JPS608536A - Carbon brake and manufacture thereof - Google Patents
Carbon brake and manufacture thereofInfo
- Publication number
- JPS608536A JPS608536A JP11539983A JP11539983A JPS608536A JP S608536 A JPS608536 A JP S608536A JP 11539983 A JP11539983 A JP 11539983A JP 11539983 A JP11539983 A JP 11539983A JP S608536 A JPS608536 A JP S608536A
- Authority
- JP
- Japan
- Prior art keywords
- carbon
- fiber
- fibers
- brake
- densification
- 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
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000000835 fiber Substances 0.000 claims abstract description 44
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 36
- 239000004917 carbon fiber Substances 0.000 claims abstract description 36
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000004744 fabric Substances 0.000 claims abstract description 11
- 239000012779 reinforcing material Substances 0.000 claims abstract 2
- 238000000280 densification Methods 0.000 claims description 25
- 238000010438 heat treatment Methods 0.000 claims description 22
- 238000005520 cutting process Methods 0.000 claims description 20
- 239000002131 composite material Substances 0.000 claims description 18
- 238000010304 firing Methods 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 239000012298 atmosphere Substances 0.000 claims description 11
- 229920001187 thermosetting polymer Polymers 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 4
- 239000000805 composite resin Substances 0.000 claims description 3
- 239000011347 resin Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 15
- 239000003575 carbonaceous material Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 239000011295 pitch Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009730 filament winding Methods 0.000 description 2
- 239000007849 furan resin Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 238000010000 carbonizing Methods 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000011134 resol-type phenolic resin Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D69/00—Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
- F16D69/02—Composition of linings ; Methods of manufacturing
- F16D69/023—Composite materials containing carbon and carbon fibres or fibres made of carbonizable material
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Composite Materials (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、ブレーキ特性の優れたカーボンブレーキに関
するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a carbon brake with excellent braking characteristics.
更に詳しくは、摺動面に対し炭素mtruが角度をもっ
て配向しているカーボンブレーキディスクあるいはカー
ボンブレーキパッドに関するものである。More specifically, it relates to a carbon brake disc or a carbon brake pad in which carbon mtru is oriented at an angle with respect to the sliding surface.
従来、カーボンブレーキディスクの厚さ方向即ち摺動向
側から圧縮成形していたため、強化炭素繊維の大部分は
摺動面にほぼ平行になっている。このため摩擦係数が低
く、またブレーキ作動中に繊維の脱落が生じ、ブレーキ
挙動が不安定になるなどの問題があった。Conventionally, carbon brake discs were compression-molded from the thickness direction, that is, from the sliding surface, so most of the reinforced carbon fibers were almost parallel to the sliding surface. For this reason, there were problems such as a low coefficient of friction and fibers falling off during braking operation, resulting in unstable braking behavior.
これを改善するため、比較的長い繊維と短い繊維とを用
い、短い繊維(5mm以下)をランダムに配向させる試
みがなされている。しかし支配的要素となる長い繊維が
18動向に対し平行であるため、十分改善の実を挙げる
に至っていない。In order to improve this, attempts have been made to use relatively long fibers and short fibers and to randomly orient the short fibers (5 mm or less). However, since the long fibers, which are the dominant element, are parallel to the 18 trend, sufficient improvement has not been achieved.
本発明者等は、このような問題について鋭意検討の結果
、大部分の繊維を摺動面に対し角度をもって配向させる
ことによって、これらの問題を改善しうろことを見出し
た。As a result of intensive studies on these problems, the present inventors have found that these problems can be improved by orienting most of the fibers at an angle with respect to the sliding surface.
即ち本発明は、
キ
(2)埋設されている炭素繊維が摺動面に対し角Ifを
もって配向しており、内周又は/及び外周を一方向炭素
繊維又は炭素繊維織物にて旋回配置してなるカーボンブ
レーキ(3)炭素繊維を強化材とする円筒状複合材であ
って、該繊維が円筒の軸と直角な面を横切るように配向
している炭素繊維強化熱硬化性樹脂複合材を円筒の軸と
直角な方向へ切断し、かつ該切断の前又は後に不活性雰
囲気中での焼成と緻密化とを行うことを特徴とするカー
ボンブレーキの製造法である。That is, the present invention provides the following features: (2) The embedded carbon fibers are oriented at an angle If with respect to the sliding surface, and the inner periphery and/or outer periphery is arranged in a rotating manner with unidirectional carbon fibers or carbon fiber fabrics. Carbon brake (3) A cylindrical composite material reinforced with carbon fibers, in which the carbon fiber reinforced thermosetting resin composite material is oriented so as to cross a plane perpendicular to the axis of the cylinder. This method of manufacturing a carbon brake is characterized by cutting the carbon brake in a direction perpendicular to the axis of the carbon brake, and performing sintering and densification in an inert atmosphere before or after the cutting.
本発明において、摺動向に対する繊維の角度とは、繊維
の実質的直線方向を示すものであり、繊維の部分的且つ
ミクロ的単位長さでの角度を示すものではない。好まし
くは繊維又はその繊維方向の延長線が一方の摺動面から
相対J−る他方の面にまで延在するような角度で配向し
ていることである。In the present invention, the angle of the fiber with respect to the sliding movement refers to the substantially linear direction of the fiber, and does not indicate the angle in the partial micro unit length of the fiber. Preferably, the fibers or their extensions in the direction of the fibers are oriented at an angle such that they extend from one sliding surface to the other opposing surface.
a+1tIliの方向を図面にて説明り゛る。The direction of a+1tIli will be explained with reference to the drawings.
第1図(イ)〜(ハ)は繊維とその方向を示し、1は繊
維、2は繊維の方向を示J−0
第1図(イ)は強化材が織物である場合の繊維とその方
向を示す。織物に使用されている繊維はサイン曲線的で
あるが、全体として繊維の方向は直線で結ぶことができ
る。この直線で表わされる方向を繊維の方向とする。(
ロ)及び(ハ)は、繊維が規則的でない場合について示
したものである。Figures 1 (a) to (c) show the fibers and their directions, 1 shows the fibers and 2 shows the fiber directions. Show direction. Although the fibers used in textiles have a sinusoidal curve, the overall direction of the fibers can be tied in a straight line. The direction represented by this straight line is the direction of the fibers. (
(b) and (c) show cases where the fibers are not regular.
本発明における繊維の方向が)習動面に対し角度をもっ
て配向しているとは、成形特摺動面の方向から加圧され
、その結果、繊維が加圧方向に対し実質的に直角方向に
配向している如き場合を除外する意味である。In the present invention, the fibers are oriented at an angle with respect to the sliding surface. This means that the fibers are oriented at an angle with respect to the sliding surface when pressure is applied from the direction of the sliding surface, and as a result, the fibers are oriented in a direction substantially perpendicular to the pressing direction. This is meant to exclude cases where it is oriented.
このような本発明によると、カーボンブレーキは、摺動
向に対し炭素繊維が角度をもって配向しているために、
ブレーキ作動時において、摩擦係数が高く、摩耗量が少
な(、繊維の脱落が生じることがほとんどなく安定した
ブレーキ作動特性を示す。According to the present invention, the carbon brake has carbon fibers oriented at an angle with respect to the sliding motion.
During brake operation, the friction coefficient is high, the amount of wear is small (and there is almost no shedding of fibers, and it exhibits stable brake operation characteristics.
本発明のカーボンブレーキは、切断、焼成、緻密化、場
合により熱処理などを行って製造される。焼成は有機物
を炭化させるために行われ、緻密化は組織を緻密にする
ために行≠われ、これは含浸と焼成の工程からなり、熱
処理は主に材料の耐熱酸化性を向上させるために行われ
るものである。The carbon brake of the present invention is manufactured by cutting, firing, densification, and optionally heat treatment. Calcining is performed to carbonize organic matter, densification is performed to make the structure denser, and this consists of the steps of impregnation and firing, and heat treatment is mainly performed to improve the thermal oxidation resistance of the material. It is something that can be done.
本発明に使用される炭素繊維は、レーヨン、ポリアクリ
ロニトリル、ピッチ等を主成分とするプレカーサーを不
活性雰囲気中800〜2000℃で炭化した炭素質繊維
あるいは2000℃以上の温度で黒鉛化した黒鉛質繊維
である。The carbon fibers used in the present invention are carbon fibers obtained by carbonizing precursors mainly composed of rayon, polyacrylonitrile, pitch, etc. at 800 to 2000°C in an inert atmosphere, or graphite fibers graphitized at temperatures of 2000°C or higher. It is a fiber.
成形硬化に使用する熱硬化性樹脂器ルフラン、フェノー
ル、ポリイミド、エポキシ等/各樹脂で、高粘度あるい
は固体である場合は適当な溶媒に溶かすか、あるいは加
熱して溶融して用(入る。Thermosetting resins used for molding and curing: Refuran, phenol, polyimide, epoxy, etc./Resins that have high viscosity or are solid must be dissolved in an appropriate solvent or melted by heating.
また、緻密化するために該複合材をフラン、フェノール
等の各樹脂あるいはコールタールピッチ等に含浸し、窒
素、アルゴン等の不活性雰囲気中で焼成する。Further, in order to make it dense, the composite material is impregnated with various resins such as furan and phenol, or coal tar pitch, and then fired in an inert atmosphere such as nitrogen or argon.
この緻密化は、該複合材を窒素、水素、アルゴン等の非
酸化性雰囲気中で700〜2000°Cに加熱し、メタ
ン、エタン、ベンゼン等の炭化水素ガスを導入して行う
ことも可能である(ケミカル嗜ペーパー・ディポジショ
ン〉。This densification can also be performed by heating the composite material to 700-2000°C in a non-oxidizing atmosphere such as nitrogen, hydrogen, or argon, and introducing a hydrocarbon gas such as methane, ethane, or benzene. Yes (Chemical Paper Deposition).
更に、炭素の配列構造を変え、耐熱酸化性を向上させる
ために、通常熱処理が行われる。この熱処理は、不活性
ガス雰囲気中2000〜3000°Cのmlにて処理1
′ることによって行われる。この熱処理は、耐熱酸化性
を向上する外、緻密化時の樹脂等の含浸を容易にする効
果もある。必要によっては所定の特性が得られる迄、緻
密化及び熱処理を繰返す。Further, heat treatment is usually performed to change the carbon arrangement structure and improve thermal oxidation resistance. This heat treatment was performed at 2000 to 3000°C in an inert gas atmosphere.
It is done by This heat treatment not only improves thermal oxidation resistance but also has the effect of facilitating impregnation with resin, etc. during densification. If necessary, densification and heat treatment are repeated until predetermined characteristics are obtained.
本発明のカーボンブレーキは航空機、鉄道車両、自動車
、オートバイ用に有用で、特に航空機用マルチタイプデ
ィスクブレーキに有用である。The carbon brake of the present invention is useful for aircraft, railway vehicles, automobiles, and motorcycles, and is particularly useful for multi-type disc brakes for aircraft.
次に本発明カーボンブレーキディスクの製造法を説明す
る。Next, a method for manufacturing the carbon brake disc of the present invention will be explained.
1)流動成形法
繊維長5〜40mmの炭素繊維と熱硬化性樹脂(例、フ
ェノール、フラン、エポキシ、ポリイミドの各樹脂など
)との混合物を円筒状軸方向く長さ方向)に流動させて
、繊維を流動方向に配向させた後、樹脂を硬化させて円
筒状成形物とする。次に該成形物を円筒の軸方向と直角
方向(半径方向)に切断、即ち輪切にすることによって
ディスク状成形物を得る。1) Flow molding method A mixture of carbon fibers with a fiber length of 5 to 40 mm and a thermosetting resin (e.g., phenol, furan, epoxy, polyimide resin, etc.) is flowed in the axial and longitudinal directions of a cylindrical shape. After orienting the fibers in the flow direction, the resin is cured to form a cylindrical molded product. Next, a disc-shaped molded product is obtained by cutting the molded product in a direction perpendicular to the axial direction (radial direction) of the cylinder, that is, into slices.
次いで該ディスク状成形物を不活性雰囲気中にて徐々に
昇温し800〜1500℃まで加熱焼成することによっ
てマトリックス樹脂を炭素質に変える。成形物の形状及
び工程上の操作性等によっては、円筒状成形物を不活性
雰囲気中で焼成した後に切断してディスク状カーボン材
にしてもよい。Next, the temperature of the disc-shaped molded product is gradually increased in an inert atmosphere and heated and fired to 800 to 1500°C, thereby converting the matrix resin into a carbonaceous material. Depending on the shape of the molded product and the operability of the process, the cylindrical molded product may be fired in an inert atmosphere and then cut into a disc-shaped carbon material.
次に該カーボン材にピッチ又はフラン樹脂等の液状有機
物を含浸後、不活性雰囲気で焼成することによって緻密
化を行なう。この緻密化は該カーボン材を高温不活性雰
囲気中に保持して導入した炭化水素ガスを熱分解して炭
素を蒸着させる前記ケミカル・ペーパー・′ディポジシ
ョン(通称CVD)法によって行ってもにい。Next, the carbon material is impregnated with a liquid organic substance such as pitch or furan resin, and then densified by firing in an inert atmosphere. This densification can also be achieved by the chemical paper deposition (commonly known as CVD) method, in which the carbon material is held in a high-temperature inert atmosphere and the introduced hydrocarbon gas is thermally decomposed to deposit carbon. .
2)フィラメントワインディング法
フェノール樹脂あるいはフラン樹脂等の熱硬化性樹脂を
含浸した炭素繊維フィラメン1〜を所定のマンドレルに
円周方向(マンドレルの軸方向と直角方向)に角度をも
って捲付(プる方法によって円筒状成形物を得た後、不
活性雰囲気中での焼成、ディスク状に切断加工、緻密化
及び熱処理をおこなって本発明のカーボンブレーキを得
る。2) Filament winding method A method in which carbon fiber filaments 1 to 1 impregnated with a thermosetting resin such as phenol resin or furan resin are wound around a predetermined mandrel at an angle in the circumferential direction (direction perpendicular to the axial direction of the mandrel). After obtaining a cylindrical molded product, the carbon brake of the present invention is obtained by firing in an inert atmosphere, cutting into a disk shape, densification, and heat treatment.
炭素繊維フィラメントの代わりに炭素m141織物等の
テープを用いてもよい。A tape such as carbon m141 fabric may be used instead of carbon fiber filaments.
3)クロスローリング法
熱硬化性樹脂を含浸した炭素繊維フィラメントクロスあ
るいは炭素I!i維スバスパンヤーンクロス定のマンド
レルに捲回積層し硬化した後、切断加工、1L緻密化、
熱処理等を行グう。3) Cross rolling method Carbon fiber filament cloth impregnated with thermosetting resin or Carbon I! i-fiber spun yarn cloth After being wound and laminated on a fixed mandrel and cured, cutting process, 1L densification,
Perform heat treatment, etc.
本発明カーボンブレーキの製造にお1プる焼成(炭化)
、緻密化、熱処理、切断等の工程は順序は特に固定され
ない。また、緻密化及び熱処理は繰返し行われることが
好ましい。Firing (carbonization) for manufacturing the carbon brake of the present invention
The order of steps such as densification, heat treatment, and cutting is not particularly fixed. Further, it is preferable that the densification and heat treatment be repeated.
更に緻密化と熱処理は、いずれを先に行ってもよい。即
ち焼成後熱処理し、その後緻密化し、或は逆に行われる
。Furthermore, either densification or heat treatment may be performed first. That is, heat treatment is performed after firing, followed by densification, or vice versa.
切断は、初めの樹脂硬化後の何れかの段階にて行われる
。しかし、切断を、緻密化前に行うと、材料が晩いため
、加工し難い。従って切断は、何回かの緻密化、熱処理
の段階で行うのがよい。切断後、緻密化することは、緻
密化効果をより高めることができる。これは、切断によ
ってより表面積が大きくなるからである。Cutting is done at some stage after initial resin curing. However, if the cutting is performed before densification, the material is slow and difficult to process. Therefore, cutting is preferably performed at several stages of densification and heat treatment. Densification after cutting can further enhance the densification effect. This is because cutting increases the surface area.
切断を容易に行うには、緻密化1稈の焼成前に行う。こ
れは炭化してない樹脂等が粘結剤として作用し脆弱な炭
素材1′31の損傷を防ぐからである。To facilitate cutting, perform cutting before firing one culm for densification. This is because the non-carbonized resin acts as a binder and prevents damage to the fragile carbon material 1'31.
本発明方法によると、同時に多数のカーボンブレーキを
製造することができ、生産効率を高めることができる。According to the method of the present invention, a large number of carbon brakes can be manufactured at the same time, and production efficiency can be improved.
以上の如く、炭素繊維が摺動面に角度をもって配向した
本発明のカーボン材の場合、炭素繊維が贋動面とほぼ平
行している従来のカーボン材と比較して、周方向あるい
は半径方向の強度が低下する傾向があるが、通常の使用
条件では問題はない。苛酷な使用条件下で高い強度が要
求される場合には、下記の如く外周又は/及び内周に一
方向炭素繊維又は炭素繊維織物を旋回積層して補強する
ことがある。 この補強はディスクブレーキ等の外周あ
るいは内周の固定用の切欠き部に特に有効である。この
切欠き部の補強の場合には、該複合材を所定形状より若
干小さめに切削加工した後、炭素繊維を旋回積層し所定
の形状を得る。 埋設している炭素繊維が摺動面に角度
をもって配向している複合材の外周あるいは内周では外
周と内周に一方向炭素繊維帷あるいは炭素繊維織物を旋
回するのは、該複合材の硬化前、硬化後、焼成後、緻密
化後あるいは熱処理後のいずれでもよい。As described above, in the case of the carbon material of the present invention in which the carbon fibers are oriented at an angle to the sliding surface, compared to the conventional carbon material in which the carbon fibers are approximately parallel to the sliding surface, the carbon fibers are oriented in the circumferential or radial direction. Although the strength tends to decrease, there is no problem under normal usage conditions. When high strength is required under severe usage conditions, unidirectional carbon fibers or carbon fiber fabrics may be laminated and reinforced on the outer periphery and/or the inner periphery as described below. This reinforcement is particularly effective for fixing notches on the outer or inner circumference of disc brakes and the like. In the case of reinforcing this notch, the composite material is cut to a size slightly smaller than a predetermined shape, and then carbon fibers are laminated in a spiral manner to obtain a predetermined shape. On the outer or inner periphery of a composite material in which the embedded carbon fibers are oriented at an angle to the sliding surface, unidirectional carbon fiber strips or carbon fiber fabrics are swirled around the outer and inner periphery to cure the composite material. It may be used before, after curing, after firing, after densification, or after heat treatment.
流動成形法の場合には、使用する雌型のキャビテイ外周
部あるいは雄型外周部に熱硬化性樹脂を含浸した炭素繊
維を旋回積層した後に、前記流動成形法で成形可能であ
る。In the case of the flow molding method, carbon fibers impregnated with a thermosetting resin can be swirled and laminated on the outer periphery of the cavity of the female mold or the outer periphery of the male mold to be used, and then molding can be performed by the flow molding method.
またマンドレルを使用する製造法は使用するマンドレル
にあらかじめ熱硬化性樹脂を含浸した一方向炭素繊維あ
るいは炭素繊維織物をその周方向に旋回積層した後、前
記フィラメントワインディング法又はクロスローリング
法で成形する。Further, in the manufacturing method using a mandrel, unidirectional carbon fibers or carbon fiber fabrics impregnated with a thermosetting resin in advance are laminated in the circumferential direction of the mandrel, and then formed by the filament winding method or cross rolling method.
あるいは、前記いずれ々)の方法で、成形した後、切断
後、焼成後、緻密化後、熱処理後の何れかの段階で熱硬
化性樹脂を含浸した炭素繊維を旋回積層させ、硬化及び
焼成等を行う。Alternatively, in any of the above methods, carbon fibers impregnated with a thermosetting resin are laminated by rotation at any stage after shaping, cutting, firing, densification, or heat treatment, and then hardening, firing, etc. I do.
以下、本発明を実施例で説明するとともに比較例を示す
。EXAMPLES Hereinafter, the present invention will be explained with reference to examples, and comparative examples will be shown.
実施例ル
ゾール型フェノール樹脂を含浸した炭素繊維フィラメン
ト束く樹脂含有!(Re)32重量%)を20mInに
切断してチョツプドストランドプリプレグを作成した。Example Contains resin for bundling carbon fiber filaments impregnated with Luzole type phenolic resin! (Re) (32% by weight) was cut into 20 mIn pieces to create chopped strand prepreg.
このプリプレグを第2図に示す金型の雌型中央部に充填
し、ホットプレスにて170”C120kg/’cm2
.60分硬化さけ、円筒状複合材を作製した。この複合
材の上端及び下端15mmを切削除去後、厚さ10mm
に輪切にし、外径115mm1内径55mm、厚さ10
mmのディスク状複合材を作製した。This prepreg was filled into the female mold center part of the mold shown in Figure 2, and heated to 170"C120kg/'cm2 using a hot press.
.. After curing for 60 minutes, a cylindrical composite material was produced. After cutting and removing 15 mm of the upper and lower ends of this composite material, the thickness was 10 mm.
Cut into rounds, outer diameter 115mm, inner diameter 55mm, thickness 10mm.
A disk-shaped composite material of mm was produced.
該複合材を窒素雰囲気中2℃/minで1000℃まで
昇温して30分保持し、有機質マトリックスを炭素質に
変えた(焼成工程)。The composite material was heated to 1000° C. at 2° C./min in a nitrogen atmosphere and held for 30 minutes to change the organic matrix to carbonaceous (firing step).
このカーボン材を緻密化するために減圧下200℃でピ
ッチを含浸した後、焼成を行lっだ。In order to make this carbon material dense, it was impregnated with pitch at 200° C. under reduced pressure, and then fired.
この含浸、焼成工程を5回繰返した後、窒素雰囲気中2
00’C/hrで2000℃に昇温後、30分保持して
熱処理を行lい、密度1.65g/ cm”、外径11
5mm 、内径55mm、厚さ10+11111のカー
ボンブレーキを作製した。After repeating this impregnation and firing process 5 times, 2
After raising the temperature to 2000℃ at 00'C/hr, heat treatment was performed by holding it for 30 minutes, resulting in a density of 1.65g/cm'' and an outer diameter of 11.
A carbon brake with a diameter of 5 mm, an inner diameter of 55 mm, and a thickness of 10+11111 mm was manufactured.
該カーボンブレーキを摺動向(ディスク面ンと直角に切
断して、その断面のm維配向を観察したところ、大部分
の繊維が摺動向にほぼ直角に配向していた。When the carbon brake was cut perpendicular to the sliding direction (disc surface) and the m-fiber orientation of the cross section was observed, most of the fibers were oriented almost perpendicular to the sliding direction.
実施例2
レゾニル型フェノール樹脂を含浸した#素繊維フィラメ
ント束(RC35重量%)を外径55+nmのマンドレ
ルにマンドレルの軸方向と60″の角度をなすようにフ
ィラメントワインディングし!c後、170℃で2時間
硬化を行ない、長さ約500111m 、外径115m
m 1内155mmの円筒状複合材を作製した。Example 2 A #plain fiber filament bundle (RC 35% by weight) impregnated with resonyl type phenolic resin was filament-winded onto a mandrel with an outer diameter of 55+nm so as to form an angle of 60'' with the axial direction of the mandrel. Cured for 2 hours, length approximately 500,111 m, outer diameter 115 m
A cylindrical composite material of 155 mm in m 1 was produced.
該複合材を実施例1と同し方法で焼成工程を行≠った。The composite material was subjected to a firing process in the same manner as in Example 1.
次いで両端部50mmを切削除去し、厚さ1101nに
輪切にし、外径115mm 、内径55mm、に加工し
た後、実施例1と同様の方法C緻密化及び熱処理を行l
い、密度1.65g/cm”のカーボンディスクを作製
した。Next, 50 mm of both ends were cut off, the pieces were cut into rings with a thickness of 1101 nm, and after being processed to have an outer diameter of 115 mm and an inner diameter of 55 mm, densification and heat treatment were performed in the same manner as in Example 1.
A carbon disk with a density of 1.65 g/cm'' was prepared.
実施例3
東邦ベスロン(株)製炭素41i維スパンヤーンuNh
(8枚朱子320g/m ’ )にフラン$741J
tt(ヒタフランV F−302、触fly’、 0,
5wt% 含有)を4oog/m2塗布して70’Cで
30分ブレギュアした後、外径55mmのマンドレルに
Vf (繊維体積含有率)が35%になる様に外径11
5m1l+まで旋回積層して 150℃2時間加熱硬化
した。Example 3 Carbon 41i fiber spun yarn uNh manufactured by Toho Bethlon Co., Ltd.
(8 sheets of satin 320g/m') for Franc $741J
tt (Hitafuran V F-302, touch fly', 0,
After applying 40og/m2 of 5 wt% (containing 5 wt%) and breguring at 70'C for 30 minutes, the outer diameter of 11 was applied to a mandrel with an outer diameter of 55 mm so that the Vf (fiber volume content) was 35%.
The layers were laminated by rotation to a thickness of 5 ml+ and heated and cured at 150°C for 2 hours.
この積層物を実施例2と同様に焼成、切削、緻密化及び
熱処理を行〆い、密度1.60g/am1のカーボンデ
ィスクを作製した。This laminate was fired, cut, densified and heat treated in the same manner as in Example 2 to produce a carbon disk with a density of 1.60 g/am1.
実施例4
実施例7において硬化後輪切した、外径115mm 、
内径501Il11厚さ10v++のディスク状複合材
の外周及び内周に、レゾール型フェノール樹脂を含浸し
た炭素繊維一方向プリプレグを周方向に厚さ1mmに旋
回積層した後、実施例1と同様に焼成、緻密化、熱処理
を打撃い、外径117mm 、内径48n+m、厚さ1
0mmのカーボンディスクを得た。Example 4 Cut after hardening in Example 7, outer diameter 115 mm,
Carbon fiber unidirectional prepreg impregnated with resol-type phenolic resin was laminated circumferentially to a thickness of 1 mm on the outer and inner peripheries of a disk-shaped composite material with an inner diameter of 501 Il 11 and a thickness of 10 V++, and then fired in the same manner as in Example 1. Densified and heat treated, outer diameter 117mm, inner diameter 48n+m, thickness 1
A 0 mm carbon disc was obtained.
比較例1
実施例1と同様に作製したチョツプドストランドプリプ
レグを第3図に示すような金型を用いて通常の圧縮成形
にて外径115mm 、内径55111m、厚さ6(l
llllnの円筒状複合材を作製した。Comparative Example 1 A chopped strand prepreg produced in the same manner as in Example 1 was subjected to ordinary compression molding using a mold as shown in FIG.
A cylindrical composite material of llllln was produced.
この複合材を実施例1と同様に切削加工、焼成、緻密化
、熱処理を行fい、密度1.65g、/Cm’ 、外径
115mm 、内径55mm、厚さ10mmの 4カー
ボンブレーキを作製した。This composite material was subjected to cutting, firing, densification, and heat treatment in the same manner as in Example 1 to produce a carbon brake having a density of 1.65 g/cm', an outer diameter of 115 mm, an inner diameter of 55 mm, and a thickness of 10 mm. .
該カーボンブレーキを摺動面と直角に切断して、その断
面のll1m配向を観察したところ、全ての繊維が摺動
向にほぼ平行に配向していた。When the carbon brake was cut at right angles to the sliding surface and the ll1m orientation of the cross section was observed, all the fibers were oriented almost parallel to the sliding direction.
比較例2
東邦ベスロン(株)製炭素繊維スパン飄7−ン織物を用
いて実施例1と同様にプリプレグを作製、して、外径1
10mm 、内径55mmに切火いて第3図に示づ金型
にて、比較例1と同様に円筒状複合材を作製した。この
複合材を実施例1と同様に切削加工、焼成、緻密化、熱
処理を行い、密度1.65(1/ CmX、外径115
mm、内径55mm、厚さ110n1のカーボンブレー
キを作製した。Comparative Example 2 A prepreg was produced in the same manner as in Example 1 using a carbon fiber spun 7-strand fabric manufactured by Toho Bethlon Co., Ltd., and the outer diameter was 1.
A cylindrical composite material having a diameter of 10 mm and an inner diameter of 55 mm was prepared in the same manner as in Comparative Example 1 using the mold shown in FIG. This composite material was subjected to cutting, firing, densification, and heat treatment in the same manner as in Example 1, and the density was 1.65 (1/CmX, outer diameter 115
A carbon brake with an inner diameter of 55 mm and a thickness of 110 nm was produced.
該カーボンブレーキを摺動向と直角に切断して、その断
面のm維配向を観察したところ、全ての繊維が摺動向に
ほぼ平行に配向していた。When the carbon brake was cut perpendicular to the sliding direction and the m-fiber orientation of the cross section was observed, all the fibers were oriented almost parallel to the sliding direction.
第1図(イ)(ロ)(ハ)は繊維方向を示り図、第2図
は実施例1で使用された金型の断面概略図、第3図は比
較例1で使用された金型の断面概略図である。
1:繊維、2:繊維の方向、3:雄型、4:圃型Figure 1 (a), (b), and (c) show the fiber direction, Figure 2 is a cross-sectional schematic diagram of the mold used in Example 1, and Figure 3 is the mold used in Comparative Example 1. FIG. 3 is a schematic cross-sectional view of the mold. 1: Fiber, 2: Fiber direction, 3: Male type, 4: Field type
Claims (4)
って配向しているカーボンブレーキ。(1) A carbon brake in which embedded carbon fibers are oriented at an angle to the sliding surface.
って配向しており、内周又は/及び外周を一方向炭素繊
維又は炭素繊維織物にて旋回配置してなるカーボンブレ
ーキ。(2) A carbon brake in which embedded carbon fibers are oriented at an angle to the sliding surface, and the inner circumference and/or outer circumference is arranged in a rotating manner using unidirectional carbon fibers or carbon fiber fabrics.
該繊維か円筒の軸と直角な面を横切るように配向してい
る炭素繊維強化熱硬化性樹脂複合材を円筒の軸と直角な
方向へ切断し、かつ該切断の前又は後に不活性雰囲気中
での焼成と緻密化とを行うことを特徴とするカーボンブ
レーキの製造法。(3) A cylindrical composite material using carbon fiber as a reinforcing material,
The carbon fiber-reinforced thermosetting resin composite material whose fibers are oriented to cross a plane perpendicular to the axis of the cylinder is cut in a direction perpendicular to the axis of the cylinder, and before or after the cutting, the carbon fiber-reinforced thermosetting resin composite is placed in an inert atmosphere before or after the cutting. A method for manufacturing a carbon brake, characterized by performing firing and densification in a carbon brake.
とする特許請求の範囲(3)の製造法。(4) The manufacturing method according to claim (3), which is characterized in that heat treatment is performed after firing and densification.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11539983A JPS608536A (en) | 1983-06-27 | 1983-06-27 | Carbon brake and manufacture thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11539983A JPS608536A (en) | 1983-06-27 | 1983-06-27 | Carbon brake and manufacture thereof |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28984990A Division JPH03194228A (en) | 1990-10-26 | 1990-10-26 | Carbon brake with reinforced periphery |
| JP28984890A Division JPH03194227A (en) | 1990-10-26 | 1990-10-26 | Carbon brake |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS608536A true JPS608536A (en) | 1985-01-17 |
| JPH0378498B2 JPH0378498B2 (en) | 1991-12-13 |
Family
ID=14661597
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11539983A Granted JPS608536A (en) | 1983-06-27 | 1983-06-27 | Carbon brake and manufacture thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS608536A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62119288A (en) * | 1985-11-19 | 1987-05-30 | Showa Denko Kk | Carbonaceous friction material |
| JPS62285973A (en) * | 1986-06-04 | 1987-12-11 | Japan Vilene Co Ltd | Sheet-form base material for friction material and production thereof |
| JPH03247628A (en) * | 1990-02-23 | 1991-11-05 | Nisshinbo Ind Inc | Non-asbestos friction material |
| JP2013091796A (en) * | 2012-12-13 | 2013-05-16 | Mitsubishi Electric Corp | Friction member and brake |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60010845T3 (en) * | 2000-02-09 | 2011-05-05 | Freni Brembo S.P.A., Curno | Shaped composite material for brakes and method for its manufacture |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5830537A (en) * | 1981-07-01 | 1983-02-23 | ル カルボン−ロレ−ヌ ソシエテ アノニム | Brake disk and its manufacture |
-
1983
- 1983-06-27 JP JP11539983A patent/JPS608536A/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5830537A (en) * | 1981-07-01 | 1983-02-23 | ル カルボン−ロレ−ヌ ソシエテ アノニム | Brake disk and its manufacture |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62119288A (en) * | 1985-11-19 | 1987-05-30 | Showa Denko Kk | Carbonaceous friction material |
| JPS62285973A (en) * | 1986-06-04 | 1987-12-11 | Japan Vilene Co Ltd | Sheet-form base material for friction material and production thereof |
| JPH03247628A (en) * | 1990-02-23 | 1991-11-05 | Nisshinbo Ind Inc | Non-asbestos friction material |
| JP2013091796A (en) * | 2012-12-13 | 2013-05-16 | Mitsubishi Electric Corp | Friction member and brake |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0378498B2 (en) | 1991-12-13 |
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