WO2004015150A2 - Materiau composite a matrice metallique renforcee par des fibres de carbone discontinues - Google Patents

Materiau composite a matrice metallique renforcee par des fibres de carbone discontinues Download PDF

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Publication number
WO2004015150A2
WO2004015150A2 PCT/US2002/015175 US0215175W WO2004015150A2 WO 2004015150 A2 WO2004015150 A2 WO 2004015150A2 US 0215175 W US0215175 W US 0215175W WO 2004015150 A2 WO2004015150 A2 WO 2004015150A2
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WIPO (PCT)
Prior art keywords
matrix composite
metal matrix
preform
plane
approximately
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PCT/US2002/015175
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English (en)
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WO2004015150A3 (fr
Inventor
James A. Cornie
Mark A. Ryals
Stephen S. Cornie
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Metal Matrix Cast Composites, Inc.
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Priority to EP02807627A priority Critical patent/EP1432840A2/fr
Publication of WO2004015150A2 publication Critical patent/WO2004015150A2/fr
Publication of WO2004015150A3 publication Critical patent/WO2004015150A3/fr

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00Details of semiconductor or other solid state devices
    • H01L23/34Arrangements for cooling, heating, ventilating or temperature compensation ; Temperature sensing arrangements
    • H01L23/36Selection of materials, or shaping, to facilitate cooling or heating, e.g. heatsinks
    • H01L23/373Cooling facilitated by selection of materials for the device or materials for thermal expansion adaptation, e.g. carbon
    • H01L23/3733Cooling facilitated by selection of materials for the device or materials for thermal expansion adaptation, e.g. carbon having a heterogeneous or anisotropic structure, e.g. powder or fibres in a matrix, wire mesh, porous structures
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C47/00Making alloys containing metallic or non-metallic fibres or filaments
    • C22C47/02Pretreatment of the fibres or filaments
    • C22C47/025Aligning or orienting the fibres
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C47/00Making alloys containing metallic or non-metallic fibres or filaments
    • C22C47/02Pretreatment of the fibres or filaments
    • C22C47/06Pretreatment of the fibres or filaments by forming the fibres or filaments into a preformed structure, e.g. using a temporary binder to form a mat-like element
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C47/00Making alloys containing metallic or non-metallic fibres or filaments
    • C22C47/08Making alloys containing metallic or non-metallic fibres or filaments by contacting the fibres or filaments with molten metal, e.g. by infiltrating the fibres or filaments placed in a mould
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C49/00Alloys containing metallic or non-metallic fibres or filaments
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper
    • 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
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001Technical content checked by a classifier
    • H01L2924/0002Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Definitions

  • the present invention relates to methods of forming metal matrix composites for thermal or structural applications, and the resulting compositions. More specifically, the invention relates to methods of infiltration casting to form metal matrix composites with controlled thermal expansion and mechanical properties, and the resulting compositions.
  • a semiconductor die typically a portion of a silicon wafer, can be directly attached to a heat sink. More commonly, the die is encased in a ceramic package that protects the die and provides electrical connections.
  • Common ceramic package materials include aluminum oxide, aluminum nitride and beryllium oxide.
  • the coefficient of thermal expansion of the semiconductor die and the ceramic package are purposely matched to avoid thermal cycle induced mechanical stress failures . Thermal cycling arises during power up and power down cycles in combination with resistive heating due to current flow in the device.
  • Heat sinks are commonly fabricated from metals, for example copper, molybdenum, tungsten and aluminum.
  • a metal heat sink is often plated with nickel prior to attachment to a ceramic package at an elevated temperature, for example, via brazing.
  • silver-filled adhesives or other conductive metal powder-filled adhesives, can be used for bonding.
  • a metal or other material for a heat sink often involves a trade-off between desirable and undesirable properties.
  • aluminum and copper have high thermal conductivity, but coefficients of thermal expansion several times greater than that of a ceramic package or semiconductor die.
  • resistive heating causes the temperature of the integrated circuit, and the attached heat sink, to fluctuate. Consequently, such metals apply mechanical stress to the heat sink bonding material during power cycling.
  • the differential expansion of the heat sink relative to the ceramic package or semiconductor die can cause failure of the bond material or cracking of the package or die.
  • some metals, such as tungsten and molybdenum have relatively small coefficients of thermal expansion. Although such metals can permit a reliable bond, they have lower thermal conductivity than aluminum or copper substrates and they are difficult to electroplate. Further, tungsten and molybdenum are undesirable for applications that require minimal weight.
  • Composites of copper and tungsten, or of copper and molybdenum can partially mitigate these deficiencies. These composites can be made by powder metallurgical methods, such as infiltrating copper into a sintered body of tungsten or molybdenum, or sintering a mixed powder of the two metals . It is difficult, however, to obtain an elongated plate by rolling a sintered ingot of tungsten or molybdenum. Alternatively, layers of metal can be joined by cladding or lamination of sheets. Cladded and laminated products require precise machining, which is difficult and increases costs.
  • some heat sinks combine a sintered ceramic with a metal matrix.
  • the fabrication process involves the formation of a ceramic preform, for example, by sintering silicon carbide powder.
  • the ceramic preform microstructure typically has a predetermined void volume fraction that is subsequently filled with molten metal, typically aluminum.
  • An aluminum ceramic heat sink can employ copper-based inserts to improve its thermal conductivity.
  • Such heat sinks can be difficult to machine and are usually limited in their ability to match coefficients of thermal expansion with integrated circuits.
  • a metal matrix composite can include an inorganic fiber material.
  • Infiltration of fibers has its own difficulties, for example, problems with fiber wetting and non-uniform fiber distribution.
  • molten metal infiltration of fibers under pressure can displace the fibers due to the fiber breakthrough pressure threshold.
  • a metal matrix composite C that includes random in-plane discontinuous carbon fibers and a method of forming an MMC from a pressure-formed preform
  • the invention can overcome numerous problems, such as: fiber collapse during molten metal infiltration; coefficient of thermal expansion ("CTE") mismatch; heat sink weight; limits on range of CTE values; difficulty in obtaining high fiber density; limits in control of fiber orientation; machinability of a heat sink; and/or heat sink cost.
  • CTE coefficient of thermal expansion
  • the invention addresses these problems through the use of one or all of the following: preforms prepared with pressures greater than the breakthrough pressure used during metal infiltration; in-plane oriented fibers; short fibers; and carbon fibers.
  • in-plane discontinuous fibers permits a high fiber volume fraction in the MMC ("in-plane" as used herein is understood as the X-Y plane, for example, the plane parallel to the bonded surface of a heat sink) . Further, by using in-plane oriented fibers, substantially all of the fibers can contribute to the control of the CTE in the X-Y plane. Though Z-direction CTE is not controlled by in-plane fibers, such control is generally unnecessary for heat sink applications because the integrated circuit or other object is attached to an X-Y oriented surface of the heat sink.
  • in-plane oriented fibers permits selection of a CTE over a wide range of values.
  • a desired volume fraction of in-plane oriented fibers is selected to obtain a desired CTE.
  • By orienting substantially all fibers in the X-Y plane a very high fiber volume fraction can be obtained. This permits selection of volume fraction over a wide range and a corresponding ability to select a wide range of CTE values.
  • Carbon fibers, in particular graphite fibers have excellent mechanical and thermal properties for use in heat sinks of the invention. In combination with an aluminum or other light metal, such heat sinks typically are easily machined, have excellent heat conductivity, and are lightweight.
  • An aluminum and graphite fiber MMC of the invention thus realizes the advantages of aluminum - lightweight, easy machinability and good heat conduction - in combination with the advantages of graphite fibers - high Young's Modulus, small to negative CTE, high tensile strength, high thermal conductivity and strong damping properties.
  • a preform that includes fibers and a binder can be prepared via application of a pressure in a preform mold that is greater than the molten alloy breakthrough pressure for the preform.
  • the binder maintains the compressed configuration of the fibers in the preform while the preform is removed from the preform mold and placed in a metal infiltration mold.
  • the metal infiltration mold can maintain the compressed fiber configuration upon removal of the binder, if the infiltration mold is sized and shaped to conform to the preform. Because the fiber configuration remains in its compressed state, it is substantially undisturbed during infiltration of molten metal at the molten metal breakthrough pressure.
  • the invention features a metal matrix composite that includes a metal alloy and random in-plane discontinuous fibers.
  • the random in-plane discontinuous fibers may be carbon, and preferably are graphite.
  • the fibers typically are milled, and preferably are ball milled.
  • the metal alloy includes aluminum, copper or magnesium.
  • the metal matrix composite has a volume fraction of random in-plane discontinuous fibers in a range of approximately 0.15 to approximately 0.6. In another embodiment, a minority of the random in-plane discontinuous fibers are oriented out of plane by an angle greater than 10°. In a preferred embodiment, the random in-plane discontinuous fibers are uniformly distributed within the metal matrix composite.
  • the metal matrix composite may include a component that enables solution hardening. In other embodiments, the metal matrix composite may include a component that enables precipitation hardening.
  • the metal matrix composite includes aluminum, silicon and magnesium. In another preferred embodiment, the metal matrix composite includes copper, chromium and zirconium.
  • the invention provides a method of manufacturing a metal matrix composite.
  • the method includes contacting random in-plane discontinuous fibers with a binder, and pressurizing the random in-plane discontinuous fibers and the binder to form a bound preform.
  • the random in-plane discontinuous fibers and the binder are pressurized to a pressure greater than the capillary breakthrough pressure of the bound preform.
  • the bound preform typically is placed in a mold, heated under a vacuum to remove the binder, then heated to above the metal liquidus and infiltrated with a molten infiltrant. The molten infiltrant is then cooled to form the metal matrix composite.
  • the method includes placement of a second bound preform adjacent to the bound preform in the mold prior to infiltration with the molten infiltrant.
  • a surface of the bound preform contacts a surface of the second bound preform, and removal of the binder prior to infiltration causes the contacted surfaces of the two preforms to merge, creating one continuous, metal matrix composite.
  • the binder may be removed (called debindering) prior to infiltration with a molten infiltrant, e.g., via evaporation.
  • the binder may partially or completely remain in the preform during infiltration.
  • a volatile component of a binder may be removed prior to infiltration, leaving a residue in the preform.
  • Figure 1 is a graph that shows the variations of CTE with in-plane volume fraction for a theoretical model and for experimental embodiments of aluminum and copper matrix composites of the invention.
  • Figures 2a and 2b are scanning electron micrographs of an experimental embodiment of a metal matrix composite having an aluminum matrix and graphite fibers.
  • Figure 2a shows a cross- section through the X-Y plane.
  • Figure 2b shows a cross-section through the X-Z plane.
  • Figures 3a-3e illustrate formation of a preform according to an embodiment of the invention.
  • Figure 3a is a cross- sectional illustration of dispensing fibers and binder into a preform mold base portion.
  • Figure 3b shows the fibers and binder residing in the preform mold base portion.
  • Figure 3c shows the fibers and binder under compression in the preform mold.
  • Figure 3d shows binding of the fibers by the binder.
  • Figure 3e shows a completed, bound preform after removal from the preform mold.
  • Figure 4 illustrates an embodiment of a stacked preform having three individual preforms layered with two graphite foils between the preforms.
  • Figures 5a and 5b illustrate an embodiment of forming a larger preform from a combination of smaller preforms.
  • Figure 3a shows a stack of preforms without any intermediate layers.
  • Figure 3b shows the larger preform after merging of the interfaces of the smaller preforms .
  • Figure 6 illustrates an embodiment of the stacked preform of Figure 4 in a metal infiltration mold.
  • Figure 7 illustrates an embodiment of a horizontally oriented preform in a metal infiltration mold.
  • a metal matrix composite that includes random in- plane discontinuous carbon fibers and a method of forming an MMC from a pressure-formed preform can solve many problems of prior art heat sinks.
  • the composite and method can alleviate such problems as: fiber collapse during molten metal infiltration; coefficient of thermal expansion (“CTE") mismatch; heat sink weight; limits on range of CTE values; difficulty in obtaining high fiber density; limits in control of fiber orientation; machinability of a heat sink; and/or heat sink cost.
  • CTE coefficient of thermal expansion
  • molten metal infiltration is understood to mean any casting process with or without an externally applied pressure to facilitate infiltration of a mold vessel cavity that contains a preform.
  • pressure infiltration casting include, but are not limited to, pressure infiltration casting such as the Advanced Pressure Infiltration Casting (APICTM) process as described in U.S. Patent Nos. 5,322,109; 5,553,658; and 5,983,973; high throughput pressure infiltration casting as described in U.S. Patent No. 6,148,899; squeeze casting; and die-casting.
  • APICTM Advanced Pressure Infiltration Casting
  • metal is understood to mean a metal or metal alloy.
  • common metals or metal alloys are, among others, aluminum, aluminum alloys, bronze, beryllium, beryllium alloys, chromium, chromium alloys, cobalt, cobalt alloys, copper, copper alloys, gold, iron, iron alloys, steel, magnesium, magnesium alloys, nickel, nickel alloys, lead, lead alloys, copper, tin, tin alloys such as tin-bismuth and tin- lead, zinc, zinc alloys, superalloys such as International
  • Nickel 100 (IN-100) or International Nickel 718 (IN-718) . and combinations thereof.
  • molten infiltrant As used herein, “molten infiltrant”, “liquid infiltrant,” “molten metal,” or “liquid metal” is understood to mean a respective material which is at least at or above approximately its liquidus temperature.
  • fugitive is understood to mean substantially removable, i.e., removable to a great extent.
  • preform is understood to mean a fibrous, non-metallic material such as, e.g., an oxide, a boride, a nitride, a carbide or a form of carbon which is to be infiltrated with an infiltrant. Infiltration of a preform by a molten metal followed by solidification produces a metal matrix composite (MMC) .
  • MMC metal matrix composite
  • bound preform is understood to mean a preform in which the fibers are held in a more or less fixed physical relationship due to the action of a binder material .
  • preform mold vessel and “preform mold” are understood to mean any container capable of holding or applying pressure to preform materials during formation of a preform.
  • metal infiltration mold vessel and “metal infiltration mold” are understood to mean any container capable of holding a preform, and confining the preform and molten metal during metal infiltration of the preform.
  • in-plane is understood to mean the X-Y plane or the plane normal to the Z direction in an X-Y-Z coordinate system. It is also understood to mean the plane that is parallel to the bonded surface of a heat sink. This is commonly referred to as the "base” plane in the electronics industry.
  • MMC components of the invention are well suited as heat sinks for use with a variety of integrated circuit semiconductor and ceramic packaging materials. These components have relatively low density, high thermal conductivity and a coefficient of thermal expansion ("CTE") that can be controlled over a wide range to match a companion integrated circuit material. Properties of common semiconductor and packaging materials are illustrated in Table I. Table I also shows the preferred heat sink CTE ranges for a good match with each of the listed materials. Table I
  • an MMC includes random in-plane discontinuous fibers. Use of discontinuous fibers, particularly fibers less than approximately 1 mm in length, permits good control of the volume fraction of the fibers in the finished MMC. Further, for in-plane oriented fibers, substantially all of the fibers contribute to control of CTE in the X-Y plane.
  • An MMC of the invention may include fibers of a narrow or wide range of fiber lengths. In some embodiments, an MMC includes fibers as short as approximately 30 ⁇ m. In some embodiments, an MMC includes chopped fibers as long as approximately 12mm.
  • Some applications do not require control of Z-direction CTE, for example, heat sinks.
  • MMC components can be fabricated with a desired X-Y plane CTE over a very wide range by selection of a corresponding fiber volume fraction.
  • the invention provides heat sinks that can be CTE-matched to a wide variety of integrated circuit materials.
  • Fibers of various materials may be used.
  • the fibers may include silicon carbide.
  • MMC components include carbon fibers, preferably graphite fibers, in a light metal matrix.
  • Carbon fibers may, e.g., be prepared from a pitch or pan precursor.
  • Preferred embodiments employ pitch precursor fibers due to a superior elastic modulus and thermal conductivity relative to pan precursor fibers.
  • Graphite fibers have excellent mechanical and thermal properties for use in heat sinks of the invention.
  • a light metal e.g., aluminum, magnesium, or copper, or their alloys
  • heat sinks are easily machined, have excellent heat conductivity and are very lightweight.
  • An aluminum and graphite fiber MMC of the invention thus realizes the advantages of aluminum - lightweight, easy machinability and good heat conduction - in combination with the advantages of graphite fibers - high Young's Modulus, small to negative CTE, high tensile strength, high thermal conductivity and strong damping properties .
  • graphite fibers In addition to high thermal conductivity, graphite fibers have the unusual feature of a high modulus of elasticity combined with a negative coefficient of thermal expansion.
  • these high modulus, negative CTE fibers can be embedded within a matrix metal alloy to restrain the matrix from expanding to its full extent during heating.
  • the fibers further prevent excessive contraction during cooling from a processing temperature, and contribute to in-plane thermal conductivity.
  • a heat sink of the invention can be soldered or brazed to an integrated circuit package to improve heat transfer.
  • the heat sink has a CTE that is preferably chosen to be slightly greater in value than the package so that the package is under compression at room or operating temperature. Package cracking or failure of the heat sink/package bond is less likely under this condition.
  • the CTE of the heat sink is also preferably chosen in view of the temperature range to be used during attachment of the heat sink to a ceramic package.
  • a eutectic copper- silicon braze alloy requires a temperature of 780 °C during attachment of a nickel plated copper alloy matrix heat sink to a metallized ceramic package.
  • a gold-germanium braze alloy requires a temperature of 380°C during attachment of an aluminum matrix heat sink to a ceramic package.
  • the discontinuous fibers can be inorganic.
  • the discontinuous fibers are carbon-based.
  • the fibers are more preferably graphite.
  • the fibers can be chopped.
  • the fibers are less than 25 mm in length.
  • the fibers are preferably less than 1 mm in length, more preferably less than 0.75 mm.
  • the fibers are milled.
  • the fibers are ball milled.
  • the fibers graphite and have an average length of approximately 0.2 mm (200 ⁇ m) and a diameter of approximately 10 ⁇ m.
  • Theoretical considerations can assist in the selection of a fiber volume fraction that will provide a desired in-plane CTE.
  • a uniaxial laminate-based theory see, e.g., R.S. Schapery, "Thermal Expansion Coefficients of Composite Materials Based on Energy Principles," J. Composite Materials, Vol. 2, pages 380-404, (1968) approximates the CTE of a composite material as :
  • ⁇ xl is the CTE of the composite in the orthogonal direction (parallel to the 0° fibers in an uniaxial laminate, units of ppm/°K)
  • ⁇ f is the axial CTE of the fiber (units of ppm/°K)
  • m is the CTE of the matrix (e.g., 24 ppm/°K for Al and 16 ppm/°K for Cu)
  • v f is the volume fraction of fibers oriented parallel to the 0° axis
  • E f is the Young' s modulus of elasticity for graphite fiber (units of GPa) .
  • E m is the Young's modulus of elasticity for the Matrix (e.g., 69 GPa for Al and 110 GPa for Cu) .
  • Such a model should be considered a lower bound approximation for orthogonally oriented fiber reinforced metals.
  • the CTE in the 0° or X direction should equal the CTE in the 90° or Y direction.
  • the in-plane CTE is 8 ppm/°K in all in-plane directions, one can simply say that the in-plane CTE is 8 ppm/°K.
  • Fibers in an MMC can be orthogonally oriented by weaving or by stacking alternating plies of uniaxially wrapped fibers to form a laminate of orthogonally oriented layers.
  • substantially uniform in-plane orthogonal properties are obtained by use of in-plane randomly oriented discontinuous fibers.
  • very few of the fibers are oriented out of plane, i.e., in the Z axis direction.
  • Other useful fibers in the ThermalGraph® family include those sold under the developmental names DKA X and DKD X. Similar fibers are available from other suppliers, such as Conoco Carbon Fibers (Houston, Texas) .
  • Theoretical curves can be used to assist control of the CTE of a reinforced metal alloy by selecting an appropriate fiber volume fraction. For example, referring to Figure 1, a CTE in a range of 4 to 12 ppm/°K would require a corresponding fiber volume fraction between approximately 0.40 and 0.18. Similarly, a P-120 reinforced copper alloy MMC would require selection of fiber volume fraction between 0.4 and 0.14 to obtain CTE values in the same range .
  • MMC components can be prepared with a wide range of CTE values.
  • a CTE can be zero or negative in value, or can be 12 ppm/°K or greater in value.
  • the ability to densely pack fibers permits fiber volume fractions to be chosen, preferably, from within a range of approximately 0.15 to 0.60. For some applications, fiber volume fraction may lie outside this range.
  • fiber volume fraction may lie outside this range.
  • a wide range of useful properties may be obtained with a fiber volume fraction in a range at least as broad as approximately 0.15 to approximately 0.55. For example, a fiber volume fraction of 0.30 provides a CTE of approximately 8.0 ppm/°K, while a fiber volume fraction of 0.40 provides a CTE of 4.0 ppm/°K.
  • Deviation of a portion of the fibers in an MMC from in- plane orientation reduces the observed CTE from that predicted by theory. Deviations from in-plane randomness in experimental samples cause the in-plane CTE of a reinforced metal alloy to be greater than that predicted theoretically. Accordingly, empirical calibration curves can be constructed that are based on experimental data. Consequently, the CTE versus volume fraction curves are more accurate for manufacturing purposes than curves obtainable from theoretical relationships such as given in Equation 1.
  • the graph in Figure 1 shows two CTE volume fraction curves for aluminum matrix and copper matrix MMC samples prepared with P-120 graphite fiber preforms.
  • the aluminum MMC curve was obtained from CTE measurements obtained during cooling of samples from 400°C to 50°C (800°C to 50°C for the copper matrix samples) .
  • P-120 reinforced aluminum samples were prepared having fiber volume fractions in a range of 0.2 to 0.4.
  • the CTE of the resulting samples varied between 13 and 4 ppm/°K.
  • the degree of deviation from theory is at least in part due to a population of fibers with some out of plane orientation. To the extent that a fiber is oriented out of plane, the elastic restraint of the fiber on the in-plane CTE of the matrix is reduced.
  • microstructure of a sample aluminum alloy MMC with 0.30 volume fraction of P-120 fibers is shown in the scanning electron micrographs of Figures 2a and 2b.
  • the sample was prepared by blending 743 grams of DKDX fibers and 119 grams of Carbowax® polyethelyne glycol 8000 from Union Carbide Chemical and Plastics Co. (Danbury, CT) as a binder.
  • the blend was loaded into a 190.5 mm X 190.5 mm press die mold and pressed to a thickness of 31.7 mm. Subsequent to heating to a temperature in a range of 80°-100°C to liquefy the binder, cooling to 10 °C solidified the binder to produce a stable, bound preform. The bound preform was infiltrated with aluminum alloy containing 12.5% silicon and 0.4% magnesium. To obtain these micrographs, polished sections were taken from the sample MMC along the X-Y plane and along the X-Z plane. The X-Y section of Figure 2a shows a substantial number of fibers laying parallel to the X-Y plane.
  • Properties of an MMC are affected by both the volume fraction and the orientation of the fibers .
  • preferred embodiments use a fibrous preform that does not "swim" or become disturbed during the inrush of molten metal .
  • These embodiments include a preform that is stable and that does not lose its shape or fiber distribution during the infiltration process .
  • a stable preform is obtained by densely packing a preform mold. After removing the packed and bound preform from the preform mold, the preform is typically placed into a metal infiltration mold, in preferred embodiments, a steel can. Preferably, the preform completely fills the metal infiltration mold or the mold cavity of the metal infiltration mold.
  • the binder When the preform is heated, the binder may begin to release the fibers . The fibers can then relax and press against the metal infiltration mold. Some binders evaporate during heating. After the binder is removed, e.g., with the assistance of an applied vacuum, and the preform has reached a molten metal infiltration temperature, molten metal infiltration can take place .
  • woven fibers in the form of a fabric cloth are cut and loaded directly into a metal infiltration mold for subsequent pressure infiltration. Since a fabric has a discrete thickness, controlling the thickness of an MMC component formed from fabric is difficult. For volume fractions above the natural woven volume fraction of a fabric, the fabric is compressed and clamped into a mold, increasing tooling costs. Moreover, it is typically difficult to pack woven fabrics to a fiber volume fraction greater than approximately 0.45. Conversely, loading molds with fabric to a fiber volume fraction less than 0.40 can lead to non-uniform distribution of the fiber plies. Even when preform cloth plies have been well compressed into a mold, non-uniform ply loading can result in warping after removal from the mold.
  • An alternative embodiment uses a continuous fiber preform.
  • a continuous fiber preform may be fabricated by drum winding continuous fibers, and fixing the wound fibers onto a transfer sheet by applying a fugitive binder.
  • plies can be stacked with orthogonal orientations, or more mixed orientations, for example, including plies oriented at 45° to other plies.
  • These embodiments can include fiber volume fractions of approximately 0.55 to 0.6 or more.
  • Another alternative preform material includes a paper-like product produced from chopped discontinuous fibers.
  • the material includes a fugitive binder to provide stability and facilitate handling.
  • the fibers in the "paper” are randomly orientated in the X-Y plane. This material can be compressed to a desired fiber volume fraction and further stabilized with additional binder.
  • a preform of the invention provides substantially uniform fiber distribution after molten metal infiltration.
  • the preform is typically prepared by compressing fibers and a binder in a preform mold.
  • the fibers are discontinuous.
  • the fibers and binder usually are mixed, then compressed at a pressure that is greater than the molten alloy breakthrough pressure for the finished preform.
  • the binder Prior to metal infiltration, the binder maintains the compressed configuration of the fibers in the preform so the preform can be removed from the preform mold and placed in a metal infiltration mold.
  • a bound preform may be stored for some time prior to metal infiltration. Preferably, the bound preforms are stored below room temperature .
  • the binder is often removed from the preform while the preform resides in the metal infiltration mold. Under the constraints of the metal infiltration mold, the preform can maintain its compressed fiber configuration. Molten metal is then infiltrated into the preform. Because the fiber configuration remains in its compressed state, it is substantially undisturbed during infiltration of molten metal at the molten metal breakthrough pressure, and proper in-plane orientation of the fibers is maintained.
  • the in-plane distribution of fibers in the preform mold is enhanced prior to compression and fixation with a binder.
  • the preform mold can be agitated, such as by vibration, prior to compression. Vibration may also break up clumps, or "hair balls", of fiber.
  • the compression of the fibers and the binder also serves to enhance the in-plane orientation of the fibers, as well as increase the volume fraction of fibers in the preform.
  • Some embodiments utilize thin sheets of paper-like or felt- like material formed from random in-plane oriented fibers.
  • a sheet is produced with a volume fraction in a range of approximately 0.05 to approximately 0.20. The sheets may be weighed to select a proper amount for a desired preform. The sheets may then be placed in a preform mold and compressed to obtain a final desired fiber volume fraction in the preform.
  • a binder material can be employed to form and maintain a preform.
  • a binder material is generally required to maintain fibers in a desired orientation and state of compression.
  • water may be a binder which is set via freezing.
  • Solid forms of polyethylene glycol (“PEG”) may be a binder as well as acrylic.
  • Solid binder materials usually -are heated to approximately or above their melting point, then cooled to solidify.
  • PEG material is Carbowax® polyethylene glycol 8000 from Union Carbide Chemical and Plastics Co. (Danbury, CT) , which is liquefied at approximately 80°-100°C.
  • Some binders are fully removed prior to molten metal infiltration.
  • Other binder materials partially or fully remain during and after molten metal infiltration.
  • a phenolic-based binder may have a volatile component removed prior to molten metal infiltration.
  • the volatile component leaves in vapor form, leaving behind a carbon-based residue.
  • non-binder organic materials may also escape from the preform during evaporation of some or all of a binder material .
  • Figures 3a through 3e illustrate in cross-section one embodiment of the formation of a preform 10.
  • a material dispenser 22 randomly dispenses discontinuous fibers 11 and a binder 12 into a preform mold base portion 20.
  • the binder 12 can be dispensed as discontinuous particles as shown, or can be mixed with the fibers by other means.
  • the fibers can be coated with binder subsequently or prior to distribution of the fibers into the preform mold.
  • One or more dispensers may be employed. In other embodiments, fibers and binder are dispensed from different dispensers .
  • the preform mold base portion 20 often is agitated.
  • the base portion 20 can be vibrated after filling with fibers 11 and binder 12.
  • agitation is applied continuously during the dispensing of the fibers and binder into the preform mold.
  • a preform mold cap portion 21 is placed in contact with the fibers 11 and binder 12. Pressure is applied via the preform mold cap portion 21 to the mixture of fibers 11 and binder 12 to compress the mixture at a pressure greater than the breakthrough pressure required to infiltrate the formed preform with the appropriate molten metal.
  • the binder 12 serves to fix the configuration of fibers obtained in this compressed state by adhering neighboring fibers 11 to one another to produce the preform 10 as shown in Figure 3d.
  • Figure 3e shows the preform 10 after it is removed from the preform mold base portion 20.
  • in a tumble mill to uniformly mix the fibers and binder.
  • the mixture then may be redispersed in a rotary brush mill to untangle the fiber clusters. A measured portion of the mixture is selected by weighing for production of an MMC of a desired size and fiber volume fraction.
  • the weighed portion of fiber and PEG binder is placed in a preform mold base portion. After leveling the mixture by vibration, the preform mold is closed and the preform is compressed to a predetermined volume to obtain the desired volume fraction of fibers in the complete preform.
  • metals and metal alloys can be used in the invention depending on the particular application.
  • Aluminum, copper and magnesium are preferred.
  • silicon it is desirable to add silicon to the metal to reduce the reactivity of the metal with graphite, which undesirably forms aluminum carbide.
  • an MMC formed from 6061 aluminum alloy with 0.45 volume fraction of graphite fibers and had approximately 4.0% carbide formation after pressure infiltration casting. Fabrication of an MMC from an aluminum alloy having approximately 7.0% by weight silicon, reduced carbide formation to approximately 0.5%. Using 12.5% silicon in the aluminum alloy, further reduced the carbide formation to approximately 0.3%.
  • the alloy includes at least approximately 7% by weight silicon, and more preferably approximately 12.5% by weight silicon.
  • the eutectic composition for an aluminum-silicon alloy has 12.5% silicon.
  • addition of silicon reduces the melting point of the alloy. This, in turn, further decreases the kinetics of carbide formation, provided that metal infiltration temperatures also are reduced.
  • the matrix alloy should also be able to withstand micro- scale deformation that can occur during thermal cycling.
  • an MMC experiences large temperature cycles during use.
  • Micro- deformation during thermal cycling can cause thermal ratcheting, i.e., a change in dimension of the MMC after each thermal cycle .
  • An accumulation of dimensional changes can lead to damage, for example, of an electronic assembly attached to an MMC heat sink. It is thus desirable to limit deformation over the use temperature ranges of an MMC, such as from approximately -30 °C to approximately 150 °C.
  • the metal matrix alloy can be hardened.
  • magnesium is added to aluminum.
  • the magnesium provides an age hardenable aluminum alloy due to formation of precipitates during cooling from, for example, a brazing temperature.
  • the precipitation hardened matrix suffers from less plastic deformation during thermal cycling.
  • An aluminum-based MMC of the invention includes 2.0% by weight or more magnesium in the alloy.
  • a preferred embodiment includes magnesium in a range of approximately 0.1% to approximately 1.0%. More preferred embodiments include magnesium in a range of approximately 0.2% to 0.5%, or approximately 0.3% to 0.4%.
  • the aluminum alloy can contain minor impurities, for example, iron, manganese and titanium.
  • chromium is often included in the alloy.
  • the chromium reacts with carbon in the fibers to form chromium carbide at the fiber-metal interface, which aids the bonding between the alloy and the fibers.
  • One embodiment includes approximately 5.0% by weight or more chromium in the alloy.
  • a preferred embodiment includes chromium in a range of approximately 0.3% to 5.0%.
  • a more preferred embodiment includes chromium in a range of approximately 0.3% to 2.0%.
  • Other more preferred embodiments include chromium in a range of approximately 0.5% to 1.5%, or approximately 0.7% to 1.0%.
  • Another embodiment includes a copper alloy having improved yield strength through addition of zirconium.
  • Zirconium promotes solid solution hardening and reduces thermal ratcheting.
  • a preferred embodiment includes zirconium in a range of approximately 0.1% to 2.0% by weight.
  • a more preferred embodiment includes zirconium in a range of approximately 0.1% to 1.0%.
  • Other more preferred embodiments include zirconium in a range of approximately 0.1% to 0.5%, or approximately 0.12% to 0.3%. Alloy additions, such as those described above, have a minimal effect on the thermal conductivity of an alloy.
  • methods of the invention overcome these difficulties by providing a preform which has been compressed at a pressure above that experienced during infiltration casting. For example, by pressing preforms to a pressure greater than the capillary breakthrough pressure, activating a binder to constrain the preform, loading the fiber and binder into a fixed volume mold, removing the binder by evacuation and heating just prior to pressure infiltration casting, a metal matrix composite can be manufactured free of breakthrough defects and at a controlled volume fraction reinforcement.
  • Preforms of the invention can be infiltrated individually or collectively.
  • Figure 4 illustrates an embodiment of multiple preforms prepared for infiltration.
  • the preforms 10 are layered with separator sheets 15, for example, graphite foil sheets, to permit production of more than one MMC component during one infiltration cycle.
  • the separator sheets may also be, e.g., slices of graphite, graphite coated steel sheets, or colloidal graphite coated sheets. The separator sheets ease separation of the MMC components after cooling of the metal.
  • one or more preforms 10 are placed adjacent to each other without separator sheets. Hence, surfaces of the preforms 10 are in direct contact .
  • the binder is removed, for example, by heating.
  • the contacted surfaces of the preforms 10 can merge with one another and permit formation of an effectively larger preform and ultimately larger MMC component .
  • a preform or stack of preforms can be infiltrated with a molten metal by any method known to one skilled in the art.
  • a stack of preforms 10 layered with separator sheets 15 is placed in a metal infiltration vessel 30.
  • a filter 33 is placed on top of the stack to prevent premature infiltration of the preform, especially if the preform is evacuated prior to introduction of the metal.
  • a filter for example, use of gated top plates or caps.
  • a preform 10 is horizontally positioned in a metal infiltration vessel 30.
  • a cap 33 with gates 39,,, for admission of molten metal, is placed on the preform 10.
  • the cap may be held in place by means known in the art which includes welding.
  • the preform (s) typically need to be isolated in a confined space so that upon removal of the binder, the fibers maintain their position, orientation and compactness .
  • the mold release agent preferably is one or more layers of colloidal carbon, e . g.
  • colloidal graphite or boron nitride which is dispersed in a suitable volatile vehicle.
  • a suitable volatile vehicle such as boron nitride or graphite.
  • other ceramic slurry coatings may be used.
  • a slurry of zirconium oxide in a slightly acidic vehicle sold under the trade name ZircwashTM may be used.
  • Other parting compounds may be used as mold release agents or washes such as boron nitride or graphite foil.
  • a preform is tightly loaded into a molten metal infiltration vessel.
  • the preform is heated to remove binder via evaporation.
  • compressive stresses stored in the preform cause the preform to relax against the walls of the vessel . Since the preform is constrained by the walls of the vessel, the vessel walls now maintain a compressive stress on the preform that is greater than the breakthrough pressure of the molten metal.
  • the process described in U.S. Patent No. 6,148,899 is used to infiltrate molten metal into a preform. Briefly, liquid metal is transferred by vacuum siphon into the metal infiltration mold vessel which is under reduced pressure. The mold vessel is placed in an autoclave and pressurized to approximately 60 atm using nitrogen gas, forcing the molten metal into the preform.
  • the mold vessel then is contacted with tin-bismuth at the eutectic composition. Heat from the vessel causes the tin- bismuth to melt. This heat transfer process increases the solidification rate of the molten metal in the preform and assists directional solidification to help eliminate shrinkage porosity.
  • the MMC component After cooling, the MMC component is removed from the vessel.
  • the MMC component can than receive other processing, for example, machining into a final desired shape for use as a heat sink, or plating in preparation for some types of brazing.

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Abstract

La présente invention concerne des procédés et des matériaux pour préparer des composants composites à matrice métallique (MMC) qui présentent un faible poids, une bonne conductivité thermique et un coefficient dans le plan de dilatation thermique pouvant être commandé. Un mode de réalisation de cette invention concerne un matériau composite à matrice métallique qui comprend un alliage métallique et des fibres discontinues se trouvant dans le plan de manière aléatoire. Dans certains modes de réalisation, l'alliage métallique comprend de l'aluminium, du cuivre ou du magnésium. Dans certains modes de réalisation, le matériau composite à matrice métallique comprend des additifs qui permettent un durcissement en solution. Dans d'autres modes de réalisation, le matériau composite à matrice métallique comprend des additifs qui permettent un durcissement par précipitation. Un autre mode de réalisation de cette invention concerne un procédé pour produire un matériau composite à matrice métallique. Ce procédé consiste à mettre en contact des fibres discontinues se trouvant dans le plan de manière aléatoire avec un liant, puis à comprimer les fibres discontinues se trouvant dans le plan de manière aléatoire et le liant afin de former une préforme liée. Cette préforme est comprimée à une pression qui est supérieure à la pression de percée capillaire de métal fondu de la préforme liée. La préforme liée est ensuite placée dans un moule, on y infiltre un produit d'infiltration fondu, puis ce produit d'infiltration fondu est refroidi afin de former le matériau composite à matrice métallique.
PCT/US2002/015175 2001-05-15 2002-05-14 Materiau composite a matrice metallique renforcee par des fibres de carbone discontinues WO2004015150A2 (fr)

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Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016076991A3 (fr) * 2014-11-13 2016-07-07 Baker Hughes Incorporated Composites renforcés, procédés de fabrication et articles obtenus à partir de ceux-ci
US9745451B2 (en) 2014-11-17 2017-08-29 Baker Hughes Incorporated Swellable compositions, articles formed therefrom, and methods of manufacture thereof
US9840887B2 (en) 2015-05-13 2017-12-12 Baker Hughes Incorporated Wear-resistant and self-lubricant bore receptacle packoff tool
US9963395B2 (en) 2013-12-11 2018-05-08 Baker Hughes, A Ge Company, Llc Methods of making carbon composites
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US10300627B2 (en) 2014-11-25 2019-05-28 Baker Hughes, A Ge Company, Llc Method of forming a flexible carbon composite self-lubricating seal
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US10344559B2 (en) 2016-05-26 2019-07-09 Baker Hughes, A Ge Company, Llc High temperature high pressure seal for downhole chemical injection applications
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US11097511B2 (en) 2014-11-18 2021-08-24 Baker Hughes, A Ge Company, Llc Methods of forming polymer coatings on metallic substrates

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6605316B1 (en) 1999-07-31 2003-08-12 The Regents Of The University Of California Structures and fabrication techniques for solid state electrochemical devices
US7461684B2 (en) 2002-08-20 2008-12-09 The Ex One Company, Llc Casting process and articles for performing same
EP1403923A1 (fr) * 2002-09-27 2004-03-31 Abb Research Ltd. Dispositif semi-conducteur dans un empaquetage à pression
US7368176B2 (en) 2003-01-23 2008-05-06 H.C. Starck Inc. Pre-plating surface treatments for enhanced galvanic-corrosion resistance
US20050118482A1 (en) * 2003-09-17 2005-06-02 Tiax Llc Electrochemical devices and components thereof
US20060086434A1 (en) 2004-10-22 2006-04-27 Metal Matrix Cast Composites, Llc Spray deposition apparatus and methods for metal matrix composites
WO2006083375A2 (fr) * 2004-11-29 2006-08-10 North Carolina State University Mousse metallique composite et procedes de preparation de celle-ci
AU2005327164B2 (en) * 2004-11-30 2010-12-02 The Regents Of The University Of California Braze system with matched coefficients of thermal expansion
RU2389110C2 (ru) * 2004-11-30 2010-05-10 Члены Правления Университета Калифорнии Структура уплотненного узла соединения для электрохимического устройства
AU2005327925B2 (en) * 2004-11-30 2011-01-27 The Regents Of The University Of California Joining of dissimilar materials
KR20060090523A (ko) * 2005-02-07 2006-08-11 삼성전자주식회사 표시 장치용 배선 및 상기 배선을 포함하는 박막트랜지스터 표시판
TWI305131B (en) * 2005-09-08 2009-01-01 Ind Tech Res Inst Heat dissipation device and composite material with high thermal conductivity
US8343686B2 (en) * 2006-07-28 2013-01-01 The Regents Of The University Of California Joined concentric tubes
DE102006043163B4 (de) 2006-09-14 2016-03-31 Infineon Technologies Ag Halbleiterschaltungsanordnungen
US20080128067A1 (en) * 2006-10-08 2008-06-05 Momentive Performance Materials Inc. Heat transfer composite, associated device and method
US8043703B2 (en) * 2007-09-13 2011-10-25 Metal Matrix Cast Composites LLC Thermally conductive graphite reinforced alloys
US7916484B2 (en) * 2007-11-14 2011-03-29 Wen-Long Chyn Heat sink having enhanced heat dissipation capacity
US8132493B1 (en) * 2007-12-03 2012-03-13 CPS Technologies Hybrid tile metal matrix composite armor
KR20100111313A (ko) * 2008-02-04 2010-10-14 더 리전트 오브 더 유니버시티 오브 캘리포니아 고온 전기화학 소자용 cu-기초 서멧
MY147805A (en) 2008-04-18 2013-01-31 Univ California Integrated seal for high-temperature electrochemical device
US8081467B2 (en) * 2008-08-20 2011-12-20 Sri Hermetics Inc. Electronics package including heat sink in the housing and related methods
JP5335339B2 (ja) * 2008-09-11 2013-11-06 株式会社エー・エム・テクノロジー 黒鉛一金属複合体とアルミニウム押出材の組合せからなる放熱体。
TWI403576B (zh) * 2008-12-31 2013-08-01 Ind Tech Res Inst 含碳金屬複合材料及其製作方法
FR2951047B1 (fr) * 2009-10-07 2011-12-09 Valeo Etudes Electroniques Module d'electronique de puissance et de procede de fabrication de ce module
WO2011153482A1 (fr) * 2010-06-04 2011-12-08 Triton Systems, Inc. Préforme de fibres courtes discontinues et billette d'aluminium renforcé de fibres et leurs procédés de fabrication
US9073116B2 (en) 2012-06-11 2015-07-07 National Oilwell Varco, L.P. Carbon foam metal matrix composite and mud pump employing same
US20140087171A1 (en) * 2012-09-21 2014-03-27 Vanguard Space Technologies, Inc. Carbon Fiber Reinforced Eutectic Alloy Materials and Methods of Manufacture
CN103710649B (zh) * 2014-01-16 2015-08-19 昌吉市银杏新材料科技有限公司 一种碳纤维增强钛合金复合材料及其制备方法
CN105296898B (zh) * 2015-09-23 2017-06-06 华南理工大学 一种金属纤维多孔骨架复合相变材料热沉及其制造方法
CN107245678B (zh) * 2017-04-12 2019-04-26 上海伊祥机械制造有限公司 一种镁合金
CN107058915B (zh) * 2017-04-20 2019-04-09 湖南中南智造新材料协同创新有限公司 一种含铬熔渗粉及其在铜铬硅改性炭/陶摩擦材料中的应用
JP6477800B2 (ja) * 2017-08-02 2019-03-06 三菱マテリアル株式会社 ヒートシンク

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3918141A (en) * 1974-04-12 1975-11-11 Fiber Materials Method of producing a graphite-fiber-reinforced metal composite
FR2546878A1 (fr) * 1983-05-31 1984-12-07 Slonina Jean Pierre Plaque support d'un substrat ceramique, leger, a forte conductivite thermique et coefficient de dilatation adapte pour toutes applications dans le domaine electronique
US5347426A (en) * 1988-09-13 1994-09-13 Pechiney Recherche Electronic device including a passive electronic component
US5437921A (en) * 1990-10-09 1995-08-01 Mitsubishi Denki Kabushiki Kaisha Electronic components mounting base material
JPH11140559A (ja) * 1997-11-05 1999-05-25 Furukawa Electric Co Ltd:The 複合材料及びその製造方法
JP2001089834A (ja) * 1999-09-22 2001-04-03 Furukawa Electric Co Ltd:The 高信頼性アルミニウム基複合板

Family Cites Families (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3936277A (en) * 1970-04-09 1976-02-03 Mcdonnell Douglas Corporation Aluminum alloy-boron fiber composite
JPS4918891B1 (fr) * 1970-12-25 1974-05-14
US3770488A (en) * 1971-04-06 1973-11-06 Us Air Force Metal impregnated graphite fibers and method of making same
US3860443A (en) * 1973-03-22 1975-01-14 Fiber Materials Graphite composite
US3953647A (en) * 1973-10-05 1976-04-27 United Technologies Corporation Graphite fiber reinforced metal matrix composite
JPS5253720A (en) * 1975-10-29 1977-04-30 Hitachi Ltd Non-orientated cu-carbon fiber compoite and its manufacturing method
US4223075A (en) * 1977-01-21 1980-09-16 The Aerospace Corporation Graphite fiber, metal matrix composite
US4341823A (en) * 1981-01-14 1982-07-27 Material Concepts, Inc. Method of fabricating a fiber reinforced metal composite
US4376803A (en) * 1981-08-26 1983-03-15 The Aerospace Corporation Carbon-reinforced metal-matrix composites
JPS5839758A (ja) * 1981-09-03 1983-03-08 Toyota Motor Corp 炭素質材−金属複合材料の製造方法
US4469757A (en) * 1982-05-20 1984-09-04 Rockwell International Corporation Structural metal matrix composite and method for making same
US4617979A (en) * 1984-07-19 1986-10-21 Nikkei Kako Kabushiki Kaisha Method for manufacture of cast articles of fiber-reinforced aluminum composite
US4578287A (en) * 1984-10-09 1986-03-25 The United States Of America As Represented By The Secretary Of The Navy Process for producing graphite fiber/aluminum-magnesium matrix composites
JPS61166934A (ja) * 1985-01-17 1986-07-28 Toyota Motor Corp 複合材料製造用短繊維成形体及びその製造方法
EP0223478B1 (fr) * 1985-11-14 1992-07-29 Imperial Chemical Industries Plc Matériau composite renforcé par fibres et comportant une matrice métallique
US4738999A (en) * 1986-03-31 1988-04-19 Lord Corporation Fiber reinforced composites
GB8713449D0 (en) * 1987-06-09 1987-07-15 Alcan Int Ltd Aluminium alloy composites
US4853294A (en) * 1988-06-28 1989-08-01 United States Of America As Represented By The Secretary Of The Navy Carbon fiber reinforced metal matrix composites
US5106702A (en) * 1988-08-04 1992-04-21 Advanced Composite Materials Corporation Reinforced aluminum matrix composite
US5085945A (en) * 1988-11-07 1992-02-04 Aluminum Company Of America Production of metal matrix composites reinforced with polymer fibers
US5040588A (en) * 1988-11-10 1991-08-20 Lanxide Technology Company, Lp Methods for forming macrocomposite bodies and macrocomposite bodies produced thereby
US5244748A (en) * 1989-01-27 1993-09-14 Technical Research Associates, Inc. Metal matrix coated fiber composites and the methods of manufacturing such composites
US5108964A (en) * 1989-02-15 1992-04-28 Technical Ceramics Laboratories, Inc. Shaped bodies containing short inorganic fibers or whiskers and methods of forming such bodies
US5578255A (en) * 1989-10-26 1996-11-26 Mitsubishi Chemical Corporation Method of making carbon fiber reinforced carbon composites
US5093050A (en) * 1989-11-17 1992-03-03 Laboratorium Fur Experimentelle Chirurgie Method for producing oriented, discontinuous fiber reinforced composite materials
DE69115891T2 (de) * 1990-02-22 1996-08-14 New Millennium Composites Ltd Faserverstärkte verbundwerkstoffe
US5120495A (en) * 1990-08-27 1992-06-09 The Standard Oil Company High thermal conductivity metal matrix composite
US5143795A (en) * 1991-02-04 1992-09-01 Allied-Signal Inc. High strength, high stiffness rapidly solidified magnesium base metal alloy composites
JPH04304333A (ja) * 1991-03-25 1992-10-27 Aluminum Co Of America <Alcoa> アルミニウムまたはアルミニウム合金をマトリクスとする複合材料およびその強化材とマトリクスとの濡れおよび結合を向上させる方法
DE69219552T2 (de) * 1991-10-23 1997-12-18 Inco Ltd Mit Nickel überzogene Vorform aus Kohlenstoff
US5384087A (en) * 1992-04-06 1995-01-24 Ametek, Specialty Metal Products Division Aluminum-silicon carbide composite and process for making the same
US5313098A (en) * 1993-04-08 1994-05-17 Alliedsignal Inc. Packaging arrangement for power semiconductor devices
US5322109A (en) * 1993-05-10 1994-06-21 Massachusetts Institute Of Technology, A Massachusetts Corp. Method for pressure infiltration casting using a vent tube
US5672433A (en) * 1993-06-02 1997-09-30 Pcc Composites, Inc. Magnesium composite electronic packages
US5407495A (en) * 1993-09-22 1995-04-18 Board Of Regents Of The University Of Wisconsin System On Behalf Of The University Of Wisconsin-Milwaukee Thermal management of fibers and particles in composites
US5410796A (en) * 1993-10-06 1995-05-02 Technical Research Associates, Inc. Copper/copper alloy and graphite fiber composite and method
US5486223A (en) * 1994-01-19 1996-01-23 Alyn Corporation Metal matrix compositions and method of manufacture thereof
US5669059A (en) * 1994-01-19 1997-09-16 Alyn Corporation Metal matrix compositions and method of manufacturing thereof
US5834115A (en) * 1995-05-02 1998-11-10 Technical Research Associates, Inc. Metal and carbonaceous materials composites
US5914156A (en) * 1995-05-02 1999-06-22 Technical Research Associates, Inc. Method for coating a carbonaceous material with a molybdenum carbide coating
US5573607A (en) * 1995-05-06 1996-11-12 Millennium Materials, Inc. Metal matrix composites of aluminum, magnesium and titanium using silicon borides
GB2301545B (en) * 1995-06-02 1999-04-28 Aea Technology Plc The manufacture of composite materials
US5814408A (en) * 1996-01-31 1998-09-29 Applied Sciences, Inc. Aluminum matrix composite and method for making same
US5664616A (en) * 1996-02-29 1997-09-09 Caterpillar Inc. Process for pressure infiltration casting and fusion bonding of a metal matrix composite component in a metallic article
US5846356A (en) * 1996-03-07 1998-12-08 Board Of Trustees Operating Michigan State University Method and apparatus for aligning discontinuous fibers
DE69708362T2 (de) * 1996-03-29 2002-08-22 Hitachi Metals, Ltd. Verfahren zur Herstellung von Aluminium-Verbundmaterial mit niedrigem thermischen Ausdehnungskoeffizient und hoher Wärmeleitfähigkeit
US5863467A (en) * 1996-05-03 1999-01-26 Advanced Ceramics Corporation High thermal conductivity composite and method
US5712014A (en) * 1996-07-01 1998-01-27 Alyn Corporation Metal matrix compositions for substrates used to make magnetic disks for hard disk drives
US5720246A (en) * 1996-07-23 1998-02-24 Minnesota Mining And Manufacturing Continuous fiber reinforced aluminum matrix composite pushrod
JP3391636B2 (ja) * 1996-07-23 2003-03-31 明久 井上 高耐摩耗性アルミニウム基複合合金
US5998733A (en) * 1997-10-06 1999-12-07 Northrop Grumman Corporation Graphite aluminum metal matrix composite microelectronic package
US6148899A (en) * 1998-01-29 2000-11-21 Metal Matrix Cast Composites, Inc. Methods of high throughput pressure infiltration casting
US6776219B1 (en) * 1999-09-20 2004-08-17 Metal Matrix Cast Composites, Inc. Castable refractory investment mold materials and methods of their use in infiltration casting
JP3721393B2 (ja) * 2000-04-28 2005-11-30 国立大学法人広島大学 多孔質プリフォーム、金属基複合材料及びそれらの製造方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3918141A (en) * 1974-04-12 1975-11-11 Fiber Materials Method of producing a graphite-fiber-reinforced metal composite
FR2546878A1 (fr) * 1983-05-31 1984-12-07 Slonina Jean Pierre Plaque support d'un substrat ceramique, leger, a forte conductivite thermique et coefficient de dilatation adapte pour toutes applications dans le domaine electronique
US5347426A (en) * 1988-09-13 1994-09-13 Pechiney Recherche Electronic device including a passive electronic component
US5437921A (en) * 1990-10-09 1995-08-01 Mitsubishi Denki Kabushiki Kaisha Electronic components mounting base material
JPH11140559A (ja) * 1997-11-05 1999-05-25 Furukawa Electric Co Ltd:The 複合材料及びその製造方法
JP2001089834A (ja) * 1999-09-22 2001-04-03 Furukawa Electric Co Ltd:The 高信頼性アルミニウム基複合板

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 1999, no. 10, 31 August 1999 (1999-08-31) -& JP 11 140559 A (FURUKAWA ELECTRIC CO LTD:THE), 25 May 1999 (1999-05-25) *
PATENT ABSTRACTS OF JAPAN vol. 2000, no. 21, 3 August 2001 (2001-08-03) -& JP 2001 089834 A (FURUKAWA ELECTRIC CO LTD:THE), 3 April 2001 (2001-04-03) *

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US10315922B2 (en) 2014-09-29 2019-06-11 Baker Hughes, A Ge Company, Llc Carbon composites and methods of manufacture
US10480288B2 (en) 2014-10-15 2019-11-19 Baker Hughes, A Ge Company, Llc Articles containing carbon composites and methods of manufacture
US9962903B2 (en) 2014-11-13 2018-05-08 Baker Hughes, A Ge Company, Llc Reinforced composites, methods of manufacture, and articles therefrom
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US9840887B2 (en) 2015-05-13 2017-12-12 Baker Hughes Incorporated Wear-resistant and self-lubricant bore receptacle packoff tool
US10125274B2 (en) 2016-05-03 2018-11-13 Baker Hughes, A Ge Company, Llc Coatings containing carbon composite fillers and methods of manufacture
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US20030024611A1 (en) 2003-02-06

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