[go: up one dir, main page]

US3213497A - Method of treating an investment mold - Google Patents

Method of treating an investment mold Download PDF

Info

Publication number
US3213497A
US3213497A US324872A US32487263A US3213497A US 3213497 A US3213497 A US 3213497A US 324872 A US324872 A US 324872A US 32487263 A US32487263 A US 32487263A US 3213497 A US3213497 A US 3213497A
Authority
US
United States
Prior art keywords
alcohol
mold
refractory
shape
investment
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
Application number
US324872A
Inventor
Robert K Scott
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Harbison Walker Refractories Co
Original Assignee
Harbison Walker Refractories Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Harbison Walker Refractories Co filed Critical Harbison Walker Refractories Co
Priority to US324872A priority Critical patent/US3213497A/en
Priority to AT877564A priority patent/AT246346B/en
Priority to DE19641433964 priority patent/DE1433964B1/en
Priority to FR993561A priority patent/FR1415980A/en
Priority to GB44769/64A priority patent/GB1027419A/en
Application granted granted Critical
Publication of US3213497A publication Critical patent/US3213497A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22C—FOUNDRY MOULDING
    • B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
    • B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
    • B22C1/205—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents of organic silicon or metal compounds, other organometallic compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22C—FOUNDRY MOULDING
    • B22C9/00—Moulds or cores; Moulding processes
    • B22C9/02—Sand moulds or like moulds for shaped castings
    • B22C9/04—Use of lost patterns

Definitions

  • this invention relates to an improvement in the process disclosed in copending application Serial No. 317,039, filed October 17, 1963 (now abandoned), and owned by the same assignee as the instant invention.
  • This invention rel-ates to the manufacture of refractory molds of the type used for making precision metal castings. More particularly, the invention relates to a process of treating refractory patterns which are subsequently to be used for casting of molten metal.
  • the single invesment casting process includes preparation of a plurality of refractory molds from the same permanent master pattern or mold.
  • the permanent mold can be termed a positive (identical to the shape to be cast); and the refractory investment is the negative into which molten metal is cast.
  • the double investment casting process is quite similar to the single investment one, in that a permanent mold is repeatedly used to make refractory invesments for the actual casting of molten metal. There is a difference, however, in the refractory investment. It has a backup .Or base portion, which can be identical to that used in the single investment mold process. However, in the double investment system, the molten metal contacting portions are coated with a layer of specially size graded refractory material to provide extremely smooth surfaces.
  • Both the single investment and double investment processes utilize substantially the same material (with the exception just noted). These materials include a refractory aggregate and a binder.
  • binder Most generally, the preparation of a binder is considered the most critical part of the process, since it had to be carefully and critically prepared according to a most precise recipe.
  • One commonly used type of binder includes a mixture of alcohol (ethyl alcohol for example), an acid (such as hydrochloric acid), a small amount of water, and an organic silicate (such as ethyl silicate), sometimes with additional ingredients added.
  • micro-crazing is beneficial, since it prevents gross cracking. It is accomplished by torching or burning the surfaces of the refractory immediately upon its reaching a self-sustaining or set state. I have not found micro-crazing desirable. I believe one completely free of even minute cracks is preferable.
  • I utilize a prehydrolyzed ethyl silicate solution and a pretreated refractory grain in a system of the type disclosed and claimed in copending application Serial No. 317,039, identified above.
  • the gel formed from this system is weak, initially; but continues to develop strength when permitted to stand.
  • a mold prepared by this and prior similar systems is allowed to stand in open air too long, evaporation of alcohol from exposed surfaces produces shrinkage of such surfaces, sufiicient to cause cracking or crazing before the gel is strong enough to prevent shrinkage.
  • a remarkably satisfactory and preferred impervious plastic sheet material which can be used according to the practice of this invention, is Saran wrap, a commercially available product.
  • This material is made from thermoplastic resins obtained by the polymerization of vinylidene chloride or co-polymerization of vinylidene chloride with lesser amounts of other unsaturated compounds.
  • other flexible film or sheet material which is impervious to air and alcohol fumes, and which will resist chemical reaction, i.e. inert to the organic and inorganic constituents of the gelling investment, can be used.
  • a rigid container if available, which can be sealed to the atmosphere, can be used, since it also will serve to enclose an alcohol-rich atmosphere about the investment.
  • refractory grain which is conventionally used for making refractory investments
  • satisfactory grain include alumina, calcined clay which analyzes mostly SiO and A1 0 on an oxide basis, mullite, silica, calcined high alumina materials such as bauxite and diaspore, fused corundum and fused mullite, sill-imanite, various spinel minerals such as chrome ore, zirconia (preferably stabilized zirconia), etc.
  • the refractories used for making investment molds should be carefully screened so as to provide a uniform product.
  • the grains may be of a size so that 50%, by weight, is in the range 6+3O mesh, the rest mostly in the 30 mesh range. From 20 to 40% can be smaller than 200 mesh. (All of these sizes are according to the United States Standard series of screens.)
  • the size graded grain is treated with a solution of a volatile organic solvent and an organic base.
  • the organic base is of the amine type, preferably having from 8 to 22 carbon atoms, and of the type of alkali metal and alkaline earth salts of chemically basic organic compounds as are discussed in the copending application above identified.
  • the refractory grain is coated by treating them with one of the amine-type materials, just discussed, so that at least a major portion of the exposed surface area of the refractory grain of the batch (at least about 50%) is covered.
  • the amount of the coating may run from 0.1 to about 2%, by weight, based on the weight of the refractory. The preferred range is 0.3 to 0.7% by weight.
  • Coated grains are treated with a gelling binder.
  • a preferred gelling binder is prepared from:
  • the resulting binder and treated refractory grain mixture is about as follows: 400 grams of a refractory consisting essentially of 20% 8 on 30 mesh calcined flint clay, the balance being -100 mesh mullite, and the mixture treated with 0.55% Duomeen C (or 0.2% diethylmethylamine-this being preferred), is mixed with 100 cc. of a binder solution containing 18% SiO by weight, derived from ethyl silicate (40% SiO content), water to allow 83% hydrolyzation (about 6 cc.
  • hydrochloric acid or other inorganic acid such as sulfuric or nitric acid to yield a pH of approximately 2 (about 1 cc.)
  • ethyl alcohol to reduce the SiO content to the above mentioned to 18% (from 50 to 55 cc. of ethyl alcohol).
  • Duomeen C is a coconut oil derivative of 1,3-propylenediamine. After thorough mixing, the resulting slurry is poured over a master pattern, where gelation occurs in about 3 minutes at 75 F.
  • a preferred refractory grain is the commercial product of commerce, identified by the trade name Flintmull GG3, a product of the Harbison-Walker Refractories Company. This commercial product is a mixture of calcined flint clay and mullite.
  • the preferred coating agent is Duomeen C, a product of the Armour Chemical Company.
  • the mixture of binder and coated refractory is poured into a master pattern, allowed to gel to a state sufiicient to resist light finger pressure, the master pattern is stripped from the refractory, and the refractory investment is inserted in a plastic bag which is tied to close the investment off from the atmosphere.
  • the time necessary for the refractory to remain covered by the plastic is visually determined; for example, when all surfaces are of a uniform color and no wet areas are obvious, the bag may be removed. I found it very satisfactory, using the preferred composition, above discussed, to remove the bag after about 1 to 2 hours, followed by air drying for a similar or longer period. If desired, the bag may remain longer; for example, overnight (12 or so hours).
  • the investment may be placed in an oven to ignite any residual alcohol.
  • the in vestment can be heated to a temperature of on the order of 2000 F. to obtain some ceramic bonding through the refractory material to thereby obtain improved strength.
  • a method of preventing micro-crazing and cracking of gelling investment molds of the type made from a slurry of (l) a refractory, and- (2) an alcohol and lower alkyl silicate bonding solution which comprises the steps of, pouring the slurry about a master pattern, allowing the slurry to initially gel only to a self-sustaining shape about said master pattern, immediately stripping the pattern from the shape, immediately encapsulating the shape in means defining an air and alcohol vapor-impervious cavity, said means sealing said cavity from the atmosphere, said cavity being larger than the mold it encapsulates and of such size and configuration as to retard the evaporation of alcohol from the mold and to promote and allow the formation of an alcohol-rich atmosphere about exposed surfaces of the mold by evaporation of alcohol from the mold, maintaining the shape in the cavity for at least about an hour until all surfaces of the mold are substantially uniform in color and with no wet areas being obvious.
  • said refractory is selected from the group consisting of alumina, calcined clay, mullite, silica, bauxite, diaspore, fused corundum, fused mullite, sillimanite, chrome ore, and mixtures thereof.
  • a method of preventing micro-crazing and cracking of gelling investment molds of the type made from a slurry of (1) a refractory, and (2) an alcohol and lower alkyl silicate bonding solution which comprises the steps of pouring the slurry about a master pattern, allowing the slurry to initially gel only to a self-sustaining shape about said master pattern, immediately stripping the pattern from the shape, immediately encapsulating the shape in an air and alcohol vapor-impervious plastic bag, said bag being sealed from the atmosphere and of such size and configuration as to retard the evaporation of the alcohol and to promote the formation of an alcohol-rich atmosphere about exposed surfaces of the mold by evaporation of alcohol from the mold, maintaining the shape in the bag until all surfaces of the mold are substantially uniform in color and with no wet areas being obvious.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mold Materials And Core Materials (AREA)

Description

Oct. 26, 1965 sco 3,213,497
METHOD OF TREATING AN INVESTMENT MOLD Filed NOV. 19, 1963 FORM CASTABLE SLURRY OF REFRACTORY AND LOWER ALKYL SILICATE IN ALCOHOL CARRIER POUR SLURRY OVER MASTER PATTERN ALLOW GELLATION OF SLURRY TO FORM SELF-SUSTAINING MOLD IMMEDIATELY REMOVE GELLED SHAPE FROM MASTER PATTERN PLACE IN AIR AND ALCOHOL IMPERVIOUS ENVELOPE AND MAINTAIN FOR AT LEAST ONE HOUR RECOVER SHAPE INVENTOR. ROBERT K. SCOTT ATTORNEY United States Patent Office 3,213,497 Patented Oct. 26, 1965 3,213,497 METHOD OF TREATING AN INVESTMENT MOLD Robert K. Scott, Forest Hills, Pa., assignor to Harhison- Walker Refractories Company, Pittsburgh, Pa., a corporation of Pennsylvania Filed Nov. 19, 1963, Ser. No. 324,872 6 Claims. (Cl. 22192) In some aspects, this invention relates to an improvement in the process disclosed in copending application Serial No. 317,039, filed October 17, 1963 (now abandoned), and owned by the same assignee as the instant invention.
This invention rel-ates to the manufacture of refractory molds of the type used for making precision metal castings. More particularly, the invention relates to a process of treating refractory patterns which are subsequently to be used for casting of molten metal.
As noted in said copending application, precision castings of molten metal and the like are used in many industries, and these castings are generally made in expendable refractory molds. There are three general classes or types of processes for making these expendable refractory molds; namely, the lost wax, the single investment, and the double investment.
The single invesment casting process includes preparation of a plurality of refractory molds from the same permanent master pattern or mold. The permanent mold can be termed a positive (identical to the shape to be cast); and the refractory investment is the negative into which molten metal is cast.
The double investment casting process is quite similar to the single investment one, in that a permanent mold is repeatedly used to make refractory invesments for the actual casting of molten metal. There is a difference, however, in the refractory investment. It has a backup .Or base portion, which can be identical to that used in the single investment mold process. However, in the double investment system, the molten metal contacting portions are coated with a layer of specially size graded refractory material to provide extremely smooth surfaces.
Both the single investment and double investment processes utilize substantially the same material (with the exception just noted). These materials include a refractory aggregate and a binder.
Most generally, the preparation of a binder is considered the most critical part of the process, since it had to be carefully and critically prepared according to a most precise recipe. One commonly used type of binder includes a mixture of alcohol (ethyl alcohol for example), an acid (such as hydrochloric acid), a small amount of water, and an organic silicate (such as ethyl silicate), sometimes with additional ingredients added.
In the above identified application, a process is taught in which specially prepared refractory grain is mixed with a prehydrolyzed binder solution, with the resulting mixture or slurry being used to cast the refractory investment which is later used for casting molten metal parts.
It is important that those portions of the investment against which molten metal is later cast be free of macro irregularities. Gas bubbles, which form on the investment surface during curing, have been one source of irregularities. The surface imperfections resulting from these bubbles, of course, result in complementary irregularities when molten metal is cast. Another distressing problem of prior methods has been the formation of hairline cracks upon set of the investment. Some workers have termed these cracks micro-crazing; but this seems misdescriptive, because the cracks can be seen by the naked eye in many instances, and, of course, results in a spiderlike network of complementary irregularities in metal cast thereagainst.
Some Workers have suggested that the micro-crazing is beneficial, since it prevents gross cracking. It is accomplished by torching or burning the surfaces of the refractory immediately upon its reaching a self-sustaining or set state. I have not found micro-crazing desirable. I believe one completely free of even minute cracks is preferable.
Accordingly, it is an object of the present invention to provide an improved method of treating investment molds, to provide improved refractory investments. It isanother object of the invention to provide an improved method of fabricating refractory investments according to the processes in which volatile and inflammable organic materials are used, while substantially reducing the risk of explosion or fire.
According to one aspect of this invention, I utilize a prehydrolyzed ethyl silicate solution and a pretreated refractory grain in a system of the type disclosed and claimed in copending application Serial No. 317,039, identified above. The gel formed from this system is weak, initially; but continues to develop strength when permitted to stand. However, when a mold prepared by this and prior similar systems is allowed to stand in open air too long, evaporation of alcohol from exposed surfaces produces shrinkage of such surfaces, sufiicient to cause cracking or crazing before the gel is strong enough to prevent shrinkage. I have discovered that investment molds of improved strength and handleability are produced if, immediately after removal of a master pattern from the gelled investment, the exposed surfaces are covered with a thin sheet or film of substantially impervious plastic material. By impervious, I mean the material is impervious to air and alcohol vapors. This impervious sheet retards the evaporation of alcohol, until the gel has developed sufficient strength so it may resist shrinkage cracking. Also, this encapsulation of the mold promotes an alcohol vapor-rich atmosphere which promotes uniform set.
A remarkably satisfactory and preferred impervious plastic sheet material, which can be used according to the practice of this invention, is Saran wrap, a commercially available product. This material is made from thermoplastic resins obtained by the polymerization of vinylidene chloride or co-polymerization of vinylidene chloride with lesser amounts of other unsaturated compounds. Of course, other flexible film or sheet material, which is impervious to air and alcohol fumes, and which will resist chemical reaction, i.e. inert to the organic and inorganic constituents of the gelling investment, can be used. A rigid container, if available, which can be sealed to the atmosphere, can be used, since it also will serve to enclose an alcohol-rich atmosphere about the investment.
The following detailed discussion should be understood as merely exemplary of practices according to my invention, and that the true measure of the spirit and scope is as defined in the claims.
Of course, practically any type of refractory grain, which is conventionally used for making refractory investments, can be used in the practice of this invention. Examples of satisfactory grain include alumina, calcined clay which analyzes mostly SiO and A1 0 on an oxide basis, mullite, silica, calcined high alumina materials such as bauxite and diaspore, fused corundum and fused mullite, sill-imanite, various spinel minerals such as chrome ore, zirconia (preferably stabilized zirconia), etc.
The refractories used for making investment molds should be carefully screened so as to provide a uniform product. For example, the grains may be of a size so that 50%, by weight, is in the range 6+3O mesh, the rest mostly in the 30 mesh range. From 20 to 40% can be smaller than 200 mesh. (All of these sizes are according to the United States Standard series of screens.) According to preferred practice,-the size graded grain is treated with a solution of a volatile organic solvent and an organic base. The organic base is of the amine type, preferably having from 8 to 22 carbon atoms, and of the type of alkali metal and alkaline earth salts of chemically basic organic compounds as are discussed in the copending application above identified. The refractory grain is coated by treating them with one of the amine-type materials, just discussed, so that at least a major portion of the exposed surface area of the refractory grain of the batch (at least about 50%) is covered. The amount of the coating may run from 0.1 to about 2%, by weight, based on the weight of the refractory. The preferred range is 0.3 to 0.7% by weight.
Coated grains are treated with a gelling binder. A preferred gelling binder is prepared from:
(1) Ethyl silicate having 40% SiO by weight,
(2) Denatured ethyl alcohol, in a quantity sulficient to dilute the ethyl silicate to obtain a fluid mixture or solution having about 18% SiO by weight and on an oxide basis,
(3) Water, in a quantity sufficient to promote hydrolyzation of the 18% SiO solution to on the order of about 60 to 80% completeness, and
(4) Sufiicient of an acid, such as hydrochloric acid, to obtain a pH of a partially hydrolyzed solution in the range from about 2 to about 4.
The resulting binder and treated refractory grain mixture, according to a preferred embodiment, is about as follows: 400 grams of a refractory consisting essentially of 20% 8 on 30 mesh calcined flint clay, the balance being -100 mesh mullite, and the mixture treated with 0.55% Duomeen C (or 0.2% diethylmethylamine-this being preferred), is mixed with 100 cc. of a binder solution containing 18% SiO by weight, derived from ethyl silicate (40% SiO content), water to allow 83% hydrolyzation (about 6 cc. of water), hydrochloric acid or other inorganic acid such as sulfuric or nitric acid to yield a pH of approximately 2 (about 1 cc.) and ethyl alcohol to reduce the SiO content to the above mentioned to 18% (from 50 to 55 cc. of ethyl alcohol). Duomeen C is a coconut oil derivative of 1,3-propylenediamine. After thorough mixing, the resulting slurry is poured over a master pattern, where gelation occurs in about 3 minutes at 75 F.
While I mention prehydrolyzed ethyl silicate and alcohol as a binder solution, it is, of course, clear other lower alkyl organic silicates of the type known to the prior art for investment molding can be used. Exemplary prior art, which discloses the known character of use of lower alkyl organic silicates and alcohols for this purpose, are as follows: Prange, 1,909,008, Shaw, United States Patent No. 2,795,022.
A preferred refractory grain is the commercial product of commerce, identified by the trade name Flintmull GG3, a product of the Harbison-Walker Refractories Company. This commercial product is a mixture of calcined flint clay and mullite. The preferred coating agent is Duomeen C, a product of the Armour Chemical Company.
In the preferred practice of the invention, the mixture of binder and coated refractory is poured into a master pattern, allowed to gel to a state sufiicient to resist light finger pressure, the master pattern is stripped from the refractory, and the refractory investment is inserted in a plastic bag which is tied to close the investment off from the atmosphere. The time necessary for the refractory to remain covered by the plastic is visually determined; for example, when all surfaces are of a uniform color and no wet areas are obvious, the bag may be removed. I found it very satisfactory, using the preferred composition, above discussed, to remove the bag after about 1 to 2 hours, followed by air drying for a similar or longer period. If desired, the bag may remain longer; for example, overnight (12 or so hours). If desired, after removal from the bag, the investment may be placed in an oven to ignite any residual alcohol. If desired, the in vestment can be heated to a temperature of on the order of 2000 F. to obtain some ceramic bonding through the refractory material to thereby obtain improved strength.
Having thus described the invention in detail, and with suflicient particularity as to enable those skilled in the art to practice it, what is desired to have protected by Letters Patent is set forth in the following claims.
I claim:
1. A method of preventing micro-crazing and cracking of gelling investment molds of the type made from a slurry of (l) a refractory, and- (2) an alcohol and lower alkyl silicate bonding solution, which comprises the steps of, pouring the slurry about a master pattern, allowing the slurry to initially gel only to a self-sustaining shape about said master pattern, immediately stripping the pattern from the shape, immediately encapsulating the shape in means defining an air and alcohol vapor-impervious cavity, said means sealing said cavity from the atmosphere, said cavity being larger than the mold it encapsulates and of such size and configuration as to retard the evaporation of alcohol from the mold and to promote and allow the formation of an alcohol-rich atmosphere about exposed surfaces of the mold by evaporation of alcohol from the mold, maintaining the shape in the cavity for at least about an hour until all surfaces of the mold are substantially uniform in color and with no wet areas being obvious.
2. The method of claim 1 in which the shape is maintained in the envelope for about one to two hours.
3. The method of claim 2 in which the shape is removed from the envelope after said one to two hour period and placed in an oven to burn off residual alcohol.
4. The method of claim 3 in which the oven is heated to a temperature sufiicient to fire the shape to obtain ceramic bonding.
5. A method according to claim 1 in which said refractory is selected from the group consisting of alumina, calcined clay, mullite, silica, bauxite, diaspore, fused corundum, fused mullite, sillimanite, chrome ore, and mixtures thereof.
6. A method of preventing micro-crazing and cracking of gelling investment molds of the type made from a slurry of (1) a refractory, and (2) an alcohol and lower alkyl silicate bonding solution, which comprises the steps of pouring the slurry about a master pattern, allowing the slurry to initially gel only to a self-sustaining shape about said master pattern, immediately stripping the pattern from the shape, immediately encapsulating the shape in an air and alcohol vapor-impervious plastic bag, said bag being sealed from the atmosphere and of such size and configuration as to retard the evaporation of the alcohol and to promote the formation of an alcohol-rich atmosphere about exposed surfaces of the mold by evaporation of alcohol from the mold, maintaining the shape in the bag until all surfaces of the mold are substantially uniform in color and with no wet areas being obvious.
References Cited by the Examiner UNITED STATES PATENTS 2,025,376 12/35 Coleman 26434O 2,979,790 4/18 Lubalin 22l92 2,795,022 6/57 Shaw 22-492 2,948,935 8/60 Carter 22192 3,148,422 9/64 Payne 22196 3,172,176 3/65 Greenwood 22193 FOREIGN PATENTS 876,805 9/ 61 Great Britain.
MARCUS U. LYONS, Primary Examiner.

Claims (1)

1. A METHOD OF PREVENTING MICRO-CRAZING AND CRACKING OF GELLING INVESTMENT MOLDS OF THE TYPE MADE FROM A SLURRY OF (1) A REFRACTORY, AND (2) AN ALCOHOL AND LOWER ALKYL SILICATE BONDING SOLUTION, WHICH COMPRISES THE STEPS OF, POURING THE SLURRY ABOUT A MASTER PATTERN, ALLOWING THE SLURRY TO INITIALLY GEL ONLY TO A SELF-SUSTAINING SHAPE ABOUT SAID MASTER PATTERN, IMMEDIATELY STRIPPING THE PATTERN FROM THE SHAPE, IMMEDIATELY ENCAPSULATING THE SHAPE IN MEANS DEFINING AN AIR AND ALCOHOL VAPOR-IMPERVIOUS CAVITY, SAID MEANS SEALING SAID CAVITY FROM THE ATMOSPHERE, SAID CAVITY BEING LARGER THAN THE MOLD IT ENCAPSULATES AND OF SUCH SIZE AND CONFIGURATION AS TO RETARD THE EVAPORATION OF ALCOHOL FROM THE MOLD AND TO PROMOTE AND ALLOW THE FORMATION OF AN ALCOHOL-RICH ATMOSPHERE ABOUT EXPOSED SURFACES OF THE MOLD BY EVAPORATION OF ALCOHOL FROM THE MOLD, MAINTAINING THE SHAPE IN THE CAVITY FOR AT LEAST ABOUT AN HOUR UNTIL ALL SURFACES OF THE MOLD ARE SUBSTANTIALLY UNIFORM IN COLOR AND WITH NO WET AREAS BEING OBVIOUS.
US324872A 1963-11-19 1963-11-19 Method of treating an investment mold Expired - Lifetime US3213497A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US324872A US3213497A (en) 1963-11-19 1963-11-19 Method of treating an investment mold
AT877564A AT246346B (en) 1963-11-19 1964-10-15 Method of preventing cracks and cracks from forming in precision molds
DE19641433964 DE1433964B1 (en) 1963-11-19 1964-10-16 Method for treating molds
FR993561A FR1415980A (en) 1963-11-19 1964-11-02 Model processing
GB44769/64A GB1027419A (en) 1963-11-19 1964-11-03 Improvements in or relating to the production of refractory moulds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US324872A US3213497A (en) 1963-11-19 1963-11-19 Method of treating an investment mold

Publications (1)

Publication Number Publication Date
US3213497A true US3213497A (en) 1965-10-26

Family

ID=23265465

Family Applications (1)

Application Number Title Priority Date Filing Date
US324872A Expired - Lifetime US3213497A (en) 1963-11-19 1963-11-19 Method of treating an investment mold

Country Status (4)

Country Link
US (1) US3213497A (en)
AT (1) AT246346B (en)
DE (1) DE1433964B1 (en)
GB (1) GB1027419A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3314117A (en) * 1965-05-10 1967-04-18 British Ind Corp Method of manufacturing a foundry core
US3445250A (en) * 1967-02-28 1969-05-20 Nalco Chemical Co Precision metal casting molds comprising alumina coated silica and a refractory
US4043853A (en) * 1976-03-05 1977-08-23 Saladino Matthew L Method of renovating a series of identical bathtubs
US5014763A (en) * 1988-11-30 1991-05-14 Howmet Corporation Method of making ceramic cores
US5126082A (en) * 1988-11-30 1992-06-30 Howmet Corporation Method of making ceramic cores and other articles

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2025376A (en) * 1932-04-12 1935-12-24 Du Pont Cellophane Co Inc Conditioned material and method of preparing same
US2795022A (en) * 1953-04-09 1957-06-11 Shaw Process Dev Corp Method of making moulds
US2948935A (en) * 1958-04-07 1960-08-16 Richard T Carter Process of making refractory shell for casting metal
US2979790A (en) * 1957-08-09 1961-04-18 Shaw Process Dev Corp Molds
GB876805A (en) * 1959-06-11 1961-09-06 Howe Sound Co Improvements in making refractory shell molds
US3148422A (en) * 1961-07-20 1964-09-15 Monsanto Chemicals Production of shell moulds
US3172176A (en) * 1964-03-26 1965-03-09 Greenwood Ronald Method of making ceramic molds

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2025376A (en) * 1932-04-12 1935-12-24 Du Pont Cellophane Co Inc Conditioned material and method of preparing same
US2795022A (en) * 1953-04-09 1957-06-11 Shaw Process Dev Corp Method of making moulds
US2979790A (en) * 1957-08-09 1961-04-18 Shaw Process Dev Corp Molds
US2948935A (en) * 1958-04-07 1960-08-16 Richard T Carter Process of making refractory shell for casting metal
GB876805A (en) * 1959-06-11 1961-09-06 Howe Sound Co Improvements in making refractory shell molds
US3148422A (en) * 1961-07-20 1964-09-15 Monsanto Chemicals Production of shell moulds
US3172176A (en) * 1964-03-26 1965-03-09 Greenwood Ronald Method of making ceramic molds

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3314117A (en) * 1965-05-10 1967-04-18 British Ind Corp Method of manufacturing a foundry core
US3445250A (en) * 1967-02-28 1969-05-20 Nalco Chemical Co Precision metal casting molds comprising alumina coated silica and a refractory
US4043853A (en) * 1976-03-05 1977-08-23 Saladino Matthew L Method of renovating a series of identical bathtubs
US5014763A (en) * 1988-11-30 1991-05-14 Howmet Corporation Method of making ceramic cores
US5126082A (en) * 1988-11-30 1992-06-30 Howmet Corporation Method of making ceramic cores and other articles

Also Published As

Publication number Publication date
GB1027419A (en) 1966-04-27
AT246346B (en) 1966-04-12
DE1433964B1 (en) 1969-09-25

Similar Documents

Publication Publication Date Title
US2380945A (en) Refractory mold
US3894572A (en) Process for forming a refractory laminate based on positive sols and refractory materials containing chemical setting agents
US2961751A (en) Ceramic metal casting process
US3878034A (en) Refractory laminate based on negative sol or silicate and positive sol
US2701902A (en) Method of making molds
US4530722A (en) Binder and refractory compositions and methods
US3270382A (en) Shell mould process
US3396775A (en) Method of making a shell mold
US3213497A (en) Method of treating an investment mold
US2795022A (en) Method of making moulds
US4201594A (en) Method for making refractory articles
US3226784A (en) Investment molding using refractory material and certain organic bases
US4602667A (en) Method for making investment casting molds
US3455368A (en) Process for the production of refractory shell molds
US2875485A (en) Precision casting mold and method of making the same
US4204872A (en) Preparation of high temperature shell molds
US3509935A (en) Method of making a refractory shell mould utilizing silicate ester binder compositions
US3148422A (en) Production of shell moulds
US3153826A (en) Precision casting molds and techniques
US3349830A (en) Method of making a casting mold
US3722574A (en) Process of making magnesium oxide cores
US3607319A (en) Process for making refractory molds
US2818619A (en) Refractory mold, method of making same and composition therefor
US3752680A (en) Refractory laminate based on positive sols and polymer lattices containing anionic surfactants
US3583468A (en) Precision metal casting molds