EP1857198B1 - Methods for attaching casting cores - Google Patents
Methods for attaching casting cores Download PDFInfo
- Publication number
- EP1857198B1 EP1857198B1 EP07251140A EP07251140A EP1857198B1 EP 1857198 B1 EP1857198 B1 EP 1857198B1 EP 07251140 A EP07251140 A EP 07251140A EP 07251140 A EP07251140 A EP 07251140A EP 1857198 B1 EP1857198 B1 EP 1857198B1
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- EP
- European Patent Office
- Prior art keywords
- casting
- core
- cores
- bringing
- casting core
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 238000005266 casting Methods 0.000 title claims description 47
- 238000000034 method Methods 0.000 title claims description 45
- 239000000919 ceramic Substances 0.000 claims description 34
- 239000002002 slurry Substances 0.000 claims description 29
- 238000007598 dipping method Methods 0.000 claims description 14
- 238000000576 coating method Methods 0.000 claims description 13
- 239000000853 adhesive Substances 0.000 claims description 12
- 230000001070 adhesive effect Effects 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 12
- 238000010304 firing Methods 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 238000000465 moulding Methods 0.000 claims description 7
- 238000005495 investment casting Methods 0.000 claims description 6
- 239000008119 colloidal silica Substances 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 229910052845 zircon Inorganic materials 0.000 claims description 4
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000003780 insertion Methods 0.000 claims description 2
- 230000037431 insertion Effects 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 239000003870 refractory metal Substances 0.000 description 11
- 229910045601 alloy Inorganic materials 0.000 description 7
- 239000000956 alloy Substances 0.000 description 7
- 239000002131 composite material Substances 0.000 description 7
- 230000013011 mating Effects 0.000 description 7
- 239000000126 substance Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 230000000712 assembly Effects 0.000 description 3
- 238000000429 assembly Methods 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000006255 coating slurry Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000002386 leaching Methods 0.000 description 3
- 238000007581 slurry coating method Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 241000588731 Hafnia Species 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910000601 superalloy Inorganic materials 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Images
Classifications
-
- 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
- B22C9/103—Multipart cores
Definitions
- the invention relates to investment casting. More particularly, the invention relates to investment casting core assemblies.
- Investment casting is commonly used in the aerospace industry. Various examples involve the casting of gas turbine engine parts. Exemplary parts include various blades, vanes, seals, and combustor panels. Many such parts are cast with cooling passageways. The passageways may be formed by sacrificial casting cores.
- Exemplary cores include ceramic cores, refractory metal cores (RMCs), and combinations thereof.
- the ceramic cores may form feed passageways whereas the RMCs may form cooling passageways extending from the feed passageways through walls of the associated part. It is understood that ceramic cores may be used to form cooling passageways and metal cores may be used to form feed passageways.
- Ceramic cores may be made by molding a "green" core and then firing to harden.
- Refractory metal cores may be made by casting or from sheetstock (e.g., by stamping or cutting/forming) or by other suitable methods.
- the cores may be assembled to each other and secured, for example, with a ceramic adhesive.
- An exemplary ceramic adhesive is alumina-based.
- the adhesive may comprise alumina powder and a binder such as colloidal silica.
- the core(s) may be overmolded with a sacrificial material (e.g., a wax) to form a pattern in a shape at least partially corresponding to that of the part to be cast.
- a shell may be formed over the pattern (e.g., a ceramic shell formed in a multi-stage stuccoing process).
- the sacrificial material may be removed (e.g., by a steam dewaxing) leaving the core within a mold chabmer formed by the shell.
- the shell may be fired to harden.
- Molten metal may be poured into the shell and allowed to solidify.
- the casting shell and core(s) are destructively removed.
- Exemplary shell removal is principally mechanical.
- Exemplary core removal is principally chemical.
- the cores may be removed by chemical leaching.
- Exemplary leaching involves use of an alkaline solution in an autoclave. Exemplary leaching techniques are disclosed in US Patents 4,141,781 , 6,241,000 , and 6,739,380 .
- GB 2 211 122 over which claim 1 is characterised, describes the joining together of blown core parts by a further blowing operation.
- EP 1 543 896 describes a method which includes capturing a refractory metal core within a shell.
- WO 00/78480 describes core elements having close tolerance mating locating features.
- EP 1 306 147 describes core elements having protruding regions and recessed pockets which provide a mechanical lock between the elements.
- the invention involves a method for attaching a first casting core to a second casting core.
- a first portion of the first casting core is brought into engagement or close proximity with a second portion of the second casting core.
- the first and second portions are dipped in a slurry to form a coating around the first and second portions.
- the coating is hardened to form a joint between the first and second portions.
- the resulting composite core may be easier to manufacture than a similarly shaped non-composite core.
- the slurry may be a ceramic slurry.
- the metallic casting core may comprise a refractory metal-based substrate (e.g., optionally coated).
- the method may be used to form a turbine blade core assembly or a turbine vane core assembly.
- the slurry may be heated to harden.
- the metallic casting core and ceramic casting core may be vibrated during the introducing.
- the bringing may be performed with the ceramic casting cores in a green state or in a fired state.
- the slurry may comprise zircon and aqueous colloidal silica.
- 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 or of alloys or intermetallics containing one or more refractory metals) and coated 24.
- Suitable coating materials include silica, alumina, zirconia, chromia, mullite and hafnia.
- the coefficient of thermal expansion (CTE) of the refractory metal and the coating are similar.
- Coatings may be applied by any appropriate line-of sight or non-line-of sight technique (e.g., chemical or physical vapor deposition (CVD, PVD) methods, plasma spray methods, electrophoresis, and sol gel methods). Individual layers may typically be 0.1 to 1 mil ( ⁇ 0.0025 to 0.025 mm) thick. Layers of Pt, other noble metals, Cr, Si, W, and/or Al, or other non-metallic materials 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.
- CVD chemical or physical vapor deposition
- PVD physical vapor deposition
- One or more ceramic cores may also be formed 26 (e.g., of or containing 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 assembly may include use of a ceramic slurry discussed below.
- 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 a furnace (e.g., containing air or other oxidizing atmosphere) in which it is heated 46 to strengthen the shell and 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 reduce or eliminate the formation of detrimental carbides in the metal casting. Removing carbon offers the additional advantage of reducing the potential for clogging the vacuum pumps used in subsequent stages of operation.
- the mold may be removed from the atmospheric furnace, allowed to cool, and inspected 48.
- the mold may be seeded 50, if necessary(e.g., by locating 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 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.
- a non-oxidizing atmosphere e.g., inert gas
- the casting furnace is heated 56 to preheat the mold. This preheating serves two purposes: to further harden and strengthen the shell; and to preheat the shell for the introduction of molten alloy to prevent thermal shock of the shell and premature solidification of the alloy.
- the molten alloy is poured 58 into the mold and the mold is allowed to cool to solidify 60 the alloy (e.g., during or 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).
- the core assembly is removed in a decoring process 68 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. Some or all of any machining or chemical or thermal treatment may be performed before the decoring.
- FIGS. 2-4 show an exemplary composite core in various stages of manufacture.
- FIG. 5 is a flowchart of the assembly/manufacture steps.
- FIG. 2 shows a pair of individually-molded ceramic cores 120 and 122.
- the exemplary cores have respective main body portions or trunks 124 and 126 and terminal portions 128 and 130. Near respective ends 132 and 134 of the terminal portions, the cores may include mating features 136 and 138. Exemplary mating features are shown as a protuberant projection 136 and complementary compartment 138. Alternative mating features include dovetail and other back-locking features, shiplap features, halflap features, and simple butt features. Although illustrated at terminal portions, the mating features may be otherwise formed (e.g., one or more pairs of mating features at intermediate locations along a core body).
- FIG. 3 shows the cores assembled/mated 180 to each other and held by a fixture 140 with their mating features engaged to each other.
- Exemplary fixtures 140 may include clamps, robotic actuators, and the like.
- the fixture 140 may hold the assembled cores during the application of slurry.
- Exemplary slurry application includes one or more dippings 182 of the terminal portions in a slurry tank to apply a slurry coating 150. If multiple dippings are used, they may be of the same slurry or different slurries from different tanks to produce a desired layering of the coating 150 (e.g., for maximized strength of joint).
- the terminal portions may be slightly thinned or recessed relative to the adjacent trunk portions so that the build-up of slurry does not excessively increase core thickness or provide discontinuities therein.
- the fixture 140 may hold the engaged portions of the cores in contact or close proximity (e.g., with a gap sufficiently sized to allow a bonding infiltration of the slurry between the two cores).
- the coating may be hardened.
- An'exemplary hardening involves drying 184 without further firing. This may be particularly useful with pre-fired ceramic components which are held together with wax pads.
- an additional ceramic core may be pre-assembled to one of the cores 120 or 122 and positioned with a wax pad. Room temperature drying of the slurry would preserve the pad.
- Alternative non-firing drying might involve heating at temperatures of up to 95°C.
- the hardening may, alternatively, include a firing (e.g., at 1200°C or greater) which may also harden the cores 120 and 122 (e.g., if assembled in a green state or an only partially fired state).
- the result of the hardening is to produce a joint 154 of sufficient strength to allow further handling and processing steps as described relative to FIG. 1 .
- these may include assembly of the resulting composite ceramic core 160 to one or more other cores such as a refractory metal core 162 ( FIG. 4 ) (e.g., via insertion 186 in a slot cut in the composite core or pre-molded therein).
- Exemplary slurries may be identical or similar to shell coating slurries. Sequences may be altered relative to application sequences for shell coating slurries to provide desired joint strength and joint surface smoothness. For example, shell coating slurry application sequences typically proceed from fine to coarse. Initial fine slurry is applied to a pattern for smoothness and subsequent coarse slurry for strength. However, it may be desired that the last layer of slurry in the coating 150 be fine for smoothness because the cores generally form internal features whereas the shells generally form external features.
- Exemplary slurries comprise a combination of zircon and aqueous colloidal silica along with appropriate surfactants and other agents (e.g., for promoting bubble rupture).
- Variations include use of the slurry coating in combination with a ceramic adhesive in the joint.
- the adhesive may be introduced during core assembly.
- Exemplary ceramic adhesives are available from Cotronics Corporation of Brooklyn, New York, under the trademark RESBOND. Use of ceramic adhesive may be particularly appropriate with pre-fired ceramic cores. The ceramic adhesive increases bond strength and may further avoid the need for a subsequent high temperature firing.
- FIG. 6 shows the assembly of a ceramic core 200 with a refractory metal core 202.
- a portion 204 of the refractory metal core is positioned within a slot 206 of a ceramic core and retained at least partially by a ceramic adhesive 208.
- a slurry coating 210 may surround the junction of these two cores to form a joint. The slurry 210 may be applied as described above.
- a portion of one or both of the cores may be masked during slurry application (e.g., spraying, painting, or dipping) or may be cleaned of slurry after such application.
- slurry application e.g., spraying, painting, or dipping
- the overdipping of the RMC-ceramic core joint isolates the unfired ceramic adhesive (if any) from contact with the casting alloy to avoid adverse chemical interaction.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
- Mold Materials And Core Materials (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/385,382 US20070221359A1 (en) | 2006-03-21 | 2006-03-21 | Methods and materials for attaching casting cores |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1857198A1 EP1857198A1 (en) | 2007-11-21 |
EP1857198B1 true EP1857198B1 (en) | 2011-09-28 |
Family
ID=38229583
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07251140A Active EP1857198B1 (en) | 2006-03-21 | 2007-03-19 | Methods for attaching casting cores |
Country Status (5)
Country | Link |
---|---|
US (1) | US20070221359A1 (zh) |
EP (1) | EP1857198B1 (zh) |
JP (1) | JP2007253237A (zh) |
CN (1) | CN101041175A (zh) |
SG (1) | SG136062A1 (zh) |
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US20110182726A1 (en) * | 2010-01-25 | 2011-07-28 | United Technologies Corporation | As-cast shroud slots with pre-swirled leakage |
US20110204205A1 (en) * | 2010-02-25 | 2011-08-25 | Ahmed Kamel | Casting core for turbine engine components and method of making the same |
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US11813665B2 (en) * | 2020-09-14 | 2023-11-14 | General Electric Company | Methods for casting a component having a readily removable casting core |
US11440146B1 (en) * | 2021-04-22 | 2022-09-13 | Raytheon Technologies Corporation | Mini-core surface bonding |
CN114406201B (zh) * | 2022-01-26 | 2023-11-14 | 阜新力达钢铁铸造有限公司 | 导轨无孔立柱的铸造方法及系统 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4141781A (en) * | 1977-10-06 | 1979-02-27 | General Electric Company | Method for rapid removal of cores made of βAl2 O3 from directionally solidified eutectic and superalloy and superalloy materials |
US4774990A (en) * | 1986-08-04 | 1988-10-04 | Mazda Motor Corporation | High pressure casting method and a casting core |
ES2005911A6 (es) * | 1987-10-22 | 1989-04-01 | Erana Agustin Arana | Mejoras introducidas en la conformacion de paquetes de machos para fundicion. |
US6241000B1 (en) * | 1995-06-07 | 2001-06-05 | Howmet Research Corporation | Method for removing cores from castings |
FR2785836B1 (fr) * | 1998-11-12 | 2000-12-15 | Snecma | Procede de fabrication de noyaux ceramiques minces pour fonderie |
US6347660B1 (en) * | 1998-12-01 | 2002-02-19 | Howmet Research Corporation | Multipiece core assembly for cast airfoil |
US6637500B2 (en) | 2001-10-24 | 2003-10-28 | United Technologies Corporation | Cores for use in precision investment casting |
EP1497059B1 (en) * | 2002-04-11 | 2008-07-23 | Rolls-Royce Corporation | Method and apparatus for removing ceramic material from cast components |
US6929054B2 (en) * | 2003-12-19 | 2005-08-16 | United Technologies Corporation | Investment casting cores |
-
2006
- 2006-03-21 US US11/385,382 patent/US20070221359A1/en not_active Abandoned
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2007
- 2007-03-08 SG SG200701726-2A patent/SG136062A1/en unknown
- 2007-03-19 EP EP07251140A patent/EP1857198B1/en active Active
- 2007-03-20 CN CNA2007100881894A patent/CN101041175A/zh active Pending
- 2007-03-20 JP JP2007071902A patent/JP2007253237A/ja active Pending
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EP1857198A1 (en) | 2007-11-21 |
US20070221359A1 (en) | 2007-09-27 |
SG136062A1 (en) | 2007-10-29 |
JP2007253237A (ja) | 2007-10-04 |
CN101041175A (zh) | 2007-09-26 |
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