The disclosure relates to manufacture of materials used for enhanced abradable coatings for a gas turbine engine.
In compressor and turbine sections of a gas turbine engine, air seals are used to seal the interface between a rotating structure, such as a hub or a blade, and a fixed structure, such as a housing or a stator. For example, typically, circumferentially arranged blade seal segments are fastened to a housing, for example, to provide the seal.
Relatively rotating components of a gas turbine engine are not at all times perfectly cylindrical or coaxial with one another during engine operation. As a result, the relatively rotating components may occasionally rub against one another. To this end, an abradable material typically is adhered to the blade seal segments or full rings and/or the rotating component.
Abradable seals in the compressor section of gas turbine engines include characteristics such as, good abradability, spall resistance, and erosion resistance. Abradable seals are required to exhibit a smooth surface, low gas permeability, and environmental durability. The seal is a sacrificial element in order to minimize blade wear, so it is abradable. The seal must also minimize gas flow leakage through the seal, so a low gas permeability is desirable.
Abradable coatings for the seals are always a compromise between abradability and erosion resistance. In order to maintain blade tip clearances over time, the seal material needs to be tough and resistant to erosion. Conventional seal materials tend to be soft and weak in order to have good abradability. Recently, MAXMETs (MAX phase reinforced metal matrix composites) have shown tremendous promise as next generation compressor abradable coatings.
MAXMET composite coatings processed by powder metallurgy routes and thermal spraying techniques have showed excellent promise due to increased erosion resistance, and significant reduction in coefficient of friction by incorporation of up to 50 vol. % MAX phases into current abradable systems. The wear response of the newly developed coatings have also showed significant changes in the rub mechanism. However, to scale up, methods of manufacture and processing parameters for enabling MAXMET applications as low and high temperature Low Pressure Compressor and High Pressure Compressor abradable coatings is currently under development. One of the challenges during use of thermal spraying methods to create abradable coatings is oxidation and low flow behavior of MAX phase particles.
In accordance with the present disclosure, there is provided a process to manufacture MAXMET particles by encapsulating the MAX phase particles in a metallic shell, the choice of which depends on the end use of the abradable coating. The metal shell minimizes oxidation of the MAX phase particles during the spray process and permits a more efficient thermal deposition of the MAXMET composite, which in turn contributes to improved erosion resistance and abradability.
In accordance with the present disclosure, there is provided a method of manufacturing a gas turbine engine air seal comprising forming at least one MAX phase particle. The method includes coating the at least one MAX phase particle with a metallic shell. The method includes applying the at least one MAX phase metallic coated particle to a surface of a substrate of the air seal to form an abradable layer of a MAXMET composite abradable material from the at least one MAX phase metallic coated particle.
In accordance with the present disclosure, there is provided chemical methods to clad MAX phase particles with a metallic shell to produce MAXMET particles for thermal spraying methods. Among these methods are, a) wet chemistry approach via a redox reaction to produce metallic shell from a metallic salt in a solution on the surface of MAX phase particles, b) combination of wet chemistry and gas reduction to make metallic particles from metal oxides resulted from solution, c) chemical vapor deposition, d) electrochemical reduction, and e) agglomeration of fine (<5-10 micron) clad MAX phase particles during the plating process to form multi-particulate MAXMET domains of approximately 16-150 micron size suitable for thermal spray deposition.
In accordance with the present disclosure, there is provided an air seal in a gas turbine engine comprising an abradable layer comprising a MAXMET composite material having MAX phase particles coated with a metallic shell.
In another and alternative embodiment the substrate is coupled to the abradable layer.
In another and alternative embodiment the metallic shell comprises Al or the metallic shell comprises Ni.
In another and alternative embodiment the MAX phase is defined by the formula Mn+1AXn where n is a number from 1 to 3.
In another and alternative embodiment a bond coat layer is adhered to at least a portion of the substrate. The abradable layer is adhered to the bond coat.
In accordance with the present disclosure, there is provided a gas turbine engine comprising a first structure. A second structure is rotatable relative to the first structure, wherein one of the first structure and second structure comprises a substrate. An abradable layer is coupled to the substrate wherein the abradable layer comprises a MAXMET composite material having MAX phase particles coated with a metallic shell.
In another and alternative embodiment the metallic shell comprises Ni or the metallic shell comprises Al. The MAX phase is defined by the formula Mn+1AXn where n is a number from 1 to 3.
In accordance with the present disclosure, there is provided a method of manufacturing a gas turbine engine air seal comprises forming at least one MAX phase particle. The method includes coating the at least one MAX phase particle with a metallic shell and applying the at least one MAX phase metallic coated particle to a surface of a substrate of the air seal to form an abradable layer of a MAXMET composite abradable material from the at least one MAX phase metallic coated particle.
In another and alternative embodiment the coating step is selected from the group consisting of a redox reaction; a combination of wet chemistry and gas reduction; chemical vapor deposition, electrochemical reduction, and agglomeration of fine (<5-10 micron) clad MAX phase particles during a plating process.
In another and alternative embodiment the method also includes the agglomeration of fine (<5-10 micron) clad MAX phase particles during the plating process to form multi-particulate MAXMET domains of approximately 16-150 micron size suitable for thermal spray deposition.
In another and alternative embodiment the step of applying the at least one MAX phase metallic coated particle to a surface of a substrate of said air seal comprises thermal spray deposition.
The details of one or more embodiments are set forth in the accompanying drawings and the description below. Other features, objects, and advantages will be apparent from the description and drawings, and from the claims.
Like reference numbers and designations in the various drawings indicate like elements.
Air seals 26 (
In one example shown in
The air seal 26 includes a bond coat 30 deposited onto the outer case 20 or other structure/substrate. In an exemplary embodiment, the bond coat 30 may be a thermally sprayed bond coat. In another example, the bond coat 30 may comprise an alloy, such as a MCrAlY composition applied by air plasma spray. A composite topcoat 32 acts as an abradable layer that is deposited on the bond coat 30 opposite the outer case 20. In an exemplary embodiment, the metallic bond coat 30 may be replaced by an adhesive layer. The adhesive may be polyurethane in the front stages of the compressor or in the fan where ambient temperature is sufficiently low (e.g., less than about 300 degrees Fahrenheit.
The Referring also to
Examples of suitable MAX phase particles 34 include, but are not limited to: ternary carbides and ternary nitrides. The atomic layers within the MAX phase particles 34 are layers of hard, strong, high modulus carbide. The atoms are also arranged in layers so that they form very weak crystallographic planes. Thus, both high modulus strong planes and very weak planes are present in matrix material 34. This results in kink band forming tendencies, which gives it both ceramic and metallic properties. The kink bands provide toughness similar to a metal, making MAX phase material 34 capable of withstanding impact damage conditions while the high modulus and high hardness of the carbide layers make MAX phase material 34 capable of withstanding fine particle erosion. At the same time, the slip planes have low strength such that MAX phase material 34 is machinable using a sharp cutting point.
The MAX phase particles 34 can be encapsulated in a metallic shell 36 to form a MAXMET composite material 38. The metallic shell 36 can comprise any variety of materials depending on the end use of the abradable composite 32. In an exemplary embodiment, the metallic shell 36 can comprise a Ni shell material for use with Ni-based abradable composite materials. In another exemplary embodiment the metallic shell 36 can comprise an Al shell for use with Al based abradable composite materials. Besides Ni and Al, depending on the applications, other metals, such as W, Co, Hf, Cr, and the like, can be applied as a coating layer.
The metallic shell 36 minimizes oxidation of the MAX phase particles 34 during the spray application process. The metallic shell 36 permits more efficient thermal deposition of the MAXMET composite material 38. The efficient thermal deposition of the MAXMET composite material 38 contributes to improved erosion resistance and abradability.
The metallic shell 36 cladding can be created by a variety of methods. For a given element, for instance, Al, certain procedures may be unique in order to create good bonding to MAX phase. Among these methods are, a) wet chemistry approach via a redox reaction to produce metallic shell from a metallic salt in a solution on the surface of MAX phase particles, b) a combination of wet chemistry and gas reduction to make metallic particles from metal oxides resulted from solution, c) chemical vapor deposition, d) electrochemical reduction, e) agglomeration of fine (<5-10 micron) clad MAX phase particles during the plating process to form multi-particulate MAXMET domains of approximately 16-150 micron size suitable for thermal spray deposition and f) electroless plating via an auto-catalytic chemical reaction to produce nickel coatings on the metal. The procedure and nickel bath (e.g. nickel chloride+hydrated sodium hypophosphite (NaPO2H2O) for electroless plating is commercially available and cost-effective. Methods c and d are ideal for fabrication of active metals with very negative electrode potentials, such as Al, Mg, and so on, which may not be able to be achieved with other methods.
The advantages of the methods described herein are easy handling, and scalability of metal synthesis/cladding. The metal shell 36 produced by these processes can minimize oxidation of the MAX phase particles 34 during the spray process and permits a more efficient thermal deposition of the MAXMET composite 38, which in turn contributes to improved erosion resistance and abradability.
One or more embodiments have been described. Nevertheless, it will be understood that various modifications may be made. For example, the present disclosure seeks to provide a method to manufacture MAXMET particles by encapsulating the MAX phase particles in a metallic shell, the choice of which depends on the end use of the abradable, e.g. Ni shell for Ni-based abradable coating materials or Al shell for Al-based abradable coating materials. The metal shell minimizes oxidation of the MAX phase particles during the spray process and permits a more efficient thermal deposition of the MAXMET composite, which in turn contributes to improved erosion resistance and abradability. Accordingly, other embodiments are within the scope of the following claims.
The instant application is a divisional application of U.S. patent application Ser. No. 14/722,263, filed May 27, 2015, which claims benefit of U.S. Patent Application No. 62/003,159, filed May 27, 2014, and entitled “Chemistry Based Methods of Manufacture for Maxmet Composite Powders”, the disclosure of which is incorporated by reference herein in its entirety as if set forth at length.
Number | Name | Date | Kind |
---|---|---|---|
4374173 | Adamovic | Feb 1983 | A |
4741973 | Condit | May 1988 | A |
6190124 | Freling et al. | Feb 2001 | B1 |
6231969 | Knight et al. | May 2001 | B1 |
6410159 | Hermanek | Jun 2002 | B1 |
6916529 | Pabla | Jul 2005 | B2 |
7135240 | Fiala et al. | Nov 2006 | B2 |
7402206 | Isberg et al. | Jul 2008 | B2 |
7572313 | Palanisamy | Aug 2009 | B2 |
8017240 | Strock | Sep 2011 | B2 |
8192850 | Brinley | Jun 2012 | B2 |
9598972 | Strock | Mar 2017 | B2 |
9850566 | Zimmermann et al. | Dec 2017 | B2 |
10036402 | Amini et al. | Jul 2018 | B2 |
20020197155 | Howard et al. | Dec 2002 | A1 |
20030228483 | Fiala et al. | Dec 2003 | A1 |
20050155454 | Fiala et al. | Jul 2005 | A1 |
20050233160 | Fiala et al. | Oct 2005 | A1 |
20050262965 | Palanisamy | Dec 2005 | A1 |
20050275143 | Toth | Dec 2005 | A1 |
20070122639 | Fiala et al. | May 2007 | A1 |
20080131686 | Strock | Jun 2008 | A1 |
20090202814 | Jabado | Aug 2009 | A1 |
20100055492 | Barsoum et al. | Mar 2010 | A1 |
20120295825 | Dorfman et al. | Nov 2012 | A1 |
20140287149 | Zimmermann | Sep 2014 | A1 |
20150308281 | Strock | Oct 2015 | A1 |
20160024955 | Amini et al. | Jan 2016 | A1 |
20160230288 | Amini et al. | Aug 2016 | A1 |
20160289844 | Strock et al. | Oct 2016 | A1 |
20160333717 | Strock | Nov 2016 | A1 |
20170030214 | Strock et al. | Feb 2017 | A1 |
20180347390 | Wilson et al. | Dec 2018 | A1 |
Number | Date | Country |
---|---|---|
1141569 | Feb 1983 | CA |
104947029 | Sep 2015 | CN |
102015212400 | Jan 2017 | DE |
1908925 | Apr 2008 | EP |
03046247 | Jun 2003 | WO |
2012000742 | Jan 2012 | WO |
2017080645 | May 2017 | WO |
Entry |
---|
USPTO STIC, Search Report, Generated 2017 for U.S. Appl. No. 14/722,263. |
USPTO STIC, Search Report, dated Aug. 25, 2017 for U.S. Appl. No. 14/722,263, pp. 1-3. |
Number | Date | Country | |
---|---|---|---|
20200003125 A1 | Jan 2020 | US |
Number | Date | Country | |
---|---|---|---|
62003159 | May 2014 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 14722263 | May 2015 | US |
Child | 16539217 | US |