The present invention relates to a coated substrate comprising a substrate material, which is coated at least in part with an oxidation-resistant coating, wherein the coating consists of or comprises a wear-resistant abrasive coating layer, which consists of coated abrasive particles embedded in an oxidation-resistant matrix material. The invention also relates to a manufacturing method thereof. Such substrate materials can, for example, consist of a single-crystalline superalloy, wherein the substrate material is a radially extending turbine blade for a turbine rotor, and wherein the coating is applied at the radially outer blade tip surface.
During transient processes, such as start, restart, shut-down or load changes in gas turbines and compressors, the distance between the rotor blades and the static components, such as heat-shields, are varying. Commonly, a rubbing of the rotor blades is circumvented by a sufficiently high distance between the rotor blades and the static components. This measure reduces the efficiency considerably.
As an alternative, oxidation- and wear-resistant abrasive coatings are applied at the rotor blade tips to prevent wear of the turbine blades upon contact with the static components, especially with the heat shields. These abrasive coatings contain abrasive particles, thereby enhancing wear resistance such that a sufficient protection of the turbine blades is provided, even if the static components are provided with a thermal barrier coating (TBC). Regularly, the abrasive particles consist of cubic boron nitride (cBN) as for example disclosed in DE 10 2010 049 399 A1. Because of its morphology and extremely high hardness, cBN has a superior cutting ability. However, at operating temperatures above 800° C. to 850° C. cBN is oxidizing with the result that a protective effect of an abrasive coating can only be provided for a very short time. cBN particles in abrasive coating can only guarantee a sufficient protection for about 1000 operation hours at temperatures above 900° C. Above 900° C. cBN particles are degraded rapidly by the oxidation process. Especially in the first turbine stages of a gas turbine, the temperatures can be between 900° C. to 1300° C.
Therefore, the object of the present invention is to provide a coated substrate that provides a long-term protection of substrate materials at elevated temperatures against wear and oxidation, and which can be produced relatively easily and fast.
The task is solved by the subject-matter of claim 1. Accordingly at least some of the abrasive particles, advantageously all of the abrasive particles, consist of α-Al2O3, wherein the abrasive particles are coated with a first particle coating layer disposed on the abrasive particles. Optionally, a second particle coating layer is disposed on the first particle coating layer. Furthermore, the matrix material of the abrasive coating consists of or comprises the oxidation-resistant compound MCrAlY, wherein M is at least one element selected from the group consisting of Ni, Co and Fe.
α-Al2O3, known as the minerals corundum or sapphire, is extremely stable against oxidation, being itself already an oxide. Although, it is less hard than cBN and possesses a lower cutting efficiency, α-Al2O3, still has a sufficient hardness (Mohs scale hardness 9).
To enhance the retention of the abrasive particles in the matrix material MCrAlY, the particles are coated with a first and optionally as well with a second particle coating layer. The first coating layer prevents a separation of the particles from the particle coating. Therefore preferably, the first particle coating layer is formed on the particles by a technique which allows chemical bonding of the layer to the particle surface. The second particle coating layer prevents a separation of the coated particles from the matrix. Therefore, a material is chosen, which binds relatively well to the first particle coating layer and the matrix material.
Hence, with the present invention a coated substrate can be provided with an enhanced lifetime of the abrasive coating compared to the state of the art at elevated temperatures. This enables a protection of turbine blades at temperatures between 900° C. to 1300° C. against wear and oxidation during the whole operation period, which is usually between 24.000 and 36.000 operating hours depending on the other damage mechanism besides oxidation.
Preferably the abrasive particles are single-crystalline. This leads to an enhanced hardness and durability of the particles. The thickness and/or the amount of the abrasive particles in the abrasive coating layer can vary widely, whereby the average particle size can be in the range of 0.1 to 1.000 microns. Preferably, the abrasive particles have an average size between 20 and 150 μm.
The first particle coating layer may consist of or comprise Ti, Zr, Hf, V, Nb, Ta, Cr, Co, Mo, Ni, alloys thereof or a carbide, boride, nitride or oxide thereof. Thereby a sufficient bonding between the particle surface and the particle coating can be achieved. Furthermore, these materials allow chemical bonding of the first particle coating layer to the particle surface as they can form an interstitial layer of metallic carbide or nitride under conventional deposition conditions. The thickness of the first particle coating layer can vary widely. Thicknesses of less 0.1 μm can be used as well as thicknesses well above five μm.
The second particle coating layer can consist of or comprises the same materials as can be used for the first particle coating layer. Preferably the thickness of the second particle coating layer is thicker than the thickness of the first particle coating layer.
If a two-layer coating is chosen, the total mass of the particle coating is preferably in an amount equivalent to 40-95 wt % of the abrasive particles prior to coating. For a single layer coating, the mass of the particle coating is usually smaller and typically in the range from 1-30 wt %.
If the substrate is a single-crystalline superalloy, according to an advantageous aspect of the invention, an intermediate coating layer is disposed between substrate material and the abrasive coating layer. This intermediate coating layer may be epitaxially bonded to the substrate material. The intermediate layer may also consist or comprise a MCrAlY alloy. This intermediate buffer coating layer binds well to the substrate material. If formed epitaxially on a single crystalline substrate material, the intermediate buffer layer has similar anisotropic material properties (e.g. Young's modulus) like the substrate. As a consequence its thermo-physical properties are matched with the substrate leading to higher cyclic lifetime. Epitaxial deposition of the intermediate buffer layer also prevents the formation of grain boundaries and defects. Furthermore, the MCrAlY material of the buffer layer enhances the oxidation resistivity of the substrate material as a crack free, stable and dense protective layer can be formed.
Preferably the matrix material and/or the intermediate coating layer consists of a MCrAlY alloy having a solidification interval between the solidus temperature and liquidus temperature ΔT0 of less than 50 K. Advantageously it is less than 40 K. This reduces the risk of cracking during solidification. This can be achieved by choosing a MCrAlY alloy which is close to a eutectic composition.
According to a further advantageous aspect of the invention, the matrix material and/or the intermediate coating layer consists of an oxidation-resistant γ/β or γ/γ′ type MCrAlY alloy, wherein the chemical composition of the alloy is selected such that upon solidification, the γ phase is firstly formed and only then the β or γ′ phase is formed. As the γ phase is firstly formed, upon solidification on the substrate material, an epitaxial bonded intermediate coating layer can be provided on the substrate material. A particularly advantageous γ/β type MCrAlY alloy has the following chemical composition: 35-40 wt % Co, 18-24 wt % Cr, 7-9 wt % Al, 0.3-0.8 wt % Y, 0.1-1 wt % Si, 0-2 wt % others, remainder Ni. This alloy has a liquidus temperature of about 1370° C.
The substrate material may consist of a single-crystalline superalloy, which can be precipitation hardened. Commonly, nickel based superalloys are used for turbine blades. Superalloys such as IN713 LC, IN 738 LC, MAR M 247, CM 247 LC, CMSX-4, MK 4 or MD 2 are suitable candidates to be used.
Usually the coating is applied at the radially outer blade tip surface, whereby the weight content of the abrasive particles in the abrasive coating layer may increase towards the radially outer direction.
The task of the invention is also solved by a method for manufacturing a coated substrate according to the present invention. Accordingly, the abrasive coating layer is formed by laser metal forming. This method is disclosed in detail in EP1 476 272 B1, the contents of which are incorporated by reference as if fully set forth. Accordingly, the coated abrasive particles and matrix material particles are mixed in a powder nozzle, transported by a carrier gas and then injected concentrically about the laser beam as a focused jet of powder into the melt pool produced by the laser beam on the blade tip. The laser metal forming process is a welding method and, in contrast to commonly used coating methods, it produces a stable, metallurgical bond with the substrate material without additional diffusion heat treatment.
If the coating also comprises an intermediate layer, the intermediate layer is firstly formed by a suitable coating method. Preferably also laser metal forming is used as it provides an inexpensive and simple method for producing coatings. Moreover, the laser metal forming can be controlled such that it is possible to achieve epitaxial deposition on single crystalline substrates.
According to another advantageous aspect of the invention, the temperature or temperature distribution in the melt pool is additionally recorded online during the laser metal forming process and this information is used by a control system, to control the laser power and thereby the temperature of the melt pool during the laser metal forming such that the temperature of the melt pool during the formation of the abrasive coating layer lies between the liquidus temperature of the substrate material and the melting temperature of the abrasive particles or the melting or liquidus temperature of the first or second particle coating layer. Thereby a very controlled growth of the coating layers with good embedding of the abrasive particles can be achieved.
If the coating also comprises an intermediate layer, the temperature of the melt pool can be controlled such that during the formation of the abrasive coating layer, the temperature lies between the liquidus temperature of the matrix material and the melting temperature of the abrasive particles or of the melting or liquidus temperature of the first or second coating layer.
According to yet another advantageous aspect of the invention, before the formation of the coating, the abrasive particles are coated. In a first step, the first particle coating layer is formed on the abrasive particles. Preferably a method is used, such that the first particle coating layer is chemically bonded to the substrate material. A suitable method is salt bath deposition. In the following optional step the secondary layers can be deposited on the first particle coating layer. A number of techniques such as electroless, electrolytic and vapour deposition techniques can be used to allow the formation of a thick second particle coating layer. Advantageously, electroless deposition is used as a thick coating layer can be produced quickly and inexpensively. The coating can also comprise more than two coating layers. The process of coating these abrasive particles is called metallization.
The invention is explained in more detail on the basis of exemplary embodiments and on the basis of the
The drawings show:
According to
The abrasive coating layer 5 consists of a matrix material 6, which consists of the compound MCrAlY, and of abrasive particles 7 consisting of single-crystalline α-Al2O3, which are embedded in the matrix material 6.
As schematically shown in
According to another embodiment shown in
For the formation of the coatings 9 according the
To produce the coating according to
Number | Date | Country | Kind |
---|---|---|---|
14196596 | Dec 2014 | EP | regional |
Number | Name | Date | Kind |
---|---|---|---|
3520656 | Yates | Jul 1970 | A |
4169020 | Stalker | Sep 1979 | A |
4289503 | Corrigan | Sep 1981 | A |
4582548 | Harris | Apr 1986 | A |
4643782 | Harris | Feb 1987 | A |
4861673 | Hara | Aug 1989 | A |
4885216 | Naik | Dec 1989 | A |
5106266 | Borns | Apr 1992 | A |
5366695 | Erickson | Nov 1994 | A |
6811898 | Ohara | Nov 2004 | B2 |
6966956 | Koizumi | Nov 2005 | B2 |
8163403 | Zurbuchen | Apr 2012 | B2 |
8647073 | Hoebel et al. | Feb 2014 | B2 |
8877122 | Aoki | Nov 2014 | B2 |
9581041 | Sinatra | Feb 2017 | B2 |
9868667 | Riman | Jan 2018 | B2 |
20020151265 | Adefris | Oct 2002 | A1 |
20030183529 | Ohara et al. | Oct 2003 | A1 |
20040180233 | Stamm | Sep 2004 | A1 |
20090117390 | Stamm et al. | May 2009 | A1 |
20090202814 | Jabado et al. | Aug 2009 | A1 |
20110103967 | Hoebel | May 2011 | A1 |
20110164961 | Taylor | Jul 2011 | A1 |
20110164963 | Taylor | Jul 2011 | A1 |
20130108421 | Sinatra et al. | May 2013 | A1 |
20130122259 | Lee | May 2013 | A1 |
Number | Date | Country |
---|---|---|
10 2010 049 399 | May 2011 | DE |
1 707 650 | Oct 2006 | EP |
1 840 245 | Oct 2007 | EP |
Entry |
---|
European Search Report dated Apr. 13, 2015, by the European Patent Office for Application No. 14196596.2:0. |
Mingxi Li et al., Microstructure of Al2O3 Nanocrystalline/Cobalt-Based Alloy Composite Coatings by Laser Deposition, Materials and Design, vol. 27, Jan. 1, 2006, pp. 1114-1119, XP027891370. |
Office Action (First Office Action) dated Nov. 29, 2018, by the Chinese Patent Office in corresponding Chinese Patent Application No. 201510886627.6, and an English Translation of the Office Action. (14 pages). |
Number | Date | Country | |
---|---|---|---|
20160160661 A1 | Jun 2016 | US |