JPS61278586A - Extrudable friction material - Google Patents

Extrudable friction material

Info

Publication number
JPS61278586A
JPS61278586A JP12012285A JP12012285A JPS61278586A JP S61278586 A JPS61278586 A JP S61278586A JP 12012285 A JP12012285 A JP 12012285A JP 12012285 A JP12012285 A JP 12012285A JP S61278586 A JPS61278586 A JP S61278586A
Authority
JP
Japan
Prior art keywords
friction
friction material
oxide powder
rubber
metal oxide
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
JP12012285A
Other languages
Japanese (ja)
Other versions
JPH0533277B2 (en
Inventor
Hidetoshi Okamoto
英俊 岡本
Misao Masuda
桝田 操
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.)
Nippon Valqua Industries Ltd
Nihon Valqua Kogyo KK
Original Assignee
Nippon Valqua Industries Ltd
Nihon Valqua Kogyo KK
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 Nippon Valqua Industries Ltd, Nihon Valqua Kogyo KK filed Critical Nippon Valqua Industries Ltd
Priority to JP12012285A priority Critical patent/JPS61278586A/en
Publication of JPS61278586A publication Critical patent/JPS61278586A/en
Publication of JPH0533277B2 publication Critical patent/JPH0533277B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Braking Arrangements (AREA)

Abstract

PURPOSE:To obtain the titled friction material which causes no high temp. fading and is excellent in mass producibility etc., by incorporating an arom. polyamide fiber and an adhesive contg. a thermosetting resin, a rubber material, etc., and a metal oxide powder as a high-temp. fading inhibitor. CONSTITUTION:An intended extrudable friction material is obtd. by incorporating an arom. polyamide fiber as a base material, an adhesive compsn. contg. a thermosetting resin (e.g.: phenolic resin), a rubber material (e.g.: butadiene rubber), etc., a metal oxide powder as a high-temp. facing inibitor (e.g.: calcined aluminum powder or zinc oxide powder). The use of the present material enables mass production of frictional materials suitable for use in buffer material of a clutch disc, a brake shoe of a washing machine, which are excellent in cushioning properties and flexibility, undergoes no lowering in friction coefficient, without use of any asbestos which has an adverse effect on human body.

Description

【発明の詳細な説明】 及皿五反±皇1 本発明は、クラッチデスクの緩衝材、洗濯機のプレキシ
−などに用いられる押出し成形可能な摩擦材に関し、さ
らに詳しくは、石綿を用いずに形成された押出し成形可
能な摩擦材に関する。
[Detailed Description of the Invention] The present invention relates to a friction material that can be extruded and used as a cushioning material for clutch desks, a plexi for washing machines, etc. The present invention relates to a formed extrudable friction material.

明の技術的背景ならびにその問題点 クラッチディスク、洗濯機の回転筒などには、緩衝作用
を持たせるために、摩擦材が用いられている。このよう
な摩擦材は、高摩擦係数を有するとともに耐摩耗性に優
れ、かつクッション性を有し、しかもたとえば回転筒に
巻きつけても折れないというような柔軟性を有すること
が望ましい。
Technical Background and Problems Friction materials are used in clutch discs, rotating cylinders of washing machines, etc. to provide a buffering effect. It is desirable that such a friction material has a high coefficient of friction, excellent wear resistance, cushioning properties, and flexibility such that it will not break even when wrapped around a rotating tube, for example.

このような摩擦材は、従来石綿を基材として製造されて
きたが、近年に至って石綿資源の枯渇およびそれに伴な
う入手難の問題が生ずるとともに、石綿の人体に対する
悪影響も指摘され、石綿の使用は再検討され始めている
Such friction materials have traditionally been manufactured using asbestos as a base material, but in recent years, asbestos resources have been depleted and the resulting difficulty in obtaining them has arisen, as well as the negative effects of asbestos on the human body have been pointed out. Its use is beginning to be reconsidered.

このため本発明者らは、摩擦材を石綿以外の基材繊維か
ら製造するべく鋭意検討したところ、次のような事実を
見出した。すなわち、石綿の代わりにガラス繊維などの
剛直な無機繊維を基材として用いて摩擦材を製造しよう
とすると、室温から50℃程度の低温での押出機による
シート状物への製造が困難となり、いちいち各摩擦材を
加熱圧縮しなければならず、このため量産性が著しく低
下してコスト上昇を招くともに、クッション性おょひ柔
軟性に優れたものが得られないという問題点が生じてし
まう。一方、石綿の代わりに、芳香族ポリアミド繊維あ
るいはフィブリル化した芳香族ポリアミド繊維を基材繊
維として用いて摩擦材を製造する場合には、低温で押出
機によりシート状に製造することが可能で量産性には優
れているが、得られる摩擦材は耐熱性に劣り、150〜
200℃程度の高温状態ではその摩擦係数が大きく低下
してしまうという重大な問題点が生じてしまう。
For this reason, the inventors of the present invention conducted intensive studies to manufacture friction materials from base fibers other than asbestos, and discovered the following fact. In other words, when trying to manufacture a friction material using rigid inorganic fibers such as glass fibers as a base material instead of asbestos, it becomes difficult to manufacture a sheet-like material using an extruder at a low temperature of about 50°C from room temperature. Each friction material must be heated and compressed one by one, which significantly reduces mass productivity and increases costs, as well as making it impossible to obtain products with excellent cushioning properties and flexibility. . On the other hand, when manufacturing friction materials using aromatic polyamide fibers or fibrillated aromatic polyamide fibers as the base fiber instead of asbestos, it is possible to manufacture sheets in the form of sheets using an extruder at low temperatures and mass production. Although it has excellent properties, the resulting friction material has poor heat resistance and is
At a high temperature of about 200° C., a serious problem arises in that the coefficient of friction decreases significantly.

本発明者らは、芳香族ポリアミド繊維を基材として含む
摩擦材の高温条件下での使用時における摩擦係数の低下
すなわち高温フェード現象を少なくすることを検討した
ところ、特定の充填剤を添加すれば、上記の問題点が一
挙に解決されることを見出して本発明を完成するに至っ
た。
The present inventors investigated how to reduce the reduction in the coefficient of friction, that is, the high-temperature fade phenomenon, when friction materials containing aromatic polyamide fibers as a base material are used under high-temperature conditions. Specifically, the present invention has been completed by discovering that the above problems can be solved all at once.

R里五亘力 本発明は、石綿以外の基材繊維から、押出し成形が可能
で量産性に優れ、しかもクッション性および柔軟性をも
有し、その上高温条件下で使用しても摩擦係数の低下が
認められないような摩擦材を提供することを目的として
いる。
The present invention enables extrusion molding from base fibers other than asbestos, has excellent mass productivity, has cushioning properties and flexibility, and has a low coefficient of friction even when used under high temperature conditions. The purpose of the present invention is to provide a friction material that does not show any decrease in friction.

及服五且1 本発明に係る摩擦材は、基材としての芳香族ポリアミド
繊維と、熱硬化性樹脂およびゴム材を含む結着組成物と
、高温フェード防止剤としての金属酸化物粉末とを含ん
でなることを特徴としている。
Applications 5 and 1 The friction material according to the present invention comprises aromatic polyamide fibers as a base material, a binder composition containing a thermosetting resin and a rubber material, and a metal oxide powder as a high temperature fade preventive agent. It is characterized by containing.

高温フェード防止剤としての金属酸化物粉末としては、
焼成アルミナ粉末、酸化亜鉛粉末、酸化鉛粉末などが主
として用いられる。
As a metal oxide powder as a high temperature anti-fade agent,
Calcined alumina powder, zinc oxide powder, lead oxide powder, etc. are mainly used.

及」匹且体煎塁贋 以下本発明に係る摩擦材について具体的に説明する。Fake original copy The friction material according to the present invention will be specifically explained below.

本発明に係る摩擦材は、基材繊維として、芳香族ポリア
ミド繊維を含んでいる。この芳香族ポリアミド繊維とし
ては、フィブリル化した芳香族ポリアミド繊維が好まし
く用いられる。このような芳香族ポリアミド繊維は、デ
ュポン社よりケブラーあるいはケブラーパルプとして市
販されている。
The friction material according to the present invention contains aromatic polyamide fibers as base fibers. As this aromatic polyamide fiber, fibrillated aromatic polyamide fiber is preferably used. Such aromatic polyamide fibers are commercially available from DuPont as Kevlar or Kevlar pulp.

このような芳香族ポリアミド繊維に、熱硬化性樹脂オよ
びゴム材からなる結着組成物が付着される。熱硬化性樹
脂としては、具体的にはフェノール樹脂、尿素樹脂、メ
ラミン樹脂、エポキシ樹脂などが用いられる。これらの
うち、フェノール樹脂が好ましく、フェノール樹脂とし
ては、ノボラック型、レゾール型、あるいはクレゾール
変性、メラミン変性、ゴム変性、カシ−変性などの変性
フェノール樹脂が用いられる。
A binding composition made of a thermosetting resin and a rubber material is attached to such aromatic polyamide fibers. As the thermosetting resin, specifically, phenol resin, urea resin, melamine resin, epoxy resin, etc. are used. Among these, phenol resins are preferred, and the phenol resins used include novolak type, resol type, and modified phenol resins such as cresol-modified, melamine-modified, rubber-modified, and oak-modified.

ゴム材としては、ブタジェンゴム(BR)、スチレン−
ブタジェンゴム(SBR)、イソプレンゴム(■R)、
エチレン−プロピレンゴム(EPM)、ブチルゴム(I
IR)、クロロプレンゴム(CR)、アクリロニトリル
−ブタジェンゴム(NBR) 、クロルスルホン化ポリ
エチレン(C3M) 、アクリルゴム(ACM> 、ウ
レタンゴム(U)、シリコーンゴム(Si)、フッ素ゴ
ム(FPM) 、多硫化ゴム(T)、ポリエーテルゴム
(FOR>などの合成ゴムならびに天然ゴムが用いられ
うるが、特にスチレン−ブタジェンゴム(SBR)、ア
クリロニトリル−ブタジェンゴム(NBR>が好ましい
Rubber materials include butadiene rubber (BR) and styrene rubber.
Butadiene rubber (SBR), isoprene rubber (■R),
Ethylene-propylene rubber (EPM), butyl rubber (I
IR), chloroprene rubber (CR), acrylonitrile-butadiene rubber (NBR), chlorosulfonated polyethylene (C3M), acrylic rubber (ACM>), urethane rubber (U), silicone rubber (Si), fluororubber (FPM), polysulfide Synthetic rubbers such as rubber (T) and polyether rubber (FOR>) as well as natural rubbers can be used, but styrene-butadiene rubber (SBR) and acrylonitrile-butadiene rubber (NBR>) are particularly preferred.

また1ゴム材中に用られる加硫剤として(よ、イオウ、
酸化亜鉛、酸化マグネシウム、有機過酸化物などが用い
られる。また加硫促進剤としては、チアゾール系促進剤
、スルフェンアミド系促進剤、ジチオカルバメート系促
進剤、アルデヒドアミンン系促進剤、グアニジン系促進
剤、チオ尿素促進剤、キサンテート系促進剤チオ尿素促
進剤、アルデヒドアンモニア系促進剤などが用いられる
Also used as a vulcanizing agent in rubber materials (sulfur,
Zinc oxide, magnesium oxide, organic peroxide, etc. are used. Vulcanization accelerators include thiazole accelerators, sulfenamide accelerators, dithiocarbamate accelerators, aldehyde amine accelerators, guanidine accelerators, thiourea accelerators, xanthate accelerators and thiourea accelerators. agents, aldehyde ammonia type accelerators, etc. are used.

本発明では、摩擦材中に高温フェード防止剤として、金
属酸化物粉末が用いられることに大きな特徴がある。金
属酸化物粉末としては、焼成アルミナ粉末、酸化亜鉛粉
末、酸化鉛粉末などが用いられるが、このうち特に焼成
アルミナ粉末が好ましい。このような金属酸化物粉末は
、150〜500メツシュ好ましくは250〜350メ
ツシュ程度の大きざを有することが好ましい。150メ
ツシュ以上の大きさの金属酸化物粉末を用いると、摩擦
材成形用組成物を押出機にて押出し成形する際に、押出
機スクリューが傷つきやすくなるため好ましくない。
The present invention is characterized in that metal oxide powder is used as a high-temperature fade preventive agent in the friction material. As the metal oxide powder, calcined alumina powder, zinc oxide powder, lead oxide powder, etc. are used, and among these, calcined alumina powder is particularly preferred. Such metal oxide powder preferably has a size of about 150 to 500 meshes, preferably about 250 to 350 meshes. If a metal oxide powder with a size of 150 mesh or more is used, the extruder screw will be easily damaged when extruding the friction material molding composition using an extruder, which is not preferable.

焼成アルミナなどの金属酸化物粉末を、摩擦材中に含有
せしめることによって、高温条件下で摩擦材を使用して
も摩擦係数はほとんど低下しなくなり、優れた摩擦特性
を有する摩擦材が得られる。
By incorporating metal oxide powder such as calcined alumina into a friction material, the coefficient of friction hardly decreases even when the friction material is used under high temperature conditions, and a friction material having excellent friction properties can be obtained.

たとえば焼成アルミナを含有せしめた摩擦材の場合には
、100℃での摩擦係数μは0.501であって、20
0 ’Cでのμは0.569である。これに対して、石
綿製摩擦材での摩擦向上剤として公知のパライト(硫酸
バラリム)を、本発明に係る芳香族ポリアミド繊維を基
材とする摩擦材に高温フェード防止剤して用いると、1
00℃での摩擦係数μは0.563であるのに対して、
200℃ではμは0.177と大きく低下してしまう。
For example, in the case of a friction material containing calcined alumina, the friction coefficient μ at 100°C is 0.501 and 20
μ at 0′C is 0.569. On the other hand, when Palite (varium sulfate), which is known as a friction improver for asbestos friction materials, is used as a high-temperature fade preventive agent in the aromatic polyamide fiber-based friction material of the present invention, 1
While the coefficient of friction μ at 00°C is 0.563,
At 200° C., μ decreases significantly to 0.177.

同様に石綿製摩擦材での摩擦向上剤であるカシューダス
トを本発明に用いて摩擦材を製造すると、100℃での
摩擦係数μは0.453であるのに対し200℃でのμ
は0.144と大きく低下してしまう。
Similarly, when a friction material is manufactured using cashew dust, which is a friction improver for asbestos friction materials, in the present invention, the friction coefficient μ at 100°C is 0.453, but the μ at 200°C is
is greatly reduced to 0.144.

このように本発明では、従来石綿製摩擦材での摩擦向上
剤として代表的な化合物たとえばパライト、カシューダ
ストを、芳香族ポリアミド繊維を基材とする摩擦材に高
温フェード防止剤として用いても、はとんど効果がない
ことは注目すべきことである。
In this way, in the present invention, even if typical compounds such as pallite and cashew dust, which are conventionally used as friction improvers in asbestos friction materials, are used as high-temperature fade preventive agents in friction materials based on aromatic polyamide fibers, It is noteworthy that this is largely ineffective.

また、本発明に係る摩擦材は、増量剤および増粘剤を含
んでいてもよく、このような増量剤および増粘剤として
は、ベントナイト、有機変性ベントナイト、微粒子シリ
カ、カルボキシメチルセルロースなどが挙げられる。
Furthermore, the friction material according to the present invention may contain an extender and a thickener, and examples of such extenders and thickeners include bentonite, organically modified bentonite, particulate silica, and carboxymethyl cellulose. .

本発明における摩擦材では、基材繊維としての芳香族ポ
リアミド繊維100重量部に対して、高温フェード防止
剤としての金属酸化物粉末は、30〜100重量部好ま
しくは40〜80重量部の量で用いられる。また、熱硬
化性樹脂、ゴム材および加硫剤を含んでなる結着剤組成
物は、芳香族ポリアミド繊維に対して、150〜300
重量部好ましくは200〜250重量部の量で用いられ
る。さらにまた、増量剤および充填剤は、芳香族ポリア
ミド繊維に対して、20〜100重量部好ましくは40
〜80重量部の量で用いられる。
In the friction material of the present invention, the amount of metal oxide powder as a high-temperature fade inhibitor is 30 to 100 parts by weight, preferably 40 to 80 parts by weight, based on 100 parts by weight of aromatic polyamide fibers as base fibers. used. Further, the binder composition containing a thermosetting resin, a rubber material, and a vulcanizing agent has a molecular weight of 150 to 300% relative to the aromatic polyamide fiber.
Parts by weight are preferably used in amounts of 200 to 250 parts by weight. Furthermore, the amount of extender and filler is 20 to 100 parts by weight, preferably 40 parts by weight, based on the aromatic polyamide fiber.
It is used in an amount of ~80 parts by weight.

次に、本発明に係る摩擦材の製造方法について説明する
が、基本的には石綿製摩擦材の製造方法と同様であって
、基材繊維としての石綿を芳香族ポリアミド繊維に代え
ればよい。すなわち、芳香族ポリアミド繊維、ゴム剤、
加硫剤、増量剤をよくロールおよびニーダ−などで混練
する。そして得られた混練物と、熱硬化性樹脂を有機溶
剤に溶解させて得られた溶液と、必要に応じて増粘剤と
をよく混練し、これに高温フェード防止剤を添加してよ
く混練して摩擦材形成用組成物を調製する。
Next, a method for manufacturing a friction material according to the present invention will be described, but it is basically the same as the method for manufacturing a friction material made of asbestos, except that asbestos as the base fiber is replaced with aromatic polyamide fiber. Namely, aromatic polyamide fiber, rubber agent,
Thoroughly knead the vulcanizing agent and extender using a roll or kneader. Then, the obtained kneaded product, a solution obtained by dissolving the thermosetting resin in an organic solvent, and a thickener if necessary are thoroughly kneaded, and a high temperature fade preventive agent is added thereto and thoroughly kneaded. A composition for forming a friction material is prepared.

得られた摩擦材形成用組成物を、押出し成形機に供給し
、この押出し成形機により押出し成形するとシート状の
摩擦材予備成形体が得られる。
The obtained composition for forming a friction material is supplied to an extrusion molding machine and extrusion molded by the extrusion molding machine to obtain a sheet-like friction material preform.

この摩擦材予備成形体を乾燥した後、加熱圧縮すれば、
摩擦材が得られる。
If this friction material preform is dried and then heated and compressed,
A friction material is obtained.

R皿五四ヌ 本発明に係る摩擦材では、芳香族ポリアミド繊維を基材
繊維として用い、金属酸化物粉末を高温フェード防止剤
として用いているので、以下のような効果が得られる。
In the friction material according to the present invention, aromatic polyamide fibers are used as base fibers and metal oxide powder is used as a high-temperature fade preventive agent, so that the following effects can be obtained.

(a>石綿以外の基材繊維から摩擦材を形成することが
できる。
(a> The friction material can be formed from base fibers other than asbestos.

(b)押出し成形が可能であるため、量産性に優れ、し
かもクッション性および柔軟性に優れた摩擦材が得られ
る。
(b) Since extrusion molding is possible, a friction material with excellent mass productivity and excellent cushioning properties and flexibility can be obtained.

(C)高温条件下で使用しても、摩擦係数が低下すると
いう高温フェード現象がほとんど認められない摩擦材が
得られる。
(C) Even when used under high-temperature conditions, a friction material can be obtained in which the high-temperature fade phenomenon in which the coefficient of friction decreases is hardly observed.

以下本発明を実施例により説明するが、本発明はこれら
実施例に限定されるものではない。
EXAMPLES The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples.

実施例 1 芳香族ポリアミド繊維100重量部と、NBRゴム10
0重量部と、硫黄10重量部と増量剤150重量部とを
ロールでよく混練した。得られた混練物と、フェノール
樹脂70重量部を有機溶剤(アセトン)150重量部に
溶解したものと増粘剤であるベントン(#27 IND
USTRIES社製)35重量部とをニーダ−で5〜2
0分混練した後、この混線物に、325メツシユの焼成
アルミナ粉末を80重量部添加して充分にニーダ−で混
練して、摩擦材形成用組成物を調製した。
Example 1 100 parts by weight of aromatic polyamide fiber and 10 parts by weight of NBR rubber
0 parts by weight, 10 parts by weight of sulfur, and 150 parts by weight of an extender were thoroughly kneaded with a roll. The obtained kneaded product, a solution of 70 parts by weight of phenolic resin in 150 parts by weight of an organic solvent (acetone), and a thickener, bentone (#27 IND
(manufactured by USTRIES) and 35 parts by weight in a kneader.
After kneading for 0 minutes, 80 parts by weight of 325 mesh calcined alumina powder was added to the mixed wire material and thoroughly kneaded in a kneader to prepare a composition for forming a friction material.

得られた摩擦材形成用組成物を押出し成形機に供給し、
押出し成形機により押出し成形して、シート状の摩擦材
予備成形体を製造した。
Supplying the obtained friction material forming composition to an extrusion molding machine,
A sheet-like friction material preform was manufactured by extrusion molding using an extrusion molding machine.

得られた摩擦材予備成形体を40〜80℃で乾燥した後
、180℃の温度で40kof /cm2の圧力で20
分間加熱圧縮して、摩擦材を製造した。
After drying the obtained friction material preform at 40 to 80°C, it was dried at a temperature of 180°C and a pressure of 40kof/cm2 for 20 minutes.
A friction material was manufactured by heating and compressing for a minute.

得られた摩擦材の摩擦係数を100℃、150℃、20
0℃の温度で測定した。またこの摩擦材を200℃に保
った後冷却し、再び100℃の温度に加熱して、摩擦係
数を測定した。結果を表1に示す。
The friction coefficient of the obtained friction material was adjusted to 100°C, 150°C, and 20°C.
Measurements were made at a temperature of 0°C. Further, this friction material was maintained at 200°C, cooled, and heated again to a temperature of 100°C, and the coefficient of friction was measured. The results are shown in Table 1.

止校五−ユ 実施例1において、焼成アルミナ粉末の代わりに、カシ
ューダスト粉末を用いた以外は、実施例1と同様にして
摩擦材を製造した。
A friction material was produced in the same manner as in Example 1, except that cashew dust powder was used instead of calcined alumina powder.

この摩擦材の高温時の摩擦係数を実施例1と同様にして
測定した。結果を表1に示す。
The friction coefficient of this friction material at high temperatures was measured in the same manner as in Example 1. The results are shown in Table 1.

比較例 2 実施例1において、焼成アルミナ粉末の代わりに、パラ
イト粉末を用いた以外は、実施例1と同様にして摩擦材
をIJ!造して、高温度の摩擦係数を測定した。結果を
表1に示す。
Comparative Example 2 A friction material was prepared in the same manner as in Example 1 except that Palite powder was used instead of calcined alumina powder in Example 1. The friction coefficient at high temperature was measured. The results are shown in Table 1.

表1 表1から、芳香族ポリアミド繊維を基材とする摩擦材で
は、焼成アルミナ粉末を添加すると、高温フェード現象
は全く認められないのに対して、石綿製摩擦材の場合の
摩擦向上剤であるカシューダスト、パライトなどを芳香
族ポリアミド繊維を基材とする摩擦材に添加しても高温
フェード現象は全く解決されていないことがわかる。
Table 1 From Table 1, in friction materials based on aromatic polyamide fibers, no high-temperature fade phenomenon is observed when calcined alumina powder is added, whereas in the case of friction materials made of asbestos, the friction improver It can be seen that even when certain cashew dust, pallite, etc. are added to friction materials based on aromatic polyamide fibers, the high-temperature fade phenomenon is not solved at all.

夫癒五−2 実施例1において、焼成アルミナ粉末の代わりに、32
5メツシユの酸化亜鉛粉末を用いた以外は実施例1と同
様にして摩擦材を製造した。
Fuyugo-2 In Example 1, instead of calcined alumina powder, 32
A friction material was produced in the same manner as in Example 1 except that 5 meshes of zinc oxide powder were used.

得られた摩擦材の高温時の摩擦係数を測定したところ、
高温フェード現象は認められなかった。
When we measured the friction coefficient of the obtained friction material at high temperatures, we found that
No high temperature fade phenomenon was observed.

衷凰■一旦 実施例1において、焼成アルミナ粉末の代わりに、32
5メツシユの酸化鉛粉末を用いた以外は実施例1と同様
にして摩擦材を製造した。
衷凰■ Once in Example 1, instead of the calcined alumina powder, 32
A friction material was produced in the same manner as in Example 1 except that 5 meshes of lead oxide powder were used.

得られた摩擦材の高温時の摩擦係数を測定したところ、
高温フェード現象は認められなかった。
When we measured the friction coefficient of the obtained friction material at high temperatures, we found that
No high temperature fade phenomenon was observed.

Claims (2)

【特許請求の範囲】[Claims] (1)基材としての芳香族ポリアミド繊維と、熱硬化性
樹脂、ゴム材を含んでなる結着剤組成物と、高温フェー
ド防止剤としての金属酸化物粉末とを含んでなることを
特徴とする押出し成形可能な摩擦材。
(1) It is characterized by comprising an aromatic polyamide fiber as a base material, a binder composition comprising a thermosetting resin and a rubber material, and a metal oxide powder as a high temperature fade preventive agent. extrudable friction material.
(2)金属酸化物粉末が、焼成アルミナ粉末、酸化亜鉛
粉末または酸化鉛粉末である特許請求の範囲第1項に記
載の押出し成形可能な摩擦材。
(2) The extrudable friction material according to claim 1, wherein the metal oxide powder is calcined alumina powder, zinc oxide powder, or lead oxide powder.
JP12012285A 1985-06-03 1985-06-03 Extrudable friction material Granted JPS61278586A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12012285A JPS61278586A (en) 1985-06-03 1985-06-03 Extrudable friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12012285A JPS61278586A (en) 1985-06-03 1985-06-03 Extrudable friction material

Publications (2)

Publication Number Publication Date
JPS61278586A true JPS61278586A (en) 1986-12-09
JPH0533277B2 JPH0533277B2 (en) 1993-05-19

Family

ID=14778507

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12012285A Granted JPS61278586A (en) 1985-06-03 1985-06-03 Extrudable friction material

Country Status (1)

Country Link
JP (1) JPS61278586A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5360587A (en) * 1992-01-15 1994-11-01 Plastics Engineering Company Preparation of friction elements and compositions therefor

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5611981A (en) * 1979-06-21 1981-02-05 Raybestos Manhattan Inc Abrasive composition
JPS5861169A (en) * 1981-09-15 1983-04-12 チオコ−ル・コ−ポレ−シヨン Aramid-containing abrasive material
JPS6020988A (en) * 1983-07-15 1985-02-02 Unitika Ltd Non-asbestos friction material and its preparation

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5611981A (en) * 1979-06-21 1981-02-05 Raybestos Manhattan Inc Abrasive composition
JPS5861169A (en) * 1981-09-15 1983-04-12 チオコ−ル・コ−ポレ−シヨン Aramid-containing abrasive material
JPS6020988A (en) * 1983-07-15 1985-02-02 Unitika Ltd Non-asbestos friction material and its preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5360587A (en) * 1992-01-15 1994-11-01 Plastics Engineering Company Preparation of friction elements and compositions therefor

Also Published As

Publication number Publication date
JPH0533277B2 (en) 1993-05-19

Similar Documents

Publication Publication Date Title
JPS622029A (en) Porous frictional material and manufacture thereof
JPS6067131A (en) Manufacture of clutch facing
JP2664738B2 (en) Friction material
JPS61278586A (en) Extrudable friction material
JP2003082331A (en) Non-asbestos friction lining
CN104175791A (en) Fiber reinforced composite wheel rim with heat dissipation capability
GB2125451A (en) Extrusion coated continuous tape
JPS61218636A (en) Production of clutch facing
JPH04173892A (en) Friction material
JPH10279777A (en) Flaky phenolic resin molding material containing carbon fiber and its production
KR20020033400A (en) Composition for friction surface, sheet molded product, and brake lining material
JPS6289784A (en) Clutch facing
JPH03185031A (en) Nonasbestos-based friction material
JPWO2003087255A1 (en) Non-asbestos friction material
JP2519722B2 (en) Clutch easing
JPS61162537A (en) Frictional material composition
KR101269486B1 (en) Natural compositions using brake pad method manufacturing
CA1204258A (en) Extrusion coated continuous tape
RU2097392C1 (en) Composition for friction materials
JPH06108040A (en) Friction material
JPH073041A (en) Production of friction material
JPS62129370A (en) Production of pencil lead
JPH09302105A (en) Frictional material
JP2000144103A (en) Rod like article for friction material and friction material
CN108641400A (en) A kind of no metal carbon fiber recombination line clutch surface and preparation method thereof