with the polymer. For such applications, plastic mold steels were developed that offer not only a good wear resistance due to the presence of carbides in a martensitic matrix, but also good corrosion resistance provided primarily by a sufficient amount of dissolved chromium. The common processing route for these high-alloyed materials is the hot isostatic pressing (HIP) of gas-atomized powders (PM-HIP). In this context, sintering plays an insignificant role, except for the processing of metalmatrix composites (MMCs). The development of novel wear-and corrosion-resistant MMCs based on plastic mold steels requires knowledge of the sintering behavior of prealloyed powders of such tool steels. It is well known that alloyed powders can be processed by supersolidus liquidphase sintering (SLPS), a method leading to almost full densification and to microstructures without significant coarsening effects. In this work, two different gas-atomized powders of plastic mold steels were investigated by computational thermodynamics, thermal analysis, sintering experiments, and microstructural characterization. The results show that both powders can be sintered to almost full density (1 to 3 pct porosity) by SLPS in a vacuum or a nitrogen atmosphere. Experimental findings on the densification behavior, nitrogen uptake, and carbide volume fractions are in good agreement with calculations performed by computational thermodynamics.
Applications in plastics processing bear increased requirements for the used materials, especially with respect to their corrosion and wear resistance. For this reason, special powder metallurgical tools steels were developed that fulfil these demands. The common processing route for their production is hot isostatic pressing (HIP) of pre-alloyed powders which is followed by hot working if semi-finished parts are to be produced. As an alternative to HIP, super solidus liquid phase sintering (SLPS) permits the consolidation of pre-alloyed tool steel powders to near net-shape parts. It can be performed in different sintering atmospheres. In this work, the plastic mould steel X190CrVMo20-4 was processed by SLPS in vacuum as well as under nitrogen atmosphere. The resulting materials were analysed with respect to their microstructure, tempering behaviour and corrosion resistance in 0.5 molar sulphuric acid in dependence of the heat treatment. As a reference, the HIPed and the HIPed and worked state were also investigated. The results show that different heat treatments alter the ranking of the sintered and the HIPed state with respect to corrosion resistance. As expected, a high tempering for maximum secondary hardness causes a significant loss of corrosion resistance. The experimental findings were supported by thermodynamic calculations based on slight alterations in chemical composition that result from the different manufacturing processes.
The use of nitrogen in martensitic stainless steels is limited by its solubility. Nitrogen solubility can be increased by alloying with elements such as Cr, Mn, and Mo and the use of pressure, such as in Pressurized ElectroSlag Remelting (PESR). Furthermore, the joint addition of C þ N increases their solubility. Solid-state nitriding can be used for case hardening or N-enrichment of steel powders before sintering. However, the resulting stabilization of austenite can be a drawback for martensitic steels. Besides cryogenic treatment below the martensite finish temperature, ausforming, that is, metal working above M s , could be promising. This contribution gives an overview about latest developments in N-rich martensitic stainless steels.
The demand for increased efficiency of industrial gas turbines and aero engines drives the search for the next generation of materials. Promising candidates for such new materials are Co-based superalloys. We characterize the microsegregation and solidification of a multi-component Co-based superalloy and compare it to a ternary CoAl-W compound and to two exemplary Ni-based superalloys by combining the experimental characterization of the as-cast microstructures with complementary modelling of phase stability. On the experimental side, we characterize the microstructure and precipitates by electron microscopy and energy-dispersive X-ray spectroscopy and determine the element distributions and microsegregation coefficients by electron probe microanalysis (EPMA). On the modelling side, we carry out solidification simulations and a structure map analysis in order to relate the local chemical composition with phase stability. We find that the microsegregation coefficients for the individual elements are very similar in the investigated Co-based and Ni-based superalloys. By interpreting the local chemical composition from EPMA with the structure map, we effectively unite the set of element distribution maps to compound maps with very good contrast of the dendritic microstructure. The resulting compound maps of the microstructure in terms of average band filling and atomic-size difference explain the formation of topologically close-packed phases in the interdendritic regions. We identify B2, C14, and D0 24 precipitates with chemical compositions that are in line with the structure map.
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