JPH0770336A - Friction material - Google Patents

Friction material

Info

Publication number
JPH0770336A
JPH0770336A JP15341393A JP15341393A JPH0770336A JP H0770336 A JPH0770336 A JP H0770336A JP 15341393 A JP15341393 A JP 15341393A JP 15341393 A JP15341393 A JP 15341393A JP H0770336 A JPH0770336 A JP H0770336A
Authority
JP
Japan
Prior art keywords
friction
substrate
binder
lead acetate
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.)
Pending
Application number
JP15341393A
Other languages
Japanese (ja)
Inventor
Toichi Sakata
淘一 坂田
秀次 ▲くわ▼島
Hideji Kuwashima
Masaaki Yasuda
雅昭 安田
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.)
Showa Denko Materials Co Ltd
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP15341393A priority Critical patent/JPH0770336A/en
Publication of JPH0770336A publication Critical patent/JPH0770336A/en
Pending legal-status Critical Current

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  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

PURPOSE:To obtain a friction material excellent in high-temp. friction properties and suitable for an automotive brake, etc., by depositing lead acetate on the surface of a fiber substrate, then impregnating or mixing the substrate with a mixture of a friction modifier and a binder, and molding and curing the resulting product. CONSTITUTION:Lead acetate is deposited on the surface of a fiber substrate such as a glass fiber or a rock wool, e.g. by impregnating the substrate with a lead acetate soln. or dispersion and drying the impregnated substrate. The substrate is then impregnated with a slurrylike mixture contg. a friction modifier such as calcium carbonate or barium sulfate and a binder such as a phenol resin to uniformly deposit the mixture on the substrate, dried to remove the solvent, thermally press-molded with a metal mold, etc., and heat-treated under specified conditions to cure the binder, thus giving a friction material which is asbestos-free and hence pollution-free.

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、自動車の動力伝達、制
動等に用いる摩擦材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material used for power transmission and braking of automobiles.

【0002】[0002]

【従来の技術】自動車に用いる摩擦材としては、一般に
ブレーキライニング、ディスクパッド及びクラッチフェ
ーシングがある。これらは従来、石綿(アスベスト)を
基材として使用していたが、アスベスト公害の問題から
非アスベスト系摩擦材の開発が望まれている。又、自動
車エンジンの性能向上に伴い摩擦材の摩擦特性(摩擦係
数、摩耗率)、機械特性の向上が望まれている。更に最
近は使用条件が苛酷になり高温時の高速回転強度も要求
されるようになってきている。現在、石綿基材の代替材
として、ガラス繊維、炭素繊維、芳香族ポリアミド繊
維、ロックウール、セラミック繊維、各種のスチームフ
ァイバー等を使用した摩擦材が開発され、一部で使用さ
れている。しかし、これらの基材は従来の石綿に比べて
高弾性で硬く、耐熱性が低いために、摩擦材にした場合
に種々の問題があり、上記した要求される性能を満足し
ない。
Brake linings, disc pads and clutch facings are generally used as friction materials for automobiles. Conventionally, asbestos (asbestos) has been used as a base material, but development of a non-asbestos friction material is desired due to the problem of asbestos pollution. Further, as the performance of automobile engines is improved, it is desired to improve the friction characteristics (friction coefficient, wear rate) and mechanical characteristics of friction materials. Furthermore, recently, the usage conditions have become severe, and high-speed rotation strength at high temperatures has been required. At present, friction materials using glass fibers, carbon fibers, aromatic polyamide fibers, rock wool, ceramic fibers, various steam fibers, etc. have been developed and used as a substitute for asbestos base materials. However, since these base materials have higher elasticity and hardness and lower heat resistance than conventional asbestos, there are various problems when used as a friction material, and the above-mentioned required performance is not satisfied.

【0003】[0003]

【発明が解決しようとする課題】石綿代替材を使用し高
温で高負荷に耐える摩擦材として、あらかじめ摩擦材自
身を高温処理したもの(例えば特開昭56−13184
6号公報、同59−113038号公報、同60−14
5302号公報等)があるが、これはコスト高や機械強
度の低下を伴う。特殊な摩擦調整剤を添加したもの(例
えば特開昭60−96625号公報、同60−9233
2号公報、同62−190232号公報等)もあるが、
従来の結合剤では耐熱性と接着性が不足しているためそ
の効果を十分発揮できない。又基材に耐熱性の高いアラ
ミド繊維やポリイミド樹脂粉を加えたものなどが開示さ
れているが、基材及び摩擦調整剤を保持する結合剤の耐
熱性は充分でなく高温強度が得られない。たとえ耐熱性
樹脂を結合剤として使用し摩擦材を得ようとしても、従
来の製造方法では工業的、技術的に困難である。
As a friction material which uses an asbestos substitute material and withstands a high load at a high temperature, the friction material itself is preliminarily treated at a high temperature (for example, JP-A-56-13184).
6, gazette 59-113038 gazette, gazette 60-14.
No. 5302, etc.), but this involves a high cost and a decrease in mechanical strength. Those to which a special friction modifier is added (for example, JP-A-60-96625 and JP-A-60-9233).
No. 2, gazette, No. 62-190232, etc.),
Since the conventional binder lacks heat resistance and adhesiveness, its effect cannot be fully exhibited. Also, a material such as aramid fiber or polyimide resin powder having high heat resistance is added to the base material, but the heat resistance of the binder holding the base material and the friction modifier is not sufficient and high temperature strength cannot be obtained. . Even if a heat resistant resin is used as a binder to obtain a friction material, the conventional manufacturing method is industrially and technically difficult.

【0004】更に、摩擦特性を改善するために摩擦調整
剤の添加量に自由度がもてるモールド成形法で製造した
摩擦材もあるが、繊維基材として短繊維を用いるため繊
維強度に難点があり、製品化はごく一部に限られてい
る。
Further, there is a friction material produced by a molding method which has a degree of freedom in the addition amount of a friction modifier for improving friction characteristics, but since short fibers are used as a fiber base material, there is a problem in fiber strength. Yes, commercialization is limited to a small part.

【0005】本発明は、上記した問題を解消し、高温高
負荷の条件下でも安定した摩擦特性を有する摩擦材を提
供するものである。
The present invention solves the above problems and provides a friction material having stable friction characteristics even under high temperature and high load conditions.

【0006】[0006]

【課題を解決するための手段】本発明は表面に酢酸鉛を
付着させた繊維基材に、摩擦調整剤及び結合剤を含む混
和物を含浸又は混合し、成形硬化してなる摩擦材に関す
る。
SUMMARY OF THE INVENTION The present invention relates to a friction material obtained by impregnating or mixing a mixture containing a friction modifier and a binder into a fiber base material having lead acetate adhered to the surface thereof, followed by molding and curing.

【0007】本発明において繊維基材の材質としては、
ガラス繊維、炭素繊維、ロックウール、セラミツク繊維
等の無機繊維、鉄線等の金属線、フェノール樹脂繊維、
芳香族ポリアミド樹脂繊維等の有機繊維などがあり、特
に制限はないが、加工の容易なこと、安価なことなどか
らガラス繊維が好ましい。繊維基材の形状としては、マ
ット、フェルト等の不織布、抄造シート、織布等のシー
ト状基材、短繊維状基材、撚糸ヤーン等の紐状基材など
がある。繊維基材は摩擦材中に25〜60重量%含有さ
せると摩擦特性のバランスが良好なので好ましい。より
好ましい値は30〜50重量%である。
In the present invention, as the material of the fiber base material,
Inorganic fiber such as glass fiber, carbon fiber, rock wool, ceramic fiber, metal wire such as iron wire, phenol resin fiber,
Organic fibers such as aromatic polyamide resin fibers are available, and there is no particular limitation, but glass fibers are preferred because they are easy to process and inexpensive. Examples of the shape of the fibrous base material include non-woven fabrics such as mats and felts, sheet-like base materials such as papermaking sheets and woven fabrics, short fibrous base materials, and string-like base materials such as twisted yarns. It is preferable that the fibrous base material is contained in the friction material in an amount of 25 to 60% by weight because the friction characteristics are well balanced. A more preferable value is 30 to 50% by weight.

【0008】本発明に用いる繊維基材はその表面に酢酸
鉛を付着させる。付着させる方法としては酢酸鉛の溶液
又は分散液に繊維基材を浸漬した後、乾燥して溶媒を除
去する方法がある。酢酸鉛の溶液又は分散液としては、
結合剤溶液に酢酸鉛を分散又は溶解させたものや水溶液
があげられるが、特に水溶液を用いるのが好ましい。
Lead acetate is attached to the surface of the fiber base material used in the present invention. As a method of attaching, there is a method of immersing the fiber base material in a solution or dispersion of lead acetate and then drying it to remove the solvent. As a solution or dispersion of lead acetate,
Examples of the binder solution include lead acetate dispersed or dissolved and an aqueous solution, and it is particularly preferable to use an aqueous solution.

【0009】付着させる酢酸鉛の量は、繊維基材に対
し、鉛量として5〜50重量%が高温時におけるガラス
繊維等の固着性、高温時の摩擦特性の面から好ましい。
より好ましくは10〜30重量%である。
The amount of lead acetate to be adhered is preferably 5 to 50% by weight with respect to the fiber base material, from the viewpoints of adhesion of glass fibers and the like at high temperatures and friction characteristics at high temperatures.
It is more preferably 10 to 30% by weight.

【0010】摩擦調整剤としては、炭酸カルシウム、珪
酸カルシウム、炭酸マグネシウム、硫酸バリウム、クレ
ー、タルク、黒鉛、カーボンブラック、アルミナ、マイ
カ、蛍石、ジルコニア、ヘマタイト、マグネタイト、シ
リカ、硫化アンチモン、三酸化アンチモン、硫化鉄、硫
化モリブデン等の各種の無機物の粉末及び短繊維、銅、
鉄、鉛等の金属の粉末、カシューダスト、メラミン樹脂
硬化物の粉末(メラミンダスト)、ゴムダスト、各種樹
脂硬化物の粉末等の有機物の粉末などが使用される。摩
擦調整剤は得られる摩擦材中に10〜60重量%含有さ
せると安定した摩擦係数が得られ、摩耗量とのバランス
に優れるので好ましい。より好ましくは20〜40重量
%である。
Friction modifiers include calcium carbonate, calcium silicate, magnesium carbonate, barium sulfate, clay, talc, graphite, carbon black, alumina, mica, fluorspar, zirconia, hematite, magnetite, silica, antimony sulfide, trioxide. Various inorganic powders such as antimony, iron sulfide, molybdenum sulfide and short fibers, copper,
Powders of metals such as iron and lead, powders of cashew dust, powders of melamine resin cured products (melamine dusts), rubber dusts, powders of various resin cured products, and the like are used. The friction modifier is preferably contained in the resulting friction material in an amount of 10 to 60% by weight because a stable friction coefficient is obtained and the balance with the wear amount is excellent. It is more preferably 20 to 40% by weight.

【0011】結合剤としては各種熱硬化性樹脂が挙げら
れるが、フェノール樹脂が好ましく用いられる。その理
由は耐熱性及び接着性に優れ、安価な上に摩擦調整剤の
メラミンダスト、三酸化アンチモン、銅粉等と組合せる
ことにより、他の熱硬化性樹脂を使用した場合よりも摩
擦特性の温度依存性を小さくできるからである。フェノ
ール樹脂の中では未変性でかつレゾール型のものがより
好ましい。又フェノール樹脂と共に耐熱性に影響しない
程度にメラミン樹脂、尿素樹脂、ポリアミドイミド樹
脂、ポリイミド樹脂、エポキシ樹脂等の熱硬化性樹脂又
は架橋性ゴムを用いてもよい。結合剤は得られる摩擦材
中に固形分として10〜50重量%含有させると繊維基
材と摩擦調整剤との結合力に優れ、摩擦係数及び摩耗率
の調整が容易なので好ましい。
As the binder, various thermosetting resins can be mentioned, but a phenol resin is preferably used. The reason is that it has excellent heat resistance and adhesiveness, is inexpensive, and combines with friction modifiers such as melamine dust, antimony trioxide, copper powder, etc. This is because the temperature dependence can be reduced. Among the phenolic resins, unmodified and resol type resins are more preferable. Further, a thermosetting resin such as a melamine resin, a urea resin, a polyamideimide resin, a polyimide resin, an epoxy resin or a crosslinkable rubber may be used together with the phenol resin to the extent that the heat resistance is not affected. The binder is preferably contained in the obtained friction material in a solid content of 10 to 50% by weight because the binding force between the fiber base material and the friction modifier is excellent and the friction coefficient and the wear rate can be easily adjusted.

【0012】以上の材料を用いて摩擦材を得る方法を述
べる。前記の方法により先ず表面に酢酸鉛を付着させた
繊維基材(鉛処理基材)を得る。次いで、繊維基材が紐
状又はシート状の場合は結合剤の溶液に摩擦調整剤を加
えて混合した混和物(スラリー)を、前記鉛処理基材に
含浸し、基材に混和物を均一に付着させた後、乾燥等に
より溶媒を除去する。又、繊維基材が短繊維状の場合
は、結合剤の溶液に摩擦調整剤及び鉛処理基材を混合し
てニーダー等で均一な混和物とし、乾燥等により溶媒を
除去する。次いで金型等に入れて熱圧成形を行い、その
後成形品を所定の加熱条件下で熱処理して結合剤を硬化
させ摩擦材を得るものである。
A method for obtaining a friction material using the above materials will be described. First, a fiber base material (lead-treated base material) having lead acetate adhered to the surface thereof is obtained by the above method. Next, when the fiber base material is in the form of a string or a sheet, the lead-treated base material is impregnated with a mixture (slurry) prepared by adding a friction modifier to a binder solution and mixing the mixture, and the mixture is uniformly applied to the base material. The solvent is removed by drying or the like. When the fibrous base material is short fibrous, the friction modifier and the lead-treated base material are mixed with the binder solution to form a uniform mixture with a kneader or the like, and the solvent is removed by drying or the like. Next, it is placed in a mold or the like and subjected to thermocompression molding, and then the molded product is heat-treated under predetermined heating conditions to cure the binder and obtain a friction material.

【0013】[0013]

〔ガラス繊維100重量部に対する鉛付着量、( )内
は酢酸鉛付着量〕
[Amount of lead attached to 100 parts by weight of glass fiber, amount of lead acetate attached in parentheses]

実施例1…………5(7.9)重量部 実施例2………10(15.7)重量部 実施例3………30(47.1)重量部 比較例1………未処理 Example 1 ... 5 (7.9) parts by weight Example 2 ... 10 (15.7) parts by weight Example 3 ... 30 (47.1) parts by weight Comparative Example 1 ..... processing

【0014】(2)摩擦調整剤の調製 硫酸バリウム(堺化学製、B・C)20重量部、タルク
(和光純薬工業製、化学用)20重量部、炭酸カルシウ
ム(竹原化学製、商品名サンライトSL−1500)2
0重量部及び珪酸カルシウム短繊維(米国NYCO社
製、商品名ウオラストナイト)40重量部を混合した無
機物粉末、メチル化メラミン樹脂(日本カーバイド製、
S−260)を150℃で1時間、180℃で4時間、
次いで210℃で2時間の順に加熱して硬化させた硬化
物を40メッシュ(約350μm)以下に粉砕したメラ
ミンダスト、酸化鉄(Fe23)粉(和光純薬工業製、
化学用、平均粒径:50〜100μm)及び銅粉(和光
純薬工業製、化学用銅箔粉、平均で厚さ2μm、短径5
0μm、長径70μm)を表1に示す重量割合で配合し
V形混合機で混合して摩擦調整剤とした。
(2) Preparation of Friction Modifier 20 parts by weight of barium sulfate (manufactured by Sakai Chemical Co., BC), 20 parts by weight of talc (manufactured by Wako Pure Chemical Industries, Ltd.), calcium carbonate (trade name, manufactured by Takehara Chemical Co., Ltd.) Sunlight SL-1500) 2
Inorganic powder in which 0 part by weight and 40 parts by weight of calcium silicate short fiber (manufactured by NYCO, Inc., trade name Wollastonite) are mixed, methylated melamine resin (manufactured by Nippon Carbide,
S-260) at 150 ° C. for 1 hour, 180 ° C. for 4 hours,
Next, melamine dust, iron oxide (Fe 2 O 3 ) powder (manufactured by Wako Pure Chemical Industries, manufactured by Wako Pure Chemical Industries, Ltd.,
For chemistry, average particle size: 50-100 μm) and copper powder (made by Wako Pure Chemical Industries, copper foil powder for chemistry, average thickness 2 μm, minor axis 5)
0 μm, major axis 70 μm) were mixed at the weight ratios shown in Table 1 and mixed by a V-type mixer to prepare a friction modifier.

【0015】[0015]

【表1】 [Table 1]

【0016】(3)摩擦材の製造 結合剤溶液としてフェノール樹脂(大日本インキ化学工
業製、TD−2040C、固形分100重量%)15重
量部をメチルエチルケトン(MEK)85重量部に溶解
した樹脂溶液(固形分15重量%)を用いた。この樹脂
溶液に前記の摩擦調整剤及び酢酸鉛処理ガラス繊維基材
を表2に示す配合比となるように加えてニーダーで均一
な混和物とした。この混和物を60℃で2時間乾燥して
成形用混和物とし、次いでこれを金型に充填し、160
℃で15分、圧力200kg/cm2で形成し5mm×50mm×
50mmの成形体を得た。その後、180℃で1時間、2
10℃で2時間、240℃で4時間の順に後硬化を行
い、成形体両面をサンダーで研摩し、摩擦材を得た。
(3) Production of friction material A resin solution prepared by dissolving 15 parts by weight of a phenol resin (TD-2040C, manufactured by Dainippon Ink and Chemicals, Inc., solid content 100% by weight) as a binder solution in 85 parts by weight of methyl ethyl ketone (MEK). (Solid content 15% by weight) was used. The friction modifier and the lead acetate-treated glass fiber base material were added to this resin solution at the compounding ratio shown in Table 2 to obtain a uniform mixture with a kneader. This admixture was dried at 60 ° C. for 2 hours to give a molding admixture, which was then filled into a mold, 160
Formed at pressure of 200kg / cm 2 for 15 minutes at ℃ 5mm × 50mm ×
A 50 mm compact was obtained. After that, at 180 ℃ for 1 hour, 2
Post-curing was carried out in the order of 10 ° C. for 2 hours and 240 ° C. for 4 hours, and both surfaces of the molded body were polished with a sander to obtain a friction material.

【0017】[0017]

【表2】 [Table 2]

【0018】実施例及び比較例で得られた摩擦材を25
mm角に切断して摩擦特性の試験片とした。この試験片を
JIS D 4411に定める定速度摩擦試験機に押し
付け圧力5kg/cm2で取り付けて運転し、250℃及び3
50℃における摩擦係数及び摩耗率(cm3/kgf・m)を
測定した。この結果を表3に示す。
The friction materials obtained in Examples and Comparative Examples were used as 25
It was cut into mm squares to obtain friction property test pieces. This test piece was mounted on a constant speed friction tester specified in JIS D 4411 by pressing at a pressure of 5 kg / cm 2 and operated at 250 ° C. and 3
The friction coefficient and wear rate (cm 3 / kgf · m) at 50 ° C. were measured. The results are shown in Table 3.

【0019】[0019]

【表3】 表2から明らかなように、比較例のものは、高温の摩耗
率が大きく摩擦性能に劣る。これに対し、実施例のもの
は摩耗率が小さい。
[Table 3] As is clear from Table 2, the comparative examples have large wear rates at high temperatures and are inferior in friction performance. On the other hand, the wear rate of the example is small.

【0020】[0020]

【発明の効果】本発明の摩擦材は、高温時の摩擦性能に
優れる。
The friction material of the present invention has excellent friction performance at high temperatures.

─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───

【手続補正書】[Procedure amendment]

【提出日】平成5年11月19日[Submission date] November 19, 1993

【手続補正1】[Procedure Amendment 1]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0002[Name of item to be corrected] 0002

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0002】[0002]

【従来の技術】自動車に用いる摩擦材としては、一般に
ブレーキライニング、ディスクパッド及びクラッチフェ
ーシングがある。これらは従来、石綿(アスベスト)を
基材として使用していたが、アスベスト公害の問題から
非アスベスト系摩擦材の開発が望まれている。又、自動
車エンジンの性能向上に伴い摩擦材の摩擦特性(摩擦係
数、摩耗率)、機械特性の向上が望まれている。更に最
近は使用条件が苛酷になり高温時の高速回転強度も要求
されるようになってきている。現在、石綿基材の代替材
として、ガラス繊維、炭素繊維、芳香族ポリアミド繊
維、ロックウール、セラミック繊維、各種のスチー
ァイバー等を使用した摩擦材が開発され、一部で使用さ
れている。しかし、これらの基材は従来の石綿に比べて
高弾性で硬く、耐熱性が低いために、摩擦材にした場合
に種々の問題があり、上記した要求される性能を満足し
ない。
Brake linings, disc pads and clutch facings are generally used as friction materials for automobiles. Conventionally, asbestos (asbestos) has been used as a base material, but development of a non-asbestos friction material is desired due to the problem of asbestos pollution. Further, as the performance of automobile engines is improved, it is desired to improve the friction characteristics (friction coefficient, wear rate) and mechanical characteristics of friction materials. Furthermore, recently, the usage conditions have become severe, and high-speed rotation strength at high temperatures has been required. Currently, as an alternative material for asbestos substrate, glass fibers, carbon fibers, aromatic polyamide fibers, rock wool, ceramic fiber, various kinds of friction material using a steam le full <br/> Aiba, etc. have been developed, with some It is used. However, since these base materials have higher elasticity and hardness and lower heat resistance than conventional asbestos, there are various problems when used as a friction material, and the above-mentioned required performance is not satisfied.

【手続補正2】[Procedure Amendment 2]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0016[Correction target item name] 0016

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0016】(3)摩擦材の製造 結合剤溶液としてフェノール樹脂(大日本インキ化学工
業製、TD−2040C、固形分100重量%)15重
量部をメチルエチルケトン(MEK)85重量部に溶解
した樹脂溶液(固形分15重量%)を用いた。この樹脂
溶液に前記の摩擦調整剤及び酢酸鉛処理ガラス繊維基材
を表2に示す配合比となるように加えてニーダーで均一
な混和物とした。この混和物を60℃で2時間乾燥して
成形用混和物とし、次いでこれを金型に充填し、160
℃で15分、圧力200kg/cm2で形成し5mm×50mm×
50mmの成形体を得た。その後、180℃で1時間、2
10℃で2時間、240℃で4時間の順に後硬化を行
い、成形体両面をサンダーで研し、摩擦材を得た。
(3) Production of friction material A resin solution prepared by dissolving 15 parts by weight of a phenol resin (TD-2040C, manufactured by Dainippon Ink and Chemicals, Inc., solid content 100% by weight) as a binder solution in 85 parts by weight of methyl ethyl ketone (MEK). (Solid content 15% by weight) was used. The friction modifier and the lead acetate-treated glass fiber base material were added to this resin solution at the compounding ratio shown in Table 2 to obtain a uniform mixture with a kneader. This admixture was dried at 60 ° C. for 2 hours to give a molding admixture, which was then filled into a mold, 160
Formed at pressure of 200kg / cm 2 for 15 minutes at ℃ 5mm × 50mm ×
A 50 mm compact was obtained. After that, at 180 ℃ for 1 hour, 2
2 hours at 10 ° C., subjected to post curing in the order of 4 hours at 240 ° C., and Migaku Ken the molded body sided Thunder, to obtain a friction material.

【手続補正3】[Procedure 3]

【補正対象書類名】明細書[Document name to be amended] Statement

【補正対象項目名】0019[Correction target item name] 0019

【補正方法】変更[Correction method] Change

【補正内容】[Correction content]

【0019】[0019]

【表3】 から明らかなように、比較例のものは、高温の摩耗
率が大きく摩擦性能に劣る。これに対し、実施例のもの
は摩耗率が小さい。
[Table 3] As is clear from Table 3 , the comparative examples have large wear rates at high temperatures and are inferior in friction performance. On the other hand, the wear rate of the example is small.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 表面に酢酸鉛を付着させた繊維基材に、
摩擦調整剤及び結合剤を含む混和物を含浸又は混合し、
成形硬化してなる摩擦材。
1. A fiber base material having lead acetate adhered to its surface,
Impregnating or mixing an admixture containing a friction modifier and a binder,
Friction material that is formed and cured.
JP15341393A 1993-06-24 1993-06-24 Friction material Pending JPH0770336A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15341393A JPH0770336A (en) 1993-06-24 1993-06-24 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15341393A JPH0770336A (en) 1993-06-24 1993-06-24 Friction material

Publications (1)

Publication Number Publication Date
JPH0770336A true JPH0770336A (en) 1995-03-14

Family

ID=15561953

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15341393A Pending JPH0770336A (en) 1993-06-24 1993-06-24 Friction material

Country Status (1)

Country Link
JP (1) JPH0770336A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107553944A (en) * 2017-08-14 2018-01-09 杭州西湖摩擦材料有限公司 A kind of preparation method of wear brake pad

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107553944A (en) * 2017-08-14 2018-01-09 杭州西湖摩擦材料有限公司 A kind of preparation method of wear brake pad

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