JPH073040A - Production of friction material - Google Patents

Production of friction material

Info

Publication number
JPH073040A
JPH073040A JP5147586A JP14758693A JPH073040A JP H073040 A JPH073040 A JP H073040A JP 5147586 A JP5147586 A JP 5147586A JP 14758693 A JP14758693 A JP 14758693A JP H073040 A JPH073040 A JP H073040A
Authority
JP
Japan
Prior art keywords
friction
friction material
weight
pts
parts
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.)
Pending
Application number
JP5147586A
Other languages
Japanese (ja)
Inventor
Toichi Sakata
淘一 坂田
Masaaki Yasuda
雅昭 安田
秀次 ▲くわ▼島
Hideji Kuwajima
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.)
Showa Denko Materials Co Ltd
Original Assignee
Hitachi 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP5147586A priority Critical patent/JPH073040A/en
Publication of JPH073040A publication Critical patent/JPH073040A/en
Pending legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

PURPOSE:To obtain a method for producing a friction material in which the friction material having a stable friction coefficient and a low wear rate even under conditions of a high temperature and load can be produced. CONSTITUTION:This method for producing a friction material is to knead or impregnate (d) a substrate composed of a fibrous material with a composition for the friction material containing (a) 20-70 pts.wt. binder, (b) 30-80 pts.wt. friction modifier [with the proviso that the total amount of the components (a) and (b) is regulated to 100 pts.wt.] and (c) carbon black in an amount of 15-50 pts.wt. based on 100 pts.wt. total amount of the components (a) and (b), then dry the kneaded or impregnated substrate, preform the dried kneaded or impregnated substrate, hot press form the preformed substrate, further heat- treat the hot press formed substrate at 230-330 deg.C for 1-8hr and subsequently cure the heat-treated substrate.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、自動車の動力伝達、制
動等に用いる摩擦材の製造法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method of manufacturing a friction material used for power transmission, braking, etc. of an automobile.

【0002】[0002]

【従来の技術】自動車に用いる摩擦材としては、ブレー
キライニング、ディスクパッド、クラッチフェーシング
等がある。これらは従来、石綿(アスベスト)を基材と
して使用していたが、アスベスト公害の問題から非アス
ベスト系摩擦材の開発が望まれている。又、自動車エン
ジンの性能向上に伴い摩擦材の摩擦特性(摩擦係数、摩
耗率)、機械特性等の向上が望まれている。更に最近は
使用条件が苛酷になり高温時の高速回転強度も要求され
るようになってきている。現在、石綿基材の代替材とし
て、ガラス繊維、炭素繊維、芳香族ポリアミド繊維、ロ
ックウール、セラミック繊維、各種のスチールファイバ
ー等を使用した摩擦材が開発され、一部で使用されてい
る。しかし、これらの基材は従来の石綿に比べて高弾性
で硬く、耐熱性が低いために、摩擦材にした場合に種々
の問題があり、上記した要求性能を満足しない。
Brake linings, disc pads, clutch facings and the like are used as friction materials for automobiles. Conventionally, asbestos (asbestos) has been used as a base material, but development of a non-asbestos friction material is desired due to the problem of asbestos pollution. Further, as the performance of automobile engines is improved, it is desired to improve the friction characteristics (friction coefficient, wear rate) and mechanical characteristics of friction materials. Furthermore, recently, the usage conditions have become severe, and high-speed rotation strength at high temperatures has been required. At present, friction materials using glass fiber, carbon fiber, aromatic polyamide fiber, rock wool, ceramic fiber, various steel fibers, etc. have been developed and used as a substitute for the asbestos base material. However, since these base materials have higher elasticity and hardness and lower heat resistance than conventional asbestos, there are various problems when used as a friction material, and the above-mentioned required performance is not satisfied.

【0003】[0003]

【発明が解決しようとする課題】石綿代替材を使用し高
温で高負荷に耐える摩擦材として、あらかじめ摩擦材自
身を高温処理したもの(例えば特開昭56−13184
6号公報、同59−113038号公報、同60−14
5302号公報等)があるが、これはコスト高や機械強
度の低下を伴う。特殊な摩擦調整剤を添加したもの(例
えば特開昭60−96625号公報、同60−9233
2号公報、同62−190232号公報等)もあるが、
結合剤の耐熱性と接着性が不足しているためその効果を
十分発揮できない。また基材に耐熱性の高いアラミド繊
維やポリイミド樹脂粉を加えたもの等が開示されている
が、基材及び摩擦調整剤を保持する結合剤の耐熱性が充
分でなく高温強度が得られない。又、摩擦特性を改善す
るために、多孔質化や軽量化が計られガラス短繊維撚り
合たせ紡績ガラス紐や、このガラス紐にアクリル繊維、
スフ、レーヨン、芳香族ポリアミド、フェノール樹脂等
の繊維を混合した混紡績ガラス紐が用いられているが、
高価格であり高温時の摩擦特性に種々の悪影響を与える
等の問題があり、製品化は一部に限られている。
As a friction material which uses an asbestos substitute material and withstands a high load at a high temperature, the friction material itself is preliminarily treated at a high temperature (for example, JP-A-56-13184).
6, gazette 59-113038 gazette, gazette 60-14.
No. 5302, etc.), but this involves a high cost and a decrease in mechanical strength. Those to which a special friction modifier is added (for example, JP-A-60-96625 and JP-A-60-9233).
No. 2, gazette, No. 62-190232, etc.),
Since the heat resistance and adhesiveness of the binder are insufficient, the effect cannot be fully exerted. Also disclosed are those in which aramid fiber or polyimide resin powder having high heat resistance is added to the base material, but the heat resistance of the binder holding the base material and the friction modifier is not sufficient and high temperature strength cannot be obtained. . In addition, in order to improve the frictional characteristics, it is made to be porous and lightweight, and short glass fibers are twisted and spun into a spun glass string, or an acrylic fiber is added to this glass string.
A mixed spun glass string is used in which fibers such as fiber, rayon, aromatic polyamide and phenol resin are mixed.
There are problems such as high price and various adverse effects on friction characteristics at high temperatures, and commercialization is limited to a part.

【0004】本発明は上記した問題を解消し、高温高負
荷の条件下でも安定した摩擦特性を有する摩擦材を提供
することを目的とする。
An object of the present invention is to solve the above problems and provide a friction material having stable friction characteristics even under high temperature and high load conditions.

【0005】[0005]

【課題を解決するための手段】本発明は、(a)結合剤
20〜70重量部及び(b)摩擦調整剤30〜80重量
部(但し(a)及び(b)の総量が100重量部となる
ようにする)並びに(a)及び(b)の総量100重量
部に対して(c)カーボンブラック15〜50重量部を
含んでなる摩擦材用組成物を、(d)繊維状物質からな
る基材に混練又は含浸させ、乾燥し、予備成形し、次い
で、熱圧形成し、さらに、230〜330℃で1〜8時
間熱処理して後硬化することを特徴とする摩擦材の製造
法に関する。
According to the present invention, (a) the binder is 20 to 70 parts by weight and (b) the friction modifier is 30 to 80 parts by weight (however, the total amount of (a) and (b) is 100 parts by weight). And (a) and (b) in a total amount of 100 parts by weight, (c) a composition for a friction material comprising 15 to 50 parts by weight of carbon black, and (d) a fibrous substance. A method for producing a friction material, comprising: kneading or impregnating a base material, drying, preforming, hot-pressing, and further heat-treating at 230 to 330 ° C. for 1 to 8 hours for post-curing. Regarding

【0006】(a)結合剤としては、特に制限はなく、
公知のものを使用することができ、例えば、フェノール
樹脂、メラミン樹脂、尿素樹脂、エポキシ樹脂、ポリア
ミドイミド前駆体樹脂、ポリイミド前駆体樹脂等の熱硬
化性樹脂、天然ゴム、クロロプレンゴム、スチレンブタ
ジエンゴム、アクリロニトリルブタジエンゴム、アクリ
ルゴム等のゴムなどが挙げられる。これらのうち、フェ
ノール樹脂及びメラミン樹脂が特性のバランスの点から
好ましく、中でもレゾール型フェノール樹脂及びメチル
化メラミン樹脂がより好ましい。又、耐熱性向上の点か
ら、ゴムが好ましい。ゴムを用いる場合は、必要に応じ
て硫黄等のゴムの架橋剤を用いてもよい。
(A) The binder is not particularly limited,
Known materials can be used, for example, thermosetting resins such as phenol resin, melamine resin, urea resin, epoxy resin, polyamideimide precursor resin, polyimide precursor resin, natural rubber, chloroprene rubber, styrene butadiene rubber. And rubber such as acrylonitrile butadiene rubber and acrylic rubber. Among these, a phenol resin and a melamine resin are preferable from the viewpoint of the balance of properties, and among them, a resol type phenol resin and a methylated melamine resin are more preferable. Further, rubber is preferable from the viewpoint of improving heat resistance. When rubber is used, a rubber crosslinking agent such as sulfur may be used if necessary.

【0007】(b)摩擦調整剤としては、特に制限はな
く、公知のものを使用することができるが、例えば、炭
酸カルシウム、炭酸マグネシウム、硫酸バリウム、珪酸
カルシウム短繊維、クレー、タルク、黒鉛、アルミナ、
マイカ、螢石、ジルコニア、ヘマタイト、マグネタイ
ト、シリカ、硫化アンチモン、硫化鉛、硫化鉄、硫化亜
鉛、硫化モリブデン、三酸化アンチモン等の無機物の粉
末、鉄、鉛、銅等の金属の粉末、カシューダスト、メラ
ミン樹脂などの熱硬化性樹脂の硬化物の粉末などの有機
物の粉末等を挙げることができる。これらは単独で又は
2種以上を組み合わせて使用される。
The friction modifier (b) is not particularly limited, and known ones can be used. Examples thereof include calcium carbonate, magnesium carbonate, barium sulfate, calcium silicate short fiber, clay, talc, graphite, alumina,
Inorganic powder of mica, fluorite, zirconia, hematite, magnetite, silica, antimony sulfide, lead sulfide, iron sulfide, zinc sulfide, molybdenum sulfide, antimony trioxide, etc., metal powder of iron, lead, copper, etc., cashew dust , Powders of organic substances such as powders of cured products of thermosetting resins such as melamine resins. These are used alone or in combination of two or more.

【0008】(c)カーボンブラックとしては、特に制
限なく公知のものを使用することができる。
As the carbon black (c), known carbon black can be used without particular limitation.

【0009】上記(a)成分は20〜70重量部の範囲
で、(b)成分は30〜80重量部の範囲で(但し、
(a)及び(b)の総量が100重量部となるようにす
る)使用される。また、(c)成分は、(a)及び
(b)成分の総量100重量部に対して15〜50重量
部(好ましくは20〜45重量部、より好ましくは35
〜45重量部)の範囲で使用することが必要である。
The component (a) is in the range of 20 to 70 parts by weight, and the component (b) is in the range of 30 to 80 parts by weight (however,
(The total amount of (a) and (b) is 100 parts by weight). Further, the component (c) is 15 to 50 parts by weight (preferably 20 to 45 parts by weight, more preferably 35) based on 100 parts by weight of the total amount of the components (a) and (b).
Up to 45 parts by weight).

【0010】(a)成分の量が少なすぎると機械強度が
劣り、多すぎると摩擦係数と摩耗量のバランスがとれな
い。(b)成分の量が少なすぎると摩擦係数が不安定と
なり、摩耗量が増大し、多すぎると摩擦係数と摩耗量の
バランスがとれない。(c)成分の量が少なすぎると耐
熱性が低下し、高温時の摩擦特性が劣り、多すぎると摩
擦係数が不安定となり、摩耗量が増大する。
If the amount of component (a) is too small, the mechanical strength will be poor, and if it is too large, the friction coefficient and the amount of wear cannot be balanced. If the amount of component (b) is too small, the friction coefficient becomes unstable and the amount of wear increases, and if it is too large, the friction coefficient and the amount of wear cannot be balanced. If the amount of the component (c) is too small, the heat resistance is lowered and the friction characteristics at high temperature are deteriorated, and if it is too large, the friction coefficient becomes unstable and the amount of wear increases.

【0011】本発明の摩擦材用樹脂組成物には、上記
(a)、(b)及び(c)の他に、必要に応じて使用さ
れる他の成分として、水、メチルエチルケトン、トルエ
ン等の有機溶剤、メチルセルロース、カルボキシメチル
セルロース、エチルセルロース、カルボキシエチルセル
ロース、ポリビニルピロリドン、ポリビニルアルコー
ル、スチレン−マレイン酸共重合ポリマー等の分散剤、
エチレングリコール、プロピレングリコール、フタル酸
ジメチル等の可塑剤、界面活性剤、密着性向上剤等の添
加剤などが挙げられる。摩擦材用組成物は、例えば、次
のようにして製造することができる。 (a)結合剤、(b)摩擦調整剤、(c)カーボンブラ
ック及び必要に応じて使用される他の成分を高速ミキサ
ー等で良く混合し、スラリー状の摩擦材用組成物を得る
ことができる。
In addition to the above (a), (b) and (c), the resin composition for a friction material of the present invention may further contain other components such as water, methyl ethyl ketone, toluene, etc. Dispersants such as organic solvents, methyl cellulose, carboxymethyl cellulose, ethyl cellulose, carboxyethyl cellulose, polyvinylpyrrolidone, polyvinyl alcohol, styrene-maleic acid copolymers,
Examples thereof include additives such as plasticizers such as ethylene glycol, propylene glycol, dimethyl phthalate, surfactants, adhesion improvers and the like. The composition for friction material can be manufactured, for example, as follows. (A) Binder, (b) friction modifier, (c) carbon black, and other components used as necessary may be well mixed with a high-speed mixer or the like to obtain a slurry-like composition for friction material. it can.

【0012】摩擦材は、例えば、次のようにして得るこ
とができる。摩擦材用組成物を、(d)繊維状物質から
なる基材に混練又は含浸し、(d)繊維状物質からなる
基材と摩擦材用組成物との混練物又は(d)繊維状物質
からなる基材に摩擦材用組成物を均一に含浸塗工し付着
させた塗工紐を得、この混練物又は塗工紐を乾燥させ溶
媒を除去し予備成形する。次いで金型等に入れて熱圧成
形(140〜180℃、50〜150kgf/cm2、5〜3
0分)を行い成形品を得、この成形品を230〜330
℃で1〜8時間熱処理して後硬化させ摩擦材を得る。熱
処理の温度と時間がこの範囲外であると、生産性、作業
性、摩擦特性(特に高温時)、機械強度が劣る。
The friction material can be obtained, for example, as follows. The composition for a friction material is kneaded or impregnated into a base material made of (d) a fibrous substance, and (d) a kneaded product of the base material made of a fibrous material and the composition for a friction material or (d) a fibrous material. A friction material composition is uniformly impregnated and coated on a base material made of to obtain a coated cord, and the kneaded product or the coated cord is dried to remove the solvent and preform. Then put it in a mold etc. and hot press molding (140-180 ° C, 50-150 kgf / cm 2 , 5-3
0 minutes) to obtain a molded product, and this molded product is 230 to 330
A heat treatment is performed at a temperature of 1 to 8 hours for post-curing to obtain a friction material. If the heat treatment temperature and time are out of this range, the productivity, workability, frictional properties (especially at high temperature) and mechanical strength will be poor.

【0013】上記した(e)繊維状物質からなる基材と
しては、特に制限なく公知のものを使用することができ
るが、例えば、ガラス繊維、炭素繊維、ロックウール、
セラミック繊維等の無機繊維、鉄線等の金属線、フェノ
ール樹脂繊維、芳香族ポリアミド樹脂繊維等の有機繊維
などを挙げることができ、加工の容易なこと、安価なこ
と等からガラス繊維が好ましい。繊維状物質からなる基
材の形態としては、チョップ、フィラメント、ロービン
グ、撚糸、ヤーン、マット、フェルト等の不織布、抄造
シート、織布等があるが制限はない。
As the base material composed of the above-mentioned (e) fibrous substance, known materials can be used without particular limitation, and examples thereof include glass fiber, carbon fiber, rock wool,
Inorganic fibers such as ceramic fibers, metal wires such as iron wires, organic fibers such as phenol resin fibers, aromatic polyamide resin fibers, and the like can be mentioned, and glass fibers are preferable because they are easy to process and inexpensive. The form of the base material made of a fibrous substance includes, but is not limited to, non-woven fabrics such as chops, filaments, rovings, twisted yarns, yarns, mats and felts, paper sheets, and woven fabrics.

【0014】(e)繊維状物質からなる基材は、最終的
に得られる摩擦材における重量比率の、繊維状物質から
なる基材/摩擦材用組成物(固形分)が、30/70〜
70/30の範囲となるような量で使用されることが好
ましい。繊維状物質からなる基材の量が少なすぎると摩
擦材の機械強度が低下する傾向があり、多すぎると摩擦
特性が不安定になり摩耗が増大すると共に摩擦の経日熱
変化により機械強度が低下する傾向がある。なお、前記
した重量比率の、繊維状物質からなる基材/摩擦材用組
成物(固形分)において、摩擦材用組成物(固形分)の
重量は、最終的に得られる摩擦材の単位当りの重量Aを
測定し、これから単位当りの繊維状物質からなる基材の
重量Bを差し引いた値A−Bとして確認することができ
る。この重量比率の微調整は、摩擦材用組成物の固形分
濃度を増減すること、含浸塗工速度を増減すること等に
より容易に行うことができる。
(E) The base material composed of the fibrous material has a weight ratio of the friction material finally obtained such that the composition of the base material composed of the fibrous material / the friction material composition (solid content) is from 30/70.
It is preferably used in an amount such that it is in the range of 70/30. If the amount of the base material made of a fibrous substance is too small, the mechanical strength of the friction material tends to decrease, and if it is too large, the friction characteristics become unstable and wear increases, and the mechanical strength changes due to the change of friction with time. Tends to decline. In the base material / friction material composition (solid content) made of a fibrous material in the above-mentioned weight ratio, the weight of the friction material composition (solid content) is per unit of the finally obtained friction material. Can be confirmed as a value A-B obtained by subtracting the weight B of the base material made of the fibrous substance per unit from this. The fine adjustment of the weight ratio can be easily performed by increasing or decreasing the solid content concentration of the friction material composition, increasing or decreasing the impregnation coating speed, and the like.

【0015】[0015]

【実施例】次に本発明を実施例によって説明する。硫酸
バリウム(堺化学製、B・C)、タルク(和光純薬工業
製、化学用)、炭酸カルシウム(竹原化学製、商品名サ
ンライトSL−1500)、珪酸カルシウム短繊維(米
国NYCO社製、商品名ウォラストナイト)40重量部
を混合した無機物粉末及び銅粉(和光純薬工業製、化学
用銅箔粉、平均で厚さ2μm、短径50μm、長径70
μm)からなる摩擦調整剤とカーボンブラック(三菱化
成♯44カーボンブラック)とを表1に示す割合で混合
して混合物を得た。また、NBR(日本ゼオン製、Ni
pool 1041)15重量部をメチルエチルケトン
(MEK)85重量部に溶解して固形分15重量%の結
合剤たるゴムの溶液を得た。また、フェノール樹脂(大
日本インキ化学工業製、TD−2040C、固形分10
0%)15重量部をメチルエチルケトン(MEK)85
重量部に溶解して固形分15重量%の結合剤たる熱硬化
性樹脂の溶液を得た。表1に示す割合で摩擦調整剤とカ
ーボンブラックとの混合物に結合剤の溶液を加えて混練
しスラリー状の摩擦材用組成物とした。
EXAMPLES The present invention will now be described with reference to examples. Barium sulfate (Sakai Chemical Co., BC), talc (Wako Pure Chemical Industries, chemical), calcium carbonate (Takehara Chemical Co., trade name Sunlight SL-1500), calcium silicate short fiber (US NYCO, Brand name Wollastonite) 40 parts by weight of inorganic powder and copper powder (Wako Pure Chemical Industries, copper foil powder for chemicals, average thickness 2 μm, minor axis 50 μm, major axis 70)
μm) and a carbon black (Mitsubishi Kasei # 44 carbon black) were mixed at a ratio shown in Table 1 to obtain a mixture. In addition, NBR (Nihon Zeon, Ni
15 parts by weight of pool 1041) was dissolved in 85 parts by weight of methyl ethyl ketone (MEK) to obtain a solution of rubber as a binder having a solid content of 15% by weight. In addition, phenol resin (manufactured by Dainippon Ink and Chemicals, TD-2040C, solid content 10
0%) 15 parts by weight of methyl ethyl ketone (MEK) 85
A thermosetting resin solution as a binder having a solid content of 15% by weight was obtained by dissolving in parts by weight. A solution of the binder was added to the mixture of the friction modifier and carbon black in the proportions shown in Table 1 and kneaded to obtain a slurry-like composition for the friction material.

【0016】[0016]

【表1】 [Table 1]

【0017】また、チョップ状のガラス繊維(富士ファ
イバーグラス製、UPG・IZA508、長さ約30m
m)をミキサーでほぐした(開繊した)ものを繊維状物
質からなる基材とした。
In addition, chopped glass fiber (made by Fuji Fiber Glass, UPG IZA508, length about 30 m
The m) was disentangled (opened) with a mixer to obtain a substrate made of a fibrous substance.

【0018】実施例1〜2 上記摩擦材用組成物(固形分)100重量部に上記繊維
状物質からなる基材を67重量部加えてニーダーで混練
し混練物を得、この混練物を60℃で2時間乾燥しME
Kを除去して予備成形し、次いでこれを金型に充填し、
160℃で15分、圧力100kgf/cm2で成形し5mm厚
さ×50mm角の成形体を得た。その後、230℃で1時
間、260℃で4時間の順に後硬化を行い、両面をサン
ダーで研磨し、摩擦材を得た。
Examples 1 and 2 67 parts by weight of the fibrous base material was added to 100 parts by weight of the friction material composition (solid content) and kneaded with a kneader to obtain a kneaded product. ME for 2 hours at ℃
Remove K and preform, then fill it in a mold,
Molding was carried out at 160 ° C. for 15 minutes at a pressure of 100 kgf / cm 2 to obtain a molded body of 5 mm thickness × 50 mm square. Then, post-curing was performed in the order of 230 ° C. for 1 hour and 260 ° C. for 4 hours, and both surfaces were polished with a sander to obtain a friction material.

【0019】比較例1〜2 表1の配合に従い、材料を配合、混合し、他は実施例1
〜2と同様にして、摩擦材を得た。
Comparative Examples 1 and 2 The materials were blended and mixed according to the formulation of Table 1, and the other components were used in Example 1.
A friction material was obtained in the same manner as in.

【0020】実施例1〜2及び比較例1〜2で得られた
摩擦材を25mm角に切断して摩擦特性評価用試験片とし
た。この試験片をJIS D4411に定める低速度摩
擦試験機に取り付け、押し付け圧力5kgf/cm2で運転
し、150℃、250℃及び350℃における摩擦係数
及び摩耗率(cm3/kgf−m)を測定した。この結果を表
2に示した。
The friction materials obtained in Examples 1 and 2 and Comparative Examples 1 and 2 were cut into 25 mm square pieces to prepare test pieces for evaluating friction characteristics. This test piece was attached to a low-speed friction tester specified in JIS D4411, operated at a pressing pressure of 5 kgf / cm 2 , and the friction coefficient and wear rate (cm 3 / kgf-m) at 150 ° C, 250 ° C and 350 ° C were measured. did. The results are shown in Table 2.

【0021】[0021]

【表2】 [Table 2]

【0022】表2から、比較例1〜2は、各温度での摩
擦係数の変動が大きく、高温の摩耗率も高く摩擦特性に
劣る。これに対し、実施例1〜2は、安定した摩擦係数
と、摩耗率が小さく優れた摩擦特性を有する。
From Table 2, Comparative Examples 1 and 2 have large fluctuations in the friction coefficient at each temperature, high wear rates at high temperatures, and poor friction characteristics. On the other hand, Examples 1 and 2 have stable friction coefficient and excellent friction characteristics with a small wear rate.

【0023】[0023]

【発明の効果】本発明によれば、高温時の摩擦特性が良
好な摩擦材が得られる。
According to the present invention, a friction material having good friction characteristics at high temperatures can be obtained.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (a)結合剤20〜70重量部及び
(b)摩擦調整剤30〜80重量部(但し(a)及び
(b)の総量が100重量部となるようにする)並びに
(a)及び(b)の総量100重量部に対して(c)カ
ーボンブラック15〜50重量部を含んでなる摩擦材用
組成物を、(d)繊維状物質からなる基材に混練又は含
浸させ、乾燥し、予備成形し、次いで、熱圧形成し、さ
らに、230〜330℃で1〜8時間熱処理して後硬化
することを特徴とする摩擦材の製造法。
1. (a) 20 to 70 parts by weight of a binder and (b) 30 to 80 parts by weight of a friction modifier (provided that the total amount of (a) and (b) is 100 parts by weight) and ( The friction material composition containing (c) 15 to 50 parts by weight of carbon black is kneaded or impregnated into a base material made of a fibrous substance with respect to 100 parts by weight of the total of (a) and (b). A method for producing a friction material, which comprises: drying, preforming, hot-pressing, and heat-treating at 230 to 330 ° C. for 1 to 8 hours for post-curing.
JP5147586A 1993-06-18 1993-06-18 Production of friction material Pending JPH073040A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5147586A JPH073040A (en) 1993-06-18 1993-06-18 Production of friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5147586A JPH073040A (en) 1993-06-18 1993-06-18 Production of friction material

Publications (1)

Publication Number Publication Date
JPH073040A true JPH073040A (en) 1995-01-06

Family

ID=15433704

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5147586A Pending JPH073040A (en) 1993-06-18 1993-06-18 Production of friction material

Country Status (1)

Country Link
JP (1) JPH073040A (en)

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