US2211133A - Method of producing casting molds - Google Patents

Method of producing casting molds Download PDF

Info

Publication number
US2211133A
US2211133A US81126A US8112636A US2211133A US 2211133 A US2211133 A US 2211133A US 81126 A US81126 A US 81126A US 8112636 A US8112636 A US 8112636A US 2211133 A US2211133 A US 2211133A
Authority
US
United States
Prior art keywords
quartz
mold
temperature
expansion
metals
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
US81126A
Inventor
Krosta Victor
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Application granted granted Critical
Publication of US2211133A publication Critical patent/US2211133A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds

Definitions

  • a-quartz means the form in which quartz is stable at a temperature below 575 C.
  • a-quartz means the form in which quartz is stable at a temperature above 575 C.
  • p-crlstobalite is the stable form thereof above 215 C.
  • Tridymite exists as a-tridymite below 117 0., as p-tridymite between 117 C. and 160 C. and as u-tridymite above 160 C.
  • p-quartz is'heated to a temerature around 1000" C. to 1400 0., it is converted irreversibly into cristobalite or tridymlte depending on-the particular temperature, time and possible catalyst, etc.
  • the mena-cristobalite is the stable form of tioned disadvantages and restrictions are overcome.
  • the invention is based uponthe conversion of u-quartz into cristobalite or tridymlte at high temperatures. This conversion is combined with a very considerable expansion which is sufllcient for the purposes in question.
  • casting molds of definite thermal expansion for founding bodies of metals or alloys with high melting point are manufactured by forming the mold of a material essentially consisting of S102 wholly or essentially in the form of a-quartz and heating the mold so that the a-quartz is converted into u-tridymite or fi-cristobalite.
  • the velocity of the a-quartz conversion depends upon a number of circumstances, for in- 'stance size of the quartz particles, provenience of the quartz, conversion temperature, duration of heat treatment etc., one uses such kinds of quartz and such conversion temperatures that the desired conversion is finished as rapidly as possible.
  • a-quartz in the form of rock-quartz 90% of which in pulverized form is mixed with 10% of the same quartz in thecolloidal state.
  • water By adding water to this mix- 25 ture the colloidal matter effects the agglutination of the mass upon drying.
  • the linear expansion amounts to 1.9%.
  • organic binding means as glue, dextrin etc., which burn at high temperatures and which are soluble in water, or organic binding means soluble in organic solutions, as for instance mastic, rosin, CCli etc. A more rapid drying of the casting mold is thereby obtained.
  • organic binding means as glue, dextrin etc., which burn at high temperatures and which are soluble in water, or organic binding means soluble in organic solutions, as for instance mastic, rosin, CCli etc. A more rapid drying of the casting mold is thereby obtained.
  • inorganic binding means provided that they do not lower the melting point of the mass.
  • the conversion of the a-quartz can be accel- 4 erated by adding catalysts which simultaneously increase the expansion obtained by the conversion.
  • a very satisfactory catalyst has been found to be water glass which also has binding properties.
  • a mass comprising Parts Pulverized rock-quartz 80 Rock-quartz in a colloidal state 10 Water glass 10 heating it up to 1300 C. over one hour and holding it at this temperature for V hour one obtains a linear expansion of 2.1%.-
  • the velocity of con version and the degree of expansion can still be improved by adding further catalysts to the mentioned m'ass.
  • By adding for instance 1% sodium wolframate the expansion is increased under equal conditions to 2.3%, while simultaneously the agglutination of the-mass is accelerated.
  • the expansion can be restricted. if desired, by using catalysts, which decompose at high temperatures, as sodium silicofiuoride or other fluorides, salts of phosphoric and boric acid etc., or mixtures thereof.
  • catalysts which decompose at high temperatures, as sodium silicofiuoride or other fluorides, salts of phosphoric and boric acid etc., or mixtures thereof.
  • the increase of the expansion during the conversion process may be influenced by using a mixture of rapidly convertible and slowly convertible quartz modifications.
  • the expansion may further be regulated by the addition of tridymite or cristobalite to the a-quartz.
  • the casting molds are indirectly heated by inserting them into muilles consisting of material of high heat conductivity, preferably silicium-carbid.
  • muilles consisting of material of high heat conductivity, preferably silicium-carbid.
  • the invention further consists in the avoidance of a chemical reaction between the melted metal and the mass of the casting mold or at least considerably reduced either by composing the mass or by treating the casting mold in a special manner.
  • reaction layer The creation of such a reaction layer can be avoided or practically avoided by two different measures.
  • One way consists in adding in advance to the mass from which the casting mold is built, substances which would be created by the reaction between melted metal and the mass, or the components of such substances which react with each other during the heating period.
  • the other way consists in that, contrary to the usual practice the temperature of the casting mold does not correspond to the melting point of the metal, but is considerably lower.
  • a melted alloy comprising 30% chromium and 70% nickel and having a temperature of about 1400 C. is founded in a casting mold the temperature of which is only about 700-800' C. It has been found that in spite of the great diflerence of 800-700 C. between the temperature of the metal and the temperature of the casting mold the metal does not coagulate untimely. For such procedure it is evident only such masses can be used which practically neither expand nor contract within the temperature interval between 700 or 800 C. and 1400 C.
  • the mass according to the invention corresponds to this condition as after the conversion of the u-quartz is completed a perceptible contraction begins below about 700 C.
  • the predetermined expansion of. the casting mold is therefore maintained within the temperature interval between about 700 C. and about 1400 C. or more.
  • Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 0., increasing the temperature of the mold to a temperature above 870 0., whereby the quartz of said mold is converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold above 870 C. for a sufficiently long period to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
  • Method of producing casting molds of deflnite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 C., increasing the temperature of the mold to a temperature of about 1300 0., whereby the quartz of said mold is converted, with expansion. into the form in which it is stable above 575 C., and maintaining the mold at about 1300 C. for a sufliciently long period to convert the quartz, with expansion, into a compound of the group consisting of tridymite and crlstobalite.
  • the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 C., increasing the temperature of the mold to a temperature of about 1300" 0., whereby the quartz of said mold is converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold at about 1300 C. for about onehalf hour to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
  • Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 C., gradually increasing the temperature of the mold to a temperature of about 1300 C. over a period of about one hour, whereby the quartz of said mold is converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold at about 1300 C. for a period of about one-half hour to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
  • Method of producing casting molds of deflnite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of rock quartz, increasing the temperature of the mold gradually over a period of about 1 hour to a temperature above 870 0. whereby the rock quartz is first converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold above 870 C. to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
  • Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of rock quartz, increasing the temperature of the mold gradually over a period of about 1 hour to a temperature of about 1300 0. whereby the rock quartz is first converted, with expansion, into the form; in which it is stable above 575 0., and maintaining the mold at about 1300 C. for a period of about one-half hour to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.

Landscapes

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

Description

Patented Aug. 13, 1940 UNITED STATES PATENT OFFICE No Drawing. Application May 21, 1936, Serial No. 81,126. In Germany May 25, 1935 11 Claims.
It is well known in the founders art that due to the contraction upon cooling cast metal bodies are always smaller than the models used. Therefore the dimensions of the models are increased in advance to such extent that the contraction upon cooling is compensated. This procedure, however, cannot be used, if natural models (plants, living beings, etc.) or artificial models of complicated form (for instance wax models for dental purposes) are to be copied in metal, as the contraction or shrinkage cannot be compensated by a corresponding increase of the model dimensions.
In the present specification the term a-quartz means the form in which quartz is stable at a temperature below 575 C. ,a-quartz means the form in which quartz is stable at a temperature above 575 C. cristobalite below 215 0., while p-crlstobalite is the stable form thereof above 215 C. Tridymite exists as a-tridymite below 117 0., as p-tridymite between 117 C. and 160 C. and as u-tridymite above 160 C. When p-quartz is'heated to a temerature around 1000" C. to 1400 0., it is converted irreversibly into cristobalite or tridymlte depending on-the particular temperature, time and possible catalyst, etc.
In case castings of relatively low melting metals or alloys with a melting point below about 1000" 30 C. are to be made the mentioned difficulty is overcome by making a wax-model of the original model and embedding it in a special mass which upon being heated to the melting temperature of the metal expands as much as the 35 metal casting contracts upon coolingwhile the wax melts and can be drawn off. In the composition of the mass use is made for instance of the reversible conversion of quartz. By converting a-quartz into B-quartz at 575 C., for instance, a linear expansion of 1.4% is obtained. In practice the quartz is mixed with gypsum which by adding water effects the hardening of the mold. Due to this expansion of the quartz, linear contractions of the metal up to about 1.5% can be compensated. V
Such masses, however, cannot be used if castings of high melting metals or alloys are desired, the melting point of which lies above 1000 C. up
to 1400 C. and more and the linear contraction to of which is higher than 1.5%. Besides this the fire-proof nature of such masses is too small; moreover, the sulphur of the gypsum easily reacts with the metal at the temperature in question.
According to the present invention, the mena-cristobalite is the stable form of tioned disadvantages and restrictions are overcome. The invention is based uponthe conversion of u-quartz into cristobalite or tridymlte at high temperatures. This conversion is combined with a very considerable expansion which is sufllcient for the purposes in question. According to the invention casting molds of definite thermal expansion for founding bodies of metals or alloys with high melting point are manufactured by forming the mold of a material essentially consisting of S102 wholly or essentially in the form of a-quartz and heating the mold so that the a-quartz is converted into u-tridymite or fi-cristobalite.
As the velocity of the a-quartz conversion depends upon a number of circumstances, for in- 'stance size of the quartz particles, provenience of the quartz, conversion temperature, duration of heat treatment etc., one uses such kinds of quartz and such conversion temperatures that the desired conversion is finished as rapidly as possible. For instance a-quartz in the form of rock-quartz is used, 90% of which in pulverized form is mixed with 10% of the same quartz in thecolloidal state. By adding water to this mix- 25 ture the colloidal matter effects the agglutination of the mass upon drying. By treating the mass at 1300 C. for one hour the linear expansion amounts to 1.9%.
In order to improve the agglutination of the mass one may use organic binding means, as glue, dextrin etc., which burn at high temperatures and which are soluble in water, or organic binding means soluble in organic solutions, as for instance mastic, rosin, CCli etc. A more rapid drying of the casting mold is thereby obtained. One can also be made of inorganic binding means, provided that they do not lower the melting point of the mass.
The conversion of the a-quartz can be accel- 4 erated by adding catalysts which simultaneously increase the expansion obtained by the conversion.
A very satisfactory catalyst has been found to be water glass which also has binding properties. By using a mass comprising Parts Pulverized rock-quartz 80 Rock-quartz in a colloidal state 10 Water glass 10 heating it up to 1300 C. over one hour and holding it at this temperature for V hour one obtains a linear expansion of 2.1%.- The velocity of con version and the degree of expansion can still be improved by adding further catalysts to the mentioned m'ass. By adding for instance 1% sodium wolframate the expansion is increased under equal conditions to 2.3%, while simultaneously the agglutination of the-mass is accelerated.
The expansion can be restricted. if desired, by using catalysts, which decompose at high temperatures, as sodium silicofiuoride or other fluorides, salts of phosphoric and boric acid etc., or mixtures thereof.
The increase of the expansion during the conversion process may be influenced by using a mixture of rapidly convertible and slowly convertible quartz modifications. The expansion may further be regulated by the addition of tridymite or cristobalite to the a-quartz.
In view of the considerable and relatively rapid expansion of the casting mold a uniform heating is required in order to avoid the creation of cracks. Therefore the casting molds are indirectly heated by inserting them into muilles consisting of material of high heat conductivity, preferably silicium-carbid. A further advantage is obtained in that the casting molds are only slowly cooled after the muiiles are removed from the furnace.
The invention further consists in the avoidance of a chemical reaction between the melted metal and the mass of the casting mold or at least considerably reduced either by composing the mass or by treating the casting mold in a special manner.
It is known that the surface of cast metal bodies produced by foundingmetals other than precious metals or alloys consisting exclusively or partly of non-precious metals is covered by a more or less thick adhering layer of oxide. This is particularly true with regard to the metals of the iron group and their alloys with metals of the 3rd to the 6th group of the periodical system of elements. Such metals and their alloys having in most cases a melting point above 1000 C. up to 1600 C., are easily converted at the melting temperature into oxide due to their high affinity with oxygen. They are able to withdraw oxygen from other substances, even from silicic anhydrite, and to react therewith to oxide. Therefore by founding such alloys in the casting molds in question one obtains cast metal bodies which eventually are covered by a strong reaction layer of oxides, silicates etc., below which lies a rough metal surface. Besides the fact, that the removal of this layer by grinding, by means of a sand-let or by chemical means in one or more runs causes a considerable loss of time, the accuracy of the cast metal bodies is essentially reduced. This disadvantage is of particular importance in the manufacture of cast metal bodies which obtain their definite form by the casting process itself, for instance such for dental purposes, which must be very accurate and which would lose their accuracy by subsequent grinding.
The creation of such a reaction layer can be avoided or practically avoided by two different measures.
One way consists in adding in advance to the mass from which the casting mold is built, substances which would be created by the reaction between melted metal and the mass, or the components of such substances which react with each other during the heating period.
The other way consists in that, contrary to the usual practice the temperature of the casting mold does not correspond to the melting point of the metal, but is considerably lower. For instance a melted alloy comprising 30% chromium and 70% nickel and having a temperature of about 1400 C. is founded in a casting mold the temperature of which is only about 700-800' C. It has been found that in spite of the great diflerence of 800-700 C. between the temperature of the metal and the temperature of the casting mold the metal does not coagulate untimely. For such procedure it is evident only such masses can be used which practically neither expand nor contract within the temperature interval between 700 or 800 C. and 1400 C. The mass according to the invention corresponds to this condition as after the conversion of the u-quartz is completed a perceptible contraction begins below about 700 C. The predetermined expansion of. the casting mold is therefore maintained within the temperature interval between about 700 C. and about 1400 C. or more.
What I claim is:
1. Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 0., increasing the temperature of the mold to a temperature above 870 0., whereby the quartz of said mold is converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold above 870 C. for a sufficiently long period to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
2. Method of producing casting molds as defined in claim 1 and in which a catalyst of the group consisting of sodium wolfraniate, silicofluorides, salts of phosphoric acid, and salts or boric acid is added to the material of the mold.
3. Method of producing casting molds as defined in claim 1 and in which a material of the group consisting of cristobalite and tridymite is included in the material of the mold.
4. Method of producing casting molds as defined in claim 1 and in which in the mass substances are included which would be created by the reaction between the melted metal and the mass.
5. Method of producing casting molds as defined in claim 1 and in which in the mass substances are included which by heating the mold produce the reaction product which would be created by the reaction between the melted metal and the mass.
6. Method of producing casting molds as defined in claim 1 and in which the casting mold is reduced to a temperature below the melting temperature of the metal before the metal is poured into the mold, for preventing reaction between the melted metal and the material of the mold.
7. Method of producing casting molds of deflnite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 C., increasing the temperature of the mold to a temperature of about 1300 0., whereby the quartz of said mold is converted, with expansion. into the form in which it is stable above 575 C., and maintaining the mold at about 1300 C. for a sufliciently long period to convert the quartz, with expansion, into a compound of the group consisting of tridymite and crlstobalite.
8. Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for,
the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 C., increasing the temperature of the mold to a temperature of about 1300" 0., whereby the quartz of said mold is converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold at about 1300 C. for about onehalf hour to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
9. Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of quartz in the form in which it is stable below 575 C., gradually increasing the temperature of the mold to a temperature of about 1300 C. over a period of about one hour, whereby the quartz of said mold is converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold at about 1300 C. for a period of about one-half hour to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
10. Method of producing casting molds of deflnite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of rock quartz, increasing the temperature of the mold gradually over a period of about 1 hour to a temperature above 870 0. whereby the rock quartz is first converted, with expansion, into the form in which it is stable above 575 C., and maintaining the mold above 870 C. to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.-
11. Method of producing casting molds of definite shape for forming bodies of metals or alloys with high melting points and compensating for the shrinkage of such metals or alloys comprising forming a mold consisting essentially of rock quartz, increasing the temperature of the mold gradually over a period of about 1 hour to a temperature of about 1300 0. whereby the rock quartz is first converted, with expansion, into the form; in which it is stable above 575 0., and maintaining the mold at about 1300 C. for a period of about one-half hour to convert the quartz, with expansion, into a compound of the group consisting of tridymite and cristobalite.
VICTOR KROSTA.
US81126A 1935-05-25 1936-05-21 Method of producing casting molds Expired - Lifetime US2211133A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2211133X 1935-05-25

Publications (1)

Publication Number Publication Date
US2211133A true US2211133A (en) 1940-08-13

Family

ID=7990305

Family Applications (1)

Application Number Title Priority Date Filing Date
US81126A Expired - Lifetime US2211133A (en) 1935-05-25 1936-05-21 Method of producing casting molds

Country Status (1)

Country Link
US (1) US2211133A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2480426A (en) * 1943-04-27 1949-08-30 John H S Skoning Method of making precision molds
DE2659168A1 (en) * 1975-12-29 1977-07-14 Sherwood Refractories CORES FOR CASTING METHODS WITH DIRECTED Solidification
US4190450A (en) * 1976-11-17 1980-02-26 Howmet Turbine Components Corporation Ceramic cores for manufacturing hollow metal castings
US4236568A (en) * 1978-12-04 1980-12-02 Sherwood Refractories, Inc. Method of casting steel and iron alloys with precision cristobalite cores
US4352390A (en) * 1978-12-04 1982-10-05 Sherwood Refractories, Inc. Precision silica cones for sand casting of steel and iron alloys
US4844148A (en) * 1986-06-10 1989-07-04 Societe Nationale D'etude Et De Construction De Moteurs D'aviation "S. N. E. C. M. A." Cristobalitic shell-mould for casting, the products and the process used for preparing the said mould

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2480426A (en) * 1943-04-27 1949-08-30 John H S Skoning Method of making precision molds
DE2659168A1 (en) * 1975-12-29 1977-07-14 Sherwood Refractories CORES FOR CASTING METHODS WITH DIRECTED Solidification
FR2336998A1 (en) * 1975-12-29 1977-07-29 Sherwood Refractories CORES FOR DIRECTIONAL SOLIDIFICATION CASTING PROCESS
US4093017A (en) * 1975-12-29 1978-06-06 Sherwood Refractories, Inc. Cores for investment casting process
US4190450A (en) * 1976-11-17 1980-02-26 Howmet Turbine Components Corporation Ceramic cores for manufacturing hollow metal castings
US4236568A (en) * 1978-12-04 1980-12-02 Sherwood Refractories, Inc. Method of casting steel and iron alloys with precision cristobalite cores
US4352390A (en) * 1978-12-04 1982-10-05 Sherwood Refractories, Inc. Precision silica cones for sand casting of steel and iron alloys
US4844148A (en) * 1986-06-10 1989-07-04 Societe Nationale D'etude Et De Construction De Moteurs D'aviation "S. N. E. C. M. A." Cristobalitic shell-mould for casting, the products and the process used for preparing the said mould

Similar Documents

Publication Publication Date Title
SE7614616L (en) METAL MOLDING, IN PARTICULAR PREPARATION OF A REFRACTORY CORE TO BE USED IN THE IMPLEMENTATION OF THE KIT
US2494403A (en) Mold composition
DE19911847A1 (en) Fine and molded casting in plastic / carbon aerogels
US2211133A (en) Method of producing casting molds
US3423216A (en) Method of making a ceramic core
US1909008A (en) Highly refractory denial mold material and method of making the same
US2209035A (en) Refractory investment
KR20080093799A (en) Plastery investment used for investment casting
US4106945A (en) Investment material
DE2313498A1 (en) PROCESS FOR MANUFACTURING CASTING FORMS FOR PRECISION CASTINGS
US5373891A (en) Investment material and mold for dental use and burnout thereof
CH498922A (en) Silica-containing binder
US2931081A (en) Mould structure and its production
US2195452A (en) Method of making articles of porcelain
US1708436A (en) Composition for dental molds
US3234607A (en) Method of forming an investment mold with potassium sulfate additive
US2211789A (en) Refractory mold material
US2341998A (en) All ceramic denture and method of producing same
US1932202A (en) Investment
MX2021002654A (en) Method of preparing a particulate refractory composition for use in the manufacture of foundry moulds and cores, corresponding uses, and reclamation mixture for thermal treatment.
AT158986B (en) Process for the production of casting molds intended for casting refractory metals and metal alloys according to models having the natural size of the casting.
GB440296A (en) Improvements in and relating to methods of casting
US2639478A (en) Process of preparing patterns
US1288035A (en) Composition of matter for use in foundry practice.
SU1400759A1 (en) Paste for reconditioning permanent and semipermanent moulds and cores