US2659654A - Composition for manufacture of sand cores - Google Patents

Composition for manufacture of sand cores Download PDF

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US2659654A
US2659654A US184907A US18490750A US2659654A US 2659654 A US2659654 A US 2659654A US 184907 A US184907 A US 184907A US 18490750 A US18490750 A US 18490750A US 2659654 A US2659654 A US 2659654A
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oil
core
binder
sand
weight
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John B Tuttle
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Standard Oil Development Co
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22C—FOUNDRY MOULDING
    • B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • 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
    • B22C1/24—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 oily or fatty substances; of distillation residues therefrom

Definitions

  • the present invention relates to. an improved composition for the manufacture of sand cores, and the like, for the casting. of metal. It. relates, particularly, to a so-called core. oil or binder of the type which is used to form sand coresfor the. casting of hollow metal products.
  • a binder As the sands used for core manufacture have no natural binding property, it is necessary to. introduce into the sand a binder. This binder is mechanically mixed with the sand that is to make, up the core prior to core formation.
  • sand cores of appropriate structural properties.
  • the binder must mix well with the sand, coating the sand particles so the core is of uniform density.
  • the binder must not create a sticky condition which would gum up the core molding boxes and it must not cause the core to swell or, crack in baking or in storage.
  • the binder must not absorb moisture from the atmosphere after it has been set in the mold Waiting for the metal to be poured. Further, the binder must impart sufii'cient bond strength to the core before it is baked to permit manual handling.
  • the binder must also permit easy removal. ofthe sand core.- from its mold prior to baking.
  • the. binder During baking, the. binder must oxidize and polymerize to yield a, sand core having sufiicient tensile strength to withstand the weight of metal when the casting is; poured and also sufiicient strength to resist: ordinary handling in the foundry, both before and: after baking. Also, the binder must decompose when the metal. is poured. With a proper binder, when the casting. is cooled, the core sand. can. be easily broken up and shaken free from the casting. These last two characteristics are in essential opposition to. each other and require careful balancing of the ingredients in any core oil. or sand binder.
  • such cores are baked with an optimum amount of the core oil binder, the preferred compositions having the property of polymerizing to a moderate extent to serve as a. binder.
  • Baking is conventionally carried out in a ventilated oven at moderately high temperatures, e. g., between 350 and 600 F. At such temperatures, volatile constituents of the core oil or binder are removed but the residue polymerizes or thickens without. undue. charring to bind the sand into a fairly strong and firm structure.
  • the molten metal temperature is. quite high, ranging from 120.0" F. for aluminum to approximately 3000 F. for iron.
  • The. temperature of the metal and the nature of. the. binder are preferably such that the binder breaks down immediately after the metal is. formed and the sand can be freely shaken out of the cast metal product.
  • hydrocarbon polymers such as those obtained by clay filtering of cracked gasoline, have desirable properties for use in core oils, paints and varnishings.
  • the patent to Chittick, No. 1,891,079 suggests the use of such a polymer in a, core oil with addition of a drying oil for such purposes.
  • such hydrocarbon polymers may be combined with a fish oil which polymerizes moderately at the baking temperature and breaks down at casting temperature to permit. ready removal of the sand core.
  • Linseed oil, soyabean oil, fish oil and related animal and vegetable oils having drying characteristics have been used in various proportions with and Without the hydrocarbon polymers mentioned above.
  • Per cent by Weight Raw linseed oil 20 Sardine oil 20 Clay filtered polymer from cracked gasoline l5 Kerosene 15 core oils after baking, and prior to casting, may be substantially increased by the used of about to 30% by weight, based on the total composition, of a relatively viscous mineral oil, preferably one of a fairly heavy lubricating grade.
  • a relatively viscous mineral oil preferably one of a fairly heavy lubricating grade.
  • Such oils should have a viscosity between 100 and 500 S. S. U. at 210 F.
  • a viscosity range of about 100 to 300 S. S. U. is ordinarily quite satisfactory and oils having a viscosity in the neighborhood of 200 S. S. U. at 210 F. are particularly preferred.
  • a drying oil such as raw linseed oil, soyabean oil, or both, is combined with an unsaturated fatty oil, preferably a fish oil such as sardine oil, either with or without the presence of wood rosin or esterified tall oil.
  • drying oil and fish oil products described above which comprise to or more of the total weight of the composition, are added from about 15 to 35% of the hydrocarbon polymer obtained by clay filtering of steam cracked gasolines, preferably 25 to 35%, and from 5 to 30% of the mineral oil mentioned above.
  • One suth polymer is derived from the steam cracking of gasoline at high temperature and low pressure, e. g., at a temperature of the range of 1100 F. to 1300 F.
  • This product is a very viscous, semi-solid, highly unsaturated plastic material.
  • the product is well known in the petroleum industry and has been unofiicially designated CTLA polymer.
  • the polymer may be derived in various ways from gasoline refining processes, one preferred method is to filter the gasoline through clay and then to extract the polymer deposited on the clay with a light solvent, such as butane, propane, or the like, after which the solvent, of course, is evaporated and the residue of fairly high molecular weight and of consistency from heavy viscous to solid is used as the polymer constituent of the binder.
  • a light solvent such as butane, propane, or the like
  • any of the previously mentioned types of mineral oils may be used as the modifiers for enhancing the strength of the core after baking. They improve the essentially brittle nature of the polymers which remain after baking. At the same time, the presence of the oil does not yield a core which breaks up with diificulty following the pouring of the metal.
  • the product is such that the oil is sufficiently non-volatile to remain as a plasticizer during the baking operation, but it decomposes with the rest of the binder under the influence of the higher temperature of the poured metal.
  • the presence of the high viscosity mineral oil permits in some cases at least, reduction in the more expensive fish oil and linseed oil components permitting even greater use of the petroleum polymers which are less expensive but per se are distinctly brittle in nature after baking.
  • Oil C in the example previously given is preferable for use when high concentrations of petroleum polymers are used. During manufacture, this oil seems to blend better with the other constituents, possibly due to its lower aniline point, and during baking it yields cores of superior tensile strength and resistance to breaking.
  • Example I by weight raw linseed oil soyabean oil wood rosin sardine oil 10.00% oil A (above) This core oil yielded satisfactory cores when oil A was present but without the addition of it, gave brittle cores.
  • Example 11 17.50% by weight raw linseed oil 17.50% sardine oil 48.75% clay filtered polymer from cracked gasoline 16.25% oil C (above)
  • the presence of the oil is necessary to secure cores that are not entirely brittle and which, at the same time, break up freely after metal pouring.
  • Example III 39.00% by weight of raw linseed oil 17.50% sardine oil 30.00% clay filtered polymer from cracked gasoline 12.57% oil A. (above) 0.42% lead linoresinate (30%) 0.31% manganese linoresinate (8%) 0.20% cobalt resinate (3% cobalt oxide)
  • the presence of the petroleum oil plasticizer in no way interferes with the behavior of the metallic driers, and yields cores of adequate strentgh which are not friable.
  • the linseed oil content was increased and the hydrocarbon polymer reduced, as compared with the prior art product previously referred to.
  • the baked core was distinctly superior in strength after baking, and still broke up easily after casting. Considerably less linseed oil may be used with entirely satisfactory results, as in Example II, or it may be eliminated altogether as in Example IV.
  • Example IV 25.00% by weight of sardine oil 25.00% soyabean oil 40.00% esterified tall oil 9.50% oil B (above) 0.50% pine oil
  • tall oil replaced the petroleum gasoline polymer and the oil plasticizer still serves its intended purposes of minimizing brittleness in baked cores.
  • the small amount of pine oil contributes an agreeable element to the odor of the binder before and during baking.
  • Example IV The use in Example IV of high boiling mineral oil, preferably lubricating oil extract, as a plasticizer, prevented crumbling and did not materially reduce ultimate strength,
  • the core oil of the present invention provides a more durable sand core, because of the plasticizer used, but does not interfere with the breaking up and ready removal of the sand core after casting.
  • modifiers known to the prior art may be used in small proportions without departing from the present invention. Such modifiers in small quantities, usually less than 1%, as cobalt, manganese and lead driers, have been quite useful, as suggested above, and the invention contemplates their inclusion when desirable.
  • the proportions of the various ingredients may be varied within the limits previously set forth, preferred proportions being about 25 to 35% by weight of the hydrocarbon polymer, or as much as 50% in some cases where strength is not quite so critical, to of the viscous mineral base oil and 15 to 22% each of soyabean oil, raw linseed oil and fish oil, such as the sardine oil.
  • the proportions of the last three ingredients may be varied very widely since they are roughly equivalent to each other in respeot to polymer formation and drying characteristics. For many reasons, one or more of the three drying oils last mentioned can be eliminated entirely, being replaced by larger proportions of one or more of the other retained ingredients. It is generally preferred, however, that at least two drying oils, in total proportions of 30 to 50% by Weight, based on the entire composition be used.
  • the cracked gasoline polymer or equivalent resinous material may be replaced partly or entirely by wood rosin or any substantially hydrocarbon resin or polymer which will retain substantial tensile strength after baking (350 to 600 F.), but will quite fully disintegrate at metal casting temperatures of 1200 to 3000 F. or so.
  • a core oil composition comprising about 30 to 50% by weight, based on the total composition, of drying oil, 15 to 35% of an unsaturated clayfiltered polymer of cracked gasoline derivation and 5 to by weight of a viscous mineral oil of at least 100 and not more than 500 S. S. U. viscosity of 210 F.
  • a core binder composition comprising at least 30% of drying oil, 15 to 35% by weight of the hydrocarbon polymer obtained by filtering cracked gasoline and 5 to 20% by weight, based on the total composition, of a viscous mineral oil 8 having a. viscosity of about -500 S. S. U. at 210 F. as a plasticizer.
  • composition according to claim 2 wherein the plasticizer is a lubricating oil extract.
  • composition according to claim 2 wherein the plasticizer is a. naphthenic lubricating oil extract of between 100 and 300 S. S. U. viscosity.
  • composition according to claim 2 wherein the plasticizer is an oil of about 200 S. S. U. viscosity.
  • a binding material for sand casting cores, and the like consisting essentially of 25 to 35% by Weight of the hydrocarbon polymer obtained by clay filtering of steam-cracked gasoline, 10 to 15% of a mineral base oil of 100 to 300 S. S. U. viscosity at 210 F. and at least two of the following: 15 to 22% soyabean oil, 15 to 22% sardine oil and 15 to 22% raw linseed oil.
  • a binding material for sand cores, and the like consisting essentially of the following ingredients by approximate weight:
  • a core oil consisting essentially of a total of 30 to 50% by Weight of one to three drying oils selected from the group consisting of linseed oil, soyabean oil and fish oil, 15 to 35% of a hydrocarbon polymer obtained by filtering cracked gasoline, which polymer retains substantial tensile strength at baking temperatures up to 600 F., and 5 to 20% of a mineral base lubricating oil of at least 100 and not over 500 S. S. U. viscosity at 210 F.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

Patented Nov. 17, 1953 CQOlWPOSITION FOR MANUFACTURE OF SAND CORES John B. Tuttle, Pelham Manor, N. Y.,. assignor to:
Standard Oil Development Company, a. corporation of Delaware No Drawing; Application September 14, 1950, SerialNo. 184,907
11. Claims} (01. ltd-38.7)
The present invention relates to. an improved composition for the manufacture of sand cores, and the like, for the casting. of metal. It. relates, particularly, to a so-called core. oil or binder of the type which is used to form sand coresfor the. casting of hollow metal products. As the sands used for core manufacture have no natural binding property, it is necessary to. introduce into the sand a binder. This binder is mechanically mixed with the sand that is to make, up the core prior to core formation.
As is well known in the art, in the manufacture ofhollow castings, such as steam radiators, automotive engine blocks, and the like, considerable skill is necessary in preparing sand cores of appropriate structural properties. The binder must mix well with the sand, coating the sand particles so the core is of uniform density. The binder must not create a sticky condition which would gum up the core molding boxes and it must not cause the core to swell or, crack in baking or in storage. The binder must not absorb moisture from the atmosphere after it has been set in the mold Waiting for the metal to be poured. Further, the binder must impart sufii'cient bond strength to the core before it is baked to permit manual handling. The binder must also permit easy removal. ofthe sand core.- from its mold prior to baking.
During baking, the. binder must oxidize and polymerize to yield a, sand core having sufiicient tensile strength to withstand the weight of metal when the casting is; poured and also sufiicient strength to resist: ordinary handling in the foundry, both before and: after baking. Also, the binder must decompose when the metal. is poured. With a proper binder, when the casting. is cooled, the core sand. can. be easily broken up and shaken free from the casting. These last two characteristics are in essential opposition to. each other and require careful balancing of the ingredients in any core oil. or sand binder.
In the prior art, it has been. common to use various compositions comprising. linseed oil, fish oil, and other fatty, vegetable and animal oils, along with. modifiers of various types in the formation of sand cores for metal castings. oils have been chosen since, during baking, they combine with oxygen in the air and are converted into a strong binder cementing the grains of sand to each other yielding a firm hard sand core.v
Commonly, such cores are baked with an optimum amount of the core oil binder, the preferred compositions having the property of polymerizing to a moderate extent to serve as a. binder.
These.
Baking is conventionally carried out in a ventilated oven at moderately high temperatures, e. g., between 350 and 600 F. At such temperatures, volatile constituents of the core oil or binder are removed but the residue polymerizes or thickens without. undue. charring to bind the sand into a fairly strong and firm structure.
To facilitate this oxidation and polymerization, it is common in the prior art to add the soaps of lead, manganese and/or cobalt to the binder to accelerate polymerization. This action is well known and is similar to the employment of these additives in the manufacture of linseed oil paints.
Later, when the. actual casting. takes place, the molten metal temperature is. quite high, ranging from 120.0" F. for aluminum to approximately 3000 F. for iron. The. temperature of the metal and the nature of. the. binder are preferably such that the binder breaks down immediately after the metal is. formed and the sand can be freely shaken out of the cast metal product.
It has also. been known in the prior art that certain hydrocarbon polymers, such as those obtained by clay filtering of cracked gasoline, have desirable properties for use in core oils, paints and varnishings. For example, the patent to Chittick, No. 1,891,079, suggests the use of such a polymer in a, core oil with addition of a drying oil for such purposes. It has also been suggested that. such hydrocarbon polymers may be combined with a fish oil which polymerizes moderately at the baking temperature and breaks down at casting temperature to permit. ready removal of the sand core.
Linseed oil, soyabean oil, fish oil and related animal and vegetable oils having drying characteristics have been used in various proportions with and Without the hydrocarbon polymers mentioned above.
An example of this prior art type of core oil is as follows:
Per cent by Weight Raw linseed oil 20 Sardine oil 20 Clay filtered polymer from cracked gasoline l5 Kerosene 15 core oils after baking, and prior to casting, may be substantially increased by the used of about to 30% by weight, based on the total composition, of a relatively viscous mineral oil, preferably one of a fairly heavy lubricating grade. Such oils should have a viscosity between 100 and 500 S. S. U. at 210 F. A viscosity range of about 100 to 300 S. S. U. is ordinarily quite satisfactory and oils having a viscosity in the neighborhood of 200 S. S. U. at 210 F. are particularly preferred.
Three types of high viscosity mineral oils have been found suitable. However, it is not intended to limit the present patent to these but they are given as examples of the products most suitable. The physical characteristics of these three preferred products appear below:
Oil A Oil B Oil C Specific Gra 'i t s 919 9471 9895 Flash Point, F 530 540 470 Pour Point, +50 S S U. at100 5, 345 9, 537 -15, 000 S S U. at 2E0 l 200 231 253 Aniline Point, F 200 180 120 ponents blended therewith, but preferably the oil used is primarily of one of these types.
According to the present invention, a drying oil, such as raw linseed oil, soyabean oil, or both, is combined with an unsaturated fatty oil, preferably a fish oil such as sardine oil, either with or without the presence of wood rosin or esterified tall oil.
To the drying oil and fish oil products described above, which comprise to or more of the total weight of the composition, are added from about 15 to 35% of the hydrocarbon polymer obtained by clay filtering of steam cracked gasolines, preferably 25 to 35%, and from 5 to 30% of the mineral oil mentioned above.
One suth polymer is derived from the steam cracking of gasoline at high temperature and low pressure, e. g., at a temperature of the range of 1100 F. to 1300 F. This product is a very viscous, semi-solid, highly unsaturated plastic material. The product is well known in the petroleum industry and has been unofiicially designated CTLA polymer.
While the polymer may be derived in various ways from gasoline refining processes, one preferred method is to filter the gasoline through clay and then to extract the polymer deposited on the clay with a light solvent, such as butane, propane, or the like, after which the solvent, of course, is evaporated and the residue of fairly high molecular weight and of consistency from heavy viscous to solid is used as the polymer constituent of the binder.
Any of the previously mentioned types of mineral oils may be used as the modifiers for enhancing the strength of the core after baking. They improve the essentially brittle nature of the polymers which remain after baking. At the same time, the presence of the oil does not yield a core which breaks up with diificulty following the pouring of the metal. The product is such that the oil is sufficiently non-volatile to remain as a plasticizer during the baking operation, but it decomposes with the rest of the binder under the influence of the higher temperature of the poured metal. The presence of the high viscosity mineral oil permits in some cases at least, reduction in the more expensive fish oil and linseed oil components permitting even greater use of the petroleum polymers which are less expensive but per se are distinctly brittle in nature after baking. Oil C in the example previously given is preferable for use when high concentrations of petroleum polymers are used. During manufacture, this oil seems to blend better with the other constituents, possibly due to its lower aniline point, and during baking it yields cores of superior tensile strength and resistance to breaking.
The invention will be more particularly understood by reference to the following specific examples:
Example I by weight raw linseed oil soyabean oil wood rosin sardine oil 10.00% oil A (above) This core oil yielded satisfactory cores when oil A was present but without the addition of it, gave brittle cores.
Example 11 17.50% by weight raw linseed oil 17.50% sardine oil 48.75% clay filtered polymer from cracked gasoline 16.25% oil C (above) Here again, the presence of the oil is necessary to secure cores that are not entirely brittle and which, at the same time, break up freely after metal pouring.
Example III 39.00% by weight of raw linseed oil 17.50% sardine oil 30.00% clay filtered polymer from cracked gasoline 12.57% oil A. (above) 0.42% lead linoresinate (30%) 0.31% manganese linoresinate (8%) 0.20% cobalt resinate (3% cobalt oxide) In this case, the presence of the petroleum oil plasticizer in no way interferes with the behavior of the metallic driers, and yields cores of adequate strentgh which are not friable. In this example, the linseed oil content was increased and the hydrocarbon polymer reduced, as compared with the prior art product previously referred to. The baked core was distinctly superior in strength after baking, and still broke up easily after casting. Considerably less linseed oil may be used with entirely satisfactory results, as in Example II, or it may be eliminated altogether as in Example IV.
Example IV 25.00% by weight of sardine oil 25.00% soyabean oil 40.00% esterified tall oil 9.50% oil B (above) 0.50% pine oil In this case, tall oil replaced the petroleum gasoline polymer and the oil plasticizer still serves its intended purposes of minimizing brittleness in baked cores. The small amount of pine oil contributes an agreeable element to the odor of the binder before and during baking.
The use in Example IV of high boiling mineral oil, preferably lubricating oil extract, as a plasticizer, prevented crumbling and did not materially reduce ultimate strength,
It should be emphasized that the core oil of the present invention provides a more durable sand core, because of the plasticizer used, but does not interfere with the breaking up and ready removal of the sand core after casting.
It will be understood that various modifiers known to the prior art may be used in small proportions without departing from the present invention. Such modifiers in small quantities, usually less than 1%, as cobalt, manganese and lead driers, have been quite useful, as suggested above, and the invention contemplates their inclusion when desirable. The proportions of the various ingredients may be varied within the limits previously set forth, preferred proportions being about 25 to 35% by weight of the hydrocarbon polymer, or as much as 50% in some cases where strength is not quite so critical, to of the viscous mineral base oil and 15 to 22% each of soyabean oil, raw linseed oil and fish oil, such as the sardine oil. The proportions of the last three ingredients may be varied very widely since they are roughly equivalent to each other in respeot to polymer formation and drying characteristics. For many reasons, one or more of the three drying oils last mentioned can be eliminated entirely, being replaced by larger proportions of one or more of the other retained ingredients. It is generally preferred, however, that at least two drying oils, in total proportions of 30 to 50% by Weight, based on the entire composition be used. The cracked gasoline polymer or equivalent resinous material may be replaced partly or entirely by wood rosin or any substantially hydrocarbon resin or polymer which will retain substantial tensile strength after baking (350 to 600 F.), but will quite fully disintegrate at metal casting temperatures of 1200 to 3000 F. or so.
What is claimed is:
1. A core oil composition comprising about 30 to 50% by weight, based on the total composition, of drying oil, 15 to 35% of an unsaturated clayfiltered polymer of cracked gasoline derivation and 5 to by weight of a viscous mineral oil of at least 100 and not more than 500 S. S. U. viscosity of 210 F.
2. A core binder composition comprising at least 30% of drying oil, 15 to 35% by weight of the hydrocarbon polymer obtained by filtering cracked gasoline and 5 to 20% by weight, based on the total composition, of a viscous mineral oil 8 having a. viscosity of about -500 S. S. U. at 210 F. as a plasticizer.
3. Composition according to claim 2 wherein the plasticizer is a lubricating oil extract.
4. Composition according to claim 2 wherein the plasticizer is a. naphthenic lubricating oil extract of between 100 and 300 S. S. U. viscosity.
5. Composition according to claim 2 wherein the plasticizer is an oil of about 200 S. S. U. viscosity.
6. A binding material for sand casting cores, and the like, consisting essentially of 25 to 35% by Weight of the hydrocarbon polymer obtained by clay filtering of steam-cracked gasoline, 10 to 15% of a mineral base oil of 100 to 300 S. S. U. viscosity at 210 F. and at least two of the following: 15 to 22% soyabean oil, 15 to 22% sardine oil and 15 to 22% raw linseed oil.
7 A binding material for sand cores, and the like, consisting essentially of the following ingredients by approximate weight:
19.00% raw linseed oil 18.75% soyabean oil 18.75% sardine oil 29.93% clay-filtered polymer from cracked gasoline 12.28% mineral oil of about 200 S. S. U. viscosity at 210 F.
8. A core oil consisting essentially of a total of 30 to 50% by Weight of one to three drying oils selected from the group consisting of linseed oil, soyabean oil and fish oil, 15 to 35% of a hydrocarbon polymer obtained by filtering cracked gasoline, which polymer retains substantial tensile strength at baking temperatures up to 600 F., and 5 to 20% of a mineral base lubricating oil of at least 100 and not over 500 S. S. U. viscosity at 210 F.
9. Composition according to claim 8 wherein said mineral base oil is primarily a Coastal bright stock.
10. Composition according to claim 8 wherein said mineral base oil is primarily a solvent extracted paraffinic oil.
11. Composition according to claim 3 wherein said mineral base oil is primarily a solvent extracted naphthenic oil.
JOHN B. TUTTLE.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,047,297 Stahl July 14, 1936 2,328,622 Crawford Sept. 7, 1943 2,468,956 Burg May 3, 1949 OTHER REFERENCES American Foundryman, October 1948, pages 40-49.

Claims (1)

1. A CORE OIL COMPOSITION COMPRISING ABOUT 30 TO 50% BY WEIGHT, BASED ON THE TOTAL COMPOSITION, OF DRYING OIL, 15 TO 35% OF AN UNSATURATED CLAYFILTERED POLYMER OF CRACKED GASOLINE DERIVATION AND 5 TO 20% BY WEIGHT OF A VISCOUS MINERAL OIL OF AT LEAST 100 AND NOT MORE THAN 500 S.S.U. VISCOSITY OF 210* F.
US184907A 1950-09-14 1950-09-14 Composition for manufacture of sand cores Expired - Lifetime US2659654A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2789331A (en) * 1953-03-30 1957-04-23 Harry W Dietert Company Method and apparatus for making molds useful in casting
US2846336A (en) * 1954-02-01 1958-08-05 Sta Vis Oil Company Method of inhibiting the adherence of moist material to metal surfaces under freezing conditions
US2861307A (en) * 1956-01-10 1958-11-25 Gen Motors Corp Shell molds
US2910748A (en) * 1957-03-11 1959-11-03 Exxon Research Engineering Co Production of binders for sand cores
US2963456A (en) * 1956-08-20 1960-12-06 Exxon Research Engineering Co Production of binders for sand cores
US3227564A (en) * 1961-01-31 1966-01-04 Catalin Ltd Foundry moulding process

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2047297A (en) * 1930-12-05 1936-07-14 Aristo Corp Core and oil therefor
US2328622A (en) * 1942-05-01 1943-09-07 Charles E Crawford Core oil and core
US2468956A (en) * 1946-10-17 1949-05-03 Socony Vacuum Oil Co Inc Core oils

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2047297A (en) * 1930-12-05 1936-07-14 Aristo Corp Core and oil therefor
US2328622A (en) * 1942-05-01 1943-09-07 Charles E Crawford Core oil and core
US2468956A (en) * 1946-10-17 1949-05-03 Socony Vacuum Oil Co Inc Core oils

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2789331A (en) * 1953-03-30 1957-04-23 Harry W Dietert Company Method and apparatus for making molds useful in casting
US2846336A (en) * 1954-02-01 1958-08-05 Sta Vis Oil Company Method of inhibiting the adherence of moist material to metal surfaces under freezing conditions
US2861307A (en) * 1956-01-10 1958-11-25 Gen Motors Corp Shell molds
US2963456A (en) * 1956-08-20 1960-12-06 Exxon Research Engineering Co Production of binders for sand cores
US2910748A (en) * 1957-03-11 1959-11-03 Exxon Research Engineering Co Production of binders for sand cores
US3227564A (en) * 1961-01-31 1966-01-04 Catalin Ltd Foundry moulding process

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