EP0377615B1 - Evaporable foam casting system utilizing a hypereutectic aluminum silicon alloy - Google Patents
Evaporable foam casting system utilizing a hypereutectic aluminum silicon alloy Download PDFInfo
- Publication number
- EP0377615B1 EP0377615B1 EP19880907541 EP88907541A EP0377615B1 EP 0377615 B1 EP0377615 B1 EP 0377615B1 EP 19880907541 EP19880907541 EP 19880907541 EP 88907541 A EP88907541 A EP 88907541A EP 0377615 B1 EP0377615 B1 EP 0377615B1
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- EP
- European Patent Office
- Prior art keywords
- alloy
- pattern
- molten alloy
- silicon
- molten
- 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.)
- Expired - Lifetime
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- 238000005266 casting Methods 0.000 title claims abstract description 20
- 239000006260 foam Substances 0.000 title claims abstract description 18
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 229910001366 Hypereutectic aluminum Inorganic materials 0.000 title claims abstract description 10
- 229910000676 Si alloy Inorganic materials 0.000 title claims abstract description 10
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 62
- 239000000956 alloy Substances 0.000 claims abstract description 62
- 230000008023 solidification Effects 0.000 claims abstract description 27
- 238000007711 solidification Methods 0.000 claims abstract description 27
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 21
- 239000010703 silicon Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 11
- 238000002425 crystallisation Methods 0.000 claims abstract description 8
- 230000008025 crystallization Effects 0.000 claims abstract description 8
- 230000008016 vaporization Effects 0.000 claims abstract description 7
- 238000001556 precipitation Methods 0.000 claims abstract description 5
- 238000009834 vaporization Methods 0.000 claims abstract description 5
- 239000011800 void material Substances 0.000 claims abstract description 5
- 238000011049 filling Methods 0.000 claims description 5
- 238000002485 combustion reaction Methods 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 239000004794 expanded polystyrene Substances 0.000 claims description 2
- 230000000717 retained effect Effects 0.000 claims description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 10
- 229910052802 copper Inorganic materials 0.000 abstract description 10
- 239000010949 copper Substances 0.000 abstract description 10
- 239000004576 sand Substances 0.000 abstract description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract description 8
- 229910052749 magnesium Inorganic materials 0.000 abstract description 8
- 239000011777 magnesium Substances 0.000 abstract description 8
- 229910052742 iron Inorganic materials 0.000 abstract description 7
- 229910052782 aluminium Inorganic materials 0.000 abstract description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 6
- 239000004793 Polystyrene Substances 0.000 abstract description 3
- 230000008030 elimination Effects 0.000 abstract description 3
- 238000003379 elimination reaction Methods 0.000 abstract description 3
- 229920002223 polystyrene Polymers 0.000 abstract description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 17
- 239000006261 foam material Substances 0.000 description 9
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 229910000838 Al alloy Inorganic materials 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- -1 aluminum-silicon-copper Chemical compound 0.000 description 3
- 230000005496 eutectics Effects 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000010125 resin casting Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin 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
- B22D21/00—Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
- B22D21/002—Castings of light metals
- B22D21/007—Castings of light metals with low melting point, e.g. Al 659 degrees C, Mg 650 degrees C
-
- 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
- B22C9/046—Use of patterns which are eliminated by the liquid metal in the mould
Definitions
- Hypereutectic aluminum silicon alloys containing from 16% to 19% by weight of silicon are known to possess good wear resistant properties, achieved by the precipitated silicon crystals which constitute the primary phase.
- United States Patent 4,603,665 describes an improved hypereutectic aluminum silicon casting alloy having particular use in casting engine blocks for marine engines.
- the alloy of the aforementioned patent contains by weight from 16% to 19% silicon, up to 1.4% iron, 0.4% to 0.7% magnesium, up to 0.3% manganese up to 0.37% copper, and the balance aluminum.
- the ternary aluminum-silicon-copper eutectic is avoided and the resulting alloy has a relatively narrow solidification temperature range.
- Evaporable foam casting is a known technique in which a pattern formed of an evaporable foam material is supported in a mold and surrounded by an unbonded particulate media, such as sand. When the molten metal contacts the pattern, the foam material vaporizes, with the vapor passing into the interstices of the sand, while the molten metal replaces the void formed by the vaporized foam material.
- U.S. Patent 4,632,169 describes a foam pattern for making an engine block in the lost foam process.
- the invention is directed to an evaporable foam casting system using a specific hypereutectic aluminum silicon alloy which, due to its composition, provides a slower solidification rate to provide high quality castings.
- the invention provides a method of casting, comprising the steps of preparing a molten alloy, casting said molten alloy into a mold into contact with an evaporable foam pattern surrounded by a finely divided media, and vaporizing the pattern by the heat of said molten alloy with the vapor passing into and being retained within said media and said molten alloy filling the void resulting from the vaporization of said pattern, characterized by employing a known hypereutectic aluminum silicon alloy containing by weight from 16% to 19% silicon whereby the heat of crystallization generated by precipitation of the silicon in said alloy as said molten alloy cools, slows the cooling rate of the molten alloy so as to retard the solidification rate of said alloy and permit said vapor to fully escape from said molten alloy, said molten alloy being maintained at a temperature below 760 o C (1400°F) and having a solidification range less than 60 o C (150°F).
- the hypereutectic aluminum silicon alloy to be used in the casting method of the invention preferably contains by weight from 16% to 19% silicon, 0.4% to 0.7% magnesium, up to 1.4% iron, up to 0.3% magnesium, up to 0.37% copper and the balance aluminum. Due to the minimum copper content, the ternary aluminum-silicon-copper eutectic is avoided and the alloy has a relatively narrow solidification range, less then 600C (150°F), and preferably less than 380C (100°F).
- the heat of the alloy will decompose the foam material to vaporize the foam, the vapor passing into the interstices of the surrounding sand and the molten alloy filling the void created by vaporization of the foam material.
- Solidification of the alloy occurs in conjunction with the heat of crystallization of primary silicon. As the alloy contains a substantial quantity of silicon, the heat of crystallization slows the solidification rate temporarily, thus allowing additional time for the elimination of pattern residue vapors from the molten alloy.
- the decrease in solidification rate also permits casting of relatively thin sections or filling isolated areas of the pattern located relatively long distances from the ingate.
- the cast alloy produced by the method of the invention has inherent soundness attributable to the relatively narrow solidification range, good corrosion resistance, and excellent wear resistance due to the precipitated silicon.
- Fig. 1 illustrates a typical evaporative foam casting system which can be utilized.
- the casting system includes a mold 1 and a pattern assembly 2 is supported within the mold and surrounded by an unbonded particulate material 3, such as sand.
- the molten alloy is introduced into the mold through a funnel 4 which communicates with inlet assembly 5 of pattern assembly 2.
- Pattern assembly 2 includes a group of patterns 6 corresponding in configuration to the part to be cast and which are formed of an evaporative foam material, such as expanded polystyrene.
- the polystyrene, polymethylmethacrylate, or alternative pattern material may be coated with a synthetic resin or a pattern wax.
- the construction of the evaporable foam resin casting system is not critical and may take any desired form.
- Patterns 6 are supported from a central sprue 7 by a plurality of ingates 8 which can be formed of the same evaporable foam material as the patterns. As illustrated in Fig. 2, the sprue is generally rectangular in horizontal cross section having a central opening 9 and an open bottom. Two vertical rows of ingates 8 are associated with each side surface of sprue 7 and each row of ingates is connected to one of the patterns 6, so that, as illustrated, eight patterns are supported from the sprue 7.
- ingates 8 are formed integrally with the respective pattern 6, and the inner flat end of each ingate is attached to the respective surface of sprue 7 through a layer of adhesive 10.
- the adhesive is a conventional type which will be vaporized by the heat of the molten alloy as it is introduced into the sprue and the vapor generated by vaporization of the adhesive will pass into the interstices of the sand.
- ingates 8 alternately, can be integrally formed with sprue 7 and thus connected to the patterns 6 through use of a layer of adhesive, or the ingates can be separate pieces and connected through adhesives to both the patterns 6 and the sprue 7.
- each side surface of sprue 7 is provided with an opening or recess 11 through which sand can flow into the interior chamber 9 of the sprue.
- opposite surfaces of the sprue are provided with openings 12 and 13, which also serve to admit sand to the internal chamber 9.
- Inlet assembly 5 includes a generally rectangular inlet member 14 formed of an evaporable foam material, such as polystyrene, and having a closed bottom, as shown in Fig. 3.
- evaporable foam material such as polystyrene
- the preferred alloy contains, by weight 16% to 19% silicon, 0.4 to 0.7% magnesium, up to 1.4% iron, up to 0.3% manganese, up to 0.37% copper, and the balance aluminum.
- the magnesium acts to strengthen the alloy, while the iron and manganese tend to harden the alloy.
- the resulting alloy has increased machineability, with more stable mechanical properties at elevated temperatures.
- the copper content is maintained below 0.37% and preferably at a minimum.
- the aluminum-silicon-copper eutectic is correspondingly eliminated with the result that the alloy has a relatively narrow solidification range, below 600C (150°F), and preferably less than 380C (100°F).
- the alloy has a yield strength of 1050 to 2100 kg/cm2 (15,000 to 30,000 psi), an ultimate tensile strength in the range of 1400 to 2450 kg/cm2 (20,000 to 35,000 psi), and an elongation of 0% to 2.0%.
- hypereutectic aluminum-silicon alloy to be used in the invention are as follows in weight percent: EXAMPLE I Silicon 16.90 Iron 0.92 Copper 0.14 Manganese 0.12 Magnesium 0.41 Aluminum 81.51 Solidification range 260C (79°F) EXAMPLE II Silicon 16.80 Iron 1.03 Copper 0.33 Manganese 0.18 Magnesium 0.50 Aluminum 81.16 Solidification range 300C (86°F)
- the silicon in the alloy precipitates as relatively large crystals which generate substantial heat of crystallization.
- the heat of crystallization generated by precipitation of the silicon crystals slows the solidification rate, by nonexternal means, while within the physical/thermodynamic constraints of nature. This allows additional time for the escape of vapors from the molten alloy, thereby minimizing gas porosity in the solidified alloy.
- the choice of silicon is ideal for this purpose because silicon has the highest heat of fusion of any element in the periodic table.
- the method of the invention permits relatively thin or complicated sections to be cast and also permits isolated areas of the pattern, located a relatively long distance from the ingate, to be cast without defects.
- the solidification rate is slowed, not by increasing the initial pouring temperature of the alloy, but through the heat of crystallization generated by the precipitation of the silicon crystals.
- the hypereutectic aluminum silicon alloy has a relatively low solidification range, less than 600C (150°F), segregation on solidification is correspondingly minimized.
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Continuous Casting (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Powder Metallurgy (AREA)
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Abstract
Description
- Aluminum alloys, due to their light weight, have been used for casting engine blocks for internal combustion engines. Hypereutectic aluminum silicon alloys containing from 16% to 19% by weight of silicon are known to possess good wear resistant properties, achieved by the precipitated silicon crystals which constitute the primary phase.
- United States Patent 4,603,665 describes an improved hypereutectic aluminum silicon casting alloy having particular use in casting engine blocks for marine engines. The alloy of the aforementioned patent contains by weight from 16% to 19% silicon, up to 1.4% iron, 0.4% to 0.7% magnesium, up to 0.3% manganese up to 0.37% copper, and the balance aluminum. By minimizing the copper content in the alloy, the ternary aluminum-silicon-copper eutectic is avoided and the resulting alloy has a relatively narrow solidification temperature range.
- Evaporable foam casting is a known technique in which a pattern formed of an evaporable foam material is supported in a mold and surrounded by an unbonded particulate media, such as sand. When the molten metal contacts the pattern, the foam material vaporizes, with the vapor passing into the interstices of the sand, while the molten metal replaces the void formed by the vaporized foam material. U.S. Patent 4,632,169 describes a foam pattern for making an engine block in the lost foam process.
- In an evaporable foam casting process, it is desirable to slow the solidification rate of the molten metal to provide time for the elimination of vapors generated by the decomposition of the pattern from the molten alloy. If the molten metal solidifies too swiftly, vapor can be entrapped in the metal, resulting in porosity and a loss of mechanical properties.
- When dealing with aluminum alloys, increasing the pouring temperature of the molten metal to slow the solidification rate is not satisfactory. Not only does an increase in the pouring temperature increase the energy requirements, but hydrogen gas is soluble in aluminum alloys and the solubility of hydrogen increases rapidly with an increase in temperature If the temperature of the molten aluminum alloy goes above 760⁰C (1400°F), excessive quantities of hydrogen can be taken into solution, and on solidifying of the alloy, the hydrogen can show up as gas porosity, which will lower the mechanical properties of the alloy.
- Attempting to slow the solidification rate of aluminum alloys during evaporable foam casting by using an alloy with a relatively large solidification range has likewise not been satisfactory. A large solidification range can result in segregation during solidification in which the early solidified alloy may have a different composition from the later solidified alloy.
- The invention is directed to an evaporable foam casting system using a specific hypereutectic aluminum silicon alloy which, due to its composition, provides a slower solidification rate to provide high quality castings.
- In particular the invention provides a method of casting, comprising the steps of preparing a molten alloy, casting said molten alloy into a mold into contact with an evaporable foam pattern surrounded by a finely divided media, and vaporizing the pattern by the heat of said molten alloy with the vapor passing into and being retained within said media and said molten alloy filling the void resulting from the vaporization of said pattern, characterized by employing a known hypereutectic aluminum silicon alloy containing by weight from 16% to 19% silicon whereby the heat of crystallization generated by precipitation of the silicon in said alloy as said molten alloy cools, slows the cooling rate of the molten alloy so as to retard the solidification rate of said alloy and permit said vapor to fully escape from said molten alloy, said molten alloy being maintained at a temperature below 760oC (1400°F) and having a solidification range less than 60oC (150°F).
- The hypereutectic aluminum silicon alloy to be used in the casting method of the invention preferably contains by weight from 16% to 19% silicon, 0.4% to 0.7% magnesium, up to 1.4% iron, up to 0.3% magnesium, up to 0.37% copper and the balance aluminum. Due to the minimum copper content, the ternary aluminum-silicon-copper eutectic is avoided and the alloy has a relatively narrow solidification range, less then 60⁰C (150°F), and preferably less than 38⁰C (100°F).
- When the molten alloy contacts the evaporable foam pattern in the mold, the heat of the alloy will decompose the foam material to vaporize the foam, the vapor passing into the interstices of the surrounding sand and the molten alloy filling the void created by vaporization of the foam material. Solidification of the alloy occurs in conjunction with the heat of crystallization of primary silicon. As the alloy contains a substantial quantity of silicon, the heat of crystallization slows the solidification rate temporarily, thus allowing additional time for the elimination of pattern residue vapors from the molten alloy. The decrease in solidification rate also permits casting of relatively thin sections or filling isolated areas of the pattern located relatively long distances from the ingate. These advantages are realized without increasing the initial pouring temperature of the molten alloy, nor through use of an alloy with a relatively large solidification range, which could cause segregation on solidifying.
- The cast alloy produced by the method of the invention has inherent soundness attributable to the relatively narrow solidification range, good corrosion resistance, and excellent wear resistance due to the precipitated silicon.
- In the drawings:
- Fig. 1 is a longitudinal section of a typical evaporable foam casting system that can be utilized;
- Fig. 2 is a section taken along line 2-2 of Fig. 1; and
- Figure 3 is a perspective view of the sprue.
- Fig. 1 illustrates a typical evaporative foam casting system which can be utilized. As illustrated, the casting system includes a mold 1 and a
pattern assembly 2 is supported within the mold and surrounded by an unbondedparticulate material 3, such as sand. The molten alloy is introduced into the mold through a funnel 4 which communicates withinlet assembly 5 ofpattern assembly 2. -
Pattern assembly 2 includes a group ofpatterns 6 corresponding in configuration to the part to be cast and which are formed of an evaporative foam material, such as expanded polystyrene. The polystyrene, polymethylmethacrylate, or alternative pattern material, may be coated with a synthetic resin or a pattern wax. - The construction of the evaporable foam resin casting system is not critical and may take any desired form.
-
Patterns 6 are supported from a central sprue 7 by a plurality ofingates 8 which can be formed of the same evaporable foam material as the patterns. As illustrated in Fig. 2, the sprue is generally rectangular in horizontal cross section having a central opening 9 and an open bottom. Two vertical rows ofingates 8 are associated with each side surface of sprue 7 and each row of ingates is connected to one of thepatterns 6, so that, as illustrated, eight patterns are supported from the sprue 7. - As shown in the drawings,
ingates 8 are formed integrally with therespective pattern 6, and the inner flat end of each ingate is attached to the respective surface of sprue 7 through a layer ofadhesive 10. The adhesive is a conventional type which will be vaporized by the heat of the molten alloy as it is introduced into the sprue and the vapor generated by vaporization of the adhesive will pass into the interstices of the sand. - As described in the aforementioned patent application, ingates 8, alternately, can be integrally formed with sprue 7 and thus connected to the
patterns 6 through use of a layer of adhesive, or the ingates can be separate pieces and connected through adhesives to both thepatterns 6 and the sprue 7. - As best illustrated in Fig. 3, the upper end of each side surface of sprue 7 is provided with an opening or recess 11 through which sand can flow into the interior chamber 9 of the sprue. In addition, opposite surfaces of the sprue are provided with
openings 12 and 13, which also serve to admit sand to the internal chamber 9. -
Inlet assembly 5 includes a generallyrectangular inlet member 14 formed of an evaporable foam material, such as polystyrene, and having a closed bottom, as shown in Fig. 3. - The alloy to be used in the process of the invention is hypereutectic aluminum silicon alloy, such as that described in U.S. Patent 4,603,665.
- The preferred alloy contains, by weight 16% to 19% silicon, 0.4 to 0.7% magnesium, up to 1.4% iron, up to 0.3% manganese, up to 0.37% copper, and the balance aluminum.
- The magnesium acts to strengthen the alloy, while the iron and manganese tend to harden the alloy. The resulting alloy has increased machineability, with more stable mechanical properties at elevated temperatures.
- The copper content is maintained below 0.37% and preferably at a minimum. As the copper content is minimized, the aluminum-silicon-copper eutectic is correspondingly eliminated with the result that the alloy has a relatively narrow solidification range, below 60⁰C (150°F), and preferably less than 38⁰C (100°F).
- The alloy has a yield strength of 1050 to 2100 kg/cm² (15,000 to 30,000 psi), an ultimate tensile strength in the range of 1400 to 2450 kg/cm² (20,000 to 35,000 psi), and an elongation of 0% to 2.0%.
- Specific examples of the hypereutectic aluminum-silicon alloy to be used in the invention are as follows in weight percent:
EXAMPLE I Silicon 16.90 Iron 0.92 Copper 0.14 Manganese 0.12 Magnesium 0.41 Aluminum 81.51 Solidification range 26⁰C (79°F) EXAMPLE II Silicon 16.80 Iron 1.03 Copper 0.33 Manganese 0.18 Magnesium 0.50 Aluminum 81.16 Solidification range 30⁰C (86°F) - When the molten alloy at a temperature below 760⁰C (1400°F) and generally at a temperature in the range of 676⁰C-760⁰C (1250°F to 1400°F) is introduced into funnel 4, it will flow downwardly to the
pattern assembly 2 and heat of the molten metal will vaporize the foam material of theinlet assembly 5, sprue 7,ingates 8, and thepatterns 6, with the resulting vapors passing into and being captured in the interstices of thesand 3. - On cooling from solution, the silicon in the alloy precipitates as relatively large crystals which generate substantial heat of crystallization. The heat of crystallization generated by precipitation of the silicon crystals slows the solidification rate, by nonexternal means, while within the physical/thermodynamic constraints of nature. This allows additional time for the escape of vapors from the molten alloy, thereby minimizing gas porosity in the solidified alloy. The choice of silicon is ideal for this purpose because silicon has the highest heat of fusion of any element in the periodic table. As the solidification rate is slowed, the method of the invention permits relatively thin or complicated sections to be cast and also permits isolated areas of the pattern, located a relatively long distance from the ingate, to be cast without defects. With the invention, the solidification rate is slowed, not by increasing the initial pouring temperature of the alloy, but through the heat of crystallization generated by the precipitation of the silicon crystals. As the hypereutectic aluminum silicon alloy has a relatively low solidification range, less than 60⁰C (150°F), segregation on solidification is correspondingly minimized.
Claims (3)
- A method of casting, comprising the steps of preparing a molten alloy, casting said molten alloy into a mold into contact with an evaporable foam pattern surrounded by a finely divided media, and vaporizing said pattern by the heat of said molten alloy with the vapor passing into and being retained within said media and said molten alloy filling the void resulting from the vaporization of said pattern, characterized by employing a known hypereutectic aluminum silicon alloy containing by weight from 16% to 19% silicon whereby the heat of crystallization generated by precipitation of the silicon in said alloy, as said molten alloy cools, slows the cooling rate of said molten alloy so as to retard the solidification rate of said alloy and permit said vapor to fully escape from said molten alloy,
said molten alloy being maintained at a temperature below 760°C (1400°F) and having
a solidification range less than 60°C (150°F). - The method of claim 1 for casting contoured components for an internal combustion engine, characterized by the steps of forming an evaporable foam pattern having a shape substantially identical to a component of an internal combustion engine, supporting said evaporable foam pattern in the mold, connecting said pattern through a sprue with the exterior of the mold, filling the mold with a generally inert finely divided media to surround said pattern, and introducing said alloy through said sprue to said pattern.
- The method of claim 2, characterized by the step of forming the pattern from expanded polystyrene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT88907541T ATE96352T1 (en) | 1987-09-08 | 1988-08-19 | BLOCKAGE CASTING PROCESS FOR CASTING A UBERENTECTIC ALUMINUM-SILICON ALLOY. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9439387A | 1987-09-08 | 1987-09-08 | |
US94393 | 1987-09-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0377615A1 EP0377615A1 (en) | 1990-07-18 |
EP0377615B1 true EP0377615B1 (en) | 1993-10-27 |
Family
ID=22244899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19880907541 Expired - Lifetime EP0377615B1 (en) | 1987-09-08 | 1988-08-19 | Evaporable foam casting system utilizing a hypereutectic aluminum silicon alloy |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0377615B1 (en) |
JP (1) | JPH03501229A (en) |
BR (1) | BR8807691A (en) |
CA (1) | CA1318106C (en) |
DE (1) | DE3885292T2 (en) |
WO (1) | WO1989002326A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9109271B2 (en) | 2013-03-14 | 2015-08-18 | Brunswick Corporation | Nickel containing hypereutectic aluminum-silicon sand cast alloy |
US9650699B1 (en) | 2013-03-14 | 2017-05-16 | Brunswick Corporation | Nickel containing hypereutectic aluminum-silicon sand cast alloys |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5000244A (en) * | 1989-12-04 | 1991-03-19 | General Motors Corporation | Lost foam casting of dual alloy engine block |
DE19731804A1 (en) * | 1997-07-24 | 1999-01-28 | Bayerische Motoren Werke Ag | Manufacturing process for a cylinder liner of an internal combustion engine |
US10370742B2 (en) | 2013-03-14 | 2019-08-06 | Brunswick Corporation | Hypereutectic aluminum-silicon cast alloys having unique microstructure |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4281705A (en) * | 1978-03-14 | 1981-08-04 | NOVEX Talalmanyfejleszto es Ertekesito Kulker. Rt. | Process for casting objects having complicated shapes |
US4603665A (en) * | 1985-04-15 | 1986-08-05 | Brunswick Corp. | Hypereutectic aluminum-silicon casting alloy |
US4632169A (en) * | 1985-05-01 | 1986-12-30 | Outboard Marine Corporation | Two cycle cylinder block foam pattern |
-
1988
- 1988-08-19 BR BR888807691A patent/BR8807691A/en unknown
- 1988-08-19 JP JP50701588A patent/JPH03501229A/en active Pending
- 1988-08-19 WO PCT/US1988/002864 patent/WO1989002326A1/en active IP Right Grant
- 1988-08-19 DE DE88907541T patent/DE3885292T2/en not_active Expired - Fee Related
- 1988-08-19 EP EP19880907541 patent/EP0377615B1/en not_active Expired - Lifetime
- 1988-08-31 CA CA000576190A patent/CA1318106C/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9109271B2 (en) | 2013-03-14 | 2015-08-18 | Brunswick Corporation | Nickel containing hypereutectic aluminum-silicon sand cast alloy |
US9650699B1 (en) | 2013-03-14 | 2017-05-16 | Brunswick Corporation | Nickel containing hypereutectic aluminum-silicon sand cast alloys |
Also Published As
Publication number | Publication date |
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WO1989002326A1 (en) | 1989-03-23 |
EP0377615A1 (en) | 1990-07-18 |
DE3885292T2 (en) | 1994-05-05 |
BR8807691A (en) | 1990-08-07 |
CA1318106C (en) | 1993-05-25 |
JPH03501229A (en) | 1991-03-22 |
DE3885292D1 (en) | 1993-12-02 |
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