JPH0555735B2 - - Google Patents
Info
- Publication number
- JPH0555735B2 JPH0555735B2 JP2646589A JP2646589A JPH0555735B2 JP H0555735 B2 JPH0555735 B2 JP H0555735B2 JP 2646589 A JP2646589 A JP 2646589A JP 2646589 A JP2646589 A JP 2646589A JP H0555735 B2 JPH0555735 B2 JP H0555735B2
- Authority
- JP
- Japan
- Prior art keywords
- friction
- graphite
- fibers
- fiber
- friction material
- 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.)
- Expired - Lifetime
Links
- 239000000835 fiber Substances 0.000 claims description 37
- 239000002783 friction material Substances 0.000 claims description 21
- 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
- 239000013078 crystal Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 4
- 238000005087 graphitization Methods 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000004760 aramid Substances 0.000 description 3
- 239000010425 asbestos Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052895 riebeckite Inorganic materials 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 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
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 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
- 239000000428 dust Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011490 mineral wool Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 244000226021 Anacardium occidentale Species 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 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
- 238000005299 abrasion Methods 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
- 239000010951 brass Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 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
- 239000011487 hemp Substances 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
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 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
- 239000000377 silicon dioxide Substances 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)
Description
[産業上の利用分野]
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。
[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。
石綿に替わる繊維基材としてガラス繊維、アル
ミナ繊維、ロツクウール、チタン酸カリウム繊維
などの無機繊維、スチール繊維、銅繊維、真ちゆ
う繊維などの金属繊維や麻、木綿、レーヨン、フ
エノール繊維、芳香族ポリアミド繊維などの有機
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。
例えばスチールフア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。
[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イスクロータに付着
し、摩擦係数を低下させるという問題点がある。
[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。
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響を与えることを知
見し、本発明を完成するに至つた。
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つて、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である。
本発明で用いる金属繊維は、スチール繊維、し
んちゆう繊維、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、ロツクウール、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、
フエノール繊維、芳香族ポリアミド繊維などの有
機繊維の1種または2種以上の短繊維が使用でき
る。
前記の繊維基材の繊維径は5μm〜100μmが好ま
しく、繊維長は0.1mm〜3mmが好ましい。本発明
で用いられる黒鉛は、結晶粒子(La,Lc)が80
〜90nmであり、その層間隔(C/2)は、
0.3357nm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、一般的には、結晶粒子(La,Lc)
及び層間距離(C/2)で表わされる。
一般的に、天然黒鉛の結晶粒子は100nm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。
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。
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、カシユーダスト、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。
つぎに本発明に用いる熱硬化性樹脂は、フエノ
ール樹脂、メラミン樹脂、エポキシ樹脂、ポリエ
ステル樹脂、フエ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エノール樹脂の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。
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。
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、バンバリーミキサー、ヘンシエル
ミキサー、ニーダあるいはV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。
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。
[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、かつ結晶粒子間のハクリ強度が強いた
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。
結晶粒子が80nm未満の場合は耐摩耗性が十分
でなく、結晶粒子が100nmを超えると熱履歴後の
摩擦係数が低くなる。
[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。
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300Kg/cm2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300Kg/
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。
表1の各例の配合によつ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。
耐摩耗性試験の方法は、JASO−C427−83[ブ
レーキ型式:PD51s、ロータ:18mmベンチレーテ
ツドタイプ、イナーシヤ(負荷):4.0Kg・f・
m・S2、制動初速度:50Km/h、減速度:0.3G]
である。
第3効力の試験の方法は、JASO−C406−82
[ブレーキ型式:PD51s、ロータ:18mmベンチレ
ーテツドタイプ、イナーシヤ(負荷):5.0Kg・
f・m・s2、第2フエード後の効力]である。
[Industrial Application Field] The present invention relates to a friction material for brakes mainly used in automobiles, railway vehicles, airplanes, industrial machines, etc. [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. . Inorganic fibers such as glass fiber, alumina fiber, rock wool, and potassium titanate fiber, metal fibers such as steel fiber, copper fiber, and brass fiber, hemp, cotton, rayon, phenol fiber, and aromatic fibers can be used as fiber base materials to replace asbestos. Fiber base materials containing organic fibers such as polyamide fibers alone or in appropriate combinations are being considered. For example, friction compositions using steel fibers, graphite, and mixtures of graphite and rubber were published in JP-A-61
It is disclosed in Publication No. 168684. Also, JP-A-62-
Publication No. 106980 discloses a friction material comprising metal fibers (metal powder), aramid fibers (aramid bulbs), a lubricant such as graphite or molybdenum disulfide, a binder, and a filler. [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. [Means for Solving the Problems] An object of the present invention is to solve the above problems and provide a friction material for brakes that has a high coefficient of friction and excellent wear resistance. The present inventors have continued their intensive research in order to solve the above problems. As a result, they discovered that the degree of crystallinity of graphite has a significant effect on its adhesion to a mating material, leading to the completion of the present invention. That is, the present invention provides a brake friction material comprising a fiber base material containing at least metal fibers, a filler, and a thermosetting resin, which comprises crystal particles (La,
The friction material for brakes is characterized by containing graphite having Lc) of 80 to 90 nm. The metal fibers used in the present invention are steel fibers, shiny fibers, and titanium fibers. Fiber base materials other than metal fibers include glass fiber, silica fiber,
Inorganic fibers such as alumina fiber, rock wool, potassium titanate fiber, linen, cotton, rayon,
One or more types of organic fibers such as phenol fibers and aromatic polyamide fibers can be used. The fiber diameter of the fiber base material is preferably 5 μm to 100 μm, and the fiber length is preferably 0.1 mm to 3 mm. The graphite used in the present invention has crystal particles (La, Lc) of 80
~90nm, and the layer spacing (C/2) is
0.3357nm is preferred. The expression "degree of graphitization" is used to indicate how close the crystal structure of graphite is to an ideal graphite crystal, and the degree of graphitization is generally defined as the degree of graphitization of crystal particles (La, Lc).
and interlayer distance (C/2). Generally, the crystal particles of natural graphite are 100 nm or more and have a high degree of graphitization, so it has good wear resistance, but it has a low coefficient of friction after heat history, which is not preferable. 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. 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. Next, the thermosetting resin used in the present invention is one or more of phenolic resin, melamine resin, epoxy resin, polyester resin, phenol-modified melamine resin, and oil, rubber, melamine, epoxy, or polyvinyl butyral-modified phenolic resin. A mixture is used. The blending amount of these thermosetting resins is preferably 5 to 15% by weight in the total friction material. Next, the method for manufacturing the asbestos-free friction material for brakes of the present invention is a conventionally used method, and is as follows. 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, a kneader, a V-type blender, or the like. This mixed raw material is filled into a mold and pressed to perform preforming. This preform is heated and pressurized to harden and bond with a thermosetting resin, and then further heat treated to produce a friction material. [Operations and Effects of the Invention] According to the friction material for brakes of the present invention, crystal particles of 80 to
Containing 90nm graphite, it has good wear resistance and strong peeling 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. If the crystal grain size is less than 80 nm, the wear resistance will not be sufficient, and if the crystal grain size exceeds 100 nm, the friction coefficient after thermal history will be low. [Example] Examples of the present invention will be shown below, but the present invention is not limited thereto. 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 was preformed for 20 seconds in a molding machine adjusted to a surface pressure of 300 kg/cm 2 at room temperature to obtain a preformed product. Rear pressure 300Kg/
The mixture was heated and pressurized for 7 minutes using a molding machine adjusted to a cm 2 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. Friction materials obtained using the formulations shown in 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. The abrasion resistance test method is JASO-C427-83 [Brake model: PD51s, rotor: 18mm ventilated type, inertia (load): 4.0Kg・f・
m・S 2 , initial braking speed: 50Km/h, deceleration: 0.3G]
It is. The third efficacy test method is JASO-C406-82
[Brake model: PD51s, rotor: 18mm ventilated type, inertia (load): 5.0Kg・
f·m·s 2 , the effectiveness after the second fade].
【表】【table】
【表】【table】
【表】
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。[Table] As shown in Table 2, the brake friction materials of Examples 1 and 2 had lower wear rates than the friction materials of Comparative Examples 1 and 2, and there was no decrease in the third effect friction coefficient. It can be seen that it is an excellent friction material with good balance.
Claims (1)
填材および熱硬化性樹脂からなるブレーキ用摩擦
材であつて、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 comprising a fiber base material containing at least metal fibers, a filler, and a thermosetting resin, the brake material comprising graphite having crystal particles (La, Lc) of 80 to 90 nm. Friction material for use.
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 JPH02209635A (en) | 1990-08-21 |
JPH0555735B2 true 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) |
Families Citing this family (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 |
JP5578391B2 (en) * | 2007-04-13 | 2014-08-27 | 日産自動車株式会社 | Non-asbestos friction material |
JP6756144B2 (en) * | 2016-04-20 | 2020-09-16 | 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
Also Published As
Publication number | Publication date |
---|---|
JPH02209635A (en) | 1990-08-21 |
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