SUPERALLOY TURBINE PART AND ASSOCIATED METHOD FOR MANUFACTURING BY BOMBARDMENT WITH CHARGED PARTICLES
20200191002 ยท 2020-06-18
Inventors
Cpc classification
F01D5/288
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F05D2230/40
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F05D2230/13
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F05D2300/175
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C23C14/3471
CHEMISTRY; METALLURGY
F05D2230/313
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F05D2230/314
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
C23C28/3455
CHEMISTRY; METALLURGY
International classification
F01D5/28
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
Abstract
The invention relates to a turbine part, such as a turbine blade or a distributor fin, for example, comprising a substrate made of a monocrystalline nickel superalloy, a metal sublayer covering the substrate, and a protective layer of metal oxide covering the sublayer, characterised in that the metal sublayer has one surface in contact with the protective layer and the surface has a mean roughness of less than 1 m.
Claims
1. A process for manufacturing a turbine component comprising: a single-crystal nickel-based superalloy substrate, a metallic bond coat covering the substrate, and a protective metal oxide layer covering the bond coat, the process comprising the steps of: a) charged-particle bombardment of a surface of the metallic bond coat in such a way that the surface has an average roughness of between 100 nm and 1 m, then b) formation of the protective layer on the surface bombarded in step a).
2. The process of claim 1, wherein the charged-particle bombardment is carried out by a plasma.
3. The process of claim 1, comprising a step of vapour-phase deposition of the metallic bond coat on the substrate before step a) of the process.
4. The process of claim 1, comprising a step of heating the component, under vacuum, to a temperature above 1000 C., between steps a) and b).
5. The process of claim 1, wherein the component is heated to between 800 C. and 1200 C. between the deposition of the metallic bond coat and step a).
6. The process of claim 1, wherein the component is rotated during step a).
7. The process of claim 1, wherein the component is kept under vacuum between steps a) and b).
8. The process of claim 1, wherein the component is heated to a temperature above 1000 C. during step b).
9. The process of claim 1, wherein step a) is carried out in a first vacuum chamber, step b) is carried out in a second vacuum chamber, and wherein the component is transported, between steps a) and b), from the first chamber to the second chamber in a passage, maintained under vacuum, connecting the two chambers.
10. A turbine component comprising: a single-crystal nickel-based superalloy substrate, a metallic bond coat covering the substrate, and a protective metal oxide layer covering the bond coat, wherein the metallic bond coat has a surface in contact with the protective layer and the surface has an average roughness of between 100 nm and 1 m.
11. The turbine component of claim 10 wherein the standard deviation of the surface roughness is less than 20% of the mean surface roughness.
12. The turbine component of 10, wherein the protective layer comprises a layer of alumina in the phase.
Description
PRESENTATION OF THE DRAWINGS
[0036] Other features and benefits will also emerge from the following description, which is purely illustrative and not limiting, and should be read in conjunction with the appended figures, among which:
[0037]
[0038]
[0039]
[0040]
[0041]
[0042]
[0043]
[0044]
DEFINITIONS
[0045] The term superalloy refers to a complex alloy with, at high temperature and high pressure, very good resistance to oxidation, to corrosion, to creep and to cyclic stresses (particularly mechanical or thermal). Superalloys have a particular application in the fabrication of components used in aeronautics, such as turbine blades, because they are a family of high-strength alloys that can work at temperatures relatively close to their melting points (typically 0.7 to 0.8 times their melting temperatures).
[0046] The base of the superalloy refers to the main metal component of the matrix. In most cases, superalloys include an iron, cobalt, or nickel base, but also sometimes a titanium or aluminium base.
[0047] Nickel-based superalloys have the advantage of offering a good compromise between oxidation resistance, breaking strength at high temperature and weight, which justifies their use in the hottest parts of turbojets.
[0048] The term vacuum refers to a primary, medium or high vacuum, i.e. characterized by a pressure between 10.sup.3 and 5 mbar. Such a vacuum can be adapted to charged-particle bombardment, for example by the formation of a plasma, at room temperature. The plasma can be argon plasma.
[0049] -Alumina is an allotropic variety of alumina corresponding to corundum, with a rhombohedral crystal structure. An -alumina layer can be formed by several -alumina grains, each of the grains delimiting an -crystalline phase.
[0050] Roughness generally refers to a measure of surface condition representative of deviations in the normal direction of the mean plane locally tangent to the surface under consideration. Average roughness, R.sub.a, is the arithmetic mean of the norm of the deviations of a surface from the average surface, or:
[0051] where y.sub.i is a measure of a deviation of the surface from the average surface.
[0052] Roughness homogeneity refers to a roughness dispersion smaller than a reference dispersion, characterized and/or measured by a standard deviation of the roughness of a surface of less than 20% of the average roughness.
DETAILED DESCRIPTION OF THE INVENTION
[0053] With reference to
[0054] In a first step 101 of the manufacturing process of the component 1, a metallic bond coat 3 is applied to a single-crystal nickel-based substrate 2. For example, one or more metal layers containing nickel and/or aluminium can be deposited by physical-vapour deposition (PVD). Such deposition may be carried out by sputtering, and/or by any other known method of PVD.
[0055] In a second step 102 of the process, the substrate with the metallic bond coat is heated to a temperature T between 800 C. and 1200 C. This heat treatment causes the metal ions of the bond coat 3 to diffuse into the substrate 2 to form an interdiffusion zone, allowing a better oxidation resistance during the use of the component.
[0056] In a third step 103 of the process, a surface of the metallic bond coat 3 is bombarded with charged particles. These particles can be ions, such as argon ions, and/or electrons. For example, a surface of the metallic bond coat 3 can be etched with plasma 7, i.e. using a plasma 7. The substrate with a metallic bond coat may be placed in a vacuum chamber, in which a continuous flow of one or more gases supplying the chemical element(s) composing the plasma is controlled. In general, one or more gases are used for metal etching. Advantageously, argon or oxygen is used. This charged-particle bombardment step removes the metastable oxides formed natively on the surface 16 of the bond coat 3.
[0057] Thus, the surface roughness 16 may be smaller than by using known methods of the prior art, such as sandblasting and electrochemical etching. For example, the surface 16 of the metallic bond coat 3 has an average roughness R.sub.a of less than 1 m, preferably less than 500 nm and preferably between 100 nm and 300 nm.
[0058] The use of charged-particle bombardment also makes it possible to etch the entire surface 16 of the component in a homogeneous way. This effect is particularly suitable for components 1 with complex geometry. For example, the standard deviation of the roughness on the surface 16 of plasma-etched bond coat 3 is less than 500 nm, preferentially less than 300 nm and preferentially less than 100 nm.
[0059] In general, the charged-particle bombardment of step 103 can be carried out by any ionic and/or electronic bombardment method that engraves a metal surface with a roughness R.sub.a of less than 1 m. It can also be performed using a femtosecond laser.
[0060] Advantageously, the component 1 is rotated during the charged-particle bombardment step 103. To this end, the component 1 can be arranged in a drum in the enclosure or on a rotating support. The rotation of the component increases the homogeneity of the roughness of the surface 16 of the bond coat 3.
[0061] As the charged-particle bombardment does not cause any mechanical contact during etching, the transport of impurities on the surface 16 of the bond coat 3 is avoided.
[0062] In a fourth step 104 of the process, the component is heated, preferably under vacuum, to a temperature above 1000 C. Thus, plasma atoms, such as argon atoms, possibly adsorbed on the surface 16 of the metallic bond coat 3, are removed or transported away from the component.
[0063] In a fifth step 105 of the process, the protective layer 4 is formed on the bombarded surface 16 of the metallic bond coat 3. The surface 16 can be a surface plasma-etched in step 103 of the process. The protective layer 4 is advantageously only composed of -alumina. To this end, the component is heated in an atmosphere containing oxygen to a temperature above 1000 C., so as to form a protective layer 4 by thermal oxidation. Preferentially, the temperature of 1000 C. is reached in less than ten minutes and preferably in less than five minutes, in order to avoid the formation of metastable oxide on the metallic bond coat 3.
[0064] The roughness R.sub.a of the surface 16 of the metallic bond coat 3, which is small compared to the usual roughness values, makes it possible to form a protective layer 4 comprising -alumina grains whose size is greater than the -alumina grains of the protective layers produced according to known methods. The protective layer 4 can for example include a layer of alumina in the phase. This layer can be formed of grains of average size, in a plane locally tangent to the surface 16, greater than 50 m. The increase in -alumina grain size increases the service life of the thermal barrier. The protective layer 4 may also include a layer of alumina exclusively in the phase.
[0065] In addition, the homogeneity of the roughness of the surface 16 of the charged-particle bombarded metallic bond coat 3 makes it possible to form the protective layer 4 at a constant kinetics on the surface 16 of the metallic bond coat 3. Thus, the protective layer 4 formed has substantially constant mechanical properties and thickness on the surface 16 of the metallic bond coat 3, which avoids mechanical stresses during use of the component, causing the protective layer 4 to flake.
[0066] All the steps of the process can advantageously be carried out under vacuum, or in general, without exposing the component to the ambient atmosphere. In particular, the component can be kept under vacuum between steps 103 and 105 of the process. This prevents the formation of unstable and/or metastable oxide on the surface 16.
[0067]
[0068]
[0069] With reference to
[0070] heating during deposition: from 100 to 900 C.;
[0071] pressure: from 0.1 Pa to 1 Pa;
[0072] power density: 2 to 15 W/cm.sup.2;
[0073] polarization: from 0 to 400 V.
The ion bombardment is carried out for 10 to 30 minutes.
[0074] With reference to
[0075] pressure: from 0.1 Pa to 1 Pa;
[0076] power density: 2 to 15 W/cm.sup.2;
[0077] polarization: from 0 to 400 V.
[0078] With reference to