The invention relates to an alloy, a powder, a production process employing the alloy or the powder, and a component comprising same.
Nickel-based superalloys are known materials for high-temperature applications as in the case of gas turbines for heat shields in combustion chambers or else for turbine blades in the hot gas pathway.
These superalloys are required at high temperatures to be oxidation-resistant and to have high mechanical strength.
An advantage for boosting the efficiency is to minimize the weight, particularly in the case of rotating components such as turbine blades.
It is an object of the invention to solve the problem stated above. The object is achieved by an alloy, a powder, a process, and a component as claimed.
The invention utilizes an improvement in the chemical composition of nickel-based superalloys in the sense of an improvement in the specific mechanical properties through adaptation of suitable elements, while retaining the capacity for crack-free processing and the productivity.
The invention is described only illustratively below. A description will now be given of the function of the individual elements included in the high-heat-resistant nickel-based alloy for the purpose of performing the above-described invention.
Carbon (C) is added and, in addition to its function as a deoxidizing element, has further functions of combining with titanium (Ti), niobium (Nb) and tantalum (Ta) to form stable MC-type primary carbides in order to suppress the coarsening of austenitic grains during a hot forming operation and to improve the high-temperature lubricity. The desired effect of the carbon (C) is achieved by adding an amount of at least 0.07%, but if added at more than 0.09% it forms the catenary microstructure of the MC-type carbide and causes hot cracks to form, originating from this part, with a consequent reduction in tooling life.
Carbon (C) is added accordingly in an amount of 0.07 wt % to 0.09 wt %, preferably 0.08 wt %.
Chromium (Cr) forms an oxide layer with extremely close adhesion on the surface during heating to high temperatures, and improves the oxidation resistance. Additionally, chromium (Cr) may also improve the hot formability.
For this effect, it must be added in an amount of more than 9.0 wt %, but if added excessively, at more than 10.0 wt %, it causes the precipitation of an a phase, which is accompanied by a reduction in the ductility.
Accordingly, the amount of chromium (Cr) is in a range above 9.0 wt % but not more than 10 wt %, very preferably at 9.5 wt %.
Tungsten (W) is an additive element which substantially strengthens the austenitic solid solution up to high temperatures.
In order to achieve these effects, tungsten (W) must be added in an amount of at least 3.0 wt %, but if added excessively, at more than 3.4 wt %, it causes the excessive precipitation of α-W and a reduction both in the oxidation resistance and in the close adhesion of an oxide film. With particular preference, accordingly, the amount of tungsten (W) is in the region of 3.2 wt %.
Molybdenum (Mo) is an element in the same group as tungsten (W), and replacing some of the tungsten (W) with molybdenum (Mo) may therefore provide the same function as that of tungsten (W). Since, however, its effect is lower than that of tungsten (W), molybdenum (Mo) is added in a range of 1.3 wt % to 1.7 wt %, more particularly at 1.5 wt %.
Aluminum (Al) is an additive element which is key to the formation of a stable γ′ phase after a tempering treatment and which is to be added in an amount of at least 5.0 wt %. Added in excess of 7.0 wt %, however, it causes an increase in the γ′ phase and lowers the hot formability. Accordingly, aluminum (Al) is situated in a range from 5.6 wt % to 6.3 wt %, preferably at 5.9 wt %.
Some of the titanium (Ti) is combined with carbon (C) to form a stable MC-type primary carbide and has a strength-enhancing function for alloys which are not γ′-hardened.
The remaining titanium (Ti) is present in the γ′ phase in the solid solution state, thereby strengthening the γ′ phase, and it serves to improve the high-temperature strength. Titanium (Ti) must therefore be added in an amount of at least 1.5 wt %, but the excessive addition thereof in excess of 3.0 wt % not only lowers the hot formability but also makes the γ′ phase unstable and causes reductions in the strength after long-term use at high temperatures. Titanium (Ti) is therefore preferably also situated in the range from 1.9 wt % to 2.3 wt %.
Additionally, aluminum (Al), tantalum (Ta) and titanium (Ti) also have an important function of improving the oxidation resistance, and form stable oxide layer systems especially when the elements are combined.
In the same way as titanium (Ti), some of both niobium (Nb) and tantalum (Ta) is combined with carbon (C) to form stable MC-type primary carbides, and they have a strength-boosting function, especially for alloys which are not γ′-hardened.
The rest both of niobium (Nb) and of tantalum (Ta) is present in solution in the γ′ phase, thereby strengthening the γ′ phase solid solution, and it serves for improving the high-temperature strength.
Accordingly, niobium (Nb) and tantalum (Ta) may be added according to requirement. Since, however, the excessive addition thereof reduces the hot formability, niobium (Nb) is situated in a range from 0.8 wt % to a minimum of 1.0 wt %.
Zirconium (Zr) and boron (B) are active for improving the high-temperature strength and ductility, through their grain boundary-active function, and at least one of them may be added to the alloy of the invention in an appropriate amount. Their effect is obtained at a low amount added.
Amounts of zirconium (Zr) and of boron (B) of more than 0.01 wt % lower the solidus temperature on heating, to the detriment of the hot formability.
Accordingly, the upper limits for zirconium (Zr) and boron (B) are 0.010 wt % and 0.010 wt %, respectively.
Hafnium (Hf) reduces the susceptibility to hot cracking during casting and improves the ductility, particularly in the case of DS materials with columnar grains in transverse direction. Hafnium (Hf) also improves the oxidation resistance. On the other hand, hafnium (Hf) lowers the initial melting temperature and because of its high reactivity may lead to reactions with the mold shell during casting. Hafnium (Hf) is therefore used at a concentration of up to max. 1.5 wt %.
Nickel (Ni) forms a stable austenitic phase and becomes a matrix both for the solid solution and for the precipitation of the γ′ phase. Moreover, since nickel (Ni) is able to form a solid solution with a large amount of tungsten (W), an austenitic matrix is obtained which has a high strength at high temperatures, and nickel is therefore the balance of the alloy.
Apart from the elements described above, it is possible to add up to 10.4 wt % of cobalt (Co) to the alloy of the invention.
In the austenite of the matrix, cobalt (Co) exists in the solid solution state, thereby achieving a certain solid solution strengthening, and it also has an effect in improving the close adhesion of the oxide film. Given that cobalt (Co) in the Ni matrix is in the solid solution state and that cobalt (Co) has virtually no adverse effect on the precipitation of the γ′ phase, cobalt (Co) is favorable. However, since cobalt (Co) is an expensive element, the addition thereof in large amounts is not preferred.
The effect of these adaptations is to ensure processability for a productive L-PBF process with improved mechanical properties and increased oxidation resistance.
In accordance with the invention, therefore, the nickel-based alloy comprises, more particularly consists of (in wt %):
The component is preferably a component of a turbine, more particularly of a gas turbine, and there more particularly in the “hot” region.
Working Examples (EX1, EX2, EX3) are shown in the table below:
Number | Date | Country | Kind |
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10 2021 204 746.7 | May 2021 | DE | national |
This application is the US National Stage of International Application No. PCT/EP2022/059718 filed 12 Apr. 2022, and claims the benefit thereof, which is incorporated by reference herein in its entirety. The International Application claims the benefit of German Application No. DE 10 2021 204 746.7 filed 11 May 2021.
Filing Document | Filing Date | Country | Kind |
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PCT/EP2022/059718 | 4/12/2022 | WO |