WO2005102962A1 - Titanium carbide as a friction and wear modifier in friction materials - Google Patents

Titanium carbide as a friction and wear modifier in friction materials Download PDF

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Publication number
WO2005102962A1
WO2005102962A1 PCT/US2005/010960 US2005010960W WO2005102962A1 WO 2005102962 A1 WO2005102962 A1 WO 2005102962A1 US 2005010960 W US2005010960 W US 2005010960W WO 2005102962 A1 WO2005102962 A1 WO 2005102962A1
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carbon
titanium carbide
weight
binder
preform
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PCT/US2005/010960
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French (fr)
Inventor
Allen H. Simpson
Nabil Abu Gharbieh
Slawomir T. Fryska
Mark L. La Forest
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Honeywell International Inc.
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Publication of WO2005102962A1 publication Critical patent/WO2005102962A1/en

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    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D69/00Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
    • F16D69/02Composition of linings ; Methods of manufacturing
    • F16D69/023Composite materials containing carbon and carbon fibres or fibres made of carbonizable material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/56Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
    • C04B35/5607Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides
    • C04B35/5611Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on refractory metal carbides based on titanium carbides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/71Ceramic products containing macroscopic reinforcing agents
    • C04B35/78Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
    • C04B35/80Fibres, filaments, whiskers, platelets, or the like
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/71Ceramic products containing macroscopic reinforcing agents
    • C04B35/78Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
    • C04B35/80Fibres, filaments, whiskers, platelets, or the like
    • C04B35/83Carbon fibres in a carbon matrix
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/48Organic compounds becoming part of a ceramic after heat treatment, e.g. carbonising phenol resins
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/52Constituents or additives characterised by their shapes
    • C04B2235/5208Fibers
    • C04B2235/5216Inorganic
    • C04B2235/524Non-oxidic, e.g. borides, carbides, silicides or nitrides
    • C04B2235/5248Carbon, e.g. graphite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5445Particle size related information expressed by the size of the particles or aggregates thereof submicron sized, i.e. from 0,1 to 1 micron
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/54Particle size related information
    • C04B2235/5418Particle size related information expressed by the size of the particles or aggregates thereof
    • C04B2235/5454Particle size related information expressed by the size of the particles or aggregates thereof nanometer sized, i.e. below 100 nm
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/21Circular sheet or circular blank
    • Y10T428/213Frictional

Definitions

  • the present invention provides a method of improving the wear rate of a carbon-carbon composite friction material.
  • the present invention at the same time provides a carbon-carbon composite friction material which has a very stable friction performance.
  • Carbon-carbon composite brakes made in accordance with the present invention have improved wear rates and stable, consistent friction performance. [0005] Accordingly, this invention provides a method of improving wear and dynamic stability in a carbon-carbon composite brake disc.
  • This method embodiment of the present invention involves manufacturing the carbon-carbon composite brake discs from preforms comprising carbon- containing fibers, resin binder, and titanium carbide particles having a particle diameter in the range of from 0.01 to 10 microns.
  • the dynamic stability of the brakes manufactured is characterized by a brake effectiveness ⁇ of less than 0.200, preferably less than 0.100, wherein ⁇ is defined by the formula __ T Average [p Av e rage - bP ⁇ N R )A p R lake, in which T Average , P Average , bprt, 2N R , A p , and R m are as defined hereinbelow.
  • is defined by the formula __ T Average [p Av e rage - bP ⁇ N R )A p R pleasant, in which T Average , P Average , bprt, 2N R , A p , and R m are as defined hereinbelow.
  • Another embodiment of the present invention is a carbon- carbon composite brake disc preform comprising carbon fibers and resin binder, wherein the preform has particulate titanium carbide uniformly distributed throughout its mass. The particles of titanium carbide in this embodiment generally range in size from 0.01 to 10 microns in diameter
  • the particles have an average particle size of 1 -2 microns and an apparent porosity in the range 0.5-0.6.
  • a particularly preferred particulate titanium carbide has an average particle size of 1 A microns and an apparent porosity of 0.545.
  • Still another embodiment of this invention is a method of making a carbon-carbon composite preform. In this method, one combines, e.g. 0.1 to 15 parts by weight titanium carbide particles ranging in size from 0.01 to 10 microns in diameter, 20 to 85 parts by weight resinous binder, and 20 to 80 parts by weight carbon fibers or carbon fiber precursors in a mold.
  • the titanium carbide particles used in this process preferably have an average particle size of 1 -2 microns and an apparent porosity in the range 0.5-0.6.
  • the mold is most preferably one that is configured to provide a preform in the shape of an aircraft landing system brake disc.
  • the particulate titanium carbide may be mixed with liquid binder, the resulting TiC/binder mixture may then be solidified, and the resulting solid TiC/binder mixture may be ground into a fine powder for use in the process.
  • Yet another embodiment of the present invention is a composition for preparing a carbon-carbon composite friction material.
  • This compositional embodiment is made up of carbon fibers or carbon fiber precursors, powdered or liquid resin binder, and titanium carbide particles ranging in size from 0.01 to 10 microns in diameter.
  • the carbon fiber or carbon fiber precursors may constitute 15-80 weight-% of the composition
  • the powdered or liquid resin binder may constitute 20-85 weight-% of the composition
  • the titanium carbide particles may constitute 0.1 -15 weight-% of the composition.
  • Titanium carbide powder may be included in a composite material during the manufacturing stage, along with the carbon fibers and matrix material.
  • the titanium carbide particles have diameters in the range 0.01 to 10 microns.
  • Particle size of titanium carbide powders may be determined in accordance with the procedures described in ASTM B-330-02. It has been found that, . although excellent friction performance can be achieved with titanium carbide particles larger than 10 microns in diameter, the wear rate of carbon-carbon composites made with such particles increases to levels that are generally unacceptable. More preferably, the particles are in the range 0.5 to 5 microns in diameter.
  • a specific example of a particulate titanium carbide that may be used in this invention is Grade 2049 TiC from Pacific Particulate Materials Ltd. of Port Coquitlam, B.C., Canada.
  • the carbon-carbon composite preforms of this invention include from 15 to 80 weight-%, preferably from 40 to 80 weight-%, more preferably from 50 to 65 weight-%, carbon fiber, from 20 to 85 weight-%, preferably from 20 to 65 weight-%, more preferably from 30 to 45 weight-%, binder, and from 0.1 to 15 weight-%, preferably from 1 to 15 weight-%, more preferably from 2 to 8 weight-%, of the titanium carbide particles. It is important that the titanium carbide (or titanium component) be dispersed or uniformly distributed throughout the entire carbon-carbon composite that will be used as friction material. This will ensure consistent friction performance throughout the life of the brake. [0011] Those skilled in the art are familiar with many methods of making carbon-carbon friction materials.
  • carbon fibers - or carbon fiber precursors such as pitch fibers or polyacrylonitrile (PAN) fibers - are used to provide architecture and strength to the composite.
  • the fibers may be of random orientation or the fibers may have a well- defined architecture, obtained e.g. by a controlled spraying of chopped fibers into a mold. Fibers ranging in length from 1 to 30 mm are normally employed in this invention. However, fibers of other lengths may be used. While it is often convenient to make use of "chopped" fibers, the only requisite of the form of the fibers is that they permit the titanium carbide particles to be uniformly distributed in the regions of the preform that will function as friction material.
  • a carbon-bearing resinous binder such as a pitch-based binder or a phenolic resin binder, is also a significant part of the present carbon-carbon composite friction materials.
  • the resin binder is carbonized during processing of the precursor mixture to prepare a preform which has a carbon matrix bonded to the reinforcement fibers.
  • titanium carbide particles are dispersed or uniformly distributed throughout the entire carbon-carbon composite, e.g., by subjecting a precursor mixture composition to mixing in a Hobart blender.
  • a precursor mixture composition e.g., by subjecting a precursor mixture composition to mixing in a Hobart blender.
  • One approach for ensuring good distribution is to mix the TiC powder with hot liquid binder, solidify the mixture by cooling, and then grinding the solid TiC/binder mixture into a fine powder. This coats the titanium carbide particles with binder and ensures that distribution of the titanium carbide in the preform is quite uniform, because when the preform is heated and pressed, the liquid flows and fills voids in the fibrous matrix of the preform.
  • Example 2 The mixture is thoroughly blended and then decanted into an annular mold, where it is pressed and heated to set the binder. Then the molded composition is charred to produce a carbon-carbon composite brake disc preform. The preform is densified by conventional CVI/CVD processing and machined to prepare a brake disc.
  • Example 2 The mixture is thoroughly blended and then decanted into an annular mold, where it is pressed and heated to set the binder. Then the molded composition is charred to produce a carbon-carbon composite brake disc preform. The preform is densified by conventional CVI/CVD processing and machined to prepare a brake disc.
  • Example 2 Example 2
  • the binder powder lots (containing TiC) and the fiber lots are deposited alternatively into the mold. Once all 3660 grams of material have been deposited into the mold in this way, the combined materials are pressed and heated to set the binder and consolidate the preform.
  • the consolidation step includes pressurization to 200 psi for 50 minutes. The temperature is maintained at a level of 215°F for 45 minutes during the consolidation step.
  • the molded composition is then charred to produce a carbon-carbon composite brake disc preform.
  • the preform is densified by conventional CVD processing and machined to prepare a brake disc having a thickness of 2.86 cm.
  • Example 3 [0016] Brake discs manufactured by conventional procedures (runs A-D) and brake discs made in accordance with the present invention (run E) were tested on a subscale dynamometer, with the following results:
  • Run E an embodiment of the present invention, demonstrated less wear. It also significantly lowered "effectiveness" as compared to Comparative Runs A-D. Reduced wear rates provide a clear economic advantage. Lower “effectiveness” increases the dynamic stability of aircraft braking systems.
  • Brake effectiveness is defined as a non-dimensional quantity relating the compressive (normal) force to the braking torque. In other words, it is a rotating machinery equivalent to the coefficient of friction. In the aircraft brake industry, the brake effectiveness is expressed as: where: a. T Averag ⁇ - Average torque generated by the brake b. P Average - Average brake hydraulic fluid pressure c. bprt - Brake pressure rotors tight, lowest pressure at which brake generates torque d. 2N R - Number of friction surfaces (twice the number of rotors N R ) e. A p - Total hydraulic fluid piston surface area f . R m - Mean brake radius.
  • aircraft brake friction materials are designed to satisfy four main functional goals: a) low effectiveness during most landing and taxi conditions; b) high effectiveness during a Rejected Take-Off (RTO) stop; c) low within stop variability (constant effectiveness values during the stop); and d) low average effectiveness variability between stops at different operating conditions.
  • Low effectiveness during landing and taxi conditions is important for maintaining vibration free brake operation, which helps to reduce unscheduled brake removals and leads to increased profitability for the brake operator.
  • An additional financial benefit usually associated with low effectiveness rates during landing and taxi is low wear rate (long brake life)
  • High effectiveness during RTO is a necessary condition for the safe operation of the aircraft during emergency braking conditions. Meeting the minimum RTO stopping distance specification is a mandatory requirement for brake qualification on the airplane. [0021] Low within stop variability requirement is necessary for smooth braking operation preferred by airplane crew and passengers and also to ensure that the peak torque generated by the brake does not exceed the structural limits of the landing gear. [0022] Low effectiveness variability under varying operating conditions is necessary to ensure good compatibility of the brake performance with the Brake Control System. Brake Control Systems can be tuned much easier to brakes that are predictable under various temperature, velocity, and pressure conditions.

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Abstract

Methods of making a carbon-carbon composite preforms, particularly suitable as brake discs in aircraft landing systems, by combining titanium carbide particles ranging in size from 0.01 to 10 microns in diameter, resinous binder, and carbon fibers or carbon fiber precursors in a mold, and subsequently subjecting the combined components to pressure and heat to carbonize the resinous binder by methods, thereby providing the carbon-carbon composite preform having particulate titanium carbide uniformly distributed throughout its mass. Prior to combining the titanium carbide and the binder with the fibers in this process, the particulate titanium carbide may be mixed with liquid binder, the resulting TiC/binder mixture may then solidified, and the resulting solid TiC/binder mixture may be ground into a fine powder for use in the process. Also, compositions for preparing a carbon-carbon composite friction materials, and methods of improving wear and dynamic stability in a carbon-carbon composite brake discs.

Description

TITANIUM CARBIDE AS A FRICTION AND WEAR MODIFIER IN FRICTION MATERIALS
PRIORITY [0001] This application claims priority under 35 U.S.C. § 1 19(e) to
U.S. Provisional Application No. 60/558,1 1 1 for "TITANIUM CARBIDE- ENHANCED CARBON-CARBON BRAKE COMPOSITES," filed on April 1 , 2004, the entire contents of which are hereby expressly incorporated by reference. FIELD OF THE INVENTION [0002] The present invention is in the field of carbon-carbon composite materials. In particular, this invention contemplates carbon- carbon composite materials that are useful as friction components, for instance in aircraft landing system brake assemblies. BACKGROUND OF THE INVENTION [0003] Many aircraft brakes are made of carbon-carbon composite materials. Aircraft brakes are subjected to high temperatures, which may change the properties of the carbon and the friction surface and lead to variation in the friction performance of the brake. Other factors that may increase variation in friction performance of carbon-carbon composite materials are variation in the carbon microstructure, variation in the fiber/matrix ratio, and differences in the energy levels of the previous stop or stops performed by the brake. Also, a desirable property of a carbon- carbon friction material is a low wear rate. The present invention provides a method of improving the wear rate of a carbon-carbon composite friction material. The present invention at the same time provides a carbon-carbon composite friction material which has a very stable friction performance. SUMMARY OF THE INVENTION [0004] It has been discovered that titanium carbide, when uniformly distributed into carbon-carbon composite preforms in the form of particles of particular particle size, provides the preforms with beneficially modified friction and wear properties. Carbon-carbon composite brakes made in accordance with the present invention have improved wear rates and stable, consistent friction performance. [0005] Accordingly, this invention provides a method of improving wear and dynamic stability in a carbon-carbon composite brake disc. This method embodiment of the present invention involves manufacturing the carbon-carbon composite brake discs from preforms comprising carbon- containing fibers, resin binder, and titanium carbide particles having a particle diameter in the range of from 0.01 to 10 microns. In accordance with the present invention, the dynamic stability of the brakes manufactured is characterized by a brake effectiveness μ of less than 0.200, preferably less than 0.100, wherein μ is defined by the formula __ T Average [p Average - bP^N R )ApR„, in which TAverage, PAverage, bprt, 2NR, Ap, and Rm are as defined hereinbelow. [0006] Another embodiment of the present invention is a carbon- carbon composite brake disc preform comprising carbon fibers and resin binder, wherein the preform has particulate titanium carbide uniformly distributed throughout its mass. The particles of titanium carbide in this embodiment generally range in size from 0.01 to 10 microns in diameter. Preferably the particles have an average particle size of 1 -2 microns and an apparent porosity in the range 0.5-0.6. A particularly preferred particulate titanium carbide has an average particle size of 1 A microns and an apparent porosity of 0.545. [0007] Still another embodiment of this invention is a method of making a carbon-carbon composite preform. In this method, one combines, e.g. 0.1 to 15 parts by weight titanium carbide particles ranging in size from 0.01 to 10 microns in diameter, 20 to 85 parts by weight resinous binder, and 20 to 80 parts by weight carbon fibers or carbon fiber precursors in a mold. The titanium carbide particles used in this process preferably have an average particle size of 1 -2 microns and an apparent porosity in the range 0.5-0.6. Subsequently, one subjects the combined components to pressure and heat to carbonize the resinous binder by methods that are in general familiar to those skilled in the art, thereby providing a carbon-carbon composite preform having particulate titanium carbide uniformly distributed throughout its mass. In this method, the mold is most preferably one that is configured to provide a preform in the shape of an aircraft landing system brake disc. Prior to combining the titanium carbide and the binder with the fibers in this process, the particulate titanium carbide may be mixed with liquid binder, the resulting TiC/binder mixture may then be solidified, and the resulting solid TiC/binder mixture may be ground into a fine powder for use in the process.
[0008] Yet another embodiment of the present invention is a composition for preparing a carbon-carbon composite friction material. This compositional embodiment is made up of carbon fibers or carbon fiber precursors, powdered or liquid resin binder, and titanium carbide particles ranging in size from 0.01 to 10 microns in diameter. In this composition, the carbon fiber or carbon fiber precursors may constitute 15-80 weight-% of the composition, the powdered or liquid resin binder may constitute 20-85 weight-% of the composition, and the titanium carbide particles may constitute 0.1 -15 weight-% of the composition. DETAILED DESCRIPTION OF THE INVENTION [0009] Titanium carbide powder may be included in a composite material during the manufacturing stage, along with the carbon fibers and matrix material. In accordance with this invention, the titanium carbide particles have diameters in the range 0.01 to 10 microns. Particle size of titanium carbide powders may be determined in accordance with the procedures described in ASTM B-330-02. It has been found that, . although excellent friction performance can be achieved with titanium carbide particles larger than 10 microns in diameter, the wear rate of carbon-carbon composites made with such particles increases to levels that are generally unacceptable. More preferably, the particles are in the range 0.5 to 5 microns in diameter. A specific example of a particulate titanium carbide that may be used in this invention is Grade 2049 TiC from Pacific Particulate Materials Ltd. of Port Coquitlam, B.C., Canada. [0010] The carbon-carbon composite preforms of this invention include from 15 to 80 weight-%, preferably from 40 to 80 weight-%, more preferably from 50 to 65 weight-%, carbon fiber, from 20 to 85 weight-%, preferably from 20 to 65 weight-%, more preferably from 30 to 45 weight-%, binder, and from 0.1 to 15 weight-%, preferably from 1 to 15 weight-%, more preferably from 2 to 8 weight-%, of the titanium carbide particles. It is important that the titanium carbide (or titanium component) be dispersed or uniformly distributed throughout the entire carbon-carbon composite that will be used as friction material. This will ensure consistent friction performance throughout the life of the brake. [0011] Those skilled in the art are familiar with many methods of making carbon-carbon friction materials. In all cases, carbon fibers - or carbon fiber precursors, such as pitch fibers or polyacrylonitrile (PAN) fibers - are used to provide architecture and strength to the composite. The fibers may be of random orientation or the fibers may have a well- defined architecture, obtained e.g. by a controlled spraying of chopped fibers into a mold. Fibers ranging in length from 1 to 30 mm are normally employed in this invention. However, fibers of other lengths may be used. While it is often convenient to make use of "chopped" fibers, the only requisite of the form of the fibers is that they permit the titanium carbide particles to be uniformly distributed in the regions of the preform that will function as friction material. Accordingly, other sorts of fibers, including "continuous" fibers, may be employed in this invention. One specific example of a carbon fiber that can be used in the present invention is Zoltek 48 K carbon fiber, available from Zoltek Corporation of St. Louis, Missouri. [0012] A carbon-bearing resinous binder, such as a pitch-based binder or a phenolic resin binder, is also a significant part of the present carbon-carbon composite friction materials. Those skilled in the art of making carbon-carbon composite friction materials are familiar with a wide variety of suitable pitch-based, phenolic, and similar resin binders. The resin binder is carbonized during processing of the precursor mixture to prepare a preform which has a carbon matrix bonded to the reinforcement fibers. [0013] In accordance with the present invention, titanium carbide particles are dispersed or uniformly distributed throughout the entire carbon-carbon composite, e.g., by subjecting a precursor mixture composition to mixing in a Hobart blender. One approach for ensuring good distribution is to mix the TiC powder with hot liquid binder, solidify the mixture by cooling, and then grinding the solid TiC/binder mixture into a fine powder. This coats the titanium carbide particles with binder and ensures that distribution of the titanium carbide in the preform is quite uniform, because when the preform is heated and pressed, the liquid flows and fills voids in the fibrous matrix of the preform. Uniform distribution of titanium carbide throughout the carbon-carbon composite friction preform ensures that the friction film generated by wear is constant through the life of a brake made from the carbon-carbon composite preform of this invention. EXAMPLES Example 1 [0014] Five parts by weight of particulate titanium carbide, having an average particle size of 1 .38 microns, an apparent porosity of 0.545, and a density of 4.93 g/cc, is added to 35 parts by weight liquid thermoplastic phenolic resin binder. To ensure adequate mixing, the titanium carbide powder and the phenolic resin powder are passed through an extruder and then re-ground into a powder. Subsequently, 60 parts by weight chopped carbon fibers are added to the powder. The mixture is thoroughly blended and then decanted into an annular mold, where it is pressed and heated to set the binder. Then the molded composition is charred to produce a carbon-carbon composite brake disc preform. The preform is densified by conventional CVI/CVD processing and machined to prepare a brake disc. Example 2
[0015] Two hundred grams of particulate titanium carbide (nominal particle size 1.4 microns) is added to 1400 grams of liquid thermoplastic phenolic resin binder to provide 1600 grams of binder. To ensure adequate mixing, the titanium carbide powder and the phenolic resin powder are passed through an extruder and then re-ground into a powder. Separately, 2060 grams of carbon fibers (Zoltec 48K, having a density of 1.78 g/cc) are provided. The fibers and the powder mixture are decanted into an annular mold, having the form of an aircraft landing system brake disc (stator), as follows. The binder powder is divided into 39 approximately equal lots and the fibers are divided into 38 approximately equal lots. The binder powder lots (containing TiC) and the fiber lots are deposited alternatively into the mold. Once all 3660 grams of material have been deposited into the mold in this way, the combined materials are pressed and heated to set the binder and consolidate the preform. The consolidation step includes pressurization to 200 psi for 50 minutes. The temperature is maintained at a level of 215°F for 45 minutes during the consolidation step. The molded composition is then charred to produce a carbon-carbon composite brake disc preform. The preform is densified by conventional CVD processing and machined to prepare a brake disc having a thickness of 2.86 cm. Example 3 [0016] Brake discs manufactured by conventional procedures (runs A-D) and brake discs made in accordance with the present invention (run E) were tested on a subscale dynamometer, with the following results:
Figure imgf000008_0002
[0017] It can be seen that Run E, an embodiment of the present invention, demonstrated less wear. It also significantly lowered "effectiveness" as compared to Comparative Runs A-D. Reduced wear rates provide a clear economic advantage. Lower "effectiveness" increases the dynamic stability of aircraft braking systems. [0018] Brake effectiveness is defined as a non-dimensional quantity relating the compressive (normal) force to the braking torque. In other words, it is a rotating machinery equivalent to the coefficient of friction. In the aircraft brake industry, the brake effectiveness is expressed as: where: a. TAveragβ- Average torque generated by the brake b. PAverage- Average brake hydraulic fluid pressure c. bprt - Brake pressure rotors tight, lowest pressure at which brake generates torque d. 2NR - Number of friction surfaces (twice the number of rotors NR) e. Ap - Total hydraulic fluid piston surface area f . Rm - Mean brake radius.
[0019] With respect to the effectiveness, aircraft brake friction materials are designed to satisfy four main functional goals: a) low effectiveness during most landing and taxi conditions; b) high effectiveness during a Rejected Take-Off (RTO) stop; c) low within stop variability (constant effectiveness values during the stop); and d) low average effectiveness variability between stops at different operating conditions. Low effectiveness during landing and taxi conditions is important for maintaining vibration free brake operation, which helps to reduce unscheduled brake removals and leads to increased profitability for the brake operator. An additional financial benefit usually associated with low effectiveness rates during landing and taxi is low wear rate (long brake life)
[0020] High effectiveness during RTO is a necessary condition for the safe operation of the aircraft during emergency braking conditions. Meeting the minimum RTO stopping distance specification is a mandatory requirement for brake qualification on the airplane. [0021] Low within stop variability requirement is necessary for smooth braking operation preferred by airplane crew and passengers and also to ensure that the peak torque generated by the brake does not exceed the structural limits of the landing gear. [0022] Low effectiveness variability under varying operating conditions is necessary to ensure good compatibility of the brake performance with the Brake Control System. Brake Control Systems can be tuned much easier to brakes that are predictable under various temperature, velocity, and pressure conditions.

Claims

What is claimed is: 1 . A method of improving wear and dynamic stability in a carbon-carbon composite brake disc, which method comprises manufacturing said carbon-carbon composite brake disc from a preform comprising 1 5 to 80 weight-% carbon-containing fibers, 20 to 85 weight- % resin binder, and 0.1 to 1 5 weight-% titanium carbide particles having a particle diameter in the range of from 0.01 to 1 0 microns.
2. The method of claim 1 , wherein the dynamic stability is characterized by a brake effectiveness of less than 0.200, wherein
Figure imgf000010_0001
where: TA.erage " Average torque generated by the brake; ^A erage " Average brake hydraulic fluid pressure; bprt - Brake pressure rotors tight, lowest pressure at which brake generates torque; 2NR - Number of friction surfaces (twice the number of rotors NR); Ap - Total hydraulic fluid piston surface area; and Rm - Mean brake radius.
3. A carbon-carbon composite brake disc preform comprising carbon fibers and resin binder, said preform having particulate titanium carbide uniformly distributed throughout its mass, wherein the particles of titanium carbide range in size from 0.01 to 1 0 microns in diameter.
4. The preform of claim 3, wherein said particulate titanium carbide has an average particle size of 1 -2 microns and an apparent porosity in the range 0.5-0.6.
5. The preform of claim 3, comprising from 1 5 to 80 weight-% carbon fiber, from 20 to 85 weight-% binder, and from 0.1 to 1 5 weight- % titanium carbide particles.
6. The preform of claim 5, comprising from 50 to 65 weight-% carbon fiber, from 30 to 45 weight-% binder, and from 2 to 8 weight-% titanium carbide particles, wherein said titanium carbide particles range in size from 0.5 to 5 microns in diameter.
7. A method of making a carbon-carbon composite preform, for example configured as an aircraft landing system brake disc, wherein said method includes: combining titanium carbide particles ranging in size from 0.01 to 10 microns in diameter, resinous binder, and carbon fibers or carbon fiber precursors in a mold, and subjecting the combined components to pressure and heat to carbonize the resinous binder, thereby providing a carbon-carbon composite preform having particulate titanium carbide uniformly distributed throughout its mass.
8. The method of claim 7, wherein, prior to combination of the titanium carbide and the binder with the fibers, the particulate titanium carbide is mixed with liquid binder, the resulting TiC/binder mixture is solidified, and the resulting solid TiC/binder mixture is ground into a fine powder.
9. The method of claim 7, which comprises combining 0.1 to 1 5 weight-% titanium carbide particles having an average particle size of 1 -2 microns and 20 to 85 weight-% resinous binder with 1 5 to 80 weight-% carbon fiber or carbon fiber precursors.
1 0. A composition for preparing a carbon-carbon composite friction material, said composition comprising 1 5 to 80 parts by weight carbon fibers or carbon fiber precursors, 20 to 85 parts by weight powdered or liquid resin binder, and 0.1 to 1 5 parts by weight titanium carbide particles ranging in size from 0.01 to 1 0 microns in diameter.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006039443A2 (en) * 2004-10-01 2006-04-13 Honeywell International Inc. Improved formulation for the manufacture of carbon-carbon composite materials
EP2028221A1 (en) * 2007-08-03 2009-02-25 Borgwarner, Inc. Friction material with silicon
EP2157330A1 (en) * 2008-08-22 2010-02-24 Honeywell International Inc. Reactive sintering to eliminate metal inserts in carbon-carbon brake discs
US7749562B1 (en) 2004-07-26 2010-07-06 Borgwarner Inc. Porous friction material comprising nanoparticles of friction modifying material
US8021744B2 (en) 2004-06-18 2011-09-20 Borgwarner Inc. Fully fibrous structure friction material
US8397889B2 (en) 2008-03-12 2013-03-19 Borgwarner Inc. Frictional device comprising at least one friction plate
US8603614B2 (en) 2004-07-26 2013-12-10 Borgwarner Inc. Porous friction material with nanoparticles of friction modifying material

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5113982B2 (en) * 2004-04-23 2013-01-09 トヨタ自動車株式会社 Method for producing carbon composite material in which metal carbide particles are dispersed
WO2006101799A2 (en) * 2005-03-16 2006-09-28 Honeywell International Inc. Carbon fiber containing ceramic particles
US20070262200A1 (en) * 2006-05-15 2007-11-15 Honeywell International Inc. Extra long life carbon-carbon friction material
US20100084075A1 (en) * 2006-10-13 2010-04-08 Honeywell International Inc. Strength enhancement of carbon-carbon composite brake pads using fiber pre-stressing
US8574470B2 (en) * 2008-10-24 2013-11-05 Honeywell International Inc. Combustion synthesis to bond metal inserts to C-C composite surfaces
RU2484035C1 (en) * 2012-01-18 2013-06-10 ОАО "Авиационная корпорация "Рубин" (ОАО "АК "Рубин") Binder for producing frictional carbon-carbon composite materials, method of producing material and material
WO2014144161A1 (en) * 2013-03-15 2014-09-18 Tribco Inc. Composite friction materials
US9272950B2 (en) 2013-12-18 2016-03-01 Honeywell International Inc. Composite materials including ceramic particles and methods of forming the same
US9725803B2 (en) 2015-07-02 2017-08-08 Goodrich Corporation Method of forming borides in carbon composites
US9970497B2 (en) 2015-12-18 2018-05-15 Goodrich Corporation Systems and methods for carbon-carbon materials incorporating yttrium and zirconium compounds
CN106763335A (en) * 2016-12-28 2017-05-31 山东正凯机械科技有限公司 A kind of preparation method of the modified carbon fiber based brake disc of lighting
US11796021B2 (en) 2020-02-05 2023-10-24 Goodrich Corporation Composites and methods of forming composites having friction and wear plugs

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3867491A (en) * 1970-06-22 1975-02-18 Carborundum Co Process for reinforced carbon bodies
EP0404571A1 (en) * 1989-06-22 1990-12-27 Toyota Jidosha Kabushiki Kaisha Sliding member
US5964320A (en) * 1996-09-10 1999-10-12 Kabushiki Kaisha Toshiba Brake shoe for elevator emergency stop
US6261692B1 (en) * 1998-07-21 2001-07-17 Korea Research Institute Of Chemical Technology Carbon-carbon composites containing ceramic power and method for preparing the same
US6390304B1 (en) * 1997-06-02 2002-05-21 Hitco Carbon Composites, Inc. High performance filters comprising inorganic fibers having inorganic fiber whiskers grown thereon
US20030180527A1 (en) * 2002-03-21 2003-09-25 Moritz Bauer Composite containing reinforcing fibers comprising carbon

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3759353A (en) * 1970-06-22 1973-09-18 Carborundum Co Disc brake containing reinforced carbon bodies
US3932568A (en) * 1973-06-26 1976-01-13 Friction Products Inc. High-energy brake and brake components
US4007814A (en) * 1976-02-05 1977-02-15 Goodyear Aerospace Corporation Carbon brake disk with cast keyslot reinforcement members
JPS5616575A (en) * 1979-07-18 1981-02-17 Toho Rayon Co Ltd Friction material and its preparation
EP0235011B1 (en) * 1986-02-05 1990-05-02 Societe Europeenne De Propulsion Friction system using composite refractory materials
US4815572A (en) * 1987-07-24 1989-03-28 Parker-Hannifin Corporation Brake system with improved brake material
US5169718A (en) * 1989-06-22 1992-12-08 Toyota Jidosha Kabushiki Kaisha Sliding member
DE4136880C2 (en) * 1991-11-09 1994-02-17 Sintec Keramik Gmbh Process for producing an oxidation-resistant component based on CFC and its application
US5383963A (en) * 1993-02-22 1995-01-24 Kubota Corporation Composite fibers of potassium hexatitanate and titanium dioxide
FR2741063B1 (en) * 1995-11-14 1998-02-13 Europ Propulsion PROCESS FOR THE INTRODUCTION INTO POROUS SUBSTRATES OF A FUSED SILICON COMPOSITION
US5878849A (en) * 1996-05-02 1999-03-09 The Dow Chemical Company Ceramic metal composite brake components and manufacture thereof
US5957251A (en) * 1996-05-02 1999-09-28 The Dow Chemical Company Brake or clutch components having a ceramic-metal composite friction material
US6110268A (en) * 1997-03-21 2000-08-29 Daimler-Benz Aktiengesellschaft Sintered brake lining and method for its manufacture
US6458466B1 (en) * 1998-04-24 2002-10-01 Dow Global Technologies Inc. Brake or clutch components having a ceramic-metal composite friction material
JP4647053B2 (en) * 1999-02-09 2011-03-09 日本碍子株式会社 SiC-C / C composite composite material, use thereof, and production method thereof
DE10131769C5 (en) * 2001-06-30 2010-02-18 Audi Ag Brake system with composite brake disc
DE10157483C2 (en) * 2001-11-23 2003-10-16 Sgl Carbon Ag Shaped body made of fiber-reinforced composite materials with a segmented cover layer, its manufacture and its use
DE10233729B4 (en) * 2002-07-24 2006-01-26 Sgl Carbon Ag Fiber-reinforced ceramic brake pads

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3867491A (en) * 1970-06-22 1975-02-18 Carborundum Co Process for reinforced carbon bodies
EP0404571A1 (en) * 1989-06-22 1990-12-27 Toyota Jidosha Kabushiki Kaisha Sliding member
US5964320A (en) * 1996-09-10 1999-10-12 Kabushiki Kaisha Toshiba Brake shoe for elevator emergency stop
US6390304B1 (en) * 1997-06-02 2002-05-21 Hitco Carbon Composites, Inc. High performance filters comprising inorganic fibers having inorganic fiber whiskers grown thereon
US6261692B1 (en) * 1998-07-21 2001-07-17 Korea Research Institute Of Chemical Technology Carbon-carbon composites containing ceramic power and method for preparing the same
US20030180527A1 (en) * 2002-03-21 2003-09-25 Moritz Bauer Composite containing reinforcing fibers comprising carbon

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8021744B2 (en) 2004-06-18 2011-09-20 Borgwarner Inc. Fully fibrous structure friction material
US7749562B1 (en) 2004-07-26 2010-07-06 Borgwarner Inc. Porous friction material comprising nanoparticles of friction modifying material
US8603614B2 (en) 2004-07-26 2013-12-10 Borgwarner Inc. Porous friction material with nanoparticles of friction modifying material
WO2006039443A2 (en) * 2004-10-01 2006-04-13 Honeywell International Inc. Improved formulation for the manufacture of carbon-carbon composite materials
WO2006039443A3 (en) * 2004-10-01 2006-06-22 Honeywell Int Inc Improved formulation for the manufacture of carbon-carbon composite materials
US7438839B2 (en) 2004-10-01 2008-10-21 Honeywell International Inc. Formulation for the manufacture of carbon-carbon composite materials
EP2028221A1 (en) * 2007-08-03 2009-02-25 Borgwarner, Inc. Friction material with silicon
US8397889B2 (en) 2008-03-12 2013-03-19 Borgwarner Inc. Frictional device comprising at least one friction plate
EP2157330A1 (en) * 2008-08-22 2010-02-24 Honeywell International Inc. Reactive sintering to eliminate metal inserts in carbon-carbon brake discs
US10100889B2 (en) 2008-08-22 2018-10-16 Honeywell International Inc. Reactive sintering to eliminate metal inserts in carbon-carbon brake discs

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