US3243397A - Mold and core coating composition from calcined hydrated aluminum silicate, mica, and bentonite - Google Patents
Mold and core coating composition from calcined hydrated aluminum silicate, mica, and bentonite Download PDFInfo
- Publication number
- US3243397A US3243397A US132294A US13229461A US3243397A US 3243397 A US3243397 A US 3243397A US 132294 A US132294 A US 132294A US 13229461 A US13229461 A US 13229461A US 3243397 A US3243397 A US 3243397A
- Authority
- US
- United States
- Prior art keywords
- slurry
- mold
- weight
- coating
- bentonite
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C3/00—Selection of compositions for coating the surfaces of moulds, cores, or patterns
Definitions
- This invention relates to a coating composition which, when applied to surfaces of foundry sand molds and cores, improves the fluidity of molten metal cast against these surfaces, reduces chill in thin sections and improves the burn-in resistance of the coated surfaces. More particularly, the invention pertains to a foundry mold or core wash containing finely divided mica, calcined hydrated aluminum silicate and bentonite suspended in a liquid carrier.
- This coating composition may be beneficially applied to molds for casting gray cast iron, mallealble iron, spheroidal graphite cast iron, aluminum alloys and magnesium alloys to improve their casting surfaces.
- a principal object of the present invention is to provide a coating for foundry sand molds and cores which materially increases the fluidity of molten casting metals contacting such molds and cores without employing superheat, preheated molds or undesirably high me'tallostatic pressures.
- sound castings of very thin section can be formed by conventional procedures.
- the term fluidity refers to that property of molten casting metal in contact with a mold which allows the metal to flow into the mold and fill it before solidification obstructs further flow of the metal.
- a foundry mold and core coating comprising a slurry of mica or vermiculite powder, finely divided calcined hydrated aluminum silicate, bentonite and a liquid carrier, such as methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, a chlorinated hydrocarbon, commercial mineral spirits or water. Small amounts of phenolic resin or sugar, sodium chloride and a wetting agent also may the beneficially included in the slurry.
- the coating composition thus provided is relatively inexpensive and can be readily applied to the mold surfaces by conventional means such as spraying, dipping or brushing.
- mol as hereinafter generally employed, means a casting form which includes both molds and cores, this invention not being limited to the former.
- sand is used in its generic sense and is not restricted to silica particles.
- the mica powder preferably constitutes approximately 40% to 75% by weight of the solids content of the coating composition, although the amount of mica may vary from as low as about to as high as 85% by weight. At least 10% by ,weight of calcined hydrated aluminum silicate or kaolinite is required where there is a prdblem of metal penetration into the mold, and the amount of this constituent may range up to about 86% of the weight of the solids in the slurry. We have found that optimum results are produced with a calcined hydrated aluminum silicate content of about to by weight.
- the phenolic resin or sugar, if either of these materials is included in the coating composition should not extceed approximately 7% by weight of the solids present. For many applications, 2% to 5% by weight of phenolic resin 3,243,397 Patented Mar. 29, 1966 is preferred, but even 0.5% by weight of the additional binder in the coating causes it to adhere more strongly to the mold.
- the bentonite should constitute no more than 15% by weight of the solids content of the slurry.
- a composition containing 3% to 7% bentonite on a solids basis provides particularly satisfactory results.
- the total amount of bentonite plus resin should not exceed approximately 20% of the weight of the solids in the slurry, and the combination of these two constituents should equal at least 5% by weight of the solids content.
- the particle size of these various powdered constituents should be finer than mesh, and much finer powders are preferred.
- the insulating film between the core or mold and the molten metal is provided principally by the mica powder in the coating, however.
- Mica is ideal for this purpose because it has a low thermal conductivity, high reflectivity for radiant heat and a very low bulk density.
- an essentially mica coating is unsatisfactory for many applications due to its poor burn-in resistance resulting from its failure to penetrate the core sunface because of the platelet shape of its particles. Consequently, it is necessary to add the calcined hydrated aluminum silicate to provide adequate burn-in resistance.
- the burn-in resistance of the coating increases appreciably as the calcined kaolinite content is raised, the mica cannot be eliminated.
- Bentonite is included in the coating composition to improve the slurry suspension, aid in bonding the mica and kaolinite particles together, and provide the coating with improved burn-in resistance.
- both bentonite and phenolic resin tend to reduce the fluidity of the molten casting metal, and it is there-fore desiralble to use only relatively small amounts of these materials.
- the phenolic resin functions as a binder to form a hard, adherent coating on the mold.
- a water-dispersible phenolic resin such as phenol-(formaldehyde resin, has proved to be highly satisfactory for use in a coating in which water is employed as a liquid carrier.
- Sugar is another resinous material which has been used successfully as a binder constituent in place of the phenolic resin.
- the coating should not be removed by normal handling nor should it be blown off with a high pressure air blast. Consequently, the minimum amount of resinous binder which should be included in the slurry is that which will provide adequate nub resistance and air-Iblast resistance.
- a coating composition containing approximately 2 or more by weight of phenolic resin binder normally has excellent resistance to rubbing and air blasting.
- Sodium chloride or hydrochloric acid may be included in the coating slurry to promote its thixotropic properties and thereby improve dipping characteristics.
- the amount of sodium chloride or HCl to be used depends upon the mineral content and pH of any water in the slurry. If the mineral content of the water is high or its pH is low, the addition of the salt or HCl becomes relatively unimportant.
- the sodium chloride should constitute about 0.05% to 3% of the solids content of the coating composition. Approximately 0.15% to 0.3% of a 20% hydrochloric acid solution has proved to be successful in increasing the thixotropy of the slurry without attendant foaming.
- the coating slurry preferably is applied to green sand molds by a spraying procedure, and when this is done it is advantageous to mix the above-described powdered constituents with a volatile organic liquid, such as commercial methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, a chlorinated hydrocarbon or naphthol spirits.
- a slurry of this type also can be used to spray baked sand molds and cores, or water may be employed as a less expensive carrier if the molds and cores are subsequently reheated to dry the coating.
- a water slurry by a dipping operation.
- any excess alcohol can be readily burned ofl.
- wetting agent When a water suspension is used in a clipping operation, it may be desirable to include a small amount of wetting agent if it is necessary to improve the penetration of the slurry into the mold.
- a low-foaming, nonionic wetting agent is preferred for this purpose.
- examples of such a wetting agent are those available under the trade names L-62 Pluronic and L61 Pluronic, products of the Wyandotte Chemical Company, Wyandotte, Michigan. Normally, as little as about 0.1% by weight of wetting agent, based on the solids content of the slurry, is beneficial in this respect; and the amount of wetting agent used ordinarily will be appreciably less than 1%.
- the above-described mold coating compositions may be prepared in the following manner: First, the bentonite is mixed with approximately 15% of the total amount of water used in the slurry. This mixture should be per mitted to stand for at least four hours so that a gel is formed. The remaining water, mica and the calcined hy drated aluminum silicate are added to the gel, and these constituents are thoroughly mixed to produce a smooth slurry. If resin or sugar is to included in the composition, this constituent should then be added to the slurry in a manner to provide minimum agitation, thereby reducing any foaming tendency. Next, the hydrochloric acid or sodium chloride, if either is to be used, is introduced and the resultant liquid composition stirred for an additional five to ten minutes. If NaCl is used it should be dissolved in a small quantity of water before being added to the slurry. When this slurry is about to be used, it should again be thoroughly agitated, and the specific gravity of the mix adjusted to provide the desired consistency.
- the coating composition by first dry blending the bentonite with about 20% to 30% of the kaolinite. This mixture may then be added to the water and the slurry stirred until smooth. Next the mica powder and the balance of the kaolinite are mixed with the slurry to produce a smooth, lump-free slurry.
- Example II Example III
- Example IV Example V
- Example VI Example VII Mica Powder t 881135 381 38 45.3 lbs .5 lb Calcined Georgia Kaolmlte--. 22 lbs 59 lbs 45.3 lbs 34.5 ugsmln ii: fiiii Western Bentonlte lbs 7.6 lbs 4.5 lbs 4 3 lbs 14 lbs 141bs' ghenollc Resin (70% 8011115) S 4.5 lbs b I ugar 91 30 grams grams 2.5 lbs I got 20% solution) i a 210 5-- 300 lbs I w n Wetting Agent-m 400 lbs 400 lbs.
- the quantity of liquid carrier used should be suflicient to provide a slurry which can be readily applied to the mold. If it is desired to dip the mold, the ratio of the liquid carrier to the solids content of the coating composition may vary between approximately 2 to l and 5 to 1. On the other hand, this ratio may be as low as l to 1 for spray coatings. Thus it will be seen that the amount of liquid in the slurry may constitute about to 83% of the total weight of the slurry, but a coating having a Water content of approximately 65% to 75% is generally preferred.
- urea formaldehyde or other soluble resins may be included in the slurry to further increase the hardness and durability of the dried coating.
- a relatively small amount of other binder materials also may be added to the slurry to improve the adhesion of the coating to the sand mold if the binder is soluble or properly dispersible in the liquid carrier.
- these binding agents are thermoplastic resins such as polyvinyl chloride, vinylidene chloride, polyvinyl alcohol and polyvinyl acetate, and thermosetting resins such as melamine formaldehyde.
- more than one polymeric binder may be used in the coating com position, but the total amount of this binder normally should not exceed about 7% by weight of the solids in the coating material.
- each of the above coating compositions had excellent dipping characteristics, dried in a reasonable period of t me and was hard and durable upon drying.
- the coatings substantially reduced chill in thin sectrons and materially aided in the cleanup of the castings.
- Use of these coatings also significantly decreased metal penetration into the mold and/or cores, thereby improvmg the surface finish of the castings in their as-cast conditlon.
- the coatings listed in Table l are less expensive than the commercially available coatings generally employed.
- Table 2 shows the results of the fluidity tests using a 13M gray cast iron in each instance.
- the coatings used in the test are the same coatings listed in Examples II through VII of Table 1 and are correspondingly identified in Table 2:
- microstructure of the Ms-inch thick sections of gray iron castings poured into the coated mold portions was slightly more refined than the microstructure of gray iron specimens cast into the i -inch thick uncoated portions of the same mold. No primary carbide was evident in either section.
- the mold coating described herein has a relatively short drying time and a wide drying temperature range. For example, a coating on port cores for gasoline engine cylinder head castings was dried in only about three minutes at 500 F. without blistering. This coating composition also has good dipping characteristics and is uniform in thickness both before and after drying, as well as being relatively inexpensive to use.
- a slurry for coating casting-defining surfaces of foundry sand molds said slurry being formed from a dry blend comprising approximately to 85 by weight of mica powder, 10% to 86% by weight of calcined hydrated aluminum silicate and 3% to by weight of bentonite to which has been added a liquid carrier in an amount sufiicient to constitute about 50% to 83% of the total weight of the slurry, the particle size of the solid constituents in said slurry not exceeding approximately 80 mesh.
- a coating slurry for application to casting-defining surfaces of a foundry mold consisting essentially of a liquid carrier and a dry blend comprising about 40% to 75% by weight of mica powder, 10% to 50% by weight of finely divided calcined hydrated aluminum silicate and 3% to 15% by weight of bentonite, said liquid carrier being selected from the group consisting of methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, mineral spirits and water in proportions such that said dry blend constitutes approximately 17% to 50% of said slurry, the particle size of the solid constituents in said slurry not exceeding approximately 80 mesh.
- a coating slurry for application to casting-defining 5 surfaces of a foundry mold consisting essentially of about 50% to 83 by weight of water and about 17% to 50% weight of a dry blend comprising approximately 10% to 85% by weight of mica powder, 10% to 86% by weight of finely divided calcined hydrated alu- 1O minum silicate, 3% to 15% by weight of bentonite and 0.5% to 7% by weight of phenol-formaldehyde resin, the combined amount of bentonite plus phenol-formaldehyde resin not exceeding of the weight of the dry blend, the particle sizes of the solid constituents in said slurry not exceeding approximately 80 mesh, said slurry containing about 0.1% to 1% by weight of wetting agent.
- a coating composition for application to casting-defining surfaces of a foundry sand mold consisting essentially of a suspension of a powder in acidic water, said powder having a particle size less than approxi-matley 80 mesh and comprising, by weight, about 10% to 85% mica, 10% to 86% calcined hydrated aluminum silicate and 3% to 15% bentonite, said suspension containing a polymeric organic binder in an amount not in excess of about 7% of the weight of said powder.
- a coating slurry for application to casting-defining surfaces of a foundry mold consisting essentially of about 50% to 83% by weight of water and about 17% to 50% by weight of a dry blend comprising approximately 10% to 85 by weight of mica powder, 10% to 86% by weight of finely divided calcined hydrated aluminum silicate, 3% to 15 by weight of bentonite and 0.5 to 7% by weight of a resinous binder, the combined amount of bentonite plus resinous binder not exceeding 20% of the weight of the dry blend, the particle sizes of the solid constituents in said slurry not exceeding approximately 80 mesh, said slurry containing sufiicient hydrochloric acid to make said slurry acidic.
- a coating slurry for application to casting-defining surfaces of a foundry sand mold to permit molten casting metal in contact with said mold to more readily flow into the mold cavity and fill it before solidification obstructs further flow of said metal said coating slurry consisting essentially of an aqueous dispersion containing approximately 17% to 50% by weight of a finely divided powder comprising about 40% to 75% by weight of mica, 20% to 50% by weight of calcined hydrated aluminum silicate and 3% to 15 by weight of bentonite, the water in said slurry containing at least one dissolved compound which makes said slurry sufiiciently acidic to promote thixotro'py of the bentonite, the particle sizes of the solid constituents in said slurry not exceeding approximately -80 mesh.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Description
United States Patent 3,243,397 MOLD AND CORE COATING COMPOSITION FROM CALCINED HYDRATED ALUMINUM SILICATE, MICA, AND BENTONITE Phillip F. Herkimer, Royal Oak, and Neil M. Lottridge,
Jr., Warren, Mich., assignors to General Motors Corporation, Detroit, Mich, a corporation of Delaware No Drawing. Filed Aug. 18, 1961, Ser. No. 132,294 6 Claims. (Cl. 26029.3)
This invention relates to a coating composition which, when applied to surfaces of foundry sand molds and cores, improves the fluidity of molten metal cast against these surfaces, reduces chill in thin sections and improves the burn-in resistance of the coated surfaces. More particularly, the invention pertains to a foundry mold or core wash containing finely divided mica, calcined hydrated aluminum silicate and bentonite suspended in a liquid carrier. This coating composition may be beneficially applied to molds for casting gray cast iron, mallealble iron, spheroidal graphite cast iron, aluminum alloys and magnesium alloys to improve their casting surfaces.
In the past it was frequently impossible to-successfully cast some thin sections of the aforementioned metals except by superheating the casting metal, preheating the mold and/or substantially increasing the metallostatic pressure. Obviously it is desirable to eliminate these procedures. A principal object of the present invention, therefore, is to provide a coating for foundry sand molds and cores which materially increases the fluidity of molten casting metals contacting such molds and cores without employing superheat, preheated molds or undesirably high me'tallostatic pressures. As a consequence, sound castings of very thin section can be formed by conventional procedures. The term fluidity, as used herein, refers to that property of molten casting metal in contact with a mold which allows the metal to flow into the mold and fill it before solidification obstructs further flow of the metal.
The above and other objects of this invention are attained with a foundry mold and core coating comprising a slurry of mica or vermiculite powder, finely divided calcined hydrated aluminum silicate, bentonite and a liquid carrier, such as methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, a chlorinated hydrocarbon, commercial mineral spirits or water. Small amounts of phenolic resin or sugar, sodium chloride and a wetting agent also may the beneficially included in the slurry. The coating composition thus provided is relatively inexpensive and can be readily applied to the mold surfaces by conventional means such as spraying, dipping or brushing.
it will be understood that the term mol as hereinafter generally employed, means a casting form which includes both molds and cores, this invention not being limited to the former. Likewise, the word sand is used in its generic sense and is not restricted to silica particles.
The mica powder preferably constitutes approximately 40% to 75% by weight of the solids content of the coating composition, although the amount of mica may vary from as low as about to as high as 85% by weight. At least 10% by ,weight of calcined hydrated aluminum silicate or kaolinite is required where there is a prdblem of metal penetration into the mold, and the amount of this constituent may range up to about 86% of the weight of the solids in the slurry. We have found that optimum results are produced with a calcined hydrated aluminum silicate content of about to by weight. The phenolic resin or sugar, if either of these materials is included in the coating composition, should not extceed approximately 7% by weight of the solids present. For many applications, 2% to 5% by weight of phenolic resin 3,243,397 Patented Mar. 29, 1966 is preferred, but even 0.5% by weight of the additional binder in the coating causes it to adhere more strongly to the mold.
Likewise, the bentonite should constitute no more than 15% by weight of the solids content of the slurry. We have found that a composition containing 3% to 7% bentonite on a solids basis provides particularly satisfactory results. The total amount of bentonite plus resin should not exceed approximately 20% of the weight of the solids in the slurry, and the combination of these two constituents should equal at least 5% by weight of the solids content. -In general, the particle size of these various powdered constituents should be finer than mesh, and much finer powders are preferred.
The presence of the calcined hydrated aluminum silicate greatly increases the burn-in resistance of a mold coating having the foregoing composition because it is a refractory material which does not fuse below approximately 3300" F. This constituent fills the porous surfaces of the mold to which the slurry is applied and mechanically stops the molten metal from penetrating these surfaces. Since the calcined kaolinite has a very low bulk density, it also thermally insulates the metal from the mold to some extent, thereby increasing the apparent fluidity of the molten metal.
The insulating film between the core or mold and the molten metal is provided principally by the mica powder in the coating, however. Mica is ideal for this purpose because it has a low thermal conductivity, high reflectivity for radiant heat and a very low bulk density. Nevertheless, an essentially mica coating is unsatisfactory for many applications due to its poor burn-in resistance resulting from its failure to penetrate the core sunface because of the platelet shape of its particles. Consequently, it is necessary to add the calcined hydrated aluminum silicate to provide adequate burn-in resistance. Although the burn-in resistance of the coating increases appreciably as the calcined kaolinite content is raised, the mica cannot be eliminated. 'If the solids in the coating do not contain at least 10% mica, complete penetration of the calcined kaolinite into the mold will not provide any measurable film on the surface of the mold or properly insulate the molten casting metal from the mold unless the slurry is excessively viscous. Without such an insulating film the fluidity of the metal is not significantly increased.
Bentonite is included in the coating composition to improve the slurry suspension, aid in bonding the mica and kaolinite particles together, and provide the coating with improved burn-in resistance. However, both bentonite and phenolic resin tend to reduce the fluidity of the molten casting metal, and it is there-fore desiralble to use only relatively small amounts of these materials.
The phenolic resin functions as a binder to form a hard, adherent coating on the mold. A water-dispersible phenolic resin, such as phenol-(formaldehyde resin, has proved to be highly satisfactory for use in a coating in which water is employed as a liquid carrier. Sugar is another resinous material which has been used successfully as a binder constituent in place of the phenolic resin. Of course, the coating should not be removed by normal handling nor should it be blown off with a high pressure air blast. Consequently, the minimum amount of resinous binder which should be included in the slurry is that which will provide adequate nub resistance and air-Iblast resistance. A coating composition containing approximately 2 or more by weight of phenolic resin binder normally has excellent resistance to rubbing and air blasting.
Sodium chloride or hydrochloric acid may be included in the coating slurry to promote its thixotropic properties and thereby improve dipping characteristics. The amount of sodium chloride or HCl to be used depends upon the mineral content and pH of any water in the slurry. If the mineral content of the water is high or its pH is low, the addition of the salt or HCl becomes relatively unimportant. In general, the sodium chloride should constitute about 0.05% to 3% of the solids content of the coating composition. Approximately 0.15% to 0.3% of a 20% hydrochloric acid solution has proved to be successful in increasing the thixotropy of the slurry without attendant foaming.
The coating slurry preferably is applied to green sand molds by a spraying procedure, and when this is done it is advantageous to mix the above-described powdered constituents with a volatile organic liquid, such as commercial methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, a chlorinated hydrocarbon or naphthol spirits. A slurry of this type also can be used to spray baked sand molds and cores, or water may be employed as a less expensive carrier if the molds and cores are subsequently reheated to dry the coating. Of course, in the case of baked sand cores, it is convenient to apply a water slurry by a dipping operation. When alcohol is used as the liquid carrier, any excess alcohol can be readily burned ofl.
When a water suspension is used in a clipping operation, it may be desirable to include a small amount of wetting agent if it is necessary to improve the penetration of the slurry into the mold. A low-foaming, nonionic wetting agent is preferred for this purpose. Examples of such a wetting agent are those available under the trade names L-62 Pluronic and L61 Pluronic, products of the Wyandotte Chemical Company, Wyandotte, Michigan. Normally, as little as about 0.1% by weight of wetting agent, based on the solids content of the slurry, is beneficial in this respect; and the amount of wetting agent used ordinarily will be appreciably less than 1%.
' scribed above.
The above-described mold coating compositions may be prepared in the following manner: First, the bentonite is mixed with approximately 15% of the total amount of water used in the slurry. This mixture should be per mitted to stand for at least four hours so that a gel is formed. The remaining water, mica and the calcined hy drated aluminum silicate are added to the gel, and these constituents are thoroughly mixed to produce a smooth slurry. If resin or sugar is to included in the composition, this constituent should then be added to the slurry in a manner to provide minimum agitation, thereby reducing any foaming tendency. Next, the hydrochloric acid or sodium chloride, if either is to be used, is introduced and the resultant liquid composition stirred for an additional five to ten minutes. If NaCl is used it should be dissolved in a small quantity of water before being added to the slurry. When this slurry is about to be used, it should again be thoroughly agitated, and the specific gravity of the mix adjusted to provide the desired consistency.
It is also possible to prepare the coating composition by first dry blending the bentonite with about 20% to 30% of the kaolinite. This mixture may then be added to the water and the slurry stirred until smooth. Next the mica powder and the balance of the kaolinite are mixed with the slurry to produce a smooth, lump-free slurry. The resinous binder or binders, the NaCl and the HCl, if used, then can be added in the manner de- Normally the coating slurry is applied to the casting-defining surfaces of the mold at room temperature.
The following Table 1 lists specific examples of coating compositions prepared in accordance with the present invention:
TABLE 1 Example I Example II Example III I Example IV Example V Example VI Example VII Mica Powder t 881135 381 38 45.3 lbs .5 lb Calcined Georgia Kaolmlte--. 22 lbs 59 lbs 45.3 lbs 34.5 ugsmln ii: fiiii Western Bentonlte lbs 7.6 lbs 4.5 lbs 4 3 lbs 14 lbs 141bs' ghenollc Resin (70% 8011115) S 4.5 lbs b I ugar 91 30 grams grams 2.5 lbs I got 20% solution) i a 210 5-- 300 lbs I w n Wetting Agent-m 400 lbs 400 lbs.
The quantity of liquid carrier used should be suflicient to provide a slurry which can be readily applied to the mold. If it is desired to dip the mold, the ratio of the liquid carrier to the solids content of the coating composition may vary between approximately 2 to l and 5 to 1. On the other hand, this ratio may be as low as l to 1 for spray coatings. Thus it will be seen that the amount of liquid in the slurry may constitute about to 83% of the total weight of the slurry, but a coating having a Water content of approximately 65% to 75% is generally preferred.
In addition to the above-described constituents or as a substitute for a portion of the phenolic resin, urea formaldehyde or other soluble resins may be included in the slurry to further increase the hardness and durability of the dried coating. A relatively small amount of other binder materials also may be added to the slurry to improve the adhesion of the coating to the sand mold if the binder is soluble or properly dispersible in the liquid carrier. Among these binding agents are thermoplastic resins such as polyvinyl chloride, vinylidene chloride, polyvinyl alcohol and polyvinyl acetate, and thermosetting resins such as melamine formaldehyde. Of course, more than one polymeric binder may be used in the coating com position, but the total amount of this binder normally should not exceed about 7% by weight of the solids in the coating material.
Each of the above coating compositions had excellent dipping characteristics, dried in a reasonable period of t me and was hard and durable upon drying. In additron, the coatings substantially reduced chill in thin sectrons and materially aided in the cleanup of the castings. Use of these coatings also significantly decreased metal penetration into the mold and/or cores, thereby improvmg the surface finish of the castings in their as-cast conditlon. Furthermore, the coatings listed in Table l are less expensive than the commercially available coatings generally employed.
When dry sand test molds were coated with the abovedescribed slurries, the fluidity of gray cast iron, malleable iron, spheroidal graphite cast iron and aluminum poured at normal casting temperatures into these molds was increased appreciably as compared with the use of similar molds which were uncoated. The fluidity of the molten metals in the molds was determined by means of a double spiral fluidity test mold in which one spiral is coated with the mold wash *while the other remains uncoated, both being fed by the same pouring basin and down sprue. The relative distances the metal travels in the spiral is a measure of the improvement in fluidity.
The following Table 2 shows the results of the fluidity tests using a 13M gray cast iron in each instance. The coatings used in the test are the same coatings listed in Examples II through VII of Table 1 and are correspondingly identified in Table 2:
The microstructure of the Ms-inch thick sections of gray iron castings poured into the coated mold portions was slightly more refined than the microstructure of gray iron specimens cast into the i -inch thick uncoated portions of the same mold. No primary carbide was evident in either section.
Likewise, tests were conducted on molten aluminum using the above-described double spiral fluidity test mold. Aluminum 356 alloy was found to have an apparent fluidity increase of approximately 225% when poured into contact with a test mold coated with the slurry of Example 1V above.
Additional tests under production conditions also showed that use of the new mold coating, by improving the surface finish of the castings, greatly reduced the amount of labor necessary in cleaning operations. Moreover, the coating prevented misruns and cold shuts. As a consequence, leakers were eliminated, and the scrap rate due to such defects was appreciably lowered. Furthermore, the mold coating described herein has a relatively short drying time and a wide drying temperature range. For example, a coating on port cores for gasoline engine cylinder head castings was dried in only about three minutes at 500 F. without blistering. This coating composition also has good dipping characteristics and is uniform in thickness both before and after drying, as well as being relatively inexpensive to use.
While our invention has been described by means of certain specific examples, it is to be understood that its scope is not to be limited thereby except as defined by the following claims.
We claim:
1. A slurry for coating casting-defining surfaces of foundry sand molds, said slurry being formed from a dry blend comprising approximately to 85 by weight of mica powder, 10% to 86% by weight of calcined hydrated aluminum silicate and 3% to by weight of bentonite to which has been added a liquid carrier in an amount sufiicient to constitute about 50% to 83% of the total weight of the slurry, the particle size of the solid constituents in said slurry not exceeding approximately 80 mesh.
2. A coating slurry for application to casting-defining surfaces of a foundry mold, said slurry consisting essentially of a liquid carrier and a dry blend comprising about 40% to 75% by weight of mica powder, 10% to 50% by weight of finely divided calcined hydrated aluminum silicate and 3% to 15% by weight of bentonite, said liquid carrier being selected from the group consisting of methyl alcohol, ethyl alcohol, isopropyl alcohol, toluene, mineral spirits and water in proportions such that said dry blend constitutes approximately 17% to 50% of said slurry, the particle size of the solid constituents in said slurry not exceeding approximately 80 mesh.
3. A coating slurry for application to casting-defining 5 surfaces of a foundry mold, said slurry consisting essentially of about 50% to 83 by weight of water and about 17% to 50% weight of a dry blend comprising approximately 10% to 85% by weight of mica powder, 10% to 86% by weight of finely divided calcined hydrated alu- 1O minum silicate, 3% to 15% by weight of bentonite and 0.5% to 7% by weight of phenol-formaldehyde resin, the combined amount of bentonite plus phenol-formaldehyde resin not exceeding of the weight of the dry blend, the particle sizes of the solid constituents in said slurry not exceeding approximately 80 mesh, said slurry containing about 0.1% to 1% by weight of wetting agent.
4. A coating composition for application to casting-defining surfaces of a foundry sand mold, said composition consisting essentially of a suspension of a powder in acidic water, said powder having a particle size less than approxi-matley 80 mesh and comprising, by weight, about 10% to 85% mica, 10% to 86% calcined hydrated aluminum silicate and 3% to 15% bentonite, said suspension containing a polymeric organic binder in an amount not in excess of about 7% of the weight of said powder.
5. A coating slurry for application to casting-defining surfaces of a foundry mold, said slurry consisting essentially of about 50% to 83% by weight of water and about 17% to 50% by weight of a dry blend comprising approximately 10% to 85 by weight of mica powder, 10% to 86% by weight of finely divided calcined hydrated aluminum silicate, 3% to 15 by weight of bentonite and 0.5 to 7% by weight of a resinous binder, the combined amount of bentonite plus resinous binder not exceeding 20% of the weight of the dry blend, the particle sizes of the solid constituents in said slurry not exceeding approximately 80 mesh, said slurry containing sufiicient hydrochloric acid to make said slurry acidic.
6. A coating slurry for application to casting-defining surfaces of a foundry sand mold to permit molten casting metal in contact with said mold to more readily flow into the mold cavity and fill it before solidification obstructs further flow of said metal, said coating slurry consisting essentially of an aqueous dispersion containing approximately 17% to 50% by weight of a finely divided powder comprising about 40% to 75% by weight of mica, 20% to 50% by weight of calcined hydrated aluminum silicate and 3% to 15 by weight of bentonite, the water in said slurry containing at least one dissolved compound which makes said slurry sufiiciently acidic to promote thixotro'py of the bentonite, the particle sizes of the solid constituents in said slurry not exceeding approximately -80 mesh.
References Cited by the Examiner UNITED STATES PATENTS 1,990,075 2/1935 Horak 10638.27 2,299,374 10/ 1942 Bickford 264-86 2,847,741 8/1958 Meves et al. 10638.27 2,857,285 10/1958 Stoddard 106-3827 2,988,525 6/1961 Clem 260-29.3 3,002,948 10/ 1961 Lawther et al.
MORRIS LIEBMAN, Primary Examiner.
MILTON STERMAN, Examiner.
A. H. KOECKERT, Assistant Examiner.
Claims (1)
1. A SLURRY FOR COATING CASTING-DEFINING SURFACES OF FOUNDRY SAND MOLDS, SAID SLURRY BEING FORMED FROM A DRY BLEND COMPRISING APPROXIMATELY 10% TO 85F% BY WEIGHT OF MICA POWDER, 10% TO 86% BY WEIGHT OF CALCINED HYDRATED ALUMINUM SILICATE AND 3% TO 15% BY WEIGHT OF BENTONITE TO WHICH HAS BEEN ADDED A LIQUID CARRIER IN AN AMOUNT SUFFICIENT TO CONSTITUTE ABOUT 50% TO 83% OF THE TOTAL WEIGHT OF THE SLURRY, THE PARTICLE SIZE OF THE SOLID CONSTITUENTS IN SAID SLURRY NOT EXCEEDING APPROXIMATELY -80 MESH.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US132294A US3243397A (en) | 1961-08-18 | 1961-08-18 | Mold and core coating composition from calcined hydrated aluminum silicate, mica, and bentonite |
GB29904/62A GB951567A (en) | 1961-08-18 | 1962-08-03 | Coating compositions for foundry sand moulds or cores |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US132294A US3243397A (en) | 1961-08-18 | 1961-08-18 | Mold and core coating composition from calcined hydrated aluminum silicate, mica, and bentonite |
Publications (1)
Publication Number | Publication Date |
---|---|
US3243397A true US3243397A (en) | 1966-03-29 |
Family
ID=22453348
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US132294A Expired - Lifetime US3243397A (en) | 1961-08-18 | 1961-08-18 | Mold and core coating composition from calcined hydrated aluminum silicate, mica, and bentonite |
Country Status (2)
Country | Link |
---|---|
US (1) | US3243397A (en) |
GB (1) | GB951567A (en) |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3364040A (en) * | 1965-02-23 | 1968-01-16 | Harbison Walker Refractories | Mold wash |
US3467618A (en) * | 1966-12-21 | 1969-09-16 | Armstrong Cork Co | Halloysite-filled phenolic molded composition |
US3520711A (en) * | 1966-08-22 | 1970-07-14 | Gen Motors Corp | Method of coating a permeable sand core body |
US3627627A (en) * | 1970-02-27 | 1971-12-14 | Chevron Res | Novel adhesive compositions |
US3910798A (en) * | 1971-10-19 | 1975-10-07 | Ici Ltd | Moulding process |
US3998917A (en) * | 1973-05-03 | 1976-12-21 | E. I. Du Pont De Nemours And Company | Ceramic compositions and articles made therefrom |
US4003425A (en) * | 1975-02-11 | 1977-01-18 | The British Cast Iron Research Assoc. | Method of and means for obtaining white cast iron |
US4226625A (en) * | 1979-06-04 | 1980-10-07 | Nalco Chemical Company | Insulating tundish veneer composition useful in casting steel |
US4319925A (en) * | 1981-03-06 | 1982-03-16 | Weston Research Corporation | Coating compositions for metal casting molds |
US4342597A (en) * | 1981-03-06 | 1982-08-03 | Weston Research Corporation | Coating compositions for liners of molten metal troughs and ladles |
US4501843A (en) * | 1984-03-23 | 1985-02-26 | Phillips Petroleum Company | Composition of polymer of olefin with mixed mineral filler |
US4587068A (en) * | 1983-06-24 | 1986-05-06 | Materials Research Corporation | Method of making ceramic tapes |
US4596838A (en) * | 1985-05-30 | 1986-06-24 | The Celotex Corporation | Mine stopping caulk |
US4687790A (en) * | 1985-05-30 | 1987-08-18 | The Celotex Corporation | Mine stopping caulk |
US4862948A (en) * | 1988-02-24 | 1989-09-05 | Borden, Inc. | Phenolic resin adhesive pastes, assemblies prepared therefrom, and processes for preparing cast metal articles using these pastes |
US5437890A (en) * | 1994-04-18 | 1995-08-01 | Edw. C. Levy Co. | Coatings for receptacles |
US20150300289A1 (en) * | 2014-04-18 | 2015-10-22 | Hyundai Motor Company | Cylinder head for engine |
BE1024286B1 (en) * | 2016-12-08 | 2018-01-12 | S.A. Lhoist Recherche Et Developpement | PROCESS FOR HANDLING TANK OR POUCH TO DOLL AND PYRO METALLURGICAL TOOLS |
WO2019224070A1 (en) * | 2018-05-25 | 2019-11-28 | Ask Chemicals Gmbh | Sizing composition, method for coating a casting mould and use of the sizing composition for coating a casting mould |
US11221181B2 (en) * | 2016-12-08 | 2022-01-11 | S.A. Lhoist Recherche Et Developpement | Method for handling a slag pot or ladle and pyrometallurgical tools |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0420781A3 (en) * | 1989-09-08 | 1992-09-02 | Bostlan, S.A. | Refractory paint for covering foundry moulds |
CN115815520B (en) * | 2023-02-14 | 2023-05-09 | 中北大学 | Core paint for aluminum alloy freezing casting and preparation process thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1990075A (en) * | 1933-02-11 | 1935-02-05 | Quandt Chemical Co | Core and mold wash |
US2299374A (en) * | 1941-04-09 | 1942-10-20 | Corning Glass Works | Method of molding nonplastic materials |
US2847741A (en) * | 1954-11-29 | 1958-08-19 | American Steel Foundries | Method of making washed shell mold |
US2857285A (en) * | 1954-08-16 | 1958-10-21 | Stephen D Stoddard | High temperature refractory coating for graphite molds |
US2988525A (en) * | 1957-07-09 | 1961-06-13 | American Colloid Co | Foundry mold composition |
US3002948A (en) * | 1957-09-12 | 1961-10-03 | American Steel Foundries | Shell mold |
-
1961
- 1961-08-18 US US132294A patent/US3243397A/en not_active Expired - Lifetime
-
1962
- 1962-08-03 GB GB29904/62A patent/GB951567A/en not_active Expired
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1990075A (en) * | 1933-02-11 | 1935-02-05 | Quandt Chemical Co | Core and mold wash |
US2299374A (en) * | 1941-04-09 | 1942-10-20 | Corning Glass Works | Method of molding nonplastic materials |
US2857285A (en) * | 1954-08-16 | 1958-10-21 | Stephen D Stoddard | High temperature refractory coating for graphite molds |
US2847741A (en) * | 1954-11-29 | 1958-08-19 | American Steel Foundries | Method of making washed shell mold |
US2988525A (en) * | 1957-07-09 | 1961-06-13 | American Colloid Co | Foundry mold composition |
US3002948A (en) * | 1957-09-12 | 1961-10-03 | American Steel Foundries | Shell mold |
Cited By (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3364040A (en) * | 1965-02-23 | 1968-01-16 | Harbison Walker Refractories | Mold wash |
US3520711A (en) * | 1966-08-22 | 1970-07-14 | Gen Motors Corp | Method of coating a permeable sand core body |
US3467618A (en) * | 1966-12-21 | 1969-09-16 | Armstrong Cork Co | Halloysite-filled phenolic molded composition |
US3627627A (en) * | 1970-02-27 | 1971-12-14 | Chevron Res | Novel adhesive compositions |
US3910798A (en) * | 1971-10-19 | 1975-10-07 | Ici Ltd | Moulding process |
US3998917A (en) * | 1973-05-03 | 1976-12-21 | E. I. Du Pont De Nemours And Company | Ceramic compositions and articles made therefrom |
US4003425A (en) * | 1975-02-11 | 1977-01-18 | The British Cast Iron Research Assoc. | Method of and means for obtaining white cast iron |
US4226625A (en) * | 1979-06-04 | 1980-10-07 | Nalco Chemical Company | Insulating tundish veneer composition useful in casting steel |
US4319925A (en) * | 1981-03-06 | 1982-03-16 | Weston Research Corporation | Coating compositions for metal casting molds |
US4342597A (en) * | 1981-03-06 | 1982-08-03 | Weston Research Corporation | Coating compositions for liners of molten metal troughs and ladles |
US4587068A (en) * | 1983-06-24 | 1986-05-06 | Materials Research Corporation | Method of making ceramic tapes |
US4501843A (en) * | 1984-03-23 | 1985-02-26 | Phillips Petroleum Company | Composition of polymer of olefin with mixed mineral filler |
US4596838A (en) * | 1985-05-30 | 1986-06-24 | The Celotex Corporation | Mine stopping caulk |
US4687790A (en) * | 1985-05-30 | 1987-08-18 | The Celotex Corporation | Mine stopping caulk |
US4862948A (en) * | 1988-02-24 | 1989-09-05 | Borden, Inc. | Phenolic resin adhesive pastes, assemblies prepared therefrom, and processes for preparing cast metal articles using these pastes |
US5437890A (en) * | 1994-04-18 | 1995-08-01 | Edw. C. Levy Co. | Coatings for receptacles |
US20150300289A1 (en) * | 2014-04-18 | 2015-10-22 | Hyundai Motor Company | Cylinder head for engine |
US9617949B2 (en) * | 2014-04-18 | 2017-04-11 | Hyundai Motor Company | Cylinder head for engine |
WO2018104448A1 (en) * | 2016-12-08 | 2018-06-14 | S.A. Lhoist Recherche Et Developpement | Method for handling a slag pot or tank and pyrometallurgical tools |
BE1024286B1 (en) * | 2016-12-08 | 2018-01-12 | S.A. Lhoist Recherche Et Developpement | PROCESS FOR HANDLING TANK OR POUCH TO DOLL AND PYRO METALLURGICAL TOOLS |
US11091650B2 (en) | 2016-12-08 | 2021-08-17 | S. A. Lhoist Recherche Et Developpement | Method for handling a slag pot or ladle and pyrometallurgical tools |
US11221181B2 (en) * | 2016-12-08 | 2022-01-11 | S.A. Lhoist Recherche Et Developpement | Method for handling a slag pot or ladle and pyrometallurgical tools |
WO2019224070A1 (en) * | 2018-05-25 | 2019-11-28 | Ask Chemicals Gmbh | Sizing composition, method for coating a casting mould and use of the sizing composition for coating a casting mould |
CN112334246A (en) * | 2018-05-25 | 2021-02-05 | Ask化学品股份有限公司 | Coating composition, method for coating a casting mould and use of said coating composition for coating a casting mould |
EP4147804A1 (en) * | 2018-05-25 | 2023-03-15 | ASK Chemicals GmbH | Sizing composition, method for coating a casting mould and use of the sizing composition for coating a casting mould |
CN112334246B (en) * | 2018-05-25 | 2023-04-28 | Ask化学品股份有限公司 | Coating composition, method for coating a casting mould, and use of said coating composition for coating a casting mould |
Also Published As
Publication number | Publication date |
---|---|
GB951567A (en) | 1964-03-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3243397A (en) | Mold and core coating composition from calcined hydrated aluminum silicate, mica, and bentonite | |
US4174331A (en) | Refractory moldable composition containing ceramic fiber and colloidal silica | |
JPH05505589A (en) | Composition for dry refractories | |
US4529028A (en) | Coating for molds and expendable cores | |
JPS59502068A (en) | Thixotropic paint composition | |
US2701902A (en) | Method of making molds | |
US3752689A (en) | Refractory laminate based on positive sols and organic or inorganic bases | |
US3445250A (en) | Precision metal casting molds comprising alumina coated silica and a refractory | |
US2491096A (en) | Casting mold | |
US3248237A (en) | Compositions of matter containing organic silicates | |
US3115414A (en) | Foundry mold coating | |
US3146113A (en) | Mould paint | |
JPH07110395B2 (en) | Consumable sand core for die casting | |
US6576330B1 (en) | Boron nitride paste composition, boron nitride “shell” coated ceramic structure, and process of manufacturing | |
US3075847A (en) | Mold coating | |
US3428465A (en) | Preparation of molds | |
US1331816A (en) | Method of casting metal | |
US3011986A (en) | Dip coat composition for metal casting comprising ceramic flour, colloidal silica, gum, alkali metal fluoride and rubber latex | |
US3816145A (en) | Trihydroxydiphenyl as an additive for foundry green molding sands | |
JPH0681839B2 (en) | Lubricant release agent | |
US1453593A (en) | Coating for metal molds | |
US3219465A (en) | Foundry mold coating | |
US3674526A (en) | Moldable metal powder compositions | |
US1955936A (en) | Foundry facing and method of making same | |
JPS5942155A (en) | Mold coating material |