JP2831491B2 - Friction material containing thermosetting resin - Google Patents
Friction material containing thermosetting resinInfo
- Publication number
- JP2831491B2 JP2831491B2 JP3168870A JP16887091A JP2831491B2 JP 2831491 B2 JP2831491 B2 JP 2831491B2 JP 3168870 A JP3168870 A JP 3168870A JP 16887091 A JP16887091 A JP 16887091A JP 2831491 B2 JP2831491 B2 JP 2831491B2
- Authority
- JP
- Japan
- Prior art keywords
- thermosetting resin
- friction material
- friction
- gel time
- flow distance
- 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 - Fee Related
Links
Landscapes
- Braking Arrangements (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は熱硬化性樹脂含有摩擦材
に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material containing a thermosetting resin.
【0002】[0002]
【従来の技術】自動車、二輪車等に用いる摩擦材には、
ブレーキライニング、ディスクパッド、クラッチフェー
ジング等がある。これら摩擦材は、一般的に、金属粉、
潤滑材、無機充填材、有機充填材等を含む摩擦調整材
と、アラミド繊維等の繊維からなる補強材とを熱硬化性
樹脂の結合材で結着して形成される。この自動車等の摩
擦材は、制動時高温になることから、高温になっても摩
擦係数(μ)の変化の少ない、いわゆる耐フェード性に
優れることが要求される。従来この耐フェード性を向上
させるために、特開昭63−293337号公報に示さ
れるように、摩擦調整材と補強材とを熱硬化性樹脂で熱
成形した成形体に無機コーティング剤を含浸させた摩擦
材が知られている。2. Description of the Related Art Friction materials used for automobiles, motorcycles and the like include:
There are brake linings, disc pads, clutch fading, etc. These friction materials are generally metal powder,
It is formed by binding a friction modifier containing a lubricant, an inorganic filler, an organic filler, and the like, and a reinforcing material made of fibers such as aramid fibers with a binder of a thermosetting resin. Since the friction material of an automobile or the like is heated to a high temperature during braking, it is required to have a so-called fade resistance with little change in the friction coefficient (μ) even at a high temperature. Conventionally, in order to improve the fade resistance, as described in JP-A-63-293337, an inorganic coating agent is impregnated in a molded article obtained by thermoforming a friction adjusting material and a reinforcing material with a thermosetting resin. Friction materials are known.
【0003】[0003]
【発明が解決しようとする課題】上記従来の摩擦材によ
れば、高温負荷時の耐フェード性や耐高温磨耗性が向上
する利点がある。しかしながら、この摩擦材は熱硬化性
樹脂によって熱成形した後、無機コーティング剤を含浸
するようにしているので製造工数が多く、コスト高とな
る問題点がある。According to the above-mentioned conventional friction material, there is an advantage that fade resistance under high temperature load and high temperature wear resistance are improved. However, since this friction material is thermoformed with a thermosetting resin and then impregnated with an inorganic coating agent, there is a problem that the number of manufacturing steps is large and the cost is high.
【0004】そこで、本発明は上記問題点を解決すべく
なされたものであり、その目的とするところは、安価で
しかも耐フェード性、耐高温磨耗性等の特性に優れる熱
硬化性樹脂含有摩擦材を提供するにある。Accordingly, the present invention has been made to solve the above problems, and it is an object of the present invention to provide a thermosetting resin-containing friction material which is inexpensive and has excellent properties such as fade resistance and high temperature wear resistance. In providing materials.
【0005】[0005]
【課題を解決するための手段】本発明は上記目的を達成
するため次の構成を備える。すなわち、充填材を含む摩
擦調整材と補強材とを熱硬化性樹脂の結合材で固着した
熱硬化性樹脂含有摩擦材において、前記結合材に、フロ
ー距離とゲルタイムの短い熱硬化性樹脂Aとこの熱硬化
性樹脂Aよりもフロー距離、ゲルタイムが共に長い熱硬
化性樹脂Bの2種類の熱硬化性樹脂を用いたことを特徴
としている。熱硬化性樹脂Aのフロー距離が10〜20
mm,ゲルタイムが10〜20秒であり、熱硬化性樹脂
Bのフロー距離が30〜40mm,ゲルタイムが60〜
80秒であると好適である。熱硬化性樹脂Aの融点が4
0〜70℃であり、熱硬化性樹脂Bの融点が71〜10
0℃であると好適である。また熱硬化性樹脂Aと熱硬化
性樹脂Bの比率は容量比で1:3〜3:1の範囲が好ま
しい。The present invention has the following arrangement to achieve the above object. That is, in a thermosetting resin-containing friction material in which a friction modifier containing a filler and a reinforcing material are fixed with a thermosetting resin binder, the binder has a thermosetting resin A having a short flow distance and a short gel time. It is characterized in that two types of thermosetting resins, thermosetting resin B, having a longer flow distance and longer gel time than thermosetting resin A are used. The flow distance of the thermosetting resin A is 10 to 20
mm, the gel time is 10 to 20 seconds, the flow distance of the thermosetting resin B is 30 to 40 mm, and the gel time is 60 to
Preferably, it is 80 seconds. Melting point of thermosetting resin A is 4
0 to 70 ° C., and the melting point of the thermosetting resin B is 71 to 10
It is preferred that the temperature is 0 ° C. The ratio between the thermosetting resin A and the thermosetting resin B is preferably in the range of 1: 3 to 3: 1 in terms of volume ratio.
【0006】[0006]
【作用】高温負荷時での耐フェード性を向上させるに
は、高温時摩擦材からガスが噴出するので、このガスの
排出を良好に行えるようにするのが1つの条件となる。
このガスの排出性は一般的に摩擦材の気孔率が高い程よ
くなる。本発明では、摩擦調整材、補強材を結着する熱
硬化性樹脂にフロー距離、ゲルタイムが短い熱硬化性樹
脂Aとこの熱硬化性樹脂Aよりフロー距離、ゲルタイム
が長い熱硬化性樹脂Bの2種類の熱硬化性樹脂を用いて
いるので、成形の際の熱硬化時、熱硬化性樹脂Aの方が
早く熱硬化し、かつ樹脂の流れ性が低いので、熱硬化性
樹脂A相互間、熱硬化性樹脂Aと熱硬化性樹脂Bとの間
で気孔が生じ、気孔率を高くすることができる。その結
果特に耐フェード性が向上した。In order to improve the fade resistance under a high temperature load, one condition is that the gas is ejected from the friction material at a high temperature, so that the gas can be discharged well.
Generally, the higher the porosity of the friction material, the better the gas exhaustability. In the present invention, the thermosetting resin for binding the friction modifier and the reinforcing material to the thermosetting resin A has a shorter flow distance and a shorter gel time, and the thermosetting resin B has a longer flow distance and a longer gel time than the thermosetting resin A. Since two types of thermosetting resins are used, the thermosetting resin A thermosets faster at the time of thermosetting during molding, and the flowability of the resin is low. Pores are generated between the thermosetting resin A and the thermosetting resin B, and the porosity can be increased. As a result, especially the fade resistance was improved.
【0007】[0007]
【実施例】以下、本発明の好適な実施例を添付図面に基
づいて詳細に説明する。本発明では、結合材にフロー距
離およびゲルタイムの短い熱硬化性樹脂Aとこの熱硬化
性樹脂Aよりもフロー距離およびゲルタイムの長い熱硬
化性樹脂Bの2種類の熱硬化性樹脂を用いる点に特徴が
ある。この場合に、熱硬化性樹脂Aはフロー距離が10
〜20mm、ゲルタイムが10〜20秒のもの、熱硬化
性樹脂Bはフロー距離が30〜40mm、ゲルタイムが
60〜80秒のものが好ましい。なおフロー距離、ゲル
タイムはJISK6910による。さらには、熱硬化性
樹脂Aは融点が40〜70℃、熱硬化性樹脂Bは融点が
70〜100℃のものが好適である。DESCRIPTION OF THE PREFERRED EMBODIMENTS Preferred embodiments of the present invention will be described below in detail with reference to the accompanying drawings. In the present invention, two types of thermosetting resins, a thermosetting resin A having a short flow distance and a short gel time and a thermosetting resin B having a long flow distance and a long gel time than the thermosetting resin A, are used as the binder. There are features. In this case, the thermosetting resin A has a flow distance of 10
~ 20mm, gel time is 10 ~ 20 seconds, thermosetting resin B has a flow distance of 30 ~ 40mm, gel time is
Those for 60 to 80 seconds are preferred. The flow distance and gel time are based on JIS K6910. Further, the thermosetting resin A preferably has a melting point of 40 to 70 ° C, and the thermosetting resin B preferably has a melting point of 70 to 100 ° C.
【0008】上記の条件を具備する熱硬化性樹脂はその
重合度等によって種々の種類のものが選定できる。例え
ば熱硬化性樹脂Aには、フェノール系ストレート樹脂、
フェノール系メラミン変成樹脂、フェノール系ゴム変成
樹脂等がある。また熱硬化性樹脂Bには、フェノール系
ゴム変成樹脂、フェノール系ストレート樹脂、フェノー
ル系メラミン変成樹脂がある。熱硬化性樹脂A、熱硬化
性樹脂Bの比率は混合性に問題がなければ特に限定され
ないが、後記する耐フェード性に優れるに必要な気孔率
を得るために、両者の比率は概ね1:3〜3:1の範囲
が好適である。また熱硬化性樹脂A、熱硬化性樹脂Bの
摩擦材全体に対応する量は概ね5〜30vol%とす
る。5%以下では成形性が悪く、30%以上では摩擦材
の耐熱性に問題が生じる。Various kinds of thermosetting resins satisfying the above conditions can be selected depending on the degree of polymerization and the like. For example, thermosetting resin A includes a phenolic straight resin,
Phenolic melamine modified resin, phenolic rubber modified resin and the like. Further, the thermosetting resin B includes a phenolic rubber modified resin, a phenolic straight resin, and a phenolic melamine modified resin. The ratio between the thermosetting resin A and the thermosetting resin B is not particularly limited as long as there is no problem with the mixing property. However, in order to obtain the porosity required for excellent fade resistance described later, the ratio between the two is approximately 1: A range of 3 to 3: 1 is preferred. In addition, the amount of the thermosetting resin A and the thermosetting resin B corresponding to the entire friction material is generally 5 to 30 vol%. If it is less than 5%, the moldability is poor, and if it is more than 30%, there is a problem in the heat resistance of the friction material.
【0009】摩擦調整材、補強材は熱硬化性樹脂による
結着性が良好でかつ所要の摩擦特性が得られればよく、
その材料、混入量は特に限定されない。摩擦調整材に
は、鉄、銅等の金属粉、黒鉛等の潤滑材、硫酸バリウム
等の無機充填材、有機ダスト等の有機充填材が用いられ
る。また補強材には、アラミド繊維その他の繊維材を用
いる。The friction-adjusting material and the reinforcing material only need to have good binding properties with the thermosetting resin and obtain the required friction characteristics.
The material and mixing amount are not particularly limited. As the friction adjusting material, metal powders such as iron and copper, lubricants such as graphite, inorganic fillers such as barium sulfate, and organic fillers such as organic dust are used. Aramid fibers and other fiber materials are used for the reinforcing material.
【0010】高温負荷時での耐フェード性を向上させる
には、高温時摩擦材からガスが噴出するので、このガス
の排出を良好に行えるようにするのが1つの条件とな
る。このガスの排出性は一般的に摩擦材の気孔率が高い
程よくなる。本発明では、摩擦調整材、補強材を結着す
る熱硬化性樹脂にフロー距離、ゲルタイムが短い熱硬化
性樹脂Aとこの熱硬化性樹脂Aよりフロー距離、ゲルタ
イムが長い熱硬化性樹脂Bの2種類の熱硬化性樹脂を用
いているので、成形の際の熱硬化時、熱硬化性樹脂Aの
方が早く熱硬化し、かつ樹脂の流れ性が低いので、熱硬
化性樹脂A相互間、熱硬化性樹脂Aと熱硬化性樹脂Bと
の間で気孔が生じ、気孔率を高くすることができる。そ
の結果耐フェード性が向上した。熱硬化性樹脂Aの使用
量が多い方が気孔率もより多くなるが、摩擦調整材、補
強材との密着性は逆に低くなる。摩擦調整材、補強材と
の密着性はフロー距離、ゲルタイムの長い熱硬化性樹脂
Bの方が良好である。気孔率の向上が図れ、かつ摩擦調
整材、補強材との密着性が良好となる範囲は、前記した
ように熱硬化性樹脂A,熱硬化性樹脂Bの比率が容量で
概ね1:3〜3:1となる範囲である。In order to improve the fade resistance under a high temperature load, one condition is to make it possible to discharge the gas satisfactorily because the gas is ejected from the friction material at a high temperature. Generally, the higher the porosity of the friction material, the better the gas exhaustability. In the present invention, the thermosetting resin for binding the friction modifier and the reinforcing material to the thermosetting resin A has a shorter flow distance and a shorter gel time, and the thermosetting resin B has a longer flow distance and a longer gel time than the thermosetting resin A. Since two types of thermosetting resins are used, the thermosetting resin A thermosets faster at the time of thermosetting during molding, and the flowability of the resin is low. Pores are generated between the thermosetting resin A and the thermosetting resin B, and the porosity can be increased. As a result, the fade resistance was improved. The higher the amount of the thermosetting resin A used, the higher the porosity, but the lower the adhesion to the friction modifier and the reinforcing material. The thermosetting resin B, which has a longer flow distance and longer gel time, has better adhesion to the friction modifier and the reinforcing material. The range in which the porosity can be improved and the adhesiveness with the friction modifier and the reinforcing material is good is that the ratio of the thermosetting resin A and the thermosetting resin B is approximately 1: 3 to The range is 3: 1.
【0011】また熱硬化性樹脂Aの融点が熱硬化性樹脂
Bの融点よりも低い方が、成形の際熱硬化性樹脂Aのほ
うが早く溶融し、ゲル化が一層早まるので気孔率の増加
により効果的である。また耐フェード性が向上した結
果、耐高温磨耗性も向上し、高速摩擦係数も大きな変動
がなかった。さらに2種類の熱硬化性樹脂を用いること
によって基体への接着強度も大きくなった。Further, when the melting point of the thermosetting resin A is lower than the melting point of the thermosetting resin B, the thermosetting resin A melts faster during molding and gelation is further accelerated, so that the porosity increases. It is effective. In addition, as a result of the improvement in the fade resistance, the high-temperature wear resistance was improved, and the high-speed friction coefficient did not change significantly. Further, by using two types of thermosetting resins, the adhesive strength to the substrate was increased.
【0012】表1に実施例と比較例の配合を示す。表2
に耐磨耗性の比較データを、表3に接着強度の比較デー
タを示す。Table 1 shows the compositions of the examples and comparative examples. Table 2
Table 3 shows comparative data of abrasion resistance, and Table 3 shows comparative data of adhesive strength.
【0013】[0013]
【表1】 [Table 1]
【0014】[0014]
【表2】 [Table 2]
【0015】[0015]
【表3】 [Table 3]
【0016】また図1に温度による摩擦係数変化(耐フ
ェード性)を、図2に高速での摩擦係数変化を示す。表
2、表3から明らかなように、本実施例では、従来品の
比較例に比して、耐摩耗性、基体への接着強度共に優
れ、また図1から明らかなように、本実施例では高温負
荷時での摩擦係数にもほとんど変化がなく耐フェード性
に優れている。さらに図2から明らかなように、本実施
例では、高速での摩擦係数変化も少なく、安定した制動
効果が得られる。上記実施例では熱硬化性樹脂Aと熱硬
化性樹脂Bとの比率を1:3に設定したが、3:1に設
定した場合にも同様の好結果が得られた。以上本発明に
つき好適な実施例を挙げて種々説明したが、本発明はこ
の実施例に限定されるものではなく、発明の精神を逸脱
しない範囲内で多くの改変を施し得るのはもちろんであ
る。FIG. 1 shows a change in friction coefficient (fade resistance) with temperature, and FIG. 2 shows a change in friction coefficient at high speed. As is clear from Tables 2 and 3, the present example is superior in both abrasion resistance and adhesive strength to a substrate as compared with the comparative example of the conventional product, and as is clear from FIG. Has almost no change in the coefficient of friction under a high temperature load and is excellent in fade resistance. Further, as is apparent from FIG. 2 , in the present embodiment, the change in the friction coefficient at high speed is small, and a stable braking effect can be obtained. In the above example, the ratio of the thermosetting resin A to the thermosetting resin B was set to 1: 3, but the same good result was obtained when the ratio was set to 3: 1. Although the present invention has been described in detail with reference to the preferred embodiments, the present invention is not limited to the embodiments, and it goes without saying that many modifications can be made without departing from the spirit of the invention. .
【0017】[0017]
【発明の効果】本発明に係る熱硬化性樹脂含有摩擦材に
よれば、製造工数も増加せず安価に提供できると共に、
気孔率が向上し、特に耐フェード性、耐高温磨耗性に優
れるという著効を奏する。According to the friction material containing a thermosetting resin according to the present invention, the friction material can be provided at a low cost without increasing the number of manufacturing steps.
The porosity is improved, and in particular, it has a remarkable effect of being excellent in fade resistance and high-temperature wear resistance.
【図1】温度による摩擦係数変化を示すグラフである。FIG. 1 is a graph showing a change in friction coefficient with temperature.
【図2】高速での摩擦係数変化を示すグラフである。FIG. 2 is a graph showing a change in friction coefficient at a high speed.
Claims (4)
硬化性樹脂の結合材で固着した熱硬化性樹脂含有摩擦材
において、前記結合材に、フロー距離とゲルタイムの短
い熱硬化性樹脂Aとこの熱硬化性樹脂Aよりもフロー距
離、ゲルタイムが共に長い熱硬化性樹脂Bの2種類の熱
硬化性樹脂を用いたことを特徴とする熱硬化性樹脂含有
摩擦材。1. A thermosetting resin-containing friction material in which a friction modifier containing a filler and a reinforcing material are fixed with a thermosetting resin binder, wherein the binder has a short flow distance and a short gel time. A thermosetting resin-containing friction material comprising two types of thermosetting resins, a resin A and a thermosetting resin B having a longer flow distance and a longer gel time than the thermosetting resin A.
0mm,ゲルタイムが10〜20秒であり、熱硬化性樹
脂Bのフロー距離が30〜40mm,ゲルタイムが60
〜80秒であることを特徴とする請求項1記載の熱硬化
性樹脂含有摩擦材2. The flow distance of the thermosetting resin A is 10 to 2
0 mm, the gel time is 10 to 20 seconds, the flow distance of the thermosetting resin B is 30 to 40 mm, and the gel time is 60.
2. A friction material containing a thermosetting resin according to claim 1, wherein the friction material has a duration of from 80 to 80 seconds.
あり、熱硬化性樹脂Bの融点が71〜100℃であるこ
とを特徴とする請求項1または2記載の熱硬化性樹脂含
有摩擦材。3. The thermosetting resin according to claim 1, wherein the melting point of the thermosetting resin A is 40 to 70 ° C., and the melting point of the thermosetting resin B is 71 to 100 ° C. Contains friction material.
が容量比で1:3〜3:1であることを特徴とする請求
項1、2または3記載の熱硬化性樹脂含有摩擦材。4. The thermosetting resin-containing composition according to claim 1, wherein the ratio of the thermosetting resin A to the thermosetting resin B is 1: 3 to 3: 1 in terms of volume ratio. Friction material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3168870A JP2831491B2 (en) | 1991-06-13 | 1991-06-13 | Friction material containing thermosetting resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3168870A JP2831491B2 (en) | 1991-06-13 | 1991-06-13 | Friction material containing thermosetting resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04366195A JPH04366195A (en) | 1992-12-18 |
JP2831491B2 true JP2831491B2 (en) | 1998-12-02 |
Family
ID=15876094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3168870A Expired - Fee Related JP2831491B2 (en) | 1991-06-13 | 1991-06-13 | Friction material containing thermosetting resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2831491B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003082331A (en) * | 2001-07-02 | 2003-03-19 | Nisshinbo Ind Inc | Non-asbestos friction lining |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61256030A (en) * | 1985-05-10 | 1986-11-13 | Toshiba Tungaloy Co Ltd | Wet friction member |
-
1991
- 1991-06-13 JP JP3168870A patent/JP2831491B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH04366195A (en) | 1992-12-18 |
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