JPH11209744A - Abrading material composition and abrading material using the same - Google Patents
Abrading material composition and abrading material using the sameInfo
- Publication number
- JPH11209744A JPH11209744A JP1627698A JP1627698A JPH11209744A JP H11209744 A JPH11209744 A JP H11209744A JP 1627698 A JP1627698 A JP 1627698A JP 1627698 A JP1627698 A JP 1627698A JP H11209744 A JPH11209744 A JP H11209744A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- resin
- boron carbide
- composition
- glassy 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
Links
Landscapes
- Braking Arrangements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、自動車、鉄道車
両、各種産業機械等の制動に用いられるディスクブレー
キパッド、ブレーキライニング等の摩擦材に適した摩擦
材組成物及び該摩擦材組成物を用いた摩擦材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material composition suitable for a friction material such as a disc brake pad and a brake lining used for braking automobiles, railway vehicles, various industrial machines, and the like, and to use of the friction material composition. Friction material.
【0002】[0002]
【従来の技術】自動車、鉄道車両、各種産業機械等に
は、その制動のためディスクブレーキパッド、ブレーキ
ライニング等の摩擦材が使用されている。この摩擦材と
して、従来は特開昭64−87930号公報、特開平2
−117985号公報等に示されるようにスチール繊維
を主構成繊維としたセミメタリック系摩擦材が主流であ
ったが、自動車産業界の軽量化、高級化への移行に沿っ
て、オートマチック車の発進時や停止時の異音発生、低
温での制動力不足、摩耗粉によるホイール汚れ等の問題
点が出て来た。ここで発生する異音は、速度が30km/
時間程度から減速していく過程で現われる摩擦材の制動
に伴うノイズ(70dB以上の音圧)であり、周波数では
約100(Hz)の乗用者に不快を感ずる領域の音であ
る。2. Description of the Related Art Friction materials such as disc brake pads and brake linings are used in automobiles, railway vehicles, various industrial machines and the like for braking. Conventionally, as this friction material, Japanese Patent Application Laid-Open No.
As shown in JP-A-117985, semi-metallic friction materials containing steel fibers as a main constituent fiber were the mainstream, but automatic vehicles were launched in line with the shift to lighter and more sophisticated automobile industries. Problems such as generation of abnormal noise at the time of stoppage and stoppage, insufficient braking force at low temperatures, and wheel contamination due to abrasion powder have come up. The abnormal noise generated here has a speed of 30 km /
This is noise (sound pressure of 70 dB or more) associated with braking of the friction material that appears in the process of decelerating from about time, and is a sound of a frequency of about 100 (Hz) in a region where a passenger feels uncomfortable.
【0003】これらの問題点を解消するため、スチール
繊維の代替として銅繊維、黄銅繊維等の非鉄金属繊維、
アラミド繊維、セラミック繊維等の有機繊維や無機繊
維、さらに安定した摩擦係数(μ≧0.42)を得るた
めに無機材料の研削剤を使用したノンスチール摩擦材へ
の移行が急速に進んできた。[0003] In order to solve these problems, non-ferrous metal fibers such as copper fiber and brass fiber are used instead of steel fiber.
The transition to organic and inorganic fibers such as aramid fibers and ceramic fibers, and non-steel friction materials using abrasives of inorganic materials in order to obtain a more stable friction coefficient (μ ≧ 0.42) has rapidly progressed. .
【0004】従来の技術では、上記の無機材料の研削剤
によって摩擦係数の安定化を図ってきたが、しかしなが
ら該研削剤は相手材の金属(ロータ)を攻撃し、その過
程でスキール音、異音等のノイズやジャダーが発生する
という欠点が生じる。ノイズやジャダーの発生を防止す
るには研削剤の使用を中止したり、使用量を低減すれば
よいが、このようにすると安定した摩擦係数を得ること
ができない。またSiO2、Al2O3、ZrO2、ZrS
iO3等の酸化物を含む研削材を用いると、ガラス状炭
素を構成している炭素が消失するという欠点が生じる。
現在の無機材料主体の研削剤以外のものを使用して、安
定した摩擦係数を有し、かつノイズやジャダーの発生を
完全に抑制した摩擦材が得られていないのが現状であ
る。In the prior art, the friction coefficient has been stabilized by the above-mentioned inorganic material abrasive. However, the abrasive attacks the metal (rotor) of the counterpart material, and in the process, squeal noise and abnormal noise are generated. There is a disadvantage that noise such as sound and judder are generated. In order to prevent the generation of noise and judder, the use of the abrasive may be stopped or the amount of the abrasive may be reduced, but in this case, a stable friction coefficient cannot be obtained. SiO 2 , Al 2 O 3 , ZrO 2 , ZrS
When an abrasive containing an oxide such as iO 3 is used, there is a disadvantage that carbon constituting glassy carbon disappears.
At present, a friction material having a stable friction coefficient and completely suppressing generation of noise and judder has not been obtained by using a material other than the current inorganic material-based abrasive.
【0005】[0005]
【発明が解決しようとする課題】請求項1記載の発明
は、安定した摩擦係数を有し、かつノイズやジャダーの
発生を抑えることができる摩擦材に適した摩擦材組成物
を提供するものである。請求項2記載の発明は、安定し
た摩擦係数を有し、かつノイズやジャダーの発生を抑え
ることが可能な摩擦材を提供するものである。SUMMARY OF THE INVENTION The present invention provides a friction material composition suitable for a friction material having a stable friction coefficient and capable of suppressing generation of noise and judder. is there. The invention described in claim 2 provides a friction material having a stable friction coefficient and capable of suppressing generation of noise and judder.
【0006】[0006]
【課題を解決するための手段】本発明は、全組成物中に
ガラス状炭素を0.3〜23重量%及び炭化ホウ素を
0.1〜15重量%含有してなる摩擦材組成物に関す
る。また、本発明は、上記の摩擦材組成物を加熱加圧し
てなる摩擦材に関する。The present invention relates to a friction material composition comprising 0.3 to 23% by weight of glassy carbon and 0.1 to 15% by weight of boron carbide in the total composition. The present invention also relates to a friction material obtained by heating and pressurizing the above friction material composition.
【0007】[0007]
【発明の実施の形態】本発明において、ガラス状炭素の
含有量は全組成物中に0.3〜23重量%、好ましくは
0.5〜22重量%、より好ましくは2〜20重量%の
範囲とされ、0.3重量%未満であると研削剤としての
効果が十分に機能せず、安定した摩擦係数を得ることが
できない。一方23重量%を超えるとノイズやジャダー
の発生を抑えることができない。ガラス状炭素は、例え
ば液状の熱硬化性樹脂を硬化させた後、不活性雰囲気中
で炭化及び高温処理(黒鉛化処理)することにより得ら
れるが、本発明においては、熱硬化性樹脂を硬化させる
前に炭化ホウ素を均一に混合した後加熱処理を行なって
硬化させ、その後不活性雰囲気中で炭化及び高温処理
(黒鉛化処理)し、これを粉砕して使用される。DETAILED DESCRIPTION OF THE INVENTION In the present invention, the content of glassy carbon in the total composition is from 0.3 to 23% by weight, preferably from 0.5 to 22% by weight, more preferably from 2 to 20% by weight. When the content is less than 0.3% by weight, the effect as a grinding agent does not function sufficiently, and a stable friction coefficient cannot be obtained. On the other hand, if it exceeds 23% by weight, generation of noise and judder cannot be suppressed. Glassy carbon can be obtained by, for example, curing a liquid thermosetting resin, and then carbonizing and high-temperature treatment (graphitization treatment) in an inert atmosphere. In the present invention, the thermosetting resin is cured. Before the boronization, the boron carbide is uniformly mixed and then subjected to a heat treatment to harden, followed by carbonization and high-temperature treatment (graphitization treatment) in an inert atmosphere, and pulverized.
【0008】ガラス状炭素を得るための熱硬化性樹脂と
しては特に制限はないが、フラン樹脂、フェノール樹
脂、エポキシ樹脂、不飽和ポリエステル樹脂、メラミン
樹脂、アルキッド樹脂、キシレン樹脂等を挙げることが
できる。また、上記の樹脂の混合物を用いてもよい。本
発明においては上記の熱硬化性樹脂の他に必要に応じ、
トリクロロ酢酸、パラトルエンスルホン酸、硫酸等の硬
化剤が添加される。必要に応じ硬化剤が添加される場
合、熱硬化性樹脂と硬化剤の配合割合は、熱硬化性樹脂
100重量部に対して硬化剤が0.3〜10重量部の範
囲が好ましく、熱硬化性樹脂100重量部に対し硬化剤
が0.3〜7重量部の範囲であることがさらに好まし
い。The thermosetting resin for obtaining the glassy carbon is not particularly limited, and examples thereof include a furan resin, a phenol resin, an epoxy resin, an unsaturated polyester resin, a melamine resin, an alkyd resin, and a xylene resin. . Further, a mixture of the above resins may be used. In the present invention, if necessary in addition to the above thermosetting resin,
A curing agent such as trichloroacetic acid, paratoluenesulfonic acid, sulfuric acid and the like is added. When a curing agent is added as necessary, the mixing ratio of the thermosetting resin and the curing agent is preferably in the range of 0.3 to 10 parts by weight of the curing agent per 100 parts by weight of the thermosetting resin. More preferably, the curing agent is in the range of 0.3 to 7 parts by weight based on 100 parts by weight of the conductive resin.
【0009】また、炭化ホウ素は全組成物中に0.1〜
15重量%、好ましくは1〜13重量%、さらに好まし
くは3〜10重量%の範囲とされ、0.1重量%未満で
あると研削剤としての効果はある程度機能するが安定し
た摩擦係数(μ≧0.42)の目標に対して(μ≧0.
35)しか得ることができない。一方15重量%を超え
るとノイズやジャダーの発生を抑えることができない。[0009] Boron carbide is contained in the total composition in an amount of from 0.1 to 0.1%.
The content is 15% by weight, preferably 1 to 13% by weight, and more preferably 3 to 10% by weight. When the content is less than 0.1% by weight, the effect as a grinding agent functions to some extent, but the stable friction coefficient (μ ≧ 0.42) for the target (μ ≧ 0.
35) can only be obtained. On the other hand, if it exceeds 15% by weight, generation of noise and judder cannot be suppressed.
【0010】本発明における摩擦材組成物は、ガラス状
炭素及び炭化ホウ素の他に結合剤、補強繊維、潤滑剤、
充填剤等が用いられ、さらに必要に応じ黄銅、しんちゅ
う等の金属粉が用いられる。本発明で用いられる結合剤
は、フェノール樹脂を用いることが好ましく、特にノボ
ラック樹脂、固形アンモニアレゾール樹脂、シリコン変
成フェノール樹脂、アクリル変成ゴムフェノール樹脂を
用いることが好ましい。本発明では上記結合剤に必要に
応じ硬化剤が添加される。結合剤は全組成物中に5〜2
0重量%含有することが好ましく、8〜14重量%含有
することがさらに好ましい。また必要に応じ添加される
硬化剤は、ヘキサメチレンテトラミン、パラホルムアル
デヒド、トリオキサン等が用いられ、結合剤中に8〜1
4重量%含有することが好ましく、10〜12重量%含
有することがさらに好ましい。[0010] The friction material composition of the present invention comprises, in addition to glassy carbon and boron carbide, a binder, a reinforcing fiber, a lubricant,
A filler or the like is used, and if necessary, metal powder such as brass or brass is used. The binder used in the present invention is preferably a phenol resin, and particularly preferably a novolak resin, a solid ammonia resol resin, a silicon-modified phenol resin, or an acrylic-modified rubber phenol resin. In the present invention, a curing agent is added to the binder as needed. The binder is present in the total composition at 5-2.
The content is preferably 0% by weight, more preferably 8 to 14% by weight. As a curing agent added as needed, hexamethylenetetramine, paraformaldehyde, trioxane, or the like is used.
The content is preferably 4% by weight, more preferably 10 to 12% by weight.
【0011】補強繊維としては、ガラス繊維、セラミッ
ク繊維、炭素繊維、鉱物繊維等の無機繊維、アラミド繊
維、ポリアミド繊維、ポリイミド繊維等の有機繊維、銅
繊維、黄銅繊維、スチール繊維等の金属繊維が用いられ
る。補強繊維は全組成物中に0.5〜16重量%含有す
ることが好ましく、3〜10重量%含有することがさら
に好ましい。Examples of the reinforcing fibers include inorganic fibers such as glass fibers, ceramic fibers, carbon fibers, and mineral fibers; organic fibers such as aramid fibers, polyamide fibers, and polyimide fibers; and metal fibers such as copper fibers, brass fibers, and steel fibers. Used. The reinforcing fiber is preferably contained in the entire composition in an amount of 0.5 to 16% by weight, more preferably 3 to 10% by weight.
【0012】また潤滑剤としては、黒鉛、硫化アンチモ
ン、硫化モリブデン等が、充填剤としては、カシューダ
スト、ゴムダスト、硫酸バリウム、炭酸カルシウム、炭
酸マグネシウム、シリカ、金属粉等が一種又は二種以上
混合して用いられる。潤滑剤は全組成物中に2〜8重量
%含有することが好ましく、3〜6重量%含有すること
がさらに好ましい。充填剤は全組成物中に10〜60重
量%含有することが好ましく、20〜50重量%含有す
ることがさらに好ましい。摩擦材組成物を構成する各成
分の使用割合は、それらの総量が100重量%になるよ
うに調整される。As the lubricant, graphite, antimony sulfide, molybdenum sulfide and the like are used. As the filler, cashew dust, rubber dust, barium sulfate, calcium carbonate, magnesium carbonate, silica, metal powder and the like are mixed. Used as The lubricant is preferably contained in the entire composition at 2 to 8% by weight, more preferably at 3 to 6% by weight. The filler is preferably contained in the entire composition in an amount of 10 to 60% by weight, more preferably 20 to 50% by weight. The usage ratio of each component constituting the friction material composition is adjusted so that the total amount thereof becomes 100% by weight.
【0013】本発明になる摩擦材は、金型内に裏金及び
摩擦材組成物を挿入及び充填した後、加熱加圧成形法で
一体成形するか又は加熱加圧成形後、接着剤を用いて裏
金と接着し、その後熱処理を行って得られる。なお摩擦
材を製造する際の加熱温度は130〜170℃が好まし
く130〜160℃がさらに好ましい。圧力は30〜6
0MPaが好ましく、35〜55MPaがさらに好ましい。熱
処理温度は100〜300℃が好ましく、150〜25
0℃がさらに好ましい。The friction material according to the present invention is obtained by inserting and filling a backing metal and a friction material composition in a mold, and then integrally molding by a heat and pressure molding method, or by using an adhesive after heating and pressure molding. It is obtained by bonding to the back metal and then performing heat treatment. The heating temperature at the time of producing the friction material is preferably from 130 to 170 ° C, more preferably from 130 to 160 ° C. Pressure is 30-6
0 MPa is preferable and 35-55 MPa is more preferable. The heat treatment temperature is preferably 100 to 300 ° C, and 150 to 25 ° C.
0 ° C. is more preferred.
【0014】[0014]
【実施例】以下本発明の実施例を説明するが、本発明は
これに制限するものではない。 実施例1〜9、比較例1〜8 黒鉛化処理後のガラス状炭素が表1及び表2になる量の
レゾール型フラン樹脂(日立化成工業(株)製、商品名V
P−13N)と炭化ホウ素を表1及び表2に示す量配合
し、均一に混合した後保温器に入れ、10℃/時間の昇
温速度で160℃まで昇温し、160℃で5時間保持し
て硬化処理を行い炭化ホウ素含有樹脂板を得た。EXAMPLES Examples of the present invention will be described below, but the present invention is not limited thereto. Examples 1 to 9 and Comparative Examples 1 to 8 Resor-type furan resins (manufactured by Hitachi Chemical Co., Ltd., trade name V
P-13N) and boron carbide were blended in the amounts shown in Tables 1 and 2, mixed uniformly, put into a warmer, heated to 160 ° C at a rate of 10 ° C / hour, and heated at 160 ° C for 5 hours. The resin was held and cured to obtain a boron carbide-containing resin plate.
【0015】次に炭化ホウ素含有樹脂板を、窒素ガス雰
囲気中で1000℃で30日保持して炭化焼成し、その
後2000℃まで昇温させ、2000℃で10時間保持
して黒鉛化処理を行い、炭化ホウ素含有ガラス状炭素を
得た。得られた炭化ホウ素含有ガラス状炭素は、厚みが
2.0〜3.5mmの範囲で、密度が1.58g/cm3、電
気比抵抗が9000μΩ−cm及び20〜400℃の熱膨
張係数が2.6×10-6deg-1であった。Next, the boron carbide-containing resin plate is carbonized and calcined at 1000 ° C. for 30 days in a nitrogen gas atmosphere, then heated to 2000 ° C., and held at 2000 ° C. for 10 hours to perform graphitization. Thus, a boron carbide-containing glassy carbon was obtained. The obtained boron carbide-containing glassy carbon has a thickness of 2.0 to 3.5 mm, a density of 1.58 g / cm 3 , an electrical resistivity of 9000 μΩ-cm, and a thermal expansion coefficient of 20 to 400 ° C. It was 2.6 × 10 −6 deg −1 .
【0016】上記で得た炭化ホウ素含有ガラス状炭素を
粉砕して平均粒径が7μmの炭化ホウ素含有ガラス状炭
素粉を得た。次いでこの炭化ホウ素含有ガラス状炭素粉
と表1及び表2に示す成分を配合し、混合機で均一に混
合して摩擦材組成物を得た。この後、140℃、圧力4
0MPaの条件で12分間加熱加圧成形し、さらに200
℃で5時間熱処理を行ってディスクブレーキパッドを得
た。The boron carbide-containing glassy carbon obtained above was pulverized to obtain a boron carbide-containing glassy carbon powder having an average particle diameter of 7 μm. Next, the boron carbide-containing glassy carbon powder and the components shown in Tables 1 and 2 were blended and uniformly mixed by a mixer to obtain a friction material composition. After this, 140 ° C, pressure 4
Heat and pressure molding for 12 minutes under the condition of 0MPa, further 200
Heat treatment was performed at 5 ° C. for 5 hours to obtain a disc brake pad.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】次に本発明になるディスクブレーキパッド
と比較例のディスクブレーキパッドとについて、比較試
験を行った。その試験結果を表3及び表4に示す。なお
試験条件は下記の通りである。 剪断強度 JASO、C427に従い、22℃及び300℃におけ
る強度を測定した。 耐摩耗性 キャリパ型式:コレットタイプ(シリンダ面積28.8
cm2) 試験条件:JASO、C427に従い、イナーシャ…4
9kgm2、制動初速度…60km/時間、減速度…2.94
m/秒2、制動前温度…250℃、制動回数…各100
0回毎の条件で摩耗量を測定した。Next, a comparative test was performed on the disc brake pad according to the present invention and the disc brake pad of the comparative example. The test results are shown in Tables 3 and 4. The test conditions are as follows. Shear strength The strength at 22 ° C and 300 ° C was measured according to JASO, C427. Wear resistance Caliper model: Collet type (cylinder area 28.8
cm 2 ) Test conditions: Inertia according to JASO, C427 ... 4
9kgm 2 , initial braking speed: 60km / h, deceleration: 2.94
m / sec. 2, braking before temperature ... 250 ℃, braking number of times ... each 100
The wear amount was measured under the condition of every 0 times.
【0020】 異音の発生状況及び効力 2000ccのオートマチック車(日産自動車(株)製、車
種名セドリック(Y32))でJASO、C402の実
車試験を行い、試験中の異音を測定し、70dB以上の異
音の発生率及び最大音圧を求めた。また効力について
は、試験中のディスクブレーキとしての効力をμ値で、
相手材表面攻撃量をロータの研削量で評価した。 成形性 ディスクブレーキパッドの外観を目視し、皺及び亀裂の
発生の有無について観察した。[0020] Abnormal noise generation status and effectiveness JASO, C402 actual vehicle test was performed on a 2000 cc automatic vehicle (model name Cedric (Y32) manufactured by Nissan Motor Co., Ltd.), and the abnormal noise during the test was measured. The occurrence rate of abnormal noise and the maximum sound pressure were determined. As for the effect, the effect as a disc brake during the test is expressed in μ value,
The amount of attack on the surface of the mating material was evaluated by the amount of grinding of the rotor. Formability The appearance of the disc brake pad was visually observed, and the occurrence of wrinkles and cracks was observed.
【0021】[0021]
【表3】 [Table 3]
【0022】[0022]
【表4】 [Table 4]
【0023】表3に示されるように、本発明になるディ
スクブレーキパッドは、皺及び亀裂の発生がなく、全て
の特性に優れることが確認された。これに対し表4に示
されるように、比較例のディスクブレーキパッドは、い
ずれかの特性に欠点が生じ、良好な結果が得られなかっ
た。As shown in Table 3, it was confirmed that the disc brake pad according to the present invention was free from wrinkles and cracks and was excellent in all properties. On the other hand, as shown in Table 4, in the disc brake pad of the comparative example, a defect occurred in any of the characteristics, and good results were not obtained.
【0024】[0024]
【発明の効果】請求項1における摩擦材組成物は、安定
した摩擦係数(μ≧0.42)を有し、かつノイズ発生
やジャダー発生を抑えることができる摩擦材を提供する
ことができる。請求項2における摩擦材は、安定した摩
擦係数(μ≧0.42)を有し、かつノイズ発生やジャ
ダー発生を抑えることが可能で、工業的に極めて好適で
ある。The friction material composition according to claim 1 can provide a friction material having a stable friction coefficient (μ ≧ 0.42) and capable of suppressing generation of noise and judder. The friction material according to claim 2 has a stable friction coefficient (μ ≧ 0.42) and can suppress generation of noise and judder, and is industrially extremely suitable.
Claims (2)
3重量%及び炭化ホウ素を0.1〜15重量%含有して
なる摩擦材組成物。1. A glassy carbon in a total composition of 0.3 to 2%.
A friction material composition containing 3% by weight and 0.1 to 15% by weight of boron carbide.
成形してなる摩擦材。2. A friction material formed by heating and pressing the friction material composition according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1627698A JPH11209744A (en) | 1998-01-29 | 1998-01-29 | Abrading material composition and abrading material using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1627698A JPH11209744A (en) | 1998-01-29 | 1998-01-29 | Abrading material composition and abrading material using the same |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH11209744A true JPH11209744A (en) | 1999-08-03 |
Family
ID=11912037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1627698A Pending JPH11209744A (en) | 1998-01-29 | 1998-01-29 | Abrading material composition and abrading material using the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH11209744A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008247963A (en) * | 2007-03-29 | 2008-10-16 | Mitsubishi Motors Corp | Lignocellulose material molding and its molding method |
-
1998
- 1998-01-29 JP JP1627698A patent/JPH11209744A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008247963A (en) * | 2007-03-29 | 2008-10-16 | Mitsubishi Motors Corp | Lignocellulose material molding and its molding method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5041471A (en) | Friction materials with universal core of non-asbestos fibers | |
KR100765638B1 (en) | Environmental friendly double-layer composition for automotive friction materials and its preparing method | |
US5712029A (en) | Friction material | |
JP2011016877A (en) | Friction material and brake shoe of brake device | |
JP6440947B2 (en) | Friction material composition, friction material using friction material composition, and friction member | |
JPH10330732A (en) | Friction material composition and friction material made therefrom | |
KR101035240B1 (en) | A low-steel type friction material and a brake for vehicle comprising the low-steel type friction material | |
US20230243395A1 (en) | Binder-Free Friction Linings, Process for Their Production and Their Use | |
JPH10195420A (en) | Friction material | |
JPH11209744A (en) | Abrading material composition and abrading material using the same | |
JP2000026839A (en) | Friction material composition, production of same, and friction material made from same | |
JP2007113642A (en) | Friction couple and friction material | |
JP4308054B2 (en) | Brake friction material | |
JP2000026838A (en) | Friction material composition and friction material using the same | |
JPH10130627A (en) | Friction material composition and production of friction material therefrom | |
JP2009298847A (en) | Friction material | |
JPH05255657A (en) | Friction material | |
JP2000204350A (en) | Friction material composition and friction material using the same | |
JP3068798B2 (en) | Friction material | |
JPH10273647A (en) | Friction material composition, its production and production of friction material using the same | |
JP2000204349A (en) | Friction material composition and friction material using the same | |
JP2002097455A (en) | Friction material composition and friction material obtained by using the same | |
JPH05320622A (en) | Friction material | |
JPH11131055A (en) | Friction material composition, its production and friction material using the composition | |
JP3228096B2 (en) | Manufacturing method of friction material |