US2368322A - Core making process - Google Patents
Core making process Download PDFInfo
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- 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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- US
- United States
- Prior art keywords
- cores
- mixture
- sand
- sodium silicate
- foundry
- 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
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- 238000000034 method Methods 0.000 title description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 38
- 239000004576 sand Substances 0.000 description 25
- 239000000203 mixture Substances 0.000 description 23
- 239000004115 Sodium Silicate Substances 0.000 description 21
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 21
- 229910052911 sodium silicate Inorganic materials 0.000 description 21
- 239000000126 substance Substances 0.000 description 15
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 10
- 229910052708 sodium Inorganic materials 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- 239000011230 binding agent Substances 0.000 description 9
- 239000000080 wetting agent Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 238000007493 shaping process Methods 0.000 description 4
- 238000009736 wetting Methods 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- PMPBFICDXLLSRM-UHFFFAOYSA-N 1-propan-2-ylnaphthalene Chemical compound C1=CC=C2C(C(C)C)=CC=CC2=C1 PMPBFICDXLLSRM-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 101100348017 Drosophila melanogaster Nazo gene Proteins 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical class O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- 241001446467 Mama Species 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000001164 aluminium sulphate Substances 0.000 description 1
- 235000011128 aluminium sulphate Nutrition 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- CJDPJFRMHVXWPT-UHFFFAOYSA-N barium sulfide Chemical compound [S-2].[Ba+2] CJDPJFRMHVXWPT-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- -1 for instance Chemical compound 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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
- B22C1/18—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 inorganic agents
- B22C1/186—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 inorganic agents contaming ammonium or metal silicates, silica sols
- B22C1/188—Alkali 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.
Landscapes
- 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.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR2368322X | 1940-02-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2368322A true US2368322A (en) | 1945-01-30 |
Family
ID=9685178
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US436540A Expired - Lifetime US2368322A (en) | 1940-02-20 | 1942-03-27 | Core making process |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2368322A (en) |
Cited By (13)
| 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 |
-
1942
- 1942-03-27 US US436540A patent/US2368322A/en not_active Expired - Lifetime
Cited By (15)
| 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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