WO2001098682A2 - Improvement of noise behavior of non-asbestos friction materials through use of fluoropolymers - Google Patents

Improvement of noise behavior of non-asbestos friction materials through use of fluoropolymers Download PDF

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Publication number
WO2001098682A2
WO2001098682A2 PCT/US2001/019398 US0119398W WO0198682A2 WO 2001098682 A2 WO2001098682 A2 WO 2001098682A2 US 0119398 W US0119398 W US 0119398W WO 0198682 A2 WO0198682 A2 WO 0198682A2
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Prior art keywords
friction material
material matrix
fluoropolymer
friction
present
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Application number
PCT/US2001/019398
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French (fr)
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WO2001098682A3 (en
Inventor
Sunil Kumar Kesavan
Original Assignee
Honeywell International Inc.
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Filing date
Publication date
Application filed by Honeywell International Inc. filed Critical Honeywell International Inc.
Priority to JP2002504407A priority Critical patent/JP2004501271A/en
Priority to EP01946462A priority patent/EP1292782A2/en
Priority to MXPA02012248A priority patent/MXPA02012248A/en
Priority to CA002413249A priority patent/CA2413249A1/en
Publication of WO2001098682A2 publication Critical patent/WO2001098682A2/en
Publication of WO2001098682A3 publication Critical patent/WO2001098682A3/en

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Classifications

    • 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
    • F16D69/025Compositions based on an organic binder
    • 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
    • F16D69/025Compositions based on an organic binder
    • F16D69/026Compositions based on an organic binder containing fibres

Definitions

  • the present invention relates generally to friction materials, and more particularly, to friction materials containing at least one fluoropolymer for use in friction linings for applications such as, but not limited to brake disk
  • Friction materials such as those typically employed in brake linings, are usually comprised of either asbestos fibers, mixtures of asbestos fibers and other heat resistant inorganic or organic fibers, asbestos-free mixtures of heat resistant inorganic or organic fibers, or metal powders such as iron powder, copper powder, steel powder or mixtures thereof, in combination with an organic monomeric or polymeric binder system (e.g., phenolic or cresylic resin).
  • an organic monomeric or polymeric binder system e.g., phenolic or cresylic resin
  • a typical friction material formulation may optionally contain one or more of the following components: thermosetting resinous binders (e.g., phenolic resins such as phenol-formaldehyde resins, epoxies, and the like) present in conventional amounts; reinforcing fibers (e.g., aramid, steel, acrylic, and the like) present in conventional amounts; metal powders (e.g., iron, copper, brass, zinc, aluminum, antimony, and the like) present in conventional amounts; solid lubricants (e.g., molybdenum disulfide, graphite, coke, stannic
  • abrasives e.g., tin oxide, magnesia, silica, iron oxide, alumina, rutile, and the like
  • organic fillers e.g., rubber particles
  • cashew nut shell particles, nitrile rubber particles, and the like present in conventional amounts; and inorganic fillers (e.g., barytes, gypsum, mica, and
  • friction materials are used in automotive brakes to slow (i.e., decelerate) and stop vehicles, by substantially converting kinetic
  • the formed friction materials run against the cast iron mating surfaces of brake rotors or drums, depending on the
  • Friction materials are typically comprised of thermoset composites containing several different materials, as previously
  • Transfer film formation is a dynamic process, i.e., the film is continuously generated and destroyed during brake use.
  • a friction material matrix comprises at least one fluoropolymer and at least one binder system.
  • a friction material matrix comprises at least one fluoropolymer present in an amount up to about 2 weight percent based on the total weight of the friction material matrix, and at least one binder system.
  • a friction material matrix comprises at least one fluoropolymer
  • fluorinated ethylene propylene selected from the group consisting of fluorinated ethylene propylene, polyvinylidene fluoride, polytetrafluoroethylene, and combinations thereof, and at least one binder system.
  • Figure 1 is a graphical illustration of the results of a dynamometer test of the noise behavior characteristics of a pair of brake pads having a
  • Figure 2 is a graphical illustration of the results of a dynamometer test of the noise behavior characteristics of a pair of brake pads having a
  • the present invention proposes the use of fluoropolymers in
  • “friction material matrix” means at least one binder system (e.g., phenolic resin), and optionally, additives such
  • reinforcing fibers as, but not limited to, reinforcing fibers, metal powders, abrasives, lubricants, organic fillers, inorganic fillers, and the like.
  • fluoropolymer means at least one polymeric material containing fluorine. Fluoropolymers are composed basically of linear polymers in which some of or all the hydrogen atoms are replaced with fluorine, and they
  • fluoropolymers rank among the best of the plastics in chemical
  • fluoropolymers In order of decreasing fluorine replacement of hydrogen, they are fluorocarbons, chlorotrifluoroethylene, and fluorohydrocarbons.
  • PTFE fluorinated ethylene propylene
  • CF 2 CF 2 ) n is made by polymerizing the tetrafluoroethylene (TFE) monomer.
  • TFE tetrafluoroethylene
  • the white-to-translucent solid polymer has an extremely high molecular weight, i.e., in the 10 6 -10 7 range, and, consequently, has a viscosity of about 10 GPa»s (10 11 P) at 380°C.
  • Its high thermal stability results from the strong carbon-fluorine bond and characterizes PTFE as a very useful high temperature polymer.
  • Its heat resistance, chemical inertness, electrical insulation properties, and its low coefficient of friction in a very wide temperature range make PTFE the most outstanding plastic in the industry.
  • PTFE is readily commercially available from Honeywell, Inc.
  • TEFLON PTFE K-10 is a free-flowing white powder having an average particle size of 560 micrometers, a bulk density of 570 g/L, a standard specific gravity of 2.16, a melting range of 320-340 C (608-644 F), is insoluble in all common solvents, and is stable to all common reagents at ordinary temperatures, and reacts with alkali metals and fluorine or reactive
  • FEP is a semi-crystalline perfluorinated polymer closely related to PTFE being a copolymer of tetrafluoroethylene and hexafluoropropylene.
  • FEP has the great practical advantage of being melt-processable, albeit at
  • FEP Compared to PTFE, FEP has similarly excellent chemical
  • FEP has better radiation resistance and much higher
  • FEP is readily commercially available from DuPont (under the tradename TEFLON FEP) and Hoechst (under the tradename HOSTAFLON
  • the fluorohydrocarbons are of two kinds: polyvinylidene fluoride
  • PVDF polyvinyl fluoride
  • fluorohydrocarbons While similar to the other fluoropolymers, fluorohydrocarbons have somewhat lower heat resistance and considerably higher tensile and cbmpressive strength.
  • PVDF is the polymer of 1 ,1-difIuoroethylene. PVDF is a semi-
  • PVDF is readily commercially available from Pennwalt Corp., (under the tradename KYNAR).
  • fluoropolymers such as, but not limited to PTFE,
  • FEP, and PVDF can be used for the purposes of this invention.
  • Fluoropolymers in either a powder or dispersion form, can be incorporated, in varying amounts, into the friction material during a wet or dry mixing process.
  • the fluoropolymer material is present in the friction material matrix in an amount of from about 0.1 to about 5 weight percent, based on the total
  • the fluoropolymer material is present in
  • the friction material matrix in an amount of up to about 2 weight percent, based on the total weight of the friction material matrix.
  • Example I a typical formulation of a friction material matrix containing at least one fluoropolymer material, in accordance with one embodiment of the present invention, is presented in Example I, below:
  • Example II a typical formulation of a friction material matrix containing at least one fluoropolymer material, in accordance with another embodiment of the present invention, is presented in Example II, below:
  • the friction materials containing at least one fluoropolymer material of the present invention reduce the tendency for brakes to generate noise (as well as vibration) by ensuring, for example, that a thin and uniform transfer film is continuously being generated at the friction couple between the brake pad and the rotor or drum.
  • a comparison test was performed.
  • a first pair of brake pads having a friction lining formulation containing no fluoropolymer material (designated HFM-1) was subjected to a dynamometer test in order to evaluate the total noise produced at various frequencies (see Figure 1).
  • the total noise of the HFM-1 formulation was significantly higher than the HFM-2 formulation, thus indicating that brake pads containing at least one fluoropolymer material in accordance with the present invention will produce less noise, especially less high frequency noise (i.e., squeal). Also noteworthy was the fact that the HFM-2 formulation did not produce any noise whatsoever above the 4000 Hz frequency.

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  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Braking Arrangements (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

Friction materials which contain at least one fluoropolymer material for use in friction linings for applications such as, but not limited to brake disk pads, are described. The fluoropolymer material, such as, but not limited to PTFE, FEP, and PVDF, is preferably present in an amount of from about 0.1 to about 5 weight percent, based on the total weight of the friction material matrix.

Description

IMPROVEMENT OF NOISE BEHAVIOR OF NON-ASBESTOS FRICTION MATERIALS THROUGH USE OF FLUOROPOLYMERS
BACKGROUND OF THE INVENTION
1. Technical Field
The present invention relates generally to friction materials, and more particularly, to friction materials containing at least one fluoropolymer for use in friction linings for applications such as, but not limited to brake disk
pads.
2. Discussion
Friction materials, such as those typically employed in brake linings, are usually comprised of either asbestos fibers, mixtures of asbestos fibers and other heat resistant inorganic or organic fibers, asbestos-free mixtures of heat resistant inorganic or organic fibers, or metal powders such as iron powder, copper powder, steel powder or mixtures thereof, in combination with an organic monomeric or polymeric binder system (e.g., phenolic or cresylic resin). Because asbestos has been alleged to be the cause of certain health problems and is no longer environmentally acceptable, most modern friction materials are made without asbestos. Thus, most current friction materials are made from synthetic and steel fibers, and iron, ceramic, and metallic powders.
A typical friction material formulation may optionally contain one or more of the following components: thermosetting resinous binders (e.g., phenolic resins such as phenol-formaldehyde resins, epoxies, and the like) present in conventional amounts; reinforcing fibers (e.g., aramid, steel, acrylic, and the like) present in conventional amounts; metal powders (e.g., iron, copper, brass, zinc, aluminum, antimony, and the like) present in conventional amounts; solid lubricants (e.g., molybdenum disulfide, graphite, coke, stannic
sulfide, antimony trisulf.de, and the like) present in conventional amounts;
abrasives (e.g., tin oxide, magnesia, silica, iron oxide, alumina, rutile, and the like) present in conventional amounts; organic fillers (e.g., rubber particles,
cashew nut shell particles, nitrile rubber particles, and the like) present in conventional amounts; and inorganic fillers (e.g., barytes, gypsum, mica, and
the like) present in conventional amounts. Other materials may be added as
well, as is known in the art.
In practice, friction materials are used in automotive brakes to slow (i.e., decelerate) and stop vehicles, by substantially converting kinetic
energy into heat. In operation, the formed friction materials run against the cast iron mating surfaces of brake rotors or drums, depending on the
configuration of the brake system. Friction materials are typically comprised of thermoset composites containing several different materials, as previously
described. The important end-use performance aspects of friction materials which are of interest to automotive manufacturers are the friction behavior,
wear life, and noise levels. Unsatisfactory noise and vibration behavior of brake systems is an important source of customer complaints and dissatisfaction. Customer dissatisfaction results in large warranty costs to
automotive manufacturers.
During use, the physiochemical changes at the interface between
the friction material and the cast iron rotors/drums of the brake system govern the performance behavior of the friction couple. When friction materials run against the cast iron surfaces in a friction couple, transfer films (also referred
to as a glaze) with complex chemical compositions are formed on the cast iron and friction material surfaces. The transfer films generated during brake use
are thermal reaction products of the cast iron and the chemical ingredients
present in the friction material.
Transfer film formation is a dynamic process, i.e., the film is continuously generated and destroyed during brake use. The chemical and
physical characteristics of the transfer film govern brake performance. The formation of a thin and uniform transfer film is desirable in brake operation.
Conversely, uneven transfer films are thought to produce undesirable levels of noise and/or vibration in brake systems, especially during braking
operations.
Therefore, there exists a need for a friction material that is
capable of continuously generating a thin and uniform transfer film, and which can be universally incorporated in a variety of compositions for the preparation
of friction materials, especially in asbestos-free, semi-metallic, and/or low- metallic friction materials, and above all, offers low-noise and low-vibration
levels during braking operations.
SUMMARY OF THE INVENTION
In accordance with one embodiment of the present invention, a friction material matrix comprises at least one fluoropolymer and at least one binder system.
In accordance with another embodiment of the present invention, a friction material matrix comprises at least one fluoropolymer present in an amount up to about 2 weight percent based on the total weight of the friction material matrix, and at least one binder system.
In accordance with still another embodiment of the present invention, a friction material matrix comprises at least one fluoropolymer
present in an amount from about 0.1 to about 5 weight percent based on the total weight of the friction material matrix, wherein the fluoropolymer is
selected from the group consisting of fluorinated ethylene propylene, polyvinylidene fluoride, polytetrafluoroethylene, and combinations thereof, and at least one binder system.
A more complete appreciation of the present invention and its
scope can be obtained from the following brief description of the drawings, detailed description of the invention, and the appended claims.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a graphical illustration of the results of a dynamometer test of the noise behavior characteristics of a pair of brake pads having a
brake lining formulation containing no fluoropolymer material; and
Figure 2 is a graphical illustration of the results of a dynamometer test of the noise behavior characteristics of a pair of brake pads having a
brake lining formulation containing at least one fluoropolymer material, in accordance with one embodiment of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
The present invention proposes the use of fluoropolymers in
friction materials to reduce or prevent unacceptable levels of brake noise during routine operation of the automobile's brake system.
As that term is used herein, "friction material matrix" means at least one binder system (e.g., phenolic resin), and optionally, additives such
as, but not limited to, reinforcing fibers, metal powders, abrasives, lubricants, organic fillers, inorganic fillers, and the like.
As that term is used herein, "fluoropolymer" means at least one polymeric material containing fluorine. Fluoropolymers are composed basically of linear polymers in which some of or all the hydrogen atoms are replaced with fluorine, and they
are characterized by relatively high crystallinity and molecular weight. As a class, fluoropolymers rank among the best of the plastics in chemical
resistance and elevated-temperature performance. Their maximum service temperature ranges up to about 500°F (260°C). They also have excellent
frictional properties and cannot be wet by many liquids. Their dielectric strength is high and is relatively insensitive to temperature and power frequency. Mechanical properties, including tensile creep and fatigue strength, are only fair, although impact strength is relatively high. There are three major classes of fluoropolymers. In order of decreasing fluorine replacement of hydrogen, they are fluorocarbons, chlorotrifluoroethylene, and fluorohydrocarbons.
There are two fluorocarbon types of note: polytetrafluoroethylene
(PTFE) and fluorinated ethylene propylene (FEP).
PTFE, a perfluorinated straight-chain high polymer having the
chemical formula (CF2CF2)n, is made by polymerizing the tetrafluoroethylene (TFE) monomer. The white-to-translucent solid polymer has an extremely high molecular weight, i.e., in the 106-107 range, and, consequently, has a viscosity of about 10 GPa»s (1011 P) at 380°C. Its high thermal stability results from the strong carbon-fluorine bond and characterizes PTFE as a very useful high temperature polymer. Its heat resistance, chemical inertness, electrical insulation properties, and its low coefficient of friction in a very wide temperature range make PTFE the most outstanding plastic in the industry. PTFE is readily commercially available from Honeywell, Inc.
(under the tradename HALON), Daikin Kogyo (under the tradename POLYFLON), DuPont (under the tradename TEFLON), Hoechst (under the tradename HOSTAFLON), and ICI (under the tradename FLUON).
One particular grade of TEFLON that is particularly preferred in the practice of the present invention is available under the tradename TEFLON PTFE K-10 (Du Pont). TEFLON PTFE K-10 is a free-flowing white powder having an average particle size of 560 micrometers, a bulk density of 570 g/L, a standard specific gravity of 2.16, a melting range of 320-340 C (608-644 F), is insoluble in all common solvents, and is stable to all common reagents at ordinary temperatures, and reacts with alkali metals and fluorine or reactive
agents yielding fluorine.
FEP is a semi-crystalline perfluorinated polymer closely related to PTFE being a copolymer of tetrafluoroethylene and hexafluoropropylene.
Its properties are similar, but generally a little inferior to, those of PTFE; but,
FEP has the great practical advantage of being melt-processable, albeit at
greater expense.
Compared to PTFE, FEP has similarly excellent chemical
resistance and electrical properties (up to very high frequencies) and good weathering resistance. FEP has better radiation resistance and much higher
impact strength than PTFE, but has lower maximum use and heat deflection temperatures and is even a little less stiff and strong.
FEP is readily commercially available from DuPont (under the tradename TEFLON FEP) and Hoechst (under the tradename HOSTAFLON
FEP).
The fluorohydrocarbons are of two kinds: polyvinylidene fluoride
(PVF2, or PVDF) and polyvinyl fluoride (PVF). While similar to the other fluoropolymers, fluorohydrocarbons have somewhat lower heat resistance and considerably higher tensile and cbmpressive strength.
PVDF is the polymer of 1 ,1-difIuoroethylene. PVDF is a semi-
crystalline polymer containing 59.4% fluorine. The symmetrical arrangement of the hydrogen and fluorine atoms in the chain contributes to the unique polarity which influences the polymer's dielectric properties and solubility.
PVDF is readily commercially available from Pennwalt Corp., (under the tradename KYNAR).
Accordingly, fluoropolymers such as, but not limited to PTFE,
FEP, and PVDF can be used for the purposes of this invention.
Fluoropolymers, in either a powder or dispersion form, can be incorporated, in varying amounts, into the friction material during a wet or dry mixing process.
In accordance with a preferred embodiment of the present
invention, the fluoropolymer material is present in the friction material matrix in an amount of from about 0.1 to about 5 weight percent, based on the total
weight of the friction material matrix. In accordance with a highly preferred embodiment of the present invention, the fluoropolymer material is present in
the friction material matrix in an amount of up to about 2 weight percent, based on the total weight of the friction material matrix.
By way of a non-limiting example, a typical formulation of a friction material matrix containing at least one fluoropolymer material, in accordance with one embodiment of the present invention, is presented in Example I, below:
EXAMPLE I
Figure imgf000009_0001
Figure imgf000010_0001
By way of a non-limiting example, a typical formulation of a friction material matrix containing at least one fluoropolymer material, in accordance with another embodiment of the present invention, is presented in Example II, below:
EXAMPLE II
Figure imgf000011_0001
The friction materials containing at least one fluoropolymer material of the present invention reduce the tendency for brakes to generate noise (as well as vibration) by ensuring, for example, that a thin and uniform transfer film is continuously being generated at the friction couple between the brake pad and the rotor or drum.
In order to evaluate the noise behavior characteristics of brake pads having a friction lining formulation containing at least one fluoropolymer material at levels in accordance with the present invention, a comparison test was performed. A first pair of brake pads having a friction lining formulation containing no fluoropolymer material (designated HFM-1) was subjected to a dynamometer test in order to evaluate the total noise produced at various frequencies (see Figure 1). A second pair of brake pads having a friction lining formulation containing at least one fluoropolymer material present at levels in accordance with the present invention, i.e., from about 0.1 to about 5 weight percent, was also subjected to a dynamometer test in order to evaluate the total noise produced at various frequencies (see Figure 2).
As can be determined from comparing Figure 1 with Figure 2, the total noise of the HFM-1 formulation, especially at 5000 Hz, was significantly higher than the HFM-2 formulation, thus indicating that brake pads containing at least one fluoropolymer material in accordance with the present invention will produce less noise, especially less high frequency noise (i.e., squeal). Also noteworthy was the fact that the HFM-2 formulation did not produce any noise whatsoever above the 4000 Hz frequency.
The foregoing description is considered illustrative only of the principles of the invention. Furthermore, because numerous modifications and changes will readily occur to those skilled in the an, it is not desired to limit the invention to the exact construction and process shown as described above. Accordingly, all suitable modifications and equivalents that may be resorted to that fall within the scope of the invention as defined by the claims that follow.

Claims

What is claimed is:
1. A friction material matrix, comprising: at least one fluoropolymer; and at least one binder system.
2. The friction material matrix of claim 1, wherein the fluoropolymer is present in an amount from about 0.1 to about 5 weight percent based on the total weight of the friction material matrix.
3. The friction material matrix of claim 1, wherein the fluoropolymer is present in an amount up to about 2 weight percent based on the total weight of the friction material matrix.
4. The friction material matrix of claim 1, wherein the fluoropolymer is selected from the group consisting of fluorinated ethylene propylene, polyvinylidene fluoride, polytetrafluoroethylene, and combinations thereof.
5. The friction material matrix of claim 1 , further comprising any one of the following components: at least one reinforcing fiber; at least one metal powder; at least one abrasive; at least one lubricant; at least one organic filler; and at least one inorganic filler.
6. A friction material matrix, comprising: at least one fluoropolymer present in an amount up to about 2 weight percent based on the total weight of the friction material matrix; and at least one binder system.
7. The friction material matrix of claim 6, wherein the fluoropolymer is selected from the group consisting of fluorinated ethylene propylene, polyvinylidene fluoride, polytetrafluoroethylene, and combinations thereof.
8. The friction material matrix of claim 6, further comprising any one of the following components:
at least one reinforcing fiber; at least one metal powder;
at least one abrasive; at least one lubricant;
at least one organic filler; and at least one inorganic filler.
9. A friction material matrix, comprising: at least one fluoropolymer present in an amount from about 0.1 to about
5 weight percent based on the total weight of the friction material matrix,
wherein the fluoropolymer is selected from the group consisting of fluorinated ethylene propylene, polyvinylidene fluoride, polytetrafluoroethylene, and combinations thereof; and at least one binder system.
10. The friction material matrix of claim 9, further comprising any one of the following components:
at least one reinforcing fiber; at least one metal powder;
at least one abrasive; at least one lubricant; at least one organic filler; and at least one inorganic filler.
PCT/US2001/019398 2000-06-16 2001-06-18 Improvement of noise behavior of non-asbestos friction materials through use of fluoropolymers WO2001098682A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2002504407A JP2004501271A (en) 2000-06-16 2001-06-18 Improving the noise behavior of non-asbestos friction materials by using fluoropolymers
EP01946462A EP1292782A2 (en) 2000-06-16 2001-06-18 Improvement of noise behavior of non-asbestos friction materials through use of fluoropolymers
MXPA02012248A MXPA02012248A (en) 2000-06-16 2001-06-18 Improvement of noise behavior of non-asbestos friction materials through use of fluoropolymers.
CA002413249A CA2413249A1 (en) 2000-06-16 2001-06-18 Improvement of noise behavior of non-asbestos friction materials through use of fluoropolymers

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US59653600A 2000-06-16 2000-06-16
US09/596,536 2000-06-16

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WO2004069954A1 (en) * 2003-02-05 2004-08-19 Hitachi Chemical Co., Ltd. Friction material composition and friction material therefrom
CN102449098A (en) * 2009-06-01 2012-05-09 日立化成工业株式会社 Friction material composition, friction material obtained from same, and friction member
CN105088744A (en) * 2015-08-31 2015-11-25 万山特区宏安摩擦材料有限公司 Modifying method of aramid fiber for carbon-based ceramic friction material
US20160245353A1 (en) * 2013-11-12 2016-08-25 Akebono Brake Industry Co., Ltd. Friction material composition and friction material

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JP2007112952A (en) * 2005-10-24 2007-05-10 Nisshinbo Ind Inc Friction material
CN111075869A (en) * 2019-12-04 2020-04-28 贵州新安航空机械有限责任公司 Composite brake shoe material formula for railway freight car and preparation process of composite brake shoe

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004069954A1 (en) * 2003-02-05 2004-08-19 Hitachi Chemical Co., Ltd. Friction material composition and friction material therefrom
EP1609837A1 (en) * 2003-02-05 2005-12-28 Hitachi Chemical Company, Ltd. Friction material composition and friction material therefrom
JPWO2004069954A1 (en) * 2003-02-05 2006-05-25 日立化成工業株式会社 Friction material composition and friction material using friction material composition
JP4613131B2 (en) * 2003-02-05 2011-01-12 日立化成工業株式会社 Friction material composition and friction material using friction material composition
JP2011017016A (en) * 2003-02-05 2011-01-27 Hitachi Chem Co Ltd Friction material composition and friction material therefrom
EP1609837A4 (en) * 2003-02-05 2011-04-13 Hitachi Chemical Co Ltd Friction material composition and friction material therefrom
US8418818B2 (en) 2003-02-05 2013-04-16 Hitachi Chemical Co., Ltd. Friction material composition and friction material therefrom
CN102449098A (en) * 2009-06-01 2012-05-09 日立化成工业株式会社 Friction material composition, friction material obtained from same, and friction member
US20160245353A1 (en) * 2013-11-12 2016-08-25 Akebono Brake Industry Co., Ltd. Friction material composition and friction material
EP3070140B1 (en) 2013-11-12 2021-04-28 Akebono Brake Industry Co., Ltd. Method of making a friction material
CN105088744A (en) * 2015-08-31 2015-11-25 万山特区宏安摩擦材料有限公司 Modifying method of aramid fiber for carbon-based ceramic friction material

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CA2413249A1 (en) 2001-12-27
MXPA02012248A (en) 2004-01-26
JP2004501271A (en) 2004-01-15
EP1292782A2 (en) 2003-03-19
WO2001098682A3 (en) 2002-04-11

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