METHOD FOR THE ADDITIVE MANUFACTURING OF AN OBJECT FROM A MARAGING STEEL POWDER

Abstract

The present invention relates to a method for producing an article out of a maraging steel, wherein the article is successively subjected to a solution annealing and heat treatment, wherein the steel has the following composition in Wt.-%: C=0.01-0.05 Si=0.4-0.8 Mn=0.1-0.5 Cr=12.0-13.0 Ni=9.5-10.5 Mo=0.5-1.5 Ti=0.5-1.5 Al=0.5-1.5 Cu=0.0-0.05

Residual iron and smelting-induced impurities.

Claims

1. A method for producing an article out of a maraging steel, wherein the article is produced out of a steel powder in an additive production process and after the additive production process, the article is subjected to an aging heat treatment, wherein the steel powder has the following composition in Wt.-%: C=0.01-0.05 Si=0.4-0.8 Mn=0.1-0.5 Cr=12.0-13.0 Ni=9.5-10.5 Mo=0.5-1.5 Ti=0.5-1.5 Al=0.5-1.5 Cu=0.0-0.05 Residual iron and smelting-induced impurities.

2. The method according to claim 1, characterized in that the powder is additively produced by means of selective laser melting (SLM), selective laser sintering (SLS), selective heat sintering (SHS), binder jetting, or the electron beam melting (EBM) method.

3. The method according to one of the preceding claims, [characterized in] that the powder is used with a grain size distribution of 5 to 150 μm, in particular 10 to 60 μm, and especially 15 to 45 μm.

4. The method according to claim 1, characterized in that the aging is carried out at 475° C. to 525° C.

5. The method according to claim 1, characterized in that the aging is carried out for 2 to 6 hours.

6. The method according to one of the preceding claims, characterized in that after the aging, the printed article has a retransformed austenite content of between 4 and 8 vol. %, in particular between 5 and 7.5 vol. %.

7. The method according to one of the preceding claims, characterized in that after the aging, the article has a hardness of >50 HRC.

8. An article produced in an additive production process out of a powder composed of a maraging steel with the following composition in Wt.-%: C=0.01-0.05 Si=0.4-0.8 Mn=0.1-0.5 Cr=12.0-13.0 Ni=9.5-10.5 Mo=0.5-1.5 Ti=0.5-1.5 Al=0.5-1.5 Cu=0.0-0.05 Residual iron and smelting-induced impurities.

9. The article according to claim 8, characterized in that the article is produced by means of selective laser melting (SLM), selective laser sintering (SLS), selective heat sintering (SHS), binder jetting, or the electron beam melting (EBM) method.

10. The article according to claim 8 or 9, characterized in that the article has a hardness of >50 HRC and a retransformed austenite content of 4 to 8 vol. %, in particular 5 to 7 vol. %.

11. A powder for use in the method according to one of claims 1 to 7, characterized in that the powder has the following composition in Wt-%: C=0.01-0.05 Si=0.4-0.8 Mn=0.1-0.5 Cr=12.0-13.0 Ni=9.5-10.5 Mo=0.5-1.5 Ti=0.5-1.5 Al=0.5-1.5 Cu=0.0-0.05 Residual iron and smelting-induced impurities and a grain size distribution of 5 to 150 μm, in particular 10 to 60 μm, and especially 15 to 45 μm.

Description

[0029] The invention will be explained by way of example based on the drawings. In the drawings:

[0030] FIG. 1 shows the influence of the titanium content;

[0031] FIG. 2 shows the influence of the molybdenum content;

[0032] FIG. 3 shows a time/temperature diagram of a heat treatment, which consists of a solution and washing procedure followed by an air-cooling to room temperature and an aging process.

[0033] FIG. 4 shows the phase diagram of iron/nickel in equilibrium;

[0034] FIG. 5 shows the hysteresis of conversion temperatures of martensite and austenite during heating and cooling;

[0035] FIG. 6 shows Table 1, which depicts the chemical composition of steels according to the invention;

[0036] FIG. 7 shows Table 2, which depicts another composition of a powder according to the invention;

[0037] FIG. 8 shows the hardness as a function of the aging temperature for different alloys;

[0038] FIG. 9 shows the austenite content as a function of the aging temperature for different alloys;

[0039] FIG. 10 shows the tensile strength and hardness values for printed, heat treated materials that are not according to the invention.

[0040] FIG. 11 shows the hardness curve as a function of the aging temperature in a printed, aged material according to the invention and in a solution annealed, aged material.

[0041] The following is a listing of the most important alloying elements and their influence on the microstructure and properties in maraging steels and in the invention in particular.

Nickel (Ni)

[0042] Nickel is the most important alloying element in maraging steels. Since the carbon content is low in maraging alloys, the addition of Ni to Fe results in the formation of a cubic Fe—Ni martensite. Controlling the Ni content is also important because Ni is an austenite-stabilizing element and Ni is thus decisive for the formation of retransformed austenite. Ni forms intermetallic precipitations with numerous elements such as Al, Ti, and Mn and therefore plays an additional decisive role as a precipitation-promoting element.

Aluminum (Al)

[0043] Aluminum is added to maraging steels as a precipitation element. It increases the solid solution strengthening and, particularly with Ni, forms intermetallic precipitations. A higher Al content can lead to the presence of δ ferrite in the microstructure, which has a negative impact on the mechanical properties and on the corrosion resistance.

Titanium (Ti)

[0044] Titanium appears to be one of the most active elements in maraging steels. It precipitates out during the aging and can be considered the most important alloying element for the formation of precipitations in maraging steels. It was used as a precipitation-promoting element in the first maraging steels that were developed and is used today in complex alloying systems.

[0045] The greatest advantage is the rapid precipitation; titanium is thus much more active, for example, than Mo in C-type and T-type maraging steels in the early stages of precipitation. The enormous influence of the Ti content on the tensile strength 18% Ni and Co-containing maraging steels is shown in FIG. 1. In addition, small quantities of Ti are added to Ti-free maraging steels in order to form carbides. The objective is to bind to the carbon C so that no other precipitation elements can form carbides.

[0046] The influence of the Ti content is shown in FIG. 1.

Molybdenum (Mo)

[0047] With an increasing Mo content, an increase in the hardness after aging can be observed (FIG. 2) since Mo forms intermetallic compounds with Ni. The precipitation behavior of Mo is strongly influenced by other elements, especially by cobalt (Co), among others. The addition of Co decreases the solubility of Mo in the matrix and Mo is also forced to form precipitations. This leads to an increase in the hardness (FIG. 2). Furthermore, Mo also increases the solid solution strengthening (FIG. 2) and improves the corrosion resistance of high Cr-containing maraging steels.

[0048] The influence of the Mo content is shown in FIG. 2.

Chromium (Cr)

[0049] Chromium is added to improve the corrosion resistance of maraging steels. This yields steels that can be used, for example, as plastic mold steels, which are exposed to a chemical attack during the production of plastics. The addition of Cr to the alloy promotes the precipitation of the Laves phase. But higher Cr contents can lead to the formation of the a phase, which has a negative effect on the mechanical properties. Furthermore, in long-term aging, spinodal segregation into Fe-rich and Cr-rich phases can occur, which reduces the notch impact strength.

Manganese (Mn)

[0050] In order to develop economical maraging steels, Mn was sometimes used to replace the more expensive Ni. Consistent with Ni, Mn forms a Mn martensite, but has less of an austenite-stabilizing effect and thus a significant quantity of δ ferrite is present in Fe—Mn alloys. This δ ferrite has a negative effect on the mechanical properties and on the corrosion resistance.

[0051] It is also already known that Mn forms intermetallic compounds with Fe and Ni.

Carbon (C)

[0052] Carbon is not an alloying element of a maraging steel. Because maraging steels cannot obtain their high strength from carbides, the carbon content is kept as low as possible during the production of the steel. For this reason, the carbon content of a maraging steel is in the range of 1/100%.

[0053] The corrosion resistance and the weldability deteriorate when carbon forms Cr-carbides in stainless maraging steels. In PH 13-8 Mo maraging steels, C forms carbides with Mo and Cr.

Copper (Cu)

[0054] Cu acts as a precipitation-promoting element in maraging steels; it does not, however, form a compound with other elements. At the beginning, it precipitates out with a cubic, body-centered structure in the Fe matrix. During the aging, it develops a 9R structure and in the end, it forms its cubic face-centered structure in equilibrium. The role of copper is to rapidly precipitate out and serve as a nucleation site for other precipitations.

Silicon (Si)

[0055] Silicon is usually considered an impurity element in steels. But in maraging steels, Si forms intermetallic phases and particularly in alloys that contain Ti, it forms the so-called Ni16Si7Ti6 G phase. The term “G phase” is used because the phase was discovered for the first time at grain boundaries; this is not the case, however, in maraging steels.

[0056] The good mechanical properties of maraging steels can be attributed to a two-stage heat treatment.

[0057] FIG. 3 shows an example of a time/temperature plan of such a heat treatment, which consists of a solution annealing procedure followed by an air-cooling to room temperature and an aging process.

[0058] If after the solution annealing procedure, a quenching from the austenitic monophase field is carried out, then a soft, but powerfully distorted Ni-martensite is formed, which can be easily machined and cold-worked if need be. The subsequent aging is typically carried out in a temperature range of 400° C. to 600° C. During the aging process, three reactions occur: [0059] (i) precipitation of intermetallic phases [0060] (ii) recovery of martensite [0061] (iii) formation of retransformed austenite

[0062] The precipitation of high-nm intermetallic phases is responsible for the immense increase in strength after the aging. Maraging steels have a series of essential advantages: [0063] only a two-stage heat treatment is required [0064] complex shapes can be easily machined in the un-aged state [0065] subsequent hardening with minimal deformation

[0066] The phase diagram of Fe—Ni in equilibrium is shown in FIG. 4. It clearly shows that Ni decreases the conversion temperature from austenite to ferrite and that in the alloys that contain more than a few percent Ni, the structure in equilibrium at room temperature consists of austenite and ferrite.

[0067] However, in practice under real cooling conditions starting from the austenitic monophase, the material does not decompose into a composition of austenite and ferrite in equilibrium. Instead, the austenite, with further cooling, is transformed into a cubic martensite.

[0068] The aging of the martensitic structure is possible due to the influence of Ni in maraging steels, which leads to a hysteresis of the conversion temperatures of martensite and austenite during the heating and cooling (FIG. 5). With an increasing Ni content, the conversion temperature of heating and cooling decreases. In this connection, the difference between the conversion temperatures depends on the Ni content.

[0069] After the solution annealing, the material is transformed to a martensite if it is cooled to below the conversion temperature. Depending on the Ni content and the other alloying elements, a certain percentage of austenite can be retransformed at room temperature. If the microstructure is reheated again to below the α-γ conversion temperature, then the martensite decomposes into an equilibrium structure composed austenite and ferrite. The speed of this reconversion reaction depends on the temperature used. Fortunately in maraging steels, this conversion is slow enough that precipitations of the intermetallic phases from the oversaturated solution form before the reconversion reaction dominates.

[0070] If on the other hand, the alloy is heated to above the α-γ conversion temperature, then the martensite is retransformed due to annealing processes.

[0071] The alloy concept according to the invention is essentially based on a concept that is built on Ni, Al, Ti, and Si (see FIG. 6) as hardening elements.

[0072] In order to increase the hardness, strength, and toughness of the alloy, the focus of the alloy development was placed essentially on two points: [0073] An increase in the hardness and strength values was achieved by modifying the precipitation densities and types. The contents of the precipitation-promoting elements Al and Ti were also increased. [0074] In order to increase the toughness, the percentage of retransformed austenite was increased. It was possible to achieve this by increasing the Ni content.

[0075] By contrast with the above-mentioned conventional methods, in particular the two-stage heat treatment, it has turned out according to the invention that particularly in maraging powders according to the invention that have been printed using the laser melting process, the solution annealing step can be eliminated and the aging step alone ensures that the desired level of strength and toughness is achieved. This was not expected, is fairly surprising, and is accompanied by the advantage that now, only an aging treatment has to be carried out, which shortens the overall process and naturally also makes it more advantageous. This is very clear from FIG. 11, which shows that in the material according to the invention, the strength level and also the solution annealing are achieved.

[0076] The invention will be described in greater detail based on the examples below.

[0077] A powder with chemical compositions according to FIG. 7 and a grain fraction of 15-45 μm is produced by means of gas atomization. To achieve this, bar stock, which has been melted in the vacuum induction furnace and possibly remelted by means of ESR (electroslag remelting) or VAR (vacuum arc remelting), is melted with the identical composition in a vacuum induction furnace and then atomized by means of inert gas (Ar, He, N). The powder fraction is adjusted by means of subsequent straining.

[0078] The resulting powder fraction is then processed to produce sample bodies in a 3D printer, which functions according to the principle of selective laser melting.

[0079] In the form of these sample bodies, the printed material is then characterized in different heat treatment states with regard to its structure, hardening/aging behavior, and mechanical properties.

[0080] In this example, the state “as printed+aged” is compared to the state “printed+solution annealed+aged.”

[0081] The solution annealing was carried out at 1000° C. for 1 h and the aging was carried out 3 h at 525° C. The hardness was then determined using the Rockwell method. The mechanical properties were determined by means of tensile testing.

[0082] FIGS. 8 and 9 show the characteristic values of a plurality of alloys with regard to hardness and toughness.

[0083] In this connection, in both of these figures, the alloys V21, V311, V321, and V322 according to Table in FIG. 6 correspond to the alloys according to the invention.

[0084] FIG. 8 shows that the corresponding alloys according to the invention lie in the upper range of hardness of all of the alloys and thus have absolutely sufficient hardness properties.

[0085] FIG. 9 shows the percentage of austenite as a function of the aging temperature. In this case, different percentages of retransformed austenite were produced, the retransformed austenite being responsible for the toughness of the material. It is clear that the alloys according to the invention are all very close to one another, particularly with an aging temperature of 525° C., and the percentages of austenite are absolutely sufficient for the high level of toughness.

[0086] If one compares this to the comparison alloy, it is clear that there are indeed alloys that have a high percentage of austenite, but if this is compared to FIG. 8, it is clear that they fall short in terms of hardness. Other alloys have a significantly lower percentage of austenite or even no austenite whatsoever and are thus very poor in toughness, even though they are better in hardness.

[0087] It is therefore clear that the invention enables a particularly successful combination of hardness and toughness. In this case, the hardness after the aging is greater than 50 HRC.

[0088] As is also clear from FIG. 10, in a Ti-free variant that is not according to the invention, the results of the mechanical testing turn out differently between “printed+aged” and “printed+solution annealed+aged.” The printed and aged material that is not according to the invention has mechanical properties that lag those of conventionally heat-treated, solution annealed, and aged material.

[0089] To achieve the best mechanical properties in these examples that are not according to the invention, after the printing, a solution annealing treatment is required before the aging.

[0090] As already stated, with the variant according to the invention (FIG. 11), it is clear that the printing and subsequent aging yields the desired result even without a solution annealing treatment.