GB2202541A - Method for manufacturing investment casting cores - Google Patents

Method for manufacturing investment casting cores Download PDF

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Publication number
GB2202541A
GB2202541A GB08804151A GB8804151A GB2202541A GB 2202541 A GB2202541 A GB 2202541A GB 08804151 A GB08804151 A GB 08804151A GB 8804151 A GB8804151 A GB 8804151A GB 2202541 A GB2202541 A GB 2202541A
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GB
United Kingdom
Prior art keywords
core
binder
sand
firing
molded
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.)
Pending
Application number
GB08804151A
Other versions
GB8804151D0 (en
Inventor
Hilton Andrew Roth
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Raytheon Technologies Corp
Original Assignee
United Technologies Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by United Technologies Corp filed Critical United Technologies Corp
Publication of GB8804151D0 publication Critical patent/GB8804151D0/en
Publication of GB2202541A publication Critical patent/GB2202541A/en
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
    • B22C1/20Compositions 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 organic agents
    • B22C1/24Compositions 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 organic agents of oily or fatty substances; of distillation residues therefrom

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Mold Materials And Core Materials (AREA)
  • Molds, Cores, And Manufacturing Methods Thereof (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

A core manufacturing process is disclosed which utilizes a low viscosity distillable binder and firing in a nonreactive refractory sand to provide debindering and sintering of the core in one operation. Cores produced utilizing the disclosed method offer significant savings in processing time while reducing the potential for breakage.

Description

Method for Manufacturing Investment Casting Cores Technical Field This invention relates to ceramic cores utilized in the investment casting process and more particularly to a method for manufacturing ceramic cores utilizing single cycle core firing in refractory sand.
Background Art Investment casting is extensively used in the production of nickel and cobalt base superalloy blades and vanes for gas turbine engines, narticularlv those requiring internal cooling passages, providing relatively precise dimensional tolerances and excellent surface finishes. In investment casting, a ceramic mold is formed around a wax pattern with a ceramic core or cores precisely positioned within the wax to simulate the required holes and passages. The wax is removed durinq a firing operation while the mold and cores remain in place, providing a mold cavity. Molten metal is added and solidified in the cavity and the ceramic cores chemically removed such as by leaching with a hot alkali solution.Utilizing removable ceramic cores avoids machining or drilling operations which may be difficult to perform on superalloy materials.
Ceramic cores are typically produced by first preparing a core molding comDosition comprising a ceramic material, such as amorphous silica, and a binder1 These materials, as well as any other components added to adjust properties, are blended, fluidized and injected into a mold, forming a core shape which is removed from the mold, placed in a furnace and heated to drive off the binder. In U.S.
Patent No. 3,234,308 to Herman, a core is disclosed which incorporates impregnation with a thermosetting resin, such as shellac, prior to debindering, to maintain the core shape after the binder is removed.
The core is subsequently fired to sinter the ceramic material, forming a solid core body while sinul tanecusly destroying the resin.
Many core manufacturers use closed ceramic setters which conform to the configuration of the core to accurately support the core and prevent the cores from warping during the firing process, with binder removal and core firing performed in two separate operations. Use of the setter technique with some binder formulations may require up to two weeks between debindering and sintering. Such a long period presents numerous opportunities for breaking or cracking the fragile core, while substantially increasing processing time. Consequently, what is needed in the art is a method of producing ceramic cores which reduces cracking and minimizes Drocessinq time.
Disclosure of Invention It is an object of the present invention to provide a method for manufacturinq investment casting cores which utilizes a single firing cycle for debindering and sintering.
It is a further object of the present invention to provide a single cycle core production process which significantly reduces the time required to produce a core.
These and other objects of the present invention are achieved by utilizing a core production process which includes the steps of preparing a core molding composition, blending with a low viscosity, distillable binder, molding the mixture to a desired shape, embeddinq the molded shape in a nonreactive refractory sand, and firing the sand and molded core disposed therein at controlled temperatures wherein the binder is drawn by capillary action into the sand where it is evaporated or decomposed. The debindered core, fully supported in the sand, is then subjected to a higher temperature at which sintering occurs.
Brief Descriation of Drawings The sole Fiqure is a graph illustrating a typical core firing program.
Best Mode for Carrying Out the Invention A ceramic core production process comprises molding compound preparation, core molding, debinderlnq and sintering. Other processing steps may be included such as powder mixing, surface treatment of the ceramic powders, binder preparation, mixinq of the treated powder mixture with the binder, forminq the molding compound, and, pelletization of the molding compound for uniform feeding in an injection molding machine.
For exemplary purposes, a core molding compound may comprise up to 35 percent by weight zircon, up to 5 percent fumed silica, up to 6.5 percent alumina fiber, balance amorphous silica, with a binder added in an amount sufficient to maintain a molded shape before firing, and a silane coupling agent added in an amount sufficient to produce optimal surface wetting of the powder by the binder. Such ingredients are discussed in the applicants copending application titled "Core Moulding Composition", Attorney Docket No.
R-2683, filed on even date herewith and herebv incorporated by reference. While an exemplary composition, it will be understood by those skilled in the art that the ingredients and proportions of the composition can be varied to produce cores with different strength and shrinkage properties. For example, silica, alumina and zircon core compositions, and mixtures thereof, may successfully utilize the method of the present invention The choice of binder formulation is usually dependent on the particular application and may comprise a mixture of paraffin waxes, lubricants and mold release agents. However, a low viscosity, distillable binder is required to practice the present inventive method.For the purposes of this application, low viscosity refers to the flowability of the binder at debinderinq temperatures and distillable refers to the ability of the binder to essentially vaporize or decompose at the debindering temperature. It should be noted that small auantities of the binder composition mav be non-distillable without deviating from this definition. For example, up to 20% of the binder mixture may remain in the core without sacrificing the benefits of the present invention. In addition, the binder chosen should exhibit a low viscosity at iniection conditions to increase moldability; about 10,000 centipoise is exemplary. One such low viscosity, distillable hinder comprises 33.38 paraffin wax havinq a meltinq point of 131-136çC, 33.3t paraffin wax havinq a meltinq point of 144-149 C and 33.34 mineral wax having a melting point of 163-1720C, with an admixture including aluminum stearate, oleic acid and beeswax added as internal lubricants, mold release agents and deflocculants.
After incorporating a low viscosity, distillable binder in the core molding composition, the bindered core composition is molded into a desired shape using either a plunger or screw-type molding machine and conventional molds. While either machine may be used, best results are generally obtained using one with electronic feedback process control of the inlection temperature, injection rate and injection pressure.
It will be understood by those skilled in the art that universal molding conditions are not obtainable and that the optimal molding conditions must be determned by trial, however, molding temperatures between 1800 and 2304F and pressures of about 4,000 to 10,000 psi are common.
The molded core is removed from the mold and placed in a firing sagger or box containing refractory sand. It is essential that the core be completely embedded in the sand for support and to assure maximum heat transfer. For exemplary purposes, alumina sand having a particle size of about 0.0017 inches is used.
However, those skilled in the art will recognize that any nonreactive refractory sand, capable of withstanding the firing temperature, may be used.
The firing sagger is placed in a furnace and a firing cycle initiated. The firing sagger is heated externally with heat transferred through the refractory sand into the core, with temperature gradients possibly forming therebetween. As the molded core is heated, the low viscosity distillable binder is drawn out of the molded core by capillary action into the adjacent sand. The binder then distills off or is decomposed, completing the debindering operation. At this point, the core is very fragile. However, since the sand is essentially fluid, it shifts as the core shrinks and maintains full surface support during the entire core firing cycle. The temperature is then increased until the sintering temperature is reached, at which point the temperature is held until the ceramic particles sinter, thereby producing a core.
Example A six pound batch of core molding compound is prepared for the inlection molding of a core. The proportions of each ingredient are disclosed in Table I.
Table I Ingredient Concentration Weiqht Percent amorphous silica 62.64 zircon 2784 fumed silica 4.12 alumina fiber (5 micron 4.16 dia x 0.125 inches long) silane coupling agent 1.24 The silane coupling agent converts the essentially polar ceramic surface of the compound to a surface of nonpolar nature which is easily wetted by the binder. For illustrative purposes, the silane coupling agent is Union Carbide Awl 105. After blendinq, the moist powder mixture is dried for three hours at about 220cm.
The ceramic powder is then mixed with a low viscosity distillable binder in a vacuum blender. The wax binder mixture comprises 33.38 paraffin wax having a meltinq point of 131-l360C, 33.38 paraffin wax having a meltinq point of 144-1490C and 33.3% mineral wax, such as ceresin, having a meltinq point of 163-172 C. In addition, an admixture of beeswax (4 parts), aluminum stearate (12 parts) and oleic acid (8 parts) is added to optimize binder properties. About 13.58 by weight binder is added to the core composition. Mixing time is batch dependent and, for this example, is about three hours at a temperature of 2200F.The molding compound is then extruded and pelletized, preferably using a die face pelletizing technique, for optimum flowability during the subsequent molding process. The pelletized moldinq compound is stored in a low humidity chamber until required for use.
Ceramic cores are then molded using a conventional plunger-type injection molding machine and conventional molds. The cores are then removed from the molds and packed into alumina sand havinq a particle size of about 0.0017 inches which is contained in a firing sagger. The sagger is placed in a programmed electronically controlled furnace and subjected to a firing cycle during which the binder is first removed from the core at low temperature without disturbing the core shape, followed by sintering of the ceramic particles at higher temperatures.
Referring to the Fiqure, an exemplary debindering and sinterinq firing Drogram is illustrated, for use with the above described core composition. The sand and cores are first subjected to a 135 oF per hour temperature ramp, from ambient to 7500F. During the ramp, the binder is removed from the core by capillary action. As the binder is drawn out into the sand, it is evaporated and/or decomposed, thereby providing debindered cores supported in the alumina sand. Any remaining traces of the binder are burned out during the next ramp to the sintering temperature of about 22500F, which proceeds at 270 F per hour.
The cores are held at the sintering temperature for approximately 3 hours, during which time complete sintering occurs between the ceramic particles and solid core bodies are formed. The cores are then furnace cooled, for example, using a 5400F per hour ramp, and the cooled cores removed from the firing sagger and prepared for core finishing and wax pattern molding.
While the preferred embodiment of the present invention is described in relation to a core composition having particular quantities of ingredients, it will be understood by those skilled in the art that various changes in composition may be made to provide additional desirable properties without varying from the scope of the present invention. It will also be understood by those skilled in the art that while a particular debindering/sintering program is illustrated, other variations in times and temperatures may be used without varying from the scope of the present invention.
Having thus described the invention, what is claimed is:

Claims (5)

  1. Claims 1. A ceramic core production process which includes the steps of preparing a core molding composition; mixing with a binder; molding said mixture at controlled temperatures and pressures, to form a molded core; and, firing the molded core to effect binder removal and sintering; the imprOvements which comprise: mixing said composition with a low viscosity, distillable binder, embedding the molded core prior to firing in a nonreactive refractory sand, and, firing the refractory sand and the molded core contained therein at controlled temperatures such that the binder is drawn out of the core into said sand, said core being fully supportable by said sand, said sand and core being subsequently subjected to a sintering temperature, whereby a solid core body is formed.
  2. 2. The process of claim 1 wherein said binder comprises 33.3% by weight paraffin wax havinq a melting point of 131-136dC, 33.38 paraffin wax having a melting point of 144-1490C. 33.3% mineral wax having a melting point of 163-l?20C with an admixture of beeswax, aluminum stearate and oleic acid added in an amount sufficient to adjust the binder properties in the core.
  3. 3. The process of claim 2 wherein said admixture comprises about 4 parts beeswax, about 12 parts aluminum stearate and about 8 parts oleic acid.
  4. 4. The process of claim 1 wherein the firing of said molded core proceeds at a first increasing temperature ramp from ambient to about 7500F, at about 1350F per hour, followed by a second increasing temperature ramp of about 2700F per hour, up to the sintering temperature of about 2SS0 F, holding for about 3 hours at about 22500F and cooling said core at a first decreasing temperature ramp of about 540F per hour.
  5. 5. The process of claim 1 wherein said molded core is embedded in alumina sand.
GB08804151A 1987-02-24 1988-02-23 Method for manufacturing investment casting cores Pending GB2202541A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1811487A 1987-02-24 1987-02-24

Publications (2)

Publication Number Publication Date
GB8804151D0 GB8804151D0 (en) 1988-03-23
GB2202541A true GB2202541A (en) 1988-09-28

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Family Applications (1)

Application Number Title Priority Date Filing Date
GB08804151A Pending GB2202541A (en) 1987-02-24 1988-02-23 Method for manufacturing investment casting cores

Country Status (4)

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JP (1) JPS63248775A (en)
FR (1) FR2615766A1 (en)
GB (1) GB2202541A (en)
IL (1) IL85507A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0590186A1 (en) * 1991-09-30 1994-04-06 H. SEELMANN & Co GmbH Investment casting core
US6808010B2 (en) 2001-03-13 2004-10-26 Howmet Research Corporation Method for treating ceramic cores
US20100236688A1 (en) * 2009-03-20 2010-09-23 Scalzo Orlando Process for joining powder injection molded parts
FR3033509A1 (en) * 2015-03-11 2016-09-16 Snecma DELIANTING METHOD USING POSITIONING JIG
FR3062323A1 (en) * 2017-01-30 2018-08-03 Safran PROCESS FOR PRODUCING A CERAMIC CORE
US10695826B2 (en) 2017-07-17 2020-06-30 Raytheon Technologies Corporation Apparatus and method for investment casting core manufacture

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109678535A (en) * 2019-01-03 2019-04-26 安徽应流久源核能新材料科技有限公司 It is a kind of using powder as Water-soluble ceramic core of raw material and preparation method thereof
CN109807289B (en) * 2019-03-20 2023-09-29 浙江宁巍机械科技有限公司 Intelligent suspension shell manufacturing production line
US20230234855A1 (en) * 2020-05-27 2023-07-27 Panasonic Intellectual Property Management Co., Ltd. Inorganic structure and method for producing same

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3234308A (en) * 1961-11-21 1966-02-08 Corning Glass Works Method of molding ceramic articles
US3330892A (en) * 1964-07-24 1967-07-11 Corning Glass Works Molding comminuted nonplastic inorganic material
US3957715A (en) * 1973-01-10 1976-05-18 Howmet Corporation Casting of high melting point metals and cores therefor
US4221748A (en) * 1979-01-25 1980-09-09 General Electric Company Method for making porous, crushable core having a porous integral outer barrier layer having a density gradient therein

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0590186A1 (en) * 1991-09-30 1994-04-06 H. SEELMANN & Co GmbH Investment casting core
US6808010B2 (en) 2001-03-13 2004-10-26 Howmet Research Corporation Method for treating ceramic cores
US20100236688A1 (en) * 2009-03-20 2010-09-23 Scalzo Orlando Process for joining powder injection molded parts
US10226818B2 (en) * 2009-03-20 2019-03-12 Pratt & Whitney Canada Corp. Process for joining powder injection molded parts
US11383299B2 (en) 2009-03-20 2022-07-12 Pratt & Whitney Canada Corp. Process for joining powder injection molded parts
FR3033509A1 (en) * 2015-03-11 2016-09-16 Snecma DELIANTING METHOD USING POSITIONING JIG
FR3062323A1 (en) * 2017-01-30 2018-08-03 Safran PROCESS FOR PRODUCING A CERAMIC CORE
US10695826B2 (en) 2017-07-17 2020-06-30 Raytheon Technologies Corporation Apparatus and method for investment casting core manufacture

Also Published As

Publication number Publication date
FR2615766A1 (en) 1988-12-02
IL85507A (en) 1991-09-16
GB8804151D0 (en) 1988-03-23
IL85507A0 (en) 1988-08-31
JPS63248775A (en) 1988-10-17

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