US2618032A - Surface treatment of molds - Google Patents

Surface treatment of molds Download PDF

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US2618032A
US2618032A US110883A US11088349A US2618032A US 2618032 A US2618032 A US 2618032A US 110883 A US110883 A US 110883A US 11088349 A US11088349 A US 11088349A US 2618032 A US2618032 A US 2618032A
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mold
graphite
mold body
suspension
liquid
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Frederick O Traenkner
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Howmet Aerospace Inc
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Aluminum Company of America
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/04Continuous casting of metals, i.e. casting in indefinite lengths into open-ended moulds
    • B22D11/041Continuous casting of metals, i.e. casting in indefinite lengths into open-ended moulds for vertical casting
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C3/00Selection of compositions for coating the surfaces of moulds, cores, or patterns

Definitions

  • the ingot passes through a mold and a small area of adhering metal can cause a long broken streak on the ingot surface. It has also been observed that adherence of metal to the mold often occurs in certain regions of the mold surface which are related to certain combinations of freezing and heat extraction that develop during solidification of the casting.
  • the material of which a mold is made generally exerts an influence upon the surface quality of the casting formed therein.
  • some materials may be "wetted" by molten metal while others are not so affected.
  • some of the materials are porous to the extent that the pores tend to be filled with molten metal as mentioned above.
  • a metal mold made from plate or heavy sheet is not sufli'ciently porous to offer any difllculty on this account, however, if the mold is a'casting or a sintered product made from powdered materials, or if it is made from non-vitrified or compressed non-metallic substances it may have a degree of porosity which ,interferes with obtaining a cast body with a ismooth surface.
  • porous molds often have certain other highly desirable qualities, it is particularly important that the dimculties associated with their porosity should be overcome and thus permit the production of highest quality castings.
  • One of the mold materials which is highly desirable in many ways is graphite but molds of this material usually are porous to some degree and therefore subject to the disadvantage stated above.
  • Mold washes and lubricants have been proposed and used for dressing mold surfaces.
  • mold washes are employed because of 8 Claims. (Cl. 22-192) their'heat insulating properties and are not used where there is relative movement between casting and the mold during the casting operation because of their low resistance to wear and relatively rough surface.
  • Liquid and semi-solid oils and greases of animal, vegetable or mineral origin have been applied to mold surfaces but such substances usually introduce problems such as buming, excessive fumes and the production of a carbonaceous deposit.
  • Solid lubricants such as graphite either alone or associated with other materials have been sprayed or brushed on mold surfaces but such coatings require frequent renewal because they-are only applied superficially and therefor are easily worn or rubbed 01!.
  • a further object is to provide a method of treating porous mold surfaces which is simple and effective in rendering the mold surfaces substantially non-porous.
  • Still another object is to provide a surface on porous molds which does not spell or become loosened in contact with molten metal.
  • Yet another object comprises the provision of a method of applying a materialto the mold surface in such a manner as to cause it to penetrate the surface of the mold .body.
  • Another object is to provide a method of treating the surface which willinsure that the surface is dry at the time it comes in contact with molten metal.
  • mold surfaces herein, it is to be understood that this refers to that surface of a mold or any part thereof which comes in c qntact with molten metal.
  • cores used in forming hollow portions of the castings are considered to be mold parts and they may be treated in the same manner as the main mold I trated by molten metal, are dry and present an exceptionally smooth long wearing surface which does not require lubrication. Because the treated mold surface has no pores of a size which can be penetrated by molten metal it is considered to be substantially non-porous.
  • the treatment introduces colloidal graphite particles into the mold pores and the subsequent baking fixes or anchors them in such a way as to prevent removal unless the mold surface itself is worn or cut away. is most cases a much better surface is developed by repeating the impregnating treatment before the baking operation.
  • the porous mold may be said to be impregnated with colloida1 graphite which is subsequently fixed or stabilized in such a manner as to firmly anchor its position.
  • the mold or mold part to be treated must possess some degree of porosity, the pores being large enough to permit the passage therethrough of colloidal graphite particles. It is obvious, of course, that the treatment is not adapted to the treatment of molds having relatively large pores for the pores must be filled with graphite particles to the extent of providing a smooth mold surface. It has been found that molds exhibiting a pore size from about 4 to 40 microns possess a very satisfactory surface for impregnation with colloidal graphite. While it is desirable that the pores be of about the same size in a given mold or mold part and that the porosity'be relatively uniformly distributed over the mold surface this is not imperative. It is essential, however, that there be enough pores of suitable size for the graphite particles to enter and become anchored therein.
  • the molds may be composed of any one of a number of materials depending upon the properties desired.
  • sintered metallic powders, or mixtures of metallic powders and ceramic materials, or non-metallic materials such as graphite may be employed. Molds made of any of these materials may be successfully treated with colloidal graphite according to my invention providing they possess the proper porosity.
  • One of the materials which has been very successfully treated is that known in the trade as dense graphite. This material has a porosity of from about 20% to about 30%; i. e. 20 to 30% of the volume consists of voids, and it has a pore size of at least 4 microns. This material when in the form of molds and treated with colloidal graphite has been used to produce aluminum alloy castings having exceptionally smooth surfaces.
  • the colloidal graphite preparation which I employ comprises graphite particles suspended in a volatile liquid or carrier.
  • the predominant portion of particles should be of colloidal size.
  • the preparation is herein referred to as a colloidal graphite suspension.
  • the suspension consists of graphite particles about 1 to 8 microns in diameter. Particles of this size are generally considered to be of colloidal size.
  • any graphite particles which are capable of being placed in colloidal suspension and which can enter the mold pores are considered to be satisfactory for the treatment of porous mold surfaces.
  • the proportion of graphite to liquid must be carefully controlled in order to secure the desired penetration of the mold. It has been found that the graphite should not exceed about by weight of the liquid in which it is suspended. A greater proportion impedes the impregnating process and does not permit the establishment or a firmly anchored coating. Smaller amounts may be employed, however, for practical purposes the quantity should not be less than about 1%.
  • the volatile carrier or vehicle should belong to the class of liquids which has a boiling point within the range of from about l00.to 500 F. and have a sumciently low viscosity to permit penetration of the pores of the mold.
  • a preferred group of liquids is that composed of a mixture of hydrocarbons in which 10% are distilled below 347 F. and .not less than below 464 F. Examples of such hydrocarbon mixtures are petroleum naphtha, and mineral spirits.
  • Other organic liquids will also serve satisfactorily such as the lower alcohols. By organic liquids is meant'hydrocarbons and their derivatives which are liquid at room temperature. Under some conditions water may be employed but special precautions may be necessary to insure complete evaporation.
  • the aforesaid liquids serve as suitable carriers for graphite and in most cases possess the necessary wetting power to facilitate penetration of the mold material, it may be desirable to add small amounts of other substances which will serve to keep the graphite particles in suspension or enhance the wetting power of the suspensions.
  • Such materials as metallic salts of long chain alkyl acids, aryl substituted long chain alkyl acids, or aromatic acids are known to have this effect upon carriers of the kind herein described.
  • Some examples of these salts are nickel, zinc or calcium naphthenates, calcium stearate, calcium phenyl stearate, wax aluminum phenate, aluminum carboxylate.
  • the added substances do not in any way interfere with the deposition of the colloidal graphite particles nor the production of the desired quality of mold surface.
  • the treatment of a mold or mold Dart consists in contacting it with a suspension of the type defined above, subsequently permitting the volatile carrier to evaporate, and finally baking the mold. While a single treatment effects an improvement, a better and more durable surface is developed by repeating the treatment at least once, and hence this is preferred.
  • the suspension may be applied in any conventional manner but usually immersion or spraying will be the most convenient method to use.
  • the mold is dried, but in my preferred practice the contacting and drying steps are repeated at least once and often twice.
  • the colloidal particles better penetrate the pores of the mold to a depth that permits subsequent firm anchorage in the pores.
  • Thedrying operation may be conducted atroom temperature or at somewhat higher temperatures, but below 300 F., the object being solely that of evaporating the carrier.
  • the period required for drying will vary with the liquid employed in the suspension and the period of exposure to the suspension. It is not necessary that the drying be carried to the point of removing all traces of the liquid, but it is essential that a major portion be evaporated. A period up to 5 or 6 hours is usually sufiicient.
  • the article After completion of at least one cycle of im aerapaa pregnation and drying the article is then subjected to a baking operation at a temperature of between 500 and 800 F. for a period of at least minutes. This -may extend to several hours. While the baking operation serves to drive off any residual vehicle or carrier it also appears. tofix or stabilize the graphite particle in the pores of the mold with the result that a firmly adherent coating is produced. Because of the firm adherence and durability of the coating obtained in the foregoing manner it may be said to be integrally bonded to the mold as compared to the superficial mold coatings of the prior art.
  • the foregoing process may be repeated. Also, after the mold has been used and some wear may have occurred the mold may be subjected to a single contact with a colloidal suspension followed by baking.
  • the mold surfaces resulting from this treatment are dry and may be used with entire safety in contact with molten metal.
  • the mold surfaces are smooth and free from pores that can be penetrated by molten metal ascompared to the untreated mold surface. Furthermore, no additional lubrication is necessary.
  • Such treated mold surfaces may be used for relatively long periods of time without renewal as compared to a surface that has not been impregnated with colloidal graphite and baked. A durable surface is of particular importance in continuous casting processes where the operation cannot be conveniently interrupted.
  • any type of metal may be cast in contact with molds treated in accordance with my invention providing the casting conditions are such as not to oxidize the coating or the mold, it has been found that aluminum and aluminum base aloy ingots having high surface quality can be cast in such molds.
  • Other non-ferrous metals such as magnesium and copper and their alloys uid boiling between 100 and 500 F., said mold body being at a temperature below the boiling point of said liquid and the period of contact between said mold body and suspension being long enough to permit penetration of said mold body by said suspension, the proportion of said graphite to said liquid not exceeding 15% by weight of the liquid, drying said treated .mold body at a temperat e between room temperature and 300 F. and pier after baking said dried mold body at 500 to 800 F. for a period of at least 15 minutes.
  • said mold body being at a temperature below the boiling point of said liquid and the period of may likewise be cast in contact with the treated molds with resulting advantage tothe surface quality of the cast product.
  • the invention may be illustrated in the following example.
  • a dense graphite mold of circular shape, open at both and bottom and having a diameter of about 14 inches was treated with a colloidal graphite suspension containing about 10% by weight of graphite.
  • the graphite mold had a porosity of about 25% and a pore size between about 4 and 40 microns.
  • the mold was immersed in the colloidal graphite suspension in petroleum naphtha for a period of 30 minutes, withdrawn and dried in air for one hour at a temperature of 250 F. Following this it was again immersed in the suspension and again dried. The process was repeated the third time and following the drying operation, the mold was baked at 700 F. for one hour.
  • the mold as inserted in the continuous casting apparatus for making aluminum base alloy ingots.
  • the ingots coming from this mold had an exceptionally smooth surface and, therefore, required no subsequent surface condition treatment to prepare them for fabricating operations.
  • the mold treated in this manner was found to retain a satisfactory surface after casting 280 ingots having a
  • the method of providing a smooth, durable, substantially non-porous graphite surface on a porous mold body having pores of 4 to 40 microns in size comprising contacting said mold body with a suspension of colloidal graphite in a liquid boiling between and 500 F., said mold body being at a temperature below 100 F. and the period of contact being long enough to permit penetration of said mold body by said suspension, the proportion of said colloidal graphite to said liquidnot exceeding 15% by weight of the liquid, drying said treated mold body at a temperature between room temperature and 300 F., repeating said contacting and drying steps at least once and thereafter baking said dried mold body at 500 to 800 F.- for aperiod of at least 15 minutes.
  • the method of providing a smooth, durable. substantially non-porous graphite surface on a porous graphite mold having a pore size between 4 and 40 microns and a porosity between 20 and 30% comprising contacting said mold with a suspension of colloidal graphite in an organic liquid boiling between 100 and 500 F., said mold being at a temperature below 100 F. and the period of contact being long enough to permit penetrationof said mold body by said suspension, the proportion of said graphite to 7 I said liquid not exceeding 15% by weight of the liquid, drying said treated mold at a temperature below 300 F., repeating said contactingand drying steps at least once and thereafter baking said dried mold at a temperature between 500 and 800 F. for a period of at least 15 minutes.
  • the method of providing a smooth, durable, substantially non-porous graphite surface on a porous graphite mold body having a. pore size of between 4 and 40 microns said method comprising immersing said mold body in a suspension of graphite particles of 1 to 8 microns in diameter in petroleum naphtha, said mold body being at a temperature below the boiling point of said naphtha and the period of immersion being long enough to permit penetration of saidmold body by said suspension, the proportion of said graphite to said petroleum naphtha being lessthan 15% by weight of the liquid, drying said mold body at a temperature between room temperature and 300 F., repeating said immersing. and drying steps at least once and baking said mold body at a temperature between 500 and 800 F. for a period of at least 15 minutes.

Description

Patented Nov. 18, 1952 UNITED STATES PA/TENT OFFICE SURFACE TREATMENT OF MOLDS Frederick 0. 'lraenkner, Massena, N. Y., assignor to Aluminum Company of America, Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Application August 17, 1949,
Serial No. 110,883
In those casting operations wherein a porous.
mold is employed and the cast article must slide over the walls of the mold cavity, the molten metal tends to enter the pores of the mold with resultant separation of a portion of the surface layer of the casting as it moves or slides through the mold. The adherence of metal to the mold results in a tearing of the casting which generally would because for rejection even though but a small part of the total surface of the cast article is thus affected. This is especially objectionable in continuous casting processes where,
the ingot passes through a mold and a small area of adhering metal can cause a long broken streak on the ingot surface. It has also been observed that adherence of metal to the mold often occurs in certain regions of the mold surface which are related to certain combinations of freezing and heat extraction that develop during solidification of the casting.
The material of which a mold is made generally exerts an influence upon the surface quality of the casting formed therein. For example, some materials may be "wetted" by molten metal while others are not so affected. Furthermore, some of the materials are porous to the extent that the pores tend to be filled with molten metal as mentioned above. Generally a metal mold made from plate or heavy sheet is not sufli'ciently porous to offer any difllculty on this account, however, if the mold is a'casting or a sintered product made from powdered materials, or if it is made from non-vitrified or compressed non-metallic substances it may have a degree of porosity which ,interferes with obtaining a cast body with a ismooth surface. Inasmuch as porous molds often have certain other highly desirable qualities, it is particularly important that the dimculties associated with their porosity should be overcome and thus permit the production of highest quality castings. One of the mold materials which is highly desirable in many ways is graphite but molds of this material usually are porous to some degree and therefore subject to the disadvantage stated above.
Mold washes and lubricants have been proposed and used for dressing mold surfaces. Generally speaking, mold washes are employed because of 8 Claims. (Cl. 22-192) their'heat insulating properties and are not used where there is relative movement between casting and the mold during the casting operation because of their low resistance to wear and relatively rough surface. Liquid and semi-solid oils and greases of animal, vegetable or mineral origin have been applied to mold surfaces but such substances usually introduce problems such as buming, excessive fumes and the production of a carbonaceous deposit. Solid lubricants such as graphite either alone or associated with other materials have been sprayed or brushed on mold surfaces but such coatings require frequent renewal because they-are only applied superficially and therefor are easily worn or rubbed 01!.-
None of these materials or methods of application have been successfully used for providing durable, very smooth coatings which are substantially non porous. 1
It is an object of this invention to provide very durable, dry, smooth surfaces on porous molds and mold parts. A further object is to provide a method of treating porous mold surfaces which is simple and effective in rendering the mold surfaces substantially non-porous. Still another object is to provide a surface on porous molds which does not spell or become loosened in contact with molten metal. Yet another object comprises the provision of a method of applying a materialto the mold surface in such a manner as to cause it to penetrate the surface of the mold .body. Another object is to provide a method of treating the surface which willinsure that the surface is dry at the time it comes in contact with molten metal. These and other objects will become apparent from the following description and claims.
In speaking of mold surfaces herein, it is to be understood that this refers to that surface of a mold or any part thereof which comes in c qntact with molten metal. Thus, for exampfie, cores used in forming hollow portions of the castings are considered to be mold parts and they may be treated in the same manner as the main mold I trated by molten metal, are dry and present an exceptionally smooth long wearing surface which does not require lubrication. Because the treated mold surface has no pores of a size which can be penetrated by molten metal it is considered to be substantially non-porous. The treatment, it is believed, introduces colloidal graphite particles into the mold pores and the subsequent baking fixes or anchors them in such a way as to prevent removal unless the mold surface itself is worn or cut away. is most cases a much better surface is developed by repeating the impregnating treatment before the baking operation. For convenience of description, the porous mold may be said to be impregnated with colloida1 graphite which is subsequently fixed or stabilized in such a manner as to firmly anchor its position.
The mold or mold part to be treated must possess some degree of porosity, the pores being large enough to permit the passage therethrough of colloidal graphite particles. It is obvious, of course, that the treatment is not adapted to the treatment of molds having relatively large pores for the pores must be filled with graphite particles to the extent of providing a smooth mold surface. It has been found that molds exhibiting a pore size from about 4 to 40 microns possess a very satisfactory surface for impregnation with colloidal graphite. While it is desirable that the pores be of about the same size in a given mold or mold part and that the porosity'be relatively uniformly distributed over the mold surface this is not imperative. It is essential, however, that there be enough pores of suitable size for the graphite particles to enter and become anchored therein.
The molds may be composed of any one of a number of materials depending upon the properties desired. For example, sintered metallic powders, or mixtures of metallic powders and ceramic materials, or non-metallic materials such as graphite may be employed. Molds made of any of these materials may be successfully treated with colloidal graphite according to my invention providing they possess the proper porosity. One of the materials which has been very successfully treated is that known in the trade as dense graphite. This material has a porosity of from about 20% to about 30%; i. e. 20 to 30% of the volume consists of voids, and it has a pore size of at least 4 microns. This material when in the form of molds and treated with colloidal graphite has been used to produce aluminum alloy castings having exceptionally smooth surfaces.
The colloidal graphite preparation which I employ comprises graphite particles suspended in a volatile liquid or carrier. The predominant portion of particles should be of colloidal size. Because of this fact, the preparation is herein referred to as a colloidal graphite suspension. In my preferred practice, the suspensionconsists of graphite particles about 1 to 8 microns in diameter. Particles of this size are generally considered to be of colloidal size. In general any graphite particles which are capable of being placed in colloidal suspension and which can enter the mold pores are considered to be satisfactory for the treatment of porous mold surfaces.
The proportion of graphite to liquid must be carefully controlled in order to secure the desired penetration of the mold. It has been found that the graphite should not exceed about by weight of the liquid in which it is suspended. A greater proportion impedes the impregnating process and does not permit the establishment or a firmly anchored coating. Smaller amounts may be employed, however, for practical purposes the quantity should not be less than about 1%.
The volatile carrier or vehicle should belong to the class of liquids which has a boiling point within the range of from about l00.to 500 F. and have a sumciently low viscosity to permit penetration of the pores of the mold. A preferred group of liquids is that composed of a mixture of hydrocarbons in which 10% are distilled below 347 F. and .not less than below 464 F. Examples of such hydrocarbon mixtures are petroleum naphtha, and mineral spirits. Other organic liquids will also serve satisfactorily such as the lower alcohols. By organic liquids is meant'hydrocarbons and their derivatives which are liquid at room temperature. Under some conditions water may be employed but special precautions may be necessary to insure complete evaporation.
Although the aforesaid liquids serve as suitable carriers for graphite and in most cases possess the necessary wetting power to facilitate penetration of the mold material, it may be desirable to add small amounts of other substances which will serve to keep the graphite particles in suspension or enhance the wetting power of the suspensions. Such materials as metallic salts of long chain alkyl acids, aryl substituted long chain alkyl acids, or aromatic acids are known to have this effect upon carriers of the kind herein described. Some examples of these salts are nickel, zinc or calcium naphthenates, calcium stearate, calcium phenyl stearate, wax aluminum phenate, aluminum carboxylate. The added substances do not in any way interfere with the deposition of the colloidal graphite particles nor the production of the desired quality of mold surface.
The treatment of a mold or mold Dart consists in contacting it with a suspension of the type defined above, subsequently permitting the volatile carrier to evaporate, and finally baking the mold. While a single treatment effects an improvement, a better and more durable surface is developed by repeating the treatment at least once, and hence this is preferred. The suspension may be applied in any conventional manner but usually immersion or spraying will be the most convenient method to use. Following contact with or exposure to the suspension the mold is dried, but in my preferred practice the contacting and drying steps are repeated at least once and often twice. By means of the multiple treatment, it has been found that the colloidal particles better penetrate the pores of the mold to a depth that permits subsequent firm anchorage in the pores. In the case of contact by immersion it is advantageous to hold the mold -or mold part in the suspension for a period of time, for example, 30 minutes. This period may extend for several hours but ordinarily such long exposure does not produce corresponding improvement over a short exposure.
Thedrying operation may be conducted atroom temperature or at somewhat higher temperatures, but below 300 F., the object being solely that of evaporating the carrier. The period required for drying will vary with the liquid employed in the suspension and the period of exposure to the suspension. It is not necessary that the drying be carried to the point of removing all traces of the liquid, but it is essential that a major portion be evaporated. A period up to 5 or 6 hours is usually sufiicient.
After completion of at least one cycle of im aerapaa pregnation and drying the article is then subjected to a baking operation at a temperature of between 500 and 800 F. for a period of at least minutes. This -may extend to several hours. While the baking operation serves to drive off any residual vehicle or carrier it also appears. tofix or stabilize the graphite particle in the pores of the mold with the result that a firmly adherent coating is produced. Because of the firm adherence and durability of the coating obtained in the foregoing manner it may be said to be integrally bonded to the mold as compared to the superficial mold coatings of the prior art.
If upon test it is found that the mold surface is not smooth, the foregoing process may be repeated. Also, after the mold has been used and some wear may have occurred the mold may be subjected to a single contact with a colloidal suspension followed by baking.
The mold surfaces resulting from this treatment are dry and may be used with entire safety in contact with molten metal. The mold surfaces are smooth and free from pores that can be penetrated by molten metal ascompared to the untreated mold surface. Furthermore, no additional lubrication is necessary. Such treated mold surfaces may be used for relatively long periods of time without renewal as compared to a surface that has not been impregnated with colloidal graphite and baked. A durable surface is of particular importance in continuous casting processes where the operation cannot be conveniently interrupted.
Although any type of metal may be cast in contact with molds treated in accordance with my invention providing the casting conditions are such as not to oxidize the coating or the mold, it has been found that aluminum and aluminum base aloy ingots having high surface quality can be cast in such molds. Other non-ferrous metals such as magnesium and copper and their alloys uid boiling between 100 and 500 F., said mold body being at a temperature below the boiling point of said liquid and the period of contact between said mold body and suspension being long enough to permit penetration of said mold body by said suspension, the proportion of said graphite to said liquid not exceeding 15% by weight of the liquid, drying said treated .mold body at a temperat e between room temperature and 300 F. and pier after baking said dried mold body at 500 to 800 F. for a period of at least 15 minutes.
weight of the liquid, drying said treated mold body at a temperature between room temperature and 300 F. and thereafter baking said dried mold body at 500 to 800 F. for a period of at least 15 minutes.
3. The method of providing a smooth, durable, substantially non-porous graphite surface on a porous graphite mold body having a pore size of between 4 and 40 microns, said method comprising immersing said mold body in a suspension of graphite particles of 1 to 8 microns in diameter in a liquid boiling between 100 and 500 F.,
said mold body being at a temperature below the boiling point of said liquid and the period of may likewise be cast in contact with the treated molds with resulting advantage tothe surface quality of the cast product.
The invention may be illustrated in the following example. A dense graphite mold of circular shape, open at both and bottom and having a diameter of about 14 inches was treated with a colloidal graphite suspension containing about 10% by weight of graphite. The graphite mold had a porosity of about 25% and a pore size between about 4 and 40 microns. The mold was immersed in the colloidal graphite suspension in petroleum naphtha for a period of 30 minutes, withdrawn and dried in air for one hour at a temperature of 250 F. Following this it was again immersed in the suspension and again dried. The process was repeated the third time and following the drying operation, the mold was baked at 700 F. for one hour. The mold as inserted in the continuous casting apparatus for making aluminum base alloy ingots. The ingots coming from this mold had an exceptionally smooth surface and, therefore, required no subsequent surface condition treatment to prepare them for fabricating operations. The mold treated in this manner was found to retain a satisfactory surface after casting 280 ingots having a. minimum length of 100 inches.
Having thus described my invention, I claim:
1. The method of providing a smooth, durable,
immersion being long enough to permit penetration of said mold body by said suspension, theproportion of said graphite to said liquid being less than 15% by weight of the liquid, drying said mold body at a temperature between room temperature and 300 F., repeating said immersing and drying steps at least once, and thereafter baking said dried mold body at a temperature between 500 and 800 F. for a period of at least 15 minutes. i
4. The method of providing a smooth, durable, substantially non-porous graphite surface on a porous mold body having pores of 4 to 40 microns in size comprising contacting said mold body with a suspension of colloidal graphite in a liquid boiling between and 500 F., said mold body being at a temperature below 100 F. and the period of contact being long enough to permit penetration of said mold body by said suspension, the proportion of said colloidal graphite to said liquidnot exceeding 15% by weight of the liquid, drying said treated mold body at a temperature between room temperature and 300 F., repeating said contacting and drying steps at least once and thereafter baking said dried mold body at 500 to 800 F.- for aperiod of at least 15 minutes.
5. The method of providing a smooth, durable. substantially non-porous graphite surface on a porous graphite mold having a pore size between 4 and 40 microns and a porosity between 20 and 30%, said method comprising contacting said mold with a suspension of colloidal graphite in an organic liquid boiling between 100 and 500 F., said mold being at a temperature below 100 F. and the period of contact being long enough to permit penetrationof said mold body by said suspension, the proportion of said graphite to 7 I said liquid not exceeding 15% by weight of the liquid, drying said treated mold at a temperature below 300 F., repeating said contactingand drying steps at least once and thereafter baking said dried mold at a temperature between 500 and 800 F. for a period of at least 15 minutes.
6. The method of providing a smooth, durable, substantially non-porous graphite surface on a porous graphite mold body having a. pore size of between 4 and 40 microns, said method comprising immersing said mold body in a suspension of graphite particles of 1 to 8 microns in diameter in petroleum naphtha, said mold body being at a temperature below the boiling point of said naphtha and the period of immersion being long enough to permit penetration of saidmold body by said suspension, the proportion of said graphite to said petroleum naphtha being lessthan 15% by weight of the liquid, drying said mold body at a temperature between room temperature and 300 F., repeating said immersing. and drying steps at least once and baking said mold body at a temperature between 500 and 800 F. for a period of at least 15 minutes.
7. The method of providing a smooth, durable, substantially non-porous graphite surface on a porous graphite mold body, the pores of which are large enough to permit the passage therethrough of colloidal graphite particles, said method comprising immersing said mold body in a suspension of colloidal graphite in an organic liquid boiling between 100 and 500 F., said mold body being at a temperature below 100 F. and the period of immersion being long enough to permit penetration of said mold body by said suspension. the proportion of said graphite to said liquid being less than 15% by weight of the liquid,
holding said mold body in said suspension for a period of at least /2 hour, drying said mold body at a temperature between room temperature and 300 F., repeating said immersion and drying F. for a period of at least 15 minutes.
steps at least once and thereafter baking said 8. The method of providing a smooth, durable, substantially non-porous graphite surface on a porous graphite mold body, the pores of which are large enough to permit passage therethrough of colloidal graphite particles, said method comprising contacting said mold body with a, suspension of colloidal graphite in a liquid boiling between and 500 F., said mold body being at a temperature below 100 F. and maintained in contact with said suspension for a period of at least hour, the proportion of said graphite to said liquid being less than 15% by weight of the liquid, drying said mold body at a temperature between room temperature and 300 F., repeating said contacting and drying steps at least once and thereafter baking said mold body at a temperature between 500 and 800 F. for a period of at least 15 minutes. V
FREDERICK O. TRAE REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 928,470 Monnot July 20, 1909 1,858,083 Goldsmith May 10, 1932 2,241,594 Gray May 13, 1941 2,245,747 Barr June 17, 1941 2,246,463 Garratt June 17, 1941- 2,376,5l8 Spence May 22, 1945 FOREIGN PATENTS v Number Country. Date 2,240 Great Britain of 1856 OTHER REFERENCES Iron Age, February 6, 1947, pages 58 and 59.

Claims (1)

1. THE METHOD OF PROVIDING A SMOOTH, DURABLE, SUBSTANTIALLY NON-POROUS GRAPHITE SURFACE ON A POROUS MOLD BODY HAVING PORES OF 4 TO 40 MICRONS IN SIZE COMPRISING CONTACTING SAID MOLD BODY WITH A SUSPENSION OF COLLOIDAL GRAPHITE IN A LIQUID BOILING BETWEEN 100 AND 500* F., SAID MOLD BODY BEING AT A TEMPERATURE BELOW THE BOILING POINT OF SAID LIQUID AND THE PERIOD OF CONTACT BETWEEN SAID MOLD BODY AND SUSPENSION BEING LONG ENOUGH TO PERMIT PENETRATION OF SAID MOLD BODY BY SAID SUSPENSION, THE PROPORTION OF SAID GRAPHITE TO SAID LIQUID NOT EXCEEDING 15% BY WEIGHT OF THE LIQUID, DRYING SAID TREATED MOLD BODY AT A TEMPERATURE BETWEEN ROOM TEMPERATURE AND 300* F. AND THEREAFTER BAKING SAID DRIED MOLD BODY AT 500 TO 800* F. FOR A PERIOD OF AT LEAST 15 MINUTES.
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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2726160A (en) * 1952-11-12 1955-12-06 Norton Co Boron nitride dispersion
US2747244A (en) * 1953-07-15 1956-05-29 Norman P Goss Porous mold for the continuous casting of metals
US2779075A (en) * 1950-10-13 1957-01-29 Griffin Wheel Co Cast article and method of making
US2812250A (en) * 1952-09-29 1957-11-05 Du Pont Production of titanium by the reduction of titanium tetrachloride by magnesium
US2870497A (en) * 1956-08-13 1959-01-27 Strauss Casting metals and alloys
US2916337A (en) * 1956-06-18 1959-12-08 Borg Warner Composite bonded article
US2956890A (en) * 1957-03-12 1960-10-18 Int Smelting & Refining Co Mold dressing
US3026214A (en) * 1957-12-13 1962-03-20 Gen Electric Co Ltd Process for production of low permeability carbon and resultant article
US3165888A (en) * 1959-09-18 1965-01-19 Edward F Keon Exhaust nozzle for reaction engines and the like
US3211560A (en) * 1961-12-18 1965-10-12 Caterpillar Tractor Co Mold wash composition and casting mold coated therewith
US3286312A (en) * 1965-03-29 1966-11-22 Little Inc A Refractory coated casting mold
US3304585A (en) * 1964-06-18 1967-02-21 Ascast Corp Graphite continuous casting mold
US3401735A (en) * 1965-03-02 1968-09-17 Foseco Int Method for making sand molds
US3487134A (en) * 1964-03-26 1969-12-30 Goodyear Tire & Rubber Method for manufacturing a textured surfaced composite foamed article and the mold therefor
US3933335A (en) * 1971-04-01 1976-01-20 Kureha Kagaku Kogyo Kabushiki Kaisha Casting mold for metals
US3962492A (en) * 1973-08-16 1976-06-08 Foseco International Limited Method of protecting refractory lining in containers for molten metal
US3994346A (en) * 1972-11-24 1976-11-30 Rem Metals Corporation Investment shell mold, for use in casting of reacting and refractory metals
US4098929A (en) * 1973-11-12 1978-07-04 Chrysler Corporation Method for improved parting from hot surfaces
US4187334A (en) * 1978-11-01 1980-02-05 Labate Michael D Process and material for treating steel walls and fans in electrical precipitation installations with micron colloidal graphite particles
US4239818A (en) * 1978-11-01 1980-12-16 Labate Michael D Process and material for treating steel walls and fans in electrical precipitation installations with micron colloidal graphite particles
US4279946A (en) * 1977-09-07 1981-07-21 Foseco International Limited Coating compositions
US4862947A (en) * 1988-08-02 1989-09-05 Pcc Airfoils, Inc. Method of casting an article
US6291407B1 (en) 1999-09-08 2001-09-18 Lafrance Manufacturing Co. Agglomerated die casting lubricant
US6432886B1 (en) 1999-09-08 2002-08-13 Mary R. Reidmeyer Agglomerated lubricant

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US928470A (en) * 1908-04-30 1909-07-20 Duplex Metals Company Mold.
US1858083A (en) * 1929-10-07 1932-05-10 George H Goldsmith Compound for preparing molds for metal castings
US2241594A (en) * 1939-12-18 1941-05-13 Standard Oil Co Mold dressing
US2245747A (en) * 1939-07-24 1941-06-17 American Cast Iron Pipe Co Method of treating centrifugal metal molds
US2246463A (en) * 1940-09-26 1941-06-17 Ind Colloids Company Treatment of mold surfaces
US2376518A (en) * 1942-05-29 1945-05-22 Int Nickel Co Method of casting metals

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US928470A (en) * 1908-04-30 1909-07-20 Duplex Metals Company Mold.
US1858083A (en) * 1929-10-07 1932-05-10 George H Goldsmith Compound for preparing molds for metal castings
US2245747A (en) * 1939-07-24 1941-06-17 American Cast Iron Pipe Co Method of treating centrifugal metal molds
US2241594A (en) * 1939-12-18 1941-05-13 Standard Oil Co Mold dressing
US2246463A (en) * 1940-09-26 1941-06-17 Ind Colloids Company Treatment of mold surfaces
US2376518A (en) * 1942-05-29 1945-05-22 Int Nickel Co Method of casting metals

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2779075A (en) * 1950-10-13 1957-01-29 Griffin Wheel Co Cast article and method of making
US2812250A (en) * 1952-09-29 1957-11-05 Du Pont Production of titanium by the reduction of titanium tetrachloride by magnesium
US2726160A (en) * 1952-11-12 1955-12-06 Norton Co Boron nitride dispersion
US2747244A (en) * 1953-07-15 1956-05-29 Norman P Goss Porous mold for the continuous casting of metals
US2916337A (en) * 1956-06-18 1959-12-08 Borg Warner Composite bonded article
US2870497A (en) * 1956-08-13 1959-01-27 Strauss Casting metals and alloys
US2956890A (en) * 1957-03-12 1960-10-18 Int Smelting & Refining Co Mold dressing
US3026214A (en) * 1957-12-13 1962-03-20 Gen Electric Co Ltd Process for production of low permeability carbon and resultant article
US3165888A (en) * 1959-09-18 1965-01-19 Edward F Keon Exhaust nozzle for reaction engines and the like
US3211560A (en) * 1961-12-18 1965-10-12 Caterpillar Tractor Co Mold wash composition and casting mold coated therewith
US3487134A (en) * 1964-03-26 1969-12-30 Goodyear Tire & Rubber Method for manufacturing a textured surfaced composite foamed article and the mold therefor
US3304585A (en) * 1964-06-18 1967-02-21 Ascast Corp Graphite continuous casting mold
US3401735A (en) * 1965-03-02 1968-09-17 Foseco Int Method for making sand molds
US3286312A (en) * 1965-03-29 1966-11-22 Little Inc A Refractory coated casting mold
US3933335A (en) * 1971-04-01 1976-01-20 Kureha Kagaku Kogyo Kabushiki Kaisha Casting mold for metals
US3994346A (en) * 1972-11-24 1976-11-30 Rem Metals Corporation Investment shell mold, for use in casting of reacting and refractory metals
US3962492A (en) * 1973-08-16 1976-06-08 Foseco International Limited Method of protecting refractory lining in containers for molten metal
US4098929A (en) * 1973-11-12 1978-07-04 Chrysler Corporation Method for improved parting from hot surfaces
US4279946A (en) * 1977-09-07 1981-07-21 Foseco International Limited Coating compositions
US4187334A (en) * 1978-11-01 1980-02-05 Labate Michael D Process and material for treating steel walls and fans in electrical precipitation installations with micron colloidal graphite particles
US4239818A (en) * 1978-11-01 1980-12-16 Labate Michael D Process and material for treating steel walls and fans in electrical precipitation installations with micron colloidal graphite particles
US4862947A (en) * 1988-08-02 1989-09-05 Pcc Airfoils, Inc. Method of casting an article
US6291407B1 (en) 1999-09-08 2001-09-18 Lafrance Manufacturing Co. Agglomerated die casting lubricant
US6432886B1 (en) 1999-09-08 2002-08-13 Mary R. Reidmeyer Agglomerated lubricant

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