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Publication numberUS2313674 A
Publication typeGrant
Publication dateMar 9, 1943
Filing dateSep 11, 1942
Priority dateSep 11, 1942
Publication numberUS 2313674 A, US 2313674A, US-A-2313674, US2313674 A, US2313674A
InventorsKinney Walter B, Salzberg Harold K
Original AssigneeBorden Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Coating foundry mold surfaces
US 2313674 A
Abstract  available in
Previous page
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Claims  available in
Description  (OCR text may contain errors)

which the molten metal flows andsets.

smoothness of the sand surfaces, the ability of Patented Mar. 9, 1943 COATING FOUNDRY MOLD SURFACES Harold K. Salzberg and Waiter B Kinney, Bainbridge, N. Y., assignors to The Borden Gompm, New York, N. Y., a corporation of New Jersey No Drawing. Application September 11, 1942,

Serial N0. 458L034 9 Claims.

metal into sand molds are in large measure dependent for their properties and quality on the character of the mold and core surfaces against The the sand and sand surfacesto conduct heat and gases and their reaction to'the heat of the metal are factors which have an important bearing on the quality. of the castings.

Foundry sand practice properly embraces the treatment of molds and cores with coatings to improve the quality of castings made in such molds. The general methods of special treatment of mold and core surfaces include (1) preparation of a special facing sand, (2) coating the sand surfaces with a prepared suspension of refractory material, (3) dusting on finely divided refractory powders, and (4) spraying the surfaces with adhesive liquids, which are usually solutions of adhesive materials.

The preparation of a special facing sand involves the mixing of a fine clean sand with water i and binders which provide the necessary strength and working properties or moldability to the sand. This sand is mixed separately from the main bulk of the sand, and often in mixing equipment set aside for the purpose. This sand. is applied to the pattern or core box first, against which it forms a thin layer, which becomes the face of the mold or core and against which the molten metal directly contacts, if no coating is subsequently applied to the facing. Facing sand is carefully prepared and closely controlled to provide the best possible mold and core surfaces.

Instead of a specially prepared facing sand, the mold or core surface may be one of a refractory material applied as a coating to an ordinary sand surface, or this coating may be applied to a special facing sand, thus combining the advantages of both methods of providing a satisfactory sand surface. These coatings in the foundry art are suspensions of fine silica, mica, graphite, zircon, clays or other refractory material, applied in liquid form by brushing, spraying or dipping the molds and cores. Upon drying they provide a smooth and heat resistant coating which largely prevents the burning of sand onto metal.

on occasion, the dispersing of the refractory material into liquid form is dispensed with and dry powdered refractory material is dusted onto the damp sand surfaces. Thus silica flour or graphite might be dusted onto parts of molds or cores which require some protection because of severe action of the flowing metal, as for instance near the gate or point of entry of the molten metal to the mold,'or around bends in the design which are subjected to severe erosion as the mold fills. Though less commonly employed, this is one method of improving core and mold surfaces.

Another method directed at the same objective involves coating, usually by spraying, of the sand surfaces with adhesive liquids. These are usually solutions of materials which are adhesive in nature, or become so on drying. The application of a spray imparts extra strength and a crust or skin to the sand on drying. Usually water soluble materials are employed, such as molasses, sulflte waste liquor, dextrine, sodium silicate solution, etc., but sometimes oils are applied or sprayed on. These same solutions at times serve as the medium for suspending finely divided refractory material to prepare coatings of the second class described above.

The demands of the production schedule or of the casting design will dictate which of the methods described is to be used in any one foundry for any certain job, but they all have the common purpose of improving the quality of the casting.

The facing sand, coating or spray must meet certain demands of performance to be acceptable by the foundry industry. The most important requirement is that of providing a sand surface which is stronger or smoother, or both stronger and smoother, than the main body of the sand. The practice of specially treating the sand surface by coating or spraying makes possible the formation of cores having shell structure, that is a structure of relatively hard and firm exterior with relatively soft interior. Cores I objectives here sought.

There are other more obvious requirements of a good facing material or coating. If the mamust preferably penetrate quickly into the sand to prevent running and to insure uniformity of strength, hardness and thickness over the entire surface of the mold or core. Strength is; developed by drying or hardening, and this drying or hardening must take place within a reasonable period of time.

A further requirement of a good facing or coat-' ing material is that, when dry, it should withstand moisture of the air; that is,'should resist the harmful efiect of moisture of the atmosphere of either the foundry or the closed mold. Oils.

are preferred for dry sand work because the oil coatings withstand damp air. The compositions utilized in the present invention also withstand the effects of moisture and provide moisture-resistant molds and cores.

the core, or mold, thus providing a two-fold advantage, viz. (1) increased strength and hardness at the surface and (2) shell structure to the core or mold. The increased strength and hardness at the surface of the sand is added protection against breakage in handling, and secondly, increased surface hardness promotes chilling of the hot metal. Shell structure in cores in 'arying degree depending upon design of casting is desirable, for a soft-centered core is more readily collapsible and more friable, thus more readily removed from the casting, than a. solid core.

Another characteristic of a spray according to the present invention, and which present core oils do not possess, is its ability to dry in the air at 7 room temperature. Green. cores, when sprayed according to the present invention, acquire a skin within a few minutes by virtue of the rapid drying of the spray coating. This skin possesses strength and serves as protection against dropping or distortion while the sand is in the green stage. Such a core or mold stands up better under the jarring and vibration incident to conveying to the core oven and therefore provides cores of the more intricate designs with dimensions within minimum tolerances.

This invention is based upon the discovery that thermosetting phenol-formaldehyde resin condensed to stages where the resin is still soluble in water proves to be a mold and core coating material possessing the necessary qualities discussed above and in addition exhibitsadvantages over materials heretofore used for the purpose.

.The dry mold or core surface bonded or coated with a water solution of thermosetting phenolformaldehyde resin differs from cores and molds bonded or coated with straight core oil in being highly collapsible by heat and therefore yielding readily to the pressure exerted by the cooling and shrinking casting. This feature of high collapsibility contributes to casting quality in reducing the amount of burned-on sand and the cracks which might form in the section of the casting as it shrinks. High collapsibility also means easy removal of burned sand from the casting. The feature of high collapsibility of core or mold is especially advantageous in the pouring of lead, aluminum or magnesium alloy castings where the metal heat is relatively low; but is also of advantage in the pouring of'other metals where shinkage percentages are high, as with certain steels, and where the design of the casting is such that shrinkage cracks are likely to occur because of unequal shrinkage in different parts of the casting.

When sprayed onto the sand surfaces of cores and molds a liquid composition made according to this invention penetrates rapidly but not deeply. Comparative measurements have been made of the depth of penetration of a spray ac cording to the present invention and of core oils conventionally used; In one test the two types of spray were applied by spray gun to green sand core test bars in amounts so that equal increase in weight of the sprayed core on the solids basis resulted. Upon visual examination the depth of penetration was found to have been as follows:

mm. Phenol-formaldehyde resin solution in water" 2 Core oil A 8 Core oil B 8 Shallow penetration results in concentration of the spray material at or near the surface of A further characteristic of a spray according to the present invention, and which core oils do not possess, is its strength in hot. cores. The synthetic resin is not a thermoplastic material and therefore is not, soft at the temperatures usually prevailing in the core oven. 0n the contrary, the sprayed cores are substantially as hard when as hot as core oven temperatures of about 400 F., as at room temperature. Therefore, the hardness of surface of the core is maintained all through the oven cycle and during handling of the hot cores.

The phenol-formaldehyde resin best suitable for this purpose is one condensed to a stage where the product is still soluble in water, for the advantages in the use of this type of coating described above accrue mainly by virtue of the fact that the composition is aqueous, and the desirable eifects which water has on foundry core and molding sands are provided. Furthermore, with water as the vehicle the cost of the coating is reduced as compared to solutions in which'organic solvents serve as vehicle.

The degree of condensation of the resin need not be narrowly defined for the resin to be useful for the purpose of this invention, solong as the reaction product of the ingredients is carried in solution in water. In fact the ingredients may be present in the initial stages of condensation, that is, in the so-called phenol alcohol stage. It is possible to obtain satisfactorily hard and strong cores from a resin in the lowest stage of condensation because the procedure of baking or drying at elevated temperatures is a part of the core making process and is accomplished under conditions which readily convert the resin from its initial stage of condensation to'the fully cured insoluble and infusible stage.

The proportion of ingredients in making the resin may vary within the range of one moi of phenol to from one to three mols of formaldehyde. When the lower proportions of formaldehyde are used, the product will be free from the objectionable sharp odor of this chemical and will, furthermore, be more stable on dilution with water, allowing a weaksolution to be used. In fact if the resin is made on the formula of one moi of phenol to one mol of formaldehyde and the reaction carried on at 0. for 30 minutes mixture of phenoland formaldehyde relying upon the heat applied to the core to condense the ingredients to the resinous stage. However, the precondensed resin is to be preferred over a mixture of the ingredients We refer to'phenol as one of the primary ingredients of this resin and do so without intention of restricting the preparation of it to phenol (CcHtOH) only. Pure or best be treated by brushing or swabbing on the liquid, and where particularly heavy coatings are desired this may be done with the concentrated commercial grades of eresol or of xylenol may be substituted for the phenol, as is well known in the art of making phen01ic" resins. Phenol yields a resin solution more soluble in water than are the resins made from commercial cresol or xylenol. I may however, substitute either of these in part or in whole for the phenol as a means of reducing cost of the product.

Condensation of the ingredients to form the resin may be carried out under either mildly alkaline or mildly acid conditions. Condensation under mildly alkaline conditions is to be preferred, however, as the degree of condensation is more readily controlled and the product more stable than when carried out under acid conditions. As an example of a resin solution suitable for the purpose of this invention, react 10 pounds of fluid, without dilution. Although the full advantages of its properties are evident-.when cores are treated before baking or drying, the application may be made to cores after baking, either while they are still hot or after they have cooled. In the latter procedure a short secondary drying of the coated core will be necessary.

The application of the-resin solutions used in the present, invention, and described above, is suflicient protection for cores and molds for many types of castings. However, where extra resistance to heat of the metal is required, the solution is made to, serve as a binder for the finely divided refractory materials commonly used in foundries, such as silica, mica, graphite, zircon, clays, etc., which are mixed into the solution by simple stirring and the mixture then reduced with water to the required consistency. Such refractory materials are available in a wide variety of types and grades, and when used in admixture with a phenol-formaldehyde resin solution the latter becomes the vehicle and the binder for the refractory material. These refractory materials are relatively inert chemically and do not destroy the i technological properties of the resin solution as to collapsibility, penetration, drying and strength described above.

The advantages to be gained by applying resin solutions to cores as herein described are not wholly lost if the solution be diluted with water solutions of certain materials instead of with water only. For instance, mixtures of resin solution and molasses or of resin solutions and water solutions of sulfite waste liquor (commercial pure phenol with 10 pounds of 37% formaldehyde (commercial formalin) by heating the mixture at90 C. under atmospheric pressure in the presence of 2 ounces of caustic soda flakes and for a period of 30 minutes. The resulting solution will contain approximately of resin solids. ,r, i

As an illustration of the practical use of the resin solution prepared as described above, small oil-bound sand cores weighing 200 grams in the green condition were sprayed on all surfaces except the plate side with the resin solution, after this had been diluted with water to a 25% resin solids content. The spraying was done from a foundrymens mouth sprayer into which air was led through the mouthpiece from a compressed air line, and was continued until the cores had gained in weight by 5 grams. During a period of one hour in the open air these cores acquired a skin, that is because superficially firm, whereas a core which was not so sprayed did not harden in the air. The sprayed cores were dried in an oven at 450 F. for a period of two hours. Upon removal from the oven and cooling, these cores were observed to have shell structure, that isv they were extremely hard and possessed sharp edges, but about 2 mm. back of the surface the sand was soft and friable. The extreme contrast between core surface and core interior. as to hardness observed in these cores could not have resulted from the drying of uncoated cores of any sand formula in practical use.

For purposes of describing the coating material used' in the present invention, we have discussed its use as a spray. The manner of'its application is not limited, however, to spraying. Occasionally the core or mold or part thereof may p as Tergitol.

lignin) can be employed which will be less expensive than if the resin solution is applied straight. Other watersoluble materials might be employed as extenders or fillers, such as sugars, dextrines and water-soluble gums. Casein solutions may be admixed with the resin solution- .in small amounts, in proportions which will not thicken the liquid beyond spraying consistency. 1

As an aid in absorption of the liquid by the sand we have added wetting agents to the resin solution and cite as anexample the agent known A phenol resin solution containing 1.5%, for example, of Tergitol has been observed to soak into the sand more quickly than in the absence of the wetting agent and the depth of penetration is somewhat increased. The primary purpose of the wetting agent, however, is to cause rapid soaking in of liquid and the increased depth of penetration is moderate and not more than one mm. in the example given above.

For the sake of brevity, the expression mold surface in the appended claims is used to designate a part or the parts of a foundry sand mold and the cores inserted or to be inserted therein, if any, with which the molten metal comes in direct contact during the pouring or casting operations; the said expression mold surface is therefore used in the appended claims as applyingtocores as well as to the sand mold itself.

In our copending case Serial No. 405,718 filed August 6, 1941, of which the present application is in part a continuation, we claim the coating of mold surfaces with emulsions, e. g., of an oil (or oily material) and a water soluble resin. In the present case we do not claim emulsions but aqueous solutions. These are applied, as in the parent case, to surfaces of the sand or sand mixtures, and are not mixed with the bulk of sand, from which the molds and/or cores are subsequently made. These aqueous solutions are T not deeply absorbed by the sand of the molds or cores, but remain on and in the surfaces, leaving the sand remote from such surfaces substantially unimpregnated and hence [substantially free of resin.

We claim:

l. A foundry sand mold, a part at least of the surface of which is coated with a coating composition containing an aqueous solution of a condensation product of a phenolic body with formaldehyde.

2. A foundry sand mold, at least a part of the surface of which is coated with an aqueous solution of phenol-formaldehyde resin condensate,

3. A foundry sand mold, at least a part of the surface of which is coated with an aqueous solution of cresol-formaldehyde resin condensate.

4. A foundry sand mold, at least a part of the surface of which is coated with an aqueous solutlon of xylenol-formaldehyde resin condensate.

5. A foundry sand mold, at least a part oi. the surface of which comprises a completely resinified body selected from the group consisting of phenol-formaldehyde, cresol-formaldehyde and' xylenol-formaldehyde reaction products, said mold surface being characterized by a substanacrae're tially higher degree of hardness than possessed by the underlying layers of sand, by a high resistance to moisture and by a high rate of collapsibility when exposed to the temperatures of molten metal.

6. In the art of producing castings of metals with sand molds, the process which comprises coating at least a part of the mold surface of a sand mold with an aqueous solution of a resinous reaction product or a phenolic body with formaldehyde.

7. In the art of producing castings of metals with sand molds, the process which comprises coating at least a part of the mold surface of a sand mold with an aqueous solution of phenolformaldehyd resin condensate.

8. In the rt of producing castings of metals with a sand mold, the process which comprises coating at least a part of the mold surface of sand molds with an aqueous solution of cresolformaldehyde resin condensate.

9. In the art of producing castings of metals with a sand mold, the process which comprises coating at least a part of the mold surface of sand molds with anaqueous solution of xylenolformaldehyde.


Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2681860 *Jan 8, 1952Jun 22, 1954Int Nickel CoMold and mold composition
US2718681 *Nov 26, 1952Sep 27, 1955Ciba LtdMethod and compositions for the production of cores for use in metal casting
US2798817 *Aug 27, 1954Jul 9, 1957Allis Chalmers Mfg CoMolding composition and method of making same
US2930089 *Nov 26, 1956Mar 29, 1960Rolls RoycePrecision casting
US3211560 *Dec 18, 1961Oct 12, 1965Caterpillar Tractor CoMold wash composition and casting mold coated therewith
US3549392 *Jan 8, 1969Dec 22, 1970Nalco Chemical CoMold coating
US3645767 *Feb 12, 1970Feb 29, 1972Monsanto ChemicalsProcess for coating ceramic molds
US4001468 *Aug 13, 1975Jan 4, 1977Ashland Oil, Inc.Method for coating sand cores and sand molds
US5558151 *Dec 18, 1995Sep 24, 1996General Motors CorporationDie casting mold having lock rings for mounting an insert to a mandrel
US5749409 *Dec 18, 1995May 12, 1998General Motors CorporationMethod of forming refractory coated foundry core
USRE32812 *May 6, 1986Dec 27, 1988Borden (Uk) LimitedFoundry moulds and cores
U.S. Classification428/451, 428/454, 427/134, 106/38.22
International ClassificationB22C1/22, B22C1/16
Cooperative ClassificationB22C1/2246
European ClassificationB22C1/22F4