US2748435A - Process for reinforcing shell molds - Google Patents
Process for reinforcing shell molds Download PDFInfo
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- US2748435A US2748435A US256309A US25630951A US2748435A US 2748435 A US2748435 A US 2748435A US 256309 A US256309 A US 256309A US 25630951 A US25630951 A US 25630951A US 2748435 A US2748435 A US 2748435A
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- 238000000034 method Methods 0.000 title claims description 21
- 230000008569 process Effects 0.000 title claims description 17
- 230000003014 reinforcing effect Effects 0.000 title description 18
- 239000000203 mixture Substances 0.000 claims description 31
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- 238000005266 casting Methods 0.000 claims description 12
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 39
- 239000004576 sand Substances 0.000 description 33
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- 235000019353 potassium silicate Nutrition 0.000 description 21
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 239000004115 Sodium Silicate Substances 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 9
- 235000019794 sodium silicate Nutrition 0.000 description 9
- 229910052911 sodium silicate Inorganic materials 0.000 description 9
- 229940032158 sodium silicate Drugs 0.000 description 9
- 239000000463 material Substances 0.000 description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 5
- 239000007789 gas Substances 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
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- 238000000429 assembly Methods 0.000 description 3
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- 238000010438 heat treatment Methods 0.000 description 3
- 238000005495 investment casting Methods 0.000 description 3
- 239000012779 reinforcing material Substances 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
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- 238000006703 hydration reaction Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000010112 shell-mould casting Methods 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
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- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- VXJCGWRIPCFWIB-UHFFFAOYSA-N hexadecasodium tetrasilicate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] VXJCGWRIPCFWIB-UHFFFAOYSA-N 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C23/00—Tools; Devices not mentioned before for moulding
Definitions
- This invention relates to reinforced sand-resin molds and cores for metal casting operations and particularly to a process for reinforcing shell-type sand-resin molds, mold sections and cores to prevent distortion of any portion of the mold or core assembly by metal pressure during casting.
- This invention contemplates the use of a novel and useful mix which may be placed on the back surfaces of thin-walled molds or cores and subsequently baked so as to constitute a reinforcing material.
- the shell molding process consists of using a thermosetting plastic or resin as a binder for the sand grains to form thin-walled molds having high gas permeability, good surface smoothness and dimensional stability.
- the molding material which is generally a dry mixture of a major proportion of silica sand and a minor proportion of a plastic binder, is used in powder form with no water being added.
- Phenol formaldehyde and melamine formaldehyde resins are typical examples of the type of thermosetting binders preferably used.
- the sand employed is preferably free of metallic oxides, clay, moisture and organic matter.
- sand-resin molds are prepared by allowing the dry mixture of sand and resin powder to come into contact with a hot metal pattern for a short period of time. A layer of the mix adheres to the metal surfaces due to the melting of the resin which entraps the sand with which it is intimately mixed, thereby reproducing pattern detail.
- Metal patterns must be employed because they are subjected to elevated temperatures. Pattern temperatures in the range of between 250 F. and 350 F. are typical, but temperatures up to 800 F. may be advantageously employed under particular conditions. Half patterns, gates and runners are usually all permanently fixed on the metal plates. The pattern temperature and the length of time the molding material is allowed to remain in contact with the hot pattern surfaces determine the resulting thickness of the mold. Mold build-up times ranging from a few seconds to approximately one minute are appropriate for various applications.
- the excess dry sand and resin are removed, and the closely adhering sandresin layer is preferably cured by heating to a temperature within the range of approximately 300 F. to 600 F. for a short period of time, usually from a few seconds to five minutes, while in contact with the metal pattern.
- This baking operation results in the conversion of the resinous material to a hard, insoluble binder which se-v curely bonds the sand grains together.
- the formed molds are, in effect, thin shells which usually have sufficient strength and stifiness to make them suitable for many casting operations if these shells are properly backed up by steel shot or other suitable materials.
- thin shell molds lack the necessary rigidity, even when certain external backing means are employed, to provide precision castings under many operating conditions, the molds frequently tending to bulge, crack, or otherwise become distorted by the pressure of the molten metal during or immediately after pouring. Not only does such mold distortion prevent casting to very close dimensional tolerance, but it also results in excessive finning at the mold parting line.
- backing up the molds with steel shot is a cumbersome and expensive process.
- a principal object of my invention is to provide an inexpensive and easily applied mix which may be placed on the back surfaces of thin-walled molds and subsequently baked so as to reinforce these molds, thus permitting the elimination of the aforementioned type of backing means and the attendant casting difii culties.
- a further object of this invention is to provide a process for reinforcing shell-type sand-resin molds by the use of the aforementioned mix and to thereby permit greater flexibility and economy in the method of backing up this type of mold.
- mold as used herein, is generally applied in its generic sense to mean a casting form which includes both molds and cores, this invention in no manner being limited to the former.
- the word pattern is used herein as including both mold patterns and core boxes.
- a layer of a mixture of sand and a waterglass solution, which functions as a binder, is placed on the back of a sand-resin mold and suitably dried or baked.
- This mixture which forms the reinforcing material, provides a very firm and close contact with the entire outside surface of the mold, thus assuring no change in the mold cavity dimensions.
- this reinforcing layer provides adequate permeability for mold gases generated at the time of metal pouring.
- the advantages of this type of mold backing also include the fact that low-cost materials are used and that only a relatively short time is required to apply it to a mold section or core.
- a waterglass solution of the desired concentration is first mixed with the sand. This may be done either by hand or machine mulling, the former method generally requiring approximately two to three minutes and the latter not more than one minute.
- the sand is readily wet by the waterglass solution and is immediately ready for application on the mold section. On the other hand, if it is desired to do so, this mix may be kept for several hours prior to use by covering it with a damp cloth.
- a layer of the moist reinforcing mix 10 having the desired thickness is then placed on the back of a shell mold section 12, a layer having a thickness of from /2" to 2" usually being satisfactory for most applications.
- the resultant reinforcing mold construction is next dried, preferably by baking in a circulating air oven at a temperature within the range of approximately 300 F. to 700 F. This assembly generally should be permitted to remain in the oven from two to five minutes.
- the waterglass-bonded sand setting readily upon heating to give asnug, firm support for all details of the mold.
- the waterglass Upon baking, the waterglass not only securely bonds together the sand particlesof the baking material, but alsocauses the back 'ing'layerto adhere to the shell mold section.
- two reinforcedshell mold sections 12 are shown inassembled position preparatory to the pour ing of the molten casting metal into the formed interjacent mold cavity 14. 6f course, these reinforced mold halves are retained in abutting position during the pouring operation by clamping or other suitable means, not shown.
- One of the reinforcing layers 10 is shown as being of a type which follows the general contour of the, supported mold section, while the other reinforcing layer. is shown as having a flush exterior surface, the lat terbeing easier to formand to support during pouring.
- the contoured type of reinforcing layer however, possesses the advantage of requiring less material to perform the same function.
- Hollow. cores may be similarly reinforced by this sandwaterglassmixture. This is accomplished by fillingthe interior space of the core with this mix and then heatingthe core and reinforcing layer in the aforementioned manner. in this connection it will be appreciated that my baked reinforcing mix possesses not only the required permeability and strength, but also the proper collapsing characteristics upon shake-out to make it suitable for suchapplications.
- sand which is preferably used to produce best results is a silica saind having an American Foundrymens Society fineness number between-3O and 150, sands having AFS fineness numbers between 40 and 60 being particularly satisfactory formost applications.
- any type of sand or comminuted refractory material may be used, such as zirconium silicate sands, metallic shot, grit, etc. Currently the relatively high cost of some of these materials is the principal objection to their use.
- waterglass I mean to include not only sodium silicate and its water solutions, but also potassium silicate and mixtures of these two silicates, the lattergenerally being referred to as double waterglass.
- sodium tetrasilicate if the silicate is to beintroduced in that form, is also meant to be included within the scope of this invention.
- sodium or potassium silicates, or mixtures thereof may be advantageously added in amounts ranging from 0.07% to 7% of thetotal weight of the resultant mix.
- the water content of the mix may vary from 0.9% to 13%.
- the remainder of the reinforcing mix is substantially all sand, this mix proving satisfactory formany applications.
- the water content in the above examples is .the sum of the water of hydration and any additional water which may be present in commercial waterglass, together with any other water which it may be desirable to add to satisfactorily wet the sand-binder reinforcing mixture.
- either the pure or commercially pure solid silicates may be employed in conjunction with the amount ofwater necessary to bring the water content to-the above percentages, or a commercial waterglass solution may be used with more water being added, if-it is foundadvan-tageous to do so, in order to provide sufficient wetting properties.
- a commercial waterglass solution containing between approximately 60% and 70% water is used, the greater the amount of this solution employed, the lesser the amount of additional water required.
- sand and waterglass reinforcing material are one which consists of approximately 98% sand, 1% commercial waterglass having a sodium silicate content of approximately 37%, and 1% additional water.
- This is equivalent to a mixture of approximately 0.4% anhydrous sodium silicate, 1.6% water and 98% sand.
- the water content is the sum of water in the free form andthat which may be present in the silicate as water of hydration.
- sand having an AFS fineness number between and may be advantageously employed, the use of this particular sand beingespecially desirable in conjunction with the aforementioned specific waterglass composition.
- A. process for forming a reinforced shell mold assembly for casting metal comprising placing a mixture of a major proportion of sand and a minor proportion of thermosetting resin in contact with a hot metallic pattern for a period of time sufficient to melt the resin and to bond-a substantialportion of the sand particles together, removing any excess sand and resin, subsequently curing the formed mold shell by baking for a short period of time while in contact with the pattern, stripping the mold shell from the pattern, applying to the back surface of said mold shell a moist layer of a mixture comprising 0.9% to 13% by weight of water, 0.07% to 7% by weight of sodium silicate and the balance substantially all sand, and thereafter baking the formed reinforced shell mold assembly for at least two minutes at a temperature between 300 F. and 700 F.
- a process for forming a reinforced shell mold assembly for casting metal comprising placing a mixture of a major proportion of sand and a minor proportion of thermosetting resin in contact with a hot metallic pattern for a period of time suificient to melt the resin and to bond a substantial portion of the sand particles together, curing the formed mold shell by heating for a short period of time while in contact with the pattern, stripping the mold shell from the pattern, applying a moist mixture comprising approximately 0.2% to 0.7% by weight of sodium silicate, 1.3% to 4% by weight of water and the balance substantially all sand to the back surface of said shell mold so as to form a reinforc- 6 ing layer having an average thickness between about onehalf inch and two inches, and thereafter baking the formed reinforced shell mold assembly for approximately two to five minutes at a temperature between 300 F. and 700" F.
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Description
June 5, 1956 w. s. HACKETT PROCESS FOR REINFORCING SHELL MOLDS Filed Nov. 14 1951 INVENTOR. X4 142??? 5%06 BY W ATTORNEYJ United States Patent 2,748,435 PROCESS F OR REINFORCING SHELL MOLDS William S. Hackett, Royal Oak, Micl1., assignor to General Motors Corporation, Detroit, Mich, a corporation of Delaware Application November 14, 1951, Serial No. 256,309
2 Claims. (Cl. 22-193) This invention relates to reinforced sand-resin molds and cores for metal casting operations and particularly to a process for reinforcing shell-type sand-resin molds, mold sections and cores to prevent distortion of any portion of the mold or core assembly by metal pressure during casting. This invention contemplates the use of a novel and useful mix which may be placed on the back surfaces of thin-walled molds or cores and subsequently baked so as to constitute a reinforcing material.
Recently developed techniques in foundry practice incorporate the use of thin-walled dispensable molds and cores composed of sand and plastic binders. These procedures, generally referred to as shell molding processes, are particularly suited to the production of precision or semi-precision castings in a wide variety of metals.
Essentially the shell molding process consists of using a thermosetting plastic or resin as a binder for the sand grains to form thin-walled molds having high gas permeability, good surface smoothness and dimensional stability. The molding material, which is generally a dry mixture of a major proportion of silica sand and a minor proportion of a plastic binder, is used in powder form with no water being added. Phenol formaldehyde and melamine formaldehyde resins are typical examples of the type of thermosetting binders preferably used. The sand employed is preferably free of metallic oxides, clay, moisture and organic matter.
These sand-resin molds are prepared by allowing the dry mixture of sand and resin powder to come into contact with a hot metal pattern for a short period of time. A layer of the mix adheres to the metal surfaces due to the melting of the resin which entraps the sand with which it is intimately mixed, thereby reproducing pattern detail. Metal patterns must be employed because they are subjected to elevated temperatures. Pattern temperatures in the range of between 250 F. and 350 F. are typical, but temperatures up to 800 F. may be advantageously employed under particular conditions. Half patterns, gates and runners are usually all permanently fixed on the metal plates. The pattern temperature and the length of time the molding material is allowed to remain in contact with the hot pattern surfaces determine the resulting thickness of the mold. Mold build-up times ranging from a few seconds to approximately one minute are appropriate for various applications.
After this short time interval, the excess dry sand and resin are removed, and the closely adhering sandresin layer is preferably cured by heating to a temperature within the range of approximately 300 F. to 600 F. for a short period of time, usually from a few seconds to five minutes, while in contact with the metal pattern. This baking operation results in the conversion of the resinous material to a hard, insoluble binder which se-v curely bonds the sand grains together. After the removal of the pattern and mold from the curing oven, the mold is stripped from the pattern.
The formed molds are, in effect, thin shells which usually have sufficient strength and stifiness to make them suitable for many casting operations if these shells are properly backed up by steel shot or other suitable materials. However, I have found that thin shell molds lack the necessary rigidity, even when certain external backing means are employed, to provide precision castings under many operating conditions, the molds frequently tending to bulge, crack, or otherwise become distorted by the pressure of the molten metal during or immediately after pouring. Not only does such mold distortion prevent casting to very close dimensional tolerance, but it also results in excessive finning at the mold parting line. Moreover, backing up the molds with steel shot is a cumbersome and expensive process.
Accordingly, a principal object of my invention is to provide an inexpensive and easily applied mix which may be placed on the back surfaces of thin-walled molds and subsequently baked so as to reinforce these molds, thus permitting the elimination of the aforementioned type of backing means and the attendant casting difii culties. A further object of this invention is to provide a process for reinforcing shell-type sand-resin molds by the use of the aforementioned mix and to thereby permit greater flexibility and economy in the method of backing up this type of mold.
Other objects and advantages of this invention will more fully appear from the following description of a preferred process for forming and applying the reinforcing mix for shell molds, reference being made to the accompanying drawing showing a sectional view of the resultant reinforced mold assembly.
It will be understood that the term mold, as used herein, is generally applied in its generic sense to mean a casting form which includes both molds and cores, this invention in no manner being limited to the former.
Similarly, unless otherwise indicated, the word pattern is used herein as including both mold patterns and core boxes.
In accordance with my invention, a layer of a mixture of sand and a waterglass solution, which functions as a binder, is placed on the back of a sand-resin mold and suitably dried or baked. This mixture, which forms the reinforcing material, provides a very firm and close contact with the entire outside surface of the mold, thus assuring no change in the mold cavity dimensions. At the same time, this reinforcing layer provides adequate permeability for mold gases generated at the time of metal pouring. The advantages of this type of mold backing also include the fact that low-cost materials are used and that only a relatively short time is required to apply it to a mold section or core.
More specifically, a waterglass solution of the desired concentration is first mixed with the sand. This may be done either by hand or machine mulling, the former method generally requiring approximately two to three minutes and the latter not more than one minute. The sand is readily wet by the waterglass solution and is immediately ready for application on the mold section. On the other hand, if it is desired to do so, this mix may be kept for several hours prior to use by covering it with a damp cloth.
Referring noW to the drawing, a layer of the moist reinforcing mix 10 having the desired thickness is then placed on the back of a shell mold section 12, a layer having a thickness of from /2" to 2" usually being satisfactory for most applications. The resultant reinforcing mold construction is next dried, preferably by baking in a circulating air oven at a temperature within the range of approximately 300 F. to 700 F. This assembly generally should be permitted to remain in the oven from two to five minutes. the waterglass-bonded sand setting readily upon heating to give asnug, firm support for all details of the mold. Upon baking, the waterglass not only securely bonds together the sand particlesof the baking material, butalsocauses the back 'ing'layerto adhere to the shell mold section.
In;the drawing, two reinforcedshell mold sections 12 are shown inassembled position preparatory to the pour ing of the molten casting metal into the formed interjacent mold cavity 14. 6f course, these reinforced mold halves are retained in abutting position during the pouring operation by clamping or other suitable means, not shown. One of the reinforcing layers 10 is shown as being of a type which follows the general contour of the, supported mold section, while the other reinforcing layer. is shown as having a flush exterior surface, the lat terbeing easier to formand to support during pouring. The contoured type of reinforcing layer, however, possesses the advantage of requiring less material to perform the same function.
Hollow. cores may be similarly reinforced by this sandwaterglassmixture. This is accomplished by fillingthe interior space of the core with this mix and then heatingthe core and reinforcing layer in the aforementioned manner. in this connection it will be appreciated that my baked reinforcing mix possesses not only the required permeability and strength, but also the proper collapsing characteristics upon shake-out to make it suitable for suchapplications.
In accordance with the invention, 1 have found it convenient to employ commercialiy available waterglass containing between 30% and 40% sodium silicate. The sand which is preferably used to produce best results is a silica saind having an American Foundrymens Society fineness number between-3O and 150, sands having AFS fineness numbers between 40 and 60 being particularly satisfactory formost applications. However, any type of sand or comminuted refractory materialmay be used, such as zirconium silicate sands, metallic shot, grit, etc. Currently the relatively high cost of some of these materials is the principal objection to their use.
By the term waterglass I mean to include not only sodium silicate and its water solutions, but also potassium silicate and mixtures of these two silicates, the lattergenerally being referred to as double waterglass. Moreover, the use of sodium tetrasilicate, if the silicate is to beintroduced in that form, is also meant to be included within the scope of this invention.
With respect to the quantity of waterglass used, sodium or potassium silicates, or mixtures thereof, may be advantageously added in amounts ranging from 0.07% to 7% of thetotal weight of the resultant mix. Depending upon the fineness of the sand employed and the amount of sodium silicate used, the water content of the mix may vary from 0.9% to 13%. The remainder of the reinforcing mix, of course, is substantially all sand, this mix proving satisfactory formany applications.
More specifically, when the waterglass is used with silica sand having AFS fineness numbers ranging from 30 to 150, particularly useful quantities of sodium silicate, for example, have been found to range from 0.2% to 0.7%, with the water content varying from 1.3% to 4% and the balance of the mixture being substantially all sand. Finer refractory materials, of course, require a somewhat greater quantity of binder.
It will be understood that the water content in the above examples is .the sum of the water of hydration and any additional water which may be present in commercial waterglass, together with any other water which it may be desirable to add to satisfactorily wet the sand-binder reinforcing mixture. Accordingly, either the pure or commercially pure solid silicates may be employed in conjunction with the amount ofwater necessary to bring the water content to-the above percentages, or a commercial waterglass solution may be used with more water being added, if-it is foundadvan-tageous to do so, in order to provide sufficient wetting properties. It also will be appreciated, of course, that when a commercial waterglass solution containing between approximately 60% and 70% water is used, the greater the amount of this solution employed, the lesser the amount of additional water required. in fact, when one of these waterglass solutions is used in a quantity which provides a relatively high silicate content in the final mix, no additional water is usually required. On the other hand, it is frequently necessary to add water to this same waterglass solution to adequately wet the sand particles when this solution is used in an amount providing a relatively low silicate content in the final mix.
Despite the necessity ofsufiiciently. wetting the sand, reinforcing mixes containing very high water contents, or which use extremely dilute solutions of waterglass, should not be employed without adequate external support because such mixes reduce the green strength of the core; Accordingly, it is highly desirable that the resultant concentration of a sodiumsilicate solution, for example, be retained between the limits of approximately 2% and these percentages representing the ratio of the weight of the pure anhydrous silicate to the total weight of the waterglass solution. On the other hand, with larger amounts of water, a longer setting time is required in order to drive off the water. I have therefore found that-a particularly useful mixture of the sand and waterglass reinforcing material is one which consists of approximately 98% sand, 1% commercial waterglass having a sodium silicate content of approximately 37%, and 1% additional water. This, of course, is equivalent to a mixture of approximately 0.4% anhydrous sodium silicate, 1.6% water and 98% sand. In this latter example, the water content is the sum of water in the free form andthat which may be present in the silicate as water of hydration. As he-rebefore stated, sand having an AFS fineness number between and may be advantageously employed, the use of this particular sand beingespecially desirable in conjunction with the aforementioned specific waterglass composition.
Upon pouring the liquid metal into the mold cavity in the usual way, the hot metal, on coming into contact with the mold, burns the plastic binder to essentially carbon. As a result of this plastic breakdown, the shake out is readily accomplished. The gases which are generated readily escape through the highly permeable sandresin shell and reinforcing layer. Inasmuchas the.above-described reinforced mold assemblies faithfully reproduce pattern details and maintain good.dimensional tolerance, this process can be used to provide. cast metal parts of extremely'thin section which can be cast to almost the precise dimensions ultimately. desired. The resultant castings have unusually smooth and clean surfaces, tine dimensions and a minimum of finat the mold parting line becauseof the un: usual surfacesmoothness, high' gas permeability and rigidity of. these mold assemblies The surfaces of these castings are also free of residual mold material, thereby eliminating the necessity of shot blasting. Hence the use of the above reinforced molds permits the production of sound precision castings in a variety of metals over a widerange of casting temperatures. Moreover, these mold assemblies can be produced and processed without objectionable dust formation.
While my invention has bendescribed by means of certainspecific examples, it will be understood that the scope of my inventionis not to be limited thereby except as defined in the appended claims.
I claim:
1. A. process for forming a reinforced shell mold assembly for casting metal, said process comprising placing a mixture of a major proportion of sand and a minor proportion of thermosetting resin in contact with a hot metallic pattern for a period of time sufficient to melt the resin and to bond-a substantialportion of the sand particles together, removing any excess sand and resin, subsequently curing the formed mold shell by baking for a short period of time while in contact with the pattern, stripping the mold shell from the pattern, applying to the back surface of said mold shell a moist layer of a mixture comprising 0.9% to 13% by weight of water, 0.07% to 7% by weight of sodium silicate and the balance substantially all sand, and thereafter baking the formed reinforced shell mold assembly for at least two minutes at a temperature between 300 F. and 700 F.
2. A process for forming a reinforced shell mold assembly for casting metal, said process comprising placing a mixture of a major proportion of sand and a minor proportion of thermosetting resin in contact with a hot metallic pattern for a period of time suificient to melt the resin and to bond a substantial portion of the sand particles together, curing the formed mold shell by heating for a short period of time while in contact with the pattern, stripping the mold shell from the pattern, applying a moist mixture comprising approximately 0.2% to 0.7% by weight of sodium silicate, 1.3% to 4% by weight of water and the balance substantially all sand to the back surface of said shell mold so as to form a reinforc- 6 ing layer having an average thickness between about onehalf inch and two inches, and thereafter baking the formed reinforced shell mold assembly for approximately two to five minutes at a temperature between 300 F. and 700" F.
References Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES FIAT Final Report No. 1168. The C Process of Making Molds and Cores for Foundry Use. Recd. in Library April 8, 1948.
Claims (1)
1. A PROCESS FOR FORMING A REINFORCED SHELL MOLD ASSEMBLY FOR CASTING METAL, SAID PROCESS COMPRISING PLACING A MIXTURE OF A MAJOR PROPORTION OF SAND AND A MINOR PROPORTION OF THERMOSETTING RESIN IN CONTACT WITH A HOT METALLIC PATTERN FOR A PERIOD OF TIME SUFFICIENT TO MELT THE RESIN AND TO BOND A SUBSTANTIAL PORTION OF THE SAND PARTICLES TOGETHER, REMOVING ANY EXCESS SAND AND RESIN, SUBSEQUENTLY CURING THE FORMED MOLD SHELL BY BAKING FOR A SHORT PERIOD OF TIME WHILE IN CONTACT WITH THE PATTERN, STRIPPING THE MOLD SHELL FROM THE PATTERN, APPLYING TO THE
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US256309A US2748435A (en) | 1951-11-14 | 1951-11-14 | Process for reinforcing shell molds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US256309A US2748435A (en) | 1951-11-14 | 1951-11-14 | Process for reinforcing shell molds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2748435A true US2748435A (en) | 1956-06-05 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US256309A Expired - Lifetime US2748435A (en) | 1951-11-14 | 1951-11-14 | Process for reinforcing shell molds |
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| Country | Link |
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| US (1) | US2748435A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2861893A (en) * | 1956-05-25 | 1958-11-25 | Brumley Donaidson Co | Foundry cores |
| US2873493A (en) * | 1954-02-18 | 1959-02-17 | Gen Motors Corp | Shell molding |
| US2903761A (en) * | 1956-07-23 | 1959-09-15 | Sirmay Emil Starn | Permanent pre-cast mold |
| US2905563A (en) * | 1956-02-29 | 1959-09-22 | Diamond Alkali Co | Alkali metal silicate binder for foundry sand molds and process |
| US2908040A (en) * | 1954-02-08 | 1959-10-13 | Us Rubber Co | Building form |
| US2931081A (en) * | 1956-03-09 | 1960-04-05 | Shaw Process Dev Corp | Mould structure and its production |
| US3017677A (en) * | 1959-07-20 | 1962-01-23 | Jr Herbert Greenewald | Composition and method of forming ceramic cores |
| US3096548A (en) * | 1963-07-09 | altieri | ||
| US3122801A (en) * | 1960-07-15 | 1964-03-03 | Glenn W Merrefield | Method of making molds |
| US3511302A (en) * | 1967-02-27 | 1970-05-12 | Robert H Barron | Method for producing a shell faced mold |
| US3648756A (en) * | 1970-05-04 | 1972-03-14 | Eaton Corp | Composite mold and method of making same |
| US3664407A (en) * | 1967-02-27 | 1972-05-23 | Robert H Barron | Apparatus for making shell molds |
| US3683995A (en) * | 1970-03-25 | 1972-08-15 | Lothar Robert Zifferer | Method of making a composite sand mold including recycling the land |
| US4050500A (en) * | 1976-03-15 | 1977-09-27 | Eaton Corporation | Method of making a shell mold |
| US4347890A (en) * | 1981-03-09 | 1982-09-07 | Pq Corporation | Method for binding particulate materials |
| US5368086A (en) * | 1992-11-02 | 1994-11-29 | Sarcol, Inc. | Method for making a ceramic mold |
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| US1889007A (en) * | 1931-02-26 | 1932-11-29 | Benjamin F Wallace | Sand core for casting metal and method of making same |
| US1914037A (en) * | 1931-06-08 | 1933-06-13 | Pont Viscoloid Company Inc Du | Molding process and apparatus |
| US1959179A (en) * | 1932-02-05 | 1934-05-15 | Essex Foundry | Mold |
| US1999382A (en) * | 1932-06-13 | 1935-04-30 | Grasselli Chemical Co | Refractory material for use in metal castings and process for making the same |
| US2322667A (en) * | 1942-07-31 | 1943-06-22 | Westinghouse Electric & Mfg Co | Mold and mold composition |
| US2368322A (en) * | 1940-02-20 | 1945-01-30 | Passelecq Georges | Core making process |
| US2398047A (en) * | 1942-12-17 | 1946-04-09 | Bernard L Schmidt | Composition for making molds |
| GB585665A (en) * | 1943-06-18 | 1947-02-18 | Horace Campbell Hall | Casting metals |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1889007A (en) * | 1931-02-26 | 1932-11-29 | Benjamin F Wallace | Sand core for casting metal and method of making same |
| US1914037A (en) * | 1931-06-08 | 1933-06-13 | Pont Viscoloid Company Inc Du | Molding process and apparatus |
| US1959179A (en) * | 1932-02-05 | 1934-05-15 | Essex Foundry | Mold |
| US1999382A (en) * | 1932-06-13 | 1935-04-30 | Grasselli Chemical Co | Refractory material for use in metal castings and process for making the same |
| US2368322A (en) * | 1940-02-20 | 1945-01-30 | Passelecq Georges | Core making process |
| US2322667A (en) * | 1942-07-31 | 1943-06-22 | Westinghouse Electric & Mfg Co | Mold and mold composition |
| US2398047A (en) * | 1942-12-17 | 1946-04-09 | Bernard L Schmidt | Composition for making molds |
| GB585665A (en) * | 1943-06-18 | 1947-02-18 | Horace Campbell Hall | Casting metals |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3096548A (en) * | 1963-07-09 | altieri | ||
| US2908040A (en) * | 1954-02-08 | 1959-10-13 | Us Rubber Co | Building form |
| US2873493A (en) * | 1954-02-18 | 1959-02-17 | Gen Motors Corp | Shell molding |
| US2905563A (en) * | 1956-02-29 | 1959-09-22 | Diamond Alkali Co | Alkali metal silicate binder for foundry sand molds and process |
| US2931081A (en) * | 1956-03-09 | 1960-04-05 | Shaw Process Dev Corp | Mould structure and its production |
| US2861893A (en) * | 1956-05-25 | 1958-11-25 | Brumley Donaidson Co | Foundry cores |
| US2903761A (en) * | 1956-07-23 | 1959-09-15 | Sirmay Emil Starn | Permanent pre-cast mold |
| US3017677A (en) * | 1959-07-20 | 1962-01-23 | Jr Herbert Greenewald | Composition and method of forming ceramic cores |
| US3122801A (en) * | 1960-07-15 | 1964-03-03 | Glenn W Merrefield | Method of making molds |
| US3511302A (en) * | 1967-02-27 | 1970-05-12 | Robert H Barron | Method for producing a shell faced mold |
| US3664407A (en) * | 1967-02-27 | 1972-05-23 | Robert H Barron | Apparatus for making shell molds |
| US3683995A (en) * | 1970-03-25 | 1972-08-15 | Lothar Robert Zifferer | Method of making a composite sand mold including recycling the land |
| US3648756A (en) * | 1970-05-04 | 1972-03-14 | Eaton Corp | Composite mold and method of making same |
| US4050500A (en) * | 1976-03-15 | 1977-09-27 | Eaton Corporation | Method of making a shell mold |
| US4347890A (en) * | 1981-03-09 | 1982-09-07 | Pq Corporation | Method for binding particulate materials |
| US5368086A (en) * | 1992-11-02 | 1994-11-29 | Sarcol, Inc. | Method for making a ceramic mold |
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