JPH0467048B2 - - Google Patents

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Publication number
JPH0467048B2
JPH0467048B2 JP28157185A JP28157185A JPH0467048B2 JP H0467048 B2 JPH0467048 B2 JP H0467048B2 JP 28157185 A JP28157185 A JP 28157185A JP 28157185 A JP28157185 A JP 28157185A JP H0467048 B2 JPH0467048 B2 JP H0467048B2
Authority
JP
Japan
Prior art keywords
friction material
iron
metal
sacrificial
friction
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.)
Expired
Application number
JP28157185A
Other languages
Japanese (ja)
Other versions
JPS62141326A (en
Inventor
Juji Kobayashi
Yoshuki Mukoyama
Mikio Mabe
Saburo Abe
Yasuo Katagiri
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.)
Hitachi Unisia Automotive Ltd
Nissan Motor Co Ltd
Resonac Corp
Original Assignee
Atsugi Unisia Corp
Hitachi Chemical Co Ltd
Nissan Motor 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 Atsugi Unisia Corp, Hitachi Chemical Co Ltd, Nissan Motor Co Ltd filed Critical Atsugi Unisia Corp
Priority to JP28157185A priority Critical patent/JPS62141326A/en
Publication of JPS62141326A publication Critical patent/JPS62141326A/en
Publication of JPH0467048B2 publication Critical patent/JPH0467048B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は自動車の動力伝達などに用いられるク
ラツチフエーシング,ブレーキライニング等の摩
擦材に関する。 (従来の技術とその問題点) 摩擦材,特にクラツチフエーシングは摩擦特性
(安定した摩擦係数),耐摩耗性,機械特性(高バ
ース強度),耐ジヤダー性,耐貼付性にすぐれる
ことが要求される。最近は上記のうち耐貼付性が
重要な特性項目となつてきている。 摩擦材にはほとんどの場合,微量の塩分が含ま
れており、この塩分は、相手材である鉄の発錆を
促進する。特に塩素イオン(Cl-)、硫酸根
(SO4 2-)を含む塩分は鉄の発錆を著しく促進す
る。摩擦材を用いた産業機械、自動車等が長期間
保管されたままの状態であると、鉄と摩擦材との
間に錆が発生し、両者が貼付くことがある。特に
寒暖の差が激しい地域では、鉄と摩擦材との間に
結露が生じやすく、この結露により鉄と摩擦材と
の間に錆が発生し上記のような貼付を起こしやす
いという問題がある。この問題を解決する方法と
して摩擦材組成物中に亜硝酸ナトリウム、リン
酸、リン酸塩、ホウ酸、ホウ酸塩等の防錆剤を添
加したり、特開昭58−81238号公に報開示されて
いるように鉄の犠性陽極となりうる金属を摩擦材
表面に溶射付着させる方法がある。 しかしながら前者の防錆法は、相対湿度が高
く、摩擦材の吸湿量が多い場合に有効であるが、
摩擦材が吸湿と乾燥をくり返すような条件下では
防錆剤が偏在するなどして充分な効果が得られな
い。実際に発錆による貼付を起こす地域の気候
は、夜間は温度が低く湿度が高いが、昼間になる
と温度が高く湿度が低くなるため、摩擦材の吸湿
と乾燥がくり返される状況下にある。後者の防錆
法は、防錆剤を添加するよりも効果的であるが、
鉄の犠性陽極となりうる金属の付着量が少ない場
合、特に5mg/cm2未満の場合、防錆効果を長期間
維持することができない。また鉄の犠性陽極とな
りうる金属の付着量が多い場合、犠性陽極作用に
必要な塩分(電解質)が摩擦材から溶出しにくく
なる。このため鉄と鉄の犠性陽極となりうる金属
とが密着しない部分、すなわち空隙ができ易く、
この空隙に結露が生じたとき犠性陽極作用による
防錆効果が不充分となる。 本発明は上記の欠点の生じない摩擦材を提供す
ることを目的とするものである。 (問題点を解決するための手段) 本発明者らは上記の欠点について種々検討した
結果、摩擦材の表面に鉄の犠性陽極となりうる金
属を5mg/cm2〜30mg/cm2付着せしめ、かつ鉄の犠
性陽極となりうる金属の層に溝及び/又は孔を設
けたところ、鉄(相手材)と鉄の犠性陽極となり
うる金属との間に空隙ができ、その空隙に結露が
生じても錆が発生せず、鉄と摩擦材との貼付によ
る問題が解消されることを確認した。 本発明は摩擦材の表面に鉄の犠性陽極となりう
る金属を5mg/cm2〜30mg/cm2付着せしめ、かつ鉄
の犠性陽極となりうる金属の層に溝及び/又は孔
を設けてなる摩擦材に関する。 本発明において鉄の犠性陽極となりうる金属と
は、錆の電気化学的な機構において、鉄と共存し
た場合に、鉄の代わりに陽極となり、鉄が錆びる
ことを防ぐ金属をいう。例えば亜鉛、アルミニウ
ム、マグネシウム等があり、これらの金属は1種
で使用しても2種以上の混合物を使用してもよく
特に制限はない。 またこれらの金属の付着は線状のもの、或は粉
末状のものを溶射して鉄及び/又は摩擦材の表面
に付着せしめてもよく、鉄の犠性陽極となりうる
金属を箔にしたものをバインダーを用いて摩擦材
の表面に接着により付着せしめるか或は金属箔を
加熱、加圧して圧着せしめてもよく特に制限はな
いが、作業性の点で摩擦材の表面に溶射して付着
せしめることが好ましい。 鉄の犠性陽極となりうる金属は、摩擦材の表面
に5mg/cm2〜30mg/cm2好ましくは10mg/cm2〜25
mg/cm2付着せしめることが必要であり、5mg/cm2
未満であると防錆効果を長期間維持することがで
きず、30mg/cm2を越えると摩擦材としての性能、
特に初期の摩擦係数が低下するなどの欠点が生じ
る。また必要以上の付着はコストアツプにもつな
がる 鉄の犠性陽極となりうる金属の層に設ける孔は
直径3mm以下であることが好ましく、1mm以下で
あればさらに好ましい。また溝は幅3mm以下であ
ることが好ましく、1mm以下であればさらに好ま
しい。なお溝及び/又は孔の数については特に制
限はない。 孔や溝の形成方法についても特に制限はない
が、例えばクラツチフエーシング、ブレーキライ
ニング等の場合は、摩擦面に犠性陽極となりうる
金属を付着せしめた後、針状の突起物を多数もつ
剣山のような器具を摩擦面に押し込んで孔をあけ
ることができる。或は鋭利な刃物ですじ状の溝を
設けてもよい。また予め金属箔に孔や空隙を設け
てから摩擦面に圧着させてもよい。さらには摩擦
材表面に溝などの凹凸を形成し、しかる後犠性陽
極となりうる金属を溶射して付着せしめてもよ
い。 溝及び/又は孔は犠性陽極作用を有効に発揮さ
せるため必要不可欠なものであり、溝及び/又は
孔を設けないと犠性陽極作用に必要な塩分が摩擦
材から溶出しないため鉄と鉄の犠性陽極となりう
る金属との間に空隙ができ易くこの空隙内に結露
が生じたとき犠性陽極作用による防錆効果が不充
分となる。 犠性陽極作用を一層効果的にするためには上記
塩分を吸湿時に摩擦材に対し、0.01〜1.0重量%
程度の濃度となるような塩分が含まれていること
が望ましい。 (実施例) 以下実施例により本発明を説明する。 実施例 1 4Kクラスアスベスト(ジヨーンズ・マンブイ
ル社製)85重量部、スフ15重量部を均一に混合
し、ついでカーデイングマシンにかけてアスベス
トウエブを作りこのアスベストウエブ82重量部に
対してカシユー殻油熱硬化物の耐摩耗粉(東北化
工製、商品名FF1800)を18重量部分散した後コ
ンデンサーにかけ、耐摩耗粉入アスベストスライ
バーとし、さらにこのものを精紡機により撚りを
かけ直径1mmの単糸とした。次にこの単糸2本と
直径0.16mmのしんちゆう線1本とを撚り合せ2.5
g/mの耐摩耗粉入りアスベストヤーンとした。 この耐摩耗粉入りアスベストヤーンにメラミン
変性フエノール樹脂(大日本インキ製)を塗工ヤ
ーンに対して20重量%となるように、含浸して付
着させ塗工ヤーンを得た。 次に塗工ヤーンをクラツチフエーシングの形状
のタブレツトに予備成形し、これを150±5℃、
加圧力300Kg/cm2で8分加熱加圧成形を行ない、
その後表面研磨し、200℃で8時間熱処理後さら
に表面研磨して図面指定の形状のクラツチフエー
シングを得た。 次に純度95%の亜鉛線を加藤メタリコン工業製
の溶射機、商品名KR−5を用いて溶融し、電圧
15V、電流20Aび空気圧5Kg/cm2の条件で上記で
得たクラツチフエーシングの表面に10mg/cm2の亜
鉛を溶射して付着せしめた。この後5mm間隔で直
径0.5mmの針状突起物をもつ器具をクラツチフエ
ーシングに押し込み、亜鉛の薄膜層に孔を設け
た。 次に亜鉛の薄膜層に孔を設けたクラツチフエー
シングを相手材のねずみ鋳鉄(JIS G5011)に面
圧2Kg/cm2で押しつけて第1表に示す条件で発錆
及び貼付力の試験を行つた。その結果を第1表に
示す。以下の実施例及び比較例も同様な方法で発
錆及び貼付力の試験を行つた。 なお実施例1で得たクラツチフエーシング中に
は0.3重量%の塩分(Ca2+,Na+,Mg2+,Cl-
SO4 2-等)が含まれていた。 実施例 2 4Kクラスアスベスト(キヤリー社製)75重量
部、スフ5重量部を均一に混合し、ついでカーデ
イングマシンにかけてアスベストウエブを作りこ
のアスベストウエブ85重量部に対してカシユー殻
油熱硬化物の耐摩耗粉(東北化工製,商品名
FF1800)18重量部を分散した後コンデンサーに
かけ、耐摩耗粉入アスベストスライバーとした。
以下実施例1と同様の工程及び実施例1と同様の
材料を用いてクラツチフエーシングを得た。 次に上記で得たクラツチフエーシングの表面に
実施例1と同様の方法で20mg/cm2の亜鉛を溶射し
て付着せしめた。以下実施例1と同様の方法で亜
鉛の薄膜層に孔を設けたクラツチフエーシングを
得た。なお実施例2で得たクラツチフエーシング
中には0.1重量%の塩分が含まれていた。 実施例 3 厚さ30〓m(21.5mg/cm2)の亜鉛箔に7.5mm間隔
で1mm×5mmの寸法の切り溝を設けた。次にこれ
を実施例1で得たクラツチフエーシングの表面に
圧力100Kg/cm2,温度150±5℃の条件で圧着して
亜鉛箔に溝を設けたクラツチフエーシングを得
た。 比較例 1 実施例1で得たクラツチフエーシングの表面に
4mg/cm2の亜鉛を溶射して付着せしめ、それ以外
は実施例1と同様の方法で亜鉛の薄膜層に孔を設
けたクラツチフエーシングを得た。 比較例 2 実施例2で得たクラツチフエーシングの表面に
33mg/cm2の亜鉛を溶射して付着せしめ、それ以外
は実施例2と同様の方法で亜鉛の薄膜層に孔を設
けたクラツチフエーシングを得た。 比較例 3 実施例1で得たクラツチフエーシングの表面に
12mg/cm2の悪鉛を溶射して付着せしめた。但し亜
鉛の薄膜層には孔、溝等は設けない。
(Field of Industrial Application) The present invention relates to friction materials such as clutch facings and brake linings used in power transmission of automobiles. (Conventional technology and its problems) Friction materials, especially clutch facings, have excellent friction properties (stable coefficient of friction), wear resistance, mechanical properties (high berth strength), anti-jadder properties, and anti-sticking properties. required. Recently, among the above properties, sticking resistance has become an important characteristic item. In most cases, friction materials contain a small amount of salt, and this salt promotes rusting of the mating material, iron. In particular, salt containing chloride ions (Cl - ) and sulfate radicals (SO 4 2- ) significantly promotes rusting of iron. If industrial machinery, automobiles, etc. that use friction materials are left in storage for a long period of time, rust may develop between the iron and the friction material, causing the two to stick together. Particularly in areas with large temperature differences, dew condensation tends to form between the iron and the friction material, and this condensation causes rust between the iron and the friction material, which tends to cause sticking as described above. As a method to solve this problem, rust preventive agents such as sodium nitrite, phosphoric acid, phosphates, boric acid, and borates are added to the friction material composition. As disclosed, there is a method of thermally spraying a metal that can be used as a sacrificial iron anode onto the surface of a friction material. However, the former rust prevention method is effective when the relative humidity is high and the amount of moisture absorbed by the friction material is large;
Under conditions where the friction material repeatedly absorbs moisture and dries, the anti-corrosion agent will be unevenly distributed and will not be sufficiently effective. The climate in areas where rusting actually occurs is low temperature and high humidity at night, but high temperature and low humidity during the day, resulting in friction materials repeatedly absorbing moisture and drying out. The latter rust prevention method is more effective than adding rust inhibitors, but
When the amount of deposited metal that can serve as a sacrificial iron anode is small, particularly when it is less than 5 mg/cm 2 , the rust prevention effect cannot be maintained for a long period of time. Furthermore, if there is a large amount of metal that can become a sacrificial iron anode attached, it becomes difficult for the salt (electrolyte) necessary for sacrificial anode action to be eluted from the friction material. For this reason, gaps are likely to form where the iron and the metal that can serve as a sacrificial anode do not come into close contact with each other.
When dew condensation occurs in this gap, the rust prevention effect due to sacrificial anode action becomes insufficient. The object of the present invention is to provide a friction material that does not suffer from the above-mentioned drawbacks. (Means for Solving the Problems) As a result of various studies on the above-mentioned drawbacks, the present inventors deposited 5 mg/cm 2 to 30 mg/cm 2 of a metal that can serve as a sacrificial iron anode on the surface of the friction material. In addition, when grooves and/or holes are provided in a layer of metal that can be used as a sacrificial iron anode, a gap is created between the iron (the other material) and the metal that can be used as a sacrificial iron anode, and dew condensation occurs in the gap. It was confirmed that no rust occurred even when the friction material was applied, and the problems caused by the adhesion of iron and friction material were resolved. In the present invention, 5 mg/cm 2 to 30 mg/cm 2 of a metal that can be used as a sacrificial iron anode is adhered to the surface of a friction material, and grooves and/or holes are provided in the metal layer that can be used as a sacrificial iron anode. Regarding friction materials. In the present invention, a metal that can serve as a sacrificial anode for iron refers to a metal that, when coexisting with iron, serves as an anode instead of iron in the electrochemical mechanism of rust, thereby preventing iron from rusting. Examples include zinc, aluminum, magnesium, etc., and these metals may be used singly or in a mixture of two or more without any particular limitation. In addition, these metals may be attached in the form of wire or powder by thermal spraying to the surface of the iron and/or friction material. It may be attached to the surface of the friction material by adhesive using a binder, or it may be crimped by heating and pressurizing a metal foil, but there is no particular restriction, but from the viewpoint of workability, it may be attached by thermal spraying to the surface of the friction material. Preferably. The metal that can be used as a sacrificial iron anode is applied to the surface of the friction material in an amount of 5 mg/cm 2 to 30 mg/cm 2 , preferably 10 mg/cm 2 to 25
It is necessary to deposit mg/ cm2 , and 5mg/ cm2
If it is less than 30mg/cm2, the rust prevention effect cannot be maintained for a long time, and if it exceeds 30mg/ cm2 , the performance as a friction material will deteriorate.
In particular, there are drawbacks such as a decrease in the initial coefficient of friction. In addition, excessive adhesion may lead to increased costs. The holes provided in the metal layer that can serve as a sacrificial iron anode are preferably 3 mm or less in diameter, and more preferably 1 mm or less in diameter. Further, the width of the groove is preferably 3 mm or less, more preferably 1 mm or less. Note that there is no particular restriction on the number of grooves and/or holes. There are no particular restrictions on the method of forming holes and grooves, but for example, in the case of clutch facings, brake linings, etc., metal that can be used as a sacrificial anode is attached to the friction surface, and then a sword mount with many needle-like protrusions is used. A hole can be made by pushing an instrument like this into the friction surface. Alternatively, streak-like grooves may be formed using a sharp knife. Alternatively, holes or gaps may be provided in the metal foil in advance and then the metal foil may be pressed against the friction surface. Furthermore, irregularities such as grooves may be formed on the surface of the friction material, and then a metal that can be used as a sacrificial anode may be deposited by thermal spraying. Grooves and/or holes are essential for effective sacrificial anode action. Without grooves and/or holes, the salt necessary for sacrificial anode action will not be leached from the friction material. A void is easily formed between the metal and the metal that can serve as a sacrificial anode, and when dew condensation occurs within this void, the rust prevention effect due to the sacrificial anode action becomes insufficient. In order to make the sacrificial anode effect even more effective, the above salt should be added to the friction material in an amount of 0.01 to 1.0% by weight when absorbing moisture.
It is desirable that the salt content be at a certain level. (Example) The present invention will be explained below with reference to Examples. Example 1 85 parts by weight of 4K class asbestos (manufactured by Johns Manbuil) and 15 parts by weight of Sufu were mixed uniformly, then processed into a carding machine to form an asbestos web, and 82 parts by weight of this asbestos web was heat-cured with cashew shell oil. After dispersing 18 parts by weight of abrasion-resistant powder (manufactured by Tohoku Kako, trade name FF1800), it was applied to a condenser to obtain asbestos sliver containing abrasion-resistant powder, which was then twisted using a spinning machine to form a single yarn with a diameter of 1 mm. Next, twist these two single yarns and one Shinchiyu wire with a diameter of 0.16 mm for 2.5
g/m of asbestos yarn containing wear-resistant powder. This asbestos yarn containing wear-resistant powder was impregnated with melamine-modified phenolic resin (manufactured by Dainippon Ink) in an amount of 20% by weight based on the coated yarn to obtain a coated yarn. Next, the coated yarn was preformed into a tablet in the shape of a clutch facing and heated at 150±5°C.
Heat and pressure molding was performed for 8 minutes at a pressure of 300Kg/ cm2 ,
Thereafter, the surface was polished, and after heat treatment at 200°C for 8 hours, the surface was further polished to obtain a clutch facing in the shape specified in the drawing. Next, a zinc wire with a purity of 95% is melted using a thermal spraying machine manufactured by Kato Metallicon Industries, trade name KR-5, and the voltage is
10 mg/cm 2 of zinc was thermally sprayed onto the surface of the clutch facing obtained above under the conditions of 15 V, 20 A current, and 5 Kg/cm 2 air pressure. After this, an instrument with needle-like protrusions 0.5 mm in diameter was pushed into the clutch facing at 5 mm intervals to create holes in the thin zinc film layer. Next, the clutch facing, which has holes in the thin zinc film layer, was pressed against the mating material, gray cast iron (JIS G5011), with a surface pressure of 2 kg/ cm2 , and rusting and sticking force tests were conducted under the conditions shown in Table 1. Ivy. The results are shown in Table 1. The following Examples and Comparative Examples were also tested for rust development and adhesion strength in the same manner. The clutch facing obtained in Example 1 contained 0.3% by weight of salt (Ca 2+ , Na + , Mg 2+ , Cl - ,
SO 4 2- etc.) were included. Example 2 75 parts by weight of 4K class asbestos (manufactured by Cary) and 5 parts by weight of Sufu were mixed uniformly, then processed into a carding machine to form an asbestos web. Wear-resistant powder (manufactured by Tohoku Kako, product name)
After dispersing 18 parts by weight of FF1800), it was applied to a condenser to obtain asbestos sliver containing wear-resistant powder.
Thereafter, a clutch facing was obtained using the same steps and materials as in Example 1. Next, 20 mg/cm 2 of zinc was deposited on the surface of the clutch facing obtained above by thermal spraying in the same manner as in Example 1. Thereafter, in the same manner as in Example 1, a clutch facing in which holes were formed in the zinc thin film layer was obtained. Note that the clutch facing obtained in Example 2 contained 0.1% by weight of salt. Example 3 Cut grooves measuring 1 mm x 5 mm were provided at 7.5 mm intervals in a zinc foil having a thickness of 30 m (21.5 mg/cm 2 ). Next, this was pressed onto the surface of the clutch facing obtained in Example 1 at a pressure of 100 kg/cm 2 and a temperature of 150±5° C. to obtain a clutch facing with grooves formed in the zinc foil. Comparative Example 1 A clutch facing was prepared in which 4 mg/cm 2 of zinc was thermally sprayed onto the surface of the clutch facing obtained in Example 1, and holes were formed in the zinc thin film layer in the same manner as in Example 1 except for the above. Got Thing. Comparative Example 2 On the surface of the clutch facing obtained in Example 2
A clutch facing with holes formed in the zinc thin film layer was obtained in the same manner as in Example 2 except that 33 mg/cm 2 of zinc was deposited by thermal spraying. Comparative Example 3 On the surface of the clutch facing obtained in Example 1
12 mg/cm 2 of bad lead was sprayed and adhered. However, no holes, grooves, etc. are provided in the zinc thin film layer.

【表】 (発明の効果) 本発明になる摩擦材は高温高湿環境下、吸湿と
乾燥がくり返される環境下においても長期間防錆
効果を維持し、また相手材である鉄との貼付きも
なく工業上極めて有効である。
[Table] (Effects of the invention) The friction material of the present invention maintains its anti-corrosion effect for a long period of time even in high temperature and high humidity environments, environments where moisture absorption and dryness are repeated, and it also maintains its anti-corrosion effect for a long period of time even in environments where moisture absorption and dryness are repeated. It is industrially extremely effective.

Claims (1)

【特許請求の範囲】 1 摩擦材の表面に鉄の犠性陽極となりうる金属
を5mg/cm2〜30mg/cm2付着せしめ、かつ鉄の犠性
陽極となりうる金属の層に溝及び/又は孔を設け
てなる摩擦材。 2 摩擦材がクラツチフエーシングである特許請
求の範囲第1項記載の摩擦材。
[Claims] 1. 5 mg/cm 2 to 30 mg/cm 2 of a metal that can be used as a sacrificial iron anode is deposited on the surface of the friction material, and grooves and/or holes are formed in the metal layer that can be used as a sacrificial iron anode. A friction material that is provided with. 2. The friction material according to claim 1, wherein the friction material is a clutch facing.
JP28157185A 1985-12-13 1985-12-13 Friction material Granted JPS62141326A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP28157185A JPS62141326A (en) 1985-12-13 1985-12-13 Friction material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28157185A JPS62141326A (en) 1985-12-13 1985-12-13 Friction material

Publications (2)

Publication Number Publication Date
JPS62141326A JPS62141326A (en) 1987-06-24
JPH0467048B2 true JPH0467048B2 (en) 1992-10-27

Family

ID=17641035

Family Applications (1)

Application Number Title Priority Date Filing Date
JP28157185A Granted JPS62141326A (en) 1985-12-13 1985-12-13 Friction material

Country Status (1)

Country Link
JP (1) JPS62141326A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01234629A (en) * 1988-03-15 1989-09-19 Daikin Mfg Co Ltd Friction material
DE3990205T1 (en) * 1988-03-15 1990-03-15 Daikin Mfg Co Ltd FRICTION MATERIAL
JP2687150B2 (en) * 1988-10-22 1997-12-08 スズキ株式会社 Disc brake rotor manufacturing method

Also Published As

Publication number Publication date
JPS62141326A (en) 1987-06-24

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