The present disclosure relates generally to methods of forming sand cores and, more particularly, to a method of forming a hollow sand core.
Sand cores are often used to manufacture parts via casting processes. The sand core serves as a mold of the desired part shape. Sand cores may be made, for example, via cold box or no bake technologies. Such processes utilize organic and/or inorganic binders which adhere to the sand, thereby strengthening the resulting core. During both the cold box and no bake processes, a catalyst is used to harden the binders.
A method of forming a hollow sand core involves placing a preform into a cavity defined in a mold, where the preform has a predetermined configuration. A granular material is then introduced into the mold cavity and around the preform. The introduced granular material is established around the preform to form the hollow sand core. The preform is deformed in a manner sufficient to enable removal of the preform from inside the hollow sand core, and then is removed from the sand core. The removal of the preform exposes a hollow portion of the sand core.
Features and advantages the present disclosure will become apparent by reference to the following detailed description and drawings, in which like reference numerals correspond to similar, though perhaps not identical, components. For the sake of brevity, reference numerals or features having a previously described function may or may not be described in connection with other drawings in which they appear.
Examples of the method disclosed herein utilize a removable preform to form and shape the interior surface of a hollow sand core. This deformable preform advantageously enables the sand core to remain intact after formation and during preform removal. Furthermore, the hollow sand core formed using the preform may be desirable, as the amount of sand needed to form the core is reduced. It is further believed that the hollow portion of the sand core also enables gases generated during the casting process to be readily removed. The process disclosed herein is particularly advantageous in that typical processes, such as cold box and no bake technologies may be used to form the hollow sand core.
Referring now to
The preform 10, 10′ is generally formed of a material that is capable of deforming from its temporary shape T (such as that shown in
It is to be understood that in some instances, the permanent shape P of the preform 10′ is not completely obtained. This may be due to the fact that the entire preform 10 is not heated above the switching or glass transition temperature, or the non-deformed portion is placed onto a mandrel for introducing pressure inside the preform 10. A non-limiting example of this embodiment is shown as reference numeral 10″ in
While expansion and contraction of the preform 10 is shown in two directions (e.g., the diameter expands/contracts), it is to be understood that expansion/contraction may cause the preform 10 to change shape in three dimensions, similar to a balloon.
Non-limiting examples of suitable materials for the preform 10 include shape memory polymers (e.g., thermoplastics such as polyolefins, polyurethanes, polyacrylates, or thermosets, such as polyolefins that have been covalently cross-linked), or elastomeric materials (e.g., natural rubber, synthetic polyisoprene, butyl rubber, halogenated butyl rubbers (e.g., chloro butyl rubber, bromo butyl rubber, etc.), polybutadiene, styrene-butadiene rubber, nitrile rubber, hydrogenated nitrile rubber, chloroprene rubber, ethylene propylene rubber, epichlorohydrin rubber, polyacrylic rubber, silicone rubber, fluorosilicone rubber, fluoroelastomers, perfluoroelastomers, polyether block amides, chlorosulfonated polyethylene, ethylene-vinyl acetate, or thermoplastic elastomers). Some elastomeric materials are also shape memory materials.
Prior to being used to form the sand core 12, the preform 10 is shaped. The shaping process used will depend, at least in part, upon the material used. Very generally, the shaping technique is selected from blow molding, injection molding, compression molding, rotational molding, extrusion, stretching, or any combination of heating and force.
In one embodiment, the materials may be initially in the permanent shape P (e.g., via extrusion). The material may then be crosslinked using irradiation or a combination of heat and chemical means (depending upon the polymer used), blow molded above the glass transition temperature of the polymer, and then cooled to below the glass transition temperature to achieve the desirable temporary shape T.
In another embodiment, the materials may be initially in an expanded form that is even larger than the desirable temporary shape T. The material may be shrunk, via heating, to reduce the size of the material to a desirable temporary shape T.
When a shape memory polymer is used, the permanent shape P (i.e., the shrunken shape) may be set by bringing the material to a temperature that is at or above its melting temperature, forming it into the desirable shape P, and then cooling it below the glass transition temperature to set the shape P. If a thermoplastic shape memory polymer (with physical crosslinks) is used, then the permanent shape P may be reshaped by bringing the material again to a temperature that is at or above the melting temperature, reforming the shape, and cooling below the glass transition temperature. However, if the material used is a thermoset shape memory polymer (with covalent crosslinks), the permanent shape P may not be reprogrammed. Rather, this embodiment of the shape memory polymer preform 10, 10′, 10″ may be reused with the set permanent shape P.
In either case, to make the temporary shape T, the shape memory polymer is deformed above the glass transition temperature, molded into the desirable shape T, and cooled below the glass transition temperature. Heating the shape memory polymer above its glass transition/switching temperature causes the polymer to become pliable. Once pliable, a force (e.g., pressure, stretching, mechanical force, etc.) may, in some instances, be applied to expand the shape memory polymer into the desirable temporary shape T. An exterior mold may be used to achieve the desirable temporary shape T when the shape memory polymer is heated and becomes deformable. As mentioned above, once in the desirable shape, the polymer is cooled to set the temporary shape T.
Once the temporary shape T is set, if the shape memory polymer is again heated to above the glass transition temperature, it will revert back to the permanent shape P. As such, once the sand core 12 is formed (discussed further hereinbelow), the shape memory polymer is heated above its glass transition temperature again to recover the permanent deformed shape P. When the shape memory polymer is heated to a temperature above its glass transition temperature, the presence of physical or covalent crosslinks allows for the reversion of the shape memory polymer from one shape (e.g., the temporary shape T) to another shape (e.g., the permanent shape P) by releasing energy i) previously imparted to the system by the deformation of the polymer, and ii) stored in the system by subsequent cooling processes.
Referring now to
In other embodiments, a low amount of pressure (e.g., 1-5 psi) may be used to maintain the rigidity of the preform 10 during the core 12 generation process. In some embodiments, the preform 10 may be pressurized and sealed prior to the core 12 generation process. In other embodiments, the preform 10 may be pressurized while in the cavity 16. One end of the preform 10 may be configured to receive such pressure (e.g., via a port formed in the core box 18), and the pressure may be constantly supplied such it is maintained throughout core 12 formation or the preform 10 may be sealed once pressurized. In some cases when pressure is constantly supplied or the preform 10 is sealed to maintain rigidity, the core forming process may be repeated using the same preform 10 multiple times without its removal from the cavity 16. This may be accomplished because either the releasing of pressure and/or heating shrinks the preform 10 to its partially or fully deformed shape 10′, 10″ within the cavity 16, and the sand core 12 may be removed therefrom.
In still other embodiments (see
Referring back to
It is to be further understood that when pressure is utilized to support the preform 10 during core 12 formation, the pressure is released prior to any casting processes.
The formed sand core 12 still has the preform 10 therein, as shown in
Regardless of when preform 10 removal is desirable, such removal may be accomplished by deforming the preform 10 to its permanent shape P (i.e., deformed preform 10′, shown in
In one embodiment, depressurization may be used to obtain the deformed (i.e., permanent shape P) preform 10′ or partially deformed preform 10″. This is generally used when pressure is used to maintain the temporary shape T during sand core 12 formation. The removal of pressure will cause the temporary shape T of the preform 10 to shrink to the permanent shape P. Once in the shrunken permanent shape P (or at least partially shrunken shape), the preform 10′ (or preform 10″) may be readily removed from one of the two ends E1, E2 through the hollow portion 14. This form of deformation is particularly suitable for the preform 10 formed of elastomeric materials.
In another embodiment, the preform 10 may be heated in order to initiate deformation. This technique may be used when a shape memory polymer preform 10 is utilized. Heating may be accomplished by introducing a fluid (e.g., gas (e.g., air, nitrogen, or any other gas that does not react with the sand core 12), liquid, etc.) having a temperature sufficient to deform or otherwise at least partially switch the state of the preform 10 into the smaller shaped preform 10′ or preform 10″. The fluid may be heated prior to being introduced or after being introduced into the preform.
It is to be understood that removal of the preform 10, 10′, 10″ will not deleteriously affect the shape of the sand core 12, at least in part because the core 12 has been cured and hardened prior to preform 10, 10′, 10″ removal.
Referring now to
In another embodiment, the permanent shape P of the preform 10′ is a smaller version of the desirable part shape, and the temporary shape T is an expanded version of the permanent shape P and is the desirable part shape. This is shown in
This embodiment may be particularly suitable when the permanent shape P has different section thicknesses along the length (not shown). When pressure is applied above the glass transition temperature of the preform 10′, the final temporary shape T will depend on, at least in part, the initial permanent shape P, the local material thickness, and the pressure applied.
The transition of the preform 10′ to its temporary shape T may also be achieved by localized crosslinking. For example, in a material where the covalent cross linking is achieved by irradiation, the irradiation may be locally applied rather than to the entire preform 10′. For another example, where the cross linking is initiated by heat, heat may be selectively applied to local areas. Once cross linked, applying pressure above the glass transition temperature will result in different rates of expansion between the cross linked locations and the under cross linked locations.
It is believed that the embodiment shown in
After the pressure is applied to achieve the desired temporary shape T, the pressure may be maintained, but the temperature changed such that it is decreased to below the glass transition temperature. This causes the temporary shape T to set so that the preform 10 becomes rigid in the core box cavity 16. The pressure may then be maintained or removed since the temporary shape 10, T is set to the desired core 12 inner shape.
In the embodiment shown in
While several embodiments have been described in detail, it will be apparent to those skilled in the art that the disclosed embodiments may be modified. Therefore, the foregoing description is to be considered exemplary rather than limiting.
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Number | Date | Country | |
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20100288460 A1 | Nov 2010 | US |