JPH04153291A - Friction material - Google Patents

Friction material

Info

Publication number
JPH04153291A
JPH04153291A JP27858390A JP27858390A JPH04153291A JP H04153291 A JPH04153291 A JP H04153291A JP 27858390 A JP27858390 A JP 27858390A JP 27858390 A JP27858390 A JP 27858390A JP H04153291 A JPH04153291 A JP H04153291A
Authority
JP
Japan
Prior art keywords
friction
graphite
filler
sic
carbon
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
JP27858390A
Other languages
Japanese (ja)
Inventor
Kiyoshi Takei
武居 精
Mamoru Tamura
守 田村
Seiichi Tashiro
田代 聖一
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.)
Ohwada Carbon Industrial Co Ltd
Original Assignee
Ohwada Carbon Industrial 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 Ohwada Carbon Industrial Co Ltd filed Critical Ohwada Carbon Industrial Co Ltd
Priority to JP27858390A priority Critical patent/JPH04153291A/en
Publication of JPH04153291A publication Critical patent/JPH04153291A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To lower the abrasion loss in an operation at low speed and to reduce the increase in the coefficient of friction at high speed by incorporating a specified amount of SiC, Al2O3 or graphite into a carbon fiber reinforced carbon composite. CONSTITUTION:A friction material made of a carbon fiber reinforced carbon composite consisting of 30-80wt.% aggregate comprising carbon fibers and 70-20wt.% filler comprising a carbonaceous material, which contains at least one of SiC, Al2O3 and graphite in an amount of 2-20wt.% based on the total weight of the filler. In the friction material, for the purpose of bonding the carbon fibers to one another, hardly graphitizable raw material, such as phenolic resin or furan resin, is used for the carbonaceous material serving as filler. The hardly graphitizable or non-graphitized carbonaceous material is readily oxidized. Therefore, conventional brake material made of CFRC is readily oxidized when heated to a high temperature due to friction under high speed and high load conditions. SiC and Al2O3 are excellent in resistance to oxidation, while graphite has better resistance to oxidation than that of non-graphitized carbonaceous material; therefore, it is supposed that they will produce an effect on the frictional performance at high temperature.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は航空機や自動車などの車輌のブレーキ材として
有効な摩擦材料に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a friction material effective as a brake material for vehicles such as aircraft and automobiles.

従来の技術 従来、航空機やレーシングカーなどのブレーキ用の材料
は宇宙用材料として開発された炭素繊維強化炭素複合材
(以下CFRCという)が使用されている。この複合材
は高熱での機械特性が従来のものと比較して良好である
からである。
BACKGROUND ART Conventionally, carbon fiber reinforced carbon composite materials (hereinafter referred to as CFRC), which were developed as materials for space use, have been used as brake materials for aircraft, racing cars, and the like. This is because this composite material has better mechanical properties at high temperatures than conventional materials.

ブレーキ用のCFRCとしては炭素繊維の織物または不
織布に熱硬化性樹脂、たとえばフェノール樹脂やフラン
樹脂を含浸させ、それを単一にあるいは積層して150
℃〜200℃の温度で100 kg/d〜200 kg
/cfflの加重をかけて成形し、それを1000°C
以上の温度で焼成し、さらに緻密化のためピッチあるい
は熱硬化性樹脂を含浸して焼成する工程を繰り返して作
られる。このようにして作られたブレーキ材は一般には
CFRC同志の摩擦により使われており、高速高荷重の
きびしい状況でのブレーキ材として優れたものであるが
、低速での摩耗量が多く、高速になると摩擦係数が上昇
する欠点があった。即ち航空機の場合、着陸の際に大き
な効果を生ずるが、飛行場内での低速運行では摩耗量が
多く、且つ車輌の場合高速で運行中のときブレーキがき
きすぎて事故を生ずるなどの欠点があった。
CFRC for brakes is made by impregnating carbon fiber woven or non-woven fabric with thermosetting resin, such as phenol resin or furan resin, either singly or in layers.
100 kg/d to 200 kg at temperatures between ℃ and 200℃
/cffl and molded at 1000°C.
It is made by repeating the process of firing at the above temperature, impregnating with pitch or thermosetting resin for densification, and firing. Brake materials made in this way are generally used due to the friction between CFRCs, and are excellent as brake materials in severe conditions at high speeds and high loads, but they suffer from a large amount of wear at low speeds, and are This has the disadvantage that the coefficient of friction increases. In other words, in the case of aircraft, it has a great effect when landing, but when operating at low speeds inside an airport, there is a lot of wear and tear, and in the case of vehicles, when operating at high speeds, there are drawbacks such as excessive braking and accidents. Ta.

発明が解決しようとする課題 本発明はこのような課題を解決するもので、低速運行で
の摩耗量が少なく、また高速での摩擦係数の増加を少な
くすることを目的とするものである。
Problems to be Solved by the Invention The present invention solves these problems, and aims to reduce the amount of wear at low speeds and to reduce the increase in the coefficient of friction at high speeds.

課題を解決するための手段 この課題を解決するために本発明は、炭素繊維30〜8
0%wtからなる骨材と、炭素70〜20%wtからな
る充填材とで構成される炭素繊維強化炭素複合材で作ら
れた摩擦材料であって、前記充填材中の全重量に対し2
〜20%wtのSiCもしくはAr103もしくは黒鉛
の少なくとも1種類を含んでいることを特徴とするもの
である。
Means for Solving the Problem In order to solve this problem, the present invention uses carbon fibers of 30 to 8
A friction material made of carbon fiber-reinforced carbon composite material consisting of aggregate consisting of 0% wt and filler consisting of 70 to 20% wt carbon, wherein 2% of the total weight of the filler is
It is characterized by containing ~20%wt of at least one of SiC, Ar103, or graphite.

すなわち、本発明は炭素繊維の織物、不織布、編物、短
繊維に熱硬化性樹脂たとえばエポキシ樹脂やフェノール
樹脂、フラン樹脂、ピッチなどを含浸させるに際し、こ
れらの樹脂98〜80%wtに対し、S I CSA 
A’ 203 、黒鉛を単独に乃至は2種類または3種
類用い、この合計が2〜20%wtになるようによく撹
拌し、混合樹脂を作る。これらのAl103 、S i
c、黒鉛の大きさは1−以下望ましくは100μ以下の
直径の粉末か、長さが3−以下の望ましくは5Hμ以下
の長さの繊維であってもよい。AI!203の粉末また
は短繊維は純度が70%以上の成分のものでも良い。S
iCの粉末または短繊維は純度が70%以上の成分でも
良い。また、Siの粉末または短繊維も純度が70%以
上の成分のものでも良く、これらは2000℃以上の加
熱によりSiCになる。従って2000℃以上でSiC
になる5iO7粉末でも良い。この混合樹脂を炭素繊維
の織物あるいはニードルパンチによるフェルトまたは短
繊維1に対し混合樹脂が2乃至0.2の範囲の割合にな
るように含浸する。
That is, in the present invention, when impregnating carbon fiber woven fabrics, nonwoven fabrics, knitted fabrics, and short fibers with thermosetting resins such as epoxy resins, phenolic resins, furan resins, pitch, etc., S is added to 98 to 80% wt of these resins. I CSA
A' 203 and graphite are used alone, or two or three types, and stirred well so that the total amount is 2 to 20% wt to prepare a mixed resin. These Al103, Si
c. The graphite may be a powder with a diameter of 1 or less, preferably 100μ or less, or a fiber with a length of 3 or less, preferably 5Hμ or less. AI! The powder or short fiber of No. 203 may have a purity of 70% or more. S
The iC powder or short fibers may have a purity of 70% or more. Further, the Si powder or short fibers may also have a purity of 70% or more, and these become SiC by heating at 2000° C. or more. Therefore, SiC
5iO7 powder may also be used. This mixed resin is impregnated in a ratio of 2 to 0.2 to one part of carbon fiber fabric, needle-punched felt, or short fibers.

このようにしてできたブリプレラグを織物の場合は数十
枚、ニードルパンチによるフェルトの場合は数枚、短繊
維の場合はそのまま金型に積層または詰めて100〜3
00kg/cdで加圧し、100〜200℃に加熱して
硬化反応させることにより炭素繊維を骨材とした炭素繊
維強化樹脂複合材ができる。そして800℃以上の温度
で不活性雰囲気中で加熱すると、前述したごとく熱硬化
性樹脂が分解して多孔性となるため、樹脂を含浸しさら
に焼成を繰り返し、比重にほぼ変化が見られない程度に
緻密化することにより、A/203を2〜20%wt含
有するか、SiCを2〜20%wt含有するか、黒鉛を
2〜20%wt含有するか、Al2O3とSiCを合わ
せて2〜20%wt含有するか、SiCと黒鉛を合わせ
て2〜20%wt含有するか、A/203と黒鉛を合わ
せて2〜20%wt含有するか、SiCとA/203と
黒鉛を合わせて2〜20%wt含有する炭素を充填材と
して、30〜70%の炭素繊維を骨材とする炭素繊維強
化炭素複合材からなる摩擦材料が得られる。焼成温度は
1000℃以上で2200℃迄の範囲であるが、200
0℃以上が望ましい。2200℃を超えるとSiCやA
l2O3が分解することがある。1000℃以下では炭
化が不充分である。SiCやA l 203、黒鉛の単
独、2種類、3種類の混合の合計が2%wt以下になる
と摩擦特性に影響が出ず、また20%wtを超えると充
填材の炭素の強度が低下し且つ炭素繊維への接着も悪く
、炭素繊維強化炭素複合材としての強度の低下を生ずる
。骨材となる炭素繊維が30%wt以下になると強度が
低下し、80%wt以上になると炭素量が少なくて強度
が低下する。
The Bripre rugs made in this way are stacked or stuffed into a mold for 100 to 300 sheets, in the case of woven fabrics, several dozen sheets, in the case of needle-punched felt, several sheets, and in the case of short fibers, they are stacked or stuffed into a mold as they are.
By applying pressure at 00 kg/cd and heating to 100 to 200°C to cause a curing reaction, a carbon fiber reinforced resin composite material using carbon fiber as an aggregate can be produced. When heated in an inert atmosphere at a temperature of 800°C or higher, the thermosetting resin decomposes and becomes porous as described above, so the resin is impregnated and fired repeatedly until the specific gravity shows almost no change. By densifying it to 20% wt content, SiC and graphite combined 2 to 20% wt, A/203 and graphite combined 2 to 20% wt, SiC, A/203 and graphite combined 2 A friction material made of a carbon fiber-reinforced carbon composite material containing carbon containing ~20% wt as a filler and 30 to 70% carbon fiber as an aggregate is obtained. The firing temperature ranges from 1000°C to 2200°C, but 200°C
A temperature of 0°C or higher is desirable. When the temperature exceeds 2200℃, SiC and A
12O3 may decompose. Carbonization is insufficient at temperatures below 1000°C. When the total of SiC, Al 203, and graphite alone, two types, and three types of mixture is less than 2%wt, there is no effect on the friction properties, and when it exceeds 20%wt, the strength of the carbon filler decreases. In addition, adhesion to carbon fibers is poor, resulting in a decrease in strength as a carbon fiber-reinforced carbon composite material. If the amount of carbon fiber used as aggregate is less than 30% wt, the strength will decrease, and if it is more than 80% wt, the carbon content will be small and the strength will decrease.

作用 以上のように、S i Cs A A’ 203 、黒
鉛を混入することにより、摩擦係数が安定して高く且つ
摩耗率が少なくなるのは次の理由によるものと考えられ
る。即ち、炭素繊維同志の結合のために、充填材の炭素
はフェノール樹脂やフラン樹脂などの難黒鉛の原料を使
用している。これらの難黒鉛乃至黒鉛化していない炭素
は酸化が早い。従って、従来のCFRCによるブレーキ
材は高速で高負荷の状況での摩擦により高い温度に発熱
すると酸化が早い。それに対し、Sl′C1Al2O3
は耐酸化性に優れ、黒鉛も黒鉛化していない炭素に比べ
耐酸化性は良好である。そのため高温での摩擦性能に効
果を生ずると思われる。
Effect As described above, the reason why the friction coefficient is stably high and the wear rate is reduced by mixing S i Cs A A' 203 and graphite is considered to be due to the following reasons. That is, in order to bond the carbon fibers together, the carbon filler uses a non-graphite material such as phenol resin or furan resin. These non-graphitic or non-graphitized carbons are oxidized quickly. Therefore, conventional CFRC brake materials oxidize quickly when they generate heat at high temperatures due to friction under high speed and high load conditions. On the other hand, Sl'C1Al2O3
has excellent oxidation resistance, and graphite also has better oxidation resistance than non-graphitized carbon. Therefore, it seems to have an effect on friction performance at high temperatures.

実施例 以下、本発明の一実施例について、詳細に説明する。Example Hereinafter, one embodiment of the present invention will be described in detail.

フェノール樹脂(ユニチカ■製ユニペックスS)をアセ
トンに1=1の割合で溶解し、それに第1表に示す如く
、S l、 A l 203 、黒鉛を混合した。
A phenolic resin (UNIPEX S manufactured by Unitika ■) was dissolved in acetone at a ratio of 1=1, and S 1 , A 1 203 and graphite were mixed therein as shown in Table 1.

上記S1、Al2O3、黒鉛を1種乃至3種含む混合樹
脂液に、6000フイラメントのアクリル系の炭素繊維
(東し■製)からなり経糸420本、緯糸420本、重
さ330gr/afの織物を含浸し、織物の重量とアセ
トンが蒸発した状態での各混合樹脂重量が1:1になる
ように8種のブリプレラグを作った。各々を金型に入れ
、200トンのホットプレス機により150 kglo
fの圧力で200℃で硬化反応させた。これを真空炉に
入れ、1G−’T o r rの真空度で2000℃に
焼成し、冷却後、フェノール樹脂に含浸し、さらに焼成
する工程を繰り返し、比重の増加が生じない迄継続し、
緻密化した。JISD4411の定速式摩擦試験機の摩
擦ディスクに第1表に示す試料徹8の混合物を含まない
フェノール樹脂のみのブリプレラグから作ったCFRC
の板を取り付け、一方試験片支持アームに5mmX25
mmX25mの大きさで第1表に示す試料N11L1〜
丸8の樹脂混合物についてJ I 5D4411の方法
に従って試験を行なった。その結果は第2表に示す通り
、何れも試料Nα8の混合物のないCFRCの従来のブ
レーキ材に比べて摩擦係数および摩耗率の何れもが優れ
ている。
A fabric made of 6000 filament acrylic carbon fiber (manufactured by Toshi) with 420 warp threads, 420 weft threads, and a weight of 330 gr/af is added to the mixed resin liquid containing one to three types of S1, Al2O3, and graphite. Eight types of brippure rugs were made so that the weight of the fabric and the weight of each mixed resin after acetone evaporated was 1:1. Each is put into a mold and 150 kglo is produced using a 200 ton hot press machine.
A curing reaction was carried out at 200° C. under a pressure of f. This is placed in a vacuum furnace and fired at 2000°C under a vacuum of 1 G-'T or r. After cooling, the process of impregnating it with phenol resin and further firing is repeated until the specific gravity does not increase.
It has become more detailed. A CFRC made from Briprelag made of only phenolic resin without the mixture of Sample Toru 8 shown in Table 1 on the friction disk of a JISD4411 constant speed friction tester.
Attach a plate of 5 mm x 25 mm to the specimen support arm.
Sample N11L1~ shown in Table 1 with a size of mm x 25m
Tests were carried out on the resin mixture of Round 8 according to the method of J I 5D4411. As shown in Table 2, the results are superior in both the friction coefficient and the wear rate compared to the conventional brake material made of CFRC without a mixture of sample Nα8.

〈以下余白〉 発明の効果 以上のように本発明によれば、5iC1AI!203、
人造黒鉛の少なくとも1種類を充填材に混入させること
により、摩擦係数が安定して高く、且つ摩耗率を下げる
ことができる。
<Margin below> Effects of the Invention As described above, according to the present invention, 5iC1AI! 203,
By mixing at least one type of artificial graphite into the filler, the coefficient of friction can be stably increased and the wear rate can be lowered.

代理人   森  本  義  弘Agent Hiroshi Mori Moto

Claims (1)

【特許請求の範囲】[Claims] 1、炭素繊維30〜80%wtからなる骨材と、炭素7
0〜20%wtからなる充填材とで構成される炭素繊維
強化炭素複合材で作られた摩擦材料であって、前記充填
材中の全重量に対し2〜20%wtのSiCもしくはA
l_2O_3もしくは黒鉛の少なくとも1種類を含んで
いることを特徴とする摩擦材料。
1. Aggregate consisting of 30-80%wt carbon fiber and carbon 7
A friction material made of a carbon fiber-reinforced carbon composite material comprising a filler of 0 to 20% wt, and 2 to 20% wt of SiC or A based on the total weight of the filler.
A friction material characterized by containing at least one type of l_2O_3 or graphite.
JP27858390A 1990-10-17 1990-10-17 Friction material Pending JPH04153291A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27858390A JPH04153291A (en) 1990-10-17 1990-10-17 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27858390A JPH04153291A (en) 1990-10-17 1990-10-17 Friction material

Publications (1)

Publication Number Publication Date
JPH04153291A true JPH04153291A (en) 1992-05-26

Family

ID=17599287

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27858390A Pending JPH04153291A (en) 1990-10-17 1990-10-17 Friction material

Country Status (1)

Country Link
JP (1) JPH04153291A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997022815A1 (en) * 1995-12-15 1997-06-26 Sab Wabco (Bromborough) Limited Friction engaging device
US20070284772A1 (en) * 2004-12-30 2007-12-13 Brembo Ceramic Brake Systems S.P.A. Shaped Composite Material
WO2014016891A1 (en) * 2012-07-23 2014-01-30 日立化成株式会社 Brake pad for yaw control, and brake member
JP2014505214A (en) * 2011-01-13 2014-02-27 ミーバ フリクテク ゲゼルシャフト ミット ベシュレンクテル ハフツング Friction material
CN105545999A (en) * 2015-12-23 2016-05-04 佛山早稻田科技服务有限公司 Frictional material
CN106167563A (en) * 2016-08-16 2016-11-30 广西南宁胜祺安科技开发有限公司 A kind of function admirable modified friction material
CN108518433A (en) * 2018-03-30 2018-09-11 王敏 A kind of preparation method of modified silicon carbide group automobile brake block

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997022815A1 (en) * 1995-12-15 1997-06-26 Sab Wabco (Bromborough) Limited Friction engaging device
US6514592B1 (en) 1995-12-15 2003-02-04 Sab Wabco Products Limited Friction engaging device
US20070284772A1 (en) * 2004-12-30 2007-12-13 Brembo Ceramic Brake Systems S.P.A. Shaped Composite Material
US8349231B2 (en) * 2004-12-30 2013-01-08 Brembo Ceramic Brake Systems S.P.A. Shaped composite material
JP2014505214A (en) * 2011-01-13 2014-02-27 ミーバ フリクテク ゲゼルシャフト ミット ベシュレンクテル ハフツング Friction material
WO2014016891A1 (en) * 2012-07-23 2014-01-30 日立化成株式会社 Brake pad for yaw control, and brake member
JPWO2014016891A1 (en) * 2012-07-23 2016-07-07 日立化成株式会社 Brake pads and brake members for yaw control
US9568061B2 (en) 2012-07-23 2017-02-14 Hitachi Chemical Company, Ltd. Brake pad for yaw control, and brake member
CN105545999A (en) * 2015-12-23 2016-05-04 佛山早稻田科技服务有限公司 Frictional material
CN106167563A (en) * 2016-08-16 2016-11-30 广西南宁胜祺安科技开发有限公司 A kind of function admirable modified friction material
CN108518433A (en) * 2018-03-30 2018-09-11 王敏 A kind of preparation method of modified silicon carbide group automobile brake block

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