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US2368322A - Core making process - Google Patents

Core making process Download PDF

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Publication number
US2368322A
US2368322A US436540A US43654042A US2368322A US 2368322 A US2368322 A US 2368322A US 436540 A US436540 A US 436540A US 43654042 A US43654042 A US 43654042A US 2368322 A US2368322 A US 2368322A
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Prior art keywords
cores
mixture
sand
sodium silicate
foundry
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US436540A
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Passelecq Georges
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    • 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
    • B22C1/16Compositions 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
    • B22C1/18Compositions 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 inorganic agents
    • B22C1/186Compositions 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 inorganic agents contaming ammonium or metal silicates, silica sols
    • B22C1/188Alkali metal silicates

Definitions

  • the masses used for this manufacture must have s'uiiicient cohesion to lend themselves to molds: on the other hand, it isnecessary that they be suiiiciently porous to allow, when the molten metal is poured, the escape of gases generated by the molten metal and by the binders utilized in suiiicient porosity. It is consequently customary out the aid of any binder.
  • the main object of the present invention is a the invention, consists essentially in constituting a mixture of foundry sand, binder or agglomerating agent and wetting emulsifying agent, it besoda (known commercially as “Breco1ane) or also the products known commercially under the denomination of "Diastersols NDS, sulphonated iauric alcohols or derivatives of formaline condensed with sulphonated naphthalenes or even natural products.
  • the process which is the object of the invention may be applied, particularly, to the constitution of foundry cores using initially ordinary silico-argillaceous foundry sands.
  • the very sand containing its binder which is the clay, is suflicient to impart to it the desired porosity by wetting it with a solution, or aqueous suspension, of the wetting-emulsifying agent,
  • Brecolane It is possible for example, to add to the sand an aqueous solution, saturated at 10%, of this wetting. agent, in a proportion of 10 to of this solution with respect to the weight of the sand.
  • a paste is obtained which may be put through a draw plate or which may mg possible for the foundry sand itself to contain the binder, after which the cores are formed by passage through a draw plate or by molding-or pouring into molds or core boxes, according to corporated to the sand, the latter is perfectly .wet and the occluded air remains in the interior of the mass, thus producing multiple pores. It is possible to use to this effect one of the many products known in industry for their wetting and emulsifying properties, such as for instance:
  • The-cylinders or cores thus formed are ,dried in a drying-room at a temperature of at least C. Argillaceous cores are at last obtained having a good resistance for the use for which they are to serve and the apparent density of which may vary from 1.20 to 1.75.
  • the process may also be applied to the fabrication of cores by using initially sands which do not have by themselves practically any agglomerating capacity, such as sands constituted by more or less pure silica.
  • a binder to the silicious sand.
  • the proportion of binder incorporated in the mixture may vary according to the degree'of plasticity or liquefaction desired. If, for instance, a solution at 36 B. of commercial sodium silicate is used, this proportionmay vary from 5 to 20% by weight of the I mixture composed of the other materials.
  • the quantity of catalyser for setting may vary with the setting speed de- Isopropyl (or butyl), naphthalene sulphonate of sired: in general, a proportion of sodium fluosilileast equal to 3.2. However, it is preferable that the ratio do not exceed the value of 3.35 so as not to hinder the reaction giving rise to the formation of nascent silica.
  • a real stoichiometric reaction may also be used by causing the flocculation of nascent silica by any reacting agent having a pH lower than that of the sodium silicate solution or containing or capable of liberating a molecule of free acid the acidity of which is at least equal to that of the silica.
  • any reacting agent having a pH lower than that of the sodium silicate solution or containing or capable of liberating a molecule of free acid the acidity of which is at least equal to that of the silica.
  • blcarbonates which, in the presence of water, give rise to free carbonic acid, or again, a sulphate, such as for instance, aluminium sulphate which, in hydrolysins, produces sulphuric acid.
  • the quantity of wettin a ent may vary with the greater or lesser degree of porosity which it is desired to obtain for the final agglomerate; if, for instance, the wetting agent known as Diastersols NBS or the one known as Brcolane be utilized, the proportion of this substance used may be chosen between 2 and 5% with respect to the weight of the sodium silicate.
  • the process, according to the invention may also be applied to the construction of molds, this application being obtained'under the same conditions as those in the fabrication of cores.
  • the mass to be molded is constituted by a mixture of sand, of sodium silicate, of fluosilicate and of wetting-emulsifying agents
  • Example 1 To 200 parts of argillaceous foundry sand are added 25 parts of an aqueous solution saturated with the wetting agent Brecolane (10%). A thorough mixing is effected in an emulsifying machine. The mixture is molded and dried at C. by gradually raising the temperature.
  • Example 2 Parts siliceous foundry sand l Sodium fluosilicate 1 The wetting agent Diastersol NDS" l
  • Example 3 Parts siliceous foundry sand 1 Sodium fiuozirconate 1 Saponin l are thoroughly mixed.
  • Example 4 100 parts by weight of siliceous foundry sand are thoroughly mixed with 0.36 part by weight of sodium fiuosilicate, 0.12 part by weight of the dispersing and wetting agent Brecola'ne and 0.12 part by weight of bentonite or colloidal clay. Then 6 parts by weight of sodium silicate at 36 B. were added to this mixture, after which the cores were molded under the usual conditions and allowed to set.
  • Example 6 Parts by weight siliceous sand 100 Paratoluene sulphochloride 0.03 Diastersol NDS 0.12
  • the process of making material for foundry cores which comprises mixing foundry sand with an aqueous solution of a wetting agent and a substance selected from the group consisting of the fluosilicates, fluotitanates, fiuozirconates and fluotungstates of sodium and potassium and thereafter incorporating in the mixture from six to ten percent of sodium silicate.
  • foundry cores which comprises mixing foundry sand with an aqueous solution of the sodium sulphonate of isopropyl naphthalene and a substance selected from the group consisting of the fluosilicates, fluotitanates, fluozirconates and -fluotungstates ofsodium and potassium and thereafter incorporating in the vmixture from six to ten percent of sodium silicate and shaping and drying the cores made thereof.
  • foundry cores which comprises mixing foundry sand with an aqueous solution of para-toluene-sulphochloride and a substance selected from the group consisting of t efluosilicates, fluotitanates,-fluozirconates and iluotungstates of sodium and potassium and thereafter incorporating in the mixture from six to ten percent of sodium silicate and shaping and drying the cores made thereof.
  • foundry cores which comprises mixing foundry sand with an aqueous solution of a wetting agent and a substance which decomposes sodium silicate and with a heat-destructible substance, thereafter incorporating in the mixture from six to ten percent of sodium silicate and shaping the cores from the mixture.
  • foundry cores which comprises mixing foundry sand with an aqueous solution of a wetting agent and a substance which decomposes sodium silicate and with a heat-dc structlble substance selected from the group consisting of sawdust and cereal hulls, thereafter incorporating in the mixture from six to ten percent of sodium silicate and shaping and drying the cores from the mixture.

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

Description

. Patented-Jan. 30, 194,5
' cone mama raocass Georges Passelecq, Paris, France; vested the Allen Property Custodian .No Drawing. Application March 27, 1942, Serial No. 436,540. In France February 20, 1940 6 Claims. (oi. 22-188) The manufacture of molds and moreparticularly foundry cores, presents, among others, ,a
double, problem to be solved; on the one hand, the masses used for this manufacture must have s'uiiicient cohesion to lend themselves to molds: on the other hand, it isnecessary that they be suiiiciently porous to allow, when the molten metal is poured, the escape of gases generated by the molten metal and by the binders utilized in suiiicient porosity. It is consequently customary out the aid of any binder.
the core. This double problem oflers greater difiiculties in so far as foundry cores are concerned because of the position these are to occupy in the midst of the metal.
Silico-argillaceous sands ordinarily utilized as foundry sands possess by themselves an agglomerating capacity which would allow their utilization for the fabrication of foundry cores, with- But experience has shown that cores thus constituted present into add to the foundry sand, for this fabrication, a consequential quantity of silica the purpose of .which is to increase the porosity and which may attain from 70 to 85% of the mixture. The addition of such a high proportion of silica necessitates, for the agglomerating process, the intervention of binders, usually constituted by organic substances such as molasses, the residual lyes of sulphited cellulose, and to which it is generally necessaryto add a considerable proportion of linseed oil, which by oxidation gives the agglomerate the desired consistency.
The main object of the present invention is a the invention, consists essentially in constituting a mixture of foundry sand, binder or agglomerating agent and wetting emulsifying agent, it besoda (known commercially as "Breco1ane) or also the products known commercially under the denomination of "Diastersols NDS, sulphonated iauric alcohols or derivatives of formaline condensed with sulphonated naphthalenes or even natural products.
The process, which is the object of the invention may be applied, particularly, to the constitution of foundry cores using initially ordinary silico-argillaceous foundry sands. In this case, the very sand containing its binder, which is the clay, is suflicient to impart to it the desired porosity by wetting it with a solution, or aqueous suspension, of the wetting-emulsifying agent,
known as Brecolane. It is possible for example, to add to the sand an aqueous solution, saturated at 10%, of this wetting. agent, in a proportion of 10 to of this solution with respect to the weight of the sand. After the mixture has been through a mixer, a pasteis obtained which may be put through a draw plate or which may mg possible for the foundry sand itself to contain the binder, after which the cores are formed by passage through a draw plate or by molding-or pouring into molds or core boxes, according to corporated to the sand, the latter is perfectly .wet and the occluded air remains in the interior of the mass, thus producing multiple pores. It is possible to use to this effect one of the many products known in industry for their wetting and emulsifying properties, such as for instance:
be used to fill more or less complicated core molds. The-cylinders or cores thus formed are ,dried in a drying-room at a temperature of at least C. Argillaceous cores are at last obtained having a good resistance for the use for which they are to serve and the apparent density of which may vary from 1.20 to 1.75.
According to the invention, the process may also be applied to the fabrication of cores by using initially sands which do not have by themselves practically any agglomerating capacity, such as sands constituted by more or less pure silica. In this case, in addition to the wetting agent, it is advisable to ,add a binder to the silicious sand. To this end, it is possible to have recourse, in particular, to sodium silicate in which case care must be taken to incorporate in the mixture a substance capable of decomposing the sodium silicate thereby giving rise to the formation of nascent silica having the power to ensure the setting of the mixture. The proportion of binder incorporated in the mixture may vary according to the degree'of plasticity or liquefaction desired. If, for instance, a solution at 36 B. of commercial sodium silicate is used, this proportionmay vary from 5 to 20% by weight of the I mixture composed of the other materials.
use such substances as, for instance, fluosilicates,
iiuotitanates, iluotungstates, fluozirconates of sodium or of potassium. The quantity of catalyser for setting may vary with the setting speed de- Isopropyl (or butyl), naphthalene sulphonate of sired: in general, a proportion of sodium fluosilileast equal to 3.2. However, it is preferable that the ratio do not exceed the value of 3.35 so as not to hinder the reaction giving rise to the formation of nascent silica.
A real stoichiometric reaction may also be used by causing the flocculation of nascent silica by any reacting agent having a pH lower than that of the sodium silicate solution or containing or capable of liberating a molecule of free acid the acidity of which is at least equal to that of the silica. Along the same line of thought, it is possible to use, in order to obtain this reaction, blcarbonates which, in the presence of water, give rise to free carbonic acid, or again, a sulphate, such as for instance, aluminium sulphate which, in hydrolysins, produces sulphuric acid. It is also possible to use a sulphide capable of liberat= ing, by hydrolysis, hydrogen sulphide which then acts as a weak acid, or an organic compound such as ortho or paratoluene sulphochloride which produces, by hydrolysis, one or several acids. Tests already eifected seem to have revealed that, in the case of a reaction of stoichiometric decomposition, the ratio SiOz/NazO of the sodium silicate may be lowered to about 2.5.
The quantity of wettin a ent may vary with the greater or lesser degree of porosity which it is desired to obtain for the final agglomerate; if, for instance, the wetting agent known as Diastersols NBS or the one known as Brcolane be utilized, the proportion of this substance used may be chosen between 2 and 5% with respect to the weight of the sodium silicate.
It is preferable, in practical applications of the invention, to effect a thorough mixture of the catalyser or substance for setting and of the wetting agent with an equal weight of sand, and then, to add the rest of the sand. After mixing in a mixer and addition of sodium silicate a sand is obtained suitable for the fabrication of cores, either by the usual method, or by vibrating for a short time. If the proportion of sodium silicate solution is sufficiently high, the mass obtained is sufliciently fluid to be poured, notably in formed molds, which allows the construction of even very complex cores, the setting'taking place due to the catalysing action of the incorporated fluosilicate. Cores thus obtained hav a good resistance and are very porous, their apparent density varying, for instance, from 1.20 to 1.60.
When it is desired to constitute cores which must have special qualities of mechanical resistance and at the same time a brittleness after molding sufficiently great to permit an easy removing of the sand-for example in the case of very long and very thin cores which cannot be upheld along their length, such as those used in the manufacture of heating radiators-it is possible, in accordance with the present invention, at the same time as a certain quantity of sodium glycol: and glycerine. As substitutes for such substances, it is also possible to use sawdust, hulls of rice or other cereals, etc. The addition of substances of this nature to the mixture to be agglomerated may also prove advantageous in those cases where, without specifically seeking to obtain a high resistance of the cores, it is profitable because of the shape of the latter, to seek a greater facility for removing the sand after molding.
As has already been said, the process, according to the invention, may also be applied to the construction of molds, this application being obtained'under the same conditions as those in the fabrication of cores. In particular, in the case where the mass to be molded is constituted by a mixture of sand, of sodium silicate, of fluosilicate and of wetting-emulsifying agents, it is possible to form the molds by usual methods, by vibrating or by pouring this mixture on to the pattern, which allows the omission of a great number of delicate operations usually necessary in the molding, of foundry parts: in particular an economy of specialized labor and of time is obtained and the operations of drying and of baking are eliminated.
Moreover. it is interesting to note that, as a result of the absence of organic binders, the gaseous emanation proceeding from the core and the mold is practically eliminated, which condition offers a notable improvement from the point of view of handling (facility, cleanliness, shophvgiene).
In order to diminish the risk of eventual sticking of the mass to be molded (cores ormolds) to the patterns or to the core boxes, it is advisable to apply on to these patterns or boxes a rubber paint such as, for instance, that found on the market.
all Hereunder are examples of carrying out the silicate is incorporated in order to ensure that invention which are given by way of illustration.
Example 1 To 200 parts of argillaceous foundry sand are added 25 parts of an aqueous solution saturated with the wetting agent Brecolane (10%). A thorough mixing is effected in an emulsifying machine. The mixture is molded and dried at C. by gradually raising the temperature.
' Example 2 Parts siliceous foundry sand l Sodium fluosilicate 1 The wetting agent Diastersol NDS" l Example 3 Parts siliceous foundry sand 1 Sodium fiuozirconate 1 Saponin l are thoroughly mixed.
I This mixture is added to 200 parts of siliceous foundry sand.
When about to be used, 20 parts of sodium silicate are thoroughly incorporated. The mixture is molded, and the setting allowed to take place.
, is desired, it is advisable-to to ten percent of sodium silicate.
' Example 4 100 parts by weight of siliceous foundry sand are thoroughly mixed with 0.36 part by weight of sodium fiuosilicate, 0.12 part by weight of the dispersing and wetting agent Brecola'ne and 0.12 part by weight of bentonite or colloidal clay. Then 6 parts by weight of sodium silicate at 36 B. were added to this mixture, after which the cores were molded under the usual conditions and allowed to set.
Example 5 Parts by weight Siliceous foundry sand 100' Barium sulphide at 80% 0.25 Diastersol NDS 0.12
are thoroughly mixed. Then 6 parts by weight of sodium silicate at 36 B. are added to this mixture, after which the cores are molded. The setting takes about three times as long as if sodium fluosilicate were used as catalyser.
Example 6 Parts by weight siliceous sand 100 Paratoluene sulphochloride 0.03 Diastersol NDS 0.12
substance which decomposes sodium silicate and thereafter incorporating in the mixture from six .2. The process of making material for foundry coreswhich comprises mixing foundry sand with an aqueous solution of a wetting agent and a substance selected from the group consisting of the fluosilicates, fluotitanates, fiuozirconates and fluotungstates of sodium and potassium and thereafter incorporating in the mixture from six to ten percent of sodium silicate.
3. The process of making foundry cores which comprises mixing foundry sand with an aqueous solution of the sodium sulphonate of isopropyl naphthalene and a substance selected from the group consisting of the fluosilicates, fluotitanates, fluozirconates and -fluotungstates ofsodium and potassium and thereafter incorporating in the vmixture from six to ten percent of sodium silicate and shaping and drying the cores made thereof.
4. The process of making foundry cores which comprises mixing foundry sand with an aqueous solution of para-toluene-sulphochloride and a substance selected from the group consisting of t efluosilicates, fluotitanates,-fluozirconates and iluotungstates of sodium and potassium and thereafter incorporating in the mixture from six to ten percent of sodium silicate and shaping and drying the cores made thereof.
5. The process of making foundry cores which comprises mixing foundry sand with an aqueous solution of a wetting agent and a substance which decomposes sodium silicate and with a heat-destructible substance, thereafter incorporating in the mixture from six to ten percent of sodium silicate and shaping the cores from the mixture.
6. The process of making foundry cores which comprises mixing foundry sand with an aqueous solution of a wetting agent and a substance which decomposes sodium silicate and with a heat-dc structlble substance selected from the group consisting of sawdust and cereal hulls, thereafter incorporating in the mixture from six to ten percent of sodium silicate and shaping and drying the cores from the mixture.
GEORGES PABSELECQ.
US436540A 1940-02-20 1942-03-27 Core making process Expired - Lifetime US2368322A (en)

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2521839A (en) * 1949-08-11 1950-09-12 Austenal Lab Inc Refractory casting mold and method of making same
US2656281A (en) * 1950-09-09 1953-10-20 Rene D Wasserman Moldable compounds for making jigs
DE923933C (en) * 1950-11-28 1955-03-14 Everard F Kohl Process for the production of shell-shaped casting molds
US2748435A (en) * 1951-11-14 1956-06-05 Gen Motors Corp Process for reinforcing shell molds
US2817128A (en) * 1952-05-15 1957-12-24 Monsanto Chemicals Foundry sand compositions and process of making
US2905563A (en) * 1956-02-29 1959-09-22 Diamond Alkali Co Alkali metal silicate binder for foundry sand molds and process
US2949375A (en) * 1957-08-20 1960-08-16 Nalco Chemical Co Siliceous casting cores
US3022555A (en) * 1962-02-27 Molds
DE975915C (en) * 1946-02-13 1962-12-06 Nicolas Herzmark Process for the production of refractory casting molds for the precision casting of metals and metal alloys
US3615755A (en) * 1970-01-14 1971-10-26 Mitsubishi Heavy Ind Ltd Method for making a mold using manganese carbonate
US4093467A (en) * 1971-04-05 1978-06-06 Abram Moiseevich Lyass Method for making foundry moulds and cores
US4226277A (en) * 1978-06-29 1980-10-07 Ralph Matalon Novel method of making foundry molds and adhesively bonded composites
WO2018097179A1 (en) * 2016-11-22 2018-05-31 旭有機材株式会社 Coated sand, manufacturing method for same, and manufacturing method for mold using same

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3022555A (en) * 1962-02-27 Molds
DE975915C (en) * 1946-02-13 1962-12-06 Nicolas Herzmark Process for the production of refractory casting molds for the precision casting of metals and metal alloys
US2521839A (en) * 1949-08-11 1950-09-12 Austenal Lab Inc Refractory casting mold and method of making same
US2656281A (en) * 1950-09-09 1953-10-20 Rene D Wasserman Moldable compounds for making jigs
DE923933C (en) * 1950-11-28 1955-03-14 Everard F Kohl Process for the production of shell-shaped casting molds
US2748435A (en) * 1951-11-14 1956-06-05 Gen Motors Corp Process for reinforcing shell molds
US2817128A (en) * 1952-05-15 1957-12-24 Monsanto Chemicals Foundry sand compositions and process of making
US2905563A (en) * 1956-02-29 1959-09-22 Diamond Alkali Co Alkali metal silicate binder for foundry sand molds and process
US2949375A (en) * 1957-08-20 1960-08-16 Nalco Chemical Co Siliceous casting cores
US3615755A (en) * 1970-01-14 1971-10-26 Mitsubishi Heavy Ind Ltd Method for making a mold using manganese carbonate
US4093467A (en) * 1971-04-05 1978-06-06 Abram Moiseevich Lyass Method for making foundry moulds and cores
US4226277A (en) * 1978-06-29 1980-10-07 Ralph Matalon Novel method of making foundry molds and adhesively bonded composites
WO2018097179A1 (en) * 2016-11-22 2018-05-31 旭有機材株式会社 Coated sand, manufacturing method for same, and manufacturing method for mold using same
CN110099761A (en) * 2016-11-22 2019-08-06 旭有机材株式会社 The manufacturing method of precoated sand and its manufacturing method and the casting mold using it
JPWO2018097179A1 (en) * 2016-11-22 2019-10-17 旭有機材株式会社 Coated sand, method for producing the same, and method for producing a mold using the same

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