US2422118A - Making cores for casting light metal alloys - Google Patents
Making cores for casting light metal alloys Download PDFInfo
- Publication number
- US2422118A US2422118A US434588A US43458842A US2422118A US 2422118 A US2422118 A US 2422118A US 434588 A US434588 A US 434588A US 43458842 A US43458842 A US 43458842A US 2422118 A US2422118 A US 2422118A
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- United States
- Prior art keywords
- core
- binder
- sand
- casting
- light metal
- 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 description 26
- 229910001092 metal group alloy Inorganic materials 0.000 title description 17
- 239000011230 binding agent Substances 0.000 description 45
- 239000004576 sand Substances 0.000 description 25
- 229910052751 metal Inorganic materials 0.000 description 23
- 239000002184 metal Substances 0.000 description 23
- 239000007795 chemical reaction product Substances 0.000 description 21
- 229920001807 Urea-formaldehyde Polymers 0.000 description 17
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 17
- 239000003795 chemical substances by application Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 6
- 235000013339 cereals Nutrition 0.000 description 6
- 230000001012 protector Effects 0.000 description 6
- 235000015112 vegetable and seed oil Nutrition 0.000 description 6
- 239000008158 vegetable oil Substances 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 4
- 238000007711 solidification Methods 0.000 description 4
- 230000008023 solidification Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- 230000027455 binding Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
- B22C1/22—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins
- B22C1/2233—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- B22C1/2246—Condensation polymers of aldehydes and ketones
-
- 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
Definitions
- the invention relates to the production of cores for casting light metal alloys such as magnesium and aluminum alloys.
- the binders heretofore used in making cores for casting light metal alloys have been vegetable oils, which harden or polymerize during the baking of th green sand core so as to knit the grains of sand together into a rigid structure.
- a core containing such a vegetable oil binder must be heated to a temperature above 400 F. in order to cause the vegetable oil to polymerize.
- the cores employed in the casting operation contain a metal protector" such as sulphur or urea.
- a metal protector is a substance that sublimes or vaporizes when the molten metal comes in contact with the core, and prevents the air that is present in the core from causing the metal to burn. If a metal protector is not present in the core, the molten metal reacts with the air or with the slight amount of moisture in the core, and causes an explosion or other damage to the cast- Since sulphur sublimes at about 350 F., it cannot be used in a core containing a vegetable oil as a binder. Such a core must be baked at a temperature above 400 F.
- the core binders heretofore known are unsatisfactory for the further reason that they do not volatilize completely upon solidification of the molten metal so as to permit the core to collapse during cooling of the casting.
- a binder which does not volatilize upon solidification of the molten metal, and thus causes the core to retain its rigidity, may cause the casting to crack during the shrinking that takes place upon cooling.
- the binders heretofore known do not completely lose their binding action during the casting operation, a, core containing such a binder isextremely difficult to remove from intricate passages in a casting such as a cylinder head for a liquid-cooled airplane engine. The operation of digging such a core out of intricate 2 passages in a casting is very tedious and timeconsuming.
- the principal object of the invention is to pro vide a novel binder for sand cores used in casting light metal alloys which sets at low baking temperatures and volatilizes substantially completely after solidification of the metal during the molding operation. More specific objects and advantages are apparent from the description, which discloses and illustrates'the invention and is not intended to impose limitations upon the claims.
- a green sandcore embodying the invention comprises a hardenable urea-formaldehyde reaction product as a binder, which sets to an infusible resin when the core is baked at a low temperature.
- the present binder decomposes and volatilizcs so completely after solidification of the molten metal that the residue of the core consists of loose sand, which can simply be poured out of the casting. Because of the complete decomposition and volatilization of the present binder. it is not necessary to restrict the percentage of binder in the core, and a sufllcient amount can be used to make the core as strong as desired.
- a core embodying the invention has a high porosity. which permits gases evolved from the niolten metal to pass off through the core, and minimizes the formation of gas flaws in the casting.
- the binder used in preparing a core in accordance with the present invention may be in the form of a solution of a urea-formaldehyde reaction product in an organic solvent which is mix d with the sand.
- the urea-formaldehyde reaction product is preferably water-soluble. so that water can be used as the solvent in the binder solution.
- the urea-formaldw hyde reaction product is in granular or powder form, because it is easier to incorporate the usual small proportion of binder uniformly with the sand by making a dry mixture of the binder and the sand.
- the water or other solvent for the urea-formaldehyde reaction product is then added to the dry mixture to produce the green sand.
- a hardening agent is preferably included in the green sand in order to accelerate the hardening or setting of the urea-formaldehyde reaction product during the baking of the core.
- hardening agent may be any substance that gives an acid reaction under the conditions of baking, such as an acid, an acid salt, or a substance that liberates acid at the baking temperture.
- the mount of the hardening agent is simply an amount such as to cause the hardening to take place at the desired rate during baking,
- the hardening agent may be omitted if desired, and the amount used should not base great as to cause substantial hardening oi the binder to occur at ordinary temperatures prior to molding of the core.
- a water-soluble urea-formaldehyde reaction product is much more stable in dry form than in the form of an aqueous solution.
- the preferred form of core binder embodying the invention is a dry stable mixture of ahardenable watersoluble urea-formaldehyde reaction product and a hardening agent therefor.
- Hardening agents that may be used to give such a stable mixture are zinc sulphate, zinc chloride, ammonium sulphate, ammonium dihydrogen phosphate, diammonium hydrogen phosphate and ammonium oxalate.
- hardening agents such as ammonium chloride, ammonium thiocyanate and various other acids and acid salts, should not be left in admixture with the dry urea-formaldehyde reaction product, because they cause it to harden radually at ordinary temperatures.
- a dry stable mixture of a hardenable watersoluble urea-formaldehyde reaction product and a hardening agent therefor, embodyin the invention is highly advantageous as a binder for use in sand cores for casting light metal alloys, because such a mixture can be-kept on hand for indefinite periods and used as needed. Since the hardening agent is already incorporated inthe mixture, it is not necessary for the foundrymen to take the responsibility of mixing the proper amount of hardening agent with the urea-formaldehyde reaction product. The amount of urea-formaldehyde reaction product used in makin up a small quantity of green sand is minute, and the proper amount of hardening agent therefor might have to be weighed out on an analytical balance.
- the amount of the urea-formaldehyde reaction product used in preparin a sand core in accordance with the present invention is simply an amount suflicient to produce a core of the desired strength, which is usually about /2 per cent or more of the weight i of dry sand. 1 per cent of the weight of dry sand is ordinarily sufflcient.
- a green sand core embodying the invention has moderate strength, but if desired the green strength of the core can be increased in the usual manner by adding cereal binders or the like.
- the green strength of a core embodying the invention is enhanced by the rigidiflcation of the outer surface of the core which occurs as thecore dries out at ordinary temperatures.
- the amount of water used in making the core depends upon the kind of sand, the amount of cereal binder, if any, and other factors, and is simply an amount sufllcient .to give the desired green strength and flow-properties of the green sand-usually from about 2 to about 6 per cent of fire weight of dry sand.
- the amount of baking necessary to'dry out the core thoroughly is usually suflicient to complete the hardening or setting of the ureauntil uniform wetting of the sand has taken place.
- the resulting green sand can be stored formaldehyde reaction product.
- a higher baking temperature may be required, but it is never necessaryto bake at a temperature above 300 F. Usually, the lower the temperature, the longer the period of baking that is required. In any case. the amount of heating should not be so great as to decompose the urea-formaldehyde reaction product.
- a core embodying the invention should not be baked more than 4 hours at 350 F. 4 hours of baking at 300 F. is ordinarily sufllcient for cores up to 6 inchesthick. Thicker cores cannot be uniformly heated throughout in 4 hours, and should therefore be baked for a longer period at a lower temperature.
- a water-soluble hardenable urea-formaldehyde reaction product may be prepared as follows: 1 mol of urea is added to a '37 uper cent aqueous solution containing 2 mols of formaldehyde that has been brought to pH 4.5-5.5 by means of sodium hydroxide. The solution is then gently refluxed long enough (about 1 hour) to carry the reaction to the desired stage. Since a ureaformaldehyde reaction product is most stable in a neutral condition, the solution is then preferably neutralized. In order to produce a solid product, the solution may be diluted with water or evaporated under vacuum to the proper concentration, and then spray-dried or vacuum drum-dried. A few per cent of a cellulose filler such as fine wood flour may be added prior to the drying operation.
- Example 1 1 part of a binder prepared in accordance with Example 1 is mixed with 100 parts of dry sand, a suitable proportion of a metal protector, and any other desired dry ingredients, such as a cereal binder, in a standard mixer such as a foundry muller. Enough water (about 4 parts) to produce a damp mixture of the desired consistency is then added, and mixing is continued until needed. No appreciable deterioration occurs in a period of 48 hours. If the surface of a pile of the reen sand becomes dried out, it can be restored to its original condition by spraying the surface lightly with water. The green sand is formedin a mold to a core of the desired shape. The core is baked at 300 F. for about 4 hours, or,
- the resulting core has a compressive strength of about 250 pounds per square inch.
- a method of casting light metal alloys that includes preparing a green sand core consisting.
- thesand when moistened can be molded into an integral core, moistning, molding, baking. and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
- a method of casting light metal alloys that includes preparing a green sand core consisting essentially of sand, water, a hardenable urea.- tormaldehyde reaction product as a binder and 'a hardening agent therefor, the proportion of binder being suflicient so that the green sand can be molded into an integral core, baking, and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
- binder being sufilcient so that the green sand can be molded into an integral core, baking, and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
- a method of casting light metal alloys that includes preparing a green sand core consisting essentially of sand, water, a cereal binder and a hardenable urea-formaldehyde reaction product as a binder, the proportion of binder being sumcient so that the green sand can be molded into an integral core, baking. and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
- a method of casting light metal alloys that includes preparing a green sand core consisting essentially of sand, water, a cereal binder, a hardenable urea-formaldehyde reaction product as a binder and a. hardening agent therefor, the proportion of binder being suflicient so that the green sand can be molded into an integral core, baking, and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Description
Patented June 10, 1947 MAKING CORES FOR CASTING LIGHT METAL ALLOYS Leonard S. Meyer, Toledo, Ohio, assignorrby mesne assignments, to
Libbey-Owens-Ford Glass Company, a corporation of Ohio No Drawing. Application March 13, 1942,
' Serial No. 434,588
6 Claims.
, The invention relates to the production of cores for casting light metal alloys such as magnesium and aluminum alloys.
The binders heretofore used in making cores for casting light metal alloys have been vegetable oils, which harden or polymerize during the baking of th green sand core so as to knit the grains of sand together into a rigid structure. However, a core containing such a vegetable oil binder must be heated to a temperature above 400 F. in order to cause the vegetable oil to polymerize.
If satisfactory results are to be obtained in casting light metal alloys, it is necessary that the cores employed in the casting operation contain a metal protector" such as sulphur or urea. A metal protector is a substance that sublimes or vaporizes when the molten metal comes in contact with the core, and prevents the air that is present in the core from causing the metal to burn. If a metal protector is not present in the core, the molten metal reacts with the air or with the slight amount of moisture in the core, and causes an explosion or other damage to the cast- Since sulphur sublimes at about 350 F., it cannot be used in a core containing a vegetable oil as a binder. Such a core must be baked at a temperature above 400 F. in order to set the vegetable oil binder, and any sulphur present would disappear during such baking. When a vegetable oil is used as the binder, it is necessary to use a metal protector in the core which does not sublime at the setting temperature of the binder. The metal protectors that have suchhigh subliming temperatures are extremely expensive, inefiicient in their action and otherwise unsatisfactory.
The core binders heretofore known are unsatisfactory for the further reason that they do not volatilize completely upon solidification of the molten metal so as to permit the core to collapse during cooling of the casting. A binder which does not volatilize upon solidification of the molten metal, and thus causes the core to retain its rigidity, may cause the casting to crack during the shrinking that takes place upon cooling. Moreover, since the binders heretofore known do not completely lose their binding action during the casting operation, a, core containing such a binder isextremely difficult to remove from intricate passages in a casting such as a cylinder head for a liquid-cooled airplane engine. The operation of digging such a core out of intricate 2 passages in a casting is very tedious and timeconsuming.
The principal object of the invention-is to pro vide a novel binder for sand cores used in casting light metal alloys which sets at low baking temperatures and volatilizes substantially completely after solidification of the metal during the molding operation. More specific objects and advantages are apparent from the description, which discloses and illustrates'the invention and is not intended to impose limitations upon the claims.
A green sandcore embodying the invention comprises a hardenable urea-formaldehyde reaction product as a binder, which sets to an infusible resin when the core is baked at a low temperature.
The present binder is not dissolved or other wise affected by the molten metal; and the decomposition of the binder is slow enough at molten metal temperatures so that no substantial decomposition has occurred by the time the molten metal has solidified in the mold. For that reason, there is no premature liberation of gas by decomposition of the binder, which might cause the formation of gas bubbles or blowhole== in the casting. Nevertheless the decomposition of the present binder is not so slow at .these temperatures that it is not completed before sub stantial cooling of the solidified metal occurs.
The present binder decomposes and volatilizcs so completely after solidification of the molten metal that the residue of the core consists of loose sand, which can simply be poured out of the casting. Because of the complete decomposition and volatilization of the present binder. it is not necessary to restrict the percentage of binder in the core, and a sufllcient amount can be used to make the core as strong as desired. A core embodying the invention has a high porosity. which permits gases evolved from the niolten metal to pass off through the core, and minimizes the formation of gas flaws in the casting.
The binder used in preparing a core in accordance with the present invention may be in the form of a solution of a urea-formaldehyde reaction product in an organic solvent which is mix d with the sand. However, the urea-formaldehyde reaction product is preferably water-soluble. so that water can be used as the solvent in the binder solution. Preferably, the urea-formaldw hyde reaction product is in granular or powder form, because it is easier to incorporate the usual small proportion of binder uniformly with the sand by making a dry mixture of the binder and the sand. The water or other solvent for the urea-formaldehyde reaction product is then added to the dry mixture to produce the green sand.
A hardening agent is preferably included in the green sand in order to accelerate the hardening or setting of the urea-formaldehyde reaction product during the baking of the core. The
hardening agent may be any substance that gives an acid reaction under the conditions of baking, such as an acid, an acid salt, or a substance that liberates acid at the baking temperture. The mount of the hardening agent is simply an amount such as to cause the hardening to take place at the desired rate during baking, The hardening agent may be omitted if desired, and the amount used should not base great as to cause substantial hardening oi the binder to occur at ordinary temperatures prior to molding of the core.
A water-soluble urea-formaldehyde reaction product is much more stable in dry form than in the form of an aqueous solution. The preferred form of core binder embodying the invention is a dry stable mixture of ahardenable watersoluble urea-formaldehyde reaction product and a hardening agent therefor.' Hardening agents that may be used to give such a stable mixture are zinc sulphate, zinc chloride, ammonium sulphate, ammonium dihydrogen phosphate, diammonium hydrogen phosphate and ammonium oxalate. Other hardening agents, such as ammonium chloride, ammonium thiocyanate and various other acids and acid salts, should not be left in admixture with the dry urea-formaldehyde reaction product, because they cause it to harden radually at ordinary temperatures. I
A dry stable mixture of a hardenable watersoluble urea-formaldehyde reaction product and a hardening agent therefor, embodyin the invention, is highly advantageous as a binder for use in sand cores for casting light metal alloys, because such a mixture can be-kept on hand for indefinite periods and used as needed. Since the hardening agent is already incorporated inthe mixture, it is not necessary for the foundrymen to take the responsibility of mixing the proper amount of hardening agent with the urea-formaldehyde reaction product. The amount of urea-formaldehyde reaction product used in makin up a small quantity of green sand is minute, and the proper amount of hardening agent therefor might have to be weighed out on an analytical balance.
For the sake of economy, the amount of the urea-formaldehyde reaction product used in preparin a sand core in accordance with the present invention is simply an amount suflicient to produce a core of the desired strength, which is usually about /2 per cent or more of the weight i of dry sand. 1 per cent of the weight of dry sand is ordinarily sufflcient.
A green sand core embodying the invention has moderate strength, but if desired the green strength of the core can be increased in the usual manner by adding cereal binders or the like. The green strength of a core embodying the invention is enhanced by the rigidiflcation of the outer surface of the core which occurs as thecore dries out at ordinary temperatures.
The amount of water used in making the core depends upon the kind of sand, the amount of cereal binder, if any, and other factors, and is simply an amount sufllcient .to give the desired green strength and flow-properties of the green sand-usually from about 2 to about 6 per cent of fire weight of dry sand.
when a hardening agent is incorporated in the core, the amount of baking necessary to'dry out the core thoroughly is usually suflicient to complete the hardening or setting of the ureauntil uniform wetting of the sand has taken place. The resulting green sand can be stored formaldehyde reaction product. If no hardenin agent 'is used, a higher baking temperature may be required, but it is never necessaryto bake at a temperature above 300 F. Usually, the lower the temperature, the longer the period of baking that is required. In any case. the amount of heating should not be so great as to decompose the urea-formaldehyde reaction product. For example, a core embodying the invention should not be baked more than 4 hours at 350 F. 4 hours of baking at 300 F. is ordinarily sufllcient for cores up to 6 inchesthick. Thicker cores cannot be uniformly heated throughout in 4 hours, and should therefore be baked for a longer period at a lower temperature.
A water-soluble hardenable urea-formaldehyde reaction product may be prepared as follows: 1 mol of urea is added to a '37 uper cent aqueous solution containing 2 mols of formaldehyde that has been brought to pH 4.5-5.5 by means of sodium hydroxide. The solution is then gently refluxed long enough (about 1 hour) to carry the reaction to the desired stage. Since a ureaformaldehyde reaction product is most stable in a neutral condition, the solution is then preferably neutralized. In order to produce a solid product, the solution may be diluted with water or evaporated under vacuum to the proper concentration, and then spray-dried or vacuum drum-dried. A few per cent of a cellulose filler such as fine wood flour may be added prior to the drying operation.
Example 1 Example 2 1 part of a binder prepared in accordance with Example 1 is mixed with 100 parts of dry sand, a suitable proportion of a metal protector, and any other desired dry ingredients, such as a cereal binder, in a standard mixer such as a foundry muller. Enough water (about 4 parts) to produce a damp mixture of the desired consistency is then added, and mixing is continued until needed. No appreciable deterioration occurs in a period of 48 hours. If the surface of a pile of the reen sand becomes dried out, it can be restored to its original condition by spraying the surface lightly with water. The green sand is formedin a mold to a core of the desired shape. The core is baked at 300 F. for about 4 hours, or,
if more than 6 inches thick, for a longer time at a lower temperature down to about 200 F. The resulting core has a compressive strength of about 250 pounds per square inch.
Various embodiments of the invention may be devised to meet various requirements.
Having described my invention, I claim: 1. A method of casting light metal alloys that includes preparing a green sand core consisting.
essentially of sand, water and a hardenable urea- ,formaldehyde reaction product as a binder, the
. thesand when moistened can be molded into an integral core, moistning, molding, baking. and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
3. A method of casting light metal alloys that includes preparing a green sand core consisting essentially of sand, water, a hardenable urea.- tormaldehyde reaction product as a binder and 'a hardening agent therefor, the proportion of binder being suflicient so that the green sand can be molded into an integral core, baking, and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
binder being sufilcient so that the green sand can be molded into an integral core, baking, and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
5. A method of casting light metal alloys that includes preparing a green sand core consisting essentially of sand, water, a cereal binder and a hardenable urea-formaldehyde reaction product as a binder, the proportion of binder being sumcient so that the green sand can be molded into an integral core, baking. and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape.
6. A method of casting light metal alloys that includes preparing a green sand core consisting essentially of sand, water, a cereal binder, a hardenable urea-formaldehyde reaction product as a binder and a. hardening agent therefor, the proportion of binder being suflicient so that the green sand can be molded into an integral core, baking, and casting a light metal alloy in contact with the core whereby said binder volatilizes substantially completely after the metal has taken its shape. LEONARD S.'M.'EYER.
REFERENCES CITED The following references are of record in the 4. A method of casting light metal alloys that Name Date Ricard Feb. 28, 1939 Wallace et a1. Sept. 24, 1940 Number
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US434588A US2422118A (en) | 1942-03-13 | 1942-03-13 | Making cores for casting light metal alloys |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US434588A US2422118A (en) | 1942-03-13 | 1942-03-13 | Making cores for casting light metal alloys |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2422118A true US2422118A (en) | 1947-06-10 |
Family
ID=23724841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US434588A Expired - Lifetime US2422118A (en) | 1942-03-13 | 1942-03-13 | Making cores for casting light metal alloys |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2422118A (en) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2465094A (en) * | 1947-05-06 | 1949-03-22 | Swan Finch Oil Corp | Binder composition for sand cores |
| US2474186A (en) * | 1947-02-07 | 1949-06-21 | Crane Co | Reinforced core |
| US2508857A (en) * | 1947-02-15 | 1950-05-23 | Dow Chemical Co | Method of reconditioning used sand |
| US2622963A (en) * | 1950-07-11 | 1952-12-23 | Whitehead Bruthers Company | Additive composition for sand molds and method of making same |
| US2657113A (en) * | 1950-02-13 | 1953-10-27 | Int Minerals & Chem Corp | Foundry composition and method |
| US2684344A (en) * | 1950-08-31 | 1954-07-20 | American Cyanamid Co | Core binding composition |
| US2718681A (en) * | 1951-11-28 | 1955-09-27 | Ciba Ltd | Method and compositions for the production of cores for use in metal casting |
| US2753608A (en) * | 1952-03-14 | 1956-07-10 | Aluminum Co Of America | Non-reactive gypsum plaster mold and method of casting therein |
| US2757095A (en) * | 1952-04-30 | 1956-07-31 | Walter Gerlinger Inc | Foundry sand, additive, and method of treating foundry sand |
| US2836867A (en) * | 1950-12-04 | 1958-06-03 | Morris Bean & Company | Process of making mold |
| US2862826A (en) * | 1956-08-13 | 1958-12-02 | Universal Marion Corp | Mold material for casting group ivb metals and method of making same |
| US2876512A (en) * | 1953-11-16 | 1959-03-10 | Ford Motor Co | Shell molding |
| US3011233A (en) * | 1959-09-04 | 1961-12-05 | Gen Electric | Refractory sulfide casting cores |
| US3075943A (en) * | 1959-09-14 | 1963-01-29 | Dow Chemical Co | Latent gaseous catalysis |
| US3108340A (en) * | 1958-03-10 | 1963-10-29 | Dow Chemical Co | Preparation of foundry cores |
| US3138836A (en) * | 1960-12-27 | 1964-06-30 | Gen Motors Corp | Foundry molds and cores and process for making same |
| US3247556A (en) * | 1960-03-28 | 1966-04-26 | Int Minerals & Chem Corp | Sand mold process using resinous binder from alkaline condensation of urea, formaldehyde, and furfuryl alcohol |
| US3380842A (en) * | 1963-09-20 | 1968-04-30 | Georgia Pacific Corp | Decorative composition and a process for its use |
| US4370463A (en) * | 1978-06-14 | 1983-01-25 | Ashland Oil, Inc. | Process for no-bake foundry application utilizing polyurethanes based on amine polyols |
| US4448907A (en) * | 1981-03-30 | 1984-05-15 | Ashland Oil, Inc. | Process for casting lightweight metals |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2148642A (en) * | 1936-12-08 | 1939-02-28 | Ricard Rene Francois Jules | Process for the manufacture of molds and cores for castings |
| US2215825A (en) * | 1938-03-16 | 1940-09-24 | Matilda Wallace | Core binder |
-
1942
- 1942-03-13 US US434588A patent/US2422118A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2148642A (en) * | 1936-12-08 | 1939-02-28 | Ricard Rene Francois Jules | Process for the manufacture of molds and cores for castings |
| US2215825A (en) * | 1938-03-16 | 1940-09-24 | Matilda Wallace | Core binder |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2474186A (en) * | 1947-02-07 | 1949-06-21 | Crane Co | Reinforced core |
| US2508857A (en) * | 1947-02-15 | 1950-05-23 | Dow Chemical Co | Method of reconditioning used sand |
| US2465094A (en) * | 1947-05-06 | 1949-03-22 | Swan Finch Oil Corp | Binder composition for sand cores |
| US2657113A (en) * | 1950-02-13 | 1953-10-27 | Int Minerals & Chem Corp | Foundry composition and method |
| US2622963A (en) * | 1950-07-11 | 1952-12-23 | Whitehead Bruthers Company | Additive composition for sand molds and method of making same |
| US2684344A (en) * | 1950-08-31 | 1954-07-20 | American Cyanamid Co | Core binding composition |
| US2836867A (en) * | 1950-12-04 | 1958-06-03 | Morris Bean & Company | Process of making mold |
| US2718681A (en) * | 1951-11-28 | 1955-09-27 | Ciba Ltd | Method and compositions for the production of cores for use in metal casting |
| US2753608A (en) * | 1952-03-14 | 1956-07-10 | Aluminum Co Of America | Non-reactive gypsum plaster mold and method of casting therein |
| US2757095A (en) * | 1952-04-30 | 1956-07-31 | Walter Gerlinger Inc | Foundry sand, additive, and method of treating foundry sand |
| US2876512A (en) * | 1953-11-16 | 1959-03-10 | Ford Motor Co | Shell molding |
| US2862826A (en) * | 1956-08-13 | 1958-12-02 | Universal Marion Corp | Mold material for casting group ivb metals and method of making same |
| US3108340A (en) * | 1958-03-10 | 1963-10-29 | Dow Chemical Co | Preparation of foundry cores |
| US3011233A (en) * | 1959-09-04 | 1961-12-05 | Gen Electric | Refractory sulfide casting cores |
| US3075943A (en) * | 1959-09-14 | 1963-01-29 | Dow Chemical Co | Latent gaseous catalysis |
| US3247556A (en) * | 1960-03-28 | 1966-04-26 | Int Minerals & Chem Corp | Sand mold process using resinous binder from alkaline condensation of urea, formaldehyde, and furfuryl alcohol |
| US3138836A (en) * | 1960-12-27 | 1964-06-30 | Gen Motors Corp | Foundry molds and cores and process for making same |
| US3380842A (en) * | 1963-09-20 | 1968-04-30 | Georgia Pacific Corp | Decorative composition and a process for its use |
| US4370463A (en) * | 1978-06-14 | 1983-01-25 | Ashland Oil, Inc. | Process for no-bake foundry application utilizing polyurethanes based on amine polyols |
| US4448907A (en) * | 1981-03-30 | 1984-05-15 | Ashland Oil, Inc. | Process for casting lightweight metals |
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