Two layered metallic bondcoat

Abstract

A component including a metallic substrate and a two layered bondcoat is provided. On the substrate a metallic bond coat especially of the type MCrAlY is preferably applied. The bond coat is a two layered metallic layer. The outer metallic bond coat has compared to the inner metallic coat a reduced amount of aluminum and/or chromium.

Description

FIELD OF INVENTION

The invention relates to a two layered metallic bondcoat.

BACKGROUND OF INVENTION

Thermal barrier coatings must offer a low thermal conductivity but also a good bonding to the substrate or to a metallic bond coat.

Also the ductility of the metallic bond coat should be improved.

SUMMARY OF INVENTION

It is therefore the aim of the invention to improve the ductility and oxidation resistance of the metallic bond coat.

The problem is solved by a two layered metallic bondcoat according to the claims.

BRIEF DESCRIPTION OF THE DRAWINGS

It shows FIG. 1, 2 a schematic view of the invention,

FIG. 3 a gas turbine,

FIG. 4 turbine blade,

FIG. 5 a combustion chamber,

FIG. 6 a list of super alloys.

DETAILED DESCRIPTION OF INVENTION

The following examples and figures are only embodiments of the invention.

A component 1, 120, 130, 155 is shown in FIG. 1.

It shows a metallic substrate 4 which is especially in the case of component like blades or vanes 120, 130 (FIG. 3) for gas turbines 100 (FIG. 2) made of a nickel based super alloy as given in FIG. 6.

On the substrate 4 a metallic bond coat 7 especially of the type MCrAlY is preferably applied.

The bond coat 7 is a two layered metallic layer 10, 13.

The inner metallic bond coat 10 is especially one of the following compositions (in wt %):

Ni-(24-26)Co-(16-18)Cr-(9-11)-Al(0.1-0.5)Y-(1-2)Re especially Ni-25Co-17Cr-10Al-0.3Y-1.5Re;Co-(29-31)Ni-(27-29)Cr-(7-9)Al-(0.4-0.8)Y-(0.5-0.9)Si, especially Co-30Ni-28Cr-8Al-0.6Y-0.7Si;Co-(27-29)Ni-(23-25)Cr-(9-11)-Al(0.4-0.8)Y, especially Co-28Ni-24Cr-10Al-0.6Y;Ni-(24-26)Co-(22-24)Cr-(9-11)-Al(0.1-0.4)Y, especially Ni-25.2Co-22.8Cr-10.1Al-0.17Y;Ni-(19-21)Co-(23-25)Cr-(6-8)Al-(0.3-0.9)Y, especially Ni-20Co-24Cr-7Al-0.6Y;Co-(34-36)Ni-(19-21)Cr-(10.5-12.5)Al-(0.08-0.4)Y-(0.1-0.5)Si, especially Co-35Ni-20Cr-11.5-Al-0.2Y-0.3Si;Ni-(11-13)Co-(20-22)Cr-(10-12)Al-(0.2-0.6)Y-(1-2)Re, especially Ni-12Co-21Cr-11Al-0.4Y-1.5Re.

The outer metallic bond coat 13 has compared to the inner metallic coat 10 a reduced amount of aluminum (Al) and/or chromium (Cr).

Preferably this upper metallic layer 13 has 16 wt %-18 wt % chromium (Cr) and/or 4 wt % to 5 wt % aluminum (Al).

The outer metallic coating 13 can have the same composition like the inner metallic coating 11 but with the above described content of aluminum (Al) and/or Chromium (Cr).

This improves the ductility of the upper metallic layer 13 which faces directly the ceramic layers.

Especially the outer layer 13 comprises, very especially consists of:

Co-(29-31)Ni-(27-29)Cr-(7-9)Al-(0.4-0.8)Y-(0.5-0.9)Si, especially Co-30Ni-28Cr-8Al-0.6Y-0.7Si;Co-(27-29)Ni-(23-25)Cr-(9-11)Al-(0.4-0.8)Y, especially Co-28Ni-24Cr-10Al-0.6Y;Preferably this upper metallic layer 13 has 16 wt %-18 wt % chromium (Cr) and/or 4 wt % to 5 wt % aluminum (Al).

The metallic outer layer 13 and the combination of inner 10 and outer layer 13 are chosen to improve the ductility.

The outer metallic layer 13 is preferably at least 10% thinner than the inner layer 10.

On the bond coat 7 an aluminum oxide layer 8 (TGO) is formed during applying the ceramic TBC or at least during operations of the coating system.

The ceramic thermal barrier coating 16 is preferably a two layered ceramic layered coating 19, 22.

Especially the ceramic TBC 16 consists only of two layers 10, 13.

The inner ceramic coating 19 on the metallic bond coat 7 over or on the substrate 4 is nanostructured and especially much thinner than the above laying ceramic layer 22. This improves the ductility and adherence of the ceramic coating.

Nanostructured means that about 70%, especially at least 90% of the grain sizes of the ceramic layer 19 are lower then 500 nm, especially ≤300 nm.

The minimum grain sizes to avoid sintering are larger than ≥100 nm and very especially ≥200 nm.

Only the inner ceramic layer 19 is nanostructured. The outer layer 22 is microstructured.

Microstructured means that at least 70%, especially at least 90% of the grain sizes of the grains are larger than 1 μm, especially larger than 20 μm.

The lower layer 19 is especially much thinner than the upper ceramic thermal barrier coating 19.

This means that the thickness of the upper layer 22 comprises at least 60%, especially 70% of the total thickness of the ceramic layer 22.

Especially the lower ceramic layer 19 has a thickness up to 100 μm with a minimum of 10 μm, especially of 20 μm.

Especially, the inner ceramic layer 19 has a porosity up to 14 vol %, especially between 9 vol % to 14 vol %.

Especially the upper ceramic layer 22 has a much higher porosity than the inner ceramic layer 19 (difference at least 10%, especially ≥20%), especially a porosity higher than 15 vol % and a porosity up to 30 vol %.

The upper layer 22 can be applied by any coating method like plasma spray, HVOF or cold gas spraying.

The nano structured ceramic layer 19 is preferably applied by a suspension, plasma spraying or solution precursor plasma spraying or any sol gel technique.

The material of the two ceramic layers 19, 22 can be the same, especially it is yttrium stabilized zirconia.

Furthermore, the inner ceramic layer 19 can be a nano structured partially stabilized zirconia and the upper layer 22 offers a different composition and is especially a ceramic layer with a structure of a pyrochlor, which is especially gadolinium zirconate (like Gd₂Zr₂O₇) or gadolinium hafnate (like Gd₂Hf₂O₇).

FIG. 4 shows a perspective view of a rotor blade 120 or guide vane 130 of a turbomachine, which extends along a longitudinal axis 121.

The turbomachine may be a gas turbine of an aircraft or of a power plant for generating electricity, a steam turbine or a compressor.

The blade or vane 120, 130 has a securing region 400, an adjoining blade or vane platform 403 and a main blade or main part 406 in succession along the longitudinal axis 121. As guide vane 130, the vane 130 may have a further platform (not shown) at its vane tip 415.

A blade or vane root 183, which is used to secure the rotor blades 120, 130 to a shaft or disk (not shown), is formed in the securing region 400. The blade or vane root 183 is designed, for example, in hammerhead form. Other configurations, such as fir-tree or dovetail root, are also possible. The blade or vane 120, 130 has a leading edge 409 and a trailing edge 412 for a medium which flows past the main blade or vane part 406.

In the case of conventional blades or vanes 120, 130, by way of example, solid metallic materials, in particular superalloys, are used in all regions 400, 403, 406 of the blade or vane 120, 130. Superalloys of this type are known, for example, from EP 1 204 776 B1, EP 1 306 454, EP 1 319 729 A1, WO 99/67435 or WO 00/44949. The blade or vane 120, 130 may in this case be produced by a casting process, also by means of directional solidification, by a forging process, by a milling process or combinations thereof.

Workpieces with a single-crystal structure or structures are used as components for machines which are exposed to high mechanical, thermal and/or chemical loads during operation. Single-crystal workpieces of this type are produced, for example, by directional solidification from the melt. This involves casting processes in which the liquid metallic alloy is solidified to form the single-crystal structure, i.e. the single-crystal workpiece, i.e. directionally. In the process, dendritic crystals are formed in the direction of the heat flux and form either a columnar-crystalline grain structure (i.e. with grains which run over the entire length of the workpiece and are referred to in this context, in accordance with the standard terminology, as directionally solidified) or a single-crystal structure, i.e. the entire workpiece consists of a single crystal. In this process, the transition to globular (polycrystalline) solidification needs to be avoided, since non-directional growth inevitably leads to the formation of transverse and longitudinal grain boundaries, which negate the good properties of the directionally solidified or single-crystal component. Where directionally solidified microstructures are referred to in general, this is to be understood as encompassing both single crystals, which do not have any grain boundaries or at most have small-angle grain boundaries, and columnar crystal structures, which do have grain boundaries running in the longitudinal direction, but do not have any transverse grain boundaries. In the case of these latter crystalline structures, it is also possible to refer to directionally solidified microstructures (directionally solidified structures). Processes of this type are known from U.S. Pat. No. 6,024,792 and EP 0 892 090 A1.

The blades or vanes 120, 130 may also have coatings protecting against corrosion or oxidation, e.g. (MCrAlX; M is at least one element selected from the group consisting of iron (Fe), cobalt (Co), nickel (Ni), X is an active element and stands for yttrium (Y) and/or silicon and/or at least one rare earth element, or hafnium (Hf)). Alloys of this type are known from EP 0 486 489 B1, EP 0 786 017 B1, EP 0 412 397 B1 or EP 1 306 454 A1.

It is also possible for a thermal barrier coating consisting, for example, of ZrO₂, Y₂O₃—ZrO₂, i.e. which is not, is partially or is completely stabilized by yttrium oxide and/or calcium oxide and/or magnesium oxide, to be present on the MCrAlX.

Columnar grains are produced in the thermal barrier coating by suitable coating processes, such as for example electron beam physical vapor deposition (EB-PVD).

The term refurbishment means that protective layers may have to be removed from components 120, 130 after they have been used (for example by sandblasting). Then, the corrosion and/or oxidation layers or products are removed. If necessary, cracks in the component 120, 130 are also repaired using the solder according to the invention. This is followed by recoating of the component 120, 130, after which the component 120, 130 can be used again.

The blade or vane 120, 130 may be of solid or hollow design. If the blade or vane 120, 130 is to be cooled, it is hollow and may also include film cooling holes 418 (indicated by dashed lines).

FIG. 5 shows a combustion chamber 110 of a gas turbine 100 (FIG. 6).

The combustion chamber 110 is configured, for example, as what is known as an annular combustion chamber, in which a multiplicity of burners 107, which are arranged around an axis of rotation 102 in the circumferential direction, open out into a common combustion chamber space 154, with the burners 107 producing flames 156. For this purpose, the combustion chamber 110 overall is of annular configuration, positioned around the axis of rotation 102.

To achieve a relatively high efficiency, the combustion chamber 110 is designed for a relatively high temperature of the working medium M of approximately 1000° C. to 1600° C. To allow a relatively long operating time even with these operating parameters, which are unfavorable for the materials, the combustion chamber wall 153 is provided with an inner lining formed from heat shield elements 155 on its side facing the working medium M. Each heat shield element 155 made from an alloy is equipped on the working medium side with a particularly heat-resistant protective layer (MCrAlX layer and/or ceramic coating) or is made from material that is able to withstand high temperatures (solid ceramic bricks). These protective layers may be similar to the turbine blades or vanes, i.e. meaning for example MCrAlX: M is at least one element selected from the group consisting of iron (Fe), cobalt (Co), nickel (Ni), X is an active element and stands for yttrium (Y) and/or silicon and/or at least one rare earth element, or hafnium (Hf). Alloys of this type are known from EP 0 486 489 B1, EP 0 786 017 B1, EP 0 412 397 B1 or EP 1 306 454 A1.

It is also possible for a, for example, ceramic thermal barrier coating to be present on the MCrAlX, consisting, for example, of ZrO₂, Y₂O₃—ZrO₂, i.e. it is not, is partially or is completely stabilized by yttrium oxide and/or calcium oxide and/or magnesium oxide.

Columnar grains are produced in the thermal barrier coating by suitable coating processes, such as for example electron beam physical vapor deposition (EP-PVD).

The term refurbishment means that protective layers may have to be removed from heat shield elements 155 after they have been used (for example by sandblasting). Then, the corrosion and/or oxidation layers or products are removed. If necessary, cracks in the heat shield element 155 are also repaired using the solder according to the invention. This is followed by recoating of the heat shield elements 155, after which the heat shield elements 155 can be used again.

Moreover, on account of the high temperatures in the interior of the combustion chamber 110, it is possible for a cooling system to be provided for the heat shield elements 155 and/or for their holding elements. The heat shield elements 155 are in this case, for example, hollow and may also include film cooling holes (not shown) which open out into the combustion chamber space 154.

FIG. 6 shows, by way of example, a gas turbine 100 in the form of a longitudinal part section. In its interior, the gas turbine 100 has a rotor 103, which is mounted such that it can rotate about an axis of rotation 102 and has a shaft, also known as the turbine rotor. An intake housing 104, a compressor 105 a, for example toroidal, combustion chamber 110, in particular an annular combustion chamber, with a plurality of coaxially arranged burners 107, a turbine 108 and the exhaust casing 109 follow one another along the rotor 103. The annular combustion chamber 110 is in communication with a, for example annular, hot-gas duct 111 where, for example, four successive turbine stages 112 form the turbine 108.

Each turbine stage 112 is formed, for example, from two blade or vane rings. As seen in the direction of flow of a working medium 113, a row 125 formed from rotor blades 120 follows a row 115 of guide vanes in the hot-gas duct 111.

The guide vanes 130 are secured to an inner housing 138 of a stator 143, whereas the rotor blades 120 of a row 125 are fitted to the rotor 103, for example by means of a turbine disk 133. A generator or machine (not shown) is coupled to the rotor 103.

When the gas turbine 100 is operating, the compressor 105 sucks in air 135 through the intake housing 104 and compresses it. The compressed air which is provided at the turbine-side end of the compressor 105 is passed to the burners 107, where it is mixed with a fuel. The mixture is then burnt in the combustion chamber 110 to form the working medium 133. From there, the working medium 133 flows along the hot-gas duct 111 past the guide vanes 130 and the rotor blades 120. The working medium 113 expands at the rotor blades 120, transferring its momentum, so that the rotor blades 120 drive the rotor 103 and the rotor drives the machine coupled to it.

When the gas turbine 100 is operating, the components which are exposed to the hot working medium 113 are subject to thermal loads. The guide vanes 130 and rotor blades 120 of the first turbine stage 112, as seen in the direction of flow of the working medium 113, together with the heat shield elements which line the annular combustion chamber 110, are subject to the highest thermal loads. To withstand the temperatures prevailing there, these components can be cooled by means of a coolant.

It is likewise possible for substrates of the components to have a directional structure, i.e. they are in single-crystal form (SX structure) or include only longitudinally directed grains (DS structure). By way of example, iron-base, nickel-base or cobalt-base superalloys are used as material for the components, in particular for the turbine blades and vanes 120, 130 and components of the combustion chamber 110. Superalloys of this type are known, for example, from EP 1 204 776 B1, EP 1 306 454, EP 1 319 729 A1, WO 99/67435 or WO 00/44949.

The blades and vanes 120, 130 may likewise have coatings to protect against corrosion (MCrAlX; M is at least one element selected from the group consisting of iron (Fe), cobalt (Co), nickel (Ni), X is an active element and stands for yttrium (Y) and/or silicon and/or at least one of the rare earth elements or hafnium). Alloys of this type are known from EP 0 486 489 B1, EP 0 786 017 B1, EP 0 412 397 B1 or EP 1 306 454 A1.

A thermal barrier coating consisting, for example, of ZrO₂, Y₂O₃—ZrO₂, i.e. it is not, is partially or is completely stabilized by yttrium oxide and/or calcium oxide and/or magnesium oxide, may also be present on the MCrAlX. Columnar grains are produced in the thermal barrier coating by suitable coating processes, such as for example electron beam physical vapor deposition (EB-PVD).

The guide vane 130 has a guide vane root (not shown here) facing the inner housing 138 of the turbine 108 and a guide vane head on the opposite side from the guide vane root. The guide vane head faces the rotor 103 and is fixed to a securing ring 140 of the stator 143.

Claims

1-26. (canceled)

27. A layer system, comprising: a substrate;a two layered metallic bond coat including an inner metallic layer and an outer metallic layer;wherein the outer metallic layer includes a lower aluminum content than the inner metallic layer, and/or that the outer metallic layer includes a lower content of chromium than the inner metallic layer.

28. The layer system as claimed in claim 27, wherein the aluminum content of the outer metallic layer is at least 10% lower than the inner metallic layer.

29. The layer system as claimed in claim 27, wherein the chromium content of the outer metallic layer is at least 10% lower than the inner metallic layer.

30. The layer system according to claim 27, wherein the inner metallic bond coat comprises a MCrAlY alloy.

31. The layer system according to claim 27, wherein the outer metallic bond coat comprises a MCrAlY alloy.

32. The layer system according to claim 27, wherein the aluminum content of the outer metallic layer is lower than the inner metallic layer, andwherein the aluminum content of the outer metallic layer is between 4 wt % and 5 wt %.

33. The layer system according to claim 27, wherein the chromium content of the outer metallic layer is lower than the inner metallic layer, andwherein the chromium content of the outer metallic layer is between 16 wt %-18 wt %.

34. The layer system according to claim 30, wherein the MCrAlY alloy of the inner metallic layer is selected from the group consisting of (in wt %): Ni-(24-26)Co-(16-18)Cr-(9-11)Al-(0.1-0.5)Y-(1-2)Re,Co-(29-31)Ni-(27-29)Cr-(7-9)Al-(0.4-0.8)Y-(0.5-0.9)Si,Co-(27-29)Ni-(23-25)Cr-(9-11)-Al(0.4-0.8)Y,Ni-(24-26)Co-(22-24)Cr-(9-11)-Al(0.1-0.4)Y,Ni-(19-21)Co-(23-25)Cr-(6-8)Al-(0.3-0.9)Y,Co-(34-36)Ni-(19-21)Cr-(10.5-12.5)Al-(0.08-0.4)Y-(0.1-0.5)Si, andNi-(11-13)Co-(20-22)Cr-(10-12)Al-(0.2-0.6)Y-(1-2)Re.

35. The layer system according to claim 27, wherein the alloy of the outer metallic layer is selected from the group consisting of (in wt %): Co-(29-31)Ni-(27-29)Cr-(7-9)Al-(0.4-0.8)Y-(0.5-0.9)Si,Co-(27-29)Ni-(23-25)Cr-(9-11)-Al(0.4-0.8)Y,Co-(29-31)Ni-(27-29)Cr-(4-5)Al-(0.4-0.8)Y-(0.5-0.9)Si,Co-(27-29)Ni-(23-25)Cr-(4-5)Al-(0.4-0.8)Y,Co-(29-31)Ni-(16-18)Cr-(7-9)Al-(0.4-0.8)Y-(0.5-0.9)Si,Co-(27-29)Ni-(16-18)Cr-(9-11)Al-(0.4-0.8)Y,Co-(29-31)Ni-(16-18)Cr-(4-5)Al-(0.4-0.8)Y-(0.5-0.9)Si, andCo-(27-29)Ni-(16-18)Cr-(4-5)Al-(0.4-0.8)Y.

36. The layer system according to claim 27, wherein the MCrAlY alloy of the outer metallic layer is selected from the group consisting of (in wt %):Ni-(24-26)Co-(16-18)Cr-(4-5)Al-(0.1-0.5)Y-(1-2)Re,Co-(29-31)Ni-(27-29)Cr-(4-5)Al-(0.4-0.8)Y-(0.5-0.9)Si,Co-(27-29)Ni-(23-25)Cr-(4-5)Al-(0.4-0.8)Y,Ni-(24-26)Co-(22-24)Cr-(4-5)Al-(0.1-0.4)Y,Ni-(19-21)Co-(23-25)Cr-(4-5)Al-(0.3-0.9)Y,Co-(34-36)Ni-(19-21)Cr-(4-5)Al-(0.08-0.4)Y-(0.1-0.5)Si, andNi-(11-13) Co-(20-22)Cr-(4-5)Al-(0.2-0.6)Y-(1-2)Re, andwherein the base which is nickel or cobalt balances the difference.

37. The layer system according to claim 27, wherein the outer metallic layer is thinner than the inner metallic layer.

38. The layer system according to claim 27, further comprising an inner ceramic layer and an outer ceramic layer.

39. The layer system according to claim 38, wherein only the inner ceramic layer is nano structured.

40. The layer system according to claim 38, wherein the inner ceramic layer is thinner than the outer ceramic layer.

41. The layer system according to claim 38, wherein the inner ceramic layer has a thickness up to 100 μm.

42. The layer system according to claim 38, wherein the inner ceramic layer has a thickness of at least 10 μm.

43. The layer system according to claim 38, wherein the inner ceramic layer has a porosity between 3 vol % to 14 vol %.

44. The layer system according to claim 38, wherein the outer metallic layer has a porosity up to 30 vol %.

45. The layer system according to claim 38, wherein the material of the two ceramic layers is the same, andwherein the material is stabilized zirconia.

46. The layer system according to claim 38, wherein the material of the outer ceramic layer is different from the material of the inner ceramic layer, andwherein the material of the outer ceramic layer has a pyrochlore structure.