JPH0712158A - Friction material - Google Patents

Friction material

Info

Publication number
JPH0712158A
JPH0712158A JP15513493A JP15513493A JPH0712158A JP H0712158 A JPH0712158 A JP H0712158A JP 15513493 A JP15513493 A JP 15513493A JP 15513493 A JP15513493 A JP 15513493A JP H0712158 A JPH0712158 A JP H0712158A
Authority
JP
Japan
Prior art keywords
friction
binder
friction material
coated
yarn
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
JP15513493A
Other languages
Japanese (ja)
Inventor
秀次 ▲くわ▼島
Hideji Kuwajima
Toichi Sakata
淘一 坂田
Masaaki Yasuda
雅昭 安田
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 JP15513493A priority Critical patent/JPH0712158A/en
Publication of JPH0712158A publication Critical patent/JPH0712158A/en
Pending legal-status Critical Current

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  • Braking Arrangements (AREA)
  • Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)

Abstract

PURPOSE:To make mechanical strength and a friction characteristic well- balanced and minimize the dispersion of various characteristics. CONSTITUTION:Friction material is formed of twist yarn formed by twisting glass fiber continuous yarn, containing admixture mainly composed of a friction conditioner and a binder, and glass fiber contiinuous yarn, mainly containing a binder, by the specified number. In this friction material, the continuous yarn mainly containing the binder has numerous micro cavities.

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、自動車や産業機械の動
力伝達、制動等に用いられる摩擦材に関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material used for power transmission and braking of automobiles and industrial machines.

【0002】[0002]

【従来の技術】自動車や産業用に用いられる摩擦材とし
ては、一般にブレーキライニング、ディスクパッド及び
クラッチフェーシングがある。これらは、従来、石綿
(アスベスト)を繊維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。また、近年、地球環境、作業環境、製造時
の安全性などの点から有機溶媒の使用が見直されてきて
いる。現在、アスベスト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の繊維基材を使
用した摩擦材が開発され、一部で実用されている。しか
し、これらの材料は、アスベストに比べて高弾性で硬
く、耐熱性が低いために種々の摩擦調整剤を加えて改善
を図っており、摩擦調整剤を基材に均一に付着させるた
めに、一般にゴムと樹脂との組成物を有機溶媒に溶解し
た溶液に摩擦調整剤を分散させた混和物が用いられてい
る。そして、有機溶媒として、近年は製造作業時の燃焼
爆発を防止するためにハロゲン系のものが多く使用され
ている。
Brake linings, disc pads and clutch facings are generally used as friction materials for automobiles and industrial applications. Conventionally, asbestos (asbestos) has been used as a fiber base material, but development of non-asbestos friction materials has been desired due to the problem of asbestos pollution. Further, in recent years, the use of organic solvents has been reconsidered from the viewpoints of the global environment, work environment, safety during production, and the like. At present, a friction material using a fiber base material such as glass fiber, carbon fiber, aromatic polyamide fiber, rock wool, ceramic fiber and various steel fibers has been developed and put into practical use as a substitute for asbestos. However, these materials are highly elastic and hard as compared with asbestos and have low heat resistance, so various friction modifiers are added to improve the properties, and in order to uniformly adhere the friction modifier to the base material, Generally, a mixture in which a friction modifier is dispersed in a solution in which a composition of rubber and a resin is dissolved in an organic solvent is used. In recent years, halogen-based organic solvents have been widely used in order to prevent combustion and explosion during manufacturing work.

【0003】一方、摩擦材の強度と摩擦特性のバランス
は、繊維基材の種類と量あるいは摩擦調整剤、結合剤の
種類と量の面から検討されている。しかしながら、これ
らの各種材料の種類や配合量を検討しても、摩擦材の強
度と摩擦特性のバランスを最適に保持するのは困難であ
る。例えば、繊維基材としてファイバー状のものを用い
た抄造法又はモールド法によるものが知られている(特
開昭61−63797号公報、特開平3−210338
号公報等)。この方法は、短く切った繊維基材と混和物
とを混合して製造する方法(一種のモールド法)である
ため、機械強度の低下が生じやすい。その他、水溶媒を
用いた摩擦材の製造法としては、摩擦調整剤を繊維基材
に付着しやすいように表面処理したもの(特開平3−6
1732公報)などが提案されているが、摩擦材の強度
と摩擦特性のバランスを最適に保持するという問題を解
決するには至っていない。
On the other hand, the balance between the strength and the friction characteristics of the friction material has been examined in terms of the type and amount of the fiber base material or the type and amount of the friction modifier and the binder. However, even if the types and blending amounts of these various materials are examined, it is difficult to maintain the balance between the strength and friction characteristics of the friction material in an optimum manner. For example, a papermaking method or a molding method using a fibrous material as a fiber base material is known (Japanese Patent Laid-Open No. 61-63797 and Japanese Laid-Open Patent Application No. 3-210338).
No. Since this method is a method (a kind of molding method) of mixing a fiber base material cut into short pieces and an admixture, a mechanical strength is likely to be lowered. In addition, as a method of manufacturing a friction material using a water solvent, a friction modifier is surface-treated so as to easily adhere to a fiber base material (Japanese Patent Laid-Open No. 3-6).
However, the problem of keeping the balance between the strength and friction characteristics of the friction material in an optimum manner has not been solved yet.

【0004】すなわち、高速回転時の破壊強度あるいは
高負荷時の破壊強度を高めるには、結合剤量を増加すれ
ばよいが、これを増加すると、高温時に摩擦係数が低下
する欠点を生じる。これを防止するには、結合剤量を減
少させる方法、空隙率を高める方法あるいは摩擦調整剤
量を増加する方法などがあるが、いずれも破壊強度が低
下しやすく、各種特性のバランスをとること及びバラツ
キを小さくすることが困難である。
That is, in order to increase the breaking strength at high speed rotation or the breaking strength at high load, it is sufficient to increase the amount of the binder, but if this amount is increased, there is a drawback that the friction coefficient decreases at high temperature. To prevent this, there are methods such as decreasing the amount of binder, increasing the porosity, and increasing the amount of friction modifier. In either case, breaking strength tends to decrease, and various properties should be balanced. Also, it is difficult to reduce the variation.

【0005】[0005]

【発明が解決しようとする課題】本発明は、前記従来技
術の欠点を解消し、機械強度と摩擦特性のバランスがと
れ、各種特性のバラツキが小さい摩擦材を提供すること
を目的とするものである。
SUMMARY OF THE INVENTION It is an object of the present invention to solve the above-mentioned drawbacks of the prior art, and to provide a friction material in which mechanical strength and friction characteristics are well balanced and variations in various characteristics are small. is there.

【0006】[0006]

【課題を解決するための手段】本発明は、摩擦調整剤及
び結合剤を主成分とする混和物を含有する連続ヤーン
と、主として結合剤を含有する連続ヤーンとを所定の本
数ずつ撚り合わせてなる撚糸からなり、主として結合剤
を含有する連続ヤーンが多数の微細な空隙を有すること
を特徴とする摩擦材に関する。
According to the present invention, a continuous yarn containing a mixture containing a friction modifier and a binder as main components and a continuous yarn containing mainly a binder are twisted together in a predetermined number. The present invention relates to a friction material characterized in that a continuous yarn mainly composed of a twisted yarn having a number of fine voids is contained.

【0007】本発明において、連続ヤーンとは、ガラス
繊維、炭素繊維、セラミック繊維等の無機質繊維及び芳
香族ポリアミド樹脂繊維、フェノール樹脂繊維、ポリア
クリロニトリル繊維等の有機質繊維からなり、これらが
単独であるいは相互に又は金属繊維などと組み合わされ
て使用される。特に、その材質を制限するものではない
が、加工が容易であり、また、安価であり、汎用性があ
ることからガラス繊維を主として用いたものが好まし
い。ここで、連続ヤーンとは、直径数μm〜数十μmの
フィラメントが集束剤で集束されたストランドが数十本
まとめられたものを指す。
In the present invention, the continuous yarn is composed of inorganic fibers such as glass fibers, carbon fibers and ceramic fibers and organic fibers such as aromatic polyamide resin fibers, phenol resin fibers and polyacrylonitrile fibers, which may be used alone or Used together or in combination with metal fibers and the like. In particular, although the material thereof is not limited, it is preferable to mainly use glass fiber because it is easy to process, inexpensive, and versatile. Here, the continuous yarn refers to a bundle of dozens of strands obtained by bundling filaments having a diameter of several μm to several tens μm with a sizing agent.

【0008】連続ヤーンを構成する繊維の、摩擦材中の
配合量は、使用した繊維の種類により変動するが、ガラ
ス繊維を連続ヤーンとして用いる場合、ガラス繊維の量
は、摩擦特性のバランス及び制御の容易さの点で摩擦材
に対して30〜60重量%含有させるのが好ましい。
The amount of the fibers constituting the continuous yarn in the friction material varies depending on the type of the fibers used. When glass fibers are used as the continuous yarn, the amount of the glass fibers depends on the balance and control of friction characteristics. From the standpoint of ease of use, it is preferable to add 30 to 60% by weight to the friction material.

【0009】本発明において、摩擦調整剤としては、特
に制限はなく、各種のものを使用することができ、例え
ば、炭酸カルシウム、炭酸マグネシウム、酸化亜鉛、硫
酸バリウム、クレー、タルク、カーボンブラック、黒
鉛、アルミナ、マイカ、螢石、ジルコニア、ヘマタイ
ト、シリカ、硫化アンチモン、硫化鉄、硫化モリブデ
ン、硫黄等の無機物の粉末、鉄、鉛、銅等の金属の粉
末、カシューダスト、ゴムダスト、各種樹脂硬化物の粉
末等の有機物の粉末、珪酸カルシウム短繊維などが使用
される。
In the present invention, the friction modifier is not particularly limited and various ones can be used, for example, calcium carbonate, magnesium carbonate, zinc oxide, barium sulfate, clay, talc, carbon black, graphite. Powders of inorganic materials such as alumina, mica, fluorite, zirconia, hematite, silica, antimony sulfide, iron sulfide, molybdenum sulfide and sulfur, powders of metals such as iron, lead and copper, cashew dust, rubber dust, cured products of various resins Powders of organic substances such as powders of calcium carbonate and short fibers of calcium silicate are used.

【0010】また、本発明に用いる結合剤としては、特
に制限はなく、各種の熱硬化性樹脂組成物及び/又はゴ
ムラテックスを使用することができる。熱硬化性樹脂組
成物としては、フェノール樹脂、メチル化メラミン樹
脂、メラミン樹脂、尿素樹脂、ポリアミドイミド樹脂、
ポリイミド樹脂、エポキシ樹脂等の樹脂組成物が挙げら
れ、これらのうちフェノール樹脂組成物、メチル化メラ
ミン樹脂組成物が好ましい。熱硬化性樹脂組成物の量
は、繊維基材と摩擦調整剤に対する結合力並びに摩擦材
の摩擦係数及び摩擦率の調整の点で一般に、摩擦材にし
たときに固形分として摩擦材に対して10〜50重量%
含有させるような量が好ましい。また、ゴムラテックス
としては、架橋性ゴムラテックスが用いられ、例えば、
ニトリルブタジエンゴム、アクリルゴム、天然ゴム、ク
ロロプレンゴムなどが挙げられる。ゴムラテックスの量
としては、一般に、得られる摩擦材に対して固形分とし
て5〜20重量%含有させるような量が好ましい。
The binder used in the present invention is not particularly limited, and various thermosetting resin compositions and / or rubber latex can be used. The thermosetting resin composition, phenol resin, methylated melamine resin, melamine resin, urea resin, polyamideimide resin,
Examples thereof include resin compositions such as polyimide resins and epoxy resins, and among these, phenol resin compositions and methylated melamine resin compositions are preferable. The amount of the thermosetting resin composition is generally in terms of the binding force to the fiber base material and the friction modifier, and the friction coefficient and the coefficient of friction of the friction material to adjust the friction material as a solid content relative to the friction material. 10-50% by weight
The amount contained is preferable. Further, as the rubber latex, a crosslinkable rubber latex is used, for example,
Examples thereof include nitrile butadiene rubber, acrylic rubber, natural rubber and chloroprene rubber. Generally, the amount of the rubber latex is preferably such that 5 to 20% by weight as a solid content is contained in the obtained friction material.

【0011】本発明の摩擦材は、上記成分の他に、必要
に応じて各種の添加剤、例えば、分散剤、可撓化剤、界
面活性剤などを含有していてもよい。特に、有機溶媒を
使用せず、水系溶媒で混和物を作製し、これを連続ヤー
ンに含浸させて塗工紐を作製する場合には、上記のよう
な添加剤を適切に活用することが好ましい。この場合、
分散剤には、主として水溶性高分子樹脂が用いられる。
このような樹脂としては、一般に増粘効果を有するメチ
ルセルロース、カルボキシメチルセルロース、ポリビニ
ルピロリドン、ポリビニルアルコール、ポリビニルメチ
ルエーテル、ポリビニルエチルエーテルなどが使用され
る。分散剤の添加量は、摩擦係数及び機械強度の点で摩
擦材に対して10重量%以下とするのが好ましく、混和
物総量中では20重量%以下とするのが好ましい。
In addition to the above components, the friction material of the present invention may contain various additives, such as a dispersant, a flexibilizer, and a surfactant, if necessary. In particular, when an admixture is prepared with an aqueous solvent without using an organic solvent and a continuous yarn is impregnated with the mixture to prepare a coated cord, it is preferable to appropriately utilize the above-mentioned additives. . in this case,
A water-soluble polymer resin is mainly used as the dispersant.
As such a resin, methyl cellulose, carboxymethyl cellulose, polyvinyl pyrrolidone, polyvinyl alcohol, polyvinyl methyl ether, polyvinyl ethyl ether, etc., which generally have a thickening effect, are used. The amount of the dispersant added is preferably 10% by weight or less with respect to the friction material in terms of friction coefficient and mechanical strength, and is preferably 20% by weight or less in the total amount of the admixture.

【0012】また、可撓化剤としては、水溶性高分子樹
脂に対して相溶性を有し、摩擦特性に影響しない物質が
好ましく、例えば、グリコール類が好適である。可撓化
剤は、混和物が塗工されたプリプレグの成形加工性を向
上するためのものであり、成形、後硬化時には飛散して
実機の摩擦材中には極力存在しないようにするのが好ま
しい。好適な可撓化剤としては、例えば、エチレングリ
コール、プロピレングリコール、ジエチレングリコール
等の低級グリコールが挙げられる。その添加量は、分散
剤の種類にもよるが、分散剤に対して80〜20重量%
が好ましい。
As the flexibilizer, a substance which is compatible with the water-soluble polymer resin and does not affect the frictional properties is preferable, and glycols are preferable. The flexibilizer is for improving the molding processability of the prepreg coated with the admixture, and is scattered during molding and post-curing so that it does not exist in the friction material of the actual machine as much as possible. preferable. Suitable flexibilizers include, for example, lower glycols such as ethylene glycol, propylene glycol and diethylene glycol. The addition amount depends on the kind of the dispersant, but is 80 to 20% by weight based on the dispersant.
Is preferred.

【0013】界面活性剤は、摩擦調整剤の分散効果及び
分散剤の安定性を増強するために用いられ、特に制限は
ないが、効果的な界面活性剤としては、アニオン系ある
いはノニオン系が好ましく用いられる。ノニオン系のポ
リエチレングリコールを用いれば好ましい。界面活性剤
の添加量は、通常は混和物の固形分に対して1〜2重量
%が好ましい。
The surfactant is used for enhancing the dispersion effect of the friction modifier and the stability of the dispersant and is not particularly limited, but anionic surfactant or nonionic surfactant is preferable as the effective surfactant. Used. It is preferable to use nonionic polyethylene glycol. Usually, the amount of the surfactant added is preferably 1 to 2% by weight based on the solid content of the mixture.

【0014】本発明は、上記のような各種の材料を適切
に組み合わせて二種類の塗工紐を作製し、それらを所定
の本数ずつ撚り合わせた撚糸を加工して摩擦材を作製す
るもので、その一つは上記各種材料からなる混和物を含
浸した塗工紐であり、他方は主として結合剤のみを含浸
した塗工紐である。
The present invention is to produce a friction material by appropriately combining the above-mentioned various materials to produce two kinds of coated cords and processing a twisted yarn in which a predetermined number of them are twisted together. One is a coated cord impregnated with a mixture of the above-mentioned various materials, and the other is a coated cord mainly impregnated with a binder.

【0015】各種材料を含有する混和物を連続ヤーンに
含浸塗工する方法としては、ドクターブレード法、ロー
ルコーター法、吹き付け法、定量ポンプによる押出塗工
法、浸漬含浸法などがあるが、混和物を略均一に含浸さ
せるには、浸漬含浸法が好適である。連続ヤーンに混和
物を略均一に含浸させる具体的な方策としては、連続ヤ
ーンを充分に開繊して混和物のスラリー中に浸漬し、含
浸させたのちこれを引き上げる方法あるいはスラリー中
で揺動させ、連続ヤーン中に略均一に含浸させる方法な
どがあるが、開繊の方法及び含浸方法には、特に制限は
ない。
As a method for impregnating and coating a mixture containing various materials on a continuous yarn, there are a doctor blade method, a roll coater method, a spraying method, an extrusion coating method using a metering pump, a dip impregnation method, and the like. The dip impregnation method is suitable for substantially uniformly impregnating. As a concrete measure for substantially uniformly impregnating the continuous yarn with the mixture, a method of sufficiently opening the continuous yarn, immersing the continuous yarn in the slurry of the mixture, impregnating it, and then pulling it up or shaking in the slurry Although there is a method of impregnating the continuous yarn substantially uniformly, the method of opening the fiber and the method of impregnation are not particularly limited.

【0016】また、主として結合剤を含有する連続ヤー
ンを作製するには、例えば、結合剤溶液をロールコータ
ー法、吹き付け法、浸漬含浸法などの方法で所定量塗工
すればよく、特にその方法を制限するものではない。
In order to produce a continuous yarn containing mainly a binder, for example, a binder solution may be applied in a predetermined amount by a method such as a roll coater method, a spraying method or a dipping impregnation method. Is not meant to be limited.

【0017】具体的に、摩擦材を得るには、例えば次の
ような方法がある。結合剤である熱硬化性樹脂の粉末を
水又は有機溶剤に分散、溶解させる。このとき必要に応
じて分散剤、可撓化剤又は界面活性剤が加えられる。次
いで、摩擦調整剤を添加して均一な分散液を作製し、さ
らにゴムラテックスと固形分調整用の水を加えて攪拌混
合して混和物を得る。得られた混和物をガラスロービン
グ等の連続ヤーンに均一に塗工して塗工物とし、この塗
工物の揮発分を乾燥等により除去して塗工紐Aとする。
なお、混和物の塗工方法としては、特に制限はないが、
浸漬含浸によるのが好ましい。また、溶媒の水を除去す
る方法にも特に制限はないが、混和物中の樹脂分が硬化
しないように注意する必要がある。
Specifically, for example, the following method can be used to obtain the friction material. A thermosetting resin powder as a binder is dispersed and dissolved in water or an organic solvent. At this time, if necessary, a dispersant, a flexibilizer or a surfactant is added. Next, a friction modifier is added to prepare a uniform dispersion, and rubber latex and water for adjusting the solid content are further added and mixed with stirring to obtain a mixture. The obtained mixture is uniformly applied to a continuous yarn such as glass roving to obtain a coated product, and a volatile component of the coated product is removed by drying or the like to obtain a coated string A.
The method for applying the mixture is not particularly limited,
Dip impregnation is preferred. The method of removing water as a solvent is not particularly limited, but it is necessary to take care so that the resin component in the mixture does not harden.

【0018】別に、結合剤の水溶液又は有機溶媒中の溶
液に連続ヤーンを含浸し、もしくは結合剤の水分散液を
連続ヤーンに均一に塗工、含浸して塗工紐Bを作製す
る。次いで、これらの二種類の塗工紐を所定の本数ずつ
撚り合わせて塗工撚糸とし、さらに、該塗工撚糸を環状
に巻き上げて予備成形品を得る。得られた環状体を金型
等に入れて熱圧成形を行い、次いで成形品を所定の加熱
条件下で熱処理して樹脂を完全に硬化させて、所望形状
の摩擦材を得ることができる。
Separately, an aqueous solution of a binder or a solution in an organic solvent is impregnated with the continuous yarn, or an aqueous dispersion of the binder is uniformly applied and impregnated on the continuous yarn to prepare a coated string B. Next, a predetermined number of these two types of coated cords are twisted together to form a coated twisted yarn, and the coated twisted yarn is further wound into a ring to obtain a preform. The obtained annular body is put in a mold or the like for thermocompression molding, and then the molded product is heat-treated under predetermined heating conditions to completely cure the resin, whereby a friction material having a desired shape can be obtained.

【0019】上記方法において、塗工物における繊維基
材と混和物との比率は、重量で繊維基材/混和物(固形
分)で30/70〜60/40とするのが好ましい。混
和物の付着量が多すぎると、摩擦材の機械強度が低下
し、付着量が少ないと、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強度が低下す
る。
In the above method, the ratio of the fibrous base material to the admixture in the coated product is preferably 30/70 to 60/40 by weight of the fibrous base material / admixture (solid content). If the adhering amount of the admixture is too large, the mechanical strength of the friction material decreases, and if the adhering amount of the admixture is small, the friction characteristics become unstable, the wear increases, and the strength decreases due to the change with time of friction.

【0020】[0020]

【作用】本発明になる摩擦材は、連続ヤーン(繊維基
材)と摩擦調整剤、結合剤(熱硬化性樹脂組成物)、ゴ
ムラテックス、分散剤、可撓化剤、界面活性剤などから
なる複合材料である。摩擦材に求められる性質は、摩擦
性能はもちろんのこと、機械的強度、耐摩耗性等があ
る。これらの性質が常に安定して一定の値を示すことが
重要であり、このためには一つの繊維基材の内部には摩
擦調整剤等の混和物が均一に含浸されており、他の繊維
基材は結合剤で強固に接着されているが、乾燥に伴う体
積減少により均一な空隙を生成することが必須要件とな
る。前記二種類の繊維基材を所定の本数ずつ撚り合わせ
て成形加工した後に主として結合剤を含有する基材及び
その周辺に空隙を生じ、この空隙が高温時に生成する液
状物を吸収する役割を果たすことで高温時の摩擦係数の
低下を防止する。なお、混和物が均一に含浸されている
連続ヤーンは強固な複合材料となるので、破壊強度及び
摩耗性は良好である。また、主として結合剤が含浸され
ており、空隙を生じさせる連続ヤーンも接着力に優れた
結合剤で繊維同士が固着さており、破壊強度の低下は少
ない。
The friction material according to the present invention comprises a continuous yarn (fiber base material), a friction modifier, a binder (thermosetting resin composition), a rubber latex, a dispersant, a flexibilizer and a surfactant. It is a composite material. The properties required of the friction material include not only friction performance but also mechanical strength, wear resistance and the like. It is important that these properties always show stable and constant values.To this end, one fiber base material is uniformly impregnated with a mixture such as a friction modifier, and The base material is firmly adhered with a binder, but it is an essential requirement that uniform voids are generated due to the volume reduction accompanying drying. A predetermined number of the above two kinds of fiber base materials are twisted together and molded, and then a base material mainly containing a binder and voids are formed around the base material, and the voids play a role of absorbing a liquid substance generated at a high temperature. This prevents the friction coefficient from decreasing at high temperatures. Since the continuous yarn in which the admixture is uniformly impregnated is a strong composite material, the breaking strength and the abrasion property are good. Further, the binder is mainly impregnated, and the continuous yarn that creates voids has the fibers bonded to each other with the binder having excellent adhesive strength, so that the breaking strength is not significantly reduced.

【0021】[0021]

【実施例】次に、実施例により本発明をさらに具体的に
説明するが、本発明はこれによって制限されるものでは
ない。
EXAMPLES Next, the present invention will be described in more detail by way of examples, but the present invention is not limited thereto.

【0022】なお、以下の実施例及び比較例に用いる各
材料は、下記のとおりである。連続ヤーンは、ガラスロ
ービング(富士ファイバーグラス製、1.8g/m)で
ある。摩擦調整剤は、酸化亜鉛(和光純薬工業製、化学
用)2重量%、硫酸バリウム(堺化学製、BC)40重
量%、カーボンブラック(三菱カーボン製、#44)6
重量%、黒鉛(英国 ABRAMWELL製)3重量%、シリカ粉
(龍森製、クリスタライト)10重量%、珪酸カルシウ
ム短繊維(米国NYCO社製、商品名ウォラスナイト)
20重量%、カシュー変性フリクションダスト(カシュ
ー株製、WD−1350)14重量%及び微粉硫黄(細
井化学製)5重量%をV型ブレンダーで均一に混合した
ものである。
The materials used in the following examples and comparative examples are as follows. The continuous yarn is glass roving (manufactured by Fuji Fiber Glass, 1.8 g / m). The friction modifier is zinc oxide (made by Wako Pure Chemical Industries, for chemicals) 2% by weight, barium sulfate (Sakai Chemical Co., BC) 40% by weight, carbon black (Mitsubishi Carbon, # 44) 6
% By weight, graphite (made by ABRAMWELL in the UK) 3% by weight, silica powder (made by Tatsumori, crystallite) 10% by weight, calcium silicate short fibers (made by NYCO in the United States, trade name Wollastonite)
20% by weight, 14% by weight of cashew-modified friction dust (manufactured by Cashew Co., Ltd., WD-1350) and 5% by weight of finely divided sulfur (manufactured by Hosoi Chemical Co., Ltd.) were uniformly mixed with a V-type blender.

【0023】結合剤としての熱硬化性樹脂組成物は、ノ
ボラックフェノール樹脂(日立化成工業製、HD−49
1、ヘキサミン7重量%含有)及びメチル化メラミン樹
脂(日本カーバイド製、S−260)である。ゴムラテ
ックスは、NBRラテックス(日本ゼオン製、LX51
3、固形分45重量%)である。分散剤は、ポリビニル
アルコール(和光純薬工業製、重合度1500)の10
重量%水溶液を用いた。可撓化剤としては、エチレング
リコール(和光純薬工業製、化学用)を用いた。界面活
性剤は、ポリエチレングリコールノニルフェノール(花
王化学製、エマルゲン910)を用いた。溶媒は、イオ
ン交換水を用いた。
The thermosetting resin composition as the binder is a novolac phenol resin (HD-49 manufactured by Hitachi Chemical Co., Ltd.).
1, containing 7% by weight of hexamine) and a methylated melamine resin (manufactured by Nippon Carbide, S-260). The rubber latex is NBR latex (manufactured by Zeon Corporation, LX51
3, solid content 45% by weight). The dispersant is polyvinyl alcohol (manufactured by Wako Pure Chemical Industries, polymerization degree: 1500) 10
A weight% aqueous solution was used. Ethylene glycol (manufactured by Wako Pure Chemical Industries, for chemicals) was used as the flexibilizer. As the surfactant, polyethylene glycol nonylphenol (Emulgen 910, manufactured by Kao Kagaku) was used. Ion-exchanged water was used as the solvent.

【0024】実施例 上記した材料を表1に示す配合表の混和物組成に従って
次の順序で混合し、混和物を作製した。すなわち、分散
剤のポリビニルアルコール水溶液に熱硬化性樹脂組成
物、可撓化剤及び界面活性剤を添加し、高速ミキサーで
攪拌混合し、均一な溶液とした。次いで、摩擦調整剤を
加えて攪拌し、均一に分散させた。その後、攪拌をプロ
ペラ攪拌に変え、ゴムラテックスを加えて攪拌しなが
ら、固形分調整用の溶媒を固形分が50重量%となるよ
うに加えて攪拌して表1に示した配合の混和物を得た。
これとは別に、表1に示す配合表の結合剤組成に従って
次の順序で材料を混合し、結合剤組成物を得た。すなわ
ち、メラミン樹脂をイオン交換水に均一に分散させ、溶
解させた後、フェノール樹脂を添加、混合して均一な結
合剤の分散液を得た。
Example The above materials were mixed in the following order according to the composition of the mixture shown in Table 1 to prepare a mixture. That is, a thermosetting resin composition, a flexibilizer and a surfactant were added to a polyvinyl alcohol aqueous solution as a dispersant, and the mixture was stirred and mixed with a high speed mixer to obtain a uniform solution. Then, a friction modifier was added and stirred to uniformly disperse. After that, the stirring was changed to propeller stirring, and while adding rubber latex and stirring, a solvent for solid content adjustment was added so that the solid content was 50% by weight and stirred to obtain a mixture having the composition shown in Table 1. Obtained.
Separately from this, the materials were mixed in the following order according to the binder composition of the recipe shown in Table 1 to obtain a binder composition. That is, a melamine resin was uniformly dispersed in ion-exchanged water and dissolved, and then a phenol resin was added and mixed to obtain a uniform binder dispersion.

【0025】連続ヤーンを充分に開繊して上記混和物あ
るいは結合剤の分散液を均一に含浸させた後、表2に記
載した条件で乾燥して塗工紐A及び塗工紐Bを得た。こ
うして得られた塗工紐A3本と塗工紐B1本とを撚り合
わせた後、環状に巻き上げて予備成形品を得た。得られ
た環状体を金型に入れ、熱圧成形を行い、次いで成形品
を220℃で熱処理して樹脂を後硬化させ、摩擦材を得
た。なお、結合剤を塗工した塗工紐Bの空隙率は、材料
の密度、体積及び重量から算出したところ37%であっ
た。
After the continuous yarn was sufficiently opened to uniformly impregnate the mixture or the dispersion liquid of the binder, it was dried under the conditions shown in Table 2 to obtain a coated cord A and a coated cord B. It was The three coated strings A thus obtained and one coated string B were twisted together and then rolled up in a ring to obtain a preform. The obtained annular body was put into a mold and subjected to thermocompression molding, and then the molded product was heat-treated at 220 ° C. to post-cure the resin to obtain a friction material. The porosity of the coated string B coated with the binder was 37% when calculated from the density, volume and weight of the material.

【0026】[0026]

【表1】 [Table 1]

【0027】[0027]

【表2】 [Table 2]

【0028】比較例 上記実施例で作製した塗工紐Aのみを4本撚り合わせた
後、実施例と同様にして成形及び熱処理を行い、摩擦材
を作製した。
Comparative Example After only four coated strings A produced in the above examples were twisted together, molding and heat treatment were carried out in the same manner as in the examples to produce friction materials.

【0029】実施例で作製した塗工紐A及びB並びに実
施例及び比較例で作製した摩擦材について下記の評価を
行い、結果を表3に示した。 (a)塗工紐の乾燥性 塗工紐A及びBをそれぞれ170℃で30分間乾燥し、
揮発分を求めて乾燥性を評価する。サンプルを3本ずつ
用いて評価を行った。 (b)塗工紐の外観 目視で観察した。 (c)塗工紐内の混和物分布 塗工紐約1mを立てに裂き、表面部と内部の混和物の分
布を目視で観察して評価した。
The coated strings A and B produced in the examples and the friction materials produced in the examples and the comparative examples were evaluated as follows, and the results are shown in Table 3. (A) Drying property of coated string Each of the coated strings A and B is dried at 170 ° C. for 30 minutes,
The dryness is evaluated by obtaining the volatile content. Evaluation was performed using three samples each. (B) Appearance of coated string It was visually observed. (C) Mixture distribution in the coated cord About 1 m of the coated cord was torn vertically, and the distribution of the admixture on the surface and inside was visually observed and evaluated.

【0030】(d)摩擦材の外観 摩擦材の表面を研磨し、厚さを3.5mmとしたときの外
観を目視で観察する。 (e)摩耗率 摩擦材から一部を切り出して試験片を作り、JIS−D
4411に定める定速度摩耗試験機に取り付けて運転
し、押し付け圧力4.9×105Pa(5kgf/cm2)で3
50℃における摩耗率(cm3/kgf・m×10-7)を測定
する。 (f)バースト強度 摩擦材を回転破壊強度試験機に取り付け、雰囲気温度2
00℃で5分間、2500回転/分で回転させ、次いで
毎秒100回転の速さで回転数を上昇させ、破壊時の回
転数を調べた。 (g)摩擦係数 300℃で測定した。
(D) Appearance of friction material The surface of the friction material is ground and the appearance is visually observed when the thickness is 3.5 mm. (E) Wear rate A part is cut out from the friction material to make a test piece, and JIS-D
It is installed in a constant-speed wear tester specified in 4411 for operation, and pressed at a pressure of 4.9 × 10 5 Pa (5 kgf / cm 2 ) for 3
The wear rate (cm 3 / kgf · m × 10 −7 ) at 50 ° C. is measured. (F) Burst strength The friction material was attached to the rotary fracture strength tester and the ambient temperature was set to 2
Rotation was performed at 2500 rpm for 5 minutes at 00 ° C., and then the rotation speed was increased at a speed of 100 rotations per second, and the rotation speed at break was examined. (G) Friction coefficient Measured at 300 ° C.

【0031】[0031]

【表3】 [Table 3]

【0032】表3に示した結果から明らかなとおり、実
施例及び比較例で製造した塗工紐内の混和物の分布は均
一であり、摩擦材の外観も良好であり、バースト強度及
び摩耗率においても両者の差は見られなかったが、30
0℃での摩擦係数においては本発明の実施例で製造した
摩擦材は、0.27〜0.30と一様に高い数値を示し
たが、比較例で製造したものは、0.18〜0.25と
バラツキが大きく、その数値も小さかった。
As is clear from the results shown in Table 3, the distribution of the admixture in the coated cords produced in Examples and Comparative Examples is uniform, the appearance of the friction material is good, and the burst strength and the wear rate are high. There was no difference between the two, but 30
With respect to the friction coefficient at 0 ° C., the friction materials produced in the examples of the present invention showed uniformly high values of 0.27 to 0.30, but those produced in the comparative examples were 0.18 to The variation was as large as 0.25, and the value was also small.

【0033】[0033]

【発明の効果】本発明になる摩擦材は、バースト強度、
摩耗率、高温での摩擦係数のいずれにおいても優れてお
り、機械的強度と摩擦特性のバランスが高いレベルでと
れており、諸性能の数値のバラツキが小さい。したがっ
て、本発明の摩擦材は、自動車も産業機械における動力
伝達装置、制動装置などに有効に利用される。また、本
発明になる摩擦材は、製造に当たって有機溶媒を使用し
なくてすむため、地球環境や作業環境を汚染せず、作業
安全性の点でも優れている。
The friction material according to the present invention has a burst strength,
It is excellent in both wear rate and friction coefficient at high temperature, has a high level of balance between mechanical strength and friction characteristics, and has little variation in various performance values. Therefore, the friction material of the present invention can be effectively used for a power transmission device, a braking device and the like in an industrial machine of an automobile. Further, since the friction material according to the present invention does not require the use of an organic solvent in the production, it does not pollute the global environment or the work environment and is excellent in work safety.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 摩擦調整剤及び結合剤を主成分とする混
和物を含有する連続ヤーンと、主として結合剤を含有す
る連続ヤーンとを所定の本数ずつ撚り合わせた撚糸から
なり、主として結合剤を含有する連続ヤーンが多数の微
細な空隙を有することを特徴とする摩擦材。
1. A twisted yarn obtained by twisting a predetermined number of continuous yarns containing a mixture containing a friction modifier and a binder as main components and continuous yarns containing the binder, mainly comprising the binder. A friction material characterized in that the continuous yarn contained therein has a large number of fine voids.
JP15513493A 1993-06-25 1993-06-25 Friction material Pending JPH0712158A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15513493A JPH0712158A (en) 1993-06-25 1993-06-25 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15513493A JPH0712158A (en) 1993-06-25 1993-06-25 Friction material

Publications (1)

Publication Number Publication Date
JPH0712158A true JPH0712158A (en) 1995-01-17

Family

ID=15599300

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15513493A Pending JPH0712158A (en) 1993-06-25 1993-06-25 Friction material

Country Status (1)

Country Link
JP (1) JPH0712158A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009149716A (en) * 2007-12-19 2009-07-09 Mitsubishi Electric Corp Friction member and method for manufacturing the same
CN102485092A (en) * 2010-11-30 2012-06-06 长尾太文 Umbrella
JP2013091796A (en) * 2012-12-13 2013-05-16 Mitsubishi Electric Corp Friction member and brake
KR20160131013A (en) * 2014-03-07 2016-11-15 발레오 마테리오 드 프릭시옹 Friction lining with improved resistance to wear, dry friction clutch comprising such a lining and methods of manufacturing such a lining and such a clutch
WO2019022012A1 (en) * 2017-07-24 2019-01-31 株式会社アドヴィックス Friction material for dry brakes

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009149716A (en) * 2007-12-19 2009-07-09 Mitsubishi Electric Corp Friction member and method for manufacturing the same
CN102485092A (en) * 2010-11-30 2012-06-06 长尾太文 Umbrella
JP2013091796A (en) * 2012-12-13 2013-05-16 Mitsubishi Electric Corp Friction member and brake
KR20160131013A (en) * 2014-03-07 2016-11-15 발레오 마테리오 드 프릭시옹 Friction lining with improved resistance to wear, dry friction clutch comprising such a lining and methods of manufacturing such a lining and such a clutch
WO2019022012A1 (en) * 2017-07-24 2019-01-31 株式会社アドヴィックス Friction material for dry brakes
JP2019023255A (en) * 2017-07-24 2019-02-14 株式会社アドヴィックス Dry brake friction material

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