JPH02209635A - Friction material for brake - Google Patents
Friction material for brakeInfo
- Publication number
- JPH02209635A JPH02209635A JP2646589A JP2646589A JPH02209635A JP H02209635 A JPH02209635 A JP H02209635A JP 2646589 A JP2646589 A JP 2646589A JP 2646589 A JP2646589 A JP 2646589A JP H02209635 A JPH02209635 A JP H02209635A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- brake
- friction
- friction material
- grain
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002783 friction material Substances 0.000 title claims abstract description 25
- 239000000835 fiber Substances 0.000 claims abstract description 48
- 239000000463 material Substances 0.000 claims abstract description 19
- 239000013078 crystal Substances 0.000 claims abstract description 16
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 229920005989 resin Polymers 0.000 claims abstract description 9
- 239000011347 resin Substances 0.000 claims abstract description 9
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 15
- 239000010439 graphite Substances 0.000 claims description 15
- 229910002804 graphite Inorganic materials 0.000 claims description 15
- 239000000945 filler Substances 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 5
- 229910000831 Steel Inorganic materials 0.000 abstract description 5
- 239000010959 steel Substances 0.000 abstract description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 abstract description 4
- 239000000428 dust Substances 0.000 abstract description 4
- 239000005060 rubber Substances 0.000 abstract description 4
- 239000003365 glass fiber Substances 0.000 abstract description 3
- 239000012784 inorganic fiber Substances 0.000 abstract description 3
- 239000000377 silicon dioxide Substances 0.000 abstract description 2
- 238000005299 abrasion Methods 0.000 abstract 1
- 238000004299 exfoliation Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- 239000004760 aramid Substances 0.000 description 3
- 239000010425 asbestos Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- 229910001369 Brass Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 229920003235 aromatic polyamide Polymers 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005087 graphitization Methods 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 244000226021 Anacardium occidentale Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Braking Arrangements (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は主に自動車、鉄道車輌、飛行機、産業機械等に
使用されるブレーキ用摩擦材に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a friction material for brakes mainly used in automobiles, railway vehicles, airplanes, industrial machinery, etc.
[従来の技術]
従来この種の摩擦材は、繊維基材として石綿が主に用い
られてきたが、最近では作業環境の改善または石綿公害
防止のため摩擦材の無石綿化が進められている。[Conventional technology] Conventionally, this type of friction material has mainly used asbestos as the fiber base material, but recently, asbestos-free friction materials have been promoted to improve the working environment and prevent asbestos pollution. .
石綿に替わる繊維基材としてガラス繊維、アルミナ繊維
、ロックウール、チタン酸カリウム繊維などの無機繊維
、スチール繊維、銅111Il維、真ちゅう繊維などの
金属繊維や麻、木綿、レーヨン、フェノール繊維、芳香
族ポリアミドya維などの有機繊維が単独または適宜組
合せた繊維基材が検討されている。As fiber base materials to replace asbestos, inorganic fibers such as glass fiber, alumina fiber, rock wool, potassium titanate fiber, metal fibers such as steel fiber, copper 111I fiber, brass fiber, hemp, cotton, rayon, phenol fiber, and aromatic fibers are used. Fiber base materials made of organic fibers such as polyamide ya fibers alone or in appropriate combinations are being considered.
例えばスチールファイバーと黒鉛および黒鉛とゴムの混
合物を用いた摩擦組成物が特開昭61−168684号
公報に開示されている。また特開昭62−106980
号公報には、金属繊維(金属粉)とアラミツド繊維(ア
ラミツドバルブ)と黒鉛、二硫化モリブデン等の潤滑剤
、結合剤および充填材からなる摩擦材が開示されている
。For example, a friction composition using a mixture of steel fiber and graphite or graphite and rubber is disclosed in JP-A-61-168684. Also, JP-A-62-106980
The publication discloses a friction material comprising metal fibers (metal powder), aramid fibers (aramid valves), a lubricant such as graphite or molybdenum disulfide, a binder, and a filler.
[発明の解決すべき問題点]
しかしながら、この種のスチール繊維等の金属繊維と黒
鉛を主成分とする摩擦材において、摩擦材の耐摩耗性向
上剤として用いられている黒鉛が高温制動時に相手材で
あるディスクロータに付着し、摩擦係数を低下させると
いう問題点がある。[Problems to be Solved by the Invention] However, in this type of friction material whose main components are metal fibers such as steel fibers and graphite, graphite, which is used as a wear resistance improver of the friction material, becomes resistant to friction during high-temperature braking. There is a problem in that it adheres to the disc rotor, which is a material, and reduces the coefficient of friction.
[問題点を解決するための手段]
本発明の目的は、上記の問題点を解決し、高摩擦係数、
耐摩耗性に優れたブレーキ用摩擦材を提供するものであ
る。[Means for Solving the Problems] An object of the present invention is to solve the above problems and provide a high coefficient of friction,
The present invention provides a brake friction material with excellent wear resistance.
本発明者等は、上記の問題点を解決すべく、鋭意研究を
続けてきた。その結果、黒鉛の結晶化度が相手材への付
着に大きな影習を与えることを知見し、本発明を完成す
るに至った。The present inventors have continued their intensive research in order to solve the above problems. As a result, it was discovered that the degree of crystallinity of graphite greatly affects its adhesion to a mating material, and the present invention was completed.
すなわち本発明は、少なくとも金属繊維を含有する繊維
基材、充填材および熱硬化性樹脂からなるブレーキ用摩
擦材であって、結晶粒子(La 、 Lc)が80〜9
0nmである黒鉛を含むことを特徴とするブレーキ用摩
擦材である。That is, the present invention provides a friction material for brakes consisting of a fiber base material containing at least metal fibers, a filler, and a thermosetting resin, wherein the crystal particles (La, Lc) are 80 to 9
This is a brake friction material characterized by containing 0 nm of graphite.
本発明で用いる金属繊維は、スチール繊維、しんちゅう
繊維、チタン繊維である。金属繊維以外の繊維基材とし
ては、ガラス繊維、シリカ繊維、アルミナ繊維、ロック
ウール、チタン酸カリウム繊維などの無機繊維および麻
、木綿、レーヨン、フェノール繊維、芳香族ポリアミド
繊維などの有機ia維の1f!!または2 fffi以
上の短繊維が使用できる。The metal fibers used in the present invention are steel fibers, brass fibers, and titanium fibers. Fiber base materials other than metal fibers include inorganic fibers such as glass fiber, silica fiber, alumina fiber, rock wool, and potassium titanate fiber, and organic IA fibers such as hemp, cotton, rayon, phenol fiber, and aromatic polyamide fiber. 1f! ! Alternatively, short fibers of 2 fffi or more can be used.
前記の繊維基材の繊維径は5μm〜1100uが好まし
く、繊維長はo、tmm〜3mmが好ましい。The fiber diameter of the fiber base material is preferably 5 μm to 1100 μm, and the fiber length is preferably o, tmm to 3 mm.
本発明で用いられる黒鉛は、結晶粒子(La 、 Lc
)が80〜900mであり、その層間隔(C/2)は0
.3357r+mが好ましい。黒鉛の結晶構造について
理想的な黒鉛結晶にどれだけ近い状態であるかの程度を
示す黒鉛化度と言う表現が用いられ、この黒鉛化度は、
−船釣には、結晶粒子(La 、 Lc)及び層間距t
Ji(C/2)で表わされる。The graphite used in the present invention has crystal grains (La, Lc
) is 80 to 900 m, and the layer spacing (C/2) is 0
.. 3357r+m is preferred. The expression "degree of graphitization" is used to indicate how close the crystal structure of graphite is to an ideal graphite crystal.
- For boat fishing, crystal grains (La, Lc) and interlayer distance t
It is expressed as Ji (C/2).
−船釣に、天然黒鉛の結晶粒子は1100n以上であり
、黒鉛化度が高いため、耐摩耗性が良好であるが、熱履
歴後の摩擦係数が低く、好ましくない。- For boat fishing, natural graphite crystal particles have a size of 1100 nm or more and a high degree of graphitization, so wear resistance is good, but the coefficient of friction after heat history is low, which is not preferable.
結晶粒子80〜90nmの黒鉛の配合量は全摩擦材に対
して5〜20重量%が好ましい。The blending amount of graphite having crystal grains of 80 to 90 nm is preferably 5 to 20% by weight based on the total friction material.
本発明において、結晶粒子が80〜90nmの黒鉛以外
の充填材として、カシューダスト、ラバーダスト、硫酸
バリウム、珪藻土、アルミナ、ドロマイト、炭酸カルシ
ウム等の摩擦調整剤を含有させることができる。In the present invention, a friction modifier such as cashew dust, rubber dust, barium sulfate, diatomaceous earth, alumina, dolomite, calcium carbonate, etc. can be included as a filler other than graphite having crystal particles of 80 to 90 nm.
つぎに本発明に用いる熱硬化性樹脂は、フェノール樹脂
、メラミン樹脂、エポキシ樹脂、ポリエステル樹脂、フ
ェノール変性メラミン樹脂およびオイル、ゴム、メラミ
ン、エポキシまたはポリビニルブチラール変性フェノー
ル樹脂の1種または2種以上の混合物が使用される。こ
れらの熱硬化性樹脂の配合量は全摩擦材中に5〜15重
量%が好ましい。Next, the thermosetting resin used in the present invention is one or more of phenol resin, melamine resin, epoxy resin, polyester resin, phenol-modified melamine resin, and oil, rubber, melamine, epoxy, or polyvinyl butyral-modified phenol resin. A mixture is used. The blending amount of these thermosetting resins is preferably 5 to 15% by weight in the total friction material.
つぎに本発明のブレーキ用無石綿摩擦材の製造方法は、
従来用いられている方法であり、次の通りである。Next, the method for manufacturing the asbestos-free friction material for brakes of the present invention is as follows:
This is a conventionally used method and is as follows.
繊維基材、充填材および粉末の熱硬化性樹脂の所定配合
量を、バンバリーミキサ−、ヘンシェルミキサー ニー
ダあるいは■型ブレンダー等で十分均一に混合して混合
原料を製造する。この混合原料を型内に充填し、押圧し
て予備成形を行う。A mixed raw material is produced by thoroughly and uniformly mixing predetermined amounts of the fiber base material, filler, and powdered thermosetting resin using a Banbury mixer, a Henschel mixer kneader, a type blender, or the like. This mixed raw material is filled into a mold and pressed to perform preforming.
この予備成形品を加熱加圧して、熱硬化性樹脂で硬化結
合させたのち、さらに熱処理をして摩擦材を製造する。This preformed product is heated and pressurized to harden and bond with a thermosetting resin, and then further heat treated to produce a friction material.
[発明の作用および効果]
本発明のブレーキ用摩擦材によれば、少なくとも金属繊
維を含有する繊維基材、充填材および熱硬化性樹脂から
なる摩擦材中に、結晶粒子が80〜90nmである黒鉛
を含有することにより、耐摩耗性もよく、かつ結晶粒子
間のパクリ強度が強いため、相手材への黒鉛の付着を抑
制し、高温制動時の摩擦係数の低下を防ぐ。[Operations and Effects of the Invention] According to the friction material for brakes of the present invention, crystal particles are 80 to 90 nm in the friction material made of a fiber base material containing at least metal fibers, a filler, and a thermosetting resin. By containing graphite, it has good wear resistance and strong cracking strength between crystal particles, which suppresses adhesion of graphite to the mating material and prevents a decrease in the coefficient of friction during high-temperature braking.
結晶粒子が80nm未溝の場合は耐摩耗性が十分でなく
、結晶粒、子が1100nを超えると熱履歴後の摩擦係
数が低くなる。If the crystal grain size is 80 nm without grooves, the wear resistance is insufficient, and if the crystal grain size exceeds 1100 nm, the friction coefficient after thermal history becomes low.
[実施例]
以下、本発明の実施例を示すが、本発明はこれに限定さ
れるものではない。[Example] Examples of the present invention will be shown below, but the present invention is not limited thereto.
実施例1〜2、および比較例1〜2
V型ブレンダーにて表1に示す組成を均一に混合して混
合原料を得た。この混合原料を常温で面圧力300 k
g/c+n’に調整した成形機にて20秒間予備成形し
予備成形品を得た。その後面圧力300 kg/cm2
金型温度150℃に調整した成形機を用いて7分間加熱
加圧した。その後250℃で2時間30分間加熱炉内で
熱処理をし、放冷後所定寸法に研摩して摩擦材を得た。Examples 1 and 2 and Comparative Examples 1 and 2 The compositions shown in Table 1 were uniformly mixed using a V-type blender to obtain mixed raw materials. This mixed raw material is heated to a surface pressure of 300 k at room temperature.
A preformed product was obtained by preforming for 20 seconds in a molding machine adjusted to g/c+n'. Rear pressure 300 kg/cm2
The molding machine was heated and pressurized for 7 minutes using a molding machine adjusted to a mold temperature of 150°C. Thereafter, it was heat-treated in a heating furnace at 250° C. for 2 hours and 30 minutes, and after being allowed to cool, it was polished to a predetermined size to obtain a friction material.
表1の各側の配合によって得た摩擦材についてブレーキ
ダイナモメータ試験機で、耐摩耗性試験と耐フエード試
験をした。試験結果を表2に示した。Friction materials obtained according to the formulations on each side of Table 1 were subjected to a wear resistance test and a fade resistance test using a brake dynamometer tester. The test results are shown in Table 2.
耐摩耗性試験の方法は、JASO−C427−83[ブ
レーキ型式: PD51g、ロータ:18mmベンチレ
ーテッドタイプ、イナーシャ(負荷):4.Okg−f
−m−52制動初速度: 50 km/h、減速度:0
.3G]である。The method of the wear resistance test was JASO-C427-83 [brake type: PD51g, rotor: 18mm ventilated type, inertia (load): 4. Okg-f
-m-52 Braking initial speed: 50 km/h, deceleration: 0
.. 3G].
第3効力の試験の方法は、JASO−C406−82[
ブレーキ型式: PD51s 、ロータ:18vnベン
チレーテツドタイプ、イナーシャ(負荷): 5 、
Okg−f−m−s2第2フェード後の効力]である。The third efficacy test method is JASO-C406-82 [
Brake model: PD51s, rotor: 18vn ventilated type, inertia (load): 5,
Okg-f-m-s2 efficacy after second fade].
(以下余白)
(表2)試験結果
表2に示されるように、実施例1.2のブレーキ用摩擦
材は、比較例1.2の摩擦材に比べ、摩耗率が小さく、
第3効力の摩擦係数の低下もなく、バランスのよい優れ
た摩擦材であることがわかる。(Margin below) (Table 2) Test Results As shown in Table 2, the brake friction material of Example 1.2 had a lower wear rate than the friction material of Comparative Example 1.2.
It can be seen that there is no decrease in the third effect friction coefficient, making it an excellent and well-balanced friction material.
特許出願人 アイシン化工株式会社 代表者宮地治夫 (表1)配合組成 (単位:重量%) (以下余白)Patent applicant: Aisin Kako Co., Ltd. Representative Haruo Miyaji (Table 1) Mixture composition (Unit: weight%) (Margin below)
Claims (1)
および熱硬化性樹脂からなるブレーキ用摩擦材であって
、結晶粒子(La、Lc)が80〜90nmである黒鉛
を含むことを特徴とするブレーキ用摩擦材。(1) A brake friction material consisting of a fiber base material containing at least metal fibers, a filler, and a thermosetting resin, characterized by containing graphite having crystal particles (La, Lc) of 80 to 90 nm. Friction material for brakes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2646589A JPH02209635A (en) | 1989-02-03 | 1989-02-03 | Friction material for brake |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2646589A JPH02209635A (en) | 1989-02-03 | 1989-02-03 | Friction material for brake |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02209635A true JPH02209635A (en) | 1990-08-21 |
JPH0555735B2 JPH0555735B2 (en) | 1993-08-17 |
Family
ID=12194269
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2646589A Granted JPH02209635A (en) | 1989-02-03 | 1989-02-03 | Friction material for brake |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02209635A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008133056A1 (en) * | 2007-04-13 | 2008-11-06 | Nissan Motor Co., Ltd. | Non-asbestos friction material |
JP2008280521A (en) * | 2007-04-13 | 2008-11-20 | Nissan Motor Co Ltd | Non-asbestos friction material |
WO2017183618A1 (en) * | 2016-04-20 | 2017-10-26 | 株式会社アドヴィックス | Non-asbestos friction material |
-
1989
- 1989-02-03 JP JP2646589A patent/JPH02209635A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008133056A1 (en) * | 2007-04-13 | 2008-11-06 | Nissan Motor Co., Ltd. | Non-asbestos friction material |
JP2008280521A (en) * | 2007-04-13 | 2008-11-20 | Nissan Motor Co Ltd | Non-asbestos friction material |
WO2017183618A1 (en) * | 2016-04-20 | 2017-10-26 | 株式会社アドヴィックス | Non-asbestos friction material |
CN109072046A (en) * | 2016-04-20 | 2018-12-21 | 株式会社爱德克斯 | Non-asbestos system friction material |
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JPH0555735B2 (en) | 1993-08-17 |
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