JPH10158631A - Friction material - Google Patents
Friction materialInfo
- Publication number
- JPH10158631A JPH10158631A JP31783496A JP31783496A JPH10158631A JP H10158631 A JPH10158631 A JP H10158631A JP 31783496 A JP31783496 A JP 31783496A JP 31783496 A JP31783496 A JP 31783496A JP H10158631 A JPH10158631 A JP H10158631A
- Authority
- JP
- Japan
- Prior art keywords
- magnesium hydroxide
- friction material
- thermosetting resin
- friction
- powder
- 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.)
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- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は摩擦材に係り、特
に、自動車や各種産業用機械のディスクパッドやブレー
キライニング等に使用される摩擦材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a friction material, and more particularly to a friction material used for a disk pad or a brake lining of an automobile or various industrial machines.
【0002】[0002]
【従来の技術】近年、自動車や各種産業用機械のディス
クパッドやブレーキライニング等に使用される摩擦材と
して、アスベストを含有しないノンアスベスト系摩擦材
の開発が進められ、多くの提案がなされている。2. Description of the Related Art In recent years, non-asbestos-based friction materials which do not contain asbestos have been developed as friction materials used for disk pads and brake linings of automobiles and various industrial machines, and many proposals have been made. .
【0003】例えば、特開平6−228327号公報に
は、アスベスト以外の補強繊維と、フェノール樹脂等の
熱硬化性樹脂と、黒鉛、硫酸バリウム等の充填材とを含
有する摩擦材において、補強繊維の一部として水酸化マ
グネシウム繊維を摩擦材全量に対して50体積%以下含
有させることで、熱履歴後の強度を上げ亀裂発生を防止
した摩擦材が提案されている。For example, Japanese Patent Application Laid-Open No. 6-228327 discloses a friction material containing a reinforcing fiber other than asbestos, a thermosetting resin such as a phenol resin, and a filler such as graphite and barium sulfate. There has been proposed a friction material in which magnesium hydroxide fibers are contained in an amount of 50% by volume or less based on the total amount of the friction material, thereby increasing the strength after heat history and preventing the occurrence of cracks.
【0004】この種の摩擦材は、一般に、外気温から4
00℃以上の高温までの温度範囲で使用されるが、使用
温度が250℃以上となると、摩擦材を構成するフェノ
ール樹脂等の熱硬化性樹脂が熱分解して摩擦材の摩擦特
性を低下させる。[0004] This kind of friction material generally has a temperature
It is used in a temperature range up to a high temperature of 00 ° C. or higher. However, when the operating temperature is 250 ° C. or higher, a thermosetting resin such as a phenol resin constituting the friction material is thermally decomposed and lowers the friction characteristics of the friction material. .
【0005】これに対して、水酸化マグネシウムは36
0℃付近で吸熱分解するため、水酸化マグネシウムを摩
擦材に配合すると、ブレーキ等によって発生した熱の一
部を吸熱し、摺動面の温度を下げ、熱硬化性樹脂の熱分
解による摩擦特性の低下を防止することができる。On the other hand, magnesium hydroxide is 36
When magnesium hydroxide is added to the friction material because it undergoes endothermic decomposition at around 0 ° C, it absorbs part of the heat generated by the brakes, etc., lowering the temperature of the sliding surface, and the frictional characteristics due to the thermal decomposition of the thermosetting resin Can be prevented from decreasing.
【0006】なお、摩擦材は一般に130〜250℃で
成形硬化されて製造されるが、水酸化マグネシウムはこ
の温度では分解されず、熱硬化性樹脂が急激に熱分解す
る350℃以上で吸熱作用を発揮する。このような吸熱
作用を示すものとして、水酸化マグネシウムの他に水酸
化アルミニウムがあるが、水酸化アルミニウムは分解温
度が200℃程度であるため成形時に分解してしまい、
350℃以上での熱硬化性樹脂の熱分解防止効果は得ら
れない。[0006] The friction material is generally produced by molding and curing at 130 to 250 ° C. However, magnesium hydroxide is not decomposed at this temperature, and the endothermic effect at 350 ° C or higher at which the thermosetting resin is rapidly thermally decomposed. Demonstrate. Aluminum hydroxide other than magnesium hydroxide exhibits such an endothermic effect. However, aluminum hydroxide is decomposed at the time of molding because its decomposition temperature is about 200 ° C.
The effect of preventing thermal decomposition of the thermosetting resin at 350 ° C. or higher cannot be obtained.
【0007】[0007]
【発明が解決しようとする課題】上述の如く、水酸化マ
グネシウムは、摩擦材が高温で使用された際に、摩擦材
の熱硬化性樹脂の熱分解を防止して、摩擦特性を安定さ
せる効果を奏するものであり、その効果は、水酸化マグ
ネシウムの配合量が多い程高いものとなる。特に、水酸
化マグネシウムを摩擦材全量に対して50体積%以上添
加することにより、優れた効果が得られる。As described above, magnesium hydroxide has an effect of preventing thermal decomposition of a thermosetting resin of a friction material and stabilizing friction characteristics when the friction material is used at a high temperature. The effect increases as the amount of magnesium hydroxide increases. In particular, excellent effects can be obtained by adding 50% by volume or more of magnesium hydroxide to the total amount of the friction material.
【0008】しかしながら、特開平6−228327号
公報記載の摩擦材で用いる水酸化マグネシウムは、繊維
形状であるため、摩擦材全量に対して50体積%以上添
加した場合には、成形原料が非常に嵩高くなる。そし
て、このような成形原料を成形すると、成形時の成形体
のスプリングバックが大きいために、成形時に亀裂が発
生し易い。However, since magnesium hydroxide used in the friction material described in JP-A-6-228327 is in the form of a fiber, if it is added in an amount of 50% by volume or more with respect to the total amount of the friction material, the raw material for molding is extremely low. Become bulky. When such a molding material is molded, cracks are likely to occur during molding due to a large springback of the molded body during molding.
【0009】このようなことから、特開平6−2283
27号公報記載の摩擦材では、水酸化マグネシウム繊維
を多量に配合することができず、このため、水酸化マグ
ネシウムによる摩擦特性の安定化効果を十分に得ること
はできないという欠点があった。For these reasons, Japanese Patent Application Laid-Open No. 6-2283 is disclosed.
In the friction material described in Japanese Patent No. 27, magnesium hydroxide fibers cannot be blended in a large amount, and therefore, there has been a drawback that the effect of stabilizing the friction characteristics by magnesium hydroxide cannot be sufficiently obtained.
【0010】本発明は上記従来の問題点を解決し、水酸
化マグネシウムの多量配合が可能で、高温での摩擦特性
が良好な摩擦材を提供することを目的とする。An object of the present invention is to solve the above-mentioned conventional problems, and to provide a friction material which can contain a large amount of magnesium hydroxide and has good friction characteristics at high temperatures.
【0011】[0011]
【課題を解決するための手段】本発明の摩擦材は、熱硬
化性樹脂との親和性を高める表面処理を施した非繊維状
水酸化マグネシウム粉体を5〜75体積%含む熱硬化性
樹脂よりなることを特徴とする。SUMMARY OF THE INVENTION A friction material according to the present invention comprises a thermosetting resin containing 5 to 75% by volume of a non-fibrous magnesium hydroxide powder which has been subjected to a surface treatment for enhancing affinity with the thermosetting resin. It is characterized by comprising.
【0012】本発明の摩擦材では、水酸化マグネシウム
として、非繊維状の水酸化マグネシウム粉体を配合する
ため、水酸化マグネシウム繊維を用いる場合のように、
成形原料が過度に嵩高くなることはなく、このため、水
酸化マグネシウムを摩擦材全量に対して多量に配合して
も成形時に亀裂を生じることなく、良好な摩擦材を製造
することができる。しかも、水酸化マグネシウム粉体は
熱硬化性樹脂との親和性を高める表面処理を施してある
ため、熱硬化性樹脂とのなじみが良く、多量に配合して
も摩擦材から剥落したり亀裂が発生したりすることもな
い。In the friction material of the present invention, since non-fibrous magnesium hydroxide powder is blended as magnesium hydroxide, as in the case of using magnesium hydroxide fiber,
The molding raw material does not become excessively bulky. Therefore, even when magnesium hydroxide is blended in a large amount with respect to the total amount of the friction material, a good friction material can be produced without cracking during molding. In addition, the magnesium hydroxide powder has been subjected to a surface treatment that enhances the affinity with the thermosetting resin, so it is well compatible with the thermosetting resin. It does not occur.
【0013】従って、高温での摩擦特性の安定化に有効
な水酸化マグネシウムを多量に配合して高温での摩擦特
性が良好な摩擦材とすることができる。Accordingly, a large amount of magnesium hydroxide, which is effective for stabilizing the friction characteristics at a high temperature, can be blended to provide a friction material having good friction characteristics at a high temperature.
【0014】本発明においては、特に、摩擦調整材とし
て三酸化アンチモン及び/又は三硫化アンチモンを10
体積%以下含有させることにより、摩擦特性をさらに安
定させることができ、また、摩擦材の摩耗を低減するこ
とができる。In the present invention, in particular, antimony trioxide and / or antimony trisulfide is used as a friction modifier in an amount of 10%.
By containing the content by volume% or less, the friction characteristics can be further stabilized, and the wear of the friction material can be reduced.
【0015】[0015]
【発明の実施の形態】以下に本発明の実施の形態を説明
する。Embodiments of the present invention will be described below.
【0016】本発明の摩擦材の結合剤となる熱硬化性樹
脂としては、フェノール樹脂、尿素樹脂、メラミン樹脂
又はこれらの変性樹脂が挙げられるが、特にフェノール
樹脂が好適である。The thermosetting resin serving as a binder for the friction material of the present invention includes a phenol resin, a urea resin, a melamine resin and modified resins thereof, and a phenol resin is particularly preferable.
【0017】本発明で用いる非繊維状の水酸化マグネシ
ウム粉体は、アスペクト比3以下、粒径0.1〜1.0
μm程度の粉体が好ましい。The non-fibrous magnesium hydroxide powder used in the present invention has an aspect ratio of 3 or less and a particle size of 0.1 to 1.0.
A powder of about μm is preferred.
【0018】本発明において、このような水酸化マグネ
シウム粉体に対して、熱硬化性樹脂との親和性を高める
ための表面処理、例えば、ステアリン酸塩等の表面処理
剤による処理、シランカップラー等のカップリング剤に
よる処理を施して熱硬化性樹脂に配合する。表面処理剤
で処理する場合、水酸化マグネシウム粉体に対してこれ
らの表面処理剤を1〜10重量%程度付着させて処理す
る。また、カップリング剤で処理する場合、水酸化マグ
ネシウム粉体に対してこれらのカップリング剤を0.1
〜5重量%程度付着させる。このような表面処理を施す
ことにより、水酸化マグネシウム粉体とフェノール樹脂
等の熱硬化性樹脂との混合及び均一分散性が向上し、製
造時や使用時の亀裂等を防止することができる。In the present invention, such a magnesium hydroxide powder is subjected to a surface treatment for enhancing the affinity with a thermosetting resin, for example, a treatment with a surface treating agent such as a stearate, a silane coupler or the like. And then blended with the thermosetting resin. In the case of treating with a surface treating agent, the surface treating agent is attached to the magnesium hydroxide powder in an amount of about 1 to 10% by weight. When treating with a coupling agent, the coupling agent is added to the magnesium hydroxide powder in an amount of 0.1%.
About 5% by weight. By performing such a surface treatment, mixing and uniform dispersibility of the magnesium hydroxide powder and a thermosetting resin such as a phenol resin are improved, and cracks or the like during production or use can be prevented.
【0019】本発明においては、このような表面処理を
施した非繊維状の水酸化マグネシウム粉体を5〜75体
積%配合する。前述の如く、この配合量は多い程、高温
での摩擦特性が安定するが、75体積%を超えて配合す
ると相対的に熱硬化性樹脂量が少なくなり、結合強度が
低下して成形時に亀裂が発生し易くなる。好ましい水酸
化マグネシウム粉体の配合量は50〜75体積%であ
る。In the present invention, the non-fibrous magnesium hydroxide powder subjected to such a surface treatment is blended in an amount of 5 to 75% by volume. As described above, the higher the blending amount, the more stable the friction characteristics at high temperatures. However, if the blending amount exceeds 75% by volume, the amount of the thermosetting resin relatively decreases, the bonding strength decreases, and cracks occur during molding. Is more likely to occur. The preferred amount of the magnesium hydroxide powder is 50 to 75% by volume.
【0020】本発明の摩擦材では、更に、摩擦調整材と
して、三酸化アンチモン及び/又は三硫化アンチモンを
含有させることでより一層高温での摩擦特性を安定化さ
せると共に耐摩耗性を高め、摩擦材の摩耗を防止するこ
とができる。三酸化アンチモン及び/又は三硫化アンチ
モンの含有量は過度に多いと、相対的に他の材料の配合
量が少なくなり摩擦材としての特性を損なうことから、
三酸化アンチモン及び/又は三硫化アンチモンの含有量
は摩擦材の10体積%以下、特に5〜8体積%であるこ
とが好ましい。The friction material of the present invention further contains antimony trioxide and / or antimony trisulfide as a friction adjusting material to further stabilize the friction characteristics at a high temperature and enhance the abrasion resistance. The wear of the material can be prevented. If the content of antimony trioxide and / or antimony trisulfide is excessively large, the compounding amount of other materials is relatively reduced and the properties as a friction material are impaired.
The content of antimony trioxide and / or antimony trisulfide is preferably 10% by volume or less, more preferably 5 to 8% by volume of the friction material.
【0021】本発明の摩擦材は、その他の成分として、
アスベスト以外の補強繊維、例えば、アラミド繊維等の
有機繊維、ガラス繊維、ロックウール、セラミックス繊
維、チタン酸カリウム繊維等の無機繊維、鉄、銅、青
銅、アルミニウム、黄銅等の金属繊維等の1種又は2種
以上;充填材、例えば、黒鉛、硫酸バリウム、二硫化モ
リブデン、カシューダスト、金属粉、アルミナ等のセラ
ミックス粉、炭酸カルシウム、ケイ酸ジルコニウム等の
1種又は2種以上等を含有していても良い。The friction material of the present invention comprises, as other components,
One kind of reinforcing fibers other than asbestos, for example, organic fibers such as aramid fibers, glass fibers, rock wool, ceramic fibers, inorganic fibers such as potassium titanate fibers, and metal fibers such as iron, copper, bronze, aluminum, and brass. Or two or more kinds; fillers, for example, one or more kinds of ceramic powders such as graphite, barium sulfate, molybdenum disulfide, cashew dust, metal powder, alumina, calcium carbonate, zirconium silicate, etc. May be.
【0022】本発明の摩擦材の好ましい配合割合は次の
通りである。 熱硬化性樹脂:8〜20体積% 非繊維状水酸化マグネシウム粉体:50〜75体積% 補強繊維:2〜25体積% 充填材:8〜30体積% 摩擦調整材(三酸化アンチモン及び/又は三硫化アンチ
モン):3〜10体積% なお、補強繊維としては、繊維径3〜300μm,繊維
長さ0.1〜5mmのものが好適である。また、充填材
としては粒径0.5〜500μm程度のものが好適であ
る。The preferred compounding ratio of the friction material of the present invention is as follows. Thermosetting resin: 8 to 20% by volume Non-fibrous magnesium hydroxide powder: 50 to 75% by volume Reinforcing fiber: 2 to 25% by volume Filler: 8 to 30% by volume Friction modifier (antimony trioxide and / or Antimony trisulfide): 3 to 10% by volume The reinforcing fibers preferably have a fiber diameter of 3 to 300 μm and a fiber length of 0.1 to 5 mm. Further, a filler having a particle size of about 0.5 to 500 μm is suitable.
【0023】本発明の摩擦材は、熱硬化性樹脂、非繊維
状水酸化マグネシウム粉体、その他、補強繊維、充填
材、摩擦調整材等を所定割合で混合し、混合材料を熱硬
化性樹脂の硬化温度、例えば熱硬化性樹脂としてフェノ
ール樹脂を用いたものであれば130〜180℃,50
〜600kg/cm2 で3〜15分間加熱加圧成形した
後、150〜200℃で3〜15時間熱処理することに
より製造することができる。The friction material of the present invention is obtained by mixing a thermosetting resin, a non-fibrous magnesium hydroxide powder, other reinforcing fibers, a filler, a friction modifier and the like at a predetermined ratio, and mixing the mixed material with the thermosetting resin. Curing temperature, for example, 130 to 180 ° C., 50 if a phenol resin is used as the thermosetting resin.
It can be manufactured by heat-press molding at 600600 kg / cm 2 for 3 to 15 minutes, followed by heat treatment at 150 to 200 ° C. for 3 to 15 hours.
【0024】[0024]
【実施例】以下に実施例及び比較例を挙げて本発明をよ
り具体的に説明するが、本発明はその要旨を超えない限
り、以下の実施例に限定されるものではない。The present invention will be described more specifically with reference to examples and comparative examples, but the present invention is not limited to the following examples unless it exceeds the gist.
【0025】なお、下記の実施例及び比較例で用いた材
料の仕様は次の通りである。The specifications of the materials used in the following Examples and Comparative Examples are as follows.
【0026】非繊維状水酸化マグネシウム粉体(表面処
理品):アスペクト比1〜3、平均粒径1μmの水酸化
マグネシウム粉体を、ステアリン酸ナトリウム5重量%
で表面処理したもの。 非繊維状水酸化マグネシウム粉体(非表面処理品):上
記表面処理品と同様のアスペクト比及び平均粒径で表面
処理を施していないもの。 水酸化マグネシウム繊維:繊維径0.1〜5μm、繊維
長さ10〜50μmの水酸化マグネシウム繊維。 熱硬化性樹脂:フェノール樹脂 銅繊維:平均繊維径60μm、平均繊維長さ3mm。Non-fibrous magnesium hydroxide powder (surface-treated product): Magnesium hydroxide powder having an aspect ratio of 1 to 3 and an average particle diameter of 1 μm was added to sodium stearate at 5% by weight.
Surface treated with. Non-fibrous magnesium hydroxide powder (non-surface-treated product): a powder having the same aspect ratio and average particle size as the above-mentioned surface-treated product but not subjected to surface treatment. Magnesium hydroxide fiber: Magnesium hydroxide fiber having a fiber diameter of 0.1 to 5 μm and a fiber length of 10 to 50 μm. Thermosetting resin: phenolic resin Copper fiber: average fiber diameter 60 μm, average fiber length 3 mm.
【0027】アラミド繊維:平均繊維径12μm、平均
繊維長さ6mmのフィブリル状 黒鉛:平均粒径150μm アルミナ:平均粒径5μm カシューダスト:平均粒径150μm 三硫化アンチモン:平均粒径50μm 三酸化アンチモン:平均粒径1μm 実施例1〜8、比較例1〜4 表1に示す配合で乾式混合機により材料を均一に分散、
混合し、混合材料を温度150℃,圧力400kg/c
m2 で10分間加熱加圧成形した後、温度210℃の熱
風乾燥機で10時間熱処理して、長さ150mm、幅5
0mm,厚さ15μmの摩擦材を製造した。Aramid fiber: Fibrillar graphite having an average fiber diameter of 12 μm and an average fiber length of 6 mm: Average particle diameter of 150 μm Alumina: Average particle diameter of 5 μm Cashew dust: Average particle diameter of 150 μm Antimony trisulfide: Average particle diameter of 50 μm Antimony trioxide: Average particle size 1 μm Examples 1 to 8 and Comparative Examples 1 to 4 Materials were uniformly dispersed by a dry mixer with the composition shown in Table 1,
Mix and mix the material at a temperature of 150 ° C and a pressure of 400 kg / c
After heating pressure forming for 10 minutes m 2, and the heat-treated at a temperature 210 ° C. in a hot-air dryer for 10 hours, the length 150 mm, width 5
A friction material having a thickness of 0 mm and a thickness of 15 μm was manufactured.
【0028】得られた摩擦材についてダイナモ試験機に
より下記条件で摩擦試験を行った。 制動初速度:100km/hr 終速度:50km/hr 制動減速度:0.4G 制動前ブレーキ温度:350℃ 成形時及び熱処理時の亀裂発生の有無及び摩擦試験結果
を表1に示す。表1より、本発明の摩擦材は、多量の水
酸化マグネシウムを配合しても亀裂発生の問題はなく、
高温での摩擦特性が良好であることがわかる。The obtained friction material was subjected to a friction test using a dynamo tester under the following conditions. Initial braking speed: 100 km / hr Final speed: 50 km / hr Braking deceleration: 0.4 G Brake temperature before braking: 350 ° C. Table 1 shows the presence or absence of cracks during molding and heat treatment, and the friction test results. From Table 1, the friction material of the present invention has no problem of crack generation even if a large amount of magnesium hydroxide is blended.
It can be seen that the friction characteristics at high temperatures are good.
【0029】[0029]
【表1】 [Table 1]
【0030】[0030]
【発明の効果】以上詳述した通り、本発明の摩擦材によ
れば、高温での摩擦特性が極めて良好な摩擦材が提供さ
れる。As described above in detail, according to the friction material of the present invention, a friction material having extremely good friction characteristics at high temperatures is provided.
Claims (2)
理を施した非繊維状水酸化マグネシウム粉体を5〜75
体積%含む熱硬化性樹脂よりなることを特徴とする摩擦
材。1. A non-fibrous magnesium hydroxide powder which has been subjected to a surface treatment for enhancing the affinity with a thermosetting resin is provided in an amount of 5 to 75%.
A friction material comprising a thermosetting resin containing about 30% by volume.
化アンチモン及び/又は三硫化アンチモンを10体積%
以下含有することを特徴とする摩擦材。2. The thermosetting resin according to claim 1, wherein the thermosetting resin contains 10% by volume of antimony trioxide and / or antimony trisulfide.
A friction material comprising:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31783496A JPH10158631A (en) | 1996-11-28 | 1996-11-28 | Friction material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31783496A JPH10158631A (en) | 1996-11-28 | 1996-11-28 | Friction material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH10158631A true JPH10158631A (en) | 1998-06-16 |
Family
ID=18092576
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31783496A Withdrawn JPH10158631A (en) | 1996-11-28 | 1996-11-28 | Friction material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH10158631A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009221400A (en) * | 2008-03-18 | 2009-10-01 | Advics Co Ltd | Friction material |
JP2017008167A (en) * | 2015-06-19 | 2017-01-12 | 株式会社アドヴィックス | Non-asbestos friction material |
JP2017141352A (en) * | 2016-02-10 | 2017-08-17 | 日立化成株式会社 | Friction material composition, friction material and friction member using the friction material composition |
-
1996
- 1996-11-28 JP JP31783496A patent/JPH10158631A/en not_active Withdrawn
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009221400A (en) * | 2008-03-18 | 2009-10-01 | Advics Co Ltd | Friction material |
JP2017008167A (en) * | 2015-06-19 | 2017-01-12 | 株式会社アドヴィックス | Non-asbestos friction material |
JP2017141352A (en) * | 2016-02-10 | 2017-08-17 | 日立化成株式会社 | Friction material composition, friction material and friction member using the friction material composition |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A300 | Withdrawal of application because of no request for examination |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 20040203 |