JPS6152434A - Friction material - Google Patents

Friction material

Info

Publication number
JPS6152434A
JPS6152434A JP16231784A JP16231784A JPS6152434A JP S6152434 A JPS6152434 A JP S6152434A JP 16231784 A JP16231784 A JP 16231784A JP 16231784 A JP16231784 A JP 16231784A JP S6152434 A JPS6152434 A JP S6152434A
Authority
JP
Japan
Prior art keywords
friction material
parts
weight
fibers
friction
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
JP16231784A
Other languages
Japanese (ja)
Other versions
JPH0261663B2 (en
Inventor
Toshiaki Sakabe
坂部 俊明
Yasuhiro Matsumoto
康弘 松本
Hisami Tsujio
辻尾 久美
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aisin Chemical Co Ltd
Aisin Corp
Original Assignee
Aisin Seiki Co Ltd
Aisin Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aisin Seiki Co Ltd, Aisin Chemical Co Ltd filed Critical Aisin Seiki Co Ltd
Priority to JP16231784A priority Critical patent/JPS6152434A/en
Publication of JPS6152434A publication Critical patent/JPS6152434A/en
Publication of JPH0261663B2 publication Critical patent/JPH0261663B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D69/00Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
    • F16D69/02Composition of linings ; Methods of manufacturing
    • F16D69/025Compositions based on an organic binder
    • F16D69/026Compositions based on an organic binder containing fibres

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Braking Arrangements (AREA)

Abstract

PURPOSE:To provide a friction material excellent in judder characteristic at the time of departure by forming the friction material by 20-30pts. of fiber processed to be bulky, 5-25pts. of binder, 10-30pts. of inorganic filler and 15- 45pts. of the other components. CONSTITUTION:The friction material is formed by 20-30pts. of heat-resisting fiber processed to be bulky, 5-25pts. of binder such as phenol resin or the like, 10-30pts. of inorganic filler such as barium sulfate, mixture of calcium carbonate, or the like, and 15-45pts. of the other components. Thus, judder will not occur at the time of departure in a specified car without damaging general characteristics of a friction material such as coefficient of friction, abrasion, strength and so on.

Description

【発明の詳細な説明】 〔産業上の利用分野) 本発明は、車両用摩擦材、特に乾式クラッチフェーシン
グ及びブレーキライニングの改良に関づ゛る。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to improvements in friction materials for vehicles, particularly dry clutch facings and brake linings.

(従来の技術) 従来、この種の摩擦材として、作lA環境の悪化を回避
するため無石綿摩擦材の開発が行なわれ、(1)スチー
ル繊維を基材としたもの、(2)有機天然繊維もしくは
一般の有機合成繊維を基材としたもの、又は(3)ガラ
ス繊維、フェノール繊維および炭素繊維等の耐熱繊維を
基材としたもの等が、その改良品として知られている。
(Prior art) Conventionally, asbestos-free friction materials have been developed as this type of friction materials in order to avoid deterioration of the production environment. Improved products are known, such as those based on fibers or general organic synthetic fibers, or (3) those based on heat-resistant fibers such as glass fibers, phenol fibers, and carbon fibers.

しかしく1)のものは重いこと、および錆の発生により
相手材に付着し、クラッチ等の特性を]lうこと等の欠
点がある。(2)のものは耐熱性および強度が劣ること
等の欠点がある。(3)のものは、結合剤との密着性が
乏しく所望の強度が得られ郵1欠点がある。
However, the method 1) has disadvantages such as being heavy and causing rust to adhere to the mating material, which may affect the characteristics of the clutch, etc. Type (2) has drawbacks such as poor heat resistance and strength. The material of (3) has poor adhesion with the binder and the desired strength cannot be obtained, but has one drawback.

そこで本発明者等は、ガラス繊維及び炭素繊維よりなる
群から選ばれた少なくとも1種又は2種以上のかさ高加
工を施した該繊維を基材とする摩擦材を発明し、該摩擦
材は公知となっている(特開昭56−167934)。
Therefore, the present inventors invented a friction material based on fibers that have been subjected to bulk processing of at least one or more types selected from the group consisting of glass fiber and carbon fiber, and the friction material is It is publicly known (Japanese Patent Laid-Open No. 56-167934).

このB環材は、強度摩擦係数、摩耗には優れていたが、
その接種々の評価をしたところ、特定の車輌で発進時シ
ャダーが発生するという欠点のあることが分った。
This B ring material had excellent strength, friction coefficient, and wear, but
When we evaluated these inoculations, we found that they had the drawback of causing shudder when starting on certain vehicles.

さらに本発明者等は、上記欠点を解消するためゴムバイ
ンダーへの配合剤を検討した結果ナーマルブラックがシ
ャダーに対して有効であることが確認できた。そこで本
発明者等は、ガラス繊維、フェノール樹脂及び炭素繊維
よりなる群から選ばれた少なくとも1種又は2種以上の
かさ高加工を施した該繊維を基材として、これに配合剤
の1つとしてサーマルブラックを配合した摩擦材を発明
し、この発明は公知となっている(特開昭58−747
75>。しかしその後の評価において、「F乗用車、4
輪駆動乗用車等における苛酷な条件下で使用すると、す
べりが発生づ°るという欠点のあることが分った。
Furthermore, the present inventors investigated compounding agents for rubber binders in order to eliminate the above-mentioned drawbacks, and as a result, they were able to confirm that Nermal Black is effective against shudder. Therefore, the present inventors used the fibers, which have been subjected to bulk processing of at least one or more types selected from the group consisting of glass fibers, phenolic resins, and carbon fibers, as a base material, and added one of the compounding agents to the fibers. As a result, he invented a friction material containing thermal black, and this invention has become publicly known (Japanese Patent Laid-Open No. 58-747).
75>. However, in the subsequent evaluation, "F passenger car, 4
It has been found that when used under severe conditions such as in a wheel-drive passenger car, it has the disadvantage that it tends to slip.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

本発明は、上記欠点をすべてバランス良く克服するもの
であり、通常I!Jv!材として要求される耐摩耗性お
よび強度等の特性を損なわずに、発進時のシャダー特性
に優れ、かつ苛酷な条°件下でもずべりを発生しないI
I擦環材提供することを目的とする。
The present invention overcomes all of the above drawbacks in a well-balanced manner, and generally I! Jv! I that has excellent shudder properties during starting without compromising properties such as abrasion resistance and strength required for the material, and does not cause slippage even under severe conditions.
The purpose is to provide a friction ring material.

〔問題点を解決するための手段〕[Means for solving problems]

本発明の摩擦材は、100ffiff1部中、かさ高加
工をしたガラス繊維、フェノール繊維および炭素繊維等
の耐熱性のある繊維群のうちの少なくとも1つから成る
m帷のかさ高加工繊維20〜3o重凶部と、結合剤5〜
25重山部と、無機フィラー10〜30重量部と、ゴム
を含むその他の成分15〜45重団部とより構成される
ことを特徴とする。
The friction material of the present invention comprises 1 part of 100ffiff, 20 to 3 m of bulky processed fibers made of at least one of a group of heat-resistant fibers such as glass fibers, phenol fibers, and carbon fibers. Serious part and binder 5~
It is characterized by being composed of 25 parts by weight, 10 to 30 parts by weight of an inorganic filler, and 15 to 45 parts by weight of other components including rubber.

本発明のII擦環材基材となるm Ili I!¥は、
300℃で耐熱性を有するUVt群をざし、具体的には
ガラス繊維、フェノール繊維、炭素繊維等である。
m Ili I! which becomes the II rubbing material base material of the present invention! ¥ is
We aim at UVt group materials that are heat resistant at 300°C, specifically glass fibers, phenol fibers, carbon fibers, etc.

この耐熱性という用語の意味する所は300’Cで!!
維の減mや収縮現象を伴わず、熱に安定であることを意
味する。本I’ll材に使用される繊維は、上記1&!
維群のうち少なくとも1種類から成る繊維であれば良く
、1種類でも2種類以上の繊維であってもよい。通常ガ
ラス繊維の1種類が用いられる。該繊維の径および長さ
等は特に限定されないが、単繊維は12μ以下が好まし
く使用時は、この単繊維を数百本収束し、ストランド等
の必要な繊維加工した後さらにかさ高加工して使用する
What this term heat resistance means is 300'C! !
This means that it is stable to heat without fiber loss or shrinkage phenomena. The fibers used in this I'll material are 1 &!
The fibers may be made of at least one type of fiber group, and may be one type or two or more types of fibers. Usually one type of glass fiber is used. The diameter and length of the fibers are not particularly limited, but it is preferable that the single fibers be 12μ or less, and when used, several hundred single fibers are converged, subjected to necessary fiber processing such as strands, and then further processed to make them bulky. use.

このかさ高加工とは、一部文献で紹介されている如く、
糸状繊維に対し羊毛に代表されるような天然繊維状のク
リンプ形態をもたば、ガラス繊維や化学繊維の風合を改
良し、伸縮性とかさ真性を付与する加工をいう。該かさ
高加工方法は、05 illの種類を例えば伸縮性、非
伸縮性の繊維等に分類し、その分類に応じて適当な方法
を選定すると良い。
This bulky processing is, as introduced in some literature,
It is a process that improves the texture of glass fibers and chemical fibers, giving them elasticity and bulk by giving filamentous fibers a natural fiber-like crimp form, such as wool. As for the bulking method, it is preferable to classify the type of 05 ill into, for example, stretchable fibers, non-stretchable fibers, etc., and select an appropriate method according to the classification.

本発明の結合剤としては、フェノール系樹脂、ブチラー
ル系樹脂、フェノキシ系樹脂、エポキシ系樹脂、メラミ
ン樹脂等を用いることかできる。
As the binder of the present invention, phenol resin, butyral resin, phenoxy resin, epoxy resin, melamine resin, etc. can be used.

フェノール系樹脂とは、例えばフェノール、クレゾール
などフェノール類の一種又はそれ以上とホルムアルデヒ
ド又はその発生源となる化合物と129111合さじて
得られる樹脂をいう。カシュウナットオイル、ポリビニ
ールブチラール、植物油、メラミン、エポキシ化合物等
で変性した変性フェノール樹脂を用いても良い。尚、耐
熱性の点では、無変性フェノール樹脂がよい。
Phenolic resin refers to a resin obtained by combining one or more phenols such as phenol and cresol with formaldehyde or a compound that is a source thereof. Modified phenolic resins modified with cashew nut oil, polyvinyl butyral, vegetable oil, melamine, epoxy compounds, etc. may also be used. In addition, unmodified phenol resin is preferable in terms of heat resistance.

本発明の無機フィラーとしては、すべり防止特性および
相手材低攻撃性の双方にバランス良く優れたものを単品
又は混合品として用いる。即ちこの両特性に優れたもの
には硫酸バリウム、炭酸カルシウム等(X群)があり、
ずべり防止特性に優れるが相手材低攻撃性には優れない
ものにはケイソウ土、アルミナ、シリカ等(Y群)があ
り、その反対の性能のものにはグラフフィト、タルク等
(7群)がある。本発明の無機フィラーとしては、(1
)X群のうちの少なくとも一種から成るもの、(2)X
群のうちの少なくとも一種に、Y群又は7群のうちの少
なくとも1!!Iを混合したもの、または(3)Y群の
うちの少なくとも一種に7群のうちの少なくとも一種の
ものを混合したものを用いることができる。なおY群の
うちの少なくとも1種から成るもの又は2群のうちの少
なくとも1種から成るものは、特性のバランスが悪いの
で使用されず、サーマルブラックについても同様である
。サーマルブラック単一では、苛酷な条件下ではすべり
を発生ずるからである。上記前はフィラーの配合成分の
種類、およびその配合割合は、目的および用途に応じて
適宜選択する。本発明の11((礪フィラーとしては、
硫酸バリウムおよび炭酸カルシウムの1又は2種である
ものが好ましい。
As the inorganic filler of the present invention, one that is excellent in both anti-slip properties and low aggressiveness of mating materials in a well-balanced manner is used singly or as a mixture. In other words, materials that are excellent in both of these properties include barium sulfate, calcium carbonate, etc. (group X).
Materials that have excellent anti-slip properties but are not excellent in low aggressiveness of mating materials include diatomaceous earth, alumina, and silica (Y group), while those with the opposite performance include graphite, talc, etc. (group 7). There is. The inorganic filler of the present invention includes (1
) consisting of at least one type of group X, (2) X
At least one of group Y or at least one of group 7! ! A mixture of I or (3) a mixture of at least one of the group Y and at least one of the seven groups can be used. Note that those consisting of at least one member of the Y group or at least one member of the two groups are not used because their properties are unbalanced, and the same applies to thermal black. This is because thermal black alone causes slippage under severe conditions. The types of components of the filler and their blending ratios are appropriately selected depending on the purpose and use. 11 of the present invention ((as a filler,
One or both of barium sulfate and calcium carbonate are preferred.

本発明に使用するゴム、その他の配合剤(例えばカシュ
ウダスト、ラバーダスト等の有機粉末、アルミニウム、
鉄、亜鉛等の金属粉末、加硫剤、加硫促進剤、加硫助剤
等)および金属線は特に限定されず、目的および用途に
より例えばクラッチフェーシング、又はブレーキライニ
ング等に応じて、種々の周知のものを選択できる。
Rubber and other compounding agents used in the present invention (e.g. organic powders such as cashew dust and rubber dust, aluminum,
Metal powders such as iron and zinc, vulcanizing agents, vulcanization accelerators, vulcanization aids, etc.) and metal wires are not particularly limited, and may be used in various ways depending on the purpose and application, such as clutch facings or brake linings. You can choose one that is well known.

ゴムはSBR又はNBR等の合成ゴムが好ましい。クラ
ッチフェーシングには比較的多分のゴムが使用される。
The rubber is preferably synthetic rubber such as SBR or NBR. A relatively large amount of rubber is used for the clutch facing.

また一般に広(使用されているスパイラルウーブン法を
用いて摩擦材を製造する場合はゴムは配合しなくてもよ
い。金属線には、真ちゅう線が好ましい。
Further, when manufacturing a friction material using the widely used spiral woven method, rubber does not need to be blended. Brass wire is preferable for the metal wire.

本摩擦材の配合成分の各配合割合は、以下にのべる、こ
の種の摩擦材に実用上要求されるすべての特性を具備す
るように設定される。またこの各配合91合は、以下の
代表的配合成分の各標準的配合割合を中心として、各成
分割合を種々かえて試験し、各々性能評価を行ない、下
記の実用上要求される特性値を具備するように決定をし
た。
The blending ratios of the components of this friction material are set so as to have all the properties practically required for this type of friction material, as described below. In addition, each of these 91 formulations was tested by changing the proportions of each component, centering on the standard proportions of the following representative compounding ingredients, and the performance of each was evaluated, and the following practically required characteristic values were obtained. I decided to equip it.

〔実用上要求される特性値〕[Practically required characteristic values]

シャター程度0.1G[F、平均IIJrs係数0゜3
〜o、45、摩耗ff16. OX 10−4mm37
kg・m以下、相手材攻撃性0.05m1ll以下、バ
ースト強度i 4000 rpm以上、発進時の実車シ
ャダーテストに優れること、苛酷な条件下での実車すべ
りのないこと。
Shutter degree 0.1G [F, average IIJrs coefficient 0°3
~o, 45, wear ff16. OX 10-4mm37
kg・m or less, aggressiveness to mating material 0.05ml or less, burst strength i 4000 rpm or more, excellent in actual vehicle shudder test when starting, and no actual vehicle slippage under severe conditions.

〔代表的配合成分とその標準的配合割合〕ガラス繊維2
5重量部、フェノール樹脂17重量部、硫酸バリウムお
よび炭酸カルシウム混合物23重■1部、5BR14重
量部、カシュダスト5重i部、架橋剤12重口部、真ち
ゅう線4重量部。
[Typical compounding ingredients and their standard compounding ratios] Glass fiber 2
5 parts by weight, 17 parts by weight of phenolic resin, 1 part by weight of barium sulfate and calcium carbonate mixture, 14 parts by weight of 5BR, 5 parts by weight of cashew dust, 12 parts by weight of crosslinking agent, 4 parts by weight of brass wire.

以上を考慮′して決定された本摩擦材の配合成分の各配
合割合は、全摩擦材100重旦全部して、以下の通りで
ある。
The blending ratios of the components of the present friction material, which were determined in consideration of the above, are as follows, including all 100 parts of the friction material.

かさ高加工をした耐熱繊維の配合割合は、20〜30重
旦部で全部。30重全部より以上ではシャダー程度が0
.1Gより以上となり、20mfi1部未満ではバース
ト強度が14000rpm未満となり、好ましくないか
らである。
The blending ratio of bulky heat-resistant fibers is 20 to 30 parts by weight. The degree of shudder is 0 for all 30 weights or more.
.. This is because if it is more than 1 G and less than 1 part of 20 mfi, the burst strength will be less than 14,000 rpm, which is not preferable.

結合剤の配合割合は、5〜25重伍部であり、好ましく
は8〜25重世部である。25iI2m部より以上では
摩擦係数が0.3未満となり、5重量部未満では該係数
が0.45より以上となり、好ましくないためである。
The blending ratio of the binder is 5 to 25 parts by weight, preferably 8 to 25 parts by weight. This is because if the amount is more than 25iI2m parts, the coefficient of friction will be less than 0.3, and if it is less than 5 parts by weight, the coefficient will be more than 0.45, which is not preferable.

無機フィラーの配合割合は、10〜30重量部であり、
好ましくは12〜30重鼠部である。10重量部未満で
は摩擦係数が0.3未満となり、30重凸部より以上で
は該係数が0.45より以−ヒとなり、好ましくないた
めである。
The blending ratio of the inorganic filler is 10 to 30 parts by weight,
Preferably it is 12 to 30 layers. This is because if it is less than 10 parts by weight, the coefficient of friction will be less than 0.3, and if it is more than 30 parts by weight, the coefficient will be less than 0.45, which is not preferable.

ゴムを含むその他の成分の配合割合は、15〜45!1
1!fi)部である。このうちゴムの配合割合は、5〜
20重呈部が好ましい。5重旦部未満では摩耗旦が6.
OXl 0−4mm37kg−mより以上となり、20
重量部より以上では摩擦係数が0.3未;菌となり好ま
しくないためである。
The blending ratio of other components including rubber is 15 to 45!1
1! fi) section. Among these, the blending ratio of rubber is 5~
20 layers are preferred. If the wear rate is less than 5, the wear rate is 6.
OXl 0-4mm 37kg-m or more, 20
If the amount is more than 1 part by weight, the coefficient of friction will be less than 0.3; this is because it may lead to bacteria, which is undesirable.

その他の成分即ち上記配合剤以外の配合剤および金属線
の配合割合は、上記配合剤の全配合旦の残部であり、通
常、その他の配合剤(架橋剤および各添加剤等)は10
〜20重囚部で口部、金属線は2〜5重旦全部ある。
The blending ratio of other components, that is, compounding agents other than the above-mentioned compounding agents and metal wires, is the balance of all the above-mentioned compounding agents, and usually the other compounding agents (crosslinking agent, each additive, etc.) are 10%
There are 2 to 5 layers of metal wire in the mouth part of the ~20 layers.

本発明の摩擦材を製造する方法には、周知の方法がいず
れも適用でき、特に制限を設けない。この代表的な例は
セミモールド法と生するもので結合剤の含浸、乾燥、ゴ
ムコート、乾燥、ループ状に巻取り、加圧加熱成形、ア
フターキュアー及び研磨等の工程を経て、摩擦材を′!
A造する方法である。
Any known method can be applied to the method of manufacturing the friction material of the present invention, and there are no particular limitations. A typical example of this is the semi-molding method, which involves impregnating the friction material with a binder, drying, rubber coating, drying, winding into a loop, pressurizing and heating molding, after-curing, and polishing. !
This is the method of building A.

〔実施例〕〔Example〕

以下、実施例により本発明を説明する。 The present invention will be explained below with reference to Examples.

実施例1 6μの繊維径を有するEガラス単繊維を収束させストラ
ンド等の開繊維加工した後、この繊維にかさ高加工を施
した。この繊維をメタノールで調合したフェノール系樹
脂溶液に含浸さぼた後、120℃でメタノールが十分に
揮発するまで約1時間乾燥させて、フェノール樹脂を被
着さびた。この後予めSBRに硫黄と促進剤CZと無機
フィラー(硫酸バリウムおにび炭酸力ルシウームa合品
)をゴムローラーで混練したものを、トルエンでゴム分
を溶解させて粘度を10000〜20000Cpsに調
整したコーテイング槽に含浸させゴムをコートする。こ
の時、同時に前記繊維に真ちゅう線を巻きつける。その
後十分に風乾させ巻取機にてループ状に巻取った後、1
65℃、100 ko/Cl12にセットした圧縮成形
機を用いて3分間加圧加熱成形する。この時最初数回ガ
ス扱きを行なう。
Example 1 E-glass single fibers having a fiber diameter of 6 μm were converged and subjected to an opening process such as a strand, and then the fibers were subjected to a bulking process. This fiber was impregnated with a phenolic resin solution prepared with methanol and then dried at 120° C. for about 1 hour until the methanol was sufficiently volatilized to rust the phenolic resin. After this, SBR is mixed with sulfur, accelerator CZ, and inorganic filler (barium sulfate and lucium carbonate a mixture) using a rubber roller, and the rubber content is dissolved with toluene to adjust the viscosity to 10,000 to 20,000 Cps. The rubber is coated by impregnating it into a coating bath. At this time, a brass wire is simultaneously wound around the fiber. After that, after thoroughly air-drying and winding it into a loop shape with a winding machine, 1
Pressure and heat molding is performed for 3 minutes using a compression molding machine set at 65° C. and 100 ko/Cl12. At this time, treat it with gas several times at first.

得られた成形品を加熱炉で150℃で6時間と、200
℃で3時間と、250℃で3時間連続加熱処理し、摩擦
面の表裏両面を研磨してI’J擦材環材た。
The obtained molded product was heated in a heating furnace at 150°C for 6 hours and then heated at 200°C.
℃ for 3 hours and 250℃ for 3 hours, and both the front and back of the friction surface were polished to obtain an I'J friction ring material.

この摩擦材全100部中には、各配合成分は重量でそれ
ぞれ第1表の如き割合で含まれていた。
In the total of 100 parts of this friction material, each component was contained in the proportions shown in Table 1 by weight.

上記yJ擦環材性能をみるために、平均摩擦係数、最小
産金係数、摩耗量、相手材攻撃性、発進時での実車シャ
ダーおよ°び苛酷条件下での実車すべりの試験を行ない
、その結果を第2表に示寸。
In order to examine the performance of the above-mentioned yJ friction material, we conducted tests on the average friction coefficient, minimum yield coefficient, amount of wear, aggressiveness of opposing materials, shudder on an actual vehicle when starting, and sliding on an actual vehicle under severe conditions. The results are shown in Table 2.

なお、この試験方法はI!J擦係数及び摩耗量は慣性ダ
イナモメータにて200″Cで試験し、シャダー及び“
すべり″は実際にIIIIW材を車(FF乗用IIおよ
び4輪駆動乗用車)に搭載し、苛酷な条件下で実車テス
トを行なった。第2表中実車スベリ試験でOはすべりな
し、×はすべりが認められたものである。
In addition, this test method is I! The J friction coefficient and wear amount were tested using an inertial dynamometer at 200"C.
``Slip'' was measured by actually mounting the IIIW material on a car (FF passenger II and 4-wheel drive passenger car) and conducting actual vehicle tests under severe conditions.Table 2: In the solid car slipping test, O means no slipping, and × means slipping. has been recognized.

実施例2〜5および比較例1〜2 実施例2〜5および比較例1〜2においては、各配合成
分の配合割合を第1表に示したものとしたこと以外は、
実施例と同様にして摩擦材を得た。
Examples 2 to 5 and Comparative Examples 1 to 2 In Examples 2 to 5 and Comparative Examples 1 to 2, except that the proportions of each compounded component were as shown in Table 1,
A friction material was obtained in the same manner as in the example.

なお比較例1においては、フィラーにケイソウ土、炭酸
カルシウム、硫酸バリウムおよびuAyJの混合品を用
い、比較例2においてはフィラーにサーマルブラックを
用い、また比較例1および2についてはカシュダストは
配合されていない。
In Comparative Example 1, a mixture of diatomaceous earth, calcium carbonate, barium sulfate, and uAyJ was used as a filler, in Comparative Example 2, thermal black was used as a filler, and in Comparative Examples 1 and 2, cash dust was not blended. do not have.

上記摩擦材の各試験を実施例1と同様にして行ない、そ
の結果を第2表に示した。この結果によれば、本実施例
1〜5のHa材はいずれも、tti記の摩擦材に実用上
要求される特性値をすべて具υ11する。即ち該本摩擦
材は、平均摩擦係数が0.39〜4.44であり、摩耗
口が6.OXlo−4mm3/kQ・m以下であり、相
手材攻撃性は0.009〜0.018mmであり、実車
シャダー性能は0.1G以下であり、実車すべりも生じ
ない。一方比較例1では相手材攻撃性は0.053mm
であり、かつ実車シャダー性能は0.120Gであり、
比較例2では実車すべりが生じ、上記実用上の特性値か
ら外れる。
Each test of the above friction material was conducted in the same manner as in Example 1, and the results are shown in Table 2. According to this result, all of the Ha materials of Examples 1 to 5 meet all the characteristic values practically required for friction materials described in tti. That is, this friction material has an average friction coefficient of 0.39 to 4.44 and a wear opening of 6. OXlo-4 mm3/kQ·m or less, the aggressiveness to the mating material is 0.009 to 0.018 mm, the actual vehicle shudder performance is 0.1 G or less, and no actual vehicle slippage occurs. On the other hand, in Comparative Example 1, the aggressiveness of the opposing material was 0.053 mm.
And the actual vehicle shudder performance is 0.120G,
In Comparative Example 2, actual vehicle slippage occurs and the characteristic values deviate from the above-mentioned practical characteristics.

以上より本摩擦材tよ、摩擦特性に優れ、かつ実車試験
において発進時でのシャダー性能に優れ、苛酷条件下で
のすべり現象をも防止した、極めて実用上有用な摩擦材
である。
From the above, this friction material has excellent friction properties, excellent shudder performance at the time of starting in actual vehicle tests, and also prevented slipping under severe conditions, making it an extremely useful friction material for practical use.

〔発明の効果〕〔Effect of the invention〕

本発明の1≠擦材は100重量部中、かさ高加工をした
ガラス繊維等の耐熱繊維のかさ高加工Ju /Ill第
1表 第2表 * 1 ・=×1O−4n+m3 /kg −m20〜
30重量部と、結合剤5〜25重量部と、無機フィラー
10〜30型組部と、ゴムを含むその他の成分15〜4
5重旦部と全部4+ll’s成されることを特徴とする
。従って本摩擦材は、シャダー程度0.1G以下、平均
摩擦係数0.3〜0.45、相手材攻撃性0.05mm
以下、摩耗m6.0X10−4 mm3 /k(1・m
以下、実車シャダーテストの良好性および苛酷な条件(
FF乗用車、4輪駆動乗用車搭載)下における実車すべ
りがないことのすべての条件を具備する。故に本摩擦材
は、摩■係数、摩耗および強度等V、擦環材しての一般
的特性を損なわずに、かつ特定の車輌で発進時ジャグ−
が発生するという欠点もなく、しかもF F乗用車、4
輪駆動乗用車等において苛酷な条件下の使用でもすべり
が発生ずるという欠点もない。即ち本IIJyA材は、
実用上極めてバランス性能に優れ、車輌用に極めて有用
である。
1≠The rubbing material of the present invention contains bulky processed heat-resistant fibers such as glass fibers in 100 parts by weight.
30 parts by weight, 5 to 25 parts by weight of binder, 10 to 30 parts of inorganic filler, and 15 to 4 parts of other components including rubber.
It is characterized by a total of 4 + ll's with 5 layers. Therefore, this friction material has a shudder level of 0.1 G or less, an average friction coefficient of 0.3 to 0.45, and an aggressiveness of opponent material of 0.05 mm.
Hereinafter, wear m6.0X10-4 mm3/k (1・m
Below, the performance of the actual vehicle shudder test and the harsh conditions (
(FWD passenger cars, 4-wheel drive passenger cars)) Meets all conditions for no actual vehicle slippage. Therefore, this friction material can be used without sacrificing the general characteristics of a friction material, such as coefficient of friction, wear, and strength, and can also be used to reduce friction when starting a specific vehicle.
It does not have the disadvantage of causing FF passenger cars, 4
There is no drawback that slippage occurs even when used under severe conditions in wheel drive passenger cars and the like. In other words, this IIJyA material is
It has excellent balance performance in practical terms and is extremely useful for vehicles.

Claims (2)

【特許請求の範囲】[Claims] (1)100重量部中、かさ高加工をしたガラス繊維、
フェノール繊維および炭素繊維等の耐熱性のある繊維群
のうちの少なくとも1つから成る繊維のかさ高加工繊維
20〜30重量部と、結合剤5〜25重量部と、無機フ
ィラー10〜30重量部と、ゴムを含むその他の成分1
5〜45重量部とより構成されることを特徴とする摩擦
材。
(1) In 100 parts by weight, bulked glass fiber,
20 to 30 parts by weight of bulky processed fibers made of at least one of heat-resistant fiber groups such as phenol fibers and carbon fibers, 5 to 25 parts by weight of a binder, and 10 to 30 parts by weight of an inorganic filler. and other ingredients including rubber1
A friction material comprising 5 to 45 parts by weight.
(2)結合剤はフェノール系樹脂であり、無機フィラー
は炭酸カルシウムおよび硫酸バリウムのうちの1種また
は2種である特許請求の範囲第1項記載の摩擦材。
(2) The friction material according to claim 1, wherein the binder is a phenolic resin, and the inorganic filler is one or two of calcium carbonate and barium sulfate.
JP16231784A 1984-07-31 1984-07-31 Friction material Granted JPS6152434A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16231784A JPS6152434A (en) 1984-07-31 1984-07-31 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16231784A JPS6152434A (en) 1984-07-31 1984-07-31 Friction material

Publications (2)

Publication Number Publication Date
JPS6152434A true JPS6152434A (en) 1986-03-15
JPH0261663B2 JPH0261663B2 (en) 1990-12-20

Family

ID=15752224

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16231784A Granted JPS6152434A (en) 1984-07-31 1984-07-31 Friction material

Country Status (1)

Country Link
JP (1) JPS6152434A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100370003C (en) * 2003-05-22 2008-02-20 日立化成工业株式会社 Friction material composition and friction material using the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5783576A (en) * 1980-09-04 1982-05-25 Valeo Friction lining
JPS5874775A (en) * 1981-10-27 1983-05-06 Aisin Chem Co Ltd Friction material

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5783576A (en) * 1980-09-04 1982-05-25 Valeo Friction lining
JPS5874775A (en) * 1981-10-27 1983-05-06 Aisin Chem Co Ltd Friction material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100370003C (en) * 2003-05-22 2008-02-20 日立化成工业株式会社 Friction material composition and friction material using the same

Also Published As

Publication number Publication date
JPH0261663B2 (en) 1990-12-20

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