JPH02212582A - Friction material - Google Patents

Friction material

Info

Publication number
JPH02212582A
JPH02212582A JP3138489A JP3138489A JPH02212582A JP H02212582 A JPH02212582 A JP H02212582A JP 3138489 A JP3138489 A JP 3138489A JP 3138489 A JP3138489 A JP 3138489A JP H02212582 A JPH02212582 A JP H02212582A
Authority
JP
Japan
Prior art keywords
fibers
friction material
weight
aramid
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
JP3138489A
Other languages
Japanese (ja)
Other versions
JP2709124B2 (en
Inventor
Katsuhiro Shibata
勝弘 柴田
Akiya Suzuki
鈴木 韶也
Yuichi Azuma
東 雄一
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.)
Honda Motor Co Ltd
Astemo Ltd
Original Assignee
Honda Motor Co Ltd
Nissin Kogyo 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 Honda Motor Co Ltd, Nissin Kogyo Co Ltd filed Critical Honda Motor Co Ltd
Priority to JP3138489A priority Critical patent/JP2709124B2/en
Publication of JPH02212582A publication Critical patent/JPH02212582A/en
Application granted granted Critical
Publication of JP2709124B2 publication Critical patent/JP2709124B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain a friction material which is easy to mold, can suitably control the fading of a brake, etc., and has high durability by using as constituents a specified amount of carbon fibers and a specified amount of aramid fibers comprising a mixture of pulpy fibers and cut fibers. CONSTITUTION:A friction material containing as fibrous material 3-30wt.% carbon fibers (A) and 2-20wt.% aramid fibers (B) comprising a mixture of pulpy fibers (a) and cut fibers (b), wherein the weight ratio of (a) to (b) in B is 0.5 or greater. The fibrillar fibers (a) serve to improve the durability of a friction material after molding, and incorporate the fibers (b) and fibers (A) or other fillers, so that these fibers and fillers are suitably dispersed and an unnecessary increase in bulk density is prevented when the friction material is molded, thus giving a friction material which is easy to mold, can suitably control the fading of a brake, and has high durability.

Description

【発明の詳細な説明】 [発明の目的] 〈産業上の利用分野〉 本発明は、自動車用ブレーキライニング、ディスクブレ
ーキパッド、クラッチフェーシング等に用いられる摩擦
材に関する。
DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] <Industrial Application Field> The present invention relates to a friction material used for automobile brake linings, disc brake pads, clutch facings, etc.

〈従来の技術〉 近年、自動車用ディスクブレーキパッドやクラッチフェ
ーシング等に用いられる摩擦材に含まれる繊維材として
、従来使用されてきた石綿よりもフェード現象が抑制さ
れ、かつ対摩耗性等に優れたカーボン繊維やアラミド繊
維等を使用することが提案されており、特開昭62−1
06980号公報にはその一例が開示されている。
<Conventional technology> In recent years, asbestos has been used as a fiber material included in friction materials used in automobile disc brake pads, clutch facings, etc., as it suppresses the fading phenomenon and has superior wear resistance than the conventionally used asbestos. It has been proposed to use carbon fiber, aramid fiber, etc.
An example of this is disclosed in Japanese Patent No. 06980.

このような摩擦材に於て、特にアラミド繊維には、比較
的強度の高い切断繊維と、フィブリル繊維内にフィラー
、レジン及び他の繊維を取込むパルプ繊維とを゛混合す
ることが好ましいが、切断繊維が多過ぎると、該繊維の
解繊に伴いかさが増大して成型が厄介になり、また、パ
ルプ繊維が多過ぎると、所望の強度を得難くなる問題が
ある。
In such friction materials, especially aramid fibers, it is preferable to mix relatively high-strength cut fibers with pulp fibers that incorporate filler, resin, and other fibers into the fibril fibers. If there are too many cut fibers, the bulk increases as the fibers are defibrated, making molding difficult. If there are too many pulp fibers, it becomes difficult to obtain the desired strength.

〈発明が解決しようとする課題〉 このような従来技術の問題点に鑑み、本発明の主な目的
は、成型し易く、ブレーキ等に於けるフェード現象が好
適に抑制され、かつ成形後の強度及び耐久性が向上した
摩擦材を提供することにある。
<Problems to be Solved by the Invention> In view of the problems of the prior art, the main objects of the present invention are to facilitate molding, to suitably suppress fade phenomena in brakes, etc., and to increase strength after molding. and to provide a friction material with improved durability.

[発明の構成] 〈課題を解決するための手段〉 このような目的は、本発明によれば、カーボン繊維を3
重量%乃至30重量%、パルプ状繊維及び切断繊維の混
合体からなるアラミド繊維を2重量%乃至20重量%含
み、前記パルプ状繊維の前記切断繊維に対する重量比が
0. 5以上であることを特徴とする摩擦材を提供する
ことにより達成される。
[Structure of the Invention] <Means for Solving the Problems> According to the present invention, such an object is achieved by using three carbon fibers.
% by weight to 30% by weight, and 2% to 20% by weight of aramid fibers consisting of a mixture of pulp fibers and cut fibers, and the weight ratio of the pulp fibers to the cut fibers is 0. This is achieved by providing a friction material characterized by a friction coefficient of 5 or more.

く作用〉 このようにすれば、アラミド繊維のパルプ繊維により成
形後の耐久性が向上し、かつそのフィブリル繊維が、切
断アラミド繊維やカーボン繊維或いは他の充填材を取り
込むことにより、各々を好適に分散させると共に成型時
に不必要にがさが増加することがない。
In this way, the durability after molding is improved by the pulp fibers of the aramid fibers, and the fibril fibers incorporate cut aramid fibers, carbon fibers, or other fillers, so that each of them can be suitably processed. In addition to being dispersed, there is no unnecessary increase in stiffness during molding.

〈実施例〉 以下、本発明の好適実施例を添付の図面について詳しく
説明する。
<Embodiments> Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings.

第1図及び第2図は、自動車用ブレーキパッド1と、該
パッドのプリフォームを成型するためのダイス2及びク
ロムモリブデン鋼からなるポンチ3を模式的に示す。
1 and 2 schematically show an automobile brake pad 1, a die 2 for molding a preform of the pad, and a punch 3 made of chrome-molybdenum steel.

ダイス2内は、その底面の面積が45cdの略扇形即ち
ブレーキパッドの形状をなし、ポンチ3は、これに対応
する形状をなしている。このダイス2内に、繊維材とし
てバルブ状アラミド繊維2.44重量%(以下wL%と
記す)、直径7μmであって全長6+amの切断アラミ
ド繊維1. 24wL%及び直径6μmであって全長3
mmのカーボン繊維3゜48wL%、摩擦係数を大きく
するための金属粉末として銅粉末17. 16vt%及
び銅−亜鉛合金粉末24.50wt%、上記金属粉末と
ロータとの部分的な凝着を防止するための固体潤滑材と
してグラファイト3.68vL%及び二硫化モリブデン
7゜69wt%、ロータを掃除する効果のある高硬度の
無機充填材として二酸化珪素4.32wL%、高温時の
パッドの摩耗及び摩擦係数の低下を防止する抑制するた
めの比較的低硬度の無機充填材として硫酸バリウム18
. 04wt%、低面圧時の摩擦係数を安定するための
有機充填材としてメラミンダスト7.53wt%、バイ
ンダとしてのフェノールレジ:/9.21wt%、pH
n整剤0. 72wt%を定法にて混合してなる混合材
120g:を計量して断面積45cmのダイス2内に充
填し、ポンチ3をもッテ高さ約80mmから15a+m
となるまテ10kg/cJで圧縮し、その後、仕上加工
して第2図に示すブレーキパッド1を形成する。
The inside of the die 2 has a bottom surface area of 45 cd and is approximately fan-shaped, that is, the shape of a brake pad, and the punch 3 has a shape corresponding to this. Inside this die 2, 2.44% by weight of bulb-shaped aramid fibers (hereinafter referred to as wL%) and 1 cut aramid fiber with a diameter of 7 μm and a total length of 6+ am were placed as fiber materials. 24 wL% and a diameter of 6 μm and a total length of 3
mm carbon fiber 3°48wL%, copper powder 17.mm as a metal powder to increase the coefficient of friction. 16vL% and copper-zinc alloy powder 24.50wt%, graphite 3.68vL% and molybdenum disulfide 7°69wt% as a solid lubricant to prevent partial adhesion between the metal powder and the rotor. Silicon dioxide 4.32wL% as a high-hardness inorganic filler with a cleaning effect, and barium sulfate 18 as a relatively low-hardness inorganic filler to prevent and suppress pad wear and decrease in friction coefficient at high temperatures.
.. 04wt%, melamine dust 7.53wt% as an organic filler to stabilize the friction coefficient at low surface pressure, phenol resin as a binder: /9.21wt%, pH
n adjustment agent 0. Weigh 120 g of a mixed material made by mixing 72 wt% using a standard method and fill it into a die 2 with a cross-sectional area of 45 cm.
The material is compressed at a rate of 10 kg/cJ, and then finished to form the brake pad 1 shown in FIG. 2.

ここで、本実施例のアラミド繊維は、ケブラー49(デ
ュポン社商標)からなるアラミド繊維である。また、本
実施例のカーボン繊維は、トレヵT300 (東し社商
標)からなる耐熱性及び強度の高いPAN系カーボン繊
維である。
Here, the aramid fiber of this example is an aramid fiber made of Kevlar 49 (trademark of DuPont). Further, the carbon fiber of this example is a PAN-based carbon fiber made of Torayca T300 (trademark of Toshisha Co., Ltd.), which has high heat resistance and strength.

第3図〜第5図は、JASOC406−82に規定され
る乗用車ブレーキ装置ダイナモメータ試験方法に基づき
、ブレーキパッド1と、従来の石綿からなる繊維材を用
いたブレーキパッドとをブレーキ試験し、その結果を比
較したグラフである。
Figures 3 to 5 show a brake test conducted on the brake pad 1 and a conventional brake pad using a fiber material made of asbestos based on the passenger car brake system dynamometer test method specified in JASOC406-82. This is a graph comparing the results.

ここで、従来の摩擦材からなるブレーキパッドに含まれ
る成分は、石綿繊維20.0wt%、炭酸カルシウム1
. 0w1%、硫酸バリウム32. 5vt%、カシュ
ーダスト及びフェノールレジン合せて23、  OwL
%、銅粉末20. 0w1%、亜鉛粉末0゜5wt%、
鉄粉末3.0w1%である。
Here, the components contained in the conventional brake pad made of friction material are asbestos fiber 20.0 wt%, calcium carbonate 1
.. 0w1%, barium sulfate 32. 5vt%, cashew dust and phenol resin total 23, OwL
%, copper powder 20. 0w1%, zinc powder 0゜5wt%,
The iron powder was 3.0w1%.

まず、JASOの規定に基づき初期計測、すり合せ前チ
エツク、第1効力試験、すり合せを行った後、第2効力
試験を行う。即ち、制動前ブレーキ温度を80℃とし、
制動初速度50km+/h、1100k/h及び130
km/hから、0.1〜0゜8Gの範囲で制動減速度を
変化させ、各制動減速度に於ける制動トルクから各々摩
擦係数(μ)を求める(第3図)。
First, based on the JASO regulations, initial measurements, pre-matching checks, first efficacy tests, and matching are performed, followed by a second effectiveness test. That is, the brake temperature before braking is 80°C,
Braking initial speed 50km+/h, 1100k/h and 130km/h
km/h, the braking deceleration is varied in the range of 0.1 to 0°8G, and the friction coefficient (μ) is determined from the braking torque at each braking deceleration (Fig. 3).

続けて、第1フエードリカバリ試験を行う。即ち、制動
前ブレーキ温度を80℃とし、制動初速度50km/h
、制動減速度0.3G一定(或いは0.3Gを得られる
圧カ一定)、制動回数3回として摩擦係数(μ)のベー
スラインをチエツクする。
Subsequently, a first fade recovery test is performed. That is, the brake temperature before braking is 80°C, and the initial braking speed is 50 km/h.
, the braking deceleration is constant at 0.3G (or the pressure at which 0.3G is obtained is constant), and the number of brakings is set to 3 to check the baseline of the friction coefficient (μ).

次に、フェード試験を行う。即ち、第1回目の制動前ブ
レーキ温度を60℃とし、制動初速度1100k/h、
制動減速度0.45G一定(或いは0.45Gを得られ
る圧カ一定)、制動間隔35秒、制動回数10回として
ブレーキ温度と、各回の摩擦係数(μ)を求める(第4
図)。また、続けてリカバリ試験を行う。即ち、制動初
速度50km/h、制動減速度0.3G一定(或いはベ
ースラインチエツクで得られた圧カ一定)、制動間隔1
20秒、制動回数15回として上記フェード試験と同様
にブレーキ温度及び摩擦係数(μ)を求める(第4図)
Next, perform a fade test. That is, the brake temperature before the first braking was 60°C, the initial braking speed was 1100 k/h,
Assuming that the braking deceleration is constant at 0.45G (or the pressure is constant to obtain 0.45G), the braking interval is 35 seconds, and the number of braking is 10 times, calculate the brake temperature and the friction coefficient (μ) for each time (4th
figure). Also, continue with the recovery test. That is, the initial braking speed is 50 km/h, the braking deceleration is constant at 0.3 G (or the pressure obtained from the baseline check is constant), and the braking interval is 1.
Calculate the brake temperature and friction coefficient (μ) in the same way as the above fade test by braking 15 times for 20 seconds (Figure 4)
.

更に、続けて第3効力試験として、第2効力試験と同様
の条件で摩擦係数(μ)を求める(第5図)。
Furthermore, as a third effectiveness test, the coefficient of friction (μ) is determined under the same conditions as the second effectiveness test (Figure 5).

第4図に良く示すように、本発明に基づく摩擦材を用い
たブレーキパッド1(実線A)は、従来の摩擦材を用い
たブレーキパッド(破線B)に比較してブレーキの温度
変化に伴う摩擦係数(μ)の変化が小さいことがわかる
。また、第3図及び第5図に良く示すように、本発明に
基づく摩擦材を用いたブレーキパッド1(実線A)は、
従来の摩擦材を用いたブレーキパッド(破線B)に比較
して熱履歴による摩擦係数(μ)の変化も小さいことが
わかる。
As clearly shown in FIG. 4, the brake pad 1 (solid line A) using the friction material according to the present invention is more sensitive to temperature changes in the brake than the brake pad (broken line B) using the conventional friction material. It can be seen that the change in the friction coefficient (μ) is small. Further, as clearly shown in FIGS. 3 and 5, the brake pad 1 (solid line A) using the friction material based on the present invention is
It can be seen that the change in the coefficient of friction (μ) due to thermal history is also smaller compared to a brake pad using a conventional friction material (broken line B).

本実施例では熱伝導率の大きなカーボン繊維を用いてい
るが、これに熱伝導率の比較的小さなアラミド繊維を組
合せることにより、ブレーキのベイパーロックを防止で
きるばかりでなく、アラミド繊維が、メタ系アラミド繊
維よりも耐熱性(摩耗クラック等に対する耐久性)の高
いバラ系アラミド繊維からなることから、カーボン繊維
と組合せることにより、耐熱性、耐久性、耐フエード性
の優れた摩擦材が得られる。また、PAN系カーボン繊
維は高温時の摩擦係数(μ)の安定化に寄与しており、
このPAN系カーボン繊維は、充分な補強効果を得るた
めに直径を15μm以下とすると良く、更に補強効果及
びカーボン繊維自体の分散効果を得るために、その全長
を0.5a+m〜9゜0+a−の範囲とすると良い。
In this example, carbon fibers with high thermal conductivity are used, but by combining them with aramid fibers with relatively low thermal conductivity, it is possible to not only prevent vapor lock of the brakes, but also to prevent the vapor lock of the brakes. Since it is made of loose aramid fiber, which has higher heat resistance (durability against abrasion cracks, etc.) than aramid fiber, by combining it with carbon fiber, a friction material with excellent heat resistance, durability, and fade resistance can be obtained. It will be done. In addition, PAN-based carbon fiber contributes to stabilizing the coefficient of friction (μ) at high temperatures.
The diameter of this PAN-based carbon fiber is preferably 15 μm or less in order to obtain a sufficient reinforcing effect, and furthermore, in order to obtain a reinforcing effect and a dispersion effect of the carbon fiber itself, its total length is 0.5 a+m to 9°0+a-. It is good to set it as a range.

本実施例では、摩擦材にパルプ状及び切断アラミド繊維
を合せて3.68wt%混合したが、実際には2〜20
vt%の範囲で混合すれば良い。ここで、アラミド繊維
が2wt%未満であると、プリフォーム成型が困難にな
り、また20wt%を越えると高温時に摩擦係数が低下
する。
In this example, a total of 3.68 wt% of pulp-like and cut aramid fibers was mixed into the friction material, but in reality, 2 to 20 wt% of pulp-like and cut aramid fibers were mixed.
It is sufficient to mix within the range of vt%. Here, if the aramid fiber content is less than 2 wt%, it becomes difficult to mold the preform, and if it exceeds 20 wt%, the friction coefficient decreases at high temperatures.

また、本実施例では、パルプ状アラミド繊維を2.44
wt%混合したが、パルプ状アラミド繊維は、耐久性を
向上させるばかりでなく、かさ密度の増大し易い切断ア
ラミド繊維を取り込み、体積増加を好適に抑制する効果
を有しており、実際には切断アラミド繊維の1/2以上
となっていれば良い。ここで、パルプ状アラミド繊維が
切断アラミド繊維の1/2未満であると、切断アラミド
繊維の解繊による体積増加を抑制できなくなり、プリフ
ォーム成型時の加圧力を増大させたり、型を大型化する
必要が生じる。尚、パルプ状アラミド繊維は、フィラー
、レジン及び比較的偏析し易いカーボン繊維等を取り込
み、好適に分散させる効果もある。
In addition, in this example, the pulp-like aramid fiber was
Although mixed in wt%, pulp-like aramid fiber not only improves durability, but also incorporates cut aramid fibers that tend to increase bulk density, and has the effect of suitably suppressing volume increase. It is sufficient if it is 1/2 or more of the cut aramid fiber. Here, if the pulp-like aramid fiber is less than 1/2 of the cut aramid fiber, it will not be possible to suppress the volume increase due to defibration of the cut aramid fiber, which will increase the pressurizing force during preform molding or increase the size of the mold. The need arises. Note that the pulp-like aramid fibers also have the effect of taking in fillers, resins, carbon fibers, etc. that are relatively easy to segregate, and dispersing them appropriately.

また、本実施例では、切断アラミド繊維を1゜24vt
%混合したが、切断アラミド繊維は、ロータの攻撃性を
低下させ、かつ耐久性を一層向上させる効果がある。こ
こで、本実施例に用いたバラ系パルプ状アラミド繊維が
高い耐久性を有していることから、例えば切断アラミド
繊維を混合しなくても充分な耐久性が得られる。
In addition, in this example, the cut aramid fiber was 1°24vt.
The cut aramid fibers have the effect of reducing rotor aggressiveness and further improving durability. Here, since the loose pulp aramid fibers used in this example have high durability, sufficient durability can be obtained even without mixing cut aramid fibers, for example.

また、本実施例では、摩擦材にPAN系のカーボン繊維
を3.48wt%混合したが、実際には3〜30wt%
の範囲で混合すれば良く、好ましくは、カーボン繊維の
重量がバルブ状アラミド繊維及び切断アラミド繊維の総
量の0.6倍以上になっていると良く、その場合、摩擦
材のフェード率が著しく向上する。ここで、カーボン繊
維が3wt%未満であると、高温時に摩擦係数が安定化
し難く、また3Qvt%を越えると常用温度に於ける摩
擦係数が低下する。
In addition, in this example, 3.48wt% of PAN-based carbon fiber was mixed in the friction material, but in reality it was 3 to 30wt%.
Preferably, the weight of carbon fiber is at least 0.6 times the total amount of bulb-shaped aramid fibers and cut aramid fibers, and in this case, the fade rate of the friction material is significantly improved. do. Here, if the carbon fiber content is less than 3 wt%, it is difficult to stabilize the friction coefficient at high temperatures, and if it exceeds 3 Qvt%, the friction coefficient at normal temperatures decreases.

また、本実施例では、摩擦材に金属粉末として銅粉末及
び銅−亜鉛合金粉末を混合したが、銅、ニッケル、銅−
亜鉛合金、鉄、銅−錫合金のうち少なくとも1種類以上
を10〜50wt%の範囲で混合すれば良い。ここで、
金属粉末が10vt%未満であると、摩擦係数を大きく
する効果が殆どなく、また50wt%を越えるとロータ
に部分的に凝着し、シャダー発生の原因となる。
In addition, in this example, copper powder and copper-zinc alloy powder were mixed as metal powder in the friction material, but copper, nickel, copper-zinc alloy powder, etc.
At least one of zinc alloy, iron, and copper-tin alloy may be mixed in a range of 10 to 50 wt%. here,
If the metal powder is less than 10wt%, it will have little effect on increasing the coefficient of friction, and if it exceeds 50wt%, it will partially adhere to the rotor, causing shudder.

また、本実施例では、摩擦材に固体潤滑材としてグラフ
ァイト及び二硫化モリブデンを混合したが、実際にはグ
ラファイト、二硫化モリブデン、硫化亜鉛、硫化鉛、三
硫化アンチモンのうち少なくとも11種類以上を5〜2
0wt%混合すれば良い。
Furthermore, in this example, graphite and molybdenum disulfide were mixed as solid lubricants in the friction material, but in reality at least 11 types of graphite, molybdenum disulfide, zinc sulfide, lead sulfide, and antimony trisulfide were mixed into the friction material. ~2
It is sufficient to mix 0wt%.

ここで、固体潤滑材が5wt%未満であると、」二足金
属粉末とロータとの凝着を防止する効果が殆どなく、ま
た20wt%を越えると摩擦係数が低下する。
Here, if the solid lubricant content is less than 5 wt%, there is little effect of preventing adhesion between the bipedal metal powder and the rotor, and if it exceeds 20 wt%, the coefficient of friction decreases.

また、本実施例では、摩擦材に高硬度の無機充填材とし
て二酸化珪素を混合し、低硬度の無機充填材として硫酸
バリウムを混合したが、実際には高硬度の無機充填材と
して、二酸化珪素、アルミナ、ムライト、酸化ジルコニ
ウム、スピネル型フェライト(Fe304)のうち少な
くとも1種類以上と、低硬度の無機充填材として硫酸バ
リウム、炭酸カルシウム、酸化第二銅のうち少なくとも
1種類以上を合せて10〜50wt%の範囲で混合すれ
ば良い。ここで、lQwL%未満であるとロータを掃除
する効果及び高温時のパッドの摩耗及び摩擦係数の低下
を抑制する効果が殆どなく、50wt%を越えると、ロ
ータの攻撃性が高(なり偏摩耗の原因となる。
In addition, in this example, silicon dioxide was mixed into the friction material as a high hardness inorganic filler, and barium sulfate was mixed as a low hardness inorganic filler, but in reality, silicon dioxide was mixed as a high hardness inorganic filler. , alumina, mullite, zirconium oxide, and spinel type ferrite (Fe304), and at least one of barium sulfate, calcium carbonate, and cupric oxide as a low hardness inorganic filler. It is sufficient to mix within a range of 50 wt%. Here, if it is less than 1QwL%, there is almost no effect of cleaning the rotor and suppressing the wear of the pad at high temperatures and the decrease in the friction coefficient, and if it exceeds 50wt%, the aggressiveness of the rotor becomes high (and uneven wear occurs). It causes.

また、本実施例では、摩擦材に有機充填材としてメラミ
ンダストを混合したが、実際には、メラミンダスト、カ
シューダスト、フェノールダストのうち少なくとも1種
類以上を3〜20vt%の範囲で混合すれば良い。ここ
で、3vL%未満であると、低面圧時の摩擦係数を安定
する効果が殆どなく、20wt%を越えると高温時の摩
擦係数低下の原因となる。
Further, in this example, melamine dust was mixed as an organic filler in the friction material, but in reality, at least one of melamine dust, cashew dust, and phenol dust should be mixed in a range of 3 to 20 vt%. good. Here, if it is less than 3 vL%, there is almost no effect of stabilizing the coefficient of friction at low surface pressures, and if it exceeds 20 wt%, it causes a decrease in the coefficient of friction at high temperatures.

更に、本実施例にて摩擦材にバインダとして混合したフ
ェノールレジンは、実際には8〜15wt%の範囲で混
合すれば良い。ここで、フェノールレジンが8wL%未
満であると、バインダとしての効果が殆どなく、また1
5wt%を越えると高温時の摩擦係数が低下する。
Furthermore, the phenol resin mixed into the friction material as a binder in this embodiment may actually be mixed in a range of 8 to 15 wt%. Here, if the phenol resin is less than 8 wL%, it has almost no effect as a binder, and 1
If it exceeds 5 wt%, the friction coefficient at high temperatures will decrease.

[発明の効果] このように本発明によれば、摩擦材に含まれるカーボン
繊維を3wt%〜30wt%の範囲とし、切断繊維及び
パルプ繊維からなるアラミド繊維を2wt%〜20vt
%の範囲とし、パルプ状繊維の切断繊維に対する重量比
を0.5以上とすることで、成型し易く、また、ブレー
キに於けるフェード現象を好適に抑制できると共に耐久
性の高い摩擦材を得ることができることから、その効果
は極めて大である。
[Effects of the Invention] As described above, according to the present invention, the carbon fibers contained in the friction material are in the range of 3wt% to 30wt%, and the aramid fibers consisting of cut fibers and pulp fibers are in the range of 2wt% to 20wt%.
% range and the weight ratio of pulp fibers to cut fibers is 0.5 or more to obtain a friction material that is easy to mold, can suitably suppress the fade phenomenon in brakes, and has high durability. Because it can be done, the effect is extremely large.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明に基づく摩擦材をもって自動車用ブレ
ーキパッドのプリフォームを成型するためのダイス及び
ポンチを模式的に示す断面図である。 第2図は、本発明に基づく摩擦材からなるブレーキパッ
ドを示す正面図である。 第3図〜第5図は、本発明に基づく摩擦材からなるブレ
ーキパッドを用いて行われたブレーキ試験の結果を示す
グラフである。 1・・・ブレーキパラ ド 2・・・ダイス 3・・・ポンチ 特 許 出 願 人 本田技研工業株式会社 同 日 信工業株式会社 代 理 人
FIG. 1 is a cross-sectional view schematically showing a die and punch for molding a preform for an automobile brake pad using a friction material according to the present invention. FIG. 2 is a front view showing a brake pad made of a friction material according to the present invention. FIGS. 3 to 5 are graphs showing the results of brake tests conducted using a brake pad made of a friction material according to the present invention. 1...Brake Parameter 2...Dice 3...Punch Patent Applicant Honda Motor Co., Ltd. Nissin Kogyo Co., Ltd. Agent

Claims (4)

【特許請求の範囲】[Claims] (1)カーボン繊維を3重量%乃至30重量%、パルプ
状繊維及び切断繊維の混合体からなるアラミド繊維を2
重量%乃至20重量%含み、 前記パルプ状繊維の前記切断繊維に対する重量比が0.
5以上であることを特徴とする摩擦材。
(1) 3% to 30% by weight of carbon fibers, 2% of aramid fibers consisting of a mixture of pulp fibers and cut fibers.
% to 20% by weight, and the weight ratio of the pulp fiber to the cut fiber is 0.
A friction material characterized by having a friction coefficient of 5 or more.
(2)前記カーボン繊維の前記アラミド繊維に対する重
量比が0.6以上であることを特徴とする特許請求の範
囲第1項に記載の摩擦材。
(2) The friction material according to claim 1, wherein the weight ratio of the carbon fiber to the aramid fiber is 0.6 or more.
(3)前記アラミド繊維がパラ系アラミド繊維からなる
ことを特徴とする特許請求の範囲第1項若しくは第2項
に記載の摩擦材。
(3) The friction material according to claim 1 or 2, wherein the aramid fibers are made of para-aramid fibers.
(4)銅、ニッケル、銅−亜鉛合金、鉄及び銅−錫合金
のうちの少なくとも1種類以上を10重量%乃至50重
量%、 グラファイト、二硫化モリブデン、硫化亜鉛、硫化鉛及
び三硫化アンチモンのうちの少なくとも1種類以上を5
重量%乃至20重量%、 二酸化珪素、アルミナ、ムライト、酸化ジルコニウム及
びスピネル型フェライト(Fe_3O_4)のうちの少
なくとも1種類以上と硫酸バリウム、炭酸カルシウム及
び酸化第二銅のうちの少なくとも1種類以上とを合せて
10重量%乃至50重量%、 メラミンダスト、カシューダスト及びフェノールダスト
のうちの少なくとも1種類以上を3重量%乃至20重量
%、 フェノールレジンを8重量%乃至15重量%含むことを
特徴とする特許請求の範囲第1項乃至第3項のいずれか
に記載の摩擦材。
(4) 10% to 50% by weight of at least one of copper, nickel, copper-zinc alloy, iron and copper-tin alloy; graphite, molybdenum disulfide, zinc sulfide, lead sulfide and antimony trisulfide; At least one type of 5
% to 20% by weight, at least one of silicon dioxide, alumina, mullite, zirconium oxide, and spinel ferrite (Fe_3O_4) and at least one of barium sulfate, calcium carbonate, and cupric oxide. It is characterized by containing a total of 10% to 50% by weight, 3% to 20% by weight of at least one of melamine dust, cashew dust, and phenol dust, and 8% to 15% by weight of phenol resin. A friction material according to any one of claims 1 to 3.
JP3138489A 1989-02-10 1989-02-10 Friction material Expired - Fee Related JP2709124B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3138489A JP2709124B2 (en) 1989-02-10 1989-02-10 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3138489A JP2709124B2 (en) 1989-02-10 1989-02-10 Friction material

Publications (2)

Publication Number Publication Date
JPH02212582A true JPH02212582A (en) 1990-08-23
JP2709124B2 JP2709124B2 (en) 1998-02-04

Family

ID=12329763

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3138489A Expired - Fee Related JP2709124B2 (en) 1989-02-10 1989-02-10 Friction material

Country Status (1)

Country Link
JP (1) JP2709124B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005121221A (en) * 2003-10-03 2005-05-12 Borgwarner Inc Mixed deposit friction material
CN105983687A (en) * 2015-02-10 2016-10-05 苏州东南电碳科技有限公司 Material for manufacturing powder metallurgy brake block of electric locomotive

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103194173B (en) * 2013-04-09 2014-07-16 吉林大学 Bionic-braking friction material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005121221A (en) * 2003-10-03 2005-05-12 Borgwarner Inc Mixed deposit friction material
CN105983687A (en) * 2015-02-10 2016-10-05 苏州东南电碳科技有限公司 Material for manufacturing powder metallurgy brake block of electric locomotive

Also Published As

Publication number Publication date
JP2709124B2 (en) 1998-02-04

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