JPH059458A - Wet friction material - Google Patents

Wet friction material

Info

Publication number
JPH059458A
JPH059458A JP4126991A JP4126991A JPH059458A JP H059458 A JPH059458 A JP H059458A JP 4126991 A JP4126991 A JP 4126991A JP 4126991 A JP4126991 A JP 4126991A JP H059458 A JPH059458 A JP H059458A
Authority
JP
Japan
Prior art keywords
friction material
resin
wet friction
friction
aramid fiber
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
JP4126991A
Other languages
Japanese (ja)
Other versions
JP3192668B2 (en
Inventor
Mikio Fujiwara
幹生 藤原
Kazuhiko Takase
和彦 高瀬
Tomohiro Kanoko
供宏 鹿子
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.)
Tungaloy Corp
Original Assignee
Toshiba Tungaloy 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 Toshiba Tungaloy Co Ltd filed Critical Toshiba Tungaloy Co Ltd
Priority to JP4126991A priority Critical patent/JP3192668B2/en
Publication of JPH059458A publication Critical patent/JPH059458A/en
Application granted granted Critical
Publication of JP3192668B2 publication Critical patent/JP3192668B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To provide the title material which contains aramide fiber and has a high coefficient of friction even at a high sliding speed and under a high load. CONSTITUTION:The title material comprises 5-40wt.% binder phase consisting of a thermosetting resin and a filler component contg. aramide fiber covered with a film of the thermosetting resin, and contains pores. The material has a higher porosity, a smaller difference between the coefficient of dynamic friction and that of static friction, and a higher abrasion resistance than those of conventinally available wet friction materials, while maintaining strengths.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、冷却効果も加味した潤
滑油の存在の下に用いられる、所謂、湿式のブレーキ又
はクラッチフェージングもしくはライニング用に適する
湿式摩擦材料に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a wet friction material suitable for so-called wet brake or clutch fading or lining, which is used in the presence of a lubricating oil having a cooling effect.

【0002】[0002]

【従来の技術】一般に、湿式摩擦材料は、有機系摩擦材
料と無機系摩擦材料に大別できる。この内、有機系摩擦
材料の代表的なものとしては、樹脂と繊維をマトリック
スとする摩擦材料がある。
2. Description of the Related Art Generally, wet friction materials can be roughly classified into organic friction materials and inorganic friction materials. Of these, a typical organic friction material is a friction material having a resin and fibers as a matrix.

【0003】摩擦材料に含有されている繊維としては、
フェノール繊維,ガラス繊維,炭素繊維,アラミド繊維
などがある。これらの内、アラミド繊維は、高強度及び
高弾性率を有していることから摩擦材料に使用されてい
る。
The fibers contained in the friction material include
Examples include phenolic fiber, glass fiber, carbon fiber, and aramid fiber. Of these, aramid fibers are used in friction materials because they have high strength and high elastic modulus.

【0004】アラミド繊維と樹脂とを含有してなる摩擦
材料としての代表的なものに、特開昭59−22137
4号公報,特開昭60−206838号公報及び特開昭
63−67436号公報がある。
A typical friction material containing an aramid fiber and a resin is disclosed in JP-A-59-22137.
4, JP-A-60-206838 and JP-A-63-67436.

【0005】[0005]

【発明が解決しようとする課題】特開昭59−2213
74号公報,特開昭60−206838号公報及び特開
昭63−67436号公報に代表されるアラミド繊維と
樹脂とを含有してなる従来の摩擦材料は、製造方法によ
り異なるが、抄造法で作製する場合には、用紙状の成形
体にする工程、この成形体を切断もしくは切断後に渦巻
状態に積層する工程などで、絡み合った網目状のアラミ
ド繊維の切断面により成形体の面粗度が低下すること、
並びに製造工程が複雑であるという問題がある。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention
Conventional friction materials containing aramid fiber and resin, represented by JP-A-74, JP-A-60-206838 and JP-A-63-67436, differ depending on the manufacturing method. In the case of production, in the step of forming a paper-shaped molded body, the step of cutting this molded body or the step of laminating it in a spiral state after cutting, etc. To fall,
In addition, there is a problem that the manufacturing process is complicated.

【0006】また、摩擦材料を金型などで型成形する場
合には、絡み合った網目状のアラミド繊維がフイブリル
状になりやすく、このために、特に乾式混合時に毛玉状
になり、次工程の金型への振り込みを困難にしている。
このために、摩擦材料に含有させるアラミド繊維の量を
制限する必要があること、仮に、多量のアラミド繊維を
含有させたとしてもアラミド繊維自体の特徴である高強
度性を引き出せないという問題がある。
Further, when the friction material is molded by a mold or the like, the entangled mesh-shaped aramid fibers are likely to be in the form of fibrils, which causes pills to form, especially during dry mixing, and the mold in the next step. Making it difficult to transfer money to.
Therefore, it is necessary to limit the amount of aramid fiber contained in the friction material, and even if a large amount of aramid fiber is contained, there is a problem that the high strength characteristic of the aramid fiber itself cannot be derived. .

【0007】さらに、摩擦材料は、高摺速時の摩擦係数
を向上させるためには気孔率を高めることが好ましいこ
とであるけれども、上述の従来の摩擦材料ではアラミド
繊維の有効な強度を引き出せてないために高気孔率にす
ることが困難であるという問題がある。
Further, it is preferable that the friction material has a higher porosity in order to improve the coefficient of friction at a high sliding speed, but in the above-mentioned conventional friction material, the effective strength of the aramid fiber can be extracted. Since it is not present, there is a problem that it is difficult to achieve high porosity.

【0008】本発明は、上述ような問題点を解決したも
ので、具体的には、樹脂を被覆させたアラミド繊維を含
有させることにより、高強度及び高気孔率を達成させ、
高摺速及び高負荷の使用条件においても高い摩擦係数を
有する湿式摩擦材料の提供を目的とするものである。
The present invention has solved the above-mentioned problems. Specifically, by containing aramid fibers coated with a resin, high strength and high porosity can be achieved.
An object of the present invention is to provide a wet friction material having a high friction coefficient even under use conditions of high sliding speed and high load.

【0009】[0009]

【課題を解決するための手段】本発明者らは、樹脂と繊
維とを含有してなる摩擦材料の強度を高めること及び気
孔率を高めることについて検討していた所、第1に、摩
擦材料に含有させる繊維は、アラミド繊維が好ましいけ
れども、アラミド繊維の切断面が鉤状になり、混合時
に、この鉤状部分の絡みにより毛玉状の塊りが形成され
ること、この毛玉状の塊りが摩擦材料の強度を低下させ
ているという知見を得たものである。
DISCLOSURE OF THE INVENTION The inventors of the present invention have studied how to increase the strength and porosity of a friction material containing a resin and fibers, and firstly, the friction material. Although the aramid fiber is preferable as the fiber to be included in the above, the cut surface of the aramid fiber becomes a hook shape, and during mixing, a pill-like lump is formed by the entanglement of the hook-like portion, and the pill-like lump is rubbed. It was found that the strength of the material was reduced.

【0010】第2に、アラミド繊維に樹脂の被膜を被覆
させると切断面における鉤状の形成が生じなく、従って
毛玉状の塊りも生じなく、これを用いて摩擦材料を作製
すると顕著に強度が向上すること、並びに高強度になる
ことから気孔率を高めても実用可能な強度が得られると
いう知見を得たものである。
Secondly, when the aramid fiber is coated with a resin film, no hook-like formation occurs on the cut surface, and therefore no pill-like lumps occur, and when a friction material is produced using this, the strength is remarkably increased. It has been found that the practical strength can be obtained even if the porosity is increased due to the improvement and the high strength.

【0011】本発明は、上述の第1及び第2の知見に基
づいて本発明を完成するに至ったものである。
The present invention has been completed based on the above-mentioned first and second findings.

【0012】すなわち、本発明の湿式摩擦材料は、5〜
40重量%の熱硬化性樹脂を結合相とし、残部がアラミ
ド繊維を含むフイラーからなる摩擦材料であって、該ア
ラミド繊維が熱硬化性樹脂の被膜で被覆されており、か
つ該摩擦材料に気孔が形成されていることを特徴とする
ものである。
That is, the wet friction material of the present invention comprises 5 to
A friction material comprising a filler containing 40% by weight of a thermosetting resin as a binder phase and the remainder containing aramid fibers, wherein the aramid fibers are covered with a film of the thermosetting resin, and the friction material has pores. Are formed.

【0013】本発明における熱硬化性樹脂は、具体的に
は、例えばフェノール樹脂,ポリイミド樹脂,エポキシ
樹脂,フラン樹脂,キシレン樹脂,ケトン樹脂,尿素樹
脂,メラミン樹脂,アニリン樹脂,スルホンアミド樹
脂,アルキド樹脂を代表例として挙げることができる。
Specific examples of the thermosetting resin in the present invention include phenol resin, polyimide resin, epoxy resin, furan resin, xylene resin, ketone resin, urea resin, melamine resin, aniline resin, sulfonamide resin, and alkyd. Resin can be mentioned as a typical example.

【0014】これらの内、結合相としての熱硬化性樹脂
は、ポリイミド樹脂,やフェノール樹脂が好ましく、ア
ラミド繊維を被覆する被膜としての熱硬化性樹脂は、例
えば、被膜が被覆されたアラミド繊維全体の数重量%具
体的には、約1重量%で効果がありこの被膜は、エポキ
シ樹脂が好ましく、特に結合相がポリイミド樹脂からな
り、アラミド繊維を被覆する被膜がエポキシ樹脂からな
る場合は、強度の向上が顕著であることから好ましいこ
とである。
Of these, the thermosetting resin as the binder phase is preferably a polyimide resin or a phenol resin, and the thermosetting resin as a coating for coating the aramid fiber is, for example, the whole aramid fiber coated with the coating. %, Specifically, about 1% by weight is effective, and this coating is preferably an epoxy resin, especially when the binder phase is composed of a polyimide resin and the coating covering the aramid fiber is composed of an epoxy resin, the strength is Is remarkable, and is preferable.

【0015】本発明におけるアラミド繊維の形状は、摩
擦材料として用いる用途及び形状により異なるけれど
も、製造工程、特にプレス成形時の金型への振込みの容
易性と摩擦材料の強度から直径9〜15μm,長さ0.
2〜1.0mmからなることが好ましく、このアラミド
繊維の含有量は、25重量%以下、好ましくは1〜10
重量%である。
The shape of the aramid fiber in the present invention varies depending on the use and shape used as the friction material, but the diameter of the aramid fiber is 9 to 15 μm in view of the ease of transfer into the mold during the manufacturing process, particularly the press molding and the strength of the friction material. Length 0.
The content of the aramid fiber is preferably 25% by weight or less, preferably 1 to 10 mm.
% By weight.

【0016】本発明におけるフイラーは、具体的には、
例えば、アルミナ,シリカ,ムライト,炭化ケイ素,フ
ッ化カルシウム,二硫化モリブデン,二硫化タングステ
ン,硫酸バリウムなどのセラミックス,天然ゴム,NB
R(アクリロニトリル・ブタジエンゴム),SBR(ス
チレン・ブタジエンゴム),アクリルゴム,ウレタンゴ
ム,シリコンゴム,フッ素ゴムなどのゴム,カーボン,
ガラス,金属,セラミックス,樹脂からなる無機繊維,
金属繊維又は有機繊維,黒鉛,膨張化黒鉛,無定形炭
素,コークスなどの炭素物質,銅,錫,鉄,鉛,黄銅又
はこれらの合金などの金属及びカシューダスト,鉱物質
物などを挙げることができる。
The filler in the present invention is specifically,
For example, alumina, silica, mullite, silicon carbide, calcium fluoride, molybdenum disulfide, tungsten disulfide, ceramics such as barium sulfate, natural rubber, NB
R (acrylonitrile / butadiene rubber), SBR (styrene / butadiene rubber), acrylic rubber, urethane rubber, silicone rubber, rubber such as fluorine rubber, carbon,
Inorganic fiber made of glass, metal, ceramics, resin,
Mention may be made of metal or organic fibers, graphite, expanded graphite, amorphous carbon, carbon materials such as coke, metals such as copper, tin, iron, lead, brass or alloys thereof, cashew dust and minerals. .

【0017】本発明の湿式摩擦材料中に存在させる気孔
は、多くなりすぎると強度低下となり、少なすぎると含
油性及び弾力性に乏しくなることから全体の10〜50
体積%が好ましく、特に30〜50体積%が好ましいこ
とである。また、この気孔は、できるだけ均一に分散さ
せておくのが好ましいことである。
If the number of pores present in the wet friction material of the present invention is too large, the strength will decrease, and if it is too small, the oil impregnation and elasticity will be poor.
Volume% is preferable, and 30 to 50 volume% is particularly preferable. It is also preferable that the pores are dispersed as uniformly as possible.

【0018】本発明の湿式摩擦材料は、結合相が5重量
%未満になると相対的にフイラーが95重量%を超えて
多くなって、強度低下が顕著になること、逆に結合相が
40重量%を超えて多くなると相対的にフイラーが60
重量%未満となって、弾力性に乏しくなること及び摩擦
が生じた時に結合相の塑性流動が大きくなって、摩擦係
数の低下を起こさせる。このために、本発明の湿式摩擦
材料における結合相は、5〜40重量%と定めたもので
ある。
In the wet friction material of the present invention, when the binder phase is less than 5% by weight, the filler is relatively increased to more than 95% by weight and the strength is significantly reduced. When it exceeds more than 60%, the filler is relatively 60.
When the content is less than wt%, the elasticity becomes poor, and when friction occurs, the plastic flow of the binder phase increases and the friction coefficient decreases. Therefore, the binder phase in the wet friction material of the present invention is defined as 5 to 40% by weight.

【0019】本発明の湿式摩擦材料は、従来から行われ
ている摩擦材料の製造方法でもって作製することができ
る。特に、本発明における気孔の形成については、含油
軸受けやフィルターなどの多孔質製品の製造方法を応用
することにより、作製することができるもので、具体的
には、熱硬化性樹脂とフィラーからなる出発物質の中に
加熱焼成時に揮散してしまう造孔物質を添加しておくこ
とである。また、気孔率は、従来と同様に、造孔物質の
量,種類及び揮散処理などの調整によりコントロールす
ることができる。
The wet friction material of the present invention can be manufactured by a conventional friction material manufacturing method. In particular, regarding the formation of pores in the present invention, it can be produced by applying a method for producing a porous product such as an oil-impregnated bearing or a filter, and specifically, a thermosetting resin and a filler. It is to add a pore-forming substance that is volatilized during heating and firing to the starting material. Further, the porosity can be controlled by adjusting the amount and type of the pore-forming substance and the volatilization treatment, as in the conventional case.

【0020】造孔物質としては、例えば、ステアリン
酸,スルファニル酸,スルファミン酸,スルファミン酸
アンモニウム,ナフトール,ニトロフェノール,パラフ
ィン,パラホルムアルデヒド,パルミチン酸,フェノー
ル,無水マレイン酸を挙げることができる。
Examples of the pore-forming substance include stearic acid, sulfanilic acid, sulfamic acid, ammonium sulfamate, naphthol, nitrophenol, paraffin, paraformaldehyde, palmitic acid, phenol and maleic anhydride.

【0021】[0021]

【作用】本発明の湿式摩擦材料は、アラミド繊維を被覆
している熱硬化性樹脂の被膜がアラミド繊維と熱硬化性
樹脂の結合相とを強固に結合させる仲介的作用をすると
共に他のフィラーとの結合をも可能とするものである。
特に、エポキシ樹脂の被膜の場合は、アラミド繊維と被
膜との親和性が高いことからアラミド繊維と被膜との結
合をも強固にする作用をしており、この被膜で被覆され
たアラミド繊維による摩擦材料の高強度化が摩擦材料自
体の気孔を高くしても実用可能な強度を保持させている
ものである。
In the wet friction material of the present invention, the coating of the thermosetting resin coating the aramid fiber has an intermediary function of firmly binding the aramid fiber and the binder phase of the thermosetting resin together with another filler. It is also possible to combine with.
In particular, in the case of a coating of epoxy resin, since it has a high affinity between the aramid fiber and the coating, it also acts to strengthen the bond between the aramid fiber and the coating. Even if the porosity of the friction material itself is increased by increasing the strength of the material, it is possible to maintain the practical strength.

【0022】[0022]

【実施例1】エポキシ樹脂の被膜を被覆したアラミド繊
維、アラミド繊維,チタン酸カリウム繊維,ガラス繊
維,カーボン繊維のそれぞれの平均直径5〜25μm,
平均長さ0.1〜1.0mmと、他にNBR,硫酸バリ
ウム,膨張化黒鉛,カシューダスト,シリカ,ポリイミ
ド樹脂とを用いて表1(重量%)の如くに配合した。こ
の表1のそれぞれの配合試料をV型ミキサーにより混合
した後、外径335mm,内径283mm,深さ5mm
の金型に充填してプレス成形した。得られた成形体を常
温から250℃まで昇温し、250℃で1時間保持し、
焼成を行った。
Example 1 Average diameters of aramid fiber, aramid fiber, potassium titanate fiber, glass fiber and carbon fiber coated with an epoxy resin film are 5 to 25 μm,
An average length of 0.1 to 1.0 mm and NBR, barium sulfate, expanded graphite, cashew dust, silica, and a polyimide resin were used and blended as shown in Table 1 (% by weight). After mixing the respective compounded samples in Table 1 with a V-type mixer, the outer diameter was 335 mm, the inner diameter was 283 mm, and the depth was 5 mm.
It was filled in the mold of No. 1 and press-molded. The obtained molded body is heated from room temperature to 250 ° C. and kept at 250 ° C. for 1 hour,
Firing was performed.

【0023】こうして得た本発明品1〜5及び比較品
1,2の抗折強度,気孔率を測定し、さらに摺速48m
/sec,吸収エネルギー10kgfm/cm2という
高摺速での1万サイクルの耐久試験時における動摩擦係
数,静摩擦係数及び摩耗率を測定し、それぞれの結果を
表2に示した。
The bending strength and the porosity of the products 1 to 5 of the present invention and the comparative products 1 and 2 thus obtained were measured, and the sliding speed was 48 m.
/ Sec and absorbed energy of 10 kgfm / cm 2, the dynamic friction coefficient, the static friction coefficient and the wear rate were measured during a durability test of 10,000 cycles at a high sliding speed. The results are shown in Table 2.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【表2】 [Table 2]

【0026】[0026]

【発明の効果】以上から、本発明の湿式摩擦材料は、被
膜が被覆されてなく、含有量も少ないアラミド繊維入り
の比較の摩擦材料に比べて、気孔率が高いにもかかわら
ず抗折強度が略同等で、動摩擦係数と静摩擦係数の差が
小さく、耐摩耗性が向上しているという効果がある。
As described above, the wet friction material of the present invention has a higher flexural strength in comparison with a comparative friction material containing no aramid fiber, which is not coated with a coating and has a small content, despite its high porosity. Are substantially equal to each other, the difference between the dynamic friction coefficient and the static friction coefficient is small, and the wear resistance is improved.

【0027】このことから、本発明の湿式摩擦材料は、
従来の摩擦材料の用途領域から高負荷又は高摺速の領域
にまで実用できる有用な材料である。
From this, the wet friction material of the present invention is
It is a useful material that can be put into practical use in a range of applications of conventional friction materials to areas of high load or high sliding speed.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 // C08L 33:24 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location // C08L 33:24

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 5〜40重量%の熱硬化性樹脂を結合相
とし、残部がアラミド繊維を含むフイラーからなる摩擦
材料において、該アラミド繊維が熱硬化性樹脂の被膜で
被覆されており、かつ該摩擦材料に気孔が形成されてい
ることを特徴とする湿式摩擦材料。
1. A friction material comprising a filler containing 5 to 40% by weight of a thermosetting resin as a binder phase and the balance comprising aramid fibers, wherein the aramid fibers are coated with a film of a thermosetting resin, and A wet friction material, wherein pores are formed in the friction material.
【請求項2】 上記アラミド繊維が全体の1〜10重量
%含むことを特徴とする湿式摩擦材料。
2. A wet friction material comprising the aramid fiber in an amount of 1 to 10% by weight based on the total weight.
【請求項3】 上記アラミド繊維が直径9〜15μm,
長さ0.2〜1.0mmからなることを特徴とする特許
請求の範囲第1項記載の湿式摩擦材料。
3. The aramid fiber has a diameter of 9 to 15 μm,
The wet friction material according to claim 1, wherein the wet friction material has a length of 0.2 to 1.0 mm.
【請求項4】 上記結合相がポリイミド樹脂からなり、
上記熱硬化性樹脂の被膜がエポキシ樹脂からなることを
特徴とする特許請求の範囲第1項記載の湿式摩擦材料。
4. The binder phase comprises a polyimide resin,
The wet friction material according to claim 1, wherein the coating film of the thermosetting resin is made of an epoxy resin.
【請求項5】 上記気孔が全体の30〜50体積%から
なることを特徴とする特許請求の範囲第1項記載の湿式
摩擦材料。
5. The wet friction material according to claim 1, wherein the pores are 30 to 50% by volume of the whole.
JP4126991A 1991-02-13 1991-02-13 Wet friction material Expired - Fee Related JP3192668B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4126991A JP3192668B2 (en) 1991-02-13 1991-02-13 Wet friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4126991A JP3192668B2 (en) 1991-02-13 1991-02-13 Wet friction material

Publications (2)

Publication Number Publication Date
JPH059458A true JPH059458A (en) 1993-01-19
JP3192668B2 JP3192668B2 (en) 2001-07-30

Family

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Application Number Title Priority Date Filing Date
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Country Link
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09119464A (en) * 1995-06-26 1997-05-06 Wagner Electric Corp Friction brake subassembly
US5662074A (en) * 1994-12-22 1997-09-02 Fuji Jukogyo Kabushiki Kaisha Exhaust port timing control apparatus for two-cycle engine
WO2006116474A2 (en) 2005-04-26 2006-11-02 Borgwarner Inc. Friction material
US7749562B1 (en) 2004-07-26 2010-07-06 Borgwarner Inc. Porous friction material comprising nanoparticles of friction modifying material
US8021744B2 (en) 2004-06-18 2011-09-20 Borgwarner Inc. Fully fibrous structure friction material
CN102261408A (en) * 2010-05-24 2011-11-30 顾贵义 Nanometer mullite automotive brake pad
US8397889B2 (en) 2008-03-12 2013-03-19 Borgwarner Inc. Frictional device comprising at least one friction plate
CN106763367A (en) * 2017-02-28 2017-05-31 佛山佳牧乐科技有限公司 Brake block friction material, brake block and brake piece preparation method
JP2020007394A (en) * 2018-07-03 2020-01-16 ポリプラスチックス株式会社 Liquid crystalline resin composition for sliding wear-resistant members, and sliding wear-resistant member including the same

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5662074A (en) * 1994-12-22 1997-09-02 Fuji Jukogyo Kabushiki Kaisha Exhaust port timing control apparatus for two-cycle engine
JPH09119464A (en) * 1995-06-26 1997-05-06 Wagner Electric Corp Friction brake subassembly
US8021744B2 (en) 2004-06-18 2011-09-20 Borgwarner Inc. Fully fibrous structure friction material
US7749562B1 (en) 2004-07-26 2010-07-06 Borgwarner Inc. Porous friction material comprising nanoparticles of friction modifying material
WO2006116474A2 (en) 2005-04-26 2006-11-02 Borgwarner Inc. Friction material
EP1874850A4 (en) * 2005-04-26 2008-06-18 Borgwarner Inc Friction material
US8397889B2 (en) 2008-03-12 2013-03-19 Borgwarner Inc. Frictional device comprising at least one friction plate
CN102261408A (en) * 2010-05-24 2011-11-30 顾贵义 Nanometer mullite automotive brake pad
CN106763367A (en) * 2017-02-28 2017-05-31 佛山佳牧乐科技有限公司 Brake block friction material, brake block and brake piece preparation method
CN106763367B (en) * 2017-02-28 2018-11-16 佛山佳牧乐科技有限公司 Brake block friction material, brake block and brake piece preparation method
JP2020007394A (en) * 2018-07-03 2020-01-16 ポリプラスチックス株式会社 Liquid crystalline resin composition for sliding wear-resistant members, and sliding wear-resistant member including the same

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