US2893102A - Article fabrication from powders - Google Patents

Article fabrication from powders Download PDF

Info

Publication number
US2893102A
US2893102A US402828A US40282854A US2893102A US 2893102 A US2893102 A US 2893102A US 402828 A US402828 A US 402828A US 40282854 A US40282854 A US 40282854A US 2893102 A US2893102 A US 2893102A
Authority
US
United States
Prior art keywords
slip
casting
powder
mold
liquid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US402828A
Inventor
William A Maxwell
Raymond S Gurnick
Allen C Francisco
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to US402828A priority Critical patent/US2893102A/en
Application granted granted Critical
Publication of US2893102A publication Critical patent/US2893102A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/58Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
    • C04B35/58085Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicides
    • C04B35/58092Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicides based on refractory metal silicides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/22Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces for producing castings from a slip
    • B22F3/222Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces for producing castings from a slip by freeze-casting or in a supercritical fluid
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B1/00Producing shaped prefabricated articles from the material
    • B28B1/007Producing shaped prefabricated articles from the material by freezing the material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B1/00Producing shaped prefabricated articles from the material
    • B28B1/24Producing shaped prefabricated articles from the material by injection moulding
    • 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
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/10Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
    • C04B35/111Fine ceramics
    • 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
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/56Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
    • C04B35/5607Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides
    • C04B35/5611Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides based on titanium carbides
    • 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
    • C04B35/62605Treating the starting powders individually or as mixtures
    • C04B35/62625Wet mixtures
    • C04B35/6263Wet mixtures characterised by their solids loadings, i.e. the percentage of solids
    • 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
    • C04B35/636Polysaccharides or derivatives thereof
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5436Particle size related information expressed by the size of the particles or aggregates thereof micrometer sized, i.e. from 1 to 100 micron
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/60Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
    • C04B2235/602Making the green bodies or pre-forms by moulding
    • C04B2235/6022Injection moulding
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/60Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
    • C04B2235/606Drying
    • 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
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/658Atmosphere during thermal treatment
    • C04B2235/6581Total pressure below 1 atmosphere, e.g. vacuum
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S425/00Plastic article or earthenware shaping or treating: apparatus
    • Y10S425/009Cooling and color

Definitions

  • This invention relates to formation of articles from powders, with particular application to powder metallurgy.
  • powder metallurgy for example, articles have been formed by cold pressing and sintering, by hot pressing, or by slip or solid castings.
  • considerable machining or grinding is necessary to form the object, and the casting method is not suitable for all applications.
  • the present invention is directed to article formation by mixing a small amount of liquid, with or-without a binder, into the powdered refractory material, injecting the material into a mold, freezing the material, drying the molded material so as not to crack or deform the molded shape, and sintering the dried form.
  • the objects of the invention therefore, include provision of a method of article formation free of pressing steps, a method permitting ready use on varied and intricate forms, a method eliminating breakage of weak intermediate structures and a method permitting facile use of a continuous manufacturing line.
  • Fig. 1 is a flow diagram indicating the process steps in article formation
  • Fig. 2 is a view showing one arrangement for deaerating a powdered charge
  • Fig. 3 is a view illustrating the injection of the material into a mold
  • Fig. 4 is a view of a turbine blade made according to the described process.
  • Molybdenum silicide is first granulated to about nine microns average size which results in maximum strength after sintering and then formed in a slip by mixture with a suflicient amount of water to form a thick nonflowing slip.
  • a suflicient amount of water In a typical example 3.55 milliliters of water is added to 20.0 grams of molybdenum disilicide powder. While not always essential it is usually desirable to include a small amount of binder, as starch, in solution in the water, about 0.4 gram to equal about 2% of the weight of the dry powder.
  • the slip (Fig. 2) is then placed in a chamber forming the injection cylinder 11 of a piston-cylinder unit 12, the piston 13 at the cylinder base being slidable therein.
  • a latch 14 may be provided to hold the pisice ton at extended limit for retention of the entire powder supply.
  • the piston 13 is attached at its base to a vibrator plate 15 which, by any appropriate means, as by a 60 cycle adjustable amplitude vibrator 16, is oscillated to keep the powder mix in a state of constant motion.
  • a vibrator plate 15 which, by any appropriate means, as by a 60 cycle adjustable amplitude vibrator 16, is oscillated to keep the powder mix in a state of constant motion.
  • the cylinder 11 is externally ridged, as at 17, and flattened at the end to form an engagement surface for the vacuum head coupling 18 in the deaeration process step, or for the die unit in the subsequent step of mold injection.
  • Tubing 19 connects the vacuum head to a vacuum pump (not shown).
  • the vacuum head coupling is applied to the contact surface of the injection cylinder, a sealing ring 20 being interposed between these units to prevent leakage. "The vacuum line is then established and the vibrator energized, thus agitating the powdered slip and aiding in gas removal therefrom.
  • the vacuum head is then separated by the die 30.
  • This die is of the usual two part construction with interior contours fashioned to the desired article form.
  • the die parts are of equal length and are flattened to engage at one end outer end 17 of the injection cylinder and at the other end the vacuum head 18, annular leakage seals 31 and 32 being provided. Applying suction and vibration to the unit, together with light hand pressure, and releasing latch 14, the slip is caused to move into the die mold spaces and pack solidly therein.
  • Both dies and the contained slip are now placed in a freezing unit such as a solid carbon dioxide bath at 40 (3.; and after ten minutes, or a time dependent on the slip mass, the die is removed from the bath, opened and the casting removed.
  • a freezing unit such as a solid carbon dioxide bath at 40 (3.; and after ten minutes, or a time dependent on the slip mass, the die is removed from the bath, opened and the casting removed.
  • Fig. 4 illustrates a turbine blade 40 made according to the described process.
  • binder While fine powders can be employed singly, it is usually desirable, as mentioned above, to add a small amount of binder in order to increase the green strength of the molded product to permit handling.
  • Any inert binder may be used which forms a suspension or solution with the admixed liquid, does not impart excessive viscosity to the slip, is not harmed by freezing or solidification and imparts adequate strength to the dry casting when used in quantities of a few percent. Binders meeting these requirements are gelatines or starches, synthetic starches being particularly satisfactory.
  • a low temperature casting material permitting easy fabrication is desirable such as plaster of Paris, rubber, plastic or metal.
  • Various casting alloys have proved satisfactory.
  • the particle size of the powder is a factor deserving attention in the process, the used powder usually having a size of optimum effectiveness.
  • the used powder usually having a size of optimum effectiveness.
  • molybdenum disilicide a nine micron average diameter is indicated, with titanium carbide, four microns, and with iron powders, diameters preferably not exceeding about 200 mesh.
  • These particle sizes are selected in order that the finished casting will exhibit maximum strength after sintering.
  • the freeze casting step has the important advantage of permitting a wide range of particle sizes as compared to the conventional slip casting methods wherein the particle sizes depend upon the time allowed for absorption and the required fluidity of the slip. Within limits the larger the particle size the lower the amount of liquid required to make a castable slip. However, the range of size is determined by suitability for the final sintering step rather than absorption time and required fluidity.
  • any liquid may be used possessing to some degree the following properties: (a) it should maintain a low viscosity when mixed with the powder to form a slip; (b) it should solidify preferably in the range from room temperature down to the limit of economical refrigeration; (c) it should not react chemically with the powder; (d) it should dry or evaporate from the solid or liquid state either in vacuum or in air; and (e) preferably, it should not be toxic or hazardous in use.
  • cyclo-hexanol has been employed and paraffin hydro-carbons solidifying at room temperature are available for use.
  • the added liquid maintains the green molded shape when frozen so as to permit handling. On sublimation of the liquid the binder holds the form until the sintering step establishes mass cohesion.
  • a skeleton mate rial such as titanium carbide, in powdered form, is cast as previously described in a shaped mold having a porosity of about 40%.
  • the casting is then semi-sintered to obtain particle bonding, the porosity being reduced to about
  • Infiltration is then carried on using molten Inconel or other high temperature alloy, the capillary action of the porous skeleton indrawing the filler metal to form a solid form.
  • the usual procedure is to place the infiltrant in physical contact with the skeleton material preferably in an evacuated chamber and inductively heat the infiltrant above the point of fusion. (See US. Patent No. 2,456,779.)
  • the advantage of the freeze-cast method as applied to infiltration is apparent in that various intricate shapes not practical with the usual pressure methods may readily be employed.
  • a process of forming articles from a refractory powder which consists in mixing a liquid with said powder to form a thick, non-flowing slip, moving the slip into a mold while subjecting the slip to vibration, freezing the slip to form a casting, removing the mold, drying the casting in a vacuous atmosphere at a temperature below the melting point of the liquid and sintering the casting.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Powder Metallurgy (AREA)

Description

July 7, 1959 w. A. MAXWELL ET AL ARTICLE FABRICATIGN FROM POWDERS Filed Jan. 7. 1954 INVENTORS William/1. Maxwell, liaymond \Sfiarm'ck ATTORNEYS M Allen QF/zzrzcisco a/ZZ, AK W N G G D V R a l R 6 E 0 T M u M ma M Mm m N k E N F R S COOL ING r J \i! WA TER VACUUM VACUUM VACUUM United States Patent ARTICLE FABRICATION FROM POWDERS William A. Maxwell, Bay Village, Raymond S. Gui-nick, Cuyahoga Falls, and Allen C. Francisco, Berea, Ohio, assignors to the United States of America as represented by the Secretary of the Navy Application January 7, 1954, Serial No. 402,828
4 Claims. (Cl. 25-156) (Granted under Title 35, US. Code (1952), see. 266) The invention described herein may be manufactured and used by or for the Government of the United States of America for governmental purposes without the payment of any royalties thereon or therefor.
This invention relates to formation of articles from powders, with particular application to powder metallurgy. In powder metallurgy, for example, articles have been formed by cold pressing and sintering, by hot pressing, or by slip or solid castings. However, with the exception of the casting method considerable machining or grinding is necessary to form the object, and the casting method is not suitable for all applications.
Briefly stated, the present invention is directed to article formation by mixing a small amount of liquid, with or-without a binder, into the powdered refractory material, injecting the material into a mold, freezing the material, drying the molded material so as not to crack or deform the molded shape, and sintering the dried form.
The objects of the invention, therefore, include provision of a method of article formation free of pressing steps, a method permitting ready use on varied and intricate forms, a method eliminating breakage of weak intermediate structures and a method permitting facile use of a continuous manufacturing line.
C Other objects and advantages of this invention will appear on reference to the following description and accompanying drawings in which:
Fig. 1 is a flow diagram indicating the process steps in article formation;
Fig. 2 is a view showing one arrangement for deaerating a powdered charge;
Fig. 3 is a view illustrating the injection of the material into a mold; and
Fig. 4 is a view of a turbine blade made according to the described process.
While the process is applicable to any ordinary powdered material, with refractory materials it has been found particularly useful, such materials as molybdenum disilicide, titanium-carbide, aluminum oxide, and iron, having been found exceptionally suitable. As an example of use the treatment of molybdenum disilicide will be described.
Molybdenum silicide is first granulated to about nine microns average size which results in maximum strength after sintering and then formed in a slip by mixture with a suflicient amount of water to form a thick nonflowing slip. In a typical example 3.55 milliliters of water is added to 20.0 grams of molybdenum disilicide powder. While not always essential it is usually desirable to include a small amount of binder, as starch, in solution in the water, about 0.4 gram to equal about 2% of the weight of the dry powder.
The slip (Fig. 2) is then placed in a chamber forming the injection cylinder 11 of a piston-cylinder unit 12, the piston 13 at the cylinder base being slidable therein. A latch 14 may be provided to hold the pisice ton at extended limit for retention of the entire powder supply.
The piston 13 is attached at its base to a vibrator plate 15 which, by any appropriate means, as by a 60 cycle adjustable amplitude vibrator 16, is oscillated to keep the powder mix in a state of constant motion. At its upper end the cylinder 11 is externally ridged, as at 17, and flattened at the end to form an engagement surface for the vacuum head coupling 18 in the deaeration process step, or for the die unit in the subsequent step of mold injection. Tubing 19 connects the vacuum head to a vacuum pump (not shown).
For the de-aeration step the vacuum head coupling is applied to the contact surface of the injection cylinder, a sealing ring 20 being interposed between these units to prevent leakage. "The vacuum line is then established and the vibrator energized, thus agitating the powdered slip and aiding in gas removal therefrom.
The vacuum head is then separated by the die 30. This die is of the usual two part construction with interior contours fashioned to the desired article form. The die parts are of equal length and are flattened to engage at one end outer end 17 of the injection cylinder and at the other end the vacuum head 18, annular leakage seals 31 and 32 being provided. Applying suction and vibration to the unit, together with light hand pressure, and releasing latch 14, the slip is caused to move into the die mold spaces and pack solidly therein.
Both dies and the contained slip are now placed in a freezing unit such as a solid carbon dioxide bath at 40 (3.; and after ten minutes, or a time dependent on the slip mass, the die is removed from the bath, opened and the casting removed.
It is now necessary to remove the moisture in the casting, which, as previously stated, is just sutlicient to produce a thick non-flowing slip. To accomplish this result without disturbance of the molded form structure the drying takes place at a pressure permitting sublimation, two to four millimeters pressure being found satisfactory for water during a time period of about four hours. Cooling of the drying chamber to hold the green casting below the melting point may be employed. After drying, the mold is sintered at around 2300 C. for one hour in a five micron vacuum. Fig. 4 illustrates a turbine blade 40 made according to the described process.
While the underlying process has been described it is desirable to point out certain useful refinements therein and to indicate desirable uses and materials.
While fine powders can be employed singly, it is usually desirable, as mentioned above, to add a small amount of binder in order to increase the green strength of the molded product to permit handling. Any inert binder may be used which forms a suspension or solution with the admixed liquid, does not impart excessive viscosity to the slip, is not harmed by freezing or solidification and imparts adequate strength to the dry casting when used in quantities of a few percent. Binders meeting these requirements are gelatines or starches, synthetic starches being particularly satisfactory.
In the die structure, a low temperature casting material permitting easy fabrication is desirable such as plaster of Paris, rubber, plastic or metal. Various casting alloys have proved satisfactory.
The particle size of the powder is a factor deserving attention in the process, the used powder usually having a size of optimum effectiveness. For example, with molybdenum disilicide a nine micron average diameter is indicated, with titanium carbide, four microns, and with iron powders, diameters preferably not exceeding about 200 mesh. These particle sizes are selected in order that the finished casting will exhibit maximum strength after sintering. The freeze casting step has the important advantage of permitting a wide range of particle sizes as compared to the conventional slip casting methods wherein the particle sizes depend upon the time allowed for absorption and the required fluidity of the slip. Within limits the larger the particle size the lower the amount of liquid required to make a castable slip. However, the range of size is determined by suitability for the final sintering step rather than absorption time and required fluidity.
Water has been used as a slip agent giving satisfactory results. However, any liquid may be used possessing to some degree the following properties: (a) it should maintain a low viscosity when mixed with the powder to form a slip; (b) it should solidify preferably in the range from room temperature down to the limit of economical refrigeration; (c) it should not react chemically with the powder; (d) it should dry or evaporate from the solid or liquid state either in vacuum or in air; and (e) preferably, it should not be toxic or hazardous in use. For example, cyclo-hexanol has been employed and paraffin hydro-carbons solidifying at room temperature are available for use. As appears from the disclosure, the added liquid maintains the green molded shape when frozen so as to permit handling. On sublimation of the liquid the binder holds the form until the sintering step establishes mass cohesion.
It is important to note that the described process does away with the usual pressing and shaping steps of powder metallurgy. Using molybdenum disilicide and the method of vibratory injection, a green shaped object is produced having a density equal to that produced by conventional pressing at 10,000 pounds per square inch. By causing the slip to flow under vibration, the amount of liquid required can be decreased and, thus, the resulting green density increased in comparison with the liquid quantities required and the densities attained in conventional slip castings. Further, the use of a viscous, non-flowing slip lessens the possibility of segregation of the refractory powders during casting.
An important use of the process is in the field of infiltration. In conventional infiltration techniques ceramals are produced by infiltering various molten metals or alloys into a porous skeleton frame, thereby making possible the reduction of strategically critical metals and an increase in operating temperatures. These prior methods involve die pressing of the skeleton powders sufficiently to produce the desired porosity, as to 40%. This skeleton may be infiltered directly or semisintered prior to infiltration.
According to the freeze-cast method a skeleton mate rial, such as titanium carbide, in powdered form, is cast as previously described in a shaped mold having a porosity of about 40%. The casting is then semi-sintered to obtain particle bonding, the porosity being reduced to about Infiltration is then carried on using molten Inconel or other high temperature alloy, the capillary action of the porous skeleton indrawing the filler metal to form a solid form. The usual procedure is to place the infiltrant in physical contact with the skeleton material preferably in an evacuated chamber and inductively heat the infiltrant above the point of fusion. (See US. Patent No. 2,456,779.) The advantage of the freeze-cast method as applied to infiltration is apparent in that various intricate shapes not practical with the usual pressure methods may readily be employed.
Modifications of the invention are possible in the light of the above teachings; and hence the invention may be practiced otherwise than as specifically described, within the scope of the appended claims.
What is claimed is:
1. A process of forming articles from a refractory powder which consists in mixing a liquid with said powder to form a thick, non-flowing slip, moving the slip into a mold while subjecting the slip to vibration, freezing the slip to form a casting, removing the mold, drying the casting in a vacuous atmosphere at a temperature below the melting point of the liquid and sintering the casting.
2. The process of forming articles from solid refractory material which consists in forming the material into a powder having an average diameter of about nine microns, mixing water with the material in the proportion of 3.55 milliliters to 20 grams of the powder to form a thick, non-flowing slip, injecting the slip into a mold by imparting vibration and suction thereto, freezing the slip to form a casting, removing the mold, drying the casting in a vacuous atmosphere at a pressure less than about four microns and a temperature below the freezing temperature of the liquid, and sintering the casting at a temperature around 2300 C.
3. The process of making articles as defined in claim 2 with the initial mix of powdered refractory material and water including a starch binder in the amount to form two percent of the dry powder-starch mix.
4. The process of forming articles from a refractory material of one of the group consisting of molybdenum disilicide, titanium carbide and aluminum oxide comprising the steps of forming the material into a powder having a particle size of optimum effectiveness during sintering, mixing a liquid with the powder to form a thick, non-flowing slip, deaerating the slip, injecting the deaerated slip into a mold by imparting vibration thereto, freezing the slip to form a casting, removing the mold, drying the casting by sublimation, and sintering the casting.
References Cited in the file of this patent UNITED STATES PATENTS 1,694,563 Ross et al. Dec. 11, 1928 2,196,258 Erdle Apr. 9, 1940 2,444,124 Wedler June 29, 1948 2,456,779 Goetzel Dec. 21, 1948 2,476,726 Haas July 19, 1949 2,622,304 Coffer Dec. 23, 1952 2,645,836 Sorensen et al. July 21, 1953 2,669,762 Blackburn et al. Feb. 23, 1954 2,765,512 Nesbit Oct. 9, 1956

Claims (1)

1. A PROCESS OF FORMING ARTICLES FROM A REFRACTORY POWDER WHICH CONSISTS IN MIXING A LIQUID WITH SAID POWDER TO FORM A THICK, NON-FLOWING SLIP, MOVING THE SLIP INTO A MOLD WHILE SUBJECTING THE SLIP TO VIBRATION, FREEZING THE SLIP TO FORM A CASTING, REMOVING THE MOLD, DRYING THE CASTING IN A VACUOUS ATMOSPHERE AT A TEMPERATURE BELOW THE MELTING POINT OF THE LIQUID AND SINTERING THE CASTING.
US402828A 1954-01-07 1954-01-07 Article fabrication from powders Expired - Lifetime US2893102A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US402828A US2893102A (en) 1954-01-07 1954-01-07 Article fabrication from powders

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US402828A US2893102A (en) 1954-01-07 1954-01-07 Article fabrication from powders

Publications (1)

Publication Number Publication Date
US2893102A true US2893102A (en) 1959-07-07

Family

ID=23593440

Family Applications (1)

Application Number Title Priority Date Filing Date
US402828A Expired - Lifetime US2893102A (en) 1954-01-07 1954-01-07 Article fabrication from powders

Country Status (1)

Country Link
US (1) US2893102A (en)

Cited By (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2944316A (en) * 1956-12-20 1960-07-12 William A Maxwell Process of casting heavy slips
US3222435A (en) * 1963-04-30 1965-12-07 Jr Edward J Mellen Injection molding of ceramic cores
US3346676A (en) * 1963-10-28 1967-10-10 Hitachi Ltd Method for the production of ceramic nuclear fuel elements
US3413383A (en) * 1964-10-28 1968-11-26 Hitachi Ltd Vibratory compaction method for the fabrication of ceramic nuclear fuel elements
US3422167A (en) * 1968-01-31 1969-01-14 Atomic Energy Commission Method for preparing metal oxide microspheres
US4000235A (en) * 1975-05-13 1976-12-28 National Forge Company Method for molding particulate material into rods
US4341725A (en) * 1977-12-13 1982-07-27 Weaver Gerald Q Molding refractory and metal shapes by slip-casting
DE3211083A1 (en) * 1982-03-25 1983-09-29 Norton Co., 01606 Worcester, Mass. Slip casting method
US4473673A (en) * 1983-05-09 1984-09-25 Wildon Industries, Inc. Cast polyester resin process and product
WO1985000130A1 (en) * 1983-06-24 1985-01-17 Udo Rieser Manufacturing of sintered ceramic moulded bodies
US4522753A (en) * 1980-07-17 1985-06-11 Massachusetts Institute Of Technology Method for preserving porosity in porous materials
US4526734A (en) * 1981-03-05 1985-07-02 Ibigawa Electric Industry Co., Ltd. Process for the production of silicon carbide sintered bodies
EP0160855A1 (en) * 1984-04-12 1985-11-13 Mitsubishi Corporation A method for the freeze-pressure molding of metallic powders
EP0161494A1 (en) * 1984-04-12 1985-11-21 Mitsubishi Corporation A method for the freeze-pressure molding of inorganic powders
EP0223081A2 (en) * 1985-10-22 1987-05-27 Mitsubishi Kasei Corporation Method for production of fiber-reinforced metal composite material
EP0345022A1 (en) * 1988-06-01 1989-12-06 Ngk Insulators, Ltd. Method for producing ceramics sintered article
US5014763A (en) * 1988-11-30 1991-05-14 Howmet Corporation Method of making ceramic cores
US5047182A (en) * 1987-11-25 1991-09-10 Ceramics Process Systems Corporation Complex ceramic and metallic shaped by low pressure forming and sublimative drying
US5047181A (en) * 1987-04-09 1991-09-10 Ceramics Process Systems Corporation Forming of complex high performance ceramic and metallic shapes
US5055436A (en) * 1988-08-19 1991-10-08 Cps Superconductor Corp. Method for preparation of superconductor powders
US5098620A (en) * 1990-06-07 1992-03-24 The Dow Chemical Company Method of injection molding ceramic greenward composites without knit lines
WO1992005022A1 (en) * 1989-03-07 1992-04-02 United Technologies Corporation Manufacture of monolithic, stiff, lightweight ceramic articles
US5126082A (en) * 1988-11-30 1992-06-30 Howmet Corporation Method of making ceramic cores and other articles
US5137540A (en) * 1989-03-07 1992-08-11 United Technologies Corporation Composite monolithic lamp and a method of making the same
US5194268A (en) * 1990-06-07 1993-03-16 The Dow Chemical Company Apparatus for injection molding a ceramic greenware composite without knit lines
US5238627A (en) * 1988-06-01 1993-08-24 Ngk Insulators, Ltd. Method for producing ceramics sintered article and molding method and molding apparatus to be used therefor
US5364570A (en) * 1991-11-16 1994-11-15 Foseco International Limited Ceramic material
DE19546904C1 (en) * 1995-12-15 1997-07-24 Fraunhofer Ges Forschung Production of flat ceramic or powder-metallurgical components structured on one side
US5753160A (en) * 1994-10-19 1998-05-19 Ngk Insulators, Ltd. Method for controlling firing shrinkage of ceramic green body
EP0887325A1 (en) * 1997-06-26 1998-12-30 General Motors Corporation Method of making fibrillose articles
US5885379A (en) * 1997-03-28 1999-03-23 The Landover Company Tempered powdered metallurgical construct and method
US6051171A (en) * 1994-10-19 2000-04-18 Ngk Insulators, Ltd. Method for controlling firing shrinkage of ceramic green body
WO2001090028A1 (en) * 2000-05-26 2001-11-29 Hiform As Moulding of ceramic moulding forms
US6368525B1 (en) * 2000-02-07 2002-04-09 General Electric Company Method for removing volatile components from a ceramic article, and related processes
US6395117B1 (en) 1994-10-19 2002-05-28 Ngk Insulators Method for producing ceramic green sheet
EP2050727A3 (en) * 2007-10-15 2012-03-14 Pacific Rundum Co., Ltd Ceramic Molded Product and Manufacturing Method Thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1694563A (en) * 1927-02-02 1928-12-11 Donald W Ross Method of molding ceramic materials
US2196258A (en) * 1936-09-21 1940-04-09 Dental Res Corp Method of molding ceramic articles
US2444124A (en) * 1944-03-04 1948-06-29 American Viscose Corp Method of freeze-drying regenerated cellulose
US2456779A (en) * 1947-01-27 1948-12-21 American Electro Metal Corp Composite material and shaped bodies therefrom
US2476726A (en) * 1945-10-01 1949-07-19 Haas Guy Casper Method for making molds
US2622304A (en) * 1950-10-02 1952-12-23 Climax Molybdenum Co Refractory
US2645836A (en) * 1949-07-01 1953-07-21 Maschf Augsburg Nuernberg Ag Molding method
US2669762A (en) * 1953-02-05 1954-02-23 Andrew R Blackburn Method for making ware by casting
US2765512A (en) * 1950-07-13 1956-10-09 Robert A Nesbit Formation of ceramic, etc., articles

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1694563A (en) * 1927-02-02 1928-12-11 Donald W Ross Method of molding ceramic materials
US2196258A (en) * 1936-09-21 1940-04-09 Dental Res Corp Method of molding ceramic articles
US2444124A (en) * 1944-03-04 1948-06-29 American Viscose Corp Method of freeze-drying regenerated cellulose
US2476726A (en) * 1945-10-01 1949-07-19 Haas Guy Casper Method for making molds
US2456779A (en) * 1947-01-27 1948-12-21 American Electro Metal Corp Composite material and shaped bodies therefrom
US2645836A (en) * 1949-07-01 1953-07-21 Maschf Augsburg Nuernberg Ag Molding method
US2765512A (en) * 1950-07-13 1956-10-09 Robert A Nesbit Formation of ceramic, etc., articles
US2622304A (en) * 1950-10-02 1952-12-23 Climax Molybdenum Co Refractory
US2669762A (en) * 1953-02-05 1954-02-23 Andrew R Blackburn Method for making ware by casting

Cited By (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2944316A (en) * 1956-12-20 1960-07-12 William A Maxwell Process of casting heavy slips
US3222435A (en) * 1963-04-30 1965-12-07 Jr Edward J Mellen Injection molding of ceramic cores
US3346676A (en) * 1963-10-28 1967-10-10 Hitachi Ltd Method for the production of ceramic nuclear fuel elements
US3413383A (en) * 1964-10-28 1968-11-26 Hitachi Ltd Vibratory compaction method for the fabrication of ceramic nuclear fuel elements
US3422167A (en) * 1968-01-31 1969-01-14 Atomic Energy Commission Method for preparing metal oxide microspheres
US4000235A (en) * 1975-05-13 1976-12-28 National Forge Company Method for molding particulate material into rods
US4341725A (en) * 1977-12-13 1982-07-27 Weaver Gerald Q Molding refractory and metal shapes by slip-casting
US4522753A (en) * 1980-07-17 1985-06-11 Massachusetts Institute Of Technology Method for preserving porosity in porous materials
US4526734A (en) * 1981-03-05 1985-07-02 Ibigawa Electric Industry Co., Ltd. Process for the production of silicon carbide sintered bodies
DE3211083A1 (en) * 1982-03-25 1983-09-29 Norton Co., 01606 Worcester, Mass. Slip casting method
US4473673A (en) * 1983-05-09 1984-09-25 Wildon Industries, Inc. Cast polyester resin process and product
WO1985000130A1 (en) * 1983-06-24 1985-01-17 Udo Rieser Manufacturing of sintered ceramic moulded bodies
EP0160855A1 (en) * 1984-04-12 1985-11-13 Mitsubishi Corporation A method for the freeze-pressure molding of metallic powders
EP0161494A1 (en) * 1984-04-12 1985-11-21 Mitsubishi Corporation A method for the freeze-pressure molding of inorganic powders
US4740352A (en) * 1984-04-12 1988-04-26 Mitsubishi Corporation Method for the freeze-pressure molding of metallic powders
US4965027A (en) * 1984-04-12 1990-10-23 Mitsubishi Corporation Method for the freeze-pressure molding of inorganic powders
EP0223081A2 (en) * 1985-10-22 1987-05-27 Mitsubishi Kasei Corporation Method for production of fiber-reinforced metal composite material
EP0223081A3 (en) * 1985-10-22 1988-01-13 Mitsubishi Chemical Industries Limited Method for production of fiber-reinforced metal composite material
US5047181A (en) * 1987-04-09 1991-09-10 Ceramics Process Systems Corporation Forming of complex high performance ceramic and metallic shapes
US5047182A (en) * 1987-11-25 1991-09-10 Ceramics Process Systems Corporation Complex ceramic and metallic shaped by low pressure forming and sublimative drying
EP0345022A1 (en) * 1988-06-01 1989-12-06 Ngk Insulators, Ltd. Method for producing ceramics sintered article
US5238627A (en) * 1988-06-01 1993-08-24 Ngk Insulators, Ltd. Method for producing ceramics sintered article and molding method and molding apparatus to be used therefor
US5055436A (en) * 1988-08-19 1991-10-08 Cps Superconductor Corp. Method for preparation of superconductor powders
US5014763A (en) * 1988-11-30 1991-05-14 Howmet Corporation Method of making ceramic cores
US5126082A (en) * 1988-11-30 1992-06-30 Howmet Corporation Method of making ceramic cores and other articles
WO1992005022A1 (en) * 1989-03-07 1992-04-02 United Technologies Corporation Manufacture of monolithic, stiff, lightweight ceramic articles
US5137540A (en) * 1989-03-07 1992-08-11 United Technologies Corporation Composite monolithic lamp and a method of making the same
US5098620A (en) * 1990-06-07 1992-03-24 The Dow Chemical Company Method of injection molding ceramic greenward composites without knit lines
US5194268A (en) * 1990-06-07 1993-03-16 The Dow Chemical Company Apparatus for injection molding a ceramic greenware composite without knit lines
US5364570A (en) * 1991-11-16 1994-11-15 Foseco International Limited Ceramic material
US6051171A (en) * 1994-10-19 2000-04-18 Ngk Insulators, Ltd. Method for controlling firing shrinkage of ceramic green body
US5753160A (en) * 1994-10-19 1998-05-19 Ngk Insulators, Ltd. Method for controlling firing shrinkage of ceramic green body
US6395117B1 (en) 1994-10-19 2002-05-28 Ngk Insulators Method for producing ceramic green sheet
DE19546904C1 (en) * 1995-12-15 1997-07-24 Fraunhofer Ges Forschung Production of flat ceramic or powder-metallurgical components structured on one side
US5885379A (en) * 1997-03-28 1999-03-23 The Landover Company Tempered powdered metallurgical construct and method
EP0887325A1 (en) * 1997-06-26 1998-12-30 General Motors Corporation Method of making fibrillose articles
US5908587A (en) * 1997-06-26 1999-06-01 General Motors Corporation Method of making fibrillose articles
US6368525B1 (en) * 2000-02-07 2002-04-09 General Electric Company Method for removing volatile components from a ceramic article, and related processes
US20020109249A1 (en) * 2000-02-07 2002-08-15 General Electric Company Method for removing volatile components from a gel-cast ceramic article
US6787074B2 (en) * 2000-02-07 2004-09-07 General Electric Company Method for removing volatile components from a gel-cast ceramic article
WO2001090028A1 (en) * 2000-05-26 2001-11-29 Hiform As Moulding of ceramic moulding forms
EP2050727A3 (en) * 2007-10-15 2012-03-14 Pacific Rundum Co., Ltd Ceramic Molded Product and Manufacturing Method Thereof

Similar Documents

Publication Publication Date Title
US2893102A (en) Article fabrication from powders
US5047181A (en) Forming of complex high performance ceramic and metallic shapes
US3066391A (en) Powder metallurgy processes and products
US3455682A (en) Isostatic hot pressing of refractory bodies
US4041123A (en) Method of compacting shaped powdered objects
US2947056A (en) Sintered alumina articles and a process for the production thereof
US5746957A (en) Gel strength enhancing additives for agaroid-based injection molding compositions
US2809891A (en) Method of making articles from aluminous metal powder
US3181947A (en) Powder metallurgy processes and products
WO2001002112A1 (en) Disintegrative core for high pressure casting, method for manufacturing the same, and method for extracting the same
JP3497461B2 (en) Method for producing porous metal
US4019913A (en) Process for fabricating silicon carbide articles
US4943413A (en) Process for producing an aluminum/magnesium alloy
US5141683A (en) Method of producing reinforced materials
JPH02185904A (en) Hot pressing of powder and granule
KR960006327B1 (en) Aluminium-silicon alloy article and the preparation process
US3328139A (en) Porous tungsten metal shapes
US3071463A (en) Method of producing sintered metal bodies
US5261941A (en) High strength and density tungsten-uranium alloys
Maxwell et al. Preliminary Investigation of the'freeze-casting'Method for Forming Refractory Powders
US5613183A (en) Manufacture of parts from particulate material
US5262122A (en) Manufacture of parts from particulate material
US2976598A (en) Method of sintering
US4445936A (en) Method of making inelastically compressible ductile particulate material article and subsequent working thereof
JP3176920B2 (en) True or pseudo equilibrium pressurization