USH1332H - Thermal conductive material - Google Patents

Thermal conductive material Download PDF

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Publication number
USH1332H
USH1332H US07/827,142 US82714292A USH1332H US H1332 H USH1332 H US H1332H US 82714292 A US82714292 A US 82714292A US H1332 H USH1332 H US H1332H
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thermal conductivity
fiber
resin
fibers
vacuum
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US07/827,142
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Clifford K. Deakyne
John G. Lavin
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DuPont Polymers Inc
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EI Du Pont de Nemours and Co
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Priority to US07/827,142 priority Critical patent/USH1332H/en
Assigned to E. I. DU PONT DE NEMOURS AND COMPANY A CORPORATION OF DE reassignment E. I. DU PONT DE NEMOURS AND COMPANY A CORPORATION OF DE ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: DEAKYNE, CLIFFORD K., LAVIN, JOHN G.
Priority to TW81106383A priority patent/TW230256B/zh
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Assigned to DUPONT POLYMERS, INC. reassignment DUPONT POLYMERS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: E. I. DU PONT DE NEMOURS AND COMPANY
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20—Conductive material dispersed in non-conductive organic material
    • H01B1/24—Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00—Use of ingredients characterised by shape
    • C08K7/02—Fibres or whiskers
    • C08K7/04—Fibres or whiskers inorganic
    • C08K7/06—Elements

Definitions

  • This invention relates to thermally conductive material and, more particularly, it relates to a carbon fiber reinforced resin matrix for use as a strong, structurally stable thermal conductive material.
  • Thermally Conductive Polymer Compositions D. M. Bigg, Polymer Composites, June 1986, Vol. 7, No. 3, pp. 125-140.
  • the fillers include spherical particles of various metals, glass or carbon black, non-spherical metal or ceramic particles and aluminum fibers. Bigg teaches that the thermal conductivity of the composite is largely determined by the resin and that in the case of fibers, the most important variables influencing composite conductivity are fiber volume fraction and fiber 1/d in the actual composite.
  • a composite material has been developed to complement the move toward miniaturization of electrical devices which exhibits high strength, structural stability and has improved thermal conductivity capability. More particularly, if a laminate is made with continuous fibers all oriented in the same direction (a "unidirectional" laminate), the thermal conductivity along the fiber axis will be determined by the "rule of mixtures". That is, it will be equal to the area of fiber times the fiber conductivity plus the area of resin times the resin conductivity. The thermal conductivity along the axis perpendicular to the fibers, however, will be dominated by the resin, and will typically be a small multiple of the resin conductivity.
  • discontinuous fibers are more complex; however, it may generally be said that the thermal conductivity of a laminate along any axis is strongly dependent upon the fraction of fibers oriented in the direction of that axis. In any practical application, the most important axis will be the one with the lowest thermal conductivity, since this will limit the flow of heat in the part. Thus, in the case of planar samples, the limiting thermal conductivity will be through-the-plane.
  • This material comprises 10 to 70% by weight carbon fiber and preferably about 15 to about 60% by weight carbon fiber, the balance being made up of a resin.
  • the ratio of the thermal conductivity of the composite (K c ) to the thermal conductivity of the resin (K p ) is above 10.
  • the carbon fibers are preferably made from a mesophase pitch by the process described in U.S. Pat. No. 4,861,653 which is incorporated by reference.
  • the fibers are in a three-dimensional arrangement, each fiber has a lamellar microstructure, and there is a distribution of diameters among the fibers ranging from about 1 micrometer to more than 10 micrometers and a number average less than 8 micrometers.
  • the fibers also are heat treated in an inert atmosphere to a temperature above 1600° C., more preferably above 2400° C.
  • Suitable resinous materials which may be used as the resin include, but are not limited to, commercially available thermoplastic and thermosetting resins.
  • Suitable processes for making useful parts include, but are not limited to, injection molding, compression molding, melt casting and blow molding.
  • the fibers described above may be incorporated into composite material at much higher volume fractions than fibers described in the prior art.
  • the thermal conductivity in the critical through-the-plane test is above about 10 (BTU)(in)/(ft 2 )(hr)(°F.) as measured on the axis of lowest thermal conductivity for the composite material or articles formed from the material.
  • the thermal conductivity performance of these articles is attributed to maintaining the three-dimensional arrangement of the fibers during forming so that at least a fraction of the fibers are oriented in any one of the axes through article.
  • FIG. 1 is a composite article formed from the material of this invention.
  • FIG. 2 is a photomicrograph of the material of this invention.
  • the component structure 10 is an injection molded motor housing made from resin reinforced with a three dimensional arrangement of mesophase pitch based discontinuous carbon fibers.
  • FIG. 2 a structure is displayed showing a resin filled with a three-dimensional fiber structure with fibers of varying lengths and dimensions. More particularly, FIG. 2 is a photograph taken on a Scanning Electron Microscope at 1000 ⁇ magnification. It is a view of the fracture surface of a tensile test bar. The bar was cut from an injection molded plaque made from the material of this invention. The resin is principally polyethylene terephthalate (PET).
  • PET polyethylene terephthalate
  • the fibers 12 are seen in a three-dimensional arrangement as cylindrical or elliptical rods of varying size.
  • the fine threads 14 are polymer. It will be observed that the fibers are oriented in many directions; indeed, they appear to be oriented quite randomly so that at least a fraction on the fibers are oriented in any one of the axes through the structure.
  • One way the composite material is made is by feeding the resin and a carbon fiber batt made according to the disclosure in above-noted patent into a single screw extruder and extruding the composite material as a strand which is then chopped and collected. The chopped strand is then used in various molding processes to form articles having high thermal conductivity.
  • Another way to form the composite material of this invention is by grinding a planar laminate into small pieces and recompressing them or forcing a very high viscosity molten resin perpendicular to the plane of a fiber assembly and moving some fibers into the third dimension.
  • T.C. Thermal conductivity
  • the composite material exhibits a three dimensional arrangement of fibers within the resin matrix as estimated from percent shrinkage data in the x, y, and z coordinate axes directions from mold size to the final part. More particularly, essentially equal percent shrinkage of the final part in the x, y, and z directions indicates three dimensional isotropic fiber reinforcement while percent shrinkage of the final part that varies by several orders of magnitude between directions suggests highly oriented reinforcing fibers.
  • a multiple six layer sandwich consisting of alternate layers of 5-mil thick Du Pont TeflonTM PFA fluorocarbon polymer film and mesophased based graphite fiber mat, made according to the procedure described in U.S. Pat. No. 4,861,653, was formed into a 7" ⁇ 7" mold of a standard compression molding machine. This multilayer sandwich was cold compressed in order to fit the fiber and film into the cavity for one minute at 1 ton, 2 ton and 2.5 ton pressures. The mold was then put into a hot press at 740° F. and the mass consolidated according to the following schedule:
  • a sample was made by compression molding a granulated molding compound.
  • the molding compound was made by interleaving equal weights of a FR-PET film (RyniteTM FR by Du Pont) (3.5 mil) and a pitch based carbon fiber mat heat-treated at 2600° C. at about 220 g/m 2 with a total of about 15 plies of mat.
  • This stack was vacuum bagged between plates and consolidated by heating to 570° F. under contact pressure, only then applying 500 psi at temperature for 10 minutes, then cooling under pressure.
  • the plate was then ground into particles using an I.M.S. model 3144-SP granulator machine with a 3/8" screen.
  • a 6" ⁇ 6" mold was filled with 120 g of predried granules with essentially random orientation. The mold was heated to 590° F. under contact pressure for 20 minutes, then 350 psi was applied for 10 minutes, then cooled under pressure. Thermal conductivity was measured according to ASTM F-433 on the axis of lowest thermal conductivity of the sample. This yielded a thermal conductivity of 47.6 (BTU)(in)/(ft 2 )(hr)(°F.) at 50° C. and 63.2 (BTU)(in)/(ft 2 )(hr)(F) at 150° C.
  • the same granulated material was also injection molded using an "8 oz. Van Dooran” lab injection molder.
  • a "gentle” screw design was used to maintain fiber length.
  • a mold with 3" ⁇ 5" plaques was used and subsequently 2" diameter disc was cut and thermal conductivity was measured according to ASTM F-433 on the axis of lowest thermal conductivity of the disc. This yielded a thermal conductivity as 22.4 (BTU)(in)/(ft 2 )(hr)(°F.).
  • Injection molded plaques were made from the formulation used in Du Pont's RyniteTM resins with glass, polyacrylonitrile-based carbon fiber (PAN) and ultra-high modulus pitch-based carbon fiber (UHM) representing the ultimate in high conductivity carbon fibers. Methods of blending the fiber with the resin varied.
  • the RyniteTM resin with glass was a commercial formulation.
  • the Rynite® resin with PAN fiber was produced by feeding resin into a rear port of an extruder, the PAN fiber into a vacuum port, blending in the extruder, being forced out through an orifice as a small diameter rod and chopped into pellets.
  • the UHM fibers were too brittle to process in a conventional sense.
  • the weight of fiber needed for the desired volume % loading was cut from the carbon fiber batts using a 7" ⁇ 7" square template.
  • the fiber was placed on a tray inside a vacuum oven at 70 degrees Centigrade and 28" Hg and left overnight to remove residual moisture.
  • 100 grams of Hercules 3501-6 epoxy resin was placed in each of two aluminum pans, and to each pan was added 10 grams of Araldite RD-2 reactive diluent, which serves to reduce the viscosity of the epoxy resin, and to allow it to flow better within the fiber assembly. This mixture was then degassed and dried in the vacuum oven along with the fiber. Care was taken to maintain the vacuum below 12" Hg to avoid foaming of the resin. Periodically the resin uniform viscosity. The resin was heated for about 2 hours.
  • the apparatus used to make the plaque was a "picture frame” stainless steel mold with a cavity 7" ⁇ 7", which was 11/2" deep.
  • the frame was placed in a "vacuum can", which had previously been sprayed with Frecote 33 mold release.
  • the vacuum can was lined with a fiberglass cloth to absorb the resin squeezed from the mold during consolidation.
  • a bottom plate, 1/2" thick was placed in the frame.
  • a Kapton® release film which has been sprayed with Frecote 33 mold release was placed on top of the bottom plate.
  • the fiber and epoxy were added.
  • 7 to 12 pieces of batt each about 1/4" thick may be required, because of the low volume density of the batt.
  • a layer of fiber was placed in the frame, and a small quantity of resin poured around the edges of the fiber sheet, and also criss-cross on the fiber surface. This step was repeated until all the fiber was in the mold. Then a release film of Kapton® which had been sprayed with Frecote 33 mold release was placed on top of the fiber, and a 7" ⁇ 7" ⁇ 1" thick ram plate placed on top of the fiber. Shims were placed on top of the mold so that when the ram plate was squeezed down to their level the plaque would be of the desired thickness.
  • tacky tape was placed along the flanged perimeter of the vacuum can to create a vacuum seal, and a large piece of Kapton® film placed over the vacuum can and pressed into the tacky tape to seal. The film was held in place with Bulldog clips.
  • the assembly was placed in a hydraulic press for curing. A vacuum connection was made to the vacuum can, and the vacuum maintained at 10 to 12" Hg.
  • the cure cycle was as follows: the assembly was heated to 70° C. and held for one hour, to allow the epoxy to soften and distribute within the fiber; it was next heated to 112° C.
  • a 2" diameter disk was cut from each of three laminates and identified as sample A, B and C and thermal conductivity measured in accordance with ASTM standard F-433 at about 50° C. on the axis of lowest thermal conductivity of each disc.
  • the compositional and thermal conductivity data of the samples is summarized below:

Abstract

A three-dimensional arrangement of carbon fibers made from mesophase pitch are used to reinforce polymer resins to form a composite material. The composite material exhibits high thermal conductivity values on all axes through the composite.

Description

This is a continuation-in-part of U.S. Ser. No. 07/570,308 filed Aug. 20, 1990, now abandoned which in turn is a continuation-in-part application of U.S. Ser. No. 07/251,783 filed Oct. 3, 1988 and now abandoned.
BACKGROUND OF THE INVENTION
This invention relates to thermally conductive material and, more particularly, it relates to a carbon fiber reinforced resin matrix for use as a strong, structurally stable thermal conductive material.
The market segment for electrical devices such as for windings of motors, transformers and solenoids is increasingly moving to miniaturization of such devices. This in turn leads to a rise in internal equipment operating temperature resulting in not only a need for higher temperature ratings on insulation materials used for these applications, but also a need for materials with improved thermal conductivity properties.
It is known to attempt to improve thermal conductivity by adding many kinds of filler as disclosed in "Thermally Conductive Polymer Compositions", D. M. Bigg, Polymer Composites, June 1986, Vol. 7, No. 3, pp. 125-140. The fillers include spherical particles of various metals, glass or carbon black, non-spherical metal or ceramic particles and aluminum fibers. Bigg teaches that the thermal conductivity of the composite is largely determined by the resin and that in the case of fibers, the most important variables influencing composite conductivity are fiber volume fraction and fiber 1/d in the actual composite.
SUMMARY OF THE INVENTION
With the recognition that fiber orientation is a key determinant of thermal conductivity in a composite material, a composite material has been developed to complement the move toward miniaturization of electrical devices which exhibits high strength, structural stability and has improved thermal conductivity capability. More particularly, if a laminate is made with continuous fibers all oriented in the same direction (a "unidirectional" laminate), the thermal conductivity along the fiber axis will be determined by the "rule of mixtures". That is, it will be equal to the area of fiber times the fiber conductivity plus the area of resin times the resin conductivity. The thermal conductivity along the axis perpendicular to the fibers, however, will be dominated by the resin, and will typically be a small multiple of the resin conductivity. The case of discontinuous fibers is more complex; however, it may generally be said that the thermal conductivity of a laminate along any axis is strongly dependent upon the fraction of fibers oriented in the direction of that axis. In any practical application, the most important axis will be the one with the lowest thermal conductivity, since this will limit the flow of heat in the part. Thus, in the case of planar samples, the limiting thermal conductivity will be through-the-plane.
This material comprises 10 to 70% by weight carbon fiber and preferably about 15 to about 60% by weight carbon fiber, the balance being made up of a resin. Preferably the ratio of the thermal conductivity of the composite (Kc) to the thermal conductivity of the resin (Kp) is above 10. The carbon fibers are preferably made from a mesophase pitch by the process described in U.S. Pat. No. 4,861,653 which is incorporated by reference. The fibers are in a three-dimensional arrangement, each fiber has a lamellar microstructure, and there is a distribution of diameters among the fibers ranging from about 1 micrometer to more than 10 micrometers and a number average less than 8 micrometers. The fibers also are heat treated in an inert atmosphere to a temperature above 1600° C., more preferably above 2400° C.
Suitable resinous materials which may be used as the resin include, but are not limited to, commercially available thermoplastic and thermosetting resins. Suitable processes for making useful parts include, but are not limited to, injection molding, compression molding, melt casting and blow molding.
Surprisingly, the fibers described above may be incorporated into composite material at much higher volume fractions than fibers described in the prior art. Also, surprisingly, the thermal conductivity in the critical through-the-plane test is above about 10 (BTU)(in)/(ft2)(hr)(°F.) as measured on the axis of lowest thermal conductivity for the composite material or articles formed from the material. The thermal conductivity performance of these articles is attributed to maintaining the three-dimensional arrangement of the fibers during forming so that at least a fraction of the fibers are oriented in any one of the axes through article.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a composite article formed from the material of this invention.
FIG. 2 is a photomicrograph of the material of this invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring now to FIG. 1, the component structure 10 is an injection molded motor housing made from resin reinforced with a three dimensional arrangement of mesophase pitch based discontinuous carbon fibers.
In FIG. 2 a structure is displayed showing a resin filled with a three-dimensional fiber structure with fibers of varying lengths and dimensions. More particularly, FIG. 2 is a photograph taken on a Scanning Electron Microscope at 1000× magnification. It is a view of the fracture surface of a tensile test bar. The bar was cut from an injection molded plaque made from the material of this invention. The resin is principally polyethylene terephthalate (PET). In the photograph, the fibers 12 are seen in a three-dimensional arrangement as cylindrical or elliptical rods of varying size. The fine threads 14 are polymer. It will be observed that the fibers are oriented in many directions; indeed, they appear to be oriented quite randomly so that at least a fraction on the fibers are oriented in any one of the axes through the structure.
One way the composite material is made is by feeding the resin and a carbon fiber batt made according to the disclosure in above-noted patent into a single screw extruder and extruding the composite material as a strand which is then chopped and collected. The chopped strand is then used in various molding processes to form articles having high thermal conductivity. Another way to form the composite material of this invention is by grinding a planar laminate into small pieces and recompressing them or forcing a very high viscosity molten resin perpendicular to the plane of a fiber assembly and moving some fibers into the third dimension.
Thermal conductivity (T.C.) is measured in accordance with ASTM Standard F-433 with a Dynatech C-Matic instrument, model TCHM-DV, and is designated as (BTU)(in)/(ft2)(hr)(°F.).
The composite material exhibits a three dimensional arrangement of fibers within the resin matrix as estimated from percent shrinkage data in the x, y, and z coordinate axes directions from mold size to the final part. More particularly, essentially equal percent shrinkage of the final part in the x, y, and z directions indicates three dimensional isotropic fiber reinforcement while percent shrinkage of the final part that varies by several orders of magnitude between directions suggests highly oriented reinforcing fibers.
EXAMPLE I
A multiple six layer sandwich consisting of alternate layers of 5-mil thick Du Pont Teflon™ PFA fluorocarbon polymer film and mesophased based graphite fiber mat, made according to the procedure described in U.S. Pat. No. 4,861,653, was formed into a 7"×7" mold of a standard compression molding machine. This multilayer sandwich was cold compressed in order to fit the fiber and film into the cavity for one minute at 1 ton, 2 ton and 2.5 ton pressures. The mold was then put into a hot press at 740° F. and the mass consolidated according to the following schedule:
5 min contact pressure
5 min 1.25 ton pressure
20 min 12.5 ton pressure
then cooled at 1.25 ton pressure.
Good consolidation was not accomplished because of the high viscosity of the PFA resin and the distance it was required to travel through the mat. The laminate was then repressed to improve consolidation by reinserting into the mold and heating to 740° F. and pressing to 37.5 tons for 20 minutes, then cooling at 1.25 tons. The volume fraction of the fiber in the composite is about 40%. A section of a laminate, made according to the above procedure, was tested according to ASTM F-433 for thermal conductivity at 50° C. and shown to be about 14 (BTU)(in)/(ft2)(hr)(°F.) versus about 1.3 for the matrix as measured through the thickness, i.e., on the axis of lowest thermal conductivity for the laminate.
EXAMPLE II
A sample was made by compression molding a granulated molding compound. The molding compound was made by interleaving equal weights of a FR-PET film (Rynite™ FR by Du Pont) (3.5 mil) and a pitch based carbon fiber mat heat-treated at 2600° C. at about 220 g/m2 with a total of about 15 plies of mat. This stack was vacuum bagged between plates and consolidated by heating to 570° F. under contact pressure, only then applying 500 psi at temperature for 10 minutes, then cooling under pressure. The plate was then ground into particles using an I.M.S. model 3144-SP granulator machine with a 3/8" screen. A 6"×6" mold was filled with 120 g of predried granules with essentially random orientation. The mold was heated to 590° F. under contact pressure for 20 minutes, then 350 psi was applied for 10 minutes, then cooled under pressure. Thermal conductivity was measured according to ASTM F-433 on the axis of lowest thermal conductivity of the sample. This yielded a thermal conductivity of 47.6 (BTU)(in)/(ft2)(hr)(°F.) at 50° C. and 63.2 (BTU)(in)/(ft2)(hr)(F) at 150° C.
The same granulated material was also injection molded using an "8 oz. Van Dooran" lab injection molder. A "gentle" screw design was used to maintain fiber length. A mold with 3"×5" plaques was used and subsequently 2" diameter disc was cut and thermal conductivity was measured according to ASTM F-433 on the axis of lowest thermal conductivity of the disc. This yielded a thermal conductivity as 22.4 (BTU)(in)/(ft2)(hr)(°F.).
The same fiber and resin were compounded using a 2" single screw with vacuum. This unit is normally used to compound glass. The screw is not as "gentle" as that used for injection molding. Strands were extruded and then chopped replacing the granulated material above. This material was then injection molded as described above and tested for thermal conductivity as described above, giving a value of 21.1 (BTU)(in)/(ft2)(hr)(°F.).
EXAMPLE III
Injection molded plaques were made from the formulation used in Du Pont's Rynite™ resins with glass, polyacrylonitrile-based carbon fiber (PAN) and ultra-high modulus pitch-based carbon fiber (UHM) representing the ultimate in high conductivity carbon fibers. Methods of blending the fiber with the resin varied. The Rynite™ resin with glass was a commercial formulation. The Rynite® resin with PAN fiber was produced by feeding resin into a rear port of an extruder, the PAN fiber into a vacuum port, blending in the extruder, being forced out through an orifice as a small diameter rod and chopped into pellets. The UHM fibers were too brittle to process in a conventional sense. They were cut into 1/2" lengths and blended with polymer pellets in the feed hopper of an extruder, fed through and chopped into pellets. Plaques 3"×5"×0.125" were made from the fiber/polymer mixtures and samples were cut from these to measure thermal conductivity at 50° C. according to ASTM Standard F-433 on the axis of lowest thermal conductivity.
The results are summarized below:
______________________________________                                    
             Thermal Conductivity                                         
             (BTU)(in)/(ft.sup.2)(hr)(°F.)                         
______________________________________                                    
PET/PAN        2.3                                                        
PET/Glass      2.3                                                        
PET/UHM Carbon 3.5                                                        
______________________________________
EXAMPLE IV
Three laminates were prepared according to Example 2, U.S. Pat. No. 4,861,653 in the following manner:
The weight of fiber needed for the desired volume % loading was cut from the carbon fiber batts using a 7"×7" square template. The fiber was placed on a tray inside a vacuum oven at 70 degrees Centigrade and 28" Hg and left overnight to remove residual moisture. The following morning 100 grams of Hercules 3501-6 epoxy resin was placed in each of two aluminum pans, and to each pan was added 10 grams of Araldite RD-2 reactive diluent, which serves to reduce the viscosity of the epoxy resin, and to allow it to flow better within the fiber assembly. This mixture was then degassed and dried in the vacuum oven along with the fiber. Care was taken to maintain the vacuum below 12" Hg to avoid foaming of the resin. Periodically the resin uniform viscosity. The resin was heated for about 2 hours.
The apparatus used to make the plaque was a "picture frame" stainless steel mold with a cavity 7"×7", which was 11/2" deep. The frame was placed in a "vacuum can", which had previously been sprayed with Frecote 33 mold release. The vacuum can was lined with a fiberglass cloth to absorb the resin squeezed from the mold during consolidation. A bottom plate, 1/2" thick was placed in the frame. A Kapton® release film which has been sprayed with Frecote 33 mold release was placed on top of the bottom plate. Next the fiber and epoxy were added. In order to make a plaque 0.1" thick, 7 to 12 pieces of batt each about 1/4" thick may be required, because of the low volume density of the batt. A layer of fiber was placed in the frame, and a small quantity of resin poured around the edges of the fiber sheet, and also criss-cross on the fiber surface. This step was repeated until all the fiber was in the mold. Then a release film of Kapton® which had been sprayed with Frecote 33 mold release was placed on top of the fiber, and a 7"×7"×1" thick ram plate placed on top of the fiber. Shims were placed on top of the mold so that when the ram plate was squeezed down to their level the plaque would be of the desired thickness. Finally, "tacky tape" was placed along the flanged perimeter of the vacuum can to create a vacuum seal, and a large piece of Kapton® film placed over the vacuum can and pressed into the tacky tape to seal. The film was held in place with Bulldog clips.
The assembly was placed in a hydraulic press for curing. A vacuum connection was made to the vacuum can, and the vacuum maintained at 10 to 12" Hg. The cure cycle was as follows: the assembly was heated to 70° C. and held for one hour, to allow the epoxy to soften and distribute within the fiber; it was next heated to 112° C. and held for an hour; next, the ram plate was pressed down to the shims--this was done slowly to avoid forcing out too much epoxy, and done in press-release cycles to move air bubbles from the center to the edge of the mold, where they could be removed by vacuum; when the ram plate was pressed to the shims the temperature was raised to 124° C., and it was held for 18 hours--once it had reached the desired temperature the vacuum was turned-off; the assembly was then cooled to ambient temperature under pressure.
A 2" diameter disk was cut from each of three laminates and identified as sample A, B and C and thermal conductivity measured in accordance with ASTM standard F-433 at about 50° C. on the axis of lowest thermal conductivity of each disc. The compositional and thermal conductivity data of the samples is summarized below:
______________________________________                                    
Sample Fiber    Temperature Thermal Conductivity                          
Ref.   Vol. %   Degrees C.  BTU (in)/(ft.sup.2) (hr) (°F.)         
______________________________________                                    
A      33.6     55.6        3.6                                           
B      35.3     55.2        4.4                                           
C      35.8     54.6        4.9                                           
______________________________________

Claims (4)

What is claimed is:
1. A thermally conductive composite material comprising a resin reinforced with a three-dimensional arrangement of discontinuous mesophase pitch based carbon fibers said material having a thermal conductivity above about 10(BTU) (in)/(ft2) (hr) (°F.) as measured on the axis of lowest thermal conductivity through the material.
2. The thermally conductive material as defined in claim 1 wherein said resin is polyethylene terephthalate polymer.
3. The thermally conductive material of claim 1 wherein said resin is fluorocarbon polymer.
4. A component made from the material of claim 1.
US07/827,142 1988-10-03 1992-01-27 Thermal conductive material Abandoned USH1332H (en)

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US57030890A 1990-08-20 1990-08-20
US07/827,142 USH1332H (en) 1988-10-03 1992-01-27 Thermal conductive material

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Cited By (9)

* Cited by examiner, † Cited by third party
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US5695847A (en) * 1996-07-10 1997-12-09 Browne; James M. Thermally conductive joining film
WO2002009939A1 (en) * 2000-07-28 2002-02-07 Tri-Mack Plastics Manufacturing Corp. Thermoplastic materials with improved thermal conductivity and methods for making the same
US20020062949A1 (en) * 1999-12-01 2002-05-30 Mccullough Kevin A. Overplated thermally conductive part with EMI sheilding
US20020111415A1 (en) * 2000-07-28 2002-08-15 Mack Edward J. Thermoplastic materials with improved thermal conductivity and methods for making the same
US20060119522A1 (en) * 2001-02-15 2006-06-08 Integral Technologies, Inc. Low cost electronic probe devices manufactured from conductive loaded resin-based materials
US20090004393A1 (en) * 2007-06-29 2009-01-01 Rodgers Steven R Thermally Conductive Structural Composite Material and Method
US20090069483A1 (en) * 2007-09-12 2009-03-12 Sumitomo Chemical Company, Limited Insulating resin composition and application thereof
US20090298976A1 (en) * 2005-10-26 2009-12-03 Hiroyuki Yano Fiber-Reinforced Composition Resin Composition, Adhesive and Sealant
US20170192303A1 (en) * 2015-12-30 2017-07-06 Lg Display Co., Ltd. Liquid crystal display device

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