Patent Application
20160214176
This invention relates generally to the field of materials technology, and more specifically to methods of forming void-containing metal forms and components formed thereof.
Thermal barrier coatings (TBCs) are utilized on hot section components of modern gas turbine engines, including the combustion and turbine section components, in order to protect the underlying base materials from high temperatures resulting from the flow of hot gases through the engine. These hot gases can be well above the melting point of the base materials which are typically superalloy materials. In the evolution of such technologies, there is an ongoing need to produce coatings having a low thermal conductivity (to impart heat resistance to coated objects) while at the same time exhibiting robust strength and durability characteristics in terms of resistance to cracking, erosion, corrosion, impact fatigue/failure, impurity infiltration and de-lamination (i.e. spallation).
Heat resistance is often the limiting feature in the performance of modern gas turbine engines. For example, it is known that an increase of 100° F. (56° C.) in the turbine's firing temperature can provide a corresponding increase of 8-13% in output and 2-4% of improvement in simple-cycle efficiency. Thus, advances in cooling and coating technologies can provide significant incentives by increasing the power density and overall efficiency of a gas turbine engine.
Based on economic, environmental and overall-performance considerations, there is significant need to develop new materials and methods for increasing the heat resistance of gas-turbine components.
Ceramic TBCs are generally applied to an intermediate bond coat overlying the metal substrate. Suitable ceramic TBC materials include zirconia-containing materials—particularly chemically-stabilized zirconias (e.g., zirconium oxides blended with other metal oxides) such as yttria-stabilized zirconias (YSZs). The bond coat typically takes the form of an intermediate adhesion layer, which is often an alloy of the formula MCrAIX (in which “M” represents Fe, Ni or Co, and “X” represents Ta, Re, Y, Zr, Hf, Si, B or C), a simple aluminide (NiAI), or a platinum-modified aluminide ((Ni, Pt)AI). Most typically, the bond coat is an intermediate layer containing an alloy of MCrAIY.
Although bond coat materials such as MCrAlYs have proven effective as an intermediate layer to enhance adhesion and to accommodate differences in the thermal expansion between superalloy substrates and ceramic TBCs, the use of such layers is disadvantageous in terms of the complexity and cost of their production. This is true, for example, because MCrAIY layers are often applied using expensive and complex processes such as vapor deposition and various spraying techniques. There is also a significant need to develop alternative materials and methods to effectively adhere ceramic TBCs to the surface of metallic gas turbine components including superalloy components.
The invention is explained in the following description in view of the drawings that show:
The present inventors have discovered methods for coating substrates, including superalloy substrates, with metallic and/or ceramic materials to produce porous (void-containing) coatings having improved properties such as reduced thermal conductivity, increased adherence, and greater resistance to cracking, impact damage and spalling. The present inventors have innovatively developed a combination of steps for manufacturing coated materials having improved thermo-protective properties as well as coated materials produced using simpler coating and bonding techniques amenable to a variety of high-temperature applications and applications requiring robust bonding between layers.
One embodiment of the present invention is a method involving the application of an energy beam to a powdered material in contact with a substrate, such that a gas-generating agent undergoes a chemical reaction to produce a gaseous substance that imparts voids (pores) to a resulting coating adhered to the substrate. Another embodiment of the present invention is a method involving the application of an energy beam to a powdered material in contact with a substrate, such that a void-generating agent undergoes a physical process that imparts voids (pores) to a resulting coating adhered to the substrate. For example, during laser sintering of a ceramic such as zirconia, a fluxing agent such as a carbonate of calcium could be added. Laser induced decomposition of this compound could generate sufficient carbon monoxide and carbon dioxide to assist physical separation of the zirconia particulates for a sufficient time to enable sintering of the particulates without their full densification.
The term “energy beam” is used herein in a general sense to describe a narrow, propagating stream of particles or packets of energy. An energy beam as used in the present invention may include a light beam, a laser beam, a particle beam, a charged-particle beam, a molecular beam, etc., which upon contact with a material imparts kinetic (thermal) and/or electronic energy (or excitation) to the material.
The term “powdered material” is used herein in a general sense to describe a mixture, grouping, or aggregation of objects in particulate form. Powdered materials may include powdered metals, powdered alloys, powdered ceramics, powdered flux materials, powdered plastics, powdered glasses, powdered composites, powdered compounds, as well as other powdered ingredients, and mixtures thereof.
The terms “metal” and “metallic material” are used herein in a general sense to describe pure metals, semi-pure metals and metal alloys.
The term “superalloy” is used herein in a general sense to describe a highly corrosion and oxidation resistant alloy that exhibits excellent mechanical strength and resistance to creep at high temperatures, as well as good surface stability. Superalloys typically include a base alloying element of nickel, cobalt or nickel-iron. Examples of superalloys include alloys sold under the trademarks and brand names Hastelloy, Inconel alloys (e.g., IN 700, IN 738, IN 792, IN 939), Rene alloys (e.g., Rene N5, Rene 80, Rene 142), Haynes alloys, Mar M, CM 247, CM 247 LC, C 263, 718, X-750, ECY 768, 282, X45, PWA 1483 and CMSX (e.g., CMSX-4, CMSX-8, CMSX-10) single crystal alloys.
The terms “ceramic” and “ceramic material” are used herein in a general sense to describe inorganic, non-metallic solids having a crystalline, partly crystalline, or amorphous structure and containing inorganic compounds such as inorganic oxides, nitrides or carbides. Especially useful ceramic materials include metal stabilized zirconias such as yttria-stabilized zirconia (YSZ) which is a crystalline ceramic structure containing zirconium dioxide and yttrium oxide.
The term “gas-generating agent” is used herein in a general sense to describe a substance or mixture of substances capable of undergoing a physical or chemical transformation to produce and/or release a gaseous substance, or to otherwise impart a void or voids to a heated, or melted, or solidifying material. In some embodiments, the gas-generating agent undergoes a chemical reaction or decomposition process upon heating to produce at least one gaseous substance. In some embodiments, the gas-generating agent reacts with an additional agent upon heating, or in the absence of heating, to produce at least one gaseous substance.
The term “gaseous substance” is used herein in a general sense to describe an element, compound, composition, or mixture thereof, which is in the gas phase and expands to fill any surrounding space or containing vessel.
The term “void-generating agent” is used herein in a general sense to describe a substance or mixture of substances capable of undergoing a physical transformation to produce a void or voids within a heated, melted, or solidifying material—or capable of causing a physical transformation to a heated, melted, or solidifying material to produce a void or voids within the resulting material.
The term “flux material” is used herein in a general sense to describe a chemical agent employed in metallurgical and welding processes as a cleaning agent, flowing agent, purifying agent and/or shielding agent. Flux materials may be organic fluxes or inorganic fluxes, and may contain metal halides (such as zinc chloride and calcium fluoride), inorganic acids (such as hydrochloric acid, phosphoric acid and hydrobromic acid), mineral acid salts, organic acids (including fatty acids such as oleic acid and stearic acid) and dicarboxylic acids, organohalides, rosin compounds (such as abietic acid, pimaric acid, and other resin acids), polyols and solvents. Especially useful flux materials are the inorganic fluxes containing borax, borates, fluoroborates, metal halides (e.g, metal fluorides, metal chlorides, halogenides), acids and amines.
The terms “voids” and “void” are used herein in a general sense to describe spaces within a solid or liquid material, in which spaces may exist a gaseous substance or a mixture of gaseous substances, or in which spaces may exist a non-gaseous substance, a mixture of non-gaseous substances, or a mixture of gaseous and non-gaseous substances, or where the spaces may be empty. Any contents of the voids or void are generally distinguishable from the surrounding matrix of the solid material, advantageously and often in a manner resulting in a reduction in the thermal conductivity of the solid material relative to the same material without the void or voids. The shape of the voids or void is not limited and may include porous volumes of various sizes and shapes having regular, irregular, symmetrical, and non-symmetrical surfaces. Within a coating produced by an embodiment of the present invention, a void or voids may vary in size, shape and distribution.
The term “substrate” is used herein in a general sense to describe an object to which a coating is applied, or in which a coating is to be applied. Suitable substrates applicable to the present invention may include metallic substrates, ceramic substrates, glass substrates, plastic substrates, composite substrates, paper substrates, etc.
The term “surface” is used herein in a general sense to describe the surface of an uncoated, coated, or partially-coated substrate or material.
The terms “melt” or “melting” are used herein in a general sense to describe physical processes that result in a phase transition of a substance from a solid phase to the liquid phase by the application of radiation (e.g., heat) or pressure resulting in a rise in the temperature of the substance to its melting point. While these terms include situations in which there may be incomplete melting resulting in a mixture of both solid and liquid phases, their use is intended to distinguish the described process from sintering processes defined below.
The terms “sinter” and “sintering” are used herein in a general sense to describe physical processes in which powders, including metallic and ceramic powders, are transformed into objects based on atomic diffusion—as opposed to melting resulting in a phase transition of the powder into a liquid phase, although some surface melting of the powder may occur. In a sintering process of the present invention, the atoms in the powder particles diffuse across the boundaries of the particles, fusing the particles together and creating one solid piece. This diffusion is caused by a gradient of chemical potential—such that atoms move from an area of higher chemical potential to an area of lower chemical potential. The atoms may follow different paths to get from one position to another. These different paths occur by different sintering mechanisms.
In some embodiments the powdered material contains a material that produces or contains the base components of a structural substrate, a bond coating, or a thermal barrier coating (TBC). Examples of the materials contained in the powdered material include metallic materials, ceramic materials, glass material and plastic materials.
In some embodiments the powdered material contains the gas-generating (or void-generating) agent; while in other embodiments the powdered material does not initially contain the gas-generating (or void-generating) agent, and the gas-generating (or void-generating) agent is added to the powdered material before or after the application of the energy beam to the powdered material.
Embodiments of the present invention include both melting and sintering processes. In melting processes the energy beam melts the powdered material to form a melt pool, in which the gaseous substance is formed or directed, and the melt pool is then allowed to cool and solidify to form a void-containing coating. In sintering process the energy beam heats the powdered material such that atomic diffusion of the powder particles occurs over a certain timeframe to produce (upon cooling) a sintered coating.
In some embodiments the void-containing coating 16 is thermal barrier coating (TBC) in the form of a porous layer of a ceramic material bonded directly to the surface of a metallic substrate (such as a superalloy substrate). In other embodiments the void-containing coating 16 is a thermal barrier coating (TBC) in the form of a porous layer of a ceramic material bonded to an intervening bond coat layer which is bonded to the surface of a metallic substrate (such as a superalloy substrate). Thus, coating methods of the present invention can advantageously be applied directly to the surface of a substrate or, alternatively, may be applied to an intermediate layer (such as a bond coat) already present on the surface of the substrate.
In some embodiments the void-containing coating 16 is a bond coat in the form of an alloy material (such as an alloy of MCrAIY) bonded directly to the surface of a metallic substrate (such as a superalloy substrate). In other embodiments the void-containing coating 16 is porous metallic or alloy material bonded directly to the surface of a metallic substrate (such as a superalloy substrate)—such that the composition of the void-containing coating 16 (in terms of its elemental composition) may be identical to that of the metallic substrate or different from that of the metallic substrate.
Some embodiments enable the formation of a ceramic thermal barrier coating bonded to the surface of a metallic (superalloy) substrate without the need for a traditional (e.g., MCrAIY) bond coat. One variation of such embodiments involves the application of an intermediate porous bond coat, containing a similar or identical composition to that of the metallic (superalloy) substrate, upon which a ceramic thermal barrier coating is applied using tradition methods or using methods of the present invention.
Key features depicted in the coated substrate of
The ability to produce a heterogeneous coating of fine pores 24, which are predominantly non-connected (non-coalesced), is an important feature which is believed to be responsible in part for the improved mechanical and thermal properties of coatings of the present invention. In terms of thermal conductivity, the ability to control pore size, distribution and (to a certain extent) shape allows the thermal characteristics of TBCs and bond coats to be tuned and modulated in key portions of hot section components. Non-coalescence of the pores 24 is believed to improve crack resistance and to reduce impact fatigue and failure, because spherically-uniform (singular) pores are known to arrest cracks which inevitably form in coating structures. Thus, when cracks do form they can be arrested by an adjoining pore—thereby, preventing propagation of the crack into the underlying substrate 20. Coalesced pores would be expected to reduce crack resistance, because their elongated shape would tend to further propagate cracks.
Other important features depicted in
Gas-generating agents (GGAs) may include any substance which when heated is capable of undergoing a chemical reaction, either by itself or in the presence of an additional agent, to form a gaseous material. The suitability of a particular gas-generating agent will depend not only on its reactivity characteristics but also on the suitability of the resulting gaseous substance as a constituent of the resulting void-containing coating. Gaseous substances may include gases such as hydrogen (H2), carbon dioxide (CO2), carbon monoxide (CO), nitrogen (N2), oxygen (O2), water (H2O), hydrofluoric acid (HF), hydrochloric acid (HCl), sulfuric acid (H2SO4), fluorine (F2), nitrogen dioxide (NO2) and sulfur dioxide (SO2). In some embodiments the gaseous substance entrapped within a void (pore) may react or otherwise interact with the surrounding material to form a largely empty void (pore).
Examples of suitable gas-generating agents include elemental metals, metal alloys, metal oxides, metal hydrides, metal carbonates, metal carbonyls, metal carbides, metal halides, metal nitrides, metal nitrates, metal sulfates and mixtures thereof.
One preferred set of gas-generating agents includes water-reactive metals and metal compounds that react with water to form at least one gaseous substance. GGAs of this type generally react with water to form hydrogen. Examples of such reactions include the reaction of titanium hydride with water as shown in equation (I), and the reaction of yttrium with water as shown in equation (II):
TiH2+2 H2O→Ti(OH)2+H2 (I)
2 Y+6 H2O→Y2(OH)3+3 H2 (II)
Suitable water-reactive metals and metal hydrides include those containing elements within Groups IA, IIA, IIIB, IVB, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA and IVA of the Periodic Table. Particularly suitable water-reactive metals and metal hydrides include those containing elements within Periods 3-6 of the Period Table—such as Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Pd, Ag, In, Sn, Hf, Os, Pt, Au, Hg and Pb. Especially preferred water-reactive metals and metal hydrides include those containing the elements Al, Ti, V, Cr, Fe, Co, Ni, Y and Zr.
Other gas-generating agents include thermally-labile compounds that decompose or otherwise react to form gaseous products such as carbon dioxide. One example of such a reaction is the thermal decomposition of copper carbonate to form carbon dioxide as shown below in equation (III):
CuCO3→CuO+CO2 (III)
Suitable metal carbonates include those containing elements within Groups IA, IIA, IIIB, IVB, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA and IVA of the Periodic Table. Particularly suitable metal carbonates include those containing elements within Periods 3-6 of the Period Table—such as Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Pd, Ag, In, Sn, Hf, Os, Pt, Au, Hg and Pb. Especially preferred metal carbonates include those containing the elements Al, Ti, V, Cr, Fe, Co, Ni, Y and Zr. Still other carbonates could include magnesium and calcium carbonate to generate gaseous products.
Another example of such a reaction is the thermal reaction of calcium fluoride with an acidic source to form hydrofluoric acid as shown below in equation (IV):
CaF2+H2SO4→CaSO4+2 HF (IV)
Suitable metal fluorides include those containing elements within Groups IA, IIA, IIIB, IV, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA and IVA of the Periodic Table. Particularly suitable metal fluorides include those containing elements within Periods 3-6 of the Periodic Table. Especially preferred metal fluorides include those commonly found in flux materials, such as calcium fluoride.
Other gas-generating agents include certain metallic oxides which, in the environment of plasma generated by a laser beam, can react to form reactive metals or metal compounds. One example of a metallic oxide capable of forming a reactive metal when heated with a laser beam is yttrium oxide (Y2O3). Suitable metal oxides include those containing elements within Groups IIIB, IVB, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA and IVA of the Periodic Table. Particularly suitable metal oxides include those containing elements within Periods 4-6 of the Period Table—such as Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Pd, Ag, In, Sn, Hf, Os, Pt, Au, Hg and Pb. Especially preferred metal oxides include those containing the elements Ti, V, Cr, Fe, Co, Ni, Y and Zr.
In some embodiments the process further includes, prior to the heating with the energy beam, a step of exposing the powdered material to humidity in order to retain water which can react with certain gas-generating agents and the laser energy to form the gaseous substance.
The proportion of the gas-generating agent in the heated region ranges from 0.1 to 50 wt. % in various embodiments.
In some embodiments a preferred porosity of the void-containing layer ranges from 1% by volume to 50% by volume. In other embodiments (e.g., certain foamed metals) a porosity of the void-containing layer is at least 50% by volume, and advantageously from 50% to 85% by volume.
The flux material 32 and the resultant slag layer 36 provide a number of functions that are beneficial to the porous metallic and/or ceramic coating 38.
First, they function to shield both the region of molten material and the solidified (but still hot) cladding 38 from the atmosphere in the region downstream of the energy beam 10. The slag floats to the surface to separate the molten or hot metal/ceramic from the atmosphere, and the flux may be formulated to produce a shielding gas in some embodiments, thereby avoiding or minimizing the use of expensive inert gas.
Second, the slag 36 acts as a blanket allowing the solidified material to cool slowly and evenly, thereby reducing residual stresses than can contribute to post weld reheat or strain age cracking.
Third, the slag 36 helps to shape the melt pool 34 to keep it close to a desired height/width ratio. In some embodiments the height/width ratio is preferably a ratio of ⅓.
Fourth, the flux material 32 provides a cleansing effect for removing trace impurities such as sulfur and phosphorous which contribute to weld solidification cracking. Such cleansing may include de-oxidation when the powdered material contains a metal powder. Because the flux powder is in intimate contact with such a metal powder, it is especially effective in accomplishing this function.
Fifth, the flux material 32 may provide an energy absorption and trapping function to more effectively convert the energy beam 10 into heat energy, thus facilitating a more precise control of heat input, such as within 1-2%, and a resultant tight control of material temperature during the melting/solidifying process.
Sixth, the flux material 32 may be formulated to compensate for loss of volatized elements during the processing or to actively contribute elements to the melt flow 34 that are not otherwise provided by the powder material itself.
Finally, as illustrated in the embodiment of
The embodiment of
The embodiment of
The embodiment of
In other embodiments the powdered material, the flux material, the heated region, the melt pool and/or the jet may contain (or additionally contain) an exothermic agent which, upon heating with the energy beam, reacts over a time period to release additional heat. Embodiments employing the exothermic agent are especially useful in laser-induced sintering processes. In these embodiments use of the exothermic agent allows the use of a lower level of laser power to be applied which enables greater temperature control of the sintering processes. Such enhanced temperature control by using an exothermic agent can provide a more homogeneous heat distribution along the depth of the powdered material—thus producing porous sintered coatings having greater homogeneity and enhanced thermal and mechanical properties.
In some embodiments the exothermic agent is contained within a flux material contained within the powdered material. In other embodiments the exothermic agent is contained within a flux material placed (layered) on top of a layer of the powdered material. In other embodiments the exothermic agent is directed into the sintering powder by use of a jet containing a propellant gas and the exothermic agent which is propelled into a heated region using a nozzle.
In some embodiments the exothermic agent is selectively placed, fed or directed into the powdered material to produce varying proportions of the exothermic agent along the length, width or depth of the powdered material—such that the degree of sintering in corresponding portions of the sintered coating is different.
The exothermic agent may be any substance that undergoes a chemical reaction to produce heat. In some embodiments the exothermic agent is metal, metal alloy or metal composition which reacts with oxygen to produce heat. One example of such a reaction is the combustion of zirconium metal with oxygen to form zirconium (II) oxide as shown below in equation (A):
Zr(s)+O2→ZrO2(s) (A)
Other examples of similar exothermic reactions which may be useful for specific applications (other material bases) include:
Fe2O3+2Al→2Fe+Al2O3 (iron thermite) (B)
3CuO+2Al→3Cu+Al2O3 (copper thermite) (C)
Mn, Cr and Si thermites and even fluoropolymers (e.g. Teflon plus Mg plus Al) may be utilized.
Suitable combustible metals include those containing elements within Groups IA, IIA, IIIB, IVB, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA and IVA of the Periodic Table. Particularly suitable combustible metals include those containing elements within Periods 3-6 of the Period Table—such as Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Pd, Ag, In, Sn, Hf, Os, Pt, Au, Hg and Pb. Especially preferred water-reactive metals and metal hydrides include those containing the elements Al, Ti, V, Cr, Fe, Co, Ni, Y and Zr. Especially preferred combustible metals include Al, Ti, Ni, Zr and Ni-Al alloys (e.g., nickel aluminides).
In some embodiments the energy beam 10 is a laser beam. In order to entrap the gaseous substance 14 produced by the gas-generating agent 8 within a re-solidifying molten metal to optimize the formation of porosity, it may be desired to achieve a relatively rapid melting and re-solidification of the melt pool 34. Therefore, in some embodiments the energy beam 10 is a pulsed laser beam rather than a continuous energy source. By pulsing relatively short bursts of relatively high levels of energy followed by periods of no energy addition, it is possible to more effectively trap relatively smaller pockets of the gaseous substance 14 in the solidifying metal than when applying the same total amount of energy with a continuous energy beam source.
In some embodiments, laser and process parameters are adjusted to achieve a stirring action to further enhance the function of the gas-generating agent 8. For example, a high density beam can create a vapor supported depression within a melt pool 34 which, when moved from side to side, can act as a stirring element. Parameters may also be adjusted to achieve waves in the melt and/or a breaking action to disrupt (break apart) coalesced bubbles in the melt pool 34.
In some embodiments the energy beam is a diode laser beam having a generally rectangular cross-sectional shape. Other known types of energy beams may also be used, such as electron beam, plasma beam, one or more circular laser beams, a scanned laser beam, an integrated laser beam, etc. A rectangular shape may be particularly advantageous for embodiments having a relatively large area to be coated. Optical conditions and hardware optics used to generate a broad area laser exposure may include but are not limited to: defocusing of the laser beam; use of diode lasers that generate rectangular energy sources at focus; use of integrating optics such as segmented mirrors to generate rectangular energy sources at focus; scanning (rastering) of the laser beam in one or more dimensions; and the use of focusing optics of variable beam diameter (e.g, 0.5 mm at focus for fine detailed work varied to 2.0 mm at focus for less detailed work). In some embodiments the motion of the optics and/or substrate may be programmed as in a selective laser melting (SLM) or selective laser sintering (SLS) process to build a custom shape layer deposit.
Some embodiments employ the use of a base alloy feed material. Such a feed material may be in the form of a wire or strip that is fed or oscillated towards the substrate 4 and is melted by the energy beam to contribute to the melt pool 34. If desired, the feed material may be preheated (e.g., electrically) to reduce the overall energy required from the energy beam 10.
Processes of the present invention may be used to manufacture various components. By example,
Other components capable of being produced by processes of the present invention include medical devices such as ceramic prosthetic devices containing void-containing layers and coatings formed in the presence of a gas-generating (or void-generating) agent.
While various embodiments of the present invention have been shown and described herein, it will be obvious that such embodiments are provided by way of example only. Numerous variations, changes and substitutions may be made without departing from the invention herein. Accordingly, it is intended that the invention be limited only by the spirit and scope of the appended claims.
This application is a continuation-in-part of U.S. patent application Ser. No. 14/274,952 filed on 12 May 2014 (attorney docket 2014P07212US), the entire contents of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14274952 | May 2014 | US |
| Child | 14333543 | US |
