JPH02209635A - Friction material for brake - Google Patents

Friction material for brake

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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
Application number
JP2646589A
Other languages
Japanese (ja)
Other versions
JPH0555735B2 (en
Inventor
Tamotsu Hayashi
保 林
Tomio Inoue
井上 富雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aisin Chemical Co Ltd
Original Assignee
Aisin Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Aisin Chemical Co Ltd filed Critical Aisin Chemical Co Ltd
Priority to JP2646589A priority Critical patent/JPH02209635A/en
Publication of JPH02209635A publication Critical patent/JPH02209635A/en
Publication of JPH0555735B2 publication Critical patent/JPH0555735B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To prevent lowering of frictional coefficient at the time of high temperature braking by having a friction material for brake made of a fiber base material containing at least metal fiber, a filling material and thermosetting resin contain black lead whose crystal grain (La, Lc) is specific. CONSTITUTION:A mixed material for a fiction material for brake is obtained by a fiber base material made of inorganic fiber such as glass fiber, silica fiber and alumina fiber containing at least metal fiber such as steel fiber and so on and organic fiber, a filling material such as cashoo dust, rubber dust, barium sulfate and so on, and thermosetting resin. Moreover, it is made to contain 5 to 20weight% of black lead grain whose crystal grain (La, Lc) is 80 to 90nm, heated by a forming machine and pressurized to grain the friction material for brake. In this way, abrasion resistance is improved and exfoliation strength between crystal grains is increased, which restrains adhesion of black lead to the other material and can prevent lowering of friction coefficient at the time of high temperature braking.

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)

【特許請求の範囲】[Claims] (1)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80〜90nm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.
JP2646589A 1989-02-03 1989-02-03 Friction material for brake Granted JPH02209635A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (4)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
JPH0555735B2 (en) 1993-08-17

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