JP2601065B2 - Friction material and heat treatment method thereof - Google Patents

Friction material and heat treatment method thereof

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Publication number
JP2601065B2
JP2601065B2 JP15794091A JP15794091A JP2601065B2 JP 2601065 B2 JP2601065 B2 JP 2601065B2 JP 15794091 A JP15794091 A JP 15794091A JP 15794091 A JP15794091 A JP 15794091A JP 2601065 B2 JP2601065 B2 JP 2601065B2
Authority
JP
Japan
Prior art keywords
friction material
heat treatment
phenylphenol
oxygen concentration
phenol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP15794091A
Other languages
Japanese (ja)
Other versions
JPH0570766A (en
Inventor
日男 馬場
光弘 井上
泰啓 原
拓二 伊藤
高明 栗田
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
Showa Denko Materials 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, Showa Denko Materials Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP15794091A priority Critical patent/JP2601065B2/en
Publication of JPH0570766A publication Critical patent/JPH0570766A/en
Application granted granted Critical
Publication of JP2601065B2 publication Critical patent/JP2601065B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)

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、摩擦材の熱処理方法に
係わり、特に自動車用ブレ−キパッドの耐フェ−ド性を
向上させるのに好適な摩擦材及び摩擦材の熱処理方法に
関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat treatment method for a friction material, and more particularly to a friction material suitable for improving the fade resistance of a brake pad for an automobile and a heat treatment method for the friction material. .

【0002】[0002]

【従来の技術】従来、自動車用ブレ−キパッドには、金
属繊維、ガラス繊維、セラミック繊維等を基材とし、こ
の基材に充填剤及び結合剤を混合して成形した摩擦材が
用いられている。
2. Description of the Related Art Conventionally, a friction material formed by mixing a filler and a binder with a base material such as a metal fiber, a glass fiber, and a ceramic fiber is used for a brake pad for an automobile. I have.

【0003】この摩擦材の熱処理方法には、非酸化雰囲
気中400〜1000℃の熱処理条件によって熱処理を
行い、熱硬化性樹脂、好ましくはフェノ−ル樹脂の結合
剤を部分的に炭化せしめ、高温時における分解生成物の
発生量の少ない熱的に安定な炭素質系物質を形成させる
ことにより、摩擦材の摩擦係数の低下原因を取り除くと
ともに、高温.高負荷時に摩擦材の劣化による制動の低
下現象(フェ−ド現象)の発生を未然に防止したものが
ある。(特開昭59−113038号公報参照)
In this heat treatment method for a friction material, heat treatment is performed in a non-oxidizing atmosphere at a heat treatment condition of 400 to 1000 ° C. to partially carbonize a binder of a thermosetting resin, preferably a phenol resin, By forming a thermally stable carbonaceous material that generates a small amount of decomposition products at the time of removal, the cause of the decrease in the friction coefficient of the friction material can be eliminated and the temperature can be increased. There is one in which the occurrence of a phenomenon of a decrease in braking (fade phenomenon) due to deterioration of a friction material under a high load is prevented. (See JP-A-59-113038)

【0004】この熱処理方法により、低速での制動時に
おける鳴きの発生を少なくし、且つ高温下での摩擦特性
を高めるようにしている。
[0004] By this heat treatment method, the generation of squeal during braking at low speed is reduced, and the friction characteristics at high temperatures are enhanced.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、レジン
モ−ルドディスクブレ−キパッドを非酸化雰囲気中にお
いて熱処理すると、基材である金属繊維が熱により劣化
し、摩擦材の強度が低下するという課題があり、また従
来のようなフェノ−ル樹脂を使用すると熱劣化により、
とくに高速時の耐摩耗性が低下するという課題があっ
た。
However, when the resin mold disk brake pad is heat-treated in a non-oxidizing atmosphere, there is a problem that the metal fibers as the base material are deteriorated by heat, and the strength of the friction material is reduced. Also, when a conventional phenol resin is used, thermal degradation causes
In particular, there is a problem that the wear resistance at high speed is reduced.

【0006】本発明は、上記課題に鑑みてなされたもの
であり、熱処理の雰囲気に低濃度の酸素を加え、繊維の
周りに補強材として酸化膜を形成させることで機械的強
度の向上を図り、また耐熱性のあるp−フェニルフェノ
−ルとフェノ−ルの共重合体樹脂を使用することで特に
高速時の耐摩耗性の向上を図ると共に、さらにp−フェ
ニルフェノ−ルとフェノ−ルの共重合体樹脂を部分的に
炭化することで耐フェド性の向上を図ることのできる摩
擦材を提供することを目的としたものである。
The present invention has been made in view of the above problems, and aims at improving mechanical strength by adding a low concentration of oxygen to a heat treatment atmosphere and forming an oxide film as a reinforcing material around fibers. In addition, by using a heat-resistant copolymer resin of p-phenylphenol and phenol, it is possible to improve the wear resistance particularly at high speeds, and to further improve p-phenylphenol and phenol. It is an object of the present invention to provide a friction material capable of improving the resistance to fade by partially carbonizing the above copolymer resin.

【0007】[0007]

【課題を解決するための手段】前記目的を達成するため
の本発明の構成を実施例に対応する図1に基づき説明す
ると、本発明は、p−フェニルフェノ−ル(1〜100
体積%)とフェノ−ル(0〜99体積%)を酸又はアル
カリ触媒を用いてホルムアルデヒドと共重合反応させ、
縮合させた耐熱性を有するp−フェニルフェノ−ルとフ
ェノ−ルの共重合体樹脂を結合剤とし、スチ−ル繊維、
アルミ繊維、銅繊維、黄銅繊維、亜鉛繊維、ニッケル繊
維、クロム繊維等のような、従来摩擦材に用いられる金
属繊維であって、酸化により強度の上昇する金属繊維を
基材とし、この基材に黒鉛、硫酸バリュウム等の充填剤
を混合して成形した摩擦材を、酸素濃度0.1〜10%
の低酸素濃度場において処理温度を250℃以上125
0℃未満とする設定条件下で熱処理を行うことを特徴と
する。
The structure of the present invention for achieving the above object will be described with reference to FIG. 1 corresponding to an embodiment. The present invention relates to p-phenylphenol (1 to 100).
Volume%) and phenol (0-99 volume%) are copolymerized with formaldehyde using an acid or alkali catalyst,
Heat-resistant condensed p-phenylphenol and phenol copolymer resin as a binder, steel fiber,
A metal fiber which is conventionally used as a friction material, such as an aluminum fiber, a copper fiber, a brass fiber, a zinc fiber, a nickel fiber, a chromium fiber, and the like. A friction material formed by mixing a filler such as graphite, barium sulfate, etc., with an oxygen concentration of 0.1 to 10%
In the low oxygen concentration field, the treatment temperature is 250 ° C or more and 125
The heat treatment is performed under a set condition of less than 0 ° C.

【0008】[0008]

【作用】本発明は、前記の手段により、熱処理された摩
擦材はその基材である繊維が酸化反応による酸化膜で補
強されることにより強度の低下を防ぎ、耐熱性樹脂であ
るp−フェニルフェノ−ル系樹脂を結合剤として使うこ
とにより、熱劣化による耐摩耗性の低下が防止できると
ともに、高温.高負荷時の摩耗係数が安定する。
According to the present invention, the friction material which has been heat-treated by the above means is prevented from decreasing in strength by reinforcing the fiber as a base material with an oxide film by an oxidation reaction, and the heat-resistant resin is p-phenyl. By using a phenolic resin as a binder, a decrease in abrasion resistance due to thermal deterioration can be prevented, and a high temperature. Stable wear coefficient under high load.

【0009】[0009]

【実施例】本発明の実施例を図に基づき以下説明する。
結合剤であるp−フェニルフェノ−ルとフェノ−ルの共
重合体樹脂は、p−フェニルフェノ−ルとフェノ−ルを
モル比1対3で、アルカリであるアンモニア触媒を用い
てホルムアルデヒドと共重合反応させ縮合することで、
本発明にかかるp−フェニルフェノ−ルとフェノ−ルの
共重合体樹脂を得る。
DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described below with reference to the drawings.
The copolymer resin of p-phenylphenol and phenol as a binder is prepared by copolymerizing p-phenylphenol and phenol at a molar ratio of 1: 3 with formaldehyde using an alkali ammonia catalyst. By polymerizing and condensing,
A copolymer resin of p-phenylphenol and phenol according to the present invention is obtained.

【0010】次ぎに、こうして得られたp−フェニルフ
ェノ−ル系樹脂、基材のスチ−ル繊維及び黒鉛やその他
の充填剤を表1に示す体積比(%)に従って配合し、こ
れを均一に混練する。
Next, the p-phenylphenol-based resin thus obtained, the steel fiber of the base material, graphite and other fillers are blended according to the volume ratio (%) shown in Table 1, and the resulting mixture is uniformly mixed. And knead it.

【0011】[0011]

【表1】 [Table 1]

【0012】次ぎに、上記複合材料を金型に充填し、温
度150℃、圧力500Kg/cm2で圧縮成形する。でき
た成形品を200℃で4時間の所定条件によりアフタ−
キュアを施した後、摩擦材の熱処理の条件として満足な
設定酸素濃度は0.1%以上10%未満、より好ましく
は1%以上5%未満が最適となった。また、処理温度は
250℃以上1250℃未満、好ましくは350℃以上
800℃未満が最適なものとなり、さらに、処理時間に
ついては4時間未満、より好ましくは30分以上2時間
以下が良い。
Next, the above-mentioned composite material is filled in a mold and compression-molded at a temperature of 150 ° C. and a pressure of 500 kg / cm 2 . The formed article is subjected to after-treatment at 200 ° C. for 4 hours under predetermined conditions.
After curing, the optimal oxygen concentration set as a condition for the heat treatment of the friction material is 0.1% or more and less than 10%, more preferably 1% or more and less than 5%. The optimum treatment temperature is 250 ° C. to less than 1250 ° C., preferably 350 ° C. to less than 800 ° C., and the treatment time is less than 4 hours, more preferably 30 minutes to 2 hours.

【0013】上記設定条件である酸素濃度と熱処理温
度、処理時間を選んだ理由は、酸素濃度が10%を越え
ると結合剤であるp−フェニルフェノ−ル系樹脂の酸化
反応が起こり始め、摩擦材の強度が弱くなるからであ
り、酸素濃度が0.1%以下の場合には、スチ−ル繊維
表面での酸化反応が僅かしか起こらず、強度を向上させ
ることが不可能となるからである。
The reason for selecting the oxygen concentration, heat treatment temperature and treatment time as the above set conditions is that when the oxygen concentration exceeds 10%, the oxidation reaction of the p-phenylphenol-based resin as a binder starts to occur, and This is because the strength of the material becomes weak, and when the oxygen concentration is 0.1% or less, the oxidation reaction on the surface of the steel fiber occurs only slightly, making it impossible to improve the strength. is there.

【0014】また、処理温度が1250℃を越えると急
激な分解が起こるため、摩擦材内部に生じたガスが外部
へ逃げ切れず、脹れや割れを生じやすくなるからであ
り、250℃以下では4時間以上の長時間の熱処理を行
っても結合剤であるp−フェニルフェノ−ル系樹脂の分
解が僅かしか起こらず、耐フェ−ド性を向上させること
が不可能になるからである。一方、処理時間は4時間以
上では、さらに処理を施しても変化は殆ど生じないとい
う理由によるものである。
Further, if the processing temperature exceeds 1250 ° C., rapid decomposition occurs, so that the gas generated inside the friction material cannot escape to the outside and tends to cause swelling or cracking. This is because even if the heat treatment is performed for a long period of time, the decomposition of the p-phenylphenol-based resin as a binder occurs only slightly, making it impossible to improve the fade resistance. On the other hand, if the processing time is 4 hours or longer, the change hardly occurs even if further processing is performed.

【0015】上記実施例において、酸素濃度による強度
保持の効果を確かめるために、その具体例として、酸素
濃度0%から10%、熱処理温度400℃、処理時間1
時間の処理を施した摩擦パッドについてその特性を調べ
てみた。酸素濃度と曲げ強度の間には図1に示すような
関係がある。図1から明かなように、酸素濃度1%から
10%の範囲で処理した摩擦パッドは、非酸化性雰囲気
(酸素濃度0%)で処理した摩擦パッドよりも曲げ強度
が向上し、低酸素濃度場での熱処理効果による強度向上
は十分実証された。
In the above embodiment, in order to confirm the effect of maintaining the strength by the oxygen concentration, specific examples thereof include an oxygen concentration of 0% to 10%, a heat treatment temperature of 400 ° C., and a treatment time of 1 hour.
The characteristics of the friction pad subjected to the time treatment were examined. There is a relationship as shown in FIG. 1 between the oxygen concentration and the bending strength. As is clear from FIG. 1, the friction pad treated in the oxygen concentration range of 1% to 10% has a higher bending strength than the friction pad treated in the non-oxidizing atmosphere (oxygen concentration 0%), and has a low oxygen concentration. The strength improvement by the heat treatment effect in the field was sufficiently demonstrated.

【0016】また、p−フェニルフェノ−ル系樹脂を使
用することによる摩擦材の耐摩耗性向上の効果を確かめ
るために、その具体例として5%酸素濃度場において熱
処理温度400℃、処理時間1時間の処理を施した摩擦
パッドの耐摩耗性について、フルスケ−ルダイナモメ−
タを用いて時速100Km、100℃で1000回制動を
行った後の摩耗量で調べてみた。試験結果を表2に示
す。
Further, in order to confirm the effect of improving the wear resistance of the friction material by using the p-phenylphenol-based resin, as a specific example, a heat treatment temperature of 400 ° C. and a treatment time of 1% in a 5% oxygen concentration field. About the wear resistance of the friction pad that has been treated for a long time, a full-scale dynamometer
It was examined by the amount of wear after braking 1000 times at 100 km / h and 100 ° C. using a motor. Table 2 shows the test results.

【0017】[0017]

【表2】 [Table 2]

【0018】表2から明かなように、一般のフェノ−ル
樹脂を用いた場合、高温熱処理を行うことで樹脂が熱劣
化し、摩耗量は従来の熱処理を行った摩擦パッドに較べ
2倍以上あり、耐摩耗性が低下しているのがわかる。し
かし、耐熱性樹脂であるp−フェニルフェノ−ル系樹脂
を結合剤として用いることで高温熱処理による熱劣化が
低下するばかりではなく、高温熱処理により、炭素化し
たp−フェニルフェノ−ル系樹脂の骨格が強固になり、
摩耗量が従来の熱処理に比べ1/2以下に改良されるこ
とがわかる。
As is clear from Table 2, when a general phenol resin is used, the resin is thermally degraded by high-temperature heat treatment, and the amount of wear is more than twice that of a friction pad that has been subjected to conventional heat treatment. It can be seen that the abrasion resistance is reduced. However, by using p-phenylphenol-based resin, which is a heat-resistant resin, as a binder, not only thermal degradation due to high-temperature heat treatment is reduced, but also p-phenylphenol-based resin carbonized by high-temperature heat treatment. The skeleton is strengthened,
It can be seen that the amount of abrasion is improved to half or less of the conventional heat treatment.

【0019】さらに、耐フェ−ド性向上の効果を確かめ
るために、その具体例として、5%酸素濃度場において
熱処理温度400℃、処理時間1時間の処理を施したデ
ィスクブレ−キパッドについてその特性を調べてみた。
Further, in order to confirm the effect of improving the fade resistance, as a specific example, the characteristics of a disk brake pad which has been subjected to a heat treatment temperature of 400 ° C. and a treatment time of 1 hour in a 5% oxygen concentration field. I checked.

【0020】この熱処理されたディスクブレ−キパッド
をJASOC406(1982年)に基づき35秒の連続制
動させたときの摩擦係数は図2に示す曲線の如くであ
る。そして、Aは上記熱処理条件を施した具体例であ
り、Bが通常の熱処理品の従来例であって、空気中で2
00℃、4時間の熱処理を行ったものである。曲線Aは
初期摩耗(制動回数nが10回以内)について、その摩
耗係数が0.43で安定しており、曲線Bに比較して顕
著な差異を示している。曲線Aの具体例によって熱処理
効果による耐フェ−ド性は十分に実証された。
The coefficient of friction when the heat-treated disk brake pad is continuously braked for 35 seconds based on JASOC 406 (1982) is as shown by the curve in FIG. A is a specific example subjected to the above heat treatment conditions, B is a conventional example of a normal heat treated product,
Heat treatment was performed at 00 ° C. for 4 hours. Curve A shows a stable wear coefficient for the initial wear (the number of braking times n is 10 or less) at 0.43, and shows a remarkable difference compared to the curve B. The example of curve A fully demonstrates the fade resistance due to the heat treatment effect.

【0021】[0021]

【発明の効果】以上説明したことから明かなように、本
発明は摩擦剤の熱処理中、雰囲気を低酸素にして摩擦パ
ッド中のスチ−ル繊維の表面に酸化膜を形成することで
スチ−ル繊維を補強し、且つ耐熱性樹脂であるp−フェ
ニルフェノ−ルとフェノ−ルの共重合体樹脂を結合剤に
使用することにより摩擦パッドの耐摩耗性を向上させ、
しかも、高温下による結合剤の熱分解をあらかじめ熱処
理によって炭化させることによって、耐フェ−ド性を向
上させることができる。
As is apparent from the above description, according to the present invention, the steel is formed by forming an oxide film on the surface of the steel fibers in the friction pad by changing the atmosphere to low oxygen during the heat treatment of the friction agent. Abrasion resistance of the friction pad is improved by using a copolymer resin of p-phenylphenol and phenol, which are heat-resistant resins, as a binder.
In addition, the thermal decomposition of the binder at a high temperature is previously carbonized by heat treatment, whereby the fade resistance can be improved.

【0022】また、高温化での摩擦材の摩擦係数を安定
させるとともに、高速時からの急制動に対して摩擦係数
を低下させることなく、制動時に発生した熱分解ガスに
よる発火現象をも抑えることができる。さらに、制動時
の鳴きを防ぐ副次的効果も有する。
Further, the present invention stabilizes the friction coefficient of the friction material at a high temperature and suppresses the ignition phenomenon caused by the pyrolysis gas generated at the time of braking without lowering the friction coefficient against sudden braking from a high speed. Can be. Further, it has a secondary effect of preventing squeal during braking.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の摩擦材の熱処理雰囲気の酸素濃度に対
する曲げ強度の関係を示す特性図。
FIG. 1 is a characteristic diagram showing a relationship between bending strength and oxygen concentration in a heat treatment atmosphere of a friction material of the present invention.

【図2】本発明の実施例と従来例における摩擦材の制動
回転数に対する摩擦係数の関係を示す特性比較図。
FIG. 2 is a characteristic comparison diagram showing a relationship between a braking coefficient and a friction coefficient of a friction material in an embodiment of the present invention and a conventional example.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 伊藤 拓二 茨城県下館市大字小川1500番地 日立化 成工業株式会社下館研究所内 (72)発明者 栗田 高明 茨城県下館市大字小川1500番地 日立化 成工業株式会社下館研究所内 ──────────────────────────────────────────────────の Continuing on the front page (72) Inventor Takuji Ito 1500 Oji Ogawa, Shimodate City, Ibaraki Pref.Hitachi Chemical Industry Co., Ltd. Industrial Co., Ltd.

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】p−フェニルフェノ−ルとフェノ−ルの共
重合体樹脂を結合剤とし、金属繊維を基材、そして黒
鉛、金属粉、無機充填剤を含有する摩擦材料をホットプ
レス法にて熱圧成形してなる摩擦材の製造法において、
前記摩擦材は酸素濃度0.1%から10%の低酸素濃度
場において温度を250℃以上1250℃未満、熱処理
時間を15分以上4時間未満とする設定条件で熱処理を
行うことを特徴とする摩擦材の熱処理方法。
A friction material containing p-phenylphenol and phenol as a binder, a metal fiber as a base material, graphite, metal powder and an inorganic filler is subjected to a hot pressing method. In the manufacturing method of friction material formed by hot pressing
The friction material is heat-treated in a low oxygen concentration field having an oxygen concentration of 0.1% to 10% under a setting condition of a temperature of 250 ° C. or more and less than 1250 ° C. and a heat treatment time of 15 minutes or more and less than 4 hours. Heat treatment method for friction material.
【請求項2】p−フェニルフェノ−ルとフェノ−ルの共
重合体樹脂を結合剤とし、金属繊維を基材、そして黒
鉛、金属粉、無機充填剤を含有する摩擦材料をホットプ
レス法にて熱圧成形してなる摩擦材において、前記摩擦
材は酸素濃度0.1%から10%の低酸素濃度場におい
て温度を250℃以上1250℃未満、熱処理時間を1
5分以上4時間未満とする設定条件で熱処理を行うこと
を特徴とする摩擦材。
2. A friction material containing p-phenylphenol and phenol copolymer resin as a binder, a metal fiber as a base material, graphite, metal powder and an inorganic filler is subjected to a hot pressing method. In a friction material formed by hot pressing under pressure, the friction material has a temperature of 250 ° C. or more and less than 1250 ° C. and a heat treatment time of 1 in a low oxygen concentration field of 0.1% to 10% oxygen concentration.
A friction material, wherein heat treatment is performed under a set condition of not less than 5 minutes and less than 4 hours.
【請求項3】金属繊維が、スチ−ル繊維であることを特
徴とする請求項1または2記載の摩擦材または摩擦材の
熱処理方法。
3. The friction material according to claim 1, wherein the metal fiber is a steel fiber.
【請求項4】p−フェニルフェノ−ルとフェノ−ルの共
重合体樹脂が、酸を触媒として合成されたものであるこ
とを特徴とする請求項2記載の摩擦材。
4. The friction material according to claim 2, wherein the copolymer resin of p-phenylphenol and phenol is synthesized using an acid as a catalyst.
【請求項5】p−フェニルフェノ−ルとフェノ−ルの共
重合体樹脂が、アルカリを触媒として合成されたもので
あることを特徴とする請求項2記載の摩擦材。
5. The friction material according to claim 2, wherein the copolymer resin of p-phenylphenol and phenol is synthesized using an alkali as a catalyst.
JP15794091A 1991-06-28 1991-06-28 Friction material and heat treatment method thereof Expired - Fee Related JP2601065B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15794091A JP2601065B2 (en) 1991-06-28 1991-06-28 Friction material and heat treatment method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15794091A JP2601065B2 (en) 1991-06-28 1991-06-28 Friction material and heat treatment method thereof

Publications (2)

Publication Number Publication Date
JPH0570766A JPH0570766A (en) 1993-03-23
JP2601065B2 true JP2601065B2 (en) 1997-04-16

Family

ID=15660796

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Link
JP (1) JP2601065B2 (en)

Also Published As

Publication number Publication date
JPH0570766A (en) 1993-03-23

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