US20090205799A1 - Casting molds for use in a directional solidification process and methods of making - Google Patents
Casting molds for use in a directional solidification process and methods of making Download PDFInfo
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- US20090205799A1 US20090205799A1 US12/033,486 US3348608A US2009205799A1 US 20090205799 A1 US20090205799 A1 US 20090205799A1 US 3348608 A US3348608 A US 3348608A US 2009205799 A1 US2009205799 A1 US 2009205799A1
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- metal oxide
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- molten
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- 238000000034 method Methods 0.000 title claims abstract description 33
- 238000007711 solidification Methods 0.000 title claims abstract description 26
- 230000008023 solidification Effects 0.000 title claims abstract description 26
- 238000005266 casting Methods 0.000 title claims abstract description 20
- 230000008569 process Effects 0.000 title abstract description 12
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 55
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 55
- 239000012768 molten material Substances 0.000 claims abstract description 38
- 239000002002 slurry Substances 0.000 claims abstract description 37
- 239000007788 liquid Substances 0.000 claims abstract description 29
- 239000002245 particle Substances 0.000 claims abstract description 25
- 239000002826 coolant Substances 0.000 claims abstract description 23
- 229910052751 metal Inorganic materials 0.000 claims abstract description 18
- 239000002184 metal Substances 0.000 claims abstract description 18
- 229910001092 metal group alloy Inorganic materials 0.000 claims abstract description 13
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- 238000002844 melting Methods 0.000 claims description 13
- 230000008018 melting Effects 0.000 claims description 13
- 229910000601 superalloy Inorganic materials 0.000 claims description 12
- 238000001816 cooling Methods 0.000 claims description 11
- 230000005496 eutectics Effects 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- 229910001338 liquidmetal Inorganic materials 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000956 alloy Substances 0.000 claims description 5
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- 229910045601 alloy Inorganic materials 0.000 claims description 4
- 239000011248 coating agent Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 4
- 229910000314 transition metal oxide Inorganic materials 0.000 claims description 4
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- 239000013078 crystal Substances 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 6
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- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
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- 229910052802 copper Inorganic materials 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
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- 239000000470 constituent Substances 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
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- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
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- 229910052733 gallium Inorganic materials 0.000 description 2
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- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
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- 229910052718 tin Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 238000004018 waxing Methods 0.000 description 2
- RUDFQVOCFDJEEF-UHFFFAOYSA-N yttrium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Y+3].[Y+3] RUDFQVOCFDJEEF-UHFFFAOYSA-N 0.000 description 2
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- -1 alumina Chemical compound 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 1
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 210000001787 dendrite Anatomy 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
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- 230000000704 physical effect Effects 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
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- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
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- 239000004576 sand Substances 0.000 description 1
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- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D27/00—Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
- B22D27/04—Influencing the temperature of the metal, e.g. by heating or cooling the mould
- B22D27/045—Directionally solidified castings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C3/00—Selection of compositions for coating the surfaces of moulds, cores, or patterns
-
- 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
Definitions
- Directional solidification casting is a method for producing gas turbine components and the like with columnar and single crystal growth structures.
- a desired single crystal growth structure is created at the base of a vertically disposed mold defining a part. Then, a single crystal solidification front is propagated through the structure under the influence of a moving thermal gradient.
- Materials that have been cast using directional solidification include steel and superalloy parts.
- the crystal grain characteristics of a superalloy can determine superalloy properties.
- the strength of a superalloy is determined in part by grain size.
- deformation processes are diffusion controlled and diffusion along grain boundaries is much higher than within grains.
- large grain structures can be stronger than fine grain structures.
- the failure of a superalloy can originate at grain boundaries oriented perpendicular to the direction of an applied stress. Casting a superalloy to produce an elongated columnar structure with unidirectional crystals aligned substantially parallel to the long axis of the casting can reduce grain boundaries normal to the primary stress axis. This grain boundary reduction can, in turn, almost entirely eliminate grain boundary failure modes.
- Dendritic refers to a form of crystal growth where forming solid extends into still molten liquid as an array of fine branched needles. Spacing between the needles in the solidification direction is called “primary dendrite arm spacing.”
- a temperature gradient can be impressed in front of an advancing solidification front to avoid nucleation and growth of parasitic dendritic grains.
- the magnitude of the required gradient is proportional to the speed of solidification. For this reason, it is desirable to control the speed of displacement of the solidification front, which can be on the order of a fraction of a centimeter to several centimeters per hour.
- Liquid metal cooled directional solidification processes have been developed to allow the speed of displacement of the solidification front to be carefully controlled.
- One such process involves passing the alloy material through a heating zone and then into a cooling zone.
- the heating zone can include an induction coil or resistance heater while the cooling zone can include a liquid metal bath.
- the liquid metal bath can be utilized both for heating and cooling to provide an improved planar solidification front for the casting of complex articles.
- a mold for casting a molten material comprises an inner surface at least partially coated with a metal oxide slurry comprising metal oxide particles, wherein the metal oxide slurry is capable of inhibiting a liquid cooling medium from contacting a molten metal or metal alloy when the molten metal or metal alloy is disposed within an interior of the mold and the mold is disposed in the liquid cooling medium.
- a method for casting a molten material comprises: disposing the molten material within an interior of a mold comprising an inner surface at least partially coated with a metal oxide slurry comprising metal oxide particles; and disposing the mold in a liquid cooling medium to cause the molten material to solidify.
- FIG. 1 is a schematic side view of a furnace for conducting a directional solidification process
- FIG. 2 is a schematic illustration of an embodiment of a barrier layer for use upon an inner surface of a mold for casting a molten material.
- FIG. 1 depicts an exemplary embodiment of a furnace 10 that can be used to cast molten materials via directional solidification processes.
- the furnace 10 can include resistance heated conductive strips 12 (e.g., graphite strips) disposed within an insulated furnace box 14 for preheating the box 14 .
- the conductive strips can be replaced by an induction coil in an alternative embodiment.
- a mold positioner 18 can hold a ceramic mold 16 having an inner surface coated with a metal oxide slurry within the furnace box 14 .
- An interior of the mold 16 can be filled with a molten material that is kept in the molten state by heating the furnace box 14 at a temperature above the melting point of the molten material.
- Directional solidification can be achieved by lowering the mold 16 containing the molten material out of the heated furnace box 14 (i.e., the hot zone) into a liquid cooling bath 20 (i.e., the cold zone) through an aperture 11 in the furnace box 14 .
- the cooling bath 20 can act as a cooling medium for the molten material.
- the cooling bath 20 can be contained in a crucible 22 of metal such as a refractory metal that is heated to a temperature below the melting point of the molten material and above the melting point of the liquid cooling medium.
- Solidification of the molten material can progress from bottom to top within mold 16 as the mold 16 is lowered into the cooling bath 20 .
- a solid-liquid interface can advance upward as heat is transferred from the molten material within the mold 16 to the liquid cooling bath 20 .
- the inner surface of the ceramic mold can be pre-coated with a slurry comprising metal oxide particles.
- the metal oxide particles can have a diameter of about 20 micrometers (microns) to about 500 microns, more specifically about 20 microns to about 100 microns, or even more specifically about 20 microns to about 50 microns.
- suitable metal oxide particles include but are not limited to particles of aluminum oxide such as alumina, alkaline earth metal oxides such as magnesium dioxide and calcium oxide, transition metal oxides such as titania, chromia, and zirconia, rare earth oxides such as yttria and ceria, and combinations comprising at least one of the foregoing metal oxides.
- the slurry can be formed by mixing the metal oxide particles with a liquid such as water.
- the slurry can then be applied to the surface of a wax pattern, which upon de-waxing, forms the inner surface of the mold, to form a barrier layer adjacent to the molten material subsequently placed within the mold.
- Filling the interior of the mold with the relatively hot molten material can cause the metal oxide slurry to cure into a solid ceramic facecoat that attaches to the surface of the molten material upon solidification.
- an additional facecoat can be disposed on the metal oxide slurry of the mold after the de-waxing procedure by rinsing the interior of the mold with an additional slurry, if so desired.
- This additional facecoat can serve as a protective coating that adheres to the molten material upon solidification. It can include a dissimilar oxide from the one used in the metal oxide slurry, such as colloidal silica, yttria, alumina, and combinations comprising at least one of the foregoing oxides.
- the ceramic facecoat can inhibit the liquid cooling medium from contacting the surface of the molten material within the mold.
- this infiltration of the liquid cooling medium can occur if the mold does not seal properly or if the mold cracks prematurely before the completion of the solidification process.
- the presence of the ceramic facecoat adjacent to the surface of the molten material can prevent or delay cross-diffusion between components of the liquid cooling medium and the molten material and any surface reactions between the two materials.
- the composition of the molten material desirably remains substantially the same and does not become contaminated during the solidification process.
- the inner surface of the mold can be pre-coated with alternating layers of a metal oxide slurry (i.e., layers 32 , 36 , 40 , 44 , and 48 ) and a stucco (i.e., layers 34 , 38 , 42 , and 46 ).
- a metal oxide slurry i.e., layers 32 , 36 , 40 , 44 , and 48
- a stucco i.e., layers 34 , 38 , 42 , and 46
- the stucco can include lime, sand, and water.
- the metal oxide slurry can be applied by, e.g., dip or spray coating.
- the stucco can be applied using a fluidized bed, by spraying coating, or by rain coating.
- Rain coating can be performed using a device (i.e., a rain sander) that picks up the stucco from a reservoir and distributes it evenly (like “rain”) over a large area.
- a rain sander i.e., a rain sander
- Suitable rain sander devices are commercially available from Pacific Kiln & Insulations Co., Inc.
- the size of the stucco particles near the bottom the stacked structure shown in FIG. 2 are smaller those near the middle and top of the stacked structure.
- the stucco particles near the bottom of the stacked structure can have a diameter of about 150 microns to about 180 microns (a mesh size of about 80 to about 100), whereas those near the middle or top of the stacked structure can have a diameter of about 250 microns to about 355 microns (a mesh size of about 42 to about 60).
- Suitable sizes of the slurry particles in the slurry layers are described above.
- the thickness of each slurry layer can be about 50% to about 75% of the diameter of the stucco particles to ensure the stucco particles are embedded in the slurry layer but do not penetrate the layer.
- stucco particles having a diameter of 180 microns can need about 90 to about 135 microns of slurry thickness to lock the particles in place.
- Examples of materials that can be cast as described above include but are not limited to metals, metal alloys, superalloys, and combinations comprising at least one of the foregoing materials.
- the term “superalloy” refers to a nickel (Ni), cobalt (Co), or iron (Fe) based heat resistant alloy that has superior strength and oxidation resistance at high temperatures.
- Superalloys can also include a metal such as chromium (Cr) to impart surface stability and one or more minor constituent such as molybdenum (Mo), tungsten (W), niobium (Nb), titanium (Ti), and/or aluminum (Al) for strengthening purposes.
- Mo molybdenum
- W tungsten
- Nb niobium
- Ti titanium
- Al aluminum
- the liquid cooling medium desirably includes a chemically inert material having a melting point significantly below that of the molten material, a relatively high thermal conductivity, and a relatively low vapor pressure.
- suitable materials for use in the liquid cooling medium include but are not limited to non-flammable, non-toxic liquid metals having a melting point less than about 700° C., eutectic or near eutectic metal alloys, and combinations comprising at least one of the foregoing cooling mediums.
- suitable materials for use in the liquid cooling medium include but are not limited to non-flammable, non-toxic liquid metals having a melting point less than about 700° C., eutectic or near eutectic metal alloys, and combinations comprising at least one of the foregoing cooling mediums.
- Non-limiting examples of such liquid metals include aluminum, tin, gallium, and indium.
- a eutectic mixture is a combination of metals in a proportion that is characterized by the lowest melting point of any mixture of the same metals.
- the eutectic point is the lowest temperature at which a eutectic mixture can exist in liquid phase.
- the eutectic point is the lowest melting point of an alloy in solution of two or more metals that is obtainable by varying the proportions of the components. Eutectic alloys have definite and minimum melting points in contrast to other combinations of the same metals.
- Non-limiting examples of eutectic or near eutectic metal alloys include binary eutectics of aluminum (Al) with copper (Cu), germanium (Ge), magnesium (Mg), or silicon (Si) and ternary eutectics of aluminum with copper and germanium, copper and magnesium, copper and silicon, or magnesium and silicon.
- Al aluminum
- eutectic alloys as well other eutectic alloys in the tin, gallium and indium systems, can be used as cooling mediums, if lower temperature or reactivity with metal is desired.
- the liquid cooling medium can be prepared as an ingot outside of the directional solidification furnace by melting and casting the alloy constituents into ingots.
- the liquid cooling medium can be prepared in situ by melting constituents within the crucible 22 .
- the terms “a” and “an” do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced items. Moreover, the endpoints of all ranges directed to the same component or property are inclusive of the endpoint and independently combinable (e.g., “about 5 wt % to about 20 wt %,” is inclusive of the endpoints and all intermediate values of the ranges of “about 5 wt % to about 20 wt %,”).
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Abstract
Molds 16 for casting molten materials using a directional solidification process and methods for forming a barrier layer between a liquid cooling medium 20 and a molten material of a casting process are provided. According to an embodiment, a mold 16 for casting a molten material comprises an inner surface at least partially coated with a metal oxide slurry 32 comprising metal oxide particles, wherein the metal oxide slurry 32 is capable of inhibiting a liquid cooling medium 20 from contacting a molten metal or metal alloy when the molten metal or metal alloy is disposed within an interior of the mold 16 and the mold 16 is disposed in the liquid cooling medium 20.
Description
- This disclosure relates generally to directional solidification casting and, more specifically, to molds for casting molten materials such as metals or metal alloys using a liquid cooled directional solidification process.
- Directional solidification casting is a method for producing gas turbine components and the like with columnar and single crystal growth structures. Generally, a desired single crystal growth structure is created at the base of a vertically disposed mold defining a part. Then, a single crystal solidification front is propagated through the structure under the influence of a moving thermal gradient.
- Materials that have been cast using directional solidification include steel and superalloy parts. In addition to composition, the crystal grain characteristics of a superalloy can determine superalloy properties. For example, the strength of a superalloy is determined in part by grain size. At high temperatures, deformation processes are diffusion controlled and diffusion along grain boundaries is much higher than within grains. Hence, at high temperatures, large grain structures can be stronger than fine grain structures. The failure of a superalloy can originate at grain boundaries oriented perpendicular to the direction of an applied stress. Casting a superalloy to produce an elongated columnar structure with unidirectional crystals aligned substantially parallel to the long axis of the casting can reduce grain boundaries normal to the primary stress axis. This grain boundary reduction can, in turn, almost entirely eliminate grain boundary failure modes.
- During directional solidification, crystals of nickel, cobalt or iron-based superalloys are characterized by a “dendritic” morphology. Dendritic refers to a form of crystal growth where forming solid extends into still molten liquid as an array of fine branched needles. Spacing between the needles in the solidification direction is called “primary dendrite arm spacing.” A temperature gradient can be impressed in front of an advancing solidification front to avoid nucleation and growth of parasitic dendritic grains. The magnitude of the required gradient is proportional to the speed of solidification. For this reason, it is desirable to control the speed of displacement of the solidification front, which can be on the order of a fraction of a centimeter to several centimeters per hour.
- Liquid metal cooled directional solidification processes have been developed to allow the speed of displacement of the solidification front to be carefully controlled. One such process involves passing the alloy material through a heating zone and then into a cooling zone. The heating zone can include an induction coil or resistance heater while the cooling zone can include a liquid metal bath. In another process, the liquid metal bath can be utilized both for heating and cooling to provide an improved planar solidification front for the casting of complex articles.
- Disclosed herein are molds for casting molten materials, methods for forming a barrier layer on an inner surface of such molds, and methods for casting a molten material. According to an embodiment, a mold for casting a molten material comprises an inner surface at least partially coated with a metal oxide slurry comprising metal oxide particles, wherein the metal oxide slurry is capable of inhibiting a liquid cooling medium from contacting a molten metal or metal alloy when the molten metal or metal alloy is disposed within an interior of the mold and the mold is disposed in the liquid cooling medium.
- In another embodiment, a method for forming a barrier layer between a molten material and a liquid cooling medium of a casting process comprises: disposing a metal oxide slurry comprising metal oxide particles upon an inner surface of the mold.
- In an additional embodiment, a method for casting a molten material comprises: disposing the molten material within an interior of a mold comprising an inner surface at least partially coated with a metal oxide slurry comprising metal oxide particles; and disposing the mold in a liquid cooling medium to cause the molten material to solidify.
- Referring now to the Figures, which are exemplary embodiments, and wherein the like elements are numbered alike:
-
FIG. 1 is a schematic side view of a furnace for conducting a directional solidification process; and -
FIG. 2 is a schematic illustration of an embodiment of a barrier layer for use upon an inner surface of a mold for casting a molten material. -
FIG. 1 depicts an exemplary embodiment of afurnace 10 that can be used to cast molten materials via directional solidification processes. As shown, thefurnace 10 can include resistance heated conductive strips 12 (e.g., graphite strips) disposed within an insulatedfurnace box 14 for preheating thebox 14. The conductive strips can be replaced by an induction coil in an alternative embodiment. Amold positioner 18 can hold aceramic mold 16 having an inner surface coated with a metal oxide slurry within thefurnace box 14. An interior of themold 16 can be filled with a molten material that is kept in the molten state by heating thefurnace box 14 at a temperature above the melting point of the molten material. Directional solidification can be achieved by lowering themold 16 containing the molten material out of the heated furnace box 14 (i.e., the hot zone) into a liquid cooling bath 20 (i.e., the cold zone) through anaperture 11 in thefurnace box 14. Thecooling bath 20 can act as a cooling medium for the molten material. Thecooling bath 20 can be contained in acrucible 22 of metal such as a refractory metal that is heated to a temperature below the melting point of the molten material and above the melting point of the liquid cooling medium. Solidification of the molten material can progress from bottom to top withinmold 16 as themold 16 is lowered into thecooling bath 20. In particular, a solid-liquid interface can advance upward as heat is transferred from the molten material within themold 16 to theliquid cooling bath 20. - As mentioned above, the inner surface of the ceramic mold can be pre-coated with a slurry comprising metal oxide particles. In an embodiment, the metal oxide particles can have a diameter of about 20 micrometers (microns) to about 500 microns, more specifically about 20 microns to about 100 microns, or even more specifically about 20 microns to about 50 microns. Examples of suitable metal oxide particles include but are not limited to particles of aluminum oxide such as alumina, alkaline earth metal oxides such as magnesium dioxide and calcium oxide, transition metal oxides such as titania, chromia, and zirconia, rare earth oxides such as yttria and ceria, and combinations comprising at least one of the foregoing metal oxides. The slurry can be formed by mixing the metal oxide particles with a liquid such as water. The slurry can then be applied to the surface of a wax pattern, which upon de-waxing, forms the inner surface of the mold, to form a barrier layer adjacent to the molten material subsequently placed within the mold. Filling the interior of the mold with the relatively hot molten material can cause the metal oxide slurry to cure into a solid ceramic facecoat that attaches to the surface of the molten material upon solidification. Optionally, an additional facecoat can be disposed on the metal oxide slurry of the mold after the de-waxing procedure by rinsing the interior of the mold with an additional slurry, if so desired. This additional facecoat can serve as a protective coating that adheres to the molten material upon solidification. It can include a dissimilar oxide from the one used in the metal oxide slurry, such as colloidal silica, yttria, alumina, and combinations comprising at least one of the foregoing oxides.
- If any of the liquid cooling medium, e.g., a liquid metal, infiltrates through the main mold member during the solidification process, the ceramic facecoat can inhibit the liquid cooling medium from contacting the surface of the molten material within the mold. By way of example, this infiltration of the liquid cooling medium can occur if the mold does not seal properly or if the mold cracks prematurely before the completion of the solidification process. The presence of the ceramic facecoat adjacent to the surface of the molten material can prevent or delay cross-diffusion between components of the liquid cooling medium and the molten material and any surface reactions between the two materials. As a result, the composition of the molten material desirably remains substantially the same and does not become contaminated during the solidification process.
- In another exemplary embodiment shown in
FIG. 2 , the inner surface of the mold can be pre-coated with alternating layers of a metal oxide slurry (i.e., 32, 36, 40, 44, and 48) and a stucco (i.e.,layers 34, 38, 42, and 46). As used herein, “stucco” refers to a material made of an aggregate, a binder, and water that is applied wet and hardens when it is dried. In one embodiment, the stucco can include lime, sand, and water. The metal oxide slurry can be applied by, e.g., dip or spray coating. The stucco can be applied using a fluidized bed, by spraying coating, or by rain coating. Rain coating can be performed using a device (i.e., a rain sander) that picks up the stucco from a reservoir and distributes it evenly (like “rain”) over a large area. Suitable rain sander devices are commercially available from Pacific Kiln & Insulations Co., Inc.layers - The size of the stucco particles near the bottom the stacked structure shown in
FIG. 2 are smaller those near the middle and top of the stacked structure. For example, the stucco particles near the bottom of the stacked structure can have a diameter of about 150 microns to about 180 microns (a mesh size of about 80 to about 100), whereas those near the middle or top of the stacked structure can have a diameter of about 250 microns to about 355 microns (a mesh size of about 42 to about 60). Suitable sizes of the slurry particles in the slurry layers are described above. The thickness of each slurry layer can be about 50% to about 75% of the diameter of the stucco particles to ensure the stucco particles are embedded in the slurry layer but do not penetrate the layer. For example, stucco particles having a diameter of 180 microns can need about 90 to about 135 microns of slurry thickness to lock the particles in place. - Examples of materials that can be cast as described above include but are not limited to metals, metal alloys, superalloys, and combinations comprising at least one of the foregoing materials. As used herein, the term “superalloy” refers to a nickel (Ni), cobalt (Co), or iron (Fe) based heat resistant alloy that has superior strength and oxidation resistance at high temperatures. Superalloys can also include a metal such as chromium (Cr) to impart surface stability and one or more minor constituent such as molybdenum (Mo), tungsten (W), niobium (Nb), titanium (Ti), and/or aluminum (Al) for strengthening purposes. The physical properties of superalloys make them particularly useful for the manufacture of gas turbine components.
- The liquid cooling medium desirably includes a chemically inert material having a melting point significantly below that of the molten material, a relatively high thermal conductivity, and a relatively low vapor pressure. Examples of suitable materials for use in the liquid cooling medium include but are not limited to non-flammable, non-toxic liquid metals having a melting point less than about 700° C., eutectic or near eutectic metal alloys, and combinations comprising at least one of the foregoing cooling mediums. Non-limiting examples of such liquid metals include aluminum, tin, gallium, and indium.
- A eutectic mixture is a combination of metals in a proportion that is characterized by the lowest melting point of any mixture of the same metals. The eutectic point is the lowest temperature at which a eutectic mixture can exist in liquid phase. The eutectic point is the lowest melting point of an alloy in solution of two or more metals that is obtainable by varying the proportions of the components. Eutectic alloys have definite and minimum melting points in contrast to other combinations of the same metals. Non-limiting examples of eutectic or near eutectic metal alloys include binary eutectics of aluminum (Al) with copper (Cu), germanium (Ge), magnesium (Mg), or silicon (Si) and ternary eutectics of aluminum with copper and germanium, copper and magnesium, copper and silicon, or magnesium and silicon. These aluminum-based eutectic alloys, as well other eutectic alloys in the tin, gallium and indium systems, can be used as cooling mediums, if lower temperature or reactivity with metal is desired.
- The liquid cooling medium can be prepared as an ingot outside of the directional solidification furnace by melting and casting the alloy constituents into ingots. Alternatively, the liquid cooling medium can be prepared in situ by melting constituents within the
crucible 22. - As used herein, the terms “a” and “an” do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced items. Moreover, the endpoints of all ranges directed to the same component or property are inclusive of the endpoint and independently combinable (e.g., “about 5 wt % to about 20 wt %,” is inclusive of the endpoints and all intermediate values of the ranges of “about 5 wt % to about 20 wt %,”). Reference throughout the specification to “one embodiment”, “another embodiment”, “an embodiment”, and so forth means that a particular element (e.g., feature, structure, and/or characteristic) described in connection with the embodiment is included in at least one embodiment described herein, and may or may not be present in other embodiments. In addition, it is to be understood that the described elements may be combined in any suitable manner in the various embodiments. It is also to be understood that the disclosure is not limited by any theories described therein. Unless defined otherwise, technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in the art to which this invention belongs.
- While the invention has been described with reference to exemplary embodiments, it will be understood that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments falling within the scope of the appended claims.
Claims (19)
1. A mold for casting a molten material, comprising: an inner surface at least partially coated with a metal oxide slurry comprising metal oxide particles, wherein the metal oxide slurry is capable of inhibiting a liquid cooling medium from contacting a molten metal or metal alloy when the molten metal or metal alloy is disposed within an interior of the mold and the mold is disposed in the liquid cooling medium.
2. The mold of claim 1 , wherein the metal oxide particles comprise aluminum oxide, an alkaline earth metal oxide, a transition metal oxide, a rare earth element oxide, or a combination comprising at least one of the foregoing metal oxides.
3. The mold of claim 1 , wherein the metal oxide particles have a diameter of about 20 micrometers to about 500 micrometers.
4. The mold of claim 1 , further comprising a primary stucco layer or another metal oxide layer disposed upon the metal oxide slurry, wherein the another metal oxide layer and the metal oxide slurry have dissimilar compositions.
5. The mold of claim 5 , further comprising at least one additional metal oxide slurry and stucco layer stack disposed upon the primary stucco layer.
6. A method for forming a barrier layer between a molten material and a liquid cooling medium of a casting process, comprising: disposing a metal oxide slurry comprising metal oxide particles upon the inner surface of the mold.
7. The method of claim 6 , wherein said disposing the metal oxide slurry comprises dip or spraying coating the inner surface of the mold.
8. The method of claim 6 , wherein the metal oxide particles comprise aluminum oxide, an alkaline earth metal oxide, a transition metal oxide, a rare earth element oxide, or a combination comprising at least one of the foregoing metal oxides.
9. The method of claim 6 , further comprising disposing a molten metal or metal alloy within an interior of the mold to cause the metal oxide slurry to react and form the barrier layer adjacent to the molten metal or metal alloy.
10. The method of claim 6 , wherein the metal oxide particles have a diameter of about 20 micrometers to about 500 micrometers.
11. The method of claim 6 , further comprising disposing a primary stucco layer or another metal oxide layer upon the metal oxide slurry, wherein the another metal oxide layer and the metal oxide slurry have dissimilar compositions.
12. The method of claim 11 , further comprising disposing at least one additional metal oxide slurry and stucco layer stack upon the primary stucco layer.
13. A method of casting a molten material, comprising:
disposing the molten material within an interior of a mold comprising an inner surface at least partially coated with a metal oxide slurry comprising metal oxide particles; and
disposing the mold in a liquid cooling medium to cause the molten material to solidify.
14. The method of claim 13 , wherein the molten material comprises a molten metal, a molten alloy, a molten superalloy, or a combination comprising at least one of the foregoing materials, and wherein the liquid cooling medium comprises a liquid metal having a melting point less than about 700° C., a liquid eutectic or near eutectic metal alloy, or a combination comprising at least one of the foregoing cooling mediums.
15. The method of claim 13 , wherein the mold is disposed in a hot zone at a temperature above a melting temperature of the molten material when the mold is filled such that the metal oxide slurry undergoes curing, and wherein the mold is moved progressively to a cold zone comprising the liquid cooling medium at a temperature below the melting temperature of the molten material, thereby effecting movement of a solidification interface through the molten material.
16. The method of claim 13 , wherein the metal oxide particles comprise aluminum oxide, an alkaline earth metal oxide, a transition metal oxide, a rare earth element oxide, or a combination comprising at least one of the foregoing metal oxides.
17. The method of claim 13 , wherein the mold further comprises a primary stucco layer or another metal oxide layer disposed upon the metal oxide slurry, wherein the another metal oxide layer and the metal oxide slurry have dissimilar compositions.
18. The method of claim 17 , wherein the mold further comprises at least one additional metal oxide slurry and stucco layer stack disposed upon the primary stucco layer.
19. The method of claim 13 , wherein the metal oxide particles have a diameter of about 20 micrometers to about 500 micrometers.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/033,486 US20090205799A1 (en) | 2008-02-19 | 2008-02-19 | Casting molds for use in a directional solidification process and methods of making |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/033,486 US20090205799A1 (en) | 2008-02-19 | 2008-02-19 | Casting molds for use in a directional solidification process and methods of making |
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| US20090205799A1 true US20090205799A1 (en) | 2009-08-20 |
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| Application Number | Title | Priority Date | Filing Date |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8323559B2 (en) | 2010-11-05 | 2012-12-04 | United Technologies Corporation | Crucible for master alloying |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4247333A (en) * | 1979-12-26 | 1981-01-27 | General Electric Company | Alumina shell molds used for investment casting in directional solidification of eutectic superalloys |
| US6467534B1 (en) * | 1997-10-06 | 2002-10-22 | General Electric Company | Reinforced ceramic shell molds, and related processes |
-
2008
- 2008-02-19 US US12/033,486 patent/US20090205799A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4247333A (en) * | 1979-12-26 | 1981-01-27 | General Electric Company | Alumina shell molds used for investment casting in directional solidification of eutectic superalloys |
| US6467534B1 (en) * | 1997-10-06 | 2002-10-22 | General Electric Company | Reinforced ceramic shell molds, and related processes |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8323559B2 (en) | 2010-11-05 | 2012-12-04 | United Technologies Corporation | Crucible for master alloying |
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