US20050230078A1 - Methods for manufacturing investment casting shells - Google Patents
Methods for manufacturing investment casting shells Download PDFInfo
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- US20050230078A1 US20050230078A1 US10/825,396 US82539604A US2005230078A1 US 20050230078 A1 US20050230078 A1 US 20050230078A1 US 82539604 A US82539604 A US 82539604A US 2005230078 A1 US2005230078 A1 US 2005230078A1
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- shell
- heating
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- composition
- strength
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C9/00—Moulds or cores; Moulding processes
- B22C9/10—Cores; Manufacture or installation of cores
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C9/00—Moulds or cores; Moulding processes
- B22C9/02—Sand moulds or like moulds for shaped castings
- B22C9/04—Use of lost patterns
- B22C9/043—Removing the consumable pattern
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C13/00—Moulding machines for making moulds or cores of particular shapes
- B22C13/08—Moulding machines for making moulds or cores of particular shapes for shell moulds or shell cores
- B22C13/085—Moulding machines for making moulds or cores of particular shapes for shell moulds or shell cores by investing a lost pattern
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C7/00—Patterns; Manufacture thereof so far as not provided for in other classes
- B22C7/02—Lost patterns
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C9/00—Moulds or cores; Moulding processes
- B22C9/12—Treating moulds or cores, e.g. drying, hardening
Definitions
- the invention relates to investment casting. More particularly, the invention relates to investment casting using molds having oxidizable cores.
- Investment casting is a commonly used technique for forming metallic components having complex geometries, especially hollow components, and is used in the fabrication of superalloy gas turbine engine components.
- Gas turbine engines are widely used in applications including aircraft propulsion, electric power generation, ship propulsion, and pumps. In gas turbine engine applications, efficiency is a prime objective.
- Cooling is typically provided by flowing relatively cool air from the compressor section of the engine through passages in the turbine components to be cooled. Such cooling comes with an associated cost in engine efficiency. Consequently, there is a strong desire to provide enhanced specific cooling, maximizing the amount of cooling benefit obtained from a given amount of cooling air. This may be obtained by the use of fine, precisely located, cooling passageway sections.
- a mold is prepared having one or more mold cavities, each having a shape generally corresponding to the part to be cast.
- An exemplary process for preparing the mold involves the use of one or more wax patterns of the part. The patterns are formed by molding wax over ceramic cores generally corresponding to positives of the cooling passages within the parts.
- a ceramic shell is formed around one or more such patterns in well known fashion. The wax may be removed such as by melting in an autoclave. The shell may be fired to strengthen the shell. This leaves a mold comprising the shell having one or more part-defining compartments which, in turn, contain the ceramic core(s) defining the cooling passages.
- Molten alloy may then be introduced to the mold to cast the part(s). Upon cooling and solidifying of the alloy, the shell and core may be mechanically and/or chemically removed from the molded part(s). The part(s) can then be machined and/or treated in one or more stages.
- the ceramic cores themselves may be formed by molding a mixture of ceramic powder and binder material by injecting the mixture into hardened metal dies. After removal from the dies, the green cores are thermally post-processed to remove the binder and fired to sinter the ceramic powder together.
- the trend toward finer cooling features has taxed core manufacturing techniques. The fine features may be difficult to manufacture and/or, once manufactured, may prove fragile.
- Commonly-assigned co-pending U.S. Pat. No. 6,637,500 of Shah et al. discloses various examples of a ceramic and refractory metal core combination. Various refractory metals, however, tend to oxidize at high temperatures in the vicinity of the temperatures used to fire the shell. Thus, the shell firing may degrade the refractory metal cores and, thereby produce potentially unsatisfactory part internal features. Accordingly, there remains room for further improvement in such cores and their manufacturing techniques.
- One aspect of the invention involves a method for forming an investment casting mold.
- a shell is formed over a pattern comprising a hydrocarbon-based body with a refractory metal-based core at least partially embedded in the body.
- the body is then substantially removed from the shell.
- the shell is strengthened by heating in a first atmosphere of a first composition.
- the shell is further strengthened by heating in a vacuum or second atmosphere of a second composition, different than the first composition.
- the heating of the further strengthening step may be a preheating prior to an introduction of molten metal to the mold.
- the first composition may be more oxidative than the second composition.
- the method may be used to fabricate a gas turbine engine airfoil element such as a blade or vane.
- the first composition may consist, in major part (e.g., by volume), of air.
- the second composition may consist, in major part, of one or more inert gases.
- the first composition may have an oxygen partial pressure of at least 15 kPa.
- the second composition may have an oxygen partial pressure of no more than 10 kPa.
- the strengthening may be effective to provide the shell with a first modulus of rupture (MOR) strength of 65-80% of a maximum MOR strength.
- the further strengthening may be effective to provide the shell with a second MOR strength of at least 85% of said maximum MOR strength. After the substantial removal of the body, the shell may have a preliminary MOR strength of no more than 50% of said maximum MOR strength.
- Another aspect of the invention involves a method for investment casting.
- a casting mold may be formed.
- Molten metal may be introduced to the mold.
- the molten metal may be permitted to solidify.
- the mold may be destructively removed.
- the temperature of the shell does not fall below a threshold (such as 1200 F) between the further strengthening and the introduction of the molten metal.
- Another aspect of the invention involves a method for forming an investment casting mold.
- One or more coating layers are applied to a sacrificial pattern having a wax first portion and a second portion comprising refractory metal.
- a steam dewaxing may remove a major portion of the pattern first portion and leave the second portion within a shell formed by the coating layers.
- There may be a first heating of the shell to harden the shell and remove residues or byproducts of the wax. This first heating may be effective to provide the shell with a first modulus of rupture (MOR) strength no more than 85% of a maximum MOR strength.
- a second heating of the shell may strengthen the shell to a second MOR strength.
- MOR modulus of rupture
- the first heating may be in an oxidizing atmosphere and the second heating may be in vacuum or an inert atmosphere.
- the second heating may be a preheating prior to molten metal introduction.
- the first MOR strength may be 65-80% of the maximum MOR strength.
- the second heating may be effective so that the second MOR strength is at least 85% of the maximum MOR strength.
- the first heating may have a peak temperature between 800 F and 1100 F.
- the second heating may have a peak temperature in excess of 1500 F.
- the first heating may have a temperature between 800 F and 1100 F for at least 2.0 hours.
- the second heating may have a temperature in excess of 1500 F for at least 1.0 hour.
- the second portion may comprise the refractory metal core, a coating on the refractory metal core, and a ceramic core secured to the refractory metal core prior to the applying.
- Another aspect of the invention involves a method for forming an investment casting mold.
- One or more coating layers are applied to a sacrificial pattern having a first portion for forming a mold void and a second portion for forming a portion of the mold.
- a major portion of the pattern first portion is removed leaving the second portion within a shell formed by the coating layers.
- the shell is initially hardened effective to provide the shell with a first modulus of rupture (MOR) strength no more than 85% of a maximum MOR strength.
- MOR modulus of rupture
- the shell is further hardened without substantial degradation of the pattern second portion.
- the method may be used to fabricate a gas turbine engine component.
- the second step may be essentially performed under an oxygen partial pressure of at least 20 kPa.
- the third step may be essentially performed under an oxygen partial pressure of no more than 5 kPa.
- Another aspect of the invention involves a system for forming an investment casting mold.
- Means are provided for forming a shell over a pattern.
- the pattern comprises a hydrocarbon-based body with a refractory metal-based core at least partially embedded in the body.
- Means are provided for substantially removing the body from the shell.
- Means are provided for strengthening the shell by heating in a first atmosphere of a first composition.
- Means are provided for further strengthening of the shell by heating in a vacuum or a second atmosphere of a second composition, different than the first composition.
- FIG. 1 is a flowchart of a first mold manufacturing process according to principles of the invention.
- FIG. 2 is a flowchart of a second mold manufacturing process according to principles of the invention.
- FIG. 1 shows an exemplary method 20 for forming an investment casting mold.
- One or more metallic core elements are formed 22 (e.g., of refractory metals such as molybdenum and niobium by stamping or otherwise cutting from sheet metal) and coated 24 .
- Suitable coating materials include silica, alumina, zirconia, chromia, mullite and hafnia.
- CTE coefficient of thermal expansion
- Coatings may be applied by any appropriate technique (e.g., CVD, PVD, electrophoresis, and sol gel techniques). Individual layers may typically be 0.1 to 1 mil thick.
- Metallic layers of Pt, other noble metals, Cr, and Al may be applied to the metallic core elements for oxidation protection, in combination with a ceramic coating for protection from molten metal erosion and dissolution.
- One or more ceramic cores are also formed 26 (e.g., of silica in a molding and firing process).
- One or more of the coated metallic core elements (hereafter refractory metal cores (RMCs)) are assembled 28 to one or more of the ceramic cores.
- RMCs refractory metal cores
- the core assembly is then overmolded 30 with an easily sacrificed material such as a natural or synthetic wax (e.g., via placing the assembly in a mold and molding the wax around it). There may be multiple such assemblies involved in a given mold.
- the overmolded core assembly (or group of assemblies) forms a casting pattern with an exterior shape largely corresponding to the exterior shape of the part to be cast.
- the pattern may then be assembled 32 to a shelling fixture (e.g., via wax welding between end plates of the fixture).
- the pattern may then be shelled 34 (e.g., via one or more stages of slurry dipping, slurry spraying, or the like).
- the drying provides the shell with at least sufficient strength or other physical integrity properties to permit subsequent processing.
- the shell containing the invested core assembly may be disassembled 38 fully or partially from the shelling fixture and then transferred 40 to a dewaxer (e.g., a steam autoclave).
- a dewaxer e.g., a steam autoclave
- a steam dewax process 42 removes a major portion of the wax leaving the core assembly secured within the shell.
- the shell and core assembly will largely form the ultimate mold.
- the dewax process typically leaves a wax or byproduct hydrocarbon residue on the shell interior and core assembly.
- the shell is transferred 44 to an atmospheric furnace (e.g., containing air or other oxidizing atmosphere) in which it is heated 46 to a first peak temperature and for a first time duration effective to prestrengthen the shell.
- the heating 46 may also remove any remaining wax residue (e.g., by vaporization) and/or converting hydrocarbon residue to carbon.
- Oxygen in the atmosphere reacts with the carbon to form carbon dioxide. Removal of the carbon is advantageous to avoid the carbon clogging the vacuum pumps used in subsequent stages of operation. This burning off of the carbon may be generally coincident with oxidation of the shell associated with the advantageous prestrengthening of the shell.
- An exemplary prestrengthening provides the shell with a fraction of its ultimate (e.g., the maximum fully-fired) modulus of rupture (MOR) strength (e.g., 50-90%, more narrowly 60-85% or 65-80%).
- MOR modulus of rupture
- industry practice generally associates firing at a temperature of at least 1500 F for a duration of at least one hour as essentially fully firing the shell to achieve essentially maximum MOR strength.
- the shell is maintained at least generally isothermal for at least this period. This may represent an increase from well below 50% of ultimate MOR strength in the relatively green state immediately post-dewax.
- the pre-harden temperature is, advantageously, sufficiently low, in view of the oxidizing nature of the atmosphere in the atmospheric furnace to avoid substantial oxidation of the metallic core element(s).
- oxidation is still a substantial potential problem due to the presence of microcracks and porosity in the coating. Oxidation can produce coating delamination or other damage and surface irregularities on the metallic core. Coating damage may allow vaporization of the metallic core elements at the high subsequent casting temperatures and/or reactions between the casting alloy and the metallic core elements. Surface irregularities caused by the oxidation may, in turn form imperfections in the associated interior surfaces of the cast part—a particular problem where fine features are being formed.
- the exemplary peak preharden temperature is less than 1150 F (e.g., 800-1100 F) for a preharden time of 2-4 hours.
- An exemplary preharden temperature and time is about 1000 F for about 3.5 hours.
- the mold may be removed from the atmospheric furnace, allowed to cool, and inspected 48 .
- the mold may be seeded 50 by placing a metallic seed in the mold to establish the ultimate crystal structure of a directionally solidified (DS) casting or a single-crystal (SX) casting. Nevertheless the present teachings may be applied to other DS and SX casting techniques (e.g., wherein the shell geometry defines a grain selector) or to casting of other microstructures.
- the mold may have The mold may be transferred 52 to a casting furnace (e.g., placed atop a chill plate in the furnace).
- the casting furnace may be pumped down to vacuum 54 or charged with a non-oxidizing atmosphere (e.g., inert gas) to prevent oxidation of the casting alloy.
- the casting furnace is heated 56 to preheat the mold.
- This preheating serves two purposes: to further harden and strengthen the shell (e.g., by at least 5% more of ultimate MOR strength); and to preheat the shell for the introduction of molten alloy to prevent thermal shock and premature solidification of the alloy.
- the preheat temperature and duration are advantageously sufficient to substantially further harden the shell above its prehardened condition. This may involve sintering of the ceramic particles within the shell.
- Advantageous MOR is in excess of 85%, and more particularly, in excess of 90 or 95% of ultimate MOR.
- Exemplary preheat times are approximately one hour (e.g., 0.25-4.0 hours, more narrowly, 0.75-2.0 hours).
- the molten alloy is poured 58 into the mold and the mold is allowed to cool to solidify 60 the alloy (e.g., after withdrawal from the furnace hot zone).
- the vacuum may be broken 62 and the chilled mold removed 64 from the casting furnace.
- the shell may be removed in a deshelling process 66 (e.g., mechanical breaking of the shell) and the core assembly removed in a decoring process 68 (e.g., a chemical process) to leave a cast article (e.g., a metallic precursor of the ultimate part).
- the cast article may be machined 70 , chemically and/or thermally treated 72 and coated 74 to form the ultimate part.
- FIG. 2 shows an alternate version 100 of the exemplary process wherein like steps are shown with like numerals.
- the alternate process separates the firing from the preheating.
- the prehardened mold is transferred 102 to a nonatmospheric furnace which may be separate from the casting furnace in which casting subsequently occurs.
- the nonatmospheric furnace may be pumped down 104 to vacuum (and/or charged with an inert atmosphere such as a noble gas or mixture thereof).
- the mold may be fired 106 at a temperature and duration similar to the preheat 56 .
- the vacuum may be broken 108 (or inert atmosphere otherwise vented) and the mold removed 110 .
- a pump down 118 may be similar to the pump down 54 .
- a preheat 120 may be similar to the preheat 56 or more abrupt as the firing function will, at least largely, already have taken place.
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Abstract
Description
- (1) Field of the Invention
- The invention relates to investment casting. More particularly, the invention relates to investment casting using molds having oxidizable cores.
- (2) Description of the Related Art
- Investment casting is a commonly used technique for forming metallic components having complex geometries, especially hollow components, and is used in the fabrication of superalloy gas turbine engine components.
- Gas turbine engines are widely used in applications including aircraft propulsion, electric power generation, ship propulsion, and pumps. In gas turbine engine applications, efficiency is a prime objective.
- Improved gas turbine engine efficiency can be obtained by operating at higher temperatures, however current operating temperatures in the turbine section exceed the melting points of the superalloy materials used in turbine components. Consequently, it is a general practice to provide air cooling. Cooling is typically provided by flowing relatively cool air from the compressor section of the engine through passages in the turbine components to be cooled. Such cooling comes with an associated cost in engine efficiency. Consequently, there is a strong desire to provide enhanced specific cooling, maximizing the amount of cooling benefit obtained from a given amount of cooling air. This may be obtained by the use of fine, precisely located, cooling passageway sections.
- A well developed field exists regarding the investment casting of internally-cooled turbine engine parts such as blades and vanes. In an exemplary process, a mold is prepared having one or more mold cavities, each having a shape generally corresponding to the part to be cast. An exemplary process for preparing the mold involves the use of one or more wax patterns of the part. The patterns are formed by molding wax over ceramic cores generally corresponding to positives of the cooling passages within the parts. In a shelling process, a ceramic shell is formed around one or more such patterns in well known fashion. The wax may be removed such as by melting in an autoclave. The shell may be fired to strengthen the shell. This leaves a mold comprising the shell having one or more part-defining compartments which, in turn, contain the ceramic core(s) defining the cooling passages. Molten alloy may then be introduced to the mold to cast the part(s). Upon cooling and solidifying of the alloy, the shell and core may be mechanically and/or chemically removed from the molded part(s). The part(s) can then be machined and/or treated in one or more stages.
- The ceramic cores themselves may be formed by molding a mixture of ceramic powder and binder material by injecting the mixture into hardened metal dies. After removal from the dies, the green cores are thermally post-processed to remove the binder and fired to sinter the ceramic powder together. The trend toward finer cooling features has taxed core manufacturing techniques. The fine features may be difficult to manufacture and/or, once manufactured, may prove fragile. Commonly-assigned co-pending U.S. Pat. No. 6,637,500 of Shah et al. discloses various examples of a ceramic and refractory metal core combination. Various refractory metals, however, tend to oxidize at high temperatures in the vicinity of the temperatures used to fire the shell. Thus, the shell firing may degrade the refractory metal cores and, thereby produce potentially unsatisfactory part internal features. Accordingly, there remains room for further improvement in such cores and their manufacturing techniques.
- One aspect of the invention involves a method for forming an investment casting mold. A shell is formed over a pattern comprising a hydrocarbon-based body with a refractory metal-based core at least partially embedded in the body. The body is then substantially removed from the shell. The shell is strengthened by heating in a first atmosphere of a first composition. The shell is further strengthened by heating in a vacuum or second atmosphere of a second composition, different than the first composition.
- In various implementations, the heating of the further strengthening step may be a preheating prior to an introduction of molten metal to the mold. The first composition may be more oxidative than the second composition. The method may be used to fabricate a gas turbine engine airfoil element such as a blade or vane. The first composition may consist, in major part (e.g., by volume), of air. The second composition may consist, in major part, of one or more inert gases. The first composition may have an oxygen partial pressure of at least 15 kPa. The second composition may have an oxygen partial pressure of no more than 10 kPa. The strengthening may be effective to provide the shell with a first modulus of rupture (MOR) strength of 65-80% of a maximum MOR strength. The further strengthening may be effective to provide the shell with a second MOR strength of at least 85% of said maximum MOR strength. After the substantial removal of the body, the shell may have a preliminary MOR strength of no more than 50% of said maximum MOR strength.
- Another aspect of the invention involves a method for investment casting. Such a casting mold may be formed. Molten metal may be introduced to the mold. The molten metal may be permitted to solidify. The mold may be destructively removed. In various implementations, the temperature of the shell does not fall below a threshold (such as 1200 F) between the further strengthening and the introduction of the molten metal.
- Another aspect of the invention involves a method for forming an investment casting mold. One or more coating layers are applied to a sacrificial pattern having a wax first portion and a second portion comprising refractory metal. A steam dewaxing may remove a major portion of the pattern first portion and leave the second portion within a shell formed by the coating layers. There may be a first heating of the shell to harden the shell and remove residues or byproducts of the wax. This first heating may be effective to provide the shell with a first modulus of rupture (MOR) strength no more than 85% of a maximum MOR strength. A second heating of the shell may strengthen the shell to a second MOR strength.
- In various implementations, the first heating may be in an oxidizing atmosphere and the second heating may be in vacuum or an inert atmosphere. The second heating may be a preheating prior to molten metal introduction. The first MOR strength may be 65-80% of the maximum MOR strength. The second heating may be effective so that the second MOR strength is at least 85% of the maximum MOR strength. The first heating may have a peak temperature between 800 F and 1100 F. The second heating may have a peak temperature in excess of 1500 F. The first heating may have a temperature between 800 F and 1100 F for at least 2.0 hours. The second heating may have a temperature in excess of 1500 F for at least 1.0 hour. The second portion may comprise the refractory metal core, a coating on the refractory metal core, and a ceramic core secured to the refractory metal core prior to the applying.
- Another aspect of the invention involves a method for forming an investment casting mold. One or more coating layers are applied to a sacrificial pattern having a first portion for forming a mold void and a second portion for forming a portion of the mold. In a first step, a major portion of the pattern first portion is removed leaving the second portion within a shell formed by the coating layers. In a second step, the shell is initially hardened effective to provide the shell with a first modulus of rupture (MOR) strength no more than 85% of a maximum MOR strength. In a third step, the shell is further hardened without substantial degradation of the pattern second portion.
- In various implementations, the method may be used to fabricate a gas turbine engine component. The second step may be essentially performed under an oxygen partial pressure of at least 20 kPa. The third step may be essentially performed under an oxygen partial pressure of no more than 5 kPa.
- Another aspect of the invention involves a system for forming an investment casting mold. Means are provided for forming a shell over a pattern. The pattern comprises a hydrocarbon-based body with a refractory metal-based core at least partially embedded in the body. Means are provided for substantially removing the body from the shell. Means are provided for strengthening the shell by heating in a first atmosphere of a first composition. Means are provided for further strengthening of the shell by heating in a vacuum or a second atmosphere of a second composition, different than the first composition.
- The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
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FIG. 1 is a flowchart of a first mold manufacturing process according to principles of the invention. -
FIG. 2 is a flowchart of a second mold manufacturing process according to principles of the invention. - Like reference numbers and designations in the various drawings indicate like elements.
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FIG. 1 shows anexemplary method 20 for forming an investment casting mold. One or more metallic core elements are formed 22 (e.g., of refractory metals such as molybdenum and niobium by stamping or otherwise cutting from sheet metal) and coated 24. Suitable coating materials include silica, alumina, zirconia, chromia, mullite and hafnia. Preferably, the coefficient of thermal expansion (CTE) of the refractory metal and the coating are similar. Coatings may be applied by any appropriate technique (e.g., CVD, PVD, electrophoresis, and sol gel techniques). Individual layers may typically be 0.1 to 1 mil thick. Metallic layers of Pt, other noble metals, Cr, and Al may be applied to the metallic core elements for oxidation protection, in combination with a ceramic coating for protection from molten metal erosion and dissolution. - One or more ceramic cores are also formed 26 (e.g., of silica in a molding and firing process). One or more of the coated metallic core elements (hereafter refractory metal cores (RMCs)) are assembled 28 to one or more of the ceramic cores. The core assembly is then overmolded 30 with an easily sacrificed material such as a natural or synthetic wax (e.g., via placing the assembly in a mold and molding the wax around it). There may be multiple such assemblies involved in a given mold.
- The overmolded core assembly (or group of assemblies) forms a casting pattern with an exterior shape largely corresponding to the exterior shape of the part to be cast. The pattern may then be assembled 32 to a shelling fixture (e.g., via wax welding between end plates of the fixture). The pattern may then be shelled 34 (e.g., via one or more stages of slurry dipping, slurry spraying, or the like). After the shell is built up, it may be dried 36. The drying provides the shell with at least sufficient strength or other physical integrity properties to permit subsequent processing. For example, the shell containing the invested core assembly may be disassembled 38 fully or partially from the shelling fixture and then transferred 40 to a dewaxer (e.g., a steam autoclave). In the dewaxer, a
steam dewax process 42 removes a major portion of the wax leaving the core assembly secured within the shell. The shell and core assembly will largely form the ultimate mold. However, the dewax process typically leaves a wax or byproduct hydrocarbon residue on the shell interior and core assembly. - After the dewax, the shell is transferred 44 to an atmospheric furnace (e.g., containing air or other oxidizing atmosphere) in which it is heated 46 to a first peak temperature and for a first time duration effective to prestrengthen the shell. The
heating 46 may also remove any remaining wax residue (e.g., by vaporization) and/or converting hydrocarbon residue to carbon. Oxygen in the atmosphere reacts with the carbon to form carbon dioxide. Removal of the carbon is advantageous to avoid the carbon clogging the vacuum pumps used in subsequent stages of operation. This burning off of the carbon may be generally coincident with oxidation of the shell associated with the advantageous prestrengthening of the shell. An exemplary prestrengthening provides the shell with a fraction of its ultimate (e.g., the maximum fully-fired) modulus of rupture (MOR) strength (e.g., 50-90%, more narrowly 60-85% or 65-80%). For typical shell materials, industry practice generally associates firing at a temperature of at least 1500 F for a duration of at least one hour as essentially fully firing the shell to achieve essentially maximum MOR strength. In common practice the shell is maintained at least generally isothermal for at least this period. This may represent an increase from well below 50% of ultimate MOR strength in the relatively green state immediately post-dewax. The pre-harden temperature is, advantageously, sufficiently low, in view of the oxidizing nature of the atmosphere in the atmospheric furnace to avoid substantial oxidation of the metallic core element(s). Despite the presence of the protective coating, oxidation is still a substantial potential problem due to the presence of microcracks and porosity in the coating. Oxidation can produce coating delamination or other damage and surface irregularities on the metallic core. Coating damage may allow vaporization of the metallic core elements at the high subsequent casting temperatures and/or reactions between the casting alloy and the metallic core elements. Surface irregularities caused by the oxidation may, in turn form imperfections in the associated interior surfaces of the cast part—a particular problem where fine features are being formed. The exemplary peak preharden temperature is less than 1150 F (e.g., 800-1100 F) for a preharden time of 2-4 hours. An exemplary preharden temperature and time is about 1000 F for about 3.5 hours. - After the prehardening, the mold may be removed from the atmospheric furnace, allowed to cool, and inspected 48. The mold may be seeded 50 by placing a metallic seed in the mold to establish the ultimate crystal structure of a directionally solidified (DS) casting or a single-crystal (SX) casting. Nevertheless the present teachings may be applied to other DS and SX casting techniques (e.g., wherein the shell geometry defines a grain selector) or to casting of other microstructures. Alternatively, the mold may have The mold may be transferred 52 to a casting furnace (e.g., placed atop a chill plate in the furnace). The casting furnace may be pumped down to
vacuum 54 or charged with a non-oxidizing atmosphere (e.g., inert gas) to prevent oxidation of the casting alloy. The casting furnace is heated 56 to preheat the mold. This preheating serves two purposes: to further harden and strengthen the shell (e.g., by at least 5% more of ultimate MOR strength); and to preheat the shell for the introduction of molten alloy to prevent thermal shock and premature solidification of the alloy. Accordingly, the preheat temperature and duration are advantageously sufficient to substantially further harden the shell above its prehardened condition. This may involve sintering of the ceramic particles within the shell. Advantageous MOR is in excess of 85%, and more particularly, in excess of 90 or 95% of ultimate MOR. This may be achieved with a preheat temperature of at least 1200 F, more particularly, at least 1400 F with an exemplary preheat temperature of about 1600 F. Exemplary preheat times are approximately one hour (e.g., 0.25-4.0 hours, more narrowly, 0.75-2.0 hours). - After preheating and while still under vacuum conditions, the molten alloy is poured 58 into the mold and the mold is allowed to cool to solidify 60 the alloy (e.g., after withdrawal from the furnace hot zone). After solidification, the vacuum may be broken 62 and the chilled mold removed 64 from the casting furnace. The shell may be removed in a deshelling process 66 (e.g., mechanical breaking of the shell) and the core assembly removed in a decoring process 68 (e.g., a chemical process) to leave a cast article (e.g., a metallic precursor of the ultimate part). The cast article may be machined 70, chemically and/or thermally treated 72 and coated 74 to form the ultimate part.
-
FIG. 2 shows analternate version 100 of the exemplary process wherein like steps are shown with like numerals. The alternate process, however, separates the firing from the preheating. Thus, after theinspection 48, the prehardened mold is transferred 102 to a nonatmospheric furnace which may be separate from the casting furnace in which casting subsequently occurs. After transfer, the nonatmospheric furnace may be pumped down 104 to vacuum (and/or charged with an inert atmosphere such as a noble gas or mixture thereof). After the pump down, the mold may be fired 106 at a temperature and duration similar to thepreheat 56. After firing, the vacuum may be broken 108 (or inert atmosphere otherwise vented) and the mold removed 110. After the removal, there may be asubsequent inspection 112, temporary storage, additional processing, and the like. Thereafter, the mold may be seeded 114 and transferred 116 to the casting furnace. A pump down 118 may be similar to the pump down 54. Apreheat 120 may be similar to thepreheat 56 or more abrupt as the firing function will, at least largely, already have taken place. - One or more embodiments of the present invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. For example, the principles may be implemented as modifications of existing or yet-developed processes in which cases those processes would influence or dictate parameters of the implementation. Accordingly, other embodiments are within the scope of the following claims.
Claims (26)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/825,396 US6951239B1 (en) | 2004-04-15 | 2004-04-15 | Methods for manufacturing investment casting shells |
| KR1020050027511A KR100619195B1 (en) | 2004-04-15 | 2005-04-01 | Methods and apparatus for forming an investment casting mold |
| SG200502024A SG116594A1 (en) | 2004-04-15 | 2005-04-05 | Methods for manufacturing investment casting shells. |
| CA002504059A CA2504059A1 (en) | 2004-04-15 | 2005-04-11 | Methods for manufacturing investment casting shells |
| RU2005111092/02A RU2299111C2 (en) | 2004-04-15 | 2005-04-15 | Method (variants) and apparatus for making casting mold for casting with use of investment patterns and method for casting with use of investment patterns (variants) |
| CNA2005100674185A CN1683098A (en) | 2004-04-15 | 2005-04-15 | Methods for manufacturing investment casting shells |
| DE602005007420T DE602005007420D1 (en) | 2004-04-15 | 2005-04-15 | Apparatus and method for producing a cast body for use in Genauguss |
| EP05252383A EP1600230B1 (en) | 2004-04-15 | 2005-04-15 | System and Method for manufacturing investment casting shells |
| AT05252383T ATE397983T1 (en) | 2004-04-15 | 2005-04-15 | APPARATUS AND METHOD FOR PRODUCING A CAST BODY FOR USE IN PRECISE CASTING |
| JP2005118007A JP2005297067A (en) | 2004-04-15 | 2005-04-15 | Method for forming investment casting mold, forming system and investment casting method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/825,396 US6951239B1 (en) | 2004-04-15 | 2004-04-15 | Methods for manufacturing investment casting shells |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| US6951239B1 US6951239B1 (en) | 2005-10-04 |
| US20050230078A1 true US20050230078A1 (en) | 2005-10-20 |
Family
ID=34940869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/825,396 Expired - Lifetime US6951239B1 (en) | 2004-04-15 | 2004-04-15 | Methods for manufacturing investment casting shells |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6951239B1 (en) |
| EP (1) | EP1600230B1 (en) |
| JP (1) | JP2005297067A (en) |
| KR (1) | KR100619195B1 (en) |
| CN (1) | CN1683098A (en) |
| AT (1) | ATE397983T1 (en) |
| CA (1) | CA2504059A1 (en) |
| DE (1) | DE602005007420D1 (en) |
| RU (1) | RU2299111C2 (en) |
| SG (1) | SG116594A1 (en) |
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| US20070068649A1 (en) * | 2005-09-28 | 2007-03-29 | Verner Carl R | Methods and materials for attaching ceramic and refractory metal casting cores |
| WO2014175940A3 (en) * | 2013-03-01 | 2015-02-26 | United Technologies Corporation | Gas turbine engine component manufacturing method and core for making same |
| WO2020030881A1 (en) * | 2018-08-07 | 2020-02-13 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Ceramic coating for foundry core |
| WO2025034166A1 (en) * | 2023-08-04 | 2025-02-13 | Agency For Science, Technology And Research | Improved formulation of water-soluble ceramic cores for investment casting to enhance high temperature structural integrity |
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- 2005-04-05 SG SG200502024A patent/SG116594A1/en unknown
- 2005-04-11 CA CA002504059A patent/CA2504059A1/en not_active Abandoned
- 2005-04-15 AT AT05252383T patent/ATE397983T1/en not_active IP Right Cessation
- 2005-04-15 DE DE602005007420T patent/DE602005007420D1/en not_active Expired - Lifetime
- 2005-04-15 CN CNA2005100674185A patent/CN1683098A/en active Pending
- 2005-04-15 JP JP2005118007A patent/JP2005297067A/en active Pending
- 2005-04-15 RU RU2005111092/02A patent/RU2299111C2/en not_active IP Right Cessation
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| US20070068649A1 (en) * | 2005-09-28 | 2007-03-29 | Verner Carl R | Methods and materials for attaching ceramic and refractory metal casting cores |
| WO2014175940A3 (en) * | 2013-03-01 | 2015-02-26 | United Technologies Corporation | Gas turbine engine component manufacturing method and core for making same |
| EP2961547A4 (en) * | 2013-03-01 | 2016-11-23 | United Technologies Corp | Gas turbine engine component manufacturing method and core for making same |
| WO2020030881A1 (en) * | 2018-08-07 | 2020-02-13 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Ceramic coating for foundry core |
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| WO2025034166A1 (en) * | 2023-08-04 | 2025-02-13 | Agency For Science, Technology And Research | Improved formulation of water-soluble ceramic cores for investment casting to enhance high temperature structural integrity |
Also Published As
| Publication number | Publication date |
|---|---|
| DE602005007420D1 (en) | 2008-07-24 |
| RU2299111C2 (en) | 2007-05-20 |
| CN1683098A (en) | 2005-10-19 |
| EP1600230B1 (en) | 2008-06-11 |
| KR20060045420A (en) | 2006-05-17 |
| EP1600230A1 (en) | 2005-11-30 |
| US6951239B1 (en) | 2005-10-04 |
| CA2504059A1 (en) | 2005-10-15 |
| SG116594A1 (en) | 2005-11-28 |
| ATE397983T1 (en) | 2008-07-15 |
| JP2005297067A (en) | 2005-10-27 |
| KR100619195B1 (en) | 2006-09-06 |
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